Mihaela Nosca is a seasoned professional with extensive experience in clinical compliance and quality management within the pharmaceutical industry. Currently serving as Director of Clinical Compliance and Inspection Readiness at CSL Seqirus since September 2018, Mihaela leads the Clinical Development Compliance and Inspection Readiness Team, providing GxP support and evaluating compliance risks within clinical trials. Prior roles include Associate Director at Astellas Pharma Europe, overseeing global quality management systems and CAPA processes, as well as Senior Project Quality Lead at PAREXEL, where Mihaela managed clinical monitoring activities. Mihaela's diverse background also includes experience in pharmacovigilance and customer care management, complemented by a medical degree from Medical University.
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