PpWe are looking for a bHead of Quality Assurance Compliance /b who is bstrategic, collaborative, and relentlessly quality-driven /b to join our bSite Quality – QA Compliance /b team, based at our bUCB campus /b located in bBraine-l’Alleud, Walloon Brabant, Belgium /b. /p h3About The Role /h3 pYou are going to set the pace for regulatory compliance and inspection readiness across our pharmaceutical manufacturing site. You will lead the site Quality Management System governance, strengthen a proactive and risk-based compliance approach, and champion a culture where quality is everyone’s responsibility. You will oversee key compliance processes—audits, deviations, corrective and preventive actions, change control, data integrity, and risk management—so you will help protect patients, products, and reliable supply. /p h3Who You Will Work With /h3 pYou will work closely with the Site Quality leadership and partner daily with Manufacturing, Technical Operations, Regulatory Affairs, and global Quality colleagues to keep the site in a sustained state of control. You will also collaborate with quality systems and continuous improvement experts who focus on optimizing quality processes, reinforcing standards, and enabling operational excellence across site activities and supporting services. /p h3What You Will Do /h3 ul liYou will drive inspection readiness and sustained compliance across manufacturing, testing, and all supporting site services. /li liYou will lead Quality Management System governance, ensuring robust oversight of deviations, corrective actions, and change control. /li liYou will coordinate regulatory and customer inspections, including preparation, hosting, and timely, high-quality response packages. /li liYou will lead internal and external audit strategy, ensuring effective follow-up, risk mitigation, and continuous improvement outcomes. /li liYou will manage the site data integrity office, define the roadmap, and strengthen oversight for equipment-related data. /li liYou will build, coach, and inspire a high-performing compliance team and develop a practical learning and training culture. /li /ul pFor this role, we are looking for the following education, experience, and skills: /p ul liYou will bring a Master’s degree in Chemistry, Life Sciences, or a closely related scientific discipline. /li liYou will have 10+ years in a regulated pharmaceutical or life-sciences environment, including 5+ years in Quality Assurance. /li liYou will demonstrate strong people leadership experience, motivating and developing teams of quality professionals. /li liYou will show expertise in quality systems governance and internal/external auditing within manufacturing environments. /li liYou will apply risk analysis and mitigation methods with confidence and sound, fact-based decision making. /li liYou will communicate fluently in French and English, influencing stakeholders with clarity, diplomacy, and accountability. /li /ul pAre 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! /p h3About Us /h3 pUCB 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. /p h3Why work with us? /h3 pAt 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. /p pAt 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. /p pUCB is an equal opportunity employer. All employment decisions will be made without regard to any characteristic protected by applicable laws. /p pShould 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. /p /p #J-18808-Ljbffr