Quality Engineer

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. As a Quality Engineer I at Baxter Healthcare Corporation, you will have a meaningful role in ensuring the quality and reliability of our healthcare products.

This is an outstanding opportunity to advance your career in a dynamic and supportive environment. Your work will directly affect the health and well‑being of patients worldwide. No matter your role at Baxter, your talent, skills, and time has a direct impact on people’s lives. Since 1931, we have been at the forefront of innovation by bringing smarter, more personalized care to patients around the world.

Now, we’re more determined than ever to make a lasting impact as we are redefining healthcare delivery across the care journey. Our Mission to Save and Sustain Lives motivates us as we create a culture in which each of us can succeed. This is where you belong.

• Perform process validation, process capability, and process control studies for assigned areas.
• Drive quality/manufacturing projects by applying Lean, problem‑solving, process control, and project management tools to achieve and sustain operational excellence.
• Support Manufacturing, Engineering, and Quality Management departments with the development and implementation of new processes and technology.
• Assist in identifying and developing process improvement projects, including automation and computerization.
• Ensure computer systems and applications align with regulatory quality standards through validation activities.
• Ensure FDA regulations are met for system upgrades and replacements.
• Ensure the quality of facility systems by writing and completing protocols and test cases for validations.
• Coordinate testing and detailing of projects.
• Perform and deliver changes to applications and assist in training for systems.
• Apply diversified knowledge of applied Statistical Analysis techniques, procedures, and criteria to carry out measurements, process, and product capability studies toward the development of new or refined equipment, materials, processes, instruments, and products.
• Communicate effectively in written and verbal form and function effectively as a team member.
• Align with plant and department environmental health and safety regulations.
• Learn, understand, and apply rigorous quality standards, established guidelines, and current Good Manufacturing Practices (cGMP).
• Notify the supervisor and take appropriate action if any safety, quality, mechanical, or discrepancy issues occur.
• Sustain a clean and safe work area using 6S principles.
• Perform all other duties and responsibilities as determined by supervision/management.

• Knowledge of applications such as Wonderware, Allen‑Bradley PLC, Access, and Microsoft Project preferred.
• ASQ Certification (CQE or CSQE) or equivalent desired.
• Strong leadership skills and the ability to work with diversified cross‑functional teams across different plant locations.
• Logical thought process and self‑motivation to work well without direct…