Quality Lab Associate

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. Are you ready to embark on an exciting journey with Baxter Healthcare Corporation as a Quality Lab Associate I?

This outstanding opportunity allows you to be part of a team that is diligent in maintaining the highest standards in healthcare. Our dedication to excellence and innovation ensures that you will be at the forefront of groundbreaking developments in the industry. We are looking for an ambitious and meticulous individual to join our team and contribute to our flawless operations.

• Perform chemical quantitative and qualitative analysis on intravenous solutions, sets, devices, raw materials, and plant water (distilled, non-distilled water) applying ‘wet’ chemistry techniques and instrument analysis.
• Use laboratory instrumentation, computer systems, and software to collect and record data.
• Must be able to use standard software applications such as MS Office Suite.
• Perform analysis requiring detailed analytical skills and understanding of chemistry principles.
• Perform investigations applying problem-solving and troubleshooting skills.
• Prepare and perform protocols.
• Investigate deviations and write exception documents.
• Ensure regulatory compliance.
• Learn, understand, and apply rigorous quality standards, established guidelines, and current Good Manufacturing Practices (cGMP).
• Complete and peer-review documentation.
• Complete all testing, including special projects/protocol testing, in a timely and appropriate manner.
• Carry out additional tasks and responsibilities as assigned by supervision/management.
• Have knowledge of both plant and department environmental health and safety regulations and align with said regulations accordingly.
• Work off shift hours and some weekends.
• 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.

• Computer proficiency is required.
• Ability to work independently.
• Good organizational and time management skills.
• Good oral and written communication skills.
• Ability to balance multiple priorities in a fast-paced environment.

• Candidate must not have color blindness as determined by the Ishihara’s Test for Color Deficiency.
• Candidates must meet near vision visual acuity requirements annually as detailed in the Baxter-Cleveland Visual Acuity procedure CL-01-01-037.

• B.S. Degree or equivalent experience in Science (Chemistry, Chemical Engineering, Physical Chemistry, Biology with Chemistry preferred).
• Quantitative analysis or equivalent lab experience within coursework.
• Experience with instrumental analysis is preferred.
• 0-3 years of experience.

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…