• The Role is responsible for reviewing the Batch Production Record, Issuance and Reviewing the Product Labels.

Release of finished products, Verification activities of finished goods at the sites.

Key Individual Accountabilities:
• Handing & tracking of QMS related activities CAPA, Deviations, Customer Complaints. OOS/OOT, Investigations.
• Ensure timely review of Batch Production record, Review & approval of investigation, verification of CAPAs, review of QC test results, batch disposition quarantine, rejections approval.
• Release/Rejection of finished products as per approved specifications.
• Calibration & Maintenance QA oversight.
• To perform cleaning verification during product change over and dispatch verification of finished as per established procedures.
• Verification of reprocessing activities in the site.




• Handling of Sale Returns.
• Complying to the laid down norms of Safety Health & Enviroment.
• Any job assigned time to time by superior based upon training on the procedure.

Required Competencies:
• Working with People
• Relating & Current working
• Adhering to principles & Values
• Adapting & responding to changes
• Coping with Pressure & Setbacks
• Achieving Personal work Goals & Objectives.
• Have the Exposure of Audits.

Education :
M.Sc. in Chemistry/ M.Pharma

Experience: 10 to 15 years. (Candidate should have API Experience)
Reporting: Manager - QA Operations

📌 Deputy Manager (Taunsa)
🏢 Centrient Pharmaceuticals Netherlands
📍 Taunsa