Galderma is seeking a Integral ESO Quality Specialist to join the External Supplier Organization for Sterile Products across Europe, collaborating with external manufacturers.
You will lead QA activities including complaint management, release testing, sterile production oversight, and documentation control in line with ISO 13485, MDR and cGMP.
The role requires 2–5 years in a regulated QA function, fluent English, and the ability to work in a dynamic, international setting with travel.
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📌 Global ESO Quality Specialist – Sterile & Compliance (Barcelona)
🏢 Galderma
📍 Barcelona
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