Quality Engineer – GMP Pharmaceutical

About the role

Join MindCapture as a Quality Engineer and support essential quality processes within a GMP‑regulated pharmaceutical site. You will work on batch record review, CAPA follow‑up, incident management and documentation support, ensuring operations remain compliant, efficient and patient‑focused.

Key responsibilities

• Review paper‑based batch records accurately and on time.
• Assist in managing CAPA actions and tracking progress.
• Support investigations linked to quality incidents and events.
• Contribute to structured root‑cause analysis activities.
• Perform impact assessments to aid decision‑making.
• Maintain and support the documentation management system.
• Coordinate training activities and ensure compliance.
• Support GMP‑aligned quality processes.

Required profile

• 1‑4 years of experience in a quality role within a GMP‑regulated pharmaceutical environment.
• Knowledge of CAPA, incident and event management.
• Experience with root‑cause analysis and impact assessment.
• Familiarity with documentation management systems and paper‑based batch record review.
• Strong communication skills in Dutch.
• Willingness to work on‑site in Puurs.
• Junior to medior mindset with a practical approach.

Required skills

• CAPA management
• Incident investigation
• Root‑cause analysis
• Impact assessment
• Documentation management systems
• Batch record review
• GMP compliance

What we offer

• Competitive salary with full benefits (meal vouchers, eco vouchers, health and group insurance, net expense allowance, company car with charging or fuel card).
• Personal growth support through tailored training and clear career development.
• Stable environment where technical skills directly improve patient care.
• Opportunity to work with high‑tech diagnostic systems at top‑tier healthcare institutions.
• Warm, collaborative culture focused on trust, ownership and long‑term impact.