ZYDUS LIFESCIENCES LTD Walk-in Interview .ZYDUS LIFESCIENCES LTD Notification full details below.Interested and eligible candidates can attend Interview on scheduled time and venue..
Vacancy details:
- Department: Vaccine Manufacturing (Cell Culture)/Quality Control (Bacterial/Viral)
- Qualification: – Post-Graduate M.Sc. in Biochemistry, Biotechnology, Microbiology, Lifesciences.
- Experience: 1-6 years of hands-on experience in relevant field, preferred Vaccine/Biotech background.
Important Details :
- Selection Process: The selection will be on the basis of Interview.
- Mode of Interview: Face to face
- Interview Rounds of Interview: HR
Greeting from ZYDUS LIFESCIENCES LTD..!
Walk In Interview for Vaccine Technology Center @ Pune
Venue:Radisson Blu Pune Hinjawadi,136/1, Near Mahindra International School, Phase1, Hinjawadi, Pune.
T: +91 020 69528000, M: +91 7888013458
Date: – 29.06.2025 (Sunday)
Timing: – 9:00 AM to 5:00 PM
Vaccine Manufacturing (Cell Culture)
Responsible for cell revival, subculture, cell counting of MRC-5 cells.
Preparation of MCB/WCB. Experience in Preparation of media and in process buffers in media mixing vessels.
Experience in handling Roller bottles, Cell stacks, TCF’s.
Experience in working in GMP conditions / production department of viral vaccines.
Preparation of SOP, BMR’s, Protocols related to cell culture / virus culture.
Experience in virus infection, virus harvesting procedures.
Experience in working with Chicken embryo fibroblast cells, pooling of embryos, seeding of RB’s .
Quality Control (Bacterial/Viral)
Candidate should have good knowledge of Product testing techniques like : Biochemical, Chromatography, Electrophoresis, Immuno assay, Cell culture & Molecular techniques
Experience in handling HPLC, Dionex, UV-Spectrophotometer, Multimode plate reader and ELISA
–Shall be well versed with Biochemical assays (Protein, O-acetyl) immuno-chemical assays and electrophoresis,
-Knowledge in calibration and qualification of equipment and instruments.
-To perform/ monitor activities in compliance with GMP/GLP/GDP and record keeping.
-Experience in preparing SOPs, Specification, STPs and Study protocols
To prepare method validation protocol and execute method validation.
Experience in handling stability studies and maintaining records.
Role shall require to coordinate with engineering/ maintenance department or third party labs as and when required.
Should possess basic skills in MS-Office, LIMS & SAP
Analyst shall be well versed with cell based assays, Virus titration, RTPCR and immuno-chemical assays.
=Instrument knowledge on pH meter, Analytical balance, Karl Fischer, Real time PCR and ELISA
Knowledge in calibration and qualification of equipment and instruments.
Experience in handling QMS elements like OOS, OOT, change control and deviation are added advantage.
To perform/Monitor activities in compliance with GMP/GLP.
Experience in preparing SOPs, specification and study protocols
To prepare protocol and execute method validation
Experience in handling stability studies and maintaining Good documentation practice.
=Role shall require to coordinate with maintenance department or third party lab as and when required.