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Convirtiéndote en agente comercial inmobiliario SAFTI:?Trabajas de forma autónoma y gestionas tu propio horario de trabajo.

Somos una compañía de Telecomunicaciones en pleno crecimiento.Durante los últimos años hemos creado más de 10.Por favor, asegúrese de leer atentamente los siguientes detalles antes de enviar cualquier solicitud.Desde DIGI necesitamos incorporar a un/a Operador NOC TV que desarrollará las sigu

Se busca profesional con experiencia en el sector de la hostelería, concretamente en gestión de canales.La persona seleccionada trabajará en San Sebastián de los Reyes, Madrid.Las principales funciones incluirán la supervisión de la conectividad entre sistemas como el PMS, Channel Manager, OTA

Se busca una persona con experiencia en limpieza general para encargarse del mantenimiento impecable de un gimnasio ubicado en Colmenar Viejo. Esta posición es ideal para quienes poseen un buen manejo de técnicas de limpieza y buscan estabilidad en su carrera profesional.

Buscamos un Director IT / Líder IT con sólida experiencia en liderazgo de equipos de departamentos tecnológicos de alto rendimiento.La persona seleccionada será responsable de dirigir, desarrollar y optimizar el área de software, garantizando la entrega de soluciones tecnológicas innovadoras,

Buscamos un Director IT / Líder IT con sólida experiencia en liderazgo de equipos de departamentos tecnológicos de alto rendimiento.

Se valorará la formación complementaria en procesos alimentarios y experiencia en liderazgo de equipos multidisciplinarios. La persona seleccionada liderará la implementación del sistema de gestión de calidad y seguridad alimentaria, supervisando todo el ciclo productivo. Con un mínimo de 7 a�

Direct message the job poster from Consultoría M&M Selección de Personal SL. Consultoría M&M Selección de Personal S. Referrals increase your chances of interviewing at Consultoría M&M Selección de Personal SL by 2x.

Buscamos un Director IT / Líder IT con sólida experiencia en liderazgo de equipos de departamentos tecnológicos de alto rendimiento.

Se busca camarero/a para trabajar en San Sebastián de los Reyes.

Desarrollo profesional en un grupo con proyectos en expansión.

Responsabilidades principales de mozo de almacén en Colmenar Viejo.

Una empresa de consultoría de IT está buscando un/a Administrador/a de Sistemas Citrix para un entorno estable en Tres Cantos.

Buscamos profesional de la limpieza con experiencia demostrable de al menos dos años para el mantenimiento de un centro deportivo. La formación específica no es un requisito, valoramos la destreza y eficacia en las tareas de limpieza industrial y mantenimiento de instalaciones deportivas. La fami

Buscamos una persona para trabajar en un almacén en Tres Cantos, dentro del sector tecnológico.Las principales responsabilidades del puesto incluirán llevar a cabo diversas tareas de gestión propias de un almacén, como la preparación y el envío de mercancías.También te encargarás de proces

Un puesto de reponedor/a está disponible para aquellos que busquen una oportunidad en el sector Retail.

¿Te apasiona la mejora de procesos y la innovación? Queremos incorporar a nuestro equipo de Mejora Continua a una persona con energía, iniciativa y ganas de crecer en un entorno dinámico y exigente. ¿Qué harás? ✔ Liderar proyectos de mejora continua en distintas áreas de la fábrica. ✔ Analizar procesos críticos para proponer mejoras y optimizaciones. ✔ Aplicar metodologías Lean Manufacturing y TPM en proyectos estratégicos. ✔ Impulsar la digitalización de procesos y la formación de equipos en excelencia operacional. ✔ Entender la estructura de costes para identificar pérdidas y desarrollar proyectos de ahorro. ¿Qué buscamos? Titulación en ingeniería. Valorable máster relacionado con mejora continua. Experiencia en metodologías de mejora continua. Dominio de TPM, Lean Manufacturing. Dominio de herramientas digitales (Power BI, Power Automate, Excel). Inglés profesional (mínimo B2). Actitud positiva, trabajo en equipo y adaptación al cambio. Si quieres formar parte de una empresa multinacional líder en su sector , con oportunidades de desarrollo y aprendizaje continuo, ¡este es tu momento! ¿Te interesa? ¡No dudes en aplicar a la posición para que podamos contarte más sobre la misma!

Te apasiona la mejora de procesos y la innovación? Queremos incorporar a nuestro equipo de Mejora Continua a una persona con energía, iniciativa y ganas de crecer en un entorno dinámico y exigente. ¿Liderar proyectos de mejora continua en distintas áreas de la fábrica. ✔ Aplicar metodologías Lean Manufacturing y TPM en proyectos estratégicos. ✔ Impulsar la digitalización de procesos y la formación de equipos en excelencia operacional. ✔ Entender la estructura de costes para identificar pérdidas y desarrollar proyectos de ahorro. ¿Titulación en ingeniería. Valorable máster relacionado con mejora continua. &##Experiencia en metodologías de mejora continua. &##Dominio de herramientas digitales (Power BI, Power Automate, Excel). &##Inglés profesional (mínimo B2). &##Actitud positiva, trabajo en equipo y adaptación al cambio. Si quieres formar parte de una empresa multinacional líder en su sector , con oportunidades de desarrollo y aprendizaje continuo, ¡este es tu momento! &##

Te apasiona la mejora de procesos y la innovación? Queremos incorporar a nuestro equipo de Mejora Continua a una persona con energía, iniciativa y ganas de crecer en un entorno dinámico y exigente. ¿Liderar proyectos de mejora continua en distintas áreas de la fábrica. ✔ Aplicar metodologías Lean Manufacturing y TPM en proyectos estratégicos. ✔ Impulsar la digitalización de procesos y la formación de equipos en excelencia operacional. ✔ Entender la estructura de costes para identificar pérdidas y desarrollar proyectos de ahorro. ¿Titulación en ingeniería. Valorable máster relacionado con mejora continua. &##Experiencia en metodologías de mejora continua. &##Dominio de herramientas digitales (Power BI, Power Automate, Excel). &##Inglés profesional (mínimo B2). &##Actitud positiva, trabajo en equipo y adaptación al cambio. Si quieres formar parte de una empresa multinacional líder en su sector , con oportunidades de desarrollo y aprendizaje continuo, ¡este es tu momento! &##

Te apasiona la mejora de procesos y la innovación? Queremos incorporar a nuestro equipo de Mejora Continua a una persona con energía, iniciativa y ganas de crecer en un entorno dinámico y exigente. ¿Liderar proyectos de mejora continua en distintas áreas de la fábrica. ✔ Aplicar metodologías Lean Manufacturing y TPM en proyectos estratégicos. ✔ Impulsar la digitalización de procesos y la formación de equipos en excelencia operacional. ✔ Entender la estructura de costes para identificar pérdidas y desarrollar proyectos de ahorro. ¿Titulación en ingeniería. Valorable máster relacionado con mejora continua. &##Experiencia en metodologías de mejora continua. &##Dominio de herramientas digitales (Power BI, Power Automate, Excel). &##Inglés profesional (mínimo B2). &##Actitud positiva, trabajo en equipo y adaptación al cambio. Si quieres formar parte de una empresa multinacional líder en su sector , con oportunidades de desarrollo y aprendizaje continuo, ¡este es tu momento! &##

We are looking for a Senior Dell Boomi Developer to join the integration team delivering a major government/public administration project. This professional will implement end‑to‑end integrations using Dell Boomi, contribute to defining reusable patterns, and work closely with the Integration Lead to ensure quality, robustness, and security across all integration flows. The role involves substantial ownership of development tasks, peer support, and participation in integration testing. Implement integrations involving ERP (Dynamics), CRM (HubSpot), storage (SharePoint/Box), CMS, LMS, and PIM tools. ~ Testing & Quality Assurance . Execute unit tests, integration tests, and end‑to‑end scenarios for the integrations developed. Collaborate with QA teams, frontend teams, and IV&V. ~ Support & Teamwork Support junior developers by reviewing code, helping unblock issues, and sharing best practices. Investigate issues in logs, Boomi process reporting, Atom/Molecule environments, and monitoring dashboards. 5–8 years of experience developing integrations using Dell Boomi or similar technologies (MuleSoft, Tibco,...) ~ Atoms/Molecules and Boomi deployment workflows ~ Solid understanding of API-based integrations, REST/SOAP, JSON, XML, and webhooks. ~ High level of English (C1) for communication with client teams.

¿Prompt Engineer con experiencia en proyectos de IA Generativa? ¿Buscas seguir creciendo en las mejores condiciones y con la mayor cercanía y flexibilidad? ¡Esto te interesa! En VASS, compañía líder en soluciones tecnológicas, buscamos Prompt Engineer para unirse de forma estable a nuestro equipo de IA. ¿Qué valoramos? Experiencia definiendo y revisando prompts, evaluando outputs de modelos y definiendo guidelines. Experiencia trabajando con equipos de datos/IA en proyectos de IA Generativa. Conocimientos en Python. Procesamiento de texto para clasificación, normalización y extracción. Gestión de proyectos. Conocimientos de APIs. ¿Qué ofrecemos? Un ambiente de trabajo colaborativo e inclusivo. Participar en proyectos de alto impacto. Modelo híbrido de trabajo con presencialidad de 1 día a la semana en las oficinas de cliente (Tres Cantos) y flexibilidad horaria. Plan de Carrera y Certificaciones: buscamos el crecimiento general y eso conlleva apoyar e incentivar el crecimiento de nuestros equipos a nivel laboral y personal. &##128640;&##128218; Si lo que acabas de leer encaja contigo y tienes interés en formar parte de un equipo innovador que impulsa la transformación digital en el sector, ¡queremos conocerte! ✨

Brindar soporte estratégico y operativo en las áreas de relaciones institucionales, comunicación corporativa y colaboración con asociaciones de pacientes, contribuyendo al desarrollo y ejecución de proyectos clave, campañas de concienciación y posicionamiento institucional. Coordinar con agencias externas la producción de notas de prensa, comunicados corporativos, materiales gráficos y audiovisuales. - Apoyar en la gestión de redes sociales y medios de comunicación. Dar soporte en la ejecución de proyectos conjuntos con asociaciones. - Formación Universitaria en Comunicación, Relaciones Internacionales, Ciencias Políticas, Ciencias de la Salud o afines. - Experiencia mínima de 2 años en funciones similares, preferentemente en el sector salud o farmacéutico. - Habilidades de comunicación, redacción, organización y trabajo transversal. - Nivel alto de inglés y dominio de herramientas digitales (Office 365, SharePoint, etc.). Vehículo de empresa. - Formación continua y desarrollo profesional. - Flexibilidad horaria y entorno colaborativo.

Brindar soporte estratégico y operativo en las áreas de relaciones institucionales, comunicación corporativa y colaboración con asociaciones de pacientes, contribuyendo al desarrollo y ejecución de proyectos clave, campañas de concienciación y posicionamiento institucional. Coordinar con agencias externas la producción de notas de prensa, comunicados corporativos, materiales gráficos y audiovisuales. - Apoyar en la gestión de redes sociales y medios de comunicación. Dar soporte en la ejecución de proyectos conjuntos con asociaciones. - Formación Universitaria en Comunicación, Relaciones Internacionales, Ciencias Políticas, Ciencias de la Salud o afines. - Experiencia mínima de 2 años en funciones similares, preferentemente en el sector salud o farmacéutico. - Habilidades de comunicación, redacción, organización y trabajo transversal. - Nivel alto de inglés y dominio de herramientas digitales (Office 365, SharePoint, etc.). Vehículo de empresa. - Formación continua y desarrollo profesional. - Flexibilidad horaria y entorno colaborativo.

JOB DESCRIPTION: Responsible for supporting global regulatory submissions and maintaining compliance with regulatory requirements for pharmaceutical products across multiple regions aligned with global regulatory strategies. This role involves preparing regulatory dossiers, coordinating with health authorities, ensuring product registration, and providing regulatory guidance to cross-functional teams. RESPONSABILITIES: Regulatory Submissions & Documentation Prepare, compile, revise, and submit global regulatory dossiers for new Marketing Authorization Applications (MAAs), variations, renewals, and lifecycle management activities. Collaborate in the preparation and/or revision of global regulatory submissions to ensure completeness, accuracy, alignment with company objectives, and compliance with the latest local and international regulations. Prepare documentation and submissions to Health Authorities, either directly or through local partners, ensuring regulatory compliance and supporting efficient product registration and maintenance. Support labelling and change control processes to ensure timely and comprehensive review and approval of packaging components (cartons, labels, Physician Insert, Patient Insert, Medication Guides). Manage other legal documentation required for registrations, such as Certificates of Pharmaceutical Product (CPPs). Maintain accurate and up-to-date regulatory documentation and regulatory files in accordance with global standards. Input regulatory intelligence, requirements, and submission data into relevant regulatory systems/databases, ensuring data accuracy and consistency. Regulatory Compliance, Strategy & Lifecycle Management Support the implementation of global regulatory strategies for assigned products to achieve regulatory approvals and maintain compliance throughout the product lifecycle. Advise and collaborate with cross-functional teams (R&D, QA, Manufacturing, etc.) on regulatory requirements to ensure successful market approval and lifecycle management. Contribute to regulatory intelligence activities and provide insights into the evolving global regulatory landscape. Regulatory Operations Contribute to the creation, maintenance, and improvement of the Regulatory Affairs Quality System, collaborating on the definition of processes and the implementation of global standard procedures. Maintain high-quality regulatory documentation and ensure compliance with procedural, regulatory, and system requirements across regions. Administrative and internal systems management (iPARTS, DACRA and any other tool). Knowledge Good knowledge of EMA, ICH, regulations and guidelines related to drug development, approval, and lifecycle management. Good knowledge of Extra EU countries’ regulation is preferred. Strong organizational skills with the ability to handle multiple regulatory projects simultaneously and manage multiple stakeholders. Good commercial and product awareness. Strong administrative and systems background, including experience with regulatory databases and document management tools. Position Impact Simultaneous management of multiple global regulatory projects with several internal and external stakeholders. High impact on regulatory compliance and ensuring product availability in the market. MINIMUM REQUIREMENTS: Minimum 3 years of experience in Regulatory roles within the Pharmaceutical Industry. Good knowledge of EMA and ICH regulations, guidelines, and regulatory processes regarding drug development, approval, and maintenance of marketing authorizations. Good knowledge of Extra EU countries’ regulation is preferred. Familiarity with eCTD submission, compilation, and publishing using specific tools. Good commercial and product awareness. Sound administrative and systems background. Ability to develop good cross-functional working relationships and tactical coordination of projects. Fluent in English, spoken and written is a must.

JOB DESCRIPTION: Responsible for supporting global regulatory submissions and maintaining compliance with regulatory requirements for pharmaceutical products across multiple regions aligned with global regulatory strategies. This role involves preparing regulatory dossiers, coordinating with health authorities, ensuring product registration, and providing regulatory guidance to cross-functional teams. RESPONSABILITIES: Regulatory Submissions & Documentation Prepare, compile, revise, and submit global regulatory dossiers for new Marketing Authorization Applications (MAAs), variations, renewals, and lifecycle management activities. Collaborate in the preparation and/or revision of global regulatory submissions to ensure completeness, accuracy, alignment with company objectives, and compliance with the latest local and international regulations. Prepare documentation and submissions to Health Authorities, either directly or through local partners, ensuring regulatory compliance and supporting efficient product registration and maintenance. Support labelling and change control processes to ensure timely and comprehensive review and approval of packaging components (cartons, labels, Physician Insert, Patient Insert, Medication Guides). Manage other legal documentation required for registrations, such as Certificates of Pharmaceutical Product (CPPs). Maintain accurate and up-to-date regulatory documentation and regulatory files in accordance with global standards. Input regulatory intelligence, requirements, and submission data into relevant regulatory systems/databases, ensuring data accuracy and consistency. Regulatory Compliance, Strategy & Lifecycle Management Support the implementation of global regulatory strategies for assigned products to achieve regulatory approvals and maintain compliance throughout the product lifecycle. Advise and collaborate with cross-functional teams (R&D, QA, Manufacturing, etc.) on regulatory requirements to ensure successful market approval and lifecycle management. Contribute to regulatory intelligence activities and provide insights into the evolving global regulatory landscape. Regulatory Operations Contribute to the creation, maintenance, and improvement of the Regulatory Affairs Quality System, collaborating on the definition of processes and the implementation of global standard procedures. Maintain high-quality regulatory documentation and ensure compliance with procedural, regulatory, and system requirements across regions. Administrative and internal systems management (iPARTS, DACRA and any other tool). Knowledge Good knowledge of EMA, ICH, regulations and guidelines related to drug development, approval, and lifecycle management. Good knowledge of Extra EU countries’ regulation is preferred. Strong organizational skills with the ability to handle multiple regulatory projects simultaneously and manage multiple stakeholders. Good commercial and product awareness. Strong administrative and systems background, including experience with regulatory databases and document management tools. Position Impact Simultaneous management of multiple global regulatory projects with several internal and external stakeholders. High impact on regulatory compliance and ensuring product availability in the market. MINIMUM REQUIREMENTS: Minimum 3 years of experience in Regulatory roles within the Pharmaceutical Industry. Good knowledge of EMA and ICH regulations, guidelines, and regulatory processes regarding drug development, approval, and maintenance of marketing authorizations. Good knowledge of Extra EU countries’ regulation is preferred. Familiarity with eCTD submission, compilation, and publishing using specific tools. Good commercial and product awareness. Sound administrative and systems background. Ability to develop good cross-functional working relationships and tactical coordination of projects. Fluent in English, spoken and written is a must.

JOB DESCRIPTION: Responsible for supporting global regulatory submissions and maintaining compliance with regulatory requirements for pharmaceutical products across multiple regions aligned with global regulatory strategies. This role involves preparing regulatory dossiers, coordinating with health authorities, ensuring product registration, and providing regulatory guidance to cross-functional teams. RESPONSABILITIES: Regulatory Submissions & Documentation Prepare, compile, revise, and submit global regulatory dossiers for new Marketing Authorization Applications (MAAs), variations, renewals, and lifecycle management activities. Collaborate in the preparation and/or revision of global regulatory submissions to ensure completeness, accuracy, alignment with company objectives, and compliance with the latest local and international regulations. Prepare documentation and submissions to Health Authorities, either directly or through local partners, ensuring regulatory compliance and supporting efficient product registration and maintenance. Support labelling and change control processes to ensure timely and comprehensive review and approval of packaging components (cartons, labels, Physician Insert, Patient Insert, Medication Guides). Manage other legal documentation required for registrations, such as Certificates of Pharmaceutical Product (CPPs). Maintain accurate and up-to-date regulatory documentation and regulatory files in accordance with global standards. Input regulatory intelligence, requirements, and submission data into relevant regulatory systems/databases, ensuring data accuracy and consistency. Regulatory Compliance, Strategy & Lifecycle Management Support the implementation of global regulatory strategies for assigned products to achieve regulatory approvals and maintain compliance throughout the product lifecycle. Advise and collaborate with cross-functional teams (R&D, QA, Manufacturing, etc.) on regulatory requirements to ensure successful market approval and lifecycle management. Contribute to regulatory intelligence activities and provide insights into the evolving global regulatory landscape. Regulatory Operations Contribute to the creation, maintenance, and improvement of the Regulatory Affairs Quality System, collaborating on the definition of processes and the implementation of global standard procedures. Maintain high-quality regulatory documentation and ensure compliance with procedural, regulatory, and system requirements across regions. Administrative and internal systems management (iPARTS, DACRA and any other tool). Knowledge Good knowledge of EMA, ICH, regulations and guidelines related to drug development, approval, and lifecycle management. Good knowledge of Extra EU countries’ regulation is preferred. Strong organizational skills with the ability to handle multiple regulatory projects simultaneously and manage multiple stakeholders. Good commercial and product awareness. Strong administrative and systems background, including experience with regulatory databases and document management tools. Position Impact Simultaneous management of multiple global regulatory projects with several internal and external stakeholders. High impact on regulatory compliance and ensuring product availability in the market. MINIMUM REQUIREMENTS: Minimum 3 years of experience in Regulatory roles within the Pharmaceutical Industry. Good knowledge of EMA and ICH regulations, guidelines, and regulatory processes regarding drug development, approval, and maintenance of marketing authorizations. Good knowledge of Extra EU countries’ regulation is preferred. Familiarity with eCTD submission, compilation, and publishing using specific tools. Good commercial and product awareness. Sound administrative and systems background. Ability to develop good cross-functional working relationships and tactical coordination of projects. Fluent in English, spoken and written is a must.

JOB DESCRIPTION: Responsible for supporting global regulatory submissions and maintaining compliance with regulatory requirements for pharmaceutical products across multiple regions aligned with global regulatory strategies. This role involves preparing regulatory dossiers, coordinating with health authorities, ensuring product registration, and providing regulatory guidance to cross-functional teams. RESPONSABILITIES: Regulatory Submissions & Documentation Prepare, compile, revise, and submit global regulatory dossiers for new Marketing Authorization Applications (MAAs), variations, renewals, and lifecycle management activities. Collaborate in the preparation and/or revision of global regulatory submissions to ensure completeness, accuracy, alignment with company objectives, and compliance with the latest local and international regulations. Prepare documentation and submissions to Health Authorities, either directly or through local partners, ensuring regulatory compliance and supporting efficient product registration and maintenance. Support labelling and change control processes to ensure timely and comprehensive review and approval of packaging components (cartons, labels, Physician Insert, Patient Insert, Medication Guides). Manage other legal documentation required for registrations, such as Certificates of Pharmaceutical Product (CPPs). Maintain accurate and up-to-date regulatory documentation and regulatory files in accordance with global standards. Input regulatory intelligence, requirements, and submission data into relevant regulatory systems/databases, ensuring data accuracy and consistency. Regulatory Compliance, Strategy & Lifecycle Management Support the implementation of global regulatory strategies for assigned products to achieve regulatory approvals and maintain compliance throughout the product lifecycle. Advise and collaborate with cross-functional teams (R&D, QA, Manufacturing, etc.) on regulatory requirements to ensure successful market approval and lifecycle management. Contribute to regulatory intelligence activities and provide insights into the evolving global regulatory landscape. Regulatory Operations Contribute to the creation, maintenance, and improvement of the Regulatory Affairs Quality System, collaborating on the definition of processes and the implementation of global standard procedures. Maintain high-quality regulatory documentation and ensure compliance with procedural, regulatory, and system requirements across regions. Administrative and internal systems management (iPARTS, DACRA and any other tool). Knowledge Good knowledge of EMA, ICH, regulations and guidelines related to drug development, approval, and lifecycle management. Good knowledge of Extra EU countries’ regulation is preferred. Strong organizational skills with the ability to handle multiple regulatory projects simultaneously and manage multiple stakeholders. Good commercial and product awareness. Strong administrative and systems background, including experience with regulatory databases and document management tools. Position Impact Simultaneous management of multiple global regulatory projects with several internal and external stakeholders. High impact on regulatory compliance and ensuring product availability in the market. MINIMUM REQUIREMENTS: Minimum 3 years of experience in Regulatory roles within the Pharmaceutical Industry. Good knowledge of EMA and ICH regulations, guidelines, and regulatory processes regarding drug development, approval, and maintenance of marketing authorizations. Good knowledge of Extra EU countries’ regulation is preferred. Familiarity with eCTD submission, compilation, and publishing using specific tools. Good commercial and product awareness. Sound administrative and systems background. Ability to develop good cross-functional working relationships and tactical coordination of projects. Fluent in English, spoken and written is a must.

ACCIONA, en su división de Facility Services, selecciona un/a Eléctrico/a en San Sebastián de los Reyes Funciones: Realizar el mantenimiento preventivo y correctivo de instalaciones en eléctricas de CPDs, centrales de distribución, grupos electrógenos, etc. Condiciones: Contrato indefinido. Jornada: de lunes a viernes, turno rotativo mañana de 7 a 15 y tardes de 12 a 20 hrs. Salario: valorable de acuerdo con el perfil del candidato/a + guardias. Ubicación: San Sebastián de los Reyes. Requisitos: Contar con formación profesional en Electricidad o afines. Con experiencia mínima de 3 años.

ACCIONA, en su división de Facility Services, selecciona un/a Técnico/a de Climatización para importante cliente ubicado en San Sebastián de los Reyes Funciones: Mantenimiento de instalaciones frigoríficas. Mantenimiento de instalaciones térmicas de edificios. Condiciones: Contrato indefinido. Jornada: de lunes a viernes, en turnos rotativos de mañana 7 a 15 h y tarde de 12 a 20 h Salario: valorable de acuerdo al perfil del candidato/a + guardias Ubicación: San Sebastián de los Reyes Requisitos: Deseable contar con formación profesional Técnico Superior de Instalaciones Térmicas y Fluidos, o Instalaciones Frigoríficas y Climatización o afines. Indispensable contar con RITE y/o manejo de gases fluorados. Conocimientos en calderas, climatización, frio industrial, gases fluorados, electricidad, fontanería.

NEGRATIN , empresa referente en el sector de las energías renovables e instalaciones, con más de 25 años de experiencia. Nos encontramos en búsqueda de un Técnico de ofertas T&D con experiencia en líneas (imprescindible). FUNCIONES: -Coordinar la preparación de ofertas para los proyectos de T&D, asegurando la integración de aspectos técnicos, económicos y comerciales -Trabajar estrechamente con los equipos de ingeniería, compras, operaciones, gestión contractual, finanzas y RRHH -Cumplimiento del presupuesto de contratación marcado por el consejo de Administración -Participar en la negociación junto con la Dirección general y la dirección de contratación los términos y condiciones con clientes SE OFRECE: Formar parte de una empresa multinacional y sostenible en el sector con posibilidades de desarrollo profesional- Formar parte de un equipo humano multidisciplinar, eficiente y altamente comprometidos Modelo híbrido Buen clima y entorno laboral Paquete retributivo acorde a la experiencia y sector Retribución flexible y beneficios sociales En Negratin, valoramos la diversidad y estamos comprometidos con la igualdad de oportunidades, garantizando un proceso de selección libre de discriminación por razones de género, promoviendo la equidad entre hombres y mujeres"

Join Satlink, a world leading technology group that develops solutions focused on ocean knowledge and sustainability, improving the management of marine resources and working closely with scientific institutions, governments, NGOs and the industry as a whole. With a family of top-tier brands, our complete porfolio of companies, technologies and data solutions deepen the understanding of the ocean ecosystem, and solve real operational challenges across all marine industries. With decades of in-house expertise, we are a trusted technology partner for +10.000 customers around the world. Within our team, we strongly value creativity, collaboration, and the continuous pursuit of innovative solutions. In this position, based at our Madrid premises, you will play a key role in driving NKE’s B2B sales across Spain, Portugal, and Latin America. You will work closely with both Satlink and NKE teams , leading strategic sales initiatives, building strong relationships with customers and partners, and supporting the growth of turnkey projects in the region. Role and Responsibilities: Develop and execute the regional NKE sales strategy for Spain, Portugal, and Latin America, targeting revenue, margin, and market growth Build country‑specific sales plans, and position Spain as a domestic market for NKE turnkey projects Implement a hybrid sales model in Spain and Portugal, maintaining direct relationships with key customers and partners Identify, onboard, and manage distributors across Latin America, monitor performance, and provide training & support on key products and tenders Lead commercial negotiations, manage key accounts, and close deals aligned with strategic objectives Oversee turnkey project scoping, proposals, and commercial governance for Spain as a new domestic market for NKE, ensuring smooth handover to the Project Management Office Coordinate closely with technical, pre‑sales, marketing, and product teams in Madrid and NKE offices to share market insights and shape local offers Support marketing initiatives and leverage synergies within Satlink and Ocean Data teams for bundled propositions Represent the company at industry shows and professional events to strengthen visibility, and develop and maintain a strong network of customers, partners, and influencers Qualifications and Education Requirements: Bachelor’s degree in Engineering, Environmental Sciences, Telecommunications, Business Administration, or equivalent 5+ years of proven experience in international B2B sales, managing distributors or strategic partners Experience in technology, environmental, water, or instrumentation sectors is desirable Experience managing clients and distributors in Spain, Portugal, and Latin America, with the ability to adapt to different business cultures Ability to develop regional sales strategies, manage key accounts, and collaborate with cross-functional teams in international environments Proactive, results-oriented mindset with a strong drive to take on commercial challenges in a growing technology environment Availability for international travel as required Languages: English (C1), Portuguese (high level), French (desirable) What We Offer Competitive fixed salary in line with the candidate’s experience and skills Young, stimulating, collaborative, and motivating work environment Opportunities for professional development and growth in a constantly evolving technology environment In compliance with Regulation (EU) 2016/679, we inform you that your personal data will be processed by Satlink S.L. for the purpose of including your application in our recruitment processes. You can exercise your data protection rights by contacting . Additional information on how your data is processed is available in our Privacy Policy at

¿Prompt Engineer con experiencia en proyectos de IA Generativa? ¿Buscas seguir creciendo en las mejores condiciones y con la mayor cercanía y flexibilidad? ¡Esto te interesa! En VASS, compañía líder en soluciones tecnológicas, buscamos Prompt Engineer para unirse de forma estable a nuestro equipo de IA. ¿Qué valoramos? Experiencia definiendo y revisando prompts, evaluando outputs de modelos y definiendo guidelines. Experiencia trabajando con equipos de datos/IA en proyectos de IA Generativa. Conocimientos en Python. Procesamiento de texto para clasificación, normalización y extracción. Gestión de proyectos. Conocimientos de APIs. ¿Qué ofrecemos? Un ambiente de trabajo colaborativo e inclusivo. Participar en proyectos de alto impacto. Modelo híbrido de trabajo con presencialidad de 1 día a la semana en las oficinas de cliente (Tres Cantos) y flexibilidad horaria. Plan de Carrera y Certificaciones: buscamos el crecimiento general y eso conlleva apoyar e incentivar el crecimiento de nuestros equipos a nivel laboral y personal. &##128640;&##128218; Si lo que acabas de leer encaja contigo y tienes interés en formar parte de un equipo innovador que impulsa la transformación digital en el sector, ¡queremos conocerte! ✨

¿Prompt Engineer con experiencia en proyectos de IA Generativa? ¿Buscas seguir creciendo en las mejores condiciones y con la mayor cercanía y flexibilidad? ¡Esto te interesa! En VASS, compañía líder en soluciones tecnológicas, buscamos Prompt Engineer para unirse de forma estable a nuestro equipo de IA. ¿Qué valoramos? Experiencia definiendo y revisando prompts, evaluando outputs de modelos y definiendo guidelines. Experiencia trabajando con equipos de datos/IA en proyectos de IA Generativa. Conocimientos en Python. Procesamiento de texto para clasificación, normalización y extracción. Gestión de proyectos. Conocimientos de APIs. ¿Qué ofrecemos? Un ambiente de trabajo colaborativo e inclusivo. Participar en proyectos de alto impacto. Modelo híbrido de trabajo con presencialidad de 1 día a la semana en las oficinas de cliente (Tres Cantos) y flexibilidad horaria. Plan de Carrera y Certificaciones: buscamos el crecimiento general y eso conlleva apoyar e incentivar el crecimiento de nuestros equipos a nivel laboral y personal. Si lo que acabas de leer encaja contigo y tienes interés en formar parte de un equipo innovador que impulsa la transformación digital en el sector, ¡queremos conocerte! ✨

Te apasiona la mejora de procesos y la innovación? Queremos incorporar a nuestro equipo de Mejora Continua a una persona con energía, iniciativa y ganas de crecer en un entorno dinámico y exigente. ¿Liderar proyectos de mejora continua en distintas áreas de la fábrica. ✔ Aplicar metodologías Lean Manufacturing y TPM en proyectos estratégicos. ✔ Impulsar la digitalización de procesos y la formación de equipos en excelencia operacional. ✔ Entender la estructura de costes para identificar pérdidas y desarrollar proyectos de ahorro. ¿Titulación en ingeniería. Valorable máster relacionado con mejora continua. &##Experiencia en metodologías de mejora continua. &##Dominio de herramientas digitales (Power BI, Power Automate, Excel). &##Inglés profesional (mínimo B2). &##Actitud positiva, trabajo en equipo y adaptación al cambio. Si quieres formar parte de una empresa multinacional líder en su sector , con oportunidades de desarrollo y aprendizaje continuo, ¡este es tu momento! &##

️ Técnico Sistemas | Híbrido – Tres Cantos Tres Cantos (Madrid) | Híbrido | ️ Infraestructura · Seguridad · Puesto de Trabajo ¿Eres un perfil senior con una visión global de sistemas, infraestructura y puesto de trabajo? Buscamos un Técnico Senior capaz de liderar despliegues, automatizaciones, entornos híbridos y administración avanzada de Active Directory. Qué harás (tu impacto) Automatización y scripting con Powershell. Despliegue de equipos mediante MDT, SCCM e Intune . Migraciones de sistemas operativos en entornos corporativos. Administración de entornos híbridos y servicios cloud. Desarrollo de aplicaciones internas (scripts, herramientas, automatización). ️ Gestión de máquinas virtuales : Proxmox, VMware, VirtualBox. Administración avanzada de Active Directory y GPOs . Gestión de almacenamiento, bases de datos y servidores . Operación en comunicaciones y seguridad del puesto . Lo que te hará brillar ✔️ Sólida experiencia en administración de sistemas y entornos híbridos. ✔️ Dominio real de Powershell y automatización. ✔️ Experiencia con herramientas de despliegue y gestión de dispositivos. ✔️ Conocimiento profundo de virtualización. ✔️ Perfil resolutivo, autónomo y con visión global de infraestructura. Por qué unirte Porque asumirás un rol clave, transversal y altamente técnico donde tu experiencia marca la diferencia. Serás la referencia técnica en un entorno moderno, seguro y de alto nivel. ¿Te interesa? Aplica tu perfil. ¡Encantados de darte más detalles! #Sistemas #ActiveDirectory #Powershell #MDT #SCCM #Intune #VMware #Proxmox #VirtualBox #InfraestructuraIT #Ciberseguridad #AdministradorSistemas #ITJobs #EmpleoIT #TresCantos #SeniorIT #TechJobs

Ria Money Transfer, a business segment of Euronet Worldwide, Inc. (NASDAQ: EEFT), delivers innovative financial services including fast, secure, and affordable global money transfers to millions of customers along with currency exchange, mobile top-up, bill payment and check cashing services, offering a reliable omnichannel experience. With over 600,000 locations in nearly 200 countries and territories, our purpose remains to open ways for a better everyday life. We believe we can create a world in which people are empowered to build the life they dream of, no matter who they are or where they are. One customer, one family, one community at a time. ABOUT THIS ROLE As a Compliance Specialist AI, in COMPLIANCE DEP your role will be: The Compliance Specialist AI supports the design, implementation, and ongoing enhancement of controls related to Machine Learning systems, ensuring alignment with applicable regulations and internal policies. The Analyst collaborates with cross-functional teams to identify risks, assess and enhance controls, evaluate datasets, and support responsible teams across the organization. ROLES & RESPONSIBILITIES • Assist in implementing compliance controls that align with global requirements. • Support the documentation, review, and maintenance of AI products such as the fraud detection model and decision engine system. • Conduct assessments for new or existing AI models and tools. • Evaluate risks related to data quality, model performance, bias, and human oversight. • Support the development of risk mitigation plans and monitor control effectiveness. Monitoring • Assist in reviewing model documentation, including testing and validation reports. • Support ongoing monitoring activities such as drift detection, and periodic compliance reviews. • Ensure evidence and audit trails are properly maintained. Issue Management & Remediation • Identify control gaps or regulatory deficiencies in AI workflows. • Track remediation activities and ensure timely closure of issues. • Prepare summaries of findings for Compliance leadership and Risk Committees. • Work closely with Product, Engineering, Legal, Data Science, Information Security, and Risk teams. • Participate in model review committees or AI governance forums. • Support training and awareness initiatives related to responsible AI and regulatory requirements. Reporting & Documentation • Prepare compliance reports, dashboards, and metrics related to AI risk and control health. • Maintain project documentation aligned with internal audit and regulatory expectations. • Support responses to regulatory inquiries and internal/external audits. POSITION REQUIREMENTS • Strong understanding of compliance, risk management, or regulatory frameworks. • Familiarity with AI/ML concepts. • High school graduated, college degree is a plus • Knowledge and experience in Microsoft Office preferred • 3 years Compliance Experience • Strong knowledge of new AI-based tools and their application in Compliance. • C1 level in English.

Ria Money Transfer, a business segment of Euronet Worldwide, Inc. (NASDAQ: EEFT), delivers innovative financial services including fast, secure, and affordable global money transfers to millions of customers along with currency exchange, mobile top-up, bill payment and check cashing services, offering a reliable omnichannel experience. With over 600,000 locations in nearly 200 countries and territories, our purpose remains to open ways for a better everyday life. We believe we can create a world in which people are empowered to build the life they dream of, no matter who they are or where they are. One customer, one family, one community at a time. ABOUT THIS ROLE As a Compliance Specialist AI, in COMPLIANCE DEP your role will be: The Compliance Specialist AI supports the design, implementation, and ongoing enhancement of controls related to Machine Learning systems, ensuring alignment with applicable regulations and internal policies. The Analyst collaborates with cross-functional teams to identify risks, assess and enhance controls, evaluate datasets, and support responsible teams across the organization. ROLES & RESPONSIBILITIES • Assist in implementing compliance controls that align with global requirements. • Support the documentation, review, and maintenance of AI products such as the fraud detection model and decision engine system. • Conduct assessments for new or existing AI models and tools. • Evaluate risks related to data quality, model performance, bias, and human oversight. • Support the development of risk mitigation plans and monitor control effectiveness. Monitoring • Assist in reviewing model documentation, including testing and validation reports. • Support ongoing monitoring activities such as drift detection, and periodic compliance reviews. • Ensure evidence and audit trails are properly maintained. Issue Management & Remediation • Identify control gaps or regulatory deficiencies in AI workflows. • Track remediation activities and ensure timely closure of issues. • Prepare summaries of findings for Compliance leadership and Risk Committees. • Work closely with Product, Engineering, Legal, Data Science, Information Security, and Risk teams. • Participate in model review committees or AI governance forums. • Support training and awareness initiatives related to responsible AI and regulatory requirements. Reporting & Documentation • Prepare compliance reports, dashboards, and metrics related to AI risk and control health. • Maintain project documentation aligned with internal audit and regulatory expectations. • Support responses to regulatory inquiries and internal/external audits. POSITION REQUIREMENTS • Strong understanding of compliance, risk management, or regulatory frameworks. • Familiarity with AI/ML concepts. • High school graduated, college degree is a plus • Knowledge and experience in Microsoft Office preferred • 3 years Compliance Experience • Strong knowledge of new AI-based tools and their application in Compliance. • C1 level in English.

Logistics Intern Are you studying Industrial Engineering or Business Administration and have a strong interest in Supply Chain & Logistics? This is a great opportunity to gain hands-on experience and start building your career in an international environment. Location: Alcobendas (Madrid) Duration: 6 months ✨ What you’ll be involved in Scheduling appointments with freight carriers and customer warehouses Processing and verifying shipping documentation Maintaining inbound and outbound shipment records Supporting daily warehouse activities and inventory stocktakes Coordinating with other departments (sales, engineering, etc.) to ensure smooth logistics operations What we’re looking for Degree or ongoing studies in Industrial Engineering or Business Administration Strong interest in Supply Chain and Logistics English level B2 or C1 Good command of Microsoft Excel Willingness to learn ERP / WMS systems Strong communication skills, sense of responsibility, and proactive attitude No previous experience required Why join us? You’ll gain exposure to real logistics operations, work closely with experienced professionals, and develop key skills for a future career in Supply Chain.

Ria Money Transfer, a business segment of Euronet Worldwide, Inc. (NASDAQ: EEFT), delivers innovative financial services including fast, secure, and affordable global money transfers to millions of customers along with currency exchange, mobile top-up, bill payment and check cashing services, offering a reliable omnichannel experience. With over 600,000 locations in nearly 200 countries and territories, our purpose remains to open ways for a better everyday life. We believe we can create a world in which people are empowered to build the life they dream of, no matter who they are or where they are. One customer, one family, one community at a time. ABOUT THIS ROLE As a Compliance Specialist AI, in COMPLIANCE DEP your role will be: The Compliance Specialist AI supports the design, implementation, and ongoing enhancement of controls related to Machine Learning systems, ensuring alignment with applicable regulations and internal policies. The Analyst collaborates with cross-functional teams to identify risks, assess and enhance controls, evaluate datasets, and support responsible teams across the organization. ROLES & RESPONSIBILITIES • Assist in implementing compliance controls that align with global requirements. • Support the documentation, review, and maintenance of AI products such as the fraud detection model and decision engine system. • Conduct assessments for new or existing AI models and tools. • Evaluate risks related to data quality, model performance, bias, and human oversight. • Support the development of risk mitigation plans and monitor control effectiveness. Monitoring • Assist in reviewing model documentation, including testing and validation reports. • Support ongoing monitoring activities such as drift detection, and periodic compliance reviews. • Ensure evidence and audit trails are properly maintained. Issue Management & Remediation • Identify control gaps or regulatory deficiencies in AI workflows. • Track remediation activities and ensure timely closure of issues. • Prepare summaries of findings for Compliance leadership and Risk Committees. • Work closely with Product, Engineering, Legal, Data Science, Information Security, and Risk teams. • Participate in model review committees or AI governance forums. • Support training and awareness initiatives related to responsible AI and regulatory requirements. Reporting & Documentation • Prepare compliance reports, dashboards, and metrics related to AI risk and control health. • Maintain project documentation aligned with internal audit and regulatory expectations. • Support responses to regulatory inquiries and internal/external audits. POSITION REQUIREMENTS • Strong understanding of compliance, risk management, or regulatory frameworks. • Familiarity with AI/ML concepts. • High school graduated, college degree is a plus • Knowledge and experience in Microsoft Office preferred • 3 years Compliance Experience • Strong knowledge of new AI-based tools and their application in Compliance. • C1 level in English.

About the Company OMODA Motors is a new brand built by Chery Group, which is a leading Chinese automobile company. OMODA operates individually from other brands of Chery Group. Its business scope covers the R&D, production and sales of passenger cars. Main Responsibilities Manage day-to-day operations of the parts department, ensuring efficient workflows and on-time parts availability Develop and execute parts supply and inventory strategies to meet business and service needs Monitor stock levels, turnover, obsolescence, and backorders to optimize inventory performance Manage supplier relationships, including OEMs and third-party vendors Negotiate pricing, terms, and logistics conditions when applicable Ensure accurate parts forecasting based on sales, service demand, and historical data Collaborate closely with Aftersales and Service teams to support workshop efficiency and customer satisfaction Implement and monitor KPIs (availability, fill rate, stock rotation, margins, obsolete stock) Ensure compliance with company policies, quality standards, and brand requirements Lead, coach, and develop the parts team (if applicable) Drive continuous improvement in systems, processes, and cost control Regular visits to Warehouse and Dealer network Act as a liaison between the market and HQ to drive continuous improvement initiatives and reporting Requirements Proven experience as a Parts Manager or similar role within the automotive sector Strong knowledge of automotive parts, logistics, and supply chain processes Experience working with OEM standards and dealer networks (preferred) Solid understanding of inventory management and forecasting Strong analytical and organizational skills Proficient in ERP/DMS systems and Excel Strong communication and leadership skills We inform you that OMODA MOTORS SPAIN S.L., a company with its registered office in Modulo 1 de la planta baja, Avda. Brusuelas 36, 28108, Alcobendas, Madrid, with CIF B56485493 (hereinafter referred to as the "Company"), will process your personal data on the basis of your express consent for the purposes of managing your job application. Your personal data will be transferred to Chery Automobile Co. Ltd (parent company of the Group), a company based in China, in order to carry out the process you have voluntarily requested. As stated in the European Data Protection Regulation (GDPR), we inform you that the Personal Information Protection Law of the People's Republic of China (PIPL) may conflict with the GDPR and in some scenarios. Your personal data will be kept for 2 years and then delete. Additionally, you may exercise your data protection rights (access, rectification, opposition, cancellation, etc.) by sending an e-mail to indicating the right you wish to exercise and your identification details. If you consider that we have not handled your personal data appropriately, you may contact the Data Protection Officer at . However, we inform you that you have the right to lodge a complaint with the Spanish Data Protection Agency if you consider that there has been a breach of data protection legislation with regard to the processing of your personal data.

About the Company OMODA Motors is a new brand built by Chery Group, which is a leading Chinese automobile company. OMODA operates individually from other brands of Chery Group. Its business scope covers the R&D, production and sales of passenger cars. Develop and execute parts supply and inventory strategies to meet business and service needs Monitor stock levels, turnover, obsolescence, and backorders to optimize inventory performance Ensure accurate parts forecasting based on sales, service demand, and historical data Ensure compliance with company policies, quality standards, and brand requirements Drive continuous improvement in systems, processes, and cost control Regular visits to Warehouse and Dealer network Proven experience as a Parts Manager or similar role within the automotive sector Experience working with OEM standards and dealer networks (preferred) Solid understanding of inventory management and forecasting Proficient in ERP/DMS systems and Excel a company with its registered office in Modulo 1 de la planta baja, Avda. Brusuelas 36, 28108, Alcobendas, Madrid, with CIF B56485493 (hereinafter referred to as the "Company"), will process your personal data on the basis of your express consent for the purposes of managing your job application. Your personal data will be transferred to Chery Automobile Co. Ltd (parent company of the Group), a company based in China, in order to carry out the process you have voluntarily requested. As stated in the European Data Protection Regulation (GDPR), we inform you that the Personal Information Protection Law of the People's Republic of China (PIPL) may conflict with the GDPR and in some scenarios. Your personal data will be kept for 2 years and then delete. Additionally, you may exercise your data protection rights (access, rectification, opposition, cancellation, etc.) If you consider that we have not handled your personal data appropriately, you may contact the Data Protection Officer at , we inform you that you have the right to lodge a complaint with the Spanish Data Protection Agency if you consider that there has been a breach of data protection legislation with regard to the processing of your personal data.

About the Company OMODA Motors is a new brand built by Chery Group, which is a leading Chinese automobile company. OMODA operates individually from other brands of Chery Group. Its business scope covers the R&D, production and sales of passenger cars. Develop and execute parts supply and inventory strategies to meet business and service needs Monitor stock levels, turnover, obsolescence, and backorders to optimize inventory performance Ensure accurate parts forecasting based on sales, service demand, and historical data Ensure compliance with company policies, quality standards, and brand requirements Drive continuous improvement in systems, processes, and cost control Regular visits to Warehouse and Dealer network Proven experience as a Parts Manager or similar role within the automotive sector Experience working with OEM standards and dealer networks (preferred) Solid understanding of inventory management and forecasting Proficient in ERP/DMS systems and Excel a company with its registered office in Modulo 1 de la planta baja, Avda. Brusuelas 36, 28108, Alcobendas, Madrid, with CIF B56485493 (hereinafter referred to as the "Company"), will process your personal data on the basis of your express consent for the purposes of managing your job application. Your personal data will be transferred to Chery Automobile Co. Ltd (parent company of the Group), a company based in China, in order to carry out the process you have voluntarily requested. As stated in the European Data Protection Regulation (GDPR), we inform you that the Personal Information Protection Law of the People's Republic of China (PIPL) may conflict with the GDPR and in some scenarios. Your personal data will be kept for 2 years and then delete. Additionally, you may exercise your data protection rights (access, rectification, opposition, cancellation, etc.) If you consider that we have not handled your personal data appropriately, you may contact the Data Protection Officer at , we inform you that you have the right to lodge a complaint with the Spanish Data Protection Agency if you consider that there has been a breach of data protection legislation with regard to the processing of your personal data.

About the Company OMODA Motors is a new brand built by Chery Group, which is a leading Chinese automobile company. OMODA operates individually from other brands of Chery Group. Its business scope covers the R&D, production and sales of passenger cars. Develop and execute parts supply and inventory strategies to meet business and service needs Monitor stock levels, turnover, obsolescence, and backorders to optimize inventory performance Ensure accurate parts forecasting based on sales, service demand, and historical data Ensure compliance with company policies, quality standards, and brand requirements Drive continuous improvement in systems, processes, and cost control Regular visits to Warehouse and Dealer network Proven experience as a Parts Manager or similar role within the automotive sector Experience working with OEM standards and dealer networks (preferred) Solid understanding of inventory management and forecasting Proficient in ERP/DMS systems and Excel a company with its registered office in Modulo 1 de la planta baja, Avda. Brusuelas 36, 28108, Alcobendas, Madrid, with CIF B56485493 (hereinafter referred to as the "Company"), will process your personal data on the basis of your express consent for the purposes of managing your job application. Your personal data will be transferred to Chery Automobile Co. Ltd (parent company of the Group), a company based in China, in order to carry out the process you have voluntarily requested. As stated in the European Data Protection Regulation (GDPR), we inform you that the Personal Information Protection Law of the People's Republic of China (PIPL) may conflict with the GDPR and in some scenarios. Your personal data will be kept for 2 years and then delete. Additionally, you may exercise your data protection rights (access, rectification, opposition, cancellation, etc.) If you consider that we have not handled your personal data appropriately, you may contact the Data Protection Officer at , we inform you that you have the right to lodge a complaint with the Spanish Data Protection Agency if you consider that there has been a breach of data protection legislation with regard to the processing of your personal data.

About the Company OMODA Motors is a new brand built by Chery Group, which is a leading Chinese automobile company. OMODA operates individually from other brands of Chery Group. Its business scope covers the R&D, production and sales of passenger cars. Develop and execute parts supply and inventory strategies to meet business and service needs Monitor stock levels, turnover, obsolescence, and backorders to optimize inventory performance Ensure accurate parts forecasting based on sales, service demand, and historical data Ensure compliance with company policies, quality standards, and brand requirements Drive continuous improvement in systems, processes, and cost control Regular visits to Warehouse and Dealer network Proven experience as a Parts Manager or similar role within the automotive sector Experience working with OEM standards and dealer networks (preferred) Solid understanding of inventory management and forecasting Proficient in ERP/DMS systems and Excel a company with its registered office in Modulo 1 de la planta baja, Avda. Brusuelas 36, 28108, Alcobendas, Madrid, with CIF B56485493 (hereinafter referred to as the "Company"), will process your personal data on the basis of your express consent for the purposes of managing your job application. Your personal data will be transferred to Chery Automobile Co. Ltd (parent company of the Group), a company based in China, in order to carry out the process you have voluntarily requested. As stated in the European Data Protection Regulation (GDPR), we inform you that the Personal Information Protection Law of the People's Republic of China (PIPL) may conflict with the GDPR and in some scenarios. Your personal data will be kept for 2 years and then delete. Additionally, you may exercise your data protection rights (access, rectification, opposition, cancellation, etc.) If you consider that we have not handled your personal data appropriately, you may contact the Data Protection Officer at , we inform you that you have the right to lodge a complaint with the Spanish Data Protection Agency if you consider that there has been a breach of data protection legislation with regard to the processing of your personal data.

Brindar soporte estratégico y operativo en las áreas de relaciones institucionales, comunicación corporativa y colaboración con asociaciones de pacientes, contribuyendo al desarrollo y ejecución de proyectos clave, campañas de concienciación y posicionamiento institucional. Coordinar con agencias externas la producción de notas de prensa, comunicados corporativos, materiales gráficos y audiovisuales. - Apoyar en la gestión de redes sociales y medios de comunicación. Dar soporte en la ejecución de proyectos conjuntos con asociaciones. - Formación Universitaria en Comunicación, Relaciones Internacionales, Ciencias Políticas, Ciencias de la Salud o afines. - Experiencia mínima de 2 años en funciones similares, preferentemente en el sector salud o farmacéutico. - Habilidades de comunicación, redacción, organización y trabajo transversal. - Nivel alto de inglés y dominio de herramientas digitales (Office 365, SharePoint, etc.). Vehículo de empresa. - Formación continua y desarrollo profesional. - Flexibilidad horaria y entorno colaborativo.

About Telcomdis Telcomdis is the EMEA Master Distributor of Motorola Licensed Products, serving a wide network of retailers, distributors and enterprise customers across Europe, the Middle East and Africa. With a broad, high‑performance international sales team and continuous growth in multi‑country operations, we are strengthening our Finance and Administration team to support our next expansion phase. Finance & Administration Manager We are looking for a hands‑on, structured and internationally‑minded Finance & Administration Manager to oversee our Finance, Accounting, Treasury, Administration and HQ Human Resources functions. This position is perfect for someone who understands international trade, VAT complexity, and multi‑currency operations, and wants to own end‑to‑end administrative and financial processes in a dynamic, growing organization. Key Responsibilities Finance & Accounting • Oversee day‑to‑day accounting, month‑end close, and financial accuracy. • Ensure compliance with Spanish GAAP and support multi‑country accounting needs. • Implement and maintain internal controls and efficient workflows. Triangular & International Operations • Manage financial treatment of triangular operations across EMEA. • Ensure accurate VAT treatment for transactions involving multiple jurisdictions. • Validate landed cost, stock valuation, and documentation for cross‑border flows. Marketplace Tax Obligations • Handle VAT obligations for marketplace sales (OSS/IOSS, deemed‑supplier rules). • Coordinate VAT collection, reporting and remittance for different platforms and countries. Tax & Compliance • Manage Spanish tax filings (VAT, CIT, Withholding). • Coordinate with advisors for tax obligations in various EMEA countries. • Ensure compliance with customs, import duties, EORI, and VIES reporting. Treasury & FX • Monitor cash flow, cash‑flow forecasting and liquidity. • Manage multi‑currency payments (EUR/USD/GBP). • Oversee banking relationships and optimize working capital. Administration • Oversee documentation, insurance, supplier contracts, certifications and general compliance. • Drive process digitalization and administrative efficiency. HR (Head Office Responsibilities) • Support hiring, onboarding, contracts, and employee documentation. • Coordinate payroll with external providers. • Maintain internal HR policies and support day‑to‑day employee relations. Requirements • 5–10 years of experience in Finance or Finance & Administration roles. • Experience in international trade, distribution, or import/export. • Understanding of triangular VAT, marketplace VAT, and multi‑jurisdiction tax compliance. • Strong financial fundamentals and administrative leadership. • High level of English (daily communication across EMEA). • ERP proficiency; Business Central highly recommended (NAV/BC). • Advanced Excel; Power BI is a plus. • Proactive, structured, detail‑oriented, and comfortable in a growing environment. What We Offer • Competitive compensation • Permanent contract • Hybrid schedule (remote Monday & Friday) • Fast‑growing, international environment

Suanfarma is a life science company dedicated to health and advancement. We focus on developing, manufacturing, and distributing high-quality active pharmaceutical ingredients, fundamental components of medicines that improve the lives of millions of people and animals every day. We’re looking for a self-motivated, highly engaged professional to act as a financial partner to the sales department, responsible for analyzing sales performance, monitoring profitability, managing trade budgets, and ensuring accurate reporting. Responsibilities: Financial analysis & reporting: prepare, monitor, and analyze P&L statements (product/customer specific), perform variance analysis to identify (i) impacts coming from volumes, prices and costs, (ii) growth drivers, and ensure reliable sales reporting. Forecast: partner with sales, supply chain, industrial and finance to produce an 18-month rolling forecast, with focus on the sales pipeline and the expected P/L results, with sales and contribution margin by customer, product, region. Budget & margin management: actively engage in the preparation of long and short-term budgets for the company. Administer trade budgets, track promotional expenses, and calculate selling prices to maximize profitability. Sales strategy support: provide actionable insights to the sales team, assist in forecasting, and advise on optimal product mix and pricing. S&OP: partner with supply chain, sales and industrial to ensure a robust S&OP process, optimizing the utilization of company resources and avoiding unnecessary inventory build-up. Operational controls: manage order-to-cash processes, ensure compliance with internal policies. Working capital: Cash matters. Actively monitor sales terms and conditions with clients, accounts receivable and accounts payable, ultimately contributing for cash generation. Data accuracy: partner with the sales and IT teams to define master data standards and ensure integrity in reporting systems, often using tools like CRM or Power BI. Requirements: Bachelor’s degree in administration, economics or engineering Proven experience in controlling activities in the industrial setting, financial planning and analysis, sales controlling. Pharma background is a plus. Knowledge of SW tools including Salesforce, Microsoft Dynamics (Business Central), Power BI Skills: Strong leadership, analytical, written and verbal communication skills Ability to work independently and be a team player Demonstrated ability to plan and organize projects Able to manage multiple complex projects and deliver in a timely manner Experience working in a team under pressure to meet deadlines Languages: ~ English (fluent), Spanish Why Join Suanfarma?: A global organization with a strong market position. An international, collaborative, and inclusive culture . Opportunities to make a real impact and grow professionally. A role with visibility and cross-functional interaction . If you’re ready for a new challenge and have the experience described above, apply for the position or send me your CV at