Global Regulatory Affairs Specialist - FDA/CMC
Curium Pharma
Curium Pharma in the United States is seeking a Regulatory Affairs Product Specialist to support US FDA submissions (NDAs, ANDAs, DMFs) and international product applications. This role oversees planning, authoring, and submitting regulatory documents while coordinating with QC, manufacturing, and quality systems. You will mentor junior staff, track regulatory changes, and maintain up-to-date knowledge of global guidelines. #J-18808-Ljbffr Curium Pharma
Vacancy posted 4 days ago
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