Design Quality Engineer (DQE) - Medical Devices - Belgium - Contract
Kortrijkonsitemid
Posted 15mo ago · via Teamtailor
About this role
We are seeking a Design Quality Engineer (DQE) to support R&D teams in transitioning from non-medical to medical device development. This role is critical in ensuring compliance with medical device regulations ( ISO 13485, 510K, IEC 62304, risk management, usability, clinical evaluation ) for key projects. Reporting to the PMO Lead, you will play a key role in technical file development, regulatory alignment, and cross-functional facilitation. Key Responsibilities Develop and maintain technical files for medical device projects. Collaborate with project managers, software architects, security teams, and usability engineers. Act as a liaison between R&D and QARA teams, ensuring regulatory clarity. Coach and mentor teams on best practices in IEC 62304 and related standards.…
What we'd score you on
reqspace match rubricFive dimensions, recruiter-grade. Upload your resume and we'll generate a written explanation of where you fit and where the gaps are.
1
Skills match
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2
Level fit
This role is mid-level. We check your trajectory against it.
3
Domain experience
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4
Recency
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5
Location fit
This role is based in Kortrijk. We weight your proximity and willingness to relocate.
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