Working closely with multidisciplinary teams including Research & Development, Engineering, Manufacturing, Regulatory Affairs, and external partners, you will contribute significantly to the development of next-generation medical technologies that improve patient outcomes and meet the highest quality standards. * Close interdisciplinary collaboration to ensure safe, effective, and reliable medical device designs. * Participate in and facilitate risk assessments, including Design and Process FMEAs. * Bachelor's degree, Master's degree, or equivalent technical qualification in Engineering, Biomedical Engineering, Life Sciences, Quality Management, or a related discipline. * Experience in Quality Management, Quality Engineering, or Product Development Quality, preferably
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