Assistant Manager Third Party Quality Assurance (Contract Mfg.)

Role & responsibilities

• 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.