Stryker is seeking a Senior Compliance Engineer, EMC to support electromagnetic compatibility testing and compliance activities for new product development and/or sustaining engineering, contributing to successful global product launches and ongoing regulatory compliance for Stryker Medical. Develop and execute EMC test plans and support design reviews. Apply EMC standards and test methods for medical devices, building proficiency in IEC 60601‑1‑2 and related global requirements. Collaborate with design, quality, and regulatory teams to identify and resolve EMC compliance needs throughout the product lifecycle.
This role is an individual contributor position focused on developing technical depth in EMC testing, standards application, and compliance processes. The EMC Engineer builds hands-on expertise through testing, analysis, and cross-functional collaboration while growing toward increased technical knowledge and responsibility.
What You Will Do
Compliance Engineering – EMC Domain responsibilities
Lead end-to-end EMC compliance Strategy for new product development programs and/or sustainment programs within Stryker Medical
Review designs with subject matter experts to develop EMC compliance plans and collaborate with design engineers to imprint good EMC design practices early in the design cycle.
Analyze designs for adherence to good EMC design practices.
Develop streamlined EMC evaluations utilizing design, data, and risk-based evaluations.
Diagnose root cause of EMC compliance issues and propose mitigation actions.
Translate global EMC standards into clear requirements.
Manage and influence third-party certification labs and NRTL partners to support global market access and meet quality, cost, and schedule expectations.
Leadership & Organizational Impact
Serve as the project lead for new product development and/or sustainment programs within Stryker Medical.
Exercise independent judgement in selecting compliance strategies and socialize direction to build alignment and consensus.
Drive design for EMI/EMC processes, and best practices across disciplines.
Travel
Up to 20%, as required to support projects, partners, and industry engagement.
What You Need (Required Qualifications )
Bachelor’s degree in electrical engineering or related discipline.
2+ years of experience required.
Preferred Qualifications
Experience with product safety regulatory certification for major standards bodies and frameworks (e.g., IEC, AAMI, and related schemes).
Experience with medical device product development lifecycle, including design controls and risk management.
Experience working with and managing third-party certification laboratories (e.g., UL, TÜV, CSA, Intertek).
Experience with device regulatory certification involving safety, EMC, and/or wireless standards.
Demonstrated ability to work independently and effectively in a matrixed organization.
Strong written, verbal, and interpersonal communication skills with the ability to influence without authority.
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