Sr. Human Factors Engineer

BD; Sandy (UT); On-site; USD 110,000 - 165,000; Full time

Job summary

BD, a global medical technology leader, is hiring a Sr. Human Factors Engineer in the USA (Utah). The role focuses on integrating human factors and user-centered design into the development of medical devices, collaborating across R&D, Regulatory, Quality, and Clinical Affairs to ensure safe, effective products.

You will lead usability studies, create risk analyses, and mentor junior staff while staying current with FDA guidance and IEC 62366 requirements. On-site collaboration is emphasized.

Qualifications

• Education: Bachelor’s degree in a relevant field.
• Experience: Minimum 5 years in human factors engineering.
• Industry Experience: 5+ years in medical device industry (Class II/III).
• Technical Knowledge: Strong understanding of human factors, usability engineering, and user-centered design.
• Research Methods: Proficient in usability testing, contextual inquiry, surveys, and interviews.
• Regulatory Knowledge: Familiar with FDA guidance, IEC 62366, ISO 14971.
• Communication: Excellent written and verbal communication.
• Cross-functional: Able to work independently and in fast-paced environments.
• Travel: ~25%.

Responsibilities

• Lead and execute human factors activities throughout the product development lifecycle.
• Conduct user research including contextual inquiry and usability testing.
• Develop user profiles, task analyses, use scenarios, and use-related risk analyses.
• Translate research findings into design requirements and recommendations.
• Collaborate with R&D, Marketing, Regulatory, Quality, and Clinical Affairs to integrate human factors considerations.
• Participate in design reviews and provide input on UI, workflow, and usability.
• Contribute to human factors plans, reports, and regulatory documentation (FDA/IEC 62366).
• Mentor junior human factors engineers and promote user-centered design culture.
• Stay current with industry best practices and regulatory requirements.

Skills

Human Factors

Usability Engineering

User-Centered Design

Research Methods

Regulatory Knowledge

Communication

Analytical

Cross-functional Collaboration

Education

Bachelor's degree in Human Factors Engineering or related

Tools

Figma

SPSS/R

Job description

We Are The People Who Give Possibilities Purpose

BD is one of the largest global medical technology companies in the world. Advancing the world of health™ is our Purpose, and it’s no small feat. It takes the imagination and passion of all of us—from design and engineering to the manufacturing and marketing of our billions of MedTech products per year, to look at the impossible and find transformative solutions that turn dreams into possibilities.

Job Description

This individual contributor role will be responsible for utilizing evidence-based tools and principles to design systems and products that match the user’s needs and environment. They align research, design, and business strategies by working with project teams and business leadership to drive user-centered product development, which is proven to reduce risks, minimize development costs, and maximize market acceptance of products.

The Sr. Human Factors Engineer will play a key role in integrating human factors principles and user-centered design methodologies into the development of Becton, Dickinson and Company's medical devices and systems. This individual will ensure that products are safe, effective, and user-friendly, ultimately improving the experience for healthcare professionals and patients.

Job Responsibilities

• Lead and execute human factors engineering activities throughout the product development lifecycle, from concept generation to post-market surveillance.
• Conduct user research activities including contextual inquiry, ethnographic studies, and usability testing to identify user needs, preferences, and pain points.
• Develop and refine user profiles, task analyses, use scenarios, and use-related risk analyses.
• Translate user research findings into actionable design recommendations and requirements.
• Collaborate with cross-functional teams including R&D, Marketing, Regulatory, Quality, and Clinical Affairs to integrate human factors considerations into product design.
• Participate in design reviews, providing expert input on user interface, workflow, and overall usability.
• Contribute to the creation of human factors plans, reports, and other regulatory documentation (e.g., IEC 62366, FDA guidance).
• Mentor junior human factors engineers and promote a culture of user-centered design within the organization.
• Stay current with industry best practices, emerging technologies, and regulatory requirements related to human factors engineering in medical devices.

Minimum Requirements

• Education: Bachelor's degree in Human Factors Engineering, Biomedical Engineering, Industrial Design, Cognitive Science, Psychology, or a related field
• Experience: Minimum of 5 years of professional experience in human factors engineering
• Industry Experience: Minimum 5 years of experience specifically in the medical device industry (e.g., Class II or Class III devices)
• Technical Knowledge: Strong understanding of human factors principles, usability engineering, and user-centered design methodologies
• Research Methods: Demonstrated proficiency in conducting human factors research methods including usability testing, contextual inquiry, surveys, and interviews
• Regulatory Knowledge: Working familiarity with relevant medical device regulations and standards such as FDA guidance, IEC 62366, and ISO 14971
• Communication Skills: Excellent written and verbal communication skills with the ability to communicate complex technical information to diverse audiences
• Core Competencies: Strong analytical and problem-solving skills, with the ability to work both independently and collaboratively in a fast-paced environment.
• Travel Requirements: ~ 25% (about once per quarter)

Preferred Qualifications

• Advanced Education: Master's degree or Ph.D. in Human Factors Engineering, Biomedical Engineering, Cognitive Science, or related field
• Leadership Experience: Demonstrated experience leading human factors activities for complex medical devices or systems (as opposed to just participating in them)
• Software Tools: experience with Figma
• Full Product Lifecycle Experience: Experience conducting human factors engineering activities throughout the entire product development lifecycle, from concept generation through post-market surveillance
• Advanced Research Methods: Experience with ethnographic studies and advanced contextual inquiry techniques beyond basic usability testing
• Documentation Expertise: Proven track record creating comprehensive human factors plans, reports, and regulatory documentation specifically for FDA submissions and IEC 62366 compliance
• Statistical Analysis: Proficiency with statistical analysis software such as SPSS, R, or similar tools
• Mentoring Experience: Previous experience mentoring junior human factors engineers or promoting user-centered design culture within an organization
• Risk Analysis: Specific experience developing and conducting use-related risk analyses in accordance with ISO 14971
• Cross-functional Collaboration: Demonstrated success working with R&D, Marketing, Regulatory, Quality, and Clinical Affairs teams on integrated product development
• Industry Knowledge: Active involvement in professional organizations or demonstrated commitment to staying current with emerging technologies and industry best practices in medical device human factors.

At BD, we prioritize on-site collaboration because we believe it fosters creativity, innovation, and effective problem-solving, which are essential in the fast-paced healthcare industry. For most roles, we require a minimum of 4 days of in-office presence per week to maintain our culture of excellence and ensure smooth operations, while also recognizing the importance of flexibility and work-life balance. Remote or field-based positions will have different workplace arrangements which will be indicated in the job posting.

For certain roles at BD, employment is contingent upon the Company’s receipt of sufficient proof that you are fully vaccinated against COVID-19. In some locations, testing for COVID-19 may be available and/or required. Consistent with BD’s Workplace Accommodations Policy, requests for accommodation will be considered pursuant to applicable law.

Why Join Us?

To find purpose in the possibilities, we need people who can see the bigger picture, who understand the human story that underpins everything we do. We welcome people with the imagination and drive to help us reinvent the future of healthcare. At BD, you’ll discover a culture in which you can learn, grow and thrive.

We believe that when people connect in person, we learn faster, collaborate more deeply, and build a stronger culture. Join us and enjoy a culture where face-to-face collaboration supports your learning, your progress, and your success.

To learn more about BD visit https://bd.com/careers.

Becton, Dickinson, and Company is an Equal Opportunity Employer. We evaluate applicants without regard to race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, and other legally protected characteristics.

Primary Work Location
USA UT - Salt Lake City

Additional Locations
USA UT - Sandy

Work Shift