Summary Highly skilled Documentation Specialist with responsibilities in the medical device industry. Knowledge of Good Manufacturing Procedures (GMP), Good Documentation Practices (GDP) and Quality Systems (QS). Provide excellent customer service and guidance to the organization by evaluating documentation to ensure that each change is scoped accurately and compliant. Subject Matter Expert (SME) in Records Management, preparing and maintaining records. * Proficient in Ariba Outlook MS Office Suite Quicken EzDoc Typing 85 WPM and 10-Key by touch

Highlights:

• Document Review
• Management
• Manufacturing
• Complaints
• Regulatory Affairs
• Procurement
• Scheduling
• Documentation
• Active Server Pages
• Quality