NEW OPPORTUNITY – Temporary QA R&D; Specialist (Pharma) 4-5 meses On-site | Sant Cugat (Barcelona)

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Contract: End August 2026 – December 2026 Oxford 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 project

Experience

Minimum 2-3 years in a similar QA R&D; GMP role

Sector: Pharmaceutical | GxP | Clinical Trials | IMPs 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
- 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




- 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
- 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) Participate in audits (internal/external) and inspections Manage submissions to AEMPS as needed (manufacturing/import/export, controlled substances) Your Profile Bachelor's or Master's degree in Pharmacy, Chemistry, Biotechnology, or similar 2-3 years of experience in QA within an R&D; or IMPs-focused xbhjioe GMP environment Solid knowledge of ICH, GxP, EU GMP Annex 13 Experience working closely with manufacturing, analytical, and regulatory teams Spanish required; English professional level Team 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 portfolio Work on-site in Sant Cugat, in close collaboration with R&D;, QA, and Regulatory teams Be part of a mission-driven, growth-oriented pharma company Interested? Apply now or reach out to our Life Sciences team at Oxford General Resources to 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