Sr Supervisor, Quality
Baxter International Inc.
Summary
As a Quality Assurance Supervisor, you will provide leadership and oversight for inspection and material release activities within a cGMP-regulated manufacturing environment. You will guide a team of QA Inspectors, ensure compliance with quality and regulatory requirements, and partner closely with Production, Engineering, and Quality teams to support operational excellence. Your success will be measured by the effectiveness of your team, the timely release of materials, audit readiness, quality performance metrics, and your ability to continuously improve processes that support both compliance and business objectives.
Job description
Your Role at Baxter
As a Quality Assurance Supervisor, you will provide leadership and oversight for inspection and material release activities within a cGMP-regulated manufacturing environment. You will guide a team of QA Inspectors, ensure compliance with quality and regulatory requirements, and partner closely with Production, Engineering, and Quality teams to support operational excellence. Your success will be measured by the effectiveness of your team, the timely release of materials, audit readiness, quality performance metrics, and your ability to continuously improve processes that support both compliance and business objectives.
What You'll Be Doing
- Lead the inspection, review, and release of incoming materials, in-process components, and finished products to ensure compliance with quality standards and regulatory requirements.
- Supervise, coach, and develop QA Inspectors, fostering a culture of accountability, continuous learning, and operational excellence.
- Plan and prioritize team workloads to support production schedules, material availability, and on-time product release objectives.
- Investigate quality events, nonconformances, corrective actions, and preventive actions to identify root causes and drive sustainable solutions.
- Partner with cross-functional teams to maintain inspection procedures, specifications, and quality systems that support compliance and manufacturing efficiency.
- Support internal audits, external inspections, and audit readiness activities while ensuring timely resolution of observations and action items.
- Analyze quality performance metrics and identify opportunities to improve processes, reduce risk, and enhance overall product quality.
What You'll Bring
Required Qualifications
- Bachelor's degree in Science, Engineering, Quality, Business, or a related field with 3-5 years of relevant experience; or 5-7 years of relevant quality experience in lieu of a bachelor's degree.
- 1-2 years of people leadership, supervisory, or team lead experience.
- Working knowledge of current Good Manufacturing Practices (cGMP), FDA regulations, and quality system requirements.
- Experience supporting quality inspections, material release activities, investigations, or quality assurance operations within a regulated environment.
- Strong problem-solving, decision-making, and organizational skills with the ability to manage multiple priorities.
- Effective verbal and written communication skills with the ability to collaborate across functions and levels of the organization.
- Proficiency with computer systems and Microsoft Office applications.
Preferred Qualifications
- Experience in medical device, pharmaceutical, biologics, or other highly regulated manufacturing environments.
- Knowledge of Good Laboratory Practices (GLP), auditing practices, and quality management systems.
- Experience supporting Lean, Six Sigma, or continuous improvement initiatives.
- Knowledge of warehouse, quarantine, or material management processes.
- Familiarity with aseptic manufacturing techniques and environments.
- Experience serving as a subject matter expert and delivering training within quality operations.
Requirements
- Bachelor's degree in Science, Engineering, Quality, Business, or a related field with 3-5 years of relevant experience; or 5-7 years of relevant quality experience in lieu of a bachelor's degree.
- 1-2 years of people leadership, supervisory, or team lead experience.
- Working knowledge of current Good Manufacturing Practices (cGMP), FDA regulations, and quality system requirements.
- Experience supporting quality inspections, material release activities, investigations, or quality assurance operations within a regulated environment.
- Strong problem-solving, decision-making, and organizational skills with the ability to manage multiple priorities.
- Effective verbal and written communication skills with the ability to collaborate across functions and levels of the organization.
- Proficiency with computer systems and Microsoft Office applications.
Benefits
- Medical Coverage
- Dental Coverage
- Life Insurance
- Accident Insurance
- Short-Term Disability Insurance
- Long-Term Disability Insurance
- Business Travel Accident Insurance
- Employee Stock Purchase Plan
- 401(k) Retirement Savings Plan
- Flexible Spending Accounts
- Educational Assistance
- Paid Holidays
- Paid Time Off
- Family and Medical Leave
- Paid Parental Leave
- Commuting Benefits
- Employee Discount Program
- Employee Assistance Program
- Childcare Benefits
- Discretionary Bonuses
Company overview
Baxter International Inc. is an American multinational healthcare company headquartered in Deerfield, Illinois, founded in 1931. As a leading global medical device manufacturer, Baxter specializes in developing and producing essential medical products for treating chronic and acute medical conditions. The company operates across three primary business segments: Medical Products and Therapies, Healthcare Systems and Technologies, and Pharmaceuticals. Baxter's extensive product portfolio includes intravenous (IV) solutions, infusion pumps, dialysis equipment for kidney disease treatment, surgical technologies, and hospital pharmaceuticals. With approximately 38,000 employees worldwide and annual revenues exceeding $10 billion, Baxter plays a critical role in global healthcare infrastructure. The company is particularly known for its leadership in IV fluid production, manufacturing approximately 60% of the intravenous fluids used in the United States. Baxter's innovations include pioneering developments in artificial kidney technology and advanced surgical products, serving healthcare providers across more than 100 countries. The company maintains a strong commitment to research and development, investing significantly in medical technology advancements that improve patient outcomes and healthcare delivery efficiency.