PbMake your mark for patients /b /ppTo strengthen our bQuality Bulle Manufacturing /bdepartment we are looking for a talented profile to fill the position of: bQuality Manager for TS, Facility and Warehousing /bb– Bulle, Switzerland. /b /ppbAbout the role /b /ppThe Quality Manager for TS, Facility and Warehousing leads, develops, and manages the quality for TS, Facility and Warehousing operational activities within the Quality Compliance organization, ensuring the deployment of Quality Culture and Compliance across Bulle site. /ppThe role ensures that the Quality Management System (QMS) with associated processes (deviations CAPA, internal audits, QMR, LPO governance, documentation training, quality life‑cycle, inspection readiness, data integrity, supplier raw material quality) are implemented, continuously improved, and aligned with regulatory expectations and UCB standards. /ppbYou will work with /b /ppThe position supports Bulle Technical Services (Instrumentation, Maintenance, Methods Support, Utilities), Bulle facility services, and Bulle Supply chain (including warehousing activities) to guarantee GxP compliance, robust data integrity, and inspection/audit readiness. /ppbWhat you will do /b /ppGeneral /pliProvide leadership and Quality oversight for Technical Services, Warehousing and Facility operations within the Bulle manufacturing site ensuring adherence to GxP, UCB Quality Program, and Health Authority requirements. /liliActively support simplification, process robustness, operational excellence and continuous improvement initiatives. /liliManage and improve quality strategies in relation to manufacturing and technical operations, regulatory changes, and evolving business needs. /liliParticipate in and contribute expertise to quality‑related projects and cross‑functional initiatives. /liliActively participate to inspection/audits (before/during/after). /lipTechnical Services (TS) /pliProvide Quality oversight for Technical Services activities (utilities, maintenance, methods/support, instrumentation), ensuring compliance with GMP and UCB Quality standards. /liliEnsure qualification/validation expectations for TS-controlled equipment and systems are defined, implemented, and maintained in accordance with current GMP guidelines and UCB Quality policies. /liliEnsure compliance of TS quality processes (e.g., change control, deviations/investigations/CAPA, qualification activities, training, and GxP documentation), including audit/inspection support as applicable. /liliIdentify, assess, and mitigate Quality risks related to Technical Services activities. /liliServe as the Quality escalation point for complex or critical Technical Services topics. /lipWarehouse and Site Supply Chain Operations /pliProvide Quality oversight for warehousing and site supply chain activities, including receipt, sampling, storage and logistic of purchased raw materials and consumables. /liliEnsure compliance of warehouse/supply chain quality processes (e.g., change control, deviations/investigations/CAPA, qualification activities, cleaning activities, training, and GxP documentation), and support audits/inspections as required. /lipFacility Operations /pliProvide Quality oversight for facility-related activities (like access control and pest control), ensuring compliance with GMP and UCB Quality standards. /liliEnsure compliance of facility quality processes (e.g., change control, deviations/investigations/CAPA, qualification activities, training and GxP documentation), and support audits/inspections as required. /lipPeople Leadership /pliTranslate global, transversal and site strategies into actionable goals for the team. /liliBuild and maintain an agile, skilled, flexible, and motivated team. /liliEnsure efficient organization, workload distribution, and competency development. /liliPromote and reinforce Quality Culture across teams and within Bulle site. /lipHSE Responsibilities /pliParticipation to periodic HSE internal audits. /liliActively participate to HSE policy deployment. /liliRespect of HSE rules (particularly respect of procedures, individual protection equipment’s use, systematic use of safety elements, wastes sorting and identification). /liliReport events (accidents and incidents) related to HSE aspects. Immediately report near misses or hazardous HSE situations. /lipbInterested? For this position you’ll need the following education, experience and skills /b /pliBachelor’s, master’s degree or an education in a relevant scientific discipline /liliExcellent written and verbal communication skills in French and English /liliSolid knowledge of the GMP‑regulated environment /liliProven ability to draft clear and accurate scientific and technical documentation /liliAbility to work independently while managing multiple priorities /liliStrong capability to coordinate complex, cross‑functional projects and meet critical deadlines /liliStrong skills in meeting preparation, facilitation, and presentations /liliDemonstrated negotiation and influencing abilities /liliHigh level of professional discretion and integrity /lipAre 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