EU Regulatory Strategy Lead

UCB; Brussel; Hybride; EUR 120 000 - 190 000; Plein temps

Avantages offerts par ce poste

Hybrid work model

Résumé du poste

UCB is seeking an EU Regulatory Strategy Team Lead to shape EU regulatory strategy for products across development, registration and lifecycle, based at our Brussels HQ. You will lead a team, influence global decisions, interact with health authorities and ensure scientifically sound, business-aligned regulatory pathways.

You will collaborate with Global Regulatory Affairs and cross-functional partners to drive clear regulatory positions while fostering growth and capability within the team.

Qualifications

• Advanced scientific degree (Master’s/PhD/MD or equivalent).
• 10+ years in Regulatory Affairs within pharma/biotech with deep EU regulatory knowledge.
• Defined and delivered regulatory strategies across development, registration and lifecycle.
• Able to build alignment with senior stakeholders in international, matrixed environments.
• Curious about digital and AI-enabled approaches in regulatory science.

Responsabilités

• Define and guide EU regulatory strategies that support global objectives and product needs across the full lifecycle.
• Ensure EU perspectives are integrated into global plans, decisions and governance discussions.
• Support effective health authority engagement by reviewing approaches and coaching colleagues.
• Manage and develop a team of EU regulatory professionals, building capability and clarity.
• Identify regulatory risks and opportunities early, align stakeholders and support escalation when needed.
• Promote standards, regulatory intelligence, resource planning and continuous improvement across the team.

Connaissances

Regulatory strategy

Leadership

Stakeholder alignment

Regulatory intelligence

Cross-functional collaboration

EU regulatory knowledge

Formation

Master’s/PhD/MD or equivalent

Description du poste

UCB is seeking an EU Regulatory Strategy Team Lead to shape EU regulatory strategy for products across development, registration and lifecycle, based at our Brussels HQ. You will lead a team, influence global decisions, interact with health authorities and ensure scientifically sound, business-aligned regulatory pathways.

You will collaborate with Global Regulatory Affairs and cross-functional partners to drive clear regulatory positions while fostering growth and capability within the team.