
Walk-in@ Pune for Vaccine Manufacturing and Quality Control
1 week ago
Division
- VTC Mfg - MMR
- Job posted on
- Jun 23, 2025
- Employee Type
- P-P8-Probationer-HO Executive
- Experience range (Years)
- 1 year - 6 years
**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**
Ø **Education: - Post-Graduate M.Sc. in Biochemistry, Biotechnology, Microbiology, Lifesciences.**
Ø **Experience: - 1-6 years of hands-on experience in relevant field, preferred Vaccine/Biotech background.**
**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)**
- 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.
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