Global Regulatory Labelling Scientist Lead - UCB S.A. - Anderlecht

Make your mark for patients.

We’re here because we want to build the future and transform patients’ lives for the better.

At UCB, our people are our experiences and achievements, our passion and drive. That’s why we’re looking for talented individuals with diverse backgrounds and experiences - not just the best and brightest, but those who care about making a meaningful difference in the lives of patients. We promote an environment of diversity, openness, and respect where people can make valuable contributions.

An exciting journey lies ahead. Will you join us in pushing the boundaries of what’s possible?

Join our Global Regulatory Affairs function, based in our Brussels (Belgium), Monheim (Germany) or Slough (UK) offices we are looking for a talented individual to fill the position of Global Labelling Scientist Lead.

As a Global Labelling Scientist, you will have the following responsibilities:

• Develop the Target Core Label (TCLP) with the program team and influence the Clinical Development to bring differentiated products to our patients, prescribers and payors
• Develop the Company Core Data Sheet (CCDS) from the emerging clinical data for the initial, subsequent indications and then through the maintenance part of the products life cycle
• Regulatory/Labelling support for risk management and other safety related activities for assigned products, in collaboration with the GRL and the PS responsible physician
• Lead the Implementation strategy of CCDS changes into worldwide labelling and clinical documentation
• Regulatory review of global promotional materials and external communication for assigned products.
• Advising global and regional teams for activities related to labelling, promotional material, external communications and related systems.

Interested? For this position you’ll need the following education, experience, and skills:

• Preferable a Life Science base Degree / Pharmacy Diploma
• At least 8 years of relevant experience in the pharmaceutical industry with preferably 6 years in Regulatory Affairs.
• Experience of global labelling strategy and working with regional teams to ensure key labelling messages are reflected in the CCDS
• Key Competencies: Influencing Skills, leading cross functional teams, and project management

Why you should apply

At UCB, we welcome passionate individuals who thrive on change and are ready make their mark for patients. Working for us, you will discover a place where you can grow and express your full potential. We place an emphasis on innovation, collaboration and impact while putting continuous efforts into cultivating a workplace culture where everyone feels included, respected and has equitable opportunities. Through meaningful recognition and a motivating atmosphere, we aim to provide an optimal experience by caring about and valuing our employees – just as we do for the patients we serve.

If you believe that you are the perfect match to join us on our pioneering adventure, then we invite you to apply and tell us more about your profile and motivation.

About us.

UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are around 7,600 people in all four corners of the globe, inspired by patients and driven by science.

At UCB, everything we do start with a simple question: “How will this create value for people living with severe disease?”. We are on a journey to become the patient-preferred biopharma leader by delivering medicines and solutions that improve lives. We want to ensure the creation of patient value, now and into the future, while contributing to a society where a population of 8 billion people and more should be able to live a good life within limited resources of one planet.

UCB and its subsidiaries encourage diversity and inclusion in the workplace; we are an Equal Opportunity Employer. We do not discriminate on the basis of race/color/religion/sex/national origin/veteran/disability/age/sexual orientation/gender identity.