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New · posted Nov 11

Baxter · Medical Devices

Quality Lab Associate I - Chemistry

  • Cleveland, MS
  • On-site
  • Full-time
  • Associate & Specialist
Save
Pay$68K–$85K
EmploymentFull-time
LocationCleveland, MS
LevelAssociate & Specialist
FunctionQuality Control
DeadlineOpen until filled

The role

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).

What you need

  • 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.

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.

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.

Skills named in this posting

What you'll do

  • 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.

Pay

$68,000 – $85,000 a year

Employer provided
How this compares

Additional Information

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.

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

Where you'll work

Cleveland, MSOn-siteOpen in Maps (opens in a new tab)

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Equal opportunity, accessibility and legal noticesBaxter's statements, word for word

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.

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.

Job intelligence

The context around this role

Live data · November 11, 2026

Salary intelligence

How the pay compares

This role's midpoint is 4% above the US median for Quality Control roles at this level.

This roleEmployer provided

$68,000 to $85,000 a year

Associate & Specialist roles in the US90 roles publishing pay

Middle half $64,000 to $88,250, median $73,500
Annual base pay
Annual base payLowMedianHigh
This role$68,000—$85,000
All US$64,000$73,500$88,250

This role: Baxter's own published range. Comparisons: the base pay employers published on open Quality Control roles at the same level on Regulatory Jobs, November 11, 2026. Nothing is estimated.

Career trajectory

Where this role sits in Quality Control

The general path across 265 open Quality Control roles on Regulatory Jobs, with the titles they carry most. Not Baxter's own promotion track.

  1. This role

    Associate & Specialist

    Often: Quality Control Analyst · Specialist, Quality Control

    $74K median137 open

  2. Next step

    Senior & Principal

    Often: Senior Scientist, Quality Control · Senior Technician Quality Control

    $95K median66 open

  3. Later

    Manager

    Often: Manager, Quality Control · Supervisor, Quality Control

    $116K median43 open

  4. Later

    Director

    Often: Associate Director, Quality Control · Senior Director, Quality Control

    $199K median19 open

Career resources on Quality Control

Skills DNA

What this role leans on

How many of the posting's 33 duty, requirement and summary lines touch each area. The posting's emphasis, not a proficiency score.

GMP and compliance: 6 linesLab testing and methods: 17 linesDocumentation and SOPs: 8 linesInvestigations and CAPA: 2 linesQuality systems and risk: 3 linesData and digital systems: 4 linesClinical trial conduct: 1 lineCollaboration and leadership: 3 linesGMPLab testingDocumentationInvestigationsQuality systemsData systemsClinical trialsTeamwork
  • Lab testing and methods17
  • Documentation and SOPs8
  • GMP and compliance6
  • Data and digital systems4
  • Quality systems and risk3
  • Collaboration and leadership3
  • Investigations and CAPA2
  • Clinical trial conduct1

Regulatory intelligence

The rules, regulations and standards behind this role

The regulations, guidance and standards that govern Quality Control work in medical devices, led by the two this posting names, each linked to the agency or standards body that publishes it.

From Regulatory News

Manufacturing and quality coverage for this profession

Company hiring pulse

Baxter on Regulatory Jobs

55
Open roles
55
Distinct roles
12
Locations

By discipline

  • Quality51 91%
  • Regulatory5 9%

By level

  • Associate & Specialist25 45%
  • Senior & Principal14 25%
  • Manager9 16%
See all 55 Baxter roles

More roles at Baxter

All 55 Baxter roles

Similar Quality Control roles elsewhere

Quality Lab Associate I - Chemistry at Baxter

Open until filled. $68K–$85K a year, employer provided.

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