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 to guide usability strategy
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 to guide usability strategy.
You will contribute to the growth of the Human Factors team by mentoring junior engineers, supporting business development, 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 to guide usability strategy.
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
Usability risk analyses and hazard identification
Client collaboration and project management
Nice-to-have
Mentoring junior engineers and interns
Delivering presentations and trainings
Supporting business development efforts
Working with healthcare professionals and lay users
Collaborative and people-focused culture
Key Requirements
5–7 years medical device industry experience
M.A./M.S. or B.A./B.S. in related field
Strong knowledge of FDA HF Guidance and IEC 62366
Experience preparing HF documentation for regulatory submissions