LOCATION(S) – REMOTE IN BELGIUM OR THE NETHERLANDS

• Are you passionate about quality and compliance in a clinical laboratory setting?
• Do you thrive in a role where you can shape quality processes and ensure regulatory excellence?
• Looking for a high-impact opportunity within a global clinical research organization?
  At Cerba Research, our Quality Assurance team is hiring. We are looking for a QA Manager – Specialty Lab to play a pivotal role in ensuring regulatory compliance and high-quality standards across our laboratory sites in France.

YOUR RESPONSIBILITIES

• Ensure regulatory adherence to GCLP, ISO 15189, GCP, and GLP standards.
• Oversee document control, procedural updates, and validation reports.
• Lead internal audits and coordinate external regulatory inspections.
• Manage non-conformance investigations and implement CAPA actions.
• Monitor quality performance metrics and identify improvement opportunities.
• Develop and deliver training programs for laboratory staff on QA standards.
• Work cross-functionally with PMs, R&D, and global QA teams to align quality initiatives.
  Travel: Regular travel to France is required – initially on a weekly basis, then reducing to every 2-3 weeks.
  You are a solutions-driven QA professional with a strong background in laboratory operations and regulatory compliance. You thrive in a dynamic environment and are comfortable leading quality initiatives.

You will need:

• QA experience in a laboratory or clinical research setting.
• Strong knowledge of GCLP, GCP, GLP. With ISO 15189/9001 being advantageous.

As a Quality Assurance Manager, you will play a key role in:

• Strengthening quality management systems across our specialty histopathology labs in France.
• Driving internal audits, supplier quality management, and CAPA implementation.
• Supporting the development and continuous improvement of QA processes.
• Collaborating with global QA teams, R&D, and project management teams to maintain compliance and efficiency