vacancies

B.Pharm / M.Pharm / M.Sc. (Chemistry or Analytical Chemistry) ; experience in a WHO-GMP compliant pharmaceutical Quality Control laboratory. Taj Pharma India

B.Pharm / M.Pharm / M.Sc . Expertise in analysis on HPLC, GC, Assay, Dissolution. Method Validation Protocol creation and execution, Expertise in handling HPLC, ICPMS, GC etc. USV Private Limited

M.Pharm / M.S / Pharm.D. or any other equivalent specializations for Department of Pharmaceutical Sciences & Technology, MRSPTU, Bathinda for the session July 2026 to December 2026.

The ideal candidate must have hands-on exposure to ophthalmic formulations, along with practical experience in autoclave operations and batch manufacturing processes. A strong understanding of GMP and quality compliance is essential.

Compilation of high quality Annual Product Reviews / Product Quality Reviews for products manufactured at various manufacturing sites and retrieve data from the Quality and regulatory databases and system

Strong understanding of CDISC standards, including the SDTM Implementation Guide and regulatory authority submission guidelines

First class post-graduate (PG) degree (including integrated PG degree) such as M.S. (Pharm)/ M.Pharm/ M.Sc/ M.Tech or Equivalent (with specialization in Pharmacology & Toxicology / Regulatory Toxicology / Pharmaceutics / Biotechnology / Life Sciences.

Diploma in Pharmacy or Bachelor of Pharmacy or Master of Pharmacy. Must have registered under Pharmacy Council and must keep the registration alive by renewing it regularly every year. 

B.Pharm or Graduation in Biomedical Sciences. Minimum 3 years experience for Operations Manager and 1 year experience for Associate Manager in pharmaceutical / medical device regulatory affairs.