Our client is a regulated manufacturing organization operating within the pharmaceutical/medical device industry, focused on quality, compliance, and continuous improvement.
Role OverviewAs 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.
Key Responsibilities- 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.
#J-18808-LjbffrSalarisomschrijving
€50000 - €70000 monthly