August 2026

M.Sc. in Biotechnology / Biochemistry / Microbiology / Zoology from a recognized University or equivalent, Selected through National Eligibility Tests - CSIR-UGC NET including Lectureship (Assistant Professorship) and GATE. CSIR-IIIM

Masters degree in Life Sciences / Biotechnology / Biochemistry / Molecular Biology / Medical Laboratory Technology. Sree Chitra Tirunal Institute for Medical Sciences and Technology. Prototype development and functional evaluation of a novel double- barrel autologous Platelet rich plasma isolation device

Pharma.D or B.Sc. Nizams Institute of Medical Sciences, located in Hyderabad, Telangana, is a premier public medical university

PGs, PharmD, MPharm Pharmacology/Pharmacy Practice with some experience in clinical research and other Life Sciences PG degrees with clinical research experience. Division of Clinical Pharmacology, Department of Pharmacology, Kasturba Medical College (KMC), Manipal.

Ph.D. in Science / Engineering with a minimum of 5 years of post-Ph.D. experience, of which at least 2 years of experience should be in start-up incubators or related organizations. BioNEST-supported Biopharma Incubation Centre (BIC), NIPER Ahmedabad

Monitor and verify the quality of raw materials, in-process materials, and finished products through regular inspections and testing. Investigate and resolve quality issues, deviations, and complaints related to manufacturing processes and products.

Oversee manufacturing and packaging operations at external manufacturing sites to ensure compliance with current Good Manufacturing Practices and applicable regulatory expectations.

This position involves active contribution to the Formulation ARD team in technical and operational activities such as hands-on support to formulation development in parenteral formulations and interpretation of analytical results. The incumbent will perform other duties as assigned.

M.Sc. / B.Pharma. Prepare documents like SOPs, specifications and non-routine documentation. Review the latest pharmacopeial updates, supplements and amendments. experience in QC department of a pharmaceutical organization with knowledge of latest regulatory standards and compliance norms