Global Regulatory Affairs Specialist - FDA Submissions
Curium Pharma
Curium Pharma is seeking a Regulatory Affairs Product Specialist in St. Louis to support US FDA applications (NDAs, ANDAs, DMFs) and international drug product submissions. You will plan, author, and compile regulatory filings, coordinate with cross-functional teams, and ensure compliance with global guidelines. The role requires a science degree, 3+ years regulatory experience, strong communication, and experience with eCTD, change controls, and MS Office. #J-18808-Ljbffr Curium Pharma
Vacancy posted 17 hours ago
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