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Support ICSR processing to ensure high-quality cases in a timely manner to meet all worldwide regulatory authority requirements

M.Sc. / B.Pharma. Prepare documents like SOPs, specifications and non-routine documentation. Review the latest pharmacopeial updates, supplements and amendments. experience in QC department of a pharmaceutical organization with knowledge of latest regulatory standards and compliance norms

B.Tech / M.Tech / B.Sc. / M.Sc. / B.Pharma. Ensure GMP compliance, system reliability, and continuous improvement to support uninterrupted production of life-saving therapies. Dr.Reddys Laboratories Career Expo

M.Sc. / B.Pharma. Operating equipment reactors, Sparkler Filter, Candle Filters, Centrifuge, Dryers as per SOP. Knowledge of GMP, cGMP, Data Integrity in USFDA and MHRA regulatory API manufacturing plants. Lupin pharma

To prepare and review new product documents like material requirement sheet, master formula card, bill of material, risk assessment reports, scale up protocol and reports, exhibit/ trial batch manufacturing record and exhibit protocols and reports etc.

Hetero is one of worlds leading producers of key Active Pharmaceutical Ingredients (APIs) and generic formulations with presence in 140+ countries and backed by 30 years of experience in the pharma sector. M.Pharm, B.Pharm, M.Sc, B.Sc

Monitor and execute the production activities in an area during the shift by maintaining cGMP and safety norms to achieve production targets

M.Pharm. M.Sc, B.Pharm, B.Tech, D.Pharm, Diploma, ITI (Candidates with regulatory plant exposure may apply)

Experience in injectables and sound knowledge of sampling, in-process checks, line clearance activities during manufacturing. Anthea Pharma Interview