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Senior Human Factors/ Usability Engineer (m/f/d)
StrykerGermanyfull_timeVerifiedPosted 26 Nov 2024
About the role
Work Flexibility: Hybrid<p></p><p></p><p>As a Senior Human Factors Engineer (m/f/d), you will leverage your deep understanding of human performance and human factors techniques to evaluate and contribute to the development of our innovative medical devices. Collaborating with cross-functional teams, you will drive the integration of human-centered design principles throughout the product lifecycle. Your work will directly impact the usability and safety of medical devices that make a difference in patient outcomes and healthcare practices.</p><p></p><p><b>What you will do:</b></p><ul><li><p>Research, evaluate and validate medical device systems for safety and effectiveness.</p></li><li><p>Develop and execute Human Factors study protocols, including user interface evaluations.</p></li><li><p>Contribute to Product Risk Management and Human Factors support across the product lifecycle.</p></li><li><p>Plan and conduct end user evaluations, analyze data, and present design recommendations.</p></li><li><p>Demonstrate a deep understanding of customer needs and product usage.</p></li><li><p>Collaborate with stakeholders (clinical specialists, industrial designers, engineers, product& program managers, marketing, technical writers and vendors) to ensure project success and foster positive working relationships as a key member of the team.</p></li></ul><p></p><p><b>What you will need:</b></p><p><b>Required:</b></p><ul><li><p>Degree in Human Factors Engineering, Usability Engineering, Cognitive Psychology, Biomedical Engineering or similar.</p></li><li><p>2+ years of work experience in a highly regulated industry.</p></li><li><p>Familiar with requirement and verification practices and Requirements Management Tools.</p></li><li><p>Collaborative Team Player with strong communication skills to effectively convey highly technical information.</p></li></ul><p></p><p><b>Preferred:</b> </p><ul><li><p>Experience with relevant standards and regulations, such as ISO 62366-1, ISO 62366-2, 21 CFR part 820, and FDA guidance.</p></li><li><p>Certifications in usability and human subjects research.</p></li></ul><p></p><p>Diversity is important to us. We welcome applications from people regardless of their ethnic, national or social origin, gender, disability, age or sexual identity. </p><p></p><p>This position is initially <b>limited until the end of 2026.</b></p><p></p><p></p>Travel Percentage: 20%<p></p><p></p><p></p><p></p><p></p><p></p><p></p><p></p>
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