M.Sc

First class post-graduate degree (including integrated PG degree) such as M.S. (Pharm) / M.Pharm or Equivalent (with specialization in Pharmacology & Toxicology/Regulatory Toxicology/Biotechnology. NIPER

Masters / Postgraduate degree in Pharmaceutical Chemistry, Chemistry, or a related discipline, with 03 years of post-qualification experience. National Drug Dependence Treatment Centre (NDDTC), AIIMS, New Delhi

The candidate should have a first-class post-graduate degree in Biochemistry/ Biotechnology/ Molecular & Human Genetics/Zoology / Animal Science / Life Sciences with qualified NET/GATE or equivalent examination. Department of Molecular and Human Genetics, Institute of Science, BHU

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

End-to-end product & process development, pilot-scale manufacturing, technical documentation, regulatory compliance.

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

Hands-on experience in Analytical Method Development, Method Validation, and Routine Analysis. 

To collaborate with internal and external stakeholders like CMC team, supply, commercial, IPR, legal, CROs, Consultants etc to ensure smooth regulatory submissions process

Senior Manager CETA, you will drive Therapeutic Area performance for CDC India by providing strategic trial insights, leading portfolio planning and execution, and ensuring operational excellence across clinical trial activities.