? NEW OPPORTUNITY – Temporary QA R&D; Specialist (Pharma) 4-5 meses
A continuación se detalla todo lo que necesita saber sobre lo que implica esta ocasión, así como lo que se espera de 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.
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 s