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.

WHAT YOU’LL BE DOING

• Performs routine quality engineering assignments of validation/qualification tasks which are typically a focused portion of larger projects. These tasks provide experience and familiarization with the quality engineering staff, methods, techniques, theories, Corporate and division SOP’s, policies and projects
• Develops or participates in the development of solutions to problems specific to assigned project
• Participates in continuous improvement projects
• Works with engineering, maintenance, manufacturing, and other functional groups on new equipment and regulatory compliance issues
• Writes, implements, and reports on validation activities. Coordinates validation issues specific to the products, manufacturing processes, cleanrooms, or critical utility systems. Writes and/or implements qualification protocols for various pieces of equipment, various classifications of cleanrooms, and critical utilities including water for injection and compressed process air
• Designs and performs routine testing, project experiments, analysis of data and reports results
• Performs engineering studies on new equipment to determine proper settings, control points, etc. including data gathering during start up and test batches
• Initiates new or revisions of protocols/operating instructions specific to the project
• Develops manufacturing process flowcharts, including defining people and material flow issues
• 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)

OTHER DUTIES AS ASSIGNED

Please note this job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee for this job. Duties, responsibilities and activities may change at any time with or without notice. Overtime is worked as require.
Applicants must be authorized to work for any employer in the U.S. We are un-able to sponsor or take over sponsorship of an employment visa at this time.

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