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 Life sciences Ltd.
USP / DSP - Production / Quality Assurance / Quality Control
Post : Executive / Senior Executive / Assistant Manager / Dy. Manager
USP & DSP - Production (M.Sc Biotech / Btech Biotech / B.E Biotech)
USP Production : Candidates must have 2-14 years of experience in aseptic handling of mammalian cell culture, media / feed preparation and its filtration, readiness of bioreactor and associated vessels (CIP. FIT. PHT. SIP), operation of bioreactor, readiness and operation of centrifuge, clarification of cells and manufacturing of monoclonal antibodies / bio therapeutic protein.
DSP Production : Candidates must have 2-14 years of experience in downstream purification process for recombinant products. TFF system, chromatography system, depth filtration procedures. CIP / SIP of the equipment.
Quality Assurance (M.Sc. Biotech / B.Pharm / M.Pharm)
QA Oversight manufacturing (IPQA) : Candidates must have 2-4 years of hands on experience in QA oversight (IPQA) related activities for drug substance manufacturing alongwith handling of process validations, cleaning validations 00S. change control, deviation, investigation. CAPA and QMS activities.
QMS : Candidates must have 6-8 years of experience with hands on experience in QMS related activities like failure investigation, quality events handling and investigations, change control, market complaint, conducting self-inspection. APQR, 00S / 00T trending etc.
Documentation cell : Candidates must have 6-8 years of experience with hands on experience in handling and controlling of various GMP documents (issuance / control / retrieval / archival). Candidates should be responsible to retain all master / executed documents in document storage room with adequate indexing and keep ready documents for the regulatory audit(s).
Assistant Manager / Dy. Manager / Associate Manager QC Chemical (M.Sc Biotech) : Candidates must have 8-12 years of experience with hands on experience in reviewing of protein analysis / instrumentation, molecular biology, bioassay and GLP activity related documents. Candidates should be responsible to review all the documents, test reports, calibration report records, logbooks, and formats in relation to the activity of protein analysis / instrumentation, molecular biology, bioassay. GLP and filling. They should also be responsible to carry out investigation of incident, deviation and OOS generated during laboratory analysis and to prepare and review ATR and COA for the batch data.
Job Location : Zydus Biotech Park at Ahmedabad
For all the above positions, candidates having exposure to regulatory requirement of documentation and cGMP / GLP is essential.
Interested candidates can send in their updated CV alongwith current and expected CTC to ruchi.lal@zyduslife.com on or before 30th April 2022.
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