Jobs at Regeneron

The Director of Government Affairs Europe will lead public policy activities, manage stakeholder relationships, and align advocacy efforts with Regeneron's business objectives across European healthcare systems.

The role involves overseeing healthcare community engagement and contracting, ensuring compliance, coordinating training, and collaborating with teams across international regions.

The Associate Director will oversee quality management systems, drive continuous improvement, and lead cross-functional teams while ensuring compliance and effective quality standards.

Lead the CMC & Combination Products regulatory team, shape global regulatory strategies for drug and device products, and oversee submissions and compliance issues.

The Associate Director will lead international product launches, managing timelines, resources, and stakeholder coordination across teams, while ensuring project delivery aligns with company goals.

The Manager is responsible for designing, developing, and delivering system application training within Global Development, collaborating closely for effective training solutions.

The Senior Manager Regulatory Intelligence monitors and interprets global regulatory changes, focusing on EU regulations and pharmacovigilance, while collaborating with cross-functional teams.