Electrical Systems Engineer (Medical Devices)

Position Overview

We are seeking a hands-on Electrical Systems Engineer to join our medical device engineering team in Minneapolis, MN . This role focuses on electrical verification and validation (V&V), hardware testing, schematic/PCB review, and troubleshooting for regulated medical devices . The candidate will work fully onsite, executing test protocols, collecting data, updating specifications, and ensuring strict adherence to Good Documentation Practices (GDP) and medical device process standards .

Key Responsibilities

• EE Testing, Verification & Validation: Create, update, and execute EE test protocols, perform verification testing, and author comprehensive test reports .

• Schematic & PCB Review: Review and analyze electrical schematics and PCB layouts .

• Hands-On Test Execution: Utilize standard benchtop laboratory equipment—including oscilloscopes, digital multimeters, and spectrum analyzers—to perform functional testing and data collection .

• EMI / EMC Support: Provide engineering support for Electromagnetic Interference (EMI) and Electromagnetic Compatibility (EMC) testing, including protocol creation, testing execution, and reporting .

• Troubleshooting & Root Cause Analysis: Diagnose, troubleshoot, and resolve electrical issues during testing, documenting findings in detailed troubleshooting reports .

• Statistical Analysis & Requirements: Utilize Minitab for test data analysis and support updates/releases for Test Requirements Specifications .

• Traceability & Compliance: Maintain strict traceability and complete all technical documentation in alignment with Good Documentation Practices (GDP) and FDA/ISO medical device regulatory standards .

Required Qualifications & Skills

• Education & Domain: Bachelor’s or Master’s degree in Electrical Engineering, Biomedical Engineering, or a related discipline.

• EE Fundamentals: Solid foundation in analog and digital electrical engineering concepts and testing techniques .

• Medical Device Process Experience: Demonstrated experience working within medical device design, development, and V&V processes .

• Tooling & Equipment: Hands-on experience with oscilloscopes, digital multimeters, spectrum analyzers, and Minitab .

• Regulatory Compliance: Strong familiarity with Good Documentation Practices (GDP), traceability metrics, and design controls .

• Communication: Excellent verbal and written technical communication skills .

• Work Arrangement: Willingness and ability to work 100% onsite (5 days per week, 8 hours per day) in Minneapolis, MN .