CV, Curriculum Vitae and Online Resumes Search

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Online Resumes with "820"

Quality Assurance Director - 20 Years of Experience - Near 33545

BSI ISO 13485:2003 Lead Auditor (TPECS) Certification - Certificate: 7930649-76913 * Hired and entrusted by B Braun McGaw of Puerto Rico and LeMaitre Vascular to implement a wide-array of corrective actions and systems resulting from 3 FDA warning letters. Subsequently after new systems implementation received 0 FDA 483 observations for a combined period of 12 years. * Built company-wide shared quality visions which complet...

Tags for this Online Resume: Documentation, Quality Assurance, Compliance, Pharmaceutical Industry, Quality, Quality Control, Regulatory Affairs, Medical Devices, Pharmaceuticals, Regulatory Compliance

Bookkeeper - 20 Years of Experience - Near 95603

System Engineer - 8 Years of Experience - Near 29461

SUMMARY OF QUALIFICATIONS A detail oriented and organized professional with over ten years' experience in Information Technology and customer service. Working knowledge of Local Area Network (LAN) procedures and security implementations, Microsoft Server 2008/2012 using Active Directory to include Domain Controllers, Microsoft Exchange Servers 2007/2013, Microsoft Lync 2013, Dell 620/720/820 Servers, DNS, DHCP, Group Policy...

Tags for this Online Resume: Servers, Active Directory, Microsoft Active Directory, VMWare, Domain Name System, Microsoft, Local Area Network, Remedy, BMC Software

General - 7 Years of Experience

KEY QUALIFICATIONS: * COMPLAINTS & TECHNICAL SUPPORT SPECIALIST WITH 5+ YEARS OF PHARMACEUTICAL AND MEDICAL DEVICE INDUSTRY experience * 5+ years of experience with product complaints including experience with Global Customer Complaints (GCC), adverse events, and auditing of complaint records * Excellent knowledge of quality standards and regulations: FDA QSR 21 CFR 803 & 820, ISO Standards 9001 / 13485 / 14971, MDD 93/42/E...

Tags for this Online Resume: Complaints, Good Clinical Practices, Medical, Pharmaceutical, Support, Technical Support, Clinical Research, Project Management, Project Manager, Research

Manager - 2 Years of Experience - Near 20716

Tags for this Online Resume: Market Research, Medical, Medical Records, Research, Allergy

Banquet Staff - 2 Years of Experience

Quality Manager - 20 Years of Experience - Near 28269

Summary of Qualifications and Accomplishments * Demonstrated excellent Quality Management/ Engineering work experience, providing technical support to customers, suppliers, cross-functional team members, and manufacturing on new and existing products. * Knowledgeable and experienced with SMT, PTH, Hybrid, Chip on Board, Power Supply, and Fiber Optic technologies to assemble, test, and box build printed circuit boards in sup...

Tags for this Online Resume: ISO 9001, Fiber Optics, Quality Assurance, Test, Welding, Capital Equipment, Consumer Products, Engineering, ISO 9001, Fiber Optics, Quality Assurance, Test, Welding, Capital Equipment, Consumer Products, Engineering

Electrical Engineer - 20 Years of Experience - Near L5L2E

Experience Summary I have over 25 years Canadian experience in Instrumentation and Control (I&C) systems and SCADA design on a wide-range of projects in the water and wastewater, chemical and petrochemical industries. My extensive consulting experience is in the field of instrumentation and control engineering. That includes process control and electrical schematics, PLC (Control Logix, Compact Logix, ControlWaves, GE Fanuc...

Tags for this Online Resume: Detail Design documentation, Process Analyzers for pH, Turbidity, FreeChlorine, Disolved Oxygen, and Chemical dosing pumps., Electrical Scahematic and PLC interface, Specification for field transducers, Specific Equipment installed in Classified Area, PLC Wiring Diagrams, Water Treatment, Instrumentation, Control Systems, Petrochemical, GE, Integrate, Security, SCADA, Instrumentation and Control

Quality Professional

Qualifications Skills: Regulatory Affairs/quality assurance: Projects, related skills and practice include: * Prepare and submit 510 (k) s for US FDA on Class I and Class II Medical Devices and assisted with the preparation of Class III submittals * Compile, document and submit Technical Files for Europe (CE Marking) per Medical Device Directive (MDD) * Perform monthly trending analysis * Developing quality systems plan inc...

Tags for this Online Resume: Manufacturing, Medical, Medical Devices, Risk Analysis, Documentation, Failure Analysis, ISO, Quality Assurance, Quality, Statistical Analysis

Computer Programmer - 20 Years of Experience - Near 71118

Tags for this Online Resume: sql, it jobs, c#, c++, software

Lawyer - 18 Years of Experience - Near 78704

Tags for this Online Resume: Equity, Litigation, Arbitration, Defense, Insurance, Insurance Defense, Probate