Global Regulatory Affairs Consultant – Medical Devices

2 giorni fa

Bardi, Emilia-Romagna, Italia Parexel Tempo pieno

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.