Executive - Quality Assurance

Executive - Quality Assurance

2 Nos.
70253
Full Time
3.0 Year(s) To 10.0 Year(s)
2.00 LPA TO 5.00 LPA
Production / Quality / Maintenance
B.Sc - Chemistry; M.Sc / MS Science - Chemistry
Job Description:

Designation : QA

Qualification : M.sc/ B.sc/ M.pharm/B.pharm

         Total experience : 2 - 5 years  

         Total Position : 2

         Gender : Male

         Location : Sachin, GIDC

         Salary Range : Upto 4 LPA

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

to carve a niche in the world of chemicals with a creative approach to chemistry, technology and systems, which will bring quantum and sustainable growth for us, our team members, and our stakeholders.

Apply Now

  • Interested candidates are requested to apply for this job.
  • Recruiters will evaluate your candidature and will get in touch with you.

Similar Jobs