Job Description
Regulatory Affa irs Specialist
This is an exciting opportunity to join an industry leading biotech company leading. The Regulatory Affairs Specialist will be responsible for supporting In Vitro Diagnostic Regulation (IVDR) transition activities that impact products currently CE Marked under the IVD Directive. This includes preparing revision of technical files as needed, updating labeling to comply with IVDR requirements, tracking regional notifications, etc.
Responsibilities:
Requirements and Desired Experience:
Compensation: $40 - $45 per hour
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