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Human Factors Engineer Medical Device Jobs in Kansas

Engenio

Human Factors Engineer

Prairie Village, KS · On-site

$75 - $90/hr

The Human Factors Engineer is a key member of the Engenious Design team. The Human Factors expert ... We create medical devices that save and improve lives such as designing and building ...

Garmin Ltd.

Human Factors UX Engineer

Olathe, KS · On-site

$70 - $90/hr

Overview We are seeking a full-time Human Factors Design Engineer 2 at Garmin's U.S. headquarters in the Greater Kansas City area. In this role, you will be responsible for leading the development ...

Actalent

Senior Med Device Mechanical Engineer

Olathe, KS · On-site

$120K - $140K/yr

... medical device environment. Essential Skills * Product development engineering experience ... Individual compensation offered for this position within this range will depend on many factors ...

Actalent

Senior Systems Engineer

Lenexa, KS · On-site

$101K - $138K/yr

Lead systems engineering activities for medical device projects, including requirements development ... Individual compensation offered for this position within this range will depend on many factors ...

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All JobsHuman Factors Engineer Medical Device JobsHuman Factors Engineer Medical Device Jobs in Kansas

Human Factors Engineer Medical Device information

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.

Are human factors engineers in demand?

Human factors engineers in medical devices are in high demand due to increasing focus on user safety, device usability, and regulatory compliance. They often work in healthcare, technology, and manufacturing sectors, utilizing skills in ergonomics, usability testing, and regulatory standards like FDA guidelines.

How much does a human factors engineer medical device make?

A human factors engineer in the medical device industry typically earns between $80,000 and $130,000 annually, depending on experience, education, and location. Senior roles or those with specialized skills in usability testing and regulatory standards can earn higher salaries, often exceeding $150,000.

What are popular job titles related to Human Factors Engineer Medical Device jobs in Kansas?

For Human Factors Engineer Medical Device jobs in Kansas, the most frequently searched job titles are:

What job categories do people searching Human Factors Engineer Medical Device jobs in Kansas look for?

The top searched job categories for Human Factors Engineer Medical Device jobs in Kansas are:

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

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

Human Factors Engineer Medical Device jobs near you
Infographic showing various Human Factors Engineer Medical Device job openings in Kansas as of August 2026, with employment types broken down into 60% Full Time, 20% Part Time, and 20% Contract. Highlights an 80% In-person, and 20% Remote job distribution.

Human Factors Engineer

Engenio

Prairie Village, KS • On-site

$75 - $90/hr

Other

Posted 17 days ago

Job description

The Human Factors Engineer is a key member of the Engenious Design team. The Human Factors expert is an insightful and empathetic observer of users and their needs, translating these insights into actionable inputs for engineers, designers, and product managers.

In this role, you will have the opportunity to directly impact the safety, usability, and effectiveness of life-changing devices by ensuring they are built around the real needs of clinicians, patients, and caregivers. You will join a collaborative, cross‑functional team working on high‑impact, high‑tech systems that improve healthcare outcomes.

This key team member is not afraid to go see how users interact with the systems we are designing, observing clinical practice in person, conducting interviews, and generally partnering with clinicians to understand their viewpoints. They are equally comfortable talking to clients, project managers, and engineering partners.

Key Responsibilities
  • Plan and conduct user research. Gather insights to uncover user needs, workflows, and pain points.
  • Create protocol plans and proctor usability studies (formative and summative).
  • Be a subject‑matter expert in relevant standards documentation including but not limited to IEC 60601, IEC 62366, ISO 14971, and AAMI/ANSI HE75.
  • Prepare thorough documentation for regulatory submissions.
  • Collaborate with designers, engineers (systems, mechanical, electrical, software), and product managers to define and implement user‑centered design solutions.
  • Enjoy a variety of projects and people while doing meaningful work.
  • See your work help real people. We create medical devices that save and improve lives such as designing and building life‑sustaining medical devices and other advanced electromechanical technology.
  • Build a portfolio to be proud of with opportunities to work on medical and consumer products.
Position Details

This is a full‑time, permanent position. This position works from our Kansas City based office during core business hours.

While we recognize that top talent comes from all over the world, we are a small team and are not able to offer visa sponsorship at this time. Candidates must be authorized to work in the United States without requiring visa sponsorship.

Because this role involves work in credentialed environments, the employee must meet all immunization and health‑screening requirements established by our clients, and their clinical partners. This may include, but is not limited to, proof of immunity or vaccination for MMR, Varicella, Hepatitis B, Tdap, annual influenza, and COVID‑19 (varies by site), as well as a tuberculosis screening.

Required Qualifications
  • BS/BA Degree in Human Factors Engineering (HFE), Usability Engineering, Human Computer Interaction (HCI), Biomedical Engineering, or equivalent.
  • 3+ years of proven experience in the planning and execution of formative and summative studies.
  • Expert in proctoring hands‑on usability studies.
  • Demonstrated ability to translate research, study results, and insights into user needs and/or design inputs.
  • Familiar with FDA, ISO, IEC, ANSI/AAMI, and other relevant usability regulations and standards.
  • Effective communication skills and capacity to collaborate with engineers, designers, and management stakeholders.
Desired Qualifications
  • Familiar with risk analysis documentation.
  • Experience in healthcare or other regulated industries.
  • Experience with Class II or Class III medical devices.
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