Evidence Quality Lead

Make your mark for patientsTo strengthen our Global Quality Assurance department, we are looking for a talented professional to fill the position of: Evidence Quality Lead – Bulle -Switzerland.About The RoleAs part of the UCB Quality organization, the Evidence Quality Lead (EQL) actively enables compliant Research, Development and Pharmacovigilance processes (i.e., GLP GCP GVP) from candidate to asset delivery, to commercial branding, with a focus on successful global launches and sustainable access for our patients. Collaborating with internal teams and external stakeholders, the EQL plays a crucial role in ensuring quality by design and maintaining continuous inspection readiness.You will work withYou will work closely with a variety of internal functions within Quality and the Business area’s you support. Additionally, you will engage with external partners and vendors to ensure the integrity of data for delegated activities.What You Will DoDevelop and Maintain the Quality Strategy at a Compound LevelCreate and sustain a quality roadmap for strategic quality objectives, covering the clinical development and post-marketing phases,Identify and manage risks using a risk-based approach across compounds, processes, systems, sites, and vendorsEnsure compliance with GxP regulations, guidance, and internal procedures while reducing complexityProactively Identify Opportunities to De-Risk at a Compound LevelPlan and execute quality activities independently to ensure subject safety and data integrity, complying with protocols and regulationsLead compliance investigations and ensure timely closure of corrective and preventative actions from deviations, audits and inspectionsEscalate issues early and ensure effective resolution or measures are in placeLead or contribute to complex projectsManage pre-inspection documentation, quality reviews, in collaboration with functional SMEs and global process owners.Monitor PerformanceConduct analytics and qualitative assessments to identify trendsMonitor quality deliverables from vendors and partners, sharing updates with internal functionsEnsure continuous inspection readiness and integrity of the data included in regulatory dossiersLead/support inspections and investigations, coordinating responses and hosting strategiesGxP Quality Advisor ResponsibilitiesReview and implement updates to GxP legislation, define best practices and assess the impact on procedures, systems and contractual arrangementsProvide expert advice to mitigate compliance risks or to address complex issues.Deliver presentations to peers, senior management, and industry audiencesAbout UsUCB 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.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 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.At 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.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. #J-18808-Ljbffr