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2 дня назад

Test Engineer II (Medical Devices)

84 800 - 127 200$
Формат работы
onsite
Тип работы
fulltime
Грейд
middle
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 II (Medical Devices): Developing and executing engineering tests that verify the safety, performance, and reliability of medical devices with an accent on mechanical, materials, functional, and laboratory testing. Focus on designing test methods and fixtures, analyzing experimental data, conducting failure investigations, and documenting verification and validation results within a medical-device quality system.

Location: North Haven, Connecticut, United States. Onsite role; candidates below the Principal level must have unrestricted U.S. work authorization at the time of hire and throughout employment. U.S. work authorization sponsorship is not available for this role.

Salary: $84,800–$127,200 per year, plus eligibility for the hirify.global Incentive Plan.

Company

hirify.global develops healthcare technologies designed to alleviate pain, restore health, and extend life.

What you will do

  • Develop, execute, and document engineering test protocols and reports for product verification and validation.
  • Design and implement test methods, fixtures, and equipment for medical device performance and reliability evaluation.
  • Perform mechanical, materials, functional, dynamic, and fatigue testing on device components and assemblies.
  • Analyze experimental data and prepare technical reports and presentations for project teams and engineering leadership.
  • Support failure analysis, root cause investigations, test method validation, and equipment qualification.
  • Operate and maintain laboratory equipment while following quality procedures and laboratory practices.

Requirements

  • Bachelor’s degree in mechanical engineering, biomedical engineering, materials science, or a related engineering discipline.
  • At least 2 years of relevant engineering, testing, or laboratory experience in the medical device field, or a master’s degree with no minimum experience requirement.
  • Experience operating a scanning electron microscope for material characterization, surface analysis, and failure investigation.
  • Experience using Instron ElectroPuls systems for dynamic and fatigue testing of medical device components and materials.
  • Experience in a cleanability laboratory supporting cleaning validation and contamination assessment.
  • Unrestricted U.S. work authorization is required; visa sponsorship is unavailable below the Principal level.

Nice to have

  • Hands-on experience with mechanical or materials testing systems.
  • Experience with fatigue, durability, or reliability testing.
  • Familiarity with microscopy techniques and materials analysis.
  • Experience with design verification and validation testing in a quality-system environment.
  • Strong technical documentation and data analysis skills.

Culture & Benefits

  • Work alongside Research & Development, Quality, Manufacturing, and Regulatory Affairs teams.
  • Health, dental, and vision insurance for eligible regular employees.
  • 401(k) plan with employer contribution and match.
  • Paid time off, paid holidays, disability coverage, life insurance, and employee assistance programs.
  • Tuition assistance or reimbursement and employee stock purchase plan.

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