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

Do you want to be part of Baxter Healthcare Corporation as a Quality Validations Engineer I? You will help maintain outstanding quality and safety standards in our workflows. You will plan, prepare, coordinate, and lead tasks related to the Validations System, ensuring they align with Good Manufacturing Practices (GMPs) and Good Documentation Practices (GDP). Emphasizing regulatory consistency and perfection, you will participate in and encourage ICare's initiatives, promoting solutions that improve product quality, safety, and efficiency. Your keen focus on detail and dedication to regulatory perfection will secure accurate execution and steady process refinement.

• Your team

• You will join a special validation team committed to maintaining the highest standards of Environment, Health, and Safety (EHS). The team grows with outstanding communication and teamwork, encouraging a safety culture and ensuring compliance with all legal and corporate requirements. Together, we are high-reaching in our goals, closely following guidelines to protect the safety and health of our personnel and the environment. Our coordinated approach ensures that we effectively complete projects and reach our objectives.

• What you'll be doing

Evaluate, build, and improve procedures related to your areas of responsibility.

Collaborate with personnel from other areas to develop and complete projects, validations, periodic reviews, continuous improvement initiatives, and analysis of exception documents.

Maintain and supervise validation quality indicators.

Ensure alignment with the standards of the Safety, Health, and Environmental Protection Program.

Provide required support to internal customers to improve the fulfillment of plant goals.

What you'll bring

• A degree or equivalent experience in Materials Engineering, Production, Industrial, Chemical, Systems, Electrical, Electronic, Electromechanical Engineering, or a related field.

• Proficiency in the English language.

Equal Employment Opportunity

Baxter is an equal opportunity employer. Baxter evaluates qualified applicants without regard to race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, protected veteran status, disability/handicap status or any other legally protected characteristic.

Reasonable Accommodations

Baxter is committed to working with and providing reasonable accommodations to individuals with disabilities globally. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application or interview process, please click on the link here and let us know the nature of your request along with your contact information.

Recruitment Fraud Notice

Baxter has discovered incidents of employment scams, where fraudulent parties pose as Baxter employees, recruiters, or other agents, and engage with online job seekers in an attempt to steal personal and/or financial information. To learn how you can protect yourself, review our Recruitment Fraud Notice.