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Baxter Logo Baxter · Research and Development

Principal Systems Verification Engineer

United States, Round Lake Employment contract 112000.00 - 154000.00 USD / Year · Job Posted May 04, 2026
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Job Description

This is where your work saves lives. As a part of Infusion Therapies & Platforms (ITP) division, the Principal Systems Verification Engineer, provides technical leadership to the System Verification team. Plans and leads project assignments in the evaluation, selection and adaptation of various techniques, procedures, and criteria with minimal guidance. Based on significant process and technical expertise, reviews and approves verification plans and methods and provides general direction to verification engineering staff. Ensures that quality is built into the design during new product development. Reports on the progress to senior management. Contributes to System Verification Engineering vision that aligns with the organization's vision and strategic plan. Exhibits creativity and innovation in completing divisional and cross-functional/business unit goals and objectives.

Job Responsibility

  • Lead planning, development and execution of system verification deliverables (test plans, test protocols, test cases, test reports, studies) and provide technical direction to the team
  • Lead validation efforts for laboratory equipment supporting infusion system testing
  • Develop and execute validation protocols, test plans, and reports in alignment with FDA, ISO, and equipment validation best practices
  • Perform IQ/OQ/PQ activities for lab equipment and ensure complete traceability from requirements through test execution
  • Contribute to the development and documentation of system requirements, systems architecture and design
  • Create best practices, process improvements and traceability to streamline testing between system, subsystem, and software verification
  • Implementing configuration and change management through the complete product life cycle, including verification and validation deliverables
  • Actively communicates and advocates team's capabilities and accomplishments
  • Create opportunities to automate testing and optimize test processes
  • Participates and/ or leads design reviews
  • Guides the team in investigations for identifying the root cause and drives action to prevent such issues recurring
  • Guide, mentor, and provide direction to junior verification and validation engineers

Requirements

  • Bachelor's degree in Mechanical, Electrical, Computer Science, Biomedical Engineering or related field
  • 5+ years of relevant industry experience
  • Strong knowledge of ISO, FDA and other regulatory standards
  • Knowledge of Design controls, lifecycle testing processes, MTBF analysis
  • Requires strong organization and communication skills, with the ability to interface with both technical and non-technical personnel
  • Ability to convince management on courses of action with minimal assistance using both written and verbal methods
  • Ability to lead teams across multiple sites

Nice to have

  • Medical device industry experience
  • Demonstrated experience with test automation

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
  • 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
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Principal Systems Verification Engineer

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Principal Systems Verification Engineer

This is where new knowledge is discovered. Baxter's Research and Development tea...
Location
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United States , Round Lake
Salary
Salary:
112000.00 - 154000.00 USD / Year
https://www.baxter.com/ Logo
Baxter
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Bachelor's degree in Mechanical, Electrical, Computer Science, Biomedical Engineering or related field.
  • 5+ years of relevant industry experience.
  • Medical device industry experience is preferred.
  • Strong organization and communication skills, with the ability to interface with both technical and non-technical personnel.
  • Strong knowledge of ISO, FDA and other regulatory standards is essential.
  • Knowledge of Design controls, lifecycle testing processes, MTBF analysis.
  • Ability to convince management on courses of action with minimal assistance using both written and verbal methods.
  • Ability to lead teams across multiple sites.
  • Demonstrated experience with test automation preferred.
Job Responsibility
Job Responsibility
  • Lead planning, development and execution of system verification deliverables (test plans, test protocols, test cases, test reports, studies) and provide technical direction to the team.
  • Lead validation efforts for laboratory equipment supporting infusion system testing.
  • Develop and execute validation protocols, test plans, and reports in alignment with FDA, ISO, and equipment validation best practices.
  • Perform IQ/OQ/PQ activities for lab equipment and ensure complete traceability from requirements through test execution.
  • Contribute to the development and documentation of system requirements, systems architecture and design.
  • Create best practices, process improvements and traceability to streamline testing between system, subsystem, and software verification.
  • Implementing configuration and change management through the complete product life cycle, including verification and validation deliverables.
  • Actively communicates and advocates team's capabilities and accomplishments.
  • Create opportunities to automate testing and optimize test processes.
  • Participate and/or lead design reviews.
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
  • Medical and dental coverage starting day one
  • Basic life, accident, short-term and long-term disability insurance
  • Business travel accident insurance
  • Employee Stock Purchase Plan (ESPP)
  • 401(k) Retirement Savings Plan (RSP) with company matching
  • Fulltime
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Principal Systems Verification Engineer

This is where your work makes a difference. At Baxter, we believe every person—r...
Location
Location
United States , Round Lake
Salary
Salary:
112000.00 - 154000.00 USD / Year
https://www.baxter.com/ Logo
Baxter
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Bachelor's degree in Mechanical, Electrical, Computer Science, Biomedical Engineering or related field
  • 5+ years of relevant industry experience
  • Medical device industry experience is preferred
  • Strong organization and communication skills, with the ability to interface with both technical and non-technical personnel
  • Strong knowledge of ISO, FDA and other regulatory standards is essential
  • Knowledge of Design controls, lifecycle testing processes, MTBF analysis
  • Ability to convince management on courses of action with minimal assistance using both written and verbal methods
  • Ability to lead teams across multiple sites
  • Demonstrated experience with test automation preferred
Job Responsibility
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  • Lead planning, development and execution of system verification deliverables (test plans, test protocols, test cases, test reports, studies) and provide technical direction to the team
  • Lead validation efforts for laboratory equipment supporting infusion system testing (e.g., Infuscale, altitude chambers, environmental chambers, and related test systems)
  • Develop and execute validation protocols, test plans, and reports in alignment with FDA, ISO, and equipment validation best practices
  • Perform IQ/OQ/PQ activities for lab equipment and ensure complete traceability from requirements through test execution
  • Contribute to the development and documentation of system requirements, systems architecture and design
  • Create best practices, process improvements and traceability to streamline testing between system, subsystem, and software verification
  • Implementing configuration and change management through the complete product life cycle, including verification and validation deliverables
  • Actively communicates and advocates team's capabilities and accomplishments
  • Create opportunities to automate testing and optimize test processes
  • Leverage and enhance existing automation framework for system testing
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  • 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
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Principal Systems Verification Engineer

This is where your work makes a difference. At Baxter, we believe every person—r...
Location
Location
United States , Round Lake
Salary
Salary:
112000.00 - 154000.00 USD / Year
https://www.baxter.com/ Logo
Baxter
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Bachelor’s degree in Mechanical, Electrical, Computer Science, Biomedical Engineering or related field
  • 5+ years of relevant industry experience
  • Medical device industry experience is preferred
  • Strong organization and communication skills, with the ability to interface with both technical and non-technical personnel
  • Strong knowledge of ISO, FDA and other regulatory standards
  • Knowledge of Design controls, lifecycle testing processes, MTBF analysis
  • Ability to convince management on courses of action with minimal assistance using both written and verbal methods
  • Ability to lead teams across multiple sites
  • Demonstrated experience with test automation preferred
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  • Lead planning, development and execution of system verification deliverables (test plans, test protocols, test cases, test reports, studies) and provide technical direction to the team
  • Lead validation efforts for laboratory equipment supporting infusion system testing
  • Develop and execute validation protocols, test plans, and reports in alignment with FDA, ISO, and equipment validation best practices
  • Perform IQ/OQ/PQ activities for lab equipment and ensure complete traceability from requirements through test execution
  • Contribute to the development and documentation of system requirements, systems architecture and design
  • Create best practices, process improvements and traceability to streamline testing between system, subsystem, and software verification
  • Implementing configuration and change management through the complete product life cycle, including verification and validation deliverables
  • Actively communicates and advocates team’s capabilities and accomplishments
  • Create opportunities to automate testing and optimize test processes
  • Leverage and enhance existing automation framework for system testing
What we offer
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  • 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)
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Principal Systems Verification Engineer

This is where your work saves lives. As a part of Infusion Therapies & Platforms...
Location
Location
United States , Round Lake
Salary
Salary:
112000.00 - 154000.00 USD / Year
https://www.baxter.com/ Logo
Baxter
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Bachelor's degree in Mechanical, Electrical, Computer Science, Biomedical Engineering or related field
  • 5+ years of relevant industry experience
  • Medical device industry experience is preferred
  • Requires strong organization and communication skills, with the ability to interface with both technical and non-technical personnel
  • Strong knowledge of ISO, FDA and other regulatory standards is essential
  • Knowledge of Design controls, lifecycle testing processes, MTBF analysis
  • Ability to convince management on courses of action with minimal assistance using both written and verbal methods
  • Ability to lead teams across multiple sites
  • Demonstrated experience with test automation preferred
  • Applicants must be authorized to work for any employer in the U.S. We are unable to sponsor or take over sponsorship of an employment visa at this time
Job Responsibility
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  • Lead planning, development and execution of system verification deliverables (test plans, test protocols, test cases, test reports, studies) and provide technical direction to the team
  • Lead validation efforts for laboratory equipment supporting infusion system testing (e.g., Infuscale, altitude chambers, environmental chambers, and related test systems)
  • Develop and execute validation protocols, test plans, and reports in alignment with FDA, ISO, and equipment validation best practices
  • Perform IQ/OQ/PQ activities for lab equipment and ensure complete traceability from requirements through test execution
  • Contribute to the development and documentation of system requirements, systems architecture and design
  • Create best practices, process improvements and traceability to streamline testing between system, subsystem, and software verification
  • Implementing configuration and change management through the complete product life cycle, including verification and validation deliverables
  • Actively communicates and advocates team's capabilities and accomplishments
  • Create opportunities to automate testing and optimize test processes. Leverage and enhance existing automation framework for system testing
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What we offer
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  • 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
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Principal Systems Engineer

This is where new knowledge is discovered. Baxter's Research and Development tea...
Location
Location
United States , Skaneateles Falls
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Salary:
112000.00 - 154000.00 USD / Year
https://www.baxter.com/ Logo
Baxter
Expiration Date
Until further notice
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Requirements
Requirements
  • Bachelor's degree in Mechanical, Electrical, Software Engineering, or a related technical discipline
  • 5+ years of relevant engineering experience, preferably in medical devices or a regulated industry
  • Strong working knowledge of ISO 14971 (Application of Risk Management to Medical Devices)
  • Strong working knowledge of IEC 62304 (Medical Device Software Lifecycle Processes)
  • Strong working knowledge of IEC/TR 80002-1 (Guidance on Software Risk Management)
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  • Strong interpersonal and communication skills, with the ability to clearly convey complex technical concepts
  • Ability to make sound decisions in the absence of complete information and navigate ambiguity effectively
  • Strategic mindset with strong attention to detail and execution discipline
  • Proven ability to manage multiple priorities and deliverables in parallel
Job Responsibility
Job Responsibility
  • Translate customer needs, business objectives, and regulatory requirements into clear, testable system-level requirements
  • Lead and execute risk management activities in accordance with ISO 14971 (Medical Device Risk Management Standard), including: Risk management planning, Risk analysis and evaluation, Risk control implementation and verification
  • Decompose system-level requirements into subsystem and module-level requirements, ensuring traceability
  • Plan and oversee reliability and robustness activities to ensure product performance over time
  • Lead cross-functional teams in identifying and mitigating technical risks, resolving issues, and managing test defects
  • Evaluate product and design changes holistically to ensure impacts are fully assessed across system, regulatory, and business dimensions
  • Drive alignment across engineering, quality, and regulatory functions on system-level decisions and deliverables
  • Support adherence to Baxter product development processes, documentation expectations, and regulatory requirements
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  • 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
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Principal Systems Engineer

This is where new knowledge is discovered. Baxter's Research and Development tea...
Location
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United States , Skaneateles Falls
Salary
Salary:
112000.00 - 154000.00 USD / Year
https://www.baxter.com/ Logo
Baxter
Expiration Date
Until further notice
Flip Icon
Requirements
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  • Bachelor's degree in Mechanical, Electrical, Software Engineering, or a related technical discipline
  • 5+ years of relevant engineering experience, preferably in medical devices or a regulated industry
  • Strong working knowledge of: ISO 14971 (Application of Risk Management to Medical Devices)
  • IEC 62304 (Medical Device Software Lifecycle Processes)
  • IEC/TR 80002-1 (Guidance on Software Risk Management)
  • Demonstrated ability to lead through influence in a cross-functional team environment
  • Strong interpersonal and communication skills, with the ability to clearly convey complex technical concepts
  • Ability to make sound decisions in the absence of complete information and navigate ambiguity effectively
  • Strategic mindset with strong attention to detail and execution discipline
  • Proven ability to manage multiple priorities and deliverables in parallel
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  • Translate customer needs, business objectives, and regulatory requirements into clear, testable system-level requirements
  • Lead and execute risk management activities in accordance with ISO 14971 (Medical Device Risk Management Standard), including: Risk management planning, Risk analysis and evaluation, Risk control implementation and verification
  • Decompose system-level requirements into subsystem and module-level requirements, ensuring traceability
  • Plan and oversee reliability and robustness activities to ensure product performance over time
  • Lead cross-functional teams in identifying and mitigating technical risks, resolving issues, and managing test defects
  • Evaluate product and design changes holistically to ensure impacts are fully assessed across system, regulatory, and business dimensions
  • Drive alignment across engineering, quality, and regulatory functions on system-level decisions and deliverables
  • Support adherence to Baxter product development processes, documentation expectations, and regulatory requirements
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  • 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
  • paid holidays
  • paid time off ranging from 20 to 35 days based on length of service
  • family and medical leaves of absence
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  • Fulltime
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Principal Systems Engineer

This is where your work saves lives. The research we do and the products we dev...
Location
Location
United States , Round Lake
Salary
Salary:
112000.00 - 154000.00 USD / Year
https://www.baxter.com/ Logo
Baxter
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Bachelor’s degree required with 5+ years of experience or Masters with 3+ years of experience.
  • Solid understanding of systems engineering principals and related disciplines, Electro/Mechanical, Digital Interface, Fluid Mechanics, Materials Science, etc.
  • Success in delivering results on technical challenges including investigative and problem-solving skills (DFSS/DMAIC/CAPA).
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  • Good communication skills, both oral and written.
Job Responsibility
Job Responsibility
  • Lead development of Design Inputs and Digital Interface Requirements.
  • Work with cross functional team members (e.g., Marketing and Clinical personnel) to translate user needs into system requirements.
  • Lead engineering resources (Electrical, Mechanical, and Software) in the decomposition of system requirements to derived requirements.
  • Contributes to resolution of competing constraints among inter-related functions (e.g., engineering, manufacturing, regulatory, marketing) required to deliver products to market.
  • Resolves interface issues and have the ability to document theory of operations of complex medical product designs.
  • Work with verification engineers to define test strategies for the development of verification plans and validation plans using requirement tracing methods.
  • Support risk analysis activities from the capture of inherent hazards through mitigation, including quantitative residual risk calculation in support of the Safety Assurance Case.
  • Implement configuration management through the complete product life cycle, including design, development, and sustaining phases.
  • Interface with Manufacturing, Service, Product Surveillance, Supply Chain, and Customer Training staff through the design transfer process.
  • Ensure compliance to the product development process and Quality System.
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
Read More
Arrow Right

Principal Systems Engineer

This is where your work saves lives. The research we do and the products we deve...
Location
Location
United States , Round Lake
Salary
Salary:
112000.00 - 154000.00 USD / Year
https://www.baxter.com/ Logo
Baxter
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Bachelor’s degree required with 5+ years of experience or Masters with 3+ years of experience
  • Solid understanding of systems engineering principals and related disciplines, Electro/Mechanical, Digital Interface, Fluid Mechanics, Materials Science, etc
  • Success in delivering results on technical challenges including investigative and problem-solving skills (DFSS/DMAIC/CAPA)
  • Prior medical device preferred, Infusion Pumps and Syringe Pumps is a plus
  • Good communication skills, both oral and written
  • Applicants must be authorized to work for any employer in the U.S.
  • No sponsorship available
Job Responsibility
Job Responsibility
  • Lead development of Design Inputs and Digital Interface Requirements
  • Work with cross functional team members to translate user needs into system requirements
  • Lead engineering resources in decomposition of system requirements to derived requirements
  • Contributes to resolution of competing constraints among inter-related functions
  • Resolves interface issues and document theory of operations of complex medical product designs
  • Work with verification engineers to define test strategies for verification and validation plans
  • Support risk analysis activities from hazard capture through mitigation, including quantitative residual risk calculation
  • Implement configuration management through complete product life cycle
  • Interface with Manufacturing, Service, Product Surveillance, Supply Chain, and Customer Training staff
  • Ensure compliance to product development process and Quality System
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
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