Apply human factors engineering to medical devices in a fully onsite Vancouver, BC contract role requiring usability expertise and risk analysis.
The Human Factors Engineer supports development and commercialization of healthcare technologies through user-centred design. You will work across engineering, clinical, quality, regulatory, and product teams throughout development. The work spans user research, usability evaluations, validation studies, requirements, and regulatory documentation.
Key Responsibilities: Develop human factors and usability engineering plans
Identify users, workflows, critical tasks, and use-related risks
Translate user needs into testable product requirements
Conduct interviews, observations, and formative usability studies




Maintain traceable, compliant usability engineering files
Requirements: Bachelor’s degree in a related discipline
Three or more years in regulated product environments
Experience planning and documenting formative studies
Experience supporting summative usability validation
Working knowledge of IEC 62366-1 practices
Bring medical-device usability engineering, user research, and regulatory documentation experience to Actalent’s Vancouver contract assignment.

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📌 Medical Device Human Factors Engineer (British Columbia)
🏢 Actalent
📍 British Columbia