Robyn Walsh has over 23 years of experience in regulatory affairs and quality assurance within the biopharmaceutical and diagnostics industries. Currently serving as Associate Director of Regulatory Affairs at MannKind Corporation, Robyn oversees regulatory operations, including the management of US filings, document submissions, and FDA interactions. Previous roles include Senior Manager in Regulatory Affairs where Robyn executed complex submissions and led authoring teams, and Manager of Quality Assurance, where Robyn developed compliance systems and maintained ISO certifications. Before MannKind, Robyn contributed as a Quality Assurance/Regulatory Affairs Associate at Tepnel Lifecodes, achieving multiple certifications, and as Special Projects Manager at the National Disease Research Interchange, where Robyn significantly increased operational efficiencies. Robyn holds an MS in Genetics from Jefferson Health and a BS in Biology and Biochemistry from Haverford College.