Descripción de la oferta
Quality Control Supervisor – StabilitiesPor favor, asegúrese de leer completamente el resumen y los requisitos de esta oportunidad de empleo que se detallan a continuación.Location: Girona | Full-time | Pharmaceutical ManufacturingWe are supporting a pharmaceutical organisation in the Girona area looking to appoint a Quality Control Supervisor – Stabilities to take ownership of stability studies and analytical method validation within a GMP-regulated environment.This is a hands-on role focused on coordinating stability programmes, ensuring compliance, and working closely with Regulatory Affairs and cross-functional teams to support product lifecycle and registration activities.The RoleYou will play a key role in planning, supervising and reviewing stability studies and analytical validation activities, while overseeing day-to-day QC laboratory operations.Key responsibilities include:Establishing and managing stability study plans and analytical method validation activitiesSupervising and coordinating QC laboratory operations related to stability programmesReviewing protocols, technical reports and regulatory documentation linked to stability and validationMonitoring study timelines, identifying risks and ensuring on-time delivery of resultsActing as a key interface between QC and Regulatory Affairs to support registration and submission activitiesPerforming data checks and ensuring accuracy of stability testing resultsManaging deviations, investigations and CAPAs within the QC environmentEnsuring all activities are carried out in compliance with GMP and quality standardsSupporting audits and regulatory inspectionsDriving continuous improvement in laboratory processes, efficiency and complianceYour ProfileWe’re looking for someone with strong experience in QC within a GMP environment, with particular exposure to stability studies and analytical method validation.You will likely have:Experience working in a GMP-regulated QC laboratoryHands-on involvement in stability studies (ICH) and/or analytical method validation xcskxlj Experience reviewing technical documentation, protocols and reportsExposure to deviations, investigations and CAPAsExperience supervising, coordinating or mentoring laboratory teamsStrong understanding of analytical techniques (e.g. HPLC, ELISA, microbiology or similar)Familiarity with systems such as LIMS, Trackwise or similarWhy ApplyHigh-impact role with ownership of stability programmes and validation activitiesOpportunity to step into or develop leadership responsibilitiesStrong exposure to Regulatory Affairs and product lifecycle activitiesCollaborative GMP environment with cross-functional visibility
