- Temporary
- Full Time
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Why join Stryker?
Looking for a place that values your unique talents? Discover Stryker's award-winning culture.
We are proud to offer you our total rewards package which includes bonuses, healthcare, insurance benefits, retirement programs, wellness programs, as well as service and performance awards – not to mention various social and recreational activities, all of which are location specific.
Job description
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.
What you will do:
Research, evaluate and validate medical device systems for safety and effectiveness.
Develop and execute Human Factors study protocols, including user interface evaluations.
Contribute to Product Risk Management and Human Factors support across the product lifecycle.
Plan and conduct end user evaluations, analyze data, and present design recommendations.
Demonstrate a deep understanding of customer needs and product usage.
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.
What you will need:
Required:
Degree in Human Factors Engineering, Usability Engineering, Cognitive Psychology, Biomedical Engineering or similar.
2+ years of work experience in a highly regulated industry.
Familiar with requirement and verification practices and Requirements Management Tools.
Collaborative Team Player with strong communication skills to effectively convey highly technical information.
Preferred:
Experience with relevant standards and regulations, such as ISO 62366-1, ISO 62366-2, 21 CFR part 820, and FDA guidance.
Certifications in usability and human subjects research.
Diversity is important to us. We welcome applications from people regardless of their ethnic, national or social origin, gender, disability, age or sexual identity.
This position is initially limited until the end of 2026.