NEW OPPORTUNITY – Temporary QA R&D Specialist (Pharma)
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#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)
#Start : ASAP | #128336; Full-time, long-term project
#Experience : Minimum 3–4 years in a similar QA R&D GMP role
#Manufacturing, packaging, and labeling instructions for IMPs
Deviation and change control management
Support the Quality Management System (QMS):
Deviation handling, CAPAs, change controls, complaints
Edition and maintenance of Quality Agreements
SOPs and controlled documents related to Quality & R&D
Archiving and documentation management for Gx P-relevant activities
Manage submissions to AEMPS as needed (manufacturing/import/export, controlled substances)
Bachelor's or Master's degree in Pharmacy, Chemistry, Biotechnology, xqysrnh or similar
~3–5 years of experience in QA within an R&D or IMPs-focused GMP environment
~ Spanish required; English professional level
~ 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
Apply now or reach out to our Life Sciences team at Oxford Global Resources to learn more: