Maegan Little
About Maegan Little
Maegan Little is a Senior Manager of Regulatory Affairs at Abeona Therapeutics, where she has worked since 2021. She has extensive experience in regulatory affairs, scientific writing, and quality assurance, with previous roles at Boehringer Ingelheim, Hikma Pharmaceuticals, and The Legal Aid Society of Cleveland.
Current Role at Abeona Therapeutics
Maegan Little serves as the Senior Manager of Regulatory Affairs at Abeona Therapeutics, a position she has held since 2021. In this role, she is responsible for overseeing regulatory submissions and ensuring compliance with industry standards. Her work involves collaborating with scientists, engineers, and project managers to develop quality products and applications for regulatory filing. This position builds on her extensive experience in regulatory affairs and quality assurance.
Previous Experience in Regulatory Affairs and Quality Assurance
Prior to her current role, Maegan Little worked at Abeona Therapeutics in various capacities, including Quality Assurance Specialist and Senior Associate in Quality Assurance from 2019 to 2021. She also held positions at Hikma Pharmaceuticals as Supervisor of Document Control and Scientific Writer, contributing to her expertise in regulatory documentation and compliance.
Educational Background and Qualifications
Maegan Little has a strong educational foundation in regulatory affairs and project management. She earned a Master of Science in Regulatory Affairs for Drugs, Biologics, and Medical Devices with a concentration in Clinical Research from Northeastern University from 2019 to 2021. Additionally, she obtained a Project Management Certificate from Kent State University in 2012. Her undergraduate studies include a Bachelor of Arts in English with a Writing Concentration from Shippensburg University of Pennsylvania.
Writing and Editing Experience
Maegan Little has a passion for writing and editing, particularly in the context of research and development documentation. She has worked as a freelance writer and editor for ten years, providing services such as writing, editing, and proofreading. Her experience includes roles at various organizations, including Boehringer Ingelheim and The Legal Aid Society of Cleveland, where she honed her skills in legal and scientific writing.
Career Progression and Roles
Maegan Little's career began in 2004 as a freelance writer and editor. She progressed through various roles in the pharmaceutical and regulatory sectors, including positions at Boehringer Ingelheim, Hikma Pharmaceuticals, and Abeona Therapeutics. Her diverse experience spans scientific writing, document control, and regulatory affairs, showcasing her adaptability and commitment to the field.