NEW OPPORTUNITY – Temporary QA R&D Specialist (Pharma)La descripción completa del puesto cubre todas las habilidades asociadas, la experiencia previa y cualquier cualificación que se espera que tengan los solicitantes. Contract: End May 2026 – December 2026Oxford Global Resources – Life Sciences Unit is 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 experienced QA R&D Specialist to join their Quality Assurance – Pharmaceutical Development team on a temporary basis.Role: QA Specialist – R&D (GMP, IMPs, Quality Systems)Start: ASAP | Full-time, long-term projectExperience: Minimum 3–4 years in a similar QA R&D GMP roleManufacturing, packaging, and labeling instructions for IMPsDeviation and change control managementSupport the Quality Management System (QMS):Deviation handling, CAPAs, change controls, complaintsEdition and maintenance of Quality AgreementsSOPs and controlled documents related to Quality & R&DArchiving and documentation management for GxP-relevant activitiesManage submissions to AEMPS as needed (manufacturing/import/export, controlled substances)Bachelor's or Master's degree in Pharmacy, Chemistry, Biotechnology, or similar~3–5 years of experience in QA within an R&D or IMPs-focused GMP environment~ Spanish required; English professional level~ Work on-site in Sant Cugat, in close collaboration with R&D, QA, and Regulatory teamsBe part of a mission-driven, growth-oriented pharma companyApply now or reach out to our Life Sciences team at Oxford Global Resources to learn more:#