SANDRA ARIZA

Sandra Ariza has extensive experience in quality control and regulatory affairs, having held significant roles at Laboratorios Legrand S.A. as Quality Control Manager and Regulatory Affairs Manager from December 2006 to August 2012, where responsibilities included managing registration processes for pharmaceuticals, dietary supplements, and cosmetics in Colombia and the Andean Region. Sandra continued her career at Abbott from September 2014 to May 2016, progressing through positions such as QA & RA Regulatory Affairs Manager for the North Region, where management of regulatory and QA operations for a team of five was key. Sandra also served as Colombia Regulatory Affairs Manager, overseeing registration processes for various health products. At Merck KGaA in Germany, Sandra worked as a Development and Research analyst from September 1999 to December 2003, leading a team of laboratory analysts. Educational credentials include a Diploma in Biotechnology, a Pharmaceutical Chemist degree, an M.Sc. in Pharmacology, and certifications in Regulatory Affairs from esteemed institutions.