Responsible for all QC and ISO activities associated with receiving, inspecting, labeling, storing, picking and shipping chemicals from various suppliers to multiple customers. Managed areas of customer service, corrective action, preparing & shipping of product using hazardous material documents, ensured excellent service from tier II suppliers, and responded to customer needs and issues. Delivered, program quality, and QA assurance while meeting customer needs.Managed and oversaw… Show more Responsible for all QC and ISO activities associated with receiving, inspecting, labeling, storing, picking and shipping chemicals from various suppliers to multiple customers. Managed areas of customer service, corrective action, preparing & shipping of product using hazardous material documents, ensured excellent service from tier II suppliers, and responded to customer needs and issues. Delivered, program quality, and QA assurance while meeting customer needs.Managed and oversaw daily activities of team working on Lockheed Martin Aerospace defense contract using a variety of industry concepts, practices and procedures to plan and accomplish goals and to perform a variety of tasks.Managed and tracked the QA Database at DFW site (Review, load Military & Bell Helicopter Textron Specs), Temperature Data-loggers, Non-Cons (Non-conforming materials) and QA hold materials.Received in materials and disposition into system.Managed material for Receiving and Recertification testing (Manage all activities for this process - between Bell Helicopter Textron and Avchem)Conducted training for employees.Internal AuditingInterfaced with Engineers and Technician in regards to database questions and testing concernsEveryday Time & Personnel Management, Vacations, Reviews etc.Traveled to other site in different states for long intervals to help get warehouse in order for internal and external audits. Show less

Specialized in Residential and Commercial real-estate. Drove Negotiations and Contracts by Closing, deals)

QA Document Management and Product Validation Liaison for Corporate Office in USAManaged ECN processDirected change control board meetingsManaged DHR (Device History Records) for US facilityPrepared goals and documentation for Gate reviewsUL contact for control of all calibrated devices in US facilityValidated Doors documentation and structureActive communicator for management between Berlin and Dallas groups for project schedulingDefined and implemented multiple… Show more QA Document Management and Product Validation Liaison for Corporate Office in USAManaged ECN processDirected change control board meetingsManaged DHR (Device History Records) for US facilityPrepared goals and documentation for Gate reviewsUL contact for control of all calibrated devices in US facilityValidated Doors documentation and structureActive communicator for management between Berlin and Dallas groups for project schedulingDefined and implemented multiple project objectives with emphasis on responsibilities for cross- sectional teams with focus on meeting schedules, prioritiesWorked with team lead to resolve any problems in a timely fashionDrove all projects assigned to final; Participated in the development of the Quality Management System (process, instructions, templates using Visio)Maintained QM system documentation Performed continuous quality assurance testing and documentation of productTrained employees on QM systemPerformed internal Quality audits between the Berlin and US facilitiesTraveled to sites to audit training, Setup and Observation of training practices and procedures Show less

Active member of several product teams as a QA representative to ensure compliance with FDA/GMP, KHID SOP (Standard Operating Procedures), PCP (Product Commercialization Process), ISO 9000, and OSHA Guidelines for medical products.Developed quality assurance test plans, procedures, corrective action processes and test summary reports per FDA regulations and IEEE standardsDirected project teams' corrective action processSupported Design Engineering for unit testing, trouble-shooting… Show more Active member of several product teams as a QA representative to ensure compliance with FDA/GMP, KHID SOP (Standard Operating Procedures), PCP (Product Commercialization Process), ISO 9000, and OSHA Guidelines for medical products.Developed quality assurance test plans, procedures, corrective action processes and test summary reports per FDA regulations and IEEE standardsDirected project teams' corrective action processSupported Design Engineering for unit testing, trouble-shooting and repair of Medical Systems software and hardware.Tested Medical products using verification/validation methods - MIM (Medical Imaging Manager), Wet and Dry Processors, Medical Laser printers.Trained all levels of employees on Image Quality, Maintained Image quality library Show less