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Human Factors Engineer Medical Device Jobs in Rochester, NY

... factors that may prove relevant during the interview process, as well as geographic market ... Experience supporting manufacturing engineering in a medical device, healthcare technology ...

Experience within battery, electronics, aerospace, defense, medical device, or other highly ... You'll work alongside talented engineering and manufacturing professionals in a collaborative ...

Electronic Engineer

Rochester, NY · On-site

$81K - $136K/yr

... and device analysis down to the component level. * Provide technical support to application ... See HR Partner with any questions. Physical Demands and Working Conditions: Ability to lift up to ...

Electronic Engineer

Rochester, NY · On-site

$81K - $136K/yr

... and device analysis down to the component level. * Provide technical support to application ... See HR Partner with any questions. • Physical Demands and Working Conditions: Ability to lift up ...

Industrial Designer

West Henrietta, NY · On-site

$55K - $65K/yr

Integrate human factors and anthropometric data into all design decisions. 3D Modelling & Rendering ... Work closely with engineers to ensure manufacturability and technical feasibility of designs.

Industrial Designer

West Henrietta, NY · Hybrid

$123K/yr

Integrate human factors and anthropometric data into all design decisions. 3D Modelling & Rendering ... Work closely with engineers to ensure manufacturability and technical feasibility of designs.

Industrial Designer

West Henrietta, NY · On-site

$123K/yr

Integrate human factors and anthropometric data into all design decisions. 3D Modelling & Rendering ... Work closely with engineers to ensure manufacturability and technical feasibility of designs.

... • Medical device or FDA-regulated product experience strongly preferred. • Strong ... The actual base salary offered may depend on a variety of factors. U.S. based employees may be ...

Showing results 41-60

Human Factors Engineer Medical Device information

See Rochester, NY salary details

$30

$56

$84

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

As of Sep 2, 2026, the average hourly pay for human factors engineer medical device in Rochester, NY is $56.63, according to ZipRecruiter salary data. Most workers in this role earn between $42.21 and $66.63 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.

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 Rochester, NY?

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

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

The top searched job categories for Human Factors Engineer Medical Device jobs in Rochester, NY are:

What cities near Rochester, NY are hiring for Human Factors Engineer Medical Device jobs?

Cities near Rochester, NY with the most Human Factors Engineer Medical Device job openings:

Infographic showing various Human Factors Engineer Medical Device job openings in Rochester, NY 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, with an average salary of $117,791 per year, or $56.6 per hour.

Engineering Technician

Carestream Health

Rochester, NY • On-site

$23 - $28/hr

Full-time

Re-posted 11 days ago


Carestream Health rating

8.3

Company rating: 8.3 out of 10

Based on 11 frontline employees who took The Breakroom Quiz

118th of 495 rated machine equipment manufacturers


Job description

Carestream Health Inc.
Innovation that sparks imagination. Continue on to your next challenge with us.
Carestream is a worldwide provider of medical imaging systems and solutions; x-ray imaging systems for non-destructive testing; manufacturing of film and precision contract coating services for a wide range of industrial, medical, electronic and other applications-all backed by a global service and support network. Carestream's diagnostic imaging technology systems are at work in 90 percent of hospitals worldwide.
At Carestream, we offer a global perspective and a world of opportunities for people who have the desire to make a positive impact. Join our team!
Compensation $23.00 to $28.00 per our depending on experience and skills related to the requirements of the job description.
*This range reflects Carestream's good faith estimate to pay fairly as starting wage. Offers will be tailored within the range based on the selected candidate's experience, industry knowledge, technical and communication skills, and other factors that may prove relevant during the interview process, as well as geographic market differentials for the position.
Position Summary:
The Engineering Technician is responsible for providing technical support to the Engineering and Manufacturing teams within an electromechanical medical device assembly environment. This role is responsible for supporting manufacturing product builds, process improvements, equipment validation, troubleshooting, document control activities, and production readiness efforts.
This position works closely with Manufacturing and Quality Engineering teams to diagnose manufacturing issues, restore production capability, and prevent recurrence through process improvements. The technician supports new and existing manufacturing lines, assists with product and equipment launches, evaluates production data, and documents findings to support manufacturing changes. Success in this role requires strong analytical and hands-on troubleshooting skills, the ability to work independently in a dynamic factory environment, and a focus on continuous improvement and operational excellence. This position will follow compliance with applicable regulatory and quality system requirements, including ISO 13485, MDSAP, FDA Quality System Regulations, and company procedures.
Location: 1049 W Ridge Road, Greece, NY 14615
Position Responsibilities:
  • Follow engineering direction to perform hands-on evaluation, repair, rework, and modification of electromechanical assemblies and components in accordance with approved procedures and quality standards.
  • Execute engineering test plans created by the manufacturing engineering team, and collect data to support product verification, process validation, root cause investigations, and process improvements.
  • Work closely with production lines to gain a thorough understanding of manufacturing processes, materials, and equipment, enabling effective troubleshooting and continuous improvement of production issues.
  • Assist the manufacturing engineering team with product and process development activities, including engineering builds, new product introductions, and manufacturing transfers.
  • Write and maintain standard operating procedures (SOPs) and assist with training Production Operators and Technicians on SOPs.
  • Support process validation activities (IQ/OQ/PQ), data collection, and continuous improvement initiatives to enhance quality, efficiency, and manufacturability.
  • Perform testing, troubleshooting, and root cause investigations of products, equipment, and manufacturing processes to resolve technical issues.
  • Create, maintain, and revise controlled manufacturing documentation, including work instructions, test methods, engineering change records, and assembly procedures.
  • Ensure compliance with ISO 13485, MDSAP, FDA regulations, and internal quality system requirements while supporting audits, CAPA activities, change control, and risk management processes.
  • Less than 10% travel.
  • Other duties as needed.

Required Skills & Education:
  • Either a High school diploma or equivalent AND 4+ years of experience working as a production or engineering technician in a manufacturing environment,

OR Associate's degree or greater in a STEM discipline AND 1+ years of experience working as a production or engineering technician in a manufacturing environment.
  • Proficient in Microsoft Office applications, including Excel 1 (data entry, formulas, charts, and basic data analysis), Word (document creation and revision), Outlook, and Teams.
  • An understanding of complex hardware equipment and the ability to troubleshoot electromechanical assemblies (identify root causes using structured problem-solving methods).
  • Demonstrated understanding of Good Documentation Practices (GDP) and document control requirements.

Desired Skills:
  • Bachelor's Degree (BS) in Electrical, Mechanical, or Manufacturing Engineering or Engineering Technology.
  • Strong Written and Verbal communication skills.
  • Experience with writing and maintaining work instructions.
  • Experience supporting manufacturing engineering in a medical device, healthcare technology, electronics, aerospace, or other regulated manufacturing environment.
  • Working knowledge of SAP or other enterprise resource planning (ERP) systems.
  • Experience with process improvement methodologies such as Lean Manufacturing, Kaizen, or Six Sigma.
  • Experience supporting engineering investigations, validation activities, or new product introduction efforts.

Work Environment:
Manufacturing Production & Labs
Physical Requirements:
Person must be willing and able to meet the following physical requirements:
  • Standing: 50-75%
  • Walking: 25-50%
  • Sitting: 1-25%
  • Bending/kneeling: 25-50%
  • Carrying, Pushing or Pulling: 25-50%
  • Lifting 20-35 pounds: 1-25%
  • Lifting 35-50 pounds: 1-25%
  • Lifting 50-100 pounds: 0%

Carestream is an Equal Opportunity Employer
Carestream is an equal opportunity organization. We recruit, employ, train, compensate, and promote without regard to race, religion, creed, color, national origin, age, gender, sexual orientation, gender identity, marital status, disability, veteran status, or any other basis protected by applicable federal, state or local law.
Applying for a job with Carestream
All Carestream employees must complete the on-line application process. Carestream is committed to working with and providing reasonable accommodations to individuals with disabilities. If you require assistance or an accommodation because of a disability to participate in the application process, please click accommodations
Requisition ID: 4807

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