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4 дня назад

Test Engineer I (Medical Devices)

70 400 - 105 600$
Формат работы
onsite
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
Test Engineer I (Medical Devices): Developing and executing verification and validation testing for complex electromechanical medical device systems with an accent on system integration, test automation, and regulatory-compliant documentation. Focus on designing test fixtures and data acquisition systems, investigating hardware and software defects, and validating products across the development lifecycle.

Location: On-site in Jacksonville, Florida, United States. Candidates must have unrestricted U.S. work authorization at the time of hire and throughout employment; sponsorship is not available for roles below Principal level.

Salary: $70,400–$105,600 per year, plus potential short-term incentive compensation.

Company

hirify.global develops healthcare technologies, including neurological, spine, chronic pain, and ear, nose, and throat medical devices.

What you will do

  • Develop and execute verification and validation test plans, protocols, analyses, and reports for system, subsystem, and component requirements.
  • Integrate software, electrical, mechanical, and electromechanical subsystems for system-level testing in development and simulated-use environments.
  • Design, validate, and maintain automated or semi-automated test fixtures, emulators, and supporting software.
  • Establish verification strategies, traceability documentation, and quality artifacts aligned with regulatory requirements.
  • Investigate and track hardware and software defects identified through manual and automated testing.
  • Collaborate with Quality, Regulatory, R&D, Operations, Program Management, and Engineering teams through multiple product lifecycle phases.

Requirements

  • Bachelor’s degree in Engineering.
  • Experience developing and executing test methods, verification activities, or validation activities for electromechanical, software-enabled, or regulated products.
  • Hands-on experience with laboratory instrumentation, product testing, data collection, and technical troubleshooting.
  • Experience creating technical documentation such as test protocols, reports, requirements traceability, design reviews, or validation records.
  • Unrestricted U.S. work authorization is required; visa sponsorship is not available for this role.
  • 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 medical device, aerospace, or another regulated product development environment.
  • Experience with LabVIEW or similar test automation tools.
  • Experience designing or validating test fixtures, prototypes, emulators, or data acquisition systems.
  • Experience with PCB design, layout review, electronics bring-up, or calibration.
  • Experience with Agile, Codebeamer, PLM, ALM, CAD/MCAD, or version control tools.

Culture & Benefits

  • Hands-on access to laboratory environments, prototype systems, and cross-functional engineering teams.
  • Minimal travel.
  • Health, dental, and vision insurance, plus health and flexible spending accounts for eligible regular employees.
  • Paid time off, paid holidays, disability coverage, life insurance, and employee assistance resources.
  • 401(k) plan with employer contribution and match, employee stock purchase plan, tuition assistance, and incentive plans.

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