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.

Your Role at Baxter

This position participates in supplier quality related supplier performance monitoring and improvement. It coordinates the resolution of quality problems of supplied parts. This position participates in supplier quality related to monitoring and improvement of supplier performance. Coordinates problem solving from parts supplied.

What you'll be doing

• Plan, coordinate, schedule, complete supplier audits domestically and internationally as the need arises.

• Follow up on supplier audits to demonstrate supplier controls required by FDA CFR 820, ISO 13485 and ISO 9000.

• Work with sourcing staff to coordinate supplier audit activities as need it.

• Develops inspection, test and test techniques to evaluate parts and works with suppliers to find solutions to identified problems.

• Create written reports and communicate the results clearly and effectively to auditee and Hillrom management.

• Manage and insure timely implementation of supplier corrective action reports (SCARs).

• Provide engineering support for non-conforming material (NMR) issues and authorization.

• Remediate Supplier files to support current and business development activity related to acquisition of new businesses.

• Verify supplier files are maintained and documented appropriately.

• Lead the supplier approval process by assessing manufacturing, Quality Systems capabilities and risks and develop Improvement plans for Critical to quality suppliers.

• Manages personnel to maintain and reduce the Incoming Inspection cycle time.

• Establishes problem solving strategies and work with Manufacturing and Quality Engineers to reduce MRB inventory

• Perform component characteristic analysis to determine inspection status changes.

What you'll bring

• B.S Degree in Engineering required, 5 year qualifying experience, including previous experience with quality auditing, specifically supplier audits.

• Excellent documentation, communication and excellent problem-solving skills desirable.

• Knowledge of FDA CFR 820, ISO 13485 and ISO 9000 requirements, strongly desired ISO 13485 Lead Auditor certification.

• Adance level of Ensglish.

We are an equal opportunity employer and value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, sex, gender, gender expression, sexual orientation, age, marital status, veteran status, or disability status. We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.

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

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