Pharma QC Analyst — ELISA, UPLC & GMP Quality

HAL Allergy Group

Leiden

On-site

EUR 42,000 - 54,000

Full time

26 hours ago
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Benefits offered by this job

Competitive salary including 13th개월s
25 vacation days

Job summary

HAL Allergy Group in Leiden seeks a QC Analyst to join our Quality Control team. You will perform a range of analytical tests, document results and ensure GMP/GcLP compliance while supporting day-to-day lab activities.

The ideal candidate has an MLO-level degree in life sciences, hands-on lab experience, and strong communication in Dutch and English. You will contribute to method validation, deviations investigations and SOP updates, while maintaining accurate records.

Qualifications

  • MLO-level education in biochemistry, biotechnology, life sciences or related lab discipline.
  • GMP/GcLP knowledge and lab safety experience is preferred.
  • Analytical mindset, accuracy and teamwork with strong documentation skills.

Responsibilities

  • Perform immunochemical analyses such as ELISA, SDS-PAGE, Western Blot and ImmunoCAP.
  • Carry out spectrophotometric analyses and protein determinations (Bradford) with phenol and supernatant measurements.
  • Run physicochemical tests (pH, osmolality, visual quality inspections).
  • Operate chromatography (UPLC) with SEC; maintain GMP/GcLP-compliant documentation.
  • Document and report analytical results accurately; review compliance.
  • Support daily lab activities: inventory, equipment status tracking, logbooks.
  • Report deviations and participate in investigations, CAPAs and change controls.
  • Assist in equipment and system validation; help update SOPs.
  • Share knowledge and train colleagues.

Skills

Dutch & English communication

Education

MLO-level education in biochemistry, biotechnology, life sciences or related laboratory discipline

Tools

LIMS
MS Office

Job description

HAL Allergy Group in Leiden seeks a QC Analyst to join our Quality Control team. You will perform a range of analytical tests, document results and ensure GMP/GcLP compliance while supporting day-to-day lab activities.

The ideal candidate has an MLO-level degree in life sciences, hands-on lab experience, and strong communication in Dutch and English. You will contribute to method validation, deviations investigations and SOP updates, while maintaining accurate records.

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