Role & responsibilities

1. To issue documents to production, quality control, i.e. BMR, ECR, AWR, Protocol, stability protocol etc.

2. To prepare SOP of the department.

3. To issue controlled copies of all SOP and other document to concerned departments.

4. To review BMR, ECR review AWR from production & quality control department.

5. To prepare and to review Process validation Protocol and report.

6. To prepare and to review Cleaning validation Protocol and report.

7. Labeling of finished product.

8. Issuance and reconciliation of finished product labels.

9. Issuing Register, logbook to respective departments.

10. Maintain and update the records of obsolete document, revision history sheet.

11. To maintain vendor qualification as per vendor list.

12. Preparation and Review of Annual product quality review and Continuous process verification report.

13. Sampling and Packing of Finished product.

14. To provide SOP training.

15.



Update the issuance register for BMR, ECR and AWR of the respective product.

16. Documents Archival.

17. To perform QA round of each and every department.

18. Perform line clearance.

19. To release the batch for further processing or distribution for sale in absence of Quality Assurance Head.

20. Approving all quality related documents in absence of Quality Assurance Head.

21. Approving specifications and master documents in absence of Quality Assurance Head.

22. Handling of customer complaints, Return Goods and Recalls.

23. Handling of Change control, Deviation, OOS, OOT and Incident.

24. Responsible to attend training programme i.e. SOP, GMP etc.

25. Handling of Audit compliance.

Preferred candidate profile

📌 Qa Executive (Badlapur & Taloja) (Panvel)
🏢 Sanvin Group
📍 Panvel