What are the responsibilities and job description for the Sr Human Factors Design Engineer – Medical Device position at Grove Technical Resources, INC?
Hiring: Sr Human Factors Design Engineer – Medical Device
Location: Fridley, MN (Onsite – Rice Creek East)
Duration: 12 Months
Type: W2 Contract
About the Role
We are seeking a Senior Human Factors Design Engineer to support a cutting-edge medical device program focused on usability, safety, and regulatory compliance. This role will play a key part in summative studies and FDA submissions.
Key Responsibilities
- Lead summative study preparation and execution
- Conduct usability testing and user research
- Perform use-related risk analysis
- Collaborate with cross-functional teams (design, quality, regulatory)
- Support regulatory submissions (FDA/TÜV)
Top Skills Required
✔ Human Factors Engineering
✔ UX Research / Usability Testing
✔ FDA / Regulatory Submission Experience
Must-Have Experience
- Formative & Summative Studies
- Human Factors / Usability Engineering
- User Experience Research
- Risk Analysis (use-related)
Nice to Have
- 510(k) submission experience
- Experience with Deep Brain Stimulation (DBS)
Experience Required
- 3 years (MS) or 5 years (BS)
- Preferred: 5–15 years in Human Factors / Medical Devices.