About this role
Director Regulatory Lifecycle Management for Biosimilars/Complex Gx Products (d/f/m) at Sandoz. Location: Ljubljana, Central Slovenia, Slovenia. Role: building team, authoring documentation, resource planning Requirements: 8+ years regulatory experience with biosimilars/biotech, 3+ years people management, scientific Masters/PhD preferred, fluent English, ability to lead teams and deliver global CMC lifecycle submissions. Category: Research and Development (R&D) Seniority: Senior Level Commitment: Full Time Workplace: Hybrid Languages: English