Maira brings 20 years of academic and industry experience in R&D leadership, CMC development, regulatory strategy, clinical trial compliance, and data management across the pharmaceutical, medical device, and biotechnology sectors. She is a subject matter expert in Canadian and U.S. regulatory requirements, with a focus on developing efficient pathways for market authorization and supporting science-based, compliant clinical data management practices. Her background includes hands-on research in immunology, bacterial genetics, probiotics, foodborne pathogens, and non-antibiotic solutions that support efforts to combat antimicrobial resistance and advance innovative products. Maira holds a Master of Science in Molecular Microbiology, a Ph.D. in Foodborne Zoonoses from the University of Guelph, and a postdoctoral fellowship in antibiotic resistance at McMaster University. She sees her work in regulatory affairs and clinical quality as a natural extension of her scientific training and commitment to evidence-based decision-making. Outside of work, Maira enjoys baking and spending time outdoors with her family, whether it's hiking, biking, kayaking, or skiing.