NEW OPPORTUNITY – Temporary QA R&D; Specialist (Pharma) 4-5 meses
La descripción completa del puesto cubre todas las habilidades asociadas, la experiencia previa y cualquier cualificación que se espera que tengan los solicitantes.
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 | 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 GMP environment
Solid knowledge of
ICH, GxP, EU xhfqzwm 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 (Barcelona)
🏢 Oxford Global Resources
📍 Barcelona