Senior Regulatory Publishing Lead — eCTD & FDA Submissions

A pharmaceutical company is seeking a Senior Regulatory Publishing Specialist in St. Louis, MO. This role involves coordinating the publishing process for FDA submissions, ensuring compliance with eCTD guidelines, and mentoring junior staff. Candidates should have a Bachelor's degree, extensive experience in regulatory publishing, and strong communication skills. The position requires proficiency in electronic submission software and an understanding of FDA regulations. A typical office working environment is expected. #J-18808-Ljbffr