Quality Assurance Officer R&D temporal

NEW OPPORTUNITY – Temporary QA R&D Specialist (Pharma)

On-site | Sant Cugat (Barcelona) Contract: End May 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 3–4 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 3–5 years of experience

in QA within an R&D or IMPs-focused 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 Global Resources

to learn more: #LifeSciences #GMP #QAJobs #IMPs #PharmaJobs #SantCugat #BarcelonaJobs #OxfordGlobalResources