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Role mission : Participate in the development and deployment of our regulatory affairs processes and report on their effectiveness and any need for improvementYour responsibilities :- Manage the international registration of medical devices to obtain the approvals needed to market our products- Ensure the creation and maintenance of technical documentation applicable to our products (CE marking files) and participate in new product development projects as a representative of the QA-RA function to ensure that applicable regulatory requirements are taken into account and met- Actively participate in maintaining the compliance of our quality management system with applicable regulatory and standards requirements, as well as the corresponding certifications (ISO 13485, CE marking, MDSAP)- Ensu...