Quality Engineer

A great opportunity has opened up with one of our clients in the medical device industry. We’re 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