Remote Regulatory Affairs, Biologics & Global Submissions

A leading pharmaceutical company is looking for a Regulatory Affairs Specialist with 7-10 years of experience in lifecycle management of drug products. The candidate should have a strong understanding of US and EU regulatory frameworks and experience in preparing and reviewing regulatory submissions. The role involves leading regulatory maintenance submissions, coordinating with stakeholders, and ensuring compliance with regulatory requirements. This position offers the flexibility of remote work. #J-18808-Ljbffr