JOB DETAILS

1. Responsible for preparation , issuance & review of BPR & BMR
2. Responsible for In - process checks during manufacturing in Tablet, to give the line clearance for start of activity in production & stores area

3. Preparation , execution and review of various qualification protocols and ensuring completion of protocol and report

4. Preparation , review , distribution of Standard Operating Procedure

5. Handling of change control , Deviation , Batch Failure , OOS , OOT , CAPA , reprocess , rework ,market complaints , return goods

6. Maintenance of control samples & documents related to control samples

7. Responsible for handling pharmaceutical ERP System like pharma suit

8. Assure ongoing compliance with quality and industry regulatory requirements

9. Plan, conduct and monitor testing and inspection of materials and products to ensure finished product quality

10. document internal ...