QA Validation

Our client is a regulated manufacturing organization operating within the pharmaceutical/medical device industry, focused on quality, compliance, and continuous improvement.

As a Quality Assurance professional, you will be responsible for managing and continuously improving the quality management system while supporting Engineering, R&D, and Production activities in a highly regulated environment.

• Manage QMS, change control, CAPA, and non-conformities
• Ensure compliance with GMP, MDR/MDD, ISO standards
• Support validation of equipment and processes
• Perform risk analyses and support design reviews
• Drive continuous improvement based on data and trends

• Bachelor’s degree or equivalent experience
• 4–6 years QA experience in pharma or medical devices
• Strong knowledge of GMP, ISO 13485, MDR/MDD
• Experience with validation and risk management
• Excellent English communication skills
• Dutch language skills
• Experience with audits or regulatory inspections
• Lean / Six Sigma knowledge

Are you looking for a QA role with ownership, variety, and impact? Apply now or reach out to learn more.