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Grifols, empresa líder global en soluciones de salud, busca un Contract Manufacturing Service Manager en Sant Cugat del Vallès, España. El rol se centra en la planificación de la producción de fabricaciones por contrato y la supervisión de acuerdos de fabricación para generar valor en la cadena de suministro. Trabajarás con equipos interfuncionales, gestionar KPIs, contratos y relaciones con clientes clave, asegurando cumplimiento, calidad y eficiencia operativa en un entorno internacional. #J-18808-Ljbffr

Would you like to join an international team working to improve the future of healthcare? Do you want to enhance the lives of millions of people? Grifols is a global healthcare company that since 1909 has been working to improve the health and well-being of people around the world.We are leaders in

Grifols, S.A in Barcelona is seeking a QA Product Release Section Manager to oversee product release activities for manufactured and distributed products. The role ensures compliance with regulatory requirements and quality standards.The ideal candidate will have a Bachelor's degree in Engineering or Health Sciences, at least 3 years of experience in Quality Assurance or Regulatory Affairs, and strong analytical skills. A flexible schedule is offered, emphasizing a diverse, inclusive workplace.

Grifols is seeking an Organizational Development Project Manager to lead strategic initiatives in organizational design, process optimization, and data management. The role focuses on redesigning structures and driving efficiency across a global matrix.You will define projects, track KPIs, and prepare executive reports while guiding a team and coordinating with HR and other functions. Fluency in English and a strong background in OD are essential.

Would you like to join an international team working to improve the future of healthcare? Do you want to enhance the lives of millions of people? Grifols is a global healthcare company that since 1909 has been working to improve the health and well-being of people around the world. We are leaders in plasma-derived medicines and transfusion medicine and develop, produce and market innovative medicines, solutions and services in more than 110 countries and regions.Creemos que la diversidad aporta valor a nuestro negocio, a nuestros equipos y a nuestra cultura. Estamos comprometidos con la igualdad de oportunidades y nuestra misión es ofrecer un entorno inclusivo donde las diferencias sumen a nuestra compañía.Ayúdanos a liderar una de las mayores empresas farmacéuticas del mundo. Somos un líder mundial en medicamentos derivados del plasma con presencia en más de 100 países y un equipo global en crecimiento de más de 20.000 personas. Por eso, necesitamos un/a Specialist Facilities Corporate como tú.Misión del RolGarantizar el correcto funcionamiento, disponibilidad y eficiencia de las instalaciones y servicios generales de diversos centros de Grifols, liderando la gestión técnica de infraestructuras, proveedores especializados y contratos de servicio. El puesto impulsará la mejora continua de los activos e instalaciones, asegurará la continuidad operativa del site y promoverá una experiencia de servicio excelente para los clientes internos, contribuyendo al cumplimiento de los objetivos de negocio.Tus responsabilidades seránSupervisar y coordinar el mantenimiento preventivo y correctivo de las instalaciones, garantizando su disponibilidad, seguridad y correcto funcionamiento.Gestionar el sistema GMAO/CMMS, asegurando la correcta planificación, documentación, seguimiento y cierre de las órdenes de trabajo.Gestionar y supervisar proveedores y empresas de servicios, velando por la calidad, el cumplimiento de los niveles de servicio y la correcta ejecución de las actividades contratadas.Garantizar la operatividad y eficiencia de las infraestructuras y sistemas críticos del centro, incluyendo climatización, instalaciones eléctricas, protección contra incendios y servicios auxiliares.Coordinar los servicios generales del centro, asegurando entornos seguros, funcionales y alineados con los estándares de calidad establecidos.Realizar el seguimiento de contratos, presupuestos e indicadores de gestión, promoviendo una utilización eficiente de los recursos y costes asociados.Velar por el cumplimiento de la normativa vigente en materia de seguridad, prevención de riesgos laborales, medioambiente y estándares corporativos.Actuar como interlocutor de referencia para los clientes internos, proporcionando un servicio cercano, eficiente y orientado a sus necesidades.Participar en auditorías, inspecciones, simulacros y proyectos de mejora relacionados con las instalaciones y servicios corporativos.Impulsar iniciativas de mejora continua, sostenibilidad y eficiencia energética, contribuyendo a la excelencia operativa y a la mejora continua de las instalaciones.Quién eresPara realizar este trabajo con éxito, una persona debe ser capaz de llevar a cabo las responsabilidades de manera satisfactoria. Los requisitos enumerados a continuación son representativos de los conocimientos, habilidades, formación y/o capacidad requeridos. Se pueden realizar adaptaciones del puesto para que las personas con diversidad funcional puedan realizar las tareas del puesto.Titulación universitaria en Ingeniería Industrial, Mecánica, Eléctrica, Química, Organización Industrial, Arquitectura o disciplinas afines.Experiencia de 3 a 5 años en la coordinación en el área de Facilities Management, gestión de infraestructuras o mantenimiento de edificios corporativos.Experiencia en coordinación de proveedores, gestión de contratos y supervisión de servicios generales.Conocimientos en mantenimiento de instalaciones técnicas, incluyendo climatización (HVAC), instalaciones eléctricas, protección contra incendios (PCI) y servicios auxiliares.Experiencia en gestión presupuestaria, control de costes, seguimiento de indicadores (KPIs) e implementación de iniciativas de mejora continua.Manejo de herramientas GMAO/CMMS para la planificación, seguimiento y control de las actividades de mantenimiento.Conocimientos de Prevención de Riesgos Laborales (PRL), seguridad industrial y normativa aplicable a edificios e instalaciones.Nivel alto de inglés (C1).Valorable experiencia en entornos multinacionales, industriales o farmacéuticos.Valorable conocimiento de SAP.Eres una persona organizada, orientada al detalle y con capacidad para gestionar diferentes tareas de forma simultánea, con orientación al cliente.Disfrutas trabajando en equipo y desarrollándote en un entorno dinámico e internacional.Lo que ofrecemosFormar parte de Grifols significa la oportunidad de trabajar en un entorno de proyección internacional dónde se promueve la igualdad de oportunidades.Significa la oportunidad de desarrollarte profesionalmente, de disponer de formación continua y de integrarte en un equipo de profesionales en el que la aportación individual de cada uno cuenta. Nuestro compromiso es mantener un entorno que favorezca el desarrollo profesional de nuestros empleados en un buen ambiente de trabajo.El capital humano de Grifols es clave tanto en el desarrollo de las actividades como en el proceso de expansión de la compañía.Creemos en el talento diverso y queremos eliminar cualquier barrera que pueda impedir tu participación. Si necesitas algún ajuste en nuestro proceso de selección, por favor, no dudes en informarnos al aplicar. Estamos aquí para ayudarte.Horario flexible: Lunes-Jueves 7-10 a 16-19h y Viernes 8-15h.Grupo Profesional: 05.Paquete de beneficios:Contrato de trabajo: IndefinidoUbicación: Sant Cugatmore about GrifolsReq ID:Type: Indefinido tiempo completoJob Category:#J-18808-Ljbffr

Would you like to join an international team working to improve the future of healthcare? Do you want to enhance the lives of millions of people? Grifols is a global healthcare company that since 1909 has been working to improve the health and well-being of people around the world. We are leaders in plasma-derived medicines and transfusion medicine and develop, produce and market innovative medicines, solutions and services in more than 110 countries and regions.We believe that diversity adds value to our business, our teams and our culture. We are committed to equal employment opportunities that foster an inclusive environment.Help us lead one of the world’s largest pharmaceutical companies. We are a world leader in plasma-derived medicines with a presence in more than 100 countries, and a growing global team of over 20 000 people. That’s why we need a Operational Excellence Specialist like you.Role MissionTo lead and drive continuous improvement, operational excellence, and project management initiatives, promoting process optimization, waste elimination, standardization of best practices, and enhanced operational performance.The successful candidate will act as a key contributor in the planning, coordination, monitoring, and communication of strategic initiatives, ensuring alignment across all involved functions and facilitating the successful execution of transformation and improvement projects that deliver business value.You will work cross-functionally with Operations, Quality, Engineering, Supply Chain, IT, and other business areas to identify improvement opportunities and develop solutions that increase productivity, quality, efficiency, and internal and external customer satisfaction.What Your Responsibilities Will BeLead and coordinate Biomat workstreams related to the implementation of the new Plasma Logistics Center (PLC).Plan, organize and monitor project activities, ensuring alignment of timelines, milestones, deliverables, resources and dependencies.Coordinate cross-functional teams and stakeholders, facilitating effective communication and collaboration across the organization.Drive process improvement, standardization, digitalization and Operational Excellence initiatives to enhance operational performance.Monitor project progress, identify risks and issues, and ensure appropriate mitigation and follow-up actions.Prepare and communicate project status updates, KPIs, governance materials and executive reports to support decision-making.Ensure compliance with GxP requirements, quality standards and applicable regulatory expectations throughout the project lifecycle.Support change management and project portfolio initiatives, promoting successful implementation and sustainable adoption of new processes and ways of working.Facilitate collaboration between cross-functional teams and help drive alignment, accountability and execution discipline across the project.Support change management activities to enable successful implementation and adoption of the future processes and ways of working.Manage and/or contribute to other projects within the Biomat project portfolio, as required, ensuring alignment with business priorities, operational excellence standards and quality requirements.Contribute to the development of the Operational Excellence strategy and support broader business transformation initiatives.Who You AreTo perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skills, education, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions).Bachelor's degree in Engineering, Biotechnology, Life Sciences, Business Administration, or a related field.Advanced level of English, Spanish, both written and spoken.3 to 5 years of experience in Operational Excellence, Continuous Improvement, PMO, Project Management, Process Excellence, or similar roles in industrial or regulated environments.Advanced proficiency in Microsoft Office and project management tools; knowledge of Power BI, Minitab, Tableau, MS Project, Smartsheet, and similar analytical tools is a plus.Proven experience leading cross-functional projects, process improvement initiatives, and organizational transformation programs.Strong knowledge of Lean, Six Sigma, Continuous Improvement methodologies, and project management principles.Experience in project planning, coordination, governance, risk management, and stakeholder management.Knowledge of GMP/GxP regulated environments is a plus.Lean Six Sigma Green Belt, Project Management, or PMO certifications are a plus.Strong analytical, communication, and problem-solving skills, with the ability to manage multiple priorities and influence stakeholders at different organizational levels.What We OfferIt is a brilliant opportunity for you, Grifols is fully aware that its employees are one of its major assets. We are committed to maintaining an atmosphere that encourages all our employees to develop their professional careers in an excellent working environment.Information about Grifols is available at www.Grifols.Com. If you are interested in joining our company and you have what it takes for such an exciting position, then don’t hesitate to apply! We look forward to receiving your application! Grifols is an equal opportunity employer.Flexible schedule: Monday-Thursday 8:00h – 17:00h and Friday 8:00 - 15:00h (with the same flexible start time).Benefits PackageContract of Employment: Permanent position.Flexibility for U Program: Remote working.Location: Parets del Vallès.www.Grifols.ComLearn more about Grifols#J-18808-Ljbffr

Grifols busca un Specialist Facilities Corporate para garantizar el correcto funcionamiento y eficiencia de las infraestructuras de sus centros, liderando la gestión técnica y contratos de servicio. Coordinarás proveedores y gestionarás la planificación en GMAO/CMMS, buscando la continuidad operativa y una experiencia de servicio excelente para clientes internos.Requisitos: Ingeniería u otra titulación afín, 3–5 años en Facilities Management, manejo de SAP y PRL, nivel de inglés alto (C1).

ResponsibilitiesManage product release activities, evaluating technical and documental compliance according to Technical Direction guidelinesParticipate in the configuration of systems related to product releaseCoordinate communications with Notified Bodies, reference laboratories and related stakeholdersManage documentation storage, control and retrieval, including externally archived documentationHandle document management quality notifications, ensuring proper tracking and workflowApprove quality notifications after evaluating their impact on batch release and product statusMonitor the status of materials affected by quality notificationsCoordinate communications with Health Authorities (e.G., AEMPS) regarding import/export activitiesIssue and manage authorizations and official letters required for import/export processesEnsure compliance with applicable regulations such as ISO 13485, IVDR and MDSAPAct as internal auditor and participate in supplier auditsParticipate in continuous improvement of the Quality Management System.RequirementsBachelor's degree in Engineering, Health Sciences or similarAt least 3 years of experience in Quality Assurance or Regulatory AffairsExperience in regulated environments under ISO13485 and/or IVDRExperience in team managementExperience in auditsExcellent communication skillsCross-functional and collaborative work with multiple departmentsAttention to detail and complianceAnalytical ability and technical judgement in impact assessmentsEnglish level is C1.Certifications & QualificationsBachelor's Degree in EngineeringBachelor's Degree in Health Sciences

¿Te gustaría un equipo internacional que trabaja para mejorar el futuro del sector de la salud? ¿Quieres contribuir a mejorar la vida de millones de personas? Grifols es una compañía global del sector de la salud que desde 1909 mejora la salud y el bienestar de las personas en todo el mundo. Somos líderes en medicamentos hemoderivados y medicina transfusional y desarrollamos, producimos y comercializamos medicamentos, soluciones y servicios innovadores en más de 110 países y regiones.Todas las habilidades, cualificaciones y experiencia relevantes que necesitará un candidato seleccionado se enumeran en la siguiente descripción.Creemos que la diversidad aporta valor a nuestro negocio, a nuestros equipos y a nuestra cultura. Estamos comprometidos con la igualdad de oportunidades y nuestra misión es ofrecer un entorno inclusivo donde las diferencias sumen a nuestra compañía.En el departamento de Validaciones de Instituto Grifols necesitamos incorporar un/a Técnico/a de Validaciones de equipos y procesos, cuya misión principal consistirá en gestionar y ejecutar los proyectos de validación asignados de acuerdo a la normativa vigente con el objetivo de asegurar la validez de los procesos productivos.Tus responsabilidades seránRealizarás la redacción, revisión y aprobación de protocolos e informes de cualificación.Realizarás la redacción, revisión y aprobación de protocolos e informes de validación.Ejecutarás estudios de cualificación y validación.Actualizarás los protocolos de validación a la normativa vigente.Editarás las desviaciones, seguimiento de CAPAs y valoración de controles de cambios.Quién eresPara realizar este trabajo con éxito, una persona debe ser capaz de llevar a cabo las responsabilidades de manera satisfactoria. Los requisitos enumerados a continuación son representativos de los conocimientos, habilidades, formación y/o capacidad requeridos. Se pueden realizar adaptaciones del puesto para que las personas con diversidad funcional puedan realizar las tareas del puesto. Posees un Grado en Ingeniería Técnica o Superior, Licenciatura en Ciencias de la Salud, siendo valorable Máster en Industria FarmacéuticaTienes experiencia de entre 1 y 3 años trabajando en posición similar.Tu nivel de inglés es avanzado (mínimo B2.2).Dominas el paquete Office y tienes conocimientos a nivel usuario de SAP.Posees disponibilidad para viajar de forma puntual.Lo que ofrecemosFormar parte de Grifols significa la oportunidad de trabajar en un entorno de proyección internacional dónde se promueve la igualdad de oportunidades. Significa la oportunidad de desarrollarte profesionalmente, de disponer de formación continua y de integrarte en un equipo de profesionales en el que la aportación individual de cada uno cuenta. Nuestro compromiso es mantener un entorno que favorezca el desarrollo profesional de nuestros empleados en un buen ambiente de trabajo. El capital humano de Grifols es clave tanto en el desarrollo de las actividades como en el proceso de expansión de la compañía. Creemos en el talento diverso y queremos eliminar cualquier barrera que pueda impedir tu participación. Si necesitas algún ajuste en nuestro proceso de selección, por favor, no dudes en informarnos al aplicar. Estamos aquí para ayudarte.Horario flexible:Lunes-Jueves 7-10 a 16-19h y Viernes ntrato de trabajo:Indefinido.Paquete de beneficios.Flexibility for U Program: 1 día de trabajo remoto a la semana. xlqxfvg Ubicación:Parets del Vallès.#J-18808-Ljbffr

Grifols, S.A in Barcelona is seeking a QA Product Release Section Manager to oversee product release activities for manufactured and distributed products. The role ensures compliance with regulatory requirements and quality standards.The ideal candidate will have a Bachelor’s degree in Engineering or Health Sciences, at least 3 years of experience in Quality Assurance or Regulatory Affairs, and strong analytical skills. A flexible schedule is offered, emphasizing a diverse, inclusive workplace.#J-18808-Ljbffr

Would you like to join an international team working to improve the future of healthcare? Do you want to enhance the lives of millions of people? Grifols is a global healthcare company that since 1909 has been working to improve the health and well-being of people around the world. We are leaders in plasma-derived medicines and transfusion medicine and develop, produce and market innovative medicines, solutions and services in more than 110 countries and regions.We believe that diversity adds value to our business, our teams, and our culture. We are committed to equal employment opportunity fostering an inclusive environment where diversity makes us be outstanding.Help us lead one of the world’s largest pharmaceutical companies. We are a world leader in plasma-derived medicines with a presence in more than 100 countries, and a growing global team of over 20.000 people. That’s why we need an Organizational Development Project Manager like you.The Project Manager is responsible for leading strategic initiatives related to organizational design, process optimization, and data management. This role oversees key projects that impact organizational structure and efficiency, ensuring that analyses and reports deliver actionable value to the business.What are your responsibilities:Leadership in Organizational Design1. Develop organizational design strategies to optimize structures and workflows.2. Analyze hierarchical levels, organizational capabilities, and resource needs to recommend structural adjustments.3. Oversee redesign initiatives, including mergers, acquisitions, or significant organizational changes.Strategic Project Management1. Define, plan, and lead key projects related to the company transformation, process improvement, or efficiency analysis.2. Monitor project progress and ensure the achievement of established KPIs.3. Act as a liaison between HR and other functional areas involved in the projects.4. Prepare executive-level reports with detailed analyses and actionable recommendations.Innovation and Continuous Improvement1. Identify opportunities for improvement in existing processes and lead their transformation.2. Act as an advisor to senior management on labor market trends and their impact on organizational strategy.Team Management1. Oversee and manage the team, ensuring clear role definitions and task assignments.2. Foster a collaborative and high-performance work environment by providing regular feedback and development opportunities.3. Monitor team performance and ensure alignment with project goals and organizational priorities.Who you areTo perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skills, education, and/or ability required. Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions).Required:Bachelor’s degree in Organizational Psychology, Business Administration, HR, or related field.5+ years of experience in Organizational Development, or related areas, ideally within a global matrix environment.Proven experience driving organizational design and transformation initiatives at enterprise scale.Experience working in or with Centers of Excellence or OD Consultancy firms is a plus.Proficient level in EnglishSkills:Strong conceptual and analytical thinking skills, with the ability to connect strategic objectives to organization and people implications.Excellent communication, facilitation, and influencing skills across diverse stakeholder groups.What we offerIt is a brilliant opportunity for you, Grifols is fully aware that its employees are one of its major assets. We are committed to maintaining an atmosphere that encourages all our employees to develop their professional careers in an excellent working environment.We believe in diverse talent and want to remove any barriers that may hinder your participation. If you require any adjustments in our selection process, please do not hesitate to inform us when applying. We are here to help.#J-18808-Ljbffr

Would you like to join an international team working to improve the future of healthcare? Do you want to enhance the lives of millions of people? Grifols is a global healthcare company that since 1909 has been working to improve the health and well‑being of people around the world. We are leaders in plasma‑derived medicines and transfusion medicine and develop, produce and market innovative medicines, solutions and services in more than 110 countries and regions.We believe that diversity adds value to our business, our teams, and our culture. We are committed to equal employment opportunities, fostering an inclusive environment where diversity makes us outstanding.Help us lead one of the world’s largest pharmaceutical companies. We are a world leader in plasma‑derived medicines with a presence in more than 100 countries, and a growing global team of over 20.000 people. That’s why we need a IT Systems Eneingeer like you.MissionThe IT Systems Engineer within IC Plasma serves a pivotal role in sustaining and advancing the technology landscape that supports plasma donor centers. This role is accountable for maintaining the reliability, performance, and compliance of the digital technology services and infrastructure that are essential to operating plasma donor centers, ensuring stable operations, minimizing disruptions, and supporting safe, efficient, and compliant collection activities.What Your Responsibilities Will BeDomain Management & Strategic Alignment Oversee the digital technology landscape for plasma donor centers and ensure alignment with enterprise architecture and security.Translate plasma operational needs into IT requirements and review infrastructure and integration standards.Contribute to long‑term roadmaps for plasma technology and infrastructure.Project Coordination & Delivery Coordinate IT activities for plasma projects from planning through deployment.Align project requirements, timelines, and deliverables across plasma operations, CoE, MSP, and internal IT.Support readiness activities, risk management and successful execution of plasma initiatives.Service Delivery, Change & Operational Excellence Manage day‑to‑day service performance, stability, and availability of plasma technologies.Coordinate change, release, and deployment activities with the CoE and MSP.Monitor service KPIs, support issue resolution, and ensure effective incident and escalation handling.Vendor, Partner & Stakeholder Coordination Serve as the primary interface between plasma operations, the CoE, the MSP, and internal IT.Ensure vendors meet SLAs and operational commitments and validate MSP changes for production safety.Facilitate requirements, communication, and governance activities.Teamwork, Knowledge Management & Culture Maintain documentation, standards, and knowledge assets aligned with CoE frameworks.Contribute to knowledge sharing and collaboration across teams and partners.Who You AreTo perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skills, education, and/or ability required. Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions).Technical SkillsBachelor’s degree in computer science, telecommunications, or a related field.Advanced English and Spanish communication skills (spoken and written).Minimum of 5 years of experience in plasma infrastructure environments, including BECS systems, donor center infrastructure, and integrations with apheresis devices.Solid understanding of plasma‑center technologies, IT frontend and backend infrastructure, networking, communication protocols, and monitoring practices.Knowledge of security and compliance practices, including secure policies, identity controls, and regulatory requirements.Experience working within ITSM frameworks (incident, change, release) and multi‑vendor delivery models (CoE, MSP).Soft SkillsStrong communication and stakeholder‑management skills across business, IT, and vendor partners.Strong relationship‑building skills to establish trust and effective collaboration across stakeholders.High level of organization, prioritization, and execution discipline in a fast‑moving environment.Problem‑solving mindset with the ability to navigate ambiguity and support decision‑making.Ability to coordinate multiple initiatives and stakeholders simultaneously.Ability to work independently and collaboratively within cross‑functional teams.What We OfferIt is a brilliant opportunity for you, Grifols is fully aware that its employees are one of its major assets. We are committed to maintaining an atmosphere that encourages all our employees to develop their professional careers in an excellent working environment.Information about Grifols is available at www.Grifols.Com.We believe in diverse talent and want to remove any barriers that may hinder your participation.If you require any adjustments in our selection process, please do not hesitate to inform us when applying.We are here to help.Grifols is an equal opportunity employer.Flexibility for U Program: Hybrid ModelFlexible schedule: Monday-Thursday 7-10 to 16-19h and Friday 8-15h (with the same flexible start time).Benefits PackageContract of Employment: Permanent positionLocation: SPAIN : España : Parets del Valles:[[cust_building]]Learn more about Grifols#J-18808-Ljbffr

Would you like to join an international team working to improve the future of healthcare? Do you want to enhance the lives of millions of people? Grifols is a global healthcare company that since 1909 has been working to improve the health and well-being of people around the world. We are leaders in plasma-derived medicines and transfusion medicine and develop, produce and market innovative medicines, solutions and services in more than 110 countries and regions.We believe that diversity adds value to our business, our teams, and our culture. We are committed to equal employment opportunities, fostering an inclusive environment where diversity makes us outstanding.Help us lead one of the world’s largest pharmaceutical companies. We are a world leader in plasma-derived medicines with a presence in more than 100 countries, and a growing global team of over 20.000 people. That’s why we need a QA Project Senior Specialist like you.To manage and coordinate cross-functional project portfolios for Laboratorios Grifols, including customer, intercompany and internal projects, from initiation through completion or operational handover. The role ensures effective planning and execution, full traceability of information, and alignment among stakeholders with business objectives, quality requirements, commitments and timelines.The position will operate in a highly regulated, cross-functional, and multidisciplinary environment, collaborating closely with Quality Assurance, Manufacturing, Planning, Regulatory Compliance, CMOs, Quality Control, Validation, Engineering, Maintenance, Technical Services, R&D, Supply Chain, and other business areas.MissionMaintain a single, consolidated and up-to-date project portfolio, categorizing projects by type, priority, criticality, status and target dates.Monitor project progress, identify risks, roadblocks, inactive initiatives and resource constraints, and elevate issues when necessary.Define and maintain governance standards, status reporting criteria and escalation processes across the project portfolio.Coordinate project teams, meetings and committees, ensuring action plans, decisions, ownership and timelines are properly documented.Manage requests, deliverables, approvals and communications associated with customer and intercompany projects.Support the monitoring of change controls, risks, deviations and action plans, ensuring compliance and traceability requirements are met.Maintain project documentation and gather information required for Product Quality Reviews (PQRs).Define and track project KPIs, analyze performance, drive continuous improvement initiatives, and ensure effective project closure and operational handover.The project portfolio may include new product introductions and industrialization initiatives, customer requests and commitments, intercompany projects, process transfers or modifications, implementation of new facilities, equipment or production lines, regulatory or technical changes, internal improvement and transformation initiatives, as well as the implementation or enhancement of systems and tools.Who you areTo perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skills, education, and/or ability required. Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions).Bachelor's degree in Science, Engineering, Pharmacy, Biotechnology or a related field.3 to 5 years of experience in project management, PMO, operational excellence or cross-functional coordination roles.Familiarity with GMP, GxP documentation, CAPA processes and change control managementProven ability to manage multiple projects simultaneously and prioritize effectively in a fast-paced environment.Strong stakeholder management skills, with the ability to collaborate and influence teams across different functions and organizational levels.Excellent organizational skills and attention to detail, ensuring accurate follow-up of actions, risks, milestones and deliverables.Strong analytical and problem-solving mindset, with the ability to identify risks, propose solutions and support decision-making.Experience working in regulated environments such as pharmaceutical, biotechnology, healthcare, chemical or manufacturing industries is highly valued.Advanced proficiency in Microsoft Excel and familiarity with project management and reporting tools such as Power BI, SAP or similar platforms.Excellent communication and presentation skills, both written and verbal.Advanced level of English.What we offerIt is a brilliant opportunity for you, Grifols is fully aware that its employees are one of its major assets. We are committed to maintaining an atmosphere that encourages all our employees to develop their professional careers in an excellent working environment.Information about Grifols is available at www.Grifols.Com.We look forward to receiving your application!We believe in diverse talent and want to remove any barriers that may hinder your participation. If you require any adjustments in our selection process, please do not hesitate to inform us when applying. We are here to help.Grifols is an equal opportunity employer.Flexibility for U Program:Hybrid ModelFlexible schedule:Monday-Thursday 7-10 to 16-19h and Friday 8-15h (with the same flexible start time).Benefits packageContract of Employment:Permanent position#J-18808-Ljbffr

¿Te gustaría unirte a un equipo internacional que trabaja para mejorar el futuro del sector de la salud? ¿Quieres contribuir a mejorar la vida de millones de personas? Grifols es una compañía global del sector de la salud que desde 1909 mejora la salud y el bienestar de las personas en todo el mundo. Somos líderes en medicamentos hemoderivados y medicina transfusional y desarrollamos, producimos y comercializamos medicamentos, soluciones y servicios innovadores en más de 110 países y regiones.Creemos que la diversidad aporta valor a nuestro negocio, a nuestros equipos y a nuestra cultura. Estamos comprometidos con la igualdad de oportunidades y nuestra misión es ofrecer un entorno inclusivo donde las diferencias sumen a nuestra compañía.Ayúdanos a liderar una de las mayores empresas farmacéuticas del mundo. Somos un líder mundial en medicamentos derivados del plasma con presencia en más de 100 países y un equipo global en crecimiento de más de 20.000 personas. Por eso, necesitamos un/a Contract Manufacturing Service Manager como tú.Este rol tiene como misión la Planificación de la producción de las fabricaciones por contrato, la supervisión y cumplimiento de los acuerdos de fabricación, la gestión integral de la relación con el equipo de supply chain de los clientes a través de reuniones periódicas y coordinación transversal, y la identificación e implementación de mejoras operativas, nuevos productos y servicios orientados a la generación de valor para el negocio.Tus responsabilidades seránPlanificación de la producción de las fabricaciones por contrato1. Diseñar y proponer el plan de producción anual a Control de Producción de Planta, para garantizar la utilización eficiente de los recursos, cumpliendo con los compromisos contractuales y maximizando la rentabilidad del negocio global.2. Controlar y monitorizar la correcta ejecución del plan y la adherencia a los planes del corto plazo de la compañía.3. Controlar y monitorizar los tiempos de fabricación y liberación de producto hasta su puesta a disposición de los contratistas.4. Proponer estrategias de producción alternativas y el mejor escenario en situaciones de cambio y/o incertidumbre.5. Control y seguimientos de inventarios para garantizar un stock de productos intermedios y acabados adecuado según los compromisos contractuales.6. Trabajar con equipos interfuncionales, identificando riesgos y oportunidades de ejecución, investigando causas de las variaciones, proponiendo soluciones y supervisando la implementación para lograr los objetivos de rendimiento; escalar los riesgos y problemas clave.Control y supervisión de la ejecución de los contratos de fabricación1. Ser enlace principal entre clientes y Biopharma Product Delivery/Control de Producción y Comercial para facilitar la resolución de deficiencias y conflictos así como la detección de oportunidades operativas para garantizar que los aspectos de fabricación se ejecuten con excelencia.2. Coordinar y colaborar con el Departamento Jurídico para la firma/renovación o adendas/cierre de los contratos para garantizar la integración oportuna y sistemática de las aportaciones y conocimientos de las partes implicadas (por ejemplo, Comercial, Finanzas, Calidad, Fabricación).3. Desarrollar y aplicar procedimientos de gestión y administración de contratos de conformidad con la política de la empresa. En su caso, contribuir a la revisión de la política o proporcionar recomendaciones.4. Colaborar con las áreas internas vinculadas, para supervisar la satisfacción de los clientes clave (por ejemplo, revisiones de negocio, encuestas, para garantizar la alineación de las expectativas, reforzar el valor de Grifols y generar confianza entre nuestros clientes.5. Gestión del rendimiento de la fabricación por contrato, incluida la consecución de los indicadores clave de rendimiento (KPIs), el cumplimiento de las obligaciones contractuales o potenciales penalizaciones y la ejecución de iniciativas de mejora continua.6. Comunicar a la Dirección la evolución del cumplimiento de los contratos.Mantenimiento de un equipo de alto rendimiento1. Reclutar, liderar, formar y desarrollar al equipo a su cargo para ejecutar las responsabilidades del departamento y garantizar la utilización eficaz de los recursos potenciando las habilidades de las personas.Optimización operativa y seguimiento de la implementación de nuevos productos y servicios que aporten valor al negocio1. Coordinación con el departamento de Operaciones de las plantas de producción para asegurar la implementación sistemática y eficiente de los nuevos productos, procesos y/o servicios.2. Definir y desplegar herramientas, procesos y sistemas de excelencia operativa que maximicen los flujos de valor en todo el ecosistema de fabricación por contrato.Quién eresPara realizar este trabajo con éxito, una persona debe ser capaz de llevar a cabo las responsabilidades de manera satisfactoria. Los requisitos enumerados a continuación son representativos de los conocimientos, habilidades, formación y/o capacidad requeridos. Se pueden realizar adaptaciones del puesto para que las personas con diversidad funcional puedan realizar las tareas del puesto.Grado UniversitarioExperiencia de 2 a 5 años en funciones similares.Inglés avanzadoCapacidad organizativa, Integridad, Auto-Desarrollo, Capacidad multi-funcional, liderazgo de equipo, pers-pectiva global, sentido de la estrategia, orientación a resultados, comunicación abierta.Conocimientos informáticos avanzados. Medio/Alto grado de dominio de las aplicaciones de Microsoft y SAP. Dominio del análisis de datos, previsión y presupuestación.Excelente comunicación escrita y verbal. Experiencia en el conocimiento del flujo E2E (plazo producción, plazos de entrega, tiempos de tránsito, para la producción y distribución de hemoderivados (opcional).Lo que ofrecemosFormar parte de Grifols significa la oportunidad de trabajar en un entorno de proyección internacional dónde se promueve la igualdad de oportunidades.Significa la oportunidad de desarrollarte profesionalmente, de disponer de formación continua y de integrarte en un equipo de profesionales en el que la aportación individual de cada uno cuenta. Nuestro compromiso es mantener un entorno que favorezca el desarrollo profesional de nuestros empleados en un buen ambiente de trabajo.El capital humano de Grifols es clave tanto en el desarrollo de las actividades como en el proceso de expansión de la compañía.Creemos en el talento diverso y queremos eliminar cualquier barrera que pueda impedir tu participación. Si necesitas algún ajuste en nuestro proceso de selección, por favor, no dudes en informarnos al aplicar. Estamos aquí para ayudarte.Horario flexible:Lunes-Jueves 7-10 a 16-19h y Viernes 8-15h, con la misma flexibilidad de entrada.Contrato de trabajo:Estable.Flexibility for U Program:Ubicación: SPAIN : España : Sant Cugat del Valles#J-18808-Ljbffr

Grifols is seeking a Production Technician to join its international team in Parets del Vallès. The role focuses on transforming production processes to improve productivity, quality, safety, and cost efficiency while complying with current regulations.Responsibilities include analyzing quality incidents, leading continuous improvement initiatives, monitoring process indicators, and supporting factory projects under the guidance of multiple managers.#J-18808-Ljbffr

Would you like to join an international team working to improve the future of healthcare? Do you want to enhance the lives of millions of people? Grifols is a global healthcare company that since 1909 has been working to improve the health and well-being of people around the world. We are leaders in plasma-derived medicines and transfusion medicine and develop, produce and market innovative medicines, solutions and services in more than 110 countries and regions.We believe that diversity adds value to our business, our teams, and our culture. We are committed to equal employment opportunities, fostering an inclusive environment where diversity makes us outstanding.MissionThe Site Procurement Senior Specialist is responsible for executing site-level procurement activities in alignment with Category Strategies, the Global Procurement Policy, and local regulatory requirements. The role acts as the primary procurement interface for the site, ensuring continuity of operations, cost control, supplier performance, and compliance. The Site Procurement Senior Specialist collaborates closely with site stakeholders, suppliers, Category Management, and Transactional Procurement teams to deliver efficient, compliant, and value-adding procurement outcomes within the defined site-managed scope.What your responsibilities will be Site Procurement Operations & Stakeholder Collaboration Act as the primary procurement interface for site stakeholders (Manufacturing, Quality, Maintenance, H&S, HR, Finance, Administration)Collaborate with Supply Chain Planning and Manufacturing to develop purchasing plans supporting daily, weekly, monthly, and annual operational needsCoordinate with site stakeholders to manage demand planning for critical materials, special delivery requirements, and annual order volumes Sourcing & Contract Management (Local / Site Scope) Execute sourcing activities for site-managed spend in line with applicable Category Strategies and Procurement PolicySupport the preparation of RFx, bid analysis, supplier evaluations, and award recommendationsNegotiate commercial and contractual terms with local/site-level suppliers within defined scope and approval limitsSupport contract drafting, negotiation, signature coordination, and renewal management for site-managed suppliers Procure-to-Pay (P2 P) & Demand Execution Support resolution of procure-to-pay exceptionsGuide and influence requesters in the use of approved procurement tools, catalogues, and sourcing channelsD. Supplier Management, Performance & Incident HandlingAct as the primary procurement escalation point for site-level supply, quality, service, or commercial incidents Initiate and manage supplier onboarding and qualification processes (SLP) for site-level suppliersEnsure suppliers comply with local homologation, quality, and regulatory requirementsCoordinate procurement activities related to site Change Controls Who you areTo perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skills, education, and/or ability required. Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions). You have proven experience in site-level procurement with a strong understanding of procurement policies, category strategies, and compliance requirements.Demonstrated ability to partner effectively with cross-functional stakeholders (Manufacturing, Quality, Supply Chain, Finance, etc.) to support operational and project needs.Solid experience in sourcing, supplier selection, and contract negotiation, with the ability to deliver value while maintaining compliance and mitigating risk.Analytical mindset with the ability to interpret spend data, track KPIs, and identify cost‑saving opportunitiesA proactive, solutions‑focused approach with a commitment to continuous improvement and operational excellence What we offerIt is a brilliant opportunity for you, Grifols is fully aware that its employees are one of its major assets. We are committed to maintaining an atmosphere that encourages all our employees to develop their professional careers in an excellent working environment.We believe in diverse talent and want to remove any barriers that may hinder your participation. If you require any adjustments in our selection process, please do not hesitate to inform us when applying. We are here to help.Grifols is an equal opportunity employer.Flexibility for U Program: Hybrid ModelContract of Employment: Permanent position#J-18808-Ljbffr

Grifols is seeking a Real Estate Manager to oversee the property portfolio at national and international levels. You will negotiate leases, identify opportunities, and coordinate with landlords, brokers, and internal teams to align with corporate objectives.The role requires a Bachelor’s degree and 5–10 years in corporate real estate, with fluency in English and Spanish and willingness to travel internationally.#J-18808-Ljbffr

Grifols busca un Specialist Facilities Corporate para garantizar el correcto funcionamiento y eficiencia de las infraestructuras de sus centros, liderando la gestión técnica y contratos de servicio.Coordinarás proveedores y gestionarás la planificación en GMAO/CMMS, buscando la continuidad oper

It is a brilliant opportunity for you, Grifols is fully aware that its employees are one of its major assets. Interact with Regulatory Authorities as it relates to safety database data transmission. Strong interpersonal skills with the ability to interact and collaborate with personnel at all levels

Grifols busca un profesional de Calidad para revisar procedimientos y supervisar el sistema de calidad de Laboratorios de Plasma.No espere a enviar su solicitud después de leer esta descripción; se espera un gran volumen de candidaturas para esta oportunidad.Se requiere experiencia en entornos reg

Grifols seeks a Pharmacovigilance Data Analysis Manager to support global PV activities and ensure high-quality deliverables that meet regulatory timelines.Envíe su CV y cualquier información adicional requerida después de haber leído esta descripción, haciendo clic en el botón de solicitud.Yo

Would you like to join an international team working to improve the future of healthcare? Do you want to enhance the lives of millions of people? Grifols is a global healthcare company that since 1909 has been working to improve the health and well-being of people around the world.We are leaders in

A in Barcelona is seeking a QA Product Release Section Manager to oversee product release activities for manufactured and distributed products.Por favor, presente su candidatura sin demora si su perfil encaja bien con este puesto, debido al alto nivel de interés.The role ensures compliance with reg

Grifols is seeking a Quality Specialist to join the GDP Compliance department.

Would you like to join an international team working to improve the future of healthcare? Do you want to enhance the lives of millions of people? Grifols is a global healthcare company that since 1909 has been working to improve the health and well-being of people around the world.We are leaders in

Grifols is seeking a Corporate Affairs Assistant to provide high-level administrative and operational support to the Corporate Affairs department in a multinational setting.Consulte la descripción del puesto a continuación.Si confía en que tiene las habilidades y la experiencia adecuadas, envíe

Formar parte de Grifols significa trabajar en un entorno internacional, con oportunidades de desarrollo y formación continua,. Se valoran Bachillerato o CFGM y experiencia en procesos de filtración, cromatografías y manejo de maquinaria, con conocimiento de GMP. Hay opciones de teletrabajo/trabaj

Grifols busca un/a Operario/a de Fibrin Sealant para incorporarse al área de Producción en España.Los candidatos deben tomarse el tiempo de leer atentamente todos los elementos de este anuncio de empleo.Por favor, envíen su solicitud sin demora.La misión es ejecutar procesos de filtración, cro

Grifols, compañía global del sector salud, busca un/a Operario/a de Tarjetas y Geles en Parets del Vallès para un contrato temporal a tiempo completo.

Operario/a 1ª Esterilizaciones. Producción la incorporación de un/a Operario/a de Esterilizaciones.

Grifols busca un Ingeniero/a de Facilities para liderar la correcta operatividad de las instalaciones y servicios generales.

Instituto Grifols es una empresa especializada en la investigación, desarrollo, producción de proteínas plasmáticas purificadas con propiedades terapéuticas que se obtienen a partir de fraccionamiento del plasma humano y en el área de Producción se precisión incorporar a un/a Operario/a de F

Instituto Grifols es una empresa especializada en la investigación, desarrollo, producción de proteínas plasmáticas purificadas con propiedades terapéuticas que se obtienen a partir de fraccionamiento del plasma humano y en el área de Producción se precisa incorporar a un/a Operario/a de Fibr

Grifols, líder global en salud, busca un Especialista en Operaciones de Calidad Regulatoria para unirse a su equipo internacional en Barcelona.Envíe su solicitud a continuación después de leer todos los detalles y la información de apoyo sobre esta oportunidad de trabajo.Esta posición apoya la

Únete a Laboratorios Grifols! Para la empresa Laboratorios Grifols, S. El capital humano de Grifols es clave tanto en el desarrollo de las actividades como en el proceso de expansión de la compañía. Te gustaría unirte a un equipo internacional que trabaja para mejorar el futuro del sector de la

Grifols busca un/a Operario/a de Esterilizaciones para unirse a su departamento de Producción en Parets del Vallès.

Garantizar el correcto funcionamiento, disponibilidad y eficiencia de las instalaciones y servicios generales de diversos centros de Grifols, liderando la gestión técnica de infraestructuras, proveedores especializados y contratos de servicio. Coordinar los servicios generales del centro, aseguran

Grifols busca un/a Operario/a de Dosificación en Parets del Vallès, dentro del área de Producción.

From Quality Assurance we are looking for a Corporate Quality Auditor who will be the responsible to perform the Corporate Quality audits to the companies of Grifols Industrial group and affiliates, in order to evaluate and ensure the compliance of Good Distribution Practices, internal procedures an

Te gustaría unirte a un equipo internacional que trabaja para mejorar el futuro del sector de la salud? ¿Quieres contribuir a mejorar la vida de millones de personas? Grifols es una compañía global del sector de la salud que desde 1909 mejora la salud y el bienestar de las personas en todo el mu

Grifols, a global healthcare leader, seeks a dedicated QA professional to strengthen our GCP/GCLP quality assurance programs in Barcelona.Asegúrese de que toda la información de su solicitud está actualizada y en orden antes de inscribirse en esta oportunidad.You will plan and conduct audits of C

From Quality Assurance we are looking for a Corporate Quality Auditor who will be the responsible to perform the Corporate Quality audits to the companies of Grifols Industrial group and affiliates, in order to evaluate and ensure the compliance of Good Distribution Practices, internal procedures an

Grifols is seeking a Corporate Quality Auditor within Quality Assurance to perform corporate quality audits across the Grifols Industrial group and affiliates, ensuring compliance with Good Distribution Practices and internal procedures.

Grifols, a leading global healthcare company, seeks a Corporate Affairs Assistant to provide comprehensive administrative and operational support from our Madrid/Sant Cugat hub.Descubra si esta oportunidad es adecuada para usted leyendo toda la información que sigue a continuación.You will manage

Would you like to join an international team working to improve the future of healthcare? Do you want to enhance the lives of millions of people? Grifols is a global healthcare company that since 1909 has been working to improve the health and well-being of people around the world.We are leaders in

Would you like to join an international team working to improve the future of healthcare? Do you want to enhance the lives of millions of people? Grifols is a global healthcare company that since 1909 has been working to improve the health and well-being of people around the world.We are leaders in

Grifols, empresa multinacional del sector salud, busca un/a Cost Controlling Controller en modalidad de prácticas para el área Biopharma.Todas las habilidades, cualificaciones y experiencia relevantes que necesitará un candidato seleccionado se enumeran en la siguiente descripción.Trabajará cod

Corporate Quality Auditor to perform audits for compliance with GDP/GXP within the Grifols Industrial group, covering various units and affiliates.