Annemarie Erickson

Annemarie Erickson has worked in various roles in the field of Regulatory Affairs since 1998. Annemarie began their career as a Trace Engineer and Manufacturing Support Technician at Hutchinson Technology Incorporated. In 2009, they worked as a Product Performance Engineer for Boston Scientific, Cardiac Rhythm on a contract basis. In 2010, they became a Senior Regulatory Specialist at the same company and was certified to (and authored) all submission types with global submissions and international affiliates. Annemarie was also the leader of an international product strategy team. In 2014, they worked as a Senior International Regulatory Specialist at Covidien LLC and as a Regulatory Affairs Project Manager at ARKRAY, Inc., where they led the Regulatory team and was the project manager for all laboratory division products with a team stretching all the way to Kyoto, Japan. Annemarie was also the Clinicals Manager. In 2016, they became a Principal Regulatory Specialist in Postmarket Compliance and was part of the Quality Assurance Leadership team of 5. Annemarie worked with BSC divisional team and governments to harmonize complaint process across all BSC divisions, and pulled Premarket and Postmarket leaders together to work toward RWE initiatives. In 2021, they became the Director of Regulatory Affairs at Diasorin Biotechnology, and in 2022, they became the Associate Director of Regulatory Affairs at Artio Medical, Inc.

Annemarie Erickson has an education history that includes a Bachelor's Degree in Industrial Technology from Iowa State University, a Bachelor's Degree in Physics from Augustana College, and Electrical Engineering from St. Cloud State University. Annemarie also has additional certifications from LinkedIn in Diversity, Inclusion, and Belonging, Communicating about Culturally Sensitive Issues, and Unconscious Bias, which they obtained in June 2021, April 2021, and April 2021 respectively.