Purpose of Position: To perform document & data control activities as per approved QMS.
1. To perform and monitor document and data control of all controlled documents (issuance, retrieval, archival and distribution). 2. To update all master documents periodically. 3. To ensure that APQRs are prepared, reviewed and approved as per approved procedure. 4. To prepare & review of all SOPs, protocols and master controlled documents. 5. To do documentation related to OOS, non-conformity, Deviation, CAPA, Change Control, market Complaint & Product Recall. 6. To review new/ revised artwork as per approved procedure. 7. To do preparation & review of MFR, BMR, Analytical documents and all other documents as per QMS. 8. To maintain records of vendor development / qualification. 9. To prepare and review validation & qualification documents. 10. Any other task assigned by reporting manager.
11. Functional reporting shall be as per Departmental Organogram.
The Job responsibilities may be revised as per company requirements as and when required.
Role:QA / QC Executive
Salary: Not Disclosed by Recruiter
Industry:Medical Services / Hospital
Functional Area:Quality Assurance
Role Category:Production & Manufacturing
Employment Type:Full Time, Permanent
UG:B.Sc in Any Specialization,B.Pharma in Pharmacy,B.Tech/B.E. in Bio-Chemistry/Bio-Technology
PG:MS/M.Sc(Science) in Biotechnology, Chemistry
Doctorate:Doctorate Not Required
J.Mitra and Co. Pvt. Ltd