Global Regulatory Affairs Director

Role: Lead global regulatory strategy and operations for biopharma products, focusing on development, commercialization, and lifecycle management. Responsibilities: provide strategic regulatory advice, influence authorities through advocacy, monitor regulatory trends, ensure compliance, and support product registration and maintenance across markets. Contribute to global development programs with interpretive expertise on legislation; represent AstraZeneca in external trade associations; foster cross-functional regulatory collaboration; promote a culture of leadership and compliance. Requirements: Bachelor’s in Life Sciences; advanced degree (MS, PharmD, PhD) preferred; 6+ years in regulatory drug development, manufacturing, or commercialization; proven leadership and project management skills; broad regulatory experience, including interactions with health authorities; strong knowledge of global regulatory procedures and legislation. HighValue: experience in drug registration, license maintenance, and regulatory strategy; leadership in global regulatory teams; knowledge of legislation impacting drug development and lifecycle management. WorkSetup: hybrid (minimum 3 days/week in-office), with flexibility; travel requirements not specified.