Systems Test Engineer - Medical Devices & R&D Lab

Philips Iberica SAU; Bothell (WA); On-site; USD 83,000 - 131,000; Full time

Benefits offered by this job

PTO (paid time off)

401k

HSA

Stock purchase plan

Education reimbursement

Job summary

Philips is seeking a Systems Test Engineer for Bothell, WA. You will analyze requirements, develop test plans, execute tests, and document results while collaborating with R&D, Product Development, and Embedded Systems teams to drive test methods and measurements in a global lab environment.

The role requires 2+ years in testing/verification, a relevant engineering degree, and readiness to work onsite in a laboratory setting, with exposure to medical device regulations (FDA/ISO)."

Qualifications

• Bachelor's degree in a related engineering field and 2+ years in product development testing/verification.
• Experience with FDA-regulated medical products (ISO13485, 21 CFR 820) is a plus.
• Strong problem-solving skills and ability to work in a global R&D environment.

Responsibilities

• Analyze system testing requirements and develop comprehensive test plans.
• Execute system tests and document results with deviations for investigation.
• Provide fault analysis and root-cause investigations to support issue resolution.
• Collaborate with cross-functional teams to define test objectives and deliverables.
• Develop and improve testing methods and measurement documentation.

Skills

Test & verification

Problem solving

Cross-functional collaboration

Education

Mechatronics Engineering

Electrical Engineering

Mechanical Engineering

Job description

Philips is seeking a Systems Test Engineer for Bothell, WA. You will analyze requirements, develop test plans, execute tests, and document results while collaborating with R&D, Product Development, and Embedded Systems teams to drive test methods and measurements in a global lab environment.

The role requires 2+ years in testing/verification, a relevant engineering degree, and readiness to work onsite in a laboratory setting, with exposure to medical device regulations (FDA/ISO)."