Mirabelle P.

Mirabelle P. is an accomplished regulatory affairs professional with extensive experience in global CMC strategies for biologics and pharmaceuticals. Currently serving as Director of Global Regulatory Affairs at AbbVie since May 2020, Mirabelle actively contributes to the development and implementation of regulatory strategies throughout the product lifecycle. Prior to AbbVie, Mirabelle held various positions at Allergan including Director and Associate Director in Global Regulatory Affairs, and Senior Manager roles. Mirabelle's earlier experience includes a Senior Manager position at Teva Parenteral Medicines, where responsibilities included establishing regulatory strategies and managing document deliverables. Mirabelle began a career in quality control and compliance as a QC Supervisor at Medeva Pharmaceuticals and later as a Quality Control Manager at a Nutritional Supplements/OTC Manufacturer. Mirabelle holds a Bachelor of Science degree in Clinical Laboratory Science from the University of Santo Tomas.