??'?? ?????? | ???? ????????? – ??????? & ?????????? ???????Mumbai | Regulated Life-Sciences Manufacturing | USFDA & WHO-PQ approvedBGR is retained by a globally respected life-sciences manufacturer (established for over three decades) with exports to the USA, Europe, Japan, and China, to identify their next Vice President – Quality & Regulatory Affairs.??? ????Second-in-command of the Quality & Regulatory function. Reporting to the Head of Quality & Regulatory, you will own day-to-day quality and regulatory operations across manufacturing, QC, QA, documentation, regulatory submissions, and supplier quality — and be groomed for succession.???? ???'?? ???
- Execute and strengthen the QMS under EN ISO 13485, ISO 9001, USFDA 21 CFR 820, and WHO-PQ
- Drive shop-floor QC across the full manufacturing cycle
- Lead internal audits and front-line responses to USFDA, notified body, WHO, and customer audits
- Own KPIs — batch rejection, RFT, deviation & CAPA closure, complaints, non-conformances
- Drive regulatory submissions, product registrations, variations, renewals, and change notifications across USA, Europe, Japan, China, and RoW
- Monitor regulatory intelligence; assess impact of evolving regulations on product compliance
- Ensure compliance with labelling, IFU, post-market surveillance,



and vigilance / adverse-event reporting
- Partner with R&D; on Design Control, DHF/DMR, ISO 14971 risk management, and IQ/OQ/PQ validation
- Run the supplier qualification, audit, and scorecard programme
- Own end-to-end customer complaint handling and CAPA closure
- Lead, coach, and build depth in a 20+ member QA / QC / RA / Documentation team???? ??'?? ??????? ???
- 12–15 years in Quality & Regulatory Affairs within a USFDA / WHO-PQ approved manufacturing environment
- Biologicals, biotech, pharma, or regulated life-sciences manufacturing background preferred
- Proven experience as a lead responder in regulatory and customer audits
- Hands-on experience with dossier preparation and regulatory submissions across US, EU, and RoW markets
- Deep working knowledge of Design Control, CAPA, Change Control, Validation, PMS, and vigilance reporting
- M.Sc. / M.Pharm in Chemistry, Microbiology, Biotechnology, or Life Sciences (Ph.D. / MBA / Six Sigma a plus)
- Solid people leadership; multi-site or multi-product exposure an added advantage???? ??? ?????? ??????A defined career path with succession into the Head of Quality & Regulatory role for the right candidate, in a market-leading, globally exporting organisation.

📌 ???? ????????? – ??????? & ?????????? ??????? (Maharashtra)
🏢 Blue Genes Research (BGR)
📍 Maharashtra