Test Engineer - Medical
IPG Photonics
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Marlborough, MA · Posted October 28, 2026
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Where Marlborough, MA ranks
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November 2026
- #5Best cities for software and engineering jobs in New England95 openings · of 24
- #8Best cities for mid-career professionals in New England52% · of 28
- #9Best cities for junior jobs in Massachusetts22% · of 20
- #12Best cities for software and engineering jobs in the Northeast95 openings · of 52
- #15Cities with the most hybrid jobs in New England10% · of 27
- #17Best cities for junior jobs in New England22% · of 28
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- Best cities for engineering pay after cost of living #1 San Mateo ($216k)
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About the job
IPG Photonics is revolutionizing the laser industry as the pioneering developer and leading producer of fiber lasers and amplifiers. Headquartered in Marlborough, MA, IPG has over 4,800 employees in more than 30 locations around the world. We aspire to work together with our employees and customers to apply light in ways that improve life.
Our mission is to develop innovative laser solutions to make the world a better place. To accomplish this mission, we are committed to attracting and retaining the best talent and an engaged and thriving workforce that drives a sustainable future for our company and society.
Working at IPG Photonics you can expect challenging projects, a motivating and friendly environment, and competitive benefits.
Position Summary
The Verification and Validation Test Engineer designs, builds, and validates test methods for verification and validation testing for medical devices and disposables in an ISO 13485 and FDA QSR compliant environment. This Role reports to Quality Management, supporting various project teams in different stages of project maturity from R&D through Production.
Key Responsibilities
Medical Device Testing: Execute Design Verification and Validation activities for complex electromechanical devices and single-use disposables.
Test Method Development: Design, develop, validate and execute test methods to inform design decisions and verify system functionality.
Documentation: Author test protocols, data sheets, and final reports. Author/assist manufacturing procedures, machine instructions.
Quality Compliance: Ensure all activities align with ISO 13485, FDA 21 CFR Part 820, and risk management standards.
Data Analysis: Apply statistical techniques like ANOVA, Gage R&R, and capability analysis to test datasets.
Communication: Present test findings to relevant stakeholders, communicate risk and countermeasure insights as applicable.