Senior Regulatory Affairs Lead: FDA Submissions & Compliance

A leading global biopharmaceutical services organization is seeking a Senior Regulatory Affairs Associate in Dover, Delaware. This role involves acting as the primary regulatory liaison and overseeing regulatory submissions, compliance, and strategic leadership for product launches. Candidates should have a Bachelor's degree in natural sciences and 3–5 years of regulatory experience. Excellent project management skills and the ability to lead cross-functional teams are essential. Join us to shape the future of healthcare compliance while making impactful contributions to a major client partnership. #J-18808-Ljbffr