Global Regulatory Affairs Specialist - MDR/IVD Expert

Hologic, Inc. is seeking a Regulatory Affairs Specialist to manage moderately complex regulatory projects and provide guidance on global regulatory requirements for new and existing products. The role covers change assessments for manufacturing, labeling, and process changes across Cytology and Molecular lines. You will prepare international submission dossiers, post-market reports, and EU CE-Mark documentation while interfacing with development teams and authorities throughout the product #J-18808-Ljbffr Hologic, Inc.