Role is responsible for implementing CMC regulatory strategies for assigned pharmaceutical products in accordance with global regulations, guidances and defined regulatory strategies.
Ensure compliance with global and local procedural documents and local implementation of Patient Safety objectives, policies, processes and procedures.
IRG subsumes the Empowerment and Equity Opportunities for Excellence in Science (EMEQ) scheme of erstwhile SERB. IRG will provide enhanced support with flexible norms.
1st Class Post Graduate Degree, including the integrated PG Degree in Biotechnology, Life Sciences/Applied Biology / Life Sciences OR Second Class Post Graduate degree including the integrated PG degrees in Sciences with Ph.D. in Biotechnology / Life Sciences / Applied Biology
Graduate, Post Graduate Degree Professional Course selected through national level examination conducted by Central Government or the agencies ICMR, DBT, DAE, DST, IIT, IISER, NISER, IISc etc. qualified.
Post Graduation in Sciences M.Pharm, Life Sciences Biotechnology, Nuclear Medicine. experience in a Research Laboratory in cell culture and animal experimentation.
Possess a Diploma or degree in Pharmacy from recognized University or institute Statutory University or a Diploma in Pharmacy of a State Govt. AND Have valid registration under the Pharmacy ACT 1948.