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 xgwbsxa 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 (San Cugat del Vallés)
🏢 Oxford Global Resources
📍 San Cugat del Vallés