SDI Limited is seeking a Technical Documentation Specialist to prepare and maintain EU MDR technical files for medical devices, ensuring traceability and regulatory alignment across product lifecycles.
The role requires collaboration with R&D;, QA, Regulatory, Manufacturing and Marketing to embed compliance within processes, and proficiency with MS Word/Excel/Project. Bayswater and Montrose site with 38-hour weeks await a detail-oriented skilled.
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📌 Medical Device Technical Documentation Specialist (ISO 13485) (Australia)
🏢 SDI
📍 Australia