Officer / Executive - Quality Assurance

Officer / Executive - Quality Assurance

5 Nos.
88635
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

--- --- Private Limited is a Private incorporated on 24 August 2021. It is classified as Non-government company and is registered at Registrar of Companies, ROC Ahmedabad. Its authorized share capital is Rs. 30,000,000 and its paid up capital is Rs. 30,000,000. It is inolved in Manufacture of other chemical products

--- --- Private Limited's Annual General Meeting (AGM) was last held on N/A and as per records from Ministry of Corporate Affairs (MCA), its balance sheet was last filed on 31 March 2023.

--- --- ---., Ltd--- --- Private Limited's Corporate Identification Number is (CIN) U24299GJ2021PTC125088 and its registration number is 125088.Its Email address is ruchit@dhanrichfinechem.com and its registered address is PLOT NO. 5901/1 CO DHANRICH FINE CHEM NR KANORIA CHEMICALS LTD GIDC ESTATE , Ankleshwar, Gujarat, India - 393002.

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