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

As Senior Manager Technical Accounting, you will lead IFRS technical analysis of complex transactions and develop accounting position papers.

In this role you will support global pharmacovigilance activities for Grifols products, ensuring high-quality safety deliverables and timely regulatory reporting. Lead projects to integrate and establish the Grifols PV system.

Lead projects to integrate and establish the Grifols PV system. In this role you will support global pharmacovigilance activities for Grifols products, ensuring high-quality safety deliverables and timely regulatory reporting.

As Senior Manager Technical Accounting, you will lead IFRS technical analysis of complex transactions and develop accounting position papers.

Deliver training on IFRS developments and accounting policies to finance teams and other departments.

In this role you will support global pharmacovigilance activities for Grifols products, ensuring high-quality safety deliverables and timely regulatory reporting. Lead projects to integrate and establish the Grifols PV system.

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

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

Grifols in Parets del Vallès seeks a senior data governance expert to lead Master Data Management and data quality initiatives in a hybrid work environment.

table.MiTabla { max-width: 1020px; }Would you like tojoin 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.What your responsibilities will beMaster Data Management & Golden RecordsHelp define, implement and evolve Master Data Management capabilities across key enterprise domains such as customer, supplier, product, material, donor, employee or location data.Support the definition of golden record rules, matching, merging, survivorship, hierarchy management and data synchronization patterns across systems. Collaborate with Data Engineering and application teams to integrate master data with ERP, CRM, analytics platforms, data lakes, data warehouses and downstream reporting solutions.Contribute to the design and operation of MDM workflows for data creation, change, approval, exception handling, de-duplication and lifecycle management.Data Governance, Quality & ComplianceSupport the implementation of data governance policies, standards, ownership, stewardship responsibilities, decision rights and escalation mechanisms. Make data standards available for Advance Analytics consumption: data AI readiness.Define and monitor data quality rules, KPIs, thresholds and remediation processes to improve accuracy, completeness, consistency, timeliness and trust.Work with business data owners and stewards to identify root causes of data issues and drive sustainable corrective actions at the source.Ensure data initiatives consider security, privacy, auditability, regulatory expectations and compliance requirements in a highly regulated environment. Experience building and maintaining data catalogs for lake house environments, ensuring that high-value analytical variables and datasets are documented, contextualized and reusable for Advanced Analytics, AI use cases and MDM initiativesExperience defining business ontologies, semantic models and controlled vocabularies to improve data consistency, interoperability, discoverability and AI-readiness across enterprise data domains.Knowledge of AI governance concepts, data governance for AI, responsible AI principles, privacy-by-design, data risk assessment and emerging regulatory expectations such as the EU AI Act.Enterprise Data Transformation & Operating ModelSupport the execution of the company data transformation roadmap, helping move the organization toward governed, trusted and reusable enterprise data capabilities.Translate strategic data objectives into actionable initiatives, deliverables, milestones and adoption plans across IT and business domains.Contribute to the definition and implementation of a hybrid / federated data operating model, balancing central standards with business domain execution.Drive coordination across Data Office, IT teams, Business stakeholders, external partners and data owners to ensure consistent execution and accountability. Metadata, Catalog, Lineage & DocumentationPromote the adoption of business glossaries, data dictionaries, metadata standards and cataloging practices to improve discoverability and common understanding of data.Support the documentation of critical data flows, lineage, transformations, ownership, usage, controls and dependencies across source systems and analytical platforms.Help establish reusable templates, standards and ways of working for documenting data architecture, MDM domains, data products, data marketplace publishing practices and governance processes.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 Computer Science, Data Science, Information Systems, Engineering or a related field.Minimum of 5 years of experience in data management, master data management, data governance, data quality, data architecture or enterprise data transformation initiatives.Experience with MDM concepts and platforms such as Reltio, SAP MDG, Informatica MDM, Semarchy, Profisee or similar solutions, data lakes and data catalog tools.Knowledge of data governance frameworks, data ownership, stewardship, data quality management, metadata management, cataloging and lineage. Experience with Microsoft Purview.Understanding of data integration patterns, APIs, ETL/ELT, data pipelines, ERP integration and analytical data platforms.Advanced English language skills, both spoken and written.Strong ownership mindset, accountability and ability to drive topics from ambiguity to execution.Excellent stakeholder management and communication skills, with the ability to influence without direct authority across business and IT teams. Collaboration.Ability to facilitate workshops, align different perspectives and convert complex data topics into clear decisions and practical actions.Comfortable operating in a matrixed, global organization and coordinating with teams across functions, geographies and time zones.Pragmatic, structured and delivery-oriented, with the ability to balance governance discipline with business agility.Continuous improvement mindset and willingness to build internal capability through knowledge transfer, documentation and enablement.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 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.Location:Parets del Vallès.#LI-Hybrid#LI-ER1Location: SPAIN : España : Parets del Valles:[[cust_building]]Learn more about Grifols

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

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.

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

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

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.

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

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

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

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, 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 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

In this role you will support global pharmacovigilance activities for Grifols products, ensuring high-quality safety deliverables and timely regulatory reporting. Lead projects to integrate and establish the Grifols PV system.

Experteer Overview In this Regulatory Affairs role, you drive worldwide regulatory strategies for product registrations, renewals, and lifecycle activities, ensuring compliance across markets. You will lead the preparation and submission of dossiers, respond to Health Authority questions, and maintain alignment with evolving regulations. You’ll supervise Regulatory Affairs Technicians and collaborate with cross-functional teams to support product lifecycle and SOP governance. This is a chance to shape regulatory pathways for therapies that improve patient outcomes on a global scale. Compensaciones / Beneficios • Assess worldwide regulatory strategies for registrations, renewals, and lifecycle activities across products and markets • Prepare, review, and submit regulatory dossiers for registrations, renewals, variations, and post-approval changes • Coordinate responses to Health Authority questions within established timelines • Manage adaptation of licenses to current regulatory requirements • Coordinate and approve packaging materials and labeling documentation for regulatory alignment • Organize and supervise Regulatory Affairs Technicians to ensure timely, high-quality work • Assess regulatory impact of changes to product, manufacturing, or processes and implement required actions • Monitor annual regulatory projects and ensure deliverables meet timelines • Represent Regulatory Affairs in communications with affiliates, partners, and Health Authorities • Maintain up-to-date regulatory knowledge and provide guidance on projects and initiatives • Coordinate preparation, review, implementation, and maintenance of Regulatory Affairs SOPs • Collaborate with cross-functional teams to provide regulatory support across the product lifecycle • Support general activities and strategic initiatives within the Regulatory Affairs Department Responsabilidades • Bachelor in Health Sciences or engineering • Experience in RRAA or technical pharmaceutical departments • Analytical skills and attention to detail; ability to summarize and evaluate information • Advanced level of Spanish and English (C1) and MS Office proficiency Requisitos principales •