M.Sc

MSc in Biotechnology/Pharmaceutical Biotechnology / Biochemistry / Bioinformatics / Life Sciences or equivalent with 3 years teaching/research experience

The candidate should be M.Sc. in Zoology/Biochemistry/Life sciences with a first-class division at both the undergraduate and postgraduate levels. Additionally, the candidate must be a resident of Uttar Pradesh

Post Graduate Degree in Molecular Biology, Microbiology, Biotechnology, Biochemistry, Virology OR in relevant subject

M.Sc. Biotechnology, Microbiology or relevant life sciences discipline appearing or passed with a minimum of 55% marks. 

Post Graduation in Science with P.G. Diploma in Clinical Research is Mandatory. Candidates with minimum 6 months experience in handling regulatory trials would be desirable.

Experience in environment monitoring, QMS, routine & non routine analysis, PET, sterility, BET & water testing.

Executing chemical reactions in mg to gm scale and to synthesize required quantities of molecules/compounds as per client specifications using efficient route and techniques.

Candidate will be responsible for preparing and managing regulatory dossiers, coordinating with regulatory authorities for EU and ASEAN markets and providing guidance on regulatory requirements to internal teams

Perform analysis of raw materials and finished products using UV, IR, HPLC, UPLC, GC, LCMS, etc. Ensure adherence to SOPs, GMP, and ALCOA principles during shift operations.