vacancies

Experience in the development and application of pharmacometric models to support drug development and regulatory submissions.

Responsible and accountable for the oversight of quality operations and GMP compliance across the TPMs under responsibility of EPD Biosimilars Operations in India.

M.Sc. (Biotechnology / Biochemistry / Microbiology / Molecular Biology/Genome Engineering/ Medical Biotechnology/ Biomedical Science / Life Science), M.Tech. (Biotechnology / Biomedical Engineering), M.Pharm. with first class.

Ph.D. or equivalent degree OR MVSc/ M.Pharm/ ME/ M.Tech with atleast 1 research paper in Science Citation Indexed (SCI) Journal

Masters Degree in Pharmaceutics or Pharmaceutical Sciences (First-class) from a recognized university. The candidate will be eligible to apply for the Ph.D. position next semester.

B.Pharm or B.Tech (Biotechnology) or Master Degree in Pharmacology / Biochemistry/ Biotechnology)

M.Sc in Chemistry / Biochemistry / BioPhysics / Biotechnology/ Pharmaceutical Science or related fields.

Master degree in Pharmaceutical or Natural Sciences with first class. GPAT / GATE / NET qualified with research experience in the field of Metabolomics/HRMS/HPLC analysis.

Post-Graduate degree in Life Sciences, Including Integrated PG degrees OR Second class Post Graduate Degree, including the integrated PG degrees with PhD