1) Improving in-process control, Issuance of Document control, To maintain core areas asper cGMP, To evaluate Batch Record Discrepancies, Control and Monitor Data integrity in Production, Stores, QC & QA, To review and sign on COA. Control of Batch release, To provide Guidance and training with respect to Sop’s, cGMP, etc, Review and Approval of calibration record and Qualification, Directing. Leading & motivating subordinates for tea work environment, To investigate for Market complaint, CAPA,OOS & Procedure Deviations, Documents Retrieval for all Depts. and records, SOP’s issuance to all Dept, Master file time to time updating od Index for all Master files, Control sample room Monitoring, Master Documents control and records, To develop team Management skills, Strong communication with Awareness and understanding required by role in QA.
Qualification – B.Sc /M.sc/B. Pharm.
Exp- Should have experience of Pharma Industry only.
Note : Candidate should be in and around Goa only
Job Types: Full-time, Regular / Permanent
Salary: ₹500,000.00 – ₹1,000,000.00 per year
Benefits:
Schedule:
Supplemental pay types:
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+91 9175929869