Perform calibration, qualification, and requalification activities for laboratory equipment, including incubators, refrigerators, ovens, and other critical systems.
Maintain the certification, traceability, and ongoing performance of calibration standards to support regulatory and corporate requirements.
Provide technical support to manufacturing and quality teams by troubleshooting measurement and instrumentation issues that impact operational performance.
Conduct qualification and requalification studies for sterilizers and other critical equipment to help ensure safe and effective processes.
Contribute to continuous improvement initiatives, including 6S, Total Productive Maintenance (TPM), and Gemba activities that enhance efficiency and reliability.
Ensure compliance with quality, environmental, health and safety, and medical device regulatory requirements while promoting a culture of operational excellence.
What You'll Bring
Required Qualifications
Technical Degree, associate degree, or bachelor's degree in Instrumentation, Automation, Metrology, Engineering, or a related technical discipline.
Experience supporting calibration, metrology, validation, instrumentation, or maintenance activities within a manufacturing or regulated environment.
Ability to interpret technical procedures, specifications, engineering documentation, and equipment requirements.
Strong attention to detail with the ability to manage multiple priorities while maintaining high-quality standards.
Working knowledge of quality systems, documentation practices, and regulatory compliance requirements.
Strong collaboration and communication skills with the ability to work effectively across cross-functional teams.
Commitment to safety, continuous improvement, and delivering accurate, timely results.
Preferred Qualifications
Experience within the medical device, pharmaceutical, biotechnology, or other highly regulated industries.
Knowledge of sterilization processes and thermal equipment qualification activities.
Experience managing calibration schedules, metrology systems, or measurement traceability programs.
Proficiency with Microsoft Office applications and technical documentation tools.
Ability to read and interpret technical documentation in English.
Previous involvement in Lean Manufacturing, TPM, 6S, or other operational excellence initiatives.
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.
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 link here and let us know the nature of your request along with your contact information.
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