Lisa Rivera is an accomplished quality professional with over 20 years of experience in the pharmaceutical industry. They held various roles, including Sr. Supervisor of Quality Assurance at Halo Pharmaceuticals and Investigations Specialist at Actavis. Currently, Rivera serves as the Associate Director of External Quality Operations at IO Biotech, having previously worked as a Quality Compliance Sr. Manager at Elevar Therapeutics and held leadership positions at Bristol Myers Squibb and Celgene. Rivera continues to advance their education at Thomas Edison State University.
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