Rebeka Stoltman
About Rebeka Stoltman
Rebeka Stoltman is the Director of Regulatory Affairs at Boston Scientific and Galil Medical. She has extensive experience in regulatory and quality management roles across various healthcare companies.
Title
Rebeka Stoltman serves as the Director of Regulatory Affairs.
Current Role at Boston Scientific
Rebeka Stoltman has been working at Boston Scientific as Director of Regulatory Affairs since 2019.
Current Role at Galil Medical
Rebeka Stoltman also holds the position of Director of Regulatory Affairs at Galil Medical, a BTG International group company, since 2017 in Arden Hills, MN.
Past Role at Boston Scientific
Before her current role, Rebeka Stoltman was the Senior Manager of Regulatory Affairs at Boston Scientific from 2012 to 2017.
Role at Coloplast
Rebeka Stoltman worked as Manager of Regulatory Affairs at Coloplast from 2007 to 2012. Prior to that, she served as a Formulation Chemist & Internal Auditor at the same company from 1998 to 2000.
Past Role at MGI PHARMA
Rebeka Stoltman was the Manager of Quality Assurance at MGI PHARMA (now Eisai) from 2004 to 2007.
Past Role at Lake Region Medical
From 2000 to 2004, Rebeka Stoltman served as Manager of Regulatory Affairs at Lake Region Medical.
Experience at LumiLife
Rebeka Stoltman worked at LumiLife as the Quality Manager from 2000 to 2002.
Role at P3 Scientific
Rebeka Stoltman held the position of Chemist at P3 Scientific (formerly Part 3) from 1996 to 1998.
Education: Bachelor of Science
Rebeka Stoltman studied Chemistry/Biochemistry and attained a Bachelor of Science degree from the University of Wisconsin-River Falls.
Education: MBA
Rebeka Stoltman earned her MBA from Cardinal Stritch University.