Panda International seeks a senior Regulatory Affairs leader to own EU MDR strategy for Class III devices, including dermal fillers, and to serve as the main liaison with the notified body. You will lead technical documentation, post-market activities, and registrations for new markets as the business grows. The role requires hands-on authorship and a track record with MDR conformance, risk management, and clinical evaluation. #J-18808-Ljbffr
📌 Global Regulatory Affairs Lead: Ivd & Software (Eixample)
🏢 Panda International
📍 Eixample
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