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Paula J. Morgan is an experienced leader in Quality and Regulatory Affairs with a comprehensive background in the medical device industry. Currently serving as Vice President of Quality and Regulatory Affairs for the Whole Blood Hemostasis Business Unit at Werfen North America since April 2017, Paula J. Morgan oversees compliance with domestic and international regulations for in vitro diagnostic and sterile Class II medical devices. Prior roles include Vice President of Clinical & Regulatory Affairs and Quality Assurance at NuVasive, where responsibilities encompassed regulatory compliance for medical devices and human tissue, and Sr. Director of Global Regulatory Affairs at the same company, focusing on global pre-market submissions. Additional experience includes leadership positions at Alphatec Spine, Zimmer Biomet, and Vista Biologicals Corporation. Paula J. Morgan holds a Bachelor of Science degree in Microbiology from the University of New Hampshire.