Quality Engineer I

Zvh; Arkansas; On-site; USD 76,000 - 95,000; Full time

Benefits offered by this job

Medical and dental coverage starting 1

Employee Stock Purchase Plan (ESPP)

401(k) Retirement Savings Plan

Paid holidays and time off

Job summary

Baxter Healthcare Corporation is seeking a Quality Engineer I to ensure quality and reliability of healthcare products. You will participate in process validation, quality initiatives, and cross‑functional collaboration to drive operational excellence.

Responsibilities include supporting manufacturing, engineering, and quality management with new processes, ensuring cGMP compliance, and contributing to 6S and safety initiatives within a dynamic team environment.

Qualifications

• BS degree in Engineering, Computer Science, or other core Science Field.
• ASQ Certification or equivalent desired.
• Experience in Quality Assurance or the Pharmaceutical industry is preferred.

Responsibilities

• Perform process validation, process capability, and process control studies.
• Drive quality/manufacturing projects using Lean, problem‑solving and project tools.
• Support Manufacturing, Engineering, and Quality Management with new processes.
• Ensure compliance with regulatory quality standards and FDA regulations.
• Coordinate testing and detail project protocols and test cases.

Skills

ASQ Certification (CQE or CSQE)

Leadership

Ability to learn applications

QA experience

Education

BS degree in Engineering, Computer Science, or other core Science Field

Tools

Wonderware

Allen-Bradley PLC

Access

Microsoft Project

Job description

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.

Key Responsibilities

• 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, Skills, and Abilities

• 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 supervision.
• Ability to quickly learn and understand applications.
• Experience in Quality Assurance or the Pharmaceutical industry desired.
• Meet visual acuity requirements as detailed in the Baxter Cleveland Visual Acuity Procedure CL‑01‑01‑037.

Physical Requirements

• Ability to lift up to 10 pounds.
• Ability to sit, stand, and/or walk for long periods.
• Ability to reach above the shoulder.
• Ability to bend/stoop.

Required Education and Experience

BS degree in Engineering, Computer Science, or other core Science Field and 0‑1 year related experience (in‑house, co‑op, or acquired outside).

Other Duties as Assigned

Please note this job description is not built to cover or contain a comprehensive listing of activities, duties, and responsibilities required of the employee for this job. Duties, responsibilities, and activities may change at any time with or without notice. Overtime is worked as required.

Compensation

We understand compensation is an important factor as you consider the next step in your career. The estimated base salary for this position is $76,000 - $95,000 annually. We may pay more or less than the anticipated range based upon market data and other factors, all of which are subject to change. Individual pay is based upon location, skills and expertise, experience, and other relevant factors.

Applicants must be authorized to work for any employer in the U.S. We cannot sponsor or transfer sponsorship of an employment visa.

Benefits at Baxter

• 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.
• 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.

Join us and enjoy the competitive compensation and benefits we offer to our employees.

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.

Know Your Rights: Workplace Discrimination is Illegal.

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.