Deborah Matos, MS, CQA, IAPP, currently serves as the Global Development QA - Processes & Systems Leader at BioNTech SE since May 2023. Prior experience includes positions as Director of Clinical Quality Assurance at Immunovant and roles at Sanofi focusing on GxP auditing and compliance management, where responsibilities encompassed managing compliance audits for clinical trials. At Sandoz, leadership and guidance in GCP regulations were provided, and independent consultancy work addressed operational and validation challenges for pharmaceutical clients. With a strong foundation in biostatistics and data sciences, Deborah held significant roles at Novartis and Ciba-Geigy throughout a robust career in clinical quality assurance. Deborah's educational background includes multiple advanced degrees and certifications in statistics, healthcare law, and data privacy from reputable institutions, underscoring expertise in regulatory compliance and data integrity.
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