Spec, Quality Supplier

This is where your work makes a difference.

At Baxter, we believe every person—regardless of who they are or where they are from—deserves a chance to live a healthy life. It was our founding belief in 1931 and continues to be our guiding principle. We are redefining healthcare delivery to make a greater impact today, tomorrow, and beyond.

Our Baxter colleagues are united by our Mission to Save and Sustain Lives. Together, our community is driven by a culture of courage, trust, and collaboration. Every individual is empowered to take ownership and make a meaningful impact. We strive for efficient and effective operations, and we hold each other accountable for delivering exceptional results.

Here, you will find more than just a job—you will find purpose and pride. 

This is where your work makes a difference.

Your Role at Baxter
Establish baseline controls and drive Continuous Improvement through the assigned suppliers.  Support sourcing projects and/or TCO’s for supplier and part qualifications as needed.

What you'll be doing

• • Develop a transfer plan based a global quality plan for the site.

• • Develops and communicates Hill-Rom’s expectations for quality performance, continuous improvement, quality systems, process controls infrastructure for high leverage/critical sustaining parts and new products sources to suppliers.

• • Performs and coordinates quality system and process control assessments.

• • Measures and communicates supplier performance on key metrics and the corresponding continuous improvement plans.

• • Participates as an active member in the New Product Development process supplier evaluation team and the sourcing core team.

• • Collaborates, trains and mentors supplier representatives in best practices, Iike quality systems, process controls methods, problem solving and statistical tools.

• • Monitors and drives corrective action and continuous improvement activities that directly impact performance for assigned suppliers.

• • Follow up supplier nonconformance material to proper disposition and implementation of actions to resolve nonconformance’s at supplier facility.

• If needed SQE will be coordinate a team of technicians to follow up supplier nonconformance’s

What you'll bring

• Bachelors of Science in Engineering or other related technical field. 

• Five (5) to 10 years in a Manufacturing, Quality Assurance, and/or Engineering role, with a minimum of 5 years in Manufacturing and/or Quality

• Experience in the medical device industry or automotive industry or high regulated enviroments,

• Experience with development and deployment on Quality System and process controls and continuous improvement methods (QSR’s, ISO9000/QS9000, ISO13485)

• Primary/Secondary party compliance auditing experience.

• Adavance level of English ( Mandatory)

• Knowledge in Core Tools

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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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