Maria Brown Email & Phone Number

Maria Brown Skills

• Global Quality System development, implementation and management
• Manufacturing Quality Assurance and Quality Control
• Product Development Quality Assurance
• Supplier Quality Management
• Quality Engineering Principles and Techniques
• Metrics; KPIs
• Global Health Authority Inspection Management
• GMP Compliance and Training
• Documentation Systems
• GMP Change Control
• Contract Manufacturing Quality Management
• Product and Process Investigation
• Root Cause Analysis
• Risk Management
• Parenteral Manufacturing Processes-Aseptic, lyophilization
• ERP System Implementation-SAP and Oracle
• 21 CFR Part 11
• GMP
• Technology Transfer
• FDA
• Change Control
• CAPA
• Cleaning Validation
• Quality Control
• Quality System
• Standard Operating Procedure (SOP)
• Corrective and Preventive Action (CAPA)
• Pharmaceutical Industry
• SOP
• Aseptic Processing
• Validation
• Trackwise
• Good Laboratory Practice (GLP)
• Quality Assurance
• U.S. Title 21 CFR Part 11 Regulation
• U.S. Food and Drug Administration (FDA)
• Regulatory Affairs
• Biotechnology
• Quality Management
• GxP
• Quality Auditing
• Verification and Validation (V&V)
• Metrics
• Erp System Implementation Sap and Oracle
• Implementation and Management
• Requirements Analysis
• Customer Service
• Parenteral Manufacturing Processes Aseptic
• Kpis
• Strategic Planning
• u.s. Food and Drug Administration Fda
• Good Laboratory Practice Glp
• Standard Operating Procedure Sop
• Global Quality System Development
• Lyophilization
• Verification and Validation V&V
• Corrective and Preventive Action Capa
• Good Manufacturing Practice Gmp
• Standard Operating Procedure
• u.s. Food and Drug Administration
• Corrective and Preventive Action
• Good Laboratory Practice
• Verification and Validation
• Good Manufacturing Practice