Ph3Evidence Quality Lead – Braine l’Alleud, Belgium /h3 pAs 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. /p h3You will work with /h3 pYou will work closely with a variety of internal functions within Quality and the Business area you support. Additionally, you will engage with external partners and vendors to ensure the integrity of data for delegated activities. /p h3What You Will Do /h3 pDevelop and Maintain the Quality Strategy at a Compound Level /p ul liCreate and sustain a quality roadmap for strategic quality objectives, covering the clinical development and post‑marketing phases /li liIdentify and manage risks using a risk‑based approach across compounds, processes, systems, sites, and vendors /li liEnsure compliance with GxP regulations, guidance, and internal procedures while reducing complexity /li /ul pProactively Identify Opportunities to De‑Risk at a Compound Level /p ul liPlan and execute quality activities independently to ensure subject safety and data integrity, complying with protocols and regulations /li liLead compliance investigations and ensure timely closure of corrective and preventative actions from deviations, audits and inspections /li liEscalate issues early and ensure effective resolution or measures are in place /li liLead or contribute to complex projects /li liManage pre‑inspection documentation, quality reviews, in collaboration with functional SMEs and global process owners /li /ul pMonitor Performance /p ul liConduct analytics and qualitative assessments to identify trends /li liMonitor quality deliverables from vendors and partners, sharing updates with internal functions /li liEnsure continuous inspection readiness and integrity of the data included in regulatory dossiers /li liLead or support inspections and investigations, coordinating responses and hosting strategies /li /ul pGxP Quality Advisor Responsibilities /p ul liReview and implement updates to GxP legislation, define best practices and assess the impact on procedures, systems and contractual arrangements /li liProvide expert advice to mitigate compliance risks or to address complex issues /li liDeliver presentations to peers, senior management, and industry audiences /li /ul h3Interested? For this position you’ll need the following education, experience, and skills /h3 ul liBachelor's degree in a relevant scientific or healthcare‑related field /li liMinimum of 10 years in the (bio)pharmaceutical industry, with at least 5 years in research, clinical development or Pharmacovigilance /li liFluent English communication (oral and written); any additional languages are a plus /li liProven track record of contributing to gene therapy clinical programs with technical and scientific expertise /li liAbility to translate regulatory and quality expectations into operations, based on knowledge of quality principles /li liExperience in GLP, GCP and/or GVP quality auditing, inspection, compliance management, and/or Medical Device regulations/operations is an asset /li liAbility to drive collaboration and engagement across the stakeholder network, motivating others to achieve results /li liSkilled in influencing others within a global matrix organization and driving informed decision‑making /li liCapable of prioritizing and focusing on critical issues using a risk‑based approach /li liManages quality and compliance issues with diligence, rigor, transparency and timeliness /li liStrong analytical skills with experience in analyzing and synthesizing complex data /li liProficient in presenting complex projects and issues clearly and succinctly /li /ul 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 h3Equal Opportunity /h3 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 EMEA‑ Please note that if your enquiry does not relate to adjustments, we will not be able to support you through this channel. /p /p #J-18808-Ljbffr