Ph.D

M.Tech/ M.E/ M.Sc in Biotechnology/ Biochemistry/ Microbiology/ Molecular Biology/ Life Sciences/ Environmental Biotechnology/ Environmental Science from a recognized university

M.Sc, Ph.D in any branch of Life Sciences, Chemistry or related field from a recognized university. Candidates with involvement in innovation/design or social entrepreneurship or social empowerment using science or technology are particularly encouraged to apply.

M.Sc any branch of Life Sciences with a minimum of 55% marks in the qualifying examination OR M.Tech. Biotechnology, Bioinformatics with a minimum of 55% marks in the qualifying examination.

M.Pharm / Ph.D in Pharmaceutics studied in Top Colleges; Test license application. Preparation of costing formula. Execution of Bio batches. Raw materials and Packing materials procurement. Pre-formulation studies. Master formula record and specification reviews. Formulation development and scale up. Stability Studies.

M.Sc. and Ph.D in Microbiology / Virology / Parasitology / Biotechnology/ Genetics / Biochemistry / Human Genomics / Molecular Biology from a recognized university/institute.

The incumbent is responsible for providing support for the development of USP documentary standards and reference standards for biological products such as peptides, Oligonucleotides, protein, carbohydrates, Complex Biologics, Vaccines, Antibiotics, and advanced therapies.

Advanced degree in Life Sciences, Pharmacy, Health Economics, Statistics, Public Health, or related field (e.g., PhD, MPH, MSc, PharmD).

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

Doctoral Degree in Science / Engineering / Technology / Pharma / MD / MS from a recognized university or equivalent.