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.

At Baxter, we are deeply connected by our mission. Every role contributes to products and therapies that improve outcomes for millions of patients worldwide. As a Quality Lab Associate I, you will perform chemical and analytical testing to support product quality, regulatory compliance, and operational excellence. This position plays a critical role in ensuring the safety, effectiveness, and quality of Baxter products through adherence to established procedures, quality systems, and Good Manufacturing Practices (cGMP).

Essential Responsibilities

• Perform quantitative and qualitative chemical analyses of intravenous solutions, administration sets, devices, raw materials, and plant water systems using wet chemistry techniques and analytical instrumentation.
• Utilize laboratory instrumentation, computerized systems, and software applications to collect, analyze, and accurately document test data.
• Apply scientific principles and analytical techniques to perform testing and interpret results with a high degree of accuracy.
• Support laboratory investigations through effective troubleshooting, root cause analysis, and problem-solving methodologies.
• Prepare, execute, and document protocol testing and special projects in accordance with approved procedures.
• Investigate deviations, document findings, and assist with the completion of exception and quality system documentation.
• Maintain compliance with applicable regulatory requirements, internal quality standards, Standard Operating Procedures (SOPs), and current Good Manufacturing Practices (cGMP).
• Complete testing activities within established timelines while maintaining data integrity and documentation accuracy.
• Perform peer review of laboratory data and documentation as required.
• Escalate safety, quality, equipment, or compliance concerns to supervision and support appropriate corrective actions.
• Maintain a clean, organized, and inspection-ready laboratory environment through 6S and continuous improvement practices.
• Demonstrate knowledge of and compliance with all applicable environmental, health, and safety requirements.
• Support business needs through flexibility in work schedules, including off-shift and weekend coverage when required.
• Perform additional duties and special assignments as needed.

Qualifications and Skills

• Strong computer proficiency, including Microsoft Office applications and laboratory computer systems.
• Ability to work independently and effectively manage multiple priorities in a fast-paced manufacturing environment.
• Strong organizational, analytical, and problem-solving skills.
• Effective written and verbal communication skills.
• Demonstrated attention to detail and commitment to data integrity and quality compliance.
• Ability to collaborate effectively within a team environment while supporting departmental objectives.

Education and Experience

• Bachelor's degree in Chemistry, Chemical Engineering, Physical Chemistry, Biology, or a related scientific discipline. Chemistry-focused coursework preferred.
• Laboratory experience gained through academic coursework, internships, co-ops, or professional experience.
• Exposure to quantitative analysis and analytical laboratory techniques required.
• Experience with analytical instrumentation is preferred.
• 0 to 3 years of relevant laboratory or quality experience.

Physical Requirements

• Must successfully meet color vision requirements as determined through the Ishihara Test for Color Deficiency.
• Must meet near-vision visual acuity requirements as defined by Baxter's Visual Acuity Procedure CL-01-01-037.
• Ability to work in a laboratory and manufacturing environment while following all required safety practices and procedures.

Additional Information

This job description is intended to provide a general overview of the position and is not intended to be an exhaustive list of all duties, responsibilities, or qualifications. Responsibilities may change based on business needs. Overtime and schedule flexibility may be required to support operational requirements.

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 our employees, and we strive to be more transparent with our pay practices. To that end, this position has a salary range of $68,000 to $85,000 and also includes an annual incentive bonus. The above range represents the expected salary range for this position. The actual salary may vary based upon several factors including, but not limited to, relevant skills/experience, time in the role, business line, and geographic/office location.

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

US Benefits at Baxter (except for Puerto Rico)

This is where your well-being matters. Baxter offers comprehensive compensation and benefits packages for eligible roles. Our health and well-being benefits include medical and dental coverage that start on day one, as well as insurance coverage for basic life, accident, short-term and long-term disability, and business travel accident insurance. Financial and retirement benefits include the Employee Stock Purchase Plan (ESPP), with the ability to purchase company stock at a discount, and the 401(k) Retirement Savings Plan (RSP), with options for employee contributions and company matching. We also offer Flexible Spending Accounts, educational assistance programs, and 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, and paid parental leave. Additional benefits include commuting benefits, the Employee Discount Program, the Employee Assistance Program (EAP), and childcare benefits. Join us and enjoy the competitive compensation and benefits we offer to our employees. For additional information regarding Baxter US Benefits, please speak with your recruiter or visit our Benefits site: Benefits | Baxter

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.

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.