IVDR Regulatory Affairs Specialist II (Temp)

A leading life science company is seeking a temporary Regulatory Affairs Specialist II to support IVDR projects and labeling conversions. The candidate should possess a Bachelor’s degree and have 3-5 years of relevant experience in the IVD industry. Responsibilities include revising technical files and participating in cross-functional meetings. This role is vital for ensuring compliance with FDA and CE marking requirements while working collaboratively to enhance product quality. #J-18808-Ljbffr