NEW OPPORTUNITY – Temporary QA R&D; Specialist (Pharma) 4-5 meses

On-site | Sant Cugat (Barcelona)

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 | Gx P | 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 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 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 GMP environment Solid knowledge of ICH, Gx P, 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 Integral Resources to learn more: #Life Sciences #GMP #QAJobs #IMPs #Pharma Jobs #Sant Cugat #Barcelona Jobs #Oxford Global Resources

📌 Quality assurance officer r&d temporal (Madrid)
🏢 Oxford Global Resources
📍 Madrid