Role & responsibilities

- Review recent product information from R&D;, including manufacturing process, testing methods, and packaging details.

- Lead technology transfer activities, ensuring products can be manufactured successfully at production sites.

- Evaluate manufacturing facilities and equipment to confirm they are suitable for producing the products.

- Participate in process validation to ensure the manufacturing process consistently produces quality products.

- Manage quality risks and investigate product failures, deviations, complaints, and non-conformances.

- Ensure Quality Management Systems (QMS) such as Change Control, CAPA, Deviations, OOS, Training, and Complaint Handling are properly followed.

- Review and approve quality documents like Master Formula Records, Batch Manufacturing Records, validation protocols, and reports.





- Coordinate with multiple teams including R&D;, Production, Vendors, Laboratories, and Contract Manufacturing Sites to ensure compliance and smooth execution.

- Lead and manage QA teams, monitor performance, and escalate critical issues to management when needed.

Preferred candidate profile

- 17-22 years of experience in Quality Assurance and Manufacturing.

- Strong knowledge of pharmaceutical manufacturing processes (solid oral, liquids, powders, semisolids).

- Experience in GMP compliance, process validation, technology transfer, and quality systems.

- Team management experience and willingness to travel extensively

📌 Manager QA Tech Transfer (Bengaluru)
🏢 Leading FMCG
📍 Bengaluru