Ashlea Ricci
About Ashlea Ricci
Ashlea Ricci is a Senior Regulatory Affairs Specialist at Teleflex Incorporated with extensive experience in the medical devices industry and a strong educational background in business administration and regulatory affairs.
Title
Ashlea Ricci is a Senior Regulatory Affairs Specialist currently working at Teleflex Incorporated in Wayne, Pennsylvania, United States.
Company
Ashlea Ricci has been with Teleflex Incorporated for over a decade, starting in June 2013. Teleflex is a global provider of medical technologies designed to improve the health and quality of people's lives.
Education and Expertise
Ashlea Ricci holds a Master of Science from The Johns Hopkins University, achieved from 2012 to 2014. She also has a Bachelor's degree in Business Administration and Management from the University of South Florida, earned between 2008 and 2012, and an Associate of Arts from Hillsborough Community College in Business Administration and Management, obtained in 2008. Additionally, she holds the RAC (US, CA) certification, indicating her expertise in regulatory affairs for both the United States and Canada.
Background in Regulatory Affairs
Ashlea Ricci has extensive experience in the field of regulatory affairs, particularly in the medical devices industry. She has held roles at multiple prominent companies prior to her current position at Teleflex Incorporated. These roles include Regulatory Affairs Associate at Bd (2012-2013), Regulatory Affairs Specialist at Conmed Corporation (2010-2012), Regulatory Affairs Associate II at Corin Group Plc (2003-2010) in the UK, and Regulatory Affairs Manager at Merz North America. Her international experience includes a seven-year tenure with Corin Group Plc in Cirencester, Gloucestershire, United Kingdom.
Achievements in the Medical Devices Industry
Ashlea Ricci has a solid track record of contributing to regulatory affairs in the medical devices sector. She has worked with products like Bd Focalpointâ and Bd Prepstainâ Sustainability and Front End Automation. Her expertise is recognized with a RAC certification, validating her knowledge and skills in regulatory processes for medical device compliance in both the US and Canada.