PMA Contractor- Regulatory affairs

PMA Contractor- Regulatory affairs Remote role – 12 months Shift: 8‑5 day shift (M‑F), flexibility in schedule if needed. Candidate can be remote in the US, West Coast preferred for PST time zone. Job Description

Regulatory affairs role – at least 5 years direct relevant PMA experience. Hands‑on experience authoring, drafting and submitting all modules for a medical device (IVD) PMA; experience with tissues is desired. Demonstrated experience working cross‑functionally to gather information and collaborate on submission documents. Additional Job Details

Hands‑on experience authoring, drafting and submitting all modules for a medical device (In Vitro Diagnostics) PMA; experience with tissues is desired.

#J-18808-Ljbffr