Global Regulatory Affairs Specialist - MedTech (Hybrid)

OrganOx Limited in Madison, NJ, is seeking a Regulatory Affairs Specialist to support global regulatory submissions, registrations, and product lifecycle activities for OrganOx devices, with emphasis on regulatory information management and cross-functional coordination. You will work with software, hardware, and disposable products teams, maintain regulatory records, and support audits and Notified Body interactions, with up to 5% travel and a hybrid work arrangement.