Remote Senior IVD/CDx Regulatory Affairs Consultant

A global biopharmaceutical organization is seeking an experienced Regulatory Affairs professional specializing in in vitro diagnostics and Companion Diagnostics. In this role, you will develop regulatory strategies, collaborate with partners, and manage submissions. Candidates should have a scientific degree and 5+ years of regulatory affairs experience, particularly with IVD and CDx. Fluent English is essential. The position can be office or home-based across various locations in Europe.