???? Mumbai (India)

???? Mumbai (India)

08 Aug
|
Blue Genes Research (BGR)
|
India

08 Aug

Blue Genes Research (BGR)

India

Mumbai | Regulated Life-Sciences Manufacturing | USFDA & WHO-PQ approved

BGR 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 workplace
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.

📌 ???? Mumbai (India)
🏢 Blue Genes Research (BGR)
📍 India

Reply to this offer

Impress this employer describing Your skills and abilities, fill out the form below and leave Your personal touch in the presentation letter.

Subscribe to this job alert:

Get the latest job offers by email for: ???? mumbai (india) / india