QA

Candidate should have experience in the field of Analytical Research and Development Involved in Analytical Method development & validations, Stability analysis, Regular analysis activities.

B.Pharm/ M.Sc; Analytical QA activities mainly to review and maintain GLP in QC review of analytical report of RM,IP,FP and stabilty data.

B. Pharma/ B. Sc/ M. Sc; Knowledge of STP/SOP, BMR/BPR, hold time study, Product Transfer, process validation, protocol preparation

Handling of QMS activities like Deviation, Incident, Investigation, CCP, Protocol Preparation, Risk Assessment etc.

B.Pharmacy / M.Pharma / M.Sc; Candidate should have experience in IPQA activities for Manufacturing and Packing area. Candidate should have experience Injectable/ Parenteral IPQA activities specially for SVP line or Oncology facility.

M.Pharm/ B.Pharm/ M.Sc; Oversee ampoule line, liquid vial line, dry powder line, and media simulation studies. Monitor and record the temperature, differential pressure, relative humidity (RH), and environmental conditions in the aseptic area of the microbiology testing area. Manage stock of dehydrated culture media, prepared media plates, and test tubes.

Should have experience in maintenance of Solid, Oral dosage form manufacturing, Topical, Blister and Cartonator Machine

Experience of QC analytical, LIMS software handling, Master preparation in LIMS, preferably ONE Lab and Labware. Candidates may also apply who has good hands on experience on Caliber, StartLIMS , Labvantage or other LIMS.

M.Pharm, B.Pharm, M.Sc, B.Sc ; Should have experience in operating and cleaning a Vial Washing machine, Depyrogenation Tunnel, Automatic Vial Filling and Sealing Machines, and Automatic PFS filling machines.