Officer / Executive - Quality Assurance

Officer / Executive - Quality Assurance

5 Nos.
96704
Full Time
4.0 Year(s) To 10.0 Year(s)
3.00 LPA TO 5.00 LPA
Production / Quality / Maintenance
Pharma/Biotech/Clinical Research
B.Sc - Chemistry; M.Sc / MS Science - Chemistry
Job Description:

1. To perform all the activities of Quality assurance departments.

2. Ensure that SOPs are available for all quality related activities and they are current.

3. Prepare and review all quality assurance related documents such as SOPs, log book, format, etc.

4. Responsible for the Release of the final products.

5. Review batch sheet, packing sheet and final product release document. 

6. Ensure the implementation of Good manufacturing practices. 

7. Ensure implementation of documentation system in the Quality control, Quality Assurance, Production, Engineering, Ware House, and other relevant departments. 

8. Ensure retention of all records relating to the manufacture, testing and packaging of the products. 

9. Prepare department organogram.

10. Issuance of all quality assurance related document and also manage record for retrieval record for document.

11. Prepare the annual product quality review for the entire product. 

12. Prepare the SOP and format related quality assurance department.

13. Review of deviation and change control activities and issuance of related document.

14. Prepare the internal audit document as per schedule and necessary corrective & preventive action is taken.

15. Act as quality representative for Quality related activities.

16. Responsible to maintain the stock of QA department.

17. Responsible to give GMP training.

18. Responsible for new employee training.

19. Review vendor qualification document.

20. To participate in equipment qualification and process validation programme.

21. To undertake any other job as may be assigned by the Lead quality assurance.

22. Review the deviations and OOS are investigated and necessary corrective and preventive actions are implemented

23. Responsible to maintain AVL and coding list.

24. Responsible to fill vendor qualification documents and give response to vendor query.

25. To prepare internal audit schedule and to implement. 

26. To prepare training schedule and its effectiveness.

27. Responsible to review of finished product analysis data.

28. Responsible to take follow up for calibration, maintenance schedule.

Key Skills :
Company Profile

--- ---, based in Bharuch, India is renowned for its dedicated team & commitment to excellence. We offer a wide range of products, including anti-diabetics, anti-cough, anti-gout agent and anticonvulsant Our capabilities extend to custom API development and contract manufacturing, highlighting our core expertise.

The company came into inception on 2022
Commercial production Started from March-2024.
A state-of-art facility for API manufacturing managed by skilled personnel.

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