Test Engineer I - Electromechanical Systems (On-site)

Medtronic plc

Jacksonville (FL)

On-site

USD 70,000 - 106,000

Full time

4 days ago
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Job summary

Medtronic plc in Jacksonville, Florida is seeking a Test Engineer I for on-site work to join the Neuroscience/ENT-focused teams. You will develop, verify, and validate complex electromechanical medical device systems, and collaborate with software, electrical, mechanical, quality, regulatory, and R&D colleagues to advance products through the development lifecycle.

The role emphasizes hands-on lab work, test fixture design, data acquisition, and rigorous documentation.

Qualifications

  • Bachelor's degree in Engineering.
  • Experience developing and executing test methods, verification activities, or validation activities for electromechanical, software-enabled, or regulated products.
  • Hands-on experience with laboratory instrumentation, product testing, data collection, and technical troubleshooting.
  • Experience creating technical documentation such as test protocols, reports, requirements traceability, design reviews, or validation records.

Responsibilities

  • Develop and execute verification and validation (V&V) test plans, protocols, analyses, and reports.
  • Integrate software, electrical, mechanical, and electro-mechanical subsystems to perform verification testing across development and simulated-use environments.
  • Design, develop, validate, and maintain automated or semi-automated test fixtures, emulators, and non-product software used to support verification activities.
  • Collaborate with cross-functional teams to support product development lifecycle.

Skills

Test method development
LabVIEW
Data collection
Troubleshooting

Education

Bachelor's degree in Engineering

Tools

LabVIEW
Data acquisition systems
PCB design/bring-up

Job description

Medtronic plc in Jacksonville, Florida is seeking a Test Engineer I for on-site work to join the Neuroscience/ENT-focused teams. You will develop, verify, and validate complex electromechanical medical device systems, and collaborate with software, electrical, mechanical, quality, regulatory, and R&D colleagues to advance products through the development lifecycle.

The role emphasizes hands-on lab work, test fixture design, data acquisition, and rigorous documentation.

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