Victoria Di Buono
About Victoria Di Buono
Victoria Di Buono is a Clinical Trial Planning Specialist at Bristol Myers Squibb with over 5 years of project leadership experience in the biomedical and pharmaceutical industries.
Company
Victoria Di Buono currently holds the position of Clinical Trial Planning Specialist at Bristol Myers Squibb. She applies her specialized knowledge in clinical trials and project management to support the development and execution of clinical trial strategies.
Title
Victoria Di Buono serves as a Clinical Trial Planning Specialist at Bristol Myers Squibb, bringing her extensive background in project management and clinical operations to the role.
Education and Expertise
Victoria Di Buono earned a Bachelor of Science degree in Biomedical/Medical Engineering from the New Jersey Institute of Technology, where she studied from 2011 to 2015. She has over five years of experience in project leadership within the biomedical and pharmaceutical industries. Her expertise includes new product development quality, technical operations for external manufacturing, NC (Nonconformance) and CAPA (Corrective and Preventive Action) root cause analyses, and executing changes in compliance with global standards and regulations.
Professional Background
Victoria Di Buono has held various roles in her career, showcasing her versatility and growth within the field. She worked as a NJIT Representative for American Collegiate Intramural Sports & Fitness from 2013 to 2015. Following this, she interned as a Neuro-Engineering Research Intern at New Jersey Institute of Technology in 2012. Her industrial career began at Ethicon, Inc. as an Associate Quality Engineer from 2015 to 2016, followed by a role as a Manufacturing Engineer from 2016 to 2018. She then progressed to Catalent Pharma Solutions, where she held several positions, including Project Coordinator (2018-2019), Sr. Project Coordinator (2019-2020), and Project Manager (2020) in Philadelphia, Pennsylvania.
Experience in Quality and Project Management
Victoria Di Buono specializes in new product development quality and technical operations for external manufacturing. Her extensive experience includes NC and CAPA root cause analyses and executing changes to meet global standards and regulations. Her project leadership experience spans over five years in the biomedical and pharmaceutical industries, with a strong background in cross-functional management and a focus on achieving cost improvement and cross-functional goals.