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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. 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. • 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., • 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)., • 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. Grifols is an equal opportunity employer. #J-18808-Ljbffr

Overview In this role you will support global pharmacovigilance activities for Grifols products, ensuring high-quality safety deliverables and timely regulatory reporting. You will lead system projects, provide safety business support, and work with IT to keep the PV platform compliant. You will drive improvements, manage PV applications, and coordinate data-related activities across teams. This position offers a chance to shape the safety data ecosystem at a world-leading pharma company. Compensaciones / Beneficios • Benefits package, • Permanent contract, • Hybrid work option, • Flexible schedule, • Location: Sant Cugat del Vallès, • Support for diverse talent and adjustments in selection process Responsabilidades, • Support drug safety applications with business administration tasks, • Deliver cost-effective PV solutions that meet business requirements, • Develop training materials and work instructions, • Coordinate and manage signal management, • Manage PV documentation (SOPs, WP, requirements, specs), • Lead change management for new processes and applications, • Interface with Regulatory Authorities on safety data transmission, • Prioritize and plan improvements based on user requests and regulations, • Ensure data consistency and integrity in the safety database, • Manage updates to submission rules and product/study configurations, • Oversee data extraction queries for PV documents, • Oversee queries to identify case intervals and counts for reports, • Coordinate IT tickets for system compliance and improvements, • Plan and prioritize scheduled IT tickets, • Lead projects to integrate and establish the Grifols PV system Requisitos principales, • Bachelor in Health Sciences or Bioscience, • Experience in pharmacovigilance (min 4 years) including PV databases, • Team management experience, • Knowledge of GMP PV practices and safety-data administration, • Proficiency in Windows and MS Office, • Familiarity with reporting tools (e.g., Business Objects), • Knowledge of E2b (R2/R3) and medical terminology (MedDRA, WhoDrug a plus), • Fluent in Spanish and English, • Strong self-start, judgment, and attention to detail, • Strong organizational, analytical, problem-solving, and communication skills, • Ability to prioritize and manage multiple tasks, • proactive, • results-oriented, • team player, • Business Objects, • Power BI, • R

Overview In this role you will support global pharmacovigilance activities for Grifols products, ensuring high-quality safety deliverables and timely regulatory reporting. You will lead system projects, provide safety business support, and work with IT to keep the PV platform compliant. You will drive improvements, manage PV applications, and coordinate data-related activities across teams. This position offers a chance to shape the safety data ecosystem at a world-leading pharma company. Compensaciones / Beneficios • Benefits package, • Permanent contract, • Hybrid work option, • Flexible schedule, • Location: Sant Cugat del Vallès, • Support for diverse talent and adjustments in selection process Responsabilidades, • Support drug safety applications with business administration tasks, • Deliver cost-effective PV solutions that meet business requirements, • Develop training materials and work instructions, • Coordinate and manage signal management, • Manage PV documentation (SOPs, WP, requirements, specs), • Lead change management for new processes and applications, • Interface with Regulatory Authorities on safety data transmission, • Prioritize and plan improvements based on user requests and regulations, • Ensure data consistency and integrity in the safety database, • Manage updates to submission rules and product/study configurations, • Oversee data extraction queries for PV documents, • Oversee queries to identify case intervals and counts for reports, • Coordinate IT tickets for system compliance and improvements, • Plan and prioritize scheduled IT tickets, • Lead projects to integrate and establish the Grifols PV system Requisitos principales, • Bachelor in Health Sciences or Bioscience, • Experience in pharmacovigilance (min 4 years) including PV databases, • Team management experience, • Knowledge of GMP PV practices and safety-data administration, • Proficiency in Windows and MS Office, • Familiarity with reporting tools (e.g., Business Objects), • Knowledge of E2b (R2/R3) and medical terminology (MedDRA, WhoDrug a plus), • Fluent in Spanish and English, • Strong self-start, judgment, and attention to detail, • Strong organizational, analytical, problem-solving, and communication skills, • Ability to prioritize and manage multiple tasks, • proactive, • results-oriented, • team player, • Business Objects, • Power BI, • R

As Senior Manager Technical Accounting, you will lead IFRS technical analysis of complex transactions and develop accounting position papers.You will support the implementation of new IFRS standards and provide guidance to finance teams to ensure consistent IFRS application.You will train stakeholde

Overview In this role you will support global pharmacovigilance activities for Grifols products, ensuring high-quality safety deliverables and timely regulatory reporting. You will lead system projects, provide safety business support, and work with IT to keep the PV platform compliant. You will drive improvements, manage PV applications, and coordinate data-related activities across teams. This position offers a chance to shape the safety data ecosystem at a world-leading pharma company. Compensaciones / Beneficios • Benefits package, • Permanent contract, • Hybrid work option, • Flexible schedule, • Location: Sant Cugat del Vallès, • Support for diverse talent and adjustments in selection process Responsabilidades, • Support drug safety applications with business administration tasks, • Deliver cost-effective PV solutions that meet business requirements, • Develop training materials and work instructions, • Coordinate and manage signal management, • Manage PV documentation (SOPs, WP, requirements, specs), • Lead change management for new processes and applications, • Interface with Regulatory Authorities on safety data transmission, • Prioritize and plan improvements based on user requests and regulations, • Ensure data consistency and integrity in the safety database, • Manage updates to submission rules and product/study configurations, • Oversee data extraction queries for PV documents, • Oversee queries to identify case intervals and counts for reports, • Coordinate IT tickets for system compliance and improvements, • Plan and prioritize scheduled IT tickets, • Lead projects to integrate and establish the Grifols PV system Requisitos principales, • Bachelor in Health Sciences or Bioscience, • Experience in pharmacovigilance (min 4 years) including PV databases, • Team management experience, • Knowledge of GMP PV practices and safety-data administration, • Proficiency in Windows and MS Office, • Familiarity with reporting tools (e.g., Business Objects), • Knowledge of E2b (R2/R3) and medical terminology (MedDRA, WhoDrug a plus), • Fluent in Spanish and English, • Strong self-start, judgment, and attention to detail, • Strong organizational, analytical, problem-solving, and communication skills, • Ability to prioritize and manage multiple tasks, • proactive, • results-oriented, • team player, • Business Objects, • Power BI, • R

Grifols busca un profesional para liderar el control de calidad en laboratorios de pruebas plasmáticas, asegurando cumplimiento con cGMP y gestionando proyectos de calidad en un entorno global. Se requieren experiencia en entornos regulados, habilidades para comunicar y coordinar mejoras, dominio del español e inglés y disponibilidad para viajar, con presencia en Egipto en aproximadamente la mitad del tiempo. #J-18808-Ljbffr

That’s why we need R&D QA Specialist & Auditor like you.

¿Te gustaría unirte a un equipo internacional que trabaja para mejorar el futuro del sector de la salud? ¿Quieres contribuir a mejorar la vida de millones de personas? Grifols es una compañía global del sector de la salud que desde 1909 mejora la salud y el bienestar de las personas en todo el mundo. Somos líderes en medicamentos hemoderivados y medicina transfusional y desarrollamos, producimos y comercializamos medicamentos, soluciones y servicios innovadores en más de 110 países y regiones. 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. To review and ensure that all procedures, testing methods and reports established in GEPD Plasma Testing Laboratories are in compliance to Egyptian regulations, and in accordance to cGMP, following Plasma Testing Specifications established and European Regulation. To manage and supervise Plasma Testing Laboratories Quality projects. To propose continuous improvement measures related to the quality systems of the Laboratories. To supervise the Quality Risk Management (QRM) process for the Laboratories. • To review and ensure that all procedures established are in accordance to cGMP., • To supervise GEPD Plasma Testing Laboratories quality system and quality culture., • To ensure investigation for incidents are initiated, as well as root cause analysis are properly in place., • To participate and support internal and external regulatory inspections and audits performed in the Laboratories., • To manage and supervise Plasma Testing Laboratories Quality projects., • Actively participate in Laboratory meetings for the follow-up of activities related to open Change Controls., • Coordinate the tasks required to be developed within the different areas of the company., • Review new procedures and processes to be implemented in the Laboratory under the scope of the Change Controls open., • To ensure continuous improvement measures related to the quality systems of the Laboratories., • To supervise the monitoring of corrective and/or preventive actions implemented within the Laboratories. Ensure their proper implementation and effectiveness., • To monitor quality system indicators., • To propose improvements in the Laboratory's processes to enhance the quality system., • To supervise the Quality Risk Management (QRM) process for the Laboratories., • To supervise Quality Risk assessment studies and reports, as well as coordinate mitigation tasks. 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 Life Sciences (Biology, Pharmacy, Biotechnology or related fields), • Minimum 3-5 years of experience in a related field., • Organized and able to manage time effectively., • Ability to work within a highly regulated, labor intensive environment., • Ability to understand, explain, follow, and enforce SOPs., • Ability to plan, communicate and execute activities for the improvement of overall operations., • Strong integrity and commitment to Quality and Compliance., • Excellent oral and written communication skills to produce clear and concise factual findings., • Advanced level of Spanish and English., • This position requires significant travel and on-site presence in Egypt, with approximately 50% of the role based in Egypt. 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 www.grifols.com. We believe in diverse talent and want to remove any barriers that may hinder your participation. If you require any adjustments in our selection process, please do not hesitate to inform us when applying. We are here to help. Grifols is an equal opportunity employer. Occasionally Remote. Contract of Employment: Permanent position. Location: Sant Cugat del Vallès. Ubicación: SPAIN : España : Sant Cugat del Valles:[[cust_building]] Conoce más sobre Grifols #J-18808-Ljbffr

Grifols, S.A in Spain seeks an experienced Regulatory Affairs professional to manage worldwide product registrations, renewals, and lifecycle strategies across markets. You will coordinate dossier submissions and ensure compliance with regulations. The role leads a team of Regulatory Affairs Technicians, collaborates across functions, and guides licensing actions while staying up to date with domestic and international requirements. #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. Ensuring compliance of the priority plan, as well as coordination of compilation, submission and following up ofproduct registration and/or renewal and/or changes/variations dossiers, and any other regulatory documentation,within the company timelines. Determine and execute actions necessary for licenses and regulatory procedures are in compliance with domestic and international licensing requirements • Assess and define worldwide regulatory strategies for product registrations, renewals, and lifecycle management activities across assigned products and markets., • Review, prepare, and submit regulatory dossiers for new registrations, renewals, variations, and other post-approval changes, ensuring compliance with applicable regulations., • Prepare, review, and coordinate responses to Health Authority questions and requests within established timelines., • Manage and coordinate the adaptation of product licenses to current regulatory requirements and evolving legislation., • Coordinate and approve packaging materials and labeling documentation, ensuring regulatory compliance and alignment with local market requirements., • Organize, coordinate, and supervise the work of Regulatory Affairs Technicians, ensuring the timely and high-quality execution of assigned activities., • Review and assess the regulatory impact of product, manufacturing, or process changes within the assigned portfolio and oversee the implementation of required regulatory actions., • Monitor and supervise the execution of annual regulatory projects and ensure deliverables are achieved according to agreed timelines., • Represent the Regulatory Affairs function in communications with affiliates, external partners, and Health Authorities, when applicable., • Maintain up-to‑date knowledge of applicable regulations and regulatory requirements, providing regulatory guidance for different projects and business initiatives., • Support general activities and strategic initiatives within the Regulatory Affairs Department., • Coordinate the preparation, review, implementation, and maintenance of Regulatory Affairs Standard Operating Procedures (SOPs)., • Collaborate with cross‑functional teams to ensure efficient regulatory support throughout the product lifecycle. 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). 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. 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 Flexible schedule: Monday-Thursday 7-10 to 16-19h and Friday 8-15h (with the same flexible start time). Contract of Employment:Permanent position. #J-18808-Ljbffr

Grifols is seeking a Pharmacovigilance Data Analysis Manager to lead global safety data initiatives across investigational and marketed products.

Seeking a Senior Cost & Controlling Analyst to perform financial analysis and control of industrial operations, optimize production costs, and support operational teams for a global healthcare company.

Seeking a Senior SAP Controlling Consultant to join an IT Finance Applications team, focusing on S/4HANA and advanced financial solutions. Responsibilities include designing, implementing, and supporting SAP CO solutions, integrating modules, and collaborating with finance stakeholders.

Manufacturing Engineer needed to lead projects for new equipment and facility implementation, manage upgrades, coordinate external suppliers, and ensure compliance with quality and safety standards in the pharmaceutical industry.

Grifols is seeking a Global Customer Shared Services Specialist to join International Customer Service. You will support contract management, pricing, master data and other service activities for international distributors and third‑party customers of Grifols. In this hybrid role, you will coordinate compliance, legal and data processes within the Global Supply Chain, liaising with multiple departments to ensure accurate and timely handling of contracts and customer records. #J-18808-Ljbffr

Grifols, a global healthcare leader, seeks a Global Quality Manager to drive policies, harmonize systems across Biopharma sites, and lead international quality initiatives. The role requires a health sciences degree, 5–10 years in quality management, and strong project management and communication

Project lead on the integration and establishment of the Grifols PV system. It is a brilliant opportunity for you, Grifols is fully aware that its employees are one of its major assets. Information about Grifols is available atwww.

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 brilliant

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. We are looking for a Global Customer Shared Services Specialist to join 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 own manufactured product and third‑party products distributed by Grifols. The primary role of the Global Customer Shared Services Specialist is to process the tasks related to Contract Management, Pricing Management, Master Data and other support activities for international distributors and third‑party customers of the Diagnostic and Healthcare Divisions. • Coordinate the Compliance and Legal aspects of the international distribution to ensure that supply of products through international distributors are according to the 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 the signature of any legal contract., • Process and collaborate with Legal, Commercial, Quality and other involved departments, 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., • Keep up to date legal contracts and process the cancellation, renewal and/or any applicable amendment according to stakeholder’s instructions., • Upload all the relevant documents to the corporate archiving tool., • Process the Master Data requests of new customers and/or update data in existing ones:, • Process the requests to create or modify the data of any International Customer in SAP as per company procedures., • Enter in SAP the approved third‑party Customer Prices provided by Commercial Division., • 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 responsible any complex issue for advice., • Maintain complete, accurate and up‑to‑date data records. 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. • Bachelor's Degree. (Business administration, Finance or similar), preferably., • Experience in similar tasks and/or in a similar area., • Advanced level of English. Excellent verbal and written communication skills in the English language., • Knowledge or experience in SAP is a plus., • MS Office., • Customer oriented., • Strong analytical and problem solving skills., • Ability to prioritize and to operate in a fast‑paced environment., • Excellent relationship building and communication skills., • Excellent attention to detail., • Proactive and results oriented. 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 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 Model Flexible schedule: Monday‑Thursday 7‑10 to 16‑19h and Friday 8‑15h (with the same flexibility start time) Contract 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. We believe that diversity adds value to our business, our teams, and our culture. We are committed to equal employment opportunity fostering an inclusive environment where diversity makes us be outstanding. Help us lead one of the world’s largest pharmaceutical companies. We are a world leader in plasma‑derived medicines with a presence in more than 100 countries, and a growing global team of over 20,000 people. That’s why we need a Global Quality Manager like you. • Issue and review Global Quality Policies and ensure its implementation in all the sites within Biopharma Business Unit, • Stay updated on industry trends and advancements in quality management practices to drive innovation and improvement, • Foster harmonization of Quality Systems across Biopharma sites, • Coordinate the implementation of electronic Quality Management Systems, • Coordinate global Quality projects and initiatives, • Coordinate global Quality working groups comprised by different key users of the sites of Biopharma, • Perform oversight of Quality Systems and elevate risks detected to Senior Management, • Evaluate new applicable regulations and ensure its timely implementation, • Continuous support to the Quality areas of Biopharma 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. • Bachelor’s Degree in Health Sciences or a related field, • 5-10 years of experience managing quality systems is required, • Analytical and problem‑solving abilities, • Excellent written and verbal communication skills, • Experience in project management, • Ability to facilitate changeDevelops collaborative working relationships, • Good understanding of regulatory requirements and quality standards relevant to Biological products, • International experience, • Willingness to travel internationally as needed, • Ambitious, results‑oriented, business‑minded person 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. Contract of Employment: Permanent position Grifols is an equal opportunity employer. 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). We believe in diverse talent and want to remove any barriers that may hinder your participation. If you require any adjustments in our selection process, please do not hesitate to inform us when applying. We are here to help. #J-18808-Ljbffr

R&D QA Specialist & Auditor to provide quality oversight of SIO pre-clinical activities, ensuring studies, processes and documentation comply with regulatory requirements and Grifols standards.

Grifols is seeking a QA Specialist & Auditor to join its international team in Sant Cugat del Vallès.

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 regulat

It is a brilliant opportunity for you, Grifols is fully aware that its employees are one of its major assets. Information about Grifols is available at believe in diverse talent and want to remove any barriers that may hinder your participation. Grifols is an equal opportunity employer.

Formar parte de Grifols significa la oportunidad de trabajar en un entorno de proyección internacional dónde se promueve la igualdad de oportunidades. El capital humano de Grifols es clave tanto en el desarrollo de las actividades como en el proceso de expansión de la compañía. Te gustaría uni

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 brilliant

Si sus habilidades, experiencia y cualificaciones coinciden con las de esta descripción del puesto, no demore su solicitud.Immunohematology (IH) / Operations Regulatory Affairs Specialist to support the Diagnostic Regulatory Affairs department.You will prepare technical documentation, manage regist

Grifols, located in Sant Cugat del Vallès, Spain, is seeking a Pharmacovigilance professional with 1 year of CRO or pharma experience and strong Spanish and English communication skills.

Grifols SA seeks a Quality Specialist to join the GDP Compliance department.

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

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

Grifols is seeking a data analytics specialist to ensure the reliable operation of analytics and reporting solutions, and to support the design and implementation of new data projects that transform information into actionable insights for informed decision-making.

Grifols, compañía global del sector de la salud con sede en Sant Cugat del Vallès, busca un/a Trainee para el equipo de R&D QA dentro de Corporate Quality. Formarás parte de un entorno internacional y contribuirás al desarrollo de procedimientos y gestión documental en I+D. La posición ofrece

Grifols is an equal opportunity employer. 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

We are looking for a Quality Specialist to join Good Distribution Practice (GDP) Compliance department at Grifols SA. It is a brilliant opportunity for you, Grifols is fully aware that its employees are one of its major assets. Grifols is an equal opportunity employer.

A busca un/a trainee para unirse al equipo de R&D QA dentro de Corporate Quality, que da soporte a I+D y producción de la Scientific Innovation Office (SIO).Si cree que es el candidato ideal para la siguiente oportunidad, envíe su solicitud después de leer la descripción completa.Trabajarás en

Lead the design, planning, and delivery of office refurbishment and fit-out projects globally for a leading healthcare company.Ensure optimized space, budget control, and regulatory compliance.

Join an international healthcare company as a Cybersecurity Assurance Specialist to support IT compliance, security, and privacy. Responsibilities include global standards, audit plans, executing audits, ensuring SOX compliance, and promoting cybersecurity culture.

Join Grifols, a global healthcare leader, as a Senior IT Systems Engineer. Improve future healthcare by managing Wintel & Virtualization platforms, defining roadmaps, and optimizing infrastructure in a hybrid work environment.

IT Business Continuity Systems Engineer to ensure data protection and backup services meet corporate and regulatory standards. Collaborate with teams, manage providers, and support audits.

Coordinate pharmaceutical engineering projects, ensuring technical quality and compliance with regulatory standards. Manage feasibility studies, equipment, and utility systems, liaising with suppliers and supervising teams.

Provide IFRS guidance to the FSSC for consistent application across Grifols. Ensure alignment with IFRS reporting requirements and Grifols accounting policies. You will also engage with external auditors and ensure alignment with Grifols policies, enabling accurate financial reporting and informed b

You will also engage with external auditors and ensure alignment with Grifols policies, enabling accurate financial reporting and informed business decisions. Provide IFRS guidance to the FSSC for consistent application across Grifols. Ensure alignment with IFRS reporting requirements and Grifols ac

In this role you will support IT compliance, security, privacy, and governance across Grifols' global operations. Compensaciones / BeneficiosBenefits packagePermanent contractHybrid modelFlexible scheduleEqual opportunity employerResponsabilidadesSupport IT compliance, security, cybersecurity an

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. It is a brilliant