Russell W.

Health product Warehouse Distribution Center

• Operation of automated production equipment, primary diagnosis of machinery failures, aiding in preventative maintenance, and sanitation of equipment. • Monitor both equipment and product according to acceptable standards. • Make real-time, accurate decisions that affect order fulfillment and product quality. • Maintain a safe work environment for all employees. • Use of Enterprise software including data input that impact production and financial systems, data retrieval, reporting, and other functions. Ensures compliance with all company policies and procedures. • Performs start-up/shut-down sanitation and limited preventative maintenance on machinery. • Ensure that work areas are clean, organized, and adhere to applicable safety rules at all times. • Check and maintain production schedules, running order and formulas. • Scale and stage ingredients according to standards. • Ensure that all product is loaded into proper containers. • Perform quality control inspections and continuously monitor product for to assure company standards. • Provide relief for scheduled breaks for Production Technicians on assigned shift.

Material Purchaser/Production Planner Premium Waters Inc., Riverside, MO. Jan 2017 - April 2017 General Responsibilities: • Through supply & demand reports generated through JD Edwards software, prioritized and planned the water bottling production scheduling. • Monitored and performed raw materials physical inventory cycle counts and inventory adjustments. • Created purchase orders as guided by Production Scheduling, Supply & Demand Reports, Sales Forecasts and trending. • Monitored changes to bottling equipment production capacity & capabilities that would effect production scheduling and raw material consumption. • Participated in operational production status meetings daily. • Generated daily reports to verify production and sales order submissions.

•Manage day to day activities project assignments, policies, procedures and schedules for QA Validation Department personnel, •Author and execute validation/qualification test protocols for processes, equipment, materials and facilities utilized in product repackaging. •Verify test process execution and documentation compliance in accordance with Good Document Practice (GDP), current Good Manufacturing Practice (cGMP) and Standard Operation Procedures (SOP’s). •Constant and continual collaboration and communication with all organizational departments including, Compliance, Regulatory, Maintenance, Quality and Production, to establish project plans and procedures, acquire technical data, develop protocols, create documentation and building schedules to assure the successful execution and completion of testing activities. •Monitor changes to qualified systems, processes, materials and equipment; identify trends and issue recommendations for testing and re-qualification. •Conduct meetings and training with upper management and validation teams. •Write, review, updated and submit Standard Operating Procedures (SOPs) •Monitor the activities and procedures of the QA Lab in regard to Product Retention and Calibration activities. •Perform internal investigations. •Participate in Operational Excellence Projects. •Generate and monitor monthly reports to support Global Quality Metrics. •Interview, hire, train, evaluate and discipline Validation Department team members; address complaints and resolve issues.

•Created protocols, addendum's and test documents with technical standards, principles, concepts, and methods for the execution of validations, qualifications and testing. •Assured document and testing processes were in compliance with Good Document Practice (GDP), Good Manufacturing Process (GMP) and Standard Operation Procedure (SOP). •Assisted, coordinated and performed all aspects of the validation execution and completion •Authored, reviewed, and distributed validation documents, memos, SOPs and specifications •Interacted with all departments to facilitate testing and validation projects •Performed quality investigations, root cause analysis, audit responses and reporting •Auditor of the Calibration Program documents to ensure all paperwork is complete, accurate and current •Assisted with the Cleaning Validation Program, as needed

•Generally assure inspection processes are performed in compliance with Good Document Practice (GDP), Good Manufacturing Process (GMP) and Standard Operation Procedure (SOP). •Conduct inspection and approvals of packaging operations and clean-up •Inspection and approval portable machines and production room equipment •Batch documentation, product, component and material verification and review •Initiation and completion of Deviations and Investigations •Machine setting verification for production run approval •Maintained production room control •Perform other duties as assigned by the QA In-Process Supervisor or Lead

•Rough and Finish Carpentry •Residential and basic Commercial Wiring •Drywall hanging, taping and finishing •Painting •Plumbing •Remodel and New Construction

•Distribution Center Supervision of outbound truck loading teams •Shipment billing •Forklift operator •Facility housekeeping and maintenance

Completing Bachelor degree.