Eva Ferrer Espuña

Eva Ferrer Espuña serves as a Regulatory Affairs Specialist at ProductLife Group since November 2024 and as a CMC and Regulatory Affairs Specialist at AEFI since January 2021, actively collaborating with Working Parties for Biologics & ATM and International Regulatory Affairs. Previously, Eva worked as a Senior Quality Assurance and Safety Specialist for Alphanumeric Systems, focusing on COVID-19 vaccine quality assurance for The Janssen Pharmaceutical Companies. Experience includes regulatory affairs roles at Clarivate, where contribution was made to the Cortellis CMC Intelligence project, and extensive work at Reig Jofre as a Senior Regulatory Affairs & CMC Specialist. Earlier positions encompassed various pharmaceutical roles including Head of Hospital Pharmacy Service and Clinical Pharmacist across multiple healthcare institutions. Educational background includes a Master's degree in Pharmaceutical Industry and OTC from CESIF and a Bachelor's degree in Pharmaceutical Sciences from Universitat de Barcelona. Working languages include German, English, and Spanish.