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Conxi Verdú has been working in the field of Regulatory Affairs and Quality Assurance since 1989. Conxi began their career at Otsuka Pharmaceutical S.A. as a Regulatory and Scientific Affairs professional. In 1992, they joined Almirall as a Senior Manager in Regulatory Affairs, where they provided regulatory strategy input to the global development teams, organized and led key milestone meetings with health authorities, and coordinated regulatory submissions of different types. In 2008, they became the Head of Regulatory Affairs and Quality Assurance at Gendiag.exe, S.L. (Ferrer Internacional, S.A.), overseeing compliance with regulatory, quality, and safety requirements applicable to company products and activities. In 2018, Conxi joined Anaconda BioMed as a Regulatory Affairs Manager, planning and managing all regulatory activities and representing the company before competent authorities and notified bodies. Most recently, in 2021, they became the Regulatory Affairs and Quality Assurance Director at Neuroelectrics.

Conxi Verdú obtained their Pharmacy Degree from the Universitat de Barcelona in 1989. In 2004-2005, they completed an Experto Universitario in Promoción de la Salud en la Comunidad from the Instituto de Salud Carlos III - Escula Nacional de Sanidad.