vacancies

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

M.Sc (Ag.)/M.Sc./M.Pharm./M.V.Sc./Bachelor of Engineering/Technology (B.E./B.Tech.) or equivalent degree in a relevant discipline (Biotechnology/Microbiology/Life Sciences/Chemical Engineering or an allied field). 1st class in Graduate and Post-Graduate examinations. Amity University

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.

Demonstrated experience managing, coaching, and developing clinical and medical professionals within a matrixed and cross-functional environment

Develops and maintains clinical software Risk Management Files that include risk management plans, hazard analyses, risk assessments and post market surveillance.

Design and develop innovative formulations for solid oral dosage forms (Tablets / Capsules / Pellets) and injectable dosage forms. 

As a subject matter expert, you would be leading the workshop discussions on configurations with concerned business leads, understand & document business requirements. Solution designing, problem solving and working closely with other leads / consultants on a project assignment would be part of core responsibilities in this role.