Louis Falcone
About Louis Falcone
Louis Falcone is the Director of Quality Assurance and Regulatory Affairs, Cardiac Assist Division at Teleflex Incorporated, with over 40 years of experience in the medical device and pharmaceutical industries.
Company
Louis Falcone is currently employed at Teleflex Incorporated, located in Wayne, Pennsylvania, United States. Within this company, he holds the position of Director of Quality Assurance and Regulatory Affairs for the Cardiac Assist Division.
Title
Louis Falcone serves as the Director of Quality Assurance and Regulatory Affairs, Cardiac Assist Division, at Teleflex Incorporated. His role primarily involves overseeing quality assurance processes and ensuring regulatory compliance within the division.
Professional Experience
Louis Falcone has gained substantial experience in quality assurance and regulatory affairs through multiple roles at different companies. Notably, he worked at Cosman Medical as Director of Regulatory Affairs and Quality Systems from 2007 to 2016 and at Iris Diagnostics/Sample Processing as Director of Quality and Regulatory Affairs from 2004 to 2007. Additionally, he held roles at Proven Process Medical Devices, Radionics Corporation, Deknatel, Elan Pharmaceutical Ltd/O'Brien Healthcare, and Baxter Dade Division Clinical Diag, with responsibilities ranging from quality systems management to analytical chemistry.
Education and Expertise
Louis Falcone holds a Bachelor of Science degree in Biology from Salem State University, obtained between 1977 and 1981. Accumulating over 40 years of experience in quality assurance and regulatory affairs within the medical device and pharmaceutical industries, he has demonstrated a strong foundation in managing quality systems, regulatory compliance, and analytical chemistry.
Background
During his extensive career, Louis Falcone has held numerous senior leadership roles in quality assurance and regulatory affairs, showcasing a consistent focus in these areas. His background includes managing quality systems and regulatory compliance efforts for a variety of medical devices and pharmaceuticals. Additionally, he has experience leading teams in both startup environments and established companies, indicating his adaptability and leadership capabilities.