Melanie Cerullo
About Melanie Cerullo
Melanie Cerullo serves as the Head of CMC and Senior Director at Wave Life Sciences, where she has worked since 2018. She has extensive experience in quality assurance and compliance, having held various leadership roles in the biotechnology and pharmaceutical industries.
Current Role at Wave Life Sciences
Melanie Cerullo serves as the Head of CMC and Senior Director at Wave Life Sciences. She has held this position since 2018, contributing to the company's efforts in the biopharmaceutical sector. Her role involves overseeing the chemistry, manufacturing, and controls aspects of the organization, ensuring compliance with industry standards and regulations. She is based in Lexington, Massachusetts.
Previous Experience at Wave Life Sciences
Prior to her current role, Melanie Cerullo was the Head of Quality and Senior Director at Wave Life Sciences from 2016 to 2018. During her tenure in Cambridge, Massachusetts, she focused on quality assurance processes, helping to establish robust quality systems within the organization.
Career Background in Quality Management
Melanie Cerullo has extensive experience in quality management within the pharmaceutical industry. She worked at Ameridose as Vice President of Quality from 2010 to 2014 and as Director of Quality from 2007 to 2010. Her earlier roles include positions at Amgen as a Quality Compliance Specialist and Quality Assurance Supervisor, as well as a Quality Control Supervisor at Nitto Denko Avecia Inc.
Educational Background
Melanie Cerullo earned her Bachelor of Science degree from Rhode Island College, studying from 1991 to 1996. She later pursued a Master's degree at Temple University, completing her studies from 2005 to 2008. Her educational background has provided her with a strong foundation in the principles of quality management and compliance in the life sciences field.
Consulting Experience
From 2014 to 2016, Melanie Cerullo worked as a consultant at The Bioprocess Institute. In this role, she provided expertise in quality assurance and compliance, contributing to various projects aimed at improving processes within the biopharmaceutical industry.