JobdescriptionLocation: Bulle, SwitzerlandActivity rate : 100%Type of contract: Temporary contract (until 31.12.2026)Start Date: ASAP You care about customers? UCB does as well! As a patient-centric company, UCB is searching for the right fit for their Patient Supply Quality Control department.In that role you will support analytical method transfers, validation, and QC readiness within a regulated, cGMP-compliant environment. Your key responsibilities:Conduct and validate analytical tests; ensure accuracy and compliance with protocols.Draft, review, and update validation protocols, risk assessments, and quality documentation.Coordinate closely with QC to ensure seamless knowledge transfer and lab readiness.Lead and contribute to continuous improvement initiatives and cross-functional projects.Act as a Subject Matter Expert (SME) on analytical methods, providing expertise across teams.Ensure strict adherence to cGMP and HSE standards; actively participate in CAPA, deviation investigations, and safety improvements.Promote HSE policies within the team, ensure safe lab practices, and report any incidents or near-misses to maintain a safe work environment. QualifikationenWhat will make you successful:Bachelor's or Master's degree with hands-on laboratory experienceProficiency in both French and English (spoken and written)Good knowledge in analytical methods (LAL, endotoxin, bioburden, etc.)Skilled in MS Office and basic statisticsStrong communicator with clear and structured thinkingHighly organized, solution-oriented, and customer-focusedPragmatic, responsible, and proactiveTeam player with a critical mindset We can offer you a new challenge in a diverse and innovative environment that gives temporary contrats the opportunity to step aside for a long period. Have we sparked your interest? Then we look forward to receiving your online application.