Medical Device Clinical QA Specialist- (EU Regulations)
Medical Device Clinical QA Specialist– (EU Regulations)
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.
- Medical device 5-7+ years
- 5-7+ years of regulatory
- Clinical Quality
- New EU Regulations
Job Type: Contract