March 2025

Certification in clinical research analysis is advantageous but not mandatory. Willingness to learn regulatory compliance is a must. Candidate with evidenced experience in clinical trial, relevant data analysis, data management and clinical statistical analyses will have additional weightage in selection.

Deciphering the role of trans encoded sRNA mediated gene regulation in stress adaptation and pathogenesis of M. tuberculosis. Effects of extreme heat on maternal, placental and fetal physiology, lactation and newborn health in India. Expertise in work using animal models, preparation, characterization of bacterial strains, molecular biology, and immunological techniques. Manage and optimize cell culture systems, including the culture of placental cells, trophoblasts, and secondary cell lines. 

A lipid perspective on immune evasion mechanisms in pancreatic cancer metastasis. Good Academic records with First Class Post Graduate Degree in any branch of life sciences. The candidate should have a minimum of one-year documented experience in handling laboratory animals and knowledge about pre-clinical models of cancer and surgical procedures. The Candidate should have qualified National Eligibility Test–CSIR-UGC-NET/LS or GATE or DBT-BET/ ICMR/DST- Inspire Fellowship

Candidates must have a PhD structural biology with experience in protein purification, biophysical, biochemical techniques and structural biology methods such as X-ray crystallography and or cryoelectron microscopy. Applicants must have excellent academic performance throughout and at least 5 years of hands- on experience in the aforementioned techniques.

The selected candidate is supposed to make her, his team and work in the core animal biotechnology areas wing. In addition to their own research programme, she, he is expected to provide support, collaborate to other research projects at NIAB and put efforts towards institute building. 

The ideal candidate will be responsible for compiling Drug Master Files DMFs and Certificates of Suitability CEPs, ensuring compliance with global market regulations and emerging market standards in accordance with ICF guidelines. This role requires strong coordination with internal stakeholders and expertise in regulatory submissions, amendments, and annual reports.

Define and implement the formulation development strategy, aligning with the broader RAD and business objectives. Lead the preparation of development reports, protocols, and documentation required for regulatory submissions. Identify and implement cutting-edge formulation technologies for new drug delivery systems. Ph.D / M.Pharm, Formulation Development NCE, Medicinal Chemistry

M.Sc / B.Pharm / M.Pharm; Computerized System Validation CSV, MES, Equipment Qualification; RM/PM, Dispensing, Inspection