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Online Resumes with "Regulatory Affair"
Clinical Regulatory Affairs
Clinical Regulatory Affairs
Biological Technician - 13 Years of Experience - Near 60030
Management, regulatory management
Tags for this Online Resume: Administartor, Human Resources, Management, Motorola, Telecommunication, Meetings Organizer, Regulatory Affairs, Arabic Language
Administrative Services Manager - 18 Years of Experience - Near 85711
SUMMARY Detail oriented manager with over 18 years of International Operation and Project Management experience in the fields of X ray Security Detection Systems, Smart Security Checkpoint applications, and Industrial Control Automation. and EXPERIENCE
Tags for this Online Resume: Services, Inventory, Recruiting, Regulatory Affairs, Research, Scheduling, Support, Technical Support, Management, Security, Asynchronous Transfer Mode (ATM), Budgetary, HR, Human Resources
Clinical Regulatory Affairs
Experienced and highly qualified Clinical Research Associate with over 10 years of experience in researching and knowledge of study startup, monitoring, and regulatory processes in the Pharmaceutical Industry. Highly proficient in performing quality assurance control on laboratory best practices while leveraging R&D experience to consistently achieve goals. Extremely focused and results-oriented in supporting complex, deadl...
Tags for this Online Resume: Data Management, Documentation, Management, Systems Administrator, Clinical Research, Health Insurance Portability And Accountability Act, Research, Project Management, Project Manager, Protocol
Compliance Officer - 5 Years of Experience - Near 75287
SUMMARY Professional with extensive experience in Regulatory Affairs/Quality Assurance in the medical device, pharmaceutical and automotive industries. Managed and supported domestic and international registrations from new product development, sustaining products to rapid response products. Project Management Market Releases Letters to File International Registrations CN reviews and sign-off Finished good inspections Excel...
Tags for this Online Resume: Assembly Line, Blue Prints, Blueprints, Calipers, CMM (Capability Maturity Model), Product Design, Product Development, Quality, Documentation, Medical
Chemist
QUALIFICATIONS * Currently working toward the Regulatory Affair Certificate. * Extensive analytical characterization and data interpretation skills. * Experienced in very different analytical tests like Assay, Release Rate, Residual Solvents, Water Content Determination, and ID by IR, and Viscosity Testing. * Expert in handling different analytical apparatus like HPLC, GC, FTIR, UV-VIS, Karl Fisher, Colorimeter, pH meter, L...
Tags for this Online Resume: Good Manufacturing Practices, Manufacturing, Compliance, Inventory, Microbiology, Research, Quality Assurance, Test, Chemistry, High Performance Liquid Chromatography (HPLC)
Study Coordinator
Summary Study Coordinator with 6 years' experience specializing in technical support of animal studies requiring GLP compliant interpretations, analysis, documentation, and reporting of results per FDA regulations beginning with protocol development support and creation of shell reports resulting in a Final product ready for FDA Regulatory Filings. Areas of Expertise / Core Competencies * Highly dependable, focused and dete...
Tags for this Online Resume: Documentation, Good Laboratory Practices, Protocol, Analytical Skills, Biomedical Industry, Quality, Quality Assurance, Coordinator, Medical Devices, Regulatory
Army - 14 Years of Experience - Near 38488
Obtain a professional career within an organization that will allow application of my skills and expertise to achieve optimum utilization of its resources and strive for continuous improvement and personal development in alignment with the organization's mission. Professional Experience Summary Regulatory Affairs Inventory Control Organization Business Administration Detail Oriented Accuracy/Efficiency Confidentiality Mento...
Tags for this Online Resume: Distribution, Data Processing, Management, Policies and Procedures, Regulatory Affairs, Research, Research and Development, Accounting, Data Entry, Microsoft
Quality Manager - 14 Years of Experience - Near 23669
Familiarity with implementation of learning and development practices. ' * Advanced knowledge with quality compliance and regulations. * Phone and in-person consultation with corporate clients. * Attention to detail. * The ability to build and maintain collaborative relationships with customers and coworkers. * Strong work ethic and high standards for performance. * A self-starter that executes with minimal supervision, thr...
Tags for this Online Resume: Compliance, Regulatory Affairs, Inventory, Medical, Medical Devices, Account Management, Accounting, Attention to Detail, Facilitator, Filing, Quality Assurance and Regulatory Affairs
Administrative Assistant - 11 Years of Experience - Near 08854
Summary * Tech Savvy Executive Administrative Assistant with 15+ years of experience in office management and special projects. * Highly proficient in Microsoft Office Suite (Word, Outlook, Excel, PowerPoint), Windows Vista, Adobe Acrobat, Adobe Acrobat Reader 7.0, ViewPoint, StartingPoint, Qumas, Lotus Notes, JDE Explorer, Concur, Ariba, Google+, ASANA, SRM, SharePoint, Windows Vista, Gelco. * Provided admin support to Vic...
Tags for this Online Resume: Executive Assistant, Billing, Regulatory Affairs, Human Resources, Purchase orders, Medical Affairs, Ariba, Contract management, Filing, Medical
Clinical Regulatory Specialist
Looking for an opportunity that will allow me to share my skills and experience for the betterment of our global community. I have worked in this arena for quite some time and I know how to avoid the pitfalls surrounding clinical trials to ensure deliverables are met and compliance and efficacy is adhered to on every level of the study timeline.
Tags for this Online Resume: Clinical Trials , IRB Submisssion, Compliance specialist, Willing to Travel, Regulatory Document Reviewer, Essential Document reviewer, Informed Consent Reviewer, Management, Clinical Research, Ethics Committee Submission experience
