Began as Quality Supervisor, promoted to Quality Manager.Investigation/Resolution of Customer ComplaintsDaily analyzation of CAPA/ NCR Headman Quarterly Management ReviewDaily communication with customers regarding technical inquiriesManage /Direct Quality Team as to daily functionsManage ISO Certification and All Regulatory functions for Class 1 Medical Device /Cosmetic Manufacturer, including:Maintain annual certification of ISO9001:2008/ISO13485:2003ISO14001- Certified Lead Auditor-RAB Accredited CourseMaintain FDA Registration 21 CFR 820 (QSR/cGMP)Audit Vendors for compliance

Managed Quality Department and Safety Program. Developed Lot Code traceability-FIFO Practice- developed strong professional relationships with customers on a daily basis. Managed a Quality Group of 7 people. Headmanned Material Review Board- Daily Nonconformance review-CAPA Implementation- Headmanned destructive testing Instron Technique for customer requirements. Laid groundwork for ISO Certification

Manufacturer of Loading Dock EquipmentBegan as general assembly position, became Plant Foreman-1984/Plant Manager-1986 and Plant Superintendant-1990. ISO Management Representative in 1998-Lead Auditor forISO9002:1994