Senior Test Engineer II: Medical Device Certification

Agiliti Health, Inc.; Wauwatosa (WI); On-site; USD 75,000 - 110,000; Full time

Benefits offered by this job

High-impact projects

Cutting-edge medical device tech

Cross-functional collaboration

Competitive compensation and growth

Meaningful impact on patient care

Job summary

Agiliti in Wisconsin is seeking a Test Engineer II to lead test and certification activities for complex medical device projects. You will develop verification plans and work with engineering, quality, and regulatory teams to ensure compliance with ISO/IEC and FDA standards.

The role requires 3–5 years of relevant experience, proficiency with SolidWorks and MPLAB/DAQ, and the ability to travel up to 25% as needed. Join a collaborative team focused on patient-ready devices.

Qualifications

• Bachelor of Science in Mechanical Engineering, Biomedical Engineering, or related field required.
• 3–5 years designing or testing products in medical/industrial sectors.
• Experience designing and running test programs for complex electromechanical devices.

Responsibilities

• Lead test and certification activities across multiple complex projects.
• Develop and execute test strategies, fixtures, and verification plans.
• Troubleshoot and validate electromechanical systems using digital tools.
• Ensure compliance with regulatory and certification standards (ISO/IEC, FDA).
• Partner with cross-functional teams to solve development challenges.
• Support prototype testing, production readiness, and root cause analysis.
• Drive continuous improvement in testing processes and technologies.
• Present project updates and lead design reviews.

Skills

Analytical Thinking

Strategic Perspective

Interpersonal Communication

Travel Availability

Leadership

Education

Bachelor of Science in Mechanical Engineering/Biomedical Engineering

Tools

SolidWorks

MPLAB/DAQ

FEA Tools

Job description

Agiliti in Wisconsin is seeking a Test Engineer II to lead test and certification activities for complex medical device projects. You will develop verification plans and work with engineering, quality, and regulatory teams to ensure compliance with ISO/IEC and FDA standards.

The role requires 3–5 years of relevant experience, proficiency with SolidWorks and MPLAB/DAQ, and the ability to travel up to 25% as needed. Join a collaborative team focused on patient-ready devices.