Job Description

Responsible for end to end management of drug product visual inspection operations (Manual and Automated) as per SOPs, Batch Manufacturing Record, QMS item and cGMP norms. Responsible for total compliance of QMS elements.

1. To coordinate team shift allocation according to the planned schedule and ensure timely approval of employee leave requests.
2. To monitor, track and review QMS elements (Change controls, CAPA, incident management, SIR, market complaints etc.) and ensure the closure of the same on time.
3. To review and compliance of Audit points.
4. To plan optical inspection operations in compliance with delivery, quality and with safety.
5. To involve in visual inspection projects activities (to prepare URS, involving in the FAT, SAT & equipment Qualification)



for current and ongoing projects.
6. To review and execute/ support the process validation protocols and its reports.
7. To review the revised batch production records MFRs SOPs etc.
8. To follow ensure clean room behaviors techniques team members.
9. To identify reporting unsafe conditions acts.
10. To coordinate packaging qualification activities and associated documentation in compliance with applicable procedures.
11. Training staff member’s relevant cGMP aspect operations.
12. To handle any other work assigned L+I Department charge.

📌 Team Lead - Visual Inspection (Bachupally)
🏢 Dr. Reddy's Laboratories
📍 Bachupally