5+

Perform line clearance. In-process venficatoon and batch reconciliation. Investigate deviations, incidents and support CAPA implementation Coordinate equipment qualification, preventive maintenance and calibration activities.

Development and validation of analytical methods for pharmaceutical products. Perform nitrosamine risk assessment, method development, and trace-level impurity analysis.

MSc / M.Tech in Biotechnology / Biochemistry / life science or equivalent with biotech/ pharma industry experience.

B.Pharm / M.Pharm / MSc Chemistry / Biotechnology. Pilot Plant, Unit Process, Spray Dryer, RCVD, Vacuum System and Solvent handling.

Washing, Tunnel (Depyrogenation Tunnel), Autoclave,Manufacturing,Filling, Sealing,Terminal Sterilization, Visual Inspection,Quality Management System (QMS), Lyophilization Dispensing

Titan, an integrated Pharmaceutical Group which is backed by the holistic approach towards catering multifarious integrated services.

B.Pharm / M.Pharm / M.Sc. (Chemistry or Analytical Chemistry) ; experience in a WHO-GMP compliant pharmaceutical Quality Control laboratory. Taj Pharma India

B.Pharm / M.Pharm / M.Sc . Expertise in analysis on HPLC, GC, Assay, Dissolution. Method Validation Protocol creation and execution, Expertise in handling HPLC, ICPMS, GC etc. USV Private Limited

The ideal candidate must have hands-on exposure to ophthalmic formulations, along with practical experience in autoclave operations and batch manufacturing processes. A strong understanding of GMP and quality compliance is essential.