Vana Bhagavan
4.6 Yrs | Medical Devices |Quality & Regulatory Affairs | Labeling | UDI | PIM | ISO 13485 | EU MDR | FDA |
- Role
- Lead Associate-regulatory Affairs at Genpact
- Location
- Srikakulam, AP, IN
- LinkedIn followers
- 500 followers
About Vana Bhagavan
Medical Device Professional with 4.6 years of experience as Quality and Regulatory affairs specialist. Expertise in Process V&V, DHF Remediation Quality Checks, Change management, Labeling, Proofreading, and Country UDI data Management in PIM UI. Skilled in Windchill, Agile, Adaptive, SAP EVEREST/Tahiti. Well-versed in ISO 13485:2016, EU MDR 2017/745, and FDA 21 CFR 820.
Experience
Lead Associate-regulatory Affairs
Jan 2025 — Present · Bengaluru, IN
LS & H Domain | Product Information Management (PIM)| MDM | SAP | Labelling | IFU | Product Life Cycle Management
Education
Aditya Institute of Technology and Management,Tekkali
B.Tech
2016 — 2020
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