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Associate , Quality

Job in Byhalia, Marshall County, Mississippi, 38611, USA
Listing for: Baxter International
Full Time position
Listed on 2026-01-12
Job specializations:
  • Quality Assurance - QA/QC
    Data Analyst, QA Specialist / Manager
Salary/Wage Range or Industry Benchmark: 60000 - 80000 USD Yearly USD 60000.00 80000.00 YEAR
Job Description & How to Apply Below
Position: Associate I, Quality
Location: Byhalia

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.

Job Description

Your role at Baxter

The Quality Associate I is responsible for providing Quality support to the Global Logistics Center. Inspects products, initiates and updates procedures, reviews temperature monitoring data, and ensures compliance with GMP/QSRs requirements, according to corporate and local Standard Operating Procedures, and all applicable FDA and state regulations.

What we offer from day 1
  • Paid Time Off and Paid Holidays
  • Medical, Dental, Disability and Life Insurance coverage
  • Vision and Voluntary Benefits
  • Paid Parental Leave
  • Retirement Savings Plan
  • Employee Stock Purchase Program
  • Flexible Health Care Spending Accounts
  • Educational Assistance Plan
What you'll be doing
  • Perform physical inspection of products and comparison/assessment to all related documentation within the warehouse as needed (certificate or analysis, packing list, bill of lading, Temptale management, etc.)
  • Initiate procedure revisions as needed to support continuous improvement. Ensure that procedures are current and that facility employees perform tasks according to procedures through direct observation.
  • Activate, distribute and file procedures related to both local and corporate changes.
  • Manage official forms distributed throughout the facility.
  • Support assigned activities to ensure compliance with the Baxter COI program.
  • Collaborate with the Training Administrator to ensure training requirements are met prior to activation of all procedures.
  • Manage the state licensure program to ensure no licenses expire.
  • Support Temperature Monitoring of the MGLC Warehouse which includes operating the Rees system, reporting all temperatures on a spreadsheet for daily management review and uploading data from the backup digital data loggers throughout the facility. Investigate and resolve any Rees system alarms and document monthly MKT requirements.
  • Manage the document retention program.
  • Support assigned responsibilities for document tracking and overall facility documentation control.
  • Prepare monthly Quality Management & Data Review Presentations.
  • Perform Internal Assessments for continuous improvement of MGLC Quality Systems.
  • Assist other members of the Quality Department and facility management team to ensure timely closure of any audit observations.
  • Serve as a back‑up for processing local hold requests using the Warehouse Management System (WMS) and JD Edwards (JDE) systems as needed.
  • Serve as a back‑up for processing corporate FCA hold requests using Cardinal Health’s FCA Tracking System, Baxter’s Warehouse Management System (WMS) and Baxter’s JD Edwards (JDE) system. Conduct audits of FCA hold product.
  • Serve as a back‑up for processing product dispositions linked to local and corporate holds and report through the appropriate people and systems to ensure timely response/closure.
  • Perform manual product releases after verification of release by manufacturing plant in Batch Release System (BRS) as necessary.
  • Support all lean implementation initiatives in the Quality Department and throughout the facility, including periodic 6S audits and closure of any assigned action items.
  • Work in collaboration with other members of the Quality Department to prepare for internal and external auditors.
  • Support the Quality Department by completing other duties, projects and/or tasks that may be assigned as needed.
What you'll bring
  • Bachelor's degreeor Associate degree required.
  • Minimum one year of relevant…
Position Requirements
10+ Years work experience
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