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.

Summary

Covering this role you'll support the management of the Supplier Quality organization, to ensure proper deployment and adherence to Global Quality Procedure applicable to Supplier Quality Assurance, execute Supplier Quality processes.

In addition, you'll take care of supplier quality assessment and follow-up of supplier failures and low performers, Improvement of supplier performance through effective partnership as well as support integration of new businesses from a Supplier Quality perspective.

What you’ll be doing

• Coordinate timely completion of the task as per due date ( e.g: Supplier Qualification, Re-evaluation, Supplier Corrective Action Request (SCAR), Supplier Notice of Change (SNC)…. )
• Prepare needed documentation and update Global supplier quality database accordingly as per Corporate Procedure (GQP) requirements
• Be in contact with suppliers to collect documentation, set up processes, discuss and solve ongoing issues.
• Identifies Baxter supplier compliance issues; helps to resolve issues in a timely manner.
• Partners with facilities and regions to ensure successful implementation and compliance to Corporate Quality Procedures / regulations.
• Own and resolve supplier related issues (RAMs/SCARs). Perform risk assessments to solve supplier issues. Work with supplier to correct.
• Support continuous improvement projects with the objective of achieving quality, reliability and cost improvements.                     

What you’ll bring

• Strong quality orientation required. Knowledge of cGMP, MDD / MDR, ISO13485, global regulatory guidelines, and validation practices.
• 2-3 years’ experience in Quality, Supplier Quality, Manufacturing, Engineering or related field
• Fluent in English.
• Education and/or Experience: Master or Engineer Level in scientific area required (Engineer, Pharmacist, or equivalent).
• Experience in Supplier Quality Management recommended.
• Effective communicator; excellent written, oral, and interpersonal communication and presentation skills
• Ability to travel 30% of the time.
• Must be able to handle multiple activities concurrently
• Good interpersonal/communication/influencing/negotiation skills.
• Ability to support projects and respond to supplier/customers (Internal and External) in a timely manner

Reasonable Accommodations

Baxter is committed to working with and providing reasonable accommodations to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application or interview process, please send an e-mail to [email protected] and let us know the nature of your request along with your contact information.

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