M.Sc

To lead and manage all regulatory affairs activities at the manufacturing site located at Mumbai and LL locations, ensuring timely regulatory submissions, compliance with regulations, and providing strategic support to institutional and international business operations.

Job Description typically involves ensuring injectable pharmaceutical products meet safety and quality standards through testing, documentation, and compliance with regulatory guidelines like GMP.

A Ph.D. in Biological Science/ Biotechnology/ Biochemistry/ Industrial Biotechnology or related including Pharma and Technology

Masters degree/ diploma in life sciences, pharmacy, public health, healthcare or other related discipline

PhD, MD, MS, MDS or equivalent degree or MVSc M.Pharm, ME, M. Tech, M.Sc with at least 3 year of research experience and one research paper in Science Citation Indexed Journal.

MSc, MTech, PhD in Biological Sciences/Biotechnology/Microbiology/Bioinformatics with 4 year post qualification relevant experience

Any Post graduate degree in life sciences, Minimum 4 years experience.

Postgraduate degree in science (M.Pharma, Life Science, Biotech, Zoology, Botany etc.) with PG Diploma in Clinical Research with two years Experience is mandatory.

Masters degree in Microbiology / Biotechnology. Basic knowledge of PGPRs, microbial community-NGS, skills, ethics to execute, deal with the experimentations