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.
About Us: Baxter’s Mission:
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 90 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 to monitoring and improvement of supplier performance. Coordinates problem solving from parts supplied.
Your team:
From your role as Sr Eng, Supplier Quality #This is where we count on your knowledge and talent to be responsible for planning, coordinating, scheduling and executing supplier audits nationally and internationally ensuring supplier quality in manufacturing processes at Baxter.
What you’ll be doing:
Plan, coordinate, Schedule, execute supplier audits domestically and internationally as required.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 audits activities as required.Develops inspection and test techniques to evaluate supplier materials.Works with suppliers to find solutions to identified problems.Manage and insure timely implementation of supplier Corrective Action Reports (SCARs). Lead the supplier approval process by assessing manufacturing, Quality Systems capabilities and risks.Manages personnel 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:
Degree in Engineering required.Knowledge of FDA CFR 820, ISO 13485 and ISO 9000 requirements, strongly desired ISO 13485 Lead Auditor certificationEnglishDesirable experience: 3 years or more of experience.previous experience with quality auditing, specifically supplier audits. Excellent documentation, communication and excellent problem-solving skills are desirable.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.
Recruitment Fraud Notice
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