EMI/EMC Test Engineer (Medical Devices) - Glasgow, DE - Fulltime/ Contract Opportunity

Zodiac Solutions; Newark (DE); On-site; USD 90,000 - 130,000; Full time

Job summary

Zodiac Solutions in Newark, DE, is seeking an EMI/EMC Test Engineer for medical devices to own EMC testing and regulatory submissions. The role partners with R&D, regulatory affairs, and systems engineering to mitigate EMC risks across the design lifecycle, including clinical and home-use environments.

The candidate will conduct pre- and full-compliance testing, coordinate with labs, and author test plans and reports for FDA 510(k)/PMA submissions and CE files.

Qualifications

• Bachelor's degree in Electrical/Biomedical Engineering or related field is required.
• 3-7 years of EMI/EMC experience, with at least 2+ years in medical devices.
• Understanding of IEC 60601-1-2 and IEC 61000-4 series as applied to medical devices.
• Experience with EMC test equipment and ability to read schematics/PCB layouts.

Responsibilities

• Plan, execute, and analyze EMC pre- and full-compliance testing per IEC 60601-1-2.
• Apply collateral standards like IEC 60601-1-11 for home healthcare environments.
• Support wireless coexistence testing for BLE and Wi-Fi per FDA guidance.
• Conduct EMC design reviews at schematic, PCB, cable/harness, and enclosure stages.
• Debug EMC failures using spectrum analyzers, EMI receivers, near-field probes, ESD devices, and surge generators.
• Coordinate with third-party labs for IEC 60601-1-2 certification testing.
• Author and maintain EMC test plans, protocols, and reports for FDA submissions and CE files.
• Link EMC test results to ISO 14971 risk management file.

Skills

EMC Testing

Reading schematics

Test equipment proficiency

Education

Bachelor's degree in Electrical/Biomedical Engineering

Tools

EMI receivers

Spectrum analyzers

ESD guns

Surge/EFT/burst generators

Near-field probes

Job description

Role: EMI/EMC Test Engineer - Medical Devices
Location: Glasgow, DE
Employment Type: Full-Time / Contract

Job Summary

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.

Required Qualifications

• 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

Key Responsibilities

• 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, T V, 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