Вакансия из Hirify Global, списка международных tech-компаний Для мэтча и отклика нужен Plus
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Обязанности и требования четко описаны, а работа связана с медицинскими устройствами и пользой для пациентов; обязательное право на работу в США ограничивает доступность вакансии.
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Только с правом на работу в США
Понятные обязанности
Медтех с пользой для пациентов
Мэтч & Сопровод
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Описание вакансии
Текст:
Hirify AI/Оригинал
TL;DR
Human Factors Engineer II (Medical Devices): Developing and evaluating drug delivery devices through human factors analysis, usability studies, risk assessment, and multidisciplinary collaboration with an accent on user needs, ergonomics, and medical device standards. Focus on leading HF documentation, identifying use-related hazards, designing usability research, and translating consumer and designer feedback into safer product concepts.
Location: Chicago, Illinois, United States; hybrid position with 3 days a week in the office.
Salary: $90,000–$110,000 USD per year.
Company
hirify.global develops and manufactures complex drug delivery systems and custom pharmaceutical devices, including inhalation, injection, nasal, dermal, and ophthalmic delivery products.
What you will do
Provide human factors services to internal and external clients within multidisciplinary development teams.
Mentor staff human factors engineers and ensure work meets internal quality standards.
Lead human factors documentation and contribute human factors expertise throughout the development process.
Analyze use workflows, goals, tasks, and user experiences to identify user needs.
Create and execute usability studies and conduct user-focused risk identification and assessment, including use FMEA.
Work with consumers and designers to evaluate concepts and existing products and identify improvement opportunities.
Requirements
Minimum BS or BSE in Human Factors, Ergonomics, Industrial Engineering, Cognitive Psychology, or extensive formal education in a related human factors area.
At least 5 years of human factors experience in the medical device or healthcare sector.
Experience conducting usability studies and hazard analysis of use-related hazards.
Experience creating experience maps, site/app maps, wireframes, and interactive prototypes.
Experience in research design related to product development.
Knowledge of or direct experience applying anthropometric data.
Awareness of or coursework in psychology, cognition, marketing, design, or product development.
Familiarity with FDA, HE 75, and ISO 62366 human factors and usability standards in medical device development.
Proficiency in Microsoft Office, Adobe Creative Suite, wireframing tools, and image/video editing; strong written and verbal communication, organization, follow-up, attention to detail, and deadline management skills.
Nice to have
Excellent verbal and written communication skills.
Strong ability to collaborate with cross-functional teams.
Ability to strongly demonstrate and communicate hirify.global values.
Culture & Benefits
Hybrid work with 3 days per week in the office.
Work focused on patient-centered drug delivery devices, accurate dosing, ergonomics, and treatment adherence.
International group with manufacturing sites in the US, France, Germany, Brazil, and Poland and an innovation center in Lyon, France.
Confidential handling of applicant information under EEO guidelines.
Employment is limited by the requirement to establish eligibility to work in the United States.
Hiring process
Submit an application with a resume; an English resume is appreciated.
Applicants may use a hirify.global employee referral, which must be submitted before applying.
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