After a journey of growth spanning 27 years as Cadila Healthcare Ltd. and the Zydus Group, we have evolved and transformed ourselves in response to the changing times. Our legacy of over 70 years in healthcare and being dedicated to life in all its dimensions is reaffirmed in our new mission, vision and purpose. Unifying ourselves under the Zydus name, Cadila Healthcare Ltd., is renamed as Zydus Lifesciences Ltd.

Biotech – R&D (Walk In Interview)

Upstream Process Group
M.Sc. (Microbiology / Biochemistry / Biotechnology) / M.Tech. with Biotechnology with 2 to 10 years of hands-on experience in upstream operations like handling mammalian cell culture process and microbial fermentation. Handling equipment such as Bioreactors, CEDEX Bioanalyzer, etc. Capable of performing activities such as handling of mammalian cell lines, cell bank preparation, media scouting and process optimization at shake flasks, small-scale bioreactors and pilot scale bioreactors to improve yields & product quality.Good Documentation skills like SOP, STP etc.
In-process analysis and stability Group
Ph.D., M.Sc., M.Tech, M.Pharm Biotechnology / Biochemistry or equivalent with 2 – 10 Years of Experience. Candidate should have hands-on experience on HPLC, gel electrophoresis, spectrophotometric, structural and biochemical techniques for biosimilar or novel biological products. Candidate is responsible for development and qualification of analytical methods, in-process analysis during upstream, downstream and drug product process development, degradation / stability studies, excipient analysis, report and protocol writing.

Formulations Group
Ph.D., M.Sc., M.Tech in Biotechnology / Biochemistry or M.Pharm Biotechnology / Pharmaceutics with 2 – 10 Years of Experience. Candidate is responsible for planning and execution of formulation development, stability / degradation studies and technology transfer for biosimilar and novel biological products. Candidate should have hands-on experience on techniques related to liquid and lyophilized formulation development. Candidate is responsible for formulation screening studies, selection of container-closure systems, analysis for formulation screening studies, stability / degradation studies and documentation. Candidate is responsible for drug product manufacturing technology transfer activity to the manufacturing site including execution of the drug product batch manufacturing in collaboration with manufacturing team.

Job Location : Ahmedabad, Gujarat

Walk in Interview
Date and Time : 07/07/2024 : 09.00 am to 04.00 pm.
Venue : Hotel Greenpark, Begumpet Road, Leelanagar, Begumpet, Hyderabad, Telangana – 500016