Executive - Quality Assurance
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.
Company Profile
--- Parenterals Ltd. is a Gujarat based pharmaceutical company, established in 1992 by Mr. Ramesh Desai, who started the company with a vision of making world class affordable medicines and to take it to the forefront of contract manufacturing units in Gujarat. A WHO GMP & an ISO 10002: 2014, 9001: 2015 certified pharmaceutical company, --- Parenterals Ltd has traversed a long way in order to be recognized as one of the fastest growing Pharmaceutical Companies in India today. Growing at a fast yet steady pace, the second-generation contract development & manufacturing organization.
Apply Now
- Interested candidates are requested to apply for this job.
- Recruiters will evaluate your candidature and will get in touch with you.