Medical Device Clinical QA Specialist- (EU Regulations)

Boston, MA

Job ID: 125198 Industry: Med

 

Medical Device Clinical QA Specialist– (EU Regulations)

Environment:

Our client is in the medical device company, that manufactures Class 1, 2 & 3 Medical Devices. They are currently looking to update some of their technical files per the new EU Regulations.

Principle Duties and Responsibilities:

The client is looking for a Clinical Quality Assurance Specialist with knowledge of the new EU Regulations. This person will be responsible for doing a GAP Analysis of their current Regulatory and Clinical files. Looking for someone who has experience with QA Regulatory Compliance and ideally a background in specifically Clinical Trials.

 

Required:
  • Medical device 5-7+ years
  • 5-7+ years of regulatory
  • Clinical Quality
  • New EU Regulations

Job Type: Contract  

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