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.
📌 Global Regulatory Affairs Consultant – Medical Devices - Bardi, Emilia-Romagna, Italy
🏢 Parexel
📍 Bardi