CrawlJobs Logo

Sr. Systems Verification Engineer, Interoperability

United States, Round Lake Employment contract 96000.00 - 132000.00 USD / Year · Job Posted May 04, 2026
Apply Position
Job Link Share

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

Looking for more opportunities?

Search for other job offers that match your skills and interests.

Similar Jobs for

Sr. Systems Verification Engineer, Interoperability

8 matching positions

Sr. Systems Verification Engineer, Interoperability

This is where new knowledge is discovered. Baxter's Research and Development tea...
Location
Location
United States , Round Lake
Salary
Salary:
96000.00 - 132000.00 USD / Year
https://www.baxter.com/ Logo
Baxter
Expiration Date
Until further notice
Flip Icon
Requirements
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
  • Experience with requirements and verification tools (e.g., DOORS, ALM tools) preferred
Job Responsibility
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
What we offer
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
  • Fulltime
Read More
Arrow Right

Sr. Systems Verification Engineer, Interoperability

As an Interoperability Engineer, you will be responsible for the verification of...
Location
Location
United States , Round Lake
Salary
Salary:
96000.00 - 132000.00 USD / Year
https://www.baxter.com/ Logo
Baxter
Expiration Date
Until further notice
Flip Icon
Requirements
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
Job Responsibility
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
What we offer
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), with the ability to purchase company stock at a discount
  • 401(k) Retirement Savings Plan (RSP), with options for employee contributions and company matching
  • Flexible Spending Accounts
  • Fulltime
Read More
Arrow Right

Sr. Systems Verification Engineer, Interoperability

This is where new knowledge is discovered. Baxter's Research and Development tea...
Location
Location
United States , Round Lake
Salary
Salary:
96000.00 - 132000.00 USD / Year
https://www.baxter.com/ Logo
Baxter
Expiration Date
Until further notice
Flip Icon
Requirements
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
Job Responsibility
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
What we offer
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), with the ability to purchase company stock at a discount
  • 401(k) Retirement Savings Plan (RSP), with options for employee contributions and company matching
  • Flexible Spending Accounts
  • Fulltime
Read More
Arrow Right

Sr. Engineer, Interoperability

Location
Location
India , Bengaluru
Salary
Salary:
Not provided
https://www.baxter.com/ Logo
Baxter
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • 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
Job Responsibility
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
  • 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
  • Fulltime
Read More
Arrow Right

Sr. Principal Engineer, PDO & Verification

Design and develop medical device systems and digital platforms, ensuring compli...
Location
Location
United States , Raleigh
Salary
Salary:
144000.00 - 216000.00 USD / Year
https://www.baxter.com/ Logo
Baxter
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Bachelor’s degree in Electronics Engineering and Communications or related field plus 8 years of related experience
  • Translate Customer/end user needs, design constraints, and regulatory mandates into comprehensive system requirements, including functional, non functional, and performance specifications for medical devices and health software
  • Perform comprehensive risk evaluation in compliance with ISO 14971, ensuring identification, analysis, and control of medical device risks
  • Analyze system behavior for complex medical products under FDA guidelines in accordance with IEC 60601-1 and IEC 80601-1 standards
  • Lead the verification and validation of medical devices and health software in strict accordance with IEC 62304 and IEC 82304, ensuring traceability, regulatory compliance, and adherence to FDA recognized software development lifecycle standards
  • Develop and maintain comprehensive verification and validation plans for medical devices and health software, including detailed test protocols, execution records, and test reports, ensuring full traceability, regulatory compliance with FDA requirements, and alignment with engineering best practices and standards such as 21CFR-820
  • Perform integration and validation testing of Kubernetes based medical device monitoring platforms across On Prem and Cloud, leveraging Docker, Kubernetes, MQTT, and RabbitMQ with secure API driven communication to ensure interoperability and compliance in regulated healthcare environments
  • Create and maintain regulatory compliant technical artifacts—including development plans, test protocols, traceability matrices, and verification/validation reports—in alignment with FDA requirements and medical device industry standards such as IEC 62304 and ISO 13485
  • Plan and prepare the test environment for integration of medical devices with Electronic Medical Record (EMR) systems, ensuring interoperability, data integrity, and patient safety in compliance with FDA regulations, IEC 62304 software lifecycle requirements, and HL7/FHIR interoperability standards
  • Expertise in IHE Patient Care Device (PCD) Alarm Communication Management Profile, which uses HL7 messaging standards to communicate between medical devices and alert management systems
Job Responsibility
Job Responsibility
  • Design and develop medical device systems and digital platforms, ensuring compliance with regulatory and business standards from concept to commercialization
  • Create and maintain product and software architecture, user interface design, and specifications that meet customer needs and regulatory requirements
  • Utilize systems engineering and design thinking to define functional and performance requirements for products and systems
  • Model behaviors across systems and conduct risk analysis from a systems perspective
  • Perform risk management activities, including analysis, evaluation, and mitigation, in accordance with ISO 14971
  • Develop and maintain verification and validation plans, test protocols, and reports to comply with FDA and industry standards
  • Conduct integration and system validation testing for Kubernetes-based digital platforms in On-Prem and Cloud environments
  • Prepare technical documentation (design plans, traceability matrices, test reports) in compliance with FDA-approved quality processes for Class I/II and MDDS products
  • Train and mentor the systems team.
What we offer
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
  • 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
  • Fulltime
Read More
Arrow Right

Sr. Principal Engineer, PDO & Verification

Baxter’s Research and Development teams work cross functionally to innovate, dev...
Location
Location
United States , Raleigh
Salary
Salary:
144000.00 - 216000.00 USD / Year
https://www.baxter.com/ Logo
Baxter
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Bachelor’s degree in Electronics Engineering and Communications or related field plus 8 years of related experience
  • Translate Customer/end user needs, design constraints, and regulatory mandates into comprehensive system requirements, including functional, non functional, and performance specifications for medical devices and health software
  • Perform comprehensive risk evaluation in compliance with ISO 14971, ensuring identification, analysis, and control of medical device risks
  • Analyze system behavior for complex medical products under FDA guidelines in accordance with IEC 60601-1 and IEC 80601-1 standards
  • Lead the verification and validation of medical devices and health software in strict accordance with IEC 62304 and IEC 82304, ensuring traceability, regulatory compliance, and adherence to FDA recognized software development lifecycle standards
  • Develop and maintain comprehensive verification and validation plans for medical devices and health software, including detailed test protocols, execution records, and test reports, ensuring full traceability, regulatory compliance with FDA requirements, and alignment with engineering best practices and standards such as 21CFR-820
  • Perform integration and validation testing of Kubernetes based medical device monitoring platforms across On Prem and Cloud, leveraging Docker, Kubernetes, MQTT, and RabbitMQ with secure API driven communication to ensure interoperability and compliance in regulated healthcare environments
  • Create and maintain regulatory compliant technical artifacts—including development plans, test protocols, traceability matrices, and verification/validation reports—in alignment with FDA requirements and medical device industry standards such as IEC 62304 and ISO 13485
  • Plan and prepare the test environment for integration of medical devices with Electronic Medical Record (EMR) systems, ensuring interoperability, data integrity, and patient safety in compliance with FDA regulations, IEC 62304 software lifecycle requirements, and HL7/FHIR interoperability standards
  • Expertise in IHE Patient Care Device (PCD) Alarm Communication Management Profile, which uses HL7 messaging standards to communicate between medical devices and alert management systems
Job Responsibility
Job Responsibility
  • Design and develop medical device systems and digital platforms, ensuring compliance with regulatory and business standards from concept to commercialization
  • Create and maintain product and software architecture, user interface design, and specifications that meet customer needs and regulatory requirements
  • Utilize systems engineering and design thinking to define functional and performance requirements for products and systems
  • Model behaviors across systems and conduct risk analysis from a systems perspective
  • Perform risk management activities, including analysis, evaluation, and mitigation, in accordance with ISO 14971
  • Develop and maintain verification and validation plans, test protocols, and reports to comply with FDA and industry standards
  • Conduct integration and system validation testing for Kubernetes-based digital platforms in On-Prem and Cloud environments
  • Prepare technical documentation (design plans, traceability matrices, test reports) in compliance with FDA-approved quality processes for Class I/II and MDDS products
  • Train and mentor the systems team
What we offer
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) with options for employee contributions and company matching
  • Flexible Spending Accounts
  • Fulltime
Read More
Arrow Right

Sr. Eng, Interoperability

This is where new knowledge is discovered. Baxter's Research and Development tea...
Location
Location
India , Bengaluru
Salary
Salary:
Not provided
https://www.baxter.com/ Logo
Baxter
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • 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
Job Responsibility
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
  • 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 we offer
What we offer
  • Support for Parents
  • Continuing Education/ Professional Development
  • Employee Heath & Well-Being Benefits
  • Paid Time Off
  • 2 Days a Year to Volunteer
  • Fulltime
Read More
Arrow Right

Sr. Eng, Interoperability

This is where new knowledge is discovered. Baxter’s Research and Development tea...
Location
Location
India , Bengaluru
Salary
Salary:
Not provided
https://www.baxter.com/ Logo
Baxter
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • 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
Job Responsibility
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
  • 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 we offer
What we offer
  • Support for Parents
  • Continuing Education/Professional Development
  • Employee Health & Well-Being Benefits
  • Paid Time Off
  • 2 Days a Year to Volunteer
  • Fulltime
Read More
Arrow Right