Haryana

Ph.D or corresponding degree in any area of Life Sciences, Medical Sciences with one year of post-qualification research experience.

Ph.D in Life Sciences, Plant Biology, Plant-Pathogen Interactions, Biochemistry, Biotechnology. Hands-on experience in basic molecular biology techniques such as DNA and RNA isolation, protein purification, routine PCRs and cloning.

Ensure the core scientific principles of the study are adhered to, including accurate data collection, participant adherence to protocols, and minimizing missing data and loss to follow-up.

proven work experience in Regulatory Affairs in the Pharmaceutical or Healthcare, or organizations in other regulated sectors. The incumbent is also responsible for acting in compliance with country policies and practices to reduce Takeda exposure to regulatory risks as well as for developing the local Regulatory team as appropriate.

Ensure that the correct suspect drug was selected within the Pharmacovigilance Safety System; Code medical terms using standardized medical dictionaries i.e. MedDRA Using medical expertise, ensure that all data has been entered and coded correctly in the Global Safety Database

Ph.D. in Biotechnology, Life Sciences with at least two years of research experience in zebrafish biology. Experience in performing zebrafish experiments and skills in molecular biology are required. Candidates with publications in the relevant field will be given preference.

PG Professional degree in Life Sciences, Pharmacology, Chemical Sciences or equivalent, M.Tech, M.Pharma or equivalent with two 2 years of post-qualification experience in the field of bioanalytical chemistry with emphasis on drug metabolism and pharmacokinetic DMPK studies.

To delineate the survival strategy of mycobacteria through antigenic determinants by inhibiting autophagy via miRNA and its significance in host directed therapy