Zydus Cadila is one of India's leading healthcare companies and a global healthcare provider with strengths all along the pharmaceutical value chain. The group’s state-of-the-art manufacturing infrastructure is spread across five states of Gujarat, Maharasahtra, Goa, Himachal Pradesh and Sikkim and the R&D Centers are spread across Ahmedabad, Baroda and Mumbai (Thane).
We invite candidates for the following positions based at Ahmedabad for our Zydus Research Centre (ZRC), Zydus Biologics (ZB) and Vaccine Technology Centre (VTC).
Supervisor to Manager - Vaccines
Quality Assurance: M.Sc. (Biotech / Microbiology) with 2-10 years of experience in Quality Assurance (QA) of vaccines/ sterile injectables. Should also have experience in QA operations/ QMS/ validation/ qualification/ documentation/ compliance.
Officer to Manager - Corporate Research Quality Assurance
Clinical Trials: M.Sc./M.Pharm with 5-12 years of experience in QA. Should carry experience of investigator site audits, review of SOPs, clinical trial study protocols (Phase I-IV), reports, raw data like informed consent forms, medical screening records, patient diaries, clinical case record forms, SMF, TMF; review of data management plan, statistical analysis plan; conduct vendor audits and host regulatory inspections.
Clinical (BA / BE, Phase I and Clinical Pathology): M.Sc/ M.Pharm with 3-5 years of experience in QA. Should carry experience of conducting various clinical audits (study based, facility based) of BA/BE & Phase/studies in GCP sections (clinical research, clinical pathology lab. PK/Stat); review of SOPs, study protocols, IBs, study data (ICFs, screening records, TMFs etc.). study reports, change controls, deviations, amendments, manuals, validation reoords; conduct vendor audits and host regulatory inspections
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Supervisor /Officer /Executive /Sr. Executive /Manager - Biologies
Quality Control: MSc. Biotechnology / Biochemistry / Microbiology with 2-15 years of hands-on experience in conducting analytical techniques in the various QC sections such as bioassay, HPIC / UPLC, CZE, UV spectrophotometer, SDS-PAGE, IEF, RT-PCR, ELISA, RM/PM testing, microbiological testing of material/products, sterlity testing, BET, environmental monitoring of Cleanroom, water system monitoring and microbiological validations/studies. Should also have knowledge of handing stability studies and GMP documentation and must be familiar with cGMP requirements and have leadership qualities.
Quality Assurance: B.Pharm/M.Pharm, M.Sc. (Biotechnology/ Biochemistry/ Microbiology) with 2-8 years of hands-on experience in IPQA activities, reviewing of batch manufacturing records, handling of qualification/ validation activity, change control, deviation, investigation, CAPA, vendor qualification activities. Must be familiar with cGMP requirements
Walk-in-interview
Date: 6th March, 2016
Time: 9 am to 5 pm
Venue: The Hotel Pride Judges Bungalow Road, S.G. Road, Bodakdev, Ahmedabad - 380 054
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