> Markdown version of [/jobs/ext/4542112-usability-engineer](https://www.wearedevelopers.com/jobs/ext/4542112-usability-engineer). Every page supports `.md` or `Accept: text/markdown`. Links point to the HTML versions so they work for humans too. Agent guide: [/agents.md](https://www.wearedevelopers.com/agents.md). --- # Usability Engineer - **Company:** Transcend Softech LLC - **Location:** Cleveland, OH, United States - **Experience:** Experienced - **Contract:** Temporary contract - **Skills:** Systems Engineering, Cognitive Psychology, Failure Mode Effects Analysis, Design of User Interfaces, Human-Computer Interaction, User-Centered Design - **Published:** November 3, 2026 - **Apply:** https://www.thejobnetwork.com/job/43931b0e-5a0f-45a2-8c8e-4bd5f2512b41/usability-engineer ## About the Role * Bachelor's or Master's degree in Industrial Design, Product Design, Cognitive Psychology, or a related field with a focus on Human Factors or Human-Computer Interaction (HCI). * 5+ years of experience in usability, human factors, or user-centered design-ideally in medical devices or other high-regulation industries (aviation, automotive, military). * Strong research and communication skills, with the ability to translate user needs into actionable design input and strategic direction. * Familiar with medical device usability and risk management standards (e.g., IEC 62366, FDA guidance, ISO 14971, EU-MDR). ## Description * Conducts usability activities across all development phases in collaboration with multidisciplinary teams including UI/UX, product design, clinical, R&D, and system engineering. * Define the usability engineering approach for projects, including planning activities, resources, and usability integration throughout development. * Conduct and lead user research, usability testing (formative and summative), task analysis, and risk assessments (usability FMEA), and generate documentation for regulatory submissions (FDA, EU-MDR, CMDE). * Identify, analyze, and document usability risks and potential use errors through comprehensive usability risk analyses. * Plan, conduct, and report usability studies in compliance with privacy, usability, and legal requirements, including NDAs, site agreements, and informed consent. * Analyze post market data and create Human Factors Engineering and usability documentation to demonstrate product safety, effectiveness, and regulatory compliance. * Collaborate with cross-functional teams-including engineering, clinical, marketing, quality, regulatory, and service-to deliver human-centered solutions that meet global medical device standards. * Work on usability documentation and report outs related to usability studies like expert review, formative evaluation and summative usability evaluations. * Create usability testing protocols, select user profiles, create usability test plans and prioritize feedback and findings into safety, critical and other categories. * Stay ahead of usability regulations (IEC 62366, ISO 14971, FDA guidance) and advise teams on compliant, user-focused product development.