NEW OPPORTUNITY – Temporary QA R&D; Specialist (Pharma) 4-5 mesesLa descripción completa del puesto cubre todas las habilidades asociadas, la experiencia previa y cualquier cualificación que se espera que tengan los solicitantes.On-site | Sant Cugat (Barcelona)Contract: End August 2026 – December 2026Oxford Global Resources – Life Sciences Unitis supporting one of the fastest-growing pharmaceutical companies headquartered in Spain, recognized for its strong commitment to innovation and R&D; excellence.We are currently looking for an experiencedQA R&D; Specialistto join theirQuality Assurance – Pharmaceutical Developmentteam on a temporary basis.Role : QA Specialist – R&D; (GMP, IMPs, Quality Systems)Location : Sant Cugat (on-site)Start : ASAP |Full-time, long-term projectExperience : Minimum 2-3 years in a similar QA R&D; GMP roleSector: Pharmaceutical | GxP | Clinical Trials | IMPsMain Responsibilities Review and/or approval of key GMP documentation generated by the Pharmaceutical Development area, including:Manufacturing, packaging, and labeling instructions for IMPsAnalytical methods, specifications (LIMS), and specification dossiersICH stability protocols/reportsMethod validation documentationShelf-life justification reports for IMPsDeviation and change control managementMaster Manufacturing Plans (MMP & MMPr)SOPs for equipment cleaning, operations,



and room proceduresQualification protocols/reports for analytical equipment Support the Quality Management System (QMS):Deviation handling, CAPAs, change controls, complaintsInvestigations of OOS, OOE, OOT and related CAPA evaluationEdition and maintenance of Quality AgreementsSOPs and controlled documents related to Quality & R&DArchiving; and documentation management for GxP-relevant activities Monitor the status of IMPs throughout the clinical supply chain (manufacturing to end-of-trial) Participate in audits (internal/external) and inspections Manage submissions to AEMPS as needed (manufacturing/import/export, controlled substances)Your ProfileBachelor’s or Master’s degree in Pharmacy, Chemistry, Biotechnology, or similar2-3 years of experiencein QA within an R&D; or IMPs-focused GMP environmentSolid knowledge ofICH, GxP, EU xkdbapo GMP Annex 13Experience working closely with manufacturing, analytical, and regulatory teamsSpanish required; English professional levelTeam player with attention to detail and problem-solving mindsetWhat’s in it for you? Join ahighly dynamic teamin a company with a strong pipeline and innovative product portfolio Workon-site in Sant Cugat , in close collaboration with R&D;, QA, and Regulatory teams Be part of amission-driven, growth-oriented pharmacompanyInterested?Apply now or reach out to ourLife Sciences team at Oxford General Resourcesto learn more:#LifeSciences #GMP #QAJobs #IMPs #PharmaJobs #SantCugat #BarcelonaJobs #OxfordGlobalResources

📌 Quality Assurance Officer R temporal (San Cugat del Vallés)
🏢 Oxford Global Resources
📍 San Cugat del Vallés