We are looking for a remote Regulatory Affairs Manager to join our Regulatory Affairs team. The Regulatory Affairs Manager implements regulatory activities related to the approval of new IVDs (in vitro diagnostics) and medical devices into the worldwide market, as directed.  Participates on product development teams and provides guidance and strategies for regulatory issues. Interacts with regulatory agencies regarding product registrations, licensures and permits, and supports regulatory compliance to QSR, ISO, CMDR, MDSAP, IVDD/IVDR, CFR and other worldwide regulatory requirements. Reviews and approves labeling and Marketing/Sales literature. This role will not require direct people management.