Make your mark for patientsTo strengthen our RD and PV Quality department we are looking for a talented profile to fill the position of: Head of RD and PV Vendor Quality – Braine l’Alleud, BelgiumAbout the roleThe Head of RD and PV Vendor Quality will lead and advocate for quality assurance in their area of responsibility, focusing on Global Vendors involved in GLP, GCP and GVP activities. This profile will ensure compliance, risk minimization, and quality by design. This role involves setting up processes and tools for vendor qualification and contract implementation, working closely with vendor quality counterparts and UCB representatives. The Head of Vendor Quality will manage a team, be part of the RD and PV Quality Leadership Team and report directly to the Head of RD and PV Quality.You will work withThe Head of RD and PV Vendor Quality will collaborate closely with various stakeholders within the RD and Pharmacovigilance Quality (RDPVQ) team. This includes working with Vendor quality counterparts, UCB functional teams, and Global Quality representatives to ensure compliance and quality assurance in GLP, GCP, and GVP activities. Additionally, the Head of RD and PV Vendor Quality will be part of the RD and PV Quality Leadership Team, reporting directly to the Head of RD and PV Quality. This role is pivotal in ensuring that processes, systems, and tools are in place for vendor qualification and compliance, contributing to the successful delivery of assets and brands.What you will doLeading a team of GLP, GCP, GVP Vendor Quality Leads (VQL)Coach, lead and empower a team of VQLsCreate strategic quality objectives that focus on enabling UCB functional areasEnsure the maintenance and lead the development of processes, systems and tools that are lean and fit for purpose, in support of the responsibilities and activities of VQLEstablish and build a network with UCB key stakeholders in relation to the GLP, GCP and GVP compliance reference system/data integrity and ensure connections with relevant VQLs are establishedEstablish good reports with Vendor Quality counterparts and ensure regulator meetings are established aimed at ensuring compliance and data integrity during the execution of delegated activitiesEnsure compliance with GxP regulations, guidance and internal procedures while reducing complexitySupport the UCB Vendor Strategy and design a qualification methodology that is lean, considers risks and the criticality of the activities outsourcedOversight on the investigation of quality issues, audit and inspection findings pertaining to activities managed by GLP GCP GVP vendors, and the timely remediation thereof, in collaboration with Vendor Quality counterparts, relevant functions within RD and PV Quality, and Global Quality. Facilitate quality optimization initiativesOversight on risks identified and the timely completion of mitigation activitiesEnsure the coordination of inspection readiness and management activities, act as the central point of contact and liaison with vendors in scope of the inspectionHost or support inspections (e.g., inspection strategy development, management of pre-inspection documentation, quality reviews, etc.)Monitor PerformanceLead and conduct analytics and qualitative assessments to identify trendsProvide feedback to functional area heads related to Key Quality/Performance Indicators and quality compliance statusMonitor quality deliverables from vendors and partners, sharing updates with internal function heads.GxP Quality AdvisorQuality Advisor for Steering or Governance committees or councils to support and ensure oversightPro-actively Identify Opportunities to De-Risk at a Candidate/Asset/Brand LevelProvide expert guidance on issues escalated to support quality improvement measuresReview and implement updates to GxP legislations and UCB controlled documents and assess the potential impact on tasks delegated to vendors.Provide expert QA advice, support and management for technical operational QA and general QA matters associated with the vendors.Define best practices and assess the impact on procedures, systems and contractual arrangementsInterested? For this position you’ll need the following education, experience and skillsBachelor’s, master’s degree or an education in a relevant scientific disciplineA minimum of 10 years of experience working in the (bio)pharmaceutical industry preferred, with a minimum of 5 years in the research, clinical development or Pharmacovigilance domainProficient in research/GLP, GCP and/or GVP regulationsAbility to translate regulatory and quality expectations into operations, based on knowledge of quality principlesExperience in GLP, GCP and/or GVP quality auditing, inspection, compliance management, and/or Medical Device regulations/operations is an assetProficient in MS Office Suite; experience with statistical programs, SAP and Veeva is an assetAbility to drive collaboration and engagement across the stakeholder network, motivating others to achieve resultsSkilled in influencing others within a global matrix organization and driving informed decision-makingCapable of prioritizing and focusing on critical issues using a risk-based approachManages quality and compliance issues with diligence, rigor, transparency and timelinessStrong analytical skills with experience in analyzing and synthesizing complex dataProficient in presenting complex projects and issues clearly and succinctlyExpertise in managing transversal quality optimization projects and resolving complex issuesExcellent planning, organizational, presentation, training, communication, and interpersonal skillsAbout usUCB 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.
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