Senior QC Chemist: Lead Chemical Testing & Compliance

Prothya Biosolutions Netherlands B.V

Netherlands

Remote

EUR 65,000 - 90,000

Full time

31 hours ago
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Benefits offered by this job

End-of-year bonus 8.33%
Holiday allowance 8.33%
Training budget €2,100 every 3 years
Travel expenses from first kilometer
Pension plan Zorg & Welzijn
Excellent transport accessibility and/

Job summary

Prothya Biosolutions Netherlands B.V is seeking a QC Senior Analyst - Chemistry to ensure GMP-compliant testing of materials and products. You will perform routine and non-routine analyses, document results, and support investigations in a collaborative QC lab environment.

You will interpret data, assist CAPA drives, maintain equipment, and help train junior staff while coordinating with QA, Manufacturing and Regulatory teams. A strong background in HPLC/GC/UV-Vis/FTIR is required.

Qualifications

  • MLO or Bachelor’s degree in chemistry or related field.
  • 5+ years in a pharmaceutical laboratory, GMP-regulated preferred.
  • Strong knowledge of HPLC, GC, UV-Vis and FTIR.

Responsibilities

  • Perform routine and non-routine chemical testing of materials and products.
  • Document results and deviations in GDP/GMP compliant records.
  • Interpret data and support investigations and CAPA activities.
  • Maintain calibration and qualification of testing equipment.
  • Collaborate with QA, Manufacturing, Regulatory in product release and audits.
  • Develop and validate testing methods to ensure accuracy and reproducibility.
  • Provide guidance and training to junior staff; oversee lab operations.

Skills

HPLC
GC
UV-Vis
FTIR
Data analysis (SAP Empower)
Attention to detail
Regulatory knowledge
Cross-functional collaboration

Education

MLO or Bachelor's degree in chemistry

Tools

SAP
Empower

Job description

Prothya Biosolutions Netherlands B.V is seeking a QC Senior Analyst - Chemistry to ensure GMP-compliant testing of materials and products. You will perform routine and non-routine analyses, document results, and support investigations in a collaborative QC lab environment.

You will interpret data, assist CAPA drives, maintain equipment, and help train junior staff while coordinating with QA, Manufacturing and Regulatory teams. A strong background in HPLC/GC/UV-Vis/FTIR is required.

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