Zydus Group Walk-in On 17th Nov 2024 for Multiple Positions

Zydus Lifesciences Ltd. 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 26,000 people worldwide, including 1,400 scientists engaged in R & D, and is driven by its mission to unlock new possibilities in lifesciences through quality healthcare solutions that impact lives.

• Vacancy details:
• Department: Production and Quality Departments (Drug Substance)
• Positions Available: Executive / Senior Executive / Assistant Manager
• Experience: 2 – 10 years
• Qualification: M.Sc. / B.Tech / B.E / M.Tech in Biotechnology/ Biochemistry/Microbiology
• Salary:₹Not Disclosed

Job Description: Greeting from Zydus Lifesciences Ltd.!!!

Important Details :

• Work Location: Ahmedabad
• Post of date :11/11/2024
• Selection Process: The selection will be on the basis of Interview.
• Mode of Interview: Face to face
• Interview Rounds of Interview: HR

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

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.