SDI Limited, a global dental products company, is seeking a Technical Documentation Specialist (Medical Devices & ISO *) to manage compliant technical files and evidence mapping across the product lifecycle. The role supports recent and legacy devices while ensuring regulatory alignment with EU MDR, FDA, and ISO standards.
Work locations include Bayswater and Montrose, with a 38-hour work week. The ideal candidate holds a science/engineering degree and 5+ years in Regulatory Affairs, QA, or
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📌 Medical Device Technical Documentation Specialist Eu Mdr/iso 13485 Melbourne (Australia)
🏢 SDI
📍 Australia
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