Medical device development and regulatory pathways
As a Senior Human Factors Engineer at ClariMed, you will lead human factors activities across the full product development lifecycle and partner directly with clients
Job Summary
As a Senior Human Factors Engineer at ClariMed, you will lead human factors activities across the full product development lifecycle and partner directly with clients.
You will contribute to the growth of the Human Factors team by mentoring junior engineers, supporting business development efforts, and representing ClariMed through presentations and thought leadership.
ClariMed offers a collaborative, people-focused culture with opportunities for growth and exposure to cutting-edge medical device technologies that have real-world impact.
Matching Summary
As a Senior Human Factors Engineer at ClariMed, you will lead human factors activities across the full product development lifecycle and partner directly with clients.
Skills & Requirements
Must-have
Human Factors principles and FDA HF Guidance
Designing and conducting usability studies
Medical device development and regulatory pathways
Technical writing for HF documentation
User research and task analysis
Usability risk analysis development
Collaboration with healthcare professionals
Nice-to-have
Mentoring junior engineers
Business development support
Presentation and training delivery
Thought leadership contributions
Working with diverse user groups
Collaborative and people-focused culture
Key Requirements
5–7 years medical device industry experience
M.A./M.S. in Human Factors or related field preferred
B.A./B.S. in related field accepted
Experience preparing HF documentation for regulatory submissions