About this role
Associate Director, Regulatory Affairs - Biosimilars (US) at Sandoz. Location: Princeton, New Jersey, United States. Role: lead strategy, prepare submissions, FDA interactions Requirements: 7+ years regulatory affairs in biopharma with US biosimilar experience; FDA submissions; strong cross-functional leadership and communication. Category: Healthcare Services - Advanced Practice Seniority: Senior Level Commitment: Full Time Workplace: Hybrid Languages: English