Quality Lab Associate I

Baxter International Inc.Cleveland, MS
$68,000 - $85,000Onsite

About The Position

Join our dedicated team at Baxter Healthcare Corporation as a Quality Lab Associate I in Cleveland, MS! This is an outstanding opportunity to work in a dynamic environment where you will play a meaningful role in ensuring the quality of our world-class products. As part of our team, you will have the chance to collaborate with experienced professionals and contribute to our mission of delivering flawless healthcare solutions.

Requirements

  • Computer proficiency is required.
  • Ability to work independently while managing multiple priorities in a fast-paced environment.
  • Good organizational and time management skills.
  • Excellent oral and written communication skills.
  • Candidate must not be color blind 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 in Science (Chemistry, Chemical Engineering, Physical Chemistry, Biology with Chemistry preferred) or equivalent experience.
  • Quantitative analysis or equivalent lab experience.
  • Experience with instrumental analysis required.
  • 2-4 years of experience.

Responsibilities

  • Perform chemical quantitative and qualitative analysis on intravenous solutions, sets, devices, raw materials, and plant water (distilled, non-distilled) using ‘wet’ chemistry techniques and instrument analysis.
  • Use laboratory instrumentation, computer systems, and software to collect and record data.
  • Apply detailed analytical skills and chemistry principles to perform accurate analysis.
  • Conduct investigations using problem-solving and troubleshooting techniques.
  • Prepare and complete protocols, and investigate deviations, writing exception documents as needed.
  • Ensure regulatory compliance by understanding and applying rigorous quality standards, detailed process guidelines, and current Good Manufacturing Practices (cGMP).
  • Complete and peer-review documentation meticulously.
  • Conduct all testing, including special projects and protocol testing, in a timely and appropriate manner.
  • Sustain a clean and safe work area using 6S principles.
  • Notify the supervisor and take appropriate action if any safety, quality, mechanical, or discrepancy issues arise.
  • Align with plant and department environmental health and safety regulations.
  • Work off-shift hours and some weekends as required.

Benefits

  • 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
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