Mechanical Systems Test Engineer, Medical Devices (V&V)

Philips; Pittsburgh (Allegheny County); On-site; USD 95,000 - 125,000; Full time

Job summary

Philips in Pittsburgh is seeking a Systems Test Engineer (Verification Engineer) focused on mechanical verification and validation of sleep apnea masks and respiratory interfaces. You will develop and execute system-level test strategies and ensure safety, reliability, and quality before patients.

You will perform hands-on testing, leverage TMV, DOE, and Gage R&R, document Test Plans and RTMs, and collaborate with cross-functional teams to drive project success in a regulated medical-device

Qualifications

• Bachelor's Degree in Mechanical Engineering or equivalent.
• Hands-on experience developing and executing mechanical product verification and validation protocols in medical devices or regulated environments.
• Proven experience with TMV, DOE, and Gage R&R studies.
• Documentation skills: Test Plans, Test Procedures, RTMs, Test Reports.
• Strong analytical problem-solving and cross-functional teamwork.

Responsibilities

• Develop, review, and execute system test plans and procedures for mechanical V&V of medical devices.
• Perform hands-on mechanical testing using specialized equipment and automation.
• Develop and validate test methods using DOE, TMV, and Gage R&R.
• Analyze requirements for testability and participate in design reviews.
• Log, track, and analyze defects; support regression testing.
• Collaborate with cross‑functional teams to manage multiple projects.

Skills

Mechanical V&V

DOE

TMV

Gage R&R

Test Plans & Reports

Problem Solving

Cross‑functional Collaboration

Education

Bachelor's Degree in Mechanical Engineering

Tools

MATLAB

Minitab

LabVIEW

Job description

Philips in Pittsburgh is seeking a Systems Test Engineer (Verification Engineer) focused on mechanical verification and validation of sleep apnea masks and respiratory interfaces. You will develop and execute system-level test strategies and ensure safety, reliability, and quality before patients.

You will perform hands-on testing, leverage TMV, DOE, and Gage R&R, document Test Plans and RTMs, and collaborate with cross-functional teams to drive project success in a regulated medical-device