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Expertise in compounding, aseptic operations, and troubleshooting equipment, with a focus on solution-oriented approaches.

Preparation and review of Protocol as per sponsor and various regulatory requirements. Preparation and review of Informed Consent Document in English and vernacular language according to protocol.

Sciences or pharmacy graduates M.Sc. / B.Pharm. / M.Pharm. in parenteral manufacturing

B. Pharma / M.Pharma. Review and submission of injectable product dossiers for TGA and Europe in CTD, ACTD formats.

Should have exposure in AMV, Routine analysis and Stability studies and should have the exposure in set-up

M.Pharm, B.Pharm, M.Sc, B.Sc, D.Pharm ; Manage blister packing and bulk bottle, Track and Trace, serialization and documentation

Plan, facilitate and conduct CMEs, symposia, trainings, workshops, scientific meetings, speaker tours, and other product specific campaigns and deliver scientific presentations with consistent messages for key products at these meetings, as required.

MSc/MPharm. PhD in Chemistry/Pharmacy from a recognized University. Scientist III, Reference Standards Evaluation

Serve as a liaison between global Research Informatics functional areas and global research scientists, prioritizing their needs and expectations