Quality Assurance Officer R&D temporal

Location: Sant Cugat Del Valles

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

Asegúrese de leer detenidamente la información sobre esta oportunidad antes de presentar su candidatura.

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 xiphteb  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:
#Life Sciences #GMP #QAJobs #IMPs #Pharma Jobs #Sant Cugat #Barcelona Jobs #Oxford Global Resources