Make your mark for patients
We are looking for a Labelling & Packaging Supply Specialist to join our Clinical Packaging & Logistics Operations Unit (Clinical Supply Chain), based in our office in Braine-l’Alleud, Belgium
About the role
You will be mainly responsible for activities linked to the development of Investigational Medicinal Products (IMP) labels and packaging solutions for clinical trials conducted by the UCB Clinical Supply Chain Department. You will play a key role in supporting strategic innovative initiatives and enhancing the overall efficiency and effectiveness of our clinical supply operations. You will be expert in adapting to evolving priorities and technologies, with a forward-thinking approach to innovation and leveraging digital tools.
Who you’ll work with
You will work within a dynamic and polyvalent team of Labelling & Packaging Supply Coordinators dedicated to set up and preproduction activities of assigned clinical trials, from labelling and packaging development activities to supply coordination activities.
What you’ll do
End-to-end label development for internal packaging activities.Support packaging development for internal packaging activities.Contributes to ensuring that legislation on clinical labelling is properly translated, understood and implemented.Strongly supports transversal projects, including but not limited to E2E Clinical Labels & new packaging solutions. Contributes to projects rolling out in collaborating with internal and external stakeholders.Proactively prospects new technologies and process insights from the outside to bring them in and improve our ways of working in order to stay ahead of the game and be ready for future business needs (digitalisation, e-labels etc…).Collaborates with Clinical supplies cross-functional teams to ensure seamless integration of labelling and packaging innovative processes with other clinical supply chain activities.Ensures inspection of labels/booklets during the reception process as a supporting activity in the teamSupport Supply Coordination activities for: CdC/BOM/PV, PrO, Batch records, similarity controls
Interested? For this role we’re looking for the following experience and skills
Bachelor’s degreeExperience of 3 years in Project ManagementKnowledge of GMP is an assetKnowledge of GMP and clinical trial supplies (protocol, blinding) is an asset.Familiarity with clinical labelling regulations (EU CTR536/2014 Annex VI) is an asset.Proficiency in computer applications (Word, Excel).Strong interest in innovative technologies and digitalization.
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 8,500 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 equitable 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.
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.
Should you require any adjustments to our process to assist you in demonstrating your strengths and capabilities contact us on EMEA-Reasonable_Accommodation@ucb.com. Please note should your enquiry not relate to adjustments; we will not be able to support you through this channel.