Zydus Lifesciences – Walk-In on 26th March 2023 for QC / Production

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Zydus Lifesciences – Walk-In on 26th March 2023 for QC / Production

The Zydus Group with an overarching purpose of empowering people with freedom to live healthier and more fulfilled lives, is an innovative, global lifesciences company that discovers, develops, manufactures, and markets a broad range of healthcare therapies. The group employs over 23000 people worldwide and is driven by its mission to unlock new possibilities in life-sciences through quality healthcare solutions that impact lives. The group aspires to become a global life-sciences company transforming lives through pathbreaking discoveries. The group has manufacturing sites and research facilities spread across five states of Gujarat, Maharashtra, Goa, Himachal Pradesh and Sikkim in India and in the US and Brazil.

Zydus Lifesciences Walk In

  • Qualification: B.Sc, MS/M.Sc
  • Experience : 02-05+years
  • Department: QC/Production
  • Role: Officer / Executive
  • Job Location: Vadodara
Time and Venue:
26th March, 10.00 AM – 4.00 PM
Zydus API Park, Zydus Lifesciences Ltd, (Formerly known as Cadila Healthcare Ltd) Behind Bright Day CBSE School, Next to Kishan Classic, Vasna Bhayli Canal Road, Vadodara
Contact – D K Patel ()

Job description:

We are recruiting for our API Production plant located at Dabhasa, Nr Vadodara.

Production (API) : Officer / Executive

The incumbent should be B Sc (Chemistry) / DCE with 2 to 5 years of relevant experience in API production. Should have exposure in handling reactors, centrifuges and clean room equipment with sound knowledge in cGMP and SOPs. Should have exposure to regulatory requirement of documentation. Adherence to Quality, Safety, Health and Environment measures and GMP norms.

Quality Control (API) : Officer / Executive

The incumbent should have B Sc / M Sc (Chemistry) with 2 to 5 years of Relevant experience in analyses the Raw materials, In-process and intermediates finished product and stability samples. Expertise in handling HPLC, GC, UV, IR, KF, Melting point etc. Preparation of STP / SPC / SOP for QC documentation on a routine basis. Ensure the compliance, Safety and 100% Good laboratory Practices. Having aware of the current pharma procedure of cGMP, GDP, GCP and GLP practices follows in QC laboratory.

Desired Candidate Profile:

  • Candidates to have exposure in pharmaceutical company (API plant) and regulatory requirements of documentation and cGMP/GLP.
  • Interested candidates may Walk-in for an interview along-with their updated CVs, CTC break up and relevant documents as per the schedule.

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