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.
Inviting candidates for Executive / Senior Executive post in Quality Control / Quality Assurance for Zydus Biologics (Zydus Biotech Park) at Ahmedabad
For all the positions mentioned candidates should have 2-6 years of experience and should be from M.Sc - Biotech / M.Sc Micro / M.Sc Biochemistry background.
QC Chemical : Candidates should have experience in analysis of protein analysis / instrumentation, molecular biology, bioassay and lab activity related documents. They would be responsible for reviewing all the documents, test reports, calibration reports records, logbooks and formats in relation to the activity of protein analysis / Instrumentation, molecular biology, bioassay and filling. They would also be responsible for carrying out investigation of incident, deviation and OOS generated during laboratory analysis.
QC Microbiologist : Should be responsible for environmental monitoring (air sampling, settle plate, surface monitoring and personnel monitoring) / water testing / bio assay / BET test / MLT / sterility testing etc.
IPQA : Candidates should have experience in QA oversight (IPQA) related activities for drug substance manufacturing along with handling of process validations, batch release activities, cleaning validations, process investigation, OOS / OOT investigation, change control, deviation, CAPA and QMS activities.
QMS : Experience in QMS related activities like failure investigation, quality events handling and investigations, change control, market complaint, conducting self- inspection, APQR, OOS / OOT trending etc.
QA Analytical : Should have experience in reviewing of analytical batch docket / reports, stability protocols and data sheets, laboratory investigation, reviewing and involvement in investigation of OOS, OOT, OOC results, handling of incidents, deviations, Change Controls in the laboratory alongwith reviewing of all types of calibration / qualification documents and reviewing / oversight implementation of all lab standard operating procedures.
Documentation cell : Experience in handling and controlling of various GMP documents (issuance / control / retrieval / archival). Candidates should be responsible for retaining all master / executed documents in document storage room with adequate indexing and keeping ready all the documents for the regulatory audit(s). For all above positions, candidates having exposure to regulatory requirement of documentation and cGMP / GLP is essential.
Job Location : Ahmedabad
The last date for applying is 20th September 2023.
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