* support medline’s supplier quality operations by executing supplier qualification, monitoring, and performance activities for a global supply base.
* this role assists with supplier assessments, documentation review, audits, and issue resolution to ensure compliance with fda regulations, iso standards, and internal quality system requirements.
* the position partners cross functionally while developing foundational expertise in supplier quality and regulatory compliance.
* 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.
#j-18808-ljbffr