Descrizione:
Freyr Solutions is seeking a Regulatory Project Manager to lead regulatory submissions for US FDA and EU EMA markets. You will coordinate cross-functional teams from Regulatory Affairs, Clinical, Quality, R&D, and Finance to ensure on-time, compliant deliverables throughout the product lifecycle.
The role requires 5+ years in regulatory affairs or project management within pharmaceutical, biotech, or medical devices, with strong budgeting and stakeholder management capabilities.
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