Quality & Regulatory Affairs (QARA) Consultant

🌍 Easy Medical Device is hiring!Position: Quality & Regulatory Affairs (QARA) Consultant 📍 Location: Morocco – Rabat 📑 Contract: Full-time🎯 About usEasy Medical Device is an international consulting firm specializing in medical device quality and regulatory compliance. With offices in Switzerland, Belgium, the UK, and Morocco, we support manufacturers in achieving compliance with international standards and regulations (ISO 13485, ISO 9001, MDR/IVDR, FDA…). 🛠️ Your responsibilitiesAs a QARA Consultant, you will be involved in:Implementing and maintaining Quality Management Systems (QMS) in compliance with ISO 13485.Developing, reviewing, and harmonizing quality procedures, work instructions, and records.Managing and improving key quality processes: CAPA, document control, change control, internal audits.Preparing and supporting clients during external audits (certification, surveillance, supplier).Leading continuous improvement projects to enhance efficiency and compliance.(As secondary support) contributing to regulatory activities related to MDR/IVDR.👤 Profile requiredBac+5 (Biomedical Engineering, Quality, Regulatory Affairs, or equivalent).Minimum 1 year of experience in Quality and Regulatory Affairs (internships included).Good knowledge of ISO 13485, ISO 9001, or equivalent.Excellent writing and analytical skills.Ability to work independently and collaboratively in an international environment.Proficiency in both French and English (spoken/written).⚠️ Note: The CV must be written in English, and the interview will be conducted in English.🚀 Why join Easy Medical Device?Work within an international and dynamic team.Participate in diverse and innovative projects for medical device manufacturers.Benefit from continuous training and professional development.Contribute to a meaningful field impacting patient health and safety.📩 How to applySend your English CV to: lelrhali@easymedicaldevice.com or via LinkedIn. Subject: Application – QARA Consultant Morocco👉 Join us and be part of a team shaping the future of compliance in the medical device industry!