2-3

Accurately translate understanding of regulatory requirements and corporate policies governing documents for regulatory submission into execution of timely and compliant analyses and presentations of safety data and benefit-risk assessment in documents.

Candidate should have completed Ph.D. in their relevant discipline. SRM College of Pharmacy, SRM Institute of Science and Technology, Kattankulattur is one of the countrys premier pharmaceutical education and research institutions.

Dossier & document preparation as per CTD, ACTD & country specific guidelines, Review of dossiers, DMF & Technical documents, Answer query raised from regulatory authority.

M.Sc. in Biological subject / Chemistry / Biochemistry. 2 years experience in Cancer Research.

Biological E. Limited (BE) invites both experienced professionals and fresh diploma holders, as well as graduates and self-driven individuals

Hetero is one of worlds leading producers of key Active Pharmaceutical Ingredients (APIs) and generic formulations with presence in 140+ countries and backed by 30 years of experience in the pharma sector.

Handle manufacturing skids, Fedegari autoclaves isolator, lyophilizers, vial washing and tunnel, vial/ ophthalmic/ PFS filling and aseptic filtration

Preparation/review of medical and scientific write up. Coordination for serious adverse event reporting and safety update to Regulatory agency

Intas is one of the leading multinational pharmaceutical formulation development, manufacturing and marketing companies in the world.