Erika Minguez

Erika Minguez possesses extensive experience in regulatory affairs and medical device auditing. As the Regulatory Affairs Director at Sinclair, Erika has overseen compliance initiatives. Previously, as the Head of Global Regulatory Affairs at Eppendorf Group, Erika managed global regulatory strategies. Erika's role as Lead Auditor and Product Reviewer for medical devices at TÜV SÜD further highlights expertise in quality assurance and regulatory compliance. Additionally, Erika began their career as a Research Assistant at Cardiovascular Engineering - Helmholtz Institute Aachen, contributing to research in the medical field.