Global Regulatory Affairs Graduate Development Program

Make your mark for patients

Global Regulatory AffairsGraduate Development Program October 2025

UCB is seekingan enthusiastic hands-on and team player graduate to jointheGraduate Development Programin Global Regulatory AffairslocatedinBrussels.

About UCB

UCB is a global biopharmaceutical company focusing on neurology and immunology. We are around 8500 people in all four corners of the globe inspired by patients and driven by science. You want to know more Have a look

About the program

This is a structured development program designed to kickstart your career and allow you togrow both personally and professionally while making an impact in the organization.

The Graduate Development Program inGlobal regulatory Affairsis a2-year rotational program consisting of4rotations of6months acrossthe Global regulatory Affairs departments.Through this program you will be exposed to different departments and gain practical hands-on experience that will allow you to build a strong foundation to pursue a career inRegulatory Affairswhile expanding your understanding of a global business.

You will gain knowledge and develop skills in a dynamic multifaceted setting where you will navigate short-term medium-term and long-term objectives. This dynamic and diverse setting will offer you new opportunities and challenges each day ensuring that no two days are the same.

Your first rotation will be inEU Global Regulatory Affairs

• Support the Lead to prepare regulatory submissions (MAAs; variations; Scientific Advice etc.)
• Reviewing regulatory documentation
• Tracking submission timelines
• Supporting regulatory strategy development
• Supporting regulatory intelligence research
• Liaising with cross-functional teams

Your next rotation will be inRegulatoryCMC

• Support in compiling CMC sections for regulatory submissions
• Support in ensuring compliance with manufacturing and quality standards
• Reviewing technical documentation for drug substance and drug product
• Supporting post-approval changes (variations) and other submissions
• Collaborating with manufacturing and quality teams
• Maintaining product lifecycle documentation

Your next rotation will be inLabeling

• Support in drafting and updating product labels and leaflets
• Ensuring compliance with labeling regulations
• Support in coordinating labeling changes with stakeholders
• Reviewing artwork for accuracy and regulatory compliance
• Supporting global labeling strategy

The final rotation will beelective designed to align both with the graduates interests and with the organizational needs in Global Regulatory Affairs.

Who youll work with

You will have the opportunity to work closely with a variety of people across our organization. You will be part of a team of dedicated professionals who are passionate about creating value for patients now and into the future. You will also have the chance to interact with experienced managers who will provide guidance and coaching throughout your addition you will be assigned a mentor who will provide support and guidance as you progress through your career as well as a buddy who will provide advice and guidance on the different aspects of working at UCB.

Finally you will also be part of UCB Early Talent community and connect with other graduates across the organization through learning and development sessions networking and social activities.

What youll learn

Throughout the 2-year program you will be assigned to different projects and teams that will allow you to

• Gain exposure to key areas of Regulatory Affairs
• Work on real projects:collaborate with Regulatory Science Leads on pipeline and marketed products throughout their lifecycle ensuring meaningful learning and exposure to regulatory processes.
• Understand regulatory strategy:learn how Regulatory Affairs professionals create innovative regulatory pathways and partnerships to expedite patient access to novel healthcare solutions.
• Develop your professional network:by driving or contributing to global Initiatives build a strong network of dedicated professionals across UCBs global regulatory community and beyond.

By working in different teams you will be exposed to a broad scope of activities helping you to gain expertise knowledge around drug development. By the end of the program you will have a well-rounded understanding of global regulatory and be equipped with the skills and knowledge to take on new challenges and build the career that is right for you. The expertise acquired will enable you to either pursue an expert career in one of these topics or pursue a generalist career path where you will profit from the holistic overview you will have gained by then.

Although you will receive support and guidance throughout the program we expect you to take ownership of your development and actively contribute not only to your own growth but also to the collective success of the team.

Interested We are looking for:

• A bachelors or masters degree in a scientific related field (e.g. life sciences pharmacy biomedical sciences)
• A previous traineeship or internship in Regulatory Affairs or a related field is highly valued
• Regulatory affairs qualification is a plus
• Strong teamwork and communication skills
• Ability to manage deadlines and work under pressure.
• A flexible curious and proactive mindset
• Good coordination and learning agility
• Digital literacy and a strong interest in automation and implementing AI solutions
• Ability to communicate effectively in English both orally and in writing

Practical information

• Start date: we are looking for graduates able to start full-time fromOctober can be considered based on the candidates availability.
• Right to work: candidates must have the right to work in Belgium to be eligible for the program.

How toapply

In order to complete your application for the Graduate Development Program you will need to:

• Officially apply for this opportunity. Please submit the entire application in English.
• Upload your resume.
• Upload a one-page presentation (PDF document) of yourself where you explain why you want to join our program (providing your name but no personal details).
• Deadline to apply 12/09

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 around 8500 people in all four corners of the globe inspired by patients and driven by science.

Why work with us
At UCB we dont just complete tasks we create value. We arent 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 thats 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.

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 . Please note should your enquiry not relate to adjustments; we will not be able to support you through this channel.