PhD in biological sciences, preferably infection biology. Prior experience in working with infectious agents and biological specimens Excellent written and verbal communication required with exceptional organizational skills

NIAB invites applications for admission to its PhD program in Biotechnology from highly motivated students for the 2025-2026 Academic Session. The institute provides opportunities for pursuing cutting-edge research using advanced technologies in frontier areas of Animal Biotechnology.

To Review Qualification Protocol and Reports of Equipment, Instrument, System.To Review Qualification Protocol and Reports of Computer System Validation CSV. Ensuring safe handling of Raw Materials and Packing Materials. Dispensing activity of RM and PM material.

EM, Media 111 visual inspection , Aseptic area monitoring, Water and Bioburden testing & Sterility testing & BET Testiug , IQ, OQ, PQ of equipment, Biological reactivity test - Moda exposure

Should have sound knowledge of BFS machine operation, aseptic area, maintenance, media fill, batch mfg., CIP, SIP, Autoclave, topical manufacturing. Candidate having experience in different packing lines of OSD & sterile manufacturing.

Fermentation Microbial, mammalian, Proficiency in aseptic technique, exposure to Centrifugation, TFF, Homogenization operation, Filter integrity testing, CGMP, Autoclave operation, media preparation

In people with this disease, small fibres of TTR protein clump together to make deposits called amyloid. Amyloid can build up around or within the nerves, heart and other organs, stopping them from working properly. Eplontersen is specifically indicated for use when the disease is causing polyneuropathy, which is damage to multiple nerves outside of the brain and central nervous system, resulting in pain, discomfort, progressive weakness and loss of sensation in the legs and arms, and mobility difficulties.

Post Graduates in Life Sciences, Pharmacy, Statistics, Social Works, Sociology, BAMS, BSMS, with MD in AYUSH to support Intramural Primary Research co- ordination and facilitate in better central procurement planning framework at ICMR headquarters

ICMR-funded project entitled Clinical Development of IIIM- 290 CDK9T1 Inhibitor for Metastatic Pancreatic Cancer, tenable at CSIR-Indian Institute of Integrative Medicine, Jammu. Research experience in natural product chemistry will be preferred.

First-class post-graduate degree included the integrated PG degree OR Second-class post-graduate degree included the integrated PG degree with Ph.D. The Role of Extra Domain A Fibronectin in NETosis-Mediated Non-Ischemic Cardiac Hypertrophy 

M.Sc in Zoology, Biochemistry, Botany, Molecular Biology, Biotechnology, Microbiology, Life Science from a recognized University or M.Sc in Forensic Science

The Clinical Research Lead will oversee and manage clinical research activities within the organization. This role involves designing, implementing, and monitoring clinical trials to ensure they meet regulatory requirements and organizational goals.

Provide strategic guidance and expertise in oncology for the development and execution of medical affairs plans focusing on Lung Cancer, GU Cancers and Hematology portfolio. Collaborate with cross-functional teams to support the successful launch and commercialization of oncology products.

To assist establishing a system in accordance with Good Manufacturing practice guidelines and responsible for follow established , new procedures, new procedures, maintaining and updating existing procedures in the department.

Research experience, knowledge in extraction and isolation techniques chromatography purification, HPLC, etc and characterization of natural products and their modifications. M.Sc, M.S. in Chemistry, Organic Chemistry, Natural Products Chemistry, Medicinal Chemistry, Pharmaceutical Chemistry from a recognized university or equivalent.

Evaluates new market complaints daily and communicates them to the various manufacturing partners, determines the criticality of complaints and makes appropriate recommendations. Escalates critical complaints and those with the potential to affect an entire batch or multiple batches. 

This is a non-supervisory position in Reference Standard Laboratory responsible for performing the required tests as part of the project and maintaining the GLP environment in the Laboratory. The incumbent will utilize his or her technical expertise, knowledge of pharmaceutical analysis in collaborative testing, efficient and effective laboratory operations.

Support affiliates in updating local requirements based on regulatory agencies guidance and input from affiliates, distributors. Manage working relationships with key stakeholders. Ensure compliance with regulatory requirements and provide strategic product direction to teams.