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)

Sector : Pharmaceutical | GxP | Clinical Trials | IMPs

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

Shelf-life justification reports for IMPs

Deviation and change control management

SOPs for equipment cleaning, operations, and room procedures

Qualification protocols/reports for analytical equipment

Support the Quality Management System (QMS):

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)

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 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? #J-18808-Ljbffr

📌 Quality Assurance Officer R&D temporal (San Cugat del Vallés)
🏢 Oxford Global Resources
📍 San Cugat del Vallés