Melisa Moore

Melisa Moore is a seasoned professional in quality assurance and compliance within the clinical and pharmaceutical sectors. Currently serving as Senior Manager of Clinical Quality at Abeona Therapeutics since November 2021, Melisa has previously held key roles including Manager of QA GxP Audits at Daiichi Sankyo, Inc. and Director of Compliance at Pharm-Olam, LLC. Melisa's expertise encompasses risk management, standards development, and process improvement, supported by earlier positions such as Validation Specialist at Eurofins Lancaster Laboratories and Senior Regulatory Coordinator at Fisher Clinical Services. Melisa's educational background includes a Bachelor of Science in Bio-Behavioral Health from Penn State and an Associate's Degree in General Studies from Reading Area Community College.