Requirements: English
Company: Barrington James
Region: Antwerpen , Flanders
A great opportunity has opened up with one of our clients in the medical device industry. Were looking for a skilled Quality Engineer to support and strengthen their Quality team. This is a permanent position based onsite not far from Antwerp, with a focus on supplier quality, risk management, and compliance within development and production.
Key Responsibilities:
- Leading quality assurance efforts throughout design and development projects
- Managing supplier qualification and conducting supplier audits (ISO 13485, MDR, ISO 14971)
- Acting as subject matter expert for product risk management
- Supporting design change evaluations to ensure compliance with regulatory standards
- Maintaining quality agreements with suppliers and external partners
- Collaborating with R&D and production teams to ensure manufacturing quality
- Acting as a back-up for the Quality Manager Product Lifecycle
- Driving continuous improvement and supporting internal/external audits
Key Requirements:
- Degree in Engineering, Life Sciences, Pharmacy or equivalent experience
- 5+ years of experience in a Quality or Supplier Quality Engineering role within medical devices (pharma is a plus)
- Strong understanding of ISO 13485, MDR, ISO 14971 (GMP knowledge a bonus)
- Proven experience in supplier qualification and auditing
- Excellent communication and stakeholder engagement skills
- Fluent in English (Dutch speaking/French is a plus)
Why Apply:
- A dynamic, forward-thinking environment
- High-impact role with autonomy and ownership
- Strong career development opportunities
- Competitive compensation package
- Up to 42 days Annual Leave
If you''re a Quality Engineer with over 5 years experience in Medical Devices, we''d love to hear from you! Apply now or reach out for more details.
Apply to be considered!
lcattcamfield@barringtonjames.com
+44 (0) 1293 243847