Medical Device Jobs

The following is a Brief selection of the active Medical Device job openings that Vohden Associates is currently recruiting for. We receive new position requirements from our client companies on a daily basis so check back often.  Please Contact Us directly for more information on these jobs and other positions that might not be posted.
 

Title:  Director of Quality and Product Development - Plastic Films - Medical

Location:  California (Los Angeles area)

Requirements for the Director of Quality position:

• Bachelors Degree in a Scientific discipline

• Minimum of 5 years experience in the manufacturing of plastic film

• Minimum of 5 years experience in quality assurance for film

• ISO 9001 and Total Quality Management expertise

• Knowledge of regulations regarding films in the Medical industry

• Fluent in Six Sigma

Job Description Highlights:

Plan, direct, and administer Quality and Product Development activities.             Direct process improvement initiatives, technical support, and projects.      Participate in Senior Management Team:  Budgeting, P&L, and Policies.   Direct all Quality activities.

Comments:

We are looking for a hands-on candidate with a Strong Quality and Six Sigma background.  Outstanding company with a record of successes.  Very competitive compensation package.  Medical device experience a plus.

Apply for this position

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Title:  Supplier Quality Specialist

Location:  Pennsylvania (Eastern)

Requirements for the Supplier Quality Specialist:

• AT LEAST a Bachelors Degree in a Scientific field.

• Minimum 5 years experience in Pharmaceutical or Medical Device

• Solid work history. 

Job Description Highlights:

Direct and manage all quality programs with respect to Supplier Qualification, Material Certifications and Qualifications for multiple manufacturing locations.  Approve new suppliers for components, finished goods, and raw materials.     Review and advise for 510(k) FDA submittals.

Comments:

Outstanding company and benefits.  Career progression opportunities.

Apply for this position

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Title:  Regulatory Affairs Specialist - Medical Device

Location:  New Jersey  (Southern or Mid-State)

Requirements for the Regulatory Affairs Specialist:

• MUST HAVE a Masters Degree or higher in a medically related discipline

•  Minimum 6 years experience in an FDA regulated environment in a Regulatory role

• Experience with CAPA

• Extensive experience and knowledge of FDA regulations and 510(k) submittals

• Good communication and leadership skills

Job Description Highlights:

The successful candidate will direct and coordinate documents and submissions to appropriate FDA and other agencies. Track and monitor control systems. Keep up to date procedures and regulations. Prepare and update product registrations, listings, licenses, and certificates. Lead CAPA investigations.

Comments:
Key is Masters Degree, 510(k) submission experience, and CAPA experience.

Apply for this position

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Title:  Controls Engineer

Location:  Pennsylvania (Eastern)

Requirements for the Controls Engineer position:

• BSEE Minimum 4 years experience.

• Must have a background in PLC controls for automation.

• Experience in Wonderware, Allen Bradley, and Panel View Systems.

Job Duties

Typical Controls Engineering position: Developing new automated control systems for automated manufacturing. Project management duties. Medical device experience a plus.

Comments:
Outstanding company with excellent benefits!  Company fosters career progression through promotion.

Apply for this position