Location: Nijmegen – The Netherlands
Work model: On-site
Employment type: Full-time
About the role
For a regulated pharmaceutical and MedTech environment in the Nijmegen region, we are looking for a QC Analyst.
In this role, you contribute to the accuracy, reliability and quality of an innovative product used by patients worldwide. You will perform analytical QC testing, maintain the QC laboratory and ensure that all work is carried out in compliance with applicable quality and regulatory standards.
You will be part of the Quality Control team and collaborate closely with manufacturing, compliance and cross-functional colleagues. This is an on-site role with flexibility for occasional evening shifts.
Key responsibilities
- Perform maintenance and calibration of HPLC equipment and general laboratory instruments.
- Ensure the cleanliness, organisation and proper maintenance of the QC laboratory.
- Conduct analytical tests, including HPLC, pH measurements, Size Exclusion Chromatography, bioburden testing and Particle Distribution Analysis.
- Conduct, interpret and document NMR analyses.
- Inspect and verify labels and incoming goods to ensure compliance with specifications and quality standards.
- Document and report test results according to standardised protocols and applicable guidelines.
- Work in compliance with GxP, safety and laboratory procedures.
- Collaborate with manufacturing, compliance and other quality-related teams.
- Contribute to continuous improvement within the QC laboratory environment.
Requirements
You are accurate, analytical and quality-minded. You understand the importance of reliable test results, traceable documentation and compliance in a regulated laboratory environment.
You can work independently, communicate clearly and remain effective in a dynamic setting. You are proactive, eager to learn and willing to contribute ideas for continuous improvement.
Your background
- Bachelor’s degree in Chemistry or a related scientific discipline.
- 2 to 3 years of experience in Quality or Quality Control is required.
- Experience with NMR is required, preferably with polymers.
- Experience with HPLC is required.
- Experience in a pharmaceutical, MedTech or other regulated environment is preferred.
- Knowledge of GxP is preferred.
- Willingness to work flexible hours, including occasional evening shifts, is essential.
- Accurate, detail-oriented and able to follow laboratory procedures carefully.
- Strong communication skills and a team-oriented working style.
- Able to work independently in a dynamic environment.
- Fluent in English, both written and spoken.
What you can expect
You will work in an international, quality-driven laboratory environment where analytical accuracy, compliance and continuous improvement are central.
The role offers varied QC work, responsibility and the opportunity to contribute to the quality of an innovative product used by patients worldwide. You can expect specialist training, development opportunities, good employment conditions and a collaborative working environment.