Laure Lambricht is a QA Associate at Celyad Oncology, where they ensure quality management for cell-based therapies and cGMP compliance. They earned a PhD in pharmaceutical and biomedical sciences from Université catholique de Louvain, focusing on cancer DNA vaccine development. Previously, Laure worked as a Senior Validation Specialist at Celyad, managing raw material qualification and validation projects. In addition to their professional experience, they are currently pursuing further education at Wageningen Universiteit en Researchcentrum.
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