Master’s degree from a recognized University/Institute in Life Sciences/Agricultural Science/Biotechnology or allied subjects; alternatively, the specified Master’s degree with selection through CSIR-UGC-NET/GATE or relevant national-level examinations conducted by Central Government departments/agencies. BRIC-NABI
Doctoral Degree in Biotechnology / Microbiology / Life Sciences. As per norms of the funding agency for research projects. North-Eastern Hill University, Shillong
Bachelors degree in pharmacy, life sciences, or a related field. Basic understanding of pharmacovigilance principles and regulatory guidelines is desirable but not required; relevant training will be provided. ICON plc
Advanced degree in Engineering, Biomedical Engineering, Life Sciences, Regulatory Affairs, or a related field. Demonstrated experience supporting regulatory submissions, registrations, compliance activities, and regulatory lifecycle management. Medtronic
Write CMC regulatory dossiers for Drug Substance filing (small and Large API Molecules) using source documents, ensuring accuracy, completeness, and compliance.
The Medical Information Specialist (MIS) position is part of the ProPharma Medical Information Contact Center and follows all corresponding regulations, industry standards, and client/internal policies regarding medical information and the collection and documentation of adverse events, special situation events, and product complaints.
First Class Postgraduate Degree in M.Sc./M.Tech/M.Pharm. in Life Sciences /Pharmaceutical Sciences / Biotechnology / Pharmacology or allied subjects with 2 years of research experience. PGIMER, Chandigarh
M.Sc. in any life science stream. Knowledge of Cell culture and Molecular biology techniques is preferred. Animal handling experience (mice). One publication. Manipal Institute of Regenerative Medicine (MIRM), MAHE Bengaluru