Details
Skills
Regulatory Affairs: MDR 2017/745, ISO 13485, ISO 14971, ISO 27001
Project Management: Medical Equipment ,Planning, Technical Team Coordination, Client Support
Biomedical R&D: Device Development, Testing, and Compliance
Technical Writing: Regulatory Documentation, Technical Files, CE Marking
IT Skills: Microsoft Office Suite, Python (Workbench 19), Data Analysis
Monitoring Tools: Scientific, Technological, and Normative Trends
Quality Management: Device Calibration, Safety Compliance, ISO Implementation
About
Biomedical Engineer with expertise in medical equipment quality control, regulatory compliance, and international project management. Fluent in French, English, and Arabic, with experience coordinating multidisciplinary projects in biomedical and hospital engineering environments. Committed to advancing healthcare infrastructure through innovation and cross-functional collaboration.
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