UCB Braine-l’Alleud, Walloon Region, BelgiumJoin or sign in to find your next jobJoin to apply for the CMC Quality Solutions Partner role at UCBUCB Braine-l’Alleud, Walloon Region, Belgium4 days ago Be among the first 25 applicantsJoin to apply for the CMC Quality Solutions Partner role at UCBMake your mark for patientsTo strengthen our CMC Quality department, we are looking for a talented profile to fill the position of: CMC Quality Solutions Partner – Braine l’Alleud, BelgiumAbout The RoleAs part of the CMC Quality Organization and reporting to the Head of CMC Quality Solutions, this position provides Analytical and GMP-quality expertise to drive continuous improvement in Quality Assurance (QA), facilitate problem-solving, and ensure effective use of the Quality Management System (QMS). The role supports CMC Quality activities by promoting robustness, efficiency, alignment, and a standardized approach across the CMC Quality Lead and CMC Quality Solutions teams. Additionally, it brings scientific and QA expertise to strategic QA activities related to the lifecycle management of commercially available products or those in late-stage development—including regulatory submissions, product launches, improvements, and phase-out—ensuring the delivery of high-quality, safe, and effective products to market.Work with: This role requires close collaboration with various functions within UCB’s Quality Organization, including Quality Systems, External & Development Supply Quality, Internal Manufacturing Quality, Distribution and Market Quality, and Devices, Primary Packaging & DHT Quality. It also involves interaction with teams such as Patient Impact, Patient Evidence, Patient Solutions, Global Regulatory Affairs, Safety, Patient Supply, and other stakeholders.What You Will DoProvide analytical expertise for supporting, reviewing, and approving controlled documents (global analytical methods, specifications, stability strategies, etc.) or CMC sections linked to regulatory submissions.Support CMC Quality Leads in product risk management.Drive or support projects affecting multiple products or process improvements, ensuring harmonized and efficient operations.Represent the CMC Quality department in QMS teams or other quality system processes.Lead the creation of simplified, efficient, and harmonized processes and procedures.Ensure effective communication and coordination across teams.Take on special assignments delegated by the Head of CMC Quality Solutions as needed.QualificationsBachelor’s or master’s degree in a relevant scientific discipline.At least 5 years of experience in pharmaceutical/biologics quality management; GMP operational experience is a plus.Fluent in English (oral and written); additional languages are a plus.Strong understanding of global pharmaceutical regulations and industry practices.Ability to analyze data independently and make effective decisions.Experience in GMP audits, inspections, project management, and data integrity assessment.Ability to work independently and in a multicultural environment.Proficiency in delivering presentations and reports to senior management.If you are ready to make a difference and contribute to our mission for patients, we would love to hear from you!About UsUCB is a global biopharmaceutical company focusing on neurology and immunology, with around 8,500 employees worldwide. We are committed to creating value for patients through science and innovation.Why work with us?We foster a culture of collaboration, innovation, and inclusion. We support your growth and offer opportunities to develop your career in a meaningful environment. UCB is an Equal Opportunity Employer and encourages diversity and inclusion.
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