Scientist

Postgraduate degree, including the integrated PG degree in life sciences. Preference will be given only to those with postgraduate degrees in M.Sc, M.Tech, two years of experience, or a Ph.D. in life sciences in the required specialisation. 

walk in interview for Life sciences candidates at BRIC-Translational Health Science and Technology Institute, THSTI is an Institute of the Biotechnology Research and Innovation Council, Department of Biotechnology, Ministry of Science & Technology, Govt. of India

First Class Post Graduate Degree including integrated PG degrees OR Second class Post Graduate Degree with PhD. Influenza vaccine to reduce cardiovascular events in patients with recent myocardial infraction: a multi-centric randomized, double blinded, double blind, placebo -controlled trial

PhD in Microbiology, Biotechnology. The candidate must have at least one first author research publication in SCI-indexed Journals. Experience in microbiology testing and assay development. Isolation of microbes from human samples DNA, RNA, plasmid isolation, real-time PCR, etc. evidenced by PhD thesis.

The candidate must possess a thorough understanding of relevant disease biology, the clinical landscape, emerging technologies, and the competitive environment. The candidate should demonstrate exceptional laboratory technical skills in cell and molecular biology, and, or in vivo pharmacology and proficient at devising strategic solutions to identify and resolve potential challenges.

PhD with 3 years experience in Biological Science, Biotechnology, Biochemistry, Bioengineering, Pharmaceutical Technology or any branch of Life Sciences Relevant to essential criteria. 

Post Graduate degree in Biotechnology Life Science subject with two year experience from recognized university. Post Graduate degree in Bio informatics subjects with two year experience from recognized university.

This is a key hands-on, non-supervisory position. In this role, the Scientist initiates and executes stability studies for reference standards using appropriate compendial methods. Additionally, the incumbent will be responsible for performing analytical method development and validations for Impurity RS and maintaining safety and GLP environment in the lab.

UNDERSTAND DESIGN, SETUP, AND EXECUTION OF IN VIVO PHARMACOLOGY MODELS FOR EXPERIMENTS ASSOCIATED WITH GROSS IMMUNOLOGY, SOLID TUMORS, AND HEME-ONCOLOGY