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Walk-In@ Pune for Vaccine Manufacturing and Quality Control

1 years

2 - 5 Lacs

Ahmedabad

Posted:1 month ago| Platform: GlassDoor logo

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Skills Required

manufacturing technology timing biotechnology microbiology testing chromatography electrophoresis spectrophotometer calibration compliance stability maintenance lims pcr documentation

Work Mode

On-site

Job Type

Part Time

Job Description

Division
VTC Mfg - MMR
Job posted on
Jun 23, 2025
Employee Type
P-P8-Probationer-HO Executive
Experience range (Years)
1 year - 6 years

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
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.


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