Kimberly Simon
About Kimberly Simon
Kimberly Simon is a Senior Regulatory Affairs Specialist at Canary Medical Inc., with a strong background in regulatory compliance for medical devices. She has previously held positions in education and regulatory affairs at various institutions, including Loyola High School and Philips.
Current Role at Canary Medical
Kimberly Simon serves as a Senior Regulatory Affairs Specialist at Canary Medical Inc. since 2022. In this role, she is responsible for ensuring compliance with U.S. FDA regulations and global standards for medical devices. Her expertise in regulatory affairs is instrumental in navigating the complexities of the medical device industry.
Previous Experience in Regulatory Affairs
Prior to her current position, Kimberly worked at Philips as a Regulatory Affairs Specialist for Image Guided Therapy Devices from 2017 to 2022. She also held the position of Regulatory Affairs Associate at Allergan for a brief period in 2013. Her experience spans multiple organizations, providing her with a comprehensive understanding of regulatory processes.
Educational Background
Kimberly Simon holds a Master of Science in Regulatory Science from the University of Southern California, which she completed from 2009 to 2011. She also earned a Bachelor of Science in Biochemistry with a minor in Music (Vocal Performance) from Loyola Marymount University between 2005 and 2009. Her educational background supports her technical expertise in regulatory affairs.
Teaching Experience
Before her career in regulatory affairs, Kimberly Simon worked as a Science Instructor for Chemistry and AP Biology at Loyola High School from 2013 to 2017. She also served as a Biochemistry and Physics Teaching Assistant at Loyola Marymount University from 2006 to 2009. Her teaching experience has equipped her with strong public speaking and presentation skills.
Technical Skills and Expertise
Kimberly possesses a strong technical background that enhances her role in regulatory affairs. She has expertise in navigating both U.S. FDA and global regulatory compliance for medical devices. Known for her adaptability and quick learning, she effectively manages various tasks within her professional environment.