Lucknow

To conduct audits and assessments of manufacturers of In Vitro Diagnostic Medical Devices (IVDs) against applicable regulatory requirements, quality management system standards, and conformity assessment procedures.

First Class Post Graduate Degree, including the integrated PG degrees in Biological Sciences, Biochemistry, Bioinformatics or Biotechnology

Candidates with a Master Degree in Chemistry / Chemical Sciences / Medicinal Chemistry / Pharmaceutical Chemistry. CSIR-CDRI

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.

MS Pharm / M. Pharm./ MTech in (Pharmacology/Pharmacology & Toxicology/Regulatory Toxicology/Biotechnology/Pharmaceutic al Chemistry/Medicinal Chemistry) or MVSc (Pharmacology/ Pathology/ Biotechnology). National Institute of Pharmaceutical Education and Research, Raebareli

M.Sc, M.Tech in Life Sciences, Microbiology, Biotechnology. Project Staff under various CSIR or externally funded projects tenable at CSIR-IITR, Lucknow.

M.Sc. in Chemistry / Chemical Sciences/Pharmaceutical Chemistry/Pharmaceutical Sciences and qualified CSIR-UGC/ICAR/ICMR NET incl. lectureship / assistant professorship or GATE. CDRI October Interview 2026

As the Experienced professional in the Medical Affairs Sub-Function, possesses well developed skills in overseeing the direction, planning, execution, clinical trials/research and the data collection activities.

Ph.D. / MD / MS / MDS or equivalent postgraduate degree OR Minimum 3 years of research, teaching, and design & development experience after M.V.Sc. / M.Pharm / M.E. / M.Tech