January 2025

To undertake proposed research involving data analysis, computational modeling and programming for the clinical data on diabetes. Experience in data analysis, computer programming and mathematical modeling is desirable.

B.Pharmacy with 50% marks and minimum 01 year experience in an analytical laboratory. Preference will be given to candidates who have experience in bioanalysis with hands on experience in HPLC and or LC- MS, MS.

Synthesis of Insulin Analogues for the Treatment of Diabetes Mellitus; PhD or equivalent degree in Chemistry, Biochemistry with at least one research paper in Science Citation Index Journal. Preference will be given to candidates with experience in solid- phase peptide synthesis.

Exploring how Theileria parasites repress host gene expression PARA- REPRESS. Post Graduate Degree in Natural Sciences with experience in research and development in industrial and academic institutions or Science and technology organizations. Candidate with experience in epigenomics, cancer biology, molecular biology, cell culture, and bioinformatics will be given preference. 

The incumbent should be aware of the product development flow from the conceptualization to tech transfer. The incumbent is responsible for R&D trials batch making for various personal care, personal hygiene products like.

M.Sc / B.Pharm / M.Pharm. Material Dispensing, Ointment, Gel Manufacturing, Filling, Packing, Track and Trace, Labelling, Cartonator, QMS. IPQA, Document Cell, OOS, OOT, Process/ Cleaning Validation, Review of BMR & BPR, Training ,QMS Investigation, CAPA, SOPs etc.

PhD in Computer Science, Computational Biology, Bioinformatics or related discipline with application of the above-mentioned skills. Demonstrated experience in development of software tools and data analysis pipelines. initiative in National Supercomputing Mission at NIBMG

He, she participates in all activities relating to preparation, submission and follow up to obtain approvals, renewals for products and its variations and line extension indications and labeling approvals of medical devices of various business units of Medtronic. He, she will be responsible for providing technical support by interpreting federal and local regulations as they apply to products, processes, practices and procedures

Supervision of aseptic area activities, shift handling, aseptic area documentation, media fill activities, aseptic behaviour monitoring, and sterile operations. Handling area cleaning and sanitation activities, supervising steam sterilizer loads, filter integrity, disinfectant preparation and filtration activity, and related documents.