Masters in pharmaceutical analysis, analytical chemistry, medicinal chemistry, Biochemistry, Biotechnology or equivalent with at least one year of hands-on experience
Knowledge of microbial testing for injectable products and environmental monitoring for sterile manufacturing area. Knowledge of instruments & equipment, method validations, finished dosage and RM testing
Post Graduate Degree in Sciences Biotechnology, Microbiology, Biochemistry, Chemistry etc OR Graduate, Post Graduate in Degree in Engineering and Technology Biotechnology, Biochemical, Bioprocess, Chemical, Food Technology, Pharmacy etc.
First Class Post Graduate Degree, including the integrated PG degrees, with three Years Experience or PhD. Second Class Post Graduate Degree, including the integrated PG degrees, with PhD and three Years Experience
Good Academic record with at least 70% marks in Masters Degree in Life sciences, Microbiology, Biotechnology, Chemistry, Physics, Biochemistry are eligible to apply.
Ensure preparation, review and submission of CTD sections in compliance with requirements of EMA, USFDA and other global markets. Timely update and preparation of dossier and documents as well as responses to the queries raised by regulatory agencies
M.Sc, M.Tech Life Science, Bioscience, Biochemistry, Zoology, Biotechnology, Forensic Science; Knowledge in cell culture, hands- on in vitro and in vivo neuronal models, molecular biology techniques, Animal handling
M.Sc in Chemistry, M.Pharm, M.S Pharm ; M.Sc in Life Sciences, allied subjects such as Biochemistry, Biotechnology Plus 2 years of research experience with NET, , GATE, Equivalent