Joseph Ostendorf, Rac
About Joseph Ostendorf, Rac
Joseph Ostendorf is a Regulatory Affairs Manager at Holaira, Inc. in Plymouth, MN, with over 11 years of experience in regulatory affairs, including previous roles at several medical device companies.
Work at Holaira, Inc.
Joseph Ostendorf has served as the Regulatory Affairs Manager at Holaira, Inc. since 2013. In this role, he has been responsible for overseeing regulatory submissions and ensuring compliance with both domestic and international regulations. His tenure at Holaira spans over 11 years, during which he has contributed significantly to the company's regulatory strategies and quality systems.
Previous Experience in Regulatory Affairs
Prior to his current position, Joseph Ostendorf held various roles in regulatory affairs across multiple organizations. He worked as a Principal Regulatory Affairs Specialist at Waters from 2010 to 2012, and as a Specialist in Regulatory Affairs at Zimmer from 2008 to 2009. Additionally, he has experience at Boston Scientific, where he served as a Technical Writer and later as a Specialist in Regulatory Affairs.
Educational Background
Joseph Ostendorf studied at the University of Minnesota, where he earned a Bachelor of Science degree in Scientific & Technical Communication from 2000 to 2004. He also attended Saint John's University for one year, focusing on Biology and Chemistry from 1999 to 2000. His educational background supports his expertise in regulatory affairs within the medical device industry.
Expertise in Regulatory Submissions
Joseph Ostendorf possesses extensive experience in developing regulatory strategies for new product development teams in the medical device sector. He has a breadth and depth of experience in both domestic and foreign regulatory submissions, which has enabled him to contribute effectively to various medical device firms throughout his career.
Career Progression in Regulatory Affairs
Throughout his career, Joseph Ostendorf has progressed through various roles in regulatory affairs. He worked at Electromed, Inc. as the Director of Regulatory Affairs from 2018 to 2019 and held multiple positions at Boston Scientific, including Technical Writer Intern and Specialist in Regulatory Affairs. His diverse experience has established a proven track record in the field.