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Skills: Supplier Quality Management, ISO 13485, ISO 9001, Supplier Auditing, Corrective and Preventive Actions (SCAR)
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Monterrey, Nuevo León, Mexico · On-site
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Monterrey, Nuevo León, Mexico · On-site
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The Supplier Quality Engineer manages supplier performance and ensures materials and services meet quality and regulatory standards. Key duties include conducting supplier audits, resolving quality issues through SCARs, and monitoring performance metrics.
A Bachelor's degree in Engineering or a related technical field is required, along with 2-4 years of experience in supplier or quality engineering. Knowledge of ISO 13485/9001 and advanced English proficiency are essential.
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.
Your role at Baxter:
The Supplier Quality Engineer (SQE) supports effective management and continuous improvement of supplier quality performance to ensure that materials, components, and services meet Baxter’s quality standards and regulatory requirements.
This role partners with internal teams and suppliers to address quality issues, support compliance with applicable standards (e.g., ISO 13485, ISO 9001), and contribute to supplier development activities. The position requires a solid understanding of manufacturing processes, quality systems, and problem-solving methodologies, with a focus on execution, collaboration, and continuous improvement.
Support the investigation and resolution of supplier-related quality issues, including audit findings and supplier corrective actions (SCARs), ensuring timely follow-up and closure.
Review and provide input on supplier change requests (e.g., process or location changes), ensuring appropriate documentation and risk considerations.
Assist in implementing supplier risk management activities and monitoring supplier performance.
Participate in supplier audits (internal and external), including preparation, execution support, and follow-up actions.
Maintain and track supplier performance metrics (scorecards), supporting data analysis and improvement initiatives.
Support qualification activities related to supplier components and engineering changes, in collaboration with cross-functional teams.
Contribute to problem-solving efforts for recurring supplier quality issues using structured methodologies.
Provide input for Supplier Business Reviews and support supplier performance discussions.
Participate in cross-functional teams (Engineering, Manufacturing, Procurement, Regulatory) to address supplier-related quality concerns.
Support periodic supplier re-evaluations and ensure documentation is complete and audit ready.
Assist in maintaining supplier quality agreements and ensuring alignment with company requirements.
Bachelor’s degree in Engineering or related technical field required.
2–4 years of experience in supplier quality, manufacturing, or quality engineering (regulated industry preferred).
Basic knowledge of ISO 13485, ISO 9001, or similar quality standards.
Exposure to supplier audits, QMS processes, and continuous improvement tools is preferred.
Advance level of English.
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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.
Recruitment Fraud Notice
Baxter has discovered incidents of employment scams, where fraudulent parties pose as Baxter employees, recruiters, or other agents, and engage with online job seekers in an attempt to steal personal and/or financial information. To learn how you can protect yourself, review our Recruitment Fraud Notice.
For nearly a century, we have delivered on our commitment to saving and sustaining the lives of patients, working alongside clinicians and providers around the world. We believe every person — regardless of who they are or where they are from — deserves a chance to live a healthy life, free from illness and full of possibility. At the intersection of progress and purpose is where we are redefining what it means to be a global medtech leader. It is where we are relentlessly pursuing healthcare transformation, fueled by our compassion for patients and providers and the challenges they face. It is where bold ideas meet the promise for meaningful change in the world around us. We are there, at every step of the journey, to help clinicians deliver the best care possible.
Offices: 1 Baxter Pkwy, Deerfield, Illinois 60015, US · 25212 IL-120, Round Lake, IL 60073, US · Calle Fernando Aranguren 830, Zapopan, JAL 45145, MX
