R&D

Regulatory-Driven Stability Studies: Design, execute, and monitor stability studies in alignment with global regulatory requirements.

Having M.D./ M.S./ M.D.S. or MBBS/ BDS/ M.VSc./ M.Sc./ M.Pharma/ M.Tech or equivalent with Ph.D. in the topic related to health research. 

Masters from a recognized University in a subject related to Biomedical Sciences OR Pharm-D degree recognized by UGC / PCI.

Masters degree in Bioinfomatics, Computational Biology, Biotechnology, Life Sciences, Genomics, Computer Science, or any allied discipline as per DST/DBT/ICMR norms for Senior Research Fellow, and two years of work experience.

Should Have Experience in Formulation development, process optimization, scale-up and technology transfer of liquid and solid dosage forms.

Basic knowledge of medical terminologies and able to understand common medical terms relevant to pharmacovigilance and adverse event reporting.

M.Tech in Biochemical Engineering, Biotechnology, Bioengineering / Bioprocess Engineering / Technology, Industrial Microbiology, M.Sc. Biotechnology, Microbiology, Industrial Microbiology.

Post Graduate in life sciences including integrated courses. Candidates with working experience of NGS, Bioinformatics, Computation biology will be given preference. Department of Microbiology, SGPGIMS, Lucknow.

Post Graduate Degree life sciences including the integrated PG degree, selected through any one of the following exams : CSIR/UGC/GATE/ICMR