Associate - Labeling Implementation - North America

Role: Associate in Global Regulatory Affairs (GRA) Labeling Implementation, focusing on US/NA market. Objectives: ensure timely, compliant implementation and maintenance of product labeling throughout the product lifecycle. Responsibilities: lead labeling change processes, liaise with cross-functional partners (Regulatory, PPD, manufacturing), oversee proof approval, train affiliates on systems/tools, monitor regulations, and provide regulatory expertise on labeling. Requirements: Bachelor's degree, 3-5 years in biotech/pharma, understanding of regulatory procedures, manufacturing, drug development, project management, strong communication, and computer skills. Preferred: scientific/health sciences degree, knowledge of regulatory landscape, supply chain, and experience in complex project execution. High-Value: focus on regulatory labeling for marketed products, cross-functional collaboration, systems expertise (BLUE, RIM), and influence on compliance and process efficiency. Work setup: not specified, but implies global/regional focus with interaction across affiliates.