Gilbert Salud
About Gilbert Salud
Gilbert Salud is a professional in Global Quality and Compliance, currently holding roles at BeiGene, Odonate Therapeutics, and Icon Bioscience, Inc.
Company
Gilbert Salud is currently associated with multiple companies in significant roles. He serves as the Global Quality and Compliance professional at BeiGene. Additionally, he holds the position of Vice President of Quality Assurance at Odonate Therapeutics in the Greater San Diego Area. Moreover, he is also the Vice President of Quality and Compliance at Icon Bioscience, Inc. in the San Francisco Bay Area. His roles at these companies underline his extensive experience and leadership in quality and compliance across the biopharmaceutical sector.
Title
Gilbert Salud holds several prominent titles in the field of quality and compliance. He is the Global Quality and Compliance professional at BeiGene. Alongside this role, he serves as the Vice President of Quality Assurance at Odonate Therapeutics and the Vice President of Quality and Compliance at Icon Bioscience, Inc. His titles reflect his expertise and leadership in managing quality and compliance in the biopharmaceutical industry.
Education and Expertise
Gilbert Salud received his education at Saint Mary’s College of California and California State University. His extensive expertise includes a comprehensive understanding of regulatory requirements for NDA/BLA/PMA/510K applications. He is well-versed in conducting GMP and QSR compliance audits for both pre-market and post-market products. His career has involved working with companies across Europe, Asia, Latin America, and the Middle East, demonstrating his global reach and versatility.
Professional Background
Gilbert Salud has held several significant roles throughout his career. Previously, he worked as a Senior Consultant at Lachman Consultant Services and Biologics Consulting. He also served as a Senior Product Quality Steward at Genentech. His tenure at the FDA included roles such as Compliance Officer and Biotech Manufacturing Team Leader, working in the Center for Drug Evaluation and Research (CDER) and the Center for Devices and Radiological Health (CDRH). His background reflects a robust foundation in regulatory affairs and quality assurance in the biopharmaceutical domain.
Achievements and Contributions
During his career, Gilbert Salud has made significant contributions to the field of quality and compliance. He has extensive experience in regulatory requirements, including NDA/BLA/PMA/510K applications, and has conducted multiple GMP and QSR compliance audits. His work spans across various geographical regions, including Europe, Asia, Latin America, and the Middle East. His roles at the FDA, Genentech, and other esteemed organizations underscore his capability in ensuring high standards of quality and compliance in the biopharmaceutical industry.