Lisa Rivera

Lisa Rivera has a diverse work experience in the pharmaceutical industry. Lisa is currently working as a Quality Compliance Manager at Elevar Therapeutics since January 2022. Prior to this, they have held various roles at Bristol Myers Squibb, including Sr. Manager, Global Quality Systems - QMS Document Management from April 2020 to December 2021, and Manager, Global GMP/GDP Compliance from June 2019 to April 2020. Before that, Lisa worked at Celgene as part of the Global Quality Operations Systems team for product complaints from October 2014 to June 2019. Lisa also has experience as a Sr. Supervisor of Quality Assurance at Halo Pharmaceuticals from November 2009 to October 2014. Lisa started their career at Actavis as an Investigations Specialist from 2002 to 2009 and gained initial industry experience as a Lab Technician at Hoffmann-La Roche from 1996 to 2002.

Lisa Rivera attended Thomas Edison State University starting in 2006, but it is unknown if they obtained a degree or studied a specific field. In terms of certifications, they obtained the Project Management (PM1001) certification from Sophia Learning in July 2021. Prior to that, in February 2019, they obtained the Professional Scrum™ with Kanban I (PSK I) certification from Scrum.org. In the future, Lisa is scheduled to obtain the GCP for Clinical Trials with Investigational Drugs and Biologics (ICH Focus) certification from the CITI Program in both February 2022 and March 2023.