December 2025

Post Graduate Degree, including the integrated PG degrees, with three years post qualification Experience or PhD.

Any M.Pharmacy / MSc with 6 to 10 Years or B.Pharmacy with 8 to 12 Years of relevant Experience in Manufacturing Downstream injectables with Strong people management experience in a regulated manufacturing operations environment.

Dossier Preparation in CTD/ACTD/eCTD/National format. Must have Parenteral and partially OSD dosage forms exposure.

Experience in IPQA,QMS, Qualification & validation. Must having experience of API Pharma Industries.

Graduation : B.Pharm with post-graduation : M.Pharm / MBA (Pharma Management). Develop and implement brand strategies and marketing plans.

Environment monitoring of aseptic area, Water sampling and testing, Sterility testing, Bioburden analysis and MLT analysis, Bacterial endotoxin test, Media preparation and handling.

Skilled in Batch Records, SOPs, BMR, and validation documentation. Proficient in calibration, routine equipment checks, and troubleshooting.

Good understanding of medical affairs function. Understanding of local regulatory policy and industrys code of practice related to drug registration, pharmaceutical promotion and clinical research.

Total 36 different medical devices are manufactured under Production Linked Incentive (PLI) Scheme for promoting domestic manufacturing of medical devices in India. These medical devices belong to different portfolios such as Imaging & Diagnostics, Critical Care & Emergency, Interventional CardioVascular, Renal Care Devices, Orthopaedic Implants, Oncology and specialist divisions.