Regulatory Publishing Specialist: eCTD Submissions

A leading nuclear medicine company is seeking a Regulatory Affairs Specialist - Publishing in St. Louis, MO. This role involves leading the electronic publishing process for regulatory submissions, ensuring eCTD sequences are compliant, and collaborating with teams to meet project deadlines. Candidates should have a bachelor’s degree and 1-3 years of related experience. Strong communication and organizational skills are a must. Join a team committed to innovation and quality in patient care. #J-18808-Ljbffr