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Mariam Motamen has extensive experience in regulatory affairs and project management across various pharmaceutical companies, currently serving as Manager of Regulatory Affairs & Quality Assurance at Bluefish Pharmaceuticals since November 2020. Previous roles include Regulatory Affairs Manager at DREHM Pharma GmbH and Regulatory Affairs Executive for Austria, Germany, and Switzerland at Norgine, where responsibilities encompassed lifecycle management and the preparation of regulatory submissions. Prior to that, Mariam held positions in project management at Baxter International Inc. and technical support at Novartis. Through a strong educational background, including a Master's degree in Drug Regulatory Affairs from The University of Bonn and a Project Management Professional (PMP) certification, Mariam has developed a robust skill set in regulatory strategy, compliance, and cross-functional project leadership.