Jobs and Careers
BA

Sr Engineer, System Verification

Baxter International Inc.
ILRL12 - RL Technology II, United States, United Statesfull_timeVerifiedPosted 3 Oct 2025
💰 $121,000/yr($88,000/yr$121,000/yr)

About the role

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. 

Your Role at Baxter

This is where your work saves lives

As a part of Infusion Therapies & Technologies division, the Senior Engineer, System Verification, contributes to system verification engineering vision that aligns with the organization's vision and strategic plan. Use proven understanding of engineering theory and best-practice in a variety of fields to lead sophisticated projects or programs within boundaries of quality, time and budget. Exhibit creativity and innovation in completing divisional and cross-functional/business unit goals and objectives. Contribute to the plans and leads project assignments in the evaluation, selection and adaptation of various techniques, procedures, and criteria with minimal mentorship. Ensures that quality is built into the design during new product development

What you'll be doing

  • Contribute to the planning, development and execution of system verification deliverables (test plans, test protocols, test cases, test reports, studies). Engage in test planning during design and development phases.

  • Contribute to the development and documentation of system requirements, systems architecture and design.

  • Ensure appropriate traceability between system, subsystem, and software verification.

  • Manage the integration of deliverables from subsystem teams, multi-functional teams (risk management, compliance, etc.) and external partners.

  • Resolve competing constraints between interrelated functions (Engineering, Risk Management, Compliance, Reliability, Clinical, Human Factors, Regulatory).

  • Implement configuration and change management through the complete product life-cycle.

  • Recommend changes to policies and establishes procedures that affect immediate department/function.

  • Build process improvements to streamline testing between system verification, subsystem and software verification.

  • Ensure all program achievements in support of all phases of the product development lifecycle are completed on time, with appropriate quality, and in compliance with relevant laboratory standards and regulations.

  • Participate and/ or leads design reviews.

  • Guide the team in investigations for identifying the root cause and drives action to prevent such issues recurring.

  • Guide, mentor, and provide directions to junior verification engineers.

  • Ensure compliance to the product development process and Quality System requirements.

  • Ensure good documentation and Good Manufacturing practices are followed in the verification process.


What You'll Bring

  • Bachelor’s Degree in Mechanical, Electrical, Computer Science, Biomedical Engineering or equivalent, MS preferred

  • 3+ years of relevant industry experience.

  • Medical device industry experience is preferred.

  • Proven organization skills and ability to collaborate with both technical and non-technical personnel.

  • Solid understanding of ISO and/or FDA and other regulatory standards.

  • Knowledge of Design controls, Lifecycle testing processes, MTBF analysis.
     

Baxter is committed to supporting the needs for flexibility in the workplace. We do so through our flexible workplace policy which includes a required minimum number of days a week onsite. This policy provides the benefits of connecting and collaborating in-person in support of our Mission. The flexible workplace policy is subject to local laws and legal requirements. At its discretion, Baxter may decide to adjust, suspend, or discontinue as business needs change.


We understand compensation is an important factor as you consider the next step in your career. At Baxter, we are committed to equitable pay for all employees, and we strive to be more transparent with our pay practices. The estimated base salary for this position is $88,000 to $12

Apply for this role

Generate a tailored application kit with a matched cover letter, interview prep, and CV highlights — in under 60 seconds.

Apply Now →Generate Application Kit

Free account required — sign up in 30s

Company

Baxter International Inc.

View company profile →