Jeroen de Vreeze

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Jeroen de Vreeze

Jeroen de Vreeze

Ing. CPIP
GMP Compliance Specialist

With over two decades of experience in sterile processing and biotechnology, Jeroen joined the CellVec team during its early inception stage as a GMP Compliance Specialist. He has been instrumental in the design and validation of CellVec’s facility and its processes as well as the creation of the organization’s Pharmaceutical Quality System. Jeroen has since supported CellVec in a variety of roles primarily focused on quality and compliance.

A Netherlands national, he spent most of his career in the United Kingdom and Singapore gaining expertise in various roles ranging from production management, project engineering, technical operations to commercial management. He successfully led operational and project-based teams in the United Kingdom, Ireland, Netherlands and Singapore implementing quality compliance and engineering projects.

Jeroen’s product experience includes sterile manufacture, medical devices, controlled drugs, tableting, IMPs and biologicals. He strives to set high standards for health and safety, product quality and financial stability for his customers to ensure a stable, continuous supply of safe product to patients.