Role missionParticipate in the development and deployment of our regulatory affairs processes and report on their effectiveness and any need for improvement Your responsibilitiesManage the international registration of medical devices to obtain the approvals needed to market our productsEnsure 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 metActively 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)Ensure effective communication with your external contacts, customers or suppliers, as well as other departments within the company, and support them in all matters relating to regulatory affairsLead projects linked to implementation of new regulatory or normative requirements and continuous improvement and contribute to regulatory and normative watchContribute to post-marketing follow-up activities (PMS)Participate in various activities of the Quality and Regulatory Affairs Department, in particular: maintaining regulatory databases, handling vigilance cases, conducting internal and supplier audits, managing modifications, analyzing data, handling CAPAsEnsures employee awareness of and training in applicable regulatory requirements Your profileAdvanced scientific or engineering training3 years' professional experience in medical device regulatory affairsKnowledge of the main standards and regulations applicable to our field (ISO 13485:2016, Regulation (EU) 2017/745, 21 CFR Part 820 and other regulations applicable in MDSAP jurisdictions)Good knowledge of MS-Office tools (Word, Excel, PowerPoint)Good level of written and spoken English (B2), Spanish or Arabic would be a plusTeam spiritExcellent analytical skillsPragmatism, proactivity, rigorExcellent communication and interpersonal skills We offerA stimulating and dynamic work environment at the cutting edge of industrial automationOpportunities for professional development and career advancementA collaborative and inclusive corporate culture that values innovation and teamworkAttractive benefits (free parking place, home office, flexible work hours, minimum 5 weeks’ vacation, health insurance participation) Entry into function : immediately or to be agreed If you recognize yourself in this job description, are dynamic and interested in taking on challenges in a growing company, then we look forward to receiving your full application. We look forward to discovering your talent and discussing how you can contribute to our success ! jid58d8bc3a jit0208a