Вакансия из Hirify Global, списка международных tech-компаний Для мэтча и отклика нужен Plus
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$70к-85к/год
$84к$93кмедиана$110к
По похожим ролям (49) ~ $93к/год
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Понятная роль для начинающего специалиста, практическая разработка продукта и работа в регулируемой медтех-сфере делают вакансию привлекательной для старта, хотя задачи охватывают несколько инженерных направлений.
?Широкий круг задач
Актуальные инструменты
Значимый продукт
Подходит для старта
Мэтч & Сопровод
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Описание вакансии
Текст:
Hirify AI/Оригинал
TL;DR
Associate Development Engineer (Medtech): Designing, developing, testing, and launching regulated clinical systems and subsystems for a histotripsy medical device with an accent on mechanical engineering, system integration, design controls, and manufacturability. Focus on remediating design specifications, conducting risk and FMEA analyses, developing R&D tests, and transferring products to manufacturing.
Location: Plymouth, Minnesota, US; hybrid
Salary: USD 70,000–85,000 / hourly
Company
hirify.global is a commercial-stage medtech company developing the Edison® System, a non-invasive sonic beam therapy platform based on histotripsy, with current liver tumor applications and clinical development across additional indications.
What you will do
Develop an understanding of the Edison system, its subsystem interactions, and the interaction between Edison software and the subsystems.
Remediate existing design specifications using input from cross-functional teams.
Design, engineer, and develop product-related mechanical systems, subsystems, and devices, including electrical, mechanical, software, and system integration tasks.
Develop engineering specifications and R&D tests; perform detailed mechanical design, design reviews, risk analysis, hazard analysis, and FMEA.
Conduct analytical evaluations including tolerance, material selection, force, stress, thermal, ex vivo, and preclinical testing.
Support design for manufacturability, manufacturing transfer, engineering builds, process validation, and product verification testing while maintaining compliant design documentation.
Requirements
Bachelor’s degree in Mechanical, Biomedical, or related Engineering.
0–2 years of related work experience, preferably in medical devices.
Experience with engineering software such as MATLAB, SolidWorks, and Minitab.
Excellent written and verbal communication skills and strong attention to detail.
Ability to work somewhat independently in a collaborative, fast-paced environment.
Nice to have
CAD experience.
Experience working within a Quality Management System.
Culture & Benefits
Full-time employment with a comprehensive benefits package.
Health, dental, and vision insurance, life insurance, and short- and long-term disability insurance.
401(k), paid time off, and additional benefits.
Equal opportunity workplace committed to diversity.
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