Materialise Medical in Plymouth is seeking a Quality Engineer to ensure the quality management system complies with FDA/QSR/MDSAP and ISO 13485. You will support SOPs, review change orders and NCMs, perform audits, and drive CAPA actions within a software-enabled medical environment.
The role emphasizes regulatory knowledge, meticulous documentation, and cross-functional collaboration with regulatory experts to maintain top-quality medical software products.
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Quality Engineer – Medical Devices (ISO 13485 + FDA) in Plymouth employer: Materialise NV
Materialise NV is an exceptional employer, offering a dynamic work culture that fosters innovation and collaboration in the orthopaedic field. With a strong focus on employee growth, you will have access to continuous professional development opportunities while working remotely from the UK, allowing for a flexible work-life balance. Join us to make a meaningful impact in healthcare by driving sales of cutting-edge custom implants and software solutions across leading orthopaedic centres.
