vacancies

The Senior Specialist, Expert License Management prepare dossiers and execute actions that support the license security and product compliance on the markets, and that meet companys and health authorities requirements. Encounter the challenges to enable representatives from all major disciplines involved to reach agreement on the license management strategy and approach.

Ph.D, MD, MS, MDS or equivalent degree or having 3 years of research experience after MVSc, M.Pharm, ME, M.Tech with at least one research paper in Science Citation Indexed journal.

To work in Clinical Trials as a Non-Medical Co-ordinator. Pharmacist for the Department of Endocrinology, Diabetes & Metabolism. B.Pharm, with Tamil Nadu Pharmacy Council Number.

Prior experience in virology or immunology is desirable. Candidates must have experience in immunological or virological assays for BSL2 or BSL3 labs. Animal handling and experimentation is desirable. 

Ph.D or Ph.D thesis submitted or defended experience Biochemistry, Biotechnology, Stem Cell Biology and Neurobiology, Neuroscience with a strong publication record and research experience in Cell Biology, Molecular Biology and Neurobiology.

Expertise in different types of purification techniques. Sound knowledge of different column chemistry used in HPLC. Responsible for troubleshooting of instruments and their calibration

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

Ensure that Bulk Viral Antigen production adheres to GMP standards on the shop floor, including line clearance, dispensing, and preparation processes. Examining and approving batch records, standard operating procedures, project plans, customer verification, and APS documents.

Post Graduation in Science M.Pharm, Life Sciences, Biotech, Zoology, Botany, etc. With PG Diploma in Clinical Research is mandatory. Candidates should have at least one-year experience as Clinical Trial / Research Coordinator is mandatory.