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7 часов назад

Test Engineer II (Medical Devices)

126 400 - 189 600$
Формат работы
hybrid
Тип работы
fulltime
Грейд
middle
Английский
b2
Страна
US/India/Canada
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): Executing verification protocols and hardware test methods for software-enabled healthcare devices with an accent on traceable documentation, lab discipline, and regulated product development. Focus on supporting automated test setups, complaint investigations, prototype fixtures, failure triage, and improving test repeatability across R&D and Quality.

Location: San Francisco, United States; hybrid with 3 days per week in the office

Salary: $126,400–$189,600 per year, plus equity and benefits.

Company

hirify.global uses AI-powered technology and human-centered care to deliver digital healthcare for musculoskeletal conditions.

What you will do

  • Execute defined test methods and verification protocols for design verification, sustaining changes, complaint investigations, and product testing.
  • Collect, organize, and document test data, discrepancies, observations, and follow-up actions in clear test reports.
  • Support QC testing, incoming checks, screening activities, and bench-level testing for in-office builds and prototype hardware.
  • Prepare devices, samples, fixtures, scripts, and lab setups for automated and semi-automated test runs; monitor results and escalate failures.
  • Maintain equipment records, fixture tracking, calibration status, and lab organization.
  • Collaborate with Quality, R&D, engineers, and program stakeholders to improve repeatability, standardize workflows, and expand automation support.

Requirements

  • Bachelor's degree, associate degree, technical certification, or equivalent practical experience in engineering, engineering technology, quality, or a related technical field.
  • 2+ years of experience in a test, laboratory, quality, manufacturing, or product development environment.
  • Experience executing written procedures or protocols and maintaining traceable sample, equipment, and test documentation.
  • Experience using common laboratory equipment and working within controlled test setups.
  • Ability to collaborate cross-functionally and strong written communication skills for documenting results and test observations.
  • Comfort working in a regulated product development environment where rigor, traceability, and process adherence are required.

Nice to have

  • Experience with hardware verification, validation, sustaining, complaint investigations, or regulated medical device development.
  • Experience with automated or semi-automated test setups, scripts, fixtures, or basic scripting for log review and failure triage.
  • Experience with root cause investigations, failure replication, prototype assembly, fixture construction, or bench test setup modifications.
  • Proficiency with soldering and hot-air rework for PCBA modifications.
  • Exposure to software or system-level testing involving hardware and software.

Culture & Benefits

  • Hybrid work model with required office attendance three days per week.
  • Medical, dental, and vision coverage for employees and eligible family members.
  • Gender-affirming care, family and fertility planning support, and travel reimbursements for unavailable healthcare.
  • Traditional or Roth 401(k) options with a 2% company match.
  • Learning and development stipend plus discounted company stock through an ESPP.

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