Medline Industries, Inc.
Mundelein, IL
Job Summary This role specializes in one or two particular subsection(s) of our Quality Management System (e.g. Device Master Records, customer complaint, product hold, recalls, incoming quality). Responsible for basic building and maintaining quality documentation and processes such as product specifications, manufacturing tolerances, engineering drawings, inspection criteria, testing reports, ERP system analysis, customer complaint analysis and validations. Job Description MAJOR RESPONSIBILITIES: Assist in the development and implementation of processes, reports, data analysis and procedures within the defined area of specialization. Collaborate with multiple groups (both internal and external) to solve complex problems and continue to ensure compliance is maintained with FDA, ISO and internal requirements. Facilitate meetings with global business units, sales, marketing, branch personnel to manage project requirements and deadlines. Track and report progress...