M.Sc

Demonstrate expertise in tablet and capsule manufacturing processes, including granulation, compression, coating, and filling. Operate production equipment such as MG, FBD, compression machines, coaters, and capsule filling machines.

Leads Pharmacovigilance and Risk Management Planning and develops strategy for approach to evaluation of issues in the clinical matrix. Leads the safety component of global regulatory submissions.

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

Masters in Pharmaceutical Sciences, MVSc, Animal Sciences OR Bachelor’s degree in Engineering or Technology or Medicine from a recognized University OR Any equivalent qualifications duly recognized by the concerned authority as per the functional requirement.

Masters in Natural or Agricultural or Pharmaceutical Sciences, Animal Sciences OR Bachelor degree in Engineering or Technology or Medicine from a recognized University or equivalent 

M.Sc, M.S. Pharm.,M.Pharm. in Biochemistry, Microbiology, Biotechnology, Life Sciences. Minimum CGPA of 6.75 for General category, OBC, 6.25 for SC. ST, 5.75 for persons with disability candidates on a 10 point scale in the qualifying examination.

Masters in Pharmaceutical Sciences, MVSc, Animal Sciences OR Bachelor degree in Engineering or Technology or Medicine from a recognized University OR Any equivalent qualifications duly recognized by the concerned authority as per the functional requirement

Masters Degree in Science with specialization in Biotechnology, Genetics and Plant Breeding, Molecular Biology, life sciences from a recognized University or equivalent. 

Master, Integrated Masters in Natural or Agricultural or Pharmaceutical Sciences, MVSc, Animal Sciences.