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5 дней назад

Engineer I (Medical Devices)

74 400 - 111 600$
Формат работы
hybrid
Тип работы
fulltime
Грейд
junior
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
Engineer I (Medical Devices/AI): Supporting peripheral vascular health product development through test method validation, design verification and validation, regulatory documentation, equipment qualification, and hands-on laboratory evaluation with an accent on manufacturable medical device solutions and AI-enabled engineering. Focus on designing technical studies, resolving product and testing issues, supporting quality and regulatory requirements, and contributing to agentic engineering initiatives.

Location: Plymouth, Minnesota, United States of America. Flexible work arrangement for U.S. candidates may combine onsite and remote work; the arrangement may change to full-time onsite based on business needs. Candidates must have unrestricted U.S. work authorization at hire and throughout employment; sponsorship is offered only for Principal-level roles and above.

Salary: $74,400.00–$111,600.00 annually, applicable to U.S. locations excluding Puerto Rico and specific California locations. The position is eligible for the hirify.global Incentive Plan.

Company

hirify.global develops healthcare technologies in the Peripheral Vascular Health operating unit to alleviate pain, restore health, and extend life.

What you will do

  • Support research and new product development across design, analysis, troubleshooting, testing, and technical support activities.
  • Design and execute studies, test strategies, test method validations, product evaluations, and hands-on laboratory work for PVH therapies.
  • Translate research findings into practical, manufacturable, and marketable product solutions.
  • Prepare, review, route, and approve technical reports and documentation in compliance with Quality Management System procedures.
  • Partner with Regulatory Affairs on submission strategies and regulatory documentation; support clinical trial-related work when needed.
  • Support production part approval, equipment replacement, qualification, revalidation, and AI-enabled or agentic engineering initiatives.

Requirements

  • Baccalaureate degree with 0 years of relevant experience.
  • Degree in mechanical engineering, biomedical engineering, or a related scientific discipline.
  • Ability to deliver complex project work with guidance, investigate technical questions, resolve generally straightforward problems, and make minor system or process improvements.
  • Ability to collaborate with internal contacts, gather and confirm information, and communicate technical findings.
  • For degrees earned outside the United States, the degree must satisfy the requirements of 8 C.F.R. § 214.2(h)(4)(iii)(A).

Nice to have

  • Experience in agentic engineering, coding, and software integration.
  • Familiarity with medical device technologies, test methods, equipment qualification, or design verification and validation.
  • Hands-on laboratory or manufacturing support experience.

Culture & Benefits

  • Work within a cross-functional R&D environment focused on peripheral vascular health therapies and patient impact.
  • Regular employees may receive health, dental, vision, life, disability, retirement, paid time off, paid holidays, employee stock purchase, tuition assistance, and well-being benefits, subject to eligibility.
  • Employees working 20 or more hours per week may receive additional insurance, healthcare spending, dependent-care, tuition, and disability benefits.
  • Benefits and compensation vary by U.S. location and may not apply fully to Puerto Rico.

Hiring process

  • Applications must be submitted through official hirify.global channels.
  • hirify.global does not request payment or sensitive personal information during early recruitment stages.

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