QA auditors
We are supporting a major GMP readiness programme across several manufacturing and QC sites in Leiden and Amsterdam. To strengthen inspection preparedness, we are assembling a team of experienced Quality Consultants who can perform daily mock audits, identify gaps, and ensure each site is fully prepared for upcoming regulatory inspections.
Dutch language skills are strongly preferred, and we are specifically looking for professionals who are already based in the Netherlands and able to travel between sites as needed.
Role Overview
We are seeking multiple Quality Consultants to support our client across several production and laboratory sites in Leiden and Amsterdam. This project is critical in preparing for upcoming Health Authority inspections. Consultants will play a key role in ensuring compliance readiness through daily oversight, structured mock audits, and hands‑on quality support.
Key Responsibilities
- Conduct daily mock inspections to assess audit readiness and identify compliance gaps.
- Perform Gemba Quality Walks with clear, documented evidence.
- Review and verify logbooks and batch‑related documentation daily.
- Check cleaning procedures and records, ensuring adherence to GMP standards.
- Assess operator SOP knowledge and practical application, documenting findings.
- Ensure dedicated "Quality Time" for operators and managers to complete required quality tasks.
- Provide real‑time feedback and support to operational teams to strengthen inspection readiness.
Requirements
- Proven GMP Quality background within pharma, biotech, ATMP, or other regulated manufacturing environments.
- Strong experience with inspections, audits, mock audits, and compliance activities.
- Ability to work full‑time on site across multiple locations (Leiden & Amsterdam).
- Dutch language skills preferred; English also required.
- Must already have the legal right to work in the EU - no sponsorship available.
- Based locally in the Netherlands and able to travel between sites as needed.
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