Mónica Escalada
Director Regulatory Affairs- Euafme Ra Biologicals Lead (Ad Interim) @Zoetis
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WORK HISTORY
Director Regulatory Affairs- Euafme Ra Biologicals Lead (Ad Interim) @Zoetis
Responsible for the Biologicals Regulatory Team for Europe Africa and Middle East -ad interim- during 2026.Responsible for Companion Animal and Livestock Biologicals RA portfolio.Team Lead for 11 colleagues.Global Project Development Lead for Biopharmaceuticals (1 molecule).
EDUCATION
University of Navarra
MPharm, Pharmacy
Ghent University
Erasmus Programme, Hospital Pharmacy
University of Cambridge
CPE (Certificate of Proficiency in English), English language
University of Navarra
MSc, Drug Research and Development
SKILLS
ABOUT MÓNICA ESCALADA
In my professional experience up to now I have developed not only a vast and robust regulatory science expertise but also project and team leadership skills, strong network building and training/mentoring/coaching others.Regulatory Affairs professional with 19 years of international Pharma experience, specialized in Biotech as well as veterinary vaccines. Expert on EMA and European procedures, especially Centralized Procedure for novel molecules. Broad knowledge of regulation in the EUAfME region and good understanding of other jurisdictions (FDA and USDA). Three years working as European Expert (non-clinical) for EMA CHMP (nominated by AEMPS). Other positions as RA Manager and RA Consultant.Experience as EU Regulatory Lead, Global Development Project Team Leader (R&D) biotech, and CMC Development Team Leader biotech.
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