NEW OPPORTUNITY – Temporary QA Specialist (Pharma)On-site | Sant Cugat (Barcelona)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)Location: Sant Cugat (on-site)Start: ASAP | Full-time, long-term projectExperience: Minimum 3–4 years in a similar QA R& D GMP roleSector: Pharmaceutical | Gx P | Clinical Trials | IMPsMain ResponsibilitiesReview and/or approval of key GMP documentation generated by the Pharmaceutical Development area, including:
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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 Gx P-relevant activities Monitor the status of IMPs throughout the clinical supply chain (manufacturing to end-of-trial)Participate in audits (internal/external) and inspectionsManage submissions to AEMPS as needed (manufacturing/import/export, controlled substances)Your Profile
Bachelor's or Master's degree in Pharmacy, Chemistry, Biotechnology, or similar3–5 years of experience in QA within an R& D or IMPs-focused GMP environmentSolid knowledge xcskxlj of ICH, Gx P, EU GMP Annex 13Experience working closely with manufacturing, analytical, and regulatory teamsSpanish required; English professional levelTeam player with attention to detail and problem-solving mindset What's in it for you?Join a highly dynamic team in a company with a strong pipeline and innovative product portfolioWork on-site in Sant Cugat, in close collaboration with R& D, QA, and Regulatory teamsBe part of a mission-driven, growth-oriented pharma companyInterested?Apply now or reach out to our Life Sciences team at Oxford Global Resources to learn more:#Life Sciences #GMP #QAJobs #IMPs #Pharma Jobs #Sant Cugat #Barcelona Jobs #Oxford General Resources