EU Regulatory Strategy Team 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

We are looking for an EU Regulatory Strategy Team Lead who is strategic, collaborative and people-centered to join our Global Regulatory Affairs team, based in our HQ in Brussels, Belgium.

About The Role

You will shape EU regulatory strategy for assigned products across development, registration and lifecycle management. You will bring EU regulatory science into global decision-making, help teams choose clear regulatory pathways and support timely patient access. You will also act as a trusted EU regulatory voice for complex questions, ensuring strategies are scientifically sound, practical and aligned with business priorities.

Who You Will Work With

You will join Global Regulatory Affairs, reporting to the Head of EU Regulatory Affairs and work closely with Global Regulatory Leads and cross-functional partners. You will lead and develop a team of EU regulatory professionals, creating an environment where colleagues can collaborate, grow and deliver consistent, high-quality regulatory outcomes. You will also oversee interactions with EU health authorities, ensuring they are clear, effective and scientifically grounded.

What You Will Do

• You will define and guide EU regulatory strategies that support global objectives and product needs across the full lifecycle.
• You will be responsible for ensuring EU perspectives are integrated into global plans, decisions and governance discussions.
• You will support effective health authority engagement by reviewing approaches, coaching colleagues and contributing to complex interactions.
• You will manage and develop a team of EU regulatory professionals, helping colleagues build capability, confidence and clarity.
• You will identify regulatory risks and opportunities early, align stakeholders on options and support clear escalation when needed.
• You will improve ways of working by promoting standards, regulatory intelligence, resource planning and continuous improvement across the team.

Interested? For this role, we are looking for the following education, experience and skills:

• You have an advanced scientific degree, such as a Master’s, PhD, MD or equivalent experience.
• You bring 10+ years of Regulatory Affairs experience in pharmaceutical or biotech settings, with deep EU regulatory knowledge.
• You have defined and delivered regulatory strategies across development, registration and lifecycle management.
• You understand EU health authority expectations and know how to prepare clear, evidence-based regulatory positions.
• You can build alignment with senior stakeholders and cross-functional partners in international, matrixed environments.
• You have led, coached or developed regulatory colleagues and are curious about digital and AI-enabled approaches in regulatory science.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About Us

UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Why work with us?

At UCB, we don’t just complete tasks, we create value. We aren’t afraid to push forward, collaborate, and innovate to make our mark for patients. We have a caring, supportive culture where everyone feels included, respected, and has equal opportunities to do their best work. We ‘go beyond’ to create value for our patients, and always with a human focus, whether that’s on our patients, our employees, or our planet. Working for us, you will discover a place where you can grow, and have the freedom to carve your own career path to achieve your full potential.

At UCB, we’ve embraced a hybrid-first approach to work, bringing teams together in local hubs to foster collaborative curiosity. Unless expressly stated in the description or precluded by the nature of the position, roles are hybrid with 40% of your time spent in the office.

UCB is an equal opportunity employer. All employment decisions will be made without regard to any characteristic protected by applicable laws.

Should you require any adjustments to our process to assist you in demonstrating your strengths and capabilities contact us on [e-mail]. Please note should your enquiry not relate to adjustments; we will not be able to support you through this channel.