Quality Inspector

1. Inspect specified product(s) at specified vendors following the priorities established by Director of Corporate Quality Control.
2. Complete each product inspection as specified in Medline product specification document(s) and applicable ECN’s and deviations.
a. Document the results of each inspection in a clear, concise and readable manner following the documentation instructions detailed in product specification and Quality procedural documents.
b. Disposition lot as dictated by the results of the inspection and the accept/reject criteria specified in applicable product specification document. Communicate lot disposition to applicable factory personnel upon completion of inspection.
c. Assure completed and reviewed inspection reports are forwarded to the Taipei office within 48 to 72 working hours of completion of inspection.
3. Maintain assigned copies of Medline documents and forms in an efficient and effective format. Add new revisions and dispose of obsolete revisions within 24 hours of receipt of new document copies from Medline Shanghai or Corporate QA. Notify Medline Shanghai in writing of receipt of new document copies within 24 hours of receipt.
a. Form copies must have form title, tracking number, and effective date clearly visible on every copy.
4. Coordinate inspection schedule with all vendors assigned to maximize number of inspections that can be performed each month.
5. Make all travel arrangements necessary to get to and from each factory for scheduled inspections.
6. Complete time records of monthly activities in the format specified by Director of Corporate QC. Submit each month’s completed records to Shanghai QA Coordinator by the 10th of the following month.
7. Complete expense reports with associated receipts on a monthly basis. Expenses not supported with a receipt may not be paid. Submit each month’s completed expense reports to ShanghaiQA Coordinator by the 10th of the following month.
8. Compliance with QSR and ISO/EN regulations and Medline policies, procedures, and work rules.
9. Monitor released documents and identify errors or omissions for correction.
10. Other projects as assigned by Director of Corporate QC or Shanghai QA Coordinator.