Mayra Acevedo
About Mayra Acevedo
Mayra Acevedo is the Director of Quality Risk Management at Bristol Myers Squibb, with extensive experience in the pharmaceutical and medical devices industries.
Company
Mayra Acevedo currently works at Bristol Myers Squibb in Summit, NJ, where she holds the position of Director of Quality Risk Management. Bristol Myers Squibb is a prominent global biopharmaceutical company recognized for its work in the development of innovative medicines for serious diseases.
Title
Mayra Acevedo is the Director of Quality Risk Management at Bristol Myers Squibb. In this role, she is responsible for overseeing and managing quality risk across the organization, ensuring adherence to regulatory standards and maintaining high-quality output in the company's products and processes.
Previous Roles at Celgene and Allergan
Before joining Bristol Myers Squibb, Mayra Acevedo worked at Celgene as an Associate Director of Supplier Management for one year from 2018 to 2019. Prior to Celgene, she was employed at Allergan in Madison, NJ, where she served as Sr. Manager of Strategic Compliance and Risk Management from 2014 to 2018, focusing on compliance and risk management in pharmaceutical operations.
Experience at Merck and Schering-Plough
Mayra's experience includes multiple roles at Merck, where she served as Quality Systems Manager from 2011 to 2014 and as MPS/RFT (Sigma) Leader from 2007 to 2011 in Kenilworth, NJ. Additionally, she spent five years as a Sr. Compliance Specialist at Schering-Plough Research Institute from 2002 to 2007 and worked as a Quality Engineer at Schering-Plough from 1999 to 2001.
Education and Expertise
Mayra Acevedo holds a BS in Industrial Engineering from the University of Puerto Rico-Mayaguez. She has extensive experience in commercial and clinical pharmaceutical and medical device industries. Her skills include Third Party Quality Management and Operational Excellence (OpEx), as well as outstanding organizational, creative thinking, and problem-solving skills.