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Luis Martinez is a seasoned professional in pharmaceutical development with extensive experience in analytical chemistry and quality control. Currently serving as a Pharmaceutical Development Coordinator at Novocol Pharma, Luis is responsible for planning and coordinating validation and method transfer activities for Active Pharmaceutical Ingredients and excipients. Previous roles include Method Development Chemist and Stability Chemist at Eurofins Alphora, where Luis managed analytical method development and executed GMP compliance studies. Luis began a career as an Analytical Chemist at the National Institutes of Health, focusing on the quality assurance of raw materials and finished products. Luis also contributed as a Patent Agent Technical Advisor at Lloreda Camacho & Co. and worked as a Quality Control Analyst at Laboratorios Prodycon S.A., specializing in environmental sample analysis. Luis holds a Bachelor of Science in Chemistry from Universidad Nacional de Colombia.