Thomas Joncret
About Thomas Joncret
Thomas Joncret is a Quality Operations Oversight professional at Bristol-Myers Squibb in New Jersey, United States, with over a decade of experience at the company.
Company
Thomas Joncret is currently employed at Bristol-Myers Squibb, a global biopharmaceutical company located in New Jersey, United States. Bristol-Myers Squibb focuses on discovering, developing, and delivering innovative medicines that help patients prevail over serious diseases. Thomas has been part of this organization for over a decade, occupying various roles that have contributed to the company's regulatory and quality operations.
Title
Thomas Joncret currently holds dual roles at Bristol-Myers Squibb. He serves as Quality Operations Oversight for Distributor Markets and also functions as the Quality Responsible Person. These positions involve overseeing the quality operations of distributed pharmaceutical products and ensuring compliance with regulatory standards.
Education and Expertise
Thomas Joncret holds both a Bachelor's and a Master's degree from the Université Catholique De Louvain. He completed his Bachelor's from 2008 to 2010 and his Master's from 2010 to 2012. His academic background includes extensive studies that have laid a strong foundation for his career in regulatory sciences and quality operations within the pharmaceutical industry.
Background
Prior to his current roles, Thomas Joncret has held numerous positions within the pharmaceutical sector. Starting at Magistra Pharma, he worked as a Pharmacist for nearly a year. He then served as a Research Assistant at Institut Malgache De Recherches Appliquées. At GSK, he completed a Management Trainee program in the United Kingdom. His career at Bristol-Myers Squibb spans multiple roles such as Regulatory Sciences Associate Benelux and Regulatory Sciences Manager, accumulating extensive experience in regulatory and quality operations.
Achievements
Throughout his tenure at Bristol-Myers Squibb, Thomas Joncret has taken on roles critical to the company's regulatory and quality frameworks. As a Regulatory Sciences Associate Benelux, he managed regional regulatory activities for three years. He later became a Regulatory Sciences Manager, a role he held for an additional three years, before progressing to his current positions. His consistent performance and long-term dedication have highlighted his contributions to upholding high standards of compliance and quality in pharmaceutical distribution.