Celestica is seeking a Quality Manager to lead Medical Device QMS and environmental controls in Valencia. You will align ISO 13485 processes with local procedures, serve as the QA SME, update documentation, and support audits by customers and regulators.The role requires extensive microbiology/lab management experience in a regulated medical device setting, with strong leadership and communication skills to interface with clients and regulators globally.
📌 Iso 13485 Quality Lead – Medical Device Compliance (Alboraya)
🏢 Celestica
📍 Alboraya
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