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Baxter QA Associate I (weekend day shift 7AM-7PM) in Bloomington, Indiana

QA Associate I (weekend day shift 7AM-7PM)

Req #:

JR - 033306


Bloomington, Indiana, United States

Job Category:

Quality Control

Date Posted:


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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.

  • Support for Parents

  • Continuing Education/Professional Development

  • Employee Health &Well-Being Benefits

  • Paid Time Off

  • 2 Days a Year to Volunteer

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Success Profile

What makes a successful Quality team member at Baxter? Take a look at some of the top traits we’re looking for and see if you’re a fit.

  • Detail Oriented

  • Continuous Learner

  • Courageous

  • Collaborative

  • Critical Thinker

  • Influential

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QA Associate I (weekend day shift 7AM-7PM)

This is where you save and sustain lives

At Baxter, we are deeply connected by our mission. No matter your role at Baxter, your work makes a positive impact on people around the world. You’ll feel a sense of purpose throughout the organization, as we know our work improves outcomes for millions of patients.

Baxter’s products and therapies are found in almost every hospital worldwide, in clinics and in the home. For over 85 years, we have pioneered significant medical innovations that transform healthcare.

Together, we create a place where we are happy, successful and inspire each other. This is where you can do your best work.

Join us at the intersection of saving and sustaining lives— where your purpose accelerates our mission.


The Quality Associate I Line Operations is a member of the Quality Assurance Line Operations Team reporting directly to the Quality Supervisor. They maintain quality oversight of the manufacturing areas by working closely with manufacturing personnel and performing various checks during manufacturing processes. They also assess regulatory and quality risks in activities and processes according to regulatory agency rules and guidelines and Baxter Standard Operating Procedures. This position strives for continuous improvement of processes and contributes to creating an environment where teamwork, productivity, safety, identity, strength, purity and quality (SISPQ) are reflected in the finished product.

Essential Duties and Responsibilities (these are primary responsibilities of the role and the incumbent will perform other duties as assigned)

  • Ensures compliance with all worldwide regulatory agency requirements and company-specific regulations related to quality of product and employee safety.

  • In-process review of records to ensure they are complete, accurate and compliant with current Good Manufacturing Practices (cGMP) requirements. Records include batch records and other documents involved in the aseptic processing of drug product.

  • Reports errors, deficiencies, discrepancies and observations to management. May stop operations when product safety is or may be compromised.

  • Performs Quality functions in classified areas, including production oversight, manufacturing process assessments, aseptic intervention oversight, and line clearances.

  • Reviews completed terminal sterilizer, lyophilizer, depyrogenation, and autoclave charts.

  • Provides review of completed work orders and proposed standard operating procedure revisions.

  • Works in collaboration with management teams to prepare for internal and external audits. Assists with timely closure of audit observations and CAPAs.

  • Initiates and authors Nonconformance Reports and corrective and preventative action responses.

  • Conducts bi-annual inspections of classified areas in preparation for facility shutdown periods.

  • Initiates standard operating procedure (SOP) revisions as needed to support continuous improvement.

  • Ensures that SOPs are current and effective and that staff performs routine tasks according to SOP through direct observation.

Job Requirements (Education, Experience and Qualifications)

  • Bachelor’s degree in a science discipline, or Bachelor’s degree in non-science discipline with at least three years of Pharmaceutical Quality or Manufacturing experience

  • Computer proficiency in Microsoft Word, Excel, and Outlook and the ability to use enterprise software (examples include: JDE, BPLM, Pilgrim, Trackwise, etc.)

Physical / Safety Requirements

  • Must wear appropriate PPE as required for various manufacturing areas

  • Must be able to gown qualify for Grade A/B areas.

  • Duties will require overtime work, including scheduled weekend shifts

  • Use of hands and fingers to manipulate office equipment is required

  • Position requires sitting for long hours, but may involve walking or standing for periods of time.


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.

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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


here and let us know the nature of your request along with your contact information.