Global Regulatory Affairs Specialist IVD Launch

A leading global healthcare company in Lake Forest, IL, is looking for a Regulatory Affairs Specialist. This role involves providing regulatory guidance for the global commercialization of in vitro diagnostic devices, collaborating with various teams to ensure compliance throughout product development. The ideal candidate will have at least 5 years of experience in regulatory affairs within the medical device industry, strong project planning skills, and the ability to mitigate regulatory risks early in the project lifecycle. #J-18808-Ljbffr