Quality Associate III,

Baxter International Inc.; Round Lake (IL); On-site; USD 96,000 - 132,000; Full time

Benefits offered by this job

Medical and dental coverage from day 1

ESPP (Employee Stock Purchase Plan)

401(k) Retirement Savings Plan

Paid time off 20–35 days

Job summary

Baxter International Inc. is seeking a Quality Associate III to manage senior-level QMS processes and drive timely, compliant investigations.

You will partner with Manufacturing, Regulatory Affairs, and other teams to ensure inspection readiness and data integrity while delivering actionable metrics and executive summaries. The role emphasizes strong analytical skills, cross-functional collaboration, and the ability to coach others in QMS best practices.

Qualifications

• Bachelors degree in science or related technical field.
• 4+ years in Quality Assurance/Quality Systems in regulated pharma/medical device.
• Experience with two or more QMS elements: change control, CAPA, nonconformance, complaints, deviations, audit readiness.
• Proven process owner or site SME for QMS processes (change control, CAPA, NCR, deviations, management review).
• Experience supporting FDA/ISO/notified body inspections.
• Ability to develop dashboards and KPI packages using Excel, Power BI, Tableau, or similar tools.
• Knowledge of FDA 21 CFR Part 820, ISO 13485, QSR, cGMP and related QMS standards.

Responsibilities

• Own or provide senior-level oversight for assigned QMS processes (change control, CAPA, customer complaints, NCRs, metrics).
• Serve as site SME for QMS processes, including workflow routing, impact assessment, and inspection readiness.
• Lead or support complex quality investigations and root-cause analyses using structured tools.
• Assess proposed changes for regulatory, product quality, patient safety, data integrity, and business impact.
• Prepare, analyze, and report QMS metrics and dashboards for leadership review.
• Collaborate cross-functionally with Manufacturing, Engineering, Regulatory Affairs, and others to resolve issues promptly.
• Support internal, corporate, customer, and regulatory audits and inspections with thorough documentation.
• Drive continuous improvement to simplify workflows and improve right-first-time documentation.

Skills

Change control

CAPA

Nonconformance

Complaints

Deviations

Audit readiness

Quality metrics

Document control

Supplier quality

Regulatory inspection support

QMS data dashboards

Cross-functional collaboration

eQMS tools

Education

Bachelor's degree in science

Tools

TrackWise

Veeva

MasterControl

ETQ

Power BI

Excel

Tableau

Smartsheet

SAP

Job description

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

As a Quality Associate III, you are unafraid of navigating through necessary internal processes to facilitate a product you deeply believe in. You can absorb and act on complex procedures and data and train your team or peers if needed. You take pride in getting things done quickly without sacrificing safety or quality. You will provide senior-level individual contributor ownership and oversight of Quality Management System processes including change control, CAPA, complaints, nonconformance records, and metrics, serving as site SME to ensure inspection readiness and regulatory compliance. Will also lead complex quality investigations, prepares management review materials, and partners cross-functionally to drive timely resolution of quality system issues while maintaining inspection-ready records in eQMS platforms.

What You'll Be Doing

• Own or provide senior-level oversight for assigned Quality Management System processes, which may include change control, CAPA, customer complaints, nonconformance records, metrics, management review inputs, and related eQMS workflows.
• Serve as site SME for assigned QMS processes, including workflow routing, impact assessment, implementation planning, completion tracking, closure quality, and inspection readiness.
• Lead or support complex quality investigations, including complaint investigations, nonconformance evaluations, root cause analysis, corrective/preventive action development, and effectiveness verification.
• Assess proposed product, process, equipment, supplier, documentation, and quality system changes for regulatory, product quality, patient safety, data integrity, and business continuity impact.
• Prepare, analyze, and report QMS metrics, including CAPA timeliness/effectiveness, complaint closure, aging records, change control execution, overdue actions, and adverse trends.
• Develop management review-ready data packages, dashboards, trend reports, and executive summaries that clearly communicate QMS performance, risks, escalations, and recommended actions.
• Partner cross-functionally with Manufacturing, Engineering, QC, Regulatory Affairs, Supplier Quality, Document Control, Medical/Clinical, and site leadership to drive timely and compliant resolution of quality system issues.
• Support internal audits, corporate audits, customer audits, and regulatory inspections by preparing records, explaining process execution, supporting back-room/front-room activities, and responding to auditor requests.
• Identify recurring QMS execution issues and lead continuous improvement initiatives to simplify workflows, improve right-first-time documentation, reduce cycle time, and strengthen compliance.
• Provide coaching, training, and practical guidance to process users, record owners, CAPA owners, change owners, and cross-functional SMEs on QMS expectations and documentation quality.
• Maintain inspection-ready records in Baxter's eQMS platforms.
• Raise significant quality issues, overdue commitments, adverse trends, or potential compliance risks through established site and corporate quality governance processes.

What You'll Bring

• Bachelor's degree in science, engineering, pharmacy, life sciences, quality, regulatory affairs, or a related technical discipline.
• 4 plus years of experience in Quality Assurance, Quality Systems, Quality Engineering, Product Surveillance, Manufacturing Quality, or Compliance in a regulated pharma, biotech, or medical device environment.
• Hands-on experience with at least two or more of the following QMS elements: change control, CAPA, nonconformance, complaints, deviations, audit readiness, management review, quality metrics, document control, supplier quality, or regulatory inspection support.
• Prior experience serving as process owner, site SME, super user, reviewer, approver, or governance-board member for change control, CAPA, complaints, NCR, deviations, or management review.
• Experience supporting FDA, ISO, notified body, corporate, customer, or health authority inspections.
• Skilled in developing dashboards, KPI packages, process-health metrics, or management review materials using Excel, Power BI, SmartSheet, Tableau, or validated/eQMS reporting tools.
• Proven ability to lead root cause analysis and investigations using structured tools such as 5 Whys, Fishbone/Ishikawa, fault tree analysis, DMAIC, risk assessment, or similar methodologies.
• Experience using eQMS or quality data systems such as TrackWise, Veeva, MasterControl, ETQ, SmartSheet, Power BI, Excel, Tableau, TcU, SAP, or equivalent.
• Strong technical writing skills with demonstrated ability to prepare clear, objective, inspection-ready investigation reports, quality assessments, executive summaries, metrics packages, and quality records.
• Ability to lead multiple complex records, projects, and deadlines with limited supervision.
• Strong communication, influencing, and cross-functional collaboration skills, including the ability to engage technical SMEs and site leadership.
• Working knowledge of applicable regulations and standards such as FDA 21 CFR Part 820, 21 CFR 210/211, ISO 13485, EU MDR, ICH, cGMP, QSR, and/or global QMS requirements, depending on product scope.
• ASQ certification such as CQE, CQA, CMQ/OE, Six Sigma Green Belt/Black Belt, RAC, or equivalent quality/process-improvement credential preferred.
• Experience in sterile drug product, combination product, device/drug-device, biologics, or high-volume regulated manufacturing environments preferred.
• Demonstrated ability to simplify QMS processes while maintaining compliance, data integrity, traceability, and inspection readiness preferred.

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 $96,000 - $132,000 annually. The estimated range is meant to reflect an anticipated salary range for the position. We may pay more or less than of the anticipated range based upon market data and other factors, all of which are subject to change. Individual pay is based on location, skills and expertise, experience, and other relevant factors. This position may also be eligible for discretionary bonuses.

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

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.

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 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.