Sr. Engineer, Interoperability Job at Baxter (Bengaluru)

Sr. Systems Verification Engineer, Interoperability

This is where new knowledge is discovered. Baxter's Research and Development tea...

Location

United States , Round Lake

Salary:

96000.00 - 132000.00 USD / Year

Baxter

Expiration Date

Until further notice

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

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

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

Sr. Systems Verification Engineer, Interoperability

As an Interoperability Engineer, you will be responsible for the verification of...

Location

United States , Round Lake

Salary:

96000.00 - 132000.00 USD / Year

Baxter

Expiration Date

Until further notice

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

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

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

Sr. Systems Verification Engineer, Interoperability

This is where new knowledge is discovered. Baxter's Research and Development tea...

Location

United States , Round Lake

Salary:

96000.00 - 132000.00 USD / Year

Baxter

Expiration Date

Until further notice

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

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

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

Sr. Systems Verification Engineer, Interoperability

This is where new knowledge is discovered. Baxter's Research and Development tea...

Location

United States , Round Lake

Salary:

96000.00 - 132000.00 USD / Year

Baxter

Expiration Date

Until further notice

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

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

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

New

Sr. Eng, Interoperability

This is where new knowledge is discovered. Baxter’s Research and Development tea...

Location

India , Bengaluru

Salary:

Not provided

Baxter

Expiration Date

Until further notice

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

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

Support for Parents
Continuing Education/Professional Development
Employee Health & Well-Being Benefits
Paid Time Off
2 Days a Year to Volunteer

Fulltime

Sr. Director, Program Engineering and Permitting

The Sr. Director of Program Engineering and Permitting oversees all large progra...

Location

United States , Denver

Salary:

185000.00 - 200000.00 USD / Year

Southeast Utilities of Georgia LLC

Expiration Date

Until further notice

Requirements

A bachelor’s degree (B.A.) in engineering, telecom or business administration is required
A minimum of 10 to 15 years of experience in engineering, permitting, telecommunications, or related industry
A minimum of 5 years of senior leadership experience in an engineering and/or telecom environment.
Equivalent combination of education/job experience
Extensive experience in civil and/or telecommunications infrastructure, with a deep background in fiber optic network design, technology standards, deployment, and construction.
Expertise in navigating complex, domestic and offshore permitting processes and coordinating with various government agencies.
Experience leading and/or participating on global teams to provide procedural consistency and exchange best practices
Comfortable navigating ambiguity and change in different international business environments
In-depth knowledge of local ordinances, codes, and evolving regulations.
Ability to work in a matrixed environment with multiple levels of accountability.

Job Responsibility

Drive the strategic vision and execution of Congruex engineering initiatives to enhance system integrations and interoperability.
Collaborates with construction and cross-functional teams on value engineering opportunities and design constructability validation
Manages domestic and offshore engineering staffing needs for large projects and holds resources accountable for performance in partnership with matrixed leadership.
Assists in developing engineering organizations for large programs during the bid phase to ensure project demands can be met effectively.
Develops a comprehensive risk and opportunities matrix during the bid phase for large construction projects, identifying potential risks, opportunities for value engineering, and mitigation strategies to ensure project success and profitability.
Supports and audits all engineering teams involved in large projects to ensure resource utilization, quality and adherence to project requirements.
Develops, writes, and maintains standards for domestic and offshore engineering and permitting processes across all large programs to ensure consistency and efficiency.
Direct all activities related to securing necessary permits, licenses, and agreements from municipalities, utility companies, and other regulatory bodies.
Lead the permit review and audit process to establish standard cadences for all programs.
Reviews and provides feedback on engineering standards and best practices to optimize project design and execution during the estimating phase.

What we offer

Medical, Dental & Vision Benefits
401(k) Program with a Company Match.
Free Wellness Resources & Marketplace Discounts
Paid Maternity & Parental Leave
Paid Basic Life Insurance & Voluntary Options

Fulltime

Sr. Principal Engineer, PDO & Verification

Design and develop medical device systems and digital platforms, ensuring compli...

Location

United States , Raleigh

Salary:

144000.00 - 216000.00 USD / Year

Baxter

Expiration Date

Until further notice

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

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

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

Sr. Principal Engineer, PDO & Verification

Baxter’s Research and Development teams work cross functionally to innovate, dev...

Location

United States , Raleigh

Salary:

144000.00 - 216000.00 USD / Year

Baxter

Expiration Date

Until further notice

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

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

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

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Sr. Engineer, Interoperability

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