What are the responsibilities and job description for the Sr Human Factors Design Engineer position at Grove Technical Resources?
Job Title: Sr Human Factors Design Engineer – Medical Device
Location: Minneapolis, MN (Onsite)
Duration: 1 year
Experience: 6–20 years
Key Skills:
• Human Factors Validation (Study Design, Protocols, Reporting)
• Use-Related Risk Analysis (URRA)
• Usability Testing (Generative, Formative, Summative)
• Critical Task Identification & Risk Traceability
• Root Cause Analysis for Use Errors
Core Responsibilities:
• Develop and update human factors documentation (URRA, Use Specifications)
• Design and execute usability validation studies based on critical tasks
• Conduct user testing and analyze usability data
• Prepare study reports and present findings
• Collaborate with design teams to improve user interaction and product safety.
Role Overview:
• Independently handle human factors engineering activities for medical devices
• Lead usability studies and ensure compliance with risk and validation standards
• Provide insights to enhance product design, safety, and user experience
• Mentor junior team members and contribute to project delivery.