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Overview In this role you will own the end-to-end delivery and evolution of a next-generation SaaS platform for study design, protocol authoring, and operational feasibility in clinical trials. You’ll bridge R&D business stakeholders, IT, and the vendor to drive design, testing, change management, and successful rollout. Post-launch, you’ll manage enhancements and adoption across a global matrix organization. This position sits at the crossroads of clinical operations, digital innovation, and enterprise IT, with a meaningful impact on patient-focused trials. Compensaciones / Beneficios • diverse and inclusive culture, • global opportunities, • personal development and career advancement, • flexible working culture, • opportunity to impact patient outcomes, • collaborative, innovative environment Responsabilidades, • Lead solution design activities and translate business requirements into functional specifications, • Support User Acceptance Testing (UAT) and facilitate alignment workshops, • Drive change management and user onboarding for platform rollout, • Manage lifecycle of the platform post go-live, including prioritizing enhancements and releases, • Monitor performance and ensure sustainable adoption and business value realization, • Collaborate with R&D users, IT partners, and external software vendor, • Contribute analytical expertise to broader digital R&D initiatives in clinical trials Requisitos principales, • 5+ years as IT Solution Lead, Application Lead, or similar in healthcare or life sciences, • Deep knowledge of clinical trial processes, including protocol design and operational planning, • Proven ability to translate complex business needs into functional specifications, • Experience in regulated environments with software development lifecycle and CSV in line with GxP, • Familiarity with clinical trial systems and data standards, • Ability to navigate a global matrix organization and build trusted relationships across R&D, IT, and external partners, • Fluent in English; proactive, solution-oriented mindset, • strong stakeholder management, • clear communication, • problem solving, • software development lifecycle (SDLC), • CSV and GxP compliance, • User Acceptance Testing (UAT)

Overview In this role you will own the end-to-end delivery and evolution of a next-generation SaaS platform for study design, protocol authoring, and operational feasibility in clinical trials. You’ll bridge R&D business stakeholders, IT, and the vendor to drive design, testing, change management, and successful rollout. Post-launch, you’ll manage enhancements and adoption across a global matrix organization. This position sits at the crossroads of clinical operations, digital innovation, and enterprise IT, with a meaningful impact on patient-focused trials. Compensaciones / Beneficios • diverse and inclusive culture, • global opportunities, • personal development and career advancement, • flexible working culture, • opportunity to impact patient outcomes, • collaborative, innovative environment Responsabilidades, • Lead solution design activities and translate business requirements into functional specifications, • Support User Acceptance Testing (UAT) and facilitate alignment workshops, • Drive change management and user onboarding for platform rollout, • Manage lifecycle of the platform post go-live, including prioritizing enhancements and releases, • Monitor performance and ensure sustainable adoption and business value realization, • Collaborate with R&D users, IT partners, and external software vendor, • Contribute analytical expertise to broader digital R&D initiatives in clinical trials Requisitos principales, • 5+ years as IT Solution Lead, Application Lead, or similar in healthcare or life sciences, • Deep knowledge of clinical trial processes, including protocol design and operational planning, • Proven ability to translate complex business needs into functional specifications, • Experience in regulated environments with software development lifecycle and CSV in line with GxP, • Familiarity with clinical trial systems and data standards, • Ability to navigate a global matrix organization and build trusted relationships across R&D, IT, and external partners, • Fluent in English; proactive, solution-oriented mindset, • strong stakeholder management, • clear communication, • problem solving, • software development lifecycle (SDLC), • CSV and GxP compliance, • User Acceptance Testing (UAT)

Overview In this role you will manage regional sourcing topics to support business development, aligning regional execution with global strategies. You will lead supplier negotiations, drive ESG integration, and develop regional sourcing roadmaps to ensure quality, cost, lead time, and risk management. You’ll collaborate across functions to deploy category strategies and roll out key initiatives like No PO No Pay, delivering measurable savings and compliance. This is an opportunity to shape regional sourcing within a global footprint and contribute to sustainable, best-in-class procurement. Compensaciones / Beneficios • Onboarding program, • Hi University learning opportunities, • Internal career opportunities, • Structured career development, • Collaborative culture, • Competitive benefits Responsabilidades, • Manage a defined group of vendors to meet quality, cost, lead time, compliance and ESG objectives; lead commercial negotiations, • Incorporate ESG requirements across sourcing activities and verify partners align with Code of Sustainable Sourcing, • Develop and manage regional sourcing roadmaps for assigned spend categories aligned with group policy; oversee initiative execution, • Report sourcing savings and compliance; promote collaboration with Category Management to leverage synergies and negotiate higher volumes, • Deploy and roll out category strategies regionally; drive performance and standardization, • Lead No PO No Pay implementation with local stakeholder alignment and timely deliverables, • Establish and maintain a supplier base to mitigate financial and operational risks; develop action plans for risk suppliers; ensure compliance with Group Purchasing Policy Requisitos principales, • Academic degree or relevant commercial/technical education, • Minimum of 5 years’ experience in purchasing and procurement techniques, • Proven track record delivering value from strategic activities, • Strong project management skills with ability to manage multiple initiatives and deadlines, • Demonstrated ability to collaborate across functions, geographies and disciplines, • Strong interpersonal skills for building partnerships with internal stakeholders and vendors, • Proven negotiation skills up to senior management with understanding of contracts and local regulations, • Fluent in English, Spanish and Catalan, • Interpersonal effectiveness, • Cross-functional collaboration, • Stakeholder management, • Purchasing techniques, • Strategic sourcing, • Contract negotiation

Overview In this role you will manage regional sourcing topics to support business development, aligning regional execution with global strategies. You will lead supplier negotiations, drive ESG integration, and develop regional sourcing roadmaps to ensure quality, cost, lead time, and risk management. You’ll collaborate across functions to deploy category strategies and roll out key initiatives like No PO No Pay, delivering measurable savings and compliance. This is an opportunity to shape regional sourcing within a global footprint and contribute to sustainable, best-in-class procurement. Compensaciones / Beneficios • Onboarding program, • Hi University learning opportunities, • Internal career opportunities, • Structured career development, • Collaborative culture, • Competitive benefits Responsabilidades, • Manage a defined group of vendors to meet quality, cost, lead time, compliance and ESG objectives; lead commercial negotiations, • Incorporate ESG requirements across sourcing activities and verify partners align with Code of Sustainable Sourcing, • Develop and manage regional sourcing roadmaps for assigned spend categories aligned with group policy; oversee initiative execution, • Report sourcing savings and compliance; promote collaboration with Category Management to leverage synergies and negotiate higher volumes, • Deploy and roll out category strategies regionally; drive performance and standardization, • Lead No PO No Pay implementation with local stakeholder alignment and timely deliverables, • Establish and maintain a supplier base to mitigate financial and operational risks; develop action plans for risk suppliers; ensure compliance with Group Purchasing Policy Requisitos principales, • Academic degree or relevant commercial/technical education, • Minimum of 5 years’ experience in purchasing and procurement techniques, • Proven track record delivering value from strategic activities, • Strong project management skills with ability to manage multiple initiatives and deadlines, • Demonstrated ability to collaborate across functions, geographies and disciplines, • Strong interpersonal skills for building partnerships with internal stakeholders and vendors, • Proven negotiation skills up to senior management with understanding of contracts and local regulations, • Fluent in English, Spanish and Catalan, • Interpersonal effectiveness, • Cross-functional collaboration, • Stakeholder management, • Purchasing techniques, • Strategic sourcing, • Contract negotiation

• Manage product release activities, evaluating technical and documental compliance according to Technical Direction guidelines, • Participate in the configuration of systems related to product release, • Coordinate communications with Notified Bodies, reference laboratories and related stakeholders, • Manage documentation storage, control and retrieval, including externally archived documentation, • Handle document management quality notifications, ensuring proper tracking and workflow, • Approve quality notifications after evaluating their impact on batch release and product status, • Monitor the status of materials affected by quality notifications, • Coordinate communications with Health Authorities (e.g., AEMPS) regarding import/export activities, • Issue and manage authorizations and official letters required for import/export processes, • Ensure compliance with applicable regulations such as ISO 13485, IVDR and MDSAP, • Act as internal auditor and participate in supplier audits, • Participate in continuous improvement of the Quality Management System., • Bachelor's degree in Engineering, Health Sciences or similar, • At least 3 years of experience in Quality Assurance or Regulatory Affairs, • Experience in regulated environments under ISO13485 and/or IVDR, • Experience in team management, • Experience in audits, • Excellent communication skills, • Cross-functional and collaborative work with multiple departments, • Attention to detail and compliance, • Analytical ability and technical judgement in impact assessments, • English level is C1., • Bachelor's Degree in Engineering, • Bachelor's Degree in Health Sciences #J-18808-Ljbffr

Werfen is a growing, family-owned, innovative company founded in 1966 in Barcelona, Spain. We are a worldwide leader in specialized diagnostics in the areas of Hemostasis, Acute Care Diagnostics, Transfusion, Autoimmunity, and Transplant. We operate directly in 30 countries, and in more than 100 territories through distributors. Our Headquarters are in Barcelona, Spain and our Technology Centers are located in the United States and Europe. Worldwide sales exceeded €2.2 billion in 2024, and our workforce is more than 7,000 strong. Solutions QA Leader focuses on organizational aspects of quality management, aiming to improve the end-to-end product development life cycle, from requirements analysis to launch and maintenance, including providing inputs and active contributions to the definition and maintenance of the Quality Management System (QMS). Working closely with the Solutions Leaders to ensure to deliver software releases with an ever-increasing level of quality. When applicable, QA Customer Liaison facilitating effective communication and understanding of QA processes, methodologies, and outcomes. • Cooperating with the Director of Quality & Regulatory Affairs - Digital Solutions to co-ordinate quality assurance activities for all SW development products assigned., • Responsible for ingraining quality as a core discipline into every aspect of the SW development teams (Squads) organizations., • Ensure that SW Development teams (Squads) are informed with the perspective of the QA processes and/or customer requirements enabling the delivery of a product or service to an agreed level of quality., • Oversee SW project documents subject to QA approval ensuring the establishment and adherence to the appropriate QMS and customer processes and procedures, including but not limited to requirements management, configuration control, secure design, risk analysis, verification and validation, traceability, etc., • Support Change Management Board (CRB) process as needed., • Advance metrics and the setting of goals that provide visibility and understanding of development effectiveness from a quality perspective., • Drive Promote continuous improvement initiatives to enhance product quality, operational efficiency, and customer satisfaction., • Collaborate in the QS software development life cycle procedures definition and maintenance. Provides input in the implementation of the process., • Point of contact for the different business unit's / client related with Quality agreements, • Take an active role in the training and dissemination of knowledge regarding quality system procedures., • Pursuing a unified approach to quality process implementation throughout the software development lifecycle across all solutions within a Factory., • Participate in software products audits and assessments as needed. The main relationships within the Werfen Group are: • Factory Lead and Solution Leaders, • Solutions QA Leaders from other factories, • SW Development Teams (Squads) and Chapter Leads, • QARA Manager and QARA Specialist, • Customer, • Validation Lead, • Application Lifecycle manager (ALM), • This position may also require cooperating with other companies inside Werfen., • Education: Engineer, computer Science or other Technical degree, or equivalent work experience., • Experience:, • A minimum of 5 years of experience in a QA related role., • Knowledge in SW Development methodologies preferably within the Healthcare sector., • Experience in the creation or revision of comprehensive software products documentation., • Additional Skills/Knowledge:, • Knowledge about applicable standards and regulations related with SW development for Health and/or Medical Device. (ISO 13485, ISO 14971, IEC 62304, IEC 82304, ISO 62366, cybersecurity), • Familiar with medical device regulations (MDR/IVDR, FDA, etc) This position has a combination of technical and leadership experience in QA area being able to collaborate seamlessly with cross-functional teams for ensuring product quality and customer and regulatory compliance. The role requires demonstrates adaptability to evolving technologies, strong communication skills, and a commitment to fostering a quality-focused culture within the organization. Besides it is needed to have: • Strong interpersonal skills with a proven ability to collaborate across teams and communicate effectively with stakeholders., • Flexibility and adaptability to a fast-changing environment/methodology, • Self-organized and self-monitor to be able to report the effort dedicated to each individual tasks inside all the different responsibilities., • Good level of Technical and Conversational English, • Commitment to continuous improvement, with a track record of implementing initiatives to enhance overall quality processes. 5% of time #J-18808-Ljbffr

Overview In this role you will own the end-to-end delivery and evolution of a next-generation SaaS platform for study design, protocol authoring, and operational feasibility in clinical trials. You’ll bridge R&D business stakeholders, IT, and the vendor to drive design, testing, change management, and successful rollout. Post-launch, you’ll manage enhancements and adoption across a global matrix organization. This position sits at the crossroads of clinical operations, digital innovation, and enterprise IT, with a meaningful impact on patient-focused trials. Compensaciones / Beneficios • diverse and inclusive culture, • global opportunities, • personal development and career advancement, • flexible working culture, • opportunity to impact patient outcomes, • collaborative, innovative environment Responsabilidades, • Lead solution design activities and translate business requirements into functional specifications, • Support User Acceptance Testing (UAT) and facilitate alignment workshops, • Drive change management and user onboarding for platform rollout, • Manage lifecycle of the platform post go-live, including prioritizing enhancements and releases, • Monitor performance and ensure sustainable adoption and business value realization, • Collaborate with R&D users, IT partners, and external software vendor, • Contribute analytical expertise to broader digital R&D initiatives in clinical trials Requisitos principales, • 5+ years as IT Solution Lead, Application Lead, or similar in healthcare or life sciences, • Deep knowledge of clinical trial processes, including protocol design and operational planning, • Proven ability to translate complex business needs into functional specifications, • Experience in regulated environments with software development lifecycle and CSV in line with GxP, • Familiarity with clinical trial systems and data standards, • Ability to navigate a global matrix organization and build trusted relationships across R&D, IT, and external partners, • Fluent in English; proactive, solution-oriented mindset, • strong stakeholder management, • clear communication, • problem solving, • software development lifecycle (SDLC), • CSV and GxP compliance, • User Acceptance Testing (UAT)

Proven track record delivering value from strategic activities. You’ll collaborate across functions to deploy category strategies and roll out key initiatives like No PO No Pay, delivering measurable savings and compliance. Lead No PO No Pay implementation with local stakeholder alignment and time

As Project Engineer, you will define and support investment and technical aspects of capital projects, managing budgets and documentation.You will oversee installation and commissioning of equipment, supervise contractors and internal teams, and ensure compliance with standards and regulations.You w

As Project Engineer, you will define and support investment and technical aspects of capital projects, managing budgets and documentation.You will oversee installation and commissioning of equipment, supervise contractors and internal teams, and ensure compliance with standards and regulations.You w

Mondelēz International in Granollers, Spain, is seeking a Project Engineer to lead capital projects and provide technical support across plants. You will define requirements, manage budgets and timelines, and coordinate internal and external resources to drive successful implementations. Engagement includes collaborating on technology trials, performing FMEA, and ensuring compliance with safety and quality standards, while supporting tender processes and commissioning activities. #J-18808-Ljbffr

As Project Engineer, you will define and support investment and technical aspects of capital projects, managing budgets and documentation.You will oversee installation and commissioning of equipment, supervise contractors and internal teams, and ensure compliance with standards and regulations.You w

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. To 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. • 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 portfolio initiatives, promoting successful implementation and sustainable adoption of new processes and ways of working., • Facilitate collaboration between cross-functional teams and help drive alignment, accountability and execution discipline across the project., • Support change management activities to enable successful implementation and adoption of the future processes and ways of working., • Manage and/or contribute to other projects within the Biomat project portfolio, as required, ensuring alignment with business priorities, operational excellence standards and quality requirements., • Contribute to the development of the Operational Excellence strategy and support broader business transformation initiatives. 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 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. 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! 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). Contract of Employment: Permanent position. Flexibility for U Program: Remote working. Location: Parets del Vallès. www.grifols.com Learn more about Grifols #J-18808-Ljbffr

Overview Join Brenntag as a Regulatory Affairs Specialist in the Barcelona/Valencia area to support regulatory, quality, and product stewardship for a broad pharma raw materials portfolio. You will deliver accurate, audit-ready documentation to pharmaceutical customers and drive regulatory deliverables for bespoke projects. The role involves cross-functional collaboration, process improvement, and occasional travel to supplier meetings and audits. You’ll help ensure materials meet EU and international pharmaceutical standards and contribute to regulatory excellence across the business. Compensaciones / Beneficios • international, collaborative environment, • continuous learning and career development, • meaningful projects with real impact, • equal employment opportunities, • global industry leader Responsabilidades, • Prepare, review and issue technical and regulatory documentation for pharma customers (Quality & Technical Agreements, Supply Chain Statements, Regulatory Questionnaires, Compliance Statements), • Ensure documents align with pharmacopoeia, IPEC Guidelines, EU GDP and GMP, • Source and evaluate regulatory, quality and technical information from internal and supplier sources, • Log, track and report customer documentation requests using KPIs and identify process improvements, • Lead regulatory deliverables for customer-specific projects and coordinate data collection for new product introductions, • Support change control evaluations and customer notifications, • Work with QHSE and supply chain to ensure compliance with standards (IPEC GMP/GDP, EXCiPACT, GDP, etc), • Contribute to global Pharma Regulatory projects and harmonisation efforts, • Deliver training on regulatory topics to commercial, supply chain and internal teams, • Perform other tasks to support regulatory and compliance success, • Cross-functional collaboration with commercial and value-added services teams Requisitos principales, • Degree in life science or equivalent experience, • Strong knowledge of APIs, excipients, biopharma materials, and traditional pharma materials, • Understanding of European National Competent Authority requirements for distribution of APIs and raw materials, • Fluent in English and Spanish (written and spoken), • Strong written communication to produce compliant documentation, • Excellent collaboration and proactive cross-functional work, • Ability to interpret regulations and resolve compliance issues, • High attention to detail and organisational skills, • Willingness to travel occasionally, • collaboration, • proactive mindset, • attention to detail, • pharmaceutical regulatory knowledge (APIs, excipients), • GMP/GDP, IPEC, EXCiPACT, • documentation and compliance drafting

Masterdata Application SpecialistApplylocations: Granollers Officetime type: Full timeposted on: Posted Yesterdayjob requisition id: JR100076## Job PurposeThe Master Data Management Specialist plays a critical role in ensuring the accuracy, consistency, governance, and lifecycle management of master data across Audens Food, with an extended scope supporting the wider GoodLife Foods Group. Acting as the key link between business stakeholders and IT, the role ensures that high-quality master data supports operational excellence, strategic initiatives, and business transformation.This position is responsible for maintaining a reliable single source of truth for Product, Customer, Supplier, and other critical business data, enabling efficient operations, regulatory compliance, and informed decision-making across the organization. The role also contributes to the successful delivery of system implementations, data integrations, and continuous improvement initiatives aimed at strengthening data governance and business processes.## Key Responsibilities* Manage and oversee the day-to-day maintenance of master data within Synergy MDM and connected enterprise systems, ensuring data integrity and operational continuity. Ensure master data is accurate, complete, and compliant with established governance policies, business standards, and quality requirements. Serve as the subject matter expert for master data management processes, supporting data quality initiatives and promoting best practices across the organization. Lead the master data workstream in ERP implementations, system integrations, data migrations, and business transformation projects. Support and coordinate integrations between Synergy MDM, ERP systems, GS1 data exchanges, APIs, and EDI interfaces to ensure seamless data flow across business applications. Collaborate closely with cross-functional stakeholders to identify, investigate, and resolve data quality issues while implementing sustainable corrective actions. Develop, maintain, and continuously improve master data documentation, governance standards, operating procedures, and user training materials.* Drive continuous improvement initiatives focused on enhancing master data processes, governance frameworks, controls, and overall data quality.## Key StakeholdersThe role requires close collaboration with a broad range of internal and external stakeholders to ensure effective master data governance and support business operations.Internal stakeholders IT Enterprise Application Manager Master Data Management Team Sales Operations Supply Chain Finance Procurement Quality Assurance* ERP and Application Support TeamsExternal stakeholders Software vendors System implementation partners* GS1 and other external data exchange partners## Role Dimensions* Preferred location: Granollers, Spain* Business scope: Multiple manufacturing sites across Audens Food and GoodLife Foods* Core systems: Synergy MDM, Izaro ERP, and other connected enterprise applications* Master data portfolio: + Approximately 1,000 product articles and 2,000 product items + Approximately 700 customer records + Approximately 3,500 supplier records* Travel: Occasional travel within Spain and to Breda, The Netherlands## Qualifications & Experience Bachelor's degree or equivalent professional experience. Minimum of 2–3 years' experience in Master Data Management, ERP systems, or enterprise business applications. Previous experience within manufacturing, FMCG, food production, or supply chain environments is highly desirable. Strong understanding of data governance principles, master data management processes, and data quality frameworks. Good knowledge of Microsoft 365 applications and basic relational database concepts. Experience working with ERP systems, APIs, EDI integrations, and GS1 data standards.* Fluent in both Spanish and English, with excellent written and verbal communication skills.* Willingness to travel occasionally as required.## Key CompetenciesThe successful candidate combines strong technical expertise with excellent analytical and interpersonal skills, enabling effective collaboration across business functions while ensuring high standards of data quality.Core competencies include: Strong analytical thinking and problem-solving capabilities. Exceptional attention to detail and commitment to data accuracy. Advanced Microsoft Excel skills, including formulas, Pivot Tables, VLOOKUP/XLOOKUP, conditional formatting, data validation, data comparison, transformation, and preparation of bulk upload files. Excellent stakeholder management and communication skills, with the ability to collaborate effectively across technical and business teams. Ability to work independently, prioritize competing demands, and manage multiple projects simultaneously. Project-oriented mindset with experience supporting business transformation and change initiatives. Proactive, pragmatic, and continuous improvement approach. Ability to translate business requirements into practical data management and system solutions that support organizational objectives.At GoodLife Foods we believe that great food brings people together and makes every moment more enjoyable. With a team of over 1,700 professionals across Europe, we are leading the way in frozen snacks and offer a diverse range of irresistible food - each made with care, expertise, and the finest ingredients. Behind all our products are great people. As we continue to grow our business, we’re building the foundation for one GoodLife Foods: a place where teams connect, processes align and our collective strengths come together. Working at GoodLife Foods means joining an organisation where diverse cultures and perspectives are celebrated while fostering one unified organisation. We strive to ensure everyone feels valued and connected. #J-18808-Ljbffr

Plant Manager Multisite - Parets & BalsarenyApplylocations: Granollers Office: Parets Plant: Balsarenytime type: Full timeposted on: Posted Todayjob requisition id: JR100073At GoodLife Foods, we believe that great food brings people together and makes every moment more enjoyable. With more than 1,650 professionals across Europe, a portfolio of 1,600 products and 14 manufacturing sites, we are a leading company in the frozen snacks and appetizers market. Every product is crafted with care, expertise and the finest ingredients.Being part of GoodLife Foods means being PROUD: pragmatic, respectful, open-minded, united and driven. These values shape the way we work together, fostering an inclusive environment where different cultures and perspectives are valued, ensuring everyone feels connected and empowered to contribute to our shared success.We are currently looking for a Plant Manager Responsible for two manufacturing facilities within the Group, Balsareny and Parets.The successful candidate will report directly to the Iberia Operations Director.POSITION MISSIONTo provide full operational leadership for two manufacturing plants of IBERIA (Parets del Vallés and Balsareny), ensuring the achievement of Safety, Quality, Service, Cost and People objectives through effective leadership, outstanding organizational skills and strong coordination of the management teams across both locations.The role is responsible for ensuring operational stability, driving continuous improvement, developing people and fostering process standardization between sites, while acting as a role model for leadership and company culture across both facilities.KEY RESPONSIBILITIES: Lead the overall operations of both manufacturing sites, ensuring the achievement of safety, quality, service, productivity and financial objectives while fostering a high-performance culture. Develop and inspire the management teams, promoting collaboration across functions and building engaged, accountable and autonomous teams. Drive operational excellence through Lean Manufacturing, continuous improvement initiatives and process standardization across both plants. Ensure compliance with health, safety, quality and food safety standards, promoting a culture of prevention, regulatory compliance and operational excellence. Oversee the financial performance of both sites, managing budgets, profitability and operational efficiency while identifying opportunities for cost optimization and sustainable growth. Lead organizational transformation by supporting the implementation of new technologies, systems and ways of working that strengthen business performance.The ideal candidate will have: Bachelor’s or Master’s degree (Engineering, Operations, or similar) 5-10 years of experience in manufacturing or operations Proven leadership experience at plant or operations level Experience in growth, transformation, or scale-up environments Experience in process-driven industries A minimum C1 level of English is required Availability to travel approximately twice per month We are looking for a leader with a strategic mindset, a results-driven approach, and excellent problem-solving and communication skills. The ideal candidate is committed to operational excellence, continuous improvement, quality, and safety.What do we offer? The opportunity to join a leading international company in the food industry. A collaborative and people-focused culture where your ideas matter. A strategic leadership role with real impact on business performance. A competitive compensation and benefits package.If you're looking to drive high-impact projects and become part of a leading international company in the food industry, we'd love to hear from you!At AudensFood, we believe in creating a workplace where everyone can grow, contribute, and feel valued. We are committed to equal opportunities, diversity, and inclusion in all their forms, fostering a culture of respect and collaboration. We believe in investing in talent, embracing diversity, and growing together. If you're proactive, committed, and excited about joining a company that is constantly evolving, we'd love to welcome you to our team! At GoodLife Foods we believe that great food brings people together and makes every moment more enjoyable. With a team of over 1,700 professionals across Europe, we are leading the way in frozen snacks and offer a diverse range of irresistible food - each made with care, expertise, and the finest ingredients. Behind all our products are great people. As we continue to grow our business, we’re building the foundation for one GoodLife Foods: a place where teams connect, processes align and our collective strengths come together. Working at GoodLife Foods means joining an organisation where diverse cultures and perspectives are celebrated while fostering one unified organisation. We strive to ensure everyone feels valued and connected. #J-18808-Ljbffr

Master Data Management & Golden Records Help 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 & Compliance Support 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 initiatives Experience 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 Model Support 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 & Documentation Promote 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. 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 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. 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. : Hybrid Model. Permanent position. www.grifols.com Learn more about Grifols #J-18808-Ljbffr

Please note that while the internal job title for this position is 'Regulatory Affairs Lead', this is an individual contributor role that does not involve team management or project leadership This position provides effective regulatory support for company's manufactured products and customer's products. Prepare and submit the documentation according to the corresponding legislation for the different countries. Be responsible for the implementation of new regulatory requirements. • Prepare the required documentation to obtain the CE mark, FDA, or other country registrations for the company's manufactured products or customer's products in accordance with current legislation. Communication and maintenance of products with Spanish authorities., • Support customers with any regulatory aspect., • Follow up and resolve requirements that emerge during registration procedures., • Maintain technical files as necessary to sustain product approval., • Review product materials, labeling, and/or specification sheets for compliance with applicable regulations and customer policies., • Be part of CFT projects as the RA representative., • Support internal and external audits, validations, and product risk analysis., • Follow management indicators/metrics for the proper performance of the department and apply appropriate corrective actions if necessary., • Support the Market Surveillance Department in compiling information for Post-Market Surveillance., • Recommend and manage, if applicable, changes to company procedures/documents (quality system and compliance) to comply with current regulations, guidelines, and/or standards., • Provide support to Customer Service regarding product import/export., • Ensure effective partnering and collaboration with R&D, Quality Operations, Design Quality, and Operations to meet project goals, maintain compliance, and complete defined regulatory submissions., • Ensure all documentation is RA-reviewed before it is shared externally with regulators and/or customers., • Collaborate with other QRA groups, R&D, and Operations to ensure successful Regulatory Inspections. To be determined based on department needs, to include interactions such as: • All departments of the company., • Customers., • Regulatory agencies., • Required: Bachelor's degree (diplomatura) in Life Sciences, Engineering, or Physical Science. Degree may be substituted by relevant skills and work experience., • Valuable: Any additional degree higher than required., • Required: 3 years in a similar position., • Software: Fluency in Office Tools (Excel & Word); basic knowledge of SAP is valuable., • Languages: Fluency in Spanish or Catalan; advanced knowledge of English (reading and speaking)., • Standards: Knowledge of IVD legislation and the healthcare sector is valuable., • Management of decisions under pressure., • Methodical and well-organized approach., • Teamwork., • Ability to express information clearly and concisely to staff, ensuring understanding., • Ability to apply a systematic approach with constant control, follow-up, and verification of results., • Analytical thinking and problem-solving., • Ability to collaborate, participate, and coordinate actively with working groups., • Reflects Werfen values in work quality and working relationships. #J-18808-Ljbffr

Why join theSourcingdepartment? At the heart of every project, ourSourcing teamsdevelop innovative strategies for the procurement of materials and services, ensuring high-quality partnerships and effective cost management. We are committed to deliveringsustainable solutionsthat meet environmental requirements while achievingbest-in-class performancein our industry. By joining our Sourcing team, you will play a key role inselecting the best suppliersandoptimizing our supply chain. You will work within a passionate team dedicated to findinginnovative and sustainable solutionsto meet the challenges of a constantly evolving sector. Within the Sourcing department, we are shaping theelectrical world of tomorrow. Join us and be part of the journey! As a Country Purchaser Regional Sourcing (m/f/d) you will report to Regional Sourcing Managerin theSourcing departmentbased inLa Roca del Vallesfor aPermanentcontract. The role of Country Purchaser is to manage country specific purchasing topics to support regional business development. To do so the jobholder drives regional execution and supply continuity aligned with global strategies and regional business needs, facilitating Hager global sourcing footprint. Duties & Responsibilities • Being accountable to manage a defined group of vendors and partnerships in order to reach Hager objectives regarding quality, costs, lead time, compliance and sustainable criteria to ensure the application of concerned sourcing strategy. To do so she/he leads the commercial negotiations., • Incorporate environmental, social and corporate governance (ESG) requirements as part of the sourcing and ensures that vendors and any other business partners are matching Hager objectives set in the Code of Sustainable Sourcing., • Develop and manage overall regional sourcing roadmaps and strategies for assigned spend categories aligned with group sourcing policy and strategies and oversee the execution of initiatives. Be accountable for reporting of sourcing savings and compliance., • Promote collaboration between Hager’s Category Management to find synergies and unlock additional sourcing opportunities and negotiate aggregated volumes to achieve commercial benefits., • Ensure deployment of category strategies in the regions., • Drive a high-level performance within a culture of collaboration, whilst focusing on process standardization, implementation of best in class practices., • Drive the implementation and regional rollout of the “No PO, No Pay” group initiative, ensuring local stakeholder alignment and compliance and provide required deliverables in time., • Establishing and maintaining a supplier base that effectively safeguards the company against financial and operational risks. This includes the development and implementation of action plans for identified risk suppliers. In addition, the position ensures full compliance with the Group Purchasing Policy throughout all relevant processes. Qualifications & Requirements • Academic degree or relevant commercial/technical education., • A minimum of 5 years’ experience of purchasing and procurement techniques., • Proven track record of delivery of value from strategic activities., • Operationally und technical savvy and having the ability to effectively manage projects simultaneously whilst meeting agreed deadlines and goals., • Demonstrated ability to navigate and collaborate across functions, businesses, geographies and disciplines., • Strong presence and interpersonal skills, with the drive to build effective partnerships with key internal stakeholders, vendors and other business partners., • Proven negotiation skills up to senior management level with understanding of contractual negotiation, development, and local regulations., • Fluent proficiency in English, Spanish and Catalan. What we offer? • Personalized onboarding experience programdesigned to make your first dayssmooth, • Opportunities to learn and grow through Hager Group's awarded HiUniversity., • Internal career opportunities, over 25% of our recruitments are through internal mobility What are the recruitment stages? • Once your CV has been selected, you will be contacted by a recruiter for an initial phone exchange., • You will be invited for a first interview with the hiring manager & the recruiter, • A second Interview will be then organized with the N+2 & the HR manager Our success relies on collective energy. Apply now and power up your future with us! #J-18808-Ljbffr

Overview Join Grifols as a Cost Controlling Senior Analyst to drive cost efficiency across manufacturing. You will partner with Production, Quality, and R&D to provide financial guidance, monitor KPIs, and ensure reliable reporting and SOX controls. Your work supports budgeting, forecasting, and cost optimization in a global health context. This role offers impact across multiple production areas and a path to shape costing strategies at a world-leading pharmaceutical company. Compensaciones / Beneficios • flexible schedule, • 2-day remote work, • permanent contract, • benefits package Responsabilidades • Analyze production process performance and monitor KPIs, • Develop and update annual standard costs for manufactured products, • Prepare financial analyses and management reports to improve plant efficiency, • Participate in budgeting and forecasting with financial analysis, • Support monthly closing activities in collaboration with FSSC, • Review financial analyses of third-party contracts across departments, • Act as financial business partner for Production, Quality, and R&D, • Calculate and analyze manufacturing product costs, • Prepare statistical reports required by official institutions (e.g., INE), • Support internal and external audits, • Design and maintain controls to ensure SOX compliance, • Maintain SAP material master data related to costing Requisitos principales • University degree in Business Administration, Economics, Finance, Accounting, or related field, • Minimum English level of B2.2, • Minimum 3 years in industrial environments, preferably pharmaceutical, with cost analysis and control experience, • Strong understanding of industrial costing and financial controlling processes, • Experience with SAP (CO) and advanced proficiency in Microsoft Excel, • Knowledge of Power BI and SAP Analytics Cloud (SAC) is a plus, • Strong interpersonal and stakeholder management skills, • Stakeholder management, • Cross-functional collaboration, • Proactive problem-solving, • SAP CO costing, • Advanced Excel, • Power BI

Senior Buyer | Cosmos Aromática Internacional (Tradebe Group) Únete a Cosmos Aromática Internacional ¿Te gustaría liderar la estrategia de compras de una compañía que está detrás de los aromas que forman parte de productos consumidos en todo el mundo? Cosmos Aromática Internacional es una empresa especializada en el desarrollo y fabricación de aromas e ingredientes para la industria alimentaria, reconocida por su capacidad de innovación, calidad y cercanía al cliente. Forma parte de la división Life Sciences de Tradebe , un grupo internacional con presencia global y más de 40 años de trayectoria. Tradebe desarrolla su actividad a través de cuatro divisiones de negocio: Environmental Services , Health & Nutrition , Life Sciences y Tradebe Port Services (TPS). Dentro de este ecosistema, Cosmos Aromática aporta conocimiento especializado en el mundo de los flavours, combinando excelencia técnica, innovación y una clara orientación al crecimiento sostenible. En este contexto, buscamos incorporar un/a Senior Buyer que lidere la estrategia de compras y aprovisionamiento de la compañía, desempeñando un papel clave en la optimización de costes, la gestión estratégica de proveedores y la garantía de suministro de materias primas esenciales para nuestro negocio. ¿Cuál será tu misión? Como Senior Buyer , serás responsable de liderar la estrategia de compras y aprovisionamiento de la compañía, garantizando el suministro eficiente de materias primas, productos y servicios en las mejores condiciones de coste, calidad, plazo y servicio. Tendrás un papel clave en la optimización de costes, la gestión estratégica de proveedores y la mejora continua de los procesos de compras, contribuyendo directamente a la competitividad y rentabilidad del negocio. Principales responsabilidades Definir e implementar la estrategia de compras y aprovisionamiento. Garantizar la disponibilidad de materias primas y servicios críticos para la operación. Analizar mercados, tendencias y evolución de costes. Identificar oportunidades de ahorro y optimización. Negociar acuerdos y condiciones comerciales con proveedores nacionales e internacionales. Gestionar, desarrollar y evaluar la cartera de proveedores. Asegurar el cumplimiento de las políticas internas, estándares de calidad y normativa aplicable. Liderar y desarrollar el equipo de Compras. Funciones Estrategia y Gestión de Compras Definir la estrategia de compras alineada con los objetivos del negocio. Elaborar y gestionar el presupuesto de compras. Analizar el gasto y desarrollar iniciativas de reducción de costes. Negociar precios, contratos, condiciones y plazos con proveedores. Gestión de Proveedores Identificar, seleccionar y homologar proveedores. Desarrollar relaciones estratégicas con partners clave. Realizar evaluaciones periódicas de desempeño. Gestionar incidencias y planes de mejora continua. Aprovisionamiento y Operaciones Coordinar el aprovisionamiento con Producción, Planificación, Calidad y Logística. Garantizar la disponibilidad de materiales según las necesidades productivas. Supervisar niveles de inventario y rotación de stock. Asegurar el cumplimiento de plazos de entrega y compromisos contractuales. Calidad, Compliance y Sostenibilidad Colaborar con Calidad para asegurar el cumplimiento de estándares ISO 22000 e IFS. Velar por el cumplimiento de los requisitos legales y normativos. Impulsar prácticas de compra sostenibles y responsables. Participar en auditorías y evaluaciones de proveedores. Reporting y Mejora Continua Elaborar informes periódicos de costes, ahorros y desempeño de proveedores. Definir y monitorizar KPIs de compras. Identificar oportunidades de mejora en procesos y herramientas. Participar en proyectos transversales de optimización y eficiencia. Grado universitario en ADE, Economía, Ingeniería o similar. Valorable Máster en Supply Chain, Compras o Dirección de Operaciones. Formación complementaria en negociación y gestión de proveedores. Más de 10 años de experiencia en compras estratégicas. Experiencia previa en posiciones de responsabilidad dentro del área de Purchasing. Valorable experiencia en entornos industriales, alimentación, ingredientes, aromas o gran consumo. Sólida experiencia en negociación con proveedores internacionales. Conocimiento de procesos de aprovisionamiento, gestión de stock y planificación. Experiencia trabajando con ERP (SAP u otros). Competencias Capacidad analítica y orientación a datos. Visión de negocio y orientación a resultados. Excelentes habilidades de negociación e influencia. Liderazgo y gestión de equipos. Proactividad y mentalidad de mejora continua. Capacidad para trabajar de forma transversal con diferentes áreas de la organización. Incorporación a una compañía internacional sólida y en crecimiento. Participación en decisiones estratégicas de negocio. Entorno dinámico, colaborativo y orientado a la innovación. Oportunidades de desarrollo profesional dentro del Grupo Tradebe. ¿Te gustaría liderar la estrategia de compras de una compañía referente en el sector de aromas y fragancias? Te estamos buscando. #J-18808-Ljbffr

Grifols is seeking a Space Planning Senior Engineer to lead the design and execution of office refurbishment projects across multiple locations in Spain. The role emphasizes optimizing space utilization and compliance with corporate strategies. The ideal candidate will have 3-5 years of experience in managing corporate space projects, a relevant degree, and strong proficiency in project management. This position offers a permanent contract, occasional remote work, and a flexible schedule. #J-18808-Ljbffr

Werfen Immunoassay is seeking a Solutions QA Leader to drive quality across software development products and ensure robust QMS alignment. Por favor, lea detenidamente la información de esta oferta de empleo para entender exactamente qué se espera de los posibles candidatos. The role partners with Directors and cross-functional teams to embed QA practices and regulatory compliance throughout the lifecycle. xqziphu The candidate will lead QA initiatives, oversee documentation, and promote continuous improvement in product quality and customer satisfaction within a complex healthcare software environment. #J-18808-Ljbffr

Merck Group in Spain seeks an Analytics Architect within the Enabling Functions Data Office to design and deliver high-impact data and AI solutions that power smarter ways of working across the organization. You will join a collaborative, internationally distributed team delivering data products at scale in a Product-Oriented Delivery model. You will work with Snowflake, AWS, Palantir Foundry and end-to-end data pipelines, focusing on governance, security, and regulatory compliance while #J-18808-Ljbffr

Your responsibilities and tasks Siga leyendo para comprender completamente lo que este trabajo requiere en cuanto a habilidades y experiencia. Si su perfil encaja, presente su candidatura. • Answer phone calls and manage customer requests, distributing calls to the appropriate team if needed. Receive customer requests via email and manage them., • Distribute requests from the shared customer service inbox to colleagues in the department., • Manage quotations: receive requests, create quotations, follow up on acceptance and act on superior instructions., • Order Management: create sales orders, purchase goods for the central warehouse and follow up on delivery., • Coordinate order delivery tracking with Supply Chain & Logistics., • Administrative management of service requests: register requests in the system, assign initial date and technician based on availability and area geographic., • Invoicing of services: produce proforma and final invoices after verifying documentation and data; track and receipt of orders for billing; issue credit notes in compliance with approval guidelines., • Manage maintenance contracts: register contract info, control intervention dates, update materials list during term; bill accordingly., • Manage incidents that arise during each phase of the “order to cash” process until resolution., • Travel management for technicians and other colleagues. Your profile and qualifications • Studies in Administration & Finance., • Minimum 1–2 years of experience in a back‑office department (Order Manager role)., • Training, knowledge and experience in administration., • Experience as part of a project‑management team is valuable., • Leadership personality experienced in leading high‑performance production organizations., • Spanish (Native)., • English (Advanced); Portuguese would be an asset., • High performance and result orientation., • Convincing personality capable of pushing for results despite resistance., • Ability to communicate with all levels within the organization. We offer • Attractive compensation package aligned with experience and responsibilities., • Private health insurance plan., • Employee Assistance Program., • Flexible working hours and a hybrid working model (up to two days per week remote)., • 23 days of vacation per year., • Great work environment as part of a collaborative team., • Continuous internal training and career development opportunities, both nationally and internationally., • Opportunity to join a company recognized as a Top Employer 2026. GEA is an equal opportunity employer. xqziphu Applicants will therefore receive consideration for employment without regard to age, sex, race, color, religion, world view, national origin, genetics, disability, gender identity, marital status, sexual orientation, veteran status or any other protected characteristic required by applicable law. Applicants with disabilities are welcome and will be given special consideration if they are equally qualified. #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. • Master Data Management & Golden Records, • Help 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 & Compliance, • Support 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 initiatives, • Experience 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 Model, • Support 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 & Documentation, • Promote 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. 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 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. 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. Hybrid Model. Contract of Employment: Permanent position. Location: Parets del Vallès. Location: SPAIN : España : Parets del Valles:((cust_building)) Learn more about Grifols #J-18808-Ljbffr

Grifols is seeking an IT Business Continuity Systems Engineer to join the IT Infrastructure Core & Services division. ¿Tiene su CV preparado? Si es así y confía en que este es el puesto ideal para usted, asegúrese de enviar su solicitud lo antes posible. The role focuses on data protection, backup governance, and regulatory compliance across on-premises and cloud environments. xqziphu You will act as SME, coordinate with MSPs, and drive improvements in service quality and audit readiness while maintaining documentation and standards. #J-18808-Ljbffr

Symrise is a global supplier of fragrances and flavors, cosmetic active ingredients as well as functional ingredients. Its customers include perfume, cosmetics, food and beverage manufacturers, the pharmaceutical industry and producers of dietary supplements and pet food. With sales of around €4.9 billion in the 2025 financial year, the company is one of the world's leading providers. The Group, headquartered in Holzminden, Germany, has more than 100 locations in Europe, Africa and the Middle East, Asia, the USA and Latin America. Together with its customers, Symrise develops new ideas and market-ready concepts for products that form an indispensable part of everyday life. Economic success and corporate responsibility are inextricably linked. Symrise - always inspiring more... We’re looking for an experienced seasoning developer to lead and support development activities for a key strategic snack customer. You will own the full lifecycle of seasoning solutions, from concept creation to industrial production support, ensuring strong technical performance and high customer satisfaction. This is a hands-on role with real impact, requiring close collaboration with cross-functional teams and direct customer interaction. • Lead the development of seasoning solutions tailored to customer product portfolios, • Create, optimize, and adapt formulations based on performance targets, customer needs, and regulatory requirements, • Ensure excellent application performance in finished products, including taste, stability, and process behavior, • Evaluate formulations through lab work, pilot trials, and industrial validation, • Support scale-up and production trials, both internally and at customer sites, • Troubleshoot production issues and implement corrective actions when needed, • Act as a key technical contact for the customer on ongoing projects and innovation initiatives, • Collaborate closely with R&D, Operations, Quality, Regulatory, Sales, and Supply Chain, • Deliver projects on time, fully documented, and aligned with internal processes and customer constraints, • Ensure compliance with safety, hygiene, and environmental standards, • Degree in Food Science, Food Engineering, Chemistry , or related field, • 5-9 years of experience in seasoning, savory, or flavor development (ideally in snacks or savory foods), • Fluent in English and Spanish (both required), • Strong understanding of seasoning functionality in industrial food production, • Hands-on experience with manufacturing trials and scale-up, • Solid knowledge of ingredients, processing technologies, and regulatory requirements, • Ability to translate market trends into relevant product development, • Experience managing cost optimization, raw material selection, and margin targets, • Confident in customer-facing situations, able to clarify needs and present solutions, • Strong cross-functional collaboration skills Become part of our open and transparent culture. It will give you the opportunity to flourish and to develop inspiring experiences that contribute to the health and well-being of consumers in 160 countries around the world. Putting our employees in the focus fuels our strong company growth above market rates and makes us an excellent place to develop your career. Come join us and embark on a fascinating journey with Symrise. #J-18808-Ljbffr

The mission of this role is to support production & warehouse managers in their daily operations and improve efficiency, standardize, and digitize highly manual processes in the Biomat production area, contributing to the operational transformation of the department. The focus will be on understanding, analysing, and optimizing operations across three key areas: Plasma Storage Freezers, Plasma Classification Room and Biological Sample Archive. • Support managers in reviewing and enhancing procedures, workflows, and documentation, ensuring full compliance with GMP, legal, environmental, and traceability requirements, while contributing to staff training and process adherence., • Extract and analyze data from SAP, WMS, and other systems to build KPIs, dashboards, and performance insights, enabling data-driven decision-making across operations., • Analyze and redesign workflows, identifying manual or inefficient processes and transforming them into automated and digital solutions, including the implementation of RPA tools., • Lead automation and digitalization projects across operational areas, working cross-functionally with IT, Engineering, Maintenance, and Operations to ensure successful deployment., • Drive continuous improvement initiatives by identifying inefficiencies, performing root cause analysis, and applying Lean Six Sigma methodologies to enhance productivity and standardization., • Oversee the Biological Sample Archive, ensuring compliant storage, traceability, and shipment of samples, while managing interactions with software vendors and system improvements., • University degree in Industrial Engineering, Mechanical Engineering, Automotive Engineering, or similar., • Master’s degree in manufacturing project management, Continuous Improvement, or similar is highly desirable., • Minimum English level of B2.2 (Essential). Ability to communicate in technical environments., • Minimum 5 years of experience in industrial operational environments, highly valued in warehousing and/or production., • Experience in process improvement, digitalization, or automation projects (RPA)., • Experience and/or knowledge of SAP and WMS., • Practical experience using Lean Six Sigma methodologies, etc. (DMAIC, Agile, Design Thinking, TPM, Shingo)., • Experience managing data analysis and statistics (Python, SQL, Tableau, Power BI)., • Strong influence and change management skills, problem solving, communication skills, numerical skills, and results orientation. Highly valued., • Permanent position (Contract of Employment)., • Flexible schedule: Monday-Thursday 8:00 – 17:00, Friday 8:00 – 15:00., • 1 day remote working flexibility., • Location: Parets del Vallès. 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 that foster an inclusive environment. We are looking for an IT Business Continuity Systems Engineer to join the IT Infrastructure Core & Services Division at 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. Role Mission You will play a key role in ensuring that data protection and backup services meet corporate standards, regulatory requirements, and audit expectations. Acting as the main liaison between the business and Managed Service Providers (MSPs), you will drive service quality, operational excellence, and continuous improvement across the data protection landscape. What Your Responsibilities Will Be • Act as the Subject Matter Expert (SME) for backup, data protection, and compliance‑related topics., • Provide technical guidance and support to infrastructure teams on backup and data protection solutions across on‑premises and cloud environments., • Collaborate with architecture teams to design, evolve, and manage the lifecycle of data protection platforms., • Contribute to the definition and implementation of solutions aligned with technical, regulatory, and corporate standards., • Lead cross‑functional workshops and discussions to ensure backup solutions are effectively integrated into the corporate technology landscape., • Own and maintain technical and functional documentation related to data protection services and processes., • Serve as the primary point of contact for quality, validation, and internal/external audit activities related to data protection., • Support audit processes by managing evidence, deviations, non‑conformities, and regulatory requirements., • Coordinate knowledge transfer activities between the backup function and other areas of the organization., • Manage and coordinate project and service demand in collaboration with project management teams and technology vendors., • Oversee the transition of new projects and solutions into managed services operations., • Monitor and follow up on major incidents, recurring issues, and support activities handled by external service providers. Who You Are To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. • Degree, Technical Engineering degree, or equivalent qualification in Computer Systems, Information Technology, or related fields., • Experience of 5 – 10 years in the administration and management of backup and data protection platforms., • Advanced knowledge of backup tools such as Dell NetWorker, PowerProtect Data Manager (PPDM), Veeam, and Commvault., • Experience managing backup infrastructure devices such as Data Domain and LTO tape libraries., • Proven experience working in complex, high‑availability corporate environments., • Experience in regulated environments and audit‑driven organizations is highly desirable., • Strong understanding of quality processes, validation, and regulatory compliance frameworks., • Advanced level of English and Spanish., • Ability to coordinate multiple initiatives and manage service demand effectively., • Strong problem‑solving and decision‑making skills., • Ability to interact effectively with technical teams, business stakeholders, and external service providers., • Strong orientation towards quality, regulatory compliance, and continuous improvement. What We Offer We are committed to maintaining an atmosphere that encourages all employees to develop their professional careers in an excellent working environment. Grifols is an equal opportunity employer. xqziphu 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 #J-18808-Ljbffr

Grifols, located in Parets del Vallès, is searching for a Cybersecurity Assurance Specialist to support IT compliance and security. With over 20,000 employees globally, you will be key in defining audit plans and promoting a cybersecurity culture across the company. The ideal candidate will possess a Bachelor’s degree in a related field and at least 5 years in cybersecurity. The role offers a permanent position with hybrid work flexibility and a supportive work environment, making it an excellent opportunity for professional growth. #J-18808-Ljbffr

Grifols is seeking a Cybersecurity Governance Specialist to join its global IT security team. You will help maintain the ISMS, develop security policies, and monitor KPIs for the Information Security Office across a multinational company. Ideal candidates have a Bachelor’s degree in a related field, 5+ years in cybersecurity, strong English and Spanish, and certifications such as CISA or CISSP are valued. This permanent, hybrid role offers an international environment. #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. 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. 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 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. 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 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. 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). xqziphu Benefits package 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 Hardware Testing Analyst like you. The 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. • Define test plans., • Execute and/or supervise test plans., • Analyze design specifications., • 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. 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). 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 experience troubleshooting 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. 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 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 Monday-Thursday 7-10 to 16-19h and Friday 8-15h (with the same flexible start time). Permanent position SPAIN : España : Parets del Valles:((cust_building)) Learn more about Grifols #J-18808-Ljbffr

Would you like to join an international team working to improve the future of healthcare? Do you want to enhance the lives of millions of people? Grifols is a global healthcare company that since 1909 has been working to improve the health and well‑being of people around the world. We are leaders in plasma‑derived medicines and transfusion medicine and develop, produce and market innovative medicines, solutions and services in more than 110 countries and regions. ¿Es usted el solicitante adecuado para esta oportunidad? Descúbralo leyendo el resumen del puesto 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 IT Validation Technician actively contributes to the execution of the defined validation methodologies which comply with company standards and regulatory requirements. This role also oversees teams and validation resources engaged in validation activities. What your responsibilities will be • Relationship Management, Planning, and Strategic Alignment, • Builds effective and trusting working relationships with all business and IT partners in areas of responsibility and collaboration., • Continuously improves knowledge of business processes, industry trends, and IT systems to better communicate IT capabilities and support IT solutions development., • Project Delivery and Management, • Proactively identifies project risks and issues, helps determine necessary escalation, mitigation, and resolution steps., • Regularly communicates deliverables status, concerns, and issues to direct Manager, the Project Manager, and the project team., • Participates in estimating project cost and time requirements, assessing capabilities and support/resource requirements in area of responsibility., • Creates, reviews, updates, and may approve CSV documentation for changes and projects as assigned in accordance with IT Methodology: Validation Plans, Risk Analysis, Validation Test Designs and Reports., • Assures the compliance of the GxP relevant IT systems with the regulatory and data integrity requirements., • IT Operational Support, • Ensures IT quality and regulatory compliance through adherence to quality control standards in all activities., • Contributes to the development, documentation, and evolution of IT policies, procedures, and tools to align with business and IT strategies and ensure sustainability of services, • Regularly communicates individual task status, open issues, and challenges to impacted stakeholders and/or direct manager., • Knowledge Sharing and Consulting, • Participates in the education of partners in industry and IT best practices in areas of responsibility and expertise., • Mentors peers and junior level staff with both challenging and routine assignments by sharing knowledge and experience., • Shares developing expertise of industry and IT best practices with peers and business partners., • May participate in the development of ongoing training for IT staff in specific areas of knowledge., • Provides support in the event of internal and external audits of validated systems, preparing supporting documentation as required., • Participates in the continuous enhancement of systems, technologies, methodologies, and services to improve IT effectiveness and system performance. 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 Life Sciences (Biology, Pharmacy, Biotechnology, Chemical or a related discipline)., • Minimum of 3 years of proven experience working within a regulated pharmaceutical environment, including GxP compliance., • Solid understanding of project management methodologies, tools, and best practices., • Knowledge of regulatory requirements and GxP standards applicable to computerized systems., • Experience supporting regulatory inspections and audit responses., • Strong attention to detail with the ability to manage multiple priorities simultaneously., • Ability to work both independently and collaboratively in cross‑functional and international teams., • Excellent organizational, communication, and problem‑solving skills., • Advanced in English, with the ability to work effectively in an international environment. Benefits package • Flexibility for U Program: Hybrid Model., • Contract of Employment: Permanent position. xqziphu 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. Maximice sus posibilidades de que su candidatura sea seleccionada asegurándose de que su CV y sus habilidades se ajustan al perfil. 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. Mission The 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 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). 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 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. Grifols is an equal opportunity employer. xqziphu Flexibility for U Program: Occasionally Remote 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 SAP / Grifols SAP as service provider: Grifols: #J-18808-Ljbffr

Would you like to join an international team working to improve the future of healthcare? Do you want to enhance the lives of millions of people? Grifols is a global healthcare company that since 1909 has been working to improve the health and well-being of people around the world. We are leaders in plasma-derived medicines and transfusion medicine and develop, produce and market innovative medicines, solutions and services in more than 110 countries and regions. We believe that diversity adds value to our business, our teams, and our culture. We are committed to equal employment opportunities, fostering an inclusive environment where diversity makes us outstanding. Help us lead one of the world’s largest pharmaceutical companies. We are leaders 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 Manufacturing Engineerlike you to join Diagnostic Grifols SA, part of the Grifols Group specialized in developing technological solutions for the pharmaceutical industry. The Manufacturing Engineering Department is part of the Production organization and provides technical support to manufacturing areas through the management of engineering projects, continuous improvement of equipment and facilities and the implementation of new production capabilities. We work cross-functionally with Manufacturing, Quality, Validation and Maintenance teams to ensure that processes, equipment, and infrastructures comply with the company's quality, safety and efficiency standards. We also collaborate closely with external engineering firms, equipment manufacturers and specialized suppliers in the design, development and implementation of new equipment, facilities and industrial services that support the organization's growth and transformation. • Lead projects involving the implementation of new manufacturing equipment, facilities and production areas., • Manage projects related to the expansion and improvement of industrial utilities and services (compressed air, HVAC, purified water, etc.)., • Coordinate engineering activities with external suppliers, contractors and internal departments., • Participate in the design and review of layouts, material flows and the configuration of new production areas., • Oversee construction and installation activities, ensuring compliance with technical requirements, GMP standards, safety regulations, timelines and budgets., • Prepare and review technical documentation associated with engineering projects., • Coordinate commissioning activities, testing execution, qualification and validation of new facilities and systems., • Act as a technical reference for industrial infrastructure projects, ensuring that implemented solutions meet both current and future manufacturing needs., • Identify opportunities for improvement in equipment, facilities and production processes., • Monitor project progress, ensuring compliance with established milestones and allocated budgets., • Participate in strategic expansion projects and the transfer of manufacturing activities to new facilities. 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 Engineering (Industrial, Mechanical, Electrical). Degree in Pharmacy or Chemical Engineering will also be considered with additional training in Project Management and/or a Master's degree in Pharmaceutical Industry., • Proven experience managing industrial projects related to manufacturing equipment and facilities, preferably within the pharmaceutical, cosmetics, biotechnology or food industries., • To have experience in industrial construction or facility expansion projects and/or experience in the design and execution of cleanrooms and GMP-compliant environments will be highly valuable. Also, to have participated in technology transfer projects or the commissioning of new manufacturing facilities., • Knowledge of industrial installations and critical utilities such as HVAC systems, compressed air, purified water, industrial gases and monitoring systems., • Experience coordinating external engineering firms, suppliers and contractors., • Knowledge of GMP regulations and requirements., • Ability to interpret engineering drawings, technical specifications and engineering documentation., • Advanced level of English., • You should also combine analytical thinking, organizational skills and strong communication abilities to transform operational needs into efficient and sustainable technical solutions., • Proactive attitude, autonomy and the ability to drive projects while coordinating multiple stakeholders in a dynamic and continuously evolving environment., • Excellent planning, organizational and project tracking skills., • Strong mindset focused on continuous improvement, problem-solving and achieving results. 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: Occasionally remote 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 #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 an AI Solutions Analyst like you. As 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. • 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. 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 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. 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, 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. Hybrid Model 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 a global healthcare company that has been working since 1909 to improve health and well‑being worldwide. We are leaders in plasma‑derived medicines and transfusion medicine and develop, produce and market innovative medicines and services in more than 110 countries. Compruebe que cumple con los requisitos de habilidades para este puesto, así como con la experiencia asociada, y luego envíe su CV a continuación. Equal Employment Opportunity Grifols is an equal‑to‑opportunity employer and is committed to fostering an inclusive environment. Adjustments can be made for applicants with disabilities. Position Overview The QA Plasma Operations & Lookback Specialist will control and oversee the acceptance process for plasma and non‑plasma raw materials in accordance with established specifications to ensure compliance with legal, regulatory and customer requirements. Responsibilities • Coordinate the surveillance process for plasma units, • Ensure that the surveillance of plasma units alerted as post‑donation information are handled according to the approved procedures, • Ensure compliance with the established deadlines in the management of alerts, • Analyze the causes that give rise to communications and inform the Technical Management when the reason requires it, • Evaluate the potential risk of plasma batches, • Analyze the data and prepare periodic reports on the process, • Other administrative tasks related to the plasma surveillance, • Control the acceptance process for raw materials, • Evaluate the supplier documentation associated with the receipt of plasma shipments and plasma fractions against the approved requirements, • Assess the maintenance of the cold chain during transportation in accordance with the specifications, • Report and verify the results of the acceptance of plasma materials according to the approved inspection plans, making decisions regarding the use of the associated shipments, • Manage discrepancies and potential deviations in the process with plasma suppliers, • Establish and maintain guidelines to be followed in the purchasing and evaluation process of quality‑subjected suppliers, advising the coordination carried out by the Purchasing Section, • Data analysis, filing and administrative tasks related to the raw materials process, • Coordinate the workflows within the lifecycle of plasma fractions to ensure their availability within the established timelines, • Manage any deviations that occur and collaborate in the investigations that arise, • Contribute xqziphu to the necessary tasks for the release of plasma fractions to customers, • Data analysis, filing, and administrative tasks related to the management process of intermediate products Qualifications • Bachelor's degree in Health Sciences (Pharmacy, Biology, Chemistry); a Master’s or postgraduate degree in the pharmaceutical sector is valuable, • 3 years of experience within Pharma Quality, • Knowledge in GMP, • Basic statistical knowledge, • Proficiency with MS Office and SAP, • Advanced level of English Schedule Monday to Friday, 14:00–22:00 (afternoon shift) Benefits Package • Permanent position, • Occasionally remote, • Location: Parets del Vallès, Spain #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. Consulte la descripción del puesto a continuación. Si confía en que tiene las habilidades y la experiencia adecuadas, envíe su solicitud hoy mismo. 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. Join Grifols! 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. Grifols S.A. is seeking a Trainee to join the IT QA Team, supporting the design and rollout of IT Quality awareness initiatives that strengthen quality and compliance across the entire IT organization. What your responsibilities will be In this role, you will play an active part in promoting a strong quality culture within IT. Your main responsibilities will include: • Supporting the design and deployment of IT QA initiatives aimed at increasing quality awareness across the IT organization., • Assisting in the implementation and continuous improvement of the IT Quality Management System, including reviewing and updating quality policies, procedures, and work instructions., • Helping analyze, track, and resolve quality events, such as deviations, change controls, and corrective and preventive actions (CAPA)., • Contributing to GxP assessments of IT suppliers and computerized systems under the guidance of the IT Quality team., • Providing support during internal and external audits and regulatory inspections.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 are currently pursuing a Bachelor’s or Master’s degree in Engineering, Telecommunications, Informatics or a related field., • You have a strong interest in the healthcare and pharmaceutical industry, particularly in Quality Management Systems (QMS), Quality Assurance or Quality Control processes., • You have solid knowledge of MS Office tools (Excel, Word, etc.). Familiarity with innovative technologies and a foundational understanding of Generative AI tools is highly valued., • You have at least a B2 level of English., • You demonstrate strong communication and stakeholder management skills, with the ability to act as a bridge between technical teams and business or pharmaceutical stakeholders., • You have an analytical mindset and are comfortable translating business needs into technology-driven solutions and improvements., • You are proactive, curious, and self-driven, with a strong willingness to learn and develop in a fast-paced and evolving environment. You bring a collaborative attitude and a genuine passion for continuous improvement and innovation.What we offer, • Study assistance, company bus and dining benefits. 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. xqziphu Grifols is an equal opportunity employer. Learn more about Grifols ( ) #J-18808-Ljbffr

Would you like to join an international team working to improve the future of healthcare? Do you want to enhance the lives of millions of people? Grifols is a global healthcare company that since 1909 has been working to improve the health and well-being of people around the world. We are leaders in plasma-derived medicines and transfusion medicine and develop, produce and market innovative medicines, solutions and services in more than 110 countries and regions. Desplácese hacia abajo para encontrar una descripción detallada de este trabajo y lo que se espera de los candidatos. Envíe su solicitud haciendo clic en el botón "Solicitar". 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 an IT Business Continuity Systems Engineer to join the IT Infrastructure Core & Services Division at Grifols SA ., company specialized in the research, development, and production of purified plasma proteins with therapeutic properties obtained from the fractionation of human plasma. Role Mission You will play a key role in ensuring that data protection and backup services meet corporate standards, regulatory requirements, and audit expectations. Acting as the main liaison between the business and Managed Service Providers (MSPs), you will drive service quality, operational excellence, and continuous improvement across the data protection landscape. What your responsibilities will be • Act as the Subject Matter Expert (SME) for backup, data protection, and compliance-related topics., • Provide technical guidance and support to infrastructure teams on backup and data protection solutions across on-premises and cloud environments., • Collaborate with architecture teams to design, evolve, and manage the lifecycle of data protection platforms., • Contribute to the definition and implementation of solutions aligned with technical, regulatory, and corporate standards., • Lead cross-functional workshops and discussions to ensure backup solutions are effectively integrated into the corporate technology landscape., • Own and maintain technical and functional documentation related to data protection services and processes., • Serve as the primary point of contact for quality, validation, and internal/external audit activities related to data protection., • Support audit processes by managing evidence, deviations, non-conformities, and regulatory requirements., • Coordinate knowledge transfer activities between the backup function and other areas of the organization., • Manage and coordinate project and service demand in collaboration with project management teams and technology vendors., • Oversee the transition of new projects and solutions into managed services operations., • Monitor and follow up on major incidents, recurring issues, and support activities handled by external service providers. 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). • Degree, Technical Engineering degree, or equivalent qualification in Computer Systems, Information Technology, or related fields., • Experience of 5-10 years in the administration and management of backup and data protection platforms., • Advanced knowledge of backup tools such as Dell NetWorker (Highly Valuable), PowerProtect Data Manager (PPDM), Veeam, and Commvault., • Experience managing backup infrastructure devices such as Data Domain and LTO tape libraries., • Proven experience working in complex, high-availability corporate environments., • Experience in regulated environments and audit-driven organizations is highly desirable., • Strong understanding of quality processes, validation, and regulatory compliance frameworks., • Advanced level of English and Spanish, • Ability to coordinate multiple initiatives and manage service demand effectively., • Strong problem-solving and decision-making skills., • Ability to interact effectively with technical teams, business stakeholders, and external service providers., • Strong orientation towards quality, regulatory compliance, and continuous improvement. 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. 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. xqziphu 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 more about Grifols Type: Indefinido tiempo completo #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. ¿Interesado en saber más sobre este trabajo? Desplácese hacia abajo y descubra qué habilidades, experiencia y cualificaciones académicas se necesitan. 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. Grifols S.A. is seeking a Trainee to join the IT QA Team, supporting the design and rollout of IT Quality awareness initiatives that strengthen quality and compliance across the entire IT organization. What Your Responsibilities Will Be In this role, you will play an active part in promoting a strong quality culture within IT. Your main responsibilities will include: • Supporting the design and deployment of IT QA initiatives aimed at increasing quality awareness across the IT organization., • Assisting in the implementation and continuous improvement of the IT Quality Management System, including reviewing and updating quality policies, procedures, and work instructions., • Helping analyze, track, and resolve quality events, such as deviations, change controls, and corrective and preventive actions (CAPA)., • Contributing to GxP assessments of IT suppliers and computerized systems under the guidance of the IT Quality team., • Providing support during internal and external audits and regulatory inspections.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 are currently pursuing a Bachelor’s or Master’s degree in Engineering, Telecommunications, Informatics or a related field., • You have a strong interest in the healthcare and pharmaceutical industry, particularly in Quality Management Systems (QMS), Quality Assurance or Quality Control processes., • You have solid knowledge of MS Office tools (Excel, Word, etc.). Familiarity with innovative technologies and a foundational understanding of Generative AI tools is highly valued., • You have at least a B2 level of English., • You demonstrate strong communication and stakeholder management skills, with the ability to act as a bridge between technical teams and business or pharmaceutical stakeholders., • You have an analytical mindset and are comfortable translating business needs into technology-driven solutions and improvements., • You are proactive, curious, and self-driven, with a strong willingness to learn and develop in a fast-paced and evolving environment. You bring a collaborative attitude and a genuine passion for continuous improvement and innovation.What We Offer, • Study assistance, company bus and dining benefits. 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. If you require any adjustments in our selection process, please do not hesitate to inform us when applying. We are here to help. xqziphu Grifols is an equal opportunity employer. Location: SPAIN : España : Parets del Valles:[[cust_building]] Learn more about Grifols #J-18808-Ljbffr

Werfen is a growing, family-owned, innovative company founded in 1966 in Barcelona, Spain. We are a worldwide leader in specialized diagnostics in the areas of Hemostasis, Acute Care Diagnostics, Transfusion, Autoimmunity, and Transplant. Through our Original Equipment Manufacturing (OEM) business line, we research, develop, and manufacture customized assays and biomaterials. We operate directly in 30 countries, and in more than 100 territories through distributors. Our Headquarters and Technology Centers are located in the US and Europe, and our workforce is more than 7,000 strong. The Systems Engineer supports R&D instruments through installation, maintenance, diagnostics, troubleshooting, modifications, and upgrades. The role links assay development and instrumentation by translating laboratory, user, and scientific needs into system-level requirements and capabilities. It applies scientific judgment to laboratory work, data analysis, deviation investigation, and interpretation of experimental and system performance. The position manages workflow, documentation, reporting, interfaces, and incident communication using company processes and systems. Working with R&D, Instrumentation, Engineering, Quality, Operations, and Technical Support, the role helps ensure instrument availability, reliable testing, and clear communication of risks, deviations, progress, and recommendations. Key Accountabilities • Act as a technical bridge between scientific development and instrumentation development, ensuring assay, laboratory, instrument, and system requirements are understood, aligned, and clearly communicated., • Perform and support laboratory procedures, experiments, system tests, and troubleshooting activities requiring scientific judgment and technical understanding., • Select appropriate experimental, analytical, and technical methods; contribute to protocols; and support interpretation of experimental and system performance data., • Detect deviations in results, system behavior, or instrument performance; identify potential causes; and recommend modifications to protocols, workflows, methods, or technical approaches., • Support internal instruments through diagnostics, troubleshooting, preventive maintenance, repair coordination, modifications, upgrades, and technical follow-up., • Compile, analyze, and interpret experimental and technical data; perform calculations; and prepare graphs, summaries, and reports to communicate findings, problems, and progress., • Provide project updates and communicate technical status, results, risks, deviations, and recommendations to supervisors, senior research staff, and cross-functional stakeholders., • Write or contribute to laboratory procedures, technical summaries, reports, reviews, protocols, and documentation under appropriate supervision and approval when required., • Ensure electronic and paper records, technical data, and work documentation are accurate and compliant with applicable guidelines, procedures, and good documentation practices., • Manage workflow, technical reporting, incident communication, autonomous task execution, escalation of risks or issues, and compliance with company processes, quality expectations, and the Ethics Code. Internal Networking This role interacts with multiple internal functions to ensure effective communication between scientific, technical, quality, and operational perspectives. To be determined based on department needs but, typical interactions may include: • R&D colleagues, including scientists, technical scientists, and development teams., • System Development and Engineering groups, including CSW and IL, involved in instrument, hardware, software, or system-level activities., • Quality Control, Quality Assurance, and Operations colleagues to support regulated development, documentation, technical investigations, and workflow alignment., • Technical Support and service-related teams to exchange information on instrument performance, issues, diagnostics, repair needs, and field-relevant feedback., • Manufacturing, logistics, and other technical departments. Minimum Knowledge & Experience required for the position • Required: Bachelor’s degree or equivalent technical qualifications in electrical/mechanical engineering or physical sciences., • Valuable: Any additional degree higher than what is required in the previous point. Any additional degree, specialization, or advanced training higher than the minimum requirement, particularly in systems engineering, biomedical engineering, instrumentation, diagnostics, laboratory sciences, or related technical/scientific areas., • Years of experience, • Experience is not required., • Valuable: Professional experience in in vitro diagnostic development, technical service, instrumentation, systems integration, or high-end life sciences/medical equipment, particularly in roles involving laboratory procedures, assay development, instrument troubleshooting, data analysis, and cross-functional technical communication. Additional Skills/knowledge: • Data analysis skills, including the ability to manage data sets, perform calculations, interpret results, and prepare graphs or technical summaries using scripting programming languages like Python or R., • Knowledge of basic software tools such as Excel, Word, and PowerPoint; knowledge of SAP is preferred., • Laboratory experience, including basic knowledge of biological and chemical laboratory procedures and the ability to operate laboratory equipment., • Working knowledge and ability to test, troubleshoot, and support electrical, mechanical, digital, or instrument-related areas., • Ability to understand and connect assay behavior, laboratory workflows, instrument performance, and system-level interactions., • Familiarity with design control processes and quality standards as required for the role. Language: • Fluency in Spanish or Catalan., • Advanced knowledge of English (reading, speaking and writing). Skills & Capabilities: • Strong attention to detail and accuracy., • Excellent analytical and troubleshooting skills, with the ability to investigate deviations, identify possible causes, and recommend corrective or improvement actions., • Ability to apply scientific methods, theoretical knowledge, and technical reasoning to tasks within one or more areas of expertise., • Ability to work in a multidisciplinary environment involving science, electronics, mechanics, software, pneumatics, fluidics, quality, and operations., • Strong teamwork and interpersonal skills, with flexibility to support multiple people, projects, and technical needs., • Clear oral and written communication skills, including the ability to explain technical or scientific issues to different audiences., • Excellent organizational, time management, and multi-tasking skills., • Ability to work independently on assigned activities with moderate guidance and to upscale risks or issues appropriately., • Curiosity, willingness to learn, and adaptability in a flexible and changing R&D environment., • Proactive, organized, resolute, and able to communicate results, problems, and progress within the group and across departments when required., • Reflects the values of Werfen and OEM in the quality of work and working relationships. Travel Requirements Sporadic travel or short-term assignment to an external may be required (up to 10% of the time). Werfen appreciates and values diversity. We are an Equal Opportunity/Affirmative Action Employer M/F/D/V. #J-18808-Ljbffr

Grifols is seeking a Software QA Engineer to join its international team in Parets del Vallès. 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. The role focuses on ensuring quality, reliability and compliance of blood typing analyser software through manual and automated testing. You will collaborate with developers, execute diverse test types, document defects, and maintain testing documentation in a rapidly evolving, FDA-regulated environment. xqziphu Hybrid work schedule is available. #J-18808-Ljbffr

Mondelēz International is seeking a Project Engineer to lead capital projects at the Granollers, Barcelona plant. ¿Está pensando en solicitar este empleo? No se demore, desplácese hacia abajo y envíe su solicitud lo antes posible para no perder la oportunidad. You will define requirements, prepare budgets and schedules, and coordinate internal and external resources to deliver on-time, within budget. xqziphu You will oversee installation, commissioning, and testing of technologies, ensure compliance with safety and quality standards, and report progress to stakeholders. #J-18808-Ljbffr

Mondelēz International in Granollers, Spain, is seeking a Project Engineer to lead capital projects and provide technical support across plants. Desplácese hacia abajo para obtener una visión general completa de lo que requerirá este trabajo. ¿Es usted el candidato adecuado para esta oportunidad? You will define requirements, manage budgets and timelines, and coordinate internal and external resources to drive successful implementations. xqziphu Engagement includes collaborating on technology trials, performing FMEA, and ensuring compliance with safety and quality standards, while supporting tender processes and commissioning activities. #J-18808-Ljbffr

Grifols seeks an IT Business Continuity Systems Engineer to join the IT Infrastructure Core & Services division in Parets del Vallès. Consulte la descripción del puesto a continuación. Si confía en que tiene las habilidades y la experiencia adecuadas, envíe su solicitud hoy mismo. You will own backup, data protection, and regulatory compliance activities, working with MSPs to ensure audit-ready outcomes. The role requires 5-10 years of experience in backup and data protection, English and Spanish proficiency, and a strong focus on quality and continuous improvement in a regulated environment. xqziphu Permanent, full-time position. #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 Assurance Specialist like you. • 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., • Define the cybersecurity annual audit plan., • Execute information security audits across the different companies within the Grifols Group worldwide., • Execution and oversight of information security controls to ensure SOX compliance., • Support for internal and external IT audits for legal compliance or information security best practice certifications (ENS, ISO 27001 and others)., • Oversee managed services., • Promote a cybersecurity culture across the entire company., • Collaborate with other cybersecurity areas to enhance the organization’s security posture. 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 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., • Leadership skills and the 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. 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. 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, • Location: SPAIN: España: Parets del Valles:((cust_building)) Information about Grifols is available at Grifols is an equal opportunity employer. #J-18808-Ljbffr