R&D

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.

MPharm in any Pharmacy discipline or PharmD. Preference will be given to candidates with background and exposure in pharmacometrics modeling. Additional benefit: Selected candidate may register for PhD under Manipal Academy of Higher Education (MAHE), Manipal on fulfilling the prescribed eligibility criteria.

M.Sc. (Life Science) or equivalent degree holders [M.Sc (Agriculture), MBBS, BDS, MVSc/ M.Pharma/ B.E./ B.Tech] with 1st class in graduate and post-graduate examination with basic knowledge of computers (word. Powerpoint, excel)

First Class Post Graduate Degree in Pharmacy / Professional Courses or any Life Sciences, including the integrated PG degrees.