Independent coordination and processing of internal deviations in collaboration with relevant departments and other interfaces. Independent monitoring of on-time processing of internal deviations and defined corrective actions (including long-term CAPAs). Independent review of 8D reports for consistency, plausibility, adequacy, and clarity, particularly with respect to: Definition of affected products or materials. Root cause analysis. Corrective and preventive actions. Effectiveness verification. Advising production regarding required rework or implementation of changes. Independent evaluation of blocked stock to determine disposition (e.g., release, rework, scrapping). Participation in processing customer complaints. Support continuous improvement initiatives (e.g., 5S). Perform additional quality assurance tasks in production as assigned (e.g., process monitoring, hygiene checks, sterilization activities, etc.). Processing time of internal deviations (critical deviations). CAPA (Corrective and Preventive Actions) overdue rate. Frequency of recurring errors.