Director, CMC Regulatory Affairs - Biologics & Combos

Regeneron Pharmaceuticals, Inc. in Dublin is seeking a Director, CMC Regulatory Affairs to lead the Haematology/Oncology CMC & Combination Products team.

You will set global regulatory strategy across the product lifecycle, from clinical registrations to market approvals and post approval management, collaborating with regulatory staff, partners, project teams, and health authorities worldwide. The role emphasizes leading submissions, guiding authorities, and shaping departmental strategy,