Walk-In@ Pune for Vaccine Manufacturing and Quality Control

Department
VTC Mfg - MMR
Job posted on
Jun 23, 2025
Employment type
P-P8-Probationer-HO Executive

Walk In Interview for Vaccine Technology Center @ Pune

Venue:
Radisson Blu Pune Hinjawadi
136/1, Near Mahindra International School, Phase1, Hinjawadi, Pune.
T: ++1 020 6+528000, M: ++1 7888013458

Date: - 2+.06.2025 (Sunday)
Timing: - +: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)
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.