Andrew Maves
About Andrew Maves
Andrew Maves is the Director of Engineering; Commissioning, Qualification, and Compliance at Bristol Myers Squibb in Phoenix, Arizona, with extensive experience in the pharmaceuticals industry.
Current Position at Bristol Myers Squibb
Andrew Maves is the Director of Engineering; Commissioning, Qualification, and Compliance at Bristol Myers Squibb. He is based in Phoenix, Arizona, United States, and is responsible for overseeing engineering functions related to commissioning, qualification, and compliance within the organization.
Previous Roles at Bristol Myers Squibb
Before his current role, Andrew Maves served as Director of Strategy and Business Operations at Bristol Myers Squibb from 2021 to 2022. Prior to that, he was the Associate Director of Technical Services from 2019 to 2021. In these roles, he contributed to strategic planning, business operations, and technical service initiatives in Phoenix, Arizona.
Experience at Celgene
Andrew Maves held several significant positions at Celgene. He was the Associate Director of Aseptic Manufacturing; Compounding in 2019 and the Associate Director of Plant Services Technical Support from 2017 to 2018. Additionally, he served as Senior Manager, Validation and Metrology from 2015 to 2017, Senior Manager, Validation in 2015, and Manager, Validation and Metrology from 2011 to 2015. Earlier, he was the Validation Supervisor at Celgene Corporation from 2010 to 2011.
Early Career in Pharmaceuticals
Andrew Maves started his career as a Validation Engineer at Watson Pharmaceuticals from 2003 to 2007, and as an Aseptic Processing Specialist at Schein Pharmaceutical from 1998 to 2003. He also worked at Abraxis BioScience as Senior Validation Scientist from 2007 to 2010. Throughout these roles, Andrew gained extensive experience in GMPs, manufacturing, and biotechnology.
Education and Certifications
Andrew Maves achieved a BS from Arizona State University, where he studied from 1999 to 2003. He also holds a Six Sigma Black Belt from Arizona State University, which he completed in 2012. These qualifications have equipped him with a robust foundation in process improvement, engineering, and technical management.
Skills and Expertise
Andrew Maves is skilled in investigation and root cause analysis techniques, change control, and validation. He has a demonstrated history of working in the pharmaceutical industry, particularly in areas related to GMPs, manufacturing, and biotechnology. His expertise is further highlighted by multiple leadership roles in engineering and technical services, focusing on commissioning, qualification, and compliance.