This is a hands on, individual contributor role for someone who enjoys owning projects end to end, collaborating cross functionally, and working in a regulated medical device environment.
What You'll Do:
- Lead usability and human factors activities across product development, with a focus on summative (validation) studies
- Plan, prepare, and execute usability studies, including protocol development, study execution, data analysis, and reporting
- Identify user related risks and support mitigation strategies through human factors engineering methods
- Partner closely with cross functional teams including R&D, Design Engineering, and Regulatory Affairs
- Support FDA and TÜV regulatory submissions, including usability validation documentation
- Apply human performance principles to optimize human machine interfaces, labeling, and training materials
- Contribute to process improvements and provide guidance or mentorship to less experienced team members as needed
- Bachelor's degree + 5 years of relevant experience
- Hands on experience with UX or usability research, especially summative usability validation
- Experience supporting FDA and/or TÜV submissions for medical devices
- Ability to work independently and manage multiple priorities in a regulated environment
- Preferred: 5-15 years of total experience in human factors or usability engineering
On-site
Full Time
Health Insurance, Life Insurance, 401k retirement plan, paid sick time
If interested and qualified, please submit your resume to careers@dr-group.com or visit our website to apply: http://dr-group.com/find-engineering-technical-jobs/
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