Вакансия из Hirify Global, списка международных tech-компаний Для мэтча и отклика нужен Plus
Пожаловаться
Зарплата и рынок
ЗП не указана
На похожих ролях по рынку
$66к$77кмедиана$101к
50 в выборке
На СНГ рынке: $1.9к/мес ($1.8к - $3к)
73
Хорошая вакансия
развернуть
Роль чётко связана с usability медицинских устройств и хирургической робототехникой, но контракт всего на три месяца и отсутствие суммы оплаты снижают предсказуемость предложения.
Кликните для подробной информации
Короткий контрактОплата не указанаПонятные задачиХирургическая робототехникаХорошие льготы
Оценка от Hirify AI
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Подключить Plus
Описание вакансии
Текст:
Hirify AI/Оригинал
TL;DR
Human Factors Engineer - Contractor (3 months) (Medical Devices): Planning and executing formative and summative usability studies for Versius surgical robotic systems with an accent on regulatory documentation, UFMEA development, and clinical usability evaluation. Focus on designing study protocols, synthesising clinical observations into actionable recommendations, and maintaining risk-management documentation for MDR- and FDA-regulated medical devices.
Location: Cambridge, UK; hybrid with a minimum of 3 days per week in the office
Company
hirify.global develops Versius, a next-generation surgical robotic system designed to transform minimal access surgery.
What you will do
Plan, moderate, and report formative and summative usability studies.
Create and deliver usability engineering documentation, including protocols and reports.
Maintain UFMEAs, critical task lists, and other risk-management documents.
Assess the impact of new usability features and requirements on existing protocols and UFMEA documentation.
Consult design teams on the appropriate level of usability activity for new system designs.
Support Human Factors activities across specific medical-device projects.
Requirements
Experience working with development teams on Human Factors and usability objectives for complex products.
Experience observing and interviewing people in clinical situations.
Experience applying Human Factors methodologies to MDR- and FDA-regulated medical devices.
Experience developing UFMEA and risk-management documentation in line with ISO 14971.
Strong communication, interpersonal, analytical, and written documentation skills.
Eligibility to work in the UK is required, and the role requires travel to the USA to support studies.
Nice to have
Experience working in a hospital environment.
Knowledge of human anatomy and surgical procedures.
Culture & Benefits
Work in a diverse, inclusive, and authentic workplace.
Contribute to a purpose-driven medical-device company focused on improving surgical care.
Benefits include a bonus, pension, healthcare, and enhanced global parental leave pay.
Будьте осторожны: если работодатель просит войти в их систему, используя iCloud/Google, прислать код/пароль, запустить код/ПО, не делайте этого - это мошенники. Обязательно жмите "Пожаловаться" или пишите в поддержку. Подробнее в гайде →