R&D

M.Sc., Botany/Microbiology/Biotechnology with/without NET /GATE Qualification.

B.Pharm, Pharm.D or equivalent with two years post-qualification experience in clinical project management and/or clinical trial/ study monitoring in a recognised organisation / institute

Provide support at BR India within Discovery Sciences, focusing on small molecule lead identification and optimization in close collaboration with Novartis colleagues in the US and Switzerland, as well as Indian CROs, to discover and advance innovative therapies addressing areas of high unmet medical need.

Coordinate with cross-functional teams to ensure seamless integration of safety data into the overall drug development process. Monitor and evaluate adverse event reports to identify potential safety signals and trends.

Candidates having M.Sc. / M. Tech / M. Pharm. / M.V.Sc. or equivalent qualification in Life Sciences or allied subjects (Biochemistry / Biotechnology / Virology / Bioinformatics / Computational Biology / Microbiology, etc.)

M.Sc in life sciences, PG diploma in Clinical Research and Pharmacovigilance 

The incumbent will be responsible for performing analytical method development and validations for USP/NF monographs and maintaining safety and GLP environment in the lab.

Review of Product Quality Complaint Investigation Reports Drug Products.Coordinate with other stakeholders involved in the complaint handling process.

PhD in Pharmacology and Toxicology / Biotechnology with GATE/GPAT/NIPER JEE. Experience in handling animal experiments and Molecular Pharmacology.