Audrey Vitale Email & Phone Number
Director of QA and QMS, Regulatory Affairs Advisor @ LifeScience PLUS, Inc
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Audrey Vitale Location
- Canaan, NH, US
Audrey Vitale Work
- 2007 -now Director of QA and QMS, Regulatory Affairs Advisor @
- 2013 -2016 QA and RA Consultant @ Network Medical Products USA, Inc.
- 1998 -2007 Regulatory Affairs Director @ Ultracell Medical Technologies, Inc
Audrey Vitale Education
- Rensselaer Polytechnic Institute
BS (Materials Engineering)
1978-1982
Audrey Vitale Skills
- Cross Functional Team Leadership
- Regulatory Affairs
- Medical Devices
- FDA
- Quality System
- Public Speaking
- Customer Service
- Sales
- CAPA
- Medical Device Directive
- CE marking
- Validation
- ISO 13485
- Manufacturing
- V&V
- 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 Cross Functional Team Leadership, Regulatory Affairs, Medical Devices, FDA, Quality System and more. Audrey Vitale has 1 emails on RocketReach.
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