Claudia Beke
About Claudia Beke
Claudia Beke is a Regulatory Affairs Manager at Bristol Myers Squibb with extensive international experience in regulatory affairs.
Current Role at Bristol Myers Squibb
Claudia Beke is currently serving as a Regulatory Affairs Manager at Bristol Myers Squibb. She joined the company in September 2021. Her role involves ensuring compliance with regulatory requirements and managing regulatory submissions.
Position at Sandoz in Tokyo
In addition to her role at Bristol Myers Squibb, Claudia Beke works as a Regulatory Affairs Associate at Sandoz in Tokyo, Japan. Her responsibilities include assisting with regulatory documentation and submissions, and ensuring adherence to local and international regulatory standards.
Past Experience at Sandoz and Bio-K+ International Inc.
Claudia Beke previously held the position of Regulatory Affairs Student at Sandoz in Holzkirchen, Bavaria, Germany, in 2015 for seven months. Before that, she completed a seven-month internship at Bio-K+ International Inc. in 2014, where she gained valuable experience in regulatory affairs.
Project Leadership at Université de Montréal
Between 2012 and 2013, Claudia Beke served as Team Lead for Projet SEUR at Université de Montréal. In this role, she led and coordinated project activities, ensuring effective team collaboration and meeting project objectives.
Educational Background
Claudia Beke holds a Master of Laws degree from Université de Sherbrooke, which she completed between 2013 and 2015. She also earned a Bachelor of Science degree from Université de Montréal, where she studied from 2009 to 2013.
International Work Experience
Claudia Beke has amassed substantial international work experience. She has worked in Tokyo, Japan as part of Sandoz, and gained professional experience in Holzkirchen, Germany during her tenure with Sandoz as a Regulatory Affairs Student in 2015.