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Online Resumes with "Regulatory Affairs "
Clinical Research
AREAS OF EXPERTISE * Clinical Trial Design * Biologics * Study Management * Medical Devices * Scientific Research * Regulatory Submissions * Program Development * KOL Relationships * Scientific Strategy * Oncology * Regulatory Strategy * Cardiovascular * Investigator Recruitment * Gastrointestinal * International Clinical Trials * Regenerative Medicine * Data Analysis * Surgery
Tags for this Online Resume: Clinical Research, Research, Pathway, Protocol, Regulatory Affairs, Infrastructure, Pharmaceutical, Publications, Selenium, Venture Capital, oncology, phase, clinical, gcp, protocol, trial, pharmaceutical, ich
Clinical Regulatory Affairs
In Between - 20 Years of Experience - Near 70084
Areas of Expertise: Research, develop, and maintain Thirty-plus years of experience in Inspection of EPA, OSHA, DOT safety, health and environmental Process Technology. regulatory affairs. Pipeline OQ compliance policies and programs. Certified Operator Qualifications Evaluator.
Tags for this Online Resume: OSHA, Compliance, Hazardous Waste, Management, Pipelines, Policies and Procedures, Procurement, D.O.T., Regulatory Affairs, Consulting, Safety
Quality Engineer - 20 Years of Experience - Near 84124
SUMMARY An analytical, detail-oriented, and highly motivated senior quality assurance regulatory affairs professional with broad experience globally in quality assurance, strategic planning, auditing, implementations, policies and procedures, compliance, systems management, project management, data analysis, and reporting. Additional aptitude in quality control, process improvement, presentations, and data management. Displ...
Tags for this Online Resume: Audit, Applications, Automotive, Database, Database Applications, Help Desk, ISO, ISO 9001, Management, Quality Assurance
Quality Assurance Director - 17 Years of Experience - Near 03062
SUMMARY A resourceful, determined and results driven global quality assurance & regulatory affairs leader with 17 years of experience in R&D, internal & contract manufacturing operation (CMO), supporting domestic & international markets.
Tags for this Online Resume: Product Development, Engineering, Management, Manufacturing, Reviews, Risk Management, Kaizen, Regulatory Affairs, Automation, Compliance, compliance, ASQ, ISO 13485, Design Control, CAPA, Quality Management System, 510k
Chemist - 15 Years of Experience - Near 92881
Experienced with trouble shooting issues in chromatography and other testing procedures resulting in effective and high quality test methods * Maintained daily, weekly, and quarterly checks of instrumentation such as stability chambers and HPLC systems as part of team responsibilities, reducing the need for a separate metrology group Scientist II (Laboratory Technical Services) 2011 Performed remediation activities for exis...
Tags for this Online Resume: Filing, Forth Programming Language, Quality Assurance, Regulatory Affairs, Test, High Performance Liquid Chromatography (HPLC), Instrumentation, Quality, Quality Control, Compliance, pharmaceutical, sop, change control, method validation, cleaning validation, hplc, fda, raw material, in-process testing, finished product, solid dose, research and development, method transfer, protocol, report
CEO of Quality/Regulatory Affairs- 19 Years of Experience - New York
SUMMARY Senior Executive with combined technical, regulatory strategy, project management and business experience to build businesses and relationships to deliver new products to market. Over 20 years of experience in medical device, pharmaceutical, biologics, and diagnostic development, including In-Vitro Diagnostic, with market leaders such as Johnson & Johnson, Watson Pharmaceuticals and Mela Sciences. Led worldwide regu...
Tags for this Online Resume: Management, Manufacturing, Product Development, Risk Management, Process Engineering, Engineering, Quality, Quality Assurance, Quality Control, Regulatory, Strategy, Clinical Development, Pharmaceutical, Medical Device, Green Belt, PnL
Health Technologist - 20 Years of Experience - Near 93035
Tags for this Online Resume: Management, Scheduling, Fraud, Inventory, Inventory Control, Logistics, Medical, Medical Terminology, Microsoft PowerPoint, healthcare, Pharmacy Compliance, Regulatory Affairs
Regulatory Affairs
Aspiring to work with a growing organization that offers a challenging environment where I can learn and carve a niche for myself and effectively contribute to the organizations target and aspirations. Firmly believe that imagination, passion and boundless curiosity always set levels and standards that exceed expectations.
Tags for this Online Resume: Computer Literate, Manufacturing, Microsoft Excel, Microsoft PowerPoint, Microsoft Word, Packaging, Diagnostics, Evaluate, Filing, Its
Quality Manager - 20 Years of Experience - Near 91709
QUALIFICATIONS AND ACHIEVEMENTS
Tags for this Online Resume: Audit, Manufacturing, Microbiology, Pharmaceutical, Quality Assurance, Test, Internal audit, Regulatory Affairs, Microbiological Testing, Management, manufacturing
Software Sales Representative - 20 Years of Experience - Near 92629
A top-performing Account Executive credited with combining sales, marketing and business development expertise to deliver substantial revenue growth in highly competitive business markets. Strong expertise in delivering revenue generated results and solving business related problems through innovative software solutions. Highly accomplished in business performance, innovative business development techniques and nurturing la...
Tags for this Online Resume: Enterprise Sales, BPM/CRM, ERP/HCM, ECM/RM, Security, Infrastructure, Orange County, Management, Email, Publishing, Regulatory Affairs, SAN (Storage Area Network), Marketing Management, Sales, Architectural, Management, Management Solutions, Risk Management, Account Manager, Business Intelligence, Content Management, Document Management, Sales
Clinical Regulatory Affairs - 13 Years of Experience - Near 19711
My background includes six years experience as a Project Manager for Regulatory Global submissions, as well as Life Cycle Management of Regulatory documents. As a Project Manager within the Submission Management Group, I provided expertise on global submission compilation and published electronic submissions compiled in RSS Application (eCTD) in accordance with Health Authority guidelines and departmental standards.
Tags for this Online Resume: Newark, DE, eCTD, RSS Application, Regulatory Publisher, Regulatory Submissions, Document Management, Legal, Management, Project Management, Publishing, Quality Assurance, Test, eCTDXpress
