Our client, a leading medical device company, is currently seeking an accomplished Regulatory Affairs Manager to join the team. Here is an overview of the role:
1) Advise various company personnel on all regulatory activities associated with FDA QSR, FDA Corrections and Removals, FDA Medical Device Reporting, ISO standards, EU MDD, Australian WAND, Japan PAL, Canadian Food and Drugs Act and ...
Exposure to compliance requirements (SOPs, GCP and ICH) Cross-functional experience with Legal, Marketing, Clinical Development, Commercial and Regulatory...
May 3 - United States
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