Holly Hallock
About Holly Hallock
Holly Hallock is the Director of Regulatory Affairs and Quality Engineering at Teleflex Incorporated, where she leads regulatory compliance and quality engineering efforts for new product development and sustaining projects.
Title and Role
Holly Hallock is the Director of Regulatory Affairs and Quality Engineering at Teleflex Incorporated. In her role, she leads regulatory affairs and quality engineering efforts, including cross-functional new product development and sustaining projects. She is also a key regulatory lead for a $1.1 billion corporate acquisition and represents Regulatory Affairs, Quality Engineering, and MDR on the Surgical Business Unit’s Senior Leadership Team.
Professional Experience at Teleflex
Holly Hallock has extensive experience at Teleflex Incorporated, having held various positions over the years. She started as a Regulatory Affairs Associate in 2011, progressing through roles such as Regulatory Affairs Specialist, Senior Regulatory Affairs Specialist, Manager of Regulatory Affairs, and Senior Manager of Regulatory Affairs and Quality Engineering. In these roles, she has been instrumental in authoring numerous successful medical device submissions for major markets, including 510(k)s, Technical File and Design Dossiers, and New and Amended Medical Device License Applications.
Educational Background
Holly Hallock holds a Master of Science in Regulatory Affairs for Drugs, Biologics, and Medical Devices from Northeastern University, completed in 2017. She also earned two Bachelor's degrees from North Carolina State University, one in Physics and the other in English Language and Literature, completed in 2010.
Early Career
Before joining Teleflex Incorporated, Holly Hallock worked as a Laboratory Assistant at North Carolina State University from 2008 to 2010. This initial experience laid the foundation for her subsequent roles in regulatory affairs and quality engineering.
Leadership and Strategic Collaboration
Holly Hallock leads 14 direct reports across three departments, supporting regulatory compliance in both domestic and global markets. She collaborates with cross-functional department leaders and regional regulatory affairs leaders to develop global corporate strategies. Additionally, she defines and executes RA/QE/MDR activities to support both business unit and corporate strategies, ensuring adherence to quality principles and regulation requirements.