NEW OPPORTUNITY – Temporary QA Specialist (Pharma)
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On-site | Sant Cugat (Barcelona)\nContract: End May 2026 – December 2026
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Oxford Integral 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.\nWe are currently looking for an experienced
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QA R&D; Specialist to join their
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Quality Assurance – Pharmaceutical Development team on a temporary basis.
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Role : QA Specialist – R&D; (GMP, IMPs, Quality Systems)\nLocation : Sant Cugat (on-site)\nStart : ASAP |
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Full-time, long-term project\nExperience : Minimum 3–4 years in a similar QA R&D; GMP role\nSector: Pharmaceutical | GxP | Clinical Trials | IMPs
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Main Responsibilities ✔️ Review and/or approval of key GMP documentation generated by the Pharmaceutical Development area, including: Manufacturing, packaging, and labeling instructions for IMPs Analytical methods, specifications (LIMS), and specification dossiers
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ICH stability protocols/reports Method validation documentation Shelf-life justification reports for IMPs Deviation and change control management Master Manufacturing Plans (MMP & MMPr) SOPs for equipment cleaning, operations, and room procedures
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Qualification protocols/reports for analytical equipment ✔️ Support the Quality Management System (QMS): Deviation handling, CAPAs, change controls, complaints Investigations of OOS, OOE, OOT and related CAPA evaluation
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Edition and maintenance of Quality Agreements SOPs and controlled documents related to Quality & R&D; Archiving and documentation management for GxP-relevant activities ✔️ Monitor the status of IMPs throughout the clinical supply chain (manufacturing to end-of-trial)
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✔️ Participate in audits (internal/external) and inspections ✔️ Manage submissions to AEMPS as needed (manufacturing/import/export, controlled substances)
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Your Profile\nBachelor’s or Master’s degree in Pharmacy, Chemistry, Biotechnology, or similar\n3–5 years of experience in QA within an R&D; or IMPs-focused GMP environment\nSolid knowledge of
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ICH, GxP, EU GMP Annex 13\nExperience working closely with manufacturing, analytical, and regulatory teams\nSpanish required; English professional level\nTeam player with attention to detail and problem-solving mindset
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What’s in it for you?\n✅ Join a highly dynamic team in a company with a strong pipeline and innovative product portfolio\n✅ Work on-site in Sant Cugat, in close collaboration with R&D;, QA, and Regulatory teams\n✅ Be part of a mission-driven, growth-oriented pharma company\nInterested?
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Apply now or reach out to our
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Life Sciences team at Oxford Global Resources to learn more:\n#LifeSciences #GMP #QAJobs #IMPs #PharmaJobs #SantCugat #BarcelonaJobs #OxfordGlobalResources