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Electrical Engineer

Job in Plymouth, Hennepin County, Minnesota, USA
Listing for: Virtue America
Full Time position
Listed on 2026-08-11
Job specializations:
  • Engineering
    Test Engineer, Electrical Engineering
Salary/Wage Range or Industry Benchmark: 85000 - 110000 USD Yearly USD 85000.00 110000.00 YEAR
Job Description & How to Apply Below

We are seeking an experienced Electrical Engineer with 5–8 years of experience to support the design, testing, troubleshooting, and lifecycle management of FDA-regulated medical devices. The ideal candidate will have hands‑on experience with IEC 60601 compliance testing
, electrical verification, and supporting hospital-based capital equipment.

Required Qualifications

  • Bachelor's Degree in Electrical Engineering.
  • 5–8 years of electrical engineering experience, preferably in the medical device industry.
  • Strong knowledge of IEC 60601 electrical safety and performance testing.
  • Experience developing, writing, and executing electrical test protocols.
  • Ability to document test results and prepare detailed engineering reports.
  • Hands‑on experience troubleshooting and resolving electrical system issues.
  • Experience supporting medical capital equipment such as:
  • EKG Systems
  • Ultrasound Equipment
  • Anesthesia Machines
  • Imaging Systems
  • Infusion Pumps
  • Other hospital console‑based medical devices

Preferred Qualifications

  • Experience supporting end‑of‑life (EOL) products.
  • Knowledge of component obsolescence management and electrical redesign activities.
  • Experience with ISO 14971 Risk Management
    .
  • Experience working in an FDA‑regulated medical device environment.
  • Familiarity with design controls, verification, validation, and product lifecycle documentation.

Key Responsibilities

  • Develop and execute electrical test plans and verification protocols.
  • Perform IEC 60601 electrical safety and compliance testing.
  • Troubleshoot electrical hardware issues and identify root causes.
  • Document test results and prepare technical reports.
  • Support sustaining engineering activities, including component obsolescence and product redesigns.
  • Collaborate with cross‑functional teams to ensure compliance with FDA regulations and quality standards.
  • Participate in risk assessments and design reviews following ISO 14971 guidelines.
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