Celestica in Valencia, Spain seeks a senior Quality & Regulatory Manager to align ISO 13485 QMS with local procedures, lead regulatory compliance, and support audits. You will drive CAPAs, oversee cleanroom operations, and manage supplier testing to ensure uninterrupted, compliant production in a general medical device environment.The role requires 10+ years in Microbiology/Lab Management within the Medical Device industry, strong regulatory knowledge, and excellent communication with regulators
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📌 Global Quality Manager, Medical Devices & ISO 13485 (Madrid)
🏢 Celestica
📍 Madrid
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