Contract: End August 2026 – December 2026

Para presentar una candidatura, simplemente lea la siguiente descripción del puesto y asegúrese de adjuntar los documentos pertinentes.

Oxford Integral 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:

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- 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):

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- 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)

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