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Human Factors Engineer Medical Device Jobs (NOW HIRING)

As a Human Factors Engineer (HFE) within ACE, part of a small, passionate, and accomplished team of ... Medical, dental, vision, basic and supplemental life insurance, paid parental leave, short and ...

As a Human Factors Engineer (HFE) within ACE, part of a small, passionate, and accomplished team of ... Medical, dental, vision, basic and supplemental life insurance, paid parental leave, short and ...

As a Human Factors Engineer (HFE) within ACE, part of a small, passionate, and accomplished team of ... Medical, dental, vision, basic and supplemental life insurance, paid parental leave, short and ...

$145 - $203/hr

As a Human Factors Engineer (HFE) within ACE, part of a small, passionate, and accomplished team of ... Medical, dental, vision, basic and supplemental life insurance, paid parental leave, short and ...

New

Sr. Human Factors Engineer

Seattle, WA ยท On-site

$145 - $203/hr

As a Human Factors Engineer (HFE) within ACE, part of a small, passionate, and accomplished team of ... Medical, dental, vision, basic and supplemental life insurance, paid parental leave, short and ...

As a Human Factors Engineer (HFE) within ACE, part of a small, passionate, and accomplished team of ... Medical, dental, vision, basic and supplemental life insurance, paid parental leave, short and ...

Showing results 41-60

Human Factors Engineer Medical Device information

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$30

$57

$85

How much do human factors engineer medical device jobs pay per hour?

As of Aug 15, 2026, the average hourly pay for human factors engineer medical device in the United States is $57.40, according to ZipRecruiter salary data. Most workers in this role earn between $42.79 and $67.55 per hour, depending on experience, location, and employer.

What is a human factors engineer in the medical device industry?

A Human Factors Engineer in the medical device industry is responsible for ensuring that medical devices are safe, effective, and easy to use by considering how people interact with technology. They apply principles of human psychology, engineering, and design to optimize device usability and minimize user errors. Their work often includes conducting usability testing, analyzing user feedback, and collaborating with product development teams to ensure regulatory compliance and improve patient outcomes.

How do human factors engineers collaborate with regulatory teams during the development of medical devices?

Human Factors Engineers frequently work alongside regulatory teams to ensure that medical devices meet stringent usability and safety requirements set by agencies like the FDA. This collaboration involves documenting user research, risk analyses, and validation studies to support regulatory submissions. Regular communication helps align design decisions with compliance standards, ensuring that the device is both user-friendly and legally marketable. As a result, Human Factors Engineers play a critical role in guiding the product through the approval process.

What are the key skills and qualifications needed to thrive as a human factors engineer in medical devices, and why are they important?

To excel as a Human Factors Engineer in Medical Devices, you need a solid background in human factors engineering, usability testing, and regulatory knowledge, typically supported by a degree in engineering, psychology, or a related field. Familiarity with tools like usability testing software, prototyping platforms, and standards such as IEC 62366 is important, along with experience in documentation for FDA submissions. Strong analytical thinking, communication, and collaboration skills help in translating user needs into safe, effective device designs. These competencies ensure medical devices are user-friendly, compliant, and minimize risks to patient safety.

What is the difference between Human Factors Engineer Medical Device vs Human Factors Specialist Medical Device?

AspectHuman Factors Engineer Medical DeviceHuman Factors Specialist Medical Device
CredentialsBachelor's or Master's in Human Factors, Psychology, or Engineering; certifications like HF/E certificationSimilar credentials, often with additional certifications in usability or ergonomics
Work EnvironmentDesign teams in medical device companies, R&D labs, regulatory environmentsUsability testing labs, clinical settings, regulatory agencies
Industry UsageDesign and optimize medical devices for usability and safetyConduct usability assessments, risk analysis, and compliance documentation

While both roles focus on usability and safety in medical devices, Human Factors Engineers typically lead design and development, whereas Human Factors Specialists often focus on usability testing and compliance. Both roles require similar credentials and work within the same industry environment, but their specific responsibilities differ slightly.

More about Human Factors Engineer Medical Device jobs

What cities are hiring for Human Factors Engineer Medical Device jobs?

Cities with the most Human Factors Engineer Medical Device job openings:

What states have the most Human Factors Engineer Medical Device jobs?

States with the most job openings for Human Factors Engineer Medical Device jobs include:

Infographic showing various Human Factors Engineer Medical Device job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 78% Full Time, 15% Part Time, and 6% Contract. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $119,382 per year, or $57.4 per hour.

Human Factors Engineering (HFE) Lead - Associate Engineering Fellow (AEF)

JobRx, Inc.

Lexington, MA โ€ข On-site

$154.40 - $242.55/hr

Other

Dental, Vision, Life, Retirement, PTO

Posted 10 days ago


Job description

Job Description

Human Factors Engineering (HFE) Lead - Associate Engineering Fellow (AEF) is responsible for Human Centered Design of Medical Devices and Combination Products. The HFE Lead - AEF will be integral to design and development of product user interface including hardware, software, packaging, labeling, and instruction material to support safe and effective use of the product for the intended use by the intended users in the anticipated use environment. The HFE AEF will lead the advancement of AI-enabled Human Factors Engineering capabilities across the organization by identifying and prioritizing high-impact digital transformation initiatives aligned with pipeline and platform device strategies.

Responsibilities
  • Leading and executing Human Factors strategy in compliance with regional regulatory guidance.
  • Driving and overseeing User Research strategy in compliance with Quality Management System.
  • Developing Human Factors Product and System level requirements in alignment with Target Product Profile.
  • Conducting exploratory research and AI-augmented research to generate high-quality user data, including digital ethnography, remote usability platforms, and synthetic user simulations.
  • Translating user needs into user experience and interface requirements and specifications.
  • Designing and executing Human Factors studies to iteratively evaluating product user interface - including hardware, software, packaging, instructional material, and training.
  • Performing use-safety engineering, apply advanced, data-driven risk management approaches, including predictive modeling and AI-assisted signal detection.
  • Developing and managing Human Factors Validation Protocols and Reports.
  • Managing Human Factors, Design, and User Research vendors.
  • Creating and implementing Human Factors regulatory strategies.
  • Developing Usability Engineering Files in compliance with IEC and ISO standards.
  • Leading development to Human Factors standard operating procedures and templates development.
  • Applying functional knowledge of applicable guidance, regulations, standards, and industry best practices to medical device and combination product design and development process.
  • Preparing documentation to support medical device and combination product development activities including design controls.
  • Partnering with cross-functional colleagues across mechanical engineering, software, clinical, regulatory, commercial, data science, digital, and quality disciplines.
  • Qualifying and managing Human Factors vendors.
  • Supporting internal and external quality audits.
  • Communicating with internal and external key stakeholders.
  • Mentoring Human Factors Engineering Leads.
Education & Qualifications
  • Doctorate degree and 7+ years of Human Factors Engineering, Biomedical Engineering, Industrial Engineering, other relevant degrees in device design or biotech industry.
  • OR, Master's degree and 13+ years of Human Factors Engineering, Biomedical Engineering, Industrial Engineering, other relevant degrees in device design or biotech industry.
  • OR, Bachelor's degree and 15+ years of Human Factors Engineering, Biomedical Engineering, Industrial Engineering, other relevant degrees in device design or biotech industry
Physical Health Requirements
  • While the role of a Human Factors Engineering Lead primarily involves cognitive and analytical tasks, good physical health is essential. Engineers may need to visit manufacturing sites or conduct user testing in clinical environments, which might involve walking, standing, or other physical activities.
  • Depending on the role and specific responsibilities, a Human Factors Engineering Lead may need to travel to clinical sites, supplier facilities, or other locations for research and testing purposes.
Travel Requirements

This position may require up to 20% yearly travel, including domestic and international.

Compensation and Benefits Summary

We understand compensation is an important factor as you consider the next step in your career. We are committed to equitable pay for all employees, and we strive to be more transparent with our pay practices.

Location: Lexington, MA

U.S. Base Salary Range: $154,400.00 - $242,550.00

The estimated salary range reflects an anticipated range for this position. The actual base salary offered may depend on a variety of factors, including the qualifications of the individual applicant for the position, years of relevant experience, specific and unique skills, level of education attained, certifications or other professional licenses held, and the location in which the applicant lives and/or from which they will be performing the job. The actual base salary offered will be in accordance with state or local minimum wage requirements for the job location.

U.S. based employees may be eligible for short-term and/or long-term incentives. U.S. based employees may be eligible to participate in medical, dental, vision insurance, a 401(k) plan and company match, short-term and long-term disability coverage, basic life insurance, a tuition reimbursement program, paid volunteer time off, company holidays, and well-being benefits, among others. U.S. based employees are also eligible to receive, per calendar year, up to 80 hours of sick time, and new hires are eligible to accrue up to 120 hours of paid vacation.

EEO Statement

Takeda is proud in its commitment to creating a diverse workforce and providing equal employment opportunities to all employees and applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, gender expression, parental status, national origin, age, disability, citizenship status, genetic information or characteristics, marital status, status as a Vietnam era veteran, special disabled veteran, or other protected veteran in accordance with applicable federal, state and local laws, and any other characteristic protected by law.

Location

Lexington, MA

It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

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