Test Engineer II - ENT - Jacksonville, FL (Onsite)

Medtronic•Jacksonville, FL

7d•Onsite

About The Position

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.

Requirements

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
For Baccalaureate degrees earned outside of the United States, a degree that satisfies the requirements of 8 C.F.R. § 214.2(h)(4)(iii)(A) is required.

Nice To Haves

Experience with Test Method Validation (TMV) in a regulated medical device
Strong statistical analysis skills, including Gauge R&R and data‑driven decision making
Proficiency in test automation frameworks, scripting languages, and test infrastructure development
Working knowledge of FDA QSR, ISO 13485, and software validation expectations

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.

Benefits

Medtronic offers a competitive Salary and flexible Benefits Package
We offer a wide range of benefits, resources, and competitive compensation plans designed to support you at every career and life stage.
Health, Dental and vision insurance
Health Savings Account
Healthcare Flexible Spending Account
Life insurance
Long-term disability leave
Dependent daycare spending account
Tuition assistance/reimbursement
Simple Steps (global well-being program)
Incentive plans
401(k) plan plus employer contribution and match
Short-term disability
Paid time off
Paid holidays
Employee Stock Purchase Plan
Employee Assistance Program
Non-qualified Retirement Plan Supplement (subject to IRS earning minimums)
Capital Accumulation Plan (available to Vice Presidents and above, or subject to IRS earning minimums)