Dayron Montoya is a highly skilled pharmaceutical professional with extensive experience in analytical methodologies and quality control across various organizations. From August 2014 to August 2015, Dayron worked at Tecnimicro, focusing on the design and validation of analytical methodologies using techniques such as HPLC and LC-MS. Following this, Dayron contributed to the stability studies of pharmaceutical products at Corpaul from August 2015 to August 2018. Dayron's expertise further expanded during tenure at West Química and Sosteli Pharma, where responsibilities included the validation of pharmaceutical methodologies and quality control of analytical techniques. Before joining Baxter International Inc. in May 2025 as a research associate, Dayron held positions at Universidad CES exploring plant biotechnology and at LifeFactors performing GMP validation of analytical methodologies. Dayron holds a degree in Pharmaceutical Chemistry from Universidad de Antioquia, emphasizing quality control and validations.
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