• ALKU
  • Vacaville, CA
  • Miscellaneous
  • Full-Time
  • 5178 Fry Rd

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Project Description:

Our client is in the process of transitioning their manufacturing facility to a new location. During the transition the client is taking the opportunity to update some of their older technical files to make sure they are in compliance.

Medical Device Project Manager

This consultant will be responsible for various tasks that involve getting the site up and running. They will be handling all necessary updates to regulatory documents from a regulatory compliance standpoint. This consultant will have ideally worked on a manufacturing site transfer before in orderhit the ground running. This person will not be responsible for any Regulatory Submissions.

Medical Device Risk Management SME Required Skills: Supplier Quality Engineer

5+ Years Experience Regulatory Compliance for Medical Device Manufacturing

Gap Assessment Experience

Medical Device Sr. Program Manager

Design Transfer Experience

Medical Device Program Manager Medical Device Project Manager Medical Device Risk Management SME Supplier Quality Engineer Medical Device Sr. Program Manager Medical Device Program Manager Medical Device Project Manager

* The salary listed in the header is an estimate based on salary data for similar jobs in the same area. Salary or compensation data found in the job description is accurate.

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