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DOMINION GLOBAL busca un/a Coordinador/a Administrativo/a para su equipo de proyectos de distribución eléctrica en Sant Feliu de Llobregat.Aumente sus posibilidades de llegar a la fase de entrevista leyendo la descripción completa del puesto y enviando su solicitud sin demora.La posición requier

Buscamos un técnico en calidad y Director técnico suplente para colaborar en la definición e implementación de las políticas/procedimientos del Sistema de Calidad de Laboratorios Salvat, asegurando su cumplimiento frente a las normativas de aplicación (GMP, GxP, ISO, ICH, etc. Como Director t�

Contrato indefinido8830 SANT BOI, EspañaMisión :Gestión de equipo: selección, formación, coaching y desarrollo de competencias de tu equipo, gestión administrativa (elaboración de plannings, etc), animación de reuniones y puntos de equipo diarios (rituales de lanzamiento de jornada, etc);Ven

Nos caracterizamos por ser una compañía dinámica, marcada por la constante innovación tecnológica y por el estudio de las nuevas perspectivas de mercado.Aunque la experiencia profesional y las cualificaciones son clave para este puesto, asegúrese de comprobar si posee las habilidades interpers

En Reig Jofre estamos buscando a un/a ¿Está pensando en solicitar este empleo? No se demore, desplácese hacia abajo y envíe su solicitud lo antes posible para no perder la oportunidad. In Process Control Manager para que pueda contribuir a los diferentes proyectos que estamos desarrollando en la planta productiva ubicada en Sant Joan Despí. Su misión principal será la de liderar el equipo de control en proceso asegurando la eficiencia operativa, el cumplimiento normativo y la mejora continua del sistema. Así mismo, garantizar la visibilidad del rendimiento del área hacia dirección y actuar como responsable último de la gestión del talento y la carga de trabajo del equipo. Funciones Definir y realizar seguimiento de los KPIs del área tales como tasa de desviaciones, cumplimiento de CAPAs o rendimiento analítico. Reporte periódico a dirección sobre el estado de los procesos y las incidencias activas. Aprobación formal de CAPAs y cierre de desviaciones de impacto elevado. Planificación semanal de la carga de trabajo del equipo y asignación de responsabilidades. Escalado y gestión de incidencias críticas con impacto en producción, calidad o regulatorio. Representación del área en auditorías internas y externas (GMP, clientes o autoridades). Gestión del desarrollo del equipo: formación, evaluación de desempeño y plan de carrera. Coordinación con otros departamentos (producción, logística, I+D y/o calidad) para la resolución de problemas transversales. Garantizar la formación, capacitación y desarrollo continuo del equipo. Liderar, coordinar, acompañar y desarrollar al equipo de In Process Control. Participar activamente en auditorías e inspecciones internas y externas. Aptitudes y experiencia requeridas: Licenciatura o Grado en Farmacia, Química, Biología, Biotecnología o disciplinas afines. Experiencia previa trabajando en Control de Calidad dentro de la industria farmacéutica. Experiencia en coordinación o liderazgo de equipos en entornos regulados. Conocimiento sólido de normativa GMP y sistemas de calidad farmacéuticos. Experiencia en gestión de desviaciones, investigaciones y acciones CAPA. Capacidad de organización, liderazgo y orientación a resultados. Nivel alto de inglés. Nosotros ofrecemos: Salario competitivo en función de la capacidad y experiencia del candidato. Horario en turno central partido. Contrato indefinido. Plan de compensación flexible (seguro médico, ticket transporte, guardería, formación…). Formar parte de una empresa líder en el sector farmacéutico. xcskxlj Si cumples con los requisitos y quieres involucrarte en un nuevo reto profesional, no lo dudes ¡Apúntate!

Experteer Overview Join Roche as an International Regulatory Affairs Professional to drive regulatory excellence for global IVD/MD instruments and software. You will collaborate with Ru0026amp;D, Quality, and Clinical teams to shape submissions, stay ahead of regulatory developments, and support product lifecycle management. This role offers meaningful global impact through enabling access to healthcare and advancing medical solutions. You’ll thrive in a collaborative, innovative environment and help define the future of regulatory strategy at Roche. Compensaciones / Beneficios • Lead and support regulatory strategies for global IVD/MD instrument and software submissions • Ensure compliance with international regulatory requirements and standards • Collaborate with cross-functional teams to drive regulatory initiatives • Provide regulatory guidance to support product development and lifecycle management • Stay informed on evolving regulatory trends and implement best practices Responsabilidades • Bachelor’s Degree in Life Sciences, Regulatory Affairs, or related field • 5 to 7 years of experience in Regulatory Affairs (Regulatory, Ru0026D, Quality and/or Clinical) • Deep knowledge of global regulatory requirements, guidelines, and procedures for IVD instruments u0026 software • Strong organizational and communication skills • Ability to multitask and manage multiple projects • Self-motivated with ability to work independently • Experience in IVD instrument and/or software development Requisitos principales • competitive compensation and benefits package • professional development and growth opportunities

ph3Buscamos: Estudiante de Project Manager - Proyecto Hincator /h3 pBarcelona · Presencial / Híbrido · Jornada completa /p h3Lo que harás: /h3 ul liGestionar la ejecución de proyectos Hincator en cliente: desde el kick-off hasta la /li liSer el punto de contacto entre el cliente (EPCs, promotores) y los equipos internos /li liCoordinar despliegues en múltiples países simultáneamente /li liDetectar incidencias en campo y resolverlas con agilidad /li liMejorar los procesos de onboarding conforme crece el volumen de proyectos /li liExperiencia en gestión de proyectos técnicos (construcción, energía o sector /li liCapacidad para manejar varios proyectos en paralelo con clientes exigentes /li liPerfil resolutivo: detecta el problema, propone la solución y la ejecuta /li liInglés profesional: los proyectos y clientes son internacionales /li liDisponibilidad para viajar a obra cuando el proyecto lo requiere /li /ul h3Se valorará: /h3 ul liExperiencia en fotovoltaica / EPCs /li liGestión de hardware en campo /li liFrancés, alemán o portugués /li /ul h3Beneficios: /h3 ul liPosibilidad de contrato indefinido /li liProyectos en 10+ países desde el primer día /li liProducto patentado reconocido por Iberdrola como el más innovador del sector en /li liDecisiones rápidas, sin burocracia /liliRecorrido real dentro de un proyecto en plena expansión internacional /li /ul /p #J-18808-Ljbffr

pQueremos incorporar UN/A LOGISTICS MANAGER para marca internacional líder en decoración para el hogar.Su misión es garantizar el flujo de mercancía fiable y eficiente en coste, desde el origen de producción en India hasta los almacenes internacionales. /ppUbicació: BARCELONA - BAIX LLOBREGAT - 08960 SANT JUST DESVERN /ppGestionar la logística de contenedores desde India a almacenes y distribuidores, incluyendo booking y planificación de envíos.Negociar tarifas y condiciones con navieras y transportistas.Supervisar aduanas, documentación de importación/exportación y compliance, asegurando que la mercancía despache y llegue a tiempo.Gestionar el seguro de la mercancía y resolver incidencias, reclamaciones y discrepancias con los transportistas. /pulliCompetències / coneixements: Experiencia negociando con navieras, transportistas y proveedores logísticos.Gestionar presupuestos y KPIs.Experiencia con sistemas ERP .Nivel profesional de inglés. /liliContracte laboral indefinit /li /ul #J-18808-Ljbffr

ppThe primary purpose of this position is to supervise and facilitate the construction phase of projects by directly managing sub‑contractors and providing oversight and project support for production, safety, and quality. Primarily focuses on General Contracting projects and serves as the on‑site project manager, schedule and sequence turf installations. Serves as regional customer service liaison; supports Sales team by attending pre‑bid meetings and presentations. /p h3What We Offer /h3 ul liFlexible working hours and hybrid work /li liAttractive rewards and benefits (health, savings, retirement) /li liLearning development opportunities /li liPaid time off and holidays /li liBenefits may vary depending on role, country and local regulations. /li /ul pTarkett is an equal opportunity employer. We value diversity in backgrounds and in experiences and promote an inclusive workplace where all employees can perform at their best. /p /p #J-18808-Ljbffr

Experteer Overview In this role you will coordinate end-to-end artwork processes for printed packaging, ensuring regulatory compliance and print readiness across EMEA. You will work with cross-functional teams to gather inputs, manage timelines, and maintain traceability of artwork versions. The position focuses on delivering accurate, brand-aligned packaging with a strong emphasis on quality and regulatory alignment. This is an opportunity to shape packaging workflows and harmonize practices across markets within a dynamic FMCG environment. Compensaciones / Beneficios • Coordinate end-to-end artwork process from briefing to final approval • Manage artwork updates for new product launches, packaging changes, regulatory updates, and continuity initiatives • Collaborate with marketing, regulatory, quality, Ru0026D, and supply chain to secure approvals • Engage repro agencies, packaging suppliers, and printers to ensure feasibility and print readiness • Review and proof artwork files for compliance and consistency • Track timelines and manage deadlines to ensure on-time delivery • Maintain version control and approval records for traceability • Support harmonization and optimization initiatives across markets • Ensure artwork status is maintained in internal systems (e.g., SAP or artwork platforms) • Troubleshoot artwork or production issues to protect launch timelines and quality Responsabilidades • 3+ years in artwork coordination, packaging production, or prepress (FMCG/beverage/regulatory industries preferred) • Understanding of printed packaging processes and print-ready file preparation • Experience managing multiple projects and stakeholders • Knowledge of printing technologies, packaging materials, and artwork workflows • Familiarity with artwork management tools; Adobe-based environments an advantage • Experience with regulatory or compliance-driven packaging is a plus • English u0026 Italian proficient • Bachelor's degree in Packaging, Graphic Arts, Design, Marketing, or related field is preferred Requisitos principales •

Cegid, referente europeo en soluciones de gestión en la nube, busca un Key Account Executive para la división Enterprise en Cataluña. Asegúrese de presentar su candidatura con toda la información solicitada, tal como se expone en la descripción del puesto a continuación. Serás responsable de identificar, abrir y desarrollar grandes cuentas estratégicas, impulsando la adopción de nuestras soluciones SaaS de HCM en organizaciones de alto potencial. Colaborarás con ventas, producto y customer success para convertir oportunidades xkdbapo complejas en relaciones sólidas, aportando valor a decisores de alto nivel y orientadas a retorno de #J-18808-Ljbffr

ppAs a Senior Process Manager within the 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 requirements, risk, configuration, defect management, and verification validation within complex development projects. /ppThere are 2 positions of this role. /ph3Responsibilities /h3ulliLead Process Governance: Provide expert guidance and support for complex system, software, and assay projects across risk, requirements, configuration, and defect management. /liliMaster Requirements Traceability: Support multi‑level requirements traceability and maintain all data within a streamlined, database‑driven approach across projects. /liliConduct Strategic Risk Assessments: Lead detailed product risk assessments by analyzing documents, reports, and market trends alongside cross‑functional teams. /liliEstablish Configuration Management: Build and maintain configuration management for complex projects, ensuring a clear overview of past, present, and future product states. /liliEnsure Regulatory Excellence: Provide specialized support to ensure that Verification Validation (VV) activities meet internal standards and global regulatory requirements such as ISO 13485. /liliDrive Radical Simplification: Proactively identify opportunities for process optimization and simplification to improve time‑to‑market without compromising quality. /liliCollaborate Globally: Thrive in an agile, multicultural setting where we experiment, learn, and trust each other to deliver the best results for patients. /li /ulh3Qualifications /h3ulliAdvanced Academic Foundation: A Master’s degree in Engineering, Life Sciences, Natural Sciences, or a related field. /liliExperience: Minimum of three years of experience in a regulated environment within product development or process management (Medical Device or Diagnostics industry preferred). /liliTechnical Mastery: A strong understanding of Design Control processes and global standards such as ISO 13485 or IEC 62304. /liliDigital Fluency: Experience with ALM tools such as Jira, Azure DevOps, or specialized requirements management software is highly valued. /liliExceptional Communication: Precise and efficient communication skills in English, enabling effective collaboration across our international sites. /li /ulpRoche is an Equal Opportunity Employer. /p /p #J-18808-Ljbffr

Hewlett Packard Enterprise is seeking an experienced PS Product Data Management leader to independently develop operational and project strategies in PDM, overseeing cross-functional topics and large program teams. You will manage master data topics, collaborate with enterprise applications (MS4, S4, Pulsar) and BI tools, and mentor teams to deliver high-adoption supply chain improvements while shaping new processes and frameworks. #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

ph3Role Purpose /h3 pAs GCS RIS Implementation Manager, you are accountable for the successful implementation of Roche’s digital products at the customer. In early product life cycle phases you will be responsible for implementing select RIS products in the ‘Nail-It’ phase of the product lifecycle. You will then be accountable for the successful onboarding and success of the affiliate implementations. /p h3Key Responsibilities /h3 ul liProvide customer project expertise to the GCS Technical Product Manager. /li liSupport the product life cycle by improving product serviceability and implementability while keeping the broader solution in mind. /li liDevelop project documentation in accordance with the scope and deliverables of the project, following best practices. /li liAlert the established escalation person(s) if problems are not resolved in a reasonable amount of time. /li liEscalate to the manager and appropriate functional heads when major issues arise that pose risk to the project’s critical path. /li liFollow or develop testing scenarios to test new or modified implementations of navify Product(s), verify test results, and drive customer acceptance. /li liStay well-informed of changes to the roadmap, features, and known features of the products within your sphere of influence. /li liLearn and share knowledge obtained for better usage of company-provided tools and software; suggest new technologies and software that may improve productivity and efficacy of the team. /li liMaintain and understand training compliance to ensure that work and interactions thereto depend on Roche’s Code of Business Conduct. /li liMaintain compliance with Roche’s TE guidelines, including cost guidelines, reporting timeliness, transparency, and correct usage of Roche’s credit card and travel tools. /li liBuild or help shape tools for teams to be more productive, with management buy‑in. /li liCreate solutions to complex issues without requiring management guidance. /li liFind solutions to issues that require resources from outside teams, document them, and integrate them into standard processes for the team. /li liMentor and onboard other members of the team. /li liDevelop templates for new documentation or improve current templates and documentation (Meeting Minutes, Project Schedule, Runbook, etc.). /li /ul h3Your profile /h3 ul liGood communication skills and proficiency in English, Spanish, and French. /li liBachelor's or master’s degree in a relevant field (IT, Lab Technician, etc.) AND /li li5+ years of relevant work experience in IT, lab organization (medical lab technician, lab manager) or hospital IT networks, interfaces, and/or database OR /li liAn equivalent mix of relevant education and work experience is required. /li liPrevious experience working in a clinical environment is highly desirable. /li liExplicit problem‑solving attitude and experience working in a customer‑oriented way in an interdisciplinary environment. /li liWillingness to travel (up to 50%) nationally and worldwide. /li liIndependent, proactive and versatile working approach, but also acting as a team player in a global team. /li /ul h3Locations /h3 pYou will be based in Sant Cugat, Spain. As this position is a global role, international business travel will be required depending on the business location of the successful candidate and ongoing business project activities. /p pRoche is an equal opportunity employer. /p pbRoche est un employeur offrant l’équité en matière d’emploi. /b /p /p #J-18808-Ljbffr

ph3Responsibilities /h3 ul liLiderar y coordinar al equipo de QA SAP, promoviendo la colaboración, el desarrollo profesional y la consecución de objetivos de calidad. /li liDefinir y supervisar la estrategia de pruebas para proyectos SAP, asegurando el cumplimiento de estándares y buenas prácticas. /li liGestionar el ciclo de vida de las pruebas mediante herramientas especializadas, asegurando la trazabilidad y el seguimiento de los resultados. /li liImpulsar la definición y evolución de los marcos de automatización de pruebas. /li liColaborar con equipos multidisciplinares para identificar, analizar y resolver incidencias relacionadas con la calidad del software. /li liRealizar el seguimiento de indicadores clave de calidad, elaborando informes y proponiendo acciones de mejora. /li liAportar mentoría y soporte al equipo, fomentando una cultura de aprendizaje continuo. /li /ul h3Requirements /h3 ul liTitulación universitaria en Informática, tecnologías de la Información o áreas afines. /li liExperiencia sólida liderando equipos de QA y participando en proyectos de implantación SAP. /li liExperiencia en automatización de pruebas y definición de estrategias de testing. /li liCapacidad demostrable para gestionar múltiples prioridades y trabajar con plazos exigentes. /li liExcelentes habilidades de comunicación, colaboración y liderazgo. /li liCapacidad analítica, orientación al detalle y resolución de problemas. /li liExperiencia con SAP Solution Manager o SAP Cloud ALM (muy positivo). /li liConocimientos y experiencia con Tricentis Tosca (muy positivo). /li liCertificaciones relacionadas con testing de software, automatización o metodologías de calidad (muy positivo). /li /ul /p #J-18808-Ljbffr

Una empresa internacional de distribución busca un/a Export Assistant en Sant Just Desvern. El candidato/a ideal tendrá experiencia en logística, deberá coordinar cargas y asegurar un retorno de información eficaz. Se valorará formación en Comercio Internacional y altos conocimientos en Microsoft Office. Esta posición ofrece flexibilidad laboral, incluyendo remoto y horarios adaptables, además de un paquete de beneficios como seguro de salud y actividades afterwork.br#J-18808-Ljbffr

Experteer Overview En un contexto de crecimiento y expansión de planta, lideras un equipo de 7 personas para gestionar métodos, mejora continua y planificación productiva. Buscas optimizar procesos, aumentar eficiencia y garantizar calidad y seguridad en un entorno de fabricación de soluciones ETO para data centers. Colaboras con otras áreas para alinear proyectos con demanda y capacidad, impulsando iniciativas de mejora y industrialización. Esta posición ofrece impacto directo en escalado productivo y resultados operativos. Compensaciones / Beneficios • Liderar y desarrollar el equipo de métodos, mejora continua y planificación de planta (7 personas) • Definir, implantar y optimizar procesos productivos con foco en eficiencia, calidad y seguridad • Liderar iniciativas de mejora continua (Lean, Six Sigma, Kaizen) y gestionar su implementación • Supervisar planificación productiva y asegurar un plan maestro alineado con demanda, capacidad y recursos • Analizar KPIs clave (productividad, OEE, lead time, costes) y definir planes de acción • Gestionar estandarización de procesos, instrucciones de trabajo y documentación técnica • Asegurar disponibilidad y optimización de herramientas, layouts y medios productivos • Liderar proyectos de industrialización y escalado productivo ante crecimiento y ampliación de planta • Evaluar ROI y viabilidad económica de proyectos Responsabilidades • Grado o Máster en Ingeniería Industrial, Mecánica, Eléctrica o similar • +5 años de experiencia gestionando equipos como manager • Experiencia en auditorías de proceso (VDA, IATF, AS9100, ISO9001 o similar) • Conocimientos sólidos en Lean Manufacturing, mapeo de procesos y herramientas de análisis de causa raíz (5 Porqués, Ishikawa) • Experiencia con herramientas digitales de fabricación (MES, PLM, ERP) • Herramientas de mejora y análisis (Excel avanzado, Power BI, estadística) • Formación técnica en instalaciones eléctricas y automatismos industriales • Nivel C1 de inglés en entorno laboral • Disponibilidad para viajar puntualmente (aprox. 1 semana/trim. Requisitos principales • modelos de trabajo flexibles • equilibrio vida/familia • ambiente inclusivo y colaborativo • oportunidades de desarrollo • ambiente dinámico • enfoque en ética y sostenibilidad

pAlmirall busca un Senior Manager en QA de GVP para garantizar la mantenimiento, desarrollo y mejora continua del Sistema de Gestión de Calidad en farmacovigilancia, asegurando cumplimiento con ICH, EU GVP y regulaciones aplicables. /ppResponsable de planificar auditorías de riesgo, coordinar auditorías en afiliados y terceros, gestionar hallazgos y preparar inspecciones de autoridades. Se trabajará desde Sant Feliu de Llobregat en un contrato indefinido, con enfoque en soluciones de QA en I+D. /p #J-18808-Ljbffr

A leading electric motorcycle manufacturer based in Sant Boi de Llobregat is looking for a motivated Purchasing Category Manager to lead the EMS and PCBA Category. This role involves strategic sourcing of high-performance electronics, building relationships with global suppliers, and managing cost and quality targets. The ideal candidate will have a minimum of 5 years of sourcing experience, expertise in high-tech electronics sectors, and a strong commitment to sustainability. Join a fast-growing team passionate about innovation.br#J-18808-Ljbffr

ph3Overview /h3 p¿Te gustaría unirte a un equipo internacional que trabaja para mejorar el futuro del sector de la salud? Grifols es una compañía global del sector de la salud que desde 1909 mejora la salud y el bienestar de las personas en todo el mundo. Somos líderes en medicamentos hemoderivados y medicina transfusional y desarrollamos, producimos y comercializamos medicamentos, soluciones y servicios innovadores en más de 110 países y regiones. /p h3Mission /h3 pTo review and ensure that all procedures, testing methods and reports established in GEPD Plasma Testing Laboratories are in compliance to Egyptian regulations, and in accordance to cGMP, following Plasma Testing Specifications established and European Regulation. To manage and supervise Plasma Testing Laboratories Quality projects. To propose continuous improvement measures related to the quality systems of the Laboratories. To supervise the Quality Risk Management (QRM) process for the Laboratories. /p h3Responsibilities /h3 ul liTo review and ensure that all procedures established are in accordance to cGMP. ul liTo supervise GEPD Plasma Testing Laboratories quality system and quality culture. /li liTo ensure investigation for incidents are initiated, as well as root cause analysis are properly in place. /li liTo participate and support internal and external regulatory inspections and audits performed in the Laboratories. /li /ul /li liTo manage and supervise Plasma Testing Laboratories Quality projects. ul liActively participate in Laboratory meetings for the follow-up of activities related to open Change Controls. /li liCoordinate the tasks required to be developed within the different areas of the company. /li liReview new procedures and processes to be implemented in the Laboratory under the scope of the Change Controls open. /li /ul /li liTo ensure continuous improvement measures related to the quality systems of the Laboratories. ul liTo supervise the monitoring of corrective and/or preventive actions implemented within the Laboratories. Ensure their proper implementation and effectiveness. /li liTo monitor quality system indicators. /li liTo propose improvements in the Laboratory's processes to enhance the quality system. /li /ul /li liTo supervise the Quality Risk Management (QRM) process for the Laboratories. ul liTo supervise Quality Risk assessment studies and reports, as well as coordinate mitigation tasks. /li /ul /li /ul h3Who You Are - Qualifications /h3 ul liBachelor’s Degree in Life Sciences (Biology, Pharmacy, Biotechnology or related fields). /li liMinimum 3-5 years of experience in a related field. /li liOrganized and able to manage time effectively. /li liAbility to work within a highly regulated, labor intensive environment. /li liAbility to understand, explain, follow, and enforce SOPs. /li liAbility to plan, communicate and execute activities for the improvement of overall operations. /li liStrong integrity and commitment to Quality and Compliance. /li liExcellent oral and written communication skills to produce clear and concise factual findings. /li liAdvanced level of Spanish and English. /li liThis position requires significant travel and on-site presence in Egypt, with approximately 50% of the role based in Egypt. /li /ul h3Benefits and Location /h3 ul liContract of Employment: Permanent position. /li liLocation: Sant Cugat del Vallès, Spain. /li liFlexibility for U Program: Occasionally Remote. /li /ul h3Equal Opportunity Statement /h3 pGrifols is an equal opportunity employer. /p /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 pAssociate Category Manager (ACM) in Sant Cugat, Spain /p h3About Our Team /h3 pAt Global Diagnostics Procurement (DOP) we are a team of about 200 enthusiastic professionals, committed to driving value with our suppliers worldwide. From locations around the world and with a diverse and multicultural team, we source, manage our supplier base, develop execute category strategies and constantly develop digitize processes that enable us to best support our business to grow sustainably. If you aspire to make an impact and want to be part of a high performing and world‑class Procurement team, this is for you. /p h3The Opportunity /h3 pAre you ready to shape the long‑term supplier strategies and project pipelines that deliver medical innovation to patients worldwide? As our Associate Category Manager you will support the development, validation, and execution of global category strategies and annual strategic initiatives. In this role you will leverage rigorous procurement analytics to transform market intelligence into actionable category guidance, ensuring global supply resilience and portfolio value. /p pWe are looking to fulfil one Associate Category Manager position per team. Successful candidates will be aligned to support one of the following dedicated procurement categories: Biologicals Chemicals, Plastics Packaging, Electronics Systems, Mechanicals, Logistics. /p ul liReporting Line: Directly reports to the respective Category Lead within the Category organization. /li liWider Team and Stakeholders: Collaborates closely with Category Managers, Sourcing Managers, Delivery Managers, Finance, Legal, and external market intelligence providers. Participates in a global ACM Community of Practice (CoP) coordinated by the Category Integration Excellence Lead to ensure consistency of methodologies, reporting standards, strategic planning processes, and cross‑category collaboration. /li liRole Type: An Individual Contributor role in support of the allocated Category, focused on strategic enablement, market data intelligence, and stakeholder management. /li liImpact: You drive category compliance, data integrity, and strategic execution across the global operations network. Specifically, you are accountable for: ul liStrategy Pipeline Support: Collation of supplier, market, and internal business data to help formulate the long‑term Category Strategy and build a proactive pipeline of future initiatives. /li liStrategic Initiative Deployment: Supporting Category Managers, Project Delivery, Delivery, and Sourcing Managers in executing and deploying complex projects in strict compliance with global standards and procedures. /li liNegotiation Contracting Preparation: Supporting contract drafting and vendor negotiations for strategic, key, or bottleneck suppliers by delivering comprehensive analytics, fact‑bases, and market benchmarks. /li liStrategic Sourcing: Support selected high‑value strategic sourcing initiatives and complex RFx activities to convert pipeline targets into realized business value. /li liReporting Analytics: Collaborating with data analytics experts to generate Category‑specific insights, generating monthly spend/savings metrics, and conducting data validation to safeguard governance. /li liImplementation Support: Converting strategic outcomes into clear category guidance documents and support materials to ensure category strategies can be effectively implemented across the organization. /li /ul /li /ul h3Who you are /h3 ul liEducation: University degree (Business or Life Sciences focus preferred). Professional purchasing (e.g., CIPS), project management (e.g., PMP, Prince2), or Finance‑related licenses are highly advantageous. /li liExperience: 2+ years of procurement or supply chain experience focused on strategic sourcing, enterprise cost reduction, or operational efficiency initiatives. /li liMarket Knowledge: Demonstrated understanding of major direct spend categories, spend levers, and supply market fundamentals. /li liSystems Analytics: Strong experience driving insights from large data sets, utilizing data visualization applications (specifically Tableau and ThoughtSpot), enterprise systems (SAP/Oracle), and eSourcing/eAuction platforms. /li liAI Digitalization: Advanced knowledge in AI application and a strong affinity to explore AI‑driven solutions broadly, particularly regarding the digital transformation of operations (Digital 2.0 / Industry 4.0). /li liMindset Soft Skills: Strong communicator capable of effective upwards management and conflict resolution. Capability to translate messy data into clear procurement specifications with a proactive, customer‑centric focus. /li liOperating Principles: Driven to live the Roche Operating Principles daily – simplifying radically, acting as one team, thinking long‑term, and prioritizing patient outcomes above all else. /li liTravel: Ability to travel domestically and internationally up to 10% of the time for supplier and internal network meetings. /li /ul pRoche is an Equal Opportunity Employer. /p /p #J-18808-Ljbffr

ph3Técnico/Técnica de Tech Transfer /h3 pNeuraxpharm busca personas que quieran marcar la diferencia y mejorar la vida de los pacientes dentro del área del SNC. Buscamos personas dispuestas a darlo todo por lograr lo extraordinario. /p pUbicación: Sant Joan Despí /p h3Principales Responsabilidades /h3 ul liDesarrollar nuevos métodos de análisis, o optimizar los existentes. /li liAsegurar que existen los medios necesarios (material, reactivos, instrumentación) para su realización. /li liRedactar la documentación de validación siguiendo las normas y criterios establecidos. /li liDar soporte al Departamento de Regulatory Affairs en la preparación de documentación a presentar a las Autoridades Sanitarias. Responder a las cuestiones generadas por éstas. /li liRealizar Estudios de Estabilidad (redacción de los protocolos e informes, gestión de las muestras y supervisión de los controles realizados por los analistas). /li /ul h3Tareas complementarias /h3 ul liRedactar los métodos analíticos necesarios para el Departamento de Control de Calidad. Puesta a punto, validación o transferencia. /li liDar soporte analítico en la transferencia de nuevos procesos de fabricación y productos a la planta. /li liDar soporte analítico en la optimización y validación de procesos de fabricación. /li liSupervisar directamente los análisis y la documentación generada por los analistas. /li liRealizar informes sobre las incidencias detectadas y/o resultados de los análisis realizados. /li liRedacción de procedimientos del Departamento. /li liControlar, gestionar y supervisar las calibraciones y averías de la instrumentación a su cargo. /li liParticipar en la formación a los analistas (inicial o continua). /li /ul h3Requisitos /h3 ul liFormación Universitaria en Química, Farmacia o equivalente. /li liImprescindible que tenga conocimientos a nivel de experto en técnicas analíticas cromatográficas. Habituado a la resolución de problemas cromatográficos. /li liExperiencia mínima de 3-5 años en un Departamento de Control de Calidad o Desarrollo Analítico, preferentemente en la Industria Farmacéutica. /li liUsuario de sistemas de datos cromatográficos y herramientas informáticas (Excel, Word, SAP y LIMS). /li liConocimientos en Sistemas de Calidad y regulación farmacéutica: GMPs, GLPs, ICH’s, Farmacopeas, etc. /li liProfesional proactivo y con alto nivel de autonomía. /li liElevada capacidad de planificación y organización, y con gran orientación al detalle. /li liEspíritu de equipo y habilidad para la comunicación con otros departamentos. /li liDominio del idioma inglés, hablado y escrito. /li /ul h3Beneficios /h3 ul liDesarrollo profesional individual en una empresa farmacéutica líder en Europa con una estrategia ambiciosa de crecimiento internacional. /li liRemuneración atractiva en función de la experiencia y las competencias aportadas. /li liUn equipo de liderazgo inspirador que impulsa tu rendimiento. /li liUna cultura inclusiva e inspiradora que promueve la diversidad en los equipos a diario con un equipo apasionado, dinámico, enfocado a los resultados y experto en su ámbito profesional. /li /ul h3Política de Diversidad e Inclusión /h3 pEn Neuraxpharm aseguramos un ambiente de trabajo inclusivo, diverso, seguro y respetuoso para todas las personas de la organización. Nuestra gente nos preocupa tanto como nuestros pacientes, y es por eso que nos comprometemos a garantizar un lugar de trabajo saludable, inclusivo y con igualdad de oportunidades, que permita a los empleados desarrollarse profesionalmente y garantice al mismo tiempo su satisfacción individual y colectiva. /p pNuestra política de Diversidad e Inclusión asegura una cultura empresarial basada en los principios de diversidad, igualdad e inclusión. Nuestra política cumple con la normativa legal europea e incluye los estándares, procesos y medidas a tomar en caso de discriminación o acoso contra cualquier empleado de la empresa. /p pAdoptamos y promovemos diferentes culturas, identidades de género, antigüedades, edades y mentalidades en el lugar de trabajo, para aportar a nuestro negocio diferentes perspectivas, estilos y experiencias. /p /p #J-18808-Ljbffr

ph3Job mission /h3 pSynthon is looking for an experienced Application Technician who, together with colleagues will be responsible for the management, continuity, optimization and further development of our Document Management System (DMS), Quality Management System (QMS) and Learning Management System (LMS). You will act as the primary point of contact and application owner for these systems, ensuring they support business processes effectively and comply with quality and regulatory requirements. /p pYou will work closely with business stakeholders, IT colleagues and external vendors, taking a leading role in application improvements, upgrades, validation activities and implementation projects. /p h3Responsibilities /h3 ul liOwn and manage the DMS, QMS and LMS application landscape throughout its lifecycle. /li liEnsure application availability, performance, reliability and compliance. /li liCoordinate and manage upgrades, releases, patches and system changes. /li liLead the resolution of complex incidents and perform root cause analyses and take preventive measures. /li liManage relationships with external vendors and monitor service levels and performance. /li liAct as the key liaison between business stakeholders, IT teams and suppliers. /li liTranslate business requirements into functional solutions and drive continuous improvement initiatives. /li liManage user access, permissions and security in accordance with company policies. /li liDevelop and maintain application documentation, procedures and training materials. /li liProvide guidance and knowledge sharing to end users and colleagues. /li /ul h3Location /h3 ul liAlternatively, HQ Nijmegen, the Netherlands. /li /ul h3Requirements /h3 pYour profile /p ul liBachelor’s degree (BSc) in IT, Information Management, Computer Science or a related field. /li liMinimum of 5 years of relevant experience in application management, functional management or a comparable role. /li liExperience with DMS, QMS, LMS or other regulated business‑critical applications. /li liExperience with vendor management and project‑based work. /li liExperience in the pharmaceutical sector is an advantage. /li /ul h3Languages /h3 pGood command of the Spanish and English language, both excellent verbal and written communication skills. /p h3Personal skills /h3 ul liAs an Application Manager, you act with a strong sense of ownership, taking responsibility for the availability and continuous improvement of your application landscape. /li liYou are committed to delivering reliable, compliant and business‑focused solutions. /li liYou possess strong analytical skills and can translate complex technical and functional issues into practical improvements. /li liYou are comfortable working with stakeholders at different organizational levels and can effectively balance business priorities, compliance requirements and technical considerations. /li liYou are proactive, results‑oriented and capable of managing multiple priorities in a dynamic environment. /li liYour strong communication skills, structured way of working and continuous improvement mindset enable you to successfully drive change and optimize application performance. /li /ul h3Sector /h3 pPharmaceutical and biopharmaceutical /p /p #J-18808-Ljbffr

ESADE Business School busca un profesional para gestionar la captación y selección de programas educativos en Sant Cugat del Vallès.

ppbWe’re reinventing the market research industry. Let’s reinvent it together. /b /ppAt Numerator, we believe tomorrow’s success starts with today’s market intelligence. We empower the world’s leading brands and retailers with unmatched insights into consumer behavior and the influencers that drive it. /ppAt Worldpanel by Numerator, we believe tomorrow’s success starts with today’s market intelligence. We empower the world’s leading brands and retailers with unmatched insights into consumer behaviour and the influencers that drive it. /ph3Role Purpose /h3pThe Client Manager is responsible for owning and developing client partnerships, delivering high-quality shopper insights, and ensuring that services provided drive measurable business impact and client satisfaction. /ph3Reasonable Adjustments /h3pWorldpanel by Numerator is committed to offering equal opportunities to all individuals, including during the recruitment process. If you require any reasonable adjustments or assistance, please advise us in advance of your interview so that we can make the necessary arrangements. /ph3Key Responsibilities /h3h3Client Partnership Relationship Management /h3ulliAct as the primary point of contact for assigned clients /liliBuild strong trusted relationships /liliUnderstand client business objectives /liliAct as a trusted advisor /li /ulh3Insight Delivery Storytelling /h3ulliDeliver impactful presentations /liliProvide business recommendations /liliRespond to client briefs /li /ulh3Service Delivery /h3ulliEnsure quality and timely delivery /liliManage reporting and client requests /liliCoordinate internal teams /liliResolve data issues /li /ulh3Commercial Growth /h3ulliIdentify upsell and cross-sell opportunities /liliSupport revenue targets /liliDevelop proposals /li /ulh3Account Development /h3ulliWork cross-functionally /liliSupport team initiatives /li /ulh3What You'll Bring to Worldpanel by Numerator /h3h3Skills Capabilities /h3ulliStrong analytical skills /liliExcellent communication and storytelling /liliCommercial acumen /liliMarket research / FMCG experience /li /ulh3KPIs /h3ulliClient satisfaction /liliDelivery accuracy /li /ulpBased in Sant Cugat del Valles, Barcelona /ppSalary Range: 34K-43K /ppJoin us in this groundbreaking venture and be part of a team that shapes the future of market research. /p /p #J-18808-Ljbffr

ph3Company Culture /h3pAt 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. 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. /ph3Position Overview /h3pThe Position At Roche, we believe it’s urgent to deliver medical solutions right now – even as we develop innovations for the future. We are passionate about transforming patients’ lives and we are brave in both decision and action. And we believe that good business means a better world. Join Our Team: Make a Difference in International Regulatory Affairs! /ppRoche is seeking a dynamic and highly motivated individual to join our team as an International Regulatory Affairs Professional. We are looking for candidates who bring an innovative and creative mindset to the table, along with a proven track record in the Regulatory Affairs field. If you are passionate about making a positive impact on global healthcare through regulatory excellence, we invite you to be part of our dedicated team. /ph3Key Responsibilities /h3ulliLeading and supporting regulatory strategies for global IVD/MD instruments and software submissions /liliEnsuring compliance with international regulatory requirements and standards /liliCollaborating with cross-functional teams, including RD, Quality, and Clinical, to drive regulatory initiatives /liliProviding regulatory guidance to support product development and lifecycle management /liliStaying abreast of evolving regulatory trends and updates, and implementing best practices /li /ulh3Requirements /h3ulliBachelor’s Degree in Life Sciences, Regulatory Affairs, or a related field /lili5 to 7 years of experience in Regulatory Affairs (Regulatory, RD, Quality and/or Clinical), with some experience in healthcare regulatory affairs /liliIn-depth knowledge of global regulatory requirements, guidelines, and procedures especially for IVD instruments software /liliStrong organizational and communication skills /liliAbility to multitask and effectively manage multiple projects simultaneously /liliSelf‑motivated and capable of working independently in a self‑management environment /liliExperience in IVD instrument and/or software development /li /ulh3Benefits /h3ulliCollaborative and innovative work environment /liliOpportunity to make a meaningful impact on patients' lives globally /liliCompetitive compensation and benefits package /liliProfessional development and growth opportunities within a leading global healthcare organization /li /ulpRoche is an Equal Opportunity Employer. /p /p #J-18808-Ljbffr

pRoche Holding AG is seeking a Sourcing Manager in Sant Cugat, Spain, to optimize sourcing operations for advanced sensor technologies. You will manage end-to-end procurement processes, ensuring global supply reliability and driving cost savings. /ppThe ideal candidate has 3–5+ years in tactical sourcing and contract management, with experience in medical devices or healthcare. Proficiency in SAP and advanced analytical skills are essential. Business-level English is required; Spanish and German are advantageous. /p #J-18808-Ljbffr

ph3Key Responsibilities /h3 ul liResponsible for the coordination and management of time to market launches, with a focus on Specialty category, of STADA AG in different regions within the Supply Chain Management /li liCoordinate all tasks, activities, resources, milestones, etc. of the product launch within deadlines and timely escape potential deviations to project plan /li liMonitor production, delivery and release steps along the supply chain /li liContinuously review and improve timings and delivery /li liEnsure adequate information flow between all internal and external stakeholders such as Global Specialty teams, Supply Planning, Production, Quality, Logistics, ESO team /li liCentral touch point for affiliates and commercial functions regarding all information on the launch status and escalation /li liMonitor track timelines with supplier as per launch tracking sheet (registrations, PO, artworks execution, production, release, shipment) /li liProvide support for launch decisions, escalations, mitigation plans and preparation of business cases /li liIdentify project risks and work out scenarios to enable a successful implementation of launches /li liEnsure oversight of supply chain changes and lead end-to-end change control management, working in a cross-functional environment /li liSupport process improvements initiatives in Global Launch Management team /li /ul h3Requirements /h3 ul liYou have a degree in business, supply chain management, chemistry or pharmacy (or related field) /li liYou bring at least 4 years of experience in operations in the pharmaceutical industry /li liYou have strong abilities in project and process management /li liYou have good understanding of local go to market requirements (regulatory, technical,…). /li liYou are fluent in English (oral and written); other languages are desirable but not a must /li liExcellent communicator who can drive multiple projects in parallel on a global multi-functional cross-cultural levels /li liEmbraces empowerment and have strong influencing skills as well as ability to achieve results in a collaborative way /li liResilience and proactive attitude, entrepreneurial spirit /li liOperational disciplines and sense of urgency, capacity to aggregate, process and analyze complex information and project activities /li liWell organized, detailed-oriented but not lose sight of the big(ger) picture /li liYou are able to think, act and initiate actions in operational, tactical and strategic terms /li liMaturity to manage multiple stakeholders on different organizational levels /li /ul pSTADA Group promotes its diverse culture, regardless of gender, age, social or ethnic origin, disabilities, religion, ideology or sexual orientation. The focus is on equal opportunities, respectful cooperation and the promotion of an inclusive working environment. /p pSTADA offers a competitive environment for personal and professional development in a growing company full of opportunities. /p /p #J-18808-Ljbffr

Experteer Overview In this role you ensure the Pharmacovigilance Quality System remains compliant and efficient, guiding audits, inspections, and documentation to support safe medicines. You work with a cross-functional team and external partners to uphold regulatory standards and continuous improvement. Your impact lies in readiness for inspections, robust audit programs, and alignment of GVP with evolving requirements. This is an opportunity to shape QA in drug safety within a patient-focused dermatology company. Compensaciones / Beneficios • Maintain the Quality System for Pharmacovigilance in line with Almirall policies, ICH, EU GVP modules, and relevant regulations • Design and manage a risk-based GVP audit plan; coordinate or oversee audits of affiliates, CROs/vendors, and internal audits • Report audit findings to management and ensure closure of significant issues • Lead preparation and management of inspections by Competent Authorities and third-party audits, developing an inspection readiness plan • Review and approve procedures and key documents to ensure compliance with Drug Safety regulations • Select and supervise outsourced QA activities related to pharmacovigilance (audits, mock inspections, training) • Involve in due diligence of development products as needed • Promote continuous improvement of the GVP Quality System based on audit findings and regulatory changes Responsabilidades • Life science degree (Pharmacy, Chemistry, Biology, etc.) Requisitos principales •

ph3Funciones /h3 h3Definición de estrategia de I+D /h3 ul liDiseñar la estrategia tecnológica y de innovación alineada con la estrategia de negocio. /li liIdentificar tendencias tecnológicas y necesidades del mercado. /li liDefinir roadmap de nuevos productos y tecnologías. /li /ul h3Desarrollo de nuevos productos /h3 ul liLiderar proyectos de desarrollo de nuevos aditivos y sus formulaciones. /li liCoordinar actividades de investigación, experimentación y validación. /li liSupervisar escalado desde laboratorio a planta piloto o producción. /li /ul h3Gestión de proyectos de innovación /h3 ul liPlanificar, priorizar y gestionar el pipeline de proyectos de I+D. /li liGestionar presupuestos de investigación. /li liCoordinar proyectos multidisciplinares (laboratorio, producción, marketing). /li /ul h3Gestión de equipo /h3 ul liLiderar el equipo de técnicos de laboratorio. /li liDefinir objetivos y evaluar desempeño del equipo. /li /ul h3Colaboración con otras áreas /h3 ul liTrabajar con product management y ventas para identificar oportunidades de mercado. /li /ul h3Requisitos /h3 h3Formación /h3 ul liDoctorado / Licenciatura en Química Orgánica. /li /ul h3Experiencia /h3 ul liLaboratorio de síntesis orgánica: experiencia en reacciones de oxidación y eterificación (hidroxilación y carboximetilación). /li liCapacidad de aprender química inorgánica (conocimiento del sector industrial). /li liExperiencia en fabricación de aditivos químicos (presión y temperatura) como dispersantes, humectantes, espesantes y coalescentes. /li liExperiencia en dirección de equipos multidisciplinares. /li liCapacidad de interlocución con proveedores. /li /ul h3Competencias clave /h3 ul liLiderazgo científico y técnico /li liGestión de innovación /li liVisión estratégica tecnológica /li liGestión de equipos multidisciplinares /li /ul h3Acerca de Caldic /h3 pEn Caldic, somos un líder global en soluciones de distribución, sirviendo a mercados diversos en todo el mundo. Unirse a nosotros significa convertirse en parte de un equipo emprendedor, colaborativo y orientado a la innovación. Operamos en 43 países de todo el mundo. Nuestras soluciones innovadoras están diseñadas para satisfacer las necesidades de industrias como alimentos, farmacéutica, cuidado personal y mercados industriales, asegurando el éxito sostenible para todos los interesados. Para más información, visite: /p h3¿Listo para unirte a nosotros? /h3 pSi estás listo para llevar tu carrera al siguiente nivel y unirte a un líder global, postúlate ahora en Caldic. /p h3Ofrecemos /h3 ul liFlexibilidad horaria. /li liAtractivo paquete de beneficios sociales. /li liAtractivo paquete retributivo (salario base + variables). /li liPlanes de formación y desarrollo profesional. /li liBuen clima laboral. /li /ul pLocation: Sant Cugat del Vallès, B, ES, 08173 /p pCity: Sant Cugat del Vallès /p pCountry/Region: ES /p /p #J-18808-Ljbffr

Grant management and reporting: Oversee post‑award grant compliance, including tracking deliverables, coordinating internal resources, drafting periodic reports, and handling audit processes. The Role /h3 pAs the International Grants and Subsidies Manager at Stark Future, you will be responsible f

ppCegides líder europeo enbsoluciones de gestión empresarial en la nube /bpara los sectores financiero (tesorería, fiscal, ERP), de recursos humanos (nóminas, gestión del talento), CPA, minorista y empresarial. En el cambiante mundo actual,Cegidy susb5.000 empleados /bhacen posible ayudando a sus 750.000 clientes a liberar su potencial gracias a soluciones empresariales innovadoras y con propósito. /ppbMakemorepossible /b,es nuestra vocación. Refleja quiénes somos, cómo y por qué hacemos las cosas como las hacemos para nuestros clientes. Gracias a ello, podemos afirmar que trabajamos cada día para dar forma a su futuro, al nuestro y al de las industrias de nuestros clientes. Un futuro que llevamos años definiendo con nuestros empleados, inventando soluciones que cambian la forma de trabajar de las personas, para un rendimiento sostenible. /ph3¿Tus principales objetivos como KeyAccount Executive? /h3pComo Key Account Executive, serás responsable de identificar, abrir y desarrollar nuevas grandes cuentas estratégicas, impulsando la adopción de nuestras soluciones SaaS de Human Capital Management (HCM) en organizaciones de alto potencial. /ppTu misión principal será generar nuevo negocio, posicionarte como partner estratégico desde las primeras interacciones y convertir oportunidades complejas en relaciones comerciales sólidas y duraderas, aportando un valor claro y medible a los decisores de alto nivel. /ppComo Key Account Executive deberás: /pulliDesarrollar y consolidar cuentas estratégicas: Identificar oportunidades de negocio y elaborar propuestas de valor personalizadas para grandes cuentas. /liliGestionar ciclos de venta complejos: Coordinar con equipos internos y asegurar el éxito en ventas de soluciones SaaS HCM de alto impacto. /liliMantener relaciones con decisores clave: Actuar como interlocutor de confianza, anticipando necesidades y riesgos estratégicos. /liliImpulsar la fidelización y adopción de soluciones: Garantizar la satisfacción del cliente y el retorno de inversión de nuestras soluciones. /liliContribuir a la estrategia comercial y al crecimiento del negocio: Colaborar con ventas, producto y customer success para identificar nuevas oportunidades. /liliPromover la mejora continua y la excelencia operativa: Definir planes de optimización y asegurar la excelencia en la gestión de cuentas estratégicas. /li /ul /p #J-18808-Ljbffr

Experteer Overview In this role you will lead and optimize critical development processes to ensure safe, effective products and regulatory compliance. You will work cross-functionally within the Design Control Excellence team to manage requirements, risk, configuration, defects, and Vu0026amp;V across complex projects. You will drive simplification for faster time-to-market while upholding quality. This is a hands-on, global role that shapes how we deliver patient-centered solutions at Roche. Compensaciones / Beneficios • Provide expert guidance on governance for complex system, software, and assay projects across risk, requirements, configuration, and defect management. • Support multi-level requirements traceability with a streamlined, database-driven approach. • Lead strategic product risk assessments with cross-functional teams. • Build and maintain configuration management for complex projects. • Ensure Verification u0026 Validation activities meet internal standards and global regulatory requirements (e.g., ISO 13485). • Identify opportunities to simplify processes to improve time-to-market without compromising quality. • Collaborate in a global, agile, cross-cultural environment to deliver results for patients. Responsabilidades • Master’s degree in Engineering, Life Sciences, Natural Sciences, or a related field. • Minimum of three years’ experience in a regulated environment within product development or process management. • Strong understanding of Design Control processes and global standards such as ISO 13485 or IEC 62304. • Digital fluency with ALM tools (e.g., Jira, Azure DevOps) and specialized requirements management software. • Excellent English communication skills for collaboration across international sites. Requisitos principales •

pul liAccountable to deliver the best-in-class end-to-end operational performance across all scorecard KPIs /li liLead a virtual cross-functional team within Customer Support to drive continuous performance improvement /li liMonitor and manage Markets delivery performance for the Commercial segment /li /ul h3Requirements /h3 ul liStrong relationship management /li liHigh analytical and creative problem-solving capabilities and techniques /li liLean6sigma knowledge methodology /li liExcellent communication skills /li liExcellent knowledge of service delivery principles and processes /li liDemonstration of resilience tenacity /li liEager to seek solutions and improve knowledge in delivery tools, always /li /ul /p #J-18808-Ljbffr

ppBarcelona |Spain | Full-time | Permanent /p h3About Us /h3 pAt STADA we pursue the purpose of "Taking care of people's health as a trusted partner." All our decisions and actions are driven by our purpose, vision and values. With our wide range of products: Generics, Consumer Healthcare and Specialties, we offer patients, doctors and pharmacists a wide range of therapeutic options. /p pAround 13,000 employees live our values of Integrity, Entrepreneurship, Agility and One STADA, in order to achieve our ambitious goals and shape a successful future for our company. We continually expand our goals in line with our ambition, and we achieve them with passion, commitment and a growth mindset. /p pDo you want to be part of a successful international pharmaceutical company and grow with us? /p h3Key Responsibilities /h3 ul liResponsible for the coordination and management of time to market launches, with a focus on Specialty category, of STADA AG in different regions within the Supply Chain Management /li liCoordinate all tasks, activities, resources, milestones, etc. of the product launch within deadlines and timely escalating potential deviations to project plan /li liMonitor production, delivery and release steps along the supply chain /li liContinuously review and improve timings and delivery /li liEnsure adequate information flow between all internal and external stakeholders such as Global Specialty teams, Supply Planning, Production, Quality, Logistics, ESO team /li liCentral touch point for affiliates and commercial functions regarding all information on the launch status and escalation /li liMonitor track timelines with supplier as per launch tracking sheet (registrations, PO, artworks execution, production, release, shipment) /li liProvide support for launch decisions, escalations, mitigation plans and preparation of business cases /li liIdentify project risks and work out scenarios to enable a successful implementation of launches /li liEnsure oversight of supply chain changes and lead end-to-end change control management, working in a cross-functional environment /li liSupport process improvements initiatives in Global Launch Management team /li /ul h3Requirements /h3 ul liYou have a degree in business, supply chain management, chemistry or pharmacy (or related field) /li liYou bring at least 4 years of experience in operations in the pharmaceutical industry /li liYou have strong abilities in project and process management /li liYou have good understanding of local go to market requirements (regulatory, technical,…). /li liYou are fluent in English (oral and written); other languages are desirable but not a must /li liExcellent communicator who can drive multiple projects in parallel on a global multi-functional cross-cultural levels /li liEmbraces empowerment and have strong influencing skills as well as ability to achieve results in a collaborative way /li liResilience and proactive attitude, entrepreneurial spirit /li liOperational disciplines and sense of urgency, capacity to aggregate, process and analyze complex information and project activities /li liWell organized, detailed-oriented but not lose sight of the big picture /li liYou are able to think, act and initiate actions in operational, tactical and strategic terms /li liMaturity to manage multiple stakeholders on different organizational levels /li /ul pSTADA Group promotes its diverse culture, regardless of gender, age, social or ethnic origin, disabilities, religion, ideology or sexual orientation. We use the strength of this diversity to develop creative ideas, expand our experience and increase innovative strength. Our focus is on equal opportunities, respectful cooperation and the promotion of an inclusive working environment. /p pSTADA offers a competitive environment for personal and professional development in a growing company full of opportunities. /p pOur future project requires dynamic and proactive professionals, capable of adding value in a changing environment. /p /p #J-18808-Ljbffr

ph3ABOUT US /h3pAt STADA we pursue the purpose of "Taking care of people's health as a trusted partner." All our decisions and actions are driven by our purpose, vision and values. With our wide range of products: Generics, Consumer Healthcare and Specialties, we offer patients, doctors and pharmacists a wide range of therapeutic options. /ppAround 13,000 employees live our values of Integrity, Entrepreneurship, Agility and One STADA, in order to achieve our ambitious goals and shape a successful future for our company. We continually expand our goals in line with our ambition, and we achieve them with passion, commitment and a growth mindset. /ppDo you want to be part of a successful international pharmaceutical company and grow with us? /ppAs part of the international bCHC marketing team /b you will drive our rapidly growing Consumer Health business by leading affiliates strategically to grow our local hero brands in the skincare category with winning marketing assets, competitive line extensions and synergetic high-impact initiatives. As International Category Manager, you will play a key role in developing and implementing marketing strategies to drive sales and increase brand awareness across global markets. /ph3What you can expect /h3pWe are seeking a marketing professional who will help us expanding STADA’s skincare footprint in Consumer Health. The ideal candidate will spearhead our skincare product lines, defining and executing marketing strategies that enhance our brand visibility, drive sales, and engage our target audience. The successful candidate will possess a blend of creative and analytical skills, with a robust understanding of the skincare industry, paired with a curious, investigative mind, taking pride in developing growth strategies and leading value accretive projects from start to finish. Knowing the Consumer Healthcare market well is a must; having a good understanding where the derma category will be heading in the coming years will be a plus. /ph3Who we are looking for /h3ulliProven Marketing and/or Sales experience (10 years or more) in the derma/skincare category in leading FMCG / CHC companies operating in an international environment /liliProven capabilities in digital marketing paired with a strong conceptual, analytical and strategic skillset /liliProven project leadership skills, delivering results in complex and ever-changing environments /liliTrack record in creating new products, concept writing testing, and developing new brands (ideally that have expanded into new markets or channels incl eCommerce) /liliSound knowledge of regulatory and legal framework of OTC medicines, medical devices, cosmetics and food supplements /liliFlexibility and agility in quickly transferring skills knowledge from one area of expertise to the other /liliStrong influencing skills and the capability to lead cross-functional teams across different regions and countries /liliStrong communication and presentation skills in English and preferably German helping you to inspire and guide teams. /liliEagerness to cultivate a growth mindset always focused on driving business value. /li /ulpbSTADA Group /b promotes its diverse culture, regardless of gender, age, social or ethnic origin, disabilities, religion, ideology or sexual orientation. We use the strength of this diversity to develop creative ideas, Expand our experience and increase innovative strength. Our focus is on equal opportunities, respectful cooperation and the promotion of an inclusive working environment. /ppbSTADA /b offers a competitive environment for personal and professional development in a growing company full of opportunities. /ppOur future project requires dynamic and proactive professionals, capable of adding value in a changing environment. /ppbFollow us on LinkedIn to receive our news! /b /p /p #J-18808-Ljbffr

What your responsibilities will be /h3 ul liIssue and review Global Quality Policies and ensure its implementation in all the sites within Biopharma Business Unit /li liStay updated on industry trends and advancements in quality management practices to drive innovation and improvement /li liFoster h

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 Are you a highly organized professional who thrives in a dynamic environment? Do you excel at multitasking, managing logistics, and providing top-tier business support? As our Learning and Business Operations Coordinator, your primary focus will be on delivering exceptional Business Support and Event/Workshop Coordination. Alongside this core responsibility, you will actively support our team in smooth Training Management operations and compliance-driven Documentation Management. Utilizing your consolidated expertise across various corporate tools and processes, you will directly contribute to the success of our Global Customer Support organization, course participants, trainers, and internal customers, ensuring our global and local teams are supported efficiently every day. Given the evolving nature of our field and our constantly growing scope of work, we are looking for a reinforcement who is agile, flexible and intrinsically motivated to: - Quickly onboard themselves into new processes and technical topics. - Embrace change and support the team in integrating new tasks. - Contribute actively to our day-to-day operations in a global setting Your Responsibilities: Business Support - Event & Workshop Management: You will be the mastermind behind our GCS events and workshops. You will coordinate all logistical aspects, including venue selection, catering, accommodation arrangements, and vendor management, while collaborating closely with stakeholders to bring event specifications to life. - Procurement: Handle the end-to-end ordering process for various corporate needs, including setting up new suppliers and efficiently coordinating approval workflows across stakeholders. - Travel Coordination: Assist with international travel arrangements and provide timely guidance for travel within the EMEA region using our Travel Management System. - Onboarding: Support the seamless onboarding of new team members Documentation Management - Workflow Management: Set up and manage timely signature workflows for regulatory-relevant documents within our electronic Document Management System (eDMS) according to required specifications. - Quality & Review: Review and modify documents with high accuracy, ensuring top-tier quality for all metadata entries in the eDMS. - Subject Matter Expert: Act as the primary point of contact for all eDMS-related inquiries, serving as a trusted partner and advisor for the entire GCS organization. - Cross-Department Collaboration: Support and collaborate with other departments to actively maintain data integrity and document quality. Training Management - Course Coordination: Assist the team in organizing and managing local and global product and non-product training courses, ensuring smooth communication with internal and external stakeholders. - LMS Administration: Handle course creation, participant registrations, training assignments, waitlist coordination, and prerequisite verification within the Learning Management System. - Data Quality & Content: Maintain training metadata and ensure the availability of relevant training content to guarantee high data quality. - Participant Assistance: Act as a helpful point of contact for training participants, assisting with logistical support, visa applications, and on-site support. - First-Level Support: Provide reliable first-level troubleshooting and support for questions regarding DIA product training, and generate ad-hoc reports as requested Your Profile To be successful in this role, you should bring a strong mix of organizational talent, attention to detail, and a service-oriented mindset. Education & Experience: - Professional Education: Successfully completed commercial vocational training or an equivalent educational background - Professional Experience: At least two years of experience in business operations, event coordination, training management, ideally within a service-oriented corporate environment. Key Skills & Attributes: - Organizational & Event Excellence: Strong organizational skills with a proven ability to manage event logistics, workshops, and business support processes independently and efficiently. - Tool & Process Proficiency: Basic knowledge of the tools and processes required for the role (prior experience with DiaDoc, myBuy and Cornerstone platforms is highly advantageous). - Accuracy & Reliability: A high standard for accuracy and quality, especially when handling compliance documentation and data entry. - Customer & Service Orientation: A strong passion for helping others, managing stakeholder relationships, and delivering excellent internal service. - Language Skills: Excellent written and spoken English skills are required. Knowledge of a second foreign language is a distinct advantage. Are you ready to coordinate our success? Apply now! 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.

ph3Responsabilidades /h3 pbGestión de OM: /b /p ul liRegistro de QSKUs (Referencia comercial de venta) en Oracle /li liGeneración de celdas (Subiventory factory locations) /li liGeneración de Job Codes (Ordenes de fabricación) /li liVinculación entre SO y Job Codes /li liActuar como SPOC de OM para el Back Office (BCF – SEIT Spain) con los diferentes HUBs Regionales de Secure Power + FO (Front Office) /li liOptimización y simplificación de los procesos actuales /li liSoporte al resto de entidades y fábricas MDC Business /li liSolicitud grabación de pedidos de Servicios a FO SEIT Spain. /li liExport Control (SPOC de la manufacturing entity – Gestión del ECCN para todos los proyectos independientemente del país destino y revisión del cumplimiento del EC 4W Diligence por parte del FO/HUB que vende al OG Customer cuando aplique para Tier 2 countries o Diversion Risk Countries) /li /ul pbGestión de transporte: /b /p ul liSolicitud de ofertas a nuestros proveedores de transporte. /li liGestión de la exportación/importación de los materiales con la aduana /li liSeguimiento de los envíos desde el inicio hasta el final /li liCreación de PO para el pago de las facturas de nuestros proveedores de transporte. /li liGestión de incidencias y daños durante el transporte (documentación, imágenes, comprobantes de entrega, seguimiento hasta resolución de la incidencia) /li liOptimización de costes logísticos (Revisión, análisis y comparativa de precios, incidencias, resultados y calidad ofrecida de los distintos proveedores) /li /ul h3Cualificaciones /h3 ul liCapacidad de análisis y entendimiento de flujos /li liCuriosidad e interés en el entendimiento de la estructura y los flujos (Triangulares, Dropshipment ...) /li liPersona dinámica que sea capaz de aportar, mejorar y automatizar los procesos actuales en un entorno de transformación y crecimiento /li liExperiencia en Tableau (Análisis con carácter informativo para revisar estados de proyectos) /li liExperiencia en puestos similares /li /ul /p #J-18808-Ljbffr

pAlmirall, S.A in Sant Feliu de Llobregat is seeking a QA Senior Manager to maintain and improve the GVP Quality Management System, ensuring compliance with ICH, EU GVP modules, and pharmacovigilance regulations. /ppYou will lead audits, inspections, and QA activities with internal and external partners, fostering continuous improvement while coordinating with safety teams. Fluent English and strong regulatory expertise are required. /p #J-18808-Ljbffr

pRoche is seeking a Senior Business Product Owner for AI Knowledge Management in Sant Cugat del Vallès to drive scalable AI-powered service solutions. You will own the product vision, align stakeholders, and lead agile teams to deliver high-impact automation and data pipelines in a global service context. /ppThe role requires a strong blend of technical and business judgment, with 5–10 years in a high-tech or service-oriented setting and expertise in AI-ready data architectures. /p #J-18808-Ljbffr

ph3Overview /h3 pbAt ScaleneWorks People Solutions /b, we're more than recruiters; we're career architects dedicated to connecting exceptional talent with top-tier opportunities. Backed by industry experts, we prioritize relationships, offer global opportunities, and champion your success every step of the way. /p pbReady to shape your future? Explore opportunities with us today. /b /p pWe are looking for a bTechnical /b bProject Manager /b for our well-known client. /p h3Responsibilities /h3 ul liManage new API integrations with clients and suppliers, ensuring design alignment, dependency tracking, and smooth implementation across teams. /li liLead planning and execution of complex technical programs that drive modernization of our platform APIs and enable agentic AI initiatives. /li liAct as the bridge between cross-functional teams (Engineering, Product, Design, Business, and RD) to align priorities and deliver customer-valued outcomes. /li liDefine and refine technical scope, architecture, and quality plans for features, solutions, or products, ensuring timely delivery and escalation when needed. /li liDevelop and maintain software roadmaps based on product vision, technical requirements, and business objectives. /li liPartner with agile development teams to prioritize, plan, and track execution across multiple programs using Scaled Agile Framework (SAFe) and Jira. /li liDrive program analysis to proactively manage risks, and influence course corrections to keep projects on track. /li liContinuously assess and improve software development lifecycle processes for efficiency and scalability. /li liCommunicate program status, progress, and challenges through clear reporting and presentations to leadership. /li liEnsure stakeholder alignment through regular engagement and feedback loops. /li /ul h3The TPM's Essential Qualifications /h3 ul liBachelor’s or Master’s degree in Computer Science, Information Technology, Business Management, or equivalent experience. /li li5–10 years of experience in technical program or project management within software or technology organizations. /li liProven ability to manage complex, cross-functional programs in an agile environment. /li liStrong understanding of API ecosystems, microservices architecture, and modern integration patterns. /li liExpertise in risk management, program analysis, and process improvement. /li liExcellent communication and leadership skills with experience presenting to senior stakeholders. /li liAbility to exercise independent judgment and make decisions within broadly defined policies and practices. /li /ul h3Preferred Skills /h3 ul liTechnical depth in software architecture, cloud platforms, and API design. /li liExperience with Scaled Agile Framework (SAFe) and Jira for program tracking and execution. /li liStrong analytical and problem-solving skills for evaluating complex technical and business challenges. /li liFamiliarity with agentic AI concepts and their application in enterprise software. /li liAbility to mentor and guide teams, fostering collaboration and innovation. /li /ul h3Ready to Take the Next Step? /h3 pIf you're ready to embark on an exciting journey with bScaleneWorks /b, we’d love to hear from you! Submit your resume today and let’s unlock new possibilities together /p /p #J-18808-Ljbffr

pSynthon in Sant Boi de Llobregat is looking for an experienced Application Technician to manage our Document Management System, Quality Management System, and Learning Management System. In this role, you will ensure the systems' compliance and assistance in business processes. /ppThe ideal candidate holds a Bachelor's degree in IT or a related field, has at least 5 years of relevant experience, and possesses strong language skills in both Spanish and English. /ppIf interested, please apply before July 31, 2026. /p #J-18808-Ljbffr

pEurofragance SLU, located in Rubí, Spain, is seeking a Supply Chain Manager to drive performance and lead the team. Your key responsibilities will include overseeing end-to-end Supply Chain operations and ensuring alignment with customer needs. /ppThe ideal candidate will hold a degree in Industrial Engineering and a Master’s in Supply Chain Management, with at least 5 years of relevant experience. Join a diverse company committed to sustainability, and enjoy benefits like flexible working hours and health services. /p #J-18808-Ljbffr

pF. Hoffmann-La Roche AG is seeking an International Regulatory Affairs Professional in Sant Cugat del Vallès, Spain. This dynamic role involves leading regulatory strategies for global submissions, ensuring compliance with international requirements, and collaborating with cross-functional teams. /ppThe ideal candidate will have a Bachelor’s Degree in Life Sciences and 5 to 7 years of experience in Regulatory Affairs. Roche offers competitive compensation and a collaborative work environment, making a meaningful impact on patients' lives globally. /p #J-18808-Ljbffr

pWorldpanel by Numerator in Sant Cugat del Vallès (Barcelona) is seeking a Client Manager to own client partnerships, deliver high‑quality shopper insights, and ensure services drive measurable business impact and client satisfaction. /ppYou will act as the primary contact for assigned clients, build trusted relationships, deliver impactful presentations and business recommendations, coordinate reporting, manage data requests, and identify upsell opportunities to help meet revenue targets. /p #J-18808-Ljbffr

ph3Role Purpose /h3 pAs GCS RIS Implementation Manager you are accountable for the successful implementation of Roche’s digital products at the customer. In early product life cycle phases you will be responsible for implementing select RIS products in the ‘Nail-It’ phase of the product lifecycle, and will then be accountable for the successful onboarding and success of the affiliate implementations. /p h3Key Responsibilities /h3 ul liProvide customer project expertise to the GCS Technical Product manager. /li liSupport the product life cycle by improving product serviceability and implementability while considering the broader solution. /li liDevelop project documentation in accordance with the scope and deliverables, following best practices. /li liEscalate issues: report unresolved problems to the established escalation person(s); raise major risks to the manager and functional heads. /li liDevelop, test, and verify testing scenarios for new or modified implementations of navify product(s), ensuring customer acceptance. /li liStay informed of roadmap changes, features, and known features within scope. /li liShare knowledge and suggest new technologies that improve productivity and efficacy. /li liMaintain training compliance and adhere to Roche’s Code of Business Conduct. /li liEnsure compliance with Roche’s TE guidelines, including cost guidelines, reporting timeliness, and correct usage of travel tools. /li liBuild or shape tools to increase team productivity, securing management buy‑in. /li liGenerate solutions to complex issues independently and incorporate them into standard processes. /li liMentor and onboard new team members. /li liDevelop templates for new documentation or improve existing templates (Meeting Minutes, Project Schedule, Runbook, etc.). /li /ul h3Qualifications /h3 ul liGood communication skills and proficiency in English, Spanish, and French. /li liBachelor’s or master’s degree in a relevant field (IT, lab technology, etc.) or equivalent mix of education and work experience. /li liAt least 5 years of relevant experience in IT, lab organization, hospital IT networks, interfaces, or databases. /li liPrevious experience working in a clinical environment is highly desirable. /li liExplicit problem‑solving attitude and customer‑oriented mindset in interdisciplinary settings. /li liWillingness to travel up to 50% nationally and worldwide. /li liIndependent, proactive and versatile working style, while being a team player in a global team. /li /ul h3Location Travel /h3 pBased in Sant Cugat, Spain. This global role requires international business travel depending on business location and project activities. /p h3Diversity Inclusion /h3 pRoche is strongly committed to a diverse and inclusive workplace. /p h3Equal Opportunity /h3 pRoche is an equal opportunity employer. bRoche is an Equal Opportunity Employer. /b /p /p #J-18808-Ljbffr