Zydus Lifesciences- Interview for Ph.D, M.Pharm, MSc, MTech in Biotech R&D, Manufacturing on 29th Sept’ 2024
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.
Walk – in interview at Bangalore (Biotech – R & D and Manufacturing based at Ahmedabad)
Biotech R&D
Protein characterization – Analytical : M.Sc. / M.Tech. (Biochemistry / Biotechnology) with at least 5 years of industrial hands-on experience in protein characterization including HPLC, structural, and biochemical techniques. Sound knowledge in analytical method development, validation, technology transfer activity and scientific report writing skills.
Upstream Process : M.Sc. (Microbiology/Biochemistry/Biotechnology)/ M. Tech. with Biotechnology with 1 to 7 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.
Downstream processing and Antibody drug conjugate : PhD / M.Sc. / M. Tech. (Biochemistry/ Biotechnology/ Life sciences) with 2 – 8 years’ hands-on experience in protein purification techniques like centrifugation, depth filtration, lab scale column purification, ultrafiltration/diafiltration. Handling of equipment’s such as AKTA Avant, AKTA Pure, AKTA Pilot, Automatic TFF system, High throughput screening system, Isolator, Membrane chromatography. Capable of performing activities such as resin screening and process optimization for Mab and ADC at small-scale and pilot scale. Good Communication and documentation (SOP /BMR /TTD/purification report) skills etc.
In-process analysis and stability group : Ph.D., M.Sc., M. Tech, M. Pharm Biotechnology / Biochemistry or equivalent with 3 – 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.
Biotech Manufacturing :
USP Production
M.Sc./ B. Tech/B. E/ M. Tech – Biotechnology/Biochemistry with 2 – 10 years of experience in handling of large-scale mammalian cell culture (SS bioreactor), media/feed preparation and its filtration. The job requires readiness of bioreactor and associated vessels (CIP, FIT, PHT, SIP), operation of bioreactor & associated vessels, readiness and operation of centrifuge, clarification of cells for manufacturing of monoclonal antibodies/ bio therapeutic protein.
DSP Production
M.Sc./B.Tech/ B. E/ M. Tech – Biotechnology/Biochemistry Candidates with 2-10 years of experience in downstream purification process for recombinant products, TFF system, chromatography system, virus filtration procedures and CIP/SIP of the equipment.
QMS Production
M.Sc./B.Tech/ B. E/ M. Tech – Biotechnology/Biochemistry Candidates with 2-15 years of experience in Preparation of risk assessment and investigation report. Meetings with cross functional team to identify the root causes of deviation, OOT and OOS. Initiation and/or review, closing of the QMS document such as deviation, change control and CAPA using Trackwise or similar software. Regular discussion with manufacturing team to reduce the human errors which leads to deviation. Preparation and/ or review of cGMP documents such as MFR, BMR, SOP etc.
For all above positions, candidates having exposure to regulatory requirement of documentation and cGMP/GLP is essential. Preference will be given to those who have thorough knowledge of all the manufacturing operations of Biosimilar products.
Walk – in interview
Date : 29th September 2024 (Sunday)
meet you in person on below address from 8 am to 4.30 pm
Starlit Suites – Bengaluru
220 Tripadvisor reviews · 3-star hotel
No E39/275, Smondo Complex, Neo Town, Near Fire Bridge, Electronic City, Bengaluru, Karnataka 560100.