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¿Quiénes somos? Grupo Farmacéutico Salvat es una compañía familiar fundada en Barcelona en 1955, con más de 70 años cuidando la salud a través de marcas emblemáticas como Cristalmina, Cetraxal, Monolitum o Salvacolina. Tenemos presencia en más de 60 países y plantas de producción en Barcelona, Madrid y Miami. Contamos con I+D propio y desarrollamos soluciones en oftalmología, otorrinolaringología y gastroenterología, además de Consumer Health y servicios CDMO, donde aspiramos a ser un referente. Estamos certificados por la FDA y reconocidos con calificación excelente en el Plan Profarma. Actualmente impulsamos el proyecto NewSalvat, una transformación para ser más ágiles, fuertes y competitivos. Nuestra cultura se basa en los valores AACT (Ambición, Accountability, Colaboración y Transparencia), apostando por el crecimiento y el talento de las personas. ¿Qué buscamos? Estamos en la búsqueda de DT suplente que comparta nuestra visión y esté listo para contribuir en proyectos desafiantes. Si tienes los conocimientos requeridos y un enfoque proactivo, ¡queremos conocerte! ATENCION: Requisito imprescindible aportar experiencia de 3 años en áreas de Garantía de calidad en la industria farmacéutica. Tu misión 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.) empleadas en las actividades de desarrollo y fabricación de medicamentos, productos sanitarios, complementos alimenticios y cosméticos, asegurando en todo momento su actualización y vigencia. Como Director técnico suplente, colaborará con DT en la liberación de lotes al mercado, revisión de los indicadores de calidad, revisión de acuerdos técnicos y documentación del sistema de calidad y comunicación con clientes, CMOs y Autoridades. Tus principales responsabilidades serán: Las tareas/responsabilidades se desarrollarán en los siguientes ámbitos: • Sistema de Calidad: funcionamiento y desarrollo de las herramientas necesarias para el mantenimiento del Sistema de calidad aplicable a los procesos de una empresa farmacéutica: control de cambios, desviaciones, CAPAs, sistema documental, PNTs y reclamaciones, • Validaciones y cualificaciones, Anexo 15 GMPs, • Seguimiento de procesos productivos, • Revisión de Calidad de Producto y CPV, • Formación interna, • Análisis de riesgos, • Indicadores de calidad, • Auditorias Requisitos • Estudios Superiores Universitarios en farmacia., • Experiencia de 3 años en áreas de Garantía de calidad en la industria farmacéutica., • Conocimientos específicos en normativa de calidad, GxP, en entorno europeo y USA., • Inglés, nivel avanzado, • Se valorará conocimientos estadísticos y en validaciones de sistemas informatizados, así como conocimiento y experiencia en normativas de Farmacovigilancia, Productos sanitarios, complementos alimenticios y cosméticos., • Nivel de responsabilidad ¿Qué te ofrecemos? • Proyecto sólido en una compañía consolidada del sector Pharma., • Entorno de transformación y con crecimiento profesional y personal., • Rol estratégico con alto impacto en negocio y en resultados., • Desarrollo profesional y liderazgo de equipos de alto rendimiento., • Entorno dinámico y orientado a resultados., • Equipos de trabajo transversales y colaborativos., • Cultura colaborativa y exigente., • Un entorno en el que valoramos la iniciativa y el impacto individual. ¿Quieres formar parte de este proyecto transformador? Aplica para más información ¡Vamos a construir juntos el futuro de Salvat!

¿Quiénes somos? Grupo Farmacéutico Salvat es una compañía familiar fundada en Barcelona en 1955, con más de 70 años cuidando la salud a través de marcas emblemáticas como Cristalmina, Cetraxal, Monolitum o Salvacolina. Tenemos presencia en más de 60 países y plantas de producción en Barcelona, Madrid y Miami. Contamos con I+D propio y desarrollamos soluciones en oftalmología, otorrinolaringología y gastroenterología, además de Consumer Health y servicios CDMO, donde aspiramos a ser un referente. Estamos certificados por la FDA y reconocidos con calificación excelente en el Plan Profarma. Actualmente impulsamos el proyecto NewSalvat, una transformación para ser más ágiles, fuertes y competitivos. Nuestra cultura se basa en los valores AACT (Ambición, Accountability, Colaboración y Transparencia), apostando por el crecimiento y el talento de las personas. ¿Qué buscamos? Estamos en la búsqueda de un/a técnico de Regulatory Affairs que comparta nuestra visión y esté listo para contribuir en proyectos desafiantes. Si tienes los conocimientos requeridos y un enfoque proactivo, ¡queremos conocerte! Tu misión Elaborar y gestionar hasta aprobación los expedientes para el registro de especialidades farmacéuticas, cosméticos, productos sanitarios, complementos alimenticios y biocidas a nivel nacional e internacional. Mantener la documentación actualizada mediante la preparación de las solicitudes de variaciones conforme a la legislación vigente. Seguimiento de la Normativa para la obtención de autorización de comercialización del producto y su mantenimiento. Tus principales responsabilidades serán: • Preparación, revisión y presentación de la documentación necesaria para solicitudes de nuevas autorizaciones, variaciones y revalidaciones ante las autoridades sanitarias (tanto nacionales como MRP y DCP), así como del seguimiento de estos trámites hasta su resolución y de las gestiones posteriores oportunas., • Preparación y seguimiento de solicitudes de registro, variaciones y revalidaciones de medicamentos en el resto del mundo (se valorará experiencia previa en registro FDA y otros países)., • Gestión de trámites para autorización y mantenimiento de complementos alimenticios, productos sanitarios, biocidas y/o cosméticos., • Seguimiento y revisión de textos de material de acondicionamiento y material publicitario., • Participación en proyectos globales de compañía en equipos multidisciplinares Requisitos • Licenciatura en ciencias de la salud (Farmacia, Química, Biología o similar), valorables estudios específicos sobre asuntos regulatorios (máster, postgrado...)., • Experiencia 2-3 años en puestos similares, • Conocimientos de la normativa en vigor para el registro y mantenimiento de los registros de medicamentos, tanto a nivel nacional como europeo, especialmente en el Módulo 3 de Calidad(valorable internacional y FDA)., • Conocimientos de la normativa de cosméticos, productos sanitarios, complementos alimenticios y biocidas., • Inglés (Nivel B2 o superior)., • Conocimientos ofimáticos avanzados (office, valorable eCTD manager, aplicaciones de gestión de agencias reguladoras). Aptitudes • Inglés, • Buenas prácticas de fabricación (GMP) de la Administración de Alimentos y Medicamentos (FDA), • Trabajo en equipo ¿Qué te ofrecemos? • Proyecto sólido en una compañía consolidada del sector Pharma., • Entorno de transformación y con crecimiento profesional y personal., • Rol estratégico con alto impacto en negocio y en resultados., • Desarrollo profesional y liderazgo de equipos de alto rendimiento., • Entorno dinámico y orientado a resultados., • Equipos de trabajo transversales y colaborativos., • Cultura colaborativa y exigente., • Un entorno en el que valoramos la iniciativa y el impacto individual. ¿Quieres formar parte de este proyecto transformador? Aplica para más información ¡Vamos a construir juntos el futuro de Salvat!

¿Quiénes somos? Grupo Farmacéutico Salvat es una compañía familiar fundada en Barcelona en 1955, con más de 70 años cuidando la salud a través de marcas emblemáticas como Cristalmina, Cetraxal, Monolitum o Salvacolina. Tenemos presencia en más de 60 países y plantas de producción en Barcelona, Madrid y Miami. Contamos con I+D propio y desarrollamos soluciones en oftalmología, otorrinolaringología y gastroenterología, además de Consumer Health y servicios CDMO, donde aspiramos a ser un referente. Estamos certificados por la FDA y reconocidos con calificación excelente en el Plan Profarma. Actualmente impulsamos el proyecto NewSalvat, una transformación para ser más ágiles, fuertes y competitivos. Nuestra cultura se basa en los valores AACT (Ambición, Accountability, Colaboración y Transparencia), apostando por el crecimiento y el talento de las personas. ¿Qué buscamos? Estamos en la búsqueda de un/a técnico de Regulatory Affairs que comparta nuestra visión y esté listo para contribuir en proyectos desafiantes. Si tienes los conocimientos requeridos y un enfoque proactivo, ¡queremos conocerte! Tu misión Elaborar y gestionar hasta aprobación los expedientes para el registro de especialidades farmacéuticas, cosméticos, productos sanitarios, complementos alimenticios y biocidas a nivel nacional e internacional. Mantener la documentación actualizada mediante la preparación de las solicitudes de variaciones conforme a la legislación vigente. Seguimiento de la Normativa para la obtención de autorización de comercialización del producto y su mantenimiento. Tus principales responsabilidades serán: • Preparación, revisión y presentación de la documentación necesaria para solicitudes de nuevas autorizaciones, variaciones y revalidaciones ante las autoridades sanitarias (tanto nacionales como MRP y DCP), así como del seguimiento de estos trámites hasta su resolución y de las gestiones posteriores oportunas., • Preparación y seguimiento de solicitudes de registro, variaciones y revalidaciones de medicamentos en el resto del mundo (se valorará experiencia previa en registro FDA y otros países)., • Gestión de trámites para autorización y mantenimiento de complementos alimenticios, productos sanitarios, biocidas y/o cosméticos., • Seguimiento y revisión de textos de material de acondicionamiento y material publicitario., • Participación en proyectos globales de compañía en equipos multidisciplinares Requisitos • Licenciatura en ciencias de la salud (Farmacia, Química, Biología o similar), valorables estudios específicos sobre asuntos regulatorios (máster, postgrado...)., • Experiencia 2-3 años en puestos similares, • Conocimientos de la normativa en vigor para el registro y mantenimiento de los registros de medicamentos, tanto a nivel nacional como europeo, especialmente en el Módulo 3 de Calidad(valorable internacional y FDA)., • Conocimientos de la normativa de cosméticos, productos sanitarios, complementos alimenticios y biocidas., • Inglés (Nivel B2 o superior)., • Conocimientos ofimáticos avanzados (office, valorable eCTD manager, aplicaciones de gestión de agencias reguladoras). Aptitudes • Inglés, • Buenas prácticas de fabricación (GMP) de la Administración de Alimentos y Medicamentos (FDA), • Trabajo en equipo ¿Qué te ofrecemos? • Proyecto sólido en una compañía consolidada del sector Pharma., • Entorno de transformación y con crecimiento profesional y personal., • Rol estratégico con alto impacto en negocio y en resultados., • Desarrollo profesional y liderazgo de equipos de alto rendimiento., • Entorno dinámico y orientado a resultados., • Equipos de trabajo transversales y colaborativos., • Cultura colaborativa y exigente., • Un entorno en el que valoramos la iniciativa y el impacto individual. ¿Quieres formar parte de este proyecto transformador? Aplica para más información ¡Vamos a construir juntos el futuro de Salvat!

¿Quiénes somos? Grupo Farmacéutico Salvat es una compañía familiar fundada en Barcelona en 1955, con más de 70 años cuidando la salud a través de marcas emblemáticas como Cristalmina, Cetraxal, Monolitum o Salvacolina. Tenemos presencia en más de 60 países y plantas de producción en Barcelona, Madrid y Miami. Contamos con I+D propio y desarrollamos soluciones en oftalmología, otorrinolaringología y gastroenterología, además de Consumer Health y servicios CDMO, donde aspiramos a ser un referente. Estamos certificados por la FDA y reconocidos con calificación excelente en el Plan Profarma. Actualmente impulsamos el proyecto NewSalvat, una transformación para ser más ágiles, fuertes y competitivos. Nuestra cultura se basa en los valores AACT (Ambición, Accountability, Colaboración y Transparencia), apostando por el crecimiento y el talento de las personas. ¿Qué buscamos? Estamos en la búsqueda de un/a técnico de Regulatory Affairs que comparta nuestra visión y esté listo para contribuir en proyectos desafiantes. Si tienes los conocimientos requeridos y un enfoque proactivo, ¡queremos conocerte! Tu misión Elaborar y gestionar hasta aprobación los expedientes para el registro de especialidades farmacéuticas, cosméticos, productos sanitarios, complementos alimenticios y biocidas a nivel nacional e internacional. Mantener la documentación actualizada mediante la preparación de las solicitudes de variaciones conforme a la legislación vigente. Seguimiento de la Normativa para la obtención de autorización de comercialización del producto y su mantenimiento. Tus principales responsabilidades serán: • Preparación, revisión y presentación de la documentación necesaria para solicitudes de nuevas autorizaciones, variaciones y revalidaciones ante las autoridades sanitarias (tanto nacionales como MRP y DCP), así como del seguimiento de estos trámites hasta su resolución y de las gestiones posteriores oportunas., • Preparación y seguimiento de solicitudes de registro, variaciones y revalidaciones de medicamentos en el resto del mundo (se valorará experiencia previa en registro FDA y otros países)., • Gestión de trámites para autorización y mantenimiento de complementos alimenticios, productos sanitarios, biocidas y/o cosméticos., • Seguimiento y revisión de textos de material de acondicionamiento y material publicitario., • Participación en proyectos globales de compañía en equipos multidisciplinares Requisitos • Licenciatura en ciencias de la salud (Farmacia, Química, Biología o similar), valorables estudios específicos sobre asuntos regulatorios (máster, postgrado...)., • Experiencia 2-3 años en puestos similares, • Conocimientos de la normativa en vigor para el registro y mantenimiento de los registros de medicamentos, tanto a nivel nacional como europeo, especialmente en el Módulo 3 de Calidad(valorable internacional y FDA)., • Conocimientos de la normativa de cosméticos, productos sanitarios, complementos alimenticios y biocidas., • Inglés (Nivel B2 o superior)., • Conocimientos ofimáticos avanzados (office, valorable eCTD manager, aplicaciones de gestión de agencias reguladoras). Aptitudes • Inglés, • Buenas prácticas de fabricación (GMP) de la Administración de Alimentos y Medicamentos (FDA), • Trabajo en equipo ¿Qué te ofrecemos? • Proyecto sólido en una compañía consolidada del sector Pharma., • Entorno de transformación y con crecimiento profesional y personal., • Rol estratégico con alto impacto en negocio y en resultados., • Desarrollo profesional y liderazgo de equipos de alto rendimiento., • Entorno dinámico y orientado a resultados., • Equipos de trabajo transversales y colaborativos., • Cultura colaborativa y exigente., • Un entorno en el que valoramos la iniciativa y el impacto individual. ¿Quieres formar parte de este proyecto transformador? Aplica para más información ¡Vamos a construir juntos el futuro de Salvat!

Galenicum invites applications for a Quality Assurance Release Expert to join our QA team in Cataluña, Spain. Descubra exactamente qué habilidades, experiencia y cualificaciones necesitará para tener éxito en este puesto antes de enviar su solicitud a continuación. You will lead release activities, review CoAs, BMRs and BPRs, and ensure documentation accuracy. The role requires GMP knowledge, 3+ years in GMP settings, and experience with QA in pharma manufacturing, plus proficiency in MS Office, SAP and TrackWise. Excellent English and Spanish are essential. xqbhyrx This position offers growth within a fast-growing company. #J-18808-Ljbffr

WE ARE HIRING! ¿Está considerando presentar su candidatura para este trabajo? Compruebe todos los detalles en esta descripción del puesto y luego haga clic en "Solicitar". Key Account Manager MedTech Neuraxpharm is looking for people who want to make a difference and improve patients’ lives within the CNS area. We want individuals who will go the extra mile and make great things happen. Being part of this team does not mean you are just working for a company, but for a cause! Neuraxpharm is looking for a Key Account Manager MedTech based in Spain Your Mission To promote, prescribe, and sell the company’s digital medical solution to epileptologists and hospitals, ensuring profitable growth and high customer satisfaction. Build strong relationships between Neuraxpharm and Key Accounts, including Physicians and Nursing teams. Support the effective communication of scientific & medical information, empowering the launch and commercialization of products. Your Major Accountabilities • Develop and implement a national sales strategy targeting reference hospitals and epileptologists., • Build strong relationships with key opinion leaders (KOLs), hospital decision-makers, and prescribers., • Achieve sales and profitability targets for the assigned country., • Collaborate with marketing and medical teams to increase awareness of the company’s solution., • Monitor market dynamics, competitors, and new business opportunities., • Participate in and contribute to projects and initiatives that increase the value and productivity of the sales team and products facilitating collaborations in the healthcare ecosystem. We Would Like You To Have • 3 years of previous experience as KAM in the Pharma Industry., • 3 years of experience in digital medical device and/or digital health., • Knowledge of epilepsy and neurology is highly desirable., • Experience in digital health or connected medical solutions., • Excellent communication and negotiation skills., • Strategic thinking, relationship management, digital health literacy., • Demonstrated ability to leverage digital tools (CRM, analytics) for account management., • Proven track record in patient-centric sales approaches., • Experience in compliance with healthcare regulations and ethical standards., • Fluent in Spanish and English desirable. About Us Neuraxpharm is a leading European specialty pharmaceutical company focused on the treatment of the central nervous system (CNS), including both psychiatric and neurological disorders. It has a unique understanding of the CNS market built over 40 years. Neuraxpharm is constantly innovating, with new products and solutions to address unmet patient needs and is expanding its portfolio through its pipeline and acquisitions. The company has c. 1,000 employees and develops and commercializes CNS products through a direct presence in more than 20 countries in Europe, two in Latin America, one in the Middle East and globally via partners in more than 50 countries. Neuraxpharm is backed by funds advised by Permira. Neuraxpharm manufactures many of its pharmaceutical products at Neuraxpharm Pharmaceuticals (formerly Laboratories Lesvi) in Spain. Be part of the team where you can count on us to deliver: • Individual Professional development in a leading European pharmaceutical company with an ambitious international growth strategy., • Attractive remuneration according to the experience and skills provided., • An inspiring leadership team that drives performance., • An inclusive culture promoting diversity across the teams that will inspire you every day with a passionate, dynamic, a result focused and an expert&excellent team! Interested in knowing more? Have a look at what Neuraxpharm culture represents and what makes us a great place to work: you want to join us, this is your opportunity! WE COUNT ON YOU, YOU COUNT ON US At Neuraxpharm’s we ensure an inclusive, diverse, safe and respectful work environment for everyone in its organization. As we care for our people as much as we do for our patients, we are committed to guaranteeing a healthy, inclusive and equal opportunity workplace that enables employees to develop their professional potential, while ensuring their individual and collective satisfaction. We are guided by a Diversity & Inclusion policy to ensure a business culture based on the principles of diversity, equality and inclusion. Our policy complies with European legal regulations and includes the necessary standards, processes and measures to be taken in the event of discrimination or harassment against any employee of the company. xcskxlj We embrace and promote different cultures, gender identities, seniorities, ages and mindsets within the workplace, to bring different perspectives, styles and experiences to our business. #J-18808-Ljbffr

IT BUSINESS PROCESS MANAGER Dé el siguiente paso en su carrera profesional ahora: desplácese hacia abajo para leer la descripción completa del puesto y envíe su solicitud. • R&D DATA SCIENCEPresenta candidaturaremote type: Corporate & Support Functionslocations: SANT FELIU DE LLOBREGATtime type: Full timeposted on: Offerta pubblicata oggijob requisition id: 001564Stiamo costruendo il futuro della dermatologia medica concentrandoci sui bisogni ancora insoddisfatti dei pazienti e dando alle persone lo spazio per pensare in modo indipendente, assumersi responsabilità e generare un impatto che conta davvero.Il nostro purpose è semplice: trasformare la vita dei pazienti rispondendo a bisogni reali. Lavoriamo con rigore, agiamo con coraggio, teniamo le cose semplici e orientiamo l’innovazione dove può davvero fare la differenza.Riconosciuti come Top Employer in Spagna dal 2008 e in Germania dal 2025, continuiamo a investire in un ambiente in cui le persone possono crescere e andare avanti.Se pensi in modo diverso, qui è il posto giusto per te. **MISSION Act as the IT solution owner and trusted partner for the R&D Data Science team, collaborating closely with bioinformatics, molecular modelling, and AI Engineering to ensure alignment, proximity, and effective day-to-day collaboration. Own and support Data Science applications, both internally developed and third-party, ensuring business alignment, prioritization, and adoption. The role is accountable for end-to-end coordination, while execution of operations, architecture, security, compliance, and support is delivered in collaboration with specialized IT teams and external vendors. This role serves as a ring-fenced resource dedicated to Data Science needs, enabling faster decision-making, better communication, and more efficient delivery of IT services. It requires a strong scientific background and solid experience in R&D Data Science environments. **TASKS AND RESPONSIBILITIES Operational: * Lead demand intake, service coordination and project delivery for Data Science-related IT needs in close collaboration with Data Science stakeholders, especially bioinformatics and modelling teams • Manage software development lifecycle of custom Data Science tools supporting the acceleration of hypothesis generation and scientific insight creation, • Act as a Single Point of Contact (SPOC) in IT for Data Science users, reducing complexity by shielding business stakeholders from interacting with multiple IT teams and ensuring seamless coordination across infrastructure, security, data and application domains, • Partner with relevant IT domains to evolve technology capabilities for R&D Data Science, supporting scientific platforms, advanced computing, omics, multimodal analytics, molecular modelling and AI/ML in line with business priorities, • Translate, review, and validate Data Science requirements into actionable IT deliverables with clear scope, timelines, and responsibilities, while safeguarding business and end-user needs through a unified model for demand intake, backlog prioritization, issue management and adoption, • Coordinate with the appropriate governance, security and compliance functions to ensure Data Science solutions align with R&D and enterprise requirements, including AI ethics, monitoring and risk management, • Coordinate with service support teams and technology vendors to ensure technical solutions meet agreed functional and performance expectations, • Ensure that appropriate documentation, knowledge transfer and service transition are in place for handover to IT support teams, • Accountable for the update of data science system maps and software developed by data science that support R&D business operations, • Work with the relevant expert teams to ensure systems and pipelines meet required standards for backup, data integrity, security and GxP compliance, • Contribute to cost-efficient technology decisions aligned with the long-term R&D business strategy, in collaboration with the relevant IT and procurement stakeholders, • Define and track KPIs to measure solution performance, adoption and business value., • Drive project management using agile methodologies and increase speed of delivery, reducing time to insight and enabling faster hypothesis generation in all possible stages of Data Science flat & self-organised model., • Represent Data Science growth needs in IT planning to help ensure that platforms and services can scale appropriately for omics, advanced analytics and AI use cases, • Coordinate the design and evolution of the end-to-end architecture for the Data Science environment with enterprise architecture and specialist IT teams, ensuring scalability, resilience and alignment with corporate standards across ideation, pilots and production solutions, • Orchestrate cross-functional delivery involving Data & AI, Infrastructure & Operations, Security and Digital Solutions, with clear ownership across the relevant IT domains **EXPERIENCE * At least 5 years of experience working in R&D Pharma in close collaboration with bioinformatics and IT teams • Deep understanding of R&D Data Science workflows (omics, bioinformatics, AI/ML pipelines, and computational modeling), • Proven ability to operate at the intersection of science and technology, translating scientific challenges into scalable IT solutions, • Experience in HPC, cloud platforms (preferably Azure), or equivalent architectures for compute-intensive workloads, • Deep knowledge of advanced computing environments, supporting analytics, scientific pipelines AI/ML, or simulation workloads, • Market vision for solutions to support data scientist in Pharma R&D environment. Broad understanding of the Pharma industry including security and GxP compliance • Python, Linux, Apache, Postgres, Bash, R, Gitlab, Shiny server, Package manager Posit Workbench & Connect, services configuration management and automation, supports custom DS application to allow developer users to install code packages, Docker CI/CD, kubernetes clusters, LakeHouse integrations (preferably DataBricks), • Demonstrated experience in designing and implementing end to end data and cloud architectures including infrastructure, data pipelines, and application integration for complex and scalable environments, • Solid experience managing full lifecycle of solutions from ideation and proof of concept to industrialization production deployment and ongoing evolution & continuous improvement, • Proven track record in leading or coordinating cross-functional teams including Data & AI, infrastructure, security and external vendors, • Proven ability to enable innovation and evaluate non-standard technologies, balancing agility with compliance and enterprise architecture in fast-evolving environments MISSION Act as the IT solution owner and trusted partner for the R&D Data Science team, collaborating closely with bioinformatics, molecular modelling, and AI Engineering to ensure alignment, proximity, and effective day-to-day collaboration. Own and support Data Science applications, both internally developed and third-party, ensuring business alignment, prioritization, and adoption. The role is accountable for end-to-end coordination, while execution of operations, architecture, security, compliance, and support is delivered in collaboration with specialized IT teams and external vendors. This role serves as a ring-fenced resource dedicated to Data Science needs, enabling faster decision-making, better communication, and more efficient delivery of IT services. xcskxlj It requires a strong scientific background and solid experience in R&D Data Science environments. #J-18808-Ljbffr

IT BUSINESS PROCESS MANAGER Si está considerando enviar una solicitud, asegúrese de pulsar el botón de solicitar de abajo después de leer la descripción completa. • R&D DATA SCIENCEBewerbenremote type: Corporate & Support Functionslocations: SANT FELIU DE LLOBREGATtime type: Full timeposted on: Vor 2 Tagen ausgeschriebenjob requisition id: 001564 **Warum Almirall? **Wir gestalten die Zukunft der medizinischen Dermatologie, indem wir uns auf unerfüllte Bedürfnisse von Patient:innen konzentrieren und Menschen den Raum geben, eigenständig zu denken, Verantwortung zu übernehmen und Wirkung zu erzielen, die wirklich zählt.Unser Anspruch ist klar: das Leben von Patient:innen zu verbessern, indem wir auf echte Bedürfnisse eingehen. Wir arbeiten mit Präzision, handeln mutig, halten die Dinge einfach und richten unsere Innovation dort aus, wo sie wirklich einen Unterschied macht.Als Top Employer in Spanien seit 2008 und in Deutschland seit 2025 investieren wir kontinuierlich in ein Umfeld, in dem Menschen wachsen und vorankommen können.Wenn du Dinge anders angehst, bist du hier richtig. **MISSION Act as the IT solution owner and trusted partner for the R&D Data Science team, collaborating closely with bioinformatics, molecular modelling, and AI Engineering to ensure alignment, proximity, and effective day-to-day collaboration. Own and support Data Science applications, both internally developed and third-party, ensuring business alignment, prioritization, and adoption. The role is accountable for end-to-end coordination, while execution of operations, architecture, security, compliance, and support is delivered in collaboration with specialized IT teams and external vendors. This role serves as a ring-fenced resource dedicated to Data Science needs, enabling faster decision-making, better communication, and more efficient delivery of IT services. It requires a strong scientific background and solid experience in R&D Data Science environments. **TASKS AND RESPONSIBILITIES Operational: * Lead demand intake, service coordination and project delivery for Data Science-related IT needs in close collaboration with Data Science stakeholders, especially bioinformatics and modelling teams • Manage software development lifecycle of custom Data Science tools supporting the acceleration of hypothesis generation and scientific insight creation, • Act as a Single Point of Contact (SPOC) in IT for Data Science users, reducing complexity by shielding business stakeholders from interacting with multiple IT teams and ensuring seamless coordination across infrastructure, security, data and application domains, • Partner with relevant IT domains to evolve technology capabilities for R&D Data Science, supporting scientific platforms, advanced computing, omics, multimodal analytics, molecular modelling and AI/ML in line with business priorities, • Translate, review, and validate Data Science requirements into actionable IT deliverables with clear scope, timelines, and responsibilities, while safeguarding business and end-user needs through a unified model for demand intake, backlog prioritization, issue management and adoption, • Coordinate with the appropriate governance, security and compliance functions to ensure Data Science solutions align with R&D and enterprise requirements, including AI ethics, monitoring and risk management, • Coordinate with service support teams and technology vendors to ensure technical solutions meet agreed functional and performance expectations, • Ensure that appropriate documentation, knowledge transfer and service transition are in place for handover to IT support teams, • Accountable for the update of data science system maps and software developed by data science that support R&D business operations, • Work with the relevant expert teams to ensure systems and pipelines meet required standards for backup, data integrity, security and GxP compliance, • Contribute to cost-efficient technology decisions aligned with the long-term R&D business strategy, in collaboration with the relevant IT and procurement stakeholders, • Define and track KPIs to measure solution performance, adoption and business value., • Drive project management using agile methodologies and increase speed of delivery, reducing time to insight and enabling faster hypothesis generation in all possible stages of Data Science flat & self-organised model., • Represent Data Science growth needs in IT planning to help ensure that platforms and services can scale appropriately for omics, advanced analytics and AI use cases, • Coordinate the design and evolution of the end-to-end architecture for the Data Science environment with enterprise architecture and specialist IT teams, ensuring scalability, resilience and alignment with corporate standards across ideation, pilots and production solutions, • Orchestrate cross-functional delivery involving Data & AI, Infrastructure & Operations, Security and Digital Solutions, with clear ownership across the relevant IT domains **EXPERIENCE * At least 5 years of experience working in R&D Pharma in close collaboration with bioinformatics and IT teams • Deep understanding of R&D Data Science workflows (omics, bioinformatics, AI/ML pipelines, and computational modeling), • Proven ability to operate at the intersection of science and technology, translating scientific challenges into scalable IT solutions, • Experience in HPC, cloud platforms (preferably Azure), or equivalent architectures for compute-intensive workloads, • Deep knowledge of advanced computing environments, supporting analytics, scientific pipelines AI/ML, or simulation workloads, • Market vision for solutions to support data scientist in Pharma R&D environment. Broad understanding of the Pharma industry including security and GxP compliance • Python, Linux, Apache, Postgres, Bash, R, Gitlab, Shiny server, Package manager Posit Workbench & Connect, services configuration management and automation, supports custom DS application to allow developer users to install code packages, Docker CI/CD, kubernetes clusters, LakeHouse integrations (preferably DataBricks), • Demonstrated experience in designing and implementing end to end data and cloud architectures including infrastructure, data pipelines, and application integration for complex and scalable environments, • Solid experience managing full lifecycle of solutions from ideation and proof of concept to industrialization production deployment and ongoing evolution & continuous improvement, • Proven track record in leading or coordinating cross-functional teams including Data & AI, infrastructure, security and external vendors, • Proven ability to enable innovation and evaluate non-standard technologies, balancing agility with compliance and enterprise architecture in fast-evolving environments MISSION Act as the IT solution owner and trusted partner for the R&D Data Science team, collaborating closely with bioinformatics, molecular modelling, and AI Engineering to ensure alignment, proximity, and effective day-to-day collaboration. Own and support Data Science applications, both internally developed and third-party, ensuring business alignment, prioritization, and adoption. The role is accountable for end-to-end coordination, while execution of operations, architecture, security, compliance, and support is delivered in collaboration with specialized IT teams and external vendors. This role serves as a ring-fenced resource dedicated to Data Science needs, enabling faster decision-making, better communication, and more efficient delivery of IT services. xqbhyrx It requires a strong scientific background and solid experience in R&D Data Science environments. #J-18808-Ljbffr

¿Quiénes somos? Grupo Farmacéutico Salvat es una compañía familiar fundada en Barcelona en 1955, con más de 70 años cuidando la salud a través de marcas emblemáticas como Cristalmina, Cetraxal, Monolitum o Salvacolina. Tenemos presencia en más de 60 países y plantas de producción en Barcelona, Madrid y Miami. Contamos con I+D propio y desarrollamos soluciones en oftalmología, otorrinolaringología y gastroenterología, además de Consumer Health y servicios CDMO, donde aspiramos a ser un referente. Estamos certificados por la FDA y reconocidos con calificación excelente en el Plan Profarma. Actualmente impulsamos el proyecto NewSalvat, una transformación para ser más ágiles, fuertes y competitivos. Nuestra cultura se basa en los valores AACT (Ambición, Accountability, Colaboración y Transparencia), apostando por el crecimiento y el talento de las personas. Si desea saber un poco más sobre esta oportunidad, o está considerando presentar su candidatura, por favor, lea la siguiente información del puesto. ¿Qué buscamos? Estamos en la búsqueda de un/a técnico de Regulatory Affairs que comparta nuestra visión y esté listo para contribuir en proyectos desafiantes. Si tienes los conocimientos requeridos y un enfoque proactivo, ¡queremos conocerte! Tu misión Elaborar y gestionar hasta aprobación los expedientes para el registro de especialidades farmacéuticas, cosméticos, productos sanitarios, complementos alimenticios y biocidas a nivel nacional e internacional. Mantener la documentación actualizada mediante la preparación de las solicitudes de variaciones conforme a la legislación vigente. Seguimiento de la Normativa para la obtención de autorización de comercialización del producto y su mantenimiento. Tus principales responsabilidades serán: • Preparación, revisión y presentación de la documentación necesaria para solicitudes de nuevas autorizaciones, variaciones y revalidaciones ante las autoridades sanitarias (tanto nacionales como MRP y DCP), así como del seguimiento de estos trámites hasta su resolución y de las gestiones posteriores oportunas., • Preparación y seguimiento de solicitudes de registro, variaciones y revalidaciones de medicamentos en el resto del mundo (se valorará experiencia previa en registro FDA y otros países)., • Gestión de trámites para autorización y mantenimiento de complementos alimenticios, productos sanitarios, biocidas y/o cosméticos., • Seguimiento y revisión de textos de material de acondicionamiento y material publicitario., • Participación en proyectos globales de compañía en equipos multidisciplinares Requisitos • Licenciatura en ciencias de la salud (Farmacia, Química, Biología o similar), valorables estudios específicos sobre asuntos regulatorios (máster, postgrado...)., • Experiencia 2-3 años en puestos similares, • Conocimientos de la normativa en vigor para el registro y mantenimiento de los registros de medicamentos, tanto a nivel nacional como europeo, especialmente en el Módulo 3 de Calidad(valorable internacional y FDA)., • Conocimientos de la normativa de cosméticos, productos sanitarios, complementos alimenticios y biocidas., • Inglés (Nivel B2 o superior)., • Conocimientos ofimáticos avanzados (office, valorable eCTD manager, aplicaciones de gestión de agencias reguladoras). Aptitudes • Inglés, • Buenas prácticas de fabricación (GMP) de la Administración de Alimentos y Medicamentos (FDA), • Trabajo en equipo ¿Qué te ofrecemos? • Proyecto sólido en una compañía consolidada del sector Pharma., • Entorno de transformación y con crecimiento profesional y personal., • Rol estratégico con alto impacto en negocio y en resultados., • Desarrollo profesional y liderazgo de equipos de alto rendimiento., • Entorno dinámico y orientado a resultados., • Equipos de trabajo transversales y colaborativos., • Cultura colaborativa y exigente., • Un entorno en el que valoramos la iniciativa y el impacto individual. ¿Quieres formar parte de este proyecto transformador? xqbhyrx Aplica para más información ¡Vamos a construir juntos el futuro de Salvat!

IT BUSINESS PROCESS MANAGER Lea atentamente toda la información sobre esta oportunidad y luego utilice el botón de solicitud de abajo para enviar su CV y su candidatura. • R&D DATA SCIENCEApplyremote type: Corporate & Support Functionslocations: SANT FELIU DE LLOBREGATtime type: Full timeposted on: Posted Todayjob requisition id: 001564We’re building the future of medical dermatology by focusing on unmet patient needs and giving people the space to think independently, take ownership and make an impact that matters.Our purpose is simple: to transform patients’ lives by addressing real needs. We work with care, act with courage, keep things simple and focus our innovation where it makes a difference.Recognised as a Top Employer in Spain since 2008 and in Germany since 2025, we continue to invest in an environment where people can grow and move forward.If you care differently, you belong here. **MISSION Act as the IT solution owner and trusted partner for the R&D Data Science team, collaborating closely with bioinformatics, molecular modelling, and AI Engineering to ensure alignment, proximity, and effective day-to-day collaboration. Own and support Data Science applications, both internally developed and third-party, ensuring business alignment, prioritization, and adoption. The role is accountable for end-to-end coordination, while execution of operations, architecture, security, compliance, and support is delivered in collaboration with specialized IT teams and external vendors. This role serves as a ring-fenced resource dedicated to Data Science needs, enabling faster decision-making, better communication, and more efficient delivery of IT services. It requires a strong scientific background and solid experience in R&D Data Science environments. **TASKS AND RESPONSIBILITIES Operational: * Lead demand intake, service coordination and project delivery for Data Science-related IT needs in close collaboration with Data Science stakeholders, especially bioinformatics and modelling teams • Manage software development lifecycle of custom Data Science tools supporting the acceleration of hypothesis generation and scientific insight creation, • Act as a Single Point of Contact (SPOC) in IT for Data Science users, reducing complexity by shielding business stakeholders from interacting with multiple IT teams and ensuring seamless coordination across infrastructure, security, data and application domains, • Partner with relevant IT domains to evolve technology capabilities for R&D Data Science, supporting scientific platforms, advanced computing, omics, multimodal analytics, molecular modelling and AI/ML in line with business priorities, • Translate, review, and validate Data Science requirements into actionable IT deliverables with clear scope, timelines, and responsibilities, while safeguarding business and end-user needs through a unified model for demand intake, backlog prioritization, issue management and adoption, • Coordinate with the appropriate governance, security and compliance functions to ensure Data Science solutions align with R&D and enterprise requirements, including AI ethics, monitoring and risk management, • Coordinate with service support teams and technology vendors to ensure technical solutions meet agreed functional and performance expectations, • Ensure that appropriate documentation, knowledge transfer and service transition are in place for handover to IT support teams, • Accountable for the update of data science system maps and software developed by data science that support R&D business operations, • Work with the relevant expert teams to ensure systems and pipelines meet required standards for backup, data integrity, security and GxP compliance, • Contribute to cost-efficient technology decisions aligned with the long-term R&D business strategy, in collaboration with the relevant IT and procurement stakeholders, • Define and track KPIs to measure solution performance, adoption and business value., • Drive project management using agile methodologies and increase speed of delivery, reducing time to insight and enabling faster hypothesis generation in all possible stages of Data Science flat & self-organised model., • Represent Data Science growth needs in IT planning to help ensure that platforms and services can scale appropriately for omics, advanced analytics and AI use cases, • Coordinate the design and evolution of the end-to-end architecture for the Data Science environment with enterprise architecture and specialist IT teams, ensuring scalability, resilience and alignment with corporate standards across ideation, pilots and production solutions, • Orchestrate cross-functional delivery involving Data & AI, Infrastructure & Operations, Security and Digital Solutions, with clear ownership across the relevant IT domains **EXPERIENCE * At least 5 years of experience working in R&D Pharma in close collaboration with bioinformatics and IT teams • Deep understanding of R&D Data Science workflows (omics, bioinformatics, AI/ML pipelines, and computational modeling), • Proven ability to operate at the intersection of science and technology, translating scientific challenges into scalable IT solutions, • Experience in HPC, cloud platforms (preferably Azure), or equivalent architectures for compute-intensive workloads, • Deep knowledge of advanced computing environments, supporting analytics, scientific pipelines AI/ML, or simulation workloads, • Market vision for solutions to support data scientist in Pharma R&D environment. Broad understanding of the Pharma industry including security and GxP compliance • Python, Linux, Apache, Postgres, Bash, R, Gitlab, Shiny server, Package manager Posit Workbench & Connect, services configuration management and automation, supports custom DS application to allow developer users to install code packages, Docker CI/CD, kubernetes clusters, LakeHouse integrations (preferably DataBricks), • Demonstrated experience in designing and implementing end to end data and cloud architectures including infrastructure, data pipelines, and application integration for complex and scalable environments, • Solid experience managing full lifecycle of solutions from ideation and proof of concept to industrialization production deployment and ongoing evolution & continuous improvement, • Proven track record in leading or coordinating cross-functional teams including Data & AI, infrastructure, security and external vendors, • Proven ability to enable innovation and evaluate non-standard technologies, balancing agility with compliance and enterprise architecture in fast-evolving environments MISSION Act as the IT solution owner and trusted partner for the R&D Data Science team, collaborating closely with bioinformatics, molecular modelling, and AI Engineering to ensure alignment, proximity, and effective day-to-day collaboration. Own and support Data Science applications, both internally developed and third-party, ensuring business alignment, prioritization, and adoption. The role is accountable for end-to-end coordination, while execution of operations, architecture, security, compliance, and support is delivered in collaboration with specialized IT teams and external vendors. This role serves as a ring-fenced resource dedicated to Data Science needs, enabling faster decision-making, better communication, and more efficient delivery of IT services. xcskxlj It requires a strong scientific background and solid experience in R&D Data Science environments. #J-18808-Ljbffr

En BESIDE apostamos por el mejor talento dentro del sector tecnológico e industrial. Contamos con una unidad de Selección Especializada en perfiles de Ingeniería para incorporarse en la plantilla de nuestros clientes. Trabajamos con un amplio rango de empresas, que nos permitirá encontrarte el puesto que más se ajuste a tus necesidades e intereses profesionales. Te podrás incorporar en las empresas más innovadoras, ofreciéndote proyectos punteros dentro de las ramas de I+D, automoción, pharma, diseño de maquinaria, desarrollo de producto, etc. No espere a enviar su solicitud después de leer esta descripción; se espera un gran volumen de candidaturas para esta oportunidad. Funciones: • Administración y gestión del día a día de los sistemas Oracle de la compañía., • Mantenimiento, monitorización y soporte de entornos Oracle RAC., • Gestión y supervisión de soluciones de alta disponibilidad mediante Oracle Data Guard., • Administración y operación de replicación de datos con Oracle GoldenGate., • Resolución de incidencias y soporte técnico en entornos Oracle de producción. Condiciones • Tres dias de teletrabajo a la semana, dos en oficina., • Horario flexible de entrada/salida; posibilidad de entrada a partir de las 7:30-9h., • Viernes jornada intensiva. Requisitos: Imprescindible • Experiencia demostrada como DBA Senior en entornos Oracle., • Conocimientos sólidos y experiencia práctica en Oracle RAC, Data Guard y GoldenGate., • Perfil orientado 100% a la administración y gestión de sistemas (no a desarrollo)., • Nivel de inglés medio. xcskxlj Se valorará • Experiencia en entornos de alta disponibilidad y misión crítica. #J-18808-Ljbffr

Sobre la posición Desde esta posición contribuirás a la planificación, coordinación y ejecución de visitas corporativas, eventos institucionales y activaciones de patrocinio, garantizando la excelencia operativa y atención al detalle en los proyectos a desarrollar. Trabajarás de forma transversal con diferentes áreas de la organización y con proveedores externos. Principales responsabilidades • Relaciones Institucionales (60%), • Organización de visitas corporativas, gestionando alojamientos, traslados, restauración y actividades complementarias., • Preparación de obsequios institucionales y materiales corporativos., • Gestión de proveedores y facturación asociada., • Elaboración de informes trimestrales sobre inversión, asistentes y servicios gestionados., • Administración y gestión (20%), • Gestionar pedidos de servicios y materiales de los proyectos ejecutados por el departamento., • Organizar acciones de empleados, como la preparación de lotes de Navidad y otras iniciativas internas., • Dar soporte administrativo y operativo a los proyectos del área., • Eventos Corporativos (10%), • Producción y ejecución de eventos corporativos., • Producción de materiales y gestión de servicios para lanzamientos de producto, reuniones internas, convenciones y actividades de team building., • Coordinación y seguimiento del plan de comunicación asociado a cada evento (save the date, invitaciones, gestión de inscripciones, registro de asistentes y seguimiento del attendee journey)., • Gestión de logística, materiales, proveedores y necesidades operativas antes, durante y después de cada evento., • Elaboración de informes de cierre de los proyectos asociados., • Dar soporte en la producción para la implementación de marca en proyectos de patrocinio., • Gestionar pedidos y materiales de activación., • Coordinar la uniformidad y materiales destinados a los equipos de activación., • Seguimiento operativo con proveedores y colaboradores., • Gestión de Ticketing e invitaciones a públicos de interés., • Gestión de catering en sedes colaboradoras.Requisitos, • Grado en Relaciones Públicas, Turismo o áreas afines., • Dominio de Microsoft Office, especialmente Excel y PowerPoint., • Se valorará experiencia previa (prácticas o hasta 2 años) en organización de eventos, hospitality, marketing o relaciones institucionales., • Disponibilidad para viajar de forma puntual y asistir a eventos cuando sea necesario., • Excelente capacidad de organización y planificación., • Atención al detalle y orientación a la calidad., • Alta discreción y confidencialidad., • Capacidad para priorizar y gestionar varios proyectos al mismo tiempo., • Capacidad para trabajar en entornos dinámicos y cambiantes., • Actitud proactiva y resolutiva., • Creatividad e iniciativa., • Excelentes habilidades de comunicación y trabajo en equipo.Valorar, • Conocimiento de Microsoft Dynamics., • Conocimiento del sector farmacéutico, healthcare o cosmética médica., • Experiencia trabajando en entornos internacionales. xqbhyrx, • Conocimiento de herramientas digitales para eventos (App de registro e interacción). #J-18808-Ljbffr

Jobtailor in Viladecans is seeking a Business Development professional to build and maintain relationships with CROs, Pharmas and Biotechs, while coordinating budgets and the sales pipeline for clinical trial services. ¿Tiene lo que se necesita para triunfar? La siguiente información debe ser leída atentamente por todos los candidatos. You will negotiate quotes and manage opportunities, plus oversee essential documents and regulatory paperwork. Fluent English is required; prior experience in pharma xcskxlj or healthcare and strong communication and client-management skills are essential to drive growth in a global #J-18808-Ljbffr

Experteer Overview In this role you will define and lead our AI strategy to drive business value across the organization. You will own end-to-end AI initiatives from ideation to production, aligning with corporate priorities and ensuring governance and data integrity. You’ll enable AI across the pharma value chain while maintaining GxP compliance and regulatory readiness. You will champion data-driven decision-making and digital transformation to sustain competitive advantage and patient impact. Compensaciones / Beneficios • Accelerate AI adoption across the organization by scaling use cases and ensuring measurable value • Own end-to-end lifecycle of AI use cases, from ideation to production and value realization • Identify, evaluate, and prioritize AI opportunities aligned with corporate strategy • Leverage external partnerships (tech providers, startups, academia) to accelerate capabilities • Orchestrate cross-functional teams and centralize delivery accountability • Collaborate with IT and digital transformation to integrate AI into enterprise systems • Ensure AI solutions are scalable, reliable, and well-integrated with business processes • Drive MLOps practices for lifecycle management, monitoring, and deployment • Establish governance and controls for responsible AI use adhering to policies and regulations • Continuously evaluate emerging AI technologies to sustain competitive advantage • Measure AI-driven value with linked financial and operational metrics Responsabilidades • 8-10+ years in AI, advanced analytics, or data-driven transformation with proven AI delivery • Strong pharma or life sciences industry experience across end-to-end value chain • Track record in defining, prioritizing, and delivering AI use cases to production with business impact • Solid understanding of ML, predictive analytics, and AI applications in pharma • Experience leading cross-functional teams in complex environments • Familiarity with GenAI capabilities and business applications • Experience with MLOps, scalability, monitoring, and lifecycle management of models • Hands-on with modern data/AI tech stacks including Cloud platforms, Data platforms, ML frameworks, and data engineering tools • Experience with enterprise AI and analytics/BI platforms • Pharma-specific systems and data environment knowledge is highly valuable • Degree in Mathematics, Physics, Statistics, Economics, Engineering, or related quantitative field • Advanced degrees in AI, Data Science, or Business Analytics valued • Language: Fluent English; Spanish/German desirable • Occasional travel availability Requisitos principales • Individual professional development • Attractive remuneration • Inspirational leadership • Inclusive culture promoting diversity • Performance-driven environment • Opportunity to impact CNS patient outcomes

Corporate Head of AI ¿Tiene lo que se necesita para triunfar? La siguiente información debe ser leída atentamente por todos los candidatos. Neuraxpharm is looking for a Corporate Head of AI based in Barcelona (hybrid role). Your Mission Define and lead the company’s Artificial Intelligence (AI) strategy, ensuring alignment with business objectives and corporate priorities, and taking end‑to‑end ownership of AI‑driven value creation across the organization. Drive the identification, prioritization, orchestration, and delivery of AI use cases, ensuring their successful deployment into production and their measurable impact on business performance. Leverage the corporate data architecture and governance framework to enable scalable and sustainable AI and advanced analytics initiatives, ensuring that data availability, quality, and consistency support industrialized AI adoption. Enable AI use consistently across the pharmaceutical value chain, from R&D and regulatory to manufacturing, medical, and commercial, ensuring strict adherence to GxP standards, data integrity principles, and evolving regulatory requirements. Promote a culture of innovation, data‑driven decision‑making, and operational excellence, positioning AI as a key enabler of digital transformation and long‑term competitive advantage. Your Major Accountabilities • Accelerate AI adoption across the organization by actively driving the understanding, implementation, and scaling of AI use cases, ensuring business teams effectively leverage AI capabilities to generate measurable value., • Own the end‑to‑end lifecycle of AI use cases, from ideation and prioritization to development, deployment, and value realization in production environments., • Identify, evaluate, and prioritize AI opportunities across all business functions, ensuring alignment with corporate strategy and focusing on initiatives with measurable business impact., • Leverage external partnerships (technology providers, startups, academic institutions) to accelerate AI capabilities and access best‑in‑class solutions., • Orchestrate cross‑functional teams to ensure successful execution of AI initiatives, acting as the central point of accountability for delivery. Partner closely with IT and digital transformation functions to ensure AI solutions are fully integrated into enterprise systems, scalable infrastructure, and core digital platforms., • Ensure that AI solutions are scalable, reliable, and integrated into existing business processes and systems, supporting long‑term adoption and sustainability., • Drive the industrialization of AI capabilities, including the implementation of best practices for model development, deployment, monitoring, and lifecycle management (MLOps – Machine Learning Operations)., • Establish governance and controls for AI usage, ensuring compliance with internal policies, ethical standards, and regulatory requirements., • Continuously evaluate emerging AI technologies and trends, identifying opportunities to enhance business performance and maintain competitive advantage., • Own the measurement and tracking of AI‑driven value, ensuring clear linkage between AI initiatives and financial and operational performance (e.g., revenue growth, cost efficiencies, productivity gains). We Would Like You To Have • 8–10+ years of experience in Artificial Intelligence (AI), advanced analytics, or data‑driven transformation roles, with proven experience delivering AI solutions in business environments., • Strong experience in the pharmaceutical or life sciences industry, with understanding of the end‑to‑end value chain (R&D, clinical development, regulatory affairs, pharmacovigilance, manufacturing, quality, supply chain, and commercial operations)., • Strong track record in defining, prioritizing, and delivering AI use cases from concept to production, including measurable business impact., • Solid understanding of machine learning (ML), predictive analytics, statistical modeling techniques and AI applications in pharma., • Experience in leading cross‑functional teams and operating in complex organizational environments, combining business, data, and technology perspectives., • Familiarity with modern AI technologies and platforms, including exposure to Generative AI (GenAI) capabilities and their application in business contexts., • Experience working with MLOps practices, ensuring scalability, monitoring, and lifecycle management of AI models in production., • Hands‑on familiarity with modern data and AI technology stacks, including Cloud platforms, Data platforms, ML frameworks, Data engineering tools., • Experience with enterprise AI and analytics/BI platforms., • Knowledge of pharma‑specific systems and data environments is highly valuable., • Degree in Mathematics, Physics, Statistics, Economics, Engineering, or a related quantitative or analytical discipline., • Advanced degrees or postgraduate studies in Artificial Intelligence, Data Science, Business Analytics, or similar fields are highly valued., • Language: Fluent English is a must and Spanish/ German desirable., • Occasional travel availability. Benefits • Individual professional development in a leading European pharmaceutical company with an ambitious international growth strategy., • Attractive remuneration according to experience and skills., • An inspiring leadership team that drives performance., • An inclusive culture promoting diversity across teams. Legal Compliance At Neuraxpharm we ensure an inclusive, diverse, safe and respectful work environment for everyone in its organization. We are committed to guaranteeing a healthy, inclusive and equal opportunity workplace that enables employees to develop their professional potential, while ensuring their individual and collective satisfaction. We are guided by a Diversity & Inclusion policy to ensure a business culture based on the principles of diversity, equality and inclusion. xcskxlj Our policy complies with European legal regulations and includes the necessary standards, processes and measures to be taken in the event of discrimination or harassment against any employee of the company. #J-18808-Ljbffr

Sr. Global Strategic Marketing Manager – Nutraceuticals No espere a enviar su solicitud después de leer esta descripción; se espera un gran volumen de candidaturas para esta oportunidad. Travel: Up to 25% globally Job Type: Full-time, Hybrid How You’ll Make An Impact • Define and lead the global strategic roadmap for nutraceutical actives, including segment prioritization and portfolio shaping, • Establish Lubrizol's "right to win" through differentiated value propositions and targeted investment strategies, • Identify and unlock new growth platforms across applications, geographies, technologies, and partnerships, • Drive disciplined portfolio management, balancing core optimization with next-generation innovation, • Lead forward-looking market intelligence to identify unmet needs, emerging trends, and structural growth opportunities, • Translate insights into actionable innovation pipelines, partnership strategies, and commercial playbooks, • Build robust, finance-aligned business cases with clear ROI and value capture mechanisms, • Orchestrate cross-functional execution to bring innovation from concept to commercialization with speed and scalability, • Lead global marketing initiatives across commercial, business development, and technical teams to deliver above-market growth, • Represent Lubrizol externally with customers, industry bodies, and partners to strengthen thought leadership and positioning Required Qualifications That Enable Your Success • Bachelor's degree in Business, Marketing, Life Sciences, or related field, • Minimum 10 years of experience in strategic marketing, business leadership, or innovation-driven roles, • Proven track record of defining and executing global growth strategies, • Experience within nutraceuticals, food, pharma, or adjacent regulated industries, • Strong understanding of nutraceutical value chains, regulatory environments, and innovation ecosystems, • Demonstrated ability xqbhyrx to lead and influence cross-functional, global teams, • Strong financial acumen with experience building investment cases and driving ROI, • Excellent communication, stakeholder management, and strategic thinking skills Preferred Qualifications That Drive You Forward • Advanced degree (MBA, MSc, or PhD) in a relevant discipline, • Experience working across multiple regions in a global organization, • Exposure to external innovation ecosystems, partnerships, or M&A projects, • Experience with commercialization of new technologies or ingredients #J-18808-Ljbffr

Mettler Toledo AG, a leader in process analytics, seeks a Market Manager to drive growth across Middle East, Africa and Europe through distributors and channel partners, strengthening customer relationships and expanding market share. Consulte la descripción del puesto a continuación. Si confía en que tiene las habilidades y la experiencia adecuadas, envíe su solicitud hoy mismo. Based in Barcelona preferred, candidates with international market experience will develop strategies, deliver training, and collaborate with engineering and xqbhyrx commercial teams to maximize value for customers in pharma, chemicals, energy, food & beverage, and water #J-18808-Ljbffr

Synthon-Hispania is seeking an experienced Application Technician to manage the DMS, QMS, and LMS landscape and ensure alignment with business processes and regulatory requirements. A continuación se detalla todo lo que necesita saber sobre lo que implica esta oportunidad, así como lo que se espera de los solicitantes. You will lead improvements, upgrades, validation activities and implementation projects, working closely with IT, stakeholders and external vendors to maintain availability, xcskxlj performance and security of the systems, including user access control and documentation. #J-18808-Ljbffr

IT BUSINESS PROCESS MANAGER La siguiente información tiene como objetivo proporcionar a los posibles candidatos una mejor comprensión de los requisitos para este puesto. • R&D DATA SCIENCESolicitarremote type: Corporate & Support Functionslocations: SANT FELIU DE LLOBREGATtime type: Full timeposted on: Publicado hace 2 díasjob requisition id: 001564Estamos construyendo el futuro de la dermatología médica centrándonos en las necesidades no cubiertas de los pacientes y dando a las personas el espacio para pensar de forma independiente, asumir responsabilidades y generar un impacto que de verdad importe.Nuestro propósito es sencillo: transformar la vida de los pacientes abordando necesidades reales. Trabajamos con rigor, actuamos con valentía, simplificamos lo complejo y enfocamos la innovación allí donde realmente marca la diferencia.Reconocidos como Top Employer en España desde 2008 y en Alemania desde 2025, seguimos invirtiendo en un entorno donde las personas pueden crecer y avanzar.Si quieres hacer las cosas de otra manera, este es tu lugar. **MISSION Act as the IT solution owner and trusted partner for the R&D Data Science team, collaborating closely with bioinformatics, molecular modelling, and AI Engineering to ensure alignment, proximity, and effective day-to-day collaboration. Own and support Data Science applications, both internally developed and third-party, ensuring business alignment, prioritization, and adoption. The role is accountable for end-to-end coordination, while execution of operations, architecture, security, compliance, and support is delivered in collaboration with specialized IT teams and external vendors. This role serves as a ring-fenced resource dedicated to Data Science needs, enabling faster decision-making, better communication, and more efficient delivery of IT services. It requires a strong scientific background and solid experience in R&D Data Science environments. **TASKS AND RESPONSIBILITIES Operational: * Lead demand intake, service coordination and project delivery for Data Science-related IT needs in close collaboration with Data Science stakeholders, especially bioinformatics and modelling teams • Manage software development lifecycle of custom Data Science tools supporting the acceleration of hypothesis generation and scientific insight creation, • Act as a Single Point of Contact (SPOC) in IT for Data Science users, reducing complexity by shielding business stakeholders from interacting with multiple IT teams and ensuring seamless coordination across infrastructure, security, data and application domains, • Partner with relevant IT domains to evolve technology capabilities for R&D Data Science, supporting scientific platforms, advanced computing, omics, multimodal analytics, molecular modelling and AI/ML in line with business priorities, • Translate, review, and validate Data Science requirements into actionable IT deliverables with clear scope, timelines, and responsibilities, while safeguarding business and end-user needs through a unified model for demand intake, backlog prioritization, issue management and adoption, • Coordinate with the appropriate governance, security and compliance functions to ensure Data Science solutions align with R&D and enterprise requirements, including AI ethics, monitoring and risk management, • Coordinate with service support teams and technology vendors to ensure technical solutions meet agreed functional and performance expectations, • Ensure that appropriate documentation, knowledge transfer and service transition are in place for handover to IT support teams, • Accountable for the update of data science system maps and software developed by data science that support R&D business operations, • Work with the relevant expert teams to ensure systems and pipelines meet required standards for backup, data integrity, security and GxP compliance, • Contribute to cost-efficient technology decisions aligned with the long-term R&D business strategy, in collaboration with the relevant IT and procurement stakeholders, • Define and track KPIs to measure solution performance, adoption and business value., • Drive project management using agile methodologies and increase speed of delivery, reducing time to insight and enabling faster hypothesis generation in all possible stages of Data Science flat & self-organised model., • Represent Data Science growth needs in IT planning to help ensure that platforms and services can scale appropriately for omics, advanced analytics and AI use cases, • Coordinate the design and evolution of the end-to-end architecture for the Data Science environment with enterprise architecture and specialist IT teams, ensuring scalability, resilience and alignment with corporate standards across ideation, pilots and production solutions, • Orchestrate cross-functional delivery involving Data & AI, Infrastructure & Operations, Security and Digital Solutions, with clear ownership across the relevant IT domains **EXPERIENCE * At least 5 years of experience working in R&D Pharma in close collaboration with bioinformatics and IT teams • Deep understanding of R&D Data Science workflows (omics, bioinformatics, AI/ML pipelines, and computational modeling), • Proven ability to operate at the intersection of science and technology, translating scientific challenges into scalable IT solutions, • Experience in HPC, cloud platforms (preferably Azure), or equivalent architectures for compute-intensive workloads, • Deep knowledge of advanced computing environments, supporting analytics, scientific pipelines AI/ML, or simulation workloads, • Market vision for solutions to support data scientist in Pharma R&D environment. Broad understanding of the Pharma industry including security and GxP compliance • Python, Linux, Apache, Postgres, Bash, R, Gitlab, Shiny server, Package manager Posit Workbench & Connect, services configuration management and automation, supports custom DS application to allow developer users to install code packages, Docker CI/CD, kubernetes clusters, LakeHouse integrations (preferably DataBricks), • Demonstrated experience in designing and implementing end to end data and cloud architectures including infrastructure, data pipelines, and application integration for complex and scalable environments, • Solid experience managing full lifecycle of solutions from ideation and proof of concept to industrialization production deployment and ongoing evolution & continuous improvement, • Proven track record in leading or coordinating cross-functional teams including Data & AI, infrastructure, security and external vendors, • Proven ability to enable innovation and evaluate non-standard technologies, balancing agility with compliance and enterprise architecture in fast-evolving environments MISSION Act as the IT solution owner and trusted partner for the R&D Data Science team, collaborating closely with bioinformatics, molecular modelling, and AI Engineering to ensure alignment, proximity, and effective day-to-day collaboration. Own and support Data Science applications, both internally developed and third-party, ensuring business alignment, prioritization, and adoption. The role is accountable for end-to-end coordination, while execution of operations, architecture, security, compliance, and support is delivered in collaboration with specialized IT teams and external vendors. This role serves as a ring-fenced resource dedicated to Data Science needs, enabling faster decision-making, better communication, and more efficient delivery of IT services. xcskxlj It requires a strong scientific background and solid experience in R&D Data Science environments. #J-18808-Ljbffr

Aufgrund der Expansion und des Wachstums unseres Shared Business Centers in Barcelona suchen wir Verstärkung im Bereich Pre Sales Support. Unser internationales Telemarketing Team steht im Austausch mit namhaften Kunden aus nahezu allen Branchen (Chemie & Rohstoffe, Pharma, Lebensmittel, FMCG, Metall- und Elektroindustrie, Transport & Logistik etc.) mit dem Ziel, Verkaufschancen zu identifizieren und zu qualifizieren. ¿Interesado en saber más sobre este trabajo? Desplácese hacia abajo y descubra qué habilidades, experiencia y cualificaciones académicas se necesitan. Kein Cold Calling. Keine Call Center Atmosphäre. Kein Micromanagement. Each Day Is Different – Unser breitgefächertes Produktportfolio, unser vielfältiger Kundenstamm, und die unterschiedlichen Marketingkampagnen machen die Rolle abwechslungsreich. Aufgaben • Durchführung von Outbound-Calls mit dem Ziel, das Interesse unserer Kunden zu gewinnen., • Proaktive Leadgenerierung im Rahmen unserer Marketingkampagnen., • Telefonische Vorstellung neuer Produkte., • Versand von Informationsmaterialien sowie anschließende Follow‑up-Aktivitäten. xqbhyrx, • Enge Zusammenarbeit mit unterschiedlichen Abteilungen, u.a. dem Produktvertrieb und Marketing. #J-18808-Ljbffr

Die Mettler Toledo AG sucht zur Verstärkung ihres Shared Business Centers in Barcelona eine(n) Pre-Sales-Support-Mitarbeiter(in). ¿Está pensando en solicitar este empleo? No se demore, desplácese hacia abajo y envíe su solicitud lo antes posible para no perder la oportunidad. Sie arbeiten im internationalen Telemarketing-Team und identifizieren sowie qualifizieren Verkaufschancen in Branchen wie Chemie, Pharma, Lebensmittel und Logistik. xqbhyrx Sie vermeiden Cold Calling, Mikromanagement und Call-Center-Atmosphäre; jeden Tag ist anders. Zu Ihren Aufgaben gehören Outbound-Anrufe, proaktive Leadgenerierung, Produktvorstellungen am Telefon und das #J-18808-Ljbffr

Aufgrund der Expansion und des Wachstums unseres Shared Business Centers in Barcelona suchen wir Verstärkung im Bereich Pre Sales Support. Unser internationales Telemarketing Team steht im Austausch mit namhaften Kunden aus nahezu allen Branchen (Chemie & Rohstoffe, Pharma, Lebensmittel, FMCG, Metall- und Elektroindustrie, Transport & Logistik etc.) mit dem Ziel, Verkaufschancen zu identifizieren und zu qualifizieren. A continuación se detalla todo lo que necesita saber sobre lo que implica esta oportunidad, así como lo que se espera de los solicitantes. Wir bieten kein Cold Calling, keine Call Center Atmosphäre und kein Micromanagement. Each Day Is Different – Unser breitgefächertes Produktportfolio, unser vielfältiger Kundenstamm, und die unterschiedlichen Marketingkampagnen machen die Rolle abwechslungsreich. Verstärken Sie unser Team mit Ihrer pro-aktiven, kommunikativen Art und übernehmen Sie folgende Aufgaben: Responsibilities • Durchführung von Outbound-Calls mit dem Ziel, das Interesse unserer Kunden zu gewinnen., • Proaktive Leadgenerierung im Rahmen unserer Marketingkampagnen., • Telefonische Vorstellung neuer Produkte., • Zusendung von Informationsmaterialien sowie anschließende Follow-up Aktivitäten. xcskxlj, • Enge Zusammenarbeit mit unterschiedlichsten Abteilungen u.a. dem Produktvertrieb und Marketing. #J-18808-Ljbffr

Laboratorios Vilardell somos la compañía farmacéutica especializada en salud digestiva con más de 90 años de historia y pioneros de la industria farmacéutica española. Nacimos en la farmacia para servir a la farmacia y seguimos trabajando para ser el laboratorio de referencia en bienestar digestivo, en España y a nivel internacional. ¿Te unes a nuestro equipo? ¿Está pensando en solicitar este empleo? No se demore, desplácese hacia abajo y envíe su solicitud lo antes posible para no perder la oportunidad. Estamos reforzando el equipo de Marketing y queremos incorporar a un/a E-Commerce Specialist. Tu misión será gestionar el portal B2B de Laboratorios Vilardell: Vilardell Farma para conseguir el crecimiento de la plataforma y un mayor rendimiento de la misma. Reportando a la Marketing Manager te encargarás de: • Garantizar una experiencia de usuario excelente, alineada al posicionamiento y la estrategia de marca en conjunto con Marketing y Comercial., • Gestionar íntegramente la plataforma B2B para asegurar la operativa: contenidos, catálogo, accesos, pedidos, incidencias, coordinación con partners, colaboración con equipo interno, actualizaciones..., • Consolidar la plataforma como canal de captación de leads y venta autónoma: optimizar formularios, landings, descargables, flujos; seguimiento de funnel..., • Trabajar la evolución del portal definiendo el roadmap y proponiendo mejoras funciones para hacerla más avanzada y escalable., • Definir y mantener un sistema de reporting periódico para controlar y analizar KPIs y estándares de calidad: ventas y comportamiento de compra, uso de portal, rendimiento…, • Actuar como figura de enlace entre la farmacia, el equipo comercial y el entorno digital, promoviendo una cultura “phygital”, • Detectar oportunidades de mejora y proponer soluciones de manera proactiva para reforzar el posicionamiento digital., • Incorporación a una empresa en expansión y crecimiento en continuo proceso de innovación y desarrollo., • Jornada laboral completa con flexibilidad horaria de entrada y salida (entrada de 08:00h a 09:30h y salida de 17:00h a 18:30h) con horario intensivo todos los viernes (entrada de 08:00h a 09:00h y salida de 14:00h a 15:00h)., • Modalidad híbrida de trabajo: oficinas ubicadas en Sant Feliu de Llobregat y posibilidad de teletrabajo (1 día a la semana). xcskxlj, • Formación Superior en Marketing digital, transformación, plataformas e-commerce., • Más de 5 años trabajando en e-commerce, preferiblemente B2B con experiencia en la gestión y evolución de plataformas digitales transaccionales, integrando sistemas y visión técnica, coordinando el contacto con las agencias externas..., • Valorable experiencia en sector salud, pharma o B2B, • Conocimiento avanzados de Prestashop, Business Central, SEO, automations, análisis de métricas como G4A, LookerStudio, Excel… #J-18808-Ljbffr

Experteer Overview In this role you will define and lead Lubrizol’s global strategic roadmap for nutraceutical actives, shaping portfolio and investment decisions. You will drive growth across regions, applications, and partnerships, balancing core optimization with next‑gen innovation. You’ll translate market intelligence into actionable pipelines and robust business cases, steering cross‑functional teams from concept to commercialization. This is a high‑impact role with global scope and a clear focus on market leadership in nutraceuticals. Compensaciones / Beneficios • Define global strategic roadmap and segment prioritization for nutraceutical actives • Shape portfolio through disciplined management and investment strategies • Identify new growth platforms across geographies, applications, technologies, and partnerships • Lead market intelligence to uncover trends, unmet needs, and growth opportunities • Translate insights into innovation pipelines, partnerships, and commercial playbooks • Build finance‑aligned business cases with clear ROI and value capture • Coordinate cross‑functional execution to scale from concept to commercialization • Drive global marketing initiatives across commercial, BD, and technical teams • Represent the company with customers, industry bodies, and partners to strengthen thought leadership Responsabilidades • Bachelor’s degree in Business, Marketing, Life Sciences, or related field • Minimum 10 years in strategic marketing, business leadership, or innovation‑driven roles • Proven track record in defining and executing global growth strategies • Experience in nutraceuticals, food, pharma, or related regulated industries • Strong understanding of nutraceutical value chains, regulatory environments, and innovation ecosystems • Demonstrated ability to lead and influence cross‑functional, global teams • Strong financial acumen with experience building investment cases and driving ROI • Excellent communication, stakeholder management, and strategic thinking skills Requisitos principales • Competitive salary with performance‑based bonus plans • Comprehensive medical, dental u0026 vision coverage • Paid holidays, vacation, and parental leave • Flexible work environment • Learning and development opportunities • Career and professional growth

If you are looking to start your career in Marketing and grow in an international pharmaceutical environment, we would love to hear from you. At Procare Health, a Spanish pharmaceutical company with international presence, we are dedicated to the development and commercialization of innovative and s

Sr. Global Strategic Marketing Manager – Nutraceuticals ¿Le interesa este puesto? Puede encontrar toda la información relevante en la descripción a continuación. Company: Lubrizol Corporation. Location: Gavà, Barcelona, Spain. Travel: Up to 25% globally. Job Type: Full-time, Hybrid. How you'll make an impact • Define and lead the global strategic roadmap for nutraceutical actives, including segment prioritization and portfolio shaping, • Establish Lubrizol’s “right to win” through differentiated value propositions and targeted investment strategies, • Identify and unlock new growth platforms across applications, geographies, technologies, and partnerships, • Drive disciplined portfolio management, balancing core optimization with next-generation innovation, • Lead forward-looking market intelligence to identify unmet needs, emerging trends, and structural growth opportunities, • Translate insights into actionable innovation pipelines, partnership strategies, and commercial playbooks, • Build robust, finance-aligned business cases with clear ROI and value capture mechanisms, • Orchestrate cross-functional execution to bring innovation from concept to commercialization with speed and scalability, • Lead global marketing initiatives across commercial, business development, and technical teams to deliver above-market growth, • Represent Lubrizol externally with customers, industry bodies, and partners to strengthen thought leadership and positioning Required Qualifications • Bachelor’s degree in Business, Marketing, Life Sciences, or related field, • Minimum 10 years of experience in strategic marketing, business leadership, or innovation-driven roles, • Proven track record of defining and executing global growth strategies, • Experience within nutraceuticals, food, pharma, or adjacent regulated industries, • Strong understanding of nutraceutical value chains, regulatory environments, and innovation ecosystems, • Demonstrated ability to lead and influence cross-functional, global teams, • Strong financial acumen with experience building investment cases and driving ROI, • Excellent communication, stakeholder management, and strategic thinking skills Preferred Qualifications • Advanced degree (MBA, MSc, or PhD) in a relevant discipline, • Experience working across multiple regions in a global organization, • Exposure to external innovation ecosystems, partnerships, or M&A projects, • Experience with commercialization of new technologies or ingredients Your Work Environment At Lubrizol, we’re committed to providing a safe, inclusive, xqbhyrx and empowering environment where you can do your best work—whether in a lab, on the production floor, or in a hybrid office setting. • Use of computers and digital tools in a hybrid office environment, • Regular collaboration with global, cross-functional teams, • Occasional international travel for customer, partner, and industry engagement, • Adherence to corporate policies, safety standards, and ethical guidelines Benefits • Competitive salary with performance-based bonus plans, • Comprehensive medical, dental & vision coverage, • Paid holidays, vacation, and parental leave, • Flexible work environment, • Learning and development opportunities, • Career and professional growth, • Inclusive culture and global collaboration #J-18808-Ljbffr

Experteer Overview In this role you will shape Lubrizol's nutraceutical actives strategy on a global scale, prioritizing segments and shaping the portfolio. You will define differentiated value propositions and investment paths to win in the market, while uncovering new growth platforms across applications, geographies, and partnerships. You will balance core optimization with next‑gen innovation and drive market intelligence to identify trends and unmet needs. Expect to translate insights into actionable pipelines, finance‑aligned business cases, and scalable cross‑functional execution in collaboration with commercial, development, and technical teams. Compensaciones / Beneficios • Define and lead the global strategic roadmap for nutraceutical actives, including segment prioritization and portfolio shaping • Establish differentiated value propositions and targeted investment strategies • Identify and unlock new growth platforms across applications, geographies, technologies, and partnerships • Drive portfolio management balancing core optimization with next-generation innovation • Lead forward-looking market intelligence to identify unmet needs and emerging trends • Translate insights into innovation pipelines, partnership strategies, and commercial playbooks • Build robust, finance-aligned business cases with clear ROI and value capture mechanisms • Orchestrate cross-functional execution to bring innovation from concept to commercialization with speed and scalability • Lead global marketing initiatives across commercial, business development, and technical teams to deliver above-market growth • Represent Lubrizol externally with customers, industry bodies, and partners to strengthen thought leadership and positioning Responsabilidades • Bachelor's degree in Business, Marketing, Life Sciences, or related field • Minimum 10 years of experience in strategic marketing, business leadership, or innovation-driven roles • Proven track record of defining and executing global growth strategies • Experience within nutraceuticals, food, pharma, or adjacent regulated industries • Strong understanding of nutraceutical value chains, regulatory environments, and innovation ecosystems • Demonstrated ability to lead and influence cross-functional, global teams • Strong financial acumen with experience building investment cases and driving ROI • Excellent communication, stakeholder management, and strategic thinking skills Requisitos principales • Competitive salary with performance-based bonus plans • Medical, dental u0026 vision coverage • Paid holidays, vacation, and parental leave • Flexible work environment • Learning and development opportunities • Career and professional growth

Experteer Overview In this role, you will drive market growth across international regions through distributors and partners, expanding our Process Analytics solutions across pharma, chemical, energy, and related industries. You will build and nurture partner networks, support strategic projects, and guide customers through technical sales cycles to improve quality, safety, and efficiency. You will train and develop partners while collaborating with cross-functional teams to maximize value. This position offers global scope, a chance to shape market strategy, and exposure to diverse industries. Compensaciones / Beneficios • Develop and execute market growth strategies via distributors and channel partners. • Build strong relationships with partners, end users, OEMs, and engineering companies. • Support strategic projects and key accounts to drive long-term business success. • Provide commercial and technical guidance throughout the sales cycle. • Deliver training, workshops, and market development initiatives to enhance partner capabilities. • Collaborate with cross-functional teams to maximize customer value and business performance. Responsabilidades • Bachelor in Chemistry, Chemical Engineering, Biochemistry, Pharmacy, Industrial Engineering, or related scientific/technical field • Minimum 3 years of international sales, business development, market development, or technical sales experience • Proven experience with distributors, channel partners, or indirect sales • Experience selling technical solutions in industrial B2B environments • Strong consultative selling and CRM knowledge • Experience with customers in pharmaceutical, chemical, energy, food u0026 beverage, water, or related process industries is desirable • Fluent English (written and spoken); French is a plus • Willingness to travel extensively (50-70% of time) • Ability to work independently within a global organization Requisitos principales • Permanent contract • Competitive salary (Fixed + Bonus) • 27 vacation days • Medical insurance • Pension plan • Restaurant card

Experteer Overview ¿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 this role you will drive the medical information strategy and contribute medical expertise to inform Medical Affairs, Marketing, and product development. You will translate clinical evidence into actionable insights for global audiences and build external expert networks to expand scientific impact. You will lead scientific communications, including publication planning, and represent Medical Affairs at conferences and forums. This position supports Radiometer’s mission to improve global healthcare with reliable, fast diagnostics in acute and emergency settings. Compensaciones / Beneficios • Lead the global medical information strategy and lifecycle of scientific content and MAPSS assets, aligning stakeholders on priorities, • Serve as trusted scientific and clinical expert in acute/emergency diagnostics for internal and external decision-making, • Drive high-impact scientific communications through publication planning and development of medical materials, • Build and manage global expert networks (KOLs/KEEs), supporting IIS initiatives and external collaborations, • Represent Medical Affairs at conferences and industry forums, delivering compliant medical insights to global stakeholders Responsabilidades • Advanced degree in Life Sciences (PhD, PharmD, MSc or equivalent) with 5+ years in Medical Affairs/Medical Information or related roles in IVD/medical devices/pharma/healthcare xqbhyrx, • Strong knowledge of medical information tools, processes, and compliance in regulated environments, • Excellent written and verbal scientific communication in English, • Solid clinical/technical understanding of IVD technologies, especially in acute/hospital settings, • Proven cross-functional collaboration and execution across Medical Affairs, Clinical, Marketing, and external stakeholders Requisitos principales • remote work arrangement

Responsibilities Las cualificaciones, habilidades y toda la experiencia relevante necesaria para este puesto se pueden encontrar en la descripción completa a continuación. • Prepare shipments, • Process shipments, • Monitor shipments Qualifications • Studies: Logistics and transport, or related., • 1-2 year of previous experience in Freight forwarding (Air Export), • Fluency in English (C1) and Spanish., • Computer skills for the use of Microsoft Office package (High Level)., • Knowledge of Dangerous Goods // Pharma // Customs will be valued, • Willingness to learn. xcskxlj, • Customer Service approach. #J-18808-Ljbffr

Pre Sales Support – Barcelona ¿Tiene lo que se necesita para triunfar? La siguiente información debe ser leída atentamente por todos los candidatos. Aufgrund der Expansion und des Wachstums unseres Shared Business Centers in Barcelona suchen wir Verstärkung im Bereich Pre Sales Support. Unser internationales Telemarketing Team steht im Austausch mit namhaften Kunden aus nahezu allen Branchen (Chemie & Rohstoffe, Pharma, Lebensmittel, FMCG, Metall- und Elektroindustrie, Transport & Logistik etc.) mit dem Ziel, Verkaufschancen zu identifizieren und zu qualifizieren. • Kein Cold Calling, • Keine Call Center Atmosphäre, • Kein Micromanagement About Mettler Toledo METTLER TOLEDO is a global leader in precision instruments and services. We are renowned for innovation and quality across laboratory, process analytics, industrial, product inspection, and retailing applications. Our sales and service network is one of the most extensive in the industry. Our products are sold in more than 140 countries, and we have a direct presence in approximately 40 countries. For more information, please visit Opening and Your Responsibilities Each Day Is Different – Unser breitgefächertes Produktportfolio, unser vielfältiger Kundenstamm, und die unterschiedlichen Marketingkampagnen machen die Rolle abwechslungsreich. Verstärken Sie unser Team mit Ihrer pro-aktiven, kommunikativen Art und übernehmen Sie folgende Aufgaben: • Durchführung von Outbound-Calls mit dem Ziel, das Interesse unserer Kunden zu gewinnen., • Proaktive Leadgenerierung im Rahmen unserer Marketingkampagnen., • Telefonische Vorstellung neuer Produkte., • Zusendung von Informationsmaterialien sowie anschließende follow-up Aktivitäten., • Enge Zusammenarbeit mit unterschiedlichsten Abteilungen u.a. dem Produktvertrieb und Marketing. What You Need to Succeed • Ausbildung: Abgeschlossene Berufsausbildung., • Berufserfahrung: Erste Erfahrung z.B. als Telemarketer, Kundenberater:in, Call Center Agent, Mitarbeiter:in im Kundenservice in einem B2B/B2C-Umfeld – gerne geben wir aber auch Quereinsteigern eine Chance!, • Kenntnisse: Gute Kenntnisse von Microsoft Office., • Wohnsitz: Barcelona., • Sprachen: Deutschkenntnisse auf Muttersprachniveau (C2), Englisch verhandlungssicher (Level B2/C1) in Wort und Schrift, gute Spanischkenntnisse sind ein Plus. Our Offer to You • Innovatives Produktportfolio: Wir sind führender Hersteller von Präzessionsmessinstrumenten für Anwendungen im Labor, der Industrie und im Handel – Unser Messportfolio wird in unterschiedlichen Branchen eingesetzt. Innovation ist für uns unverzichtbar, um unseren Kunden eine Verbesserung ihres Produktionsumfelds zu garantieren., • Sicherheit & Karrierechancen: Wir sind Marktführer in einer krisensicheren Wachstumsbranche und legen großen Wert auf eine umfassende Einarbeitung: eLearnings, Classroom Trainings, Kennenlernen funktionsübergreifender Abteilungen etc., • Attraktives Vergütungspaket: Unbefristeter Vertrag, wettbewerbsfähiges Zielgehalt (Festgehalt + Bonus), Work-at-home-program, 27 Urlaubstage/Jahr, flexible Arbeitszeiten und die Möglichkeit, jeden Freitag und den ganzen Sommer über früh Feierabend zu machen (8h-15h), interessantes Paket an Sozialleistungen, freie Parkplätze direkt vor der Tür, kostenloses Frühstück und frisches Obst, Restaurantkarte, Krankenversicherung und Rentenplan., • Eigenverantwortung & WIR‑Gefühl: Direkte Berichtslinie zum Telemarketing Manager, kurze Entscheidungswege, angenehmes Arbeitsklima, regelmäßige Teamevents und Workshops., • Fachliche und persönliche Weiterentwicklung: Wir investieren in Ihre kontinuierliche Weiterentwicklung durch eine moderne Learning Plattform sowie kontinuierliche Classroom Trainings in den Bereichen Telemarketing, Self‑Management, Fremdsprachen (Englisch, Deutsch) etc. Equal Opportunity Employment We are an equal opportunity employer and value diversity at our company. We give consideration for employment without regard to race, color, religion, sex, age, national origin, disability, sexual orientation, gender identity, genetic information, or any other protected classification. xcskxlj You can find more details in the Equal Employment Opportunity Policy. #J-18808-Ljbffr

Galenicum is seeking a Stability Technician to join our Laboratory Team in Spain. ¿Todo listo para enviar su solicitud? Por favor, lea la descripción al menos una vez antes de hacer clic en "Solicitar". You will revise stability reports for R&D projects, manage stability studies with CMOs, and ensure timely analysis and documentation. The role requires GLP/GMP analytical development experience and coordination across departments. xcskxlj Educational background in life sciences (Pharmacy preferred) and fluent English and Spanish are required. #J-18808-Ljbffr

mesoestetic Pharma Group en Cataluña busca un/a profesional para planificar, coordinar y ejecutar visitas corporativas, eventos institucionales y activaciones de patrocinio. ¿Tiene las habilidades necesarias para este puesto? Lea todos los detalles a continuación y presente su candidatura hoy mismo. Trabajarás con distintas áreas y proveedores para asegurar la excelencia operativa. xcskxlj Entre tus funciones estarán la organización logística de visitas (alojamientos, traslados, catering), la producción de materiales y el seguimiento de los informes de inversión y asistencia. #J-18808-Ljbffr

¿Quiénes somos? Grupo Farmacéutico Salvat es una compañía familiar fundada en Barcelona en 1955, con más de 70 años cuidando la salud a través de marcas emblemáticas como Cristalmina, Cetraxal, Monolitum o Salvacolina. Tenemos presencia en más de 60 países y plantas de producción en Barcelona, Madrid y Miami. Contamos con I+D propio y desarrollamos soluciones en oftalmología, otorrinolaringología y gastroenterología, además de Consumer Health y servicios CDMO, donde aspiramos a ser un referente. Estamos certificados por la FDA y reconocidos con calificación excelente en el Plan Profarma. Actualmente impulsamos el proyecto NewSalvat, una transformación para ser más ágiles, fuertes y competitivos. Nuestra cultura se basa en los valores AACT (Ambición, Accountability, Colaboración y Transparencia), apostando por el crecimiento y el talento de las personas. Desplácese hacia abajo para encontrar una descripción detallada de este trabajo y lo que se espera de los candidatos. Envíe su solicitud haciendo clic en el botón "Solicitar". ¿Qué buscamos? Estamos en la búsqueda de DT suplente que comparta nuestra visión y esté listo para contribuir en proyectos desafiantes. Si tienes los conocimientos requeridos y un enfoque proactivo, ¡queremos conocerte! ATENCION: Requisito imprescindible aportar experiencia de 3 años en áreas de Garantía de calidad en la industria farmacéutica. Tu misión 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.) empleadas en las actividades de desarrollo y fabricación de medicamentos, productos sanitarios, complementos alimenticios y cosméticos, asegurando en todo momento su actualización y vigencia. Como Director técnico suplente, colaborará con DT en la liberación de lotes al mercado, revisión de los indicadores de calidad, revisión de acuerdos técnicos y documentación del sistema de calidad y comunicación con clientes, CMOs y Autoridades. Tus principales responsabilidades serán: Las tareas/responsabilidades se desarrollarán en los siguientes ámbitos: • Sistema de Calidad: funcionamiento y desarrollo de las herramientas necesarias para el mantenimiento del Sistema de calidad aplicable a los procesos de una empresa farmacéutica: control de cambios, desviaciones, CAPAs, sistema documental, PNTs y reclamaciones, • Validaciones y cualificaciones, Anexo 15 GMPs, • Seguimiento de procesos productivos, • Revisión de Calidad de Producto y CPV, • Formación interna, • Análisis de riesgos, • Indicadores de calidad, • Auditorias Requisitos • Estudios Superiores Universitarios en farmacia., • Experiencia de 3 años en áreas de Garantía de calidad en la industria farmacéutica., • Conocimientos específicos en normativa de calidad, GxP, en entorno europeo y USA., • Inglés, nivel avanzado, • Se valorará conocimientos estadísticos y en validaciones de sistemas informatizados, así como conocimiento y experiencia en normativas de Farmacovigilancia, Productos sanitarios, complementos alimenticios y cosméticos., • Nivel de responsabilidad ¿Qué te ofrecemos? • Proyecto sólido en una compañía consolidada del sector Pharma., • Entorno de transformación y con crecimiento profesional y personal., • Rol estratégico con alto impacto en negocio y en resultados., • Desarrollo profesional y liderazgo de equipos de alto rendimiento., • Entorno dinámico y orientado a resultados., • Equipos de trabajo transversales y colaborativos., • Cultura colaborativa y exigente., • Un entorno en el que valoramos la iniciativa y el impacto individual. ¿Quieres formar parte de este proyecto transformador? xqbhyrx Aplica para más información ¡Vamos a construir juntos el futuro de Salvat!

Tiselab busca un/a profesional de ventas técnicas para la zona Norte (Cataluña, Levante y Norte de España). La experiencia que se espera de los solicitantes, así como las habilidades y cualificaciones adicionales necesarias para este trabajo, se enumeran a continuación. Formarás parte del equipo comercial y reportarás a la Directora Comercial, gestionando clientes y proyectos de microbiología para la industria farmacéutica. xcskxlj Realizarás venta de medios y placas de cultivo, muestreadores ambientales y soluciones de monitorización, manteniendo contacto regular con clientes y proponiendo ofertas. #J-18808-Ljbffr

Neuraxpharm in Barcelona is seeking a Corporate Head of AI to define and lead the company’s AI strategy with end‑to‑end ownership of AI‑driven value creation. Asegúrese de leer detenidamente la información sobre esta oportunidad antes de presentar su candidatura. The role combines governance, data integrity, and scalable AI across R&D, regulatory, manufacturing and commercial functions. You will drive AI use cases from ideation to production, partner with IT and external providers, and foster a culture of data‑driven decision making to support xqbhyrx digital transformation and long‑term competitive #J-18808-Ljbffr Hay opciones de teletrabajo/trabajo desde casa disponibles para este puesto.

Almirall, S.A. Por favor, lea detenidamente la siguiente descripción del puesto para asegurarse de que encaja con el perfil antes de enviar su solicitud. cerca un IT Business Process Manager per il team R&D Data Science a Sant Feliu de Llobregat. Ruolo di punto di contatto tra DS, bioinformatica e AI Engineering per allineare le applicazioni DS interne ed esterne, guidando consegna e adozione. Richiesta forte background scientifico, almeno 5 anni in ambiente R&D Pharma e competenze in infrastrutture cloud, pipeline DS e conformità. Ruolo chiave per accelerare insight e innovazione. xqbhyrx #J-18808-Ljbffr Hay opciones de teletrabajo/trabajo desde casa disponibles para este puesto.

Experteer Overview In this role, you will lead the medical strategy for ophthalmic surgical product development, focusing on Phase IIIB/IV studies and cross‑functional collaboration. You will partner with global development teams, marketing, sales, and healthcare providers to shape medical strategy, evidence generation, and launch plans. Your work drives patient outcomes by ensuring scientifically sound, non‑promotional information and robust publications. This position offers impact across regional strategies, post‑market studies, and scientific communications in a global, patient‑focused environment. Compensaciones / Beneficios • Support the execution of medical affairs strategic plans • Develop regional medical affairs strategy for the assigned therapeutic area • Provide medical and scientific input for product messaging and claims • Support post‑market/phase IV studies strategy and preregistration study input • Contribute to launch strategies, lifecycle management, and indications expansion • Create medical publications content (whitepapers, manuscripts, posters, articles, video scripts) • Handle medical inquiries and maintain peer‑to‑peer relationships with Medical Experts and stakeholders • Plan and execute medical advisory board meetings • Provide fair and balanced scientific information to healthcare professionals • Support internal training for academic or healthcare professionals • Assist with medical promotional review as needed Responsabilidades • Bachelor's Degree or equivalent experience; 7+ years of relevant life sciences experience • Advanced clinical degree preferred (OD or MD ophthalmologist) • MS/PhD in life sciences with strong clinical research background • English language proficiency (read/write/speak) • Estimated travel ~10% • Location flexible within Europe • Experience in medical affairs, ophthalmology, and phase IIIB/IV study design and execution Requisitos principales •

Almirall in Sant Feliu de Llobregat is seeking an IT Business Process Manager for R&D Data Science to own IT solutions and partner with bioinformatics, molecular modelling, and AI Engineering. Si los siguientes requisitos del puesto y la experiencia coinciden con sus habilidades, por favor, asegúrese de enviar su solicitud sin demora. You will ensure alignment, prioritisation, and effective day-to-day collaboration across IT teams and external vendors. xqbhyrx The role requires leading end-to-end IT delivery for Data Science tools, driving adoption, governance, and compliance in a fast-evolving pharma environment. #J-18808-Ljbffr

Almirall SA en Sant Feliu de Llobregat busca un/a Senior Manager de Market Access para liderar proyectos transversales con instituciones, sociedades científicas y asociaciones de pacientes. La persona ideal posee experiencia de 7+ años en pharma/biotech xcskxlj y grado universitario, preferentemen

STADA Group in Sant Just Desvern, Spain, seeks a project coordinator for supply chain management in pharmaceutical launches.

The InsudPharma group is aware that business management must align with the needs and demands of society, and therefore assumes the commitment to equal opportunities and treatment between men and women, as stated in the current regulations on the matter - Organic Law 3/2007, and we do not discrimina

Inventory Planner & Procurement Specialist.La persona seleccionada será responsable de garantizar la disponibilidad de materiales y productos, optimizando los niveles de inventario y asegurando un suministro eficiente para los mercados de España y Portugal.Tiene las siguientes habilidades, experie