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Exclusive Walk-In Interview For Multiple R&D Vacancies @ Zydus Cadila, Pune |Salary Upto Rs 7 Lakh p.a

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, Maharashtra, Goa, Himachal Pradesh and Sikkim and the R &D Centres are spread across Ahmedabad, Baroda and Mumbai (Thane)

Position 1

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Officer to Manager Vaccines

  • Quality Assurance (Vaccine): 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.
  • Quality Control (Vaccine): M.Sc. (Biotech / Microbiology / Chemistry) with 2-10 years of experience in Quality Control (QC) of vaccines/sterile injectables. Should have experience in QC Finished product testing / raw material testing / microbiological testing.

Position 2

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 & 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 I 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 records; Conduct of vendor audits and host regulatory inspections.
  • Non Clinical: M.Sc. / M.Pharm with 8 – 12 years of experience in QA (GLP). Should carry experience of review of SOPs, Study plan, final study reports; Conduct of Study based, process based & Facility based audits; Host regulatory inspections; be able to perform trend analysis of Audit findings, analyze and track Deviations, Non-conformances, Out of Specification, Change Controls and CAPA; conduct Quality Review Meetings.
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Position 3

Officer to Manager – Biologics

  • Quality Control : MSc. Biotechnology / Biochemistry/Microbiology with 2-15 years of hands on experience of conducting various analytical techniques in the various QC sections such as Bioassay, HPLC/UPLC, CZE, UV Spectrophotometer, SDS-PAGE, IEF, RT-PCR, ELISA, RM/PM testing, microbiological testing of material/products, sterility testing, BET, environmental monitoring of cleanroom, water system monitoring and microbiological validations/studies, should also have knowledge of handling stability studies and GMP documentation. Must be familiar with cGMP requirements and have good leadership quality.
  • Quality Assurance: B. Pharm / M. Pharm- M.Sc.( Biotechnology/Biochemistry / Microbiology ) with 2-8 years of hands on experience of 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.
  • Manufacturing (Downstream Process): MSc. Biotechnology / Biochemistry, M. Tech/B.Tech with Biotechnology / Biochemistry / Biochemical engineering with 2-8 years of hands on experience of handling equipment such as Chromatography systems, Ultrafiltration systems, Filtration Techniques etc. Should also have knowledge of GMP documentation. Must be familiar with cGMP requirements.
  • Manufacturing (Upstream Process): MSc. Biotechnology / Biochemistry, M. Tech/B.Tech with Biotechnology / Biochemistry / Biochemical engineering with 2-8 years of hands on experience of handling equipment such as Bioreactor, Disc Stack Centrifugation, Filtration Techniques etc. Should also have knowledge of GMP documentation. Must be familiar with cGMP requirements.
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Experience : 2 – 7 Years

Compensation : 2,25,000 – 7,00,000 P.A

How to Apply : 

Attend Walk-In Interview :

  • Date : 15.05.2016
  • Time : 9.00 HRS to 17.00 HRS
  • Venue : Lemon Tree Hotel, Hinjawadi
    P4, Rajiv Gandhi Infotech Park Phase 1, Hinjawadi, PuneInterested candidates may also email their resume to [email protected] or send it by courier to the Human Resource Department , Zydus Research Center ,Sarkhej Bavla NH 8 A , Moraiya, Taluka Sanand, Ahmedabad382213 within 7 days.

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