Life Sciences

Post Graduate Degree in Science M.Pharma, Life Science, M.Sc., Biotech, Zoology, Botany etc and P.G. Diploma in Clinical Research with 1-year experience as trial, research coordinator is mandatory.

A Comprehensive Approach to Address Antimicrobial Resistance. Masters in Chemistry, Pharmaceutical Chemistry from a recognized University or equivalent. Experience in mammalian Cell culture, protein expression and purification. Centre for Marine Therapeutics

PG Diploma in Public Health, OR M.Sc Life Sciences branch with M.Phil, PhD, AND with at least 5 years work experience after highest degree.

Identification of potent antimicrobial compounds from medicinal plants against multidrug resistant ESKAPE bacteria isolated from different water sources in and around Jhansi district. Screening of various herbal, plants based raw materials for fungal growth associated with mycotoxin contamination. 

Masters or M. Tech or M. Pharm in any branches of Agricultural Sciences, Biology, Life Sciences, Pharmacy any specialization, Veterinary Sciences, Computer Sciences, Bioinformatics and Biotechnology.

Able to conceptualize and design novel vectors across expression systems including bacterial, yeast, mammalian, gene modification techniques. Experience in mass spectrometry for protein, antibody analysis.

Conduct in-depth research and analysis of rare disease markets, including competitive landscape, market dynamics, and emerging trends. Develop and maintain a comprehensive understanding of the rare disease market, including key players, product portfolios, and future opportunities. Collaborate with cross-functional teams to gather and synthesise relevant data and insights to support strategic decision-making.

QA Specialist will serve as QA technical subject matter expert for CSV process, such as MES, KNEAT, DCS, including but not limited to GMP enterprise systems, manufacturing systems and computerized equipment, laboratory systems and computerized equipment and validation software tools.

Represent Regulatory Affairs as team member of product development projects from Concept through Commercialization. Review pre-clinical, and clinical protocols and associated reports to be used in submissions for assigned projects.