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.