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Overview

Company
Artech
Location
Minneapolis, MN 55401
Employment type
On-site
  • CPQ Product Engineer
  • Business Analyst
  • VP, FP&A Advice & Wealth Management (AWM) & Insurance
  • Microsoft Power BI, Data Governance with Life and annuities domain
  • Project Engineer II
  • Validation Engineer
Back to Jobs
A
ArtechVerified Employer

Business Services & Consulting • Minneapolis, MN 55401

Sr Human Factors Design Eng

Minneapolis, MN 55401On-sitePosted 19 hours ago
Business Services & Consulting

About the Role

Sr Human Factors Design Eng

Seeking a Senior Human Factors Engineer to support usability engineering and risk management for Class III implantable neurostimulator medical devices.

Key responsibilities include:

  • Planning and executing human factors usability validation studies (protocol design, execution, data analysis, reporting)
  • Developing and maintaining Use-Related Risk Analysis (URRA)
  • Collaborating with cross-functional design and engineering teams to improve safe device usability
  • Identifying use-related risks and supporting design updates for medical device safety
  • Applying human factors principles to evaluate and optimize humanmachine interactions

Must have skills:

  • Human factors/usability engineering in medical devices
  • Usability validation testing (study design, execution, analysis, reporting)
  • Use-Related Risk Analysis (URRA) development and updates
  • Experience with Class III or complex medical devices preferred
  • Strong collaboration with engineering and cross-functional teams

Qualifications:

  • Bachelor's degree (or higher) in Human Factors, Engineering, or related field
  • 4+ years experience (or 2+ years with advanced degree)
  • Experience in regulated medical device environment

Sr Human Factors Design Eng

Seeking a Senior Human Factors Engineer to support usability engineering and risk management for Class III implantable neurostimulator medical devices.

Key responsibilities include:

  • Planning and executing human factors usability validation studies (protocol design, execution, data analysis, reporting)
  • Developing and maintaining Use-Related Risk Analysis (URRA)
  • Collaborating with cross-functional design and engineering teams to improve safe device usability
  • Identifying use-related risks and supporting design updates for medical device safety
  • Applying human factors principles to evaluate and optimize humanmachine interactions

Must have skills:

  • Human factors/usability engineering in medical devices
  • Usability validation testing (study design, execution, analysis, reporting)
  • Use-Related Risk Analysis (URRA) development and updates
  • Experience with Class III or complex medical devices preferred
  • Strong collaboration with engineering and cross-functional teams

Qualifications:

  • Bachelor's degree (or higher) in Human Factors, Engineering, or related field
  • 4+ years experience (or 2+ years with advanced degree)
  • Experience in regulated medical device environment

What You'll Do

Planning and executing human factors usability validation studies (protocol design, execution, data analysis, reporting)
Developing and maintaining Use-Related Risk Analysis (URRA)
Collaborating with cross-functional design and engineering teams to improve safe device usability
Identifying use-related risks and supporting design updates for medical device safety
Applying human factors principles to evaluate and optimize humanmachine interactions
Human factors/usability engineering in medical devices

Skills & Technologies

Business Services & Consulting

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