G Giles Location: Loxahatchee, FL 33470 ... plete revamping of ISO 9001:2000 System including major Operation Manual and Quality Manual rewrite. Implementation of Electro Static Discharge and NASA Hand Soldering Program. Turbo Combustor Technologies, Stuart, FL May 2004 - November 2004 Receiving Inspection · Performed chemical analysis, measurement and other material specification compliance testing. · Controlled certification paperwork and filing. Sermatech International, Boynton Beach, FL March 1998 - June 2003 Assistant Quality Manager, Tech, Etc... · Auditor for in-house, FAA and ISO Audits. · Calibration Technician (hand tools to Plasma Booths). · Records Administrator for Quality Records. · M ...
97 hits
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L Swisher Location: Tampa, FL 33647 ... ts for the Medical Device, Pharmaceutical and Nutritional Industries include: · Quality Systems (CAPA, Training, Supplier Quality, Internal Auditing, Document Control, · Training - Quality Systems Regulations, Good Documentation Practices, Corrective and Preventative Actions, New Hire Orientation · Supplier Quality Audits · Laboratory Investigation Reviews · Non-Conforming Material Reviews · Procedure Reviews and Re-Writes · FDA Readiness Plans Manager of Quality J and J Scientific Products, Inc.; Tampa, Florida - 2007 Responsibilities included: · Responsible for overall activities including quality assurance, quality control and regulatory affairs. · Deve ...
95 hits
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R Atkins Location: Jupiter, FL 33458 ... in domestic and international markets in medical device and consumer packaged goods. A results driven, hands-on leader with proven success in the areas of business Start up, Regulatory Compliance, Quality System Development, GMP Auditing, Supply Chain, Team Development and Training. A proven record of achieving measurable results within organizations by driving down operational costs, improving team performance and eliminating quality compliance issues through the use of Lean and Six Sigma methods.CORE COMPETENCIESTeam LeadershipInvent ory ERP SystemsOrganizat ional Restructuring FDA & ISO 13485 ComplianceSuppli er Quality ManagementRisk ManagementFDA GMP Training ProgramsProcess Val ...
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K Vampran Location: Kissimmee, FL 34746 ... ns, procedure manuals, training, Monthly reports. Analytical: Department correspondence with engineers, Blueprints and revisions, reviewing customer surveys, Section planning, reviewing studies/processe s, details Inspections. Testing: Calibration, mechanical, electrical, bometric Tolerance, surface plate layout. Leadership/ Management: Interviewing/Hir ing establishing. Product goals, counseling /advising, ethical standards Company goals/objectives , loss prevention initiatives. .Professional Experience 1999-Present Daniel’s Manufacturing Co. Quality Control Inspector / Quality Assurance Inspector Full-time quality inspector for commercial military aircraft Repair and emer ...
91 hits
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F Pineda Location: Miami, FL 33185 ... uditing, overseeing, coaching, implementing and executing Food Safety Quality Control Operations and sanitation programs in compliance with all Federal, State, Local regulations pertinent for different types of GMP Food processing and distributing plants and those at retail level.PROFESIONA L EXPERIENCE Chemstar Corp. Lithia Springs, GaField Service Technician 2009- Perform Food Safety and Sanitation Audits along with the maintenance, installation and upgrades of chemical dispensing units used in food retail establishments. Coaching/Trainin g personnel on a daily basis in the proper and safe handling of chemicals to be used and for all pertinent food safety and sanitation issues. Daily repo ...
89 hits
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W Wiley Location: Saint Augustine, FL 32092 ... administration, capability studies, and process analysis for efficiency improvement and scrap reduction, and design review coordination for new product introduction. Utilize statistical tracking systems to indicate product quality trends. Plan and coordinate quality system for all Quality, registrations, (standards Australia, ISO 9001, ISO 13485, CE Mark, Japan Standard).Key Accomplishments: Managed cross functional team that standardized lens parameter finished goods testing for product release that decreased the amount of lenses tested yearly by 40%.Developed Technical justification for adopting ISO specification for High Minus Spherical product power measurements.Dev eloped and managed ...
87 hits
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J Munsch Location: Gulf Breeze, FL 32561 ... rtunity to grow along with the organization. Employment History Pegasus Laboratories, Inc. 2001-2006 Compliance Technician, Quality Assurance Manager Pensacola, FL Supervised, mentored and evaluated direct report associates. Issued production instructions as set forth in the master production schedule. Assumed responsibility for quality of all products received and manufactured. Reviewed and approved all required documentation prior to release for distribution. Prepared and submitted regulatory forms and documentation required for compliance. Observed personnel to ensure compliance with established regulations. Created, reviewed and approved standard operating procedures. ...
85 hits
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D Pase Location: Casselberry, FL 32707 ... Dept of AgricultureFour plant processing assignment covering a 175 mile routeAssured HACCP programs were in complianceWorked with plant management to assure product safety Used computer to research regulations and file reports Completed all GMP, SSOP, and HACCP courses offered by USDA Quality Control SupervisorJan 1978 - March 1985 - Perdue Farms Salisbury MDSupervised 8 QA InspectorsAssure d products met Quality standardsWorked with plant management to produce high quality productsEducatio n Keystone College - LaPlume PAGraduated - May 2006Associates in Business Admi ...
83 hits
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K Godwin Location: Merritt Island, FL 32953 ... Ensure ASRC Aerospace contract's quality assurance program and quality assurance provisions are well defined in the Quality Management System for continuous improvement throughout the company. Responsible for the development, implementation and audit process for the AS9100 Quality Management System Aerospace requirements throughout the company. Review and revise internal documentation for compliance. Participate in design reviews, technical interchange, and pre award meetings. Maintain C/PAR database for corrective and preventive actions to ensure the appropriate root cause analysis is identified and properly implemented. Conduct supplier audits for procurement of complex, critical and high ...
81 hits
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T Omdahl Location: Orlando, FL 32819 ... Mr. Tracy P. Omdahl Quality Assurance / Regulatory Affairs / Reliability D REGULATORY SUMMARY £ Experience with US, Canada and EU medical device regulations, developments and trends including Pacific Rim and Latin America country product registration. International medical device product registrations for global projects from around the world, including â Brazil ANVISA & InMetro â Central and South America â EU CE notified body marking for class II and class III products â China SFDA â Australia TGA â Mexico Secretaria de Salud â Canada CMDR / CMDCAS / CAMCAS â Russia device registration and Gost Mark â Japan MGLW. DMAH, MAH and registration of foreign manufacturers â Device classifi ...
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