**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.
Join an organization and a team where your work matters.
Join us now!
**Your role at Baxter**
**What you'll be doing**:
- Ensure the implementation and compliance of the Supplier Quality subsystems in accordance with the General Policies, as well as the compliance with all required deadlines.
These include: Supplier Evaluation and Selection, Maintenance of existing suppliers, Supplier Complaints (SCAR), Supplier Audits, Supplier Action and Risk Mitigation Plans (RAM), Supplier Change Notifications, and Supplier Terminations.
- Maintain and manage the NSR (New Supplier Requests) system, as well as their execution for all suppliers in Americas.




- Compliance with and management of Regional and Global Metrics.
- Coordination of training and access to SQLM for all Latin American and Caribbean users.
Regional Train of Trainers for the Supplier Quality process.
- Regional SME (Subject Matter Expert) for Global Supplier Quality processes.
- Compliance with applicable BPDs and SOPs.
- Perform SQLM-TW system maintenance activities related to SQ Opex.
**What you'll bring**
- Biochemical Engineering, QFB, or related fields.
- 5 to 8 years in Quality Systems, preferably in Supplier Quality.
- Knowledge of international standards ISO **** / ISO *****.
- Trend analysis.
- Project management skills managing multiple issues of moderate to high complexity relatively independently with mínimal supervision/instructions.
- Experience in a medical device, pharmaceutical, or highly regulated environment is a plus.
- Knowledge and experience of Quality Management Systems, GMPs, regulatory guidelines, and statistics is preferred.
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**Reasonable Accommodations**
**Recruitment Fraud Notice**
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To learn how you can protect yourself, review our Recruitment Fraud Notice.

📌 Quality System Specialist (Xico)
🏢 Baxter
📍 Xico