JobdescriptionFor our client, we are looking for a QC Analyst (FR) to join their team in Neuchâtel.Work Conditions:On-site role in Neuchâtel6-month contract via Randstad (17/03/2025 - 16/09/2025)French mandatory (English is a plus)Variable working hours, including weekends (1 out of 4 to 6) and on-call periodsJob ResponsibilitiesAs the entry point for the Quality Control (QC) laboratories, you will be responsible for providing the necessary samples, stability materials, and articles for analysis. You will ensure the proper handling, documentation, and distribution of samples while maintaining compliance with Good Manufacturing Practices (GMP) and internal procedures.Your main tasks will include:Sample Handling & LogisticsControl, aliquot, identify, record, distribute, store, or dispose of samples in compliance with GMP and standard operating procedures (SOPs)Ensure proper reception, processing, and distribution of samples according to established guidelinesReceive and register samples in tracking systems (LIMS or similar) within defined timelinesPerform sample destruction and transfers as requiredStability & Validation StudiesParticipate in validation protocols and stability studies, from sample reception to analysis, stabilization, and disposalEnsure proper documentation and traceability of stability samplesStock & Equipment ManagementManage the stock of consumables and reagents for the laboratoryOversee equipment maintenance, calibration, and temperature alarm monitoringEnsure proper logbook completion and reviewRegulatory Compliance & EHSAdhere to GMP guidelines and internal quality proceduresSupport regulatory audits by maintaining accurate documentationFollow EHS (Environment, Health & Safety) regulations and actively report any deviationsSupport for QC TeamsAssist with non-testing tasks such as preparation of analysis solutions, freezer transfers, and autoclaving activitiesCollaborate with cross-functional teams for efficient sample processingJob Requirements? Education & ExperiencePrevious experience in sample management, stability studies, or QC logistics within a GMP-regulated environmentFamiliarity with Good Manufacturing Practices (GMP), stability management, and laboratory sample handlingExperience with LIMS or other sample tracking systems is a plus? Technical & Soft SkillsStrong attention to detail and ability to follow SOPs preciselyExcellent organizational and multitasking skillsProactive mindset in ensuring regulatory compliance and safety standardsAbility to work both independently and in collaboration with QC and regulatory teamsThis is a great opportunity to join a dynamic and high-quality environment. If you meet the requirements and are interested, apply now!Luciana Sardo