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Descripción del puestoEl Instituto Grifols S.A. necesita un/a Trainee para el departamento de Process Development.Responsabilidades- Integrarse en un equipo de Desarrollo y participar en el diseño, la ejecución y evaluación de procesos de purificación de proteínas en el laboratorio y/o en la Planta Piloto.- Colaborar en la elaboración de instrucciones de proceso, tabulación de datos primarios y análisis e interpretación técnica de resultados de proceso.- Dar soporte en la preparación de muestras, en la preparación de los procesos experimentales y en la gestión de las analíticas.- Participar en el diseño de estudios, alineados con los proyectos en curso en el área de CMC.- Ayudar con la realización de presentaciones de los proyectos, con objeto de actualizar el progreso de los estudios.- Colaborar con otros departamentos de Plasma R&D como Bioanalytics y Discovery Research, aprendiendo las funciones de cada área.- Redactar protocolos de estudios y informes técnicos de estudios finalizados.Requisitos- Estudiante de Máster en Biotecnología, Bioquímica, Ingeniería Biomédica, Ingeniería Química o estudios relacionados.- Valorable experiencia o conocimientos en purificación de proteínas.- Nivel de inglés C1.- Disponibilidad de realizar un convenio a través de tu centro de estudios por un mínimo de 8 meses.- Proactivo/a, con ganas de aprender, flexible y cómodo/a en ambiente dinámico e innovador.Beneficios- Ayuda al estudio, comedor y autobús de empresa.- Oportunidad de formarte en un entorno altamente regulado e internacional.- Integrarte en un equipo multidisciplinar con posibilidades reales de aprender y desarrollarte en la industria farmacéutica.Inclusión y diversidadCreemos que la diversidad aporta valor a nuestro negocio, a nuestros equipos y a nuestra cultura. Estamos comprometidos con la igualdad de oportunidades y con ofrecer un entorno inclusivo donde las diferencias sumen a nuestra compañía.#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. It is a brillia

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 an AI Solutions Analyst like you.MissionAs an AISolutionsAnalyst in our multinational company, you will play a key role in identifying, designing, and developing AI processes and solutions in the AI‑based user solution stack that generates tangible business value. Your mission will be to translate business challenges into scalable AI solutions and automations, leveraging modern AI capabilities to enhance efficiency, innovation, and decision‑making across the organization.You will be responsible for the governance of AI low‑code solutions, driving productivity, process optimization and AI‑enabled initiatives across the organization. You will identify business needs, translate them into scalable digital solutions using Microsoft 365, Power Platform and Copilot technologies, and promote adoption. You will also ensure alignment with governance, compliance and enterprise standards while measuring impact and supporting continuous improvement.What your responsibilities will be- Identify, design and implement productivity, automation and AI‑enabled use cases that deliver measurable impact across business units, with a strong focus on the Microsoft 365, Copilot and Power Platform ecosystem.- Translate business needs into practical digital solutions by combining AI capabilities with low‑code, automation, and analytics to improve operational efficiency, collaboration and decision‑making.- Promote the adoption of AI capabilities across the company by designing and executing awareness, training and change‑management initiatives.- Collaborate closely with IT teams, business stakeholders, governance teams and external partners to ensure the effective development, integration and adoption of productivity, automation and AI‑enabled solutions.- Support the implementation and continuous evolution of governance practices, including strategy, policies, lifecycle management, roles, monitoring, support models and compliance.- Assess the feasibility, value, risks and scalability of proposed low‑code, automation and AI use cases, ensuring that solutions are sustainable, aligned with enterprise standards and consistent with AI governance principles.- Stay continuously informed about new Microsoft capabilities, especially in Copilot Studio, generative AI, Microsoft Foundry, Power Platform, Azure and Microsoft 365, assessing their potential application in the business context.- Measure and report the performance, adoption and business impact of implemented initiatives, sharing insights and recommendations for improvement, scaling and continuous optimization.- Promote AI adoption and low‑code tools across the company, designing and executing awareness, training, and change‑management initiatives to scale up the productivity.- Work with business and IT teams to optimise existing manual or fragmented processes through automation, workflow and agent orchestration.- Communicate complex concepts in a clear, engaging, and business‑oriented manner to both technical and non‑technical audiences.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 or Master’s degree in Computer Science, Information Systems, Engineering, Artificial Intelligence, Business Technology or a related field.- Hands‑on experience designing, developing or implementing business solutions using Microsoft technological stack, including Copilot Studio, Power Automate, Power Apps, Power BI, Dataverse and M. Foundry. Experience with AI projects is highly valued.- Strong understanding of enterprise productivity technologies, low‑code development, workflow automation, data integration, and AI agentic solutions.- Good understanding of Microsoft architecture and governance concepts, including environments, connectors, DLP policies, security roles, solution lifecycle management, monitoring and support models.- Ability to translate business needs into scalable, secure and maintainable digital solutions, demonstrating a strong problem‑solving, analytical and business‑oriented mindset.- Outstanding communication and teamwork skills, with the ability to collaborate effectively with diverse global teams and explain technical, automation and AI concepts in an accessible way.- Demonstrated curiosity and passion for exploring new Microsoft technologies, AI capabilities and productivity solutions that can generate tangible business value.- Experience driving AI awareness and productivity adoption, change‑management initiatives, or digital transformation programs is highly valued.- Advanced 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. If you are interested in joining our company and you have what it takes for such an exciting position, thendon’thesitate to apply!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 ModelHybrid ModelFlexible scheduleMonday‑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

Company OverviewGrifols is a global healthcare company with a focus on plasma‑derived medicines and transfusion medicine, operating in more than 110 countries.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.Job Title and MissionQA Plasma Operations & Lookback SpecialistThe role's mission is to control and oversee the acceptance process for plasma and non‑plasma raw materials, ensuring compliance with legal, regulatory and customer requirements.Responsibilities- Surveillance Process for Plasma Units- Ensure that the surveillance of plasma units alerted as post‑donation information is handled according to the approved procedures.- Ensure compliance with the established deadlines for managing alerts.- Analyze the causes that give rise to communications and inform Technical Management when necessary.- Evaluate the potential risk of plasma batches.- Analyze data and prepare periodic reports on the process.- Other administrative tasks related to plasma surveillance.- Acceptance Process for Raw Materials- Evaluate supplier documentation for plasma shipments and fractions against approved requirements.- Assess maintenance of the cold chain during transportation per specifications.- Report and verify results of raw material acceptance per inspection plans, deciding on use of shipments.- Manage discrepancies and potential deviations with suppliers.- Establish and maintain guidelines for purchasing and evaluating quality‑subjected suppliers, advising Purchasing Section coordination.- Data analysis, filing and administrative tasks related to raw materials process.- Coordinate workflows within the lifecycle of plasma fractions to ensure availability within timelines.- Manage deviations and collaborate in investigations.- Contribute to tasks for release of plasma fractions to customers.- Data analysis, filing, and administrative tasks related to intermediate product management.Qualifications- Bachelor's degree in Health Sciences (Pharmacy, Biology, Chemistry); Master or Postgraduate degree in the pharmaceutical sector is valuable.- 3 years of experience within Pharma Quality.- Knowledge of GMP.- Basic statistical knowledge.- Proficiency in MS Office and SAP.- Advanced level of English.Benefits and ScheduleSchedule: Monday to Friday from 14h to 22h (Afternoon shift). Flexibility for U Program: Occasionally remote.Benefits package: Contract of Employment: Permanent position.We are an equal opportunity employer.We believe in diverse talent and welcome you to inform us if adjustments are required during the selection process.#J-18808-Ljbffr

Do you want to join an international team working to improve the future of healthcare? Do you want to improve the lives of millions of people? Grifols is a global healthcare company which, since its foundation in Barcelona in 1909, has been working to improve the health and well‑being of people all over the world. Our four divisions - Bioscience, Diagnostic, Hospital and Bio Supplies - develop, produce and market innovative medicines, solutions and services in more than 100 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 Cybersecurity Governance Specialist like you.What your responsibilities will be- Support the IT Organization on matters related to IT compliance, security, cybersecurity and privacy.- Support the development and implementation of global standards related to IT compliance and security.- Monitoring and modulation of cyberawareness campaigns across Grifols worldwide.- Promote a cybersecurity culture across the entire company.- Maintain and develop the ISMS (Information Security Management System).- Manage Information Security Office Dashboard.- Generate documentation and reports for senior management.- Monitor KRIs and KPIs for the Information Security Office.- Oversee managed services.- Develop and update security policies and procedures.- Support Grifols IT certification initiatives.- Collaborate with other cybersecurity areas to enhance the organization's security posture.- Train employees in security practices and cybersecurity awareness.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 Skills:- Bachelor's degree in computer science, Systems Engineering, Cybersecurity, or a related field.- Advanced English and Spanish language skills (spoken and written)- Minimum of 5 years of experience in cybersecurity roles.- Deep knowledge of cybersecurity frameworks (NIST, ISO27k, ENS, SOX, Cyber Essentials).- Cybersecurity certifications (CISA, ISO27k Lead Auditor, CISM, CISSP, CRISC, etc.) are highly valued.Soft Skills:- Ability to work as part of a team.- Excellent communication skills and the ability to work under pressure.- Strong teamwork and collaboration skills.- Problem‑solving and critical‑thinking abilities.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.Flexibility for U ProgramHybrid ModelFlexible scheduleMonday-Thursday 7-10 to 16-19h and Friday 8-15h (with the same flexible start time).Benefits packageContract of EmploymentPermanent positionGrifols is an equal opportunity employer.#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 Hardware Testing Analyst like you.MissionThe Hardware Testing Analyst is responsible for planning, designing, and executing hardware test activities for electronic and mechanical systems in compliance with quality management procedures. The role contributes to ensuring product reliability, performance, and regulatory compliance through rigorous testing, analysis, and continuous improvement.What your responsibilities will be- Define test plans.- Execute and/or supervise test plans.- Assess design limits and constraints.- Design test cases.- Design and develop test fixtures and test benches.- Execute and/or supervise test cases.- Reproduce reported issues and failures.- Identify root causes and similar failure modes.- Generate test reports and communicate results.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.We are looking for a proactive and hands-on engineer with strong analytical skills and a passion for problem-solving.- Bachelor's Degree in Mechanical Engineering, Industrial Engineering, Electronics Engineering, or a related field.- Advanced level of English.- Hands-on experience of 3-5 years in designing and executing verification and validation testing activities.- Hands-on experiencetroubleshooting complex electromechanical systems.- Experience can come from various industries, including healthcare, electronics, automotive, industrial equipment, or electro-mechanical products.- Dynamic, analytical, and critical thinker with the ability to challenge development assumptions and proactively identify improvement opportunities.- Experience with tools such as Jama and Jira is considered an asset.- Experience with reliability testing.- You have the ability to interpret technical documentation, specifications, and engineering drawings.- Knowledge of standards and regulations related to electrical equipment safety, transportation, medical devices, or similar regulated industries is considered a plus.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 atwww.Grifols.Com.We believe in diverse talent and want to remove any barriers that may hinder your participation.Grifols is an equal opportunity employer.Flexibility for U Program: Occasionally RemoteFlexible 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

Grifols, S.A. in Spain is seeking an AI Solutions Analyst to identify, design and implement AI-driven processes within the Microsoft 365, Copilot Studio, Power Platform ecosystem. You will translate business challenges into scalable low-code solutions while ensuring governance and compliance across the organization.Experience with AI projects and enterprise productivity technologies is highly valued. You will work with global teams, drive adoption, and help optimize workflows and#J-18808-Ljbffr

Grifols, S.A in Parets del Vallès, Spain, is looking for an Automation Specialist to support and coordinate automation processes within the production environment. You will plan and execute maintenance on control systems, supervise industrial networks, manage spare parts records and SCADA updates, and provide automation support for projects.CFGS (Mechatronics or Industrial Automation) and 3–5 years in a similar role are required with intermediate English.#J-18808-Ljbffr

Grifols, S.A en Barcelona busca un/a Trainee para trabajar en el departamento de Software (Devops) en I+D de Instrumentos de Inmunohematología. El candidato ideal está estudiando un Grado o Máster en Ingeniería Informática o Telecomunicaciones, tiene un nivel de inglés avanzado y es apasionado de la programación. Las responsabilidades incluyen apoyo en testing automático, participación en la automatización de pruebas y documentación en un entorno Agile. Se ofrece ayuda al estudio y otras oportunidades de formación.#J-18808-Ljbffr

Grifols is seeking an IT Business Continuity Systems Engineer to join the IT Infrastructure Core & Services division. The role focuses on data protection, backup governance, and regulatory compliance across on-premises and cloud environments.You will act as SME, coordinate with MSPs, and drive improvements in service quality and audit readiness while maintaining documentation and standards.

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 Software QA Engineer like you.MissionTo ensure the quality, reliability, and compliance of blood typing analyzer software applications by executing and maintaining testing activities, identifying and documenting defects, and collaborating closely with development teams to deliver safe, effective, and high-quality solutions that meet customer and regulatory requirements.What your responsibilities will be- Collaborate with the development team to plan and refine upcoming work.- Execute and maintain manual and automatic test plans for blood typing analyser applications following the established quality policies and standards.- Identify and document bugs.- Participate in various types of testing, including functional, regression, smoke, exploratory and acceptance.- Create and maintain the technical documentation following the established quality policies and standards.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 a Certificate of Higher Education (CFGS), a degree or master in Computer Science, Telecommunications or other relevant degree.- You have at least 1-3 year of experience in software quality & testing.- Experience with any of the following frameworks will be highly valued: Selenium, Playwright, Rest Assured, Cucumber, or Gherkin.- You are highly motivated to work collaboratively with the team to deliver a high quality product to our customers.- You are an open minded, positive, pragmatic and a team player.- You can communicate openly and clearly in English (B2 level).- Having experience working in an agile/scrum environment is a plus- Having experience working in FDA regulated environments is a plus.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 atwww.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

Grifols S.A. busca incorporar a un/a Trainee para el AI Center of Excellence (AI CoE), apoyando en la gestión de casos de uso, análisis de adopción de IA y iniciativas de gobierno y Responsible AI.Participarás en la comunicación y difusión del uso de IA en la organización y colaborarás con equipos IT, Data, Legal y negocio. La posición ofrece una oportunidad de adquirir experiencia práctica en proyectos reales de IA dentro de un entorno corporativo multinacional en España, con ubicación en#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.For Material Planning department of Instituto Grifols SA, a company specialized in the research, development, and production of purified plasma proteins with therapeutic properties obtained from the fractionation of human plasma, there is a need for the incorporation of a Material Planning Specialist.What your responsibilities will be- You will secure the supply of raw materials and packaging to meet production requirements.- Identify the materials required to ensure scheduled production.- Execute and follow up order requisitions for required materials.- Follow up on incoming orders and claim orders in delay.- Review stocks and consumptions to achieve the optimal level of raw material inventory.- You will coordinate with other departments the production objectives, minimizing costs and managing incidences.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 Bachelor’s Degree in Industrial Engineering, Chemical Engineering, Business (ADE, Economics) or similar.- You have at least 3 years of experience in a similar position.- You are fluent in Spanish and English (B2.2.).- You have advanced knowledge in Excel. Experience with SAP is a plus.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!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.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

Grifols, S. A in Parets del Vallès is looking for a Cloud Operations Engineer. The role involves supporting the design and operation of cloud platforms, actively participating in cloud transformations, and ensuring that services are reliable and secure. Candidates must have a Bachelor's degree and experience with Azure and AWS.Grifols values diversity and offers a hybrid work model along with a permanent contract. Strong communication skills in English and Spanish are essential.

Grifols, S.A. is seeking a Senior Category Specialist for HR Procurement on a temporary basis. You will define and implement procurement strategies for HR and Other Corporate Services, leading strategic sourcing with internal stakeholders and key suppliers to maximize value and reduce costs.This role collaborates across a global matrix organization to ensure policy compliance and service excellence. The ideal candidate has 5+ years of experience in indirect procurement, strong English, and a#J-18808-Ljbffr

¿Te gustaría unirte a un equipo internacional que trabaja para mejorar el futuro del sector de la salud? Grifols es una compañía global del sector de la salud que desde 1909 mejora la salud y el bienestar de las personas en todo el mundo.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.Técnico/a de ValidacionesEn el departamento de Validaciones del Instituto Grifols buscamos incorporar a un/a Técnico/a de Validaciones de equipos y procesos, cuya misión principal consiste 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 serán- Redacción, revisión y aprobación de protocolos e informes de cualificación.- Redacción, revisión y aprobación de protocolos e informes de validación.- Ejecución de estudios de cualificación y validación.- Actualización de los protocolos de validación según la normativa vigente.- Edición de desviaciones, seguimiento de CAPAs y valoración de controles de cambios.Requisitos- Grado en Ingeniería Técnica o Superior, Licenciatura en Ciencias de la Salud, con valorable Máster en Industria Farmacéutica.- Experiencia de 1 a 3 años en posición similar.- Inglés avanzado (mínimo B2.2).- Manejo del paquete Office y conocimientos de SAP a nivel usuario.- Disponibilidad para viajar de forma puntual.Datos del puestoHorario flexible: Lunes-Jueves 7‑10 a 16‑19h y Viernes 8‑15h.Contrato de trabajo: Indefinido.Flexibility for U Program: 1 día de trabajo remoto a la semana.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.#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 Automation Specialist like you.The primary mission of this role is to provide support and coordinate automation processes, spare parts management and planned maintenance activities within the production environment of Laboratorios Grifols S.A.What your responsibilities will be- Plan and execute maintenance activities related to control systems and programmable controllers.- Supervise and maintain the industrial network infrastructure.- Manage program changes, including supervision and authorization processes.- Update automation-related hardware and develop replacement plans to prevent equipment obsolescence.- Maintain factory SCADA systems and oversee the implementation of new SCADA solutions.- Provide programming and automation support for engineering projects.- Maintain and supervise user roles and access permissions across systems.- Create and monitor tasks derived from preventive maintenance plans.- Generate work orders originating from preventive maintenance activities.- Manage the creation, modification and deletion of spare parts records.- Support shift personnel in identifying, locating and clarifying spare parts requirements.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).- You have CFGS (Mechatronics, Industrial Automation or similar).- You have between 3-5 years of experience in a similar role.- You have intermediate 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.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.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

Grifols is seeking an Operational Excellence Specialist to coordinate the Biomat area and the end-to-end flow across multiple functions within Project Lliçà. The role focuses on leading continuous improvement, standardizing best practices, and driving transformation initiatives to deliver business value.You will work with Operations, Quality, Engineering, Supply Chain, IT and other areas to identify opportunities and deliver solutions that increase productivity, quality, and customer#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.As an Operational Excellence Specialist, you will be responsible for coordinating the Biomat area and the end-to-end flow across multiple functional areas within the framework of the Project Lliçà.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 be- Lead 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 porfolio 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 porfolio, 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.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 package- Contract of Employment: Permanent position- Flexibility for U Program: Remote working#J-18808-Ljbffr

Grifols is seeking an IT Validation Technician to support execution of validation methodologies meeting company standards and regulatory requirements. This role oversees validation activities and resources across IT projects.The ideal candidate holds a Life Sciences degree and 1–3 years in a regulated pharma environment (GxP). Strong project management, detail orientation, and English proficiency are essential for success in a global setting.#J-18808-Ljbffr

Grifols, S.A in Parets del Vallès is seeking a Material Planning Specialist to join its team. This role involves securing the supply of raw materials and packaging and coordinating with other departments to meet production goals.The ideal candidate holds a Bachelor's Degree in Industrial Engineering, Chemical Engineering, or Business, and has at least 3 years of relevant experience. Fluency in Spanish and English, along with advanced Excel skills, is required. This is a permanent position with a commitment to employee development.#J-18808-Ljbffr

Senior Category Specialist - HR Procurement - TemporaryWould 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 presence in more than 100 countries, and a growing global team of over 20.000 people. That’s why we need a Senior Category Specialist - HR Procurement - Temporary like you.Role MissionThe Senior Category Specialist - HR Procurement and Other Corporate Services will be responsible for supporting the definition and implementation of the procurement strategy for the Human Resources and Other Corporate Services category, driving strategic sourcing initiatives that maximize value, optimize costs, mitigate risks, and ensure the delivery of high‑quality services across the organization. Working closely with internal stakeholders and strategic suppliers, this role will drive supplier performance, innovation, and continuous improvement while ensuring alignment with business priorities and procurement policies.What your responsibilities will be- Support the definition and implementation of category strategies for Human Resources and Other Corporate Services, ensuring procurement initiatives are aligned with business objectives and long‑term organizational needs.- Lead end‑to‑end strategic sourcing processes, including market analysis, RFI/RFP/RFQ, supplier evaluation, negotiation, and contract award.- Build and maintain strong relationships with strategic suppliers, driving supplier performance, innovation, and continuous improvement.- Negotiate commercial agreements and contractual terms to optimize total cost of ownership while ensuring service quality and business continuity.- Identify cost optimization opportunities through spend analysis, supplier consolidation, and sourcing strategies.- Partner closely with HR and cross‑functional stakeholders to understand business requirements and translate them into procurement solutions.- Assess and mitigate supplier, commercial, and operational risks while ensuring compliance with internal policies and applicable regulations.- Monitor supplier performance through KPIs and governance routines, driving corrective actions and continuous improvement initiatives where required.- Support procurement transformation initiatives, promoting process standardization, digitalization, and procurement best practices.- Ensure compliance with corporate procurement policies, quality standards, and sustainability objectives.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 Business Administration, Supply Chain Management, Engineering or a related field.- Advanced English (essential).- At least 5 years of experience supporting the definition and implementation of category strategies for indirect categories, preferably within Human Resources and Other Corporate Services.- Experience performing spend analysis, supplier evaluation and category planning.- Experience working within multinational and matrix organizations.- Knowledge of procurement tools such as SAP, Ariba, Coupa or similar procurement platforms.- Strong analytical mindset with the ability to transform data into sourcing strategies and business decisions.- Excellent stakeholder management, negotiation and communication skills.- Proactive, collaborative and results‑oriented, with a continuous improvement mindset and the ability to influence without direct authority.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 scheduleMonday‑Thursday 7:00‑10:00 a 16:00‑19:00h and Friday 8:00‑15:00h.Benefits packageContract of EmploymentTemporary Full-Time#J-18808-Ljbffr

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

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 Network Security Engineer will be responsible for supporting the design, implementation, and continuous enhancement of the organization’s network security infrastructure across global on‑premises, cloud, and hybrid environments.What your responsibilities will be- Support the design, implementation and enhancements of network security solutions across global on‑premises, cloud and hybrid environments- Define processes, procedures, and guidelines for driving the evolution of networks to be automated, orchestrated and software based- Manage and support key security technologies including NGFW, VPN, WAF, NAC, SWG and DNS security solutions- Participate in network security transformation initiatives such as Zero Trust, network segmentation and firewall modernization- Proactively identify weak areas and inefficiencies across network security infrastructures and services- Review and approve technical designs, specifications, and statement of work documents- Support the deployment, configuration and lifecycle management of network security technologies across on‑premises and cloud environments- Provide L3 support, troubleshoot complex security issues and contribute to vulnerability remediation activities- Support secure connectivity between data centers, branch offices, cloud environments and third‑party networks- Collaborate with Infrastructure, Cloud, Architecture and Cybersecurity teams to ensure secure, resilient and compliant network servicesWho 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 Information Technology, Computer Science or a related field, or equivalent professional experience- Minimum 3–5 years of experience in Network Security, Security Engineering, Network Engineering or Infrastructure Security roles within complex enterprise environments- Hands‑on experience with Check Point, Palo Alto, Fortinet, Netskope and F5 WAF technologies- Strong knowledge of NGFW, VPN, IDS/IPS, WAF, NAC and cloud‑connected security environments- Experience supporting security modernization initiatives, including Zero Trust and network segmentation projects- Strong analytical, troubleshooting and stakeholder management skills- Professional proficiency in English and Spanish- Relevant certifications such as PCNSE, CCSA, Fortinet FCP, CCNA/CCNP Security or ITIL are highly valuedBenefits and CompensationFlexibility for U Program: Hybrid Model. Flexible schedule: Monday-Thursday 7-10 to 16-19 h and Friday 8-15 h with the same flexible start time. Contract of Employment: Permanent position.Grifols is an equal opportunity employer.#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 Workplace Project Manager like you.Your primary mission will be to lead the design execution, planning and delivery of office refurbishment and fit-out projects across multiple locations, ensuring optimized space utilization, regulatory compliance, budget control and alignment with corporate strategy.ResponsibilitiesSpace Planning and Project Management:- End-to-end management of projects across multiple locations (from concept to delivery).- Design and planning of corporate spaces tailored to local needs.Project Management and Execution:- Coordination with internal and external stakeholders (Facilities, IT, Security, suppliers).- Cost and timeline control, ensuring deadlines and budget compliance.- Site supervision and validation of corporate standards.- Risk management and issue resolution throughout projects.- Resource optimization and continuous improvement of design and execution processes.QualificationsTo 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 provided to enable individuals with disabilities to perform the essential functions.- Bachelor’s or Master’s degree in Architecture, Building Engineering, Engineering or a related field.- Project Management certification is a plus.- 3-5 years of experience in managing office, retail or corporate space projects. Experience in structured corporate environments is a plus.- Proven experience in space planning, refurbishment and fit-out projects.- Experience managing multi-site projects is highly desirable.- Strong background in coordinating multidisciplinary teams and external vendors.- Proficiency in design tools such as AutoCAD or similar is a plus.- Experience in budget management and project scheduling.- Site supervision and construction management experience.- Fluent English (minimum B2/C1), both written and spoken.- Strong organizational skills with the ability to manage multiple projects simultaneously.- Results-driven mindset with a focus on deadlines, cost control and quality.- Excellent communication and stakeholder management skills.- Strong problem-solving abilities and adaptability.- Continuous improvement mindset, with a focus on process optimization.- Willingness to travel across different locations (15%-50%).Benefits & ScheduleFlexibility for U Program: Occasionally remoteFlexible schedule: Monday-Thursday 7-10 to 16-19h and Friday 8-15h (with the same flexible start time).Professional Group: 6Contract of Employment: Permanent positionWe believe in diverse talent and want to remove any barriers that may hinder your participation.Grifols is an equal opportunity employer.#J-18808-Ljbffr

Grifols, S.A in Spain is seeking a Software QA Engineer to ensure the quality, reliability and regulatory compliance of blood typing analyzer software applications. You will execute tests, document defects and work closely with development teams to deliver high‑quality solutions that meet customer and regulatory requirements.The role requires 1–3 years in software quality and testing, a relevant degree, and experience with Selenium/Playwright/Cucumber or Gherkin.#J-18808-Ljbffr

Grifols, S.A. is seeking an IT Business Continuity Systems Engineer to enhance data protection and backup services. The role demands expertise in backup tools and coordination within the IT Infrastructure Core & Services Division.The ideal candidate will lead initiatives to ensure compliance and service quality, effectively interact with technical teams and managed service providers. With a flexible working schedule, Grifols offers a permanent contract with a focus on continuous improvement.#J-18808-Ljbffr

Grifols, S.A is seeking a Senior IT Systems Engineer to enhance the future of healthcare through innovation and technology. The role includes acting as the Technical Product Owner for virtualization platforms and managing continuous improvement on service lifecycle.The ideal candidate will hold a Bachelor's degree in Information Technology or a related field and possess comprehensive knowledge in Wintel technologies, automation, and high availability environments, alongside strong communication skills.Flexible working hours and a permanent position offer an engaging work culture at Grifols.#J-18808-Ljbffr

Grifols is seeking a QA Plasma Operations & Lookback Specialist in Parets del Vallès, Spain. You will control the acceptance process for plasma and non-plasma raw materials, ensuring compliance with legal and regulatory requirements.The role requires a Bachelor’s degree in Health Sciences and at least 3 years of experience in Pharma Quality. Proficiency in English and knowledge of GMP is essential. Occasional remote work is available.

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 Network Security Engineer like you.MissionThe Network Security Engineer will be responsible for supporting the design, implementing, and continuously enhancing the organization's network security infrastructure across global on-premises, cloud, and hybrid environments.What your responsibilities will beSupport the design, implementation and enhancements of network security solutions across global on-premises, cloud and hybrid environmentsDefine processes, procedures, and guidelines for driving the evolution of Networks to be automated, orchestrated and software based.Manage and support key security technologies including NGFW, VPN, WAF, NAC, SWG and DNS Security solutions.Participate in network security transformation initiatives such as Zero Trust, network segmentation and firewall modernization.Proactively identify weak areas and inefficiencies across network security infrastructures and services.Review and approve technical designs, specifications, and statement of work documents.Support the deployment, configuration and lifecycle management of network security technologies across on-premises and cloud environments.Provide L3 support, troubleshoot complex security issues and contribute to vulnerability remediation activities.Support secure connectivity between data centers, branch offices, cloud environments and third-party networks.Collaborate with Infrastructure, Cloud, Architecture and Cybersecurity teams to ensure secure, resilient and compliant network services.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 Information Technology, Computer Science or a related field, or equivalent professional experience.Minimum 3-5 years of experience in Network Security, Security Engineering, Network Engineering or Infrastructure Security roles within complex enterprise environments.Hands-on experience with Check Point, Palo Alto, Fortinet, Netskope and F5 WAF technologies.Strong knowledge of NGFW, VPN, IDS/IPS, WAF, NAC and cloud-connected security environments.Experience supporting security modernization initiatives, including Zero Trust and network segmentation projects.Strong analytical, troubleshooting and stakeholder management skills.Professional proficiency in English and Spanish.Relevant certifications such as PCNSE, CCSA, Fortinet FCP, CCNA/CCNP Security or ITIL are highly valued.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!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 (http://www.Grifols.Com/es/web/international/home)#LI-Hybrid#LI-ER1Req ID: 544118Type: Indefinido tiempo completoJob Category: SISTEMAS DE INFORMACION

Grifols seeks a Pharmacovigilance professional to provide operational support for global PV activities, ensuring high-quality safety data analysis, data review, and regulatory deliverables across investigational and marketed products. The role includes safety data extraction, development of safety reports, and collaboration with Regulatory Affairs, IT, and QA to maintain compliance. xcskxlj Para ser considerado para una entrevista, por favor, asegúrese de que su solicitud se ajusta plenamente a las especificaciones del puesto que se encuentran a continuación. Strong Excel/SQL skills and English fluency are required. #J-18808-Ljbffr

Product Development & Support IH SpecialistWould 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.The Product Development and Support department at Diagnostic Grifols S.A. is seeking a Product Development and Support Specialist to join our team.What your responsibilities will be- Tracking the design and development of new products, ensuring that the customer’s voice is a central driver in decision‑making and that coherent input is integrated across software, hardware, and reagent components, while collaborating with other departments to maintain alignment with established product objectives. Defining requirements for the products to be developed, gathering the needs of all stakeholders.- Testing the instruments in development to detect errors and propose improvements.- Preparing and executing usability studies of the developed products.- Designing and writing technical information for Application Technicians and conducting training courses on the portfolio.- Writing user manuals for the developed products.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.- You have a degree in Biomedical Engineering, Biotechnology or Science.- You have 1 to 3 years of experience in product development, with knowledge of the pharmaceutical and/or medical device industry being a plus.- Knowledge on donor screening and/or immunohematology will be a plus.- You have an advanced English level- You possess strong analytical and problem-solving skills, with the ability to troubleshoot complex technical issues.- You excel in teamwork and possess excellent communication skills.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.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

Para el equipo de Regulatory Operations. Este equipo es una parte integral del equipo de Regulatory Affairs de la Diagnostic Division, y su función principal es estandarizar y proporcionar soporte en los diferentes procesos regulatorios del área. Además, de asegurar que todos los equipos estén actualizados sobre las últimas versiones de las regulaciones aplicables a productos IVD. Se precisa la incorporación de un/a trainee. ¿Tiene las habilidades necesarias para este puesto? Lea todos los detalles a continuación y presente su candidatura hoy mismo. Responsabilidades • Darás soporte en la estandarización de procesos dentro del área de Regulatory Affairs. Esto incluye la creación de guías y procedimientos, así como la formación y apoyo a los equipos para garantizar que todas sigan las mismas prácticas y estándares., • Colaborarás en el mantenimiento de listados y bases de datos de licencias, así como en la implementación de proyectos liderados desde Regulatory Operations. Requisitos • Eres estudiante de Grado en Ciencias de la Salud o de Máster de Industria Farmacéutica o similares., • Posees un nivel de inglés avanzado equivalente al C1., • Dispones de conocimientos medios/avanzados del paquete Office., • Te consideras una persona motivada, dinámica y colaborativa. Te atreves a compartir tu visión y cuentas con buenas habilidades comunicativas., • Desarrollo de competencias clave altamente valoradas., • Oportunidad de formarte en un entorno altamente regulado e internacional., • Integrarte en un equipo multidisciplinar, con posibilidades reales de aprender y desarrollarte en la industria farmacéutica. Beneficios • Realizar prácticas en Grifols supone una oportunidad única para complementar la formación académica con experiencia práctica en control de costes, gestión financiera de nuevos productos y transformación de sistemas en una compañía industrial de referencia., • Oportunidad de formarte en un entorno altamente regulado e internacional., • Integrarte en un equipo multidisciplinar, con posibilidades reales de aprender y desarrollarte en la industria farmacéutica., • Trabajo en un entorno con proyección internacional donde se promueve la igualdad de oportunidades. Creemos que la diversidad aporta valor a nuestro negocio, a nuestros equipos y a nuestra cultura. xcskxlj Estamos comprometidos con la igualdad de oportunidades y nuestra misión es ofrecer un entorno inclusivo donde las diferencias sumen a nuestra compañía. Ubicación: SPAIN: España: Sant Cugat del Valles: [[cust_building]] #J-18808-Ljbffr

Para el equipo de Regulatory Operations. Este equipo es una parte integral del equipo de Regulatory Affairs de la Diagnostic Division, y su función principal es estandarizar y proporcionar soporte en los diferentes procesos regulatorios del área. Además, de asegurar que todos los equipos estén actualizados sobre las últimas versiones de las regulaciones aplicables a productos IVD. Se precisa la incorporación de un/a trainee. ¿Tiene las habilidades necesarias para este puesto? Lea todos los detalles a continuación y presente su candidatura hoy mismo. Responsabilidades • Darás soporte en la estandarización de procesos dentro del área de Regulatory Affairs. Esto incluye la creación de guías y procedimientos, así como la formación y apoyo a los equipos para garantizar que todas sigan las mismas prácticas y estándares., • Colaborarás en el mantenimiento de listados y bases de datos de licencias, así como en la implementación de proyectos liderados desde Regulatory Operations. Requisitos • Eres estudiante de Grado en Ciencias de la Salud o de Máster de Industria Farmacéutica o similares., • Posees un nivel de inglés avanzado equivalente al C1., • Dispones de conocimientos medios/avanzados del paquete Office., • Te consideras una persona motivada, dinámica y colaborativa. Te atreves a compartir tu visión y cuentas con buenas habilidades comunicativas., • Desarrollo de competencias clave altamente valoradas., • Oportunidad de formarte en un entorno altamente regulado e internacional., • Integrarte en un equipo multidisciplinar, con posibilidades reales de aprender y desarrollarte en la industria farmacéutica. Beneficios • Realizar prácticas en Grifols supone una oportunidad única para complementar la formación académica con experiencia práctica en control de costes, gestión financiera de nuevos productos y transformación de sistemas en una compañía industrial de referencia., • Oportunidad de formarte en un entorno altamente regulado e internacional., • Integrarte en un equipo multidisciplinar, con posibilidades reales de aprender y desarrollarte en la industria farmacéutica., • Trabajo en un entorno con proyección internacional donde se promueve la igualdad de oportunidades. Creemos que la diversidad aporta valor a nuestro negocio, a nuestros equipos y a nuestra cultura. xcskxlj Estamos comprometidos con la igualdad de oportunidades y nuestra misión es ofrecer un entorno inclusivo donde las diferencias sumen a nuestra compañía. Ubicación: SPAIN: España: Sant Cugat del Valles: [[cust_building]] #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 Cloud Operations Engineer will be responsible for supporting the design, deployment, automation, operation and continuous improvement of Grifols’ cloud platforms and services across hybrid and multi‑cloud environments.This role will contribute to the successful execution of the company’s cloud transformation initiatives, including Journey to Cloud programs, cloud migrations, infrastructure modernization, automation, Kubernetes adoption and Infrastructure as Code practices.The position will work closely with IT Infrastructure, Architecture, Cybersecurity, Application teams, Service Management and external partners to ensure that cloud services are reliable, secure, scalable, cost‑efficient and aligned with business, compliance and operational requirements.What your responsibilities will be- Cloud Operations and Platform Engineering- Operate, maintain and continuously improve cloud environments across Microsoft Azure, Amazon Web Services AWS, Oracle Cloud Infrastructure.- Support the deployment and management of cloud infrastructure, including compute, storage, networking, identity, security and monitoring services.- Ensure cloud platforms are available, secure, resilient and aligned with operational standards.- Participate in the definition and evolution of cloud operating models, standards, guardrails and best practices.- Support hybrid cloud scenarios and integration between on‑premises infrastructure and public cloud platforms.- Contribute to the adoption of cloud‑native technologies and modern infrastructure practices.- Infrastructure as Code and Automation- Design, develop and maintain Infrastructure as Code using Terraform or equivalent automation frameworks.- Automate repetitive operational tasks to improve efficiency, consistency and reliability.- Contribute to the creation of reusable cloud modules, templates and deployment patterns.- Support CI/CD pipelines for infrastructure deployment and cloud platform changes.- Promote automation‑first principles within Cloud Operations and infrastructure teams.- Kubernetes and Container Platforms- Operate and support Kubernetes‑based platforms, including managed Kubernetes services such as Azure Kubernetes Service AKS and Amazon Elastic Kubernetes Service EKS.- Support containerized workloads, platform reliability, cluster lifecycle management and integration with cloud‑native services.- Collaborate with application and DevOps teams to enable secure and scalable container adoption.- Support monitoring, logging, backup, security and operational governance for Kubernetes environments.- Journey to Cloud and Cloud Migration- Participate in cloud migration and modernization initiatives, supporting assessment, planning, execution and post‑migration optimization.- Collaborate with architecture and application teams to evaluate workload readiness, migration patterns and landing zone requirements.- Support the migration of workloads from on‑premises platforms to cloud environments.- Contribute to reducing technical debt and improving infrastructure standardization.- Identify risks, dependencies and operational impacts during migration activities.- FinOps and Cost Optimization- Monitor cloud consumption and identify opportunities for cost optimization.- Support tagging, reporting, budgeting and cost visibility practices.- Collaborate with Procurement, Finance and technical teams to improve cloud cost governance.- Recommend optimization actions while maintaining performance, security and availability.- Promote responsible cloud consumption across teams and projects.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 Information Technology, Computer Science, or a related field.- Solid experience in cloud infrastructure, cloud operations, systems engineering or platform engineering roles.- Hands‑on experience with Microsoft Azure and Amazon Web Services AWS required, with Oracle Cloud Infrastructure OCI as a strong plus.- Experience operating cloud environments in enterprise, regulated or complex IT organisations.- Experience participating in cloud migration, infrastructure modernisation or Journey to Cloud initiatives.- Practical experience with Terraform or other Infrastructure as Code tools.- Experience with Kubernetes and container platforms, preferably AKS and/or EKS.- Knowledge of CI/CD concepts and automation pipelines.- Excellent written and verbal communication skills in both English and Spanish.Valuable Certifications- Microsoft Certified: Azure Solutions Architect Expert.- AWS Certified Solutions Architect – Associate.- AWS Certified Solutions Architect – Professional.- HashiCorp Terraform Associate.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 atwww.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!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 Model.Benefits packageContract of Employment:Permanent position.#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. Asegúrese de que toda la información de su solicitud está actualizada y en orden antes de inscribirse en esta oportunidad. Mission The RRAA Specialist will be responsible for the preparation of technical documentation, submission and following up of product registration and/or renewal, variations dossiers, as well as other regulatory documentation. Responsibilities • Prepare, compile, and maintain registration dossiers and other regulatory documentation for medicinal products and medical devices within the assigned portfolio., • Prepare, review, and submit regulatory documentation for new registrations, renewals, variations, and other regulatory procedures., • Review and validate dossiers prepared by other team members, ensuring accuracy, quality, and regulatory compliance., • Monitor the progress of regulatory submissions and registration procedures, liaising with regulatory authorities when required., • Maintain up‑to‑date knowledge of current regulations and regulatory requirements applicable to medicinal products and medical devices, ensuring ongoing compliance., • Coordinate the translation of regulatory documentation, ensuring accuracy, consistency, and compliance with local market requirements., • Collaborate with cross‑functional teams and external partners to ensure timely and high‑quality regulatory submissions. Qualifications • Bo thorn the necessary bachelor's degree in Health Sciences or engineering., • Experience in RRAA or technical departments within the pharmaceutical industry., • Analytical skills, attention to detail, and ability to summarize and evaluate., • Advanced level of Spanish and English (C1) and proficiency in MS Office (Excel). Benefits • Hybrid Model: Flexible remote/on‑site schedule., • Flexible schedule: Monday–Thursday 7–10 to 16–19h and Friday 8–15h., • Permanent position., • Location: Sant Cugat del Vallès, Spain. 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 let us know. xcskxlj Grifols is an equal opportunity employer. #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. ¡Inscríbase sin demora! Se espera un gran volumen de solicitantes para el puesto que se detalla a continuación, no espere para enviar su CV. 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 Technical Drug Safety Officer like you. Your role mission: Provides operational support for global pharmacovigilance activities for Grifols investigational and marketed products. Ensures pharmacovigilance deliverables are of the highest quality and meet global regulatory reporting timelines. Responsible for data reviews and management of the integrated database utilized by worldwide Grifols pharmacovigilance personnel. What Your Responsibilities Will Be • To participate in the safety data collection, review, processing, evaluation, analysis and compilation:, • Processing Grifols marketed products adverse event case reports (including definition of submissions required and conducting follow-up with reporters)., • Compilation and reconciliation of information in order to prepare documentation required by pharmacovigilance legislation:, • Review of the weekly literature review., • Review of the updates in pharmacovigilance legislation., • Compliance with archiving tasks for deliverables and relevant documents., • Compilation of information for and participation in preparation of periodic safety update reports., • Ensure quality and compliance with the legal requirements for pharmacovigilance tasks and responsibilities:, • Support to the pharmacovigilance staff involved in audits and inspections, • Provide training to concerned personnel based on the training plan and managing training documentation and deliverables within relevant company departments, • Support to the review and update of the SOPs, working practices or conventions, • PV database operating activities:, • Use of queries for data extraction for different PV documents., • Ensure data consistency and integrity within the safety database., • Support to updates in the database configuration..Who You Are To 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 Health Sciences (Pharmacy, Biology, Chemistry), being valuable to have a Master or Postgraduate degree in the pharmaceutical sector and/or in Pharmacovigilance., • You have 1-2 experience in a similar position within pharma industry (CRO or pharmaceutical company), being high valuable., • You have knowledge of MS Office and SAP program., • You have advanced level of English.What We Offer It 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 believe in diverse talent and want to remove any barriers that may hinder your participation. We are here to help. Grifols is an equal opportunity employer. Schedule: Monday-Thursday 7-10 to 16-19h and Friday 8-15h (with the same flexible start time). xcskxlj Benefits Package • Contract of Employment: Permanent position, • Flexibility for U Program: Hybrid, • Location: Sant Cugat del Vallès, • Location: SPAIN : Spain : Sant Cugat del Valles:[[cust_building]], • Schedule: Monday-Thursday 7-10 to 16-19h and Friday 8-15h (with the same flexible start time). Learn more about Grifols #J-18808-Ljbffr

Overview ¿Te interesaría seguir desarrollándote como Responsable de Presupuestos de Instalaciones Eléctricas en una empresa que trabaja para grandes clientes industriales de referencia como Pfizer, Grifols, Hipra o Nestlé y liderando la profesionalización y optimización de un área clave para el negocio? Desde Oxigent Technologies seleccionamos un/a RESPONSABLE DE PRESUPUESTOS (INSTALACIONES ELÉCTRICAS) para participar en un proyecto estable ubicado en Salt (Girona). En el caso de ser la persona seleccionada, tu misión será liderar el área de estudios de instalaciones industriales, coordinando un equipo de 4 técnicos y definiendo nuevas metodologías, plantillas y herramientas para garantizar la rentabilidad y viabilidad de cada proyecto. ¿Tiene las siguientes habilidades, experiencia e impulso para tener éxito en este puesto? Descúbralo a continuación. Responsabilidades • Liderar, coordinar y supervisar al equipo técnico de presupuestos y oficina técnica (4 personas)., • Elaborar, revisar y validar presupuestos completos de instalaciones industriales (materiales, mano de obra, equipos, subcontratas, costes y márgenes)., • Diseñar y sistematizar metodologías, plantillas de cálculo y criterios para la profesionalización del área de estudios., • Analizar la viabilidad técnico-económica de proyectos eléctricos y mecánicos (BT/MT, cuadros, cableado, automatización)., • Coordinarse con obra, compras y producción, dando soporte técnico en incidencias, desviaciones o cambios de alcance. Requisitos • Formación técnica: Ingeniería Industrial, Eléctrica o similar (valorables perfiles CFGS Industrial/Electricidad con amplia experiencia)., • Experiencia acreditada: Al menos 5-6 años en estudios, presupuestos u oficina técnica de instalaciones eléctricas y/o mecánicas en sector industrial., • Experiencia en gestión: Haber coordinado equipos o actuado como referente técnico de oficina técnica., • Conocimientos técnicos: Dominio en lectura de planos/esquemas, cálculo de costes y conceptos de instalaciones industriales (BT/MT, cuadros, canalizaciones)., • Carnet de conducir Qué te ofrecemos • Contratación indefinida a través de Oxigent Technologies, • Salario según experiencia aportada: Entre 35.000 y 37.000 € brutos anuales, • Horario de trabajo: Jornada completa presencial (8:00h a 17:00h)., • Cheque Formación para desarrollarte en las áreas profesionales que más te interesen., • Seguro médico privado., • Retribución flexible aplicable a seguro médico, restaurante, transporte, guardería y formación., • Aplicación de acceso a gimnasios y actividades deportivas en toda España con descuentos., • ¡Y muchos otros beneficios! ¡Únete al equipo de Oxigent! xcskxlj Empresa comprometida con la sostenibilidad y la igualdad de oportunidades, donde el talento y la tecnología no entienden de género. #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. Obtenga más información sobre este puesto leyendo los detalles a continuación y luego envíe su solicitud para ser considerado. 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. Mission Provides operational support for global Pharmacovigilance (PV) activities for Grifols investigational and marketed products. Ensures Drug Safety, Pharmacovigilance deliverables are of the highest quality and meet global Regulatory Reporting timelines. Responsible for Safety Data Analysis, Data Review, and management of the integrated Safety Database utilized by worldwide Grifols pharmacovigilance personnel. What Your Responsibilities Will Be • Participate in the safety data collection, review, processing, evaluation, analysis and compilation:, • Extraction, review and analysis of information from the pharmacovigilance database, performing Safety Information Analytics, Safety Data Analysis, Data Extraction, Data Review, and Data Management., • Compilation and reconciliation of information in order to prepare documentation required by pharmacovigilance legislation:, • Process and review safety data to develop Aggregate Safety Reports., • Support responses to requests from regulatory agencies, ensuring Regulatory Compliance., • Coordinate and manage creation of SQL queries for Data Extraction used in different PV documents., • Develop training documentation and/or work instructions to determine methods and procedures., • Work as Signal Analyst during Signal Detection and Signal Management activities, including extraction of signal detection reports and ensuring document filing and archiving., • Ensure quality and compliance with the legal requirements for pharmacovigilance tasks and responsibilities:, • Support pharmacovigilance staff involved in audits and inspections (Quality Assurance, GVP Compliance)., • Provide training to concerned personnel based on the training plan., • Support the review and update of SOPs., • Interact with Regulatory Affairs Department regarding Aggregate Safety Reports and other documents required by Regulatory Authorities., • PV database operating activities:, • Use SQL queries for Data Extraction for different PV documents., • Ensure Data Consistency, Data Integrity, and Data Quality within the Safety Database., • Support updates in the database configuration, collaborating with IT and Database Administration activities. Who You Are • Bachelor's degree in Health Sciences (Pharmacy, Biology, Chemistry), with a Master's or Postgraduate degree in the pharmaceutical sector and/or Pharmacovigilance, Bioinformatics, Biostatistics, or Data Analytics considered an asset., • 1–2 years of experience in a similar position within the pharmaceutical industry (CRO or pharmaceutical company)., • Experience with Excel, Excel Macros, SQL, Business Objects, RStudio, Data Analytics, or Business Intelligence tools is highly valued., • Knowledge of E2B(R2), E2B(R3), MedDRA, WHO Drug Dictionary, and medical terminology is considered an advantage., • Advanced level of English. What We Offer It 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. Grifols is an equal opportunity employer. Flexibility for U Program Hybrid Model. Benefits Package Contract of Employment Permanent position. xqbhyrx Location Sant Cugat del Vallès, Spain. For more information, visit J-18808-Ljbffr

Grifols, S.A. busca un/a Técnico/a de Validaciones para gestionar y ejecutar proyectos de validación de equipos y procesos, asegurando la validez de los procesos productivos conforme a normativa vigente.La posición implica redacción y revisión de protocolos e informes, ejecución de estudios de cualificación y validación, y actualización de documentos según normativa. Se requiere ingeniería o grado en ciencias de la salud, 1–3 años de experiencia, inglés avanzado y SAP a nivel usuario.#J-18808-Ljbffr

About the company Las cualificaciones, habilidades y toda la experiencia relevante necesaria para este puesto se pueden encontrar en la descripción completa a continuación. 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. Mission The RRAA Specialist will be responsible of the preparation of technical documentation, submission and following up of product registration and/or renewal, variations dossiers, as well as other regulatory documentation. What your responsibilities will be • Prepare, compile, and maintain registration dossiers and other regulatory documentation for medicinal products and medical devices within the assigned portfolio., • Prepare, review, and submit regulatory documentation for new registrations, renewals, variations, and other regulatory procedures., • Review and validate dossiers prepared by other team members, ensuring accuracy, quality, and regulatory compliance., • Monitor the progress of regulatory submissions and registration procedures, liaising with regulatory authorities when required., • Maintain up-to-date knowledge of current regulations and regulatory requirements applicable to medicinal products and medical devices, ensuring ongoing compliance., • Coordinate the translation of regulatory documentation, ensuring accuracy, consistency, and compliance with local market requirements., • Collaborate with cross-functional teams and external partners to ensure timely and high-quality regulatory submissions. Who you are To 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 a Bachelor's Degree in Health Sciences or engineering., • You have experience in RRAA or technical departments within the pharmaceutical industry., • You have analytical skills, attention to detail, and ability to summarize and evaluate., • You have Advanced level of Spanish and English (C1) and of MS Office (Excel). Flexibility for U Program Hybrid Model Flexible schedule Monday-Thursday 7-10 to 16-19h and Friday 8-15h (with the same flexible start time). Benefits package Contract of Employment: Permanent position. xcskxlj Grifols is an equal opportunity employer. #J-18808-Ljbffr

Grifols, S.A. ¿Posee las habilidades y la experiencia adecuadas para este puesto? Siga leyendo para descubrirlo y envíe su solicitud. is seeking a Pharmacovigilance Specialist to support global safety data activities. You will participate in data collection, analysis and documentation across investigational and marketed products, ensuring regulatory compliance and high-quality deliverables. The role requires 1–2 years in pharma, strong Excel/SQL skills, and advanced English, with a hybrid work model and a permanent contract offering room for professional growth within Grifols' PV team. xqbhyrx #J-18808-Ljbffr Hay opciones de teletrabajo/trabajo desde casa disponibles para este puesto.

Grifols, S.A is seeking a Network Security Engineer to design, implement and continuously enhance security across on‑prem, cloud and hybrid environments. You will drive automation, establish secure network policies and support key technologies such as NGFW, VPN and WAF.Qualified candidates bring 3–5 years in network security, experience with major vendors, and strong English/Spanish communication. Hybrid work model and permanent position offered.#J-18808-Ljbffr

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

table.MiTabla { max-width: 1020px;!important Los candidatos deben tomarse el tiempo de leer atentamente todos los elementos de este anuncio de empleo. Por favor, envíen su solicitud sin demora. 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 Automation Specialist like you. The primary mission of this role is to provide support and coordinate automation processes, spare parts management and planned maintenance activities within the production environment of Laboratorios Grifols S.A. What your responsibilities will be Plan and execute maintenance activities related to control systems and programmable controllers. Supervise and maintain the industrial network infrastructure. Manage program changes, including supervision and authorization processes. Update automation-related hardware and develop replacement plans to prevent equipment obsolescence. Maintain factory SCADA systems and oversee the implementation of new SCADA solutions. Provide programming and automation support for engineering projects. Maintain and supervise user roles and access permissions across systems. Create and monitor tasks derived from preventive maintenance plans. Generate work orders originating from preventive maintenance activities. Manage the creation, modification and deletion of spare parts records. Support shift personnel in identifying, locating and clarifying spare parts requirements. Who you are To 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). You have CFGS (Mechatronics, Industrial Automation or similar). You have between 3-5 years of experience in a similar role. You have intermediate level of English. What we offer It 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 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! 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. xqbhyrx Schedule: Schedule: Monday-Thursday 7-10 to 16-19h and Friday 8-15h (with the same flexible start time). Benefits package Contract of Employment: Permanent position Location: Parets del Vallès : SPAIN : España : Parets del Valles: [[cust_building]] Learn more about Grifols

Grifols is seeking a Technical Drug Safety Officer in Sant Cugat del Vallès, Spain, to support global pharmacovigilance activities. Asegúrese de presentar su candidatura con toda la información solicitada, tal como se expone en la descripción del puesto a continuación. This role involves safety data management, compliance assurance, and participation in audits. The ideal candidate holds a Bachelor's degree in Health Sciences and has 1–2 years of pharma industry experience. The position offers a permanent contract and hybrid working conditions. xcskxlj #J-18808-Ljbffr Hay opciones de teletrabajo/trabajo desde casa disponibles para este puesto.

Grifols is seeking an RRAA Specialist to prepare technical documentation, submit product registrations and renewals, and manage variations dossiers for medicinal products and medical devices. You will review dossiers, monitor submission progress, coordinate translations, and stay current with regulatory requirements across the portfolio. Todos los candidatos deben asegurarse de leer atentamente la siguiente descripción del puesto y la información antes de enviar su solicitud. The role is based in Sant Cugat del Vallès with a hybrid work model. xcskxlj #J-18808-Ljbffr Hay opciones de teletrabajo/trabajo desde casa disponibles para este puesto.

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, and we are committed to equal employment opportunities that foster an inclusive environment. ¿Tiene las siguientes habilidades, experiencia e impulso para tener éxito en este puesto? Descúbralo a continuación. We are looking for a Global Customer Shared Services Specialist to join the International Customer Service department. Integrated within the Global Supply Chain, International Customer Service is a key part of the supply chain focused on customer fulfilment of our own manufactured product and third‑party products distributed by Grifols. Responsibilities • Coordinate the compliance and legal aspects of the international distribution to ensure that the supply of products through international distributors is according to internal policies and external regulations., • Process, supporting the Corporate Compliance teams, the due‑diligence requests for international distributors in a timely manner to the North American Compliance Department prior to the signature of any legal contract., • Collaborate with Legal, Commercial, Quality and other involved departments on the preparation, revision, approval and signature process of commercial agreements and other legal documentation according to corporate guidelines and external regulations., • Coordinate the legalization and/or translation of documents when required., • Keep up to date the third‑party customers’ annual compliance certificates in cooperation with Commercial teams., • Maintain and process the cancellation, renewal or any applicable amendment of legal contracts according to stakeholder instructions., • Upload all the relevant documents to the corporate archiving tool., • Process master‑data requests of new customers and/or update data for existing ones., • Process the requests to create or modify the data of any international customer in SAP as per company procedures., • Enter approved third‑party customer prices provided by the Commercial Division into SAP., • Provide an excellent service level to our customers and stakeholders to ensure customer satisfaction., • Work collaboratively and liaise with other departments for seamless operations in the area., • Process the requests received from customers and stakeholders correctly and in a timely manner., • Keep customers and stakeholders informed in a professional manner ensuring accuracy., • Escalate to line manager any complex issue for advice., • Maintain complete, accurate and up‑to‑date data records. Qualifications • Bachelor’s Degree (Business Administration, Finance or related field), preferably., • Experience in similar tasks and/or in a similar area., • Advanced level of English. Excellent verbal and written communication skills in English., • Knowledge or experience in SAP is a plus., • Proficiency with MS Office., • Customer‑oriented mindset., • Strong analytical and problem‑solving skills., • Ability to prioritize and operate in a fast‑paced environment., • Excellent relationship‑building and communication skills., • Excellent attention to detail., • Proactive and results‑oriented. Benefits & Other Information It is a brilliant opportunity for you. We are fully aware that our employees are one of our major assets and are committed to maintaining an atmosphere that encourages professional career development in an excellent working environment. 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 adjustments in our selection process, please let us know when applying; we are here to help. We believe in diversity and inclusion. Grifols is an equal opportunity employer. Flexibility for U Program: Hybrid Model. Flexible schedule: Monday–Thursday 7:10 – 16:19 and Friday 8:00 – 15:00 (with the same flexibility start time). Benefits Package: Contract of Employment: Permanent position. xcskxlj Location: Sant Cugat del Vallès, Spain. More information: J-18808-Ljbffr