P NEW OPPORTUNITY – QA RD Specialist (Pharma) | On-site – Sant Cugat, Barcelona /ppOxford Global Resources – Life Sciences Unit is currently supporting one of the fastest-growing pharmaceutical companies headquartered in Spain, with a strong focus on innovation and RD. /ppWe are looking for an experienced QA professional to join their Quality Assurance – Pharmaceutical Development team. /pp Role: QA Specialist – RD (GMP, IMPs, Quality Systems) /pp Location: Sant Cugat (on-site) /pp Start: ASAP | Full-time, long-term project /pp Experience: Minimum 3–4 years in a similar QA RD GMP role /pp Sector: Pharmaceutical | GxP | Clinical Trials | IMPs /pp Main Responsibilities /pp Review and/or approval of key GMP documentation generated by the Pharmaceutical Development area, including: /pulliManufacturing, packaging, and labeling instructions for IMPs /liliAnalytical methods, specifications (LIMS), and specification dossiers /liliICH stability protocols/reports /liliMethod validation documentation /liliShelf-life justification reports for IMPs /liliDeviation and change control management /liliMaster Manufacturing Plans (MMP MMPr) /liliSOPs for equipment cleaning, operations, and room procedures /liliQualification protocols/reports for analytical equipment /li /ulp Support the Quality Management System (QMS): /pulliDeviation handling, CAPAs, change controls, complaints /liliInvestigations of OOS, OOE, OOT and related CAPA evaluation /liliEdition and maintenance of Quality Agreements /liliSOPs and controlled documents related to Quality RD /liliArchiving and documentation management for GxP-relevant activities /li /ulp Monitor the status of IMPs throughout the clinical supply chain (manufacturing to end-of-trial) /pp Participate in audits (internal/external) and inspections /pp Manage submissions to AEMPS as needed (manufacturing/import/export, controlled substances) /pp Your Profile /pulliBachelor’s or Master’s degree in Pharmacy, Chemistry, Biotechnology, or similar /lili3–5 years of experience in QA within an RD or IMPs-focused GMP environment /liliSolid knowledge of ICH, GxP, EU GMP Annex 13 /liliExperience working closely with manufacturing, analytical, and regulatory teams /liliSpanish required; English professional level /liliTeam player with attention to detail and problem-solving mindset /li /ulp What’s in it for you? /pp Join a highly dynamic team in a company with a strong pipeline and innovative product portfolio /pp Work on-site in Sant Cugat, in close collaboration with RD, QA, and Regulatory teams /pp Be part of a mission-driven, growth-oriented pharma company /ppInterested? /ppApply now or reach out to our Life Sciences team at Oxford Global Resources to learn more: /pp#LifeSciences #GMP #QAJobs #IMPs #PharmaJobs #SantCugat #BarcelonaJobs #OxfordGlobalResources /p