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Acerca de la Empresa Para una comprensión completa de esta oportunidad y de lo que se requerirá para ser un candidato exitoso, siga leyendo. ¿Quieres trabajar en el Nuevo Hospital Veterinari Abat Marcet en Terrassa? El nuevo Hospital Veterinari Abat Marcet cuenta con un total de 1000m2, amplias instalaciones con dos quirófanos con equipamiento para traumatología y endoscopia, seis salas de Hospitalización, Laboratorio, Radiología, Ecografía, Ecocardiografía, TAC, y Sala de Formación. Requisitos: • Licenciatura/Grado en Veterinaria.., • Se valorará formación específica en la especialidad de anestesía (posgrados, másteres, estancias, cursos avanzados, etc.), • Experiencia mínima de tres años en el área de anestesia veterinaria, • Persona con gran vocación por los animales, dotes comunicativas, empática, habituada a trabajar en equipo y con capacidades de fidelización del cliente. Condiciones contractuales: • Contrato indefinido., • Salario a partir de 30.000 € brutos/anuales en función de la experiencia, • Se podrá requerir una mínima participación en medicina general cuando el servicio lo requiera., • Jornada completa, • Turnos de mañana, • Se ofrece formación en la especialidad de anestesia a cargo de la empresa., • Seguro médico privado pagado por la empresa + importantes beneficios sociales, • Oportunidades de desarrollo profesional y pertenencia a un grupo de clínicas y hospitales veterinarios con más de 150 centros en la actualidad. xcskxlj ¡Si tu perfil encaja con lo que hemos descrito, nos encantaría conocerte!

Dos personas para bajar un piso.Es fácil Tiene el somier metálico y de maderas.El metal serviría para chatarra.Es porque yo sola no lo puedo bajar ni tirarul br/liTipo(s) de residuos a recoger /li Sofá, cama, mobiliario br/li¿Los residuos necesitan medidas especificas de seguridad para su retir

Descripción del puesto Buscamos un Representante de Atención al Cliente con un nivel profesional de inglés para unirse a nuestro equipo de Industrial Solutions en Terrassa, Barcelona.El candidato seleccionado gestionará los pedidos de compra y desarrollará relaciones sólidas con los clientes,

Tiene las cualificaciones y habilidades adecuadas para este trabajo? Descúbralo a continuación y pulse en "solicitar" para ser considerado.En Fonomed, empresa vinculada al Grupo BancSabadell, trabajamos para ofrecer soluciones de comunicación y gestión que aportan eficiencia, calidad y cercanía

Adecco busca un/a Formador/a EPLAN en Sabadell para unirse al equipo técnico de una empresa innovadora en soluciones de software para ingeniería eléctrica. La misión principal será la formación de clientes en herramientas EPLAN, así como la optimización de procesos de diseño eléctrico. Se

Compromiso con la Diversidad En Solenis apostamos por una cultura inclusiva que reconoce y valora la diversidad, donde cada persona es valorada por su talento y potencial.

Con la recién apertura de una sucursal en Francia, buscan un/a Administrativo/a para su departamento de Customer Service.

Creación de plantillas de ofertas y colaboración en la creación de especificaciones técnicas Generación y redacción de ofertas comerciales Realizar seguimiento de la actividad de ventas Negociar precios y condiciones con los clientes Evaluar y analizar resultados * Control de indicador

En Ferchau, valoramos el talento, la dedicación y la innovación.

RAS Interim busca cubrir un puesto en su almacén ubicado en Sabadell, con incorporación inmediata.Se valorará experiencia en carga/descarga y manejo de carretillas; se requiere carnet vigente y disponibilidad para trabajar en equipo.Se ofrece contrato inicial por ETT y posibilidad de renovación,

Claire Joster somos una compañía de selección especializada donde buscamos el encaje de candidatos/as y empresas procurando el bienestar de las personas. Pertenecemos al Grupo Eurofirms, primera empresa nacional de gestión de personas. La experiencia que se espera de los solicitantes, así como las habilidades y cualificaciones adicionales necesarias para este trabajo, se enumeran a continuación. Desde Claire Joster nos encontramos en la búsqueda de un/a Técnico SAT para una empresa dedicada al procesado de materiales, ubicada en Sant Cugat de vallés. Funciones: Instalar y ejecutar la puesta en marcha de los equipos vendidos. Realizar los mantenimientos preventivos de los equipos ya instalados de su cartera de clientes consolidada. Asistencia para la reparación de averías. Redactar informes de estados de los activos. Asesoramiento al cliente frente la resolución de las averías. Requisitos: Imprescindible formación FP superior electro-mecánico, automatización industrial. Se valorará ingeniería técnica. Se valora experiencia en puesto similar. Tener conocimientos informáticos. Perfil proactivo, con ambición a tener una formación constante, con capacidad de autogestión y resolución. Carnet de conducir y disponibilidad para viajar en territorio nacional. Se ofrece: Contrato indefinido a jornada completa. Salario en función de experiencia. Vehículo de empresa. Gastos pagados. Seguro médico privado. Formación continua. Horario: 08h a 17h Si tienes ganas de seguir aprendiendo y creciendo profesionalmente, ¡es tu oportunidad! xcskxlj Aplica a la oferta y nos pondremos en comunicación contigo a la mayor brevedad.

En Vectem desarrollamos y fabricamos productos cosméticos desde nuestras instalaciones de Rubí. Con más de 60 años de experiencia y en una etapa de crecimiento, queremos incorporar un/a formulador/a al equipo de I+D. Sea uno de los primeros solicitantes, lea la descripción completa del puesto a continuación y luego envíe su candidatura para que sea considerada. Buscamos una persona con al menos dos años de experiencia práctica en formulación cosmética, especialmente en productos de cuidado facial, corporal o capilar. Tu misión Desarrollarás nuevos productos cosméticos y acompañarás cada fórmula desde las primeras pruebas de laboratorio hasta su industrialización. Trabajarás en contacto directo con Producción, Calidad, proveedores y laboratorios externos. ¿Qué harás? Formular, reformular y optimizar productos de skin care y/o hair care. Diseñar y ejecutar pruebas de laboratorio y preparar muestras. Evaluar resultados y realizar el seguimiento de estudios de estabilidad y compatibilidad. Elaborar fórmulas, métodos de fabricación, listados INCI e informes técnicos. Seleccionar y evaluar nuevas materias primas junto con proveedores. Coordinar ensayos externos de eficacia, challenge test y compatibilidad envase-producto. Participar en lotes piloto, escalado industrial y primeros lotes de fabricación. Investigar incidencias de producto y proponer mejoras de fórmula o proceso. Qué necesitamos Al menos dos años de experiencia práctica en formulación cosmética. Experiencia desarrollando productos de cuidado de la piel y/o del cabello. CFGS o titulación universitaria relacionada con Química, Farmacia, Biología, Biotecnología, Ingeniería Química o similar. Conocimientos de GMP e ISO 22716. Capacidad para analizar resultados, documentar conclusiones y trabajar con autonomía. Inglés suficiente para consultar documentación técnica y comunicarse con proveedores. xcskxlj Valoraremos también experiencia en escalado industrial, evaluación sensorial, selección de materias primas o gestión de proyectos de desarrollo. Se ofrece: • Contrato indefinido, • Jornada completa, • Cheque restaurante, • Flexibilidad horaria, • Jornada intensiva los viernes

At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters. The Position The Opportunity The Digital Innovation and Operational Services Chapter is a global team in R&D that focuses on internal improvement: increasing productivity, efficiency, and the ability of the R&D organization to collaborate across its global organizational interfaces. Our work involves reducing complexity of our systems, harmonizing processes, tools, and business practices, and building connections across geographical and organizational silos. The Role We are seeking an R&D Enterprise Tools Operations Specialist I to join our global service and support team. You are well organized and detail-oriented. You will be the reliable service provider handling critical system requests within our core business tools, ensuring our scientists and engineers worldwide can focus on developing innovative products for patients. This role requires building organizational know-how—understanding who our internal customers are, how they work, and solving problems in a way that anticipates their support needs. You are quick in learning new software systems and tools, enjoy helping your coworkers every day, and are motivated to innovate internal processes to automate tasks, you will fit right into our team! Your key Responsibilities As a part of a global centralized expert support team, execute enterprise tool system tasks based on R&D customer requests, leveraging expert knowledge of business tools, compliance requirements, and R&D teams and processes. - Execute R&D System Requests: Fulfill customer tool requests using expertise in business systems and compliance standards. - Provide Timely Expert Support: Offer professional, empathetic, and quick solutions to R&D operational issues and system problems. You may be the primary contact for R&D scientists and engineers in the use of our internal enterprise systems. - Expert in our Global Business Applications: Act as the subject matter expert for one or more complex R&D business applications. - Specialize in R&D Business Processes: Develop deep expertise in key processes (e.g., records management, lab data, training system data, change requests) for timely and accurate execution. - Maximize Scientist Productivity: Use your expertise across business data and organizational structure to streamline operations and save significant time for R&D scientists. - Anticipate Customer Needs: Build organizational know-how of R&D roles and priorities to deliver proactive system support. - Maintain Global Service Excellence: Demonstrate a strong, collaborative customer service mindset within a diverse, global team. - Drive Process Improvement: Identify manual steps and actively suggest opportunities for digitization and improvement. - Automate Administrative Tasks: Apply or develop automation and AI tools to reduce administrative load on R&D staff. - Ensure Data Integrity and Compliance: Guarantee all activities strictly adhere to regulated R&D processes, supporting audits and data retrieval. Who you are: Education: Bachelor’s degree, preferably in a technical, scientific, or business discipline. Experience: 2+ years of professional experience in an operations, technical support, or system administration role, or equivalent academic projects / internships Language Skills: Excellent written and verbal English Language skills are required to support our global organization. German language skills are a plus. System Proficiency: - Demonstrated ability to quickly learn new software, systems, and processes is essential. - Prior experience in enterprise business applications is highly desirable (e.g., Electronic Document Management Systems, Learning Management Systems, or Project Management tools). - Education and/or experience in data analysis, use and/or creation of AI chatbots, AI prompt engineering and/or development of AI agents is desirable Tools : Experience with SAP, Cornerstone, Google Suite and Office Suite Execution & Focus: A proven ability to complete complex, detailed tasks accurately and efficiently. You have a rigorous and detail-oriented approach to following established processes. People Skills: Demonstrated ability to work well with others in a hybrid virtual and global team environment Schedule flexibility: To support the global nature of our work (e.g. collaboration between the US and Europe), customer and stakeholder meetings periodically require participation in meetings during the early evening hours (e.g. until 1900 for Europe positions, starting at 0700 PST for US positions ). Who we are A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact. Let’s build a healthier future, together. Roche is an Equal Opportunity Employer.

At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters. The Position The Opportunity The Digital Innovation and Operational Services Chapter is a global team in R&D that focuses on internal improvement: increasing productivity, efficiency, and the ability of the R&D organization to collaborate across its global organizational interfaces. Our work involves reducing complexity of our systems, harmonizing processes, tools, and business practices, and building connections across geographical and organizational silos. We are seeking a R&D Enterprise Tools Operations Specialist to join our global support team. You are well organized and detail-oriented. You will be the reliable service provider handling critical system requests within our core business tools, ensuring our scientists and engineers worldwide can focus on developing innovative products for patients. This role requires building organizational know-how—understanding who our internal customers are, how they work, and solving problems in a way that anticipates their support needs. You are quick in learning new software systems and tools, enjoy helping your coworkers every day, and are motivated to innovate internal processes to automate tasks, you will fit right into our team! Key Responsibilities As a part of a global centralized expert support team, execute enterprise tool system tasks based on R&D customer requests, leveraging expert knowledge of business tools, compliance requirements, and R&D teams and processes. - Execute R&D System Requests: Fulfill customer tool requests using expertise in business systems and compliance standards. - Provide Timely Expert Support: Offer professional, empathetic, and quick solutions to R&D operational issues and system problems. - Expert in our Global Business Applications: Act as the subject matter expert for one or more complex R&D business applications. - Specialize in R&D Processes: Develop deep expertise in key processes (e.g., records management, lab data, change requests) for high-accuracy execution. - Maximize Scientist Productivity: Use your expertise across business data and organizational structure to streamline operations and save significant time for R&D scientists. - Anticipate Customer Needs: Build organizational know-how of R&D roles and priorities to deliver proactive system support. - Maintain Global Service Excellence: Demonstrate a strong, collaborative customer service mindset within a diverse, global team. - Drive Process Improvement: Identify manual steps and actively suggest opportunities for digitization and improvement. - Automate Administrative Tasks: Apply or develop automation and AI tools to reduce administrative load on R&D staff. - Ensure Data Integrity and Compliance: Guarantee all activities strictly adhere to regulated R&D processes, supporting audits and data retrieval. Requirements: - Education: Bachelor’s degree, preferably in a technical, scientific, or business discipline. - Experience: 2+ years of professional experience in an operations, technical support, or system administration role, or equivalent academic projects / internships - Language Skills: Excellent written and verbal English Language skills are required to support our global organization. German language skills are a plus. - System Proficiency: Ability to quickly learn new software, systems, and processes is essential. - - Prior experience in enterprise business applications is desirable (e.g., Electronic Document Management Systems, Learning Management Systems, or Project Management tools). - Education and experience in data structures, databases, automation, scripting, AI prompt engineering and/or development of AI agents is desirable - Tools : Experience with SAP, Cornerstone, Google Suite and Office Suite is a plus. - Execution & Focus: A proven ability to complete complex, detailed tasks accurately and efficiently. You have a rigorous and detail-oriented approach to following established processes. - People Skills: Demonstrated ability to work well with others in a hybrid virtual and global team environment Who we are A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact. Let’s build a healthier future, together. Roche is an Equal Opportunity Employer.

Experteer Overview In this role you will serve as a Solutions Engineer bridging sales, design and manufacturing to deliver customer-specific tooling solutions across the EMEA region. You will develop concepts, evaluate technical and economic feasibility, and drive tool performance for customers. You will collaborate with design and production teams and communicate with customers to ensure timely, high-quality results. This position offers the opportunity to influence tooling decisions and delivery outcomes in a global industrial technology company. Compensaciones / Beneficios • Process customer-specific tool requests and prepare offers • Create concept drawings considering technical and economic factors • Lead small projects and take technical responsibility for tools • Liaise with design to develop 3D concepts and drawings • Present tool solutions to internal and external stakeholders • Provide technical clarifications with sales and customers • Make or buy decisions • Clarify and monitor delivery dates • Update technical databases • Analyze cutting data and tool life for customer-specific tools Responsabilidades • Fluent in English and very good German • Mechanical engineer or engineering technician with relevant experience • Knowledge of metal cutting tools desirable • SAP and PLM knowledge preferable • Strong MS Office skills, especially Excel • AutoCAD or NX knowledge preferable • Team-oriented, quick learner with attention to detail • Structured and reliable work approach Requisitos principales • Lunch Ticket COBEE • ADESLAS - Additional health insurance • Hybrid work model

Experteer Overview As Sourcing Lead in Sant Cugat, you will steer global sourcing for NPC, Sensors u0026amp; Cartridges and External Manufacturing, balancing strategy with execution. You’ll lead a multi-disciplinary team, drive digital procurement transformation, and partner with executive leadership to optimize the supplier network. The role centers on delivering measurable value, governance, and process improvements across a global portfolio. This is a high-impact opportunity to shape Roche's sourcing ecosystem and enable near-patient diagnostics at scale. Compensaciones / Beneficios • Lead global sourcing operations for NPC, Sensors u0026 Cartridges, and EM portfolios • Manage and coach a local team of up to 16 Sourcing Managers and one Business Capability Lead • Drive digital procurement transformation and collaborate with executive leadership • Define and monitor KPIs for OTIF delivery and governance across the portfolio • Execute compliant sourcing, conduct market research, and benchmark NPI • Oversee a portfolio of contracts (CDAs, SOWs, MSAs) with varying complexity • Govern the iCollab platform to advance supplier integration with Planning and RSS • Resolve high-stakes conflicts and provide monthly/quarterly updates to leadership • Partner with Digital u0026 Process teams to deploy AI and digital solutions and drive process improvements Responsabilidades • University degree in Business or Life Sciences • MBA and CIPS certification highly preferred • 7–10 years in Direct Procurement (Medtech, Automotive, Electronics, Pharmaceuticals, or Chemicals) • 3–5 years in a Shared Service or CoE environment • Deep sourcing knowledge and portfolio management in ADI, Reagents, and Instruments • Strong affinity for AI-driven digital transformation of operations • ERP experience with SAP and BI tools like Tableau • Lean and/or Six Sigma mindset with proven change-management and executive relationship skills Requisitos principales •

pRalarsa - Part of Cary Group busca incorporar un/a Administrativo/a de Facturación para su equipo de Invoicing, ubicado en sus oficinas centrales. La persona seleccionada gestionará facturación, tramitación y reclamación de servicios, asegurando atención eficaz al cliente, tanto interno como externo. /ppEmitir, revisar y validar facturas, registrar información en plataformas y coordinar con talleres, franquicias y aseguradoras. /p #J-18808-Ljbffr

pCegid busca un Sales Manager de Canal y Alianzas Mid‑Market para liderar la estrategia de canal y alianzas, impulsando el crecimiento de MRR y la captación de nuevos clientes. Ubicaciones: oficinas de Sant Cugat o Las Rozas, Madrid. /ppEntre sus funciones se incluyen implementar el Partners Program, identificar y activar nuevos partners estratégicos, y dirigir al equipo de Partner Managers, con foco en KPIs y crecimiento sostenible a través de co-venta y co‑marketing. /p #J-18808-Ljbffr

pHewlett Packard Enterprise (HP) is seeking a Sales Compensation Planning Expert to lead the design, governance, and continuous improvement of global sales planning processes across the channel business. You will own end-to-end quota and coverage strategy, aligning targets with capacity and market potential while driving standardization and automation. /ppThe role sits at the intersection of Sales, Finance, and Sales Compensation, enabling scalable, data-driven planning across HP’s multi-channel /p #J-18808-Ljbffr

pAscendion is seeking a CRM/Operations professional to manage end-to-end CRM processes for a global business unit with minimal supervision. You will review regional and global planning processes, gather requirements, and develop dashboards and reports to streamline operations and drive performance. /ppThe role requires 5–7 years in CRM or operations, with a four-year degree in a related field. PMP/Lean Six Sigma is a plus and you will liaise across business, sales, and technical teams to deliver /p #J-18808-Ljbffr

ppBarcelona /p pBuscamos un/a bField Service Engineer /b para dar soporte técnico a sistemas de bRadioterapia y Neurociencia /b en distintos centros hospitalarios del territorio nacional. Serás la persona responsable de garantizar que los equipos funcionan con precisión y fiabilidad, combinando intervenciones en campo, soporte remoto y una gestión autónoma de tu agenda. /p pSi te motiva trabajar con tecnología de alto nivel, tener autonomía y formar parte de un entorno donde tu labor contribuye directamente a la atención de pacientes, esta posición puede ser un gran paso en tu carrera. /p pUbicación: bBarcelona /b /p h3Responsabilidades /h3 ul liRealizar mantenimiento preventivo y correctivo de los equipos instalados en hospitales y centros especializados. /li liAtender incidencias y consultas técnicas por teléfono, online o presencialmente, priorizando la satisfacción del cliente. /li liDocumentar tus intervenciones de forma clara y rigurosa para asegurar trazabilidad y cumplimiento normativo. /li liColaborar en la instalación y puesta en marcha de nuevos sistemas. /li liGestionar tu planificación diaria con autonomía, manteniendo una comunicación fluida con el equipo técnico. /li liRealizar desplazamientos dentro del territorio asignado (viajes planificados y no planificados). /li /ul h3Requisitos /h3 ul liGrado en Ingeniería Electrónica, Biomédica, Mecánica, Telecomunicaciones o Física. Se valorará experiencia equivalente. /li li1–2 años de experiencia en servicio técnico, mantenimiento o soporte de equipos complejos. Se valorará tener experiencia en entorno hospitalario, alta tecnología, TAC, Acelerador Lineal, Resonancia Magnética. /li liConocimientos en instrumentación y herramientas de medida (osciloscopio, multímetro, etc.). /li liBuen nivel de español e inglés. /li liCapacidad para trabajar de forma autónoma, organizada y orientada a la resolución de problemas. /li liComodidad trabajando tanto solo como en coordinación con otros equipos. /li liFlexibilidad horaria y disponibilidad para desplazamientos. /li /ul h3Qué ofrecemos /h3 ul liAutonomía real para organizar tu trabajo y tus rutas. /li liTecnología de vanguardia en un entorno sanitario altamente especializado. /li liFormación continua en sistemas avanzados de Radioterapia y Neurociencia. /li liEstabilidad y proyecto a largo plazo, con un equipo cercano y colaborativo. /li liUn rol donde tu trabajo tiene un impacto directo en la calidad asistencial de los pacientes. /li /ul /p #J-18808-Ljbffr

ph3Cumplimiento de Calidad de Producto - Validaciones asépticas /h3pDentro del departamento de QA Systems Product la responsabilidad es implementar y mantener sistemas que garanticen el cumplimiento GMP de los productos y procesos (APQRs, CSVC, revisión y aprobación de documentos y datos maestros…). /ppbFunciones y Responsabilidades: /b /pulliEvaluar y aprobar los documentos relacionados con el ciclo de vida de validación de procesos de fabricación y packaging, limpieza de equipos y transporte de productos asépticos y orales de acuerdo a las normativas cGMP, FDA, procedimientos corporativos y locales (VMP, VPP, RA, Control Strategy, PPQs, CPV, CTV, monitorizaciones de limpiezas y sus revisiones periódicas). /liliEvaluar y aprobar los documentos relacionados con el ciclo de vida de cualificación de equipos y sistemas informatizados, instalaciones y servicios de acuerdo a las normativas cGMP, FDA, procedimientos corporativos y locales. /liliAsegurar el cumplimiento GMP y regulatorio de los procedimientos asociados a fabricación, limpieza de equipos y transporte mediante la revisión de contenidos documentales (SOP). /liliDiseñar e implementar los informes periódicos de producto (PQR/APR) para productos fabricados en las plantas de Sant Cugat de acuerdo con las normativas cGMP, FDA y requerimientos corporativos y locales. /liliRevisar y aprobar los documentos relacionados con el ciclo de vida de validación de métodos analíticos y las prescripciones de análisis. /liliAsegurar el cumplimiento GMP y regulatorio del contenido del sistema ERP (especificaciones de análisis, estándares, recetas de fabricación y datos maestros). /li /ulpbPerfil y Requisitos: /b /pulliExperiencia de más de 5 años en industria farmacéutica (áreas deseadas Calidad y/o Validaciones). /liliImprescindible formación o conocimientos en sistema de validaciones y tecnologías asépticas. /liliMuy valorable experiencia con Productos Combinados y su normativa. /liliInglés y castellano fluido hablado y escrito. /liliPersona con rápida adaptación a los cambios, flexibilidad, atención al detalle, organizada, autónoma y con buenas habilidades de comunicación, pedagogía y empatía. /li /ulpEn Boehringer Ingelheim, valoramos y apreciamos la diversidad de talento dentro de nuestra organización. A pesar de ello, nos vemos en la necesidad de informar a los/as candidatos/as interesados/a que, para esta posición, no podemos considerar solicitudes que impliquen movimientos internacionales /ppEstamos continuamente trabajando porque queremos diseñar para ti la mejor experiencia. Estos son algunos ejemplos de cómo te cuidaremos: /pulliHorario flexible /liliSeguro de vida y accidente /liliSeguro médico a un precio competitivo /liliInversión en formación y desarrollo /liliCuidado de la salud /liliPortal de ofertas para colaboradores /li /ul /p #J-18808-Ljbffr

ppAt Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters. /p h3The Position /h3 h3The Opportunity /h3 pAs a Senior Process Manager within our Design Control Excellence (DCE) team in Sant Cugat, you will be responsible for the essential development processes that ensure our life‑saving products are safe, effective, and compliant. You will play a key role in executing requirement, risk, configuration, defect management, and verification validation within complex development projects. This is an opportunity to join a growing innovation hub where you will work in a cross‑functional environment to ensure compliant execution while continuously optimizing efficiency to meet evolving organizational needs. /p ul liLead Process Governance: Provide expert guidance and support for complex system, software, and assay projects across risk, requirements, configuration, and defect management /li liMaster Requirements Traceability: Support multi‑level requirements traceability and ensure all data is maintained within a streamlined, database‑driven approach across projects /li liConduct Strategic Risk Assessments: Lead detailed product risk assessments by analyzing documents, reports, and market trends alongside cross‑functional teams /li liEstablish Configuration Management: Build and maintain configuration management for complex projects, ensuring a clear overview of past, present, and future product states /li liEnsure Regulatory Excellence: Provide specialized support to ensure that Verification Validation (VV) activities meet both internal standards and global regulatory requirements like ISO 13485 /li liDrive Radical Simplification: Proactively identify opportunities for process optimization and simplification to improve time‑to‑market without compromising quality /li liCollaborate Globally: Thrive in an agile, multicultural setting where we experiment, learn, and trust each other to deliver the best results for patients /li /ul h3Who You Are /h3 pYou are a proactive and service‑oriented professional who excels at solving complex problems independently. You bring strong analytical thinking and the ability to communicate precisely in a collaborative, global environment. /p h3To be successful in this role, you bring: /h3 ul liAdvanced Academic Foundation: A Master’s degree in Engineering, Life Sciences, Natural Sciences, or a related field /li liExperience: Minimum of three years of experience in a regulated environment within product development or process management (Medical Device or Diagnostics industry preferred) /li liTechnical Mastery: A strong understanding of Design Control processes and global standards such as ISO 13485 or IEC 62304 /li liDigital Fluency: Experience with ALM tools such as Jira, Azure DevOps, or specialized requirements management software is highly valued /li liExceptional Communication: Precise and efficient communication skills in English, enabling effective collaboration across our international sites /li /ul pThere are 2 positions of this role. /p pAt Roche, you’ll thrive in a culture that values different perspectives and creates a place of belonging, where we challenge ourselves to excel and achieve strong results, together. /p h3Who we are /h3 pA healthier future drives us to innovate. Together, more than 100,000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life‑changing healthcare solutions that make a global impact. /p pLet’s build a healthier future, together. /p pRoche is an Equal Opportunity Employer. /p /p #J-18808-Ljbffr

ppWould you like to join an international team working to improve the future of healthcare? Do you want to enhance the lives of millions of people? Grifols is a global healthcare company that since 1909 has been working to improve the health and well-being of people around the world. We are leaders in plasma-derived medicines and transfusion medicine and develop, produce and market innovative medicines, solutions and services in more than 110 countries and regions. /p pbWe believe that diversity adds value to our business, our teams and our culture. We are committed to equal employment opportunities that foster an inclusive environment. /b /p pWe are looking for a Corporate Quality Specialist who will be part of the change and digital transformation, getting involved in the supervision of Grifols' quality systems through data analysis and the preparation of technical reports, as well as promoting and participating in projects for the harmonization and continuous improvement of quality systems. /p h3What your responsibilities will be /h3 ul liReview and update the corporate quality system /li liDraft and review quality system documents (policies, SOPs, reports, etc.) /li liImplementation of electronic quality system /li liData analysis and reporting /li liDraft, review and approve technical reports /li liStudy quality systems and compare them with current regulations /li liReview quality standards and monitor their implementation at Grifols /li liProvide support in the management of global quality projects: coordinate multidisciplinary teams, incorporate AI tools, etc. /li liDraft, review and approve technical documentation /li /ul h3Who you are /h3 pTo perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skills, education, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. /p ul liBachelor's degree in Health Sciences or a related field /li li3 years of pharma quality experience (Quality Systems, Quality Assurance, CVS and/or Audit) /li liExperience collaborating in digital transformation projects and/or in software implementation /li liAdvanced English Level /liliExcellent written and verbal communication skills /li liGood understanding of regulatory requirements and quality standards relevant to our products (biopharma, medical devices) /li liDevelop collaborative working relationships /li liResults‑oriented and proactive mindset /li liWillingness to travel internationally as needed (maximum 30%) /li /ul h3What we offer /h3 pIt is a brilliant opportunity for you, Grifols is fully aware that its employees are one of its major assets. We are committed to maintaining an atmosphere that encourages all our employees to develop their professional careers in an excellent working environment. /p pInformation about Grifols is available at If you are interested in joining our company and you have what it takes for such an exciting position, then don’t hesitate to apply! We look forward to receiving your application! /p pWe believe in diverse talent and want to remove any barriers that may hinder your participation. If you require any adjustments in our selection process, please do not hesitate to inform us when applying. We are here to help. /p pGrifols is an equal opportunity employer. /p pbFlexibility for U Program: /b Hybrid Model /p pbFlexible schedule: /b Monday-Thursday 7‑10 to 16‑19h and Friday 8‑15h (with the same flexible start time). /p pbBenefits Package /b /p pbContract of Employment: /b Permanent position /p /p #J-18808-Ljbffr

Estamos buscando operarios/as de alimentación para trabajar en una importante empresa en Sant Quirze. En Adecco creemos en la igualdad de oportunidades y apostamos por el Talento Sin Etiquetas Requisitos Funciones principales: - Manejo de maquinaria sencilla. - Alimentación de las máquinas con chocolate o pasta. -Limpieza del puesto de trabajo. ¿Qué ofrecemos? Contrato temporal con Adecco. Horario: - Turno de mañana: 6:00h a 14:00. - Turno de tarde (a concretar). Salario 9.69€ b/h

pAB-BIOTICS, una empresa líder en suplementos y productos farmacéuticos, está buscando un Artwork Manager altamente motivado y creativo para gestionar la producción de empaques. /ppEl candidato ideal contará con al menos 2 años de experiencia, dominio en diseño gráfico y excelentes habilidades de comunicación. Además, la empresa ofrece flexibilidad para el trabajo remoto y oportunidades de desarrollo profesional. /p #J-18808-Ljbffr

ppAt Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters. /p h3The Position /h3 h3What will your main responsibilities be? /h3 ul liInternal advisory: Support the resolution of employee queries related to the collective bargaining agreement, employment rights, leave policies, vacation entitlements, and Spanish labour legislation /li liEmployee and labour relations: Assist in the preparation of documentation and reports for Employee Representatives (Works Council), labour inspections, and collective bargaining processes. Prepare meeting minutes and presentations related to employment and labour relations topics /li liCase management and compliance: Support the administration and follow-up of disciplinary processes, organisational restructuring initiatives, administrative conciliation procedures, and employment litigation matters, while ensuring compliance with Spanish labour legislation and internal policies /li liReporting and international projects: Prepare labour relations reports and documentation in English, contributing to the monitoring of key metrics and supporting the global People Culture team /li /ul h3What are we looking for? /h3 ul liEducation: You are currently pursuing a Bachelor's degree in Labour Relations and Human Resources, Law, or a Master's/Postgraduate qualification specialising in Labour Law or Employment Law in Spain /li liLanguages: Fluent English (minimum B2/C1 level), both written and spoken, with the ability to collaborate with international teams and interpret corporate documentation /li liEligibility: You must be eligible to sign an internship agreement (Convenio de Prácticas) with a university or educational institution in Spain /li liKey competencies: Strong attention to detail, analytical mindset, ability to handle confidential information with discretion, excellent communication skills, and a proactive attitude /li liTechnical skills: Proficiency in Microsoft Office (particularly Excel and PowerPoint). Knowledge of HR systems such as Workday will be considered an advantage /li /ul h3Who we are /h3 pA healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact. /p pLet’s build a healthier future, together. /p pbRoche is an Equal Opportunity Employer. /b /p /p #J-18808-Ljbffr

pCegid busca un/a desarrollador/a Java/SQL para diseñar, desarrollar y mantener aplicaciones empresariales en un entorno tecnológico en la nube. Colaborarás con Product Managers, UX y Arquitectos para transformar requisitos funcionales en soluciones técnicas eficientes. /ppTrabajarás en un equipo Agile SCRUM, garantizando la calidad mediante pruebas y depuración, y contribuirás a la automatización de pruebas y a la mejora continua de procesos. /p #J-18808-Ljbffr

pGFT is a digital transformation pioneer and has an open position for a Solution Architect. You will lead solution design, chose technology stacks, supervise the technical team, and document the enterprise environment to guide software architecture and API design. /ppThe role requires a Bachelor’s degree in computer science or related field, at least five years in IT, and the ability to work with a distributed team. Cloud basics are desirable and the company supports a diverse, inclusive environment. /p #J-18808-Ljbffr

ppHave you started in Computer Validation with a knack for IT systems? Do you thrive in an environment where you can shape strategy and support the validation of our technical solutions? If so, Boehringer Ingelheim has an exciting opportunity for you. We're inviting you to join our Compliance and Validation team, a place where you can make a real impact. /p pThis position offers more than a job; it's an opportunity to support our manufacturing processes and digital initiatives with your specialized knowledge in Computer Validation. As a key player, you'll support the change in meeting our dynamic business needs and play a pivotal role in supporting our IT systems and our manufacturing and laboratory processes. /p h3Tasks And Responsibilities /h3 ul liAssist in Developing Validation Strategies: Support the creation and implementation of validation strategies, help define processes, and assist in setting timelines for activities. /li liSupport Validation Activities: Assist in ensuring all activities are conducted according to strategies, help review protocols, and monitor tests. /li liEnsure Compliance with Regulations: Support the validation of computer systems in compliance with regulations and adapt strategies as necessary. /li liDocumentation and Reporting: Help maintain documentation of all activities, prepare reports, document issues and resolutions, and maintain records. /li liTraining and Development: Participate in training and development on validation processes and provide support to the team. /li /ul h3Requirements /h3 ul liEducation: Bachelor's degree in IT, health care degree, or similar. /li liExperience: 1-2 years in computer systems validation (or related field). /li liTechnical Understanding: Basic understanding of the technology being validated, including hardware, software, and network systems. /li liRegulatory Knowledge: Familiarity with relevant regulations and standards for computer system validation, such as FDA 21 CFR Part 11 and EU Annex 11 are a plus. /li liCommunication: Ability to effectively communicate with team members and stakeholders. /li liDocumentation Skills: Ability to prepare accurate validation documentation and reports. /li liKnowledge in Cloud Validation, Documentation Automation, Task Automation or Test Automation is a plus. /li /ul h3Benefits /h3 ul liFlexible working conditions /li liLife and accident insurance /li liHealth insurance at a competitive price /li liInvestment in your learning and development /li liGym membership discounts /li /ul /p #J-18808-Ljbffr

pRoche in Sant Cugat del Vallès is seeking a Senior Process Manager within the Design Control Excellence team to drive essential development processes ensuring safety, efficacy and regulatory compliance for life-saving products. /ppYou will lead governance across risk, requirements, configuration, defect management and VV, contributing to streamlined, database-driven project data and global regulatory alignment. /p #J-18808-Ljbffr

Amcor is seeking an Industrial Design Leader based in Sant Cugat del Vallès, Spain. In this role, you will lead a global team focused on innovative packaging design. The ideal candidate will have over 8 years of experience in a relevant field, demonstrating strong leadership in cross-functional teams. Join Amcor to shape sustainable packaging solutions that benefit customers and consumers alike. The position is full-time with an on-site work environment.br#J-18808-Ljbffr

ppb¡Nuestros equipos de comercial siguen creciendo! /b /p pSi buscas incorporarte a un ambiente joven y dinámico en el que cada día es distinto, e impulsar la financiación de proyectos I+D+i, en LEYTON encontrarás precisamente esto /p p.Llevamos más de 25 años en activo, y con casi 3.000 empleados en nuestras sedes internacionales, estamos posicionados como la consultoría líder mundial en financiación I+D+i. Para continuar logrando un desarrollo constante, buscamos incorporar un perfil como bCash Collector /b para nuestras oficinas de bSant Cugat del Vallés /b. /p pSi te gusta el trato con clientes, eres una persona resolutiva y te motiva trabajar por objetivos, esta puede ser tu oportunidad. /p h3¿Cuál será tu misión? /h3 pFormarás parte del departamento bde Cash Collection /b, gestionando una cartera de clientes asignada y asegurando el correcto seguimiento y recuperación de las facturas pendientes de cobro. /p pSerás responsable de acompañar todo el proceso de reclamación de deuda, desde el vencimiento de la factura hasta su cobro efectivo. /p h3¿Qué harás en tu día a día? /h3 ul liGestionar una cartera de clientes asignada por zona geográfica. /li liRealizar el seguimiento de facturas vencidas y próximas a vencimiento. /li liContactar con clientes para solicitar y actualizar previsiones de pago. /li liGestionar incidencias relacionadas con la facturación. /li liNegociar compromisos y fechas de pago. /li liCoordinarte con los diferentes departamentos internos para resolver bloqueos de cobro. /li liGestionar provisiones y realizar seguimiento hasta el cierre de cada expediente. /li liCFGS en Administración y Finanzas, ADE o similar. /li liValorable experiencia previa en atención al cliente, administración, recobro o gestión de deuda. /li liNivel usuario de Microsoft Office. /li liBuen dominio de Excel y Outlook. /li liValorable conocimiento de Galileo u otras herramientas de gestión. /li /ul /p #J-18808-Ljbffr

ph3La position /h3 pAs a Senior Process Manager within our Design Control Excellence (DCE) team in Sant Cugat, you will be responsible for the essential development processes that ensure our life‑saving products are safe, effective, and compliant. You will play a key role in executing requirement, risk, configuration, defect management and verification validation within complex development projects. This is an opportunity to join a growing innovation hub where you will work in a cross‑functional environment to ensure compliant execution while continuously optimizing efficiency to meet evolving organizational needs. /p ul libLead Process Governance: /b Provide expert guidance and support for complex system, software, and assay projects across risk, requirements, configuration, and defect management. /li libMaster Requirements Traceability: /b Support multi‑level requirements traceability and ensure all data is maintained within a streamlined, database‑driven approach across projects. /li libConduct Strategic Risk Assessments: /b Lead detailed product risk assessments by analyzing documents, reports, and market trends alongside cross‑functional teams. /li libEstablish Configuration Management: /b Build and maintain configuration management for complex projects, ensuring a clear overview of past, present, and future product states. /li libEnsure Regulatory Excellence: /b Provide specialized support to ensure that Verification Validation (VV) activities meet both internal standards and global regulatory requirements like ISO 13485. /li libDrive Radical Simplification: /b Proactively identify opportunities for process optimization and simplification to improve time‑to‑market without compromising quality. /li libCollaborate Globally: /b Thrive in an agile, multicultural setting where we experiment, learn, and trust each other to deliver the best results for patients. /li /ul h3Who You Are /h3 pYou are a proactive and service‑oriented professional who excels at solving complex problems independently. You bring strong analytical thinking and the ability to communicate precisely in a collaborative, global environment. /p pbTo be successful in this role, you bring: /b /p ul libAdvanced Academic Foundation: /b A Master’s degree in Engineering, Life Sciences, Natural Sciences, or a related field. /li libExperience: /b Minimum of three years of experience in a regulated environment within product development or process management (Medical Device or Diagnostics industry preferred). /li libTechnical Mastery: /b A strong understanding of Design Control processes and global standards such as ISO 13485 or IEC 62304. /li libDigital Fluency: /b Experience with ALM tools such as Jira, Azure DevOps, or specialized requirements management software is highly valued. /li libExceptional Communication: /b Precise and efficient communication skills in English, enabling effective collaboration across our international sites. /li /ul pThere are 2 positions of this role. /p pbRoche est un employeur offrant l'équité en matière d'emploi. /b /p /p #J-18808-Ljbffr

INMOBILIARIA SITUADA EN SABADELL, NECESITA INCORPORAR UN/A ADMINISTRATIVO/VA DE GESTIÓN DE ALQUILERES. TU MISIÓN PRINCIPAL SERÁ ASEGURAR UNA GESTIÓN ADMINISTRATIVA DE LA CARTERA DE ALQUILERES Y RESOLVER LAS INCIDENCIAS CON EFICACIA. SI TE APASIONA EL TRATO HUMANO, ERES UNA PERSONA RESOLUTIVA Y DOMINAS LA ADMINISTRACIÓN INMOBILIARIA, ¡ESTA POSICIÓN ES PARA TI! Datos de contacto: CÓDIGO DE OFERTA: 092026022543 La inscripción a esta oferta se efectúa a través del portal Feina Activa (https://feinaactiva.gencat.cat/web/guest/home ), donde encontrará más información sobre los detalles del puesto de trabajo. Puede acceder a la oferta indicando la referencia (Referencia número:92321111) en la búsqueda avanzada de Feina Activa. Para optar a las ofertas de este portal, se precisa una inscripción previa en él.

ph3About the Team /h3pDiagnostics Direct Procurement (DOP) is a team of about 200 professionals committed to driving value with suppliers worldwide. The team sources, manages the supplier base, develops and executes category strategies, and continually digitises processes to support sustainable business growth. /ph3Role Overview /h3pAs the Global Category Manager for Engineering Services based in Sant Cugat, Spain, you will steer the long‑term category roadmap and command the high‑value supplier ecosystems that drive our global instrument development projects. /ppReporting line: Directly reports to the Global Category Lead Capex / Engineering Services / IT within the Category organization. /ppWider team and stakeholders: Engages directly with cross‑functional teams composed of representatives from Category, Procurement Center of Excellence, RD, and other global business partners. Serves as a key business partner contact point for senior functional and business stakeholders in RD. /ppRole type: Individual Contributor with global category leadership position focused on strategic vision, category development, pipeline building, and relationship ecosystem management. /ph3Impact /h3pYou deliver commercial impact by anchoring cost and developing a resilience pipeline of projects, in addition to securing our sustainability priorities. /ph3Key Responsibilities /h3ulliStrategy Annual Pipeline: Collate market intelligence, supplier data and business requirements to formulate a formalized, global Category Strategy and initiative pipeline aligned with leaders across the organization. /liliCommercial Negotiations: Lead high‑value commercial and contractual negotiations for strategic suppliers within the category. /liliSupplier Ecosystems: Manage key global suppliers, establish development and innovation programs, monitor value targets, and manage supplier risks. /liliGuidance Content: Develop and maintain category guidance documents to translate strategy into clear, executable content for procurement colleagues and business users. /liliBusiness Partnering: Build deep relationships with senior stakeholders, particularly in RD, challenge demand/specifications to maximize value, and manage risk/CSR reviews. /liliTeam Budget Oversight: Coach procurement colleagues, provide professional development, manage a shared Associate Category Manager, and track budget spend. /li /ulh3Required Qualifications Experience /h3ulliEducation: University degree required (Business or Life Sciences focus preferred). A post‑graduate business‑related qualification is preferred. /liliExperience: 5+ years of in‑depth strategic and operational procurement experience with extensive knowledge of category management and advanced strategic sourcing. /liliRegulated Industry: 5+ years of overall business experience working within a regulated industry like Diagnostics with familiarity of relevant legal and quality risks. /liliMarket Expertise: Deep sub‑category subject matter knowledge of Software Development (e.g., Instrument OS Embedded Systems, Software Maintenance), Hardware Engineering (e.g., Product Design) and Testing (e.g., SW/HW Testing, Testing Automation, Verification Validation (VV)). /liliSystems Analytics: Expert proficiency in navigating enterprise systems, P2P tools, and procurement systems for sourcing events and contract negotiations (e.g., eSourcing, eAuction). /liliAI Digitalization: Advanced knowledge in AI application and a strong affinity to explore AI‑driven solutions broadly, particularly regarding the digital transformation of operations. /liliFinancial Acumen: Proven financial and business acumen, grounded in total cost of ownership (TCO) and cost modeling. /liliLeadership Change: Strong communication, project management, and change management skills with a demonstrated ability to lead global cross‑functional teams in a fluid environment. /liliLanguages: Business‑level fluency in English is required. /liliTravel: High flexibility and willingness to travel domestically and internationally up to 30%. /li /ulh3Equal Opportunity Employer /h3pRoche is an Equal Opportunity Employer. /p /p #J-18808-Ljbffr

En nuestra oficina técnica ofrecemos servicios en función de las necesidades de cada cliente, ya que en BETWEEN nos podemos hacer responsables de todas las tareas de desarrollo relacionadas con el ciclo de vida de su producto. Seleccionamos un/a bTécnico/a de Mantenimiento Electrónico /b para in

Marketing Manager /h3 pEnergiot is looking for a Marketing Manager to join our team in Barcelona and help lead the next stage of our marketing and communications strategy. Develop and manage Account‑Based Marketing (ABM) and inbound marketing campaigns to generate qualified leads. The main goal of

pAMMEGA busca un/a Responsable de Producción para dirigir el Taller Central en Barberà del Vallès. Liderarás equipos, planificarás y coordinarás procesos de fabricación de bandas transportadoras, asegurando calidad, seguridad y servicio al cliente. /ppReportarás al Director de Operaciones y liderarás iniciativas de mejora continua, desarrollando a tu equipo mediante formación y estandarización de procesos, con foco en entrega a tiempo y eficiencia. /p #J-18808-Ljbffr

pMoventia busca un Controller Financiero con fuerte componente analítico para apoyar su negocio internacional y liderar procesos en el área de transporte de viajeros. La posición implica supervisar el cierre mensual y asegurar la calidad de la información financiera presentada. /ppEl candidato ideal debe tener formación en ADE o económicas, experiencia en control financiero, y un dominio avanzado de Excel. Se requiere también un conocimiento fluido del francés para interactuar con diferentes áreas del negocio y asegurar las mejores prácticas contables. /p #J-18808-Ljbffr

DESDE MIM GRUP, EMPRESA DEDICADA E INTEGRADA EN EL MANTENIMIENTO INDUSTRIAL, ENFOCADA EN EL SECTOR INTRALOGÍSTICO (INDUSTRIA 4.ALMACENES AUTOMATIZADOS) PRECISAMOS INCORPORAR PERFILES DE MANTENIMIENTO/LUBRICACIÓN INDUSTRIAL PARA GESTIONAR, ASEGURAR Y CONSERVAR LA PRODUCCIÓN Y LA MAQUINARIA DE NUES

Sener busca incorporar un/a Ingeniero/a de Implantación APS (Ortems) en Cerdanyola del Vallès. Este rol implica mejorar e integrar herramientas de producción, gestionar los recursos y colaborar con diferentes áreas. Se requiere Grado/Máster en Organización Industrial y experiencia en la implantación de sistemas como APS, ERP y MES. Ofrecemos oportunidades en proyectos innovadores, horarios flexibles y un entorno que promueve igualdad y desarrollo profesional.br#J-18808-Ljbffr

pSener Aerospace Defence busca un/a Técnico/a de Producción de Equipos Electrónicos Embarcados en Cerdanyola del Vallès. /ppSe requiere experiencia en producción electrónica y conocimiento de normativas IPC. Ofrecemos participación en proyectos de alto nivel tecnológico, un plan retributivo flexible y un programa de bienestar físico y emocional. /ppPromovemos la igualdad de oportunidades y el desarrollo profesional. /p #J-18808-Ljbffr

ppEn Sener Aeroespacial y Defensa queremos incorporar en nuestro equipo a una posición estable de Técnico/a producción componentes electrónicos SMT Manual para proyectos de Aeroespacial y Defensa en nuestro centro de Cerdanyola del Valles (Barcelona). /p pSomos una compañía de ingeniería pionera en el diseño de tecnología satelital y equipos para la exploración espacial. En Defensa abordamos el diseño y producción de equipos y sistemas, incluidos los no tripulados. Nuestra pasión por la precisión nos ha llevado a situarnos como colaboradores de confianza de las principales agencias espaciales, organismos gubernamentales y empresas. /p h3Qué harás: /h3 ul liRealizar operaciones de ensamblaje y montaje manual de componentes electrónicos SMT sobre PCB. /li liPreparación de materiales, herramientas y equipos necesarios para la producción. /li liEjecutar tareas de soldadura manual y retrabajos de componentes SMT. /li liInterpretar instrucciones de trabajo, planos, listas de materiales (BOM) y documentación técnica. /li liVerificar visualmente la correcta colocación y soldadura de componentes electrónicos. /li liIdentificar y reportar defectos, incidencias de producción. /li liRellenar registros de producción y documentación asociada. /li liGarantizar el cumplimiento de los estándares ESD. /li liMantener el puesto de trabajo limpio, ordenado y seguro. /li liAsegurar el cumplimiento de los procedimientos de calidad y prevención de riesgos laborales. /li /ul h3Qué esperamos de ti: /h3 ul liFP en Electrónica o formación similar. /li liExperiencia en procesos de fabricación electrónica y SMT. /li liConocimientos de soldadura electrónica y manejo de componentes SMT. /li liCapacidad de interpretación de instrucciones técnicas. /li liAtención al detalle y orientación a la calidad. /li /ul h3Qué te ofrecemos: /h3 ul liContrato indefinido. /li liHorario: turnos rotativos de mañana y tarde. /li liIntegrar en un equipo multidisciplinar y altamente cualificado participando en proyectos innovadores tecnológicamente a nivel internacional. /li liContinua tu desarrollo profesional con nosotros y accede a un amplio abanico formativo (formación técnica, en habilidades, idiomas...). /li liCuídate con nuestro programa de bienestar físico y emocional: deportes, talleres, fisioterapia, etc. /li liOptimiza tu salario con nuestro plan retributivo flexible (tarjeta de comida, seguro médico privado, tickets guardería...) y cuenta con nuestro seguro de vida y accidentes. /li liPortal de descuentos para ti y plan de acogida específico para nuestros empleados internacionales. /li liPromovemos la igualdad de oportunidades, diversidad e inclusión de todas las personas y estamos certificados como Entidad Familiarmente Responsable (efr). Además, desde la Fundación Sener colaboramos en actividades que fomentan la búsqueda del conocimiento y contribuyen al desarrollo socialmente responsable de la ingeniería. /li /ul pSi te sientes identificado/a, te esperamos....¡En Sener queremos llegar tan lejos como quieras llegar tú! /p p#LI-NM1 /p /p #J-18808-Ljbffr

Sener Aerospace Defence busca un/a Técnico/a de Producción SMT Automático en Cerdanyola del Vallès. Serás responsable de la operación de líneas SMT automáticas y el control de calidad. Se requieren al menos 2 años de experiencia en producción industrial y formación en Electricidad/Electrónica. Ofrecemos un entorno innovador y oportunidades de desarrollo profesional, además de un plan retributivo flexible, seguro médico, y programas de bienestar físico y emocional.br#J-18808-Ljbffr

ppEn Sener Aeroespacial y Defensa deseamos incorporar en nuestro equipo a una posición estable de Técnico/a Producción Montaje Electrónico para proyectos de Aeroespacial y Defensa en nuestro centro de Cerdanyola del Valles (Barcelona). /p pSomos una compañía de ingeniería pionera en el diseño de tecnología satelital y equipos para la exploración espacial. En Defensa abordamos el diseño y producción de equipos y sistemas, incluidos los no tripulados. Nuestra pasión por la precisión nos ha llevado a situarnos como colaboradores de confianza de las principales agencias espaciales, organismos gubernamentales y empresas. /p h3Qué harás: /h3 ul liManejo de máquinas de línea de montaje automático de equipos electrónicos /li liIntegración de equipos (montaje, pegados, tornillería, etc.) /li liPreparación de material para alimentar la línea de montaje /li liImprescindible tener disponibilidad para trabajar enturnos rotativos de mañana, tarde y noche (cambio de turno cada 2 semanas) /li /ul h3Qué esperamos de ti: /h3 ul liEstudios de FP Electrónica o estudios afines /li liNo se requiere experiencia en el puesto (se formará a la persona que se incorpore) /li liConocimientos de ofimática /li liNivel básico de inglés /li liDestreza manual para el manejo de piezas pequeñas /li liCapacidad de atención al detalle /li liDisponibilidad horaria para realizar turnos rotativos de mañana, tarde y noche /li liVehículo propio para poder ajustarse al horario /li liTrabajo en equipo /li /ul h3Qué te ofrecemos: /h3 ul liContrato indefinido /li liHorario: turnos rotativos de mañana, tarde y noche (cambio de turno cada 2 semanas) /li liIntégrate en un equipo multidisciplinar y altamente cualificado participando en proyectos innovadores tecnológicamente a nivel internacional. /li liContinua tu desarrollo profesional con nosotros y accede a un amplio abanico formativo (formación técnica, en habilidades, idiomas...). /li liCuídate con nuestro programa de bienestar físico y emocional: deportes, talleres, fisioterapia, etc. /li liOptimiza tu salario con nuestro plan retributivo flexible (tarjeta de comida, seguro médico privado, tickets guardería...) y cuenta con nuestro seguro de vida y accidentes. /li liPortal de descuentos para ti y plan de acogida específico para nuestros empleados internacionales. /li liPromovemos la igualdad de oportunidades, diversidad e inclusión de todas las personas y estamos certificados como Entidad Familiarmente Responsable (efr). Además, desde la Fundación Sener colaboramos en actividades que fomentan la búsqueda del conocimiento y contribuyen al desarrollo socialmente responsable de la ingeniería. /li /ul pSi te sientes identificado/a, te esperamos....¡En Sener queremos llegar tan lejos como quieras llegar tú! /p /p #J-18808-Ljbffr

pClaire Joster busca un/a Project Manager para su sede en Sabadell. La persona seleccionada será responsable de gestionar y coordinar proyectos en la industria química y alimentaria, asegurando un enfoque en resultados y autonomía en la planificación. /ppSe requiere experiencia previa en procesos industriales y un nivel alto de inglés (C1). La empresa ofrece horario flexible, retribución acorde a la valía y comisiones. Además, se ofrece acceso a clases de inglés in company. /p #J-18808-Ljbffr

ph3HP Sales Compensation Design Strategy Manager /h3pHP seeks an expert Sales Compensation Design Manager to lead the design, governance, and execution of sales incentive and quota programs across a complex, multi‑channel go‑to‑market model. The role sits at the intersection of strategy, analytics, and execution, ensuring compensation frameworks drive the right sales behaviors, support margin and growth objectives, and scale globally with consistency and transparency. /ph3Key Responsibilities /h3ulliLead end‑to‑end design of global sales compensation plans across direct, indirect, overlay, and specialist roles. /liliManage a team of regional experts to drive global coordination of strategies, programs and processes. /liliEnsure plans are aligned to HP’s growth strategy, product mix, margin objectives, and channel model. /liliBalance simplicity, scalability, and motivational impact while maintaining governance and compliance. /liliTranslate strategic priorities into measurable incentive mechanics (rates, accelerators, thresholds, SPIFFs). /li /ululliOwn annual and in‑year quota planning cycles across regions, segments, and roles. /liliDevelop quota methodologies that ensure fairness, achievability, and differentiation, grounded in data and historical performance. /liliPartner with Sales Operations, Finance, and GTM leaders to align quotas to revenue targets and capacity models. /liliDrive consistent quota allocation processes, timelines, and approval frameworks globally. /li /ululliEstablish performance analytics to evaluate plan effectiveness, quota attainment, pay‑for‑performance, and ROI. /liliIdentify trends, risks, and unintended behaviors and recommend plan or quota adjustments. /liliDeliver clear executive‑level insights and scenario modeling to support decision‑making. /li /ululliAct as a trusted advisor to senior Sales and Finance leadership. /liliLead and develop a high‑performing compensation and quota planning team. /liliInfluence across a matrixed organization without direct authority. /liliNavigate ambiguity and competing priorities with executive presence and clarity. /li /ulh3Required Qualifications /h3ulli10+ years of progressive experience in sales compensation and quota planning. /liliProven leadership experience in a large, international, matrixed organization. /liliDeep expertise in compensation plan design and quota methodologies across multiple sales roles and international complexity. /liliStrong analytical skills with the ability to translate data into executive‑ready insights. /liliExperience leading annual planning cycles with complex stakeholder alignment. /liliAdvanced knowledge of SPM/ICM platforms (e.g., SAP SuccessFactors, Xactly, Varicent, Forma). /li /ulh3Preferred Qualifications /h3ulliExperience in technology, hardware, or hybrid product/services sales models. /liliFluency in Business English (both verbal and written). /liliBachelor or Master’s degree in Business, Finance, or related field. /liliDemonstrated experience leading transformations in highly complex matrixed organizations. /li /ulh3Success Metrics (First 12–18 Months) /h3ulliOn‑time, high‑quality delivery of annual compensation and quota cycles. /liliImproved quota attainment correlation to performance and reduced plan complexity. /liliIncreased confidence and trust from Sales leadership in incentive fairness and effectiveness. /liliMeasurable reduction in manual processes and exception handling. /liliClear linkage between incentives, sales behavior, and business outcomes. /li /ulh3Location Work Conditions /h3pFull‑time. Shift – No shift premium (Spain). Travel and relocation supported as required. /ph3Equal Employment Opportunity /h3pHP, Inc. provides equal employment opportunity to all employees and prospective employees, without regard to race, color, religion, sex, national origin, ancestry, citizenship, sexual orientation, age, disability, or status as a protected veteran, marital status, familial status, physical or mental disability, medical condition, pregnancy, genetic predisposition or carrier status, uniformed service status, political affiliation or any other characteristic protected by applicable national, federal, state, and local law(s). Please be assured that you will not be subject to any adverse treatment if you choose to disclose the information requested. This information is provided voluntarily. The information obtained will be kept in strict confidence. For more information, review HP’s EEO Policy or read about your rights as an applicant under the law here: “Know Your Rights: Workplace Discrimination is Illegal.” /p /p #J-18808-Ljbffr