vacancies

Hetero is one of worlds leading producers of key Active Pharmaceutical Ingredients (APIs) and generic formulations with presence in 140+ countries and backed by 30 years of experience in the pharma sector

Handling QMS as per Regulatory requirements. Handling Deviations, CAPA, Change Controls, OOS investigations. Responsible to process internal quality audits.

Evaluate change control requests and assess their impact on product stability. Review laboratory test results (CoAs), investigate OOS/OOT findings, and prepare non¬conformity reports.

B.Pharm and / or M.Pharm from a recognized institution. Minimum 2 years of relevant experience in Clinical Trials, Clinical Research, Clinical Trial Pharmacy Management, and/or Clinical Trial Data Management.

MSc. in Chemistry / Analytical Sciences / Bio-chemistry / Biotechnology or M.Pharm. To carry out scientific work on instrumental analysis and tobacco protocol development.

Academic & administrative responsibilities. Deserving candidates with strong academic & administrative profile

M.S. (Pharm) / M Tech / M.Sc in field aligned with Pharma or Chemistry or Biotechnology. Experience Handled small protein purification and analysis.

M.Sc./M.Tech. in Life Sciences/Biotechnology/Molecular Biology/Biochemistry/ Bioinformatics/Genomics / Pharmacy or any other related subject, and National level SRF eligibility test such as NET, GATE, etc. qualified with 2 years of research experience. 

Preference will be given for Nursing Graduates/ PGs, Pharm D, MPharm (Pharmacology/Pharmacy Practice) with some experience in clinical research, Other Life Sciences PG degrees with clinical research experience