Sue Dahlquist

Sue Dahlquist

Vice President, Regulatory Affairs and Quality Assurance

Sue Dahlquist has more than 25 years of experience in the life sciences and medical device industry, including over 15 years in regulatory affairs. Her experience includes successful planning and execution of global regulatory strategies for new product development and regulatory compliance throughout the product life cycle. Prior to joining MicroMedicine, she held positions at Smith & Nephew, Boston Scientific, and Organogenesis, leading regulatory teams in the areas of cell therapy, gynecology, sports medicine, and trauma.