Test and Verification Officer M/F

This job offer is entrusted to France Travail by LINDUSTRIE-RECRUTE.FR The Test and Verification Officer participates in the development and verification of custom instruments and/or machines in the Life Sciences field. In detail, your missions consist of: Participating in the definition of the test and verification strategy for instruments developed according to the ISO13485 standard Performing development tests on modules or instruments during feasibility and development phases Defining test protocols and performing tests during Factory Acceptance Tests (FAT, at the MGA site) and Site Acceptance Tests (SAT, at the client site) for custom machines Defining test protocols and performing tests during the integration and verification phases for instruments developed according to the ISO13485 standard Outsourcing tests (Safety, EMC, Transport) to external service providers or notified bodies Writing test protocols and recording the results obtained in compliance with regulatory requirements and good laboratory practices Synthesizing and communicating the status of test execution and their results to Internal Project Managers and Clients, the Development Team, and R&D Managers Participating in the resolution of problems encountered by the project group, and being proactive regarding solutions to be implemented Participating in the technical transfer to production (training on adjustments and controls, use of test benches, ECME, and software) Identifying the measuring devices and consumables necessary for performing development and verification tests, and ensuring the monitoring of consumable stocks In connection with the Quality department, participating in the monitoring and management of control, measurement, and testing equipment Occasionally, providing transversal leadership to other test and verification officers You are an engineer with approximately 10 years of experience in validation, verification, or development of complex systems, ideally in the medical device field or in a highly regulated environment. You possess excellent writing skills and an analytical mind that allow you to produce clear, structured documentation in compliance with quality requirements. At ease in the laboratory, you master measuring and metrology instruments, as well as hardware and software testing methodologies. You know how to develop systems combining hardware and software and you appreciate multidisciplinary technical environments mixing mechanics, electronics, software, embedded software, or fluidics. You are familiar with the quality and regulatory requirements applicable to medical devices, including standards such as ISO 13485, ISO 62304, ISO 14971, and IEC 61010-1, and you know how to integrate them into your daily work. You demonstrate a good ability to synthesize, communicate easily both in writing and orally, and you enjoy teamwork. Finally, you are able to operate in an international context thanks to a good level of English. ? Our package: Annual remuneration over 13 months (44K-47K adaptable according to your profile) Restaurant vouchers of 9.50 euros (60% employer share) Profit-sharing Employee Savings Plan (25% employer match) Weekly base of 37.5 hours: 4.33 overtime hours increased by 25% + 6 RTT days/year. 2 attendance rest days Our other advantages: Our CSE: organization of events + Employee Club: platform for benefits, discounts, and offers (theme park tickets, shows, concerts, cinema tickets, travel, shopping, sports leisure, culture) MGAme: challenges and ev