Quality Control Analyst — Vaccine QC & Method Transfer

Gi Life Sciences

Land van Cuijk

On-site

EUR 28,792 - 47,988

Full time

14 days+

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Job summary

Gi Life Sciences in Boxmeer (Netherlands) is seeking a Quality Control Analyst to strengthen our QC Transfer team. You will perform and report biological QC tests on vaccines and related products, ensuring compliance with GMP in a regulated lab environment.

The role offers full-time, 40 hours per week with standard daytime hours, training and development in a highly specialized QC setting, and opportunities to contribute to method transfers and continuous improvement.

Qualifications

  • Completed laboratory education at least MBO level 4 in microbiology or biology.
  • At least 3 years of experience in a QC and/or GMP laboratory.
  • Hands-on experience with ELISA, PCR, microbiology, and cell culture.
  • Strong communication skills in Dutch and English, both spoken and written.
  • Accurate, quality-minded, proactive, flexible, and a strong team player.

Responsibilities

  • Perform, review, and report biological QC tests on intermediate and final products related to vaccines.
  • Apply techniques such as ELISA, cell culture, titrations, microbiological tests, PCR, and immunofluorescence.
  • Enter and manage test results in electronic data-processing and QC systems.
  • Review, verify, and release test results according to procedures and quality standards.
  • Identify, document, and report deviations in line with GMP procedures.
  • Contribute to method transfers, Tier meetings, and improvement projects using Lean and Six Sigma tools.

Skills

Quality control
GMP knowledge
Biological testing
Dutch language
English language

Education

MBO level 4 in microbiology or biology

Tools

ELISA
PCR
Cell culture
Microbiology

Job description

Gi Life Sciences in Boxmeer (Netherlands) is seeking a Quality Control Analyst to strengthen our QC Transfer team. You will perform and report biological QC tests on vaccines and related products, ensuring compliance with GMP in a regulated lab environment.

The role offers full-time, 40 hours per week with standard daytime hours, training and development in a highly specialized QC setting, and opportunities to contribute to method transfers and continuous improvement.

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