Sr. Eng, Interoperability

This is where

your work makes a difference.

At Baxter, we believe every person—regardless of who they are or where they are from—deserves a chance to live a healthy life. It was our founding belief in 1931 and continues to be our guiding principle. We are redefining healthcare delivery to make a greater impact today, tomorrow, and beyond.

Our Baxter colleagues are united by our Mission to Save and Sustain Lives. Together, our community is driven by a culture of courage, trust, and collaboration. Every individual is empowered to take ownership and make a meaningful impact. We strive for efficient and effective operations, and we hold each other accountable for delivering exceptional results.

Here, you will find more than just a job—you will find purpose and pride. 

Interoperability Engineer II

Saving and Sustaining Lives Through Connected Healthcare

This is where you save and sustain lives

At Baxter, we are deeply connected by our mission. No matter your role at Baxter, your work makes a positive impact on people around the world. You’ll feel a sense of purpose throughout the organization, as we know our work improves outcomes for millions of patients. Baxter’s products and therapies are found in almost every hospital worldwide, in clinics and in the home. For over 85 years, we have pioneered medical innovations that transform healthcare. This is where you can do your best work—at the intersection of saving and sustaining lives.

Your role at Baxter

As an

Interoperability Engineer

, you will be responsible for the

verification of medical device digital interoperability

. You will ensure that Baxter devices meet defined system and interface requirements for interoperating with

other medical devices and healthcare IT systems

, such as hospital infrastructure, middleware, and digital applications.

This role applies a

systems engineering foundation

with a strong emphasis on

requirements‑based verification

, interface testing, and system integration activities. The position does

not

own validation activities, but collaborates closely with teams responsible for clinical and user validation.

Your team

You will work within a cross‑functional environment that includes Systems Engineering, Software Engineering, Verification, Quality, Cybersecurity, IT, and Clinical stakeholders. The team values disciplined execution, collaboration, and clear ownership to deliver compliant and reliable interoperable medical device solutions.

What you’ll be doing

• Own and maintain

interoperability verification requirements

, including traceability from platform requirements to verification evidence

• Develop and execute

verification plans, test cases, and test procedures

for interoperability-related requirements

• Perform

platform-level verification testing

for device‑to‑device and device‑to‑IT connectivity enabled features

• Collaborate with Systems and Software Engineering teams to ensure interoperability designs are

verifiable and testable

• Assess interoperability-related changes and determine

verification impact and required test coverage

• Troubleshoot and support resolution of interoperability defects identified during verification and integration testing

• Generate clear, compliant

verification documentation and evidence

to support design control and regulatory needs

• Apply understanding of

clinical workflows and intended use

when defining representative verification scenarios

• Demonstrate working knowledge of

FDA, ISO, IEC, and software lifecycle standards

as they apply to verification of connected medical devices

• Contribute to continuous improvement of interoperability verification methods, tools, and best practices

What you’ll bring

• Bachelor’s degree in Engineering (Systems, Biomedical, Computer, Electrical, or related discipline)

• 3+ years of experience in medical device or regulated product development, with a

focus on verification activities

• Systems engineering background with strong experience in

requirements management, traceability, and verification planning

• Hands‑on experience with

system, interface, or integration verification testing

• Familiarity with medical device interoperability concepts, healthcare IT integration, or connected systems

• Experience participating in design control and change management processes

• Strong technical documentation, organization, and analytical skills

• Effective written and verbal communication skills for cross‑functional collaboration

• Experience with requirements and verification tools (e.g., DOORS, ALM tools) preferred

• Exposure to healthcare data exchange mechanisms or interface specifications is a plus

Equal Employment Opportunity

Baxter is an equal opportunity employer. Baxter evaluates qualified applicants without regard to race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, protected veteran status, disability/handicap status or any other legally protected characteristic.

Reasonable Accommodations

Baxter is committed to working with and providing reasonable accommodations to individuals with disabilities globally. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application or interview process, please click on the https://forms.microsoft.com/Pages/ResponsePage.aspx?id=Nd3GyB-HME-FrGU185glFONjsWP56EBPkq0TvnZuTOFUQk8wUzgwWENFVU5YOFdEOTFEM0pTN0VOVy4u link here and let us know the nature of your request along with your contact information.

Recruitment Fraud Notice

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