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1 день назад

Human Factors Expert

Тип работы
fulltime
Грейд
senior
Английский
b2
Страна
US
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
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Описание вакансии

Текст:
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TL;DR
Human Factors Expert (Medical Devices): Designing and validating user interfaces, usability studies, and human factors strategies for drug delivery systems and medical devices with an accent on user research, risk analysis, and regulatory documentation. Focus on leading contextual inquiries, task analyses, usability testing, and design mitigations that improve safety, ease of use, and regulatory approval.

Location: North Chicago, Illinois, United States; willingness to travel up to 20% required.

Company

hirify.global develops innovative medicines, drug delivery systems, and medical devices addressing serious health challenges.

What you will do

  • Lead human factors engineering strategies for combination product and medical device development projects.
  • Design and conduct contextual inquiries, interviews, surveys, usability tests, and other usability assessments.
  • Perform task, workflow, and use-related risk analyses and evaluate design mitigations.
  • Collaborate with system engineers to define user needs, requirements, and user interface specifications.
  • Design device user interfaces and instructional materials.
  • Prepare human factors documentation for regulatory submissions and present findings to scientific and non-scientific stakeholders.

Requirements

  • Master’s degree with 14+ years of related experience or PhD with 8+ years of related experience in Human Factors, Industrial Engineering, Human-Computer Interaction, Psychology, or an equivalent discipline.
  • Strong knowledge of human factors methods and principles.
  • At least 8–10 years of experience in user interface design and usability testing.
  • Experience innovating and contributing to new or improved product releases.
  • Strong communication, problem-solving, analytical, and collaboration skills.
  • Ability to work with internal colleagues, external collaborators, and third-party human factors firms.

Nice to have

  • Experience in pharmaceutical or medical device product development.
  • Working knowledge of medical devices, regulations, and standards.

Culture & Benefits

  • Work with Human Factors, Engineering, Medical, Compliance, and Regulatory specialists.
  • Opportunities to develop and implement improved human factors engineering approaches.
  • Knowledge sharing, mentoring, and training across the function.
  • Travel of up to 20% may be required.

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