Ingeniero de Calidad de Proveedores
Medline-P090
Conduct supplier audits to verify compliance with ISO 9001, ISO 13485, and applicable regulatory requirements related to high-risk vendors. Support supplier qualification, re‑qualification, and disqualification activities for moderate to high‑risk suppliers, including documentation review and approval routing. Review and approve supplier quality records and compliance documentation in accordance with internal procedures. Execute Supplier Corrective Action Requests (SCARs) by tracking actions, verifying evidence, and documenting effectiveness under supervision. Assist with supplier communication related to quality requirements, documentation requests, and corrective actions to Medline’s internal business partners and external suppliers Provide technical guidance and training to suppliers on quality standards and best practices. Support containment activities and investigations related to supplier nonconformances Utilize root cause analysis and risk management tools to prevent recurrence of issues. Maintain accurate and timely records of supplier audits, performance reviews, nonconformances, and corrective actions. Prepare routine reports, dashboards, and summaries for supplier quality performance and compliance tracking.
Abril 22 2026 en Mexicali
