Technical Supervisor Job in Cadila Pharmaceuticals Ltd at Jammu

• Major Purpose of the Job: Preparation and Execution of Validation and Qualification protocols and reports. • Principal Tasks:- 1. Preparation of Qualification Documents like IQ, OQ, PQ and Summary report. 2. Execution of Qualification Activities. 3. Preparation and Execution of Process Validation Protocol and Report. 4. Handling of Market complaint. 5. Preparation and execution of Hold time validation Protocol and Report. 6. In process checking of all manufacturing and packing activities. • Responsibilities: 1. Preparation and execution of qualification protocols and report. 2. Execution of qualification activities. 3. Preparation and execution of process validation protocol and report. 4. Maintaining of all quality documents. 5. Implementation and monitoring of all cGMP activities in manufacturing area. 6. In process checking of manufacturing and packing. 7. In process sampling at different stages of manufacturing and packing. 8. Reviewing of batch manufacturing record after completion of processing. 9. Giving line clearance for all activities at shop floor. 10. Any other Job as and when assigned by Head QA.