Melissa Schneider
About Melissa Schneider
Melissa Schneider is a Regulatory Affairs Specialist at Boston Scientific with extensive experience in clinical data management and FDA regulations for medical devices.
Title
Melissa Schneider holds the position of Regulatory Affairs Specialist at Boston Scientific. In this role since 2015, she contributes her expertise to steer regulatory strategies for medical devices.
Career at Biothera
Before her tenure at Boston Scientific, Melissa worked at Biothera as a Sr. Regulatory Affairs Specialist from 2006 to 2015. Based in Eagan, MN, she spent 9 years in this role, where she honed her skills in regulatory compliance and strategically managed regulatory submissions.
Early Career Experiences
Melissa's career began with positions focused on data management and clinical monitoring. She worked at Guidant Corporation as a Clinical Data & Monitoring Assistant from 2003 to 2004 in Arden Hills, MN. She then transitioned to MGI Pharma, where she worked in data management from 2005 to 2006. These roles provided her with foundational experience in clinical data management, which she leveraged in her later regulatory roles.
Education and Expertise
Melissa studied at the University of Wisconsin-La Crosse, where she achieved a BS in Biology. Her educational background laid a scientific groundwork, which she applied throughout her career. She has developed significant expertise in navigating FDA regulations specific to the medical device sector.
Expertise in Regulatory Affairs
Melissa Schneider brings a wealth of experience in clinical data management, enhancing compliance and efficiency in regulatory processes. At Boston Scientific, she plays a significant role in crafting regulatory strategies for medical devices, ensuring adherence to FDA regulations.