Audit Medline Asia suppliers according to Medline internal audit SOP and applicable regulations (ISO 13485, FDA regulations, QSR part 820, MDR 2017/745, ISO 9001, ASTM standards, etc.).
Draft and publish high‑quality audit reports in a timely manner.
Conduct CAPA follow‑up and review evidence for suppliers promptly.
Provide support and guidance to vendors for improving their quality management systems per Medline internal audit SOP and applicable regulations.
Respond to vendor questions and provide training, instruction, and guidance to suppliers.
Support pre‑audit activities and 3rd‑party audit projects assigned by the supervisor/manager.
Follow up with vendors to address problems identified during audits and support them on CAPA reviews.
Handle additional assignments related to the Quality Management System, supplier audit, or other related responsibilities as assigned by ...
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