A client of ours is looking to bring on a Senior Regulatory Affairs Specialist to work on cutting edge Class II and Class III medical devices.
Essential Requirements
- 4+ years of Regulatory Affairs Experience in the Medical Device space
- Experience as lead author on a major FDA submission (510k or PMA preferred)
- B.S in Biology, Chemistry, Biomedical Engineering or a similar field
- U.S Ad / Promo experience
- International regulatory experience (LATAM, EU, APAC, Health Canada)
- Preference given to candidates based in Massachusetts, but candidates can be based anywhere in the United States; this role is remote.
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Senior Regulatory Affairs Specialist
A client of ours is looking to bring on a Senior Regulatory Affairs Specialist to work on cutting edge Class II and Class III medical devices. Regulatory Affairs Experience in the Medical Device space. International regulatory experience (LATAM, EU, APAC, Health Canada). ...
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