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Spec, Quality Supplier

https://www.baxter.com/ Logo

Baxter

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Location:
Mexico , Monterrey

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Category:
Quality Control

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Contract Type:
Not provided

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Salary:

Not provided
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Job Description:

This is where you make a difference in our patients’ safety. As a member of the Baxter Quality team, you will play an essential part in our mission of saving and sustaining lives. Quality is important throughout the entire product lifecycle and works collaboratively with all areas of the organization. Because Quality touches everything Baxter does, a role in Quality provides many opportunities for growth, learning and a successful career that has a daily impact on people’s lives.

Job Responsibility:

  • 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
  • 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

Requirements:

  • 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
What we offer:
  • Support for Parents
  • Continuing Education/ Professional Development
  • Employee Heath & Well-Being Benefits
  • Paid Time Off
  • 2 Days a Year to Volunteer

Additional Information:

Job Posted:
March 19, 2026

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