Senior Human Factors Engineer

Grove Technical Resources, Inc.; Minneapolis (MN); On-site; USD 96,000 - 165,000; Full time

Job summary

The Grove Technical Resources, Inc. is seeking a Senior Human Factors Design Engineer to support the development of Class III implantable neurostimulators and related medical devices.

You will plan and conduct usability validation studies, develop URRA documentation, and collaborate with cross-functional teams to improve device usability and safe use. The role emphasizes human-centered design, risk management, and user-focused research methods.

Qualifications

• 5–20 years of relevant human factors engineering or medical device usability experience.
• Strong experience in usability validation and URRA.
• Experience with medical device design, risk management, and human-centered design principles.

Responsibilities

• Plan and conduct human factors usability validation studies, including protocol development, study execution, data analysis, and report writing.
• Develop and revise Use-Related Risk Analysis (URRA) documentation.
• Collaborate with cross-functional engineering and product development teams to improve device usability and ensure safe use.
• Develop research methodologies and evaluate user interactions with medical devices.

Skills

Human factors engineering

Usability validation

Use-Related Risk Analysis (URRA)

User-centered design

Data analysis

Education

Bachelor's degree or higher in a relevant field

Job description

Location: Minneapolis, MN

Duration: 12 Months

Job Description:

We are seeking an experienced Senior Human Factors Design Engineer to support the development of Class III implantable neurostimulators and associated medical devices.

Key Responsibilities:

• Plan and conduct human factors usability validation studies, including protocol development, study execution, data analysis, and report writing.
• Develop and revise Use-Related Risk Analysis (URRA) documentation.
• Collaborate with cross-functional engineering and product development teams to improve device usability and ensure safe use.
• Develop research methodologies and evaluate user interactions with medical devices.

Required Qualifications:

• 5–20 years of relevant human factors engineering or medical device usability experience.
• Strong experience in usability validation and Use-Related Risk Analysis (URRA).
• Experience with medical device design, risk management, and human-centered design principles.
• Bachelor's degree or higher in a relevant field.