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        <title><![CDATA[Quality Engineer]]></title>
        <description><![CDATA[


Job Title :Quality Engineer
Job Code :4129
Location :WHEELING IL US 60090
Job Description :
Accellent, Inc. is a fully integrated provider of design, supply chain management and strategic sourcing services to the Medical Device industry. Accellentwww.accellent.com, a recognized market leader, is a fast-growing outsource manufacturing and design solution company specializing in high growth areas such as Cardiology, Endoscopy and Orthopaedics. The top Medical Device companies partner with Accellent to provide innovation, advanced technology, speed to market, low cost labor and strategic sourcing.
We&rsquo;re looking for team players with a can-do attitude to share in our vision and corporate values. Accellent offers competitive salaries; a comprehensive benefits package, and a stimulating work environment.
Currently, we are searching for a Quality Engineer (New Process Development) to join our Wheeling, IL facility.

Quality assists in the design and implementation of policies and procedures for testing and evaluating the precision and accuracy of products and/or equipment. The Quality Engineer will be expected to provide support to Operations, interact with customers and provide support for Engineering, Quality Systems and Process engineering. Specializations may include but are not limited to: design control; material and process control; product reliability; software quality engineering; and/or metrology.
This position will be integral in meeting the Quality Management System requirements. It requires creativity and foresight to work with operations and product development teams to ensure compliance to the Quality Manual, Design Control, Supplier Management and other appropriate procedures for a variety of medical devices from concept through market introduction. The ideal candidate is a self-motivated individual who is excited by the prospect of working in a dynamic, fast-paced environment.
Job Requirements :
Qualifications
1.   2+ years experience in the Medical Device or other regulated industry, such as QSR and ISO 13485, with increasing responsibility.
2.   2+ years prior experience in Quality New Product Development role required, as well as prior demonstrated project management experience needed
3.   Experience with FDA and ISO 13485 Certification inspections is a plus.
4.   Must be adept in use of computer software for the analysis of data, preferably Microsoft Excel and statistical packages (Minitab preferred). 
5.   Quality Engineering certification (CQE) preferred or equivalent body of knowledge in areas which include but are not limited to Statistics, SPC, Geometric Dimensioning &amp; Tolerancing; Sampling, Design of Experiments, etc. Ability to analyze, understand and effectively communicate this technical material. Experience with Lean Manufacturing and Six Sigma is a plus.
6.   Ability to organize and judge priorities in a dynamic, fast-paced environment and work independently with minimal supervision.
7.   Must possess excellent verbal &amp; written communication skills, which include but are not limited to presentation, organizational and management skills.
Career Level :Experienced (Non-Manager)
Education :Bachelor's Degree
% of Travel Required :0-10%
Shift/Hours :First Shift (Day)
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        <expiration_date>2010-03-25</expiration_date>
        <employer><![CDATA[Accellent Inc.]]></employer>
        <location><![CDATA[WHEELING, IL, 60070, USA]]></location>
    </job>
    <job>
        <title><![CDATA[Warehouseman]]></title>
        <description><![CDATA[


Job Title :Warehouseman
Job Code :4167
Location :Juarez Chih MX 32470
Job Description :
Position Scope/Summary
&middot;    Participates in inventory duties
Key Result Accountabilities
* Performs maintenance to forklift before and after use.
* Prepares production Kits as required.
* Give support to production group (extra).
* Maintains the random location inventory system.
&middot;    Receive &amp; locate raw materials.
Environmental Working Conditions  
&middot;    Maintain order &amp; cleanliness in warehouse.
Qualifications
&middot;    Basicknowledge of computeruse
&middot;    Ability to use a calculator
&middot;    1-3 years experience as warehouseman preferred.   
&middot;    Forklift operator certification and licensed.
Job Requirements :
N/a
Career Level :Experienced (Non-Manager)
Education :High School or equivalent
% of Travel Required :None
Shift/Hours :First Shift (Day)
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        <expiration_date>2010-03-25</expiration_date>
        <employer><![CDATA[Accellent Inc.]]></employer>
        <location><![CDATA[, USA]]></location>
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    <job>
        <title><![CDATA[Laser Operator - Days]]></title>
        <description><![CDATA[


Job Title :Laser Operator - Days
Job Code :4181
Location :Brooklyn Park MN US 55429
Job Description :
Accellent, Inc. is a fully integrated provider of design, supply chain management and strategic sourcing services to the Medical Device industry. Accellentwww.accellent.com, a recognized market leader, is a fast-growing outsource manufacturing and design solution company specializing in high growth areas such as Cardiology, Endoscopy and Orthopaedics. The top Medical Device companies partner with Accellent to provide innovation, advanced technology, speed to market, low cost labor and strategic sourcing.
We&rsquo;re looking for team players with a can-do attitude to share in our vision and corporate values. Accellent offers competitive salaries; a comprehensive benefits package, and a stimulating work environment.
Currently, we are searching for a Laser Operator to join our Brooklyn Park facility.
Job Requirements :
Setup, troubleshoot, operate, and perform maintenance (when required) to machines
Include the following: (other duties may be assigned)
Responsible for keeping the machines running, performing daily maintenance, and keeping the area around the machines clean
Operate the machine as efficiently as possible
Produce high quality components to print specifications
Read part prints and understand dimensions
Use and understand how inspection equipment works - making sure it is correct and calibrated
Do whatever is needed to insure quality - including sorting for features that are uncontrollable
Maintain correct lot control numbers of components and assemblies
Communicate with opposite shift operator to insure smooth transition between shifts
Follow company policies and rules
Provide support within the organization as experience and time allow
 Key Result Accountabilities
Supervisory Responsibilities:
Needs to work in an atmosphere with little supervision.
Work with management staff to ensure high customer quality and schedule deadlines and requirements are met.
Language Skills:
Must be able to communicate with facility personnel.
Reasoning Ability:
The ability to complete projects and problem solve independently.
Mathematical Skills:
Must have basic math skills

 Environmental Working Conditions
 Reasonable accommodations may be made to enable individuals with disabilities to perform the essential      

 Qualifications
 High school diploma or equivalent is preferred
Career Level :Experienced (Non-Manager)
Education :High School or equivalent
% of Travel Required :None
Shift/Hours :First Shift (Day)
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            <industry><![CDATA[Health Products & Services]]></industry>
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        <expiration_date>2010-03-25</expiration_date>
        <employer><![CDATA[Accellent Inc.]]></employer>
        <location><![CDATA[Brooklyn Park, MN, 55445, USA]]></location>
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    <job>
        <title><![CDATA[Maintenance Manager]]></title>
        <description><![CDATA[


Job Title :Maintenance Manager
Job Code :4099
Location :Arvada CO US 80002
Job Description :
JOB PURPOSE: Direct and manage resources to provide, maintain, and improve manufacturing equipment and facilities to achieve safety, quality, production, productivity, lean manufacturing goals and 5S goals.
RESPONSIBILITIES:
1. Supervise and direct maintenance personnel in achieving company goals for improvement projects.
2. Perform trouble shooting in both electrical and mechanical issues on grinding, straightening and wire coiling equipment as well as secondary equipment. Schedule and perform PMs, as well as PLC and other types of specialty repairs.
3. Develop and enhance preventive maintenance program.
4. Lead strategic planning directed at raising the level of maintenance performance with an emphasis on continuous improvement for technicians skill level
5. Communicate with outside vendors in locating and ordering parts for plant equipment and buildings.
6. Interface with other departments in selecting appropriate procedures and timing for equipment repair.
7. Provide and maintain a cost effective spare parts inventory for production equipment and facilities.
8. Establish and maintain an effective Maintenance Management system
9. Maintain maintenance shop and spare parts inventory area in accordance with lean manufacturing and the 5S philosophy.
10. Organize and establish effective preventative maintenance schedules for equipment and buildings with a goal of 100% up time.
11. Manage environmental quality standards to meet local, state and federal regulations achieving best industrial practices.
12. Must have the ability to use Microsoft Office Suite and learn and apply other software applications as required.
13. Must have a demonstrated knowledge of electrical and mechanical systems
14. Must have the ability to troubleshoot and develop preventative plans.
15. Identify and resolve recurring downtime or inefficient operational issues
16. Evaluate cost saving opportunities and improvements for equipment to increase longevity and reliability
17. Manage maintenance budget
18. Develop and maintain strong internal and external working relationships with team members, vendors and customers
Job Requirements :
QUALIFICATIONS: Minimum five years maintenance supervisory and/or management experience in a manufacturing facility. A degree in Industrial Manufacturing, Engineering or related discipline preferred. Prior experience in a medical device manufacturing environment desired. Prior maintenance experience in building and HVAC a plus. Knowledge of safety and environmental regulatory standards strongly preferred.
Career Level :Manager (Manager/Supervisor of Staff)
Education :High School or equivalent
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            <industry><![CDATA[Health Products & Services]]></industry>
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        <expiration_date>2010-03-25</expiration_date>
        <employer><![CDATA[Accellent Inc.]]></employer>
        <location><![CDATA[Arvada, CO, 80005, USA]]></location>
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    <job>
        <title><![CDATA[Sr. Manufacturing Engineer]]></title>
        <description><![CDATA[


Job Title :Sr. Manufacturing Engineer
Job Code :4096
Location :Brooklyn Park MN US 55429
Job Description :
Accellent, Inc. is a fully integrated provider of design, supply chain management and strategic sourcing services to the Medical Device industry. Accellentwww.accellent.com, a recognized market leader, is a fast-growing outsource manufacturing and design solution company specializing in high growth areas such as Cardiology, Endoscopy and Orthopedics. The top Medical Device companies partner with Accellent to provide innovation, advanced technology, speed to market, low cost labor and strategic sourcing. 
We&rsquo;re looking for team players with a can-do attitude to share in our vision and corporate values. Accellent offers competitive salaries; a comprehensive benefits package, and a stimulating work environment. 
Currently, we are searching for a Sr. Manufacturing Engineer to join our Brooklyn Park, MN facility.
About the Opportunity:
Job Requirements :


Position Scope/Summary
Directs, coordinates, and exercises functional authority for planning, organization, control, integration, and completion of engineering activities within the Injection Molding function.
Key Results &amp; Accountabilities
Follows and develops Quality and Regulatory requirements including Accellent policies, procedures, and
appropriate regulatory requirements.
Plans, Develops, and Executes Process and Test Method Validations (IQ, OQ, PQ, PPQ) in accordance
with Accellent procedures and guidelines.
Communicates ideas, information, and recommendations clearly, effectively and frequently (oral and written)
within Accellent, with outside suppliers or partners and with Accellent customers during formal and informal
interactions.
Prepares or reviews documentation with a high degree of accuracy, completeness, and effectiveness using
common Accellent engineering tools &amp; templates were available. (Examples include specifications,
manufacturing procedures, ECOs, and technical reports or analysis)
Applies and Promotes Lean manufacturing techniques to continuously improve cycle times and process
flows. Identifies, supports, or directs the execution of improvement efforts to reduce waste in all
manufacturing and business processes.
Uses structured problem solving techniques and statistical methods for data driven analysis and decisions.
Applies and leads DMAIC &ndash; Six Sigma approaches to solve issues and reduce variation in all manufacturing
and business processes.
Plans, executes and manages project activities with cross functional teams. Project types can include new
product development and introduction, manufacturing transfers, continuous improvement and cost reduction
initiatives.
Exhibits the Accellent values (Customer focus, Continuous Improvement, Performance, Accountability,
Teamwork and Integrity) in all activities. 
Demonstrates leadership through mentoring of junior staff, responsiveness to business needs and motivation
of diverse, cross functional teams including influencing both internal and external members to achieve
positive business results
Demonstrates technical ability through the application of engineering skills, approaches and knowledge.
Takes financial responsibility for activities to create positive impact to the business
Performs all duties and directs others creating a safe working environment for our employees and our
communities.
Performs other duties as necessary. 
Qualifications
Bachelor of Science in Engineering/technical field and a minimum of 5 years experience (1+ years in the
medical device industry). Post graduate work will be taken into account.
Experience with implantable medical molding assemblies and micro molding applications in a clean room
environment.
Background in molding process development on horizontal and vertical press equipment. 
To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. 
The requirements listed here and in the Engineering Career Matrix are representative of the knowledge,
skill, and/or abilities required. Reasonable accommodations may be made to enable individuals with
disabilities to perform the essential functions.
 In addition, the individual must have a working knowledge of ISO and applicable customer and regulatory
 standards.

Environmental Working Conditions
The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
While performing the duties of this job, the employee is frequently exposed to moving mechanical parts. The employee is occasionally exposed to high, precarious places; fumes or airborne particles; toxic or caustic chemicals; risk of electrical shock; and vibration. The noise level in the work environment is usually moderate.
Qualifications 


It is impossible to list every requirement for, or responsibility of, any position. Similarly we cannot identify all the skills a position may require since job responsibilities and the Company&rsquo;s needs may change over time. Therefore, the above job description is not comprehensive or exhaustive. The Company reserves the right to adjust, add to or eliminate any aspect of the above description. The Company also retains the right to require all employees to undertake additional or different job responsibilities when necessary to meet business needs. Employee Signature


Due to the expected number of responses, only those most qualified will be contacted. No recruiters please; all unsolicited third-party submissions will be rejected.

Accellent is an Equal Opportunity/Affirmative Action employer and we value diversity in our workforce. As such we provide equal opportunity for all applicants without regard to race, religion, gender, national origin, age, marital status, veteran status, or disability. To learn more about Accellent and our career opportunities, please visit us atwww.accellent.com

Career Level :Experienced (Non-Manager)
Education :Bachelor's Degree
% of Travel Required :0-10%
Shift/Hours :First Shift (Day)
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        <expiration_date>2010-03-25</expiration_date>
        <employer><![CDATA[Accellent Inc.]]></employer>
        <location><![CDATA[Brooklyn Park, MN, 55445, USA]]></location>
    </job>
    <job>
        <title><![CDATA[Principal Engineer]]></title>
        <description><![CDATA[


Job Title :Principal Engineer
Job Code :4077
Location :Wilmington MA US 01887
Job Description :
Accellent, Inc. is a fully integrated provider of design, supply chain management and strategic sourcing services to the Medical Device industry. Accellentwww.accellent.com, a recognized market leader, is a fast-growing outsource manufacturing and design solution company specializing in high growth areas such as Cardiology, Endoscopy and Orthopaedics. The top Medical Device companies partner with Accellent to provide innovation, advanced technology, speed to market, low cost labor and strategic sourcing.
We&rsquo;re looking for team players with a can-do attitude to share in our vision and corporate values. Accellent offers competitive salaries; a comprehensive benefits package, and a stimulating work environment.
Currently, we are searching for a Principal Engineer to join our Wilmington, MA facility.
About the Opportunity:
Under direction, performs work of considerable difficulty in advanced engineering work, which involves program responsibility. This work involves the application of considerable professional engineering knowledge and skills to the direction of a major engineering project as an ongoing program function. Duties may involve the supervision, coordination and scheduling of subordinate technical staff and the coordination of program or project activities with other divisions or facilities. Assignments are broad in scope with the opportunity for the use of independent judgment.
Key Result Accountabilities
* ?
Interfaces directly and regularly with customers (internal and external) technical staff. Will typically be assigned projects that are of the highest priority and revenue potential with high visibility by Accellent customers. Often is included in critical technical discussions with customers to bring deep insight to a problem or opportunity and establish a high level of credibility for Accellent through demonstrated knowledge and expertise.
?
Exhibits highest level of expertise in chosen technical fields, often sited as an expert in the field. Expertise is exhibited by technical journal and industry publications and/or relevant patents.
* ?
Evaluates, when required, proposed projects for feasibility and applicability of Accellent technology. Will typically be assigned projects when are less defined and require (1) The development of new Accellent Technology and/or processes, (2) The Improvement and Further Resolution of Existing Accellent Technology, and/or (3) Development of new Supplier Processes or Components as required to meet Project Goals.
* ?
Leads in the development of new products and implementation of processes as assigned for Customers and/or Internal Projects.
* ?
Reviews existing processes to identify and implement cost, quality, and productivity improvements through advanced approaches.
?
Follows and develops Quality and Regulatory requirements including Accellent policies, procedures, and appropriate regulatory requirements.
Job Description
Plans, Develops, and Executes Process and Test Method Validations (IQ, OQ, PQ, PPQ) in accordance with Accellent procedures and guidelines
* ?
Communicates ideas, information, and recommendations clearly, effectively and frequently (oral and written) within Accellent, with outside suppliers or partners and with Accellent customers during formal and informal interactions.
* ?
Prepares or reviews documentation with a high degree of accuracy, completeness, and effectiveness using common Accellent engineering tools &amp; templates were available. (Examples include specifications, manufacturing procedures, ECOs, and technical reports or analysis)
* ?
Applies and Promotes Lean manufacturing techniques to continuously improve cycle times and process flows. Identifies, supports, or directs the execution of improvement efforts to reduce waste in all manufacturing and business processes.
* ?
Uses structured problem solving techniques and statistical methods for data driven analysis and decisions.
* ?
Applies and leads DMAIC &ndash; Six Sigma approaches to solve issues and reduce variation in all manufacturing and business processes.
* ?
Plans, executes and manages project activities with cross functional teams. Project types can include new product development and introduction, manufacturing transfers, continuous improvement and cost reduction initiatives.
* ?
Exhibits the Accellent values (Customer focus, Continuous Improvement, Performance, Accountability, Teamwork and Integrity) in all activities.
* ?
Demonstrates leadership through mentoring of junior staff, responsiveness to business needs and motivation of diverse, cross functional teams including influencing both internal and external members to achieve positive business results
* ?
Demonstrates technical ability through the application of engineering skills, approaches and knowledge.
* ?
Takes financial responsibility for activities to create positive impact to the business
* ?
Performs all duties and directs others creating a safe working environment for our employees and our communities.
* ?
Performs other duties as necessary.Approval Date: 02/16/09 Effective Date: 02/16/09 Page 2 of 2
* ?
Environmental Working Conditions
The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
Job DescriptionApproval Date: 02/16/09 Effective Date: 02/16/09 Page 3 of 2
While performing the duties of this job, the employee is frequently exposed to moving mechanical parts. The employee is occasionally exposed to high, precarious places; fumes or airborne particles; toxic or caustic chemicals; risk of electrical shock; and vibration. The noise level in the work environment is usually moderate.
Position Scope/Summary
Job Requirements :
To perform this job successfully, an individual must e able to perform each essential duty satisfactorily. The requirements listed are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.



Due to the expected number of responses, only those most qualified will be contacted. No recruiters please; all unsolicited third-party submissions will be rejected.

Accellent is an Equal Opportunity/Affirmative Action employer and we value diversity in our workforce. As such we provide equal opportunity for all applicants without regard to race, religion, gender, national origin, age, marital status, veteran status, or disability. To learn more about Accellent and our career opportunities, please visit us atwww.accellent.com
Career Level :Experienced (Non-Manager)
Education :Master's Degree
% of Travel Required :0-10%
Shift/Hours :First Shift (Day)
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        <expiration_date>2010-03-25</expiration_date>
        <employer><![CDATA[Accellent Inc.]]></employer>
        <location><![CDATA[Wilmington, MA, 01887, USA]]></location>
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    <job>
        <title><![CDATA[Finsher]]></title>
        <description><![CDATA[


Job Title :Finsher
Job Code :4075
Location :Orchard Park NY US 14127
Job Description :
1.   Knowledgeable about finishing techniques, which include but are not limited to using foredoms, gesswein, tumbling, burlytic, cleaning, grinding, miyano operations, Lapmaster, red wheeling, hand deburring, tumble blasting, sand blasting, clean room operations, molding machines, furnaces, waterbaths, dryers, trim, scrape or deburr parts using hand tools and equipment.
2.   Responsible for performing work that meets or exceeds our production standards and scrap rates that will achieve our metric goals for scrap, Fill Rate, Rework, Customer Lot Acceptance (CLA), and Customer Complaints, etc.
3.   Knowledge of shop control system in order to review and print paperwork needed for job and input data for work completed on various jobs.
4.   Use Smart Scope, comparator, micrometers, blade micrometers, counting scales and/or profilometer for measuring and counting parts, as necessary.
5.   Knowledge of reading and using Collection Plans in order to conduct frequency checks.
6.   Understand MVR procedures.
7.   Be able to rotate into other Finishing jobs with competency and confidence.
8.   Ability to work well in a team environment.
9.   Other duties as necessary.
10. Keep work area clean.
Job Requirements :
1.   Able to use microscope and other measuring equipment.
2.   Able to use computer, pulling up instructions and reading them.
3.   Able to follow instructions, both written and verbal.
4.   Able to count parts.
Career Level :Entry Level
Education :Vocational
Shift/Hours :First Shift (Day)
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        <expiration_date>2010-03-25</expiration_date>
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        <location><![CDATA[Orchard Park, NY, 14127, USA]]></location>
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    <job>
        <title><![CDATA[IS Site Administrator]]></title>
        <description><![CDATA[


Job Title :IS Site Administrator
Job Code :3995
Location :Arvada CO US 80002
Job Description :
Accellent, Inc. is a fully integrated provider of design, supply chain management and strategic sourcing services to the Medical Device industry. Accellentwww.accellent.com, a recognized market leader, is a fast-growing outsource manufacturing and design solution company specializing in high growth areas such as Cardiology, Endoscopy and Orthopaedics. The top Medical Device companies partner with Accellent to provide innovation, advanced technology, speed to market, low cost labor and strategic sourcing. 
We&rsquo;re looking for team players with a can-do attitude to share in our vision and corporate values. Accellent offers competitive salaries; a comprehensive benefits package, and a stimulating work environment. 

The IS Site Administrator provides technical leadership, management and direction to the Arvada, CO, Englewood CO, and Upland CA sites and is responsible for the installation, maintenance, and support of computers, networks, and telephone systems for the sites which include.
This position is based at our Arvada, CO site.
Responsibilities:
* Coordinate daily support issues of sites to ensure systems are operational with high degree of reliability.
* Installation, maintenance, administration, and support of software (ERP, Microsoft Exchange, etc.), computers (servers, PCs), peripherals, networks and topologies, and communications equipment. 
* Maintain documented inventory of software licenses, inventory of computers and other hardware, network, system and network backup procedures, and any other IS processes.
* Implement methodology to ensure that hardware, software, and telephone systems are monitored for problems and that patches, service packs, or maintenance releases stay current.
* Provide Project Management for key Information Services projects.
* Establish and follow procedures to keep the computing, network, and telephone systems running in excellent condition.
* Keep business units informed of current and future IS activities and projects so that they have a clear understanding of IS&rsquo; plans.
* Develop and publish metrics of reliability of network, servers, applications, and telephone system.
* Proactively go out and determine what needs are of the user base.
* Interface effectively with vendors.

Job Requirements :

Requirements:

* College degree; Computer Science preferred.
* At least 5 years experience in planning, installing and supporting computer software and hardware, networking, and communications equipment.
* At least 3 years experience managing IS Operations staff.
* At least 2 years experience supporting validated systems. Must be familiar with CFR Part 11 and other regulatory requirements.
* Proficient in Microsoft Office, databases, PCs, and telecommunication systems.
* At least one year Project Management experience.
* Experience working across organizational boundaries.
* Excellent verbal and written communication skills. Ability to communicate effectively through all levels of an organization.
* Experience with ERP systems and manufacturing environment. Ability to understand the needs of a manufacturing site.
* Strong interpersonal skills and highly skilled team player. Must be customer service oriented.

Accellent is an Equal Opportunity/Affirmative Action employer and we value diversity in our workforce. As such we provide equal opportunity for all applicants without regard to race, religion, gender, national origin, age, marital status, veteran status, or disability. To learn more about Accellent and our career opportunities, please visit us atwww.accellent.com 

Career Level :Experienced (Non-Manager)
Education :Bachelor's Degree
Shift/Hours :First Shift (Day)
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            <industry><![CDATA[Health Products & Services]]></industry>
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        <expiration_date>2010-03-25</expiration_date>
        <employer><![CDATA[Accellent Inc.]]></employer>
        <location><![CDATA[Arvada, CO, 80005, USA]]></location>
    </job>
    <job>
        <title><![CDATA[Sr. Manufacturing Engineer]]></title>
        <description><![CDATA[


Job Title :Sr. Manufacturing Engineer
Job Code :3988
Location :Wheeling IL US 60090
Job Description :

Accellent, Inc. is a fully integrated provider of design, supply chain management and strategic sourcing services to the Medical Device industry. Accellentwww.accellent.com, a recognized market leader, is a fast-growing outsource manufacturing and design solution company specializing in high growth areas such as Cardiology, Endoscopy and Orthopaedics. The top Medical Device companies partner with Accellent to provide innovation, advanced technology, speed to market, low cost labor and strategic sourcing. 
We&rsquo;re looking for team players with a can-do attitude to share in our vision and corporate values. Accellent offers competitive salaries; a comprehensive benefits package, and a stimulating work environment. 
The Sr. Manufacturing Engineer will be expected to provide hands on engineering support for Operations. Interacts with customers and provides support for Engineering and Quality Systems. 
This position is located in our Wheeling, Illinois site.
Responsibilities:
* Follows and develops Quality and Regulatory requirements including Accellent policies, procedures, and appropriate regulatory requirements.
* Develops and Executes Process and Test Method Validations (IQ, OQ, PQ, PPQ) in accordance with Accellent procedures and guidelines
* Communicates ideas, information, and recommendations clearly, effectively and frequently (oral and written) within Accellent, with outside suppliers or partners and with Accellent customers during formal and informal interactions.
* Prepares or reviews documentation with a high degree of accuracy, completeness, and effectiveness using common Accellent engineering tools &amp; templates were available. (Examples include specifications, manufacturing procedures, ECOs, and technical reports or analysis)
* Applies Lean manufacturing techniques to continuously improve cycle times and process flows. Identifies, and supports the execution of improvement efforts to reduce waste in all manufacturing and business processes.
* Uses structured problem solving techniques and statistical methods for data driven analysis and decisions.
* Applies DMAIC &ndash; Six Sigma approaches to solve issues and reduce variation in all manufacturing and business processes.
* Plans and executes project activities within a cross functional team. Project types can include new product development and introduction, manufacturing transfers, continuous improvement and cost reduction initiatives.
* Exhibits the Accellent values (Customer focus, Continuous Improvement, Performance, Accountability, Teamwork and Integrity) in all activities.
* Demonstrates leadership through mentoring of junior staff and responsiveness to business needs to achieve positive results
* Demonstrates technical ability through the application of engineering skills, approaches and knowledge.
* Performs all duties and directs others creating a safe working environment for our employees and our communities.
* Performs other duties as necessary.
,
Job Requirements :
* 
* 
Job Requirements:

* BS in Engineering
* 7-10 years engineering work experience in a machining environment.
* Swiss Style machining experience required
* Vertical machining experience
* Wire EDM experience
* Laser welding
* CNC programming experience


Accellent is an Equal Opportunity/Affirmative Action employer and we value diversity in our workforce. As such we provide equal opportunity for all applicants without regard to race, religion, gender, national origin, age, marital status, veteran status, or disability. To learn more about Accellent and our career opportunities, please visit us atwww.accellent.com 

Career Level :Experienced (Non-Manager)
Education :Bachelor's Degree
% of Travel Required :0-10%
Shift/Hours :First Shift (Day)
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        <location><![CDATA[Wheeling, IL, 60070, USA]]></location>
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    <job>
        <title><![CDATA[Maintenance Technician]]></title>
        <description><![CDATA[


Job Title :Maintenance Technician
Job Code :3964
Location :Collegeville PA US 19426
Job Description :
Accellent, Inc. is a fully integrated provider of design, supply chain management and strategic sourcing services to the Medical Device industry. Accellentwww.accellent.com, a recognized market leader, is a fast-growing outsource manufacturing and design solution company specializing in high growth areas such as Cardiology, Endoscopy and Orthopaedics. The top Medical Device companies partner with Accellent to provide innovation, advanced technology, speed to market, low cost labor and strategic sourcing.
We&rsquo;re looking for team players with a can-do approach to share in our vision and corporate values. Accellent offers competitive salaries; a comprehensive benefits package, and a stimulating work environment.
Currently, we are searching for a Maintenance Technician for our Collegeville facility.
About the Opportunity:
Position Scope / SummaryThe Maintenance Technician is responsible for the upkeep of all equipment, HVAC and electrical systems and routine maintenance, utilizing the preventive maintenance schedule. Will install, move and disassemble machinery and equipment.
* Key Result Accountabilities
* Conduct preventive maintenance per the schedule for all equipment assigned, to reduce downtime and prevent failures.
* Perform unscheduled servicing of equipment after a problem is discovered. Install, move and disassemble machinery and equipment as necessary.
* Employ the strategies of 5S in order to maintain an efficient work area; clean, well ordered and maintaining the right types and amounts of spare parts.
* Maintain accurate records of maintenance issues on all equipment.
* Follow the proper methods and procedures for the handling of non-hazardous waste in the plant and removal of waste from the plant.
* Being trained in the complete operation of the waste liquid treatment plant including proper procedures to be followed in case of leaks, spills, or other emergencies - Procedure #4563, Waste Liquid Treatment Facility #3505. May also be trained in Hazardous Waste Handling, Procedure #1043 and Groundwater Abatement System Periodic Inspection Procedure T PR 57-16.
* Completing and maintaining proficiency with all required safety training and all corresponding safety training updates Deal with outside contractors for routine maintenance items/service contracts when necessary.
* Ensure cleaning schedules are adhered to per PM-015 and maintenance schedules.
* Responding to emergency call-ins on a 24 hour basis and working on a rotational weekend shift.
* Maintain a clean and safe work area.
* Other duties as necessary.
Job Requirements :
Qualifications

* Minimum 5+ years in a Maintenance Technician position at a manufacturing facility, responsible for maintaining equipment and systems.
* Pass Maintenance fundamentals Test with Grade of 80% minimum.
* Experience in the following trades or skills: Electrical, electronic, gas or arc welding, pipe fitting, hydraulic piping, machinist, air conditioning and heating, plumbing, blueprint reading, disassembly and assembly of machines or components, lubrication and servicing of machines and equipment, rigging, sheet metal fabrication.Prior experience installing, moving and disassembling equipment and machinery.
* Able to use all the tools necessary to conduct the work involved with maintaining Accellent&rsquo;s equipment and building systems.
* Able to use the computer, specifically spreadsheets, word processing and data base programs as well as experience with PM systems.
* Able to give and follow instructions, both written and verbal.
* Effectively communicate with all levels of employees, as well as outside contractors.
* Excellent organizational skills; able to manage multiple priorities with many time constraints.Environmental Working Conditions
The physical demands described herein are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform essential functions. Ability to spend time using your hands to handle, control, reach, or feel objects, tools or controls. Will spend extended periods of time standing and walking throughout the shop. Will be required to wear respirator in confined spaces. Required to wear all Safety PPE. Occasionally required to sit, stoop, kneel, bend, crouch, bend and twist. Ability to lift up to 80 lbs.
Career Level :Experienced (Non-Manager)
Education :Certification
Shift/Hours :First Shift (Day)
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    <job>
        <title><![CDATA[Ortho Platform Leader]]></title>
        <description><![CDATA[


Job Title :Ortho Platform Leader
Job Code :3900
Location :1. Warsaw IN US 46580
2. Memphis TN US 38197
Job Description :
Accellent, Inc. is a fully integrated provider of design, supply chain management and strategic sourcing services to the Medical Device industry. Accellentwww.accellent.com, a recognized market leader, is a fast-growing outsource manufacturing and design solution company specializing in high growth areas such as Cardiology, Endoscopy and Orthopaedics. The top Medical Device companies partner with Accellent to provide innovation, advanced technology, speed to market, low cost labor and strategic sourcing.
We&rsquo;re looking for team players with a can-do attitude to share in our vision and corporate values. Accellent offers competitive salaries; a comprehensive benefits package, and a stimulating work environment.
Currently, we are searching for an Orthopedics Business Leader to join our leadership team.
About the Opportunity:
The Ortho Business leader serves as the Orthopedic technical market leader for the Accellent enterprise.
Reporting to our SVP of Engineering and Technical Solutions, the Ortho Business Leader will:
* provide Strategic planning and Market Development to support the Senior Leadership Team, Orthopedic operations, and the sales and marketing organization
* interact with Orthopedic customers and prospective customers, strategic alliance partners, and acquisition candidates.
* responsible for the achievement of the company&rsquo;s revenue and profit objectives for the Orthopedic market.
* provide direct management of the Accellent TBDL Ortho Field Sales Resources.
Key result accountabilities for the Ortho Business Leader to achieve include:
Strategic Planning:
* Owns the Orthopedic Strategic Plan.
* Overall responsibility for development, communication and execution of the strategic plan for the Orthopedic business
* Responsible for developing both strategic and tactical plans to grow Accellent&rsquo;s Ortho business ahead of the market, pushes those plans through the Senior Leadership Team for approval, then directs the execution of those plans through Accellent&rsquo;s functional management teams.
* Strategic Market Planning and Analysis, including assisting sales in Pricing and Margin Guidelines for Ortho Segment, Establishing and Supporting Opportunity Screening process for implants and instruments.
* Align and Integrate Ortho strategic plans with company strategy, assist in aligning Forecast with Market Potential.
* Assists facilities in understanding strategic opportunities.Sales Support:
* Responsible for the overall revenue growth of the Ortho business.
* Owns the Ortho Sales Forecast
* Directly supports Accellent&rsquo;s Ortho sales efforts worldwide.
* Direct Management and Responsibility for Accellent&rsquo;s Ortho TBDL Team and Resources
* Coordinates multi-functional activities related to identification and execution of sales pipeline opportunities.
* Works through the sales and marketing organization to a) increase profits from Ortho product sales, and b) to grow Accellent&rsquo;s Ortho revenue ahead of the market.
* Develops and maintains strong relationships with customer decision makers to attain estimated future projects/requirements.
* Assists sales people in developing sales plans for strategic sales.
* Travels with sales people on strategic sales initiatives
* Assists with the development of Ortho sales leads.
* Responsible for ultimately increasing Ortho customer satisfaction.
* Act as primary trainer and/or assist with ongoing Ortho-related training (FSE, Technical Resources, etc.) Driving an appropriate training program to scale a Orthopedic Technical Sales Team.
* Train Sales on Orthopedic market and productMarketing:&middot;
* Responsible for staying current in and reporting on all facets of Accellent&rsquo;s Orthopedic business, Accellent&rsquo;s Orthopedic customers, general Orthopedic product design, manufacturing, and supply trends, and macro trends in the Orthopedic industry for the purpose of advising Accellent leaders and growing the Orthopedic business.
* Supports marketing team on matters related to Orthopedic marketing strategy and tactics, including but not limited to promotional activities, advertising, messaging, branding, trade shows, sample kits, and sales training.
* Provide Strategic Market Analysis and Go-to-Market Support, including: Market and Competitive Analysis to support business development activity, Product/Market and Customer Analysis to support sales and marketing activity, Develop targeted marketing initiatives to support enterprise revenue goals.
* Align with sales and marketing on Orthopedic market trendsBusiness Development:&middot;
* Responsible for the development and execution of the capability strategy for the Orthopedic business.
* Define and support internal capability developmento Coordinate strategic alliances as required to support development efforts.o Determine acquisition strategy as necessary to support capability development.&middot; Responsible for supporting Orthopedic business development efforts throughout all stages of the sales process, including but not limited to a) qualifying new sales opportunities, b) assisting the sales team with the preparation of a competitive quote, c) assisting sales with the delivery and technical explanation of key quotations d) assistingwith the sales process where new opportunities are discovered, e) getting the customer to formalize their purchase decision with purchase orders or contracts, and f) assisting in the execution of any orders.
* Advise the company on the development, implementation, and ongoing management of a NPD/Quick Turn prototype effort via Accellent Idea Centers in support of the Ortho Market Development.
* Identify and filter opportunities for NPD/Quick Turn to drive long term manufacturing revenue.
* Influence coordination and collaboration of Accellent manufacturing facilities in support of programs and product launches&middot;
* Work extensively with customer R&amp;D and D&amp;D Teams to provide DFMA, Product, and Manufacturing inputs to select Ortho Customers.Performance Tracking and Reporting:
* Responsible for overall performance tracking for the Orthopedic Business.
* Responsible for developing a competitive database, organizing the collection efforts for such data, analyzing the information, and disseminating that information as appropriate. &middot; Provides activity reports and ad hoc management reports related to the position.
* Responsible for the overall management of expenses within budget.

Job Requirements :
* Strong understanding of medical device industry, contract manufacturing industry, and Orthopedic industry.
* 5 &ndash; 10 Years of Orthopedic product and manufacturing experience.
* Superior communication skills, oral and written. Superior presentation skills.
* Ability to analyze, understand and effectively communicate technical material to both technical and non-technical audiences
* Superior leadership and collaboration skills, particularly geared towards matrixed (indirect) leadership and influence.
* Operates independently, without direct supervision, needs minimal direction/self starter.
* Highly organized.
* Able to develop and execute basic marketing plans.
* Full understanding of corporate strategy and capabilities.
* Strong in Excel &amp; PowerPoint. CAD &amp; Design programs a plus
* Possesses a bachelor&rsquo;s degree in a related field (Masters degree preferred.)
* Highly personable, outgoing, people-oriented personality.
* Builds and maintains a high degree of credibility with others throughout the organization.
* Personal credit card (for use in booking travel)
Due to the expected number of responses, only those most qualified will be contacted. No recruiters please; all unsolicited third-party submissions will be rejected.

Accellent is an Equal Opportunity/Affirmative Action employer and we value diversity in our workforce. As such we provide equal opportunity for all applicants without regard to race, religion, gender, national origin, age, marital status, veteran status, or disability. To learn more about Accellent and our career opportunities, please visit us atwww.accellent.com
Career Level :Manager (Manager/Supervisor of Staff)
Education :Bachelor's Degree
% of Travel Required :50-60%
Shift/Hours :First Shift (Day)
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        <location><![CDATA[Warsaw, IN, 46582, USA]]></location>
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    <job>
        <title><![CDATA[Technical Business Leader (Med Dev/Catheter Design)]]></title>
        <description><![CDATA[


Job Title :Technical Business Leader (Med Dev/Catheter Design)
Job Code :3898
Location :Los Angeles CA US 90052
Job Description :

Accellent, Inc. is a fully integrated provider of design, supply chain management and strategic sourcing services to the Medical Device industry. Accellentwww.accellent.com, a recognized market leader, is a fast-growing outsource manufacturing and design solution company specializing in high growth areas such as Cardiology, Endoscopy and Orthopaedics. The top Medical Device companies partner with Accellent to provide innovation, advanced technology, speed to market, low cost labor and strategic sourcing.
We&rsquo;re looking for team players with a can-do attitude to share in our vision and corporate values. Accellent offers competitive salaries; a comprehensive benefits package, and a stimulating work environment.
Currently, we are searching for a Technical Business Development Leader (Technical Sales Engineer/TBDL) to join in the Los Angeles, CA area. This is an excellent opportunity for a candidate in an engineering or program management role with customer-facing experience.
About the Opportunity:
The role of a TBDL is to tactically execute the strategy, contracts, and programs of key identified customers. It is a management promotable role and should be viewed as a training ground for greater responsibility. It has indirect visibility to senior management of both the customer and to Accellent and serves to assure that customer expectations are met.
Position Summary
To assist in increased revenue and profitability of assigned customers. To enhance the reputation and business relationship between customer and Accellent. To execute, monitor and report on all programs contracts and agreements between the customer and Accellent.
Key Result Accountabilities
* Responsible for the individual facilities/divisions of Platinum customers including executing corporate direction, implementing strategic deals and revenue growth.
* Responsible for all aspects of customer satisfaction within a specified geographic territory.
* Responsible for the implementation of strategic directions indicated by the CAD.
* Identifies key initiatives and opportunities to the CAD.
* All aspects of customer satisfaction and communication of issues to the CAD and or management.
Job Requirements :
* BS Engineering or equivalent degree.
* Must be able to call on and influence senior &amp; mid-level OEM management.
* Must have a broad understanding of the OEM&rsquo;s specific market and needs.
* Possess a deep understanding of company strategy and capabilities.
* Demonstrated success in managing multi tasks in multiple geographic locations.
* Must be able operate at an ever increasing level of efficiency.
* Demonstrated understanding of and negotiation for profitability and long term relationships.
* Very well developed problem solving skills.
* Minimum 5 years in medical device/tech sales or sales support.
* Robust understanding of catheter-based applications.
* Professional-level computer skills, Outlook (email ettiquette, email management), Excel (charting, graphing, reporting), Word (communications, presentations, etc.) and PowerPoint (professional-looking presentation creation, etc.)
* CAD and design programs a plus.
This position is a field-based (home office) sales position - travel requirements within territory will require routine travel of 50%+ of the time to ensure highest customer satisfaction.
Due to the expected number of responses, only those most qualified will be contacted. No recruiters please; all unsolicited third-party submissions will be rejected.
Accellent is an Equal Opportunity/Affirmative Action employer and we value diversity in our workforce. As such we provide equal opportunity for all applicants without regard to race, religion, gender, national origin, age, marital status, veteran status, or disability. To learn more about Accellent and our career opportunities, please visit us atwww.accellent.com
Career Level :Experienced (Non-Manager)
Education :Bachelor's Degree
% of Travel Required :40-50%
Shift/Hours :First Shift (Day)
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    <job>
        <title><![CDATA[Coiling Technician]]></title>
        <description><![CDATA[


Job Title :Coiling Technician
Job Code :3616
Location :Brooklyn Park MN US 55429
Job Description :
Accellent, Inc. is a fully integrated provider of design, supply chain management and strategic sourcing services to the Medical Device industry. Accellentwww.accellent.com, a recognized market leader, is a fast-growing outsource manufacturing and design solution company specializing in high growth areas such as Cardiology, Endoscopy and Orthopaedics. The top Medical Device companies partner with Accellent to provide innovation, advanced technology, speed to market, low cost labor and strategic sourcing. 
We&rsquo;re looking for team players with a can-do attitude to share in our vision and corporate values. Accellent offers competitive salaries; a comprehensive benefits package, and a stimulating work environment. 
Currently, we are searching for an Coiling Technician to join our Brooklyn Park, MN facility.
About the Opportunity:
Job Requirements :
     Position Scope/Summary
 Two years of relevant experience with coiling including:
* Setting up coils and coil winding process
* Inspecting coils and assessing process capability
* Selecting/grinding Mandresl and coil tooling  Additional background and expeirence would include:

* Fabricate complex prototypes including, but not limited to:
* Complex surface parts that would typically be molded
* Small, precision metal components
* Assemblies that contain many parts
* Design fixtures
* Design and build custom manufacturing equipment
* Evaluate vendor and supplier capability to meet our needs and requirements.
* Effectively communicate with the customer and vendors
* Propose experimental designs and conduct tests; perform or supervise validation testing
* Provide DFMA feedback in an organized manner
* Prepare cost studies for products
* Train technicians, assemblers, and associate technician in their specific specialty field
* Document components, prepare DCOs
* Provide &ldquo;rapid&rdquo; response to internal and external customer requests. This includes quote turn around and component delivery in hours/days.
* Work within a team environment to meet or exceed facility metrics such as On time delivery, quote turn around, customer satisfaction and profitability.
     Key Result Accountabilities
  Supervisory Responsibilities:
  Needs to work in an atmosphere with little 
  supervision.
  Language Skills:
  Must be able to communicate with facility
  personnel.
  Reasoning Ability:
  The ability to complete projects and problem solveindependently. 
     Environmental Working Conditions
     Reasonable accommodations may be made to enable individuals with disabilities to perform the
     essential functions.

  Qualifications
&middot;    Strong CAD/CAM experience, Pro/E or Solidworks knowledge a plus
&middot;    Strong Vertical Milling experience
&middot;    Good organization, written, and verbal communication skills
&middot;    Broad capability in machine shop practices
&middot;    Turning - Swiss-style and conventional
&middot;    EDM
&middot;    Capable of independent thinking and problem solving
&middot;    Capable of taking initiative in recognizing corrective actions
&middot;    An understanding of machine shop math is required
&middot;    4 year college degree or equivalent work experience preferred.


  It is impossible to list every requirement for, or responsibility of, any position. Similarly we cannot identify all the skills a position may require since job responsibilities and the Company&rsquo;s needs may change over time. Therefore, the above job description is not comprehensive or exhaustive. The Company reserves the right to adjust, add to or eliminate any aspect of the above description. The Company also retains the right to require all employees to undertake additional or different job responsibilities when necessary to meet business needs.
Accellent is an equal opportunity employer.



Career Level :Experienced (Non-Manager)
Education :Vocational
% of Travel Required :0-10%
Shift/Hours :First Shift (Day)
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        <expiration_date>2010-03-25</expiration_date>
        <employer><![CDATA[Accellent Inc.]]></employer>
        <location><![CDATA[Brooklyn Park, MN, 55445, USA]]></location>
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    <job>
        <title><![CDATA[Quality Engineer]]></title>
        <description><![CDATA[


Job Title :Quality Engineer
Job Code :3534
Location :Houston PA US 15342
Job Description :
This position is required in order to plan and validate processes from the quote and contract review stage through shipment to ensure the product meets customer requirements in all respects. The incumbent will determine and clarify customer inspection requirements and develop, use, and improve our quality system to meet those requirements.
Key Result Accountabilities
1.   Continuous Improvement: Identify and validate process controls on key production processes to assure consistent and repeatable process outputs. Seek new inspection methods with inspection equipment providers/vendors. Work with toolmakers/R&amp;D to design new and/or improved inspection gauging or fixturing. Provide sponsorship and act as change facilitator for SPC, FMEA, DOE, and process validation systems with the net result of inspection velocity. Innovate and improve the quality system to achieve a Best in Class medical device process development system.*
2.   Process Validation: Develop and implement IQ, OQ, and PQ protocols to ensure
compliance with the Quality System.*
3.   Quality System Metrics: Develop methods and systems to provide quality indicators to the organization, training the organization on those methods and systems.*
4.   Corrective and Preventative Action: Work with customers and vendors to complete root cause analysis and to determine and implement Corrective and Preventive Actions. Perform trending of quality indicators, both internal and external, and lead continuous improvement efforts relating to our indicators.*
5.   Training: Train production personnel on the Quality System and FDA requirements.*
6.   Contract Review: Participate in quote and PO review process to identify unclear, incomplete or difficult requirements prior to engineering the product. Assist engineering Team in interpreting all types of blueprints, standards, and customer specifications into engineering requirements for implementation in Accellent Work Instructions.*
7.   Regulatory Compliance: Ensure we comply with FDA&rsquo;s Quality System Regulation.*
8.   Bring any questions on interpretation of conformance to the attention of the Quality Assurance Manager.*
9.   Perform other duties as assigned by supervisory personnel.
Job Requirements :
Two years experience as a Quality Engineer in a medical devisce manufacturing environment requjired. Strong math skills and mechanical aptitude.  Computer skills required. Strong organizational skills and the ability to multi-task. Attention to fine detail and tolerances required.
Career Level :Experienced (Non-Manager)
Education :Bachelor's Degree
% of Travel Required :None
Shift/Hours :First Shift (Day)
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        <expiration_date>2010-03-25</expiration_date>
        <employer><![CDATA[Accellent Inc.]]></employer>
        <location><![CDATA[Houston, PA, 15342, USA]]></location>
    </job>
    <job>
        <title><![CDATA[Director, Financial Planning & Analysis]]></title>
        <description><![CDATA[Job Title :Director, Financial Planning & Analysis
Job Code :3424
Location :Wheeling IL US 60090
Job Description :
Accellent, Inc. is a fully integrated provider of design, supply chain management and strategic sourcing services to the Medical Device industry. Accellentwww.accellent.com, a recognized market leader, is a fast-growing outsource manufacturing and design solution company specializing in high growth areas such as Cardiology, Endoscopy and Orthopaedics. The top Medical Device companies partner with Accellent to provide innovation, advanced technology, speed to market, low cost labor and strategic sourcing. 
We&rsquo;re looking for team players with a can-do attitude to share in our vision and corporate values. Accellent offers competitive salaries; a comprehensive benefits package, and a stimulating work environment. 
Currently, we are searching for a Director, Financial Planning &amp; Analysis based out of the Chicagoland area.
About the Opportunity:

As Director of Financial Planning &amp; Analysis, you'll be responsible for providing overall financial leadership for a multi-factory operation. You will be accountable for delivering financial and operating results, budgeting, forecasting, and business development support. You will also provide counsel to the business leader and business leadership team on all financial matters that focuses on maximizing the revenue growth, profitability and cash flow generation, as well the activities associated with the revenue generation, cost management, operational improvement, capital expenditure investment activities and asset management.
Position Responsibilities
* Responsible for high quality, accurate, on time, insight driven financial and operations analysis and reporting - translate insights to recommendations and actions.
* Lead the development of a Rolling 12 Month Forecast (R12M) and Annual Operating plans
* Evaluate the impact of R12M forecasts, new product introduction, business strategies as well as regulatory actions on the business and recommend actions with business leaders to improve financial performance.
* Operate in a professional and credible manner evidenced by providing timely and accurate analysis of budgets, financial reports and financial trends
* Enhance and/or develop, implement and enforce policies and procedures of the organization that will improve the overall operation and effectiveness of the function and organization
* Provide technical financial advice and knowledge to others within the financial discipline. Interface with the Finance and Accounting teams as well as internal and external audit teams
* Provide strategic financial input and leadership on issues affecting the organization; i.e., evaluation of potential alliances, investments, contracts, etc.
* Lead initiatives to enhance all financial metrics as defined by Accellent
* Travel is required; approximately 50% of the time
Key Competencies and Success Factors
* Self directed, action oriented, forward-thinking and creative individual with high ethical standards
* Strategic visionary with strong financial skills, analytical ability, good judgment and strong operational focus
* Organized, team player who is an effective influencer
* Demonstrate the ability to lead change in the face of adversity; to challenge the status quo constructively
* An intelligent and articulate individual who can relate to people at all levels of an organization and possesses excellent communication skills
* Demonstrate the ability to be a good educator who is trustworthy and willing to share information and serve as a mentor 
* Decisive individual who possesses a &quot;big picture&quot; perspective
* Ability to meet deadlines and function in a matrix environment
* Independent ability to generate business decision support; this is a stand-alone FP&amp;A role without direct reports.
Qualifications:
* Bachelor's Degree required; MBA preferred
* Proficient knowledge and skill in ERP computer applications
* Excellent computer skills, including the development of complex modeling
* Five to ten years of finance experience is required;experience within a manufacturing company with multi-facility responsibility is a must
Due to the expected number of responses, only those most qualified will be contacted. No recruiters please; all unsolicited third-party submissions will be rejected.
Accellent is an Equal Opportunity/Affirmative Action employer and we value diversity in our workforce. As such we provide equal opportunity for all applicants without regard to race, religion, gender, national origin, age, marital status, veteran status, or disability. To learn more about Accellent and our career opportunities, please visit us atwww.accellent.com
Job Requirements :
~
Career Level :Manager (Manager/Supervisor of Staff)
Education :Bachelor's Degree
% of Travel Required :50-60%
Shift/Hours :First Shift (Day)
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        <industries>
            <industry><![CDATA[Health Products & Services]]></industry>
        </industries>
        <expiration_date>2010-03-25</expiration_date>
        <employer><![CDATA[Accellent Inc.]]></employer>
        <location><![CDATA[Wheeling, IL, 60070, USA]]></location>
    </job>
    <job>
        <title><![CDATA[Engineering Program Manager]]></title>
        <description><![CDATA[


Job Title :Engineering Program Manager
Job Code :4334
Location :Wheeling IL US 60090
Job Description :
Accellent, Inc. is a fully integrated provider of design, supply chain management and strategic sourcing services to the Medical Device industry. Accellentwww.accellent.com, a recognized market leader, is a fast-growing outsource manufacturing and design solution company specializing in high growth areas such as Cardiology, Endoscopy and Orthopaedics. The top Medical Device companies partner with Accellent to provide innovation, advanced technology, speed to market, low cost labor and strategic sourcing. 
We&rsquo;re looking for team players with a can-do attitude to share in our vision and corporate values. Accellent offers competitive salaries; a comprehensive benefits package, and a stimulating work environment. 
Currently, we are searching for an Engineering Program Manager to join our Wheeling, IL facility.
About the Opportunity:
Under minimal direction, the Program Manager performs work of considerable difficulty in advanced engineering focused on program responsibility. This involves the application of considerable professional engineering knowledge and skills to direct major engineering project as an ongoing program function.

Responsibilities:

* Plans, executes and manages program activities utilizing cross functional teams within a matrix organization.
* Translate customer inputs into the definition of scope, budget and resource requirements for engineering programs resulting in the delivery of a program proposal.
* Coordinate and assemble project teams, manage program budgets, ensure program milestones and deliverables are achieved through the management of the triple constraints of time, cost and scope.
* Manage programs across multiple manufacturing sites.
* Manage new product development introduction, manufacturing transfers, continuous improvement and cost reduction initiatives.
* Develop customer relationships to help foster effective communication, establish program expectation and minimize program risks.
* Ability to communicate effectively with all levels of external customer, suppliers and internal stakeholders including senior management.
* Identify program risks and develop risk mitigation strategies to maintain program expectations.
* Identify, create and communicate change of scope requests to program stakeholders.
* Instill leadership principles and accountability within projects teams.
* Foster open communication within the project teams to ensure barriers to program success are removed.
Job Requirements :

* Bachelor of Science in Engineering required (Mechanical Engineering, Plastics Engineering preferred).
* Minimum of 10 years experience (engineering, manufacturing, project management).
* Medical device manufacturing industry experience strongly preferred.
* Demonstrated ability to understand, follow and develop both Quality and Regulatory requirements.
* Proven track record of proactively managing risk to achieve business and customer objectives.
* Knowledge of accounting and financial planning techniques. Proficience in understanding and reporting financial program status as well as managing the details related to the financial status within the program.
* Excellent communication skills, strong customer relationships, leadership skills and team building competencies. Must be able to distill complex technical content into brief, concise and understandable language when communicating status to management and the customer.
* Demonstrated leadership - mentoring of junior staff, motivation of diverse, cross functional teams.
* The ability to work with all levels of staff through all company business units.
* Excellent problem solving skills are required . 
* Flexibility to travel up to 25%
* Ability to work to a deadline and to handle multiple tasks simultaneously. Experience with Microsoft Office including Microsoft Word, Excel, PowerPoint and Project


Due to the expected number of responses, only those most qualified will be contacted. No recruiters please; all unsolicited third-party submissions will be rejected.

Accellent is an Equal Opportunity/Affirmative Action employer and we value diversity in our workforce. As such we provide equal opportunity for all applicants without regard to race, religion, gender, national origin, age, marital status, veteran status, or disability. To learn more about Accellent and our career opportunities, please visit us atwww.accellent.com
Career Level :Experienced (Non-Manager)
Education :Bachelor's Degree
% of Travel Required :0-10%
Shift/Hours :First Shift (Day)
]]></description>
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            <industry><![CDATA[Health Products & Services]]></industry>
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        <expiration_date>2010-03-25</expiration_date>
        <employer><![CDATA[Accellent Inc.]]></employer>
        <location><![CDATA[Wheeling, IL, 60070, USA]]></location>
    </job>
    <job>
        <title><![CDATA[Quality Control Supervisor]]></title>
        <description><![CDATA[


Job Title :Quality Control Supervisor
Job Code :4260
Location :Wheeling IL US 60090
Job Description :
Position Scope/Summary
Oversight of Quality Control function for the site focused on incoming, and finished goods inspection. Oversee calibration and enhance Quality System. Represent Accellent in a professional and exemplary manner before our customers, employees and community at large.
Key Result Accountabilities
&middot;    Responsible for supervision and day to day activities of the quality control inspectors.
&middot;    Oversee the Quality Control functions including Device History Records (DHR), inspection database, using and implementing ANSI Z1.4 standard.
&middot;    Responsible for implementing and monitoring reduced / audit inspections and associated database.
&middot;    Provides input on supplier performance to Supply chain and QA Manager.
&middot;    Oversee the Calibration functions including use of Gage tracking program and calibration scheduling.
&middot;    Communicate with shift personnel to facilitate inspection (day/nights)
&middot;    Demonstrate and lead team&rsquo;s sense of urgency with respect to achieving Quality metrics.
&middot;    Provide leadership and training to all applicable quality personnel.
&middot;    Determines best utilization of resources to meet schedule requirements.
&middot;    Prepares performance reviews for all applicable personnel at regular intervals
&middot;    Responsible for performance reviews and recommending personnel actions, such as promotions, transfers, discharges and disciplinary measures such as verbal and written verbal warnings.
&middot;    Provide feedback to the Quality Manager regarding individual performance issues.
&middot;    Identify improvement opportunities and recommend priorities.
&middot;    Act as a facilitator with quality personnel to generate ideas individually and collectively, then discuss recommendation with the Quality Manager.
&middot;    Analyzes and resolves work problems, or assists workers in solving work problems.
&middot;    Oversees and complies to work rules including those pertaining with safety, health, quality system, and Accellent Quality Management System.
&middot;    Implement improvement suggestions as appropriate to increase Quality performance.
&middot;    Suggest plans to motivate workers to achieve work related and professional goals
&middot;    Schedule overtime.
Environmental Working Conditions
Employee must comply withand enforceall safety policies and safe work procedures established by the company. Employee will be required to deliver safety training, serve on the facility safety committee and perform hazard analysis and resolution. Job tasks may also involve:  
&middot;    Using and providing employees with personal protective equipment such as safety glasses, goggles, gloves, and other equipment as established in company policies and safe work procedures.
&middot;    Training employees to work safely with cutting &amp; machining fluids, solvents, lubricants and other hazardous chemicals.
&middot;    Establishing, training employees and enforcing safe work procedures for all operations under their control. 
&middot;    Performing accident investigation and appropriate follow up.
Employee will be expected to serve as an example for all employees with respect to safety.
Job Requirements :
Requirements needed from WHL
Qualifications
&middot;    High school diploma [GED}, Technical degree or 10 years relevant experience.
&middot;    5 years of supervisory experience.
&middot;    Demonstrated decision-making and problem solving abilities.
&middot;    Policies and Procedures: Must conform to all established procedures and work activities.
&middot;    Analytical problem solving: Uses a systematic approach to solving problems by researching and evaluating alternative solutions.
&middot;    Good communication skills.
&middot;    Versatility: Must be able to respond to changing priorities with minimum disruption.
&middot;    Initiative: Must be able to function with minimum supervision.
&middot;    Leadership: Must be able to lead discussions and meeting with customers, outside vendor, suppliers and staff.
&middot;    Complete all job specific required training.
&middot;    Perform duties to achieve overall business unit metrics.
&middot;    Comply with all safety regulations, wears appropriate safety equipment as required in each area of the facility.
&middot;    Capable of certification as CQT, CQE, or CQA.
&middot;    Teamwork skills to facilitate training and group problem solving.
It is impossible to list every requirement for, or responsibility of, any position. Similarly we cannot identify all the skills a position may require since job responsibilities and the Company&rsquo;s needs may change over time. Therefore, the above job description is not comprehensive or exhaustive.  The Company reserves the right to adjust, add to or eliminate any aspect of the above description. The Company also retains the right to require all employees to undertake additional or different job responsibilities when necessary to meet business needs.
Career Level :Manager (Manager/Supervisor of Staff)
Education :Associate Degree
% of Travel Required :0-10%
Shift/Hours :First Shift (Day)
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            <industry><![CDATA[Health Products & Services]]></industry>
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        <expiration_date>2010-03-25</expiration_date>
        <employer><![CDATA[Accellent Inc.]]></employer>
        <location><![CDATA[Wheeling, IL, 60070, USA]]></location>
    </job>
    <job>
        <title><![CDATA[Machinist - Second Shift]]></title>
        <description><![CDATA[


Job Title :Machinist - Second Shift
Job Code :4254
Location :SALEM VA US 24153
Job Description :
Accellent, Inc. is a fully integrated provider of design, supply chain management and strategic sourcing services to the Medical Device industry. Accellentwww.accellent.com, a recognized market leader, is a fast-growing outsource manufacturing and design solution company specializing in high growth areas such as Cardiology, Endoscopy and Orthopaedics. The top Medical Device companies partner with Accellent to provide innovation, advanced technology, speed to market, low cost labor and strategic sourcing.
We&rsquo;re looking for team players with a can-do attitude to share in our vision and corporate values. Accellent offers competitive salaries; a comprehensive benefits package, and a stimulating work environment.
Currently, we are searching for a Machinist to join our Salem, Virginia facility. 

Essential Duties and Responsibilities:
1.)    Achieve training certifications as specified in the training database for this job.
2.)    Perform tasks and procedures daily as required to move jobs through the micro machining area.
     a.)    Run machines at their optimum capacity to keep jobs up to date per micro machining scheduling board by achieving pieces per hour scheduled.
     
     b.)    Perform all in process inspections and tool changes during job runs.
     
     c.)    Perform final processing of jobs and forwarding to the next department.
     
     d.)    Document jobs on a daily basis including set-up sheets, material accountability, run time
           log, and any other spreadsheets or forms.
3.)    Assist in the development and continual improvement of the manufacturing processes and systems by supporting and participating in daily production activities.
     a.)    Identify and communicate opportunities to make improvements to the area.
b.)    Transfers knowledge, information, observations, and other communication throughout the department (and shop if needed).
4.)    Maintain equipment and work area in a organized, clean, and safe manner.
     
     a.)    Maintain tools and equipment in proper working condition. 
     b.)    Completes Maintenance Requests, as necessary, using the Lotus Notes system.
7.)    Maintain material accountability, within the manufacturing area, by keeping all product and scrap tagged with the proper labels identifying work order number and type of material.
8.)    Maintains segregation of work order material and documentation by allowing only one job per workstation.
9.)    Initiates Deviation Reports, using Lotus Notes system, to identify / document / disposition nonconforming material during any state of manufacture.
Job Requirements :

Knowledge Skills and Abilities (KSA):
1.)    The ability to strictly adhere to Standard Operating Procedures, including all safety, health, and environmental procedures.
2.)    Knowledge and ability to operate a computer.
3.)    Knowledge of basic math skills including addition, subtraction, multiplication, division, percentages, proportions, and fractions.
4.)    Ability to use various measuring equipment including micrometers, laser micrometers, electronic balance, calipers, dial indicators , ELF, and Ram optical.
5.)    Good communication and time management skills.
6.)    Basic CNC/manual machining knowledge.
Physical Demands:
The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
1.)    Frequently required to stand; walk; sit; use hands to feel objects or handle tools or controls for extended periods of time. Also required to reach with hands and arms; stoop, kneel or crouch. 
2.)    Specific vision abilities required by the job include close vision, distance vision, peripheral vision, and depth perception. 
3.)    Manual dexterity and eye/hand coordination required.
4.)    May be required to occasionally lift or move up to 75 pounds.
5.)    Will be required to handle cleaning agents such as acetone and/or acid including nitric and muriatic acids on a daily basis. Follow the proper safety procedures for the handling and disposal of the above liquids with the proper safety equipment. Also required to handle lathe coolant on a daily basis.
Education / Experience:
1.)    2 year technical/associate degree preferred. High School Diploma or GED required. 
2.)    Previous machining experience (manual or CNC). 
3.)    Computer skills required for in house software including Visual Mfg, Lotus Notes, and Microsoft Office.
Due to the expected number of responses, only those most qualified will be contacted. No recruiters please; all unsolicited third-party submissions will be rejected.
Accellent is an Equal Opportunity Employer. To learn more about Accellent and our career opportunities, please visit us atwww.accellent.com
Career Level :Experienced (Non-Manager)
Education :High School or equivalent
% of Travel Required :0-10%
Shift/Hours :Second Shift (Afternoon)
]]></description>
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        <expiration_date>2010-03-25</expiration_date>
        <employer><![CDATA[Accellent Inc.]]></employer>
        <location><![CDATA[SALEM, VA, 24157, USA]]></location>
    </job>
    <job>
        <title><![CDATA[EDM Operator]]></title>
        <description><![CDATA[


Job Title :EDM Operator
Job Code :4232
Location :Brooklyn Park MN US 55429
Job Description :
Accellent, Inc. is a fully integrated provider of design, supply chain management and strategic sourcing services to the Medical Device industry. Accellentwww.accellent.com, a recognized market leader, is a fast-growing outsource manufacturing and design solution company specializing in high growth areas such as Cardiology, Endoscopy and Orthopaedics. The top Medical Device companies partner with Accellent to provide innovation, advanced technology, speed to market, low cost labor and strategic sourcing.
We&rsquo;re looking for team players with a can-do attitude to share in our vision and corporate values. Accellent offers competitive salaries; a comprehensive benefits package, and a stimulating work environment.
Currently, we are searching for a Wire EDM Operator to join our Brooklyn Park, MN facility.
About the Opportunity:

Operate EDM and other shop equipment to produce parts or add features to parts according to blueprints.
Include the following:
* Keep EDM machines running, inspect parts, have acceptable attendance, check parts from the operator before you, keep your work area clean.
* Provide support within the organization as experience and time allow.
* Other duties may be assigned.
Job Requirements :
Key Result Accountabilities
Language Skills:
Basic reading, writing, and communication skills.
Mathematical Skills:
Basic, Trigonometry helpful, ability to learn algebra.
Reasoning Ability:
Have the ability to work with all types of workers. Be able to troubleshoot and solve minor problems.
Physical Demands: 
The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job.
Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
 
 Qualifications
2 year vocational degree in CNC Machining preferred, but not required.
Ability to read a micrometer, read blue prints and use a microscope required.
 Experience manufacturing small parts with tight tolerances preferred


Due to the expected number of responses, only those most qualified will be contacted. No recruiters please; all unsolicited third-party submissions will be rejected.

Accellent is an Equal Opportunity/Affirmative Action employer and we value diversity in our workforce. As such we provide equal opportunity for all applicants without regard to race, religion, gender, national origin, age, marital status, veteran status, or disability. To learn more about Accellent and our career opportunities, please visit us atwww.accellent.com
Career Level :Experienced (Non-Manager)
Education :High School or equivalent
% of Travel Required :0-10%
Shift/Hours :First Shift (Day)
]]></description>
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            <industry><![CDATA[Health Products & Services]]></industry>
        </industries>
        <expiration_date>2010-03-25</expiration_date>
        <employer><![CDATA[Accellent Inc.]]></employer>
        <location><![CDATA[Brooklyn Park, MN, 55445, USA]]></location>
    </job>
    <job>
        <title><![CDATA[Sr. Quality Engineer (Molding)]]></title>
        <description><![CDATA[


Job Title :Sr. Quality Engineer (Molding)
Job Code :4229
Location :Juarez Chih MX 32470
Job Description :
Accellent, Inc. is a fully integrated provider of design, supply chain management and strategic sourcing services to the Medical Device industry. Accellentwww.accellent.com, a recognized market leader, is a fast-growing outsource manufacturing and design solution company specializing in high growth areas such as Cardiology, Endoscopy and Orthopaedics. The top Medical Device companies partner with Accellent to provide innovation, advanced technology, speed to market, low cost labor and strategic sourcing. 
We&rsquo;re looking for team players with a can-do attitude to share in our vision and corporate values. Accellent offers competitive salaries; a comprehensive benefits package, and a stimulating work environment. 
Currently, we are searching for a to join our facility.
About the Opportunity 

Position Scope/Summary
Quality assists in the design and implementation of policies and procedures for testing and evaluating the precision and accuracy of products and/or equipment. The Sr. Quality Engineer will be expected to provide support to Operations, interact with customers and provide support for Engineering, Quality Systems and Process engineering. 
Specializations may include but are not limited to: design control; material and process control; product reliability; software quality engineering; and/or metrology.
This position will be integral in meeting the Quality Management System requirements. It requires creativity and foresight to work with operations and product development teams to ensure compliance to the Quality Manual, Design Control, Supplier Management and other appropriate procedures for a variety of medical devices from concept through market introduction. The ideal candidate is a self-motivated individual who is excited by the prospect of working in a dynamic, fast-paced environment.
Key Result Accountabilities
&middot;    Maintain company compliance with FDA Quality System Regulations and ISO 13485 standards. Experience with FDA and ISO inspections and registration is a plus.
&middot;    Actively participates in internal audits, management review and other activities covered under Accellent Quality Manual, Policies and Procedures.
&middot;    Provide customer related quality and regulatory inquiries support.
&middot;    Compiles and writes training material and conducts training sessions on quality control activities.
&middot;    Provide QE direction, analysis and recommendations for Product Development to successfully launch new products into active production in a timely and cost effective manner. Directs development and maintenance of internal/external standards relative to Design and Development,
&middot;    Lead implementation of continuous improvement projects or act as subject matter expert for SPC, FMEA, DOE and process validation.
&middot;    Lead and provide Project Management support as needed.
&middot;    Develops and initiates standard methods for inspection, testing, and evaluation, utilizing knowledge in related engineering fields.
&middot;    Devices sampling procedures and designs and develops forms and instructions for recording, evaluating, and reporting quality and reliability data.
&middot;    Performs measurement system analyses to evaluate test and inspection equipment.
&middot;    Leads disposition of discrepant material and devises process to assess product quality and reliability.
&middot;    Monitors and directs engineering group on calibration requirements and implementation of systems to support equipment calibration.
&middot;    Lead supplier approval and qualification of new/revised items which includes inspection method development and validation as well as correlation with supplier&rsquo;s methods, supplier audits, management of supplier corrective and preventative actions and assist in FMEA. 
&middot;    Direct support for FDA and ISO inspections and registration.
&middot;    Directs workers engaged in measuring, testing, and tabulating data concerning quality and reliability.
&middot;    All other duties as assigned.
&middot;    Up to 10% travel may be required.
Environmental Working Conditions
Employee must comply with all safety policies and safe work procedures established by the company. Job tasks may also involve:      
&middot;    Using personal protective equipment such as safety glasses, goggles, gloves, and other equipment as established in company policies and safe work procedures.
&middot;    Working near cutting &amp; machining fluids, solvents, lubricants and other hazardous chemicals using appropriate safety controls.
Employee will be expected to attend safety training, and may serve on the facility safety committee and participate in hazard analysis and resolution.
Qualifications
&middot;    3-5 years experience as a Quality Engineer working directly in plastic injection molding tight tolerance medical parts and familiarity with sub-assemblies and contract manufacturing.
&middot;    Must have experience writing and carrying out IQ/OQ/PQ validation protocols.
&middot;    Experience in a medical device or FDA regulated environment, regulatory validation experience for Class II and Class III Medical Devices, including 510K submissions.
&middot;    Experience with FDA and ISO 13485 Certification inspections is a plus.
&middot;    Must be adept in use of computer software for the analysis of data, preferably Microsoft Excel and statistical packages (Minitab preferred). 
&middot;    Quality Engineering certification (CQE) preferred or equivalent body of knowledge in areas which include, but are not limited to Statistics, SPC, Geometric Dimensioning/Tolerancing; Sampling, Design of Experiments, etc. Ability to analyze, understand and effectively communicate this technical material. Experience with Lean Manufacturing and Six Sigma is a plus.
&middot;    Ability to organize and judge priorities in a dynamic, fast-paced environment and work independently with minimal supervision.
&middot;    Must possess excellent verbal &amp; written communication skills, which include but are not limited to presentation, organizational and management skills.
Job Requirements :



Due to the expected number of responses, only those most qualified will be contacted. No recruiters please; all unsolicited third-party submissions will be rejected.

Accellent is an Equal Opportunity/Affirmative Action employer and we value diversity in our workforce. As such we provide equal opportunity for all applicants without regard to race, religion, gender, national origin, age, marital status, veteran status, or disability. To learn more about Accellent and our career opportunities, please visit us atwww.accellent.com
Career Level :Experienced (Non-Manager)
Education :Bachelor's Degree
% of Travel Required :0-10%
Shift/Hours :First Shift (Day)
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        <expiration_date>2010-03-25</expiration_date>
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        <location><![CDATA[, USA]]></location>
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    <job>
        <title><![CDATA[Voice of Customer Manager (Manufacturing)]]></title>
        <description><![CDATA[


Job Title :Voice of Customer Manager (Manufacturing)
Job Code :4227
Location :Arvada CO US 80002
Job Description :

Accellent, Inc. is a fully integrated provider of design, supply chain management and strategic sourcing services to the Medical Device industry. Accellentwww.accellent.com, a recognized market leader, is a fast-growing outsource manufacturing and design solution company specializing in high growth areas such as Cardiology, Endoscopy and Orthopaedics. The top Medical Device companies partner with Accellent to provide innovation, advanced technology, speed to market, low cost labor and strategic sourcing.
We&rsquo;re looking for team players with a can-do attitude to share in our vision and corporate values. Accellent offers competitive salaries; a comprehensive benefits package, and a stimulating work environment.
Currently, we are searching for a to join a Customer Operations Manager to join our Arvada, CO facility.
Position Scope/Summary
The Customer Operations Manager will be expected to provide leadership, direction, and solution-oriented thinking to the Customer Operations Team. This team will be technically knowledgeable of the site&rsquo;s products, services and local processes and be able to use that understanding to provide solutions to customer requirements.
This position will ensure advocacy for the customer and work closely with Operations, Planning, Engineering, Quality, Technical Solutions, Customer Solutions, and Sales to provide solutions that fulfill our customers&rsquo; needs with speed, accuracy, and exceptional communication. This position will work directly with &ldquo;factory direct&rdquo; customers to service their quoting, order entry, and general service needs. The manager will be a member of the Site Leadership Team and a key partner with the Director of Operations.
Key Result AccountabilitiesChampion the voice of the customer as a member of the Site Leadership Team.
* Work with the Site Leadership team to instill customer advocacy within the facility.
* Serve as the voice of customer during customer production meetings and interactions with facility personnel
* Represent Accellent and the site to the customer and Sales as appropriate in conjunction with customer communication, visits and issue resolution.
Partner with Customers and Sales organization to meet customer requirements and grow sales
* Develop and foster customer relationships by working directly with Factory Direct customers and partnering with Sales and/or CSR&rsquo;s for Strategic and Multi-Site customers
* Communicate with customers and other Accellent functions (i.e. Sales, Customer Service, Technical Solutions) to fully understand customer requirements.
* Demonstrate responsiveness and leadership in interactions with customers, Sales and CSR&rsquo;s.
* Ensure that all customer contractual obligations are implemented and maintained as required
* In relation toCorporate/Multi-site Customers: a. Provide information and input to Sales/CSR team as needed to grow sales and meet customer requirements. b. Provide data for Quarterly Business Reviews and participate in reviews c. Provide information and input to the annual and monthly forecasting process, including reconciliation to the monthly facility forecast. 6. In relation to Factory Direct Customers: a. Develop and manage sales goals for Factory Direct Customers b. Identify and develop sales growth opportunities for Factory Direct Customers c. Coordinate with Customer Operations at other facilities to develop cross-facility sales opportunities. d. Prepare and deliver sales presentations and customer visits to support sales efforts. e. Develop and administer customer contracts and supply agreements f. Responsible for timely and accurate forecasting for Factory Direct CustomersEnsure Customer Operations Processes are executed accurately and within established timeframes
* Order Entry/Confirmation a. Execute contract review and order entry process for Factory Direct Customers b. Support CSR group with information needs for contract review, order entry and confirmation process c. Work with Site Planning and Operations to establish and communicate standard product lead times.
* Change Order and expedite requests a. Work with facility personnel (Planning, Operations and Purchasing) to meet customer requests for items such as order expedites and change requests b. Communicate and monitor plans for expedite requests and recovery plans to Sales, CSR&rsquo;s, Customers and Operations as required to meet commitments
* Quoting a. Execute quotation process for Repeat and Standard Products b. Support Technical Solutions group for New Product quotations c. Liaison with TS on New Product quotations and new cost model development and deployment
* Configuration Engineering a. Execute configuring items/BOMs/Routings to support CS and Operations. b. Manage configuration changes as required by customers, Customer Operations or Operations. c. Provide information and input to the quoting process
* Align and maintain local processes and procedures with the Global Customer Operations processes and procedures. 6. Work with the Customer Operations Team members to identify process improvement opportunities to better serve the customersLead and manage Site Customer Operations Team
* Ensure that Customer Operations Team has the training and knowledge to utilize Oracle (or designated system) for quoting, order entry, and configuration engineering
* Provide leadership to Customer Operations Team members including guidance, prioritization, training and support for daily activities.
* Drive team performance towards key metric targets, including Order Acknowledgement Cycle Time, Quote Cycle Time
* Coordinate and maintain Customer Operations back up system within the team
* Ensure team adherence to all ISO Certification requirements; participate in Customer Service related audits as requiredEnvironmental Working ConditionsThe work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
Job Requirements :
To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.  It is impossible to list every requirement for, or responsibility of, any position. Similarly we cannot identify all the skills a position may require since job responsibilities and the Company&rsquo;s needs may change over time. Therefore, the above job description is not comprehensive or exhaustive. The Company reserves the right to adjust, add to or eliminate any aspect of the above description. The Company also retains the right to require all employees to undertake additional or different job responsibilities when necessary to meet business needs.
Due to the expected number of responses, only those most qualified will be contacted. No recruiters please; all unsolicited third-party submissions will be rejected.
Accellent is an Equal Opportunity/Affirmative Action employer and we value diversity in our workforce. As such we provide equal opportunity for all applicants without regard to race, religion, gender, national origin, age, marital status, veteran status, or disability. To learn more about Accellent and our career opportunities, please visit us atwww.accellent.com
Career Level :Manager (Manager/Supervisor of Staff)
Education :Bachelor's Degree
% of Travel Required :0-10%
Shift/Hours :First Shift (Day)
]]></description>
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        <industries>
            <industry><![CDATA[Health Products & Services]]></industry>
        </industries>
        <expiration_date>2010-03-25</expiration_date>
        <employer><![CDATA[Accellent Inc.]]></employer>
        <location><![CDATA[Arvada, CO, 80005, USA]]></location>
    </job>
    <job>
        <title><![CDATA[Operator]]></title>
        <description><![CDATA[


Job Title :Operator
Job Code :4337
Location :Orchard Park NY US 14127
Job Description :
Position Scope / Summary
Operators are responsible for running primary machines to produce parts according to customer specifications.
Key Result Accountabilities
1.   Run machines assigned to achieve a utilization of at least 75% for the shift.
2.   Responsible for performing work that meets or exceeds our production standards and scrap rates that will achieve the metric goals for scrap, EBITDA, Fill Rate, Rework etc...
3.   Measure parts accurately according to the blueprint and collection plan.
4.   Knowledge of reading and using Collection Plan and blueprints in order to conduct frequency checks, both visually and dimensionally, using the appropriate measuring equipment.
5.   Be able to start, stop and produce single parts on the machine.
6.   Offset machines as needed. (when you are qualified to do so; an offset test will be given)
7.   Knowledge of Shop Control System in order to review and print paperwork needed for job and input data for work completed on various jobs.
8.   Create batches.
9.   Understand MVR procedures.
10. Keep work area clean.
11. Able to perform routine/daily maintenance of machines such as sumping machines, oil levels/ refills, filters for air cleaners and pumps.
12. Know who to go to for assistance.
13. Able to move around the team assigned, to run various jobs with competence and confidence.
14. Acquire the training needs to get the skills and knowledge necessary to get book 1 signed off. This book MUST be signed off. It is the company&rsquo;s responsibility to provide the training, but it is operator&rsquo;s responsibility to make sure book is signed off in a timely manner.
15. Other duties as necessary.
Environmental Working Conditions
&middot;    The physical demands described herein are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform essential functions.
&middot;    Ability to spend time using your hands to handle, control, or feel objects, tools or controls.
&middot;    Will spend extended periods of time standing and walking throughout the shop.
&middot;    Occasionally required to sit, stoop, kneel, bend, crouch, bend and twist.
&middot;    Ability to lift 1pound up to 50 lbs.

Job Requirements :
Qualifications
1.   Able to use microscope and other measuring equipment, to include micrometers, comparator, SmartScope, profilometer, thread gages, pins, etalon, and digital linear gage.
2.   Able to use computer, pulling up instructions and reading them.
3.   Able to use basic shop math.
4.   Able to read and understand blueprints.
5.   Able to follow instructions, both written and verbal.
6.   Able to count and box parts.
Career Level :Experienced (Non-Manager)
Education :Certification
% of Travel Required :0-10%
Shift/Hours :First Shift (Day)
]]></description>
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        <industries>
            <industry><![CDATA[Health Products & Services]]></industry>
        </industries>
        <expiration_date>2010-03-25</expiration_date>
        <employer><![CDATA[Accellent Inc.]]></employer>
        <location><![CDATA[Orchard Park, NY, 14127, USA]]></location>
    </job>
    <job>
        <title><![CDATA[Operator]]></title>
        <description><![CDATA[


Job Title :Operator
Job Code :4339
Location :Orchard Park NY US 14127
Job Description :
Position Scope / Summary
Operators are responsible for running primary machines to produce parts according to customer specifications.
Key Result Accountabilities
1.   Run machines assigned to achieve a utilization of at least 75% for the shift.
2.   Responsible for performing work that meets or exceeds our production standards and scrap rates that will achieve the metric goals for scrap, EBITDA, Fill Rate, Rework etc...
3.   Measure parts accurately according to the blueprint and collection plan.
4.   Knowledge of reading and using Collection Plan and blueprints in order to conduct frequency checks, both visually and dimensionally, using the appropriate measuring equipment.
5.   Be able to start, stop and produce single parts on the machine.
6.   Offset machines as needed. (when you are qualified to do so; an offset test will be given)
7.   Knowledge of Shop Control System in order to review and print paperwork needed for job and input data for work completed on various jobs.
8.   Create batches.
9.   Understand MVR procedures.
10. Keep work area clean.
11. Able to perform routine/daily maintenance of machines such as sumping machines, oil levels/ refills, filters for air cleaners and pumps.
12. Know who to go to for assistance.
13. Able to move around the team assigned, to run various jobs with competence and confidence.
14. Acquire the training needs to get the skills and knowledge necessary to get book 1 signed off. This book MUST be signed off. It is the company&rsquo;s responsibility to provide the training, but it is operator&rsquo;s responsibility to make sure book is signed off in a timely manner.
15. Other duties as necessary.
Environmental Working Conditions
&middot;    The physical demands described herein are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform essential functions.
&middot;    Ability to spend time using your hands to handle, control, or feel objects, tools or controls.
&middot;    Will spend extended periods of time standing and walking throughout the shop.
&middot;    Occasionally required to sit, stoop, kneel, bend, crouch, bend and twist.
&middot;    Ability to lift 1pound up to 50 lbs.
Job Requirements :
Qualifications
1.   Able to use microscope and other measuring equipment, to include micrometers, comparator, SmartScope, profilometer, thread gages, pins, etalon, and digital linear gage.
2.   Able to use computer, pulling up instructions and reading them.
3.   Able to use basic shop math.
4.   Able to read and understand blueprints.
5.   Able to follow instructions, both written and verbal.
6.   Able to count and box parts.
Career Level :Experienced (Non-Manager)
Education :Certification
% of Travel Required :0-10%
Shift/Hours :Third Shift (Night)
]]></description>
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            <industry><![CDATA[Health Products & Services]]></industry>
        </industries>
        <expiration_date>2010-03-25</expiration_date>
        <employer><![CDATA[Accellent Inc.]]></employer>
        <location><![CDATA[Orchard Park, NY, 14127, USA]]></location>
    </job>
    <job>
        <title><![CDATA[Production Operator]]></title>
        <description><![CDATA[


Job Title :Production Operator
Job Code :4341
Location :Galway Galway IE
Job Description :
* 
Position Scope
Involved in the execution of manufacturing operations to modify materials so that they comply with component, assembly and product drawings.
Position Summary
&middot;    Performs tasks in accordance with written work instructions to produce components and assemblies in accordance with drawings and specifications provided by the company or its customers.
&middot;    Regular and timely attendance is an essential responsibility of any general operative.
&middot;    Identifies and highlights methods of performing tasks in an efficient and cost effective manner. Identifies and makes suggestions for improvement to production and business processes to ensure continuous improvement.
&middot;    Reads drawings and job paperwork for product specifications.
&middot;    Repeatedly feeds and handles fine wire in a variety of wire manufacturing operations.
&middot;    Observes machine operation and verifies conformance of machined parts to drawing specifications. Performs in-process inspections to assure conformance of product. Adjusts machinery as needed to assure that part meets specifications.
o   Support and carry out all self-directed team meetings with the operators assign area.
o   Maintain and improve 5s standards within the Accellent
o   Participate in the daily scheduling of jobs through the department.
o   Communicate with other personnel as required to meet the production schedule
o   Support supervisor in reinforcing all company procedure compliance and optimization.
* Production efficiency
* Ensure raw material is issued correctly to production jobs in the ERP system
* Monitor VMI (Vendor managed Inventory) programs.
* Monitor production cycle times by process
Key Result Accountabilities
&middot;    Perform Duties and work through Self Directed Teams to Achieve Accellent Galway Operation's Goals including Fill Rate, Customer Lot Acceptance and Cycle Time.  
&middot;    Perform duties to ensure the day to day production department meets all customer requirements
&middot;    Ability to carry out instructions outlined in Standard Operating Procedures.
&middot;    Ability to ensure execution of the daily production schedule.
&middot;      Adhere to all company polices
Environmental Working Conditions
Normally works in a machine shop or the assembly area. Incumbent will be subject to environmental conditions existing in all these areas.
Health and Safety Responsibilities
* Employees shall comply with and understand the Accellent safety rules, safety statement, policies, procedures and/or all regulations related to health and safety as detailed by Accellent.
* Each employee is responsible for their own health, safety and welfare and that of others affected by their actions, errors or omissions at work.
* To ensure that Health and Safety will be considered fundamental to the design and operation of work.
&middot;    Attend and actively participate in toolbox talks
&middot;   Ensure all relevant activities conducted are planned so that they are conducted in a safe manner.
&middot;   Ensure systems of work that are planned, organized, performed and maintained through safe work instructions.understand the Accellent safety rules, safety statement, policies, procedures and/or all regulations related to health and safety as detailed by Accellent.
* Each employee is responsible for their own health, safety and welfare and that of others affected by their actions, errors or omissions at work.
* Defects/Issues with plant, equipment or system of work must be reported to management.
* To ensure that Health and Safety will be considered fundamental to the design and operation of work.
Job Requirements :
Qualifications
&middot;    Educated to leaving certificate standard or equivalent.
&middot;    Experience in a previous manufacturing environment is desirable.
&middot;    An intermediate level of English is required
&middot;    A good understanding of basic math calculations is essential. Demonstrated ability to read and interpret measurement instruments (micrometers, rulers, comparators etc.) and engineering drawings is advantageous.
&middot;    Will be able to work individually and/or as part of a manufacturing team to execute production plans and tasks in an efficient manner that ensures the customers gets a quality product at the required time.
&middot;    Good interpersonal skills and a demonstrated ability and willingness to get along with fellow workers are essential.
Career Level :Entry Level
Education :High School or equivalent
% of Travel Required :0-10%
Shift/Hours :First Shift (Day)
]]></description>
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        <industries>
            <industry><![CDATA[Health Products & Services]]></industry>
        </industries>
        <expiration_date>2010-03-25</expiration_date>
        <employer><![CDATA[Accellent Inc.]]></employer>
        <location><![CDATA[, USA]]></location>
    </job>
    <job>
        <title><![CDATA[Production Operator]]></title>
        <description><![CDATA[


Job Title :Production Operator
Job Code :4342
Location :Galway Galway IE
Job Description :
* 
Position Scope
Involved in the execution of manufacturing operations to modify materials so that they comply with component, assembly and product drawings.
Position Summary
&middot;    Performs tasks in accordance with written work instructions to produce components and assemblies in accordance with drawings and specifications provided by the company or its customers.
&middot;    Regular and timely attendance is an essential responsibility of any general operative.
&middot;    Identifies and highlights methods of performing tasks in an efficient and cost effective manner. Identifies and makes suggestions for improvement to production and business processes to ensure continuous improvement.
&middot;    Reads drawings and job paperwork for product specifications.
&middot;    Repeatedly feeds and handles fine wire in a variety of wire manufacturing operations.
&middot;    Observes machine operation and verifies conformance of machined parts to drawing specifications. Performs in-process inspections to assure conformance of product. Adjusts machinery as needed to assure that part meets specifications.
o   Support and carry out all self-directed team meetings with the operators assign area.
o   Maintain and improve 5s standards within the Accellent
o   Participate in the daily scheduling of jobs through the department.
o   Communicate with other personnel as required to meet the production schedule
o   Support supervisor in reinforcing all company procedure compliance and optimization.
* Production efficiency
* Ensure raw material is issued correctly to production jobs in the ERP system
* Monitor VMI (Vendor managed Inventory) programs.
* Monitor production cycle times by process
Key Result Accountabilities
&middot;    Perform Duties and work through Self Directed Teams to Achieve Accellent Galway Operation's Goals including Fill Rate, Customer Lot Acceptance and Cycle Time.  
&middot;    Perform duties to ensure the day to day production department meets all customer requirements
&middot;    Ability to carry out instructions outlined in Standard Operating Procedures.
&middot;    Ability to ensure execution of the daily production schedule.
&middot;      Adhere to all company polices
Environmental Working Conditions
Normally works in a machine shop or the assembly area. Incumbent will be subject to environmental conditions existing in all these areas.
Health and Safety Responsibilities
* Employees shall comply with and understand the Accellent safety rules, safety statement, policies, procedures and/or all regulations related to health and safety as detailed by Accellent.
* Each employee is responsible for their own health, safety and welfare and that of others affected by their actions, errors or omissions at work.
* To ensure that Health and Safety will be considered fundamental to the design and operation of work.
&middot;    Attend and actively participate in toolbox talks
&middot;   Ensure all relevant activities conducted are planned so that they are conducted in a safe manner.
&middot;   Ensure systems of work that are planned, organized, performed and maintained through safe work instructions.understand the Accellent safety rules, safety statement, policies, procedures and/or all regulations related to health and safety as detailed by Accellent.
* Each employee is responsible for their own health, safety and welfare and that of others affected by their actions, errors or omissions at work.
* Defects/Issues with plant, equipment or system of work must be reported to management.
* To ensure that Health and Safety will be considered fundamental to the design and operation of work.
Job Requirements :
Qualifications
&middot;    Educated to leaving certificate standard or equivalent.
&middot;    Experience in a previous manufacturing environment is desirable.
&middot;    An intermediate level of English is required
&middot;    A good understanding of basic math calculations is essential. Demonstrated ability to read and interpret measurement instruments (micrometers, rulers, comparators etc.) and engineering drawings is advantageous.
&middot;    Will be able to work individually and/or as part of a manufacturing team to execute production plans and tasks in an efficient manner that ensures the customers gets a quality product at the required time.
&middot;    Good interpersonal skills and a demonstrated ability and willingness to get along with fellow workers are essential.
Career Level :Entry Level
Education :High School or equivalent
% of Travel Required :0-10%
Shift/Hours :Second Shift (Afternoon)
]]></description>
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        <industries>
            <industry><![CDATA[Health Products & Services]]></industry>
        </industries>
        <expiration_date>2010-03-25</expiration_date>
        <employer><![CDATA[Accellent Inc.]]></employer>
        <location><![CDATA[, USA]]></location>
    </job>
    <job>
        <title><![CDATA[Production Operator]]></title>
        <description><![CDATA[


Job Title :Production Operator
Job Code :4343
Location :Galway Galway IE
Job Description :
* 
Position Scope
Involved in the execution of manufacturing operations to modify materials so that they comply with component, assembly and product drawings.
Position Summary
&middot;    Performs tasks in accordance with written work instructions to produce components and assemblies in accordance with drawings and specifications provided by the company or its customers.
&middot;    Regular and timely attendance is an essential responsibility of any general operative.
&middot;    Identifies and highlights methods of performing tasks in an efficient and cost effective manner. Identifies and makes suggestions for improvement to production and business processes to ensure continuous improvement.
&middot;    Reads drawings and job paperwork for product specifications.
&middot;    Repeatedly feeds and handles fine wire in a variety of wire manufacturing operations.
&middot;    Observes machine operation and verifies conformance of machined parts to drawing specifications. Performs in-process inspections to assure conformance of product. Adjusts machinery as needed to assure that part meets specifications.
o   Support and carry out all self-directed team meetings with the operators assign area.
o   Maintain and improve 5s standards within the Accellent
o   Participate in the daily scheduling of jobs through the department.
o   Communicate with other personnel as required to meet the production schedule
o   Support supervisor in reinforcing all company procedure compliance and optimization.
* Production efficiency
* Ensure raw material is issued correctly to production jobs in the ERP system
* Monitor VMI (Vendor managed Inventory) programs.
* Monitor production cycle times by process
Key Result Accountabilities
&middot;    Perform Duties and work through Self Directed Teams to Achieve Accellent Galway Operation's Goals including Fill Rate, Customer Lot Acceptance and Cycle Time.  
&middot;    Perform duties to ensure the day to day production department meets all customer requirements
&middot;    Ability to carry out instructions outlined in Standard Operating Procedures.
&middot;    Ability to ensure execution of the daily production schedule.
&middot;      Adhere to all company polices
Environmental Working Conditions
Normally works in a machine shop or the assembly area. Incumbent will be subject to environmental conditions existing in all these areas.
Health and Safety Responsibilities
* Employees shall comply with and understand the Accellent safety rules, safety statement, policies, procedures and/or all regulations related to health and safety as detailed by Accellent.
* Each employee is responsible for their own health, safety and welfare and that of others affected by their actions, errors or omissions at work.
* To ensure that Health and Safety will be considered fundamental to the design and operation of work.
&middot;    Attend and actively participate in toolbox talks
&middot;   Ensure all relevant activities conducted are planned so that they are conducted in a safe manner.
&middot;   Ensure systems of work that are planned, organized, performed and maintained through safe work instructions.understand the Accellent safety rules, safety statement, policies, procedures and/or all regulations related to health and safety as detailed by Accellent.
* Each employee is responsible for their own health, safety and welfare and that of others affected by their actions, errors or omissions at work.
* Defects/Issues with plant, equipment or system of work must be reported to management.
* To ensure that Health and Safety will be considered fundamental to the design and operation of work.
Job Requirements :
Qualifications
&middot;    Educated to leaving certificate standard or equivalent.
&middot;    Experience in a previous manufacturing environment is desirable.
&middot;    An intermediate level of English is required
&middot;    A good understanding of basic math calculations is essential. Demonstrated ability to read and interpret measurement instruments (micrometers, rulers, comparators etc.) and engineering drawings is advantageous.
&middot;    Will be able to work individually and/or as part of a manufacturing team to execute production plans and tasks in an efficient manner that ensures the customers gets a quality product at the required time.
&middot;    Good interpersonal skills and a demonstrated ability and willingness to get along with fellow workers are essential.
Career Level :Entry Level
Education :High School or equivalent
% of Travel Required :0-10%
Shift/Hours :First Shift (Day)
]]></description>
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        <industries>
            <industry><![CDATA[Health Products & Services]]></industry>
        </industries>
        <expiration_date>2010-03-25</expiration_date>
        <employer><![CDATA[Accellent Inc.]]></employer>
        <location><![CDATA[, USA]]></location>
    </job>
    <job>
        <title><![CDATA[Machinist (West) - Weekend Shift]]></title>
        <description><![CDATA[


Job Title :Machinist (West) - Weekend Shift
Job Code :4357
Location :Salem VA US 24153
Job Description :
Accellent, Inc. is a fully integrated provider of design, supply chain management and strategic sourcing services to the Medical Device industry. Accellenta recognized market leader, is a fast-growing outsource manufacturing and design solution company specializing in high growth areas such as Cardiology, Endoscopy and Orthopaedics. The top Medical Device companies partner with Accellent to provide innovation, advanced technology, speed to market, low cost labor and strategic sourcing. 
We&rsquo;re looking for team players with a can-do attitude to share in our vision and corporate values. Accellent offers competitive salaries; a comprehensive benefits package, and a stimulating work environment. 
Currently, we are searching for a Machinist for our weekend only shift (Friday, Saturday, and Sunday) to join our Salem, Virginia facility. 




Essential Duties and Responsibilities: 
1.)     Must achieve all training certifications required in the training database for this job.
2.)     Perform the tasks and procedures required to move jobs through the department in a timely manner.

3.)     Maintain production and material control systems as needed to ensure proper job and material tracking is  maintained

4.)     Complete off-schedule notifications.

5.)     Maintain work area and equipment in a clean, neat, and organized fashion.

6.)     Champion the Accellent's Values and assist in developing an understanding of these values in fellow employees.

Job Requirements :
Knowledge Skills and Abilities (KSA):
1.) Ability to effectively communicate with other operators.
2.) Mechanical aptitude and ability to work with a wide variety of equipment.
3.) The ability to strictly adhere to Standard Operating Procedures, including all safety, health, and environmental procedures.
4.) Knowledge of basic math skills including addition, subtraction, multiplication, division, percentages, proportions, and fractions.
5.) The ability to use various measuring devices including micrometers, laser micrometers, electronic balance, calipers, and pin gauges.
6.) Capable of performing basic computer tasks.


Due to the expected number of responses, only those most qualified will be contacted. No recruiters please; all unsolicited third-party submissions will be rejected.

Accellent is an Equal Opportunity/Affirmative Action employer and we value diversity in our workforce. As such we provide equal opportunity for all applicants without regard to race, religion, gender, national origin, age, marital status, veteran status, or disability. To learn more about Accellent and our career opportunities, please visit us atwww.accellent.com
Career Level :Experienced (Non-Manager)
Education :High School or equivalent
% of Travel Required :0-10%
Shift/Hours :Weekend
]]></description>
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        <industries>
            <industry><![CDATA[Health Products & Services]]></industry>
        </industries>
        <expiration_date>2010-03-25</expiration_date>
        <employer><![CDATA[Accellent Inc.]]></employer>
        <location><![CDATA[Salem, VA, 24157, USA]]></location>
    </job>
    <job>
        <title><![CDATA[Project Engineer]]></title>
        <description><![CDATA[


Job Title :Project Engineer
Job Code :4364
Location :Laconia NH US 03247
Job Description :
Accellent, Inc. is a fully integrated provider of design, supply chain management and strategic sourcing services to the Medical Device industry. Accellentwww.accellent.com, a recognized market leader, is a fast-growing outsource manufacturing and design solution company specializing in high growth areas such as Cardiology, Endoscopy and Orthopaedics. The top Medical Device companies partner with Accellent to provide innovation, advanced technology, speed to market, low cost labor and strategic sourcing. 
Currently, we are searching for aProject Engineer tojoin our Laconia, NH facility.

The Project Engineer provides support to the Laconia Manufacturing Engineering Team and leadership for device assembly transfers and sustaining activities. The position is responsible for planning (scheduling, resourcing and costs) of the project from initiation through production launch. The Project Engineer leads the project team functions to successfully fulfill project requirements and addresses team needs throughout the project life. The Project Engineer leads scheduling discussions for the company during customer meetings and provides timely information to the customer on the progress of their projects. The Project Engineer is responsible for the creation, transfer and review of manufacturing documentation and can lead elements of equipment installation and process validation in partnership with quality engineering members. Identify manufacturing and customer requirements by review of product specifications and manufacturing documentation.
Responsibilities:
&middot;    Lead in problem-solving and trouble-shooting of processes, materials, and tooling to improve efficiency and cost of quality
&middot;    Lead in the start up, debugging and process optimization for new production processes
&middot;    Can lead in the preparation of specifications for materials, devise and run tests to ensure product quality
&middot;    Manage inter-business unit components and/or assembly projects
&middot;    Ensure projects adhere to Accellent control procedures
&middot;    Utilize planning software, typically MS Project, for management of projects
&middot;    Act as primary point of contact with the customer
&middot;    Responsible for the project design history file and adherence to Accellent Quality Standards and FDA QSRs for design controls and quality systems.
&middot;    Comply with work rules including those pertaining to safety, health, quality and Accellent Quality Management Systems.
&middot;    Manage technical transfers including, but not limited to, line layout, BOM, routers, work instructions and equipment.
Job Requirements :
. 
Job Requirements:
* BS ME or equivalent in an engineering technology
* 10 years' experience in component manufacturing and two years' experience in project planning. Medical device experience is desired.
* Catheter product experience and/or medical device product and manufacturing experience highly desired
* Six Sigma and/or Lean continuous process improvement experience desired.
* Proficient in the use of the principles and theories of science, engineering and mathematics to solve technical problems and implement creative solutions under minimal supervision.
* A solid understanding of product assembly and manufacturing operations also is required.
* Experience interfacing with suppliers, customers.
* Make appropriate decisions based on a variety of input and options. He/she must be able to write, follow and/or modify procedures as required for a project or for standard procedures.
* Able to write minutes, reports and general documentation that are clear and concise.
* Work well in a team environment and be able to facilitate discussions, conference calls and meetings with customers, suppliers and co-workers as related to the job. Proficiency with Microsoft Office including Microsoft Word, Excel and PowerPoint and familiarity with Microsoft Access, Mini Tab, Project and the Internet are expected.
* This is a hands-on position. Project Engineers frequently exert ten or more pounds of force and require visual acuity and hearing ability with or without accommodation for reading machine dial gauges, blue-prints and precision measuring and monitoring machine sounds for diagnostic purposes. 

Due to the expected number of responses, only those most qualified will be contacted. No recruiters please; all unsolicited third-party submissions will be rejected.

Accellent is an Equal Opportunity/Affirmative Action employer and we value diversity in our workforce. As such we provide equal opportunity for all applicants without regard to race, religion, gender, national origin, age, marital status, veteran status, or disability. To learn more about Accellent and our career opportunities, please visit us atwww.accellent.com
Career Level :Experienced (Non-Manager)
Education :Bachelor's Degree
% of Travel Required :0-10%
Shift/Hours :First Shift (Day)
]]></description>
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        <industries>
            <industry><![CDATA[Health Products & Services]]></industry>
        </industries>
        <expiration_date>2010-03-25</expiration_date>
        <employer><![CDATA[Accellent Inc.]]></employer>
        <location><![CDATA[Laconia, NH, 03246, USA]]></location>
    </job>
    <job>
        <title><![CDATA[Machinist]]></title>
        <description><![CDATA[


Job Title :Machinist
Job Code :4376
Location :SALEM VA US 24153
Job Description :
Accellent, Inc. is a fully integrated provider of design, supply chain management and strategic sourcing services to the Medical Device industry. Accellentwww.accellent.com, a recognized market leader, is a fast-growing outsource manufacturing and design solution company specializing in high growth areas such as Cardiology, Endoscopy and Orthopaedics. The top Medical Device companies partner with Accellent to provide innovation, advanced technology, speed to market, low cost labor and strategic sourcing.
We&rsquo;re looking for team players with a can-do attitude to share in our vision and corporate values. Accellent offers competitive salaries; a comprehensive benefits package, and a stimulating work environment.
Currently, we are searching for a Machinist to join our Salem, Virginia facility. 

Essential Duties and Responsibilities:
1.)    Achieve training certifications as specified in the training database for this job.
2.)    Perform tasks and procedures daily as required to move jobs through the micro machining area.
     a.)    Run machines at their optimum capacity to keep jobs up to date per micro machining scheduling board by achieving pieces per hour scheduled.
     
     b.)    Perform all in process inspections and tool changes during job runs.
     
     c.)    Perform final processing of jobs and forwarding to the next department.
     
     d.)    Document jobs on a daily basis including set-up sheets, material accountability, run time
           log, and any other spreadsheets or forms.
3.)    Assist in the development and continual improvement of the manufacturing processes and systems by supporting and participating in daily production activities.
     a.)    Identify and communicate opportunities to make improvements to the area.
b.)    Transfers knowledge, information, observations, and other communication throughout the department (and shop if needed).
4.)    Maintain equipment and work area in a organized, clean, and safe manner.
     
     a.)    Maintain tools and equipment in proper working condition. 
     b.)    Completes Maintenance Requests, as necessary, using the Lotus Notes system.
7.)    Maintain material accountability, within the manufacturing area, by keeping all product and scrap tagged with the proper labels identifying work order number and type of material.
8.)    Maintains segregation of work order material and documentation by allowing only one job per workstation.
9.)    Initiates Deviation Reports, using Lotus Notes system, to identify / document / disposition nonconforming material during any state of manufacture.
Job Requirements :

Knowledge Skills and Abilities (KSA):
1.)    The ability to strictly adhere to Standard Operating Procedures, including all safety, health, and environmental procedures.
2.)    Knowledge and ability to operate a computer.
3.)    Knowledge of basic math skills including addition, subtraction, multiplication, division, percentages, proportions, and fractions.
4.)    Ability to use various measuring equipment including micrometers, laser micrometers, electronic balance, calipers, dial indicators , ELF, and Ram optical.
5.)    Good communication and time management skills.
6.)    Basic CNC/manual machining knowledge.
Physical Demands:
The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
1.)    Frequently required to stand; walk; sit; use hands to feel objects or handle tools or controls for extended periods of time. Also required to reach with hands and arms; stoop, kneel or crouch. 
2.)    Specific vision abilities required by the job include close vision, distance vision, peripheral vision, and depth perception. 
3.)    Manual dexterity and eye/hand coordination required.
4.)    May be required to occasionally lift or move up to 75 pounds.
5.)    Will be required to handle cleaning agents such as acetone and/or acid including nitric and muriatic acids on a daily basis. Follow the proper safety procedures for the handling and disposal of the above liquids with the proper safety equipment. Also required to handle lathe coolant on a daily basis.
Education / Experience:
1.)    2 year technical/associate degree preferred. High School Diploma or GED required. 
2.)    Previous machining experience (manual or CNC). 
3.)    Computer skills required for in house software including Visual Mfg, Lotus Notes, and Microsoft Office.
Due to the expected number of responses, only those most qualified will be contacted. No recruiters please; all unsolicited third-party submissions will be rejected.
Accellent is an Equal Opportunity Employer. To learn more about Accellent and our career opportunities, please visit us atwww.accellent.com
Career Level :Experienced (Non-Manager)
Education :High School or equivalent
% of Travel Required :0-10%
Shift/Hours :Second Shift (Afternoon)
]]></description>
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            <industry><![CDATA[Health Products & Services]]></industry>
        </industries>
        <expiration_date>2010-03-25</expiration_date>
        <employer><![CDATA[Accellent Inc.]]></employer>
        <location><![CDATA[SALEM, VA, 24157, USA]]></location>
    </job>
    <job>
        <title><![CDATA[Technical Business Development Leader]]></title>
        <description><![CDATA[


Job Title :Technical Business Development Leader
Job Code :4387
Location :1. Cincinnati OH US 45999
2. Chicago IL US 60652
Job Description :
Accellent, Inc. is a fully integrated provider of design, supply chain management and strategic sourcing services to the Medical Device industry. Accellentwww.accellent.com, a recognized market leader, is a fast-growing outsource manufacturing and design solution company specializing in high growth areas such as Cardiology, Endoscopy and Orthopaedics. The top Medical Device companies partner with Accellent to provide innovation, advanced technology, speed to market, low cost labor and strategic sourcing.
We&rsquo;re looking for team players with a can-do attitude to share in our vision and corporate values. Accellent offers competitive salaries; a comprehensive benefits package, and a stimulating work environment.
Currently, we are searching for a Technical Business Development Leader to join our team..
About the Opportunity:
The role of a Technical Business Development Leader is to obtain new business opportunities by providing technical and engineering support to customers leveraging Accellent&rsquo;s processing capabilities and technical expertise. The Technical Business Development Leader will engage customers with sound technical consultation and will define, support, close, monitor, and report on development-related and new business opportunities, programs, contracts and agreements. Through their technical leadership, the TBDL will develop and grow the business relationship between our customers and Accellent, increasing our revenue and profitability. 
The ideal candidate will be a degreed engineer with a robust background in the design, program management or manufacturing engineering of endoscopic medical devices.
The TBDL will focus on:
New Opportunity Identification and Qualification
* Applies a broad knowledge of Accellent's services, products and manufacturing capabilities to scope and develop large opportunities and close sales.
* Work with customer&rsquo;s technical/engineering group to develop new products utilizing Accellent&rsquo;s capabilities and core competencies.
* Coordinate with the Accellent Project Managers and Directors of Sales to translate customers&rsquo; requirements into actionable activities for Accellent.
* Responsible for customer-facing activities related to execution of prototypes and pre-production builds.
* Provide input from customers to assist with cost estimating and project scheduling for development projects.
* Support proposal activity for new business.
* Identify cost reduction initiatives for customer&rsquo;s and develop and win new business opportunities.
* Directly responsible for growing Accellen&rsquo;t Risk Adjusted Sales Pipeline and Market Revenue.Technical Sales Activities
* Lead technical discussions and promote Accellent capabilities to new and existing customers using available tools such as technical fairs and forums.
* Proactively identify and scope new business opportunities with active involvement in customer&rsquo;s R&amp;D, product development, and operations teams.
* Effectively work with Accellent Technical Solutions and manufacturing facilities to identify, scope, and sell appropriate supply chain solutions to our customers.
* Ensure project confidentiality and coordinate Non-Disclosure Agreements with customersAccount Management Support
* Work with the Sales Account Management teams to understand the full scope of customer&rsquo;s business including executing corporate direction, identifying design and development opportunities, providing technical consultation, implementing strategic deals and revenue growth.
* Work directly with customers to identify and provide solutions to their supply chain management challenges, including development, design, and manufacturing requirements.
* Responsible for technical and NPD customer satisfaction.
* Communicate effectively across Accellent all customer concerns and obtain additional assistance / support when required.Strategic Market Segment Development
* Responsible for the implementation of strategic directions defined by the Business Platform Leader.
* Identifies key initiatives and opportunities to the Business Platform Leader
* Identify capability gaps within market segments and help to prioritize development of missing capabilities.
* Assist in identifying technology trends and market dynamics.
* Support marketing efforts, as required, for example supporting trade shows
* Actively participate in the development of the Accellent Technology Plan 
Job Requirements :
* Bachelor degree in Mechanical Engineering, Materials Engineering, or similar discipline.
* 5-7 years experience in an engineering position required.
* Minimum, 5 years experience in the manufacture preferably of endoscopic devices and/or components.
* Minimum: 2 years experience in project planning and scheduling.
* Ability to call on and influence customer&rsquo;s technical/engineering group.
* Must have a good understanding of the OEM&rsquo;s specific market and needs.
* Possess a deep understanding of company strategy and capabilities.
* Ability to manage multiple tasks in multiple geographic locations.
* Ability to understand and negotiate for profitability and long term relationships.
* Ability to provide critical analysis of a concept or problem and provide an appropriate resolution. Must be able to provide novel and creative solutions for device design, manufacturing, and assembly.
* Ability to communicate well with clients, suppliers, and coworkers and work well in a team environment.
* Excellent communication skills with the ability to clearly communicate issues and potential resolutions in a timely manner to management or clients.
* Ability to respond to changing priorities with minimum disruption.
* Ability to find solutions with minimal supervision and seek guidance or direction when appropriate
* Ability to provide technical leadership in discussions, conference calls and meetings with customers and staff as related to the job responsibilities.
* Ability to read, understand, and interpret technical drawings, models, and schematics.
* Proficient computer skills, Outlook, Excel, Project, Word &amp; PowerPoint. CAD &amp; Design programs a plus.
Due to the expected number of responses, only those most qualified will be contacted. No recruiters please; all unsolicited third-party submissions will be rejected.
Accellent is an Equal Opportunity/Affirmative Action employer and we value diversity in our workforce. As such we provide equal opportunity for all applicants without regard to race, religion, gender, national origin, age, marital status, veteran status, or disability. To learn more about Accellent and our career opportunities, please visit us atwww.accellent.com
Career Level :Experienced (Non-Manager)
Education :Bachelor's Degree
% of Travel Required :50-60%
Shift/Hours :First Shift (Day)
]]></description>
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        <industries>
            <industry><![CDATA[Health Products & Services]]></industry>
        </industries>
        <expiration_date>2010-03-25</expiration_date>
        <employer><![CDATA[Accellent Inc.]]></employer>
        <location><![CDATA[Cincinnati, OH, 45217, USA]]></location>
    </job>
    <job>
        <title><![CDATA[Manufacturing Engineer]]></title>
        <description><![CDATA[


Job Title :Manufacturing Engineer
Job Code :4469
Location :Trenton GA US 30752
Job Description :
Accellent, Inc. is a fully integrated provider of design, supply chain management and strategic sourcing services to the Medical Device industry. Accellentwww.accellent.com, a recognized market leader, is a fast-growing outsource manufacturing and design solution company specializing in high growth areas such as Cardiology, Endoscopy and Orthopaedics. The top Medical Device companies partner with Accellent to provide innovation, advanced technology, speed to market, low cost labor and strategic sourcing. 
We&rsquo;re looking for team players with a can-do attitude to share in our vision and corporate values. Accellent offers competitive salaries; a comprehensive benefits package, and a stimulating work environment. 
We are seeking a Manufacturing Engineer for our Trenton, GA facility.
The Engineer will be expected to provide hands on Engineering support for Operations. Interacts with customers and provides support for Engineering and Quality Systems.
Responsibilities:
* Follows and develops Quality and Regulatory requirements including Accellent policies, procedures, and appropriate regulatory requirements.
* Develops and Executes Process and Test Method Validations (IQ, OQ, PQ, PPQ) in accordance with Accellent procedures and guidelines
* Communicates ideas, information, and recommendations clearly, effectively and frequently (oral and written) within Accellent, with outside suppliers or partners and with Accellent customers during formal and informal interactions.
* Prepares or reviews documentation with a high degree of accuracy, completeness, and effectiveness using common Accellent engineering tools &amp; templates were available. (Examples include specifications, manufacturing procedures, ECOs, and technical reports or analysis)
* Applies Lean manufacturing techniques to continuously improve cycle times and process flows. Identifies, and supports the execution of improvement efforts to reduce waste in all manufacturing and business processes.
* Uses structured problem solving techniques and statistical methods for data driven analysis and decisions.
* Applies DMAIC &ndash; Six Sigma approaches to solve issues and reduce variation in all manufacturing and business processes.
* Plans and executes project activities within a cross functional team. Project types can include new product development and introduction, manufacturing transfers, continuous improvement and cost reduction initiatives.
* Exhibits the Accellent values (Customer focus, Continuous Improvement, Performance, Accountability
Job Requirements :



Accellent is an Equal Opportunity/Affirmative Action employer and we value diversity in our workforce. As such we provide equal opportunity for all applicants without regard to race, religion, gender, national origin, age, marital status, veteran status, or disability. To learn more about Accellent and our career opportunities, please visit us atwww.accellent.com

Requirements:
* BS Mechanical Engineering or Chemical Engineering
* 3-5 years engineering experience preferably in a manufacturing environment
* Six Sigma Green Belt certification
* Continuous process improvement experience.
Career Level :Experienced (Non-Manager)
Education :Bachelor's Degree
% of Travel Required :0-10%
Shift/Hours :First Shift (Day)
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            <industry><![CDATA[Health Products & Services]]></industry>
        </industries>
        <expiration_date>2010-03-25</expiration_date>
        <employer><![CDATA[Accellent Inc.]]></employer>
        <location><![CDATA[Trenton, GA, 30752, USA]]></location>
    </job>
    <job>
        <title><![CDATA[Machine Operator]]></title>
        <description><![CDATA[


Job Title :Machine Operator
Job Code :4473
Location :Houston PA US 15342
Job Description :
Accellent, Inc. is a fully integrated provider of design, supply chain management and strategic sourcing services to the Medical Device industry. Accellentwww.accellent.com, a recognized market leader, is a fast-growing outsource manufacturing and design solution company specializing in high growth areas such as Cardiology, Endoscopy and Orthopaedics. The top Medical Device companies partner with Accellent to provide innovation, advanced technology, speed to market, low cost labor and strategic sourcing. 
We&rsquo;re looking for team players with a can-do attitude to share in our vision and corporate values. Accellent offers competitive salaries; a comprehensive benefits package, and a stimulating work environment. 
Currently, we are searching for a to join our facility.
About the Opportunity:




Job Title: 
Machine Operator 
Department: 
Manufacturing
Reports To: 
Manufacturing Manager 
Location: 
Pittsburgh
FLSA Status: 
Non-Exempt 
Division: 
Orthopaedics
Classification: 
Date: 
April 2008
Education: 
High School diploma or equivalent 
Organizational
Relationships: 
Internally  - Department employees, quality control employees, other operations employees
Externally  - Auditors
Position Scope/Summary
Performance of assigned manufacturing operations and related activities.
Key Result Accountabilities
* Perform manufacturing operations according to the company&rsquo;s Quality System and ensure satisfaction of customer requirements and specifications.*
* Perform required machinery/equipment maintenance.*
* Follow and maintain production schedules.*
* Completion of all required paperwork including identification and traceability.*
* Perform required in-process inspection and testing to ensure component compliance with customer requirements and specifications.*
* Monitor tooling/fixturing supply levels.
* Notify Shift Leader or Manufacturing Manager of any nonconformance or discrepant parts/materials.*
* Work with Shift Leaders on the development of manufacturing processes.
* Maintain a clean and safe work environment.
* Perform machinery set-ups as scheduled/required.*
* Follow company rules, regulations, and safety guidelines.
* Perform other duties as assigned by supervisory personnel.
*Essential function of the job

Qualifications
Strong math skills and mechanical aptitude. Computer skills preferred. Attention to fine detail and tolerances required.
Job Requirements :

Environmental Working Condition


Physical Demands
(without accommodations) 
Not at All
0% of workday 
Occasional
1-30% of workday 
Frequent
31-60% of workday 
Constant
61-100% of workday
Sitting 

X 

Standing 

X
Walking 

X
Climbing stairs/ladders 
X 

Push/Pull 
X 

Bending at waist (forward or sideways) 
X 

Simple grasping both hands 

X
Fine manipulation both hands 

X 

Lifting/Carrying items 0-10lbs. 

X 

Lifting/Carrying items 11-25lbs. 

X 

Lifting/Carrying items 26-50lbs. 
X 

Lifting/Carrying items 51-75lbs. 
X 

Lifting/Carrying items over 75lbs. 
X 

Functional near, far, color vision aided or unaided 

X
Functional hearing, aided or unaided 

X
Functional verbal communication skills 

X
Other 





Personal Protective Equipment required 

X



It is impossible to list every requirement for, or responsibility of, any position. Similarly we cannot identify all the skills a position may require since job responsibilities and the Company&rsquo;s needs may change over time. Therefore, the above job description is not comprehensive or exhaustive.  The Company reserves the right to adjust, add to or eliminate any aspect of the above description. The Company also retains the right to require all employees to undertake additional or different job responsibilities when necessary to meet business needs.

Due to the expected number of responses, only those most qualified will be contacted. No recruiters please; all unsolicited third-party submissions will be rejected.

Accellent is an Equal Opportunity/Affirmative Action employer and we value diversity in our workforce. As such we provide equal opportunity for all applicants without regard to race, religion, gender, national origin, age, marital status, veteran status, or disability. To learn more about Accellent and our career opportunities, please visit us atwww.accellent.com
Environmental Working Condition


Physical Demands
(without accommodations) 
Not at All
0% of workday 
Occasional
1-30% of workday 
Frequent
31-60% of workday 
Constant
61-100% of workday
Sitting 

X 

Standing 

X
Walking 

X
Climbing stairs/ladders 
X 

Push/Pull 
X 

Bending at waist (forward or sideways) 
X 

Simple grasping both hands 

X
Fine manipulation both hands 

X 

Lifting/Carrying items 0-10lbs. 

X 

Lifting/Carrying items 11-25lbs. 

X 

Lifting/Carrying items 26-50lbs. 
X 

Lifting/Carrying items 51-75lbs.
Career Level :Entry Level
Education :High School or equivalent
% of Travel Required :None
Shift/Hours :Third Shift (Night)
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        <industries>
            <industry><![CDATA[Health Products & Services]]></industry>
        </industries>
        <expiration_date>2010-03-25</expiration_date>
        <employer><![CDATA[Accellent Inc.]]></employer>
        <location><![CDATA[Houston, PA, 15342, USA]]></location>
    </job>
    <job>
        <title><![CDATA[Machine Operator]]></title>
        <description><![CDATA[


Job Title :Machine Operator
Job Code :4474
Location :Houston PA US 15342
Job Description :
Accellent, Inc. is a fully integrated provider of design, supply chain management and strategic sourcing services to the Medical Device industry. Accellentwww.accellent.com, a recognized market leader, is a fast-growing outsource manufacturing and design solution company specializing in high growth areas such as Cardiology, Endoscopy and Orthopaedics. The top Medical Device companies partner with Accellent to provide innovation, advanced technology, speed to market, low cost labor and strategic sourcing. 
We&rsquo;re looking for team players with a can-do attitude to share in our vision and corporate values. Accellent offers competitive salaries; a comprehensive benefits package, and a stimulating work environment. 
Currently, we are searching for a to join our facility.
About the Opportunity:




Job Title: 
Machine Operator 
Department: 
Manufacturing
Reports To: 
Manufacturing Manager 
Location: 
Pittsburgh
FLSA Status: 
Non-Exempt 
Division: 
Orthopaedics
Classification: 
Date: 
April 2008
Education: 
High School diploma or equivalent 
Organizational
Relationships: 
Internally  - Department employees, quality control employees, other operations employees
Externally  - Auditors
Position Scope/Summary
Performance of assigned manufacturing operations and related activities.
Key Result Accountabilities
* Perform manufacturing operations according to the company&rsquo;s Quality System and ensure satisfaction of customer requirements and specifications.*
* Perform required machinery/equipment maintenance.*
* Follow and maintain production schedules.*
* Completion of all required paperwork including identification and traceability.*
* Perform required in-process inspection and testing to ensure component compliance with customer requirements and specifications.*
* Monitor tooling/fixturing supply levels.
* Notify Shift Leader or Manufacturing Manager of any nonconformance or discrepant parts/materials.*
* Work with Shift Leaders on the development of manufacturing processes.
* Maintain a clean and safe work environment.
* Perform machinery set-ups as scheduled/required.*
* Follow company rules, regulations, and safety guidelines.
* Perform other duties as assigned by supervisory personnel.
*Essential function of the job
Qualifications
Strong math skills and mechanical aptitude. Computer skills preferred. Attention to fine detail and tolerances required.

Job Requirements :

Environmental Working Condition


Physical Demands
(without accommodations) 
Not at All
0% of workday 
Occasional
1-30% of workday 
Frequent
31-60% of workday 
Constant
61-100% of workday
Sitting 

X 

Standing 

X
Walking 

X
Climbing stairs/ladders 
X 

Push/Pull 
X 

Bending at waist (forward or sideways) 
X 

Simple grasping both hands 

X
Fine manipulation both hands 

X 

Lifting/Carrying items 0-10lbs. 

X 

Lifting/Carrying items 11-25lbs. 

X 

Lifting/Carrying items 26-50lbs. 
X 

Lifting/Carrying items 51-75lbs. 
X 

Lifting/Carrying items over 75lbs. 
X 

Functional near, far, color vision aided or unaided 

X
Functional hearing, aided or unaided 

X
Functional verbal communication skills 

X
Other 





Personal Protective Equipment required 

X



It is impossible to list every requirement for, or responsibility of, any position. Similarly we cannot identify all the skills a position may require since job responsibilities and the Company&rsquo;s needs may change over time. Therefore, the above job description is not comprehensive or exhaustive.  The Company reserves the right to adjust, add to or eliminate any aspect of the above description. The Company also retains the right to require all employees to undertake additional or different job responsibilities when necessary to meet business needs.

Due to the expected number of responses, only those most qualified will be contacted. No recruiters please; all unsolicited third-party submissions will be rejected.

Accellent is an Equal Opportunity/Affirmative Action employer and we value diversity in our workforce. As such we provide equal opportunity for all applicants without regard to race, religion, gender, national origin, age, marital status, veteran status, or disability. To learn more about Accellent and our career opportunities, please visit us atwww.accellent.com
Career Level :Entry Level
Education :High School or equivalent
% of Travel Required :None
Shift/Hours :Third Shift (Night)
]]></description>
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        <industries>
            <industry><![CDATA[Health Products & Services]]></industry>
        </industries>
        <expiration_date>2010-03-25</expiration_date>
        <employer><![CDATA[Accellent Inc.]]></employer>
        <location><![CDATA[Houston, PA, 15342, USA]]></location>
    </job>
    <job>
        <title><![CDATA[Sr. Supervisor Inventory Control]]></title>
        <description><![CDATA[


Job Title :Sr. Supervisor Inventory Control
Job Code :4477
Location :1. El Paso Texas US 79906
2. Juarez Chih MX 32420
Job Description :
Position Scope/Summary
The responsibility of a lead shipping/receiving person includes, but is not limited to: providing leadership and direction to a team of (1-4) personnel, as well as assigning work in specified work areas. Training ofmaterial handlersas required. &ldquo;On the job training&rdquo; and subsequent certification to all of the procedures pertinent to their specific assigned job level. Improving and/or maintaining warehouse organization in respect to safety, quality of work, product flow, product identification, FIFO, inventory control, and housekeeping. Leading Inventory Control process including cycle counting, identification of discrepancies, and discrepancy resolution. Timely response to customer needs including expedites of shipments, physical counts, control of customer supplied inventories.
Key Result Accountabilities
* Support management with the implementation of new policies and procedures, and direct team members ensuring complete conformance.
* Must be fully proficient in all duties related to shipping, receiving, and inventory control.
* Provide leadership and direction to assigned area of responsibility ensuring quality standards are met and daily assignments are carried out.
* Insure that staff follows all processes and instructions as dictated by quality procedures.
* Has the responsibility of establishing and following documentation for normal material handling requirements (receiving, inventory control and shipping).
* Responsible for labeling accuracy with proper description and information for shipping/receiving and inventory control purposes.
* Must train or assist personnel where applicable.
* Develop and possess the ability to initiate and accurately complete the required documentation (i.e. certificates of compliance, packing lists, shipping labels, foreign invoices, daily shipping lists, inventory labels, etc.)
* Possess and/or obtain necessary skills to accurately perform all required duties.
* Performs job duties with little or no supervision or assistance.
* Acts as a resource during audits or customer visits for questions and answers or practical demonstrations.
* Maintains cleanliness of work area, machines, tools, and equipment. (5S program in support of lean)
* Insure alignment of department resources in support of lean manufacturing and cell support teams.
* Performs job duties with little or no supervision or assistance.
&middot; Responsible for the safe operation and set-up of all warehousing equipment including lift trucks, pallet jacks, shrink wrappers, and scales. 
&middot; Responsible for performing routing preventive maintenance as assigned by Facilities Maintenance Manager.
&middot; Responsible for reporting any suspected machine malfunctions to the immediate supervisor of the area in which he/she is working.
&middot; Accurate documentation, reporting, time card maintenance.
&middot; Responsible for following material requisitioning procedures for kitting (issuance ) of raw materials , moving of all raw material and work in process materials.
&middot; Responsible for following all lot control procedures as defined by Q.A. Department.
&middot; Manages shop floor material transactions
&middot; Prints work order/ job travelers as needed.
&middot; Performs material transactions as required to include issuing material to jobs.
&middot; Monitors material transactions for accuracy and maintenance of traceability.
&middot; Reviews completed jobs for transaction integrity and uses information for necessary training and continued improvement.
&middot; Follow all instructions contained in work order packets including: MPR&rsquo;s, MPS&rsquo;s, and Work Instructions.
&middot; Complies with work rules including those pertaining to safety, health, Quality System, and the Accellent Quality Management System.
&middot; Overtime as required.
Qualifications
* Ability to read, write and speak fluent English
* Associates / Undergraduate degree and 5 years prior related experience in a manufacturing/scheduling/planning environment, or a combination of experience and education
* Prior inventory control experience preferred
* Familiar with computer based planning and scheduling systems (Oracle experience preferred)
* Ability to assimilate information quickly and possesses strong decision making abilities and organizational skills
* Must be capable of assimilating Accellent systems and procedures quickly
* Able to work in a fast paced and evolving environment
* Working knowledge of material handling equipment and processes, as well as work center capacities
* Ability to coordinate internal and external vendor services and customer needs
* Strong experience with MS Word and Excel
* Solid understanding of ISO and Quality System Procedures
* Complete all job specific required training
* Perform duties to achieve overall business unit metrics
* Compliance all safety regulations, wears appropriate safety equipment as required in each area of the facility
* Prior experience working in a manufacturing environment strongly preferred
* Prior supervisory experience a must
* Prior experience in a Lean Manufacturing environment a plus.

Environmental Working Conditions
The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job, the employee regularly works near moving mechanical parts and is regularly exposed to vibration. The noise level in the work environment is usually loud.

Employee must comply with all safety policies and safe work procedures established by the company. Job tasks may also involve:  
&middot;    Using personal protective equipment such as safety glasses, goggles, gloves, and other equipment as established in company policies and safe work procedures.
&middot;    Working with cutting &amp; machining fluids, solvents, lubricants and other hazardous chemicals using appropriate safety controls.
&middot;    Lifting up to 50 pounds.
&middot;    Frequent carrying, bending, standing, sitting, and repetitive motion.
Employee will be expected to attend safety training, serve on the facility safety committee and participate in hazard analysis and resolution.
Job Requirements :
n/a
Career Level :Experienced (Non-Manager)
Education :Associate Degree
Shift/Hours :First Shift (Day)
]]></description>
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            <industry><![CDATA[Health Products & Services]]></industry>
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        <expiration_date>2010-03-25</expiration_date>
        <employer><![CDATA[Accellent Inc.]]></employer>
        <location><![CDATA[El Paso, TX, 79977, USA]]></location>
    </job>
    <job>
        <title><![CDATA[Supply Chain Manager]]></title>
        <description><![CDATA[


Job Title :Supply Chain Manager
Job Code :4388
Location :Collegeville PA US 19426
Job Description :
Accellent, Inc. is a fully integrated provider of design, supply chain management and strategic sourcing services to the Medical Device industry. Accellentwww.accellent.com, a recognized market leader, is a fast-growing outsource manufacturing and design solution company specializing in high growth areas such as Cardiology, Endoscopy and Orthopaedics. The top medical device companies partner with Accellent to provide innovation, advanced technology, speed to market, low cost labor and strategic sourcing.
We&rsquo;re looking for team players with a can-do attitude to share in our vision and corporate values. Accellent offers competitive salaries, a comprehensive benefits package, and a stimulating work environment.
Currently, we are searching for a Supply Chain Manager to join our Supply Chain team at the Collegeville, PA facility.
The Supply Chain Manager is a member of the facility leadership team with functional responsibility for S&amp;OP (Master Planning) ,capacity planning, materials management/flow, tactical procurement, production scheduling, inventory control, warehousing and logistics. This individual will help to drive key critical performance drivers (CPDs) such as fill rate, on-time delivery, back order, quality lot acceptance and financial metrics such as inventory turns, standard cost variances, absorption and budget. The person will represent Accellent in a professional and exemplary manner before our suppliers, employees and community at large. POSITION RESPONSIBILITY
* Drive the sites Sales and Operations planning process to develop mid to long range operating plans, which drives the demand and capacity planning function which the incumbent is responsible for. Assist in capital expenditure (CAPEX)justification and approval working with peers within operations
* Works with Accellent Customers and Customer Operations Management (COM) in the establishment and management of Kanban and Consigned Finished Goods Inventory programs, and insures that proper Demand and Capacity Plans are implemented to support these requirements at their site
* Management responsibilities for demand and capacity planning, production scheduling and execution, inventory, purchasing and supplier service level management Responsible for integrating production schedules with business planning and forecasting. Balance of ERP/MRP capability with pull / lean methodology. Must be a driver of lean manufacturing and a lean culture.
* Responsible for inventory accuracy (raw, outside services , WIP and finished goods) and cycle count programs. Working closely with finance, maintain appropriate inventory levels to meet customer demand while meeting Accellent financial objectives.
* Manage and support outside service providers to meet Accellent business requirements.
* Participate in daily lean huddles as well as ,participate on project teams as required.
* Responsible for the planning systems for all raw materials, internal operations, subcontract operations and outside supporting services.
* Responsible for production order execution and working with operations to insure that our on time delivery , cycle time and fill rate goals are met.
* Responsible for site procurement activities (raw materials, outside services (OSV) as well as expense items).
* Managing and maintaining supplier programs, including the implementation of Kanban Replenishment , Consigned Vendor Managed Inventory (VMI) Programs in areas such as raw materials, tooling, etc.
* Global Sourcing &ndash; actively participates with Accellent Global Sourcing Commodity Management team on Strategic Supplier partnerships and agreements in support of Accellent Strategic Goals.
* Participates with Strategic Sourcing Commodity management on Supplier Relationship Management (Quarterly Business Reviews (QBR) with key suppliers for the site, as well as participates in Global Sourcing supplier relationship management (SRM) meetings as required.
* Supplier Performance Management &ndash; responsible for working with site operations quality and global sourcing on supplier report cards to insure that plans of action are developed and implemented for improving poor performing suppliers.
* Weekly / Monthly reporting on Key Performance Indicators (KPI&rsquo;s) for the Supply Chain function for their site.
* Participates in Global Supply Chain meetings within Accellent to foster cross site teamwork and development of our Global Supply Chain capabilities.
* Explore new technologies and processes, to reduce non-value added procurement and planning activities.
* Responsible for training and career development of all site Supply Chain employees.
* Manage department to meet all quality and financial system requirements.
* Participate in the contract review of all new products / processes.
Job Requirements :
ORGANIZATIONAL RELATIONSHIPS
Internally - Customer Operations , Operations, Quality, Global Sourcing, Proj Mgt/Quoting and Engineering departments. Member of facility leadership team
Externally - Customers, outside suppliers and other Accellent facilities
EDUCATION, TYPE AND YEARS OF EXPERIENCE, AND SKILL REQUIREMENTS
* To perform this job successfully, an individual must have the necessary education and work experience. Recognizing that education and work experience are relative to the experience, environments, the review of an individual&rsquo;s accomplishments is critical to filling the position successfully.
* Prior Supply Chain leadership role is a must.
* 4 year degree. MBA a plus.
* Minimum of 5 - 8 years experience in increasing levels of responsibility within Materials and Purchasing Management. 3-5 years of management or supervision experience.
* Prior Demand and Capacity Planning experience required, must have a prior hands on experience within Masterscheduling, Capacity Planning and production planning
* Prior Purchasing and experience required
* CPIM / CPM certification a plus.
* Experienced Six Sigma Black Belt / Green Belt, prior experience working in a lean manufacturing environment
* Experience with ERP/MRP systems (Oracle, SAP, JD Edwards)
* Strong verbal and written communication skills, analytical skills, statistical and mathematical abilities and interpersonal skills.
* Advanced Computer skills using Microsoft Word, Excel, Powerpoint and Project
* Excellent communication skills, strong organizational skills and a tremendous sense of getting things done. Self-motivation and problem solving skills are extremely important in this position.OTHER JOB REQUIRMENTS REQUIREMENTS
It is impossible to list every requirement for, or responsibility of, any position. Similarly we cannot identify all the skills a position may require since job responsibilities and the Company&rsquo;s needs may change over time. Therefore, the above job description is not comprehensive or exhaustive. The Company reserves the right to adjust, add to or eliminate any aspect of the above description. The Company also retains the right to require all employees to undertake additional or different job responsibilities when necessary to meet business needs.
PHYSICAL DEMANDS:
* The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
* While performing the duties of this job, the employee is regularly required to sit and talk or hear.
* The employee is occasionally required to stand; walk; use hands to finger, handle, or feel; reach with hands and arms; and taste or smell.
* The employee must occasionally lift and/or move up to 25 pounds. Specific vision abilities required by this job include close vision, and ability to adjust focus.WORK ENVIRONMENT:
* The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
* While performing the duties of this job, the employee is occasionally exposed to moving mechanical parts.
* The noise level in the work environment is usually moderate. Occasional travel will be required.
Career Level :Manager (Manager/Supervisor of Staff)
Education :Bachelor's Degree
]]></description>
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        <expiration_date>2010-03-25</expiration_date>
        <employer><![CDATA[Accellent Inc.]]></employer>
        <location><![CDATA[Collegeville, PA, 19426, USA]]></location>
    </job>
    <job>
        <title><![CDATA[Sr. Quality Engineer - Contract]]></title>
        <description><![CDATA[


Job Title :Sr. Quality Engineer - Contract
Job Code :4390
Location :Wilmington MA US 01887
Job Description :
Accellent, Inc. is a fully integrated provider of design, supply chain management and strategic sourcing services to the Medical Device industry. Accellentwww.accellent.com, a recognized market leader, is a fast-growing outsource manufacturing and design solution company specializing in high growth areas such as Cardiology, Endoscopy and Orthopaedics. The top Medical Device companies partner with Accellent to provide innovation, advanced technology, speed to market, low cost labor and strategic sourcing. 
We&rsquo;re looking for team players with a can-do attitude to share in our vision and corporate values. Accellent offers competitive salaries; a comprehensive benefits package, and a stimulating work environment. 
Currently, we are searching for a Sr. Quality Engineer to join our Wilimington, MA facility.  This a temporary position.
About the Opportunity:
Position Scope / Summary
Quality assists in the design and implementation of policies and procedures for testing and evaluating the precision and accuracy of products and/or equipment. The Sr. Quality Engineer will be expected to provide support to Operations, interact with customers and provide support for Engineering, Quality Systems and Process engineering. 
Specializations may include but are not limited to: design control; material and process control; product reliability; software quality engineering; and/or metrology.
This position will be integral in meeting the Quality Management System requirements. It requires creativity and foresight to work with operations and product development teams to ensure compliance to the Quality Manual, Design Control, Supplier Management and other appropriate procedures for a variety of medical devices from concept through market introduction. The ideal candidate is a self-motivated individual who is excited by the prospect of working in a dynamic, fast-paced environment.
Key Result Accountabilities
1.   Maintain company compliance with FDA Quality System Regulations and ISO 13485 standards. Experience with FDA and ISO inspections and registration is a plus.
2.   Actively participates in internal audits, management review and other activities covered under Accellent Quality Manual, Policies and Procedures.
3.   Provide customer related quality and regulatory inquiries support.
4.   Compiles and writes training material and conducts training sessions on quality control activities.
5.   Provide QE direction, analysis and recommendations for Product Development to successfully launch new products into active production in a timely and cost effective manner. Directs development and maintenance of internal/external standards relative to Design and Development,
6.   Lead implementation of continuous improvement projects or act as subject matter expert for SPC, FMEA, DOE and process validation.
7.   Lead and provide Project Management support as needed.
8.   Develops and initiates standard methods for inspection, testing, and evaluation, utilizing knowledge in related engineering fields.
9.   Devises sampling procedures and designs and develops forms and instructions for recording, evaluating, and reporting quality and reliability data.
10. Performs measurement system analyses to evaluate test and inspection equipment.
11. Leads disposition of discrepant material and devises process to assess product quality and reliability.
12. Monitors and directs engineering group on calibration requirements and implementation of systems to support equipment calibration.
13. Lead supplier approval and qualification of new/revised items which includes inspection method development and validation as well as correlation with supplier&rsquo;s methods, supplier audits, management of supplier corrective and preventative actions and assist in FMEA. 
14. Direct support for FDA and ISO inspections and registration.
15. Directs workers engaged in measuring, testing, and tabulating data concerning quality and reliability.
16. All other duties as assigned.
17. Up to 10% travel may be required.
Environmental Working Conditions
Employee must comply with all safety policies and safe work procedures established by the company. Job tasks may also involve:  
             
&middot;    Using personal protective equipment such as safety glasses, goggles, gloves, and other equipment as established in company policies and safe work procedures.
&middot;    Working near cutting &amp; machining fluids, solvents, lubricants and other hazardous chemicals using appropriate safety controls.
Employee will be expected to attend safety training, and may serve on the facility safety committee and participate in hazard analysis and resolution.
Job Requirements :

* Medical Device background with a clear understanding of ISO 13485:2003 and 21 CFR Part 820
* Creation of Master Validation plans,
* Writing validation protocols,
* FMEA and DOE
* Oversight of IP, OQ, PQ at Manufacturing site (travel may be required)
* WritingPQ report
* Test method development and validation reporting
* Experience with software based products and associated Verification and Validation 21CFR Part 11 (1 individual)
Due to the expected number of responses, only those most qualified will be contacted. No recruiters please; all unsolicited third-party submissions will be rejected.

Accellent is an Equal Opportunity/Affirmative Action employer and we value diversity in our workforce. As such we provide equal opportunity for all applicants without regard to race, religion, gender, national origin, age, marital status, veteran status, or disability. To learn more about Accellent and our career opportunities, please visit us atwww.accellent.com
Career Level :Experienced (Non-Manager)
Education :Bachelor's Degree
% of Travel Required :0-10%
Shift/Hours :First Shift (Day)
]]></description>
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            <industry><![CDATA[Health Products & Services]]></industry>
        </industries>
        <expiration_date>2010-03-25</expiration_date>
        <employer><![CDATA[Accellent Inc.]]></employer>
        <location><![CDATA[Wilmington, MA, 01887, USA]]></location>
    </job>
    <job>
        <title><![CDATA[Swiss Operator -  B12]]></title>
        <description><![CDATA[


Job Title :Swiss Operator - B12
Job Code :4393
Location :Brooklyn Park MN US 55429
Job Description :
Accellent, Inc. is a fully integrated provider of design, supply chain management and strategic sourcing services to the Medical Device industry. Accellentwww.accellent.com, a recognized market leader, is a fast-growing outsource manufacturing and design solution company specializing in high growth areas such as Cardiology, Endoscopy and Orthopaedics. The top Medical Device companies partner with Accellent to provide innovation, advanced technology, speed to market, low cost labor and strategic sourcing.
We&rsquo;re looking for team players with a can-do attitude to share in our vision and corporate values. Accellent offers competitive salaries; a comprehensive benefits package, and a stimulating work environment.
Currently, we are searching for a Swiss Operator - Weekend Shift to join our Brooklyn Park facility.
Job Requirements :
Position Scope/Summary
Setup, troubleshoot, operate and perform maintenance when required to machines.
Include the following:
Responsible for keeping the machines running and work area clean.
Operate the machine as efficiently as possible.
Produce high quality components to print specifications. 
Read part prints and understand dimensions.
Use and understand how inspection equipment works making sure it is correct and is calibrated.
Do whatever is needed to insure quality - including sorting for features that are uncontrollable.
Obtain material from material rack.
Communicate with opposite shift operator to insure smooth transition between shifts.
Follow all company policies and rules.
Provide support within the organization as experienceand time allow.
Other duties may be assigned.
 Key Result Accountabilities
Supervisory Responsibilities:
Needs to work in an atmosphere with little supervision.
Language Skills:
Must be able to communicate with inspection personnel as well as other operators.
Mathematical Skills:
Must have basic math skills.
Reasoning Ability:
Must be able to reason cause and effect on parts.
Strong organizational skills.

 Environmental Working Conditions
Reasonable accommodations may be made to enable individuals with disabilities to perform the 
essential functions.
                              
 Qualifications
Must be able to read a print and use inspection equipment necessary to do the job.
  It is impossible to list every requirement for, or responsibility of, any position. Similarly we cannot
  identify all the skills a position may require since job responsibilities and the Company&rsquo;s needs may
  change over time. Therefore, the above job description is not comprehensive or exhaustive. 
 The Company reserves the right to adjust, add to or eliminate any aspect of the above description. 
 The Company also retains the right to require all employees to undertake additional or different job
 responsibilities when necessary to meet business needs.
Due to the expected number of responses, only those most qualified will be contacted. No recruiters please; all unsolicited third-party submissions will be rejected.

Accellent is an Equal Opportunity/Affirmative Action employer and we value diversity in our workforce. As such we provide equal opportunity for all applicants without regard to race, religion, gender, national origin, age, marital status, veteran status, or disability. To learn more about Accellent and our career opportunities, please visit us atwww.accellent.com

Career Level :Experienced (Non-Manager)
Education :High School or equivalent
% of Travel Required :None
Shift/Hours :Weekend
]]></description>
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        <industries>
            <industry><![CDATA[Health Products & Services]]></industry>
        </industries>
        <expiration_date>2010-03-25</expiration_date>
        <employer><![CDATA[Accellent Inc.]]></employer>
        <location><![CDATA[Brooklyn Park, MN, 55445, USA]]></location>
    </job>
    <job>
        <title><![CDATA[Swiss Operator -  B12]]></title>
        <description><![CDATA[


Job Title :Swiss Operator - B12
Job Code :4395
Location :Brooklyn Park MN US 55429
Job Description :
Accellent, Inc. is a fully integrated provider of design, supply chain management and strategic sourcing services to the Medical Device industry. Accellentwww.accellent.com, a recognized market leader, is a fast-growing outsource manufacturing and design solution company specializing in high growth areas such as Cardiology, Endoscopy and Orthopaedics. The top Medical Device companies partner with Accellent to provide innovation, advanced technology, speed to market, low cost labor and strategic sourcing.
We&rsquo;re looking for team players with a can-do attitude to share in our vision and corporate values. Accellent offers competitive salaries; a comprehensive benefits package, and a stimulating work environment.
Currently, we are searching for a Swiss Operator - Weekend Shift to join our Brooklyn Park facility.
Job Requirements :
Position Scope/Summary
Setup, troubleshoot, operate and perform maintenance when required to machines.
Include the following:
Responsible for keeping the machines running and work area clean.
Operate the machine as efficiently as possible.
Produce high quality components to print specifications. 
Read part prints and understand dimensions.
Use and understand how inspection equipment works making sure it is correct and is calibrated.
Do whatever is needed to insure quality - including sorting for features that are uncontrollable.
Obtain material from material rack.
Communicate with opposite shift operator to insure smooth transition between shifts.
Follow all company policies and rules.
Provide support within the organization as experienceand time allow.
Other duties may be assigned.
 Key Result Accountabilities
Supervisory Responsibilities:
Needs to work in an atmosphere with little supervision.
Language Skills:
Must be able to communicate with inspection personnel as well as other operators.
Mathematical Skills:
Must have basic math skills.
Reasoning Ability:
Must be able to reason cause and effect on parts.
Strong organizational skills.

 Environmental Working Conditions
Reasonable accommodations may be made to enable individuals with disabilities to perform the 
essential functions.
                              
 Qualifications
Must be able to read a print and use inspection equipment necessary to do the job.
  It is impossible to list every requirement for, or responsibility of, any position. Similarly we cannot
  identify all the skills a position may require since job responsibilities and the Company&rsquo;s needs may
  change over time. Therefore, the above job description is not comprehensive or exhaustive. 
 The Company reserves the right to adjust, add to or eliminate any aspect of the above description. 
 The Company also retains the right to require all employees to undertake additional or different job
 responsibilities when necessary to meet business needs.
Due to the expected number of responses, only those most qualified will be contacted. No recruiters please; all unsolicited third-party submissions will be rejected.

Accellent is an Equal Opportunity/Affirmative Action employer and we value diversity in our workforce. As such we provide equal opportunity for all applicants without regard to race, religion, gender, national origin, age, marital status, veteran status, or disability. To learn more about Accellent and our career opportunities, please visit us atwww.accellent.com

Career Level :Experienced (Non-Manager)
Education :High School or equivalent
% of Travel Required :None
Shift/Hours :Weekend
]]></description>
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        </industries>
        <expiration_date>2010-03-25</expiration_date>
        <employer><![CDATA[Accellent Inc.]]></employer>
        <location><![CDATA[Brooklyn Park, MN, 55445, USA]]></location>
    </job>
    <job>
        <title><![CDATA[Swiss Operator -  B12]]></title>
        <description><![CDATA[


Job Title :Swiss Operator - B12
Job Code :4396
Location :Brooklyn Park MN US 55429
Job Description :
Accellent, Inc. is a fully integrated provider of design, supply chain management and strategic sourcing services to the Medical Device industry. Accellentwww.accellent.com, a recognized market leader, is a fast-growing outsource manufacturing and design solution company specializing in high growth areas such as Cardiology, Endoscopy and Orthopaedics. The top Medical Device companies partner with Accellent to provide innovation, advanced technology, speed to market, low cost labor and strategic sourcing.
We&rsquo;re looking for team players with a can-do attitude to share in our vision and corporate values. Accellent offers competitive salaries; a comprehensive benefits package, and a stimulating work environment.
Currently, we are searching for a Swiss Operator - Weekend Shift to join our Brooklyn Park facility.
Job Requirements :
Position Scope/Summary
Setup, troubleshoot, operate and perform maintenance when required to machines.
Include the following:
Responsible for keeping the machines running and work area clean.
Operate the machine as efficiently as possible.
Produce high quality components to print specifications. 
Read part prints and understand dimensions.
Use and understand how inspection equipment works making sure it is correct and is calibrated.
Do whatever is needed to insure quality - including sorting for features that are uncontrollable.
Obtain material from material rack.
Communicate with opposite shift operator to insure smooth transition between shifts.
Follow all company policies and rules.
Provide support within the organization as experienceand time allow.
Other duties may be assigned.
 Key Result Accountabilities
Supervisory Responsibilities:
Needs to work in an atmosphere with little supervision.
Language Skills:
Must be able to communicate with inspection personnel as well as other operators.
Mathematical Skills:
Must have basic math skills.
Reasoning Ability:
Must be able to reason cause and effect on parts.
Strong organizational skills.

 Environmental Working Conditions
Reasonable accommodations may be made to enable individuals with disabilities to perform the 
essential functions.
                              
 Qualifications
Must be able to read a print and use inspection equipment necessary to do the job.
  It is impossible to list every requirement for, or responsibility of, any position. Similarly we cannot
  identify all the skills a position may require since job responsibilities and the Company&rsquo;s needs may
  change over time. Therefore, the above job description is not comprehensive or exhaustive. 
 The Company reserves the right to adjust, add to or eliminate any aspect of the above description. 
 The Company also retains the right to require all employees to undertake additional or different job
 responsibilities when necessary to meet business needs.
Due to the expected number of responses, only those most qualified will be contacted. No recruiters please; all unsolicited third-party submissions will be rejected.

Accellent is an Equal Opportunity/Affirmative Action employer and we value diversity in our workforce. As such we provide equal opportunity for all applicants without regard to race, religion, gender, national origin, age, marital status, veteran status, or disability. To learn more about Accellent and our career opportunities, please visit us atwww.accellent.com

Career Level :Experienced (Non-Manager)
Education :High School or equivalent
% of Travel Required :None
Shift/Hours :Weekend
]]></description>
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            <industry><![CDATA[Health Products & Services]]></industry>
        </industries>
        <expiration_date>2010-03-25</expiration_date>
        <employer><![CDATA[Accellent Inc.]]></employer>
        <location><![CDATA[Brooklyn Park, MN, 55445, USA]]></location>
    </job>
    <job>
        <title><![CDATA[Laser Welding - Lead]]></title>
        <description><![CDATA[


Job Title :Laser Welding - Lead
Job Code :4397
Location :Brooklyn Park MN US 55429
Job Description :
Accellent, Inc. is a fully integrated provider of design, supply chain management and strategic sourcing services to the Medical Device industry. Accellentwww.accellent.com, a recognized market leader, is a fast-growing outsource manufacturing and design solution company specializing in high growth areas such as Cardiology, Endoscopy and Orthopaedics. The top Medical Device companies partner with Accellent to provide innovation, advanced technology, speed to market, low cost labor and strategic sourcing.
We&rsquo;re looking for team players with a can-do attitude to share in our vision and corporate values. Accellent offers competitive salaries; a comprehensive benefits package, and a stimulating work environment.
Currently, we are searching for a Laser Welding-Lead Night Shift to join our Brooklyn Park facility.
Job Requirements :

 Position Scope/Summary 
* Coordinate and manage Laser workstations and employees
* Include the following: (other duties may be assigned)
* Training of employees
* Managing employees and keeping them on task
* Responsible for keeping the machines running efficiently so due dates can be met
* Perform set-up checks, daily maintenance, and keep the area around the machines clean
* Produce high quality components to print specifications
* Read part prints and understand dimensions
* Use and understand how inspection equipment works - making sure it is correct and calibrated
* Do whatever is needed to assure quality - including sorting for features that are uncontrollable
* Maintain correct lot control numbers of components and assemblies
* Communicate with opposite shift operators/leads to assure smooth transition between shifts
* Follow company policies and rules
* Provide support within the organization as experience and time allow 
 Key Result Accountabilities
Supervisory Responsibilities:
Needs to work in an atmosphere with little supervision.
Work with management staff to ensure high customer quality and schedule deadlines and requirements are met.
Language Skills:
Must be able to communicate with inspection personnel as well as other operators.
Mathematical Skills:
Must have basic math skills.
Reasoning Ability:
Must be able to reason cause and effect on parts.
Strong organizational skills.

 Environmental Working Conditions
Reasonable accommodations may be made to enable individuals with disabilities to perform the 
essential functions.
                              
 Qualifications
Must be able to read a print and use inspection equipment necessary to do the job.
  It is impossible to list every requirement for, or responsibility of, any position. Similarly we cannot
  identify all the skills a position may require since job responsibilities and the Company&rsquo;s needs may
  change over time. Therefore, the above job description is not comprehensive or exhaustive. 
 The Company reserves the right to adjust, add to or eliminate any aspect of the above description. 
 The Company also retains the right to require all employees to undertake additional or different job
 responsibilities when necessary to meet business needs.
Due to the expected number of responses, only those most qualified will be contacted. No recruiters please; all unsolicited third-party submissions will be rejected.

Accellent is an Equal Opportunity/Affirmative Action employer and we value diversity in our workforce. As such we provide equal opportunity for all applicants without regard to race, religion, gender, national origin, age, marital status, veteran status, or disability. To learn more about Accellent and our career opportunities, please visit us atwww.accellent.com

Career Level :Experienced (Non-Manager)
Education :High School or equivalent
% of Travel Required :None
Shift/Hours :Second Shift (Afternoon)
]]></description>
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        <industries>
            <industry><![CDATA[Health Products & Services]]></industry>
        </industries>
        <expiration_date>2010-03-25</expiration_date>
        <employer><![CDATA[Accellent Inc.]]></employer>
        <location><![CDATA[Brooklyn Park, MN, 55445, USA]]></location>
    </job>
    <job>
        <title><![CDATA[Finisher]]></title>
        <description><![CDATA[


Job Title :Finisher
Job Code :4401
Location :Orchard Park NY US 14127
Job Description :


Job Title: 
Finisher 
Department: 
Manufacturing
Reports To: 
Team Leader 
Location: 
OrchardPark
FLSA Status: 
Non-Exempt 
Facility: 
Endo (Cardio, Endo, Ortho)
Classification: 
Hourly (factory) 
Date: 

Education: 
High School Diploma or GED
Organizational Relationships: 
Internally  - All levels of Employees, especially Lead Finishers, Operators, Sr. Operators, B&rsquo;s, A&rsquo;s, QC techs and PIC person on team.
Externally - Customers, Auditors
Position Scope / Summary
Finishers are responsible for performing operations per work instructions on parts in order to meet customer specifications.
Key Result Accountabilities
1.   Knowledgeable about finishing techniques, which include but are not limited to using foredoms, gesswein, tumbling, burlytic, cleaning, grinding, miyano operations, Lapmaster, red wheeling, hand deburring, tumble blasting, sand blasting, clean room operations, molding machines, furnaces, waterbaths, dryers, trim, scrape or deburr parts using hand tools and equipment.
2.   Responsible for performing work that meets or exceeds our production standards and scrap rates that will achieve our metric goals for scrap, Fill Rate, Rework, Customer Lot Acceptance (CLA), and Customer Complaints, etc.
3.   Knowledge of shop control system in order to review and print paperwork needed for job and input data for work completed on various jobs.
4.   Use Smart Scope, comparator, micrometers, blade micrometers, counting scales and/or profilometer for measuring and counting parts, as necessary.
5.   Knowledge of reading and using Collection Plans in order to conduct frequency checks.
6.   Understand MVR procedures.
7.   Be able to rotate into other Finishing jobs with competency and confidence.
8.   Ability to work well in a team environment.
9.   Other duties as necessary.
10. Keep work area clean.
Job Requirements :
Environmental Working Conditions
&middot;    The physical demands described herein are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform essential functions.
&middot;    Ability to spend time using your hands to handle, control, or feel objects, tools or controls.
&middot;    Will spend extended periods of time sitting and/or standing.
&middot;    Occasionally required to stoop, kneel, bend, crouch, bend and twist.
&middot;    Ability to lift 1pound up to 10 lbs.
Qualifications
1.   Able to use microscope and other measuring equipment.
2.   Able to use computer, pulling up instructions and reading them.
3.   Able to follow instructions, both written and verbal.Able to count parts
Career Level :Entry Level
Education :High School or equivalent
% of Travel Required :0-10%
Shift/Hours :Second Shift (Afternoon)
]]></description>
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        <industries>
            <industry><![CDATA[Health Products & Services]]></industry>
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        <expiration_date>2010-03-25</expiration_date>
        <employer><![CDATA[Accellent Inc.]]></employer>
        <location><![CDATA[Orchard Park, NY, 14127, USA]]></location>
    </job>
    <job>
        <title><![CDATA[Operator B]]></title>
        <description><![CDATA[


Job Title :Operator B
Job Code :4403
Location :Orchard Park NY US 14127
Job Description :


Job Title: 
Operator 
Department: 
Manufacturing
Reports To: 
Team Leader 
Location: 
OrchardPark
FLSA Status: 
Non-exempt 
Facility: 
Endo (Cardio, Endo, Ortho)
Classification: 
Hourly (factory) 
Date: 

Education: 
High School Graduate, Graduation from a machining certificate program, BOCES Machine Shop program, ECC or Metalworking Institute program in machining is preferable.
Organizational Relationships: 
Internally  - All levels of Employees, but especially Sr. Operators, B&rsquo;s, A&rsquo;s and QC Techs on team.
Externally - Customers, Auditors
Position Scope / Summary
Operators are responsible for running primary machines to produce parts according to customer specifications.
Key Result Accountabilities
1.   Run machines assigned to achieve a utilization of at least 75% for the shift.
2.   Responsible for performing work that meets or exceeds our production standards and scrap rates that will achieve the metric goals for scrap, EBITDA, Fill Rate, Rework etc...
3.   Measure parts accurately according to the blueprint and collection plan.
4.   Knowledge of reading and using Collection Plan and blueprints in order to conduct frequency checks, both visually and dimensionally, using the appropriate measuring equipment.
5.   Be able to start, stop and produce single parts on the machine.
6.   Offset machines as needed. (when you are qualified to do so; an offset test will be given)
7.   Knowledge of Shop Control System in order to review and print paperwork needed for job and input data for work completed on various jobs.
8.   Create batches.
9.   Understand MVR procedures.
10. Keep work area clean.
11. Able to perform routine/daily maintenance of machines such as sumping machines, oil levels/ refills, filters for air cleaners and pumps.
12. Know who to go to for assistance.
13. Able to move around the team assigned, to run various jobs with competence and confidence.
14. Acquire the training needs to get the skills and knowledge necessary to get book 1 signed off. This book MUST be signed off. It is the company&rsquo;s responsibility to provide the training, but it is operator&rsquo;s responsibility to make sure book is signed off in a timely manner.
15. Other duties as necessary.
Job Requirements :
Environmental Working Conditions
&middot;    The physical demands described herein are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform essential functions.
&middot;    Ability to spend time using your hands to handle, control, or feel objects, tools or controls.
&middot;    Will spend extended periods of time standing and walking throughout the shop.
&middot;    Occasionally required to sit, stoop, kneel, bend, crouch, bend and twist.
&middot;    Ability to lift 1pound up to 50 lbs.



Job Title: 
Operator continued
Qualifications
1.   Able to use microscope and other measuring equipment, to include micrometers, comparator, SmartScope, profilometer, thread gages, pins, etalon, and digital linear gage.
2.   Able to use computer, pulling up instructions and reading them.
3.   Able to use basic shop math.
4.   Able to read and understand blueprints.
5.   Able to follow instructions, both written and verbal.Able to count and box parts
Career Level :Experienced (Non-Manager)
Education :Certification
]]></description>
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            <industry><![CDATA[Health Products & Services]]></industry>
        </industries>
        <expiration_date>2010-03-25</expiration_date>
        <employer><![CDATA[Accellent Inc.]]></employer>
        <location><![CDATA[Orchard Park, NY, 14127, USA]]></location>
    </job>
    <job>
        <title><![CDATA[Machine Operator - Wire]]></title>
        <description><![CDATA[


Job Title :Machine Operator - Wire
Job Code :4351
Location :SALEM VA US 24153
Job Description :
Accellent, Inc. is a fully integrated provider of design, supply chain management and strategic sourcing services to the Medical Device industry. Accellentwww.accellent.com, a recognized market leader, is a fast-growing outsource manufacturing and design solution company specializing in high growth areas such as Cardiology, Endoscopy and Orthopaedics. The top Medical Device companies partner with Accellent to provide innovation, advanced technology, speed to market, low cost labor and strategic sourcing.
We&rsquo;re looking for team players with a can-do attitude to share in our vision and corporate values. Accellent offers competitive salaries; a comprehensive benefits package, and a stimulating work environment.
Currently, we are searching for a Machine Operator for our Wire Department to join our Salem, Virginia facility. Employees must be able to:

1.)    Must achieve all training certifications required in the training database for this job.
2.)    Perform the tasks and procedures required to move jobs through the department in a timely manner.
3.)    Maintain and update production and material control systems as needed to ensure proper job and material tracking is maintained
4.)    Complete off-schedule notifications.
5.)    Maintain work area and equipment in a clean, neat, and organized fashion.
6.)    Champion Accellent's Values and assist in developing an understanding of these values in fellow employees.
Job Requirements :

IV. Knowledge Skills and Abilities (KSA):
1.)    Ability to effectively communicate with other operators.
2.)    Mechanical aptitude and ability to work with a wide variety of equipment.
3.)    The ability to strictly adhere to Standard Operating Procedures, including all safety, health, and environmental procedures.
4.)    Knowledge of basic math skills including addition, subtraction, multiplication, division, percentages, proportions, and fractions.
5.)    The ability to use various measuring devices including micrometers, laser micrometers, electronic balance, calipers, and pin gauges.
6.)    Capable of performing basic computer tasks.
Due to the expected number of responses, only those most qualified will be contacted. No recruiters please; all unsolicited third-party submissions will be rejected.
Accellent is an Equal Opportunity Employer. To learn more about Accellent and our career opportunities, please visit us atwww.accellent.com
Career Level :Experienced (Non-Manager)
Education :High School or equivalent
% of Travel Required :0-10%
Shift/Hours :Second Shift (Afternoon)
]]></description>
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            <industry><![CDATA[Health Products & Services]]></industry>
        </industries>
        <expiration_date>2010-03-25</expiration_date>
        <employer><![CDATA[Accellent Inc.]]></employer>
        <location><![CDATA[SALEM, VA, 24157, USA]]></location>
    </job>
    <job>
        <title><![CDATA[Engineer]]></title>
        <description><![CDATA[


Job Title :Engineer
Job Code :4353
Location :Salem VA US 24153
Job Description :

Accellent, Inc. is a fully integrated provider of design, supply chain management and strategic sourcing services to the Medical Device industry. Accellent, www.accellent.com, a recognized market leader, is a fast-growing outsource manufacturing and design solution company specializing in high growth areas such as Cardiology, Endoscopy and Orthopedics. The top Medical Device companies partner with Accellent to provide innovation, advanced technology, speed to market, low cost labor and strategic sourcing.
We&rsquo;re looking for team players with a can-do attitude to share in our vision and corporate values. Accellent offers competitive salaries; a comprehensive benefits package, and a stimulating work environment.

Position Scope / Summary
Currently, we are searching for a degreed engineer for our operations, focused on secondary profiling of CNC parts to include: EDM, Micro-Blast, and Laser Cutting processes to join our Salem, Virginia facility. This position will involve tool/fixture design and development. CNC experience is preferred. Knowledge of Solidworks required.
Job Requirements :
&bull; Follows and develops Quality and Regulatory requirements including Accellent policies, procedures, and appropriate regulatory requirements.
&bull; Develops and Executes Process and Test Method Validations (IQ, OQ, PQ, PPQ) in accordance with Accellent procedures and guidelines
&bull; Communicates ideas, information, and recommendations clearly, effectively and frequently (oral and written) within Accellent, with outside suppliers or partners and with Accellent customers during formal and informal interactions.
&bull; Prepares or reviews documentation with a high degree of accuracy, completeness, and effectiveness using common Accellent engineering tools &amp; templates were available. (Examples include specifications, manufacturing procedures, ECOs, and technical reports or analysis)
&bull; Applies Lean manufacturing techniques to continuously improve cycle times and process flows. Identifies, and supports the execution of improvement efforts to reduce waste in all manufacturing and business processes.
&bull; Uses structured problem solving techniques and statistical methods for data driven analysis and decisions.
&bull; Applies DMAIC &ndash; Six Sigma approaches to solve issues and reduce variation in all manufacturing and business processes.
&bull; Plans and executes project activities within a cross functional team. Project types can include new product development and introduction, manufacturing transfers, continuous improvement and cost reduction initiatives.
&bull; Exhibits the Accellent values (Customer focus, Continuous Improvement, Performance, Accountability, Teamwork and Integrity) in all activities.
&bull; Demonstrates leadership through mentoring of junior staff and responsiveness to business needs to achieve positive results
&bull; Demonstrates technical ability through the application of engineering skills, approaches and knowledge.
&bull; Performs all duties and directs others creating a safe working environment for our employees and our communities.
&bull; Performs other duties as necessary.

Environmental Working Conditions
The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
While performing the duties of this job, the employee is frequently exposed to moving mechanical parts. The employee is occasionally exposed to high, precarious places; fumes or airborne particles; toxic or caustic chemicals; risk of electrical shock; and vibration. The noise level in the work environment is usually moderate.

Qualifications
It is impossible to list every requirement for, or responsibility of, any position. Similarly we cannot identify all the skills a position may require since job responsibilities and the Company&rsquo;s needs may change over time. Therefore, the above job description is not comprehensive or exhaustive. The Company reserves the right to adjust, add to or eliminate any aspect of the above description. The Company also retains the right to require all employees to undertake additional or different job responsibilities when necessary to meet business needs.

Due to the expected number of responses, only those most qualified will be contacted. No recruiters please; all unsolicited third-party submissions will be rejected.

Accellent is an Equal Opportunity/Affirmative Action employer and we value diversity in our workforce. As such we provide equal opportunity for all applicants without regard to race, religion, gender, national origin, age, marital status, veteran status, or disability. To learn more about Accellent and our career opportunities, please visit us at
www.accellent.com

Career Level :Experienced (Non-Manager)
Education :Bachelor's Degree
% of Travel Required :0-10%
Shift/Hours :First Shift (Day)
]]></description>
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            <industry><![CDATA[Health Products & Services]]></industry>
        </industries>
        <expiration_date>2010-03-25</expiration_date>
        <employer><![CDATA[Accellent Inc.]]></employer>
        <location><![CDATA[Salem, VA, 24157, USA]]></location>
    </job>
    <job>
        <title><![CDATA[Engineer (Wire Department)]]></title>
        <description><![CDATA[


Job Title :Engineer (Wire Department)
Job Code :4354
Location :Salem VA US 24153
Job Description :

Accellent, Inc. is a fully integrated provider of design, supply chain management and strategic sourcing services to the Medical Device industry. Accellent, www.accellent.com, a recognized market leader, is a fast-growing outsource manufacturing and design solution company specializing in high growth areas such as Cardiology, Endoscopy and Orthopedics. The top Medical Device companies partner with Accellent to provide innovation, advanced technology, speed to market, low cost labor and strategic sourcing.
We&rsquo;re looking for team players with a can-do attitude to share in our vision and corporate values. Accellent offers competitive salaries; a comprehensive benefits package, and a stimulating work environment.

Position Scope / Summary
Currently, we are searching for an engineer to provide technical support to our wire manufacturing operations in Salem, VA. A degree in Metallurgical/Material Science Engineering or an engineer with extensive metal working experience is required for this position. Specfic knowledge of the heat treatment of metals, fine wire drawing and a mimimum of three yeras of experience are preferred.
Job Requirements :
&bull; Follows and develops Quality and Regulatory requirements including Accellent policies, procedures, and appropriate regulatory requirements.
&bull; Develops and Executes Process and Test Method Validations (IQ, OQ, PQ, PPQ) in accordance with Accellent procedures and guidelines
&bull; Communicates ideas, information, and recommendations clearly, effectively and frequently (oral and written) within Accellent, with outside suppliers or partners and with Accellent customers during formal and informal interactions.
&bull; Prepares or reviews documentation with a high degree of accuracy, completeness, and effectiveness using common Accellent engineering tools &amp; templates were available. (Examples include specifications, manufacturing procedures, ECOs, and technical reports or analysis)
&bull; Applies Lean manufacturing techniques to continuously improve cycle times and process flows. Identifies, and supports the execution of improvement efforts to reduce waste in all manufacturing and business processes.
&bull; Uses structured problem solving techniques and statistical methods for data driven analysis and decisions.
&bull; Applies DMAIC &ndash; Six Sigma approaches to solve issues and reduce variation in all manufacturing and business processes.
&bull; Plans and executes project activities within a cross functional team. Project types can include new product development and introduction, manufacturing transfers, continuous improvement and cost reduction initiatives.
&bull; Exhibits the Accellent values (Customer focus, Continuous Improvement, Performance, Accountability, Teamwork and Integrity) in all activities.
&bull; Demonstrates leadership through mentoring of junior staff and responsiveness to business needs to achieve positive results
&bull; Demonstrates technical ability through the application of engineering skills, approaches and knowledge.
&bull; Performs all duties and directs others creating a safe working environment for our employees and our communities.
&bull; Performs other duties as necessary.

Environmental Working Conditions
The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
While performing the duties of this job, the employee is frequently exposed to moving mechanical parts. The employee is occasionally exposed to high, precarious places; fumes or airborne particles; toxic or caustic chemicals; risk of electrical shock; and vibration. The noise level in the work environment is usually moderate.

Qualifications
It is impossible to list every requirement for, or responsibility of, any position. Similarly we cannot identify all the skills a position may require since job responsibilities and the Company&rsquo;s needs may change over time. Therefore, the above job description is not comprehensive or exhaustive. The Company reserves the right to adjust, add to or eliminate any aspect of the above description. The Company also retains the right to require all employees to undertake additional or different job responsibilities when necessary to meet business needs.

Due to the expected number of responses, only those most qualified will be contacted. No recruiters please; all unsolicited third-party submissions will be rejected.

Accellent is an Equal Opportunity/Affirmative Action employer and we value diversity in our workforce. As such we provide equal opportunity for all applicants without regard to race, religion, gender, national origin, age, marital status, veteran status, or disability. To learn more about Accellent and our career opportunities, please visit us at
www.accellent.com

Career Level :Experienced (Non-Manager)
Education :Bachelor's Degree
% of Travel Required :0-10%
Shift/Hours :First Shift (Day)
]]></description>
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        <industries>
            <industry><![CDATA[Health Products & Services]]></industry>
        </industries>
        <expiration_date>2010-03-25</expiration_date>
        <employer><![CDATA[Accellent Inc.]]></employer>
        <location><![CDATA[Salem, VA, 24157, USA]]></location>
    </job>
    <job>
        <title><![CDATA[Buyer/Planner III (Sr)]]></title>
        <description><![CDATA[


Job Title :Buyer/Planner III (Sr)
Job Code :4449
Location :Brooklyn Park MN US 55429
Job Description :
Essential Duties and Areas of Accountability:
Planning Responsibilities:
* Primarily responsible for the creation of the Master Demand Plan (MasterSchedule) for the site working with the Site Supply Chain Manager/Supervisor, as well as the Accellent Director of Supply Chain
* Responsible for the Creation and Management of the Forecast Demand files within Accellent's ERP system
* Creates, Schedules and maintains production orders within the Accellent ERP system for assigned work centers to load the factory to ensure manufacturing output goals are obtained for their site.
* Responsible for working with assigned work center supervisors in the proper tracking and reporting on OTD (on time delivery) cycle time and yield for production orders on a weekly basis.
* Responsible for determining the daily required production rate (takt time) for their assigned work centers, as well as working with the corresponding work center supervisors in the tracking and reporting on daily/weekly performance for their assigned areas
* Manage material flow in facility and through vendors who perform outside processingPurchasing Responsibilities:
* Prepares instructions and oversees purchasing systems and procedures; reviews purchase order claims and contracts for conformance to company policy
* Responsible for tactical procurement in support of the sites production schedules, as well as purchase order releases on blanket agreements negotiated with the Accellent Global Sourcing
* Prepares management reports as required (Inventory ABC analysis/cost savings program;raw material cost track, etc.); Tracks and updates operating/expense budget
* Procures all products to necessary dock dates to ensure on-time production starts per production schedule
* Ensures materials are utilized to minimize excess and obsolescence exposure
* Works with Global Sourcing to develop cost reduction programs with suppliers to ensure an annual reduction is achieved per facility objectives for both common Accellent materials working with Global sourcing as well as direct spend activities
* Timely sourcing and cost effective procurement of raw materials, factory/office supplies, as well as outside services.
* Analyzes contractual commitments, customer specifications, design changes, and other data to plan and develop planning and procurement activities from conceptual stage through life-cycle of product
* Responsible for site procurement activities (raw materials, outside services (OSV) as well as expense items)
* Managing and maintaining supplier programs, including the implementation of Kanban Replenishment, Consigned Vendor Managed Inventory (VMI) Programs in areas such as raw materials, tooling, etc.
* Global Sourcing - actively participates with Accellent Global Sourcing Commodity Management team on Strategic Supplier partnerships and agreements in support of Accellent Strategic Goals.
* Participates with Strategic Sourcing Commodity management on Supplier Relationship Management (SRM) quarterly/bi-annual reviews with key suppliers for the site, as well as participates in Global Sourcing SRM meetings as required.
* Supplier Performance Management - responsible for working with site operations quality and global sourcing on supplier report cards to insure that plans of action are developed and implemented for improving poor performanceQualifications:
To perform this job successfully, an individual must be able to perform eash essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
Education and/or Experience:
Bachelor's degree from four-year College or University; and five plus years related experience and/or training; or equivalent combination of education and experience.

Job Requirements :
Essential Duties and Areas of Accountability:
Planning Responsibilities:
* Primarily responsible for the creation of the Master Demand Plan (MasterSchedule) for the site working with the Site Supply Chain Manager/Supervisor, as well as the Accellent Director of Supply Chain
* Responsible for the Creation and Management of the Forecast Demand files within Accellent's ERP system
* Creates, Schedules and maintains production orders within the Accellent ERP system for assigned work centers to load the factory to ensure manufacturing output goals are obtained for their site.
* Responsible for working with assigned work center supervisors in the proper tracking and reporting on OTD (on time delivery) cycle time and yield for production orders on a weekly basis.
* Responsible for determining the daily required production rate (takt time) for their assigned work centers, as well as working with the corresponding work center supervisors in the tracking and reporting on daily/weekly performance for their assigned areas
* Manage material flow in facility and through vendors who perform outside processingPurchasing Responsibilities:
* Prepares instructions and oversees purchasing systems and procedures; reviews purchase order claims and contracts for conformance to company policy
* Responsible for tactical procurement in support of the sites production schedules, as well as purchase order releases on blanket agreements negotiated with the Accellent Global Sourcing
* Prepares management reports as required (Inventory ABC analysis/cost savings program;raw material cost track, etc.); Tracks and updates operating/expense budget
* Procures all products to necessary dock dates to ensure on-time production starts per production schedule
* Ensures materials are utilized to minimize excess and obsolescence exposure
* Works with Global Sourcing to develop cost reduction programs with suppliers to ensure an annual reduction is achieved per facility objectives for both common Accellent materials working with Global sourcing as well as direct spend activities
* Timely sourcing and cost effective procurement of raw materials, factory/office supplies, as well as outside services.
* Analyzes contractual commitments, customer specifications, design changes, and other data to plan and develop planning and procurement activities from conceptual stage through life-cycle of product
* Responsible for site procurement activities (raw materials, outside services (OSV) as well as expense items)
* Managing and maintaining supplier programs, including the implementation of Kanban Replenishment, Consigned Vendor Managed Inventory (VMI) Programs in areas such as raw materials, tooling, etc.
* Global Sourcing - actively participates with Accellent Global Sourcing Commodity Management team on Strategic Supplier partnerships and agreements in support of Accellent Strategic Goals.
* Participates with Strategic Sourcing Commodity management on Supplier Relationship Management (SRM) quarterly/bi-annual reviews with key suppliers for the site, as well as participates in Global Sourcing SRM meetings as required.
* Supplier Performance Management - responsible for working with site operations quality and global sourcing on supplier report cards to insure that plans of action are developed and implemented for improving poor performanceQualifications:
To perform this job successfully, an individual must be able to perform eash essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
Education and/or Experience:
Bachelor's degree from four-year College or University; and five plus years related experience and/or training; or equivalent combination of education and experience.

Career Level :Experienced (Non-Manager)
Education :Bachelor's Degree
]]></description>
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            <industry><![CDATA[Health Products & Services]]></industry>
        </industries>
        <expiration_date>2010-03-25</expiration_date>
        <employer><![CDATA[Accellent Inc.]]></employer>
        <location><![CDATA[Brooklyn Park, MN, 55445, USA]]></location>
    </job>
    <job>
        <title><![CDATA[Swiss Machinist -  Platinum Nights]]></title>
        <description><![CDATA[


Job Title :Swiss Machinist - Platinum Nights
Job Code :4332
Location :Brooklyn Park MN US 55429
Job Description :
Accellent, Inc. is a fully integrated provider of design, supply chain management and strategic sourcing services to the Medical Device industry. Accellentwww.accellent.com, a recognized market leader, is a fast-growing outsource manufacturing and design solution company specializing in high growth areas such as Cardiology, Endoscopy and Orthopaedics. The top Medical Device companies partner with Accellent to provide innovation, advanced technology, speed to market, low cost labor and strategic sourcing.
We&rsquo;re looking for team players with a can-do attitude to share in our vision and corporate values. Accellent offers competitive salaries; a comprehensive benefits package, and a stimulating work environment.
Currently, we are searching for a Swiss Machinist Nights to join our Brooklyn Park facility.
Job Requirements :
Position Scope/Summary
Setup, troubleshoot, operate and perform maintenance when required to machines.
Include the following:
Responsible for keeping the machines running and work area clean.
Operate the machine as efficiently as possible.
Produce high quality components to print specifications. 
Read part prints and understand dimensions.
Use and understand how inspection equipment works making sure it is correct and is calibrated.
Do whatever is needed to insure quality - including sorting for features that are uncontrollable.
Obtain material from material rack.
Communicate with opposite shift operator to insure smooth transition between shifts.
Follow all company policies and rules.
Provide support within the organization as experienceand time allow.
Other duties may be assigned.
 Key Result Accountabilities
Supervisory Responsibilities:
Needs to work in an atmosphere with little supervision.
Language Skills:
Must be able to communicate with inspection personnel as well as other operators.
Mathematical Skills:
Must have basic math skills.
Reasoning Ability:
Must be able to reason cause and effect on parts.
Strong organizational skills.

 Environmental Working Conditions
Reasonable accommodations may be made to enable individuals with disabilities to perform the 
essential functions.
                              
 Qualifications
Must be able to read a print and use inspection equipment necessary to do the job.
  It is impossible to list every requirement for, or responsibility of, any position. Similarly we cannot
  identify all the skills a position may require since job responsibilities and the Company&rsquo;s needs may
  change over time. Therefore, the above job description is not comprehensive or exhaustive. 
 The Company reserves the right to adjust, add to or eliminate any aspect of the above description. 
 The Company also retains the right to require all employees to undertake additional or different job
 responsibilities when necessary to meet business needs.
Due to the expected number of responses, only those most qualified will be contacted. No recruiters please; all unsolicited third-party submissions will be rejected.

Accellent is an Equal Opportunity/Affirmative Action employer and we value diversity in our workforce. As such we provide equal opportunity for all applicants without regard to race, religion, gender, national origin, age, marital status, veteran status, or disability. To learn more about Accellent and our career opportunities, please visit us atwww.accellent.com

Career Level :Experienced (Non-Manager)
Education :High School or equivalent
% of Travel Required :None
Shift/Hours :Third Shift (Night)
]]></description>
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        <industries>
            <industry><![CDATA[Health Products & Services]]></industry>
        </industries>
        <expiration_date>2010-03-25</expiration_date>
        <employer><![CDATA[Accellent Inc.]]></employer>
        <location><![CDATA[Brooklyn Park, MN, 55445, USA]]></location>
    </job>
    <job>
        <title><![CDATA[CNC Machinist - Cell 12]]></title>
        <description><![CDATA[


Job Title :CNC Machinist - Cell 12
Job Code :4331
Location :Brooklyn Park MN US 55429
Job Description :
Accellent, Inc. is a fully integrated provider of design, supply chain management and strategic sourcing services to the Medical Device industry. Accellentwww.accellent.com, a recognized market leader, is a fast-growing outsource manufacturing and design solution company specializing in high growth areas such as Cardiology, Endoscopy and Orthopaedics. The top Medical Device companies partner with Accellent to provide innovation, advanced technology, speed to market, low cost labor and strategic sourcing. 
We&rsquo;re looking for team players with a can-do attitude to share in our vision and corporate values. Accellent offers competitive salaries; a comprehensive benefits package, and a stimulating work environment. 
Currently, we are searching for a CNC Machinist to join our Brooklyn Park, MN facility.
About the Opportunity:
Position Scope/Summary

Operate EDM, Swiss and other shop equipment to produce parts or add features to parts according to blueprints.
Include the following:
To keep machines running, inspect parts, have acceptable attendance, check parts from the operator before you, keep your work area clean.
Provide support within the organization as experience and time allow.
Other duties may be assigned.
Job Requirements :
Key Result Accountabilities
Language Skills:
Basic reading, writing, and communication skills.
Mathematical Skills:
Basic, Trigonometry helpful, ability to learn algebra.
Reasoning Ability:
Have the ability to work with all types of workers. Be able to troubleshoot and solve minor problems.
Physical Demands: 
The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
Environmental Working Conditions
The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. 
Due to the expected number of responses, only those most qualified will be contacted. No recruiters please; all unsolicited third-party submissions will be rejected.
Accellent is an Equal Opportunity/Affirmative Action employer and we value diversity in our workforce. As such we provide equal opportunity for all applicants without regard to race, religion, gender, national origin, age, marital status, veteran status, or disability. To learn more about Accellent and our career opportunities, please visit us atwww.accellent.com
It is impossible to list every requirement for, or responsibility of, any position. Similarly we cannot identify all the skills a position may require since job responsibilities and the Company&rsquo;s needs may change over time. Therefore, the above job description is not comprehensive or exhaustive. The Company reserves the right to adjust, add to or eliminate any aspect of the above description. The Company also retains the right to require all employees to undertake additional or different job responsibilities when necessary to meet business needs.
Career Level :Experienced (Non-Manager)
Education :Vocational
% of Travel Required :None
Shift/Hours :Second Shift (Afternoon)
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            <industry><![CDATA[Health Products & Services]]></industry>
        </industries>
        <expiration_date>2010-03-25</expiration_date>
        <employer><![CDATA[Accellent Inc.]]></employer>
        <location><![CDATA[Brooklyn Park, MN, 55445, USA]]></location>
    </job>
    <job>
        <title><![CDATA[Program Manager]]></title>
        <description><![CDATA[


Job Title :Program Manager
Job Code :4207
Location :Brooklyn Park MN US 55429
Job Description :
Job Description:*
Accellent, Inc. is a fully integrated provider of design, supply chain management and strategic sourcing services to the Medical Device industry. Accellentwww.accellent.com, a recognized market leader, is a fast-growing outsource manufacturing and design solution company specializing in high growth areas such as Cardiology, Endoscopy and Orthopedics. The top Medical Device companies partner with Accellent to provide innovation, advanced technology, speed to market, low cost labor and strategic sourcing.
We&rsquo;re looking for team players with a can-do attitude to share in our vision and corporate values. Accellent offers competitive salaries; a comprehensive benefits package, and a stimulating work environment.
Currently, we are searching for a Program Manager to join our Brooklyn Park, MN facility.

Position Scope/Summary
Under minimal direction, performs work of considerable difficulty in advanced engineering work focus on program responsibility. This work involves the application of considerable professional engineering knowledge and skills to the direction of a major engineering project as an ongoing program function. Duties may involve the supervision, coordination and scheduling of subordinate technical staff and the coordination of program or project activities with other facilities. Assignments are broad in scope with the opportunity for the use of independent judgment
Job Requirements :
Key Result Accountabilities
* Interfaces directly and regularly with customers (internal and external) staff. Will typically be assigned projects that are of the highest priority and revenue potential with high visibility by Accellent customers. Often is included in critical business discussions with customers to bring deep insight to a problem or opportunity and establish a high level of credibility for Accellent through demonstrated program management knowledge and expertise.
* Proactively manage the risk associated with projects so that Accellent and the customer&rsquo;s business objectives are achieved
* Minimize the uncertainties associated with projects relative to scope changes, customer expectations, business issues and other intangibles to enable successful completion of projects.
* Work with sales to define customer needs and develop a comprehensive plan to meet their needs. Involve and coordinate the input of all key functional groups and contributors to the proposed work plan.
* Enable customer involvement on projects to insure that Accellent is viewed as a collaborative extension of their engineering department.
* Establish and maintain customer communications and credibility as the Accellent champion who is responsible to insure successful development and manufacturing launch.
* Work effectively at all levels of Accellent to influence multiple resources towards successful completion of projects while having ultimate accountability for successful execution.
* Follows and develops Quality and Regulatory requirements including Accellent policies, procedures, and appropriate regulatory requirements.
* Communicates ideas, information, and recommendations clearly, effectively and frequently (oral and written) within Accellent, with outside suppliers or partners and with Accellent customers during formal and informal interactions.
* Prepares or reviews documentation with a high degree of accuracy, completeness, and effectiveness using common Accellent engineering tools &amp; templates were available. (Examples include specifications, manufacturing procedures, ECOs, and technical reports or analysis)
* Applies and Promotes Lean manufacturing techniques to continuously improve cycle times and process flows. Identifies, supports, or directs the execution of improvement efforts to reduce waste in all manufacturing and business processes.
* Uses structured problem solving techniques and statistical methods for data driven analysis and decisions.
* Applies and leads DMAIC &ndash; Six Sigma approaches to solve issues and reduce variation in all manufacturing and business processes.
* Plans, executes and manages project activities with cross functional teams. Project types can include new product development and introduction, manufacturing transfers, continuous improvement and cost reduction initiatives.
* Exhibits the Accellent values (Customer focus, Continuous Improvement, Performance, Accountability, Respect, Teamwork and Integrity) in all activities.
* Demonstrates leadership through mentoring of junior staff, responsiveness to business needs and motivation of diverse, cross functional teams including influencing both internal and external members to achieve positive business results
* Demonstrates technical ability through the application of engineering skills, approaches and knowledge.
* Takes financial responsibility for activities to create positive impact to the business
* Performs all duties and directs others creating a safe working environment for our employees and our communities.
* Other duties as assigned.
Environmental Working Conditions
The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
While performing the duties of this job, the employee is frequently exposed to moving mechanical parts. The employee is occasionally exposed to high, precarious places; fumes or airborne particles; toxic or caustic chemicals; risk of electrical shock; and vibration. The noise level in the work environment is usually moderate.
Qualifications
* BS in Engineering/Technical Field, advanced degree (masters, PhD, Lean or Six sigma Black Belet certification) preferred
* 10+ years experience (5+ in medical device industry)
* Injection Molding experience
* To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed here and in the Engineering Career Matrix are representative of the knowledge, skill, and/or abilities required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
* In addition, the individual must have a working knowledge of ISO and applicable customer and regulatory standards.
Environmental Working Conditions
The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
While performing the duties of this job, the employee is frequently exposed to moving mechanical parts. The employee is occasionally exposed to high, precarious places; fumes or airborne particles; toxic or caustic chemicals; risk of electrical shock; and vibration. The noise level in the work environment is usually moderate.

It is impossible to list every requirement for, or responsibility of, any position. Similarly we cannot identify all the skills a position may require since job responsibilities and the Company&rsquo;s needs may change over time. Therefore, the above job description is not comprehensive or exhaustive. The Company reserves the right to adjust, add to or eliminate any aspect of the above description. The Company also retains the right to require all employees to undertake additional or different job responsibilities when necessary to meet business needs. Employee Signature

Due to the expected number of responses, only those most qualified will be contacted. No recruiters please; all unsolicited third-party submissions will be rejected.
Accellent is an Equal Opportunity/Affirmative Action employer and we value diversity in our workforce. As such we provide equal opportunity for all applicants without regard to race, religion, gender, national origin, age, marital status, veteran status, or disability. To learn more about Accellent and our career opportunities, please visit us atwww.accellent.com

Career Level :Experienced (Non-Manager)
Education :Bachelor's Degree
% of Travel Required :0-10%
Shift/Hours :First Shift (Day)
]]></description>
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            <industry><![CDATA[Health Products & Services]]></industry>
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        <expiration_date>2010-03-25</expiration_date>
        <employer><![CDATA[Accellent Inc.]]></employer>
        <location><![CDATA[Brooklyn Park, MN, 55445, USA]]></location>
    </job>
    <job>
        <title><![CDATA[NC Lathe, Set-Up Operator]]></title>
        <description><![CDATA[


Job Title :NC Lathe, Set-Up Operator
Job Code :4209
Location :Wheeling IL US
Job Description :
Accellent, Inc. is a fully integrated provider of design, supply chain management and strategic sourcing services to the Medical Device industry. Accellentwww.accellent.com, a recognized market leader, is a fast-growing outsource manufacturing and design solution company specializing in high growth areas such as Cardiology, Endoscopy and Orthopaedics. The top Medical Device companies partner with Accellent to provide innovation, advanced technology, speed to market, low cost labor and strategic sourcing. 
We are seeking a candidate to become an integral part of a high performing team. Candidate must be able to program and machine tight tolerance Medical and Aerospace production parts. Candidates must also be proficient at programming and set up of SQT 200MY (or similar) Mazak CNC lathe machines. Experience with Geometric Dimensions and Tolerances along with reading and interpreting blueprints is required. Experience with Programming and setup of Mazak Vertical Machining Centers a plus.
Essential Job Functions:
Program &amp; Set Up Mazak SQT 200MY (or similar) lathes
Machining Experience 5+ years
Provide hands-on manufacturing expertise for machined products
Ability to read and interpret engineering drawings &amp; specifications
Part inspection including SPC data collection
Maintain organization to ISO operation procedures.
Complete all job specific required training.
Perform duties to achieve overall business unit metrics.
Comply with all safety regulations, wears appropriate safety equipment as required in each area of the facility
General housekeeping
Preferred Background:
Program &amp; Set Up Mazak vertical machining centers a plus
Mastercam experience a plus
CMM experience a plus
     



   
Job Requirements :
  
   Qualifications
* Minimum 4+ years of shop manual machine experience
* Ability to use typical inspection equipment.
* In depth knowledge of most conventional equipment and machines
* Ability to read most blueprints and operation sheets
* Good understanding of shop math . Ability to use trigonometry and on blueprints and operation sheets
* Good understanding of geometric tolerances.
* Maintain organization to ISO operation procedures.
* Complete all job specific required training.
* Perform duties to achieve overall business unit metrics.
* Comply to all safety regulations, wears appropriate safety equipment as required in each area of the facility.

Due to the expected number of responses, only those most qualified will be contacted. No recruiters please; all unsolicited third-party submissions will be rejected.

Accellent is an Equal Opportunity/Affirmative Action employer and we value diversity in our workforce. As such we provide equal opportunity for all applicants without regard to race, religion, gender, national origin, age, marital status, veteran status, or disability. To learn more about Accellent and our career opportunities, please visit us atwww.accellent.com
Career Level :Experienced (Non-Manager)
Education :High School or equivalent
% of Travel Required :0-10%
Shift/Hours :Second Shift (Afternoon)
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            <industry><![CDATA[Health Products & Services]]></industry>
        </industries>
        <expiration_date>2010-03-25</expiration_date>
        <employer><![CDATA[Accellent Inc.]]></employer>
        <location><![CDATA[Wheeling, IL, 60070, USA]]></location>
    </job>
    <job>
        <title><![CDATA[Senior Engineer]]></title>
        <description><![CDATA[


Job Title :Senior Engineer
Job Code :4212
Location :Arvada CO US 80002
Job Description :
Accellent, Inc. is a fully integrated provider of design, supply chain management and strategic sourcing services to the Medical Device industry. Accellentwww.accellent.com, a recognized market leader, is a fast-growing outsource manufacturing and design solution company specializing in high growth areas such as Cardiology, Endoscopy and Orthopaedics. The top Medical Device companies partner with Accellent to provide innovation, advanced technology, speed to market, low cost labor and strategic sourcing. 
We&rsquo;re looking for team players with a can-do attitude to share in our vision and corporate values. Accellent offers competitive salaries, a comprehensive benefits package, and a stimulating work environment. 
Currently, we are searching for a Senior Engineer to join our Arvada facility.

Position Scope/Summary
Directs, coordinates, and exercises functional authority for planning, organization, control, integration, and completion of engineering activities within area of assigned responsibility.
Key Results &amp; Accountabilities 
Follows and develops Quality and Regulatory requirements including Accellent policies, procedures, and appropriate regulatory requirements. 
Plans, Develops, and Executes Process and Test Method Validations (IQ, OQ, PQ, PPQ) in accordance with Accellent procedures and guidelines.
Communicates ideas, information, and recommendations clearly, effectively and frequently (oral and written) within Accellent, with outside suppliers or partners and with Accellent customers during formal and informal interactions. 
Prepares or reviews documentation with a high degree of accuracy, completeness, and effectiveness using common Accellent engineering tools &amp; templates were available. (Examples include specifications, manufacturing procedures, ECOs, and technical reports or analysis). 
Applies and Promotes Lean manufacturing techniques to continuously improve cycle times and process flows. Identifies, supports, or directs the execution of improvement efforts to reduce waste in all manufacturing and business processes. 
Uses structured problem solving techniques and statistical methods for data driven analysis and decisions.
Applies and leads DMAIC &ndash; Six Sigma approaches to solve issues and reduce variation in all manufacturing and business processes.
Plans, executes and manages project activities with cross functional teams. Project types can include new product development and introduction, manufacturing transfers, continuous improvement and cost reduction initiatives.
Job Requirements :
Job Description
Exhibits the Accellent values (Customer focus, Continuous Improvement, Performance, Accountability, Teamwork and Integrity) in all activities 
Demonstrates leadership through mentoring of junior staff, responsiveness to business needs and motivation of diverse, cross functional teams including influencing both internal and external members to achieve positive business results . 
Demonstrates technical ability through the application of engineering skills, approaches and knowledge. 
Takes financial responsibility for activities to create positive impact to the business. 
Performs all duties and directs others creating a safe working environment for our employees and our communities. 
Performs other duties as necessary.
Environmental Working Conditions
The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
While performing the duties of this job, the employee is frequently exposed to moving mechanical parts. The employee is occasionally exposed to high, precarious places; fumes or airborne particles; toxic or caustic chemicals; risk of electrical shock; and vibration. The noise level in the work environment is usually moderate.
Qualifications
To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed here and in the Engineering Career Matrix are representative of the knowledge, skill, and/or abilities required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
In addition, the individual must have a working knowledge of ISO and applicable customer and regulatory standards.
It is impossible to list every requirement for, or responsibility of, any position. Similarly we cannot identify all the skills a position may require since job responsibilities and the Company&rsquo;s needs may change over time. Therefore, the above job description is not comprehensive or exhaustive. The Company reserves the right to adjust, add to or eliminate any aspect of the above description. The Company also retains the right to require all employees to undertake additional or different job responsibilities when necessary to meet business needs.


Due to the expected number of responses, only those most qualified will be contacted. No recruiters please; all unsolicited third-party submissions will be rejected.

Accellent is an Equal Opportunity/Affirmative Action employer and we value diversity in our workforce. As such we provide equal opportunity for all applicants without regard to race, religion, gender, national origin, age, marital status, veteran status, or disability. To learn more about Accellent and our career opportunities, please visit us atwww.accellent.com

Career Level :Experienced (Non-Manager)
Education :Bachelor's Degree
% of Travel Required :10-20%
Shift/Hours :First Shift (Day)
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            <industry><![CDATA[Health Products & Services]]></industry>
        </industries>
        <expiration_date>2010-03-25</expiration_date>
        <employer><![CDATA[Accellent Inc.]]></employer>
        <location><![CDATA[Arvada, CO, 80005, USA]]></location>
    </job>
    <job>
        <title><![CDATA[Account Manager - Medical Device Manufacturing]]></title>
        <description><![CDATA[


Job Title :Account Manager - Medical Device Manufacturing
Job Code :4222
Location :Cincinatti OH US 45223
Job Description :
Accellent, Inc. is a fully integrated provider of design, supply chain management and strategic sourcing services to the Medical Device industry. Accellentwww.accellent.com, a recognized market leader, is a fast-growing outsource manufacturing and design solution company specializing in high growth areas such as Cardiology, Endoscopy and Orthopaedics. The top Medical Device companies partner with Accellent to provide innovation, advanced technology, speed to market, low cost labor and strategic sourcing.
We&rsquo;re looking for team players with a can-do attitude to share in our vision and corporate values. Accellent offers competitive salaries; a comprehensive benefits package, and a stimulating work environment.
Currently, we are searching for a to join a Technical (Manufacturing Engineering) Account Manager to join our corporate sales team.
About the Opportunity:
Based in the Cincinnatti-area, the Account Manager is responsible for tartgeted retention, satisfaction increasing revenues and profitability of established Key Account(s).
The Account Manager role is an excellent opportunity for a candidate with a strong engineering, manufacturing sales (OEM) or design engineer from a medical device environment.
The Account Manager focus includes the retention of existing revenues as well as identifying, qualifying and closing new business for incremental revenue realization. To enhance the reputation and business relationship between customer and the company.
Key Result Accountabilities
* Overall responsibility for the revenue growth of assigned customers through value add solutions and contract negotiation.
* Retain and increase the profitable penetration of existing accounts
* Establish, maintain, and grow strong relationships with decision makers at assigned customers.
* Responsible for accomplishing sales objectives to include revenue growth, identifying and prioritizing opportunities, securing resources, executing sales strategies and pull-through tactics to meet planned and company objectives.
* Develop and execute specific account strategies to promote revenue growth and increase market share.
* Identify, engage and maintain relationships with key influencers/decision makers through active customer involvement. Primary call points are &ldquo;C&rdquo; level executives and other senior managers who can influence large transfers of outsourcing business to the company.
* Keeps informed on new products, services, and other general information of interest to customers, through successful completion of Sales Training, shop floor experience, local training, and self-study.
* Stays informed of customer business opportunities, account changes, current conditions, future prospects, active measurements, and competitive landscape to protect revenue from competitors.
* Provides direction and guidance to Field Sales Engineer/s, primarily on ways of implementing strategic deals and ensuring service levels for assigned accounts are met.
* Develop technical expertise related to company and industry.
* Presents customer key performance indicators (KPIs) to review overall service performance for the quarter.
* Responsible for maintaining expenses within budget.
* Responsible for generating required reporting.
This is a field-based, home office position with an expected 25%-50% travel (territory and assigned account dependant) 
Job Requirements :
* Bachelors Degree a. Related discipline or engineering degree preferred
* Business to business sales experience (min 2-5years) a. Medical Device Industry preferred b. Proven successful track record c. Completion of formal sales training program(s) a plus
* Demonstrated selling and account management skills
* Ability to translate strategy into tactical implementation and to motivate people to execute on the strategy
* Able to effectively call on &ldquo;C&rdquo; level and senior management across multiple functions (Operations, Engineering, Marketing) of major OEM Medical Manufacturers.
* Demonstrated ability to work collaboratively with and influence peers and management.
* Able to direct a cross functional team to work in concert to deliver goods and services.
* Highly motivated, disciplined/self starter
* Strong interpersonal, communication, presentation and organizational skills. The ability to build effective relationships.
* Able to analyze, understand and effectively communicate technical material
* Proficient computer skills (Outlook, Excel, Word, PowerPoint); CAD &amp; Design programs a plus
* Able to assess the financial impact of deals &amp; opportunities.
* Skilled in negotiation at highest level.
* Strong understanding of the medical device industry and/or contract manufacturing industry.
Due to the expected number of responses, only those most qualified will be contacted. No recruiters please; all unsolicited third-party submissions will be rejected.

Accellent is an Equal Opportunity/Affirmative Action employer and we value diversity in our workforce. As such we provide equal opportunity for all applicants without regard to race, religion, gender, national origin, age, marital status, veteran status, or disability. To learn more about Accellent and our career opportunities, please visit us atwww.accellent.com
Career Level :Experienced (Non-Manager)
Education :Bachelor's Degree
% of Travel Required :40-50%
Shift/Hours :First Shift (Day)
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            <industry><![CDATA[Health Products & Services]]></industry>
        </industries>
        <expiration_date>2010-03-25</expiration_date>
        <employer><![CDATA[Accellent Inc.]]></employer>
        <location><![CDATA[Cincinatti, OH, 45217, USA]]></location>
    </job>
    <job>
        <title><![CDATA[Finisher]]></title>
        <description><![CDATA[


Job Title :Finisher
Job Code :4309
Location :Orchard Park NY US 14127
Job Description :
Key Result Accountabilities
1.   Knowledgeable about finishing techniques, which include but are not limited to using foredoms, gesswein, tumbling, burlytic, cleaning, grinding, miyano operations, Lapmaster, red wheeling, hand deburring, tumble blasting, sand blasting, clean room operations, molding machines, furnaces, waterbaths, dryers, trim, scrape or deburr parts using hand tools and equipment.
2.   Responsible for performing work that meets or exceeds our production standards and scrap rates that will achieve our metric goals for scrap, Fill Rate, Rework, Customer Lot Acceptance (CLA), and Customer Complaints, etc.
3.   Knowledge of shop control system in order to review and print paperwork needed for job and input data for work completed on various jobs.
4.   Use Smart Scope, comparator, micrometers, blade micrometers, counting scales and/or profilometer for measuring and counting parts, as necessary.
5.   Knowledge of reading and using Collection Plans in order to conduct frequency checks.
6.   Understand MVR procedures.
7.   Be able to rotate into other Finishing jobs with competency and confidence.
8.   Ability to work well in a team environment.
9.   Other duties as necessary.
10. Keep work area clean.
1.   
Job Requirements :
1.   Able to use microscope and other measuring equipment.
2.   Able to use computer, pulling up instructions and reading them.
3.   Able to follow instructions, both written and verbal.
4.   Able to count parts.

Career Level :Entry Level
Education :High School or equivalent
Shift/Hours :Second Shift (Afternoon)
]]></description>
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            <industry><![CDATA[Health Products & Services]]></industry>
        </industries>
        <expiration_date>2010-03-25</expiration_date>
        <employer><![CDATA[Accellent Inc.]]></employer>
        <location><![CDATA[Orchard Park, NY, 14127, USA]]></location>
    </job>
    <job>
        <title><![CDATA[Assembler]]></title>
        <description><![CDATA[


Job Title :Assembler
Job Code :4310
Location :Laconia NH US 03246
Job Description :
Accellent, Inc. is a fully integrated provider of design, supply chain management and strategic sourcing services to the Medical Device industry. Accellentwww.accellent.com, a recognized market leader, is a fast-growing outsource manufacturing and design solution company specializing in high growth areas such as Cardiology, Endoscopy and Orthopaedics. The top Medical Device companies partner with Accellent to provide innovation, advanced technology, speed to market, low cost labor and strategic sourcing. 
We&rsquo;re looking for team players with a can-do attitude to share in our vision and corporate values. Accellent offers competitive salaries; a comprehensive benefits package, and a stimulating work environment. 
Currently, we are searching for a to join our facility.
About the Opportunity:
Temporary Assembler - standard job description applies


Job Requirements :




Due to the expected number of responses, only those most qualified will be contacted. No recruiters please; all unsolicited third-party submissions will be rejected.

Accellent is an Equal Opportunity/Affirmative Action employer and we value diversity in our workforce. As such we provide equal opportunity for all applicants without regard to race, religion, gender, national origin, age, marital status, veteran status, or disability. To learn more about Accellent and our career opportunities, please visit us atwww.accellent.com
Career Level :Experienced (Non-Manager)
Education :High School or equivalent
% of Travel Required :0-10%
Shift/Hours :First Shift (Day)
]]></description>
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        <industries>
            <industry><![CDATA[Health Products & Services]]></industry>
        </industries>
        <expiration_date>2010-03-25</expiration_date>
        <employer><![CDATA[Accellent Inc.]]></employer>
        <location><![CDATA[Laconia, NH, 03246, USA]]></location>
    </job>
    <job>
        <title><![CDATA[Assembler]]></title>
        <description><![CDATA[


Job Title :Assembler
Job Code :4312
Location :Laconia NH US 03246
Job Description :
Accellent, Inc. is a fully integrated provider of design, supply chain management and strategic sourcing services to the Medical Device industry. Accellentwww.accellent.com, a recognized market leader, is a fast-growing outsource manufacturing and design solution company specializing in high growth areas such as Cardiology, Endoscopy and Orthopaedics. The top Medical Device companies partner with Accellent to provide innovation, advanced technology, speed to market, low cost labor and strategic sourcing. 
We&rsquo;re looking for team players with a can-do attitude to share in our vision and corporate values. Accellent offers competitive salaries; a comprehensive benefits package, and a stimulating work environment. 
Currently, we are searching for a to join our facility.
About the Opportunity:
Temporary Assembler - standard job description applies


Job Requirements :




Due to the expected number of responses, only those most qualified will be contacted. No recruiters please; all unsolicited third-party submissions will be rejected.

Accellent is an Equal Opportunity/Affirmative Action employer and we value diversity in our workforce. As such we provide equal opportunity for all applicants without regard to race, religion, gender, national origin, age, marital status, veteran status, or disability. To learn more about Accellent and our career opportunities, please visit us atwww.accellent.com
Career Level :Experienced (Non-Manager)
Education :High School or equivalent
% of Travel Required :0-10%
Shift/Hours :First Shift (Day)
]]></description>
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        <industries>
            <industry><![CDATA[Health Products & Services]]></industry>
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        <expiration_date>2010-03-25</expiration_date>
        <employer><![CDATA[Accellent Inc.]]></employer>
        <location><![CDATA[Laconia, NH, 03246, USA]]></location>
    </job>
    <job>
        <title><![CDATA[Supply Chain Supervisor]]></title>
        <description><![CDATA[


Job Title :Supply Chain Supervisor
Job Code :4327
Location :Houston PA US 15342
Job Description :
Position Scope/Summary
The responsibility of a supervisor inventory control includes, but is not limited to: providing leadership and direction to a team of (1-4) personnel, as well as assigning work in specified work areas. Training of material handlers as required. &ldquo;On the job training&rdquo; and subsequent certification to all of the procedures pertinent to their specific assigned job level (Receiving, Inventory Control, Shipping &amp; Cycle Count). Improving and/or maintaining warehouse organization in respect to safety, quality of work, product flow, product identification, FIFO, inventory control, and housekeeping. Lead Inventory Control process including cycle counting, identification of discrepancies, and discrepancy resolution. Timely response to customer needs including expedites of shipments, physical counts, control of customer supplied inventories.
Key Result Accountabilities
* Support management with the implementation of new policies and procedures, and direct team members ensuring complete conformance.
* Must be fully proficient in all duties related to shipping, receiving, and inventory control.
* Provide leadership and direction to assigned area of responsibility ensuring quality standards are met and daily assignments are carried out.
* Insure that staff follows all processes and instructions as dictated by quality procedures.
* Has the responsibility of establishing and following documentation for normal material handling requirements (receiving, inventory control and shipping).
* Responsible for labeling accuracy with proper description and information for shipping/receiving and inventory control purposes.
* Must train or assist personnel where applicable.
* Develop and possess the ability to initiate and accurately complete the required documentation (i.e. certificates of compliance, packing lists, shipping labels, foreign invoices, daily shipping lists, inventory labels, etc.)
* Possess and/or obtain necessary skills to accurately perform all required duties.
* Performs job duties with little or no supervision or assistance.
* Acts as a resource during audits or customer visits for questions and answers or practical demonstrations.
* Maintains cleanliness of work area, machines, tools, and equipment. (5S program in support of lean)
* Insure alignment of department resources in support of lean manufacturing and cell support teams.
* Performs job duties with little or no supervision or assistance.
&middot; Responsible for the safe operation and set-up of all warehousing equipment including lift trucks, pallet jacks, shrink wrappers, and scales. 
&middot; Responsible for performing routing preventive maintenance as assigned by Facilities Maintenance Manager.
&middot; Responsible for reporting any suspected machine malfunctions to the immediate supervisor of the area in which he/she is working.
&middot; Accurate documentation, reporting, time card maintenance.
&middot; Responsible for following material requisitioning procedures for kitting (issuance ) of raw materials , moving of all raw material and work in process materials.
&middot; Responsible for following all lot control procedures as defined by Q.A. Department.
&middot; Manages shop floor material transactions
&middot; Prints work order/ job travelers as needed.
&middot; Performs material transactions as required to include issuing material to jobs.
&middot; Monitors material transactions for accuracy and maintenance of traceability.
&middot; Reviews completed jobs for transaction integrity and use information for necessary training and continued improvement.
&middot; Follow all instructions contained in work order packets including: MPR&rsquo;s, MPS&rsquo;s, and Work Instructions.
&middot; Complies with work rules including those pertaining to safety, health, Quality System, and the Accellent Quality Management System.
&middot; Overtime as required.
Qualifications
* Ability to read, write and speak fluent English
* Associates / Undergraduate degree and 5 years prior related experience in a manufacturing/scheduling/planning environment, or a combination of experience and education
* Prior inventory control experience preferred
* Familiar with computer based planning and scheduling systems (Oracle experience preferred)
* Ability to assimilate information quickly and possesses strong decision making abilities and organizational skills
* Must be capable of assimilating Accellent systems and procedures quickly
* Able to work in a fast paced and evolving environment
* Working knowledge of material handling equipment and processes, as well as work center capacities
* Ability to coordinate internal and external vendor services and customer needs
* Strong experience with MS Word and Excel
* Solid understanding of ISO and Quality System Procedures
* Complete all job specific required training
* Perform duties to achieve overall business unit metrics
* Compliance all safety regulations, wears appropriate safety equipment as required in each area of the facility
* Prior experience working in a manufacturing environment strongly preferred
* Prior supervisory experience a must
* Prior experience in a Lean Manufacturing environment a plus.
Job Requirements :
Qualifications
* Ability to read, write and speak fluent English
* Associates / Undergraduate degree and 5 years prior related experience in a manufacturing/scheduling/planning environment, or a combination of experience and education
* Prior inventory control experience preferred
* Familiar with computer based planning and scheduling systems (Oracle experience preferred)
* Ability to assimilate information quickly and possesses strong decision making abilities and organizational skills
* Must be capable of assimilating Accellent systems and procedures quickly
* Able to work in a fast paced and evolving environment
* Working knowledge of material handling equipment and processes, as well as work center capacities
* Ability to coordinate internal and external vendor services and customer needs
* Strong experience with MS Word and Excel
* Solid understanding of ISO and Quality System Procedures
* Complete all job specific required training
* Perform duties to achieve overall business unit metrics
* Compliance all safety regulations, wears appropriate safety equipment as required in each area of the facility
* Prior experience working in a manufacturing environment strongly preferred
* Prior supervisory experience a must
* Prior experience in a Lean Manufacturing environment a plus.
Career Level :Experienced (Non-Manager)
Education :Bachelor's Degree
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        <expiration_date>2010-03-25</expiration_date>
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        <location><![CDATA[Houston, PA, 15342, USA]]></location>
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    <job>
        <title><![CDATA[Buyer/ Planner]]></title>
        <description><![CDATA[


Job Title :Buyer/ Planner
Job Code :4326
Location :Houston PA US 15342
Job Description :
Schedules, orders and coordinates the delivery of parts/materials, equipment and services used in product manufacturing according to production plans. Controls the inventory of assigned production parts/materials in accordance with management objectives. Expedites requirements as needed (e.g., order action, shortage/pre-shortage, late order reports). Establishes standard cost on assigned production parts/materials for approval by management. Assist in the selection of particular vendors/suppliers with whom to place orders and acts as a primary contact with vendors/suppliers. Resolves problems with assigned production parts/materials, equipment or supplier orders. As a cross-functional team member, represents supply base and takes actions necessary to support quoting, production, cost savings initiatives, quality/complaint investigations and other supply chain related activities.
ESSENTIAL DUTIES, AND AREAS OF ACCOUNTABILITY:
In addition to regular and timely attendance, these include the following. Other duties may be assigned.
Demonstrates company core values; strong team player as measured by peers (behavior and work ethic). Complies with work rules including those pertaining to safety, health, Quality System, and the Accellent Quality Management System.

Planning Responsibilities:
       
* Works with Site Sr. Buyer Planner (Master Planner) in the review and updating of the master plan demand plans for their assigned areas as required.
* Creates, Schedules and maintains production orders within the ACC ERP system for assigned work centers to load the factory to ensure manufacturing cycle times goals are obtained for their site.
* Responsible for working with assigned work center supervisors in the proper tracking and reporting on OTD (on time delivery ) cycle time and yield for production orders on a weekly basis
* Responsible for determining the daily required production rate (take time) for their assigned work centers , as well as working with the corresponding work center supervisors in the tracking and reporting on daily / weekly performance for their assigned areas.
Purchasing Responsibilities
* Prepares instructions and oversees purchasing systems and procedures; reviews purchase order claims and contracts for conformance to company policy.
* Responsible for tactical procurement in support of the sites production schedules, as well as purchase order releases on blanket agreements negotiated with the Accellent Global Sourcing.
* Prepares management reports as required (Inventory ABC analysis/cost savings program; raw material cost track, etc.); Tracks and updates operating/expense budget.
* Procures all products to necessary dock dates to ensure on-time production starts per production schedule.
* Ensures materials are utilized to minimize excess and obsolescence exposure.
* Works with Global Sourcing to develop cost reduction programs with suppliers to ensure an annual reduction is achieved per facility objectives for both common Accellent materials working with Global sourcing as well as direct spend activities.
* Timely sourcing and cost effective procurement of raw materials, factory/office supplies, as well as outside services.
* Analyzes contractual commitments, customer specifications, design changes, and other data to plan and develop planning and procurement actitivities from conceptual stage through life-cycle of product.
* Responsible for site procurement activities (raw materials, outside services (OSV) as well as expense items).
* Managing and maintaining supplier programs, including the implementation of Kanban Replenishment, Consigned Vendor Managed Inventory (VMI) Programs in areas such as raw materials, tooling, etc.
* Global Sourcing &ndash; actively participates with Accellent Global Sourcing Commodity Management team on Strategic Supplier partnerships and agreements in support of Accellent Strategic Goals.
* Participates with Strategic Sourcing Commodity management on Supplier Relationship Management (SRM quarterly / bi-annual reviews with key suppliers for the site, as well as participates in Global Sourcing SRM meetings as required.
* Supplier Performance Management &ndash; responsible for working with site operations quality and global sourcing on supplier report cards to insure that plans of action are developed and implemented for improving poor performing suppliers.
* In support of facility inventory turn objectives, develops supplier consignment program to ensure necessary materials are on site (in aggregate including WIP and finished goods).
* Responsible for assisting and in development implementation/maintenance of Lean Manufacturing initiatives, including Kanban/Pull systems with vendors and production.
* Leads cross-functional teams chartered to perform Supply Chain related continual improvement and/or problem solving.


Job Requirements :

QUALIFICATIONS:
To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
EDUCATION and/or EXPERIENCE:
Bachelor's degree from four-year College or University; and three plus years related experience and/or training; or equivalent combination of education and experience.
OTHER QUALIFICATIONS:
Excellent PC skills and working knowledge of fully integrated computerized manufacturing and accounting system.      
CPIM / CPM preferred
LANGUAGE SKILLS:
Excellent communication skills. Ability to read, analyzes, and interprets common scientific and technical journals, financial reports, customer prints or other specifications, and legal documents. Ability to respond to common inquiries or complaints from customers, regulatory agencies, or members of the business community. Ability to effectively present information to all levels in the organization and top management.
MATHEMATICAL SKILLS:
Ability to apply concepts such as fractions, percentages, ratios, and proportions to practical situations. In addition, basic knowledge of statistical process control techniques.
REASONING ABILITY:
Ability to define problems, collect data, establish facts, and draw valid conclusions. Ability to interpret an extensive variety of technical instructions in mathematical or diagram form and deal with several abstract and concrete variables.
Career Level :Experienced (Non-Manager)
Education :Bachelor's Degree
% of Travel Required :None
Shift/Hours :First Shift (Day)
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        <expiration_date>2010-03-25</expiration_date>
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        <location><![CDATA[Houston, PA, 15342, USA]]></location>
    </job>
    <job>
        <title><![CDATA[Production Associate - Operator]]></title>
        <description><![CDATA[


Job Title :Production Associate - Operator
Job Code :4323
Location :Upland CA US 91786
Job Description :
Accellent, Inc. is a fully integrated provider of design, supply chain management and strategic sourcing services to the Medical Device industry. Accellentwww.accellent.com, a recognized market leader, is a fast-growing outsource manufacturing and design solution company specializing in high growth areas such as Cardiology, Endoscopy and Orthopaedics. The top Medical Device companies partner with Accellent to provide innovation, advanced technology, speed to market, low cost labor and strategic sourcing. 
We&rsquo;re looking for team players with a can-do attitude to share in our vision and corporate values. Accellent offers competitive salaries; a comprehensive benefits package, and a stimulating work environment. 
Currently, we are searching for a to join our facility.
About the Opportunity:



1.0       JOB SUMMARY
1.1       The Machine Operator is to cycle and run machines that requirefull time attention. Operator may be required to remove each part as it is molded, put inserts into mold or put in hand loaded inserts. On operator assigned machines, operator is required to stay at machine, while machine is running, unless relieved by another operator.
2.0       PRIMARY RESPONSIBILITIES
2.1       Must be able to read and follow all procedures (KOP&rsquo;s, MOP&rsquo;s COP&rsquo;s GMP&rsquo;s)
2.2       Must be able to read and follow all work instructions.
2.3       Cycle machine as trained. (FormQ102)
2.4       Inspect parts for defects and cosmetics issues.
2.5       Pack parts at machine per customer specification.
2.6       Maintain Medical Parts Program where necessary.
2.7       Assist packers with line clearances. (FormM055F)
2.8       Input rejects from machines if needed.
2.9       Communicates with Supervisor, Technician, and QA any issues with parts or machines.
3.0       ADDITIONAL DUTIES AND BACK-UP RESPONSIBILITIES
3.1       Must be willing to work overtime and weekends.
3.2       Willing to work any other assigned duties as instructed by Supervisor or Lead.
3.3       Must be willing to train other employees
3.4       Must relieve for breaks and lunches as needed.
3.5       Must be safety conscious and work in a safe manner at all times. Follow all safety rules and standards.
3.6       Maintain clean working environments throughout production and assembly areas.
Job Requirements :

1.0       JOB REQUIREMENTS
1.1       Education: High school diploma or equivalent.
1.2       Experience: Entry Level.
1.3       Specialized Knowledge: Manufacturing in the medical field helpful, but not required.Physical Demands: Must be able to lift 30 lbs. Must be able to stand for entire shift.  Must be able to bend, twist, and squat. Must have good vision, aided by glasses if necessary



Due to the expected number of responses, only those most qualified will be contacted. No recruiters please; all unsolicited third-party submissions will be rejected.

Accellent is an Equal Opportunity/Affirmative Action employer and we value diversity in our workforce. As such we provide equal opportunity for all applicants without regard to race, religion, gender, national origin, age, marital status, veteran status, or disability. To learn more about Accellent and our career opportunities, please visit us atwww.accellent.com
Career Level :Entry Level
Education :High School or equivalent
% of Travel Required :None
Shift/Hours :Third Shift (Night)
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            <industry><![CDATA[Health Products & Services]]></industry>
        </industries>
        <expiration_date>2010-03-25</expiration_date>
        <employer><![CDATA[Accellent Inc.]]></employer>
        <location><![CDATA[Upland, CA, 91786, USA]]></location>
    </job>
    <job>
        <title><![CDATA[Part-Time Janitor]]></title>
        <description><![CDATA[


Job Title :Part-Time Janitor
Job Code :4320
Location :Laconia NH US 03246
Job Description :
Accellent, Inc. is a fully integrated provider of design, supply chain management and strategic sourcing services to the Medical Device industry. Accellentwww.accellent.com, a recognized market leader, is a fast-growing outsource manufacturing and design solution company specializing in high growth areas such as Cardiology, Endoscopy and Orthopaedics. The top Medical Device companies partner with Accellent to provide innovation, advanced technology, speed to market, low cost labor and strategic sourcing. 
We&rsquo;re looking for team players with a can-do attitude to share in our vision and corporate values. Accellent offers competitive salaries; a comprehensive benefits package, and a stimulating work environment. 
Currently, we are searching for a Part-time Janitor to join our facility.
About the Opportunity:
The Part-Time Janitor is responsible for preventative, corrective and maintenance of facilities work in support of the overall goal of maintaining a clean, comfortable and safe working environment. Principal responsibilities include performing scheduled and as-needed cleaning for the facility including mopping/drying, trash/debris removal, emptying receptacles, etc. In addition, the Part-Time Janitor conducts on-the-spot and routine inspections of the facility and grounds including the hallways, common areas, restrooms, etc. The Part-time Janitor handles urgent requests and completes any and all assigned facility support, clean-up, maintenance of repair on a priority basis, putting safety above all. The Part-Time Janitor is responsible for such minor repairs to the facilities and premises as painting, patching, changing out lamps and ballasts, light plumbing/wiring/ventilation repairs, moving materials, changing out ceiling tiles, rug repair, and other similar tasks as needed. The Part-Time Janitor performs seasonal work such as snow removal in the winter and mowing the lawn/trimming shrubs in the warm weather. The Part-Time Janitor helps to ensure that all building and maintenance policies, procedures, SOP's, codes regulations, etc. are followed and enforced including safety systems and standards.


Job Requirements :
The successful candidate will be able to function effectively in a team environment composed of technical, production and management personnel to resolve issues quickly, economically and work/adapt in a constantly changing environment with minimal supervision. Strong interpersonal communication skills along with a demonstrated ability to follow documented procedures are required. Two or more years' experience performing routine maintenance is essential. Background with electrical maintenance in a manufacturing /industrial environment is a strong plus. The successful candidate will be able to demonstrate trouble-shooting skills and commitment to safety and quality. Computer proficiency and the ability to maintain both automated and paper record-keeping systems are required. The ability to use Microsoft Office is strongly preferred. The ability to read and understand ACAD drawings or blueprints is a plus.



Due to the expected number of responses, only those most qualified will be contacted. No recruiters please; all unsolicited third-party submissions will be rejected.

Accellent is an Equal Opportunity/Affirmative Action employer and we value diversity in our workforce. As such we provide equal opportunity for all applicants without regard to race, religion, gender, national origin, age, marital status, veteran status, or disability. To learn more about Accellent and our career opportunities, please visit us atwww.accellent.com
Career Level :Experienced (Non-Manager)
Education :High School or equivalent
% of Travel Required :0-10%
Shift/Hours :First Shift (Day)
]]></description>
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            <industry><![CDATA[Health Products & Services]]></industry>
        </industries>
        <expiration_date>2010-03-25</expiration_date>
        <employer><![CDATA[Accellent Inc.]]></employer>
        <location><![CDATA[Laconia, NH, 03246, USA]]></location>
    </job>
    <job>
        <title><![CDATA[Quality Control Inspector II]]></title>
        <description><![CDATA[


Job Title :Quality Control Inspector II
Job Code :4315
Location :Laconia NH US
Job Description :
Accellent, Inc. is a fully integrated provider of design, supply chain management and strategic sourcing services to the Medical Device industry. Accellentwww.accellent.com, a recognized market leader, is a fast-growing outsource manufacturing and design solution company specializing in high growth areas such as Cardiology, Endoscopy and Orthopaedics. The top Medical Device companies partner with Accellent to provide innovation, advanced technology, speed to market, low cost labor and strategic sourcing. 
We&rsquo;re looking for team players with a can-do attitude to share in our vision and corporate values. Accellent offers competitive salaries; a comprehensive benefits package, and a stimulating work environment. 
Currently, we are searching for a to join our facility.
About the Opportunity:

The Quality Inspector II performs calibration, sterile product release, and other non-standard inspection duties as well as prepares documents /records associated with these functions.The Quality Inspector II examinesproduct prior to shipment to the sterilizer and after receipt from the sterilizer; performs first piece inspection of sectioned weld samples; issues copies of engineering drawings as specified in applicable procedures; and issues set-up material to set-up personnel.
 




Job Requirements :

A minimum of 2 years experience in an inspection environment is required. .




Due to the expected number of responses, only those most qualified will be contacted. No recruiters please; all unsolicited third-party submissions will be rejected.

Accellent is an Equal Opportunity/Affirmative Action employer and we value diversity in our workforce. As such we provide equal opportunity for all applicants without regard to race, religion, gender, national origin, age, marital status, veteran status, or disability. To learn more about Accellent and our career opportunities, please visit us atwww.accellent.com
Career Level :Experienced (Non-Manager)
Education :High School or equivalent
% of Travel Required :0-10%
Shift/Hours :First Shift (Day)
]]></description>
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            <industry><![CDATA[Health Products & Services]]></industry>
        </industries>
        <expiration_date>2010-03-25</expiration_date>
        <employer><![CDATA[Accellent Inc.]]></employer>
        <location><![CDATA[Laconia, NH, 03246, USA]]></location>
    </job>
    <job>
        <title><![CDATA[Finisher]]></title>
        <description><![CDATA[


Job Title :Finisher
Job Code :4335
Location :Orchard Park NY US 14127
Job Description :
Key Result Accountabilities
1.   Knowledgeable about finishing techniques, which include but are not limited to using foredoms, gesswein, tumbling, burlytic, cleaning, grinding, miyano operations, Lapmaster, red wheeling, hand deburring, tumble blasting, sand blasting, clean room operations, molding machines, furnaces, waterbaths, dryers, trim, scrape or deburr parts using hand tools and equipment.
2.   Responsible for performing work that meets or exceeds our production standards and scrap rates that will achieve our metric goals for scrap, Fill Rate, Rework, Customer Lot Acceptance (CLA), and Customer Complaints, etc.
3.   Knowledge of shop control system in order to review and print paperwork needed for job and input data for work completed on various jobs.
4.   Use Smart Scope, comparator, micrometers, blade micrometers, counting scales and/or profilometer for measuring and counting parts, as necessary.
5.   Knowledge of reading and using Collection Plans in order to conduct frequency checks.
6.   Understand MVR procedures.
7.   Be able to rotate into other Finishing jobs with competency and confidence.
8.   Ability to work well in a team environment.
9.   Other duties as necessary.
10. Keep work area clean.
Environmental Working Conditions
&middot;    The physical demands described herein are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform essential functions.
&middot;    Ability to spend time using your hands to handle, control, or feel objects, tools or controls.
&middot;    Will spend extended periods of time sitting and/or standing.
&middot;    Occasionally required to stoop, kneel, bend, crouch, bend and twist.
&middot;    Ability to lift 1pound up to 10 lbs.
Job Requirements :
Qualifications
1.   Able to use microscope and other measuring equipment.
2.   Able to use computer, pulling up instructions and reading them.
3.   Able to follow instructions, both written and verbal.
4.   Able to count parts.
Career Level :Entry Level
Education :High School or equivalent
% of Travel Required :0-10%
Shift/Hours :First Shift (Day)
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            <industry><![CDATA[Health Products & Services]]></industry>
        </industries>
        <expiration_date>2010-03-25</expiration_date>
        <employer><![CDATA[Accellent Inc.]]></employer>
        <location><![CDATA[Orchard Park, NY, 14127, USA]]></location>
    </job>
    <job>
        <title><![CDATA[Sr. Quality Engineer - Contract]]></title>
        <description><![CDATA[


Job Title :Sr. Quality Engineer - Contract
Job Code :4386
Location :Wilmington MA US 01887
Job Description :
Accellent, Inc. is a fully integrated provider of design, supply chain management and strategic sourcing services to the Medical Device industry. Accellentwww.accellent.com, a recognized market leader, is a fast-growing outsource manufacturing and design solution company specializing in high growth areas such as Cardiology, Endoscopy and Orthopaedics. The top Medical Device companies partner with Accellent to provide innovation, advanced technology, speed to market, low cost labor and strategic sourcing. 
We&rsquo;re looking for team players with a can-do attitude to share in our vision and corporate values. Accellent offers competitive salaries; a comprehensive benefits package, and a stimulating work environment. 
Currently, we are searching for a Sr. Quality Engineer to join our Wilimington, MA facility.  This a temporary position.
About the Opportunity:
Position Scope / Summary
Quality assists in the design and implementation of policies and procedures for testing and evaluating the precision and accuracy of products and/or equipment. The Sr. Quality Engineer will be expected to provide support to Operations, interact with customers and provide support for Engineering, Quality Systems and Process engineering. 
Specializations may include but are not limited to: design control; material and process control; product reliability; software quality engineering; and/or metrology.
This position will be integral in meeting the Quality Management System requirements. It requires creativity and foresight to work with operations and product development teams to ensure compliance to the Quality Manual, Design Control, Supplier Management and other appropriate procedures for a variety of medical devices from concept through market introduction. The ideal candidate is a self-motivated individual who is excited by the prospect of working in a dynamic, fast-paced environment.
Key Result Accountabilities
1.   Maintain company compliance with FDA Quality System Regulations and ISO 13485 standards. Experience with FDA and ISO inspections and registration is a plus.
2.   Actively participates in internal audits, management review and other activities covered under Accellent Quality Manual, Policies and Procedures.
3.   Provide customer related quality and regulatory inquiries support.
4.   Compiles and writes training material and conducts training sessions on quality control activities.
5.   Provide QE direction, analysis and recommendations for Product Development to successfully launch new products into active production in a timely and cost effective manner. Directs development and maintenance of internal/external standards relative to Design and Development,
6.   Lead implementation of continuous improvement projects or act as subject matter expert for SPC, FMEA, DOE and process validation.
7.   Lead and provide Project Management support as needed.
8.   Develops and initiates standard methods for inspection, testing, and evaluation, utilizing knowledge in related engineering fields.
9.   Devises sampling procedures and designs and develops forms and instructions for recording, evaluating, and reporting quality and reliability data.
10. Performs measurement system analyses to evaluate test and inspection equipment.
11. Leads disposition of discrepant material and devises process to assess product quality and reliability.
12. Monitors and directs engineering group on calibration requirements and implementation of systems to support equipment calibration.
13. Lead supplier approval and qualification of new/revised items which includes inspection method development and validation as well as correlation with supplier&rsquo;s methods, supplier audits, management of supplier corrective and preventative actions and assist in FMEA. 
14. Direct support for FDA and ISO inspections and registration.
15. Directs workers engaged in measuring, testing, and tabulating data concerning quality and reliability.
16. All other duties as assigned.
17. Up to 10% travel may be required.
Environmental Working Conditions
Employee must comply with all safety policies and safe work procedures established by the company. Job tasks may also involve:  
             
&middot;    Using personal protective equipment such as safety glasses, goggles, gloves, and other equipment as established in company policies and safe work procedures.
&middot;    Working near cutting &amp; machining fluids, solvents, lubricants and other hazardous chemicals using appropriate safety controls.
Employee will be expected to attend safety training, and may serve on the facility safety committee and participate in hazard analysis and resolution.
Job Requirements :

* Medical Device background with a clear understanding of ISO 13485:2003 and 21 CFR Part 820
* Creation of Master Validation plans,
* Writing validation protocols,
* FMEA and DOE
* Oversight of IP, OQ, PQ at Manufacturing site (travel may be required)
* WritingPQ report
* Test method development and validation reporting
* Experience with software based products and associated Verification and Validation 21CFR Part 11 (1 individual)
Due to the expected number of responses, only those most qualified will be contacted. No recruiters please; all unsolicited third-party submissions will be rejected.

Accellent is an Equal Opportunity/Affirmative Action employer and we value diversity in our workforce. As such we provide equal opportunity for all applicants without regard to race, religion, gender, national origin, age, marital status, veteran status, or disability. To learn more about Accellent and our career opportunities, please visit us atwww.accellent.com
Career Level :Experienced (Non-Manager)
Education :Bachelor's Degree
% of Travel Required :0-10%
Shift/Hours :First Shift (Day)
]]></description>
        <link><![CDATA[http://jcnlx.com/87317bcc65364eeeac9a73eaa2d9467c105]]></link>
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        <industries>
            <industry><![CDATA[Health Products & Services]]></industry>
        </industries>
        <expiration_date>2010-03-25</expiration_date>
        <employer><![CDATA[Accellent Inc.]]></employer>
        <location><![CDATA[Wilmington, MA, 01887, USA]]></location>
    </job>
    <job>
        <title><![CDATA[Sr. Quality Engineer (Sterilization & Validation)]]></title>
        <description><![CDATA[


Job Title :Sr. Quality Engineer (Sterilization & Validation)
Job Code :4231
Location :Juarez Chih MX 32470
Job Description :
Accellent, Inc. is a fully integrated provider of design, supply chain management and strategic sourcing services to the Medical Device industry. Accellentwww.accellent.com, a recognized market leader, is a fast-growing outsource manufacturing and design solution company specializing in high growth areas such as Cardiology, Endoscopy and Orthopaedics. The top Medical Device companies partner with Accellent to provide innovation, advanced technology, speed to market, low cost labor and strategic sourcing. 
We&rsquo;re looking for team players with a can-do attitude to share in our vision and corporate values. Accellent offers competitive salaries; a comprehensive benefits package, and a stimulating work environment. 
Currently, we are searching for a to join our facility.
About the Opportunity:

Position Scope/Summary
Quality assists in the design and implementation of policies and procedures for testing and evaluating the precision and accuracy of products and/or equipment. The Sr. Quality Engineer will be expected to provide support to Operations, interact with customers and provide support for Engineering, Quality Systems and Process engineering. 
Specializations may include but are not limited to: design control; material and process control; product reliability; software quality engineering; and/or metrology.
This position will be integral in meeting the Quality Management System requirements. It requires creativity and foresight to work with operations and product development teams to ensure compliance to the Quality Manual, Design Control, Supplier Management and other appropriate procedures for a variety of medical devices from concept through market introduction. The ideal candidate is a self-motivated individual who is excited by the prospect of working in a dynamic, fast-paced environment.
Key Result Accountabilities
&middot;    Maintain company compliance with FDA Quality System Regulations and ISO 13485 standards. Experience with FDA and ISO inspections and registration is a plus.
&middot;    Actively participates in internal audits, management review and other activities covered under Accellent Quality Manual, Policies and Procedures.
&middot;    Provide customer related quality and regulatory inquiries support.
&middot;    Compiles and writes training material and conducts training sessions on quality control activities.
&middot;    Provide QE direction, analysis and recommendations for Product Development to successfully launch new products into active production in a timely and cost effective manner. Directs development and maintenance of internal/external standards relative to Design and Development,
&middot;    Lead implementation of continuous improvement projects or act as subject matter expert for SPC, FMEA, DOE and process validation.
&middot;    Lead and provide Project Management support as needed.
&middot;    Develops and initiates standard methods for inspection, testing, and evaluation, utilizing knowledge in related engineering fields.
&middot;    Devices sampling procedures and designs and develops forms and instructions for recording, evaluating, and reporting quality and reliability data.
&middot;    Performs measurement system analyses to evaluate test and inspection equipment.
&middot;    Leads disposition of discrepant material and devises process to assess product quality and reliability.
&middot;    Monitors and directs engineering group on calibration requirements and implementation of systems to support equipment calibration.
&middot;    Lead supplier approval and qualification of new/revised items which includes inspection method development and validation as well as correlation with supplier&rsquo;s methods, supplier audits, management of supplier corrective and preventative actions and assist in FMEA. 
&middot;    Direct support for FDA and ISO inspections and registration.
&middot;    Directs workers engaged in measuring, testing, and tabulating data concerning quality and reliability.
&middot;    All other duties as assigned.
&middot;    Up to 10% travel may be required.
Environmental Working Conditions
Employee must comply with all safety policies and safe work procedures established by the company. Job tasks may also involve:      
&middot;    Using personal protective equipment such as safety glasses, goggles, gloves, and other equipment as established in company policies and safe work procedures.
&middot;    Working near cutting &amp; machining fluids, solvents, lubricants and other hazardous chemicals using appropriate safety controls.
Employee will be expected to attend safety training, and may serve on the facility safety committee and participate in hazard analysis and resolution.
Qualifications
&middot;    3-8 years experience in the Medical Device or other regulated industry, such as QSR and ISO 13485, with increasing responsibility.
&middot;    Experience with FDA and ISO 13485 Certification inspections is a plus.
&middot;    3 plus years Project Management experience, supervising diverse teams. 
&middot;    Must be adept in use of computer software for the analysis of data, preferably Microsoft Excel and statistical packages (Minitab preferred). 
&middot;    Quality Engineering certification (CQE) preferred or equivalent body of knowledge in areas which include, but are not limited to Statistics, SPC, Geometric Dimensioning/Tolerancing; Sampling, Design of Experiments, etc. Ability to analyze, understand and effectively communicate this technical material. Experience with Lean Manufacturing and Six Sigma is a plus.
&middot;    Ability to organize and judge priorities in a dynamic, fast-paced environment and work independently with minimal supervision.
&middot;    Must possess excellent verbal &amp; written communication skills, which include but are not limited to presentation, organizational and management skills.
Senior Quality Engineer (sterilization) additional responsibilities:
Coordinate, schedule, implement, approve and monitor aspects of all environmental and sterility assurance activities in compliance with regulatory and company policies and procedures. Review and approve sterility validation protocols and reports. Prepare quarterly dose audit and bioburden samples, annual E&amp;O samples and audit of post sterile paperwork when needed. Conduct audits of post sterile product paperwork. Prepare, obtain, and ship pre-sterile microbial content samples. Monitor test data from testing facilities. Interface with inside and outside contacts by providing technical support to other departments in regards to microbiology, biocompatibility and sterilization. Gather various test data; maintain data and trends, logs, lists, and records. Review data using statistical methods and take necessary actions as required. Monitor, set up and coordinate the program sampling by taking viable and non-viable samples at the applicable facilities in accordance with company policies and procedures. Train and mentor technicians, and ensure employees are following company policies and procedures.
Experience with medical device steam, ethylene oxide, radiation sterilization procedures, and routine finished product sterility release are highly desired. Must possess strong organizational, troubleshooting and investigatory skills for sterilization, bio burden, and environmental deviations and excursions. Knowledge of safe work practices in handling chemicals and biological materials, and medical device regulations and industrial sterilization and microbiological controls are also highly desired.
Responsible for validation and qualification (IQ, OQ, and PQ) of equipment and processes. This position will develop, author, and execute protocols and summarize results in final reports. Supports projects required for the expansion, improvement and modernization of the production facility. Establish time lines and determine resources need to complete protocols. Implement projects within budget and schedule. Ensure that validated or qualified equipment and processes are maintained under change control. This position will coordinate outside contract services utilized for any validation or qualification activities. He/she will utilize skills and experience in Medical Device, or related areas to implement and maintain quality systems that ensure all aspects of product manufacturing and release meet analytical, production, packaging, and labeling specifications in accordance with all applicable ISO and GMP guidelines, or regulatory, company and customer requirements. Communicate expectations for quality performance, continuous improvement, quality systems, process controls infrastructure for critical sustaining parts and new products.Experience in completing Process Validation&rsquo;s as per CDRH Guidance is highly desired.  
Job Requirements :



Due to the expected number of responses, only those most qualified will be contacted. No recruiters please; all unsolicited third-party submissions will be rejected.

Accellent is an Equal Opportunity/Affirmative Action employer and we value diversity in our workforce. As such we provide equal opportunity for all applicants without regard to race, religion, gender, national origin, age, marital status, veteran status, or disability. To learn more about Accellent and our career opportunities, please visit us atwww.accellent.com
Career Level :Experienced (Non-Manager)
Education :Bachelor's Degree
% of Travel Required :0-10%
Shift/Hours :First Shift (Day)
]]></description>
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        <industries>
            <industry><![CDATA[Health Products & Services]]></industry>
        </industries>
        <expiration_date>2010-03-25</expiration_date>
        <employer><![CDATA[Accellent Inc.]]></employer>
        <location><![CDATA[, USA]]></location>
    </job>
    <job>
        <title><![CDATA[Manufacturing Engineering Technician - Swiss Programming]]></title>
        <description><![CDATA[


Job Title :Manufacturing Engineering Technician - Swiss Programming
Job Code :4161
Location :Wheeling IL US 60090
Job Description :
Accellent, Inc. is a fully integrated provider of design, supply chain management and strategic sourcing services to the Medical Device industry. Accellentwww.accellent.com, a recognized market leader, is a fast-growing outsource manufacturing and design solution company specializing in high growth areas such as Cardiology, Endoscopy and Orthopaedics. The top Medical Device companies partner with Accellent to provide innovation, advanced technology, speed to market, low cost labor and strategic sourcing. 
We&rsquo;re looking for team players with a can-do attitude to share in our vision and corporate values. Accellent offers competitive salaries; a comprehensive benefits package, and a stimulating work environment. 
Currently, we are searching for a Manufacturing Engineer with a Swiss Programming background to join our facility.

Job Requirements :



Due to the expected number of responses, only those most qualified will be contacted. No recruiters please; all unsolicited third-party submissions will be rejected.

Accellent is an Equal Opportunity/Affirmative Action employer and we value diversity in our workforce. As such we provide equal opportunity for all applicants without regard to race, religion, gender, national origin, age, marital status, veteran status, or disability. To learn more about Accellent and our career opportunities, please visit us atwww.accellent.com
Career Level :Experienced (Non-Manager)
Education :Bachelor's Degree
% of Travel Required :0-10%
Shift/Hours :First Shift (Day)
]]></description>
        <link><![CDATA[http://jcnlx.com/61dfba3e13f949d4a7e46fcd3f21843a105]]></link>
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        <guid isPermaLink="false"><![CDATA[accellent-4161]]></guid>
        <industries>
            <industry><![CDATA[Health Products & Services]]></industry>
        </industries>
        <expiration_date>2010-03-25</expiration_date>
        <employer><![CDATA[Accellent Inc.]]></employer>
        <location><![CDATA[Wheeling, IL, 60070, USA]]></location>
    </job>
    <job>
        <title><![CDATA[Quality Assurance Manager]]></title>
        <description><![CDATA[


Job Title :Quality Assurance Manager
Job Code :4160
Location :Upland CA US 91786
Job Description :
Accellent, Inc. is a fully integrated provider of design, supply chain management and strategic sourcing services to the Medical Device industry. Accellentwww.accellent.com, a recognized market leader, is a fast-growing outsource manufacturing and design solution company specializing in high growth areas such as Cardiology, Endoscopy and Orthopaedics. The top Medical Device companies partner with Accellent to provide innovation, advanced technology, speed to market, low cost labor and strategic sourcing. 
We&rsquo;re looking for team players with a can-do attitude to share in our vision and corporate values. Accellent offers competitive salaries; a comprehensive benefits package, and a stimulating work environment. 
Currently, we are searching for a to join our facility.
About the Opportunity:
POSITION SCOPE / SUMMARY
The company provides design and outsourced manufacturing, assembly, and supply chain management to the medical device industry. With approximately 20 locations, Accellent employs 3000 people in 5 countries. Quality oversees the development of quality systems, standards and protocols for quality assurance testing models. Quality assists in the design and implementation of policies and procedures for quality systems, product and process controls, testing and evaluating the precision and accuracy of products and/or equipment. The Quality Manager will be expected to provide leadership and management for QA activity in a manufacturing facility; interact with customers and provide leadership support for Engineering, Quality Systems and Process engineering. 
KEY RESPONSIBILITIES
1.      Serves as management representative.
2.      Work collaboratively with Engineering, Operations, and other functional groups to successfully and seamlessly deliver to customers an integrated set of services and products.
3.      Work collaboratively with site management team to successfully and seamlessly deliver to customers an integrated set of services and products.
4.      Be a resource and mentor to other members of the management team, with a responsibility to develop people and support corporate goals of employee engagement.
5.      Talent acquisition and development. Recommends and executes personnel actions including promotions, performance reviews and any disciplinary measures. 
6.      Responsible for business improvement programs and initiatives such as Complaint reduction, Quality System improvements (CAPA, NCR, Training, etc), cost improvement programs through Lean Manufacturing techniques and drive successful business excellence programs for manufacturing to support business opportunities.
7.      Ensures output, timeliness, quality and Cost to standards consistent with customer requirements and company strategy.
8.      Support strategies to help drive improvements in operational capability required to support corporate growth and strategies.
9.      Reduce manufacturing operations costs through innovation and productivity gains.
10.    Create a continuous improvement culture that strives to satisfy customer requirements for fill-rates and zero defects.
11.    Complies with all work rules including those pertaining to safety, health, quality and Accellent Quality Management System.
12.    Develop and drive implementation of the quality system architecture, staffing, and associated processes to ensure adequate checks and balances exist as well as establishing the appropriate independence of the quality function. 
13.    Leads management reviews, to ensure the quality system is suitable and effective to satisfy regulatory requirements and the company's quality policy and objectives and other applicable procedures and practices at all levels of the organization. 
14.    Develops and drives a work culture fostering a highly ethical environment grounded in credibility and trust and fully committed to patient safety, compliance, quality and customer focus.
15.    Builds a strong quality team through staffing, leadership and training serving as a role model that drives improved compliance practices.
16.    Performs other duties as necessary.

Job Requirements :
QUALIFICATIONS
1.      Bachelors degree in engineering or technical equivalent degree
2.      10 years experience in manufacturing, preferably medical devices, including at least three years leadership responsibilities with increasing responsibility in quality assurance and associated fields.
3.      Must be familiar and understand recognized regulatory standards such as ( where applicable)
* US &ndash; CFR 21 part 820 (FDA QSR, GMP)
* ISO 13485 - (EN) ISO 13485
* Medical Device Directive (MDD) 93/42/EEC
* Active Implantable Medical Device Directive (AIMD) 90/385/EEC
* In Vitro Diagnostic Medical Device Directive (IVDD) 98/79/EC
* ISO 13485 under Canadian Medical Device Conformity Assessment System (CMDCAS)
* ISO 14971
* AS9100
* ISO 9001
4.      Able to be technically comprehensive and knowledgeable including standard business ERP system principles, as well as technical aspects such as statistics, documentation, SPC, Geometric Tolerencing and mechanical drawings and associated software packages. 
5.      Familiar with Six Sigma and/or a history of lean manufacturing, Kaizen and 5S, etc. Six-Sigma certified or willing to obtain certification preferred.
6.      Must possess excellent verbal &amp; written communication skills, as well as presentation, organizational and management skills.
7.      History of recruiting and retaining exceptional talent.



Due to the expected number of responses, only those most qualified will be contacted. No recruiters please; all unsolicited third-party submissions will be rejected.

Accellent is an Equal Opportunity/Affirmative Action employer and we value diversity in our workforce. As such we provide equal opportunity for all applicants without regard to race, religion, gender, national origin, age, marital status, veteran status, or disability. To learn more about Accellent and our career opportunities, please visit us atwww.accellent.com
Career Level :Manager (Manager/Supervisor of Staff)
Education :Bachelor's Degree
% of Travel Required :10-20%
Shift/Hours :First Shift (Day)
]]></description>
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        <industries>
            <industry><![CDATA[Health Products & Services]]></industry>
        </industries>
        <expiration_date>2010-03-25</expiration_date>
        <employer><![CDATA[Accellent Inc.]]></employer>
        <location><![CDATA[Upland, CA, 91786, USA]]></location>
    </job>
    <job>
        <title><![CDATA[3rd Op Visual Inspector - Days]]></title>
        <description><![CDATA[


Job Title :3rd Op Visual Inspector - Days
Job Code :4157
Location :Brooklyn Park MN US 55429
Job Description :
Accellent, Inc. is a fully integrated provider of design, supply chain management and strategic sourcing services to the Medical Device industry. Accellentwww.accellent.com, a recognized market leader, is a fast-growing outsource manufacturing and design solution company specializing in high growth areas such as Cardiology, Endoscopy and Orthopedics. The top Medical Device companies partner with Accellent to provide innovation, advanced technology, speed to market, low cost labor and strategic sourcing. 
We&rsquo;re looking for team players with a can-do attitude to share in our vision and corporate values. Accellent offers competitive salaries; a comprehensive benefits package, and a stimulating work environment. 
Currently, we are searching for a 3rd Op Visual Inspector to join our Brooklyn Park facility.
About the Opportunity:
Job Requirements :
 Position Scope/Summary
Manufacture components and assemblies for  customers as instructed.
Include the following:
Deburr, chamfer, visual, blowout, sort, poke, drill out, assemble, weld, flow rate check, and tray parts.
Provide support within the organization as experience and time allow.
Other duties may be assigned.
 Key Result Accountabilities
Physical Demands: 
The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
 Environmental Working Conditions
The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
 Qualifications
To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed Above are representative of the knowledge, skill, and/or ability required.
Career Level :Entry Level
Education :High School or equivalent
% of Travel Required :0-10%
Shift/Hours :First Shift (Day)
]]></description>
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        <industries>
            <industry><![CDATA[Health Products & Services]]></industry>
        </industries>
        <expiration_date>2010-03-25</expiration_date>
        <employer><![CDATA[Accellent Inc.]]></employer>
        <location><![CDATA[Brooklyn Park, MN, 55445, USA]]></location>
    </job>
    <job>
        <title><![CDATA[Set-up/Process Technician - Overmolding]]></title>
        <description><![CDATA[


Job Title :Set-up/Process Technician - Overmolding
Job Code :4044
Location :Wheeling IL US 60090
Job Description :
Accellent, Inc. is a fully integrated provider of design, supply chain management and strategic sourcing services to the Medical Device industry. Accellentwww.accellent.com, a recognized market leader, is a fast-growing outsource manufacturing and design solution company specializing in high growth areas such as Cardiology, Endoscopy and Orthopaedics. The top Medical Device companies partner with Accellent to provide innovation, advanced technology, speed to market, low cost labor and strategic sourcing. 
We&rsquo;re looking for team players with a can-do attitude to share in our vision and corporate values. Accellent offers competitive salaries; a comprehensive benefits package, and a stimulating work environment. 
Currently, we are searching for a to join our facility.
About the Opportunity:


Job Requirements :




Due to the expected number of responses, only those most qualified will be contacted. No recruiters please; all unsolicited third-party submissions will be rejected.

Accellent is an Equal Opportunity/Affirmative Action employer and we value diversity in our workforce. As such we provide equal opportunity for all applicants without regard to race, religion, gender, national origin, age, marital status, veteran status, or disability. To learn more about Accellent and our career opportunities, please visit us atwww.accellent.com
Career Level :Experienced (Non-Manager)
Education :High School or equivalent
% of Travel Required :0-10%
Shift/Hours :First Shift (Day)
]]></description>
        <link><![CDATA[http://jcnlx.com/7777afdce0974daa9f44ed8d225fd553105]]></link>
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        <industries>
            <industry><![CDATA[Health Products & Services]]></industry>
        </industries>
        <expiration_date>2010-03-25</expiration_date>
        <employer><![CDATA[Accellent Inc.]]></employer>
        <location><![CDATA[Wheeling, IL, 60070, USA]]></location>
    </job>
    <job>
        <title><![CDATA[Quality Engineer - Plastics]]></title>
        <description><![CDATA[


Job Title :Quality Engineer - Plastics
Job Code :4043
Location :Wheeling IL US 60090
Job Description :

Accellent, Inc. is a fully integrated provider of design, supply chain management and strategic sourcing services to the Medical Device industry. Accellentwww.accellent.com, a recognized market leader, is a fast-growing outsource manufacturing and design solution company specializing in high growth areas such as Cardiology, Endoscopy and Orthopaedics. The top Medical Device companies partner with Accellent to provide innovation, advanced technology, speed to market, low cost labor and strategic sourcing.
We&rsquo;re looking for team players with a can-do attitude to share in our vision and corporate values. Accellent offers competitive salaries; a comprehensive benefits package, and a stimulating work environment.
Currently, we are searching for a Quality Engineer (Plastics) to join our Wheeling, IL facility.
Position Scope / Summary
Quality assists in the design and implementation of policies and procedures for testing and evaluating the precision and accuracy of manufactured products and/or equipment. The Quality Engineer will be expected to provide support to Operations, interact with customers and provide support for Engineering, Quality Systems and Process engineering. Specializations may include but are not limited to: design control; material and process control; product reliability; software quality engineering; and/or metrology.
This position will be integral in meeting the Quality Management System requirements. It requires creativity and foresight to work with operations and product development teams to ensure compliance to the Quality Manual, Design Control, Supplier Management and other appropriate procedures for a variety of medical devices from concept through market introduction. The ideal candidate is a self-motivated individual who is excited by the prospect of working in a dynamic, fast-paced environment.
Key Result Accountabilities
* Maintain company compliance with FDA Quality System Regulations and ISO 13485 standards. Experience with FDA and ISO inspections and registration is a plus.
* Actively participates in internal audits, management review and other activities covered under Accellent Quality Manual, Policies and Procedures.
* Provide customer-related quality and regulatory inquiries&rsquo; support.
* Compiles and writes training material and conducts training sessions on quality control activities.
* Provide QE direction, analysis and recommendations for Product Development to successfully launch new products into active production in a timely and cost effective manner. Directs development and maintenance of internal/external standards relative to Design and Development,
* Lead implementation of continuous improvement projects or act as subject matter expert for SPC, FMEA, DOE and process validation.
* Lead and provide Project Management support as needed.
* Develops and initiates standard methods for inspection, testing, and evaluation, utilizing knowledge in related engineering fields.
* Devises sampling procedures and designs and develops forms and instructions for recording, evaluating, and reporting quality and reliability data.
* Performs measurement system analyses to evaluate test and inspection equipment.
* Leads disposition of discrepant material and devises process to assess product quality and reliability.
* Monitors and directs engineering group on calibration requirements and implementation of systems to support equipment calibration.
* Support supplier approval and qualification of new/revised items which includes inspection method development and validation as well as correlation with supplier&rsquo;s methods, supplier audits, management of supplier corrective and preventative actions and assist in FMEA.
* Support for FDA and ISO inspections and registration.
* Supports or may perform measuring, testing, and tabulating data concerning quality and reliability.
* All other duties as assigned.
* Minimal travel may be required.
Job Requirements :
Qualifications
&middot;   Bachelors (or higher) in engineering
&middot;   4+ years in Quality Engineering total minimum experience, including:
o   2+ years experience in the Medical Device or other regulated industry, such as QSR and ISO 13485, with increasing responsibility.
o   2+ years prior experience in Quality New Product Development role required, as well as prior demonstrated project management experience needed
o   Plastics to include mold validation process
&middot;   Experience with FDA and ISO 13485 Certification inspections is a plus.
&middot;   Must be adept in use of computer software for the analysis of data, preferably Microsoft Excel and statistical packages (Minitab preferred).
&middot;   Quality Engineering certification (CQE) preferred or equivalent body of knowledge
&middot;   Demonstrated working and applied knowledge in areas which include but are not limited to Statistics, SPC, Geometric Dimensioning &amp; Tolerancing; Sampling, Design of Experiments, etc. Ability to analyze, understand and effectively communicate this technical material.
&middot;   Experience with Lean Manufacturing and Six Sigma is a plus.
&middot;   Ability to organize and judge priorities in a dynamic, fast-paced environment and work independently with minimal supervision.
&middot;   Must possess excellent verbal &amp; written communication skills, which include but are not limited to presentation, organizational and management skills.
Accellent is an Equal Opportunity/Affirmative Action employer and we value diversity in our workforce. As such we provide equal opportunity for all applicants without regard to race, religion, gender, national origin, age, marital status, veteran status, or disability. To learn more about Accellent and our career opportunities, please visit us atwww.accellent.com




Career Level :Experienced (Non-Manager)
Education :Bachelor's Degree
% of Travel Required :0-10%
Shift/Hours :First Shift (Day)
]]></description>
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        <industries>
            <industry><![CDATA[Health Products & Services]]></industry>
        </industries>
        <expiration_date>2010-03-25</expiration_date>
        <employer><![CDATA[Accellent Inc.]]></employer>
        <location><![CDATA[Wheeling, IL, 60070, USA]]></location>
    </job>
    <job>
        <title><![CDATA[Technical Business Development Leader]]></title>
        <description><![CDATA[


Job Title :Technical Business Development Leader
Job Code :4027
Location :Warsaw IN US 46580
Job Description :
Accellent, Inc. is a fully integrated provider of design, supply chain management and strategic sourcing services to the Medical Device industry. Accellentwww.accellent.com, a recognized market leader, is a fast-growing outsource manufacturing and design solution company specializing in high growth areas such as Cardiology, Endoscopy and Orthopaedics. The top Medical Device companies partner with Accellent to provide innovation, advanced technology, speed to market, low cost labor and strategic sourcing.
We&rsquo;re looking for team players with a can-do attitude to share in our vision and corporate values. Accellent offers competitive salaries; a comprehensive benefits package, and a stimulating work environment.
Currently, we are searching for a Technical Business Development Leader to join our Company.
About the Opportunity:
The role of a Technical Business Development Leader is to obtain new business opportunities by providing technical and engineering support to customers leveraging Accellent&rsquo;s processing capabilities and technical expertise. The Technical Business Development Leader will engage customers with sound technical consultation and will define, support, close, monitor, and report on development-related and new business opportunities, programs, contracts and agreements. Through their technical leadership, the TBDL will develop and grow the business relationship between our customers and Accellent, increasing our revenue and profitability.
Key Result AccountabilitiesNew Opportunity Identification and Qualification
* Applies a broad knowledge of Accellent's services, products and manufacturing capabilities to scope and develop large opportunities and close sales.
* Work with customer&rsquo;s technical/engineering group to develop new products utilizing Accellent&rsquo;s capabilities and core competencies.
* Coordinate with the Accellent Project Managers and Directors of Sales to translate customers&rsquo; requirements into actionable activities for Accellent.
* Responsible for customer-facing activities related to execution of prototypes and pre-production builds.
* Provide input from customers to assist with cost estimating and project scheduling for development projects.
* Support proposal activity for new business.
* Identify cost reduction initiatives for customer&rsquo;s and develop and win new business opportunities.
* Directly responsible for growing Accellen&rsquo;t Risk Adjusted Sales Pipeline and Market Revenue.
* Technical Sales Activities
* Lead technical discussions and promote Accellent capabilities to new and existing customers using available tools such as technical fairs and forums. &middot; Proactively identify and scope new business opportunities with active involvement in customer&rsquo;s R&amp;D, product development, and operations teams.
* Effectively work with Accellent Technical Solutions and manufacturing facilities to identify, scope, and sell appropriate supply chain solutions to our customers.
* Ensure project confidentiality and coordinate Non-Disclosure Agreements with customersAccount Management Support
* Work with the Sales Account Management teams to understand the full scope of customer&rsquo;s business including executing corporate direction, identifying design and development opportunities, providing technical consultation, implementing strategic deals and revenue growth.
* Work directly with customers to identify and provide solutions to their supply chain management challenges, including development, design, and manufacturing requirements.
* Responsible for technical and NPD customer satisfaction.
* Communicate effectively across Accellent all customer concerns and obtain additional assistance / support when required.Strategic Market Segment Development
* Responsible for the implementation of strategic directions defined by the Business Platform Leader. Also, identifies key initiatives and opportunities to the Business Platform Leader
* Identify capability gaps within market segments and help to prioritize development of missing capabilities.
* Assist in identifying technology trends and market dynamics.
* Support marketing efforts, as required, for example supporting trade shows
* Actively participate in the development of the Accellent Technology Plan
* Comply with all work rules including those pertaining to safety, health and the Accellent Quality System.
Environmental Working Conditions 1. Ability to travel 50% of the time. 2. Ability to analyze, understand and effectively communicate deep technical material. 3. Ability to work in a demanding user environment.
Position Scope/Summary
Job Requirements :
* Bachelor degree in Mechanical Engineering, Materials Engineering, or similar discipline.
* 5-7 years experience in an engineering position required.
* Minimum: 5 years experience in the manufacture of components. Medical device experience preferred.
* Minimum: 2 years experience in project planning and scheduling.
* Ability to call on and influence customer&rsquo;s technical/engineering group.
* Must have a good understanding of the OEM&rsquo;s specific market and needs.
* Possess a deep understanding of company strategy and capabilities.
* Ability to manage multiple tasks in multiple geographic locations.
* Ability to understand and negotiate for profitability and long term relationships.
* Ability to provide critical analysis of a concept or problem and provide an appropriate resolution. Must be able to provide novel and creative solutions for device design, manufacturing, and assembly.
* Ability to communicate well with clients, suppliers, and coworkers and work well in a team environment.
* Excellent communication skills with the ability to clearly communicate issues and potential resolutions in a timely manner to management or clients.
* Ability to respond to changing priorities with minimum disruption.
* Ability to find solutions with minimal supervision and seek guidance or direction when appropriate
* Ability to provide technical leadership in discussions, conference calls and meetings with customers and staff as related to the job responsibilities.
* Ability to read, understand, and interpret technical drawings, models, and schematics.
* Proficient computer skills, Outlook, Excel, Project, Word &amp; PowerPoint. CAD &amp; Design programs a plus.Due to the expected number of responses, only those most qualified will be contacted. No recruiters please; all unsolicited third-party submissions will be rejected.
Accellent is an Equal Opportunity/Affirmative Action employer and we value diversity in our workforce. As such we provide equal opportunity for all applicants without regard to race, religion, gender, national origin, age, marital status, veteran status, or disability. To learn more about Accellent and our career opportunities, please visit us atwww.accellent.com
Career Level :Experienced (Non-Manager)
Education :Bachelor's Degree
% of Travel Required :50-60%
Shift/Hours :First Shift (Day)
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        <expiration_date>2010-03-25</expiration_date>
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        <location><![CDATA[Warsaw, IN, 46582, USA]]></location>
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    <job>
        <title><![CDATA[3rd Op Visual Inspector - Nights]]></title>
        <description><![CDATA[


Job Title :3rd Op Visual Inspector - Nights
Job Code :4023
Location :Brooklyn Park MN US 55429
Job Description :
Accellent, Inc. is a fully integrated provider of design, supply chain management and strategic sourcing services to the Medical Device industry. Accellentwww.accellent.com, a recognized market leader, is a fast-growing outsource manufacturing and design solution company specializing in high growth areas such as Cardiology, Endoscopy and Orthopaedics. The top Medical Device companies partner with Accellent to provide innovation, advanced technology, speed to market, low cost labor and strategic sourcing. 
We&rsquo;re looking for team players with a can-do attitude to share in our vision and corporate values. Accellent offers competitive salaries; a comprehensive benefits package, and a stimulating work environment. 
Currently, we are searching for a 3rd Op Visual Inspector to join our Brooklyn Park facility.
About the Opportunity:
Job Requirements :
 Position Scope/Summary
Manufacture components and assemblies for  customers as instructed.
Include the following:
Deburr, chamfer, visual, blowout, sort, poke, drill out, assemble, weld, flow rate check, and tray parts.
Provide support within the organization as experience and time allow.
Other duties may be assigned.
 Key Result Accountabilities
Physical Demands: 
The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
 Environmental Working Conditions
The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
 Qualifications
To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed Above are representative of the knowledge, skill, and/or ability required.
Career Level :Entry Level
Education :High School or equivalent
% of Travel Required :0-10%
Shift/Hours :Third Shift (Night)
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            <industry><![CDATA[Health Products & Services]]></industry>
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        <expiration_date>2010-03-25</expiration_date>
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        <location><![CDATA[Brooklyn Park, MN, 55445, USA]]></location>
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    <job>
        <title><![CDATA[Temporary Maintenance Technician]]></title>
        <description><![CDATA[


Job Title :Temporary Maintenance Technician
Job Code :4010
Location :SALEM VA US 24153
Job Description :
Accellent, Inc. is a fully integrated provider of design, supply chain management and strategic sourcing services to the Medical Device industry. Accellentwww.accellent.com, a recognized market leader, is a fast-growing outsource manufacturing and design solution company specializing in high growth areas such as Cardiology, Endoscopy and Orthopaedics. The top Medical Device companies partner with Accellent to provide innovation, advanced technology, speed to market, low cost labor and strategic sourcing.
We&rsquo;re looking for team players with a can-do attitude to share in our vision and corporate values. Accellent offers competitive salaries; a comprehensive benefits package, and a stimulating work environment.
Currently, we are searching for a Maintenance Technician to join our Salem, Virginia facility. 

Essential Duties and Responsibilities:
1.) Perform all responsibilities defined for a Maintenance Equipment Mechanic.
2.) Must be an exemplary performer.
3.) Must be able to prioritize department repair and Improvement projects to satisfy internal or external customers.
4.) Ability to trouble-shoot, repair &amp; fabricate equipment in the following areas: Electrical Systems, Programmable Logic Controllers, Mechanical Systems, Pneumatic Systems, Hydraulic Systems.
a.) In conjunction with supervisors and operators in all areas.
b.) Communicates and updates all plans and projects as appropriate.
5.) Plans and executes all phases of equipment repair to minimize the effect on operations and maximize machine capabilities.
6.) Provides training on all equipment for personnel that will ensure we are true to Accellent values.
7.) Manage maintenance personnel and assist in the development and continual improvement of personnel to assure department is ready to meet the demands of Accellent.
a.) Be a mentor.
b.) Assist in the development of each team member to their maximum potential.
c.) Work as part of a team to implement new procedures or equipment.
d.) Involve service technicians as needed to maintain and repair equipment.
e.) Identify and actively pursue educational needs of the department.
f..) Provide training as appropriate.
8.) Assist in the development and continual improvement of the processes and systems in manufacturing from a maintenance perspective.
a.) Identify and actively pursue opportunities to make improvements in manufacturing area.
b.) Work with R&amp;D / Engineering to implement new equipment.
c.) Assist with the creation and development of Standard Operating Procedures as necessary.
d.) Work with Engineering to create Preventive Maintenance schedules.
e.) Share &amp; document knowledge of equipment with maintenance and production personnel.
f.) Identify trends in downtime and propose changes to the Preventive Maintenance schedule.
9.) Maintain inventory of spare parts for equipment by using the purchasing system and the CMMS (Computer Maintenance Management System).
a.) Develop optimum inventory levels based on historical and anticipated usage.
b.) Assure cost effective purchasing of spare parts.
c.) Effectiveness of maintenance dollars spent.
Job Requirements :

Knowledge Skills and Abilities (KSA):
1.) Leader, planner, multitasking, prioritize-utilizing numerous inputs, project management.
a.) Effectively allocate resources in the manufacturing area.
b.) Develop the capabilities of an individual to grow to their fullest potential.
c.) Create plans of actions to address downward fluctuations in performance of departments and individuals.
2.) Ability to interpret the following: Blue prints, engineering drawings, mechanical drawings, ladder logic, hydraulic schematics, electrical schematics, air or gas schematics and water schematics.
V. Physical Demands:
The physical demands described herein are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform essential functions.
1.) The employee must occasionally lift or move 75 pounds.
2.) May be required to work in areas up to 30 feet above the floor.
3.) May be required to work in tight spaces.
4.) May be required to handle &amp; place very small components.
5.) Frequently required to stand; walk; sit; use hands to feel objects or handle tools or controls; reach with hands and arms; stoop, kneel or crouch.
VI. Education / Experience:
6.) Prior supervisory experience is desirable.
1.) High school graduate or GED equivalent.
2.) Extensive knowledge of mechanical equipment systems and practices.
3.) Building, plumbing and electrical codes and regulations pertaining to mechanical maintenance knowledge are a plus.
4.) Service and repair all types of mechanical systems.
5.) Read and interpret blueprints and mechanical drawings. 
Due to the expected number of responses, only those most qualified will be contacted. No recruiters please; all unsolicited third-party submissions will be rejected.
Accellent is an Equal Opportunity Employer. To learn more about Accellent and our career opportunities, please visit us atwww.accellent.com
Career Level :Experienced (Non-Manager)
Education :High School or equivalent
% of Travel Required :0-10%
Shift/Hours :First Shift (Day)
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        <expiration_date>2010-03-25</expiration_date>
        <employer><![CDATA[Accellent Inc.]]></employer>
        <location><![CDATA[SALEM, VA, 24157, USA]]></location>
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    <job>
        <title><![CDATA[Senior Quality Engineer]]></title>
        <description><![CDATA[


Job Title :Senior Quality Engineer
Job Code :4306
Location :Laconia NH US 03246
Job Description :
Accellent, Inc. is a fully integrated provider of design, supply chain management and strategic sourcing services to the Medical Device industry. Accellentwww.accellent.com, a recognized market leader, is a fast-growing outsource manufacturing and design solution company specializing in high growth areas such as Cardiology, Endoscopy and Orthopaedics. The top Medical Device companies partner with Accellent to provide innovation, advanced technology, speed to market, low cost labor and strategic sourcing. 

The Sr. Quality Engineer will be expected to provide support to Operations, interact with customers and provide support for Engineering, Quality Systems and Process engineering. Quality assists in the design and implementation of policies and procedures for testing and evaluating the precision and accuracy of products and/or equipment.
Specializations may include but are not limited to: design control; material and process control; product reliability; software quality engineering; and/or metrology.
This position will be integral in meeting the Quality Management System requirements. It requires creativity and foresight to work with operations and product development teams to ensure compliance to the Quality Manual, Design Control, Supplier Management and other appropriate procedures for a variety of medical devices from concept through market introduction. The ideal candidate is a self-motivated individual who is excited by the prospect of working in a dynamic, fast-paced environment.
This position is located in Laconia, NH.

Responsibilities:
&middot;    Maintain company compliance with FDA Quality System Regulations and ISO 13485 standards. Experience with FDA and ISO inspections and registration is a plus.
&middot;    Actively participates in internal audits, management review and other activities covered under Accellent Quality Manual, Policies and Procedures.
&middot;    Provide customer related quality and regulatory inquiries support.
&middot;    Compiles and writes training material and conducts training sessions on quality control activities.
&middot;    Provide QE direction, analysis and recommendations for Product Development to successfully launch new products into active production in a timely and cost effective manner. Directs development and maintenance of internal/external standards relative to Design and Development,
&middot;    Lead implementation of continuous improvement projects or act as subject matter expert for SPC, FMEA, DOE and process validation.
&middot;    Lead and provide Project Management support as needed.
&middot;    Develops and initiates standard methods for inspection, testing, and evaluation, utilizing knowledge in related engineering fields.
&middot;    Devises sampling procedures and designs and develops forms and instructions for recording, evaluating, and reporting quality and reliability data.
&middot;    Performs measurement system analyses to evaluate test and inspection equipment.
&middot;    Leads disposition of discrepant material and devises process to assess product quality and reliability.
&middot;    Monitors and directs engineering group on calibration requirements and implementation of systems to support equipment calibration.
&middot;    Lead supplier approval and qualification of new/revised items which includes inspection method development and validation as well as correlation with supplier&rsquo;s methods, supplier audits, management of supplier corrective and preventative actions and assist in FMEA. 
&middot;    Direct support for FDA and ISO inspections and registration.
&middot;    Directs workers engaged in measuring, testing, and tabulating data concerning quality and reliability.
&middot;    All other duties as assigned.
&middot;    Up to 10% travel may be required.

Accellent is an Equal Opportunity/Affirmative Action employer and we value diversity in our workforce. As such we provide equal opportunity for all applicants without regard to race, religion, gender, national origin, age, marital status, veteran status, or disability. To learn more about Accellent and our career opportunities, please visit us atwww.accellent.com 

Job Requirements :
Requirements:
&middot;    3-8 years experience in the Medical Device manufacturing industry (prefer disposable medical device manufacturing)
&middot;    BS Engineering desired
&middot;    Experience with FDA and ISO 13485 Certification inspections is a plus.
&middot;    3 plus years Project Management experience, supervising diverse teams. 
&middot;    Must be adept in use of computer software for the analysis of data, preferably Microsoft Excel and statistical packages (Minitab preferred). 
&middot;    Quality Engineering certification (CQE) preferred or equivalent body of knowledge in areas which include, but are not limited to Statistics, SPC, Geometric Dimensioning/Tolerancing; Sampling, Design of Experiments, etc. Ability to analyze, understand and effectively communicate this technical material. Experience with Lean Manufacturing and Six Sigma is a plus.
&middot;    Ability to organize and judge priorities in a dynamic, fast-paced environment and work independently with minimal supervision.
&middot;    Must possess excellent verbal &amp; written communication skills, which include but are not limited to presentation, organizational and management skills.
Accellent is an Equal Opportunity/Affirmative Action employer and we value diversity in our workforce. As such we provide equal opportunity for all applicants without regard to race, religion, gender, national origin, age, marital status, veteran status, or disability. To learn more about Accellent and our career opportunities, please visit us atwww.accellent.com 





Career Level :Manager (Manager/Supervisor of Staff)
Education :Bachelor's Degree
% of Travel Required :0-10%
Shift/Hours :First Shift (Day)
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            <industry><![CDATA[Health Products & Services]]></industry>
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        <expiration_date>2010-03-25</expiration_date>
        <employer><![CDATA[Accellent Inc.]]></employer>
        <location><![CDATA[Laconia, NH, 03246, USA]]></location>
    </job>
    <job>
        <title><![CDATA[Swiss Machinist -  Platinum]]></title>
        <description><![CDATA[


Job Title :Swiss Machinist - Platinum
Job Code :4304
Location :Brooklyn Park MN US 55429
Job Description :
Accellent, Inc. is a fully integrated provider of design, supply chain management and strategic sourcing services to the Medical Device industry. Accellentwww.accellent.com, a recognized market leader, is a fast-growing outsource manufacturing and design solution company specializing in high growth areas such as Cardiology, Endoscopy and Orthopaedics. The top Medical Device companies partner with Accellent to provide innovation, advanced technology, speed to market, low cost labor and strategic sourcing.
We&rsquo;re looking for team players with a can-do attitude to share in our vision and corporate values. Accellent offers competitive salaries; a comprehensive benefits package, and a stimulating work environment.
Currently, we are searching for a Swiss Machinist to join our Brooklyn Park facility.
Job Requirements :
Position Scope/Summary
Setup, troubleshoot, operate and perform maintenance when required to machines.
Include the following:
Responsible for keeping the machines running and work area clean.
Operate the machine as efficiently as possible.
Produce high quality components to print specifications. 
Read part prints and understand dimensions.
Use and understand how inspection equipment works making sure it is correct and is calibrated.
Do whatever is needed to insure quality - including sorting for features that are uncontrollable.
Obtain material from material rack.
Communicate with opposite shift operator to insure smooth transition between shifts.
Follow all company policies and rules.
Provide support within the organization as experienceand time allow.
Other duties may be assigned.
 Key Result Accountabilities
Supervisory Responsibilities:
Needs to work in an atmosphere with little supervision.
Language Skills:
Must be able to communicate with inspection personnel as well as other operators.
Mathematical Skills:
Must have basic math skills.
Reasoning Ability:
Must be able to reason cause and effect on parts.
Strong organizational skills.

 Environmental Working Conditions
Reasonable accommodations may be made to enable individuals with disabilities to perform the 
essential functions.
                              
 Qualifications
Must be able to read a print and use inspection 
equipment necessary to do the job.
  It is impossible to list every requirement for, or responsibility of, any position. Similarly we cannot identify all the skills a position may require since
  job responsibilities and the Company&rsquo;s needs may change over time. Therefore, the above job description is not comprehensive or exhaustive. The Company
  reserves the right to adjust, add to or eliminate any aspect of the above description. The Company also retains the right to require all
 employees to undertake additional or different job responsibilities when necessary to meet business needs.
Due to the expected number of responses, only those most qualified will be contacted. No recruiters please; all unsolicited third-party submissions will be rejected.

Accellent is an Equal Opportunity/Affirmative Action employer and we value diversity in our workforce. As such we provide equal opportunity for all applicants without regard to race, religion, gender, national origin, age, marital status, veteran status, or disability. To learn more about Accellent and our career opportunities, please visit us atwww.accellent.com

Career Level :Experienced (Non-Manager)
Education :High School or equivalent
% of Travel Required :None
Shift/Hours :First Shift (Day)
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            <industry><![CDATA[Health Products & Services]]></industry>
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        <expiration_date>2010-03-25</expiration_date>
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        <location><![CDATA[Brooklyn Park, MN, 55445, USA]]></location>
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    <job>
        <title><![CDATA[Shipping Clerk - Days]]></title>
        <description><![CDATA[


Job Title :Shipping Clerk - Days
Job Code :4293
Location :Brooklyn Park MN US 55429
Job Description :
Accellent, Inc. is a fully integrated provider of design, supply chain management and strategic sourcing services to the Medical Device industry. Accellent
Job Requirements :
Job Requirements:*
Position Scope/Summary
Provide support within the organization as experience and time allow. Compares identifying information and counts, weighs, or measures items of incoming and outgoing shipments to verify information against bills of lading, invoices, orders, or other records. Determines method of shipment. Affixes shipping labels on packed cartons. Assembles cardboard containers or selects pre-assembled containers. Inserts items into containers. Packages in a manner so that the product safely reaches its destination without damage. Posts weights and shipping charges, and affixes postage. Unpacks and examines incoming shipments, rejects damaged items, records shortages, and corresponds with shipper to rectify damages and shortages. Routes items to departments. Examines outgoing shipments to ensure shipments meet specifications. Maintains inventory of shipping materials and supplies.
Key Result Accountabilities
Supervisory Responsibilities: Needs to work in an atmosphere with little supervision.To aid in the training and the addition of staffing for the shipping department. Language Skills: Must be able to communicate with facility personnel.
Reasoning Ability: The ability to complete projects and problem solve independently.
Environmental Working Conditions
Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

Career Level :Entry Level
Education :High School or equivalent
% of Travel Required :None
Shift/Hours :First Shift (Day)
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            <industry><![CDATA[Health Products & Services]]></industry>
        </industries>
        <expiration_date>2010-03-25</expiration_date>
        <employer><![CDATA[Accellent Inc.]]></employer>
        <location><![CDATA[Brooklyn Park, MN, 55445, USA]]></location>
    </job>
    <job>
        <title><![CDATA[Account Manager]]></title>
        <description><![CDATA[


Job Title :Account Manager
Job Code :4274
Location :Brooklyn Park MN US 55429
Job Description :
Accellent, Inc. is a fully integrated provider of design, supply chain management and strategic sourcing services to the Medical Device industry. Accellentwww.accellent.com, a recognized market leader, is a fast-growing outsource manufacturing and design solution company specializing in high growth areas such as Cardiology, Endoscopy and Orthopaedics. The top Medical Device companies partner with Accellent to provide innovation, advanced technology, speed to market, low cost labor and strategic sourcing. 
We&rsquo;re looking for team players with a can-do attitude to share in our vision and corporate values. Accellent offers competitive salaries; a comprehensive benefits package, and a stimulating work environment. 
Currently, we are searching for an Account Manager to join our Sales team.

Position Scope/Summary
The Account Manager is responsible for increasing revenues and profitability of identified accounts. This includes the retention of existing revenues as well as identifying, qualifying and closing new business for incremental revenue realization. To enhance the reputation and business relationship between customer and the company.
Key Result Accountabilities
1.   Overall responsibility for the revenue growth of assigned customers through value add solutions and contract negotiation.
2.   Retain and increase the profitable penetration of existing accounts
3.   Establish, maintain, and grow strong relationships with decision makers at assigned customers.
4.   Responsible for accomplishing sales objectives to include revenue growth, identifying and prioritizing opportunities, securing resources, executing sales strategies and pull-through tactics to meet planned and company objectives.
5.   Develop and execute specific account strategies to promote revenue growth and increase market share.
6.   Identify, engage and maintain relationships with key influencers/decision makers through active customer involvement. Primary call points are &ldquo;C&rdquo; level executives and other senior managers who can influence large transfers of outsourcing business to the company.
7.   Keeps informed on new products, services, and other general information of interest to customers, through successful completion of Sales Training, shop floor experience, local training, and self-study.
8.   Stays informed of customer business opportunities, account changes, current conditions, future prospects, active measurements, and competitive landscape to protect revenue from competitors. 
9.   Provides direction and guidance to Field Sales Engineer/s, primarily on ways of implementing strategic deals and ensuring service levels for assigned accounts are met.
10. Develop technical expertise related to company and industry.
11. Presents customer key performance indicators (KPIs) to review overall service performance for the quarter.
12. Responsible for maintaining expenses within budget.
13. Responsible for generating required reporting.

Environmental Working Conditions
-    Field based with home office
-    25%-50% Travel (territory and assigned account dependant)
Job Requirements :

Qualifications
1.   Bachelors Degree
a.   Related discipline or engineering degree preferred
2.   Business to business sales experience (min 2-5years)
a.   Medical Device Industry preferred
b.   Proven successful track record
c.   Completion of formal sales training program(s) a plus
3.   Demonstrated selling and account management skills
4.   Ability to translate strategy into tactical implementation and to motivate people to execute on the strategy
5.   Able to effectively call on &ldquo;C&rdquo; level and senior management across multiple functions (Operations, Engineering, Marketing) of major OEM Medical Manufacturers.
6.   Demonstrated ability to work collaboratively with and influence peers and management. 
7.   Able to direct a cross functional team to work in concert to deliver goods and services.
8.   Highly motivated, disciplined/self starter
9.   Strong interpersonal, communication, presentation and organizational skills. The ability to build effective relationships.
10. Able to analyze, understand and effectively communicate technical material
11. Proficient computer skills (Outlook, Excel, Word, PowerPoint)
12. Able to assess the financial impact of deals &amp; opportunities.
13. Skilled in negotiation at highest level.
14. Strong understanding of the medical device industry and/or contract manufacturing industry.
15. Basic computer skills, Outlook, Excel, Word &amp; PowerPoint. CAD &amp; Design programs a plus
Due to the expected number of responses, only those most qualified will be contacted. No recruiters please; all unsolicited third-party submissions will be rejected.

Accellent is an Equal Opportunity/Affirmative Action employer and we value diversity in our workforce. As such we provide equal opportunity for all applicants without regard to race, religion, gender, national origin, age, marital status, veteran status, or disability. To learn more about Accellent and our career opportunities, please visit us atwww.accellent.com
Career Level :Entry Level
Education :Bachelor's Degree
% of Travel Required :30-40%
Shift/Hours :First Shift (Day)
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            <industry><![CDATA[Health Products & Services]]></industry>
        </industries>
        <expiration_date>2010-03-25</expiration_date>
        <employer><![CDATA[Accellent Inc.]]></employer>
        <location><![CDATA[Brooklyn Park, MN, 55445, USA]]></location>
    </job>
    <job>
        <title><![CDATA[Inprocess Inspector Operations 2]]></title>
        <description><![CDATA[


Job Title :Inprocess Inspector Operations 2
Job Code :4273
Location :Orchard Park NY US 14127
Job Description :

Job Title: 
In Process Inspector Quality 2 
Department: 
Quality
Reports To: 
Quality Assurance Manager 
Location: 

FLSA Status: 
Non exempt 
Division: 

Classification: 
Date: 
11/15/08
Education: 
High School graduate, GED or equivalent experience required. Vocational or technical schooling preferred.
Organizational
Relationships: 
Internally  - All facility employees
Externally - Auditors, customers and vendors
Position Scope/Summary
Perform first piece, in process and final inspection or test on a wide variety of parts and document results. Indicate inspection status, maintain product traceability and non-conforming material control. Participate in internal audits, statistical process control and assist control of process documentation, records and equipment calibration
Key Result Accountabilities
Perform required inspections, measurements and testing of incoming parts, production first piece, in-process and finished product per established criteria.
Record results on appropriate documentation. Communicate any discrepancies to the person(s) responsible for corrective/preventive action activity. 
Perform various dimensional inspections using specific dies, gages, microscopes, micrometers and other dimensional inspection systems.
Indicate inspection status of parts with assigned labels and stamps.
Maintain product identification and traceability.
Control non-conforming product in accordance with documented procedures and verify timely corrective and preventative action.
Protect product during handling and storage in the performance of work.
Monitor factory environmental conditions, record data and identify adverse conditions.
Assist with distribution and control of process documentation and quality records.
Assist with control of measuring and test equipment calibration.
Participate in internal quality audits to verify compliance with documented procedures and specifications, record results and verify audit corrective action.
Assist with statistical methods of verifying and controlling process capability.
Provide leadership to production personnel on quality issues.
Comply with and reinforce the requirements of the Quality Manual and Standard Operating Procedures, ISO 9002, FDA Quality System Regulations and other customer standards.
Follow Occupational Safety and Health regulations, including laser safety practices. Performs job duties with little or no supervision or assistance.
Job Requirements :
Qualifications
Minimum 2 years experience as an inspector or 4 years manufacturing experience as a machine operator in a manufacturing or production environment. Prior medical device, aerospace, automotive or regulatedQualifications
Minimum 2 years experience as an inspector or 4 years manufacturing experience as a machine operator in a manufacturing or production environment. Prior medical device, aerospace, automotive or regulated manufacturing environment preferred..
Certificate(s) of training related to this field of work (medical device industry or quality assurance) preferred
Prior experience interpreting technical drawings &amp; specifications required.
Proficient in the use of measuring and test equipment.
Career Level :Experienced (Non-Manager)
Education :Certification
Shift/Hours :Second Shift (Afternoon)
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        <expiration_date>2010-03-25</expiration_date>
        <employer><![CDATA[Accellent Inc.]]></employer>
        <location><![CDATA[Orchard Park, NY, 14127, USA]]></location>
    </job>
    <job>
        <title><![CDATA[In Process Inspector Operations 2]]></title>
        <description><![CDATA[


Job Title :In Process Inspector Operations 2
Job Code :4271
Location :Orchard Park NY US 14127
Job Description :

Job Title: 
In Process Inspector Quality 2 
Department: 
Quality
Reports To: 
Quality Assurance Manager 
Location: 

FLSA Status: 
Non exempt 
Division: 

Classification: 
Date: 
11/15/08
Education: 
High School graduate, GED or equivalent experience required. Vocational or technical schooling preferred.
Organizational
Relationships: 
Internally  - All facility employees
Externally - Auditors, customers and vendors
Position Scope/Summary
Perform first piece, in process and final inspection or test on a wide variety of parts and document results. Indicate inspection status, maintain product traceability and non-conforming material control. Participate in internal audits, statistical process control and assist control of process documentation, records and equipment calibration
Key Result Accountabilities
Perform required inspections, measurements and testing of incoming parts, production first piece, in-process and finished product per established criteria.
Record results on appropriate documentation. Communicate any discrepancies to the person(s) responsible for corrective/preventive action activity. 
Perform various dimensional inspections using specific dies, gages, microscopes, micrometers and other dimensional inspection systems.
Indicate inspection status of parts with assigned labels and stamps.
Maintain product identification and traceability.
Control non-conforming product in accordance with documented procedures and verify timely corrective and preventative action.
Protect product during handling and storage in the performance of work.
Monitor factory environmental conditions, record data and identify adverse conditions.
Assist with distribution and control of process documentation and quality records.
Assist with control of measuring and test equipment calibration.
Participate in internal quality audits to verify compliance with documented procedures and specifications, record results and verify audit corrective action.
Assist with statistical methods of verifying and controlling process capability.
Provide leadership to production personnel on quality issues.
Comply with and reinforce the requirements of the Quality Manual and Standard Operating Procedures, ISO 9002, FDA Quality System Regulations and other customer standards.
Follow Occupational Safety and Health regulations, including laser safety practices. Performs job duties with little or no supervision or assistance.
Job Requirements :
Qualifications
Minimum 2 years experience as an inspector or 4 years manufacturing experience as a machine operator in a manufacturing or production environment. Prior medical device, aerospace, automotive or regulated manufacturing environment preferred..
Certificate(s) of training related to this field of work (medical device industry or quality assurance) preferred
Prior experience interpreting technical drawings &amp; specifications required.
Proficient in the use of measuring and test equipment.
Demonstrate ability to check dimensions, surface relationships, finish material defects and mechanical strength of product following appropriate training
Prior experience in the use of PC&rsquo;s and Microsoft Office software applications required.
Career Level :Experienced (Non-Manager)
Education :Certification
Shift/Hours :Third Shift (Night)
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        <expiration_date>2010-03-25</expiration_date>
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        <location><![CDATA[Orchard Park, NY, 14127, USA]]></location>
    </job>
    <job>
        <title><![CDATA[Sales Operations Manager - Twin Cities]]></title>
        <description><![CDATA[


Job Title :Sales Operations Manager - Twin Cities
Job Code :4268
Location :Brooklyn Park MN US 55428
Job Description :
Accellent, Inc. is a fully integrated provider of design, supply chain management and strategic sourcing services to the Medical Device industry. Accellentwww.accellent.com, a recognized market leader, is a fast-growing outsource manufacturing and design solution company specializing in high growth areas such as Cardiology, Endoscopy and Orthopaedics. The top Medical Device companies partner with Accellent to provide innovation, advanced technology, speed to market, low cost labor and strategic sourcing. 
We&rsquo;re looking for team players with a can-do attitude to share in our vision and corporate values. Accellent offers competitive salaries; a comprehensive benefits package, and a stimulating work environment. 
Currently, we are searching for a Sales Operations Manager to lead our Inside Sales Operations from our Brooklyn Park, MN facility.
About the Opportunity:
The Sales Operations Manager will be the leader in ensuring that all sales tools (forecasting and reporting) are in place and operational to support the activities and outcomes of our sales force. This is a new role for our organization, and the successful candidate will lead the implementation of our in-development dashboard and CRM tools (Oracle-based). We are looking for a proactive leader that can manage the tools, recommend action to leaders within Accellent based on proactive and on-going trend analysis.
Position Scope/Summary
The company provides design and outsourced manufacturing, assembly, and supply chain management to the medical device industry. With approximately 19 locations, Accellent employs 3500 people in 5 countries. The Sales Operations Manager is responsible for Sales Planning Support, Marketing, Tools &amp; Systems and Core Sales Process..
Key Result Accountabilities
Core Sales Process
1.   Manage sales pipeline including all standard reporting on pipeline.
2.   Assist in account reviews &amp; annual account planning.
3.   Track performance of reps and teams against quotas account plans, and targets.
4.   Manage other sales metrics.
5.   Assist in key customer visit preparation.
6.   Support in research on customers, markets, or background of potential opportunities.
Tools &amp; Systems
1.   Build requirements for continuous improvement of existing sales tools (e.g. pipeline, npd tab, quoting system).
2.   Serve as sales lead for any further tool development (including CRM system implementation).
Sales Planning Support
1.   Run analysis for compensation plans / budgeting process.
2.   Analyze performance data to identify variances, underperforming teams and flag areas to focus.
3.   Contribute to problem solving on key issues &amp; barriers but not replacing the manager of the sales group. 
4.   Escalate issues as needed. 
Marketing
1.   Maintain value proposition &ldquo;pitch books&rdquo; or other collateral.
2.   Assist sales management in creation of any standard marketing materials for sales team.
3.   Market intelligence reports for particular industries.
1.   Complies with all work rules including those pertaining to safety, health, quality and Accellent Quality Management Systems.
2.   Performs other duties as necessary.
Job Requirements :
* Bachelor&rsquo;s Degree in Economics, Marketing, Sales Management or related field with a minimum of 5+ years of related experience, medical device manufacturing experience a plus. 
* Inside Sales Management experience required with proven success in managing dashboards, reporting and trend analysis for a complex sales team.
* CRM implementation experience highly desired.
* A minimum of 5+ years direct sales or account management and process management experience.
* Solid financial, analytical and critical thinking skills.
* Self-starter, works well under pressure and can effectively manage competing priorities
* Clearly understands the financial and broader stakeholder issues driving strategic decision-making across all functional areas. Thinks for the business, not for the function, while simultaneously and effectively managing the day-to-day delivery of exceptional results.
* Open and transparent leadership and peer group interaction style. Welcomes input from others in the continuous improvement of his or her span of control.
* Strong interpersonal, communication, presentation and organizational skills. The ability to build effective relationships.
* Knowledgeable about the highly regulated nature of this business and comfortable functioning within such an environment.
* Proficient computer skills (MS Outlook, Excel, Word, PowerPoint, Access)
* Able to assess the financial impact of deals &amp; opportunities.

Due to the expected number of responses, only those most qualified will be contacted. No recruiters please; all unsolicited third-party submissions will be rejected.

Accellent is an Equal Opportunity/Affirmative Action employer and we value diversity in our workforce. As such we provide equal opportunity for all applicants without regard to race, religion, gender, national origin, age, marital status, veteran status, or disability. To learn more about Accellent and our career opportunities, please visit us atwww.accellent.com
Career Level :Experienced (Non-Manager)
Education :Bachelor's Degree
% of Travel Required :0-10%
Shift/Hours :First Shift (Day)
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        </industries>
        <expiration_date>2010-03-25</expiration_date>
        <employer><![CDATA[Accellent Inc.]]></employer>
        <location><![CDATA[Brooklyn Park, MN, 55445, USA]]></location>
    </job>
    <job>
        <title><![CDATA[Senior Manufacturing Engineer]]></title>
        <description><![CDATA[


Job Title :Senior Manufacturing Engineer
Job Code :3305
Location :Upland CA US 91786
Job Description :
Accellent, Inc. is a fully integrated provider of design, supply chain management and strategic sourcing services to the Medical Device industry. Accellentwww.accellent.com, a recognized market leader, is a fast-growing outsource manufacturing and design solution company specializing in high growth areas such as Cardiology, Endoscopy and Orthopaedics. The top Medical Device companies partner with Accellent to provide innovation, advanced technology, speed to market, low cost labor and strategic sourcing.
We&rsquo;re looking for team players with a can-do attitude to share in our vision and corporate values. Accellent offers competitive salaries; a comprehensive benefits package, and a stimulating work environment.
Currently, we are searching for aSenior Manufacturing Engineer to join our Upland, CAfacility.
About the Opportunity:Reporting the the Engineering Manager, the Senior Manufacturing Engineer works with the Upland operations team to direct, coordinate, and exercises functional authority for planning, organization, control, integration, and completion of engineering activities within area of assigned responsibility.
Our Senior Manufacturing Engineer:
* Follows and develops Quality and Regulatory requirements including Accellent policies, procedures, and appropriate regulatory requirements.
* Plans, Develops, and Executes Process and Test Method Validations (IQ, OQ, PQ, PPQ) in accordance with Accellent procedures and guidelines  Communicates ideas, information, and recommendations clearly, effectively and frequently (oral and written) within Accellent, with outside suppliers or partners and with Accellent customers during formal and informal interactions.
* Prepares or reviews documentation with a high degree of accuracy, completeness, and effectiveness using common Accellent engineering tools &amp; templates were available. (Examples include specifications, manufacturing procedures, ECOs, and technical reports or analysis)
* Applies and Promotes Lean manufacturing techniques to continuously improve cycle times and process flows. Identifies, supports, or directs the execution of improvement efforts to reduce waste in all manufacturing and business processes.
* Uses structured problem solving techniques and statistical methods for data driven analysis and decisions.
* Applies and leads DMAIC &ndash; Six Sigma approaches to solve issues and reduce variation in all manufacturing and business processes.
* Plans, executes and manages project activities with cross functional teams.
* Project types can include new product development and introduction, manufacturing transfers, continuous improvement and cost reduction initiatives.
* Practices and demonstrates the Accellent values (Customer focus, Continuous Improvement, Performance, Accountability, Teamwork and Integrity) in all activities.
* Demonstrates leadership through mentoring of junior staff, responsiveness to business needs and motivation of diverse, cross functional teams including influencing both internal and external members to achieve positive business results
* Demonstrates technical ability through the application of engineering skills, approaches and knowledge.
* Takes financial responsibility for activities to create positive impact to the business   Performs all duties and directs others creating a safe working environment for our employees and our communities.


Job Requirements :

* BS in Engineering, or equivalent, plus a minimum of five (5) years experience in plastic injection molding is required.
* A minimum of one year in medical device manufacturing and experience in transferring products from design to manufacturing is highly desirable.
* Strong understanding of various manufacturing processes including: precision plastic injection molding, insert molding, mold construction, plastic joining technologies, prototyping, precision machining, stampings, assembly, and packaging.
* Good understanding of polymer material properties and the practical application of these principles in establishing robust manufacturing processes, troubleshooting processes, and consulting with customers on material selection.
* Must have working knowledge of Microsoft Office, MiniTab, and SolidWorks. Knowledge of Access, MoldFlow, and Enterprise IQMS is desirable.Must be able to apply engineering concepts, original thinking, cause and effect, and ingenuity to solve problems.
* Must have good decision making and organizational skills.
* Must be able to manage and deliver results on multiple priorities simultaneously.
* Must have good verbal and written communications skills.
* Must be skilled statistical practitioner and apply statistical analysis to determine process capabilities, compare populations via hypothesis testing, utilize process control charting, and use the output of these analysis&rsquo; to improve operations. Six Sigma Belt is highly desirable.
* Knowledge and experience in performing Design of Experiments (DOE) desirable.
Due to the expected number of responses, only those most qualified will be contacted. No recruiters please; all unsolicited third-party submissions will be rejected.
Accellent is an Equal Opportunity/Affirmative Action employer and we value diversity in our workforce. As such we provide equal opportunity for all applicants without regard to race, religion, gender, national origin, age, marital status, veteran status, or disability. To learn more about Accellent and our career opportunities, please visit us atwww.accellent.com
Career Level :Experienced (Non-Manager)
Education :Bachelor's Degree
% of Travel Required :0-10%
Shift/Hours :First Shift (Day)
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        </industries>
        <expiration_date>2010-03-25</expiration_date>
        <employer><![CDATA[Accellent Inc.]]></employer>
        <location><![CDATA[Upland, CA, 91786, USA]]></location>
    </job>
    <job>
        <title><![CDATA[Continuous Improvement Leader - Med Dev Manufacturing]]></title>
        <description><![CDATA[


Job Title :Continuous Improvement Leader - Med Dev Manufacturing
Job Code :3268
Location :Trenton GA US 30752
Job Description :
Accellent, Inc. is a fully integrated provider of design, supply chain management and strategic sourcing services to the Medical Device industry. Accellentwww.accellent.com, a recognized market leader, is a fast-growing outsource manufacturing and design solution company specializing in high growth areas such as Cardiology, Endoscopy and Orthopaedics. The top Medical Device companies partner with Accellent to provide innovation, advanced technology, speed to market, low cost labor and strategic sourcing.
We&rsquo;re looking for team players with a can-do attitude to share in our vision and corporate values. Accellent offers competitive salaries; a comprehensive benefits package, and a stimulating work environment.


We are searching for aContinuous Improvement Leaderto join ourteam to continue our LEAN cultural transformation. This opportunity will be based at our Trenton, GA facility. Relocation assistance is available.

About the Opportunity:
The Continuous Improvement Leaders will be integral in driving Accellent's continuing commitment to a culture of LEAN thinking and continuous process improvement. The selected LEAN experts will provide leadership, training and support to their assigned Site in an effort to achieve &ldquo;Best-in-Class&rdquo; performance by eliminating waste in all manufacturing and business processes, radically improving cycle times to our customers and creating an environment focused on continuous improvement. Our Continuous Improvement Leaders will drive high visibility projects and will be embedded in our site leadership.

Primary Responsibilities:
* Lead the training of the Site employees in Lean Enterprise principles, ensuring they have a solid working knowledge of how to apply these tools &amp; techniques to achieve process improvements in the manufacturing &amp; office environment.
* Perform facility-wide training in Lean Manufacturing tools, including the use of Kaizen events, Value-Stream Mapping, Single-Piece Flow, TPM, Setup Reduction, 5S, Kanban, etc.
* Apply a &ldquo;train the trainer&rdquo; approach to progressively educate managers, supervisors and cell leaders to conduct independent Lean initiatives.
* Develop and deploy the annual facility Lean Process Excellence plan, consistent with the Hoshin Planning cycle and addressing annual division performance improvement objectives.
* Lead the delivery of significant, quantifiable, annualized cost savings.
* Take accountability for the success of identified cost reduction. 
* Drive cost reduction efforts through cycle time reduction, process improvement, setup reduction, etc.Develop and improve manufacturing processes through the use of Lean Sigma. 
* Drive the development of product flow and make recommendations on the efficient lay-out of the manufacturing floor and track the resulting benefit of those implemented changes.
* Lead the Site deployment of daily, weekly, and monthly metrics, ensuring that collection and monitoring of this information is meaningful in the identification of areas requiring process improvement or corrective action.
* Lead problem solving efforts both internally and externally, working closely with customers and QA on internal and external corrective and preventive actions.
* Assist Supply Chain Management in the development of partnerships with suppliers and maximizing the use of VMI programs, Kanbans, and consignment inventory with key customers.
* Act as an intergral membership of the site Leadership Team.
Secondary Responsibilities:
* Drive six sigma process improvement methodologies as the facility wide &ldquo;thinking tool.&rdquo; Be the facility wide champion for data based decision making.
* Lead the training of the workforce in Six Sigma tools &amp; techniques to ensure all associates are capable of participating in a process improvement project team.
* Assist QA with process capability validation, the implementation and qualification of new equipment (i.e. new machines, automation) and the certification of primary and secondary processes using statistical methods, capability studies, etc.
* Assist the Controller in tracking the financial impact and benefits of Lean and Six Sigma initiatives, establishing metrics consistent with Lean Thinking.
* Stay apprised of product costs and variance reports.
* Assist in the establishment of standard costs for new and existing products, where impacted by Lean deployment initiatives.
* Assist in financial justification of new equipment as it applies to Lean deployment or process improvement.
* Benchmark industry-wide application of business process improvements to assure Accellent maintains a leadership position in medical devices.
* Coordinate with peers at other Accellent facilities in the training of Lean Sigma principles and implementation of Lean tools and techniques.
* Maintain a current knowledge base and personal development plan to retain leadership skill set in the Lean Sigma disciplines.
The Continuous Improvement Leaders will have two customer groups. 
* Internal functions such as:  Customer Solutions, Quoting, Operations, Quality, Project Management and Engineering, Production Control departments. 
* External: Customers, suppliers and other Accellent facilities.
Job Requirements :
The successful candidate for the Continuous Improvement Leader will possess:
* An undergraduate degree in Engineering, Industrial Technology or Business (as a minimum) - an applicable advanced degree is desirable.
* A minimum of five years experience in deployment of Lean Manufacturing and/or Six Sigma tools. 3-5 years of management or supervision experience a plus.
* Demonstrated track record of Lean implementation yielding measurable performance improvement or transformation from traditional batch manufacturing processes.
* Experience in a &ldquo;Made-to-Order&rdquo; product environment a plus.
* Formal Lean training required. Black Belt certification a plus.
* Demonstrated strong verbal and written communication skills, analytical skills, statistical and mathematical abilities and interpersonal skills.
* Experience in cost conscious manufacturing environments (automotive, consumer electronics, appliances) considered a plus.
* The ability to handle highly confidential information in an appropriate manner.
* The ability to work with all levels of staff throughout all Accellent facilities.Medical Device manufacturing experience is not required. If you have Lean leadership experience in a high-mix, low volume environment, with demonstrated success of shaping and supporting cultural transformation, then we want to hear from you!
Due to the expected number of responses, only those most qualified will be contacted with preference given to candidates within geographic proximity first. No recruiters please; all unsolicited third-party submissions will be rejected.
Accellent is an Equal Opportunity/Affirmative Action employer and we value diversity in our workforce. As such we provide equal opportunity for all applicants without regard to race, religion, gender, national origin, age, marital status, veteran status, or disability. To learn more about Accellent and our career opportunities, please visit us atwww.accellent.com
Career Level :Experienced (Non-Manager)
Education :Bachelor's Degree
% of Travel Required :0-10%
Shift/Hours :First Shift (Day)
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        </industries>
        <expiration_date>2010-03-25</expiration_date>
        <employer><![CDATA[Accellent Inc.]]></employer>
        <location><![CDATA[Trenton, GA, 30752, USA]]></location>
    </job>
    <job>
        <title><![CDATA[Assembler]]></title>
        <description><![CDATA[


Job Title :Assembler
Job Code :4463
Location :TRENTON GA US 30752
Job Description :
Assemblers has the general responsibility of assembly and production of catheter component sub-assemblies and assemblies. 
Assembler is expected to work with all relevant personnel to effectively meet or exceed expectations for product quality.
Assemblers must also have knowledge of visual and dimensional inspection techniques, and ability to interpret customer drawings and prints.
Job Requirements :
* Has the responsibility of following established documentation for final processing.
* Must accurately document all work performed on processing check sheet and/or work order.
* Performs necessary assembly process steps to complete assigned work.
* Performs in-process inspection on all parts for the purpose of identifying defects and notifying proper personnel of serious defected material
* Must be able to read and interpret customer prints and specifications.
* Performs various dimensional inspection using specific dies or gauges, or dimensional inspection systems and micrometers.
* Responsible for labeling material with proper description and information for shipping and inventory control purposes.
* Maintains cleanliness of work area, machines, tools, and equipment.
* Performs job duties with little or no supervision or assistance.
Career Level :Entry Level
Education :High School or equivalent
% of Travel Required :None
Shift/Hours :First Shift (Day)
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        <expiration_date>2010-03-25</expiration_date>
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        <location><![CDATA[TRENTON, GA, 30752, USA]]></location>
    </job>
    <job>
        <title><![CDATA[Assembler]]></title>
        <description><![CDATA[


Job Title :Assembler
Job Code :4464
Location :TRENTON GA US 30752
Job Description :
Assemblers has the general responsibility of assembly and production of catheter component sub-assemblies and assemblies. 
Assembler is expected to work with all relevant personnel to effectively meet or exceed expectations for product quality.
Assemblers must also have knowledge of visual and dimensional inspection techniques, and ability to interpret customer drawings and prints.
Job Requirements :
* Has the responsibility of following established documentation for final processing.
* Must accurately document all work performed on processing check sheet and/or work order.
* Performs necessary assembly process steps to complete assigned work.
* Performs in-process inspection on all parts for the purpose of identifying defects and notifying proper personnel of serious defected material
* Must be able to read and interpret customer prints and specifications.
* Performs various dimensional inspection using specific dies or gauges, or dimensional inspection systems and micrometers.
* Responsible for labeling material with proper description and information for shipping and inventory control purposes.
* Maintains cleanliness of work area, machines, tools, and equipment.
* Performs job duties with little or no supervision or assistance.
Career Level :Entry Level
Education :High School or equivalent
% of Travel Required :None
Shift/Hours :Second Shift (Afternoon)
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            <industry><![CDATA[Health Products & Services]]></industry>
        </industries>
        <expiration_date>2010-03-25</expiration_date>
        <employer><![CDATA[Accellent Inc.]]></employer>
        <location><![CDATA[TRENTON, GA, 30752, USA]]></location>
    </job>
    <job>
        <title><![CDATA[Process Engineer]]></title>
        <description><![CDATA[


Job Title :Process Engineer
Job Code :4466
Location :Trenton GA US 30752
Job Description :
Accellent, Inc. is a fully integrated provider of design, supply chain management and strategic sourcing services to the Medical Device industry. Accellentwww.accellent.com, a recognized market leader, is a fast-growing outsource manufacturing and design solution company specializing in high growth areas such as Cardiology, Endoscopy and Orthopaedics. The top Medical Device companies partner with Accellent to provide innovation, advanced technology, speed to market, low cost labor and strategic sourcing. 
We&rsquo;re looking for team players with a can-do attitude to share in our vision and corporate values. Accellent offers competitive salaries; a comprehensive benefits package, and a stimulating work environment. 
Currently, we are searching for a Process Engineer to join our facility.
About the Opportunity:
Development and/or management of high priority Customer and/or Internal Projects as assigned to produce products and develop processes to ensure quality, cost targets, schedules, etc are met. Support Engineering and Manufacturing with design, documentation, validation and implementation of fixtures, equipment, processes and product. (Manufacturing encompasses all component, assembly and extrusion processes.)
Job Requirements :
* Assure that all products being produced from Manufacturing for internal or external customers meets all requirements. This will include regular contact to address and correct any issues that may arise in a normal manufacturing environment.
* Excellent process knowledge of Manufacturing and able to provide technical services to internal and external customers.
* Review existing processes to identify and implement cost, quality, and productivity improvements.
* Support Manufacturing Specialists in the development and execution of new processes and products.
* Manage projects involving design and processes improvements that involve single or multi-site involvement. Activities may include proposal development, quoting and cost estimating, charter and scope definition, project planning, and project budgeting. Responsible for directing the activities of the team including work assignment, progress monitoring and status communication the status.
* Provide leadership for, and direct the activities of, the project team.
* Work with Manufacturing in the procurement, set-up, validation and execution of new product lines and equipment.
* Implement, validate and train operators with new tooling/equipment in manufacturing and assure all documentation is correct and complete.
* Evaluate proposed projects for feasibility and applicability of Accellent Cardiology technology. Will typically be assigned projects when are less defined and require (1) The development of new technology and/or processes, (2) The improvement and further resolution of existing technology, and/or (3) Development of new supplier processes or components as required to meet Project Goals.



Due to the expected number of responses, only those most qualified will be contacted. No recruiters please; all unsolicited third-party submissions will be rejected.

Accellent is an Equal Opportunity/Affirmative Action employer and we value diversity in our workforce. As such we provide equal opportunity for all applicants without regard to race, religion, gender, national origin, age, marital status, veteran status, or disability. To learn more about Accellent and our career opportunities, please visit us atwww.accellent.com
Career Level :Experienced (Non-Manager)
Education :Bachelor's Degree
% of Travel Required :0-10%
Shift/Hours :First Shift (Day)
]]></description>
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        <industries>
            <industry><![CDATA[Health Products & Services]]></industry>
        </industries>
        <expiration_date>2010-03-25</expiration_date>
        <employer><![CDATA[Accellent Inc.]]></employer>
        <location><![CDATA[Trenton, GA, 30752, USA]]></location>
    </job>
    <job>
        <title><![CDATA[Q.A. Inspector]]></title>
        <description><![CDATA[


Job Title :Q.A. Inspector
Job Code :4407
Location :Juarez Chih MX 32470
Job Description :
Accellent, Inc. is a fully integrated provider of design, supply chain management and strategic sourcing services to the Medical Device industry. Accellentwww.accellent.com, a recognized market leader, is a fast-growing outsource manufacturing and design solution company specializing in high growth areas such as Cardiology, Endoscopy and Orthopaedics. The top Medical Device companies partner with Accellent to provide innovation, advanced technology, speed to market, low cost labor and strategic sourcing.
We&rsquo;re looking for team players with a can-do attitude to share in our vision and corporate values. Accellent offers competitive salaries; a comprehensive benefits package, and a stimulating work environment.
Currently, we are searching for a to join our facility.
About the Opportunity:
Position Scope/Summary
* Responsible for raw material component inspection and testing (as required per component Specification), all required documentation, all required system transactions, and proper archiving of
* All inspected/tested raw material Device History Record per established Quality System controls.
                                               
Key Result Accountabilities
* Responsible for coordinating, tracking, and trending supplier certified raw material components.
* Responsible for miscellaneous Quality Assurance supporting roles relative to Accellent Manufacturing/processing.
Environmental Working Conditions 
&middot;    Ability to work in a demanding user environment
&middot;    Ability to provide and communicate data necessary for timely, team oriented product disposition(s).
Qualifications
* Ability to read, analyze, and understand Quality System documents; to include but not limited to: Company Policies, Standard Operating Procedures, component specifications, Quality Work Instructions, etc.
* Ability to utilize current business software applications; to include but not limited to: word Processing software, spreadsheet/statistical applications, web browsing applications, etc.
* Ability to use and understand applicable Inspection Measuring and Testing Equipment, to include Appropriate sampling plans/strategies.
* A minimum of 2 years experience in a Quality Assurance/Control function.


Job Requirements :




Due to the expected number of responses, only those most qualified will be contacted. No recruiters please; all unsolicited third-party submissions will be rejected.

Accellent is an Equal Opportunity/Affirmative Action employer and we value diversity in our workforce. As such we provide equal opportunity for all applicants without regard to race, religion, gender, national origin, age, marital status, veteran status, or disability. To learn more about Accellent and our career opportunities, please visit us atwww.accellent.com
Career Level :Entry Level
Education :High School or equivalent
% of Travel Required :0-10%
Shift/Hours :Second Shift (Afternoon)
]]></description>
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        <expiration_date>2010-03-25</expiration_date>
        <employer><![CDATA[Accellent Inc.]]></employer>
        <location><![CDATA[, USA]]></location>
    </job>
    <job>
        <title><![CDATA[Rotational Engineer]]></title>
        <description><![CDATA[


Job Title :Rotational Engineer
Job Code :4415
Location :Wilmington MA US 01887
Job Description :
Accellent, Inc. is a fully integrated provider of design, supply chain management and strategic sourcing services to the Medical Device industry. Accellentwww.accellent.com, a recognized market leader, is a fast-growing outsource manufacturing and design solution company specializing in high growth areas such as Cardiology, Endoscopy and Orthopaedics. The top Medical Device companies partner with Accellent to provide innovation, advanced technology, speed to market, low cost labor and strategic sourcing. 
We&rsquo;re looking for team players with a can-do attitude to share in our vision and corporate values. Accellent offers competitive salaries; a comprehensive benefits package, and a stimulating work environment. 
Currently, we are searching for a Rotational Engineer to join our team.

Job Requirements :
Position Scope/Summary
Provides design, manufacturing, process control, process improvement, quality systems and or lean excellence engineering support. Performs engineering functions related to manufacturing processes, quality systems, process documentation and lean excellence. May be assigned to Endoscopy, Cardiology or Orthopaedics division depending on academic background, professional interest and company need. 
Key Result Accountabilities
1.   Design, develop, implement, enhance and maintain manufacturing processes and process improvements for use in the production of customer components.
2.   Revise manufacturing processes and documentation, as required, for the purpose of improvement in quality and or in manufacturing efficiencies.
3.   Design, develop, implement, enhance and maintain improvements in inspection methods and procedures to ensure a controllable, cost effective manufacturing process that meets or exceeds customer needs.
* Communicate with customer engineering and/or design departments to identify and resolve issues thataffect or are affected by the manufacturing or quality system process.
5.  Keep current on state of the art engineering design and lean excellence initiatives that impact medical device industry.
6.  Perform other duties as assigned.
Qualifications
* Minimum 3.2 Grade Point Average (4.0 scale) or equivalent required. Magna Cum Laude or Summa Cum Laude preferred. Prior academic experience as a team leader or group leader for class projects strongly preferred.
* Prior experience as an engineering intern or co-operative student in a domestic manufacturing setting is a plus. Medical device manufacturing or experience as an intern or co-operative student in a highly regulated domestic manufacturing environment strongly preferred.
* Prior experience using automated engineering software is preferred.
* Excellent communication, time management and organization skills are required.
5.   Ability to travel and to relocate is required.




Due to the expected number of responses, only those most qualified will be contacted. No recruiters please; all unsolicited third-party submissions will be rejected.


Accellent is an Equal Opportunity/Affirmative Action employer and we value diversity in our workforce. As such we provide equal opportunity for all applicants without regard to race, religion, gender, national origin, age, marital status, veteran status, or disability. To learn more about Accellent and our career opportunities, please visit us at
www.accellent.com
Career Level :Entry Level
Education :Bachelor's Degree
% of Travel Required :30-40%
Shift/Hours :First Shift (Day)
]]></description>
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        <expiration_date>2010-03-25</expiration_date>
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        <location><![CDATA[Wilmington, MA, 01887, USA]]></location>
    </job>
    <job>
        <title><![CDATA[Rotational Engineer]]></title>
        <description><![CDATA[


Job Title :Rotational Engineer
Job Code :4417
Location :Wilmington MA US 01887
Job Description :
Accellent, Inc. is a fully integrated provider of design, supply chain management and strategic sourcing services to the Medical Device industry. Accellentwww.accellent.com, a recognized market leader, is a fast-growing outsource manufacturing and design solution company specializing in high growth areas such as Cardiology, Endoscopy and Orthopaedics. The top Medical Device companies partner with Accellent to provide innovation, advanced technology, speed to market, low cost labor and strategic sourcing. 
We&rsquo;re looking for team players with a can-do attitude to share in our vision and corporate values. Accellent offers competitive salaries; a comprehensive benefits package, and a stimulating work environment. 
Currently, we are searching for a Rotational Engineer to join our team.

Job Requirements :
Position Scope/Summary
Provides design, manufacturing, process control, process improvement, quality systems and or lean excellence engineering support. Performs engineering functions related to manufacturing processes, quality systems, process documentation and lean excellence. May be assigned to Endoscopy, Cardiology or Orthopaedics division depending on academic background, professional interest and company need. 
Key Result Accountabilities
1.   Design, develop, implement, enhance and maintain manufacturing processes and process improvements for use in the production of customer components.
2.   Revise manufacturing processes and documentation, as required, for the purpose of improvement in quality and or in manufacturing efficiencies.
3.   Design, develop, implement, enhance and maintain improvements in inspection methods and procedures to ensure a controllable, cost effective manufacturing process that meets or exceeds customer needs.
* Communicate with customer engineering and/or design departments to identify and resolve issues thataffect or are affected by the manufacturing or quality system process.
5.  Keep current on state of the art engineering design and lean excellence initiatives that impact medical device industry.
6.  Perform other duties as assigned.
Qualifications
* Minimum 3.2 Grade Point Average (4.0 scale) or equivalent required. Magna Cum Laude or Summa Cum Laude preferred. Prior academic experience as a team leader or group leader for class projects strongly preferred.
* Prior experience as an engineering intern or co-operative student in a domestic manufacturing setting is a plus. Medical device manufacturing or experience as an intern or co-operative student in a highly regulated domestic manufacturing environment strongly preferred.
* Prior experience using automated engineering software is preferred.
* Excellent communication, time management and organization skills are required.
5.   Ability to travel and to relocate is required.




Due to the expected number of responses, only those most qualified will be contacted. No recruiters please; all unsolicited third-party submissions will be rejected.


Accellent is an Equal Opportunity/Affirmative Action employer and we value diversity in our workforce. As such we provide equal opportunity for all applicants without regard to race, religion, gender, national origin, age, marital status, veteran status, or disability. To learn more about Accellent and our career opportunities, please visit us at
www.accellent.com
Career Level :Entry Level
Education :Bachelor's Degree
% of Travel Required :30-40%
Shift/Hours :First Shift (Day)
]]></description>
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            <industry><![CDATA[Health Products & Services]]></industry>
        </industries>
        <expiration_date>2010-03-25</expiration_date>
        <employer><![CDATA[Accellent Inc.]]></employer>
        <location><![CDATA[Wilmington, MA, 01887, USA]]></location>
    </job>
    <job>
        <title><![CDATA[Environmental Health and Safety Engineer]]></title>
        <description><![CDATA[


Job Title :Environmental Health and Safety Engineer
Job Code :4418
Location :Collegeville PA US 19426
Job Description :
Accellent, Inc. is a fully integrated provider of design, supply chain management and strategic sourcing services to the Medical Device industry. Accellentwww.accellent.com, a recognized market leader, is a fast-growing outsource manufacturing and design solution company specializing in high growth areas such as Cardiology, Endoscopy and Orthopaedics. The top medical device companies partner with Accellent to provide innovation, advanced technology, speed to market, low cost labor and strategic sourcing.
We&rsquo;re looking for team players with a can-do attitude to share in our vision and corporate values. Accellent offers competitive salaries, a comprehensive benefits package, and a stimulating work environment.
Currently, we are searching for a Facility and EHS Engineer to join our Facility Management team at the Collegeville, PA facility.
About the Opportunity
The Facility and EHS Engineer reports to the Manager of Engineering Facilities for plant safety, compliance with government regulations, fire protection, facilities inspections, insurance liaison, and manpower planning including outside contractor liaison. In addition, this position assists with manufacturing and facility engineering projects.  
Responsibilities 
&middot;    Manage and coordinate all plant safety activities and programs, i.e. accident investigation, coordinate safety committee, update/ maintain all safety procedures, equipment training/certification, maintain programs for plant and personnel safety protection.
&middot;    Initiate and coordinate necessary actions to correct unsafe conditions throughout the facility.
&middot;    Identify new equipment and manufacturing technologies to improve equipment and the overall facility. 
&middot;    Establish and maintain procedures to assure compliance with OSHA, EPA, DEP and other governmental agencies.
&middot;    Coordinate, develop and schedule periodic maintenance of key facility mechanical and production equipment.
&middot;    Establish and maintain fire prevention procedures, select and recommend new equipment and direct activities as needed.
&middot;    Coordinate and monitor facility inspections by insurance and government agencies.
&middot;    Initiate and maintain practices, procedures to achieve plant wide good energy practices.
&middot;    Coordinate outside vendors for maintenance, construction and plant facilities including but not limited todisposal; delivery, storage and disposal of gases used in manufacturing processes; site water grounds maintenance; and certifications required for regulatory purposes. Procure outside contractors to complement Engineering or maintenance tasks as assigned.
&middot;    Coordinate and follow- up with all procedure revisions and maintenance of the Engineering Department Procedures and Files.
&middot;    Monitor the Energy Management System.
&middot;    Apply and promote lean manufacturing techniques.
&middot;    Plan, execute and manage projects activities with cross functional teams.
&middot;    Demonstrate technical ability through the application of engineering skills, approaches and knowledge.
&middot;    Perform other duties and necessary.
Job Requirements :
Qualifications
&middot;    BS degree in EHS Sciences, Engineering or equivalent
&middot;    Minimum 5 years vendor and interdepartmental project management experience
&middot;    Minimum 5 years safety and security experience
&middot;    Knowledge of lean manufacturing techniques
&middot;    Demonstrated experience in an industrial manufacturing environment
&middot;    Demonstrated experience with OSHA VPP certification
&middot;    Demonstrated experience with ISO 14001
&middot;    Experience in maintaining air and water permits within a manufacturing plant
&middot;    Preferred experience in metal processing equipment and facilities or equivalent 
&middot;    Preferred experience with governmental environmental documentation
&middot;    Preferred ability to write and submit environmental year end reports
&middot;    Preferred CAD experience

Environmental Working Conditions: 
The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
While performing the duties of this job, the employee is frequently exposed to moving mechanical parts. The employee is occasionally exposed to high, precarious places; fumes or airborne particles; toxic or caustic chemicals; risk of electrical shock; and vibration. The noise level in the work environment is usually moderate.
Career Level :Experienced (Non-Manager)
Education :Bachelor's Degree
]]></description>
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            <industry><![CDATA[Health Products & Services]]></industry>
        </industries>
        <expiration_date>2010-03-25</expiration_date>
        <employer><![CDATA[Accellent Inc.]]></employer>
        <location><![CDATA[Collegeville, PA, 19426, USA]]></location>
    </job>
    <job>
        <title><![CDATA[Machine Operator]]></title>
        <description><![CDATA[


Job Title :Machine Operator
Job Code :4423
Location :Watertown CT US 06779
Job Description :
Accellent, Inc. is a fully integrated provider of design, supply chain management and strategic sourcing services to the Medical Device industry. Accellentwww.accellent.com, a recognized market leader, is a fast-growing outsource manufacturing and design solution company specializing in high growth areas such as Cardiology, Endoscopy and Orthopaedics. The top Medical Device companies partner with Accellent to provide innovation, advanced technology, speed to market, low cost labor and strategic sourcing. 
We're looking for team players with a can-do attitude to share in our vision and corporate values. Accellent offers competitive salaries; a comprehensive benefits package, and a stimulating work environment. 
Currently, we are searching for a  to join our  facility.
About the Opportunity:
 Operate and monitor eyelet machines
 
 
 
Job Requirements :


Previous eyelet machine operator experience


Due to the expected number of responses, only those most qualified will be contacted. No recruiters please; all unsolicited third-party submissions will be rejected.
 
 
Accellent is an Equal Opportunity/Affirmative Action employer and we value diversity in our workforce. As such we provide equal opportunity for all applicants without regard to race, religion, gender, national origin, age, marital status, veteran status, or disability. To learn more about Accellent and our career opportunities, please visit us atwww.accellent.com
Career Level :Experienced (Non-Manager)
Education :High School or equivalent
% of Travel Required :0-10%
Shift/Hours :Second Shift (Afternoon)
]]></description>
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            <industry><![CDATA[Health Products & Services]]></industry>
        </industries>
        <expiration_date>2010-03-25</expiration_date>
        <employer><![CDATA[Accellent Inc.]]></employer>
        <location><![CDATA[Watertown, CT, 06779, USA]]></location>
    </job>
    <job>
        <title><![CDATA[Quality Assurance Technician]]></title>
        <description><![CDATA[


Job Title :Quality Assurance Technician
Job Code :4427
Location :Houston PA US 15342
Job Description :
Accellent, Inc. is a fully integrated provider of design, supply chain management and strategic sourcing services to the Medical Device industry. Accellentwww.accellent.com, a recognized market leader, is a fast-growing outsource manufacturing and design solution company specializing in high growth areas such as Cardiology, Endoscopy and Orthopaedics. The top Medical Device companies partner with Accellent to provide innovation, advanced technology, speed to market, low cost labor and strategic sourcing. 
We&rsquo;re looking for team players with a can-do attitude to share in our vision and corporate values. Accellent offers competitive salaries; a comprehensive benefits package, and a stimulating work environment. 
Currently, we are searching for a to join our facility.
About the Opportunity:



Job Title: 
Quality Assurance Technician 
Department: 
Quality Assurance
Reports To: 
Quality Assurance Manager 
Location: 
Pittsburgh
FLSA Status: 
Non-Exempt 
Division: 
Orthopaedics
Classification: 
Date: 
10/21/09
Education: 
High School diploma or equivalent (some college preferred)
Organizational
Relationships: 
Internally -Department employees, operations employees, Engineering, Customer Solutions
Externally  -Customers, Suppliers, auditors

Position Scope/Summary
Responsible for verifying product conformance to contract specifications.
Key Result Accountabilities
1.   Maintain a clean and safe work environment.
   2.  Assist Quality Assurance Manager in developing Quality Assurance inspection and work
      instructions.
3.   Correctly operate necessary inspection equipment.*
4.   Perform in-process first-piece inspection as directed.*
5.   Perform final inspection and tests on company and supplier-manufactured components.*
6.   Maintain and calibrate inspection equipment as directed.*
7.   Maintain product identity and traceability.*
8.   Direct or Participate in measurement system analysis studies, PFMEA&rsquo;s, Process Capability Studies. 
9.   Initiate Corrective &amp; Preventive Action Reports as necessary.*
10. Follow all applicable company and/or customer supplied procedures and policies.
11. Perform other duties as assigned by supervisory personnel.
*Essential functions of the job

Job Requirements :

Qualifications
Strong math skills and mechanical aptitude. Computer skills preferred. Strong organizational skills and the ability to multi-task. Attention to fine detail and tolerances required.
Environmental Working Conditions


Physical Demands
(without accommodations) 
Not at All
0% of workday 
Occasional
1-30% of workday 
Frequent
31-60% of workday 
Constant
61-100% of workday
Sitting 

X
Standing 
X 

Walking 
X 

Climbing stairs/ladders 
X 

Push/Pull 
X 

Bending at waist (forward or sideways) 
X 

Simple grasping both hands 

X
Fine manipulation both hands 

X
Lifting/Carrying items 0-10lbs. 

X 

Lifting/Carrying items 11-25lbs. 

X 

Lifting/Carrying items 26-50lbs. 
X 

Lifting/Carrying items 51-75lbs. 
X 


Lifting/Carrying items over 75lbs. 
X 


Functional near, far, color vision aided or unaided 

X
Functional hearing, aided or unaided 

X
Functional verbal communication skills 

X
Other 





Personal Protective Equipment required 
X 





It is impossible to list every requirement for, or responsibility of, any position. Similarly we cannot identify all the skills a position may require since job responsibilities and the Company&rsquo;s needs may change over time. Therefore, the above job description is not comprehensive or exhaustive.  The Company reserves the right to adjust, add to or eliminate any aspect of the above description. The Company also retains the right to require all employees to undertake additional or different job responsibilities when necessary to meet business needs.


Due to the expected number of responses, only those most qualified will be contacted. No recruiters please; all unsolicited third-party submissions will be rejected.

Accellent is an Equal Opportunity/Affirmative Action employer and we value diversity in our workforce. As such we provide equal opportunity for all applicants without regard to race, religion, gender, national origin, age, marital status, veteran status, or disability. To learn more about Accellent and our career opportunities, please visit us atwww.accellent.com
Career Level :Experienced (Non-Manager)
Education :High School or equivalent
% of Travel Required :None
Shift/Hours :First Shift (Day)
]]></description>
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            <industry><![CDATA[Health Products & Services]]></industry>
        </industries>
        <expiration_date>2010-03-25</expiration_date>
        <employer><![CDATA[Accellent Inc.]]></employer>
        <location><![CDATA[Houston, PA, 15342, USA]]></location>
    </job>
    <job>
        <title><![CDATA[Buyer/Planner III (Sr)]]></title>
        <description><![CDATA[


Job Title :Buyer/Planner III (Sr)
Job Code :4434
Location :Orchard Park NY US 14127
Job Description :
Position Scope/Position Summary
This job description is not intended to be all-inclusive and the employee will perform other reasonably related duties as assigned by immediate supervisor or other management members or their designees. This job description does not constitute a written or implied contract of employment and this organization reserves the right to revise and/or change job duties as the need arises.
Schedules, orders and coordinates the delivery of parts/materials, equipment and services used in product manufacturing according to production plans. Controls the inventory of assigned production parts/materials in accordance with management objectives. Expedites requirements as needed (e.g., order action, shortage/pre-shortage, late order reports). Establishes standard cost on assigned production parts/materials for approval by management. Assist in the selection of particular vendors/suppliers with whom to place orders and acts as a primary contact with vendors/suppliers. Resolves problems with assigned production parts/materials, equipment or supplier orders. As a cross-functional team member, represents supply base and takes actions necessary to support quoting, production, cost savings initiatives, quality/complaint investigations and other supply chain related activities.
ESSENTIAL DUTIES, AND AREAS OF ACCOUNTABILITY:
In addition to regular and timely attendance, these include the following. Other duties may be assigned.
Demonstrates company core values; strong team player as measured by peers (behavior and work ethic). Complies with work rules including those pertaining to safety, health, Quality System, and the Accellent Quality Management System.
Planning Responsibilities
       
* Primarily responsible for the creation of the Master Demand Plan (MasterSchedule) for the site working with the Site Supply Chain Manager / Supervisor, as well as the Accellent Director of Supply Chain
* Responsible for the Creation and Management of the Forecast Demand Files within Accellent&rsquo;s ERP system.
* Creates, Schedules and maintains production orders within the Accellent ERP system for assigned work centers to load the factory to ensure manufacturing output goals are obtained for their site.
* Responsible for working with assigned work center supervisors in the proper tracking and reporting on OTD (on time delivery ) cycle time and yield for production orders on a weekly basis
* Responsible for determining the daily required production rate (takt time) for their assigned work centers , as well as working with the corresponding work center supervisors in the tracking and reporting on daily / weekly performance for their assigned areas.
* Manage material flow in facility and through vendors who perform outside processing.
* Schedules work centers and issue a dispatch list to work centers/cells, or trains corresponding work center supervisors on process.
* Check and verify availability of material and available capacity internally and at vendors.
* Route work to minimize machine time and set-ups and achieve desired throughput goals as defined in the performance metrics.
* Provides up-to-date documentation for facility packages and outside services.
* Expedites operations that delay schedules and alter schedules to meet unforeseen conditions.
* Monitor and report on raw materials, purchased, and manufactured parts and components, as required
* Scheduling of sub-assemblies and complete units to meet specified shipping dates.
* Conduct production-planning meetings and communicate issues/concerns to senior mgt.
&middot;    Communicate customer due date changes to site COS (Customer Operations Specialist)
&middot;    Utilize customer forecasts to create forecasts within ERP and adequately plan demand and capacity
&middot;    Monitor and adjust schedules based on variances to output
&middot;    Assist in planning for utilization and capacity
* Maintain organization to ISO operation procedures.
* Complete all job specific required training.
* Perform duties to achieve overall business unit metrics.
* Represent Accellent in a professional and exemplary manner before our suppliers, employees and community at large.
* Comply with all safety regulations, wears appropriate safety equipment as required in each area of the facility.
Purchasing Responsibilities
* Prepares instructions and oversees purchasing systems and procedures; reviews purchase order claims and contracts for conformance to company policy.
* Responsible for tactical procurement in support of the sites production schedules, as well as purchase order releases on blanket agreements negotiated with the Accellent Global Sourcing.
* Prepares management reports as required (Inventory ABC analysis/cost savings program; raw material cost track, etc.); Tracks and updates operating/expense budget.
* Procures all products to necessary dock dates to ensure on-time production starts per production schedule.
* Ensures materials are utilized to minimize excess and obsolescence exposure.
* Works with Global Sourcing to develop cost reduction programs with suppliers to ensure an annual reduction is achieved per facility objectives for both common Accellent materials working with Global sourcing as well as direct spend activities.
* Timely sourcing and cost effective procurement of raw materials, factory/office supplies, as well as outside services.
* Analyzes contractual commitments, customer specifications, design changes, and other data to plan and develop planning and procurement actitivities from conceptual stage through life-cycle of product.
* Responsible for site procurement activities (raw materials, outside services (OSV) as well as expense items).
* Managing and maintaining supplier programs, including the implementation of Kanban Replenishment, Consigned Vendor Managed Inventory (VMI) Programs in areas such as raw materials, tooling, etc.
* Global Sourcing &ndash; actively participates with Accellent Global Sourcing Commodity Management team on Strategic Supplier partnerships and agreements in support of Accellent Strategic Goals.
* Participates with Strategic Sourcing Commodity management on Supplier Relationship Management (SRM quarterly / bi-annual reviews with key suppliers for the site, as well as participates in Global Sourcing SRM meetings as required.
* Supplier Performance Management &ndash; responsible for working with site operations quality and global sourcing on supplier report cards to insure that plans of action are developed and implemented for improving poor performing suppliers.
* In support of facility inventory turn objectives, develops supplier consignment program to ensure necessary materials are on site (in aggregate including WIP and finished goods).
* Responsible for assisting and in development implementation/maintenance of Lean Manufacturing initiatives, including Kanban/Pull systems with vendors and production.
* Leads cross-functional teams chartered to perform Supply Chain related continual improvement and/or problem solving.

Job Requirements :
QUALIFICATIONS:
To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
EDUCATION and/or EXPERIENCE:
Bachelor's degree from four-year College or University; and five plus years related experience and/or training; or equivalent combination of education and experience.
OTHER QUALIFICATIONS:
Excellent PC skills and working knowledge of fully integrated computerized manufacturing and accounting system.      
CPIM / CPM preferred
LANGUAGE SKILLS:
Excellent communication skills. Ability to read, analyzes, and interprets common scientific and technical journals, financial reports, customer prints or other specifications, and legal documents. Ability to respond to common inquiries or complaints from customers, regulatory agencies, or members of the business community. Ability to effectively present information to all levels in the organization and top management.
MATHEMATICAL SKILLS:
Ability to apply concepts such as fractions, percentages, ratios, and proportions to practical situations. In addition, basic knowledge of statistical process control techniques.
REASONING ABILITY:
Ability to define problems, collect data, establish facts, and draw valid conclusions. Ability to interpret an extensive variety of technical instructions in mathematical or diagram form and deal with several abstract and concrete variables.
PHYSICAL DEMANDS:
The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
While performing the duties of this job, the employee is regularly required to sit and talk or hear. The employee is occasionally required to stand; walk; use hands to finger, handle, or feel; reach with hands and arms; and taste or smell. The employee must occasionally lift and/or move up to 25 pounds. Specific vision abilities required by this job include close vision, and ability to adjust focus.
WORK ENVIRONMENT:
The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
While performing the duties of this job, the employee is occasionally exposed to moving mechanical parts. The noise level in the work environment is usually moderate.
Occasional travel will be required.

Career Level :Experienced (Non-Manager)
Education :Bachelor's Degree
% of Travel Required :0-10%
Shift/Hours :First Shift (Day)
]]></description>
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        <expiration_date>2010-03-25</expiration_date>
        <employer><![CDATA[Accellent Inc.]]></employer>
        <location><![CDATA[Orchard Park, NY, 14127, USA]]></location>
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    <job>
        <title><![CDATA[Inspector]]></title>
        <description><![CDATA[


Job Title :Inspector
Job Code :4437
Location :Brooklyn Park MN US 55429
Job Description :
Accellent, Inc. is a fully integrated provider of design, supply chain management and strategic sourcing services to the Medical Device industry. Accellentwww.accellent.com, a recognized market leader, is a fast-growing outsource manufacturing and design solution company specializing in high growth areas such as Cardiology, Endoscopy and Orthopaedics. The top Medical Device companies partner with Accellent to provide innovation, advanced technology, speed to market, low cost labor and strategic sourcing.
We&rsquo;re looking for team players with a can-do attitude to share in our vision and corporate values. Accellent offers competitive salaries; a comprehensive benefits package, and a stimulating work environment.
Currently, we are searching for an Inspector to join our Brooklyn Park, Minnesota facility.
About the Opportunity:
Position Scope/Summary:Performs inspection or test on a wide variety of parts and document results. Indicates inspection status, maintains product traceability and non-conforming material control.
Job Requirements :
Key Result Accountabilities:
* Perform required inspections, measurements and testing of incoming parts, production first piece, in-process and finished product per established criteria. Record results on appropriate documentation.
* Communicate any discrepancies to the person(s) responsible for corrective/preventive action activity.
* Perform various dimensional inspections using specific dies, gages, microscopes, micrometers and other dimensional inspection systems.
* Indicate inspection status of parts with assigned labels and stamps.
* Maintain product identification and traceability.
* Control non-conforming product in accordance with documented procedures and verify timely corrective and preventative action.
* Protect product during handling and storage in the performance of work.
* Monitor factory environmental conditions, record data and identify adverse conditions.
* Assist with distribution and control of process documentation and quality records.
* Assist with control of measuring and test equipment calibration.
* Participate in internal quality audits to verify compliance with documented procedures and specifications, record results and verify audit corrective action.
* Assist with statistical methods of verifying and controlling process capability.
* Provide leadership to production personnel on quality issues.
* Comply with and reinforce the requirements of the Quality Manual and Standard Operating Procedures, ISO 9002, FDA Quality System Regulations and other customer standards.
* Follow Occupational Safety and Health regulations, including laser safety practices.
* Performs job duties with little or no supervision or assistance.Qualifications:
* Experience operating/programming smart scopes with touch laser, vision and probe set x2 is required
* Prior inspection experience 
* Prior medical device or regulated manufacturing environment preferred.
* Prior experience interpreting technical drawings &amp; specifications required.
* Proficient in the use of measuring and test equipment.
* Demonstrate ability to check dimensions, surface relationships, finish material defects and mechanical strength of product following appropriate training
* Prior experience in the use of PC&rsquo;s and Microsoft Office software applications required.
Environmental Working Conditions:
Employee must comply with all safety policies and safe work procedures established by the Company. Job tasks may also involve: Using personal protective equipment such as safety glasses, goggles, gloves, and other equipment as established in Company policies and safe work procedures. Working near cutting &amp; machining fluids, solvents, lubricants and other hazardous chemicals using appropriate safety controls. Carrying, bending, standing, sitting, and repetitive motion may be applicable.
It is impossible to list every requirement for, or responsibility of, any position. Similarly we cannot identify all the skills a position may require since job responsibilities and the Company&rsquo;s needs may change over time. Therefore, the above job description is not comprehensive or exhaustive. The Company reserves the right to adjust, add to or eliminate any aspect of the above description. The Company also retains the right to require all employees to undertake additional or different job responsibilities when necessary to meet business needs.


Due to the expected number of responses, only those most qualified will be contacted. No recruiters please; all unsolicited third-party submissions will be rejected.
Accellent is an Equal Opportunity/Affirmative Action employer and we value diversity in our workforce. As such we provide equal opportunity for all applicants without regard to race, religion, gender, national origin, age, marital status, veteran status, or disability. To learn more about Accellent and our career opportunities, please visit us atwww.accellent.com

Career Level :Experienced (Non-Manager)
Education :High School or equivalent
% of Travel Required :None
Shift/Hours :First Shift (Day)
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        <expiration_date>2010-03-25</expiration_date>
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        <location><![CDATA[Brooklyn Park, MN, 55445, USA]]></location>
    </job>
    <job>
        <title><![CDATA[Senior Maintenance Technician]]></title>
        <description><![CDATA[


Job Title :Senior Maintenance Technician
Job Code :4438
Location :Upland CA US 91786
Job Description :
Accellent, Inc. is a fully integrated provider of design, supply chain management and strategic sourcing services to the Medical Device industry. Accellentwww.accellent.com, a recognized market leader, is a fast-growing outsource manufacturing and design solution company specializing in high growth areas such as Cardiology, Endoscopy and Orthopaedics. The top Medical Device companies partner with Accellent to provide innovation, advanced technology, speed to market, low cost labor and strategic sourcing. 
We&rsquo;re looking for team players with a can-do attitude to share in our vision and corporate values. Accellent offers competitive salaries; a comprehensive benefits package, and a stimulating work environment. 
Currently, we are searching for a to join our facility.
About the Opportunity:



1.0       JOB SUMMARY
1.1       The Senior Maintenance Technician is responsible for the repair and maintenance of all production equipment &amp; machinery.
1.2       The Senior Maintenance Technician is responsible for the repair, maintenance and appearance of the facility.
2.0       PRIMARY RESPONSIBILITIES
2.1       Completes the repairs and maintenance of production equipment and machinery.
2.2       The duties will include trouble shooting equipment &amp; machinery, allocating the proper spare parts to complete the repair and to maintain appropriate maintenance documentation.
2.3       Responds to production and/of facility emergencies to maintain production output.
2.4       Establishes priorities based on available information, work processes and current production commitments.
2.5       Performs preventative maintenance on production equipment and machinery as defined by the set of procedures.
2.6       Follow established procedures to maintain lubrication levels and/or to lubricate and adjust production equipment as necessary.
2.7       Responds to safety emergencies and situations requiring immediate attention.
.
3.0       ADDITIONAL DUTIES AND BACK-UP RESPONSIBILITIES
3.1       Supports production as requested by the production supervisor and/or the maintenance supervisor. Including but not limited to, screw and barrel cleanings, making water hoses, relocating equipment, responding to oil and water spills.
3.2       Maintains and repairs the facility as necessary, including drywall repair and small building projects and plumbing fixture repair.
Job Requirements :

1.0       JOB REQUIREMENTS
1.1       Education: Two-year college degree in general education or technical certifications as specified in 4.2 or equivalent work experience.
1.2       Specialized training in, electricity high &amp; low voltage systems, machine control, programmable controllers and be able to read electrical blue prints and schematics. Specialized training in hydraulics systems and components and be able to read hydraulic blue prints and schematics.
1.3       Experience: Ten years in manufacturing maintenance environment.
1.4       Specialized Knowledge:  Must be proficient in hydraulic systems and components, pneumatic systems and components, electrical systems for high and low voltage applications and plumbing systems and components. Must be proficient with robotics, robot controllers, robot wiring interfaces, instruction manual interpretation and robot trouble shooting &amp; repair.
1.5       Physical Demands: Walking, lifting, bending and stooping, must be able to climb step stools &amp; ladders.
1.6       Strong written and oral communication skills and must be able to communicate with multiple levels of staff throughout the organization.
1.7       Must be available on call responding to after hours/weekend maintenance repairs.
1.8       Ability to manage and prioritize multiple tasks.
1.9       Ability to establish priorities based on available information, work processes, goal/objectives, regulations, and policies.
1.10      Ability to manage process-driven tasks without supervisory reminders.
1.11      Possesses a strong commitment to performing tasks correctly the first time.



Due to the expected number of responses, only those most qualified will be contacted. No recruiters please; all unsolicited third-party submissions will be rejected.

Accellent is an Equal Opportunity/Affirmative Action employer and we value diversity in our workforce. As such we provide equal opportunity for all applicants without regard to race, religion, gender, national origin, age, marital status, veteran status, or disability. To learn more about Accellent and our career opportunities, please visit us atwww.accellent.com
Career Level :Experienced (Non-Manager)
Education :Associate Degree
% of Travel Required :0-10%
Shift/Hours :First Shift (Day)
]]></description>
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        <expiration_date>2010-03-25</expiration_date>
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        <location><![CDATA[Upland, CA, 91786, USA]]></location>
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    <job>
        <title><![CDATA[Lead Quality Assurance 3 (Principal Quality Tech)]]></title>
        <description><![CDATA[


Job Title :Lead Quality Assurance 3 (Principal Quality Tech)
Job Code :4528
Location :Brooklyn Park MN US 55429
Job Requirements :
Qualifications:
* 7 years equivalent experience in similar regulated field; Medical Device experience strongly preferred Accellent (or equivalent) certified mechanical first piece inspector
* Accellent (or equivalent) certified laser first piece inspector
* Accellent (or equivalent) CMM certified operator
* Understanding of quality concepts
* Perform duties to achieve overall business unit metrics
* Ability to interpret complex blueprints
* Ability to calibrate all necessary gages that do not require outside calibration
* Ability to understand and comply with the Quality Systems Regulations (QSR) and ISO 13485:2003 standards
* Experience with MS-Word, Excel, Access, and Power Point for word processing and documentation support
* Must be able to complete multiple prioritized tasks with minimal direct supervision while maintaining focus on preventative activities
* Complete and job-specific required training
* ASQ certifications as CMI, CQIA, CQT, CCT or CQA required or with exception, 10 years experience in Quality and/or Operations (if a combination, 7 minimum in Quality)
* Good teamwork and communication skills to facilitate training and group problem solving
* Ability to lead a cross functional team.



Career Level :Experienced (Non-Manager)
Education :High School or equivalent
% of Travel Required :None
Shift/Hours :First Shift (Day)
]]></description>
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        <expiration_date>2010-03-25</expiration_date>
        <employer><![CDATA[Accellent Inc.]]></employer>
        <location><![CDATA[Brooklyn Park, MN, 55445, USA]]></location>
    </job>
    <job>
        <title><![CDATA[Production Operator]]></title>
        <description><![CDATA[


Job Title :Production Operator
Job Code :4534
Location :Collegeville PA US 19426
Job Description :
Accellent, Inc. is a fully integrated provider of design, supply chain management and strategic sourcing services to the Medical Device industry. Accellentwww.accellent.com, a recognized market leader, is a fast-growing outsource manufacturing and design solution company specializing in high growth areas such as Cardiology, Endoscopy and Orthopaedics. The top Medical Device companies partner with Accellent to provide innovation, advanced technology, speed to market, low cost labor and strategic sourcing.
We&rsquo;re looking for team players with a can-do approach to share in our vision and corporate values. Accellent offers competitive salaries; a comprehensive benefits package, and a stimulating work environment.
Currently, we are searching for a Production Operator for our Collegeville facility.
About the Opportunity:
A. Operate the specific equipment assigned per Department Supervisor/Shift Foreperson/Leadperson per accepted work instructions and acceptable efficiency levels.
B. Regularly perform minor and major set-ups and adjustments of all equipment to which assigned, when appropriate training has been completed. Performance of these tasks may require specific physical capabilities or subject the operator to special environmental situations.
C. Inspect and produce products at an acceptable quality level.
D. Maintain orderly and safe working conditions, and perform all duties in accordance with established good manufacturing practices.
E. Exhibit commitment toward continuous improvement of quality, efficiency, and customer service performance.
F. Perform other assigned tasks as necessary from time to time.
G. In the event of a temporary transfer to another department, this position may require the Operator to perform either &ldquo;A&rdquo; or &ldquo;B&rdquo; operator duties. (See Exhibit &ldquo;A&rdquo;, which lists examples of machines, tooling and inspection equipment required for this position.)

H. Responsible for the accuracy of shop floor production reporting
Job Requirements :
Job Requirements:
A. Competency to the Eighth Grade level in reading comprehension and math computation.
B. Ability to establish good working relationships with all levels of Operations personnel, as well as support departments, such as Maintenance and Inspection.
ENVIRONMENTAL WORKING CONDITIONS:
A. The physical requirements listed in this section include, but are not limited, to the motor/physical abilities and skills required of this position in order to successfully undertake the essential duties and responsibilities of this position. In accordance with the Americans with Disabilities Act (ADA), reasonable accommodations may be made to empower individuals with disabilities to undertake the essential duties and responsibilities of the position.

B. While undertaking the essential duties and responsibilities of the position, the employee must consistently stand (usually throughout an entire work shift), frequently bend at the waste, move to various departments within the plant, listen, speak, and sometimes sit. For most jobs, the employee will also be required to frequently lift and/or move material/items weighing at least 10 lbs. (multiple times per day) and to periodically lift and/or move material/items weighing over 35 lbs. (several times per week). For some jobs, the employee will be required to frequently lift and/or move material/items weighing over 35 lbs. (several times per day). In addition, the employee will be required to work in a facility with varying temperatures in varying work areas, sometimes below 60 degrees or above 100 degrees.
Career Level :Entry Level
Education :High School or equivalent
]]></description>
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        <expiration_date>2010-03-25</expiration_date>
        <employer><![CDATA[Accellent Inc.]]></employer>
        <location><![CDATA[Collegeville, PA, 19426, USA]]></location>
    </job>
    <job>
        <title><![CDATA[Poduction Operator]]></title>
        <description><![CDATA[


Job Title :Poduction Operator
Job Code :4535
Location :Collegeville PA US 19426
Job Description :
sourcing services to the Medical Device industry. Accellentwww.accellent.com, a recognized market leader, is a fast-growing outsource manufacturing and design solution company specializing in high growth areas such as Cardiology, Endoscopy and Orthopaedics. The top Medical Device companies partner with Accellent to provide innovation, advanced technology, speed to market, low cost labor and strategic sourcing.
We&rsquo;re looking for team players with a can-do approach to share in our vision and corporate values. Accellent offers competitive salaries; a comprehensive benefits package, and a stimulating work environment.
Currently, we are searching for a Production Operator for our Collegeville facility.
About the Opportunity:
A. Operate the specific equipment assigned per Department Supervisor/Shift Foreperson/Leadperson per accepted work instructions and acceptable efficiency levels.
B. Regularly perform minor and major set-ups and adjustments of all equipment to which assigned, when appropriate training has been completed. Performance of these tasks may require specific physical capabilities or subject the operator to special environmental situations.
C. Inspect and produce products at an acceptable quality level.
D. Maintain orderly and safe working conditions, and perform all duties in accordance with established good manufacturing practices.
E. Exhibit commitment toward continuous improvement of quality, efficiency, and customer service performance.
F. Perform other assigned tasks as necessary from time to time.
G. In the event of a temporary transfer to another department, this position may require the Operator to perform either &ldquo;A&rdquo; or &ldquo;B&rdquo; operator duties. (See Exhibit &ldquo;A&rdquo;, which lists examples of machines, tooling and inspection equipment required for this position.)
H. Responsible for the accuracy of shop floor production reporting

Job Requirements :
Job Requirements
A. Competency to the Eighth Grade level in reading comprehension and math computation.
B. Ability to establish good working relationships with all levels of Operations personnel, as well as support departments, such as Maintenance and Inspection.
ENVIRONMENTAL WORKING CONDITIONS:
A. The physical requirements listed in this section include, but are not limited, to the motor/physical abilities and skills required of this position in order to successfully undertake the essential duties and responsibilities of this position. In accordance with the Americans with Disabilities Act (ADA), reasonable accommodations may be made to empower individuals with disabilities to undertake the essential duties and responsibilities of the position.
B. While undertaking the essential duties and responsibilities of the position, the employee must consistently stand (usually throughout an entire work shift), frequently bend at the waste, move to various departments within the plant, listen, speak, and sometimes sit. For most jobs, the employee will also be required to frequently lift and/or move material/items weighing at least 10 lbs. (multiple times per day) and to periodically lift and/or move material/items weighing over 35 lbs. (several times per week). For some jobs, the employee will be required to frequently lift and/or move material/items weighing over 35 lbs. (several times per day). In addition, the employee will be required to work in a facility with varying temperatures in varying work areas, sometimes below 60 degrees or above 100 degrees
Career Level :Entry Level
Education :High School or equivalent
]]></description>
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        <expiration_date>2010-03-25</expiration_date>
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        <location><![CDATA[Collegeville, PA, 19426, USA]]></location>
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    <job>
        <title><![CDATA[Production Operator]]></title>
        <description><![CDATA[


Job Title :Production Operator
Job Code :4536
Location :Collegeville PA US 19426
Job Description :
Accellent, Inc. is a fully integrated provider of design, supply chain management and strategic sourcing services to the Medical Device industry. Accellentwww.accellent.com, a recognized market leader, is a fast-growing outsource manufacturing and design solution company specializing in high growth areas such as Cardiology, Endoscopy and Orthopaedics. The top Medical Device companies partner with Accellent to provide innovation, advanced technology, speed to market, low cost labor and strategic sourcing.
We&rsquo;re looking for team players with a can-do approach to share in our vision and corporate values. Accellent offers competitive salaries; a comprehensive benefits package, and a stimulating work environment.
Currently, we are searching for a Production Operator for our Collegeville facility.
About the Opportunity:
A. Operate the specific equipment assigned per Department Supervisor/Shift Foreperson/Leadperson per accepted work instructions and acceptable efficiency levels.
B. Regularly perform minor and major set-ups and adjustments of all equipment to which assigned, when appropriate training has been completed. Performance of these tasks may require specific physical capabilities or subject the operator to special environmental situations.
C. Inspect and produce products at an acceptable quality level.
D. Maintain orderly and safe working conditions, and perform all duties in accordance with established good manufacturing practices.
E. Exhibit commitment toward continuous improvement of quality, efficiency, and customer service performance.
F. Perform other assigned tasks as necessary from time to time.
G. In the event of a temporary transfer to another department, this position may require the Operator to perform either &ldquo;A&rdquo; or &ldquo;B&rdquo; operator duties. (See Exhibit &ldquo;A&rdquo;, which lists examples of machines, tooling and inspection equipment required for this position.)
H. Responsible for the accuracy of shop floor production reporting 


Job Requirements :
Job Requirements
A. Competency to the Eighth Grade level in reading comprehension and math computation.
B. Ability to establish good working relationships with all levels of Operations personnel, as well as support departments, such as Maintenance and Inspection.
ENVIRONMENTAL WORKING CONDITIONS:
A. The physical requirements listed in this section include, but are not limited, to the motor/physical abilities and skills required of this position in order to successfully undertake the essential duties and responsibilities of this position. In accordance with the Americans with Disabilities Act (ADA), reasonable accommodations may be made to empower individuals with disabilities to undertake the essential duties and responsibilities of the position.

B. While undertaking the essential duties and responsibilities of the position, the employee must consistently stand (usually throughout an entire work shift), frequently bend at the waste, move to various departments within the plant, listen, speak, and sometimes sit. For most jobs, the employee will also be required to frequently lift and/or move material/items weighing at least 10 lbs. (multiple times per day) and to periodically lift and/or move material/items weighing over 35 lbs. (several times per week). For some jobs, the employee will be required to frequently lift and/or move material/items weighing over 35 lbs. (several times per day). In addition, the employee will be required to work in a facility with varying temperatures in varying work areas, sometimes below 60 degrees or above 100 degrees
Career Level :Entry Level
Education :High School or equivalent
]]></description>
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        <expiration_date>2010-03-25</expiration_date>
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        <location><![CDATA[Collegeville, PA, 19426, USA]]></location>
    </job>
    <job>
        <title><![CDATA[Cell 14 Machine Operator]]></title>
        <description><![CDATA[


Job Title :Cell 14 Machine Operator
Job Code :4489
Location :Brooklyn Park MN US 55429
Job Description :
Accellent, Inc. is a fully integrated provider of design, supply chain management and strategic sourcing services to the Medical Device industry. Accellentwww.accellent.com, a recognized market leader, is a fast-growing outsource manufacturing and design solution company specializing in high growth areas such as Cardiology, Endoscopy and Orthopaedics. The top Medical Device companies partner with Accellent to provide innovation, advanced technology, speed to market, low cost labor and strategic sourcing.
We&rsquo;re looking for team players with a can-do attitude to share in our vision and corporate values. Accellent offers competitive salaries; a comprehensive benefits package, and a stimulating work environment.
Currently, we are searching for a Cell 14 Machine Operator to join our Brooklyn Park facility.
About the Opportunity:

Position Scope/Summary:
Manufacture components and assemblies for customers as instructed. 
Job Requirements :
Key Result Accountabilities:
* This position includes the following functions: Deburr, chamfer, visual, blowout, sort, poke, drill out, assemble, weld, flow rate check, and tray parts;
* Provide support within the organization as experience and time allow;
* Other duties may be assigned.

Due to the expected number of responses, only those most qualified will be contacted. No recruiters please; all unsolicited third-party submissions will be rejected.
Accellent is an Equal Opportunity/Affirmative Action employer and we value diversity in our workforce. As such we provide equal opportunity for all applicants without regard to race, religion, gender, national origin, age, marital status, veteran status, or disability. To learn more about Accellent and our career opportunities, please visit us atwww.accellent.com
Career Level :Experienced (Non-Manager)
Education :High School or equivalent
% of Travel Required :None
Shift/Hours :Weekend
]]></description>
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            <industry><![CDATA[Health Products & Services]]></industry>
        </industries>
        <expiration_date>2010-03-25</expiration_date>
        <employer><![CDATA[Accellent Inc.]]></employer>
        <location><![CDATA[Brooklyn Park, MN, 55445, USA]]></location>
    </job>
    <job>
        <title><![CDATA[Cell 14 Machine Operator]]></title>
        <description><![CDATA[


Job Title :Cell 14 Machine Operator
Job Code :4491
Location :Brooklyn Park MN US 55429
Job Description :
Accellent, Inc. is a fully integrated provider of design, supply chain management and strategic sourcing services to the Medical Device industry. Accellentwww.accellent.com, a recognized market leader, is a fast-growing outsource manufacturing and design solution company specializing in high growth areas such as Cardiology, Endoscopy and Orthopaedics. The top Medical Device companies partner with Accellent to provide innovation, advanced technology, speed to market, low cost labor and strategic sourcing.
We&rsquo;re looking for team players with a can-do attitude to share in our vision and corporate values. Accellent offers competitive salaries; a comprehensive benefits package, and a stimulating work environment.
Currently, we are searching for a Cell 14 Machine Operator to join our Brooklyn Park facility.
About the Opportunity:

Position Scope/Summary:
Manufacture components and assemblies for customers as instructed. 
Job Requirements :
Key Result Accountabilities:
* This position includes the following functions: Deburr, chamfer, visual, blowout, sort, poke, drill out, assemble, weld, flow rate check, and tray parts;
* Provide support within the organization as experience and time allow;
* Other duties may be assigned.

Due to the expected number of responses, only those most qualified will be contacted. No recruiters please; all unsolicited third-party submissions will be rejected.
Accellent is an Equal Opportunity/Affirmative Action employer and we value diversity in our workforce. As such we provide equal opportunity for all applicants without regard to race, religion, gender, national origin, age, marital status, veteran status, or disability. To learn more about Accellent and our career opportunities, please visit us atwww.accellent.com
Career Level :Experienced (Non-Manager)
Education :High School or equivalent
% of Travel Required :None
Shift/Hours :Second Shift (Afternoon)
]]></description>
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        <industries>
            <industry><![CDATA[Health Products & Services]]></industry>
        </industries>
        <expiration_date>2010-03-25</expiration_date>
        <employer><![CDATA[Accellent Inc.]]></employer>
        <location><![CDATA[Brooklyn Park, MN, 55445, USA]]></location>
    </job>
    <job>
        <title><![CDATA[Customer Operations Manager]]></title>
        <description><![CDATA[


Job Title :Customer Operations Manager
Job Code :4492
Location :Brooklyn Park MN US 55429
Job Description :
Accellent, Inc. is a fully integrated provider of design, supply chain management and strategic sourcing services to the Medical Device industry. Accellentwww.accellent.com, a recognized market leader, is a fast-growing outsource manufacturing and design solution company specializing in high growth areas such as Cardiology, Endoscopy and Orthopaedics. The top Medical Device companies partner with Accellent to provide innovation, advanced technology, speed to market, low cost labor and strategic sourcing.
We&rsquo;re looking for team players with a can-do attitude to share in our vision and corporate values. Accellent offers competitive salaries; a comprehensive benefits package, and a stimulating work environment.
Currently, we are searching for a Customer Operations Manager to join our Brooklyn Park, MN facility.
About the Opportunity:
The Customer Operations Manager will be expected to provide leadership, direction, and solution-oriented thinking to the Customer Operations Team. This team will be technically knowledgeable of the site&rsquo;s products, services and local processes and be able to use that understanding to provide solutions to customer requirements. This position will ensure advocacy for the customer and work closely with Operations, Planning, Engineering, Quality, Technical Solutions, Customer Solutions, and Sales to provide solutions that fulfill our customers&rsquo; needs with speed, accuracy, and exceptional communication. This position will work directly with &ldquo;factory direct&rdquo; customers to service their quoting, order entry, and general service needs. The manager will be a member of the Site Leadership Team and a key partner with the Director of Operations.
Job Requirements :
 Key Result Accountabilities
 Champion the voice of the customer as a member of the Site Leadership Team.
1.   Work with the Site Leadership team to instill customer advocacy within the facility.
2.   Serve as the voice of customer during customer production meetings and interactions with facility personnel
3.   Represent Accellent and the site to the customer and Sales as appropriate in conjunction with customer communication, visits and issue resolution.
 Partner with Customers and Sales organization to meet customer requirements and grow sales
1.   Develop and foster customer relationships by working directly with Factory Direct customers and partnering with Sales and/or CSR&rsquo;s for Strategic and Multi-Site customers
2.   Communicate with customers and other Accellent functions (i.e. Sales, Customer Service, Technical Solutions) to fully understand customer requirements.
3.   Demonstrate responsiveness and leadership in interactions with customers, Sales and CSR&rsquo;s.
4.   Ensure that all customer contractual obligations are implemented and maintained as required
5.   In relation toCorporate/Multi-site Customers:
a.   Provide information and input to Sales/CSR team as needed to grow sales and meet customer requirements.
b.   Provide data for Quarterly Business Reviews and participate in reviews
c.   Provide information and input to the annual and monthly forecasting process, including reconciliation to the monthly facility forecast.
6.   In relation to Factory Direct Customers:
a.   Develop and manage sales goals for Factory Direct Customers
b.   Identify and develop sales growth opportunities for Factory Direct Customers
c.   Coordinate with Customer Operations at other facilities to develop cross-facility sales opportunities.
d.   Prepare and deliver sales presentations and customer visits to support sales efforts.
e.   Develop and administer customer contracts and supply agreements
f.   Responsible for timely and accurate forecasting for Factory Direct Customers
Ensure Customer Operations Processes are executed accurately and within established timeframes
1.   Order Entry/Confirmation
a.   Execute contract review and order entry process for Factory Direct Customers
b.   Support CSR group with information needs for contract review, order entry and confirmation process
c.   Work with Site Planning and Operations to establish and communicate standard product lead times.
2.   Change Order and expedite requests
a.   Work with facility personnel (Planning, Operations and Purchasing) to meet customer requests for items such as order expedites and change requests
b.   Communicate and monitor plans for expedite requests and recovery plans to Sales, CSR&rsquo;s, Customers and Operations as required to meet commitments
3.   Quoting
a.   Execute quotation process for Repeat and Standard Products
b.   Support Technical Solutions group for New Product quotations
c.   Liaison with TS on New Product quotations and new cost model development and deployment
4.   Configuration Engineering
a.   Execute configuring items/BOMs/Routings to support CS and Operations.
b.   Manage configuration changes as required by customers, Customer Operations or Operations.
c.   Provide information and input to the quoting process
5.   Align and maintain local processes and procedures with the Global Customer Operations processes and procedures.
6.   Work with the Customer Operations Team members to identify process improvement opportunities to better serve the customers
Lead and manage Site Customer Operations Team
1.   Ensure that Customer Operations Team has the training and knowledge to utilize Oracle (or designated system) for quoting, order entry, and configuration engineering
2.   Provide leadership to Customer Operations Team members including guidance, prioritization, training and support for daily activities. 
3.   Drive team performance towards key metric targets, including Order Acknowledgement Cycle Time, Quote Cycle Time
4.   Coordinate and maintain Customer Operations back up system within the team
5.   Ensure team adherence to all ISO Certification requirements; participate in Customer Service related audits as required
Education/Experience:
* 
4 year Bachelor&rsquo;s Degree or equivalent experience;
* 
3+ years experience in medical device or related field

Qualifications
To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed are
 representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with 
disabilities to perform the essential functions.


Due to the expected number of responses, only those most qualified will be contacted. No recruiters please; all unsolicited third-party submissions will be rejected.

Accellent is an Equal Opportunity/Affirmative Action employer and we value diversity in our workforce. As such we provide equal opportunity for all applicants without regard to race, religion, gender, national origin, age, marital status, veteran status, or disability. To learn more about Accellent and our career opportunities, please visit us atwww.accellent.com
Career Level :Manager (Manager/Supervisor of Staff)
Education :Bachelor's Degree
% of Travel Required :10-20%
Shift/Hours :First Shift (Day)
]]></description>
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        <expiration_date>2010-03-25</expiration_date>
        <employer><![CDATA[Accellent Inc.]]></employer>
        <location><![CDATA[Brooklyn Park, MN, 55445, USA]]></location>
    </job>
    <job>
        <title><![CDATA[VMC Machine Operator]]></title>
        <description><![CDATA[


Job Title :VMC Machine Operator
Job Code :4494
Location :Brooklyn Park MN US 55429
Job Description :
Accellent, Inc. is a fully integrated provider of design, supply chain management and strategic sourcing services to the Medical Device industry. Accellentwww.accellent.com, a recognized market leader, is a fast-growing outsource manufacturing and design solution company specializing in high growth areas such as Cardiology, Endoscopy and Orthopaedics. The top Medical Device companies partner with Accellent to provide innovation, advanced technology, speed to market, low cost labor and strategic sourcing.
We&rsquo;re looking for team players with a can-do attitude to share in our vision and corporate values. Accellent offers competitive salaries; a comprehensive benefits package, and a stimulating work environment.
Currently, we are searching for a VMC Machine Operator to join our Brooklyn Park facility.
About the Opportunity:
Position Scope/Summary:
Program, setup, troubleshoot, and operate Multi-axis Milling Centers in a production environment, including the following: Read part prints and understand dimensions; Set-up, maintain, and operate CNC machining centers; Troubleshoot and document set-ups and adjust programs; Adjust offsets to maintain dimensional integrity; Produce high quality components and insure proper inspection to meet quality standards; Use inspection equipment to verify parts meet print specifications; Maintain clean/organized working area; Follow company policies and rules; Provide support within the organization as experience and time allow; Other duties may be assigned.
Job Requirements :
Key Result Accountabilities:
* Must be able to work in an atmosphere with little supervision;
* Must be able to communicate with inspection personnel as well as other operators;
* Must have advanced shop math skills;
* Must be able to reason cause and effect on parts.Environmental Working Conditions:
Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
Qualifications:

* Must be able to program, setup, and operate 4-Axis CNC Milling Centers;
* Must understand programs on all types of CNC machines;
* Must know Geometric Dimensioning and Tolerancing;
* Must have knowledge of typical inspection equipment;
* Must be able to read blue prints and use inspection equipment necessary to do the job;
* Ability to generate part progrmas using CAM software preferred;
* Ability to design and build special tooling required for jobs preferred.Education:
* Technical College Degree in Machining or equivalent work experience preferred;
* Five plus years of experience in CNC Milling preferred.
Due to the expected number of responses, only those most qualified will be contacted. No recruiters please; all unsolicited third-party submissions will be rejected.
Accellent is an Equal Opportunity/Affirmative Action employer and we value diversity in our workforce. As such we provide equal opportunity for all applicants without regard to race, religion, gender, national origin, age, marital status, veteran status, or disability. To learn more about Accellent and our career opportunities, please visit us atwww.accellent.com
Career Level :Experienced (Non-Manager)
Education :High School or equivalent
% of Travel Required :None
Shift/Hours :First Shift (Day)
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        <industries>
            <industry><![CDATA[Health Products & Services]]></industry>
        </industries>
        <expiration_date>2010-03-25</expiration_date>
        <employer><![CDATA[Accellent Inc.]]></employer>
        <location><![CDATA[Brooklyn Park, MN, 55445, USA]]></location>
    </job>
    <job>
        <title><![CDATA[Machine Operator (Electro-Polish 3rd shift)]]></title>
        <description><![CDATA[


Job Title :Machine Operator (Electro-Polish 3rd shift)
Job Code :4496
Location :Wheeling Illinois US
Job Description :
Accellent, Inc. is a fully integrated provider of design, supply chain management and strategic sourcing services to the Medical Device industry. Accellentwww.accellent.com, a recognized market leader, is a fast-growing outsource manufacturing and design solution company specializing in high growth areas such as Cardiology, Endoscopy and Orthopaedics. The top Medical Device companies partner with Accellent to provide innovation, advanced technology, speed to market, low cost labor and strategic sourcing. 
We&rsquo;re looking for team players with a can-do attitude to share in our vision and corporate values. Accellent offers competitive salaries; a comprehensive benefits package, and a stimulating work environment. 

 Key Result Accountabilities
&middot;    Set-up and/or operate basic jobs with assistance (i.e. 1 tool) on some of the equipment within a cell or department using set-up sheets, blueprints and/or operation sheets per customer requirements.
&middot;    Inspection of work accurately with assistance from co-workers.
&middot;    Performs basic set-up and operation manual machines when required.
&middot;    Basic adjustments to maintain dimensional integrity.
&middot;    Uses basic shop math to assist in all aspects of the job
&middot;    Complies with work rules including those pertaining to safety, health, quality system, and Accellent Quality Management System.
&middot;    Verify the revision level for the current operation (operation sheets, blue prints)
&middot;    Verify PC count and all applicable documentation for completion of previous operations.
&middot;    To complete all applicable documentation for the current operation (i.e. Shop traveler sign off and first pc, inspection record sheet, and/or AQL and NCMR)
&middot;    Participates on various teams to achieve performance metrics.
&middot;    Maintains machine maintenances and log.


Job Requirements :
Some previous related experience strongly preferred, along with previous experience working in a manufacturing environment is preferred. The ability to speak, read and write English is required, along with computer and/or related application software experience. May be required to stand and/or walk regularly and exert some physical effort typically not to exceed 25 lbs. This position is located in a factory environment with a strong emphasis on safety, quality and training.

Due to the expected number of responses, only those most qualified will be contacted. No recruiters please; all unsolicited third-party submissions will be rejected.

 Qualifications
&middot;    This position requires a high school diploma or GED or equivalent experience required.
&middot;    Attended Trade school or 0-2 yrs shop experience.
&middot;    Ability to use basic inspection equipment and techniques.
&middot;    Ability to read basic blueprints and/or operation sheets.
&middot;    Basic shop math skills.
&middot;    Must pass novice on the operator certification test.
&middot;    Maintain organization to ISO operation procedures.
&middot;    Complete all job specific required training.
&middot;    Perform duties to achieve overall business unit metrics.
&middot;    Comply with all safety regulations, wears appropriate safety equipment as required in each area of the facility.

Accellent is an Equal Opportunity/Affirmative Action employer and we value diversity in our workforce. As such we provide equal opportunity for all applicants without regard to race, religion, gender, national origin, age, marital status, veteran status, or disability. To learn more about Accellent and our career opportunities, please visit us atwww.accellent.com
Career Level :Entry Level
Education :High School or equivalent
% of Travel Required :0-10%
Shift/Hours :Third Shift (Night)
]]></description>
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            <industry><![CDATA[Health Products & Services]]></industry>
        </industries>
        <expiration_date>2010-03-25</expiration_date>
        <employer><![CDATA[Accellent Inc.]]></employer>
        <location><![CDATA[Wheeling, IL, 60070, USA]]></location>
    </job>
    <job>
        <title><![CDATA[Material Handler III]]></title>
        <description><![CDATA[


Job Title :Material Handler III
Job Code :4499
Location :Eden NY US 14057
Job Description :


Job Title: 
Material Handler and Receiving 
Department: 
Maintenance
Reports To: 
Purchasing Leader 
Location: 
OrchardPark
FLSA Status: 
Non-exempt 
Facility: 
Endo (Cardio, Endo, Ortho)
Classification: 
Hourly (factory) 
Date: 

Education: 
High School Graduate or GED
Organizational Relationships: 
Internally  - All levels of Employees
Externally - Outside contractors, suppliers.
Position Scope / Summary
The Material Handler is responsible for supplying stock, packing and tooling to the primary machines to ensure the smooth and continuous operation of machining at the facility.
Key Result Accountabilities
1.   Follow the daily schedule of duties assigned by your supervisor. Maintain accurate daily work log.
2.   Cone bar stock.
3.   Supply bar stock to primary machines as requested by operators.
4.   Receive material into Oracle database.
5.   Release bar stock from receiving warehouse.
6.   Employ the strategies of 5S in order to maintain an efficient work area; clean and well ordered.
7.   Responsible for daily bar stock and tooling cycle counts.
8.   Receive and maintain returnable supplier packing.
9.   Move Finish Goods to shipping warehouse.
10. Recover and maintain bar stock from machines.
11. Other duties as necessary.
Environmental Working Conditions
&middot;    The physical demands described herein are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform essential functions.
&middot;    Ability to spend time using your hands to handle, control, or feel objects, tools or controls.
&middot;    Will spend extended periods of time standing and walking throughout the shop.
&middot;    Able to sit, stoop, kneel, bend, crouch, bend and twist.
&middot;    Ability to lift 1pound up to 60 lbs.



Job Requirements :
Qualifications
1.   Able to use the computer to input and access data.
2.   Able to follow instructions, both written and verbal, with little supervision on daily repetitive tasks.
3.   Effectively communicate with all levels of employees.
4.   Good organizational skills; able to manage several priorities as assigned by a supervisor.




Career Level :Experienced (Non-Manager)
Education :Certification
% of Travel Required :0-10%
Shift/Hours :First Shift (Day)
]]></description>
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            <industry><![CDATA[Health Products & Services]]></industry>
        </industries>
        <expiration_date>2010-03-25</expiration_date>
        <employer><![CDATA[Accellent Inc.]]></employer>
        <location><![CDATA[Eden, NY, 14057, USA]]></location>
    </job>
    <job>
        <title><![CDATA[Supply Chain Manager]]></title>
        <description><![CDATA[


Job Title :Supply Chain Manager
Job Code :4504
Location :Brooklyn Park MN US 55429
Job Description :
Accellent, Inc. is a fully integrated provider of design, supply chain management and strategic sourcing services to the Medical Device industry. Accellentwww.accellent.com, a recognized market leader, is a fast-growing outsource manufacturing and design solution company specializing in high growth areas such as Cardiology, Endoscopy and Orthopaedics. The top Medical Device companies partner with Accellent to provide innovation, advanced technology, speed to market, low cost labor and strategic sourcing. 
We&rsquo;re looking for team players with a can-do attitude to share in our vision and corporate values. Accellent offers competitive salaries; a comprehensive benefits package, and a stimulating work environment. 
Currently, we are searching for a Supply Chain Manager to join our facility.
About the Opportunity:
The Supply Chain Manager is a member of the facility leadership team with functional responsibility for S&amp;OP (Master Planning),capacity planning, materials management/flow, tactical procurement, production scheduling, inventory control, warehousing and logistics. This individual will help to drive key critical performance drivers (CPDs) such as fill rate, on-time delivery, back order, quality lot acceptance and financial metrics such as inventory turns, standard cost variances, absorption and budget. The person will represent Accellent in a professional and exemplary manner before our suppliers, employees and community at large.
Job Requirements :

POSITION RESPONSIBILITY
* Drive the sites Sales and Operations planning process to develop mid to long range operating plans, which drives the demand and capacity planning function which the incumbent is responsible for. Assist in capital expenditure (CAPEX) justification and approval working with peers within operations
* Works with Accellent Customers and Customer Operations Management (COM) in the establishment and management of Kanban and Consigned Finished Goods Inventory programs, and insures that proper Demand and Capacity Plans are implemented to support these requirements at their site
* Management responsibilities for demand and capacity planning, production scheduling and execution, inventory, purchasing and supplier service level management Responsible for integrating production schedules with business planning and forecasting. Balance of ERP/MRP capability with pull / lean methodology. Must be a driver of lean manufacturing and a lean culture.
* Responsible for inventory accuracy (raw, outside services , WIP and finished goods) and cycle count programs. Working closely with finance, maintain appropriate inventory levels to meet customer demand while meeting Accellent financial objectives.
* Manage and support outside service providers to meet Accellent business requirements.
* Participate in daily lean huddles as well as on project teams as required.
* Responsible for the planning systems for all raw materials, internal operations, subcontract operations and outside supporting services.
* Responsible for production order execution and working with operations to insure that our on time delivery , cycle time and fill rate goals are met.
* Responsible for site procurement activities (raw materials, outside services (OSV) as well as expense items).
* Managing and maintaining supplier programs, including the implementation of Kanban Replenishment , Consigned Vendor Managed Inventory (VMI) Programs in areas such as raw materials, tooling, etc.
* Global Sourcing &ndash; actively participates with Accellent Global Sourcing Commodity Management team on Strategic Supplier partnerships and agreements in support of Accellent Strategic Goals.
* Participates with Strategic Sourcing Commodity management on Supplier Relationship Management (Quarterly Business Reviews (QBR) with key suppliers for the site, as well as participates in Global Sourcing supplier relationship management (SRM) meetings as required.
* Supplier Performance Management &ndash; responsible for working with site operations quality and global sourcing on supplier report cards to insure that plans of action are developed and implemented for improving poor performing suppliers.
* Weekly / Monthly reporting on Key Performance Indicators (KPI&rsquo;s) for the Supply Chain function for their site.
* Participates in Global Supply Chain meetings within Accellent to foster cross site teamwork and development of our Global Supply Chain capabilities.
* Explore new technologies and processes, to reduce non-value added procurement and planning activities.
* Responsible for training and career development of all site Supply Chain employees.
* Manage department to meet all quality and financial system requirements.
* Participate in the contract review of all new products / processes.
ORGANIZATIONAL RELATIONSHIPS
Internally  - Customer Operations , Operations, Quality, Global Sourcing, Proj Mgt/Quoting and Engineering departments. Member of facility leadership team
Externally  - Customers, outside suppliers and other Accellent facilities
Education, Years of Experience, and Skill Requirements
* To perform this job successfully, an individual must have the necessary education and work experience. Recognizing that education and work experience are relative to the experience, environments, the review of an individual&rsquo;s accomplishments is critical to filling the position successfully.
* Prior Supply Chain leadership role is a must.
* 4 year degree. MBA a plus.
* Minimum of 5 - 8 years experience in increasing levels of responsibility within Materials and Purchasing Management. 3-5 years of management or supervision experience.
* Prior Demand and Capacity Planning experience required, must have a prior hands on experience within Masterscheduling, Capacity Planning and production planning
* Prior Purchasing and experience required
* CPIM / CPM certification a plus.
* Experienced Six Sigma Black Belt / Green Belt, prior experience working in a lean manufacturing environment
* Experience with ERP/MRP systems (Oracle, SAP, JD Edwards)
* Strong verbal and written communication skills, analytical skills, statistical and mathematical abilities and interpersonal skills.
* Advanced Computer skills using Microsoft Word, Excel, Powerpoint and Project
* Excellent communication skills, strong organizational skills and a tremendous sense of getting things done. Self-motivation and problem solving skills are extremely important in this position. 
JOB SPECIFIC TRAINING REQUIREMENTS
It is impossible to list every requirement for, or responsibility of, any position. Similarly we cannot identify all the skills a position may require since job responsibilities and the Company&rsquo;s needs may change over time. Therefore, the above job description is not comprehensive or exhaustive.  The Company reserves the right to adjust, add to or eliminate any aspect of the above description. The Company also retains the right to require all employees to undertake additional or different job responsibilities when necessary to meet business needs.

Due to the expected number of responses, only those most qualified will be contacted. No recruiters please; all unsolicited third-party submissions will be rejected.

Accellent is an Equal Opportunity/Affirmative Action employer and we value diversity in our workforce. As such we provide equal opportunity for all applicants without regard to race, religion, gender, national origin, age, marital status, veteran status, or disability. To learn more about Accellent and our career opportunities, please visit us atwww.accellent.com
Career Level :Manager (Manager/Supervisor of Staff)
Education :Bachelor's Degree
% of Travel Required :10-20%
Shift/Hours :First Shift (Day)
]]></description>
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            <industry><![CDATA[Health Products & Services]]></industry>
        </industries>
        <expiration_date>2010-03-25</expiration_date>
        <employer><![CDATA[Accellent Inc.]]></employer>
        <location><![CDATA[Brooklyn Park, MN, 55445, USA]]></location>
    </job>
    <job>
        <title><![CDATA[Swiss Machinist]]></title>
        <description><![CDATA[


Job Title :Swiss Machinist
Job Code :4505
Location :Brimfield MA US 01010
Job Description :
Accellent, Inc. is a fully integrated provider of design, supply chain management and strategic sourcing services to the Medical Device industry.

Accellent (www.accellent.com), a recognized market leader, is a fast-growing outsource manufacturing and design solution company specializing in high growth areas such as Cardiology, Endoscopy and Orthopaedics. The top Medical Device companies partner with Accellent to provide innovation, advanced technology, speed to market, low cost labor and strategic sourcing. 
We&rsquo;re looking for team players with a can-do attitude to share in our vision and corporate values. Accellent offers competitive salaries; a comprehensive benefits package, and a stimulating work environment. 
Currently, we are searching for a to join our Brimfield, MA facility.
About the Opportunity:
&middot;    Set-up and operate all jobs on all Swiss (Star 20 and 32, Citizen L20) equipment within a cell accordance to set-up sheets,  blueprints and operation sheets per customer requirements.
&middot;    Set-up and operate all jobs on manual machines when required.
  Able to interface with fanuc controls.
&middot;    Troubleshoot set-ups and adjust programs when necessary, document changes per procedure.
&middot;    Writes programs for Santec machines if applicable.
&middot;    Makes adjustments of offsets to maintain dimensional integrity.
&middot;    Inspect all dimensions without assistance to meet quality standards
&middot;    Build tooling / fixturing when necessary.
&middot;    First piece inspection for machining operations.
&middot;    Verify the revision level for the current operation (Programs, operation sheets, blue prints)
&middot;    Verify Pc. Count and all applicable documentation for completion of previous operations.
&middot;    To complete all applicable documentation for the current operation (i.e. Shop traveler sign off and first pc, inspection record sheet, and/or AQL and NCMR)
&middot;    Submit requests to update travelers with changes to routings and runtimes.
&middot;    Documentation of new or revised set-ups on set-up sheets.
&middot;    Maintains machine maintenances and log.
&middot;    Train lesser grade individuals on all aspects of Swiss machining and proper inspection methods.
&middot;    Complies with work rules including those pertaining to safety, health, quality system, and Accellent Quality Management System.
Participates on various teams to achieve performance metrics.


Job Requirements :

&middot;    This position requires a high school diploma or GED.
&middot;    5+ years experience
&middot;    Ability to understand all blueprints
&middot;    Able to understand programs on all types of CNC machines
&middot;    Knowledge of all typical inspection equipment.
&middot;    Advanced shop math skills
&middot;    Able to understand geometric tolerances
&middot;    Ability to use trigonometry on blueprints
Ability to program or learn to program
&middot;    Maintain organization to ISO operation procedures.
&middot;    Complete all job specific required training.
&middot;    Perform duties to achieve overall business unit metrics.
Comply to all safety regulations, wears appropriate safety equipment as required in each area of the facility

Due to the expected number of responses, only those most qualified will be contacted. No recruiters please; all unsolicited third-party submissions will be rejected.

Accellent is an Equal Opportunity/Affirmative Action employer and we value diversity in our workforce. As such we provide equal opportunity for all applicants without regard to race, religion, gender, national origin, age, marital status, veteran status, or disability. To learn more about Accellent and our career opportunities, please visit us atwww.accellent.com
Career Level :Experienced (Non-Manager)
Education :High School or equivalent
% of Travel Required :0-10%
Shift/Hours :First Shift (Day)
]]></description>
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            <industry><![CDATA[Health Products & Services]]></industry>
        </industries>
        <expiration_date>2010-03-25</expiration_date>
        <employer><![CDATA[Accellent Inc.]]></employer>
        <location><![CDATA[Brimfield, MA, 01010, USA]]></location>
    </job>
    <job>
        <title><![CDATA[Technical Solutions Representative]]></title>
        <description><![CDATA[


Job Title :Technical Solutions Representative
Job Code :4513
Location :Juarez Chih MX 32420
Job Description :
Position Scope/Summary
In their area of expertise/responsibility, the TSR is responsible for the analysis of quote requests and the generation/coordination of accurate manufacturing approaches, costs &amp; lead-time estimates, within the targeted quote time-frame. In order to fully understand the Customers&rsquo; quoting requirements and subsequently provide a timely and accurate quote, this role will proactively engage with Sales, the Customer (where appropriate), Customer Solutions, Technical Directors, Technical Solutions Manager, other TSRs, Engineering, Operations and Quality.
Key Result Accountabilities
1.   Read and interpret customer supplied quote requirements, including all specifications, design prints, quantity/lead-time needs to determine manufacturing feasibility and optimal process approach. 
2.   Will correspond with Customer Solutions, Sales and the Customer (where appropriat