We anticipate the application window for this opening will close on - 4 Apr 2026

 

At Medtronic you can begin a life-long career of exploration and innovation, while helping champion healthcare access and equity for all. You’ll lead with purpose, breaking down barriers to innovation in a more connected, compassionate world.

A Day in the Life

The ENT Operating Unit is a global leader in innovative solutions that improve patient access, outcomes, and satisfaction. We partner closely with clinicians to deliver technologies across image-guided surgery, nerve monitoring, powered instruments, and emerging therapies that enhance patient care worldwide. 

As a Test Engineer II, you will play a critical role in developing and validating hardware and embedded software for ENT products. You’ll collaborate with cross-functional teams to design, execute, and automate testing strategies that ensure product quality, performance, and regulatory compliance. 

 

Key Responsibilities 

• Develop and execute V&V test plans and protocols and produce audit-ready reports. Assess Design Inputs (DIs) and define effective verification strategies to ensure compliance.  

• Follow internal quality processes and generate required documentation, including traceability matrices and V&V summary reports, to meet regulatory standards.  

• Develop and validate non-product software for test fixtures, including supporting documentation.  

• Identify, document, and track defects from manual and automated testing; support root cause analysis and recommend solutions.  

• Conduct code reviews to ensure adherence to coding standards and proper handling of edge cases.  

• Collaborate cross-functionally (electronics lab, mechanical, electrical, and NPD teams) to design and build test fixtures for system verification.  

• Create and release fixture validation specifications, test plans, and reports in PLM systems.  

• Develop and execute TMV protocols, ensuring methods are robust, repeatable, and reproducible.  

• Perform Gauge R&R and other statistical analyses to validate test methods.  

• Define acceptance criteria aligned with engineering and quality requirements.  

• Ensure all TMV and V&V activities comply with FDA QSR and ISO 13485 standards. 

 

Location: Jacksonville, FL (Onsite) 
 

Onsite Requirement: We bring bold ideas forward with speed and decisiveness, and in-person collaboration is vital to how we work. As part of our commitment to innovation, this position requires 5 days a week onsite presence to accelerate problem-solving, build trust across teams, and elevate the capabilities of our program management community. 

Must Have (Required Qualifications): 

• Bachelor’s degree in Computer Science, Electrical Engineering, or related field with minimum of 2 years of testing experience within medical devices or regulated environment, OR 

• Master's degree in Computer Science, Electrical Engineering, or related field with minimum of 0 years of testing experience within medical devices or regulated environment 

Nice to Have (Preferred Skills); 

• Experience with Test Method Valid