- Conduct GMP audits, vendor qualification, risk assessments, and CAPA follow-ups.
- Monitor critical manufacturing and packing activities at third-party sites.
- Review BMR/BPR, COA, specifications, and analytical data for batch compliance.
- Investigate deviations, OOS/OOT results, non-conformances, and quality complaints.
- Ensure compliance with approved MFR, SOPs, GMP, and regulatory requirements.
- Provide final QA disposition/release and ensure batches are cleared for dispatch.
Preferred candidate profile
Responsible for ensuring GMP compliance, product quality, and QA oversight at third-party/contract manufacturing sites. The role involves vendor qualification, GMP audits, batch manufacturing monitoring, documentation review, and final QA release of products before dispatch
Experience : 5-9 years in Quality Assurance within Pharmaceutical manufacturing.
📌 Assistant Manager Third Party Quality Assurance (Contract Mfg.) (Mumbai)
🏢 Nutragenix Healthcare Private
📍 Mumbai
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