Human Factors Engineer

INFOSYS NOVA HOLDINGS LLC; Seattle (WA); On-site; USD 98,000 - 140,000; Full time

Job summary

INFOSYS NOVA HOLDINGS LLC is seeking a Human Factors Engineer in Seattle, WA, onsite, to support the development of medical devices and combination products. You will ensure user needs, safety, and usability are integrated throughout the product lifecycle and collaborate with engineering, marketing, medical, and regulatory teams.

The role focuses on user research, usability studies, use-related risk assessments, and FDA regulatory submissions, with opportunities to publish and educate on HF

Qualifications

• 5-8 years of experience with medical devices and FDA submissions.
• Experience in early-stage human factors research/activities in innovation/early phase projects.
• Planning and executing usability studies and preparing FDA submission documents.

Responsibilities

• Provide expert HF engineering guidance based on usability activity results.
• Lead planning and execution of user research studies and usability tests.
• Perform use-related risk assessments and document HF evaluations.
• Draft technical documents for usability files and regulatory submissions.

Skills

Human Factors Engineering

User research

Usability testing

Regulatory submissions

Job description

If you are unable to complete this application due to a disability, contact this employer to ask for an accommodation or an alternative application process.

Onsite Services Admin Professional Seattle, WA, US

3 days ago Requisition ID: 1379

Salary Range: $98,000.00 To $140,000.00 Annually

HUMAN FACTORS ENGINEER

JOB SUMMARY

We are seeking a Human Factors Engineer to support the development of innovative medical devices and combination products by ensuring user needs, safety, and usability are integrated throughout the product development lifecycle. This individual will partner closely with cross-functional teams including engineering, marketing, medical, and regulatory affairs to plan, execute, and document human factors activities that support product design decisions and regulatory submissions. The role will focus on conducting user research, leading usability studies, performing use-related risk assessments, and ensuring compliance with FDA guidance and applicable human factors standards.

KEY RESPONSIBILITES INCLUDE:

• Provide expert Human Factors Engineering guidance based on usability activity results and Human Factors Engineering principles
• Provide use-related input into the creation of product and system requirements based on user needs and Human Factors Engineering expertise
• Partner with marketing, medical, engineering and others to plan and conduct Human Factors Engineering activities, including but not limited to:
  • Conceptualizing, organize, and lead the conduct of user research studies (e.g., contextual inquires, dairy studies, observational studies)
  • Lead the development of protocols, study designs, and execution of formative and summative (HF Validation) usability studies
  • Conduct heuristic evaluations and expert reviews
  • Conduct use-related risk analysis
  • Lead the reporting and disposition of Human Factors Engineering evaluation findings
  • Draft technical documents (e.g., use-specification) for usability files within the DHF and as guidance for late-stage development
  • Author Human Factors Engineering / Usability Engineering reports for regulatory submission
• Serve as an opinion leader, internally and externally, including seeking opportunities to publish and speak publicly about Human Factors Engineering
• Conducts Human Factors Engineering educational workshops and seminars to multi-functional audiences
• Assist in internal Human Factors Engineering staff training and process improvement activities
• Assist in maintaining procedures and tools on best practices related to Human Factors Engineering

It is also important that individuals in this role ensure the following:

• User capabilities and limitations and associated use-related risks are appropriately addressed in planning, requirements development, and design & engineering
• User performance characteristics and their associated benefits and risks assist in deciding among design alternatives
• Compliance to relevant standards (IEC 62366, ANSI/AAMI HE75, etc.) and FDA guidance is adequately addressed in Human Factors Engineering processes and deliverables

QUALIFICATIONS

Education/Experience

• 5-8 years of experience with medical devices and FDA submissions
• Experience in early-stage human factors research/activities in innovation/early phase projects
• Planning and executing usability studies, and preparing FDA submission documents
• Combination product or medical mobile app experience is a bonus but not necessary