EU Regulatory Science Lead

UCB; Brussel; Hybrid; EUR 120,000 - 180,000; Full time

Benefits offered by this job

Hybrid work model

Job summary

UCB in Brussels is seeking an EU Regulatory Science Lead to drive regulatory strategy for assigned products across development, approval and lifecycle management. You will be the main EU regulatory contact, engaging with EMA and national authorities to support timely submissions and informed decisions.

You will collaborate with Global Regulatory Affairs and cross-functional teams to translate complex requirements into practical plans, manage risks, and adapt to evolving EU regulations with a

Qualifications

• Degree in life sciences, pharmacy, medicine, law or regulatory field.
• Strong experience in EU regulatory affairs across development and lifecycle.
• Ability to translate complex regulatory information for diverse audiences.

Responsibilities

• Develop and implement EU regulatory strategies aligned with business objectives.
• Coordinate EU submission activities in line with regulations, guidelines, timelines and agreed strategies.
• Manage EU regulatory risks by identifying options, recommending practical actions and supporting mitigation plans.
• Act as the key EU contact for assigned products, including EMA and national agency interactions where needed.
• Communicate clear regulatory plans, risks and updates to leadership, affiliates and cross-functional stakeholders.
• Maintain awareness of evolving EU regulations, guidelines, competitor activity and potential impact on product plans.

Skills

EU regulatory

Regulatory strategy

Cross-functional

Regulatory communication

Digital tools awareness

Education

Life sciences / Pharmacy degree

Job description

We are looking for an EU Regulatory Science Lead who is strategic, collaborative and adaptable to join our Global Regulatory Affairs team, based in our Brussels, Belgium offices.

About The Role

You will drive the EU regulatory strategy and activities for assigned products across development, approval and lifecycle activities. You will be the main regulatory contact for EU health authority interactions, including the EMA where relevant. You will help shape practical plans, identify regulatory risks, and work with global and regional partners to support timely submissions and informed decision-making.

Who You Will Work With

You will work closely with the Global Regulatory Lead, EU affiliates, Global Regulatory Affairs colleagues, submission teams, and cross-functional partners across development, clinical, medical, safety, quality and commercial teams. You will also collaborate with EU health authorities and contribute regional insight into global regulatory planning.

What You Will Do

• You will develop and implement EU regulatory strategies aligned with business objectives and global regulatory plans.
• You will be responsible for coordinating EU submission activities in line with regulations, guidelines, timelines and agreed strategies.
• You will manage EU regulatory risks by identifying options, recommending practical actions and supporting mitigation plans.
• You will act as the key EU contact for assigned products, including EMA and national agency interactions where needed.
• You will communicate clear regulatory plans, risks and updates to leadership, affiliates and cross-functional stakeholders.
• You will maintain awareness of evolving EU regulations, guidelines, competitor activity and potential impact on product plans.

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

• You have a degree in life sciences, pharmacy, medicine, law or another relevant scientific or regulatory field.
• You bring strong experience in EU regulatory affairs, including product development, marketing authorisations and lifecycle management.
• You understand EU regulatory frameworks, procedures, health authority expectations and the evolving policy environment.
• You can translate complex regulatory information into clear recommendations for different audiences.
• You work well across functions, cultures and organisational boundaries, building alignment through evidence and credibility.
• You are curious and aware about digital tools, data science and AI, and their potential impact on regulatory science.
• You can adjust to changing conditions, learn quickly, and remain effective in evolving regulatory and scientific landscapes.
• You are self-aware and looking for continuous learning and growth of self and others, by seeking and giving constructive feedback.

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.