NEW OPPORTUNITY – Temporary QA Specialist (Pharma)
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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 xpzdshu 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:
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