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Quality Lab Associate I - Micro

Req # JR - 186650 Location Cleveland, Mississippi, United States Job Category Quality Date posted 11/06/2025
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Overview

This is where you make a difference in our patients’ safety. As a member of the Baxter Quality team, you will play an essential part in our mission of saving and sustaining lives. Quality is important throughout the entire product lifecycle and works collaboratively with all areas of the organization. Because Quality touches everything Baxter does, a role in Quality provides many opportunities for growth, learning and a successful career that has a daily impact on people’s lives.

  • Support for Parents

  • Continuing Education/ Professional Development

  • Employee Heath & Well-Being Benefits

  • Paid Time Off

  • 2 Days a Year to Volunteer

Success Profile

What makes a successful Quality team member at Baxter? Take a look at some of the top traits we’re looking for and see if you’re a fit.

  • Detail Oriented
  • Continuous Learner
  • Courageous
  • Collaborative
  • Critical Thinker
  • Influential

Quality Lab Associate I - Micro

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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

This is where your creativity addresses challenges

You perform advanced micro testing on medical products through all stages of the manufacturing process. You will also be responsible for reviewing the work of the Quality Technicians and perform investigations as needed.

Your Team at Baxter

Cleveland’s technology and automation are groundbreaking. It is the U.S. sole source for plastic pour bottles, glass IV, and various reconstitution devices. This facility has a number of major product lines with a diverse array of automated manufacturing technologies ranging from bottle solution filling, injection molding, and device assembly.

Our Cleveland plant has been an integral part of Baxter for over 70 years. The work is challenging and rewarding, as Baxter offers competitive compensation and benefits. Baxter encourages and values every employee and believes that all can make a contribution to advancing healthcare for patients; work to be proud of.

What we offer from Day One

  • Medical, Dental and Vision coverage
  • 160 hours of Paid Time Off and Paid Holidays
  • 401K match
  • Employee Stock Purchase Program
  • Paid Parental Leave
  • Tuition Reimbursement

What you'll be doing:

  • Ensure that all environmental monitoring is performed in accordance with regulations.
  • Be able to perform the following Microbiological tests as deemed necessary in role of responsibility: Compressed Air (Viable and Non-Viable), Micro Air, Surfaces, Distilled and Non-Distilled Water, Aerosol Challenge of HEPA Filters, Particle Counts (Room Air and Hoods), Sterilizer Cooling Water, LAF Velocities/Hourly Air Changes/Air Flow Patterns, Bioburden (Solution and Device), Media and Reagents Preparation and Quality Control Testing, Validation of lab instruments/processes (i.e. autoclave, air sampler, particle counter), Perform area audits, Sterility Testing, Plate Reading/Gram Stains, Data Entry, Filter Integrity Testing, Bacterial Endotoxin Testing.
  • Perform sample test result evaluation and implement corrective action/preventative action when necessary.
  • Coordinate and schedule various testing and lab functions.
  • Monitor, evaluate, and trend data.
  • Work with personnel from all areas of the plant.
  • Ensure regulatory compliance.
  • Must have knowledge of both plant and departmental environmental health and safety regulations and follow said regulations accordingly.
  • Use laboratory instrumentation and computer systems to collect and record data.
  • Perform analysis requiring precise analytical skills and understanding of Microbiological principles.
  • Performing investigations and problem solving.
  • Preparing and performing protocols.
  • Investigating deviations and writing exception documents.
  • Completing and reviewing documentation.
  • Complete all testing, including special projects / protocol testing in a timely and appropriate manner.
  • Must perform all other duties and responsibilities as determined by supervision/management.
  • Must be able to work off-shift hours and some weekends.
  • Learn, understand and apply thorough quality standards, Standard Operating Procedures (SOPs) 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.

What you'll bring

  • B.S. Degree in Life Science (Biology/Microbiology or Chemistry) required
  • Lab experience beyond coursework
  • Experience with Microbiological Testing techniques, preferred.
  • Previous experience in FDA regulated industry, preferred.
  • 2-5 Years experience
  • Computer competency, required
  • Ability to work independently
  • Good organizational and time management skills
  • Good oral and written communication skills.
  • Ability to handle multiple priorities in a fast-paced environment
  • Ability to lift up to 20 pounds, lift above the shoulder up to 20 pounds
  • Ability to bend/stoop, climb ladders, stand and/or walk for long periods of time
  • Ability to work in unfavorable conditions (hot/cold temperatures)
  • Requires manual hand dexterity
  • Candidate must not be color blind as determined by the Isihara’s Test for Color Deficiency
  • Candidates must meet near vision visual acuity requirements annually as documented in the Baxter-Cleveland Visual Acuity procedure CL-01-01-037

Applicants must be authorized to work for an employer in the U.S. We are unable to sponsor or take over sponsorship of an employment visa at this time.

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 $64,000 - $88,000 annually. The estimated range is meant to reflect an anticipated salary range for the position. We may pay more or less than that of the anticipated range based upon market data and other factors, all of which are subject to change. Individual pay is based on upon location, skills and expertise, experience, and other relevant factors. For questions about this, our pay philosophy, and available benefits, please speak to the recruiter if you decide to apply and are selected for an interview.

Other Duties as Assigned

Please note this job description is not designed to cover or contain a comprehensive listing of activities, duties or 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.

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.

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Address

Explore this location 911 N Davis
Cleveland, MS 38732
United States of America
Explore This Location

Hear from Our Employees

Our company is enriched by a diverse population of individuals in more than 100 countries that work to solve, innovate, manufacture and drive better healthcare options for patients around the world.

Meet Christelle, Senior Quality Manager in Malta

“I was an Engineering Graduate with a Master's in Business Administration, and was more inclined toward working with people than with machines. When I came across an opportunity to work with Baxter as a Quality Engineer, it was the perfect combination: a manufacturing environment and a role that required me to collaborate with multiple teams daily. Baxter's mission of saving and sustaining lives gives me all the purpose and fulfilment I need.”

Meet Lorena, Senior QA Associate in London, UK

“I am registered pharmacist in the UK with experience with drug products and final product release. I am very dedicated to my work and accurate in details to ensure correct assessment is provided to our customers to ensure patients' safety.”

Meet Gary, Quality Research Manager in Singapore

“I have always enjoyed working at Baxter and I find here to be a great place to work! Management truly cares for you, and invests time and resources to support your career goals and aspirations. My current role provides me the opportunity to work with culturally diverse teams, bringing different talents together, learning from one another and working toward a common goal and mission.”

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