| Resume alert | Resumes 91 - 100 of 105 |
Quality Assurance Engineer
Trinity, FL, 34655
... 13485 and 510(k) filing experience • Sterile and Non-sterile filling equipment • Batch, extrusion and continuous operations • FDA electronic OTC drug registration • FDA electronic facility registration • Materials Requirement Planning (MRP) • Allen ... - 2010 Jul 08
... 13485 and 510(k) filing experience • Sterile and Non-sterile filling equipment • Batch, extrusion and continuous operations • FDA electronic OTC drug registration • FDA electronic facility registration • Materials Requirement Planning (MRP) • Allen ... - 2010 Jul 08
Project Manager Medical Device
Tampa, FL, 33618
... Implementation Project Leader - Document management system for FDA regulated, consumer, as well as medical device company, specializing in disinfectant wipes. . Implementation Project Leader - Document Management system for Global Fortune 500 ... - 2010 May 29
... Implementation Project Leader - Document management system for FDA regulated, consumer, as well as medical device company, specializing in disinfectant wipes. . Implementation Project Leader - Document Management system for Global Fortune 500 ... - 2010 May 29
Quality Control Manager
New Port Richey, FL, 34655
... o FDA, DEA, and EPA experience. o Establishes specifications for finished products. o Dedicated to success o Hazardous materials management certified. PROFESSIONAL EXPERIENCE BioTec Films LLC - Tampa, FL (A manufacturer of food grade thin films) 10 ... - 2010 May 16
... o FDA, DEA, and EPA experience. o Establishes specifications for finished products. o Dedicated to success o Hazardous materials management certified. PROFESSIONAL EXPERIENCE BioTec Films LLC - Tampa, FL (A manufacturer of food grade thin films) 10 ... - 2010 May 16
Customer Service Medical
Largo, FL, 33770
... Trained to the following FDA & ISO regulations: 21 CFR Part 210/211, 21 CFR Part 820, ISO 13485/ISO9000- Medical Device Regulations, ISO 14971- Risk Management System for Medical Devices, ANSI/AAMI/ISO 11134- Sterilization of Health Care Products). ... - 2010 May 13
... Trained to the following FDA & ISO regulations: 21 CFR Part 210/211, 21 CFR Part 820, ISO 13485/ISO9000- Medical Device Regulations, ISO 14971- Risk Management System for Medical Devices, ANSI/AAMI/ISO 11134- Sterilization of Health Care Products). ... - 2010 May 13
Quality Control Manager
Wesley Chapel, FL, 33543
... Organized and maintained the volumes of documents required by FDA. . Responsible for special product shipments packaged per DOT regulations. . Assumed responsibilities for GMP, environmental health and safety procedure awareness, and compliance. ... - 2010 May 12
... Organized and maintained the volumes of documents required by FDA. . Responsible for special product shipments packaged per DOT regulations. . Assumed responsibilities for GMP, environmental health and safety procedure awareness, and compliance. ... - 2010 May 12
Marketing Professional
Largo, FL, 33771
... surveys and internal problem resolution training * Made recommendations regarding new product development, including FDA approvals, packaging and integration of new product to new and existing markets * Copywriting and design management for ... - 2010 May 10
... surveys and internal problem resolution training * Made recommendations regarding new product development, including FDA approvals, packaging and integration of new product to new and existing markets * Copywriting and design management for ... - 2010 May 10
Engineer Electrical
Palm Harbor, FL, 34683
... Knowledge of FDA Quality Systems Regulations, IPC-610 and ISO 13485. Fully bilingual, English and Spanish. PROFESSIONAL EXPERIENCE Kaman Precision Products Inc. Product Assurance Engineer (2010 – Present) Responsible in both manufacturing and ... - 2010 May 09
... Knowledge of FDA Quality Systems Regulations, IPC-610 and ISO 13485. Fully bilingual, English and Spanish. PROFESSIONAL EXPERIENCE Kaman Precision Products Inc. Product Assurance Engineer (2010 – Present) Responsible in both manufacturing and ... - 2010 May 09
Sr. Principal Systems Engineer
Dunedin, FL, 34698
... ENGINEERING Engineering Service Requirements Analysis Design Verification and Validation Process Improvement and Automation Fault Tree Analysis / Risk Mitigation QUALITY SYSTEMS FDA QSR / MDD / ISO9001 Lean Six Sigma Greenbelt Maturity Models / CMM ... - 2010 May 05
... ENGINEERING Engineering Service Requirements Analysis Design Verification and Validation Process Improvement and Automation Fault Tree Analysis / Risk Mitigation QUALITY SYSTEMS FDA QSR / MDD / ISO9001 Lean Six Sigma Greenbelt Maturity Models / CMM ... - 2010 May 05
Customer Service Manager
Clearwater, FL, 33761
... FDA & DEA Regulations . AS400, MRP/ERP, & KRONOS [pic] PROFESSIONAL EXPERIENCE HunterDouglas, Southeast, Pinellas Park, Florida . 2005-2009 A leading global window fashion company. Production Manager Oversee all facets of daily operations for ... - 2010 May 02
... FDA & DEA Regulations . AS400, MRP/ERP, & KRONOS [pic] PROFESSIONAL EXPERIENCE HunterDouglas, Southeast, Pinellas Park, Florida . 2005-2009 A leading global window fashion company. Production Manager Oversee all facets of daily operations for ... - 2010 May 02
Sales Service
Odessa, FL, 33556
... This lead to global role out of these services to meet FDA regulatory requirements and additional income within the company Thomas mcphee Page 2 AnaChem Ltd, Luton, England 1995 - 2000 Family business acquired by Diploma plc - UK & Ireland's leading ... - 2010 Mar 11
... This lead to global role out of these services to meet FDA regulatory requirements and additional income within the company Thomas mcphee Page 2 AnaChem Ltd, Luton, England 1995 - 2000 Family business acquired by Diploma plc - UK & Ireland's leading ... - 2010 Mar 11