pFreyr 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, RD, and Finance to ensure on-time, compliant deliverables throughout the product lifecycle.
/ppThe role requires 5+ years in regulatory affairs or project management within pharmaceutical, biotech, or medical devices, with strong budgeting and stakeholder management capabilities.
/p #J-*****-Ljbffr
📌 Regulatory Program Lead – Us & Eu Submissions (Bardi)
🏢 Freyr Solutions
📍 Bardi
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