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Audrey Vitale Location
Canaan, NH, US
Audrey Vitale Work
Director of QA and QMS, Regulatory Affairs Advisor @ (July 2007 - Present)
QA and RA Consultant @ Network Medical Products USA, Inc. (January 2013 - April 2016)
Regulatory Affairs Director @ Ultracell Medical Technologies, Inc (January 1998 - January 2007)
Audrey Vitale Education
Rensselaer Polytechnic Institute
BS (Materials Engineering)
1978-1982
Audrey Vitale Skills
CAPA
CE marking
Cross-functional Team Leadership
FDA
ISO 13485
Manufacturing
Medical Device Directive
Medical Devices
Quality System
Regulatory Affairs
V&V
Validation
Cross Functional Team Leadership
Public Speaking
Customer Service
Sales
Ce Mark
Regulations
Distributors
Asia
R&d
Plastics
ISO 9001
Production Process
Middle East
Sales and Marketing
Documentation
Regulatory Approvals
Registrations
Consulting
Materials
Compliance
Writing
South America
Internal Audit
Process Efficiency
Corporate Office
Market
Technology Transfer
Vigilance
Product Quality
Quality Management
Oracle Enterprise Manager
International Marketing
Quality Assurance
Regulatory Compliance
Medicine
Country
Responsibility
Strategic Planning
Sold
Materials Science
Usa
Training
Troubleshooting
Branding
Glass
Auditing
European Union
Quality System Compliance
International
Canada
System
Testing
Lsp
Audrey Vitale Summary
Audrey Vitale, based in Canaan, NH, US, is currently a Director of QA and QMS, Regulatory Affairs Advisor at LifeSciencePLUS, Inc.. Audrey Vitale brings experience from previous roles at Network Medical Products USA, Inc. and Ultracell Medical Technologies, Inc. Audrey Vitale holds a 1978 - 1982 BS in Materials Engineering @ Rensselaer Polytechnic Institute. With a robust skill set that includes CAPA, CE marking, Cross-functional Team Leadership, FDA, ISO 13485 and more. Audrey Vitale has 1 emails on RocketReach.
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