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Prêt(e) à jouer un rôle clé dans l’avenir des thérapies géniques pour les maladies rares ? Bienvenue chez Généthon, laboratoire pionnier et leader de la thérapie génique, fondé par l’AFM-Téléthon. Ici, nous ne suivons pas les chemins tracés, nous les créons. Chaque jour, nos 240 professionnels – chercheurs, ingénieurs, techniciens et experts – unissent leurs talents et leur passion pour relever des défis complexes et ouvrir de nouvelles voies dans la recherche et les traitements. Ensemble, nous transformons des avancées scientifiques en solutions concrètes pour les personnes atteintes de maladies rares. Les maladies rares ont besoin de talents singuliers. La Direction juridique accompagne l’ensemble des activités de Généthon en apportant une expertise juridique exigeante, pragmatique et tournée vers la réussite des projets scientifiques, opérationnels et stratégiques. Poste ouvert dans le cadre d'un CDI Rattaché(e) à la Directrice juridique, vous intervenez comme partenaire juridique de proximité des équipes internes. Vous contribuez activement à la sécurisation juridique des activités de Généthon, tout en accompagnant des projets variés dans un environnement de recherche, d’innovation et de partenariats internationaux. Vos missions principales 1. Accompagnement juridique des équipes internes • Conseiller et accompagner les équipes scientifiques et l’ensemble des fonctions de développement et supports dans leurs projets, • Analyser les enjeux et risques juridiques des opérations soumises, proposer des solutions adaptées et opérationnelles, • Contribuer à la diffusion d’une culture juridique claire, accessible et pragmatique 1. Rédaction et négociation contractuelle • Rédiger, négocier et assurer le suivi de contrats variés en français et en anglais, • Adapter et faire évoluer les modèles contractuels existants, • Contribuer à l’amélioration continue des processus contractuels 1. Structuration juridique • Participer à l’élaboration de procédures, documents de référence et outils juridiques, • Contribuer à la veille législative, réglementaire et jurisprudentielle sur les sujets suivis, • Diffuser les informations juridiques utiles aux services concernés Préparation, rédaction et suivi de documents juridiques Préparation, négociation et rédaction des contrats (simples et/ou complexes), révision et suivi jusqu’à la signature dans le domaine de la Recherche, des Essais cliniques, de la fabrication pharmaceutique et pour les activités de support et transversales, en français et en anglais Elaboration de documents types (contrats, clauses documents corporate), procédures. Conseil aux opérationnels Sensibiliser les clients internes aux contraintes juridiques qui régissent leur activité, Evaluer les risques juridiques des opérations soumises, Assurer une veille législative, réglementaire et jurisprudentielle sur des sujets spécifiques et diffuser les informations utiles aux services concernés. Profil : Formation et expérience • Formation de niveau Bac+5 en Droit avec une spécialisation en droit de la Santé., • 5 ans d’expérience, • Niveau d’anglais professionnel requis (écrit et oral) Compétences et qualités • Solide capacité d’analyse juridique et compréhension d’environnements complexes, • Rigueur, fiabilité, sens des priorités et adaptabilité, • Intérêt pour la santé et les sciences, • Esprit de synthèse et capacité à proposer des solutions pragmatiques, • Aisance relationnelle, sens du service interne et pédagogie, • Goût pour le travail en équipe et les projets transverses Pourquoi rejoindre Généthon ? Un impact direct : vos idées et actions contribueront à changer la vie des patients atteints de maladies rares. Une expertise reconnue et pluridisciplinaire : 20 nationalités, 80 métiers différents, une richesse humaine au service d’un même objectif. Une mission inspirante dans un cadre enrichissant : innover pour guérir avec des opportunités de développement et un environnement inclusif Nous consacrons notre énergie à changer le monde et à innover pour guérir. Et vous ? LES MALADIES RARES ONT BESOIN DE TALENTS SINGULIERS

Job Type Full-time Description At CloudHQ, our mission is to deliver flexible, efficient, and resilient data center solutions to businesses worldwide. Founded by a pioneer in data center REITs, we are a rapidly growing organization with state-of-the-art data center sites globally in locations such as Ashburn, London, Frankfurt, Paris, Milan, Osaka, and São Paulo. As we embark on an exciting phase of global growth, we are looking for top-tier talent to drive our success and shape the future of CloudHQ. Role Overview The France Data Center Operations Lead is responsible for all operational activities across France, ensuring compliance, efficiency, and alignment with global strategies. This role requires strategic leadership, financial oversight, and team development across multiple sites. Key Responsibilities General Management and Leadership • Lead and manage all data center operations in France, ensuring alignment with regional and global strategies., • Develop and execute country-level operational plans, including cost optimization, compliance, and efficiency initiatives., • Build and lead high-performing teams across operations, properties, security, and compliance functions., • Coach, mentor, and develop direct managers, fostering leadership capabilities and succession planning., • Promote a culture of safety, compliance, and operational excellence across all sites., • Represent the company in industry forums, regulatory engagements, and with strategic partners. Operational Oversight • Ensure operational excellence across all sites, maintaining uptime, reliability, and adherence to global standards., • Define and monitor KPIs and performance metrics for operational efficiency and quality., • Drive continuous improvement in processes, sustainability, and risk management., • Collaborate with technical leadership for infrastructure scalability and resilience, without direct technical ownership., • Implement risk management strategies, including disaster recovery and business continuity plans. Financial and Regulatory Management • Manage country-level budgets, including planning, forecasting, and cost control., • Ensure compliance with local laws, regulations, and corporate governance standards., • Liaise with legal, finance, and compliance teams to mitigate risks and maintain operational integrity. Sustainability and Innovation • Lead initiatives for energy efficiency and carbon reduction across data center operations., • Explore and adopt innovative technologies to optimize operational performance and sustainability. Required Skills And Experience Education • Bachelor’s degree in Business, Operations Management, Engineering, or a related field., • MBA or equivalent preferred. Requirements Experience • Minimum of 10 years in operations management, with at least 5 years in a leadership role managing complex, multi-site environments., • Proven experience in data center operations or similar mission-critical infrastructure environments. Leadership Skills • Ability to lead cross-functional teams and develop managers., • Strong strategic thinking and decision-making capabilities. Technical Expertise • Deep understanding of data center infrastructure, including:, • Electrical systems (UPS, generators, PDUs), • Mechanical systems (HVAC, CRAC/CRAH), • Network connectivity (fiber, structured cabling), • Familiarity with DCIM (Data Center Infrastructure Management) and BMS (Building Management Systems) tools., • Knowledge of industry standards, including ISO 27001, ISO 50001, ASHRAE, TIA-942, and Uptime Institute Tier Standards., • Ability to implement disaster recovery and business continuity plans., • Understanding of energy efficiency metrics (e.g., PUE) and sustainability best practices. Other Skills • Strong financial acumen, including budgeting and forecasting., • Excellent communication and stakeholder management skills., • Ability to work effectively in a fast-paced, global environment. Language • Native French speaker with fluent English and professional business proficiency.

To support its growth, GenoTher – Medical Genetics Biocluster is recruiting a Scientific Project Manager, who will serve as an Associate to the Scientific Director of GenoTher. This position is intended for an experienced scientist who aims to contribute to the structuring and valorization of translational research in genetic medicine. The successful candidate will act as a strategic scientific interface between academic research, technological platforms, and innovation dynamics within the biocluster, working in close support of the Chief Scientific Officer (CSO). They will actively contribute to the coordination of the biocluster’s scientific activities and the animation of its scientific ecosystem Poste basé à : Évry (91) – Genopole Type de contrat : CDI – statut cadre Disponibilité : Juin 2026 About GenoTher : A biocluster of excellence accredited under the France 2030 plan, GenoTher supports project leaders in gene therapy to develop innovative solutions and address the challenges of this rapidly growing sector. Our mission is to foster therapeutic and technological innovation, provide access to cutting-edge platforms and expertise, and strengthen France’s leadership in gene therapy. Key Responsibilities 1. Scientific coordination and community building • Contribute to the coordination of the biocluster’s scientific activities., • Organize and structure thematic working groups., • Plan and coordinate meetings, workshops, and scientific events., • Draft meeting minutes, reports, and synthesis documents., • Ensure effective information flow across stakeholders (academic, technological, industrial)., • Monitor the implementation and follow-up of agreed actions., • Contribute to the animation of scientific networks and collaborations. 1. Coordination of translational scientific projects • Monitor collaborative projects with strong translational potential (proof of concept, maturation, preclinical stages)., • Support academic teams in transitioning from fundamental research to translational applications (gene therapy, genome editing, emerging modalities)., • Contribute to alignment between projects, technological platforms, and strategic priorities., • Identify scientific, technological, and translational bottlenecks. 1. Scientific expertise and strategic analysis • Provide high-level expertise in genetic medicine, including:, • genome editing technologies (CRISPR, base/prime editing, next-generation tools),, • delivery technologies, especially LNPs and non-viral approaches,, • integration of AI/data-driven methods in biomedical R&D., • Conduct state-of-the-art analyses, benchmarks, and scientific positioning notes., • Contribute to the preparation of strategic briefs, analyses, and decision-making materials., • Support the definition of R&D strategic priorities. 1. Interface between research, valorization, and innovation • Support evaluation of project valorization potential (maturation, partnerships, technology transfer)., • Interact with innovation stakeholders (TTOs, industry, investors, …)., • Contribute to the preparation of scientific dossiers for funding, partnerships, or incubation., • Promote a collaborative and translational culture within the ecosystem. 1. Support to the Scientific Direction • Prepare decision-support notes, strategic presentations, and governance materials., • Contribute to the organization and facilitation of scientific committees., • Provide recommendations on emerging scientific and technological trends. Profile Education and experience • PhD in biology, biotechnology, genetic medicine, or related field., • 10+ years of experience with exposure to translational research and/or innovation., • Proven experience at the research–innovation interface. Scientific skills • Expertise in genetic medicine and advanced therapies., • Strong knowledge of genome editing technologies., • Familiarity with LNPs and non-viral delivery systems., • Understanding of AI/computational approaches in biomedical research., • Ability to assess complex, multidisciplinary projects. Transversal skills • Excellent analytical, writing, and synthesis abilities., • Strong autonomy, critical thinking, and strategic mindset., • Organizational and coordination skills., • Ability to work in multi-stakeholder environments., • Strong networking and scientific communication skills., • Fluency in French is required (spoken and written); professional English is mandatory. Salary: Based on profile and experience Additional benefits: Health insurance with attractive coverage Remote working up to 2 days per week Why join us? Joining GenoTher means becoming part of an ambitious project dedicated to therapeutic innovation, within a dynamic and collaborative environment. You will have the opportunity to work with leading stakeholders and contribute to building a center of excellence in gene therapy.