Priyanshu Sharma
Medical Device Reporting | US FDA | Regulatory Affairs | Post Market Surveillance | Healthcare
- Role
- Senior Associate at Genpact
- Location
- Gurugram, HR, IN
- LinkedIn followers
- 500 followers
Experience
Senior Associate
Jan 2026 — Present · Gurugram, IN
Manage and submit required regulatory reports to the U.S. FDA, including Medical Device Reports (MDRs), in a timely and accurate manner.Ensure strict adherence to the FDA Quality System Regulation (21 CFR Part 820) by overseeing quality events, CAPA activities, and compliance audits.
Education
Meerut Institute of Engineering and Technology(MIET)
Bachelor of Technology - BTech, Biotechnology
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