A leading clinical consulting company in Belgium is seeking a Senior Consultant RA IVD to provide regulatory consulting and strategic advisory services. The ideal candidate will have at least 8 years of experience in regulatory affairs within the IVD sector and proven expertise with EU IVDR/MDR and FDA frameworks. Responsibilities include managing regulatory documentation, client training sessions, and project management. This role offers a competitive salary and opportunities for professional growth within an international environment. #J-18808-Ljbffr