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Human Factors Engineer Medical Device Jobs in Indiana

Flotec

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Machinist / Inspector - Medical Device Manufacturing

Avon, IN · On-site

$40K - $55K/yr

Read and interpret engineering drawings, work instructions, inspection plans, routings, and manufacturing documentation. * Verify dimensional accuracy, surface finish, threads, features, and critical ...

Siri InfoSolutions Inc

Manufacturing Engineer

Warsaw, IN · On-site

$70K - $90K/yr

Role : Medical Device Manufacturing Engineer Location: Warsaw, IN Duration: 6+ months Experience Required 4 - 6 years (Prior Zimmer Biomet experience is preferred) Technical/Functional Skills:

Hearst UK

Medical Coder Specialist

Indianapolis, IN · On-site

Medical Device In The Quality Department In Some Jobs You Take Orders. In This One, You Write ... Partnering with our information system developer and healthcare institution customers, you'll help ...

Hearst

Medical Coder Specialist

Indianapolis, IN · On-site

Medical Device In The Quality Department Join the healthcare information technology team that ... Partnering with our information system developer and healthcare institution customers, you'll help ...

Hearst

Medical Coder Specialist

Carmel, IN · On-site

Partnering with our information system developer and healthcare institution customers, you'll help ... Evaluates medical device content to ensure the accuracy of HCPCS mappings. * Follows up with ...

Hearst Health

Medical Coder Specialist

Carmel, IN · On-site

Partnering with our information system developer and healthcare institution customers, you'll help ... Evaluates medical device content to ensure the accuracy of HCPCS mappings. * Follows up with ...

Hearst

Medical Coder Specialist

Carmel, IN

Partnering with our information system developer and healthcare institution customers, you'll help ... Evaluates medical device content to ensure the accuracy of HCPCS mappings. * Follows up with ...

Hearst

Medical Coder Specialist

Carmel, IN

Partnering with our information system developer and healthcare institution customers, you'll help ... Evaluates medical device content to ensure the accuracy of HCPCS mappings. * Follows up with ...

First Databank

Medical Coder Specialist

Carmel, IN

Partnering with our information system developer and healthcare institution customers, you'll help ... Evaluates medical device content to ensure the accuracy of HCPCS mappings. * Follows up with ...

Hearst

Medical Coder Specialist

Indianapolis, IN · On-site

Partnering with our information system developer and healthcare institution customers, you'll help ... Evaluates medical device content to ensure the accuracy of HCPCS mappings. * Follows up with ...

Hearst

Medical Coder Specialist

Carmel, IN

Partnering with our information system developer and healthcare institution customers, you'll help ... Evaluates medical device content to ensure the accuracy of HCPCS mappings. * Follows up with ...

Imh

$14.50 - $18.75/hr

Medical Device Design and Prototyping * Computational Fluid Dynamics (CFD) and Fluid Mechanics research or practical experience The Advanced Visualization Engineering Intern supports the IMPACT ...

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

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 Indiana?

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

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

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

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

Cities in Indiana 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 Indiana as of August 2026, with employment types broken down into 1% As Needed, 78% Full Time, 15% Part Time, and 6% Contract. Highlights an 91% Physical, 1% Hybrid, and 8% Remote job distribution.

Embedded Systems Engineer for Medical Device Startup

Levisonics, Inc.

Fishers, IN • On-site

Full-time

Medical, Dental, Vision, PTO

Re-posted 3 days ago

Job description

About Us: We are a dynamic and innovative medical device startup developing a point-of-care portable blood coagulation testing device.
Job Summary: We are seeking a talented and experienced Embedded Systems Engineer to join our team and lead the design and development of embedded computing systems, guiding our devices from prototypes to commercial readiness. The ideal candidate will have a Bachelor's or Master's degree in Electrical Engineering, Computer Engineering, or a related field, with at least 5 years of experience (Ph.D. preferred). You will drive embedded hardware/software development for real-time systems, emphasizing proficiency in C, C++, and/or assembly language for hardware interfacing and optimization. Experience in hardware architectures, sensors, actuators, and communication protocols is crucial, alongside a knack for evaluating and selecting optimal components. Hands-on experience with embedded processors and display integration, as well as a strong grasp of design modification processes to enhance device durability, are also required. Proficiency in coding and optimizing for resource-constrained environments is a plus. As the first embedded engineer on our team, you will play a pivotal role in advancing our blood coagulation testing device from prototype to production. This role is critical to the success of our product and involves working on multiple federal grants and projects. You will be responsible for both hardware and software components, ensuring our device is efficient, reliable, and ready for market.
Startup Environment: Operating in a fast-paced startup, we value innovation, adaptability, and proactive mindsets. Ideal team members thrive under pressure, manage multiple projects, and adapt as company needs evolve. We are looking for individuals who are passionate about working in a startup setting and thrive in dynamic and challenging situations. We value individuals who are not just seeking a job but are driven by a genuine passion for creating impactful solutions and driving change in the medical device industry. If you are excited about the opportunity to make a meaningful impact and are ready to roll up your sleeves and tackle challenges head-on, we encourage you to apply.
Key Responsibilities:
  1. Design & build portable battery system for power supply.
  2. Improve sample handling system design.
  3. Implement an independent embedded processing system and streamlined user interface for straightforward operation.
  4. Upgrade embedded processing system.
  5. Develop efficient injection/fluid handling systems.
  6. Identify and implement efficient computing by selecting and implementing embedded computers to run inside the medical device.
  7. Ensure the embedded system replaces the laptop.
  8. Integrate various hardware and software components together.
  9. Enable battery operation of the device.
  10. Design and develop sample handling systems and cartridges.
  11. Lead end-to-end projects for multiple federal grants and develop innovative solutions.
  12. Collaborate with other team members in taking device prototypes to market.
  13. Participate in FDA-related activities and follow quality protocols.
  14. Participate in grant writing or other fundraising activities as needed.
  15. Perform other relevant tasks as needed for the company.

Minimum Qualifications:
  • Bachelors in Electrical Engineering, Computer Engineering, or a related field and minimum 5 years of experience.
  • Proven experience in embedded systems engineering, preferably in the medical device industry.
  • Knowledge of sensors and commercial medical devices.
  • Proficiency in C, C++, and/or assembly language for embedded software development.
  • Experience with battery systems, fluid handling systems, and embedded processing systems.
  • Familiarity with CAD design, particularly using software like SolidWorks.
  • Understanding of calibration techniques.
  • Familiarity with injection molding and 3D printing for rapid prototyping.
  • Ability to design devices for manufacturing at scale.
  • Knowledge of cybersecurity as it relates to medical devices.
  • Familiarity with rheology/acoustics topics is a plus.
  • Strong problem-solving and analytical skills.
  • Ability to learn new concepts proactively and break down work effectively.
  • Familiarity with Agile methodologies and efficient project management.
  • Demonstrated accountability, effective planning, and team leadership.
  • Innovative thinker with a track record of generating new ideas.
  • Strong written and verbal communication skills.

Preferred Qualifications:
  • Masters or Ph.D. in Electrical Engineering, Computer Engineering, or a related field.
  • Experience selecting and implementing embedded processors and displays.
  • Prior startup or medical device development experience
  • Experience in medical device regulatory compliance (FDA).

What We Offer:
  • Competitive salary
  • Health, dental, and vision insurance coverage
  • Generous paid time off
  • Professional development opportunities
  • Potential to receive stock options
  • Opportunities for growth within the company
  • Flexible work arrangements, including remote work options
  • Dynamic and innovative startup environment
  • Opportunity to make a meaningful impact in the medical device industry

Apply