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Usability Engineer

Job in Cleveland, Cuyahoga County, Ohio, 44101, USA
Listing for: Transcend Softech LLC
Full Time position
Listed on 2026-09-25
Job specializations:
  • Engineering
    Biomedical Engineer, Regulatory Compliance Specialist, Quality Engineering
Salary/Wage Range or Industry Benchmark: 90000 - 120000 USD Yearly USD 90000.00 120000.00 YEAR
Job Description & How to Apply Below

Position:
Usability Engineer

Location:

Cleveland OH Duration: 6 Months Experience 4 7 Years Usability Engineer IGT MOSResponsibilities:

  • 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.
Skills:
  • 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).
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