Aldo is a seasoned executive with thorough expertise in Information Governance, Quality & Compliance. A recognized thought leader and accomplished change agent with a reputation for innovation and creativity. Customer-focused with a natural talent for cultivating collaborative, trust-based client relationships. Validation and Quality Assurance leader with extensive domestic and international experience implementing and maintaining computerized and laboratory systems in the pharmaceutical/biotechnology industry. Successful in leading validation projects in areas of Good Manufacturing Practices (GMP) and Good Clinical Practices (GCP). Expertise in performing capability audits of vendors to ensure that products and services meet defined standards. In depth knowledge of Quality Management Systems with a proven record of establishing Audit and CAPA management, Periodic Reviews and readiness practices for business process and computerized systems. His specialties include: FDA (21 CFR Part 11) and EU regulations, Document Management, Risk Management, Audit Management, and Laboratory systems.