Quality Officer – Pharmaceutical Projects

About the role

We are seeking a Quality Officer to join our pharmaceutical projects in Belgium. You will ensure that products and processes meet GMP regulations and internal quality standards while supporting continuous improvement across cross‑functional teams.

Key responsibilities

• Ensure compliance with GMP requirements and company quality standards.
• Review and approve quality documentation such as procedures, records, and reports.
• Support investigations of deviations, non‑conformities, and CAPA implementation.
• Participate in internal audits and assist during regulatory inspections.
• Monitor quality processes, identify improvement opportunities, and contribute to the QMS.
• Collaborate with Production, QC, Engineering, Validation, and Supply Chain teams.
• Support change controls, risk assessments, and quality‑related projects.

Required profile

• Bachelor's or Master's degree in Pharmacy, Chemistry, Biology, Biotechnology, Engineering or a related scientific field.
• Experience in a quality role within the pharmaceutical or another GMP‑regulated industry.
• Strong analytical, problem‑solving, communication and teamwork skills.
• Proactive, detail‑oriented and quality‑driven mindset.
• Good command of English; Dutch and/or French are a plus.

Required skills

• Good knowledge of GMP regulations.
• Experience with deviations, CAPA, change controls and quality documentation.

What we offer

• Permanent employment contract with stability and security.
• Individual profit sharing.
• One‑on‑one coaching and tailored training.
• Access to a strong technical network and an entrepreneurial lab.