IVD Regulatory Device Associate — Hybrid

A biotechnology company seeks a GRA Device Associate in Cambridge, MA to support global regulatory strategies for in-vitro diagnostics. This role involves preparing regulatory submissions and ensuring compliance while collaborating with cross-functional teams. The ideal candidate has over 6 years in the pharmaceutical industry with a solid background in IVD regulatory experience. Strong communication skills and the ability to thrive in a hybrid environment are crucial. Preferred education includes a Bachelor’s or higher in a scientific or engineering discipline. #J-18808-Ljbffr