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Sr. Systems Verification Engineer, Interoperability

https://www.baxter.com/ Logo

Baxter

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Location:
United States , Round Lake

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Category:
Research and Development

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Contract Type:
Employment contract

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Salary:

96000.00 - 132000.00 USD / Year
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Job Description:

This is where new knowledge is discovered. Baxter's Research and Development teams work cross functionally to innovate, develop and introduce creative solutions for patients needs globally. From Scientists to Engineers, your work creates the products that save and sustain lives. 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.

Job Responsibility:

  • 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

Requirements:

  • Bachelor's degree in Engineering (Systems, Biomedical, Computer, Electrical, or related discipline)
  • 3+ years of experience in 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
  • 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

Nice to have:

  • Familiarity with medical device interoperability concepts, healthcare IT integration, or connected systems
  • Experience with requirements and verification tools (e.g., DOORS, ALM tools)
What we offer:
  • Support for Parents
  • Continuing Education/ Professional Development
  • Employee Heath & Well-Being Benefits
  • Paid Time Off
  • 2 Days a Year to Volunteer
  • medical and dental coverage that start on day one
  • insurance coverage for basic life, accident, short-term and long-term disability, and business travel accident insurance
  • Employee Stock Purchase Plan (ESPP)
  • 401(k) Retirement Savings Plan (RSP)
  • Flexible Spending Accounts
  • educational assistance programs
  • time-off benefits such as paid holidays
  • paid time off ranging from 20 to 35 days based on length of service
  • family and medical leaves of absence
  • paid parental leave
  • commuting benefits
  • Employee Discount Program
  • Employee Assistance Program (EAP)
  • childcare benefits
  • annual incentive bonus

Additional Information:

Job Posted:
May 04, 2026

Employment Type:
Fulltime
Work Type:
On-site work
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