data analysistechnical writingiotsolidworkselectrical engineeringsystems engineeringmedical devicesbiomedical engineeringlab testingverification testing
Вакансия из Hirify Global, списка международных tech-компаний Для мэтча и отклика нужен Plus
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Зарплата и рынок
$67к-101к/год
$84к$93кмедиана$110к
По похожим ролям (47) ~ $93к/год
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Чётко очерченная junior-роль даёт практический опыт в R&D медицинских устройств в зрелой продуктовой компании; при оценке стоит учесть работу на месте и физические требования.
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Работа на местеПонятные задачиСфера медтехаПрактика в R&DТребование к нагрузке
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Описание вакансии
Текст:
Hirify AI/Оригинал
TL;DR
Associate Systems Engineer (Medical Devices): Supporting the design and development of wearable medical devices and pump technology with an accent on product requirements, device integration, verification testing, and design documentation. Focus on designing feasibility tests, troubleshooting design issues, authoring engineering documentation, and executing design verification for regulatory clearance and commercial release.
Location: Onsite in Acton, Massachusetts, United States; must be able to sit or stand for 8 hours a day.
Annual base salary: $67,100.00–$100,625.00 for U.S.-based positions; incentive compensation may also apply.
Company
hirify.global develops wearable medical devices, including the Omnipod insulin management platform, for people with diabetes and other conditions.
What you will do
Support all phases of the design and development lifecycle for wearable medical devices and pump technology.
Collaborate with Systems Engineers to troubleshoot design issues, analyze designs, and identify improvement methods.
Write and interpret product requirements, support device integration, and participate in product and technical reviews.
Author and review Engineering Change Orders, engineering build requests, feasibility protocols, and reports; manage engineering materials.
Design and set up feasibility tests in a laboratory environment and execute design verification testing.
Support design improvements, FDA and international clearance, commercial release, and triage brainstorming sessions.
Requirements
Bachelor’s degree in Biomedical Engineering, Electrical Engineering, Computer Science, or another engineering discipline.
Ability to work in a fast-paced, dynamic environment with a commitment to continuous learning.
Passion for improving the lives of others.
Technical writing and effective communication skills.
Experience with laboratory testing equipment.
Proficiency with Microsoft Word, Excel, and PowerPoint.
Ability to sit or stand for 8 hours per day.
Nice to have
1–2 years of experience as a Systems Engineer or Project Engineer in the medical device or another regulated industry, or equivalent experience.
Working knowledge of engineering principles and scientific methods.
General understanding of communication technology, mobile technology, IoT, medical devices, and regulations.
Experience with product lifecycle tools such as Jira, Helix, Bamboo, or Bitbucket.
Experience with data analysis using MATLAB.
Experience with SolidWorks or Pro-Engineer.
Hands-on, inquisitive approach with the ability to challenge designs.
Planning, organization, and prioritization skills in a dynamic environment.
Culture & Benefits
Fast-paced environment focused on continuous learning and improving patients’ lives.
Medical, dental, and vision insurance.
401(k) with company match.
Paid time off and employee wellness programs.
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