Principal Regulatory Affairs Specialist - Acton
1 month ago

Job summary
The Principal Regulatory Affairs Specialist will lead strategic regulatory initiatives and projects as subject matter expert which support both domestic and international market authorization and compliance including working with Marketing, New Product Development, Manufacturing and Engineering.Responsibilities
- Lead strategic regulatory initiatives and projects to ensure regulatory approval and compliance of medical devices in both domestic and international markets.
- Provide regulatory affairs expertise for aspects of product development, product manufacturing, and/or clinical studies including pre-market, post-market physician initiated studies.
Job description
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