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AreyoureadytobuildandleadanintegratedS&OPprocessacrossaninternationalfoodbusiness?GoodLifeFoodsislookingforaSeniorGroupS&OPManagerwhocanconnectcommercialambitions,operationalcapabilitiesandfinancialprioritiesintoonereliableplan. Yourrole AsSeniorGroupS&OPManager,youwilldevelopandimplementagroup-wideS&OPstrategy,governancemodelandoperatingrhythmacross14factoriesandsixcommercialareas. Yourgoalistocreateasingle,financiallyalignedplanthatbalancesdemand,productioncapacity,inventory,servicelevelsandprofitability.Thisisbothatransformationandleadershiprole.YouwilldesignthefutureS&OPorganisation,strengthenprocessesandtools,andensureconsistentadoptionacrosscountriesandfunctions.YouwillleadaninternationalteamofeightDemandPlanners,SupplyPlannersandanS&OPToolsSpecialist,basedinGranollers(Spain). YouwillreportdirectlytotheChiefSupplyChainOfficer. Yourresponsibilities: Developandimplementacentralised,group-wideS&OPstrategyandgovernancemodel. Establishclearroles,responsibilities,decisionrightsandKPIsacrosscentralandlocalteams. Leadtheend-to-endS&OPcycle,includingdemand,supply,inventoryandcapacityplanning. ChairkeymonthlyS&OPmeetingsandpreparedecisionsforExecutiveBoardlevel. Improveforecastaccuracy,supply-planreliability,servicelevelsandstockhealth. ConnectSales,Manufacturing,SupplyChain,Finance,LogisticsandInnovationaroundoneintegratedplan. Developeffectiveplanningprocesses,dataanalyticsandsupportingITtools. Lead,coachanddeveloptheinternationalS&OPteam. Drivechangeandembedconsistentwaysofworkingthroughouttheorganisation. Yourprofile: Abachelor’sormaster’sdegreeinSupplyChainManagement,Logistics,BusinessAdministration,Economicsorarelatedfield. Atleast10yearsofrelevantexperienceinS&OP,demandplanningorsupplychainplanning,preferablywithinFMCGorfoodmanufacturing. Provenexperiencebuildingorsignificantlyimprovinganend-to-endS&OPprocess. Strongleadershipexperiencewithinaninternationalandmultidisciplinaryenvironment. Asolidunderstandingofbothdemandandsupplyplanning,includingtheirfinancialimpact. StronganalyticalcapabilitiesandexperienceinERPandplanningsystems,ExcelandPowerBI. Theabilitytoinfluenceseniorstakeholdersandturncomplexinformationintocleardecisions. Native-levelSpanishandprofessionalfluencyinEnglish;knowledgeofDutchisanadvantage. WillingnesstotravelregularlytoourlocationsacrossEurope. Whatweoffer: Ahigh-impactleadershippositionattheheartofGoodLifeFoods’internationaloperations.YouwillhavethemandatetoshapeourfutureS&OPorganisation,buildcapabilitiesandcreatelastingimprovementsacrosstheentiregroup. AtGoodLife Foods webelieveincreatingaworkplacewhereeveryonecangrow,contribute,andfeelvalued.Wepromoteequalopportunities,diversity,andinclusioninalltheirforms,fosteringanenvironmentofrespectandcollaboration. #J-18808-Ljbffr

We're Hiring | Regulatory Affairs Specialist – Barcelona / ValenciaEMEA Pharma Business UnitAt Brenntag, the global market leader in chemicals and ingredients distribution, we're looking for a Regulatory Affairs Specialist to join our team in Barcelona o Valencia.If you're passionate about regulatory compliance, enjoy working in an international environment, and want to make an impact by supporting regulatory excellence across the business, we'd love to hear from you.Role OverviewAs a key member of the Pharma team, you will support the EMEA division on all regulatory, quality, compliance, legal, and product stewardship topics related to the supply of a large portfolio of raw materials into the pharmaceutical industry. ¿Es este su próximo empleo? Descúbralo leyendo la descripción completa a continuación y no dude en enviar su candidatura. Your primary responsibility is to provide accurate, timely, and audit‑ready documentation to pharmaceutical customers and to support regulatory deliverables for bespoke product projects.The role is primarily office‑based, with occasional travel required for supplier meetings, customer visits, audits, or internal workshops.You will collaborate closely with commercial, supply chain, QHSE, and supplier partners to ensure that all materials supplied meet applicable pharmaceutical regulations and industry standards.Key ResponsibilitiesCustomer Documentation & Regulatory SupportPrepare, review, and issue technical and regulatory documentation required by pharmaceutical customers, including:Quality & Technical AgreementsSupply Chain StatementsRegulatory QuestionnairesCompliance Statements (e.g., TSE/BSE, GMO, allergens, nitrosamines, residual solvents, elemental impurities)Ensure all documentation is accurate, consistent and aligned with applicable frameworks (i.e. relevant pharmacopoeia, IPEC Guidelines, EU GDP and GMP guidelines.Information Gathering & Supplier EngagementSource regulatory, quality, and technical information internally and from suppliers to fulfil customer requests.Evaluate supplier documentation for completeness, compliance, and suitability for pharmaceutical use.Customer Request ManagementLog, track, and report customer documentation requests using defined KPIs.Support continuous improvement by identifying trends, gaps, and opportunities to streamline documentation processes.Support for Customer Value Added Service ProjectsLead and manage regulatory deliverables for customer-specific projects.Coordinate regulatory assessments, supplier data collection, and compliance documentation for new product introductions or customised specifications.Support change control evaluations and customer notifications.Regulatory Compliance & Standards ImplementationWork with QHSE and supply chain teams to ensure compliance with applicable standards (IPEC GMP/GDP, EXCiPACT, GDP, and other regulatory frameworks).Support implementation of new regulatory requirements and internal standards across the business unit.Cross-Functional CollaborationPartner with commercial and value-added services teams to provide regulatory expertise for customer projects and commercial initiatives.Contribute to global Pharma Regulatory team projects, harmonisation efforts, and continuous improvement activities.Training & Knowledge SharingDeliver training to commercial, supply chain, and internal teams on regulatory topics relevant to supply of materials into the pharmaceutical industry.Act as a subject matter expert for documentation, compliance, and regulatory expectations.Additional ResponsibilitiesPerform any other tasks within capability to support the commercial, regulatory, and compliance success of the Pharma business unit.Your ProfileQualifications & ExperienceDegree in a life science discipline (chemistry, biochemistry, pharmaceutical sciences) or equivalent relevant experience.Strong knowledge of pharmaceutical industry requirements for APIs, excipients, biopharma materials, and traditional pharma raw materials.Understanding of European National Competent Authority requirements for distribution of APIs, excipients, and raw materials.Skills & CompetenciesFluent in English and Spanish (spoken and written).Strong written communication skills with the ability to produce clear, accurate, and compliant documentation.Excellent collaboration skills with the ability to work proactively across all levels and functions.Ability to interpret regulations, resolve compliance issues, and respond to complex regulatory queries.High attention to detail and strong organisational skills.Willingness to undertake occasional travel for customer meetings, supplier visits, audits, or internal workshops. What we offer: The opportunity to join a global industry leader. An international, collaborative, and dynamic work environment. Continuous learning and career development opportunities. The chance to contribute to meaningful projects that make a real impact.Interested in joining us, or know someone who might be a great fit? We'd love to hear from you! Feel free to apply or share this opportunity with your network.Brenntag provides equal employment opportunities to qualified applicants and employees of all backgrounds and identities to create a workplace where difference is valued because it forms a resilient and more innovative organization. We do not discriminate on the basis of age, disability, gender identity, sexual orientation, ethnicity, race, religion or belief, parental and family status, or any other protected characteristic. xsgfvud We welcome applications from women, men and non-binary candidates of all ethnicities and socio-economic backgrounds.Brenntag TA TeamSummaryLocation: Massalfassar,Spain; Granollers,SpainType: Full time

Kärcher is a leading German multinational company specializing in cleaning solutions. It stands out in the market thanks to its maximum performance, innovation, and quality. Currently, the company employs over 15,000 people and has a presence in 70 different countries. We continue to grow and improve thanks to the effort, commitment, and dedication of every single person who is part of this great team. Do you want to be a part of the Kärcher world? Now is your opportunity! We are looking for a Project Manager to join our technical team in Granollers. This role will plan, coordinate, and ensure the successful execution of optimization and continuous improvement projects assigned by the Kärcher Spain Technical Service Management. • Assigned Project Management: Directly responsible for the practical implementation of projects (e.g., the launch of OneView)., • Resource Coordination: Organize the necessary resources (technical staff, materials, training) to execute the project, maintaining fluid communication among all internal stakeholders., • Measurement and Monitoring: Actively monitor the progress of the implementation, reporting deviations and proposing immediate corrective actions to ensure the project stays on course., • Analysis and Data: Collect and analyze performance metrics (e.g., repair time, spare part usage) to detect bottlenecks and opportunities for improvement at the workshop level., • Continuous Technical Training: Always stay informed and technically trained regarding the Kärcher product from a technical perspective., • Bachelor's Degree in Industrial Engineering, • Desirable +2 years of demonstrable experience in Project Management., • Fluency in English The opportunity to work for a company with a highly prestigious and market-leading brand in a stable position, alongside a team that maintains an excellent working environment and prioritizes teamwork and collaboration. • 100% subsidized private medical insurance., • Employee discount on brand products., • 1 remote work day per week (after the 6-month onboarding period). Do you think you are a good fit? Are you looking for a WOW career path at Kärcher? Apply now and build a cleaner world with us. We are looking forward to meeting you! Together towards a Cleaner World At Kärcher Spain, we are an employer committed to equal opportunities. We seek to attract, develop, and retain the most talented people within a diverse team. We do not discriminate on the grounds of race, color, religion or belief, sex, sexual orientation, identity... #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

BOLD in Spain seeks a Senior Aerodynamics Surface Design Engineer to bridge aerodynamic theory and practical CAD work. You'll collaborate with Aerodynamicists, CFD Analysts, and Manufacturing to translate concepts into detailed CATIA models and prototypes for wind tunnel testing. The role emphasizes cross‑functional teamwork, rigorous design reviews, and strict FIA compliance, with a focus on wings, diffusers, sidepods, and other surfaces. #J-18808-Ljbffr

Merck Group in Spain (Catalunya) seeks a Senior AI/ML Platform Engineer and Technical Lead to build and evolve our AI/ML platform powering enterprise capabilities. Ideal candidates have 8+ years in software/platform engineering, 2+ years in production LLM ops, and strong cloud-native experience acro

BOLD is committed to shaping the future of high-performance mobility from Formula 1 to aviation and marine. In our mission to deliver innovative and impactful products in the mobility sector, we are building the company whilst working with clients in exciting engineering and manufacturing challenges. As a Supplier Quality Engineer, you will liaise with all our current and future suppliers. You will validate any new parts or suppliers against production and customer requirements as well as our quality standards. You will manage supplier nonconformities based on root cause analysis in order to avoid recurrence. • Evaluate and validate new suppliers to be part of BOLD's supplier panel., • Analyze and evaluate special customer-relevant quality requirements., • Provide input and liaise with suppliers during the RFI and RFQ stages of the acquisition phase., • Analyze and implement requirements for purchased parts in new developments and technical changes., • Manage supplier PPAP and purchased part related APQP., • Supplier Quality Management from acquisition phase to SOP and during production., • Perform Supplier audits and assist engineering and procurement teams from the quality point of view., • Product and process validation for new components at supplier site -, • Initiate and follow through to completion any supplier NCR., • Travel up to 60% to suppliers (mainly in Spain)., • 5+ years of experience as Supplier Quality Engineer., • Bachelor's degree (or higher) in Electric, Electronic or Industrial Engineering, or equivalent professional work experience., • Experience with Automotive and/or Aerospace standards at production level with IATF16949, AS9100 certification., • Deep knowledge and experience in the use of core tools (problem solving, APQP, PPAP, FMEA, 8D, etc.)., • Driver's license and own vehicle., • Expertise in electric and/or electronic components., • Experience with battery packs., • Understanding the testing requirements and validating battery products at a high level., • Auditor VDA 6.3., • Competitive compensation., • Flexible compensation, • Health insurance., • Kindergarten., • Regular events and team building activities. BOLD is an equal opportunity company. We believe in a merit and competence culture where the best ideas thrive regardless of age, disability, race, religion, or belief, gender, sexual orientation, marital status, or family circumstances. #J-18808-Ljbffr

Masterdata Application SpecialistApplylocations: Granollers Officetime type: Full timeposted on: Posted Yesterdayjob requisition id: JR ## 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

Merck Healthcare in Spain (Catalonia) is seeking an Agentic AI Platform Architect to design, implement, and operate a cloud-native backend platform that enables autonomous AI agents. You will write production code, build pipelines, deploy services, and guide a team across the globe. You will own the platform architecture, work with EKS, Terraform, Helm, Argo CD, and GitOps, ensuring security, scalability, and operability. Strong AWS experience and IaC, plus GenAI familiarity, are essential. #J-18808-Ljbffr

Lubrizol Corporation in Spain seeks a Quality Control Manager to lead quality control and quality assurance activities, ensuring robust laboratory practices and compliance across manufacturing processes. You will supervise analytical method development, calibration, and investigations of non-conformities, while coaching the team and collaborating with Operations, R&D, and external partners to drive continuous improvement. #J-18808-Ljbffr

Evonik in Spain is seeking a senior project manager to lead cross‑functional chemistry and nanotechnology initiatives. You will coordinate applied innovation, regulatory, engineering and manufacturing teams to ensure on‑time, on‑budget delivery of complex projects. You’ll drive risk management, reporting to senior leadership, and foster international collaboration in a hybrid work environment that supports professional growth within a global science and engineering company. #J-18808-Ljbffr

Jobtailor in Spain seeks a Senior Management Accountant to lead budgeting, forecasting and financial reporting for the site and group.You will drive cost efficiency, support investment appraisal, and develop KPI analytics with Hyperion/Essbase experience.Candidates with ACA/ACCA/CIMA qualifications

Work Your Magic with us! Ready to explore, break barriers, and discover more? We know you’ve got big plans – so do we! Our colleagues across the globe love innovating with science and technology to enrich people’s lives with our solutions in Healthcare, Life Science, and Electronics. Sea uno de los primeros solicitantes, lea la descripción completa del puesto a continuación y luego envíe su candidatura para que sea considerada. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That's why we are always looking for curious minds that see themselves imagining the unimaginable with us. Your Role: At the heart of our global supply chain strategy, this role offers you the opportunity to shape how we source, qualify, and partner with key suppliers — driving measurable impact on supply security, financial performance, and sustainability across our operations within the region of EMEA.As Sourcing Manager, you will lead the end-to-end strategic sourcing process for key suppliers, translating category strategies into actionable plans that directly support our business objectives. Working closely with Category Managers, you will identify opportunities, negotiate favorable terms, qualify suppliers, and build long-term partnerships that fuel growth and innovation. You will be accountable for supplier identification, performance management, and issue resolution, ensuring compliant, reliable, and high-quality outcomes at every stage.You will develop, implement, and champion sourcing strategies aligned with industrial and commercial objectives, integrating quality and risk management considerations throughout. Balancing agility with discipline, you will deliver results at pace without compromising on standards. Drawing on your understanding of manufacturing processes and Good Manufacturing Practice requirements, you will continuously seek opportunities to reduce total cost of ownership while maintaining high levels of supplier performance.You will build trusted relationships with cross-functional teams and senior stakeholders, analyze market trends, evaluate alternatives, and actively contribute to supplier diversification and supply chain resilience. This position is based in Mollet del Vallès, Spain, and requires up to 15% business travel.Who You AreMaster's degree in Business Administration, Supply Management, Supply Chain, Procurement, or Life Sciences, or equivalent experience, engineering or technical background is of great advantageMinimum of 5 years of experience in Strategic Sourcing, Category Management, or Procurement within the Life Sciences industry, with strong expertise in strategic supplier management, sourcing strategy development, and supplier relationship management; or a minimum of 5 years of experience in Supply Chain, Supplier Performance Management, or Operations, with proven expertise in supplier governance, performance reviews, continuous improvement, and supply assurance.Experience within a multinational company in the Life Sciences, Pharmaceutical, or Medical Devices sectors, ideally in a matrixed and international environment.Proven ability to manage the full sourcing process end-to-end, including supplier identification, negotiations, qualification, and performance management.Excellent negotiation, communication, and stakeholder management skills, with the ability to influence across all organizational levels.Demonstrated experience leading cross-functional initiatives involving multiple stakeholders and functions.Strong analytical and problem-solving capabilities, enabling data-driven decision-making in complex situations.Proficiency with Microsoft Office applications and experience with ERP systems such as SAP, Oracle, or equivalent; project management knowledge is an advantage.Fluent in French and English, both written and spoken; Spanish is considered an asset.What we offer: We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We believe that this variety drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress! xsgfvud Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

Work Your Magic with us! Ready to explore, break barriers, and discover more? We know you’ve got big plans – so do we! Our colleagues across the globe love innovating with science and technology to enrich people’s lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That's why we are always looking for curious minds that see themselves imagining the unimaginable with us. Your Role: At the heart of our global supply chain strategy, this role offers you the opportunity to shape how we source, qualify, and partner with key suppliers — driving measurable impact on supply security, financial performance, and sustainability across our operations within the region of EMEA. As Sourcing Manager, you will lead the end-to-end strategic sourcing process for key suppliers, translating category strategies into actionable plans that directly support our business objectives. Working closely with Category Managers, you will identify opportunities, negotiate favorable terms, qualify suppliers, and build long-term partnerships that fuel growth and innovation. You will be accountable for supplier identification, performance management, and issue resolution, ensuring compliant, reliable, and high-quality outcomes at every stage. You will develop, implement, and champion sourcing strategies aligned with industrial and commercial objectives, integrating quality and risk management considerations throughout. Balancing agility with discipline, you will deliver results at pace without compromising on standards. Drawing on your understanding of manufacturing processes and Good Manufacturing Practice requirements, you will continuously seek opportunities to reduce total cost of ownership while maintaining high levels of supplier performance. You will build trusted relationships with cross-functional teams and senior stakeholders, analyze market trends, evaluate alternatives, and actively contribute to supplier diversification and supply chain resilience. This position is based in Mollet del Vallès, Spain, and requires up to 15% business travel. • Master's degree in Business Administration, Supply Management, Supply Chain, Procurement, or Life Sciences, or equivalent experience, engineering or technical background is of great advantage, • Minimum of 5 years of experience in Strategic Sourcing, Category Management, or Procurement within the Life Sciences industry, with strong expertise in strategic supplier management, sourcing strategy development, and supplier relationship management; or a minimum of 5 years of experience in Supply Chain, Supplier Performance Management, or Operations, with proven expertise in supplier governance, performance reviews, continuous improvement, and supply assurance., • Experience within a multinational company in the Life Sciences, Pharmaceutical, or Medical Devices sectors, ideally in a matrixed and international environment., • Proven ability to manage the full sourcing process end-to-end, including supplier identification, negotiations, qualification, and performance management., • Excellent negotiation, communication, and stakeholder management skills, with the ability to influence across all organizational levels., • Demonstrated experience leading cross-functional initiatives involving multiple stakeholders and functions., • Strong analytical and problem-solving capabilities, enabling data-driven decision-making in complex situations., • Proficiency with Microsoft Office applications and experience with ERP systems such as SAP, Oracle, or equivalent; project management knowledge is an advantage., • Fluent in French and English, both written and spoken; Spanish is considered an asset. What we offer: We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We believe that this variety drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress! #J-18808-Ljbffr

table.MiTabla { max-width: 1020px;}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.Solicitar este puesto es sencillo. Desplácese hacia abajo y haga clic en "Solicitar" para ser considerado para esta posición.We are leaders in plasma-derived medicines and transfusion medicine and develop, produce and market innovative medicines, solutions and services in more than 110 countries and regions.We believe that diversity adds value to our business, our teams, and our culture.We are committed to equal employment opportunities, fostering an inclusive environment where diversity makes us outstanding.Help us lead one of the world’s largest pharmaceutical companies.We are a world leader in plasma-derived medicines with a presence in more than 100 countries, and a growing global team of over 20.000 people.That’s why we need a IT Systems Eneingeer like you.MissionThe IT Systems Engineer within ICS Plasma serves a pivotal role in sustaining and advancing the technology landscape that supports plasma donor centers.This role is accountable for maintaining the reliability, performance, and compliance of the digital technology services and infrastructure that are essential to operating plasma donor centers, ensuring stable operations, minimizing disruptions, and supporting safe, efficient, and compliant collection activities.What your responsibilities will beDomain Management & Strategic AlignmentOversee the digital technology landscape for plasma donor centers and ensure alignment with enterprise architecture and security.Translate plasma operational needs into IT requirements and review infrastructure and integration standards.Contribute to long‑term roadmaps for plasma technology and infrastructure.Project Coordination & DeliveryCoordinate IT activities for plasma projects from planning through deployment.Align project requirements, timelines, and deliverables across plasma operations, CoE, MSP, and internal IT.Support readiness activities, risk management and successful execution of plasma initiatives.Service Delivery, Change & Operational ExcellenceManage day‑to‑day service performance, stability, and availability of plasma technologies.Coordinate change, release, and deployment activities with the CoE and MSP.Monitor service KPIs, support issue resolution, and ensure effective incident and escalation handling.Vendor, Partner & Stakeholder CoordinationServe as the primary interface between plasma operations, the CoE, the MSP, and internal IT.Ensure vendors meet SLAs and operational commitments and validate MSP changes for production safety.Facilitate requirements, communication, and governance activities.Teamwork, Knowledge Management & CultureMaintain documentation, standards, and knowledge assets aligned with CoE frameworks.Contribute to knowledge sharing and collaboration across teams and partners. Who you areTo perform this job successfully, an individual must be able to perform each essential duty satisfactorily.The requirements listed below are representative of the knowledge, skills, education, and/or ability required.Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions).Technical Skills:Bachelor’s degree in computer science, telecommunications, or a related field.Advanced English and Spanish communication skills (spoken and written).Minimum of 5 years of experience in plasma infrastructure environments, including BECS systems, donor center infrastructure, and integrations with apheresis devices.Solid understanding of plasma-center technologies, IT frontend and backend infrastructure, networking, communication protocols, and monitoring practices.Knowledge of security and compliance practices, including secure policies, identity controls, and regulatory requirements.Experience working within ITSM frameworks (incident, change, release) and multi-vendor delivery models (CoE, MSP).Soft SkillsStrong communication and stakeholder‑management skills across business, IT, and vendor partners. Strong relationship‑building skills to establish trust and effective collaboration across stakeholders.High level of organization, prioritization, and execution discipline in a fast‑moving environment.Problem-solving mindset with the ability to navigate ambiguity and support decision-making.Ability to coordinate multiple initiatives and stakeholders simultaneously.Ability to work independently and collaboratively within cross-functional teams.What we offerIt is a brilliant opportunity for you, Grifols is fully aware that its employees are one of its major assets.We are committed to maintaining an atmosphere that encourages all our employees to develop their professional careers in an excellent working environment. Information about Grifols is available at If you are interested in joining our company and you have what it takes for such an exciting position, then don’t hesitate to apply! We look forward to receiving your application! We believe in diverse talent and want to remove any barriers that may hinder your participation.If you require any adjustments in our selection process, please do not hesitate to inform us when applying.We are here to help.Grifols is an equal opportunity employer. xsgfvud Flexibility for U Program: Hybrid ModelFlexible schedule: Monday-Thursday 7-10 to 16-19h and Friday 8-15h (with the same flexible start time).Benefits packageContract of Employment: Permanent positionLocation: SPAIN : España : Parets del Valles:[[cust_building]]Learn more about Grifols#LI-Hybrid#LI-ER1

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

A leading healthcare company in Spain is seeking a qualified professional to support production and warehouse operations by enhancing procedures and implementing digital solutions. This role demands a minimum of 5 years of experience in industrial environments and strong skills in data analysis, process improvement, and project management. The candidate should hold a university degree in Industrial Engineering or similar, with experience in automation projects such as RPA. A flexible work schedule and one day of remote work are included. #J-18808-Ljbffr

GoodLife Foods is seeking a Senior Group S&OP Manager to develop and implement a group-wide S&OP strategy, governance model and operating rhythm across 14 factories and six commercial areas. You will lead an international team and report to the Chief Supply Chain Officer from Granollers, Spain. The role balances demand, production capacity, inventory and profitability to deliver a single, financially aligned plan. #J-18808-Ljbffr

Merck Group in Spain and Italy seeks an Investment Project Sourcing Manager within Technical Sourcing to lead end-to-end sourcing for complex technical investment projects across three global sectors, spanning architecture, engineering, construction, and lab equipment. You’ll align internal stakeholders with suppliers to optimize cost, quality, and delivery in a fast-moving, international setting. Fluency in Spanish, Italian, and English, 5+ years in multinational procurement or engineering, and #J-18808-Ljbffr

Work Your Magic with us! Ready to explore, break barriers, and discover more? We know you’ve got big plans – so do we! Our colleagues across the globe love innovating with science and technology to enrich people’s lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That's why we are always looking for curious minds that see themselves imagining the unimaginable with us. United As One for Patients, our purpose in Healthcare is to help create, improve and prolong lives. We develop medicines, intelligent devices and innovative technologies in therapeutic areas such as Oncology, Neurology and Fertility. Our teams work together across 6 continents with passion and relentless curiosity in order to help patients at every stage of life. Joining our Healthcare team is becoming part of a diverse, inclusive and flexible working culture, presenting great opportunities for personal development and career advancement across the globe. Clinical trials are at the heart of bringing new therapies to patients — and the decisions made in early study design have a lasting impact on their success. As Solution Lead for the Study Design Platform, you will own the end-to-end delivery and continuous evolution of a next‑generation Software as a Service platform that enables smarter, data‑driven decisions in clinical study planning, protocol authoring, and scenario‑based operational feasibility analysis. You will join the Digital, Data & IT (DDIT) R&D team within our Healthcare sector, working at the intersection of clinical operations, digital innovation, and enterprise IT. During the implementation phase, you will act as the critical bridge between R&D business stakeholders, the IT team, and the software vendor. You will lead solution design activities, translate complex business requirements into clear functional specifications and process flows, support User Acceptance Testing (UAT), facilitate alignment workshops, and drive change management and user onboarding to ensure a successful platform rollout. Beyond go‑live, you will take ownership of lifecycle management: prioritizing enhancements, supporting releases, monitoring solution performance, and ensuring sustainable adoption and business value realization. Working across a global matrix organization, you will collaborate closely with R&D users, IT partners, and the software provider — and may also contribute your analytical expertise to broader digital R&D initiatives in the clinical trial space. This position is based in Spain, preferably Barcelona or Madrid, but other locations in Spain may also be considered. • You hold a Master's degree in life sciences, computer science, or a related field, or bring equivalent professional experience., • You have 5 or more years of experience as an IT Solution Lead, Application Lead, or in a comparable role within the healthcare or life sciences industry., • You bring in-depth knowledge of clinical trial processes, including protocol design, operational planning (country and site selection), and study conduct., • You have a proven track record of translating complex business needs into functional specifications and communicating effectively with both technical and non-technical stakeholders., • You have hands‑on experience contributing to IT solution delivery in regulated environments, with a solid understanding of software development lifecycles and computerized system validation (CSV) in line with GxP requirements., • You are familiar with clinical trial systems and clinical trial data standards, and can navigate a global matrix organization to build trusted relationships across R&D, IT, and external partners., • You are fluent in English (written and spoken) and bring a proactive, solution‑oriented mindset — you take ownership, anticipate challenges, and drive issues through to resolution. We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We believe that this variety drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress! Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity! #J-18808-Ljbffr

table.MiTabla { max-width: 1020px;}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.Se pueden requerir diversas habilidades interpersonales y experiencia para el siguiente puesto. Por favor, asegúrese de consultar la descripción a continuación con atención.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.What your responsibilities will beSupport 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.Who you areTo perform this job successfully, an individual must be able to perform each essential duty satisfactorily.The requirements listed below are representative of the knowledge, skills, education, and/or ability required.Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions).Technical Skills: Bachelor's degree in computer science, Systems Engineering, Cybersecurity, or a related field. Advanced English and Spanish language skills (spoken and written) Minimum of 5 years of experience in cybersecurity roles. Deep knowledge of cybersecurity frameworks (NIST, ISO27k, ENS, SOX, Cyber Essentials). Cybersecurity certifications (CISA, ISO27k Lead Auditor, CISM, CISSP, CRISC, etc.) are highly valued. Soft Skills: 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. What we offerIt is a brilliant opportunity for you, Grifols is fully aware that its employees are one of its major assets.We are committed to maintaining an atmosphere that encourages all our employees to develop their professional careers in an excellent working environment. Information about Grifols is available at If you are interested in joining our company and you have what it takes for such an exciting position, then don’t hesitate to apply! We look forward to receiving your application! We believe in diverse talent and want to remove any barriers that may hinder your participation.If you require any adjustments in our selection process, please do not hesitate to inform us when applying.We are here to help.Grifols is an equal opportunity employer. xsgfvud Flexibility for U Program: Hybrid ModelFlexible schedule: Monday-Thursday 7-10 to 16-19h and Friday 8-15h (with the same flexible start time).Benifits packageContract of Employment: Permanent positionLocation: SPAIN : España : Parets del Valles:[[cust_building]]Learn more about Grifols#LI-Hybrid#LI-ER1

Mollet del Valles (Barcelona), Spain Hybrid Working Global tech company founded in 2011 Our mission is to shape the future through technology The role As an Antenna / RF Design Engineer, you will be responsible for the end-to-end design, simulation, and validation of antennas and RF front-end systems. You will play a key role in ensuring the technical and functional feasibility of our products, working closely with a multidisciplinary team to guarantee that all technical specifications, quality standards, design to cost focus and project timelines are strictly met. Key responsabilities Antennas and RF Circuit Design: Take part in the design and development of antennas and RF front-end architectures from MHz to mmW application: front ends, LNA, RF filters including Power Amplifiers (PAs), Low Noise Amplifiers (LNAs), filters, mixers, combiners, antennas among others, following the IDS (Idneo Development System) Electromagnetic Simulation: Conduct RF and EM simulations using softwares like ADS, Microwave Office, HFSS, Feko. Laboratory Testing & Validation: Define and execute test plans for RF / HW verification in the RF laboratory during each development loop. Utilize advanced instrumentation including Vector Network Analyzers (VNAs), Spectrum Analyzers, radio generators and perform antenna measurements in anechoic chambers. PCB Layout: Oversee and guide the PCB layout routing for RF circuits, ensuring strict RF guidelines for signal integrity, grounding, impedance and isolation for all RF traces. Design Optimization: Analyze and optimize RF designs to maximize performance while keeping focus on cost. Lifecycle & Industrialization: Collaborate with the manufacturing and industrialization teams to ensure a successful transition of prototypes into mass production. Technical Documentation: Manage product modifications and generate comprehensive technical documentation, design reports, and test procedures throughout the development cycle. (*) The described functions are only the most representative for this position; therefore, they should not be understood as all the inherent functions related to this job position. Experience & Technical Knowledge: At least 2+ years of solid experience designing Antennas and/or RF front ends (PAs, LNAs, filters, mixers, combiners) Education: Bachelor’s, Master’s, or Ph.D. degree in Telecommunications Engineering, Electronics Engineering, or a closely related field with a specialization in RF/Microwave engineering. Software Tools: Proven experience in EDA simulation software (e.g., AWR, ADS) and EM simulation tools (e.g., FEKO, HFSS). Languages: Advanced level of English (written and spoken) Availability: Willingness to travel occasionally for project collaboration and testing campaigns. Highly Valued Prior professional experience in RF design for Automotive, Aerospace or Defense applications (e.g., satellite communications, radar systems, or compliance with military / automotive standards). Hands-on experience in Antenna design, integration, and tuning. Solid understanding of wireless communication technologies and standards (LTE, 5G, UWB, Bluetooth, Wi-Fi, GNSS, Broadcasting, V2X, Radar, ….) We are engineering the future #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

Mollet del Valles (Barcelona), Spain Hybrid Working Global tech company founded in 2011 Our mission is to shape the future through technology Design, develop, and test embedded C/C++ firmware and real-time software architectures for cutting-edge automotive, medtech, and industrial devices, ensuring full functional safety compliance, high code quality, and seamless integration in alignment with Idneo standards and product excellence goals. Design the detailed architecture and embedded software modules in C and C++ programming languages for microcontrollers and microprocessors (ARM Cortex-M/A, TriCore, etc.). Develop low-level drivers (MCAL/HAL), hardware abstraction layers, and communication protocol stacks (CAN, CAN-FD, LIN, Ethernet, SPI, I2C, UART, BLE, Wi-Fi). Implement application logic running on Real-Time Operating Systems (RTOS such as FreeRTOS, Zephyr, SafeRTOS) or Bare-Metal architectures. Configure and integrate industry-standard software stacks (e.g., AUTOSAR Classic/Adaptive) when applicable according to project needs. Execute debugging on the target board utilizing laboratory equipment such as oscilloscopes, logic analyzers, JTAG/SWD debuggers, emulators, and CAN network tools (Vector CANoe/CANalyzer, PeakCAN). Actively cooperate with the Hardware and Validation teams to troubleshoot anomalies and support the commissioning of new prototypes. Apply secure and maintainable coding guidelines following the MISRA C / MISRA C++ standards and static/dynamic code analysis rules. Ensure strict compliance with software quality processes under ASPICE (Automotive SPICE) or ISO 9001/13485 models. Actively participate in the implementation of functional safety standards depending on the industry (ISO 26262 for automotive, IEC 62304 for medical devices, or IEC 61508 for industrial). Perform unit testing, integration testing, and code coverage analysis (using tools like VectorCAST, Cantata, or GoogleTest) to guarantee software reliability. Manage versions properly using control tools (Git, SVN) and track tasks/bugs effectively through issue tracking systems (Jira, Confluence). Document software design specifications, architecture, and test plans in accordance with the project's delivery phases. Participate in peer-to-peer Code Reviews to ensure consistency, high quality, and adherence to development best practices across the team. (*) The described functions are only the most representative for this position; therefore, they should not be understood as all the inherent functions related to this job position. University Degree in Electronic Engineering, Telecommunications or Computer Science Minimum of 3 years of proven experience in embedded software development using C/C++. Technical Knowledge: Solid programming skills in C/C++ Experience working with RTOS and Bare-metal architectures. Knowledge of communication buses (CAN, SPI, I2C, UART) Proficiency in Git, Jira, GCC/IAR/Keil compilers, and Vector CANoe/CANalyzer. Fluent English (minimum B2 level, C1 highly desirable), both written and spoken. The most important is attitude, ownership and problem solving abilities when a new technology comes up. We are engineering the future #J-18808-Ljbffr

AreyoureadytobuildandleadanintegratedS&OPprocessacrossaninternationalfoodbusiness?GoodLifeFoodsislookingforaSeniorGroupS&OPManagerwhocanconnectcommercialambitions,operationalcapabilitiesandfinancialprioritiesintoonereliableplan. AsSeniorGroupS&OPManager,youwilldevelopandimplementagroup-wideS&OPstrategy,governancemodelandoperatingrhythmacross14factoriesandsixcommercialareas. Yourgoalistocreateasingle,financiallyalignedplanthatbalancesdemand,productioncapacity,inventory,servicelevelsandprofitability.Thisisbothatransformationandleadershiprole.YouwilldesignthefutureS&OPorganisation,strengthenprocessesandtools,andensureconsistentadoptionacrosscountriesandfunctions.YouwillleadaninternationalteamofeightDemandPlanners,SupplyPlannersandanS&OPToolsSpecialist,basedinGranollers(Spain). YouwillreportdirectlytotheChiefSupplyChainOfficer. • Developandimplementacentralised,group-wideS&OPstrategyandgovernancemodel., • Establishclearroles,responsibilities,decisionrightsandKPIsacrosscentralandlocalteams., • Leadtheend-to-endS&OPcycle,includingdemand,supply,inventoryandcapacityplanning., • ChairkeymonthlyS&OPmeetingsandpreparedecisionsforExecutiveBoardlevel., • Improveforecastaccuracy,supply-planreliability,servicelevelsandstockhealth., • ConnectSales,Manufacturing,SupplyChain,Finance,LogisticsandInnovationaroundoneintegratedplan., • Developeffectiveplanningprocesses,dataanalyticsandsupportingITtools., • Lead,coachanddeveloptheinternationalS&OPteam., • Drivechangeandembedconsistentwaysofworkingthroughouttheorganisation., • Abachelor’sormaster’sdegreeinSupplyChainManagement,Logistics,BusinessAdministration,Economicsorarelatedfield., • Atleast10yearsofrelevantexperienceinS&OP,demandplanningorsupplychainplanning,preferablywithinFMCGorfoodmanufacturing., • Provenexperiencebuildingorsignificantlyimprovinganend-to-endS&OPprocess., • Strongleadershipexperiencewithinaninternationalandmultidisciplinaryenvironment., • Asolidunderstandingofbothdemandandsupplyplanning,includingtheirfinancialimpact., • StronganalyticalcapabilitiesandexperienceinERPandplanningsystems,ExcelandPowerBI., • Theabilitytoinfluenceseniorstakeholdersandturncomplexinformationintocleardecisions., • Native-levelSpanishandprofessionalfluencyinEnglish;knowledgeofDutchisanadvantage., • WillingnesstotravelregularlytoourlocationsacrossEurope. Ahigh-impactleadershippositionattheheartofGoodLifeFoods’internationaloperations.YouwillhavethemandatetoshapeourfutureS&OPorganisation,buildcapabilitiesandcreatelastingimprovementsacrosstheentiregroup. AtGoodLife Foods webelieveincreatingaworkplacewhereeveryonecangrow,contribute,andfeelvalued.Wepromoteequalopportunities,diversity,andinclusioninalltheirforms,fosteringanenvironmentofrespectandcollaboration. Webelieveintalent,diversity,andgrowingtogether.Ifyouareaproactiveandcommittedprofessionalwhoiseagertobepartofaconstantlyevolvingcompany,wewouldlovetohearfromyou! #J-18808-Ljbffr

Work Your Magic with us! Ready to explore, break barriers, and discover more? We know youve got big plans - so do we! Our colleagues across the globe love innovating with science and technology to enrich people's lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. Thats why we are always looking for curious minds that see themselves imagining the unimaginable with us. Investment Projects are where strategy meets execution, and this role sits right at that intersection. As an Investment Project Sourcing Manager within Technical Sourcing, you will lead end-to-end sourcing execution for complex technical investment projects across three global business sectors, primarily across sites in Spain and Italy with the flexibility to support projects across the broader EMEA region. Your work directly shapes the quality, cost, and delivery outcomes of strategic investments spanning architecture and engineering services, construction, and the installation of laboratory, infrastructure, and production equipment. You will serve as the critical link between internal stakeholders and the external supply base, translating business needs into sourcing strategies that maximize value through cost savings, risk reduction, and supplier performance. From early project involvement and procurement planning through supplier qualification, negotiation, contract management, and performance follow-up, you will own the full sourcing lifecycle with a focus on continuous improvement and cross-functional collaboration. Working across a diverse, international environment, you will build and maintain strong supplier relationships, resolve commercial disputes, and contribute to the evolution of category strategies by staying ahead of market trends and supply chain dynamics. If you bring a structured mindset, strong negotiation skills, and the drive to deliver results in a fast-moving global organization, this role offers real impact across the business. • Bachelor's degree in Business Administration, Engineering, or a related field, or an equivalent combination of education and relevant experience., • Minimum 5 years of experience in procurement or engineering roles within multinational companies, with a preference for investment project sourcing in the chemical, pharmaceutical, or life science industry., • Demonstrated ability to lead end-to-end sourcing processes including procurement planning, supplier qualification, competitive bidding, negotiation, and contract management for complex technical investment projects., • Strong project management skills with the ability to work effectively in cross-functional and geographically diverse teams, managing multiple priorities in parallel., • Experience identifying, managing, and mitigating supply chain risks, with the ability to anticipate market trends and translate them into actionable sourcing strategies., • Excellent communication and stakeholder management skills, with the ability to engage and align across different seniority levels and functions in a complex global organization., • Fluency in Spanish, Italian, and English (written and spoken) is required., • Willingness and ability to travel up to 30%, primarily within EMEA. We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We believe that this variety drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress! #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. Overview 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. Responsibilities 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. Qualifications 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

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. Position part of the procurement team focused in improving and re-evaluating the procurement activities, optimizing the organization's supply base and increasing its overall value proposition. Focused on the total cost of ownership, this position also considers product quality, customer needs, organizational goals and market conditions as an essential part of the procurement process. Actions are driven by a rigorous and collaborative approach, based on fact analysis and market intelligence, following the Strategic Sourcing Framework. Key Accountabilities Ensure the availability of raw material, both; short and long term, through regular monitorization of critical raw materials and a continuous analysis of risks to define risk mitigation actions. Regular reporting and analysis of the main purchasing KPIs, such as • OTIF, • Expired material, • Obsolescence, • Monthly stock report Main responsible for the price negotiation and the management of materials savings initiatives in line with profit plan and overall business objectives. Negotiation of supply agreements as needed to support the critical business needs: • Monitorization and renewal of existing Supply and Quality Agreements, • Ensures Supply and Quality Agreements are positioned appropriately before business is initiated with new vendors Improve the value-to-price relationship with suppliers following Strategic Sourcing Framework • Quarterly communication of raw material forecast, • Follow up calls with all the vendors, • Annual visit plan with key vendors, • Attendance to main exhibitions Supports Supplier Quality department to accomplish the goals defined in supplier quality system • Annual risk analysis of raw materials and definition of key vendors list, • Analysis of vendors performance Ensure the maximum quality of the purchased products Follow up of technical problems with Supplier Quality, Technical Support, R&Dor Manufacturing departments Contribute to keep updated the material and supplier database Strategic activities: • Development and implementation of the Strategic Sourcing strategy, • Develop key performance measures for chosen suppliers and negotiate on multiple variables to award longer-term strategic contracts that result in significant cost reduction and improved service levels, • Monitor current category market conditions, technology roadmaps and identify supply/demand challenges & opportunities., • Identification of new suppliers in collaboration with R&D during the development of new products, • Identification of potential risk and definition of mitigation action plans, • Involvement in the total cost analysis for new product developments Internal Networking To be determined based on department needs, to include interactions such as: • Supplier Quality: Control change notification management and vendor's complaints support, • Manufacturing: Support in solving technical issues related to raw material or packaging performance, • R&D: Support in the development of new products and identifying suppliers for new assays, • Supply Chain Department; Including warehouse and planning, • Sales and Marketing: Benchmarking of vendors, • Quality Control Minimum Knowledge & Experience required for the position Education: • Required:Bachelor'sdegree(Diplomatura)inthebiologicalorrelatedsciences.Degreemaybesubstitutedbyrelevantskillsandworkexperience, • Valuable:Anyadditionaldegreehigherthantherequired Experience: Minknowledge • Software:FluencyinOfficeTools(Excel&Word),ValuableadvancedknowledgeinSAP, • Language:FluencyinSpanishorCatalan.AdvancedknowledgeofEnglish(reading,writingandspeaking) AdditionalSkills/Knowledge: • Software:FluencyinOfficeTools(Excel&Word),ValuableAdvancedknowledgeinSAP, • Language:FluencyinSpanishorCatalan.MediumknowledgeofEnglishreading,writingandspeaking) Skills & Capabilities The ideal candidate for this position will exhibit the following skills and competencies: • Management of decisions under pressure., • Methodical and well-organized person., • Teamwork., • Ability to express information clearly and concisely to the staff, ensuring their understanding., • Ability to apply a systematic approach and constant control, follow-up and verification of the results., • Ability to collaborate, participate and coordinate actively with working groups., • Good reporting and analysis capabilities., • Reflects values of Werfen in the quality of work and working relationship. Travel Requirements 5% of the time Werfen appreciates and values diversity. We are an Equal Opportunity/Affirmative Action Employer M/F/D/V. #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. At Grifols SA, we are looking for a Real Estate Manager, reporting directly to the company's Senior Real Estate Manager, responsible for managing all properties at both the national and international levels. • You will manage and oversee the real estate property portfolio, including cost negotiations, contract monitoring, and maintaining up-to-date information in the database., • You will negotiate lease contracts and renegotiations., • You will identify real estate opportunities., • You will foster strong relationships between internal stakeholders, Landlords & Brokers., • You will oversee the administration and management of real estate assets., • You will be responsible for the strategic planning of the property portfolio to ensure company objectives are met., • You will optimize space utilization., • You will monitor properties across international subsidiaries., • You have a Bachelor’s Degree., • You have 5-10 years of experience in a similar position within Corporate Real Estate and/or Real Estate Consulting., • You have an advanced English and Spanish level., • You are a proactive and goal-oriented individual with a collaborative mindset., • You are highly organized, capable of multitasking and provide effective follow-up., • You have availability to travel internationally. 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. Hybrid Model Monday-Thursday 7-10 to 16-19h and Friday 8-15h (with the same flexible start time) Contract of Employment: Permanent position Location: Parets del Vallés Location: SPAIN : España : Parets del Valles:((cust_building)) Learn more about Grifols #J-18808-Ljbffr

table.MiTabla { max-width: 1020px;}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.La siguiente información tiene como objetivo proporcionar a los posibles candidatos una mejor comprensión de los requisitos para este puesto.We are leaders in plasma-derived medicines and transfusion medicine and develop, produce and market innovative medicines, solutions and services in more than 110 countries and regions.We believe that diversity adds value to our business, our teams, and our culture.We are committed to equal employment opportunities, fostering an inclusive environment where diversity makes us outstanding.What your responsibilities will beMaster Data Management & Golden RecordsHelp define, implement and evolve Master Data Management capabilities across key enterprise domains such as customer, supplier, product, material, donor, employee or location data.Support the definition of golden record rules, matching, merging, survivorship, hierarchy management and data synchronization patterns across systems.Collaborate with Data Engineering and application teams to integrate master data with ERP, CRM, analytics platforms, data lakes, data warehouses and downstream reporting solutions.Contribute to the design and operation of MDM workflows for data creation, change, approval, exception handling, de-duplication and lifecycle management.Data Governance, Quality & ComplianceSupport the implementation of data governance policies, standards, ownership, stewardship responsibilities, decision rights and escalation mechanisms.Make data standards available for Advance Analytics consumption: data AI readiness.Define and monitor data quality rules, KPIs, thresholds and remediation processes to improve accuracy, completeness, consistency, timeliness and trust.Work with business data owners and stewards to identify root causes of data issues and drive sustainable corrective actions at the source.Ensure data initiatives consider security, privacy, auditability, regulatory expectations and compliance requirements in a highly regulated environment.Experience building and maintaining data catalogs for lake house environments, ensuring that high-value analytical variables and datasets are documented, contextualized and reusable for Advanced Analytics, AI use cases and MDM initiativesExperience defining business ontologies, semantic models and controlled vocabularies to improve data consistency, interoperability, discoverability and AI-readiness across enterprise data domains.Knowledge of AI governance concepts, data governance for AI, responsible AI principles, privacy-by-design, data risk assessment and emerging regulatory expectations such as the EU AI Act.Enterprise Data Transformation & Operating ModelSupport the execution of the company data transformation roadmap, helping move the organization toward governed, trusted and reusable enterprise data capabilities.Translate strategic data objectives into actionable initiatives, deliverables, milestones and adoption plans across IT and business domains.Contribute to the definition and implementation of a hybrid / federated data operating model, balancing central standards with business domain execution.Drive coordination across Data Office, IT teams, Business stakeholders, external partners and data owners to ensure consistent execution and accountability.Metadata, Catalog, Lineage & DocumentationPromote the adoption of business glossaries, data dictionaries, metadata standards and cataloging practices to improve discoverability and common understanding of data.Support the documentation of critical data flows, lineage, transformations, ownership, usage, controls and dependencies across source systems and analytical platforms.Help establish reusable templates, standards and ways of working for documenting data architecture, MDM domains, data products, data marketplace publishing practices and governance processes.Who you areTo perform this job successfully, an individual must be able to perform each essential duty satisfactorily.The requirements listed below are representative of the knowledge, skills, education, and/or ability required.Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions).Bachelor’s degree in Computer Science, Data Science, Information Systems, Engineering or a related field.Minimum of 5 years of experience in data management, master data management, data governance, data quality, data architecture or enterprise data transformation initiatives.Experience with MDM concepts and platforms such as Reltio, SAP MDG, Informatica MDM, Semarchy, Profisee or similar solutions, data lakes and data catalog tools.Knowledge of data governance frameworks, data ownership, stewardship, data quality management, metadata management, cataloging and lineage.Experience with Microsoft Purview.Understanding of data integration patterns, APIs, ETL/ELT, data pipelines, ERP integration and analytical data platforms.Advanced English language skills, both spoken and written.Strong ownership mindset, accountability and ability to drive topics from ambiguity to execution.Excellent stakeholder management and communication skills, with the ability to influence without direct authority across business and IT teams.Collaboration.Ability to facilitate workshops, align different perspectives and convert complex data topics into clear decisions and practical actions.Comfortable operating in a matrixed, global organization and coordinating with teams across functions, geographies and time zones.Pragmatic, structured and delivery-oriented, with the ability to balance governance discipline with business agility.Continuous improvement mindset and willingness to build internal capability through knowledge transfer, documentation and enablement.What we offerIt is a brilliant opportunity for you, Grifols is fully aware that its employees are one of its major assets.We are committed to maintaining an atmosphere that encourages all our employees to develop their professional careers in an excellent working environment. Information about Grifols is available at If you are interested in joining our company and you have what it takes for such an exciting position, then don’t hesitate to apply! We look forward to receiving your application! We believe in diverse talent and want to remove any barriers that may hinder your participation.If you require any adjustments in our selection process, please do not hesitate to inform us when applying.We are here to help.Grifols is an equal opportunity employer. Flexibility for U Program: Hybrid Model.Benefits packageContract of Employment: Permanent position. xsgfvud Location: Parets del Vallès.#LI-Hybrid#LI-ER1Location: SPAIN : España : Parets del Valles:[[cust_building]]Learn more about Grifols

Country Manager Spain & Portugal Business Support Full-time Higher Professional Education Granollers, SpainApply now## Ready to lead strategic growth, inspire a diverse team, and shape the future of our business?An exciting opportunity awaits as we seek a dedicated Country Manager for Spain & Portugal to spearhead our presence in the livestock industry. In this role, you’ll lead strategic initiatives, manage a dynamic team, and contribute to our global organization’s growth, all while fostering sustainability in our business practices.## What are you going to do?As the Country Manager Spain & Portugal, you will be responsible for overseeing and driving the company’s commercial objectives, growth, and market presence within Spain & Portugal. The role will encompass a wide range of responsibilities, including but not limited to:Key Responsibilities: Strategic Leadership: Develop and implement a strategic business plan to achieve the company’s objectives in the livestock industry, ensuring sustainable growth and profitability Team Management: Lead and inspire according to the company’s style a diverse team of professionals, providing guidance, coaching, and support to achieve operational excellence Market Analysis: Continuously monitor market trends, competition, and customer needs to identify new opportunities and adapt strategies accordingly Sales and Marketing: Oversee the sales and marketing efforts to promote our livestock services and products, expand our customer base, and achieve revenue targets Financial Management: Manage the financial aspects of the business, including budgeting, forecasting, and cost control, to ensure sustainable profitability Customer Relationship Management: Build and maintain strong relationships with key customers and distributors, to enhance the company’s reputation and market presence Reporting: Provide regular reports to the corporate office on the country’s performance, market insights, and strategic recommendations## What we are looking for? Bachelor’s degree in business, agriculture (Livestock), or a related field Proven experience in sales leadership in a senior management role within the livestock industry Excellent communication, negotiation, and interpersonal skills Proven track record of successfully leading and managing cross-functional teams Strong understanding of livestock production practices Results-oriented with a track record of meeting sales targets Ability to analyze data and market trends to make informed decisions Excellent strategic thinking and problem-solving abilities Besides Spanish, fluent in at least English language (written and spoken) High grade of the Spanish livestock market will be appreciated## What we offer? Competitive salary and performance-based bonuses Opportunity to lead a dynamic team and make a significant impact in the livestock industry Career development and growth prospects within a global organization* A commitment to sustainability business practicesWhat makes us special?At The Schippers Group, we believe that prevention is better than cure. We are committed to leading the livestock sector in preventing diseases and ensuring animal welfare. With over 500 colleagues worldwide and a brand-new headquarters in Hapert, Netherlands, we have a global reach and local dedication. If you want to be part of a company with impact and a passion for positive change, you’ve come to the right place!Martijn MichielsHR Business Partner Send Whatsapp messagePrint jobApply now #J-18808-Ljbffr

Job Description Are You Ready to Make It Happen at Mondelēz International? Join our Mission to Lead the Future of Snacking.As an organization we are committed to developing the next generation of Makers and Bakers.Joining us at an early career stage in our fast paced and ever changing environment w

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GoodLife Foods is seeking a Senior Group S&OP Manager to connect demand, supply, and finance across 14 factories and six commercial areas in Europe. You will develop a group-wide S&OP strategy, governance, and operating rhythm, based in Granollers (Spain), leading an international team of eight planners and an S&OP Tools Specialist, reporting to the Chief Supply Chain Officer. The role focuses on transforming processes, embedding best practices and driving long-term profitability while ensuring #J-18808-Ljbffr

Are you ready to build and lead an integrated S&OP process across an international food business? GoodLife Foods is looking for a Senior Group S&OP Manager who can connect commercial ambitions, operational capabilities and financial priorities into one reliable plan. As Senior Group S&OP Manager, you will develop and implement a group-wide S&OP strategy, governance model and operating rhythm across 14 factories and six commercial areas. Your goal is to create a single, financially aligned plan that balances demand, production capacity, inventory, service levels and profitability. This is both a transformation and leadership role. You will design the future S&OP organisation, strengthen processes and tools, and ensure consistent adoption across countries and functions. You will lead an international team of eight Demand Planners, Supply Planners and an S&OP Tools Specialist, based in Granollers (Spain). You will report directly to the Chief Supply Chain Officer. • Develop and implement a centralised, group-wide S&OP strategy and governance model., • Establish clear roles, responsibilities, decision rights and KPIs across central and local teams., • Lead the end-to-end S&OP cycle, including demand, supply, inventory and capacity planning., • Chair key monthly S&OP meetings and prepare decisions for Executive Board level., • Improve forecast accuracy, supply-plan reliability, service levels and stock health., • Connect Sales, Manufacturing, Supply Chain, Finance, Logistics and Innovation around one integrated plan., • Develop effective planning processes, data analytics and supporting IT tools., • Lead, coach and develop the international S&OP team., • Drive change and embed consistent ways of working throughout the organisation., • A bachelor’s or master’s degree in Supply Chain Management, Logistics, Business Administration, Economics or a related field., • At least 10 years of relevant experience in S&OP, demand planning or supply chain planning, preferably within FMCG or food manufacturing., • Proven experience building or significantly improving an end-to-end S&OP process., • Strong leadership experience within an international and multidisciplinary environment., • A solid understanding of both demand and supply planning, including their financial impact., • Strong analytical capabilities and experience in ERP and planning systems, Excel and Power BI., • The ability to influence senior stakeholders and turn complex information into clear decisions., • Native-level Spanish and professional fluency in English; knowledge of Dutch is an advantage., • Willingness to travel regularly to our locations across Europe. A high-impact leadership position at the heart of GoodLife Foods' international operations. You will have the mandate to shape our future S&OP organisation, build capabilities and create lasting improvements across the entire group. We look forward to hearing from you! At GoodLife Foods we would love to hear from you! At GoodLife Foods we believe that great food brings people together and makes every moment more enjoyable. We promote equal opportunities, diversity, and inclusion in all their forms, fostering an environment of respect and collaboration. We believe in talent, diversity, and growing together. 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

Jobtailor in Spain seeks a highly capable QA/Regulatory Affairs professional to lead product release activities, ensuring ISO13485/IVDR/MDSAP compliance and effective document control.You will coordinate with Notified Bodies, labs and health authorities, manage quality notifications, and drive conti

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. 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. Here is the clean, formatted text in English, ready to copy and paste: 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. Werfen Companies. Customers. Regulatory agencies. Suppliers. 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 has the discretion of substituting relevant work experience for a degree and/or making exceptions to the years of experience requirement) Management of decisions under pressure. Methodical and well-organized approach. Teamwork. Time management skills. 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. Up to 5% of time. #J-18808-Ljbffr

Benefits packageContract of Employment: Permanent positionLocation: SPAIN : España : Parets del Valles:[[cust_building]]Learn more about Grifols#LI-ER1. MiTabla { max-width: 1020px;}Would you like to join an international team working to improve the future of healthcare? Do you want to enhance th

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. The People Partner role has been designed to strengthen the Immunoassay & Digital Solutions People Function model by owning Employee Journey, Employer Branding, People Analytics, Digital HR, Culture & Engagement and continuous improvement initiatives, enabling People Business Partners to focus on strategic business partnership while accelerating the team's digital, AI and data-driven capabilities. Reporting to the VP People Function Immunoassay and Digital Solutions, the People Partner Digital & Analytics is responsible for leading and continuously improving key People Function initiatives across the employee lifecycle, acting as a strategic partner for employee experience, employer branding, talent initiatives, culture, engagement, people data quality, digitalization and analytics. The role is designed to strengthen the People Function operating model by increasing execution capacity, improving process scalability, enabling data-driven decision-making, and supporting the evolution of the team toward more digital, analytical and AI-enabled ways of working. The People Partner works closely with the People Business Partners to deliver impactful people initiatives, strengthen the employee journey, improve digital adoption and ensure operational excellence across People processes. The position plays a critical role in helping the People Function become increasingly employee-centric, scalable and data-driven. • Own and continuously improve the employee journey across key lifecycle moments., • Maintain and continuously improve employee-facing materials, employee manuals and internal People resources., • Drive employee experience improvements through employee feedback, process reviews and data analysis., • Support employee engagement, culture and wellbeing initiatives across the site., • Design and deploy employer branding initiatives across digital and offline channels., • Develop and manage strategic partnerships with universities, business schools and external talent communities to expand brand visibility., • Lead the design and evolution of internship, graduate and early talent programs, • Support Talent Acquisition activities in partnership with People Business Partners, hiring managers and external providers., • Contribute to enhancing candidate and hiring manager experience throughout recruitment processes., • Monitor employer branding and talent attraction metrics, translating insights into actions that improve talent visibility, candidate engagement and hiring outcomes., • Maintain and continuously improve People KPI dashboards and reporting tools., • Ensure People data accuracy, consistency and quality across systems and reports., • Translate People data into actionable insights supporting business and People decisions., • Monitor workforce, talent, employee journey and engagement metrics., • Support workforce planning, talent discussions and organizational reviews through data-driven insights., • Ensure audit readiness and compliance of People data and documentation., • Act as a digital champion and change agent within the People Function, promoting a culture of innovation, experimentation and continuous improvement., • Lead the identification, evaluation and implementation of digital solutions to enhance People processes, employee experience and operational efficiency., • Promote AI-enabled ways of working and support the responsible adoption of Generative AI tools across the People Function., • Identify automation opportunities that eliminate manual activities, improve data quality and reduce administrative workload., • Act as key user, superuser and internal advisor for HRIS, digital People platforms and employee experience technologies., • Partner with People Operations, IT and Global People teams to optimize workflows, system integrations, reporting capabilities and user adoption., • Drive digital literacy initiatives and support the development of digital, data and AI capabilities across local People teams., • Explore emerging HR technologies, market trends and best practices, translating innovation opportunities into practical People solutions., • Support the evolution of the People Function's digital, analytics and AI capabilities, contributing to the transformation of HR into a data-driven and technology-enabled function., • Coordinate, lead and contribute cross-functional People Function initiatives and projects related to culture, engagement, wellbeing and CSR, ensuring alignment with People strategy and business priorities. Support deployment of global People initiatives locally, ensuring effective adoption and communication., • Partner with People Business Partners to identify opportunities to improve employee and manager experience., • Contribute to team benchmarking, innovation and capability-building initiatives in digitalization and AI., • Review, simplify and continuously improve People processes., • Maintain job descriptions, process documentation and People Function materials., • Ensure compliance with quality, audit and governance requirements., • Improve role clarity, ownership and handoffs across People Business Partners, People Operations, People Partner and Administration Support roles., • Identify opportunities to transfer, simplify or automate low-value activities. The People Partner works closely with: • VP People Function., • People Business Partners., • People Operations teams., • Managers and employees across the site., • Global People Function teams., • Universities, business schools, RPO partners and external talent providers., • Bachelor's Degree in Psychology, Human Resources, Business Administration, Labor Relations, Data Analytics, Information Systems, Digital Business, Digital Transformation or related disciplines., • Master's Degree or postgraduate studies in Human Resources, Digital Transformation, People Analytics, Business Analytics, HR Technology or Artificial Intelligence applied to business are desirable., • Additional certifications in People Analytics, Digital HR, Artificial Intelligence, Data Visualization, Automation, Digital Transformation, Agile Methodologies or Project Management will be considered a plus., • 3-6 years of experience in Human Resources, People Partner, Employee Experience, Employer Branding, Talent Acquisition, People Analytics or related People Function roles., • Experience in multinational environments is highly valued., • Experience within highly digital environments such as technology hubs is highly valued., • Experience in sectors such as pharmaceutical, biotechnology, diagnostics, healthcare or similar industries is desirable., • Proven capability to design and implement employee lifecycle initiatives and talent programs., • Experience working with People KPIs, dashboards and HR systems., • People Analytics & Data Visualization: advanced capability in Excel and Power BI to manage People KPIs, build dashboards, interpret workforce trends and translate data into clear, actionable insights., • Generative AI & Digital Productivity: confident and responsible use of Microsoft Copilot and other AI-enabled tools to improve analysis, content creation, knowledge management and day-to-day People Function effectiveness., • HRIS & Digital People Platforms: strong working knowledge of SAP or comparable HRIS platforms, including data structures, reporting, employee lifecycle processes and digital talent solutions., • Process Automation & Low-Code Tools: ability to identify automation opportunities and use tools such as Power Automate and Power Apps to streamline workflows, approvals, notifications and recurring People processes., • Digital Employee Experience & Engagement: ability to leverage digital collaboration, listening and engagement platforms to improve employee journeys, adoption, communication and the overall manager and employee experience., • Fluent Spanish and advanced English (minimum B2). The ideal candidate will demonstrate: • Strong business and people orientation., • Employee experience and customer-centric mindset., • Digital curiosity and AI learning agility., • Strong analytical and data storytelling capabilities., • Influence and relationship-building skills., • Excellent planning and organizational skills., • Continuous improvement mindset., • Adaptability, flexibility and learning agility., • High degree of ownership and accountability., • Commitment to Werfen Values. Travel is not expected to be recurring; however, availability to travel when required is expected. #J-18808-Ljbffr

Work Your Magic with us! Ready to explore, break barriers, and discover more? We know you’ve got big plans – so do we! Our colleagues across the globe love innovating with science and technology to enrich people’s lives with our solutions in Healthcare, Life Science, and Electronics. Obtenga más información sobre este puesto leyendo los detalles a continuación y luego envíe su solicitud para ser considerado. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That's why we are always looking for curious minds that see themselves imagining the unimaginable with us. Your Role: Investment Projects are where strategy meets execution, and this role sits right at that intersection. As an Investment Project Sourcing Manager within Technical Sourcing, you will lead end-to-end sourcing execution for complex technical investment projects across three global business sectors, primarily across sites in Spain and Italy with the flexibility to support projects across the broader EMEA region. Your work directly shapes the quality, cost, and delivery outcomes of strategic investments spanning architecture and engineering services, construction, and the installation of laboratory, infrastructure, and production equipment. You will serve as the critical link between internal stakeholders and the external supply base, translating business needs into sourcing strategies that maximize value through cost savings, risk reduction, and supplier performance. From early project involvement and procurement planning through supplier qualification, negotiation, contract management, and performance follow-up, you will own the full sourcing lifecycle with a focus on continuous improvement and cross-functional collaboration. Working across a diverse, international environment, you will build and maintain strong supplier relationships, resolve commercial disputes, and contribute to the evolution of category strategies by staying ahead of market trends and supply chain dynamics. If you bring a structured mindset, strong negotiation skills, and the drive to deliver results in a fast-moving global organization, this role offers real impact across the business.Who You AreBachelor's degree in Business Administration, Engineering, or a related field, or an equivalent combination of education and relevant experience.Minimum 5 years of experience in procurement or engineering roles within multinational companies, with a preference for investment project sourcing in the chemical, pharmaceutical, or life science industry.Demonstrated ability to lead end-to-end sourcing processes including procurement planning, supplier qualification, competitive bidding, negotiation, and contract management for complex technical investment projects.Strong project management skills with the ability to work effectively in cross-functional and geographically diverse teams, managing multiple priorities in parallel.Experience identifying, managing, and mitigating supply chain risks, with the ability to anticipate market trends and translate them into actionable sourcing strategies.Excellent communication and stakeholder management skills, with the ability to engage and align across different seniority levels and functions in a complex global organization.Fluency in Spanish, Italian, and English (written and spoken) is required.Willingness and ability to travel up to 30%, primarily within EMEA.What we offer: We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We believe that this variety drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress! xsgfvud Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

Work Your Magic with us! Ready to explore, break barriers, and discover more? We know you’ve got big plans – so do we! Our colleagues across the globe love innovating with science and technology to enrich people’s lives with our solutions in Healthcare, Life Science, and Electronics. Si le interesa solicitar este empleo, por favor, asegúrese de cumplir los siguientes requisitos que se enumeran a continuación. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That's why we are always looking for curious minds that see themselves imagining the unimaginable with us. Your RoleData and AI are reshaping the way global organizations operate, and this role sits at the heart of that transformation. As a Software Engineer within our Enabling Functions Data Office, you will design and deliver high-impact data and AI solutions that power smarter ways of working across the organization. You will be part of a collaborative, internationally distributed team of engineers and architects, working within a Product-Oriented Delivery model to bring Analytics, AI, and data products to life at scale.In this role, you will:Design, build, and maintain scalable applications, data pipelines, and platform components that translate complex business requirements from enabling functions such as HR, procurement, and legal into future-ready technical solutions.Develop robust applications and interfaces that replace manual processes with seamless, intuitive user experiences.Take ownership of data platforms, ensuring cost efficiency, governance, security, and compliance across the full data lifecycle.Partner closely with stakeholders across your delivery pod to understand business needs and shape the technical direction of solutions.Shape the future of data engineering within Enabling Functions, leveraging platforms such as Snowflake, AWS, and Palantir Foundry.Contribute to a growing Spain-based hub within a global team, with the opportunity to work on diverse and high-visibility AI use cases spanning automation, carbon footprint analytics, procurement intelligence, and more.Who You Are You bring several years of proven expertise and experience in software engineering, including application design, development, and delivery within enterprise environments, with a strong foundation in writing clean, maintainable, and secure code.You are proficient in development platforms and languages such as Python and Spark, and you apply modern engineering practices including version control, CI/CD pipelines, and automated testing as a matter of course.You have hands-on experience with data platform technologies such as Palantir Foundry, Snowflake, and PySpark, and you are confident designing and delivering end-to-end data pipelines.You have a solid understanding of data pipeline architecture, data governance, data lineage, privacy and security controls, and compliance standards in enterprise-scale environments.You communicate complex technical concepts clearly and confidently to non-technical stakeholders, and you are comfortable translating business requirements into actionable technical solutions.Familiarity with AI workflows, MLOps, AI safety and guardrails, or CI/CD for AI components is a plusYou hold a university degree or equivalent qualification in a relevant technical or engineering discipline.You are comfortable working in a distributed, international team environment and are open to occasional travel within Europe.Strong communication skills in English ; proficiency in German is a plus.What we offer: We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We believe that this variety drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress! xsgfvud Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

What makes you a good fit Location: Montornès del Vallès, Barcelona, Spain. Some perks of joining HenkelFlexible work scheme with flexible hours, hybrid work model, and work from anywhere policy for up to 30 days per yearDiverse national and international growth opportunitiesGlobal wellbeing stand

En Adecco queremos conocerte! Una importante empresa del sector alimentación, busca incorporar en su planta ubicada en Parets del Vallés, operarios/as para el sector de alimentación. Trabajarás en una empresa líder del sector alimentación, Mondelez España, como operario/a en diferentes puest

Actitud proactiva para identificar y eliminar riesgos en el área de trabajo. Formación y capacitación interna para el desarrollo de habilidades técnicas y de liderazgo. Además, se espera que colabore activamente en la detección y eliminación de riesgos, garantizando un ambiente de trabajo seg

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