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Baxter Logo Baxter · Quality Control

Associate II, Quality (7pm-7am)

United States, Marion Employment contract 88000.00 - 121000.00 USD / Year · Job Posted July 04, 2026
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Job Description

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.

Job Responsibility

  • Leads ongoing, daily departmental operations
  • May include the supervision of assigned personnel in achieving defined quality goals in an efficient, accurate and timely manner
  • Interview/hire, evaluate, train and develop direct reports
  • Perform in-depth internal assessments and evaluations by collecting and analyzing accurate, objective evidence regarding risks and their magnitude
  • Work closely with production supervisors, quality, engineering and other internal groups to accomplish the above and influence necessary actions
  • Determine the logic, adequacy and effectiveness of processes, systems and related requirements
  • Develop plans to correct identified risks including areas of non-conformance
  • Inform management and implement approved corrective action plans
  • Serve as Subject Matter Expert (SME) by maintaining a high level of expertise in current regulatory requirements
  • Provide training and coaching to local employees and others as needed on relevant area(s)
  • When required, assist other Quality areas in the successful performance of these activities
  • Write, review, analyze and revise written Standard Operating Procedures (SOPs) and submit procedural changes as needed to meet Corporate, Divisional, Plant, Regulatory Requirements, etc.
  • Participate in external assessments and audits by evaluating and solving product/process problems by providing technical, analytical and supervisory skills Support process with timely closure of observations/audit items
  • Oversees audits of various reports (Protocols, Qualifications, Regulatory Submissions, etc.) Participate in QA/QC multi-site projects in the role of contributor, coordinator or lead
  • Other duties, tasks or projects as assigned
  • Sustain a clean and safe work area using 6S principles
  • Learn, understand and apply rigorous quality standards, Standard Operating Procedures (SOPs) and Current Good Manufacturing Practices (cGMP)

Requirements

  • High School Diploma, GED, or equivalent required
  • Must be at least 18 years of age
  • BS in engineering/science or equivalent work experience
  • 3-5 years exp. in Quality with a medical device/Pharma company or other similarly regulated industry
  • Strong interpersonal skills and great attention to detail are necessary
  • Must be a strong team player with good problem solving, and good verbal and written communication skills
  • Must have the ability to manage people, encourage teamwork and drive decisions
  • Must be able to handle multiple projects concurrently, have computer experience and have knowledge of FDA Regulations, Application of Good Laboratory Practices, and Application of Good Manufacturing Practices
  • Understand verbal and written safety and quality instructions and read and comprehend written work instructions including words and drawings
  • Must have basic English written and oral communication skills adequate to communicate with other team members

What we offer

  • 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
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