Parexel is seeking a Regulatory Affairs professional to lead regulatory strategy for medical devices and drug-device combinations. You will serve as regulatory representative for global project teams and drive interactions with health authorities and Notified Bodies.
Flexible home/office setup with EU MDR-focused tasks across regions. You will develop regulatory strategies, manage submissions, maintain regulatory databases, and collaborate with CMC and QA.
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📌 Global Regulatory Affairs Consultant – Medical Devices (Bardi)
🏢 Parexel
📍 Bardi
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