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# EMI/EMC Test Engineer

- **Company:** TekFortune INC
- **Location:** Glasgow, DE, United States
- **Experience:** Experienced
- **Contract:** Permanent contract
- **Skills:** Systems Engineering, Software Debugging, Firmware, Software Engineering, Wi-Fi Technology, Hfss, Pcb Layout, Ansys
- **Published:** September 11, 2026
- **Apply:** https://www.dice.com/job-detail/15dff988-9828-46c3-8f44-e19aabe0572d

## About the Role

* Bachelor's degree in Electrical/Biomedical Engineering or related field
 * 3-7 years of EMI/EMC experience, with at least 2+ years specific to medical devices
 * Working knowledge of IEC 60601-1-2 and its test methods (IEC 61000-4 series as applied to medical devices)
 * Understanding of "essential performance" and "basic safety" concepts as they relate to EMC pass/fail criteria
 * Experience with EMC test equipment: EMI receivers, spectrum analyzers, ESD guns, surge/EFT/burst generators, near-field probes
 * Ability to read schematics/PCB layouts, particularly isolation barriers and patient-applied parts
 * Strong technical writing skills for regulatory-grade documentation, * Experience supporting FDA 510(k) or PMA submissions, or EU MDR technical documentation
 * Familiarity with ISO 14971 (risk management) and IEC 62304 (software lifecycle, if device includes firmware)
 * Experience with wireless coexistence testing for connected/IoT medical devices
 * Exposure to home-use/lay-person environment EMC (IEC 60601-1-11)
 * Familiarity with EMC simulation tools (ANSYS HFSS, CST)

Soft Skills

 * Comfortable working within a regulated, design-controlled environment (documentation discipline, traceability)
 * Strong cross-functional collaboration with regulatory affairs, quality, and systems engineering
 * Able to communicate EMC risk clearly to non-EMC stakeholders (e.g., regulatory, clinical teams)

## Description

We are seeking an EMI/EMC Test Engineer to own electromagnetic compatibility and electromagnetic interference testing for our medical device portfolio, ensuring compliance with IEC 60601-1-2 and supporting FDA/international regulatory submissions. The role works closely with R&D, systems engineering, and regulatory affairs to identify and mitigate EMC risks throughout the design lifecycle, particularly for devices operating in clinical and home-use environments., * Plan, execute, and analyze EMC pre-compliance and full-compliance testing per IEC 60601-1-2 (radiated/conducted emissions, radiated/conducted immunity, ESD, EFT/burst, surge, magnetic field immunity, dips & interruptions)

 * Apply collateral/particular standards as applicable (e.g., IEC 60601-1-11 for home healthcare environments, IEC 60601-2-XX device-specific standards)
 * Support wireless coexistence testing for connected medical devices (BLE, Wi-Fi) per FDA guidance on RF wireless technology
 * Conduct EMC design reviews at schematic, PCB layout, cable/harness, and enclosure stages - especially around patient-connected circuits and isolation boundaries
 * Debug EMI/EMC failures using spectrum analyzers, EMI receivers, near-field probes, ESD simulators, and surge/EFT generators
 * Coordinate with accredited third-party test labs (e.g., UL, TÜV, Intertek) for formal IEC 60601-1-2 certification testing
 * Author and maintain EMC test plans, protocols, and reports suitable for FDA 510(k)/PMA submissions and CE technical files (MDR)
 * Link EMC test results to risk management file (ISO 14971) - document hazards, mitigations, and residual risk related to electromagnetic disturbances
 * Recommend and validate design mitigations (shielding, filtering, grounding, isolation) without compromising patient safety or essential performance
 * Support root-cause investigation for field complaints or CAPAs related to EMC issues
 * Maintain traceability between EMC test evidence and Design History File (DHF) per IEC 62304/design control requirements
 * Track evolving global regulatory requirements (FDA, EU MDR, Health Canada, etc.) affecting EMC for medical devices