Zydus Biologics – Walk-In Interviews for Production / QC / IPQA on 17th Nov’ 2024

Zydus Lifesciences Limited, The Zydus Group with an overarching purpose of empowering people with freedom to live healthier and more fulfilled lives, is an innovative, global Lifescience 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.

Walk-In Interviews in Pune on 17th Nov 2024 (Sunday) for Production and Quality Departments (Drug Substance) at Zydus Biologics, Ahmedabad.

Job Description:

• Positions Available: Executive / Senior Executive / Assistant Manager
• Qualification: M.Sc. / B.Tech / B.E / M.Tech in Biotechnology/ Biochemistry/Microbiology
• Job Location: Ahmedabad
• Experience: 2 – 10 Years

Walk-In Interview Details:

• Date: 17th Nov 2024 (Sunday)
• Time: 8:30 AM to 5:00 PM
• Venue: Hotel Radisson Blu, 136/1 Hinjewadi Phase 1 Rd, behind Mahindra International School, Phase 1, Hinjawadi Rajiv Gandhi Infotech Park, Hinjawadi, Pune, Pimpri-Chinchwad, Maharashtra 411057.
• Contact Number: 020-69528000

Job Profiles:

USP Production:

• Experience with large-scale mammalian cell culture (SS bioreactor), media/feed preparation, and filtration. Role includes bioreactor readiness, CIP/FIT/PHT/SIP procedures, centrifuge operation, and clarification of cells for monoclonal antibody/bio-therapeutic protein manufacturing.

DSP Production:

• Experience in downstream purification for recombinant products, including TFF systems, chromatography, virus filtration, and CIP/SIP equipment.

QMS Production:

• Proficiency in risk assessment and investigation reporting, root cause analysis, and QMS document management (e.g., deviations, CAPA) using Trackwise or similar systems. Regular collaboration with the manufacturing team to mitigate human errors and ensure accurate cGMP document preparation.

IPQA

• Experience in QA oversight for drug substance manufacturing, warehouse, and shop floor activities.

Q.C. Chemical Analyst

• Experience in protein analysis, HPLC, capillary electrophoresis, molecular biology, and bioassays. Responsibilities include reviewing lab documentation, conducting incident/deviation/OOS investigations during lab analysis, and ensuring compliance with lab procedures.

Additional Requirements for All Positions

• Candidates must have experience with regulatory documentation and cGMP/GLP standards. Preference will be given to candidates knowledgeable in Biosimilar product manufacturing operations.

Note:

1. Employees will work in shifts based on allocation. Shift deployment for male candidates will be A/B/C.
2. Candidates should bring: a recent resume, relevant qualification certificates/mark sheets, PAN Card, Aadhar Card, latest increment letter, previous experience letters (if any), and last three months’ salary slips.

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