Rebecca Alcantara

Rebecca Alcantara has over 19 years of diverse work experience in the pharmaceutical and healthcare industry. Rebecca most recently served as the Director of Global Supplier Quality & Compliance at Curia (formerly AMRI) since September 2020. Prior to that, from September 2018 to September 2020, they were the Director of Quality and Compliance at Ashfield, part of UDG Healthcare plc. Rebecca also held various roles at Merck, including Senior Specialist from May 2017 to September 2018. Rebecca spent a significant portion of their career at Charles River Laboratories, where they held several roles, including Senior Manager of Regulatory Compliance from May 2013 to May 2017, Regulatory Compliance Manager from July 2011 to May 2013, Senior Quality Assurance Auditor from November 2006 to July 2011, and QA Auditor II from May 2006 to November 2006. Rebecca started their career as a Cell Culture Team Leader at Charles River Laboratories in 2001. Their responsibilities included managing regulatory compliance programs, overseeing document control, conducting audits, and assisting with regulatory filings.

Rebecca Alcantara earned a Bachelor of Science degree in Biology from Delaware Valley University in the years 1996 to 2000.