vacancies

Responsible for the design, planning, operation and monitoring of the downstream group and this for development activities as well as for scale-up and GMP production 

Schedule and assign projects to Regulatory Affairs team to ensure business timelines are met. Review, compile and dispatch new product submissions and pre-launch variations. 

M.Sc - Microbiology / Biotechnology / B.E / B.Tech (Biotechnology), USV IS HIRING for Drug Substance Biologics Manufacturing Plant

BA / BS degree with at least 3 years clinical trial experience or direct equivalent experience or advanced degree (MS / PhD /PharmD ) with at least 2 years clinical trial experience.

Exposure to regulatory requirements in healthcare and life sciences, delivering guidance to ensure organizations meet necessary standards.

MSc in Biological Sciences / MPharm from a recognized University/Institution or equivalent, and research experience in cell culture, molecular biology techniques, animal handling, clinical sample analysis and related work. CSIR-Indian Institute of Integrative Medicine, Jammu

PhD. in Chemical / Biological/ Pharmaceutical Sciences in relevant fields from a UGC/AICTE recognized University / Institute. National Dope Testing Laboratory

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

NIMHANS is conducting a Walk in Selection for Postdoctoral Fellow, Junior Research Fellow. Experience in mass spectrometry for metabolomics/proteomics and associated down steam analyses. Enzyme kinetics, immunoblotting, immunocytochemistry