Salary
💰 €35,000 - €43,000 per year
About the role
- Conduct analytical testing using validated procedures and calibrated instruments (including HPLC with Chromeleon 6.8/7.2)
- Perform finished product (FP) release analysis and evaluate test results against specifications
- Ensure compliance with GLP, GMP, approved SOPs and good documentation practices
- Prepare analytical reports, CoAs, audit reports, and method transfer documentation
- Complete and maintain accurate online documentation and GMP records
- Maintain laboratory cleanliness, safety, and dispose of samples/solutions per SOPs
- Support calibration, qualification, and validation activities; draft/review SOPs and maintain lab equipment
- Participate in continuous improvement projects, cost-saving and process simplification initiatives
- Report to Head QA/QC and interact with QA, Lab Planning, Lab Assistants, and external service engineers
Requirements
- European citizenship or valid EU work authorization (based in the Netherlands preferred)
- B.Sc., M.Sc., or B.Pharm (Chemistry)
- 1–2 years experience in pharmaceutical QC
- Preferred: 1 year experience in MDI / DPI / Nasal / Respiratory formulations
- Proficient in HPLC analysis and Chromeleon 6.8 / 7.2
- Knowledge of GLP, GMP, SOPs, and good documentation practices
- Experience with finished product (FP) release analysis and testing against specifications
- Ability to prepare analytical reports, Certificates of Analysis (CoAs), and method transfer documentation
- Experience in sample handling, preparation, and laboratory safety
- English language proficiency