Contract: End August 2026 – December 2026 Oxford General 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) Manufacturing, packaging, and labeling instructions for IMPs Deviation and change control management Support the Quality Management System (QMS): Edition and maintenance of Quality Agreements SOPs and controlled documents related to Quality & R&D; Archiving and documentation management for GxP-relevant activities Manage submissions to AEMPS as needed (manufacturing/import/export, controlled substances) ~ 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 GMP environment ~ Spanish required; English professional level ~ Work on-site in Sant Cugat, in close collaboration with R&D;, QA, and Regulatory teams

📌 Quality Assurance Officer R&D Temporal (Cataluña)
🏢 Oxford Global Resources
📍 Cataluña