Systems Test Engineer — Medical Device Verification

Philips

Bothell (WA)

On-site

USD 83,000 - 131,000

Full time

14 days+

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Benefits offered by this job

PTO
401k (up to 7% match)
HSA (company contribution)
Stock purchase plan
Education reimbursement

Job summary

Philips Bothell-based Systems Test Engineer role focuses on conducting testing and verification for R&D and T&V laboratories. You will work with cross-functional teams to transform concepts into testable solutions and contribute to new testing methods and measurement documentation.

The role emphasizes hands-on mechanical testing of Oral Healthcare devices, with a 3-day in-office requirement and the potential for global collaboration in Philips testing laboratories.

Qualifications

  • 2+ years of experience in product development testing and verification.
  • Strong problem-solving skills and use of problem-solving tools.
  • Experience with FDA-regulated medical devices is a plus (ISO13485, 21CFR820).

Responsibilities

  • Analyze system testing requirements and develop test plans to ensure coverage and compliance with standards.
  • Execute system tests per procedures and document deviations for investigation.
  • Evaluate test outcomes and deliver reports with insights on performance and improvements.
  • Support troubleshooting and root-cause analysis for project teams.
  • Collaborate with cross-functional teams to define test objectives, scope, and deliverables.
  • Develop testing solutions and equipment for Philips testing laboratories.

Skills

System testing
Verification
Problem solving

Education

Bachelor's degree in Mechatronics, Electrical, Electronic, Mechanical Engineering

Job description

Philips Bothell-based Systems Test Engineer role focuses on conducting testing and verification for R&D and T&V laboratories. You will work with cross-functional teams to transform concepts into testable solutions and contribute to new testing methods and measurement documentation.

The role emphasizes hands-on mechanical testing of Oral Healthcare devices, with a 3-day in-office requirement and the potential for global collaboration in Philips testing laboratories.

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