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Te interesa conducir para una empresa con camiones nuevos y trabajo estable? Entonces aplica hoy mismo a .Transportamos exclusivamente para una empresa global del sector de venta por catálogo y comercio electrónico.Actualmente estamos buscando empleados a tiempo completo debido a

Te interesa conducir para una empresa con camiones nuevos y trabajo estable? Entonces aplica hoy mismo a .Transportamos exclusivamente para una empresa global del sector de venta por catálogo y comercio electrónico.Actualmente estamos buscando empleados a tiempo completo debido a

Overview Play a pivotal role in bringing the new ONE Deco vision to life by orchestrating global projects such as product innovation and optimizing operational processes. As a Global Program Manager within ONE Deco, you’ll drive innovation and excellence in product development and operational processes across all brands in the decorative segment. Key Responsibilities Act as portfolio manager for assigned Decorative Segment annual strategic projects. Orchestrate One Deco strategic projects encompassing cross‑brand and cross‑functional elements. Lead and update the One Deco segment product pipeline. Handle Segment Innovation and Sustainability projects, ensuring a powerful, innovative, and sustainable global Deco pipeline (PaintGreen) roll‑out and anchor Segment Product Development governance and operations (ColourGate) Supply to Rethink Innovation and delivery of differentiated solutions. Harmonize segment product management community and follow‑ups. Ensure annual project results and long‑term strategic progress with a focus on innovation, sustainability, and operational excellence initiatives. Qualifications Top‑tier project manager with cross‑functional project experience and a consistent record of success. Broad understanding of company processes and stakeholders; solid knowledge of technical products and operational execution. Global, collaborative attitude with fluency in English and excellent partner and interpersonal skills. Experience coordinating across functions, geographies, and cultures, and ability to take action with flexibility and creativity across many time zones. Strong influencing skills and a global mindset. Ability to work independently and as part of a close‑knit team. Additional Information At Hempel, we are committed to promoting a workplace that celebrates and values unique backgrounds, perspectives, and talents. We provide training and initiatives to support an inclusive culture, ensuring every employee feels respected and empowered to bring their authentic selves to work. Senior Level: Senior Level Interested in applying? Submit your application letter with a CV in English via our recruitment system. #J-18808-Ljbffr

Do you want to join an international team working to improve the future of healthcare? Do you want to improve the lives of millions of people? Grifols is a global healthcare company which, since its foundation in Barcelona in 1909, has been working to improve the health and well‑being of people al

With more than 150 years of industry-leading experience, the businesses of SGS & Co and SGK are uniting to form SGX—a powerful force in innovative packaging production. Building on the legacy of trusted service since 1947 and 1953, SGX will deliver the full suite of packaging graphics, plate and cylinder production, and metal deco services to brand owners, retailers, and printers—all with a focus on reducing complexity, delivering flawless in-market execution, and leveraging global reach to drive consistency and impact at scale.Position Summary-Ever wondered how products make it from an idea to the shelf?We are looking for an Administrative Assistant Intern to support our team. This is a coordination-focused role within the packaging production process, ideal for someone interested in how brands come to life across physical products.This is a hands-on support role focused on practical administrative tasks that help packaging projects run smoothly and on time: tracking shipments, coordinating colour proof deliveries, preparing supporting documentation, and liaising with suppliers.Job Responsibilities-You'll work closely with the Production Manager and Back Office Coordinators and get hands-on experience supporting the team's day-to-day operations, including:- Jump in on day-to-day admin for agency managers: booking travel, helping with events, tracking shipments, and ordering office supplies.- Support packaging projects with the practical stuff that keeps things moving such as documents, coordination, follow-ups, and status tracking.- Help keep proofing and despatching procees efficient by staying in sync with admin teams around the world and making sure information flows smoothly.- Be a go-to contact for suppliers: sharing updates, chasing answers, and keeping requests on track.- Check colour proofs for quality, then organise their preparation and shipment so the right materials arrive at the right time.What This Role Is AboutWe are looking for someone with a strong interest in administration, organisation, coordination, and business support functions. This is not a design or project management role.Requirements-- Currently studying Business Administration, Management, Operations, International Business, Marketing or a related field- You are interest in administrative coordination and operational processes- You are interest in project coordination and how brands/products are delivered to market- Strong organisational skills and attention to detail- You like teamwork and have good interpersonal skills- Rigorous and motivated, you are looking for an instructive internship where you will be untrusted with a wide variety of missions- Spanish and English fluentIdeal ProfileThis internship is especially suitable for students who enjoy structure, organisation, and making sure processes run efficiently — the behind-the-scenes engines that keep business moving.Location & Timeline:- Carrer de Laureà Miró, 143, Esplugas de Llobregat (Barcelona)- 6 months internship, on Full-time basis- Onsite work arrangement- Salary 900€/ month gross- Mission to be filled: ASAP- Job Type: Full-time- EU visa required- University agreement neededThe businesses of SGS & Co and SGK have united to form Propelis, a go-to-market ecosystem that enables marketers to move their brands forward with greater speed, clarity, and confidence. Our broad range of integrated solutions include brand creative, packaging, print solutions, branded environments, and content production. Services are delivered through our family of brands: SGX, Marks, Equator, Collide, and 5Flow. With a combined legacy spanning more than 150 years, Propelis commences operations with 10,000 employees in 30+ countries, nearly $1 billion in annual sales, and a diverse client base of over 2,000 leading companies.

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. Mission The Site Procurement Senior Specialist is responsible for executing site-level procurement activities in alignment with Category Strategies, the Global Procurement Policy, and local regulatory requirements. The role acts as the primary procurement interface for the site, ensuring continuity of operations, cost control, supplier performance, and compliance. The Site Procurement Senior Specialist collaborates closely with site stakeholders, suppliers, Category Management, and Transactional Procurement teams to deliver efficient, compliant, and value-adding procurement outcomes within the defined site-managed scope. What your responsibilities will be Site Procurement Operations & Stakeholder Collaboration Act as the primary procurement interface for site stakeholders (Manufacturing, Quality, Maintenance, H&S, HR, Finance, Administration) Collaborate with Supply Chain Planning and Manufacturing to develop purchasing plans supporting daily, weekly, monthly, and annual operational needs Coordinate with site stakeholders to manage demand planning for critical materials, special delivery requirements, and annual order volumes Sourcing & Contract Management (Local / Site Scope) Execute sourcing activities for site-managed spend in line with applicable Category Strategies and Procurement Policy Support the preparation of RFx, bid analysis, supplier evaluations, and award recommendations Negotiate commercial and contractual terms with local/site-level suppliers within defined scope and approval limits Support contract drafting, negotiation, signature coordination, and renewal management for site-managed suppliers Procure-to-Pay (P2P) & Demand Execution Support resolution of procure-to-pay exceptions Guide and influence requesters in the use of approved procurement tools, catalogues, and sourcing channels D. Supplier Management, Performance & Incident Handling Act as the primary procurement escalation point for site-level supply, quality, service, or commercial incidents Initiate and manage supplier onboarding and qualification processes (SLP) for site-level suppliers Ensure suppliers comply with local homologation, quality, and regulatory requirements Coordinate procurement activities related to site Change Controls Who you are To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skills, education, and/or ability required. Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions). You have proven experience in site-level procurement with a strong understanding of procurement policies, category strategies, and compliance requirements. Demonstrated ability to partner effectively with cross-functional stakeholders (Manufacturing, Quality, Supply Chain, Finance, etc.) to support operational and project needs. Solid experience in sourcing, supplier selection, and contract negotiation, with the ability to deliver value while maintaining compliance and mitigating risk. Analytical mindset with the ability to interpret spend data, track KPIs, and identify cost‑saving opportunities A proactive, solutions‑focused approach with a commitment to continuous improvement and operational excellence What we offer It is a brilliant opportunity for you, Grifols is fully aware that its employees are one of its major assets. We are committed to maintaining an atmosphere that encourages all our employees to develop their professional careers in an excellent working environment. 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 Contract of Employment: Permanent position #J-18808-Ljbffr

Grifols, S.A. is seeking a Firmware Engineer to design, develop, and maintain firmware for analytical instruments, working with microcontrollers and instrument electronics. You will collaborate with hardware and R&D teams, implement firmware, run tests, document processes, and support quality standards in a global healthcare environment. The role requires 3–4 years in firmware, strong C/C++ skills, and experience with Renesas or Xilinx MCUs, E2Studio, and Vivado/Vitis. #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. 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 Are 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. 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

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. Your Role 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. Who You Are 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 Gx P 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. 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! Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity! #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. Your Role: at the heart of clinical data management lies a critical challenge: turning complex, evolving business needs into precise, actionable system requirements. As a Requirements Engineer for Clinical Trial Systems, you will play a pivotal role in shaping the quality and integrity of a global Operational Data Repository programme — directly enabling faster, more reliable clinical trial execution across the organisation. In this role, you will own the review, improvement, and creation of Functional Requirement Specifications, ensuring they are precise, complete, and aligned with both business intent and technical feasibility. You will identify gaps, resolve ambiguities, and simplify complex business rules without losing their essential meaning. Working at the intersection of clinical operations and information technology, you will facilitate structured requirement reviews with cross-functional stakeholders and drive meaningful improvements to documentation standards, traceability, and requirement governance. Your work will directly influence the reliability and scalability of the data platforms that underpin clinical trial operations. Who You Are You bring 5 or more years of experience as a Business Analyst, with a strong track record of delivering high-quality requirement specifications in complex, cross-functional environments. A professional certification such as Certified Business Analysis Professional, PMI Professional in Business Analysis, or International Requirements Engineering Board certification is an advantage. You have 3 or more years of hands-on experience with clinical trial data and processes, giving you a solid understanding of how data flows through clinical operations and what is required to support compliant, audit-ready systems. You are skilled at facilitating requirement workshops and stakeholder reviews, translating diverse perspectives into clear, consistent, and actionable documentation. You have practical experience working with data platforms, system integrations, and application programming interfaces, and you understand the technical constraints that shape feasible requirements. You have worked in regulated environments and are familiar with Good Practice standards applicable to clinical data systems, including the expectations around validation, traceability, and change control. You bring strong analytical skills and a meticulous attention to detail, with the ability to identify inconsistencies, redundancies, and gaps across large sets of requirements. You hold a degree in Information Technology, Life Sciences, Business, or a related field, or bring equivalent professional experience that demonstrates the same depth of knowledge. You demonstrate AI literacy: you understand how artificial intelligence technologies work, their practical applications and limitations, and the ethical considerations around bias, fairness, privacy, and accountability — enabling you to critically assess AI-driven tools and make informed, responsible decisions in your role. 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

Would you like to join an international team working to improve the future of healthcare? Do you want to enhance the lives of millions of people? Grifols is a global healthcare company that since 1909 has been working to improve the health and well-being of people around the world. We are leaders in plasma-derived medicines and transfusion medicine and develop, produce and market innovative medicines, solutions and services in more than 110 countries and regions. We believe that diversity adds value to our business, our teams and our culture. We are committed to equal employment opportunities that foster an inclusive environment. Help us lead one of the world’s largest pharmaceutical companies. We are a world leader in plasma-derived medicines with presence in more than 100 countries, and a growing global team of over 20.000 people. That’s why we need a Production Technicianlike you. Role Mission Transform production processes, focusing your activity on improving productivity, quality, safety, and process costs, while always ensuring compliance with current regulations. What your responsibilities will be Analyze and document quality incidents, develop corrective action proposals, and implement those actions. Participate in the factory's continuous improvement program, attending daily meetings to monitor the relevant processes assigned by the manager. Monitoring process indicators, analyzing and identifying opportunities for improvement, developing proposals for action to the manager, and implementing them according to the manager's guidelines. Performing tasks associated with factory projects, according to established deadlines and costs. You will have three reporting lines: to the factory engineering manager, the production area, and your direct manager. Knowledge and application of work standards (GMP, PNT, INS, BPL, according to defined procedures. Compliance with and monitoring of established quality, safety, hygiene, and environmental standards. Who you are To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skills, education, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions). Bachelor's degree in Industrial, Mechanical, or Process Engineering. Master's degree in Continuous Improvement – Six Sigma (desirable). English level B2. You have 3 years of experience in similar roles leading continuous improvement projects for productive areas. You are a dynamic, proactive person who can carry out projects independently with a sense of responsibility. You are organized and methodical, and you enjoy working in a team. What we offer It is a brilliant opportunity for you, Grifols is fully aware that its employees are one of its major assets. We are committed to maintaining an atmosphere that encourages all our employees to develop their professional careers in an excellent working environment. Information about Grifols is available at If you are interested in joining our company and you have what it takes for such an exciting position, then don’t hesitate to apply! We look forward to receiving your application! We believe in diverse talent and want to remove any barriers that may hinder your participation. If you require any adjustments in our selection process, please do not hesitate to inform us when applying. We are here to help.

SARIA es una empresa global y líder especialista en el reciclaje de residuos animales y vegetales. Como Grupo SARIA, creamos valor para nuestros socios y el medio ambiente al actuar como un proveedor de servicios confiable y fabricante de productos de calidad para las industrias agrícola, energética, de alimentación animal, alimentaria, de catering y farmacéutica. Nuestra amplia cartera de productos y servicios se basa en la transformación de subproductos animales y residuos orgánicos en materias primas de alta calidad para nuevas aplicaciones, conservando los escasos recursos naturales existentes y realizando, mediante nuestro modelo de negocio, una importante contribución a la sostenibilidad ambiental. En SARIA, estamos construyendo una cultura en la que todos puedan sentirse como en casa, con independencia de su género, edad, cultura, orientación sexual, religión y discapacidad. Juntos, tenemos éxito como un equipo global. Queremos fomentar la innovación y capacitar a nuestros equipos para compartir nuevas formas de pensar, aprovechando al máximo el talento diverso. Al mismo tiempo, como empresa familiar, valoramos una mentalidad práctica y queremos que cada empleado crezca y desarrolle al máximo sus habilidades. Es esta combinación la que nos diferencia como empleador y caracteriza la vida en SARIA. En Grupo SARIA garantizamos la igualdad de trato y de oportunidades en todos nuestros procesos de selección. Todas las candidaturas serán valoradas conforme a criterios objetivos relacionados exclusivamente con las competencias, experiencia y aptitudes requeridas para el puesto Nos ilusiona que te conviertas en parte de nuestro equipo y te unas por completo a la aventura que se avecina. Si quieres trabajar con nosotros y formar parte de nuestro equipo como: Senior Procurement Category Management: Logistics, debes saber lo siguiente. Los objetivos de la posición son los siguientes: Desarrollo e implantación de estrategia y gestión de compras con foco en las categorías de Logística (por ej.: subcontrata de transporte, compra de camiones, combustible, neumáticos, etc.) para todas las empresas del Grupo Saria. Liderar el desarrollo e implementación de estrategias de compras específicas para las diferentes categorías asignadas (por ej.: subcontrata de transporte, compra de camiones, combustible, neumáticos, etc.) - Llevar a cabo tareas de sourcing, licitaciones y negociaciones con proveedores de manera independiente y autónoma. - Elaborar estrategias de negociación adecuadas para cada categoría, sector y proyecto, que permitan alcanzar los objetivos de optimización de costes a la vez que promuevan relaciones sostenibles con los proveedores y el desarrollo de estos. - Generar acuerdos marco estratégicos con proveedores, así como llevar a cabo su correcta implementación y seguimiento. - Ser el principal motor y gestor del cambio, tener poder de influencia y estar en constante comunicación con los responsables de logística, directores de planta y responsables de los distintos departamentos a nivel nacional para asesorarlos en las compras y en la búsqueda de potenciales áreas de optimización en el aprovisionamiento. Buscamos profesionales con sólida experiencia mínima de Mínimo 10 años en entorno multinacional corporativo y/o industrial, en el área de Procurement a cargo de diversas categorías de producto. Será muy valorado experiencia específica como Category Management en logística (por ej.: subcontrata de transporte, compra de camiones, combustible, neumáticos, etc.). Título universitario en ingeniería industrial, administración de empresas, Supply Chain o similares Formación y conocimientos adicionales: Muy valorable Master o Post grado en Compras, Supply Chain o Project Management. Experto en Excel para realizar análisis de datos y generación de informes concluyentes. Valorable experiencia con herramientas de BI. Inglés fluido hablado y escrito (C1). Incorporación a multinacional líder en su sector, en un ambiente de trabajo dinámico. Tendrás a tu disposición beneficios como seguro médico, descuentos en servicios y/o productos, Ticket restaurante, guardería y transporte. Uniéndote a nuestro equipo te acompañaremos en tu proceso de aprendizaje y desarrollo. Grupo Saria adopta, en la medida de lo posible, medidas que favorecen la conciliación de la vida laboral, personal y familiar, promoviendo un entorno de trabajo basado en la corresponsabilidad y el bienestar de las personas #J-18808-Ljbffr

Would you like to join an international team working to improve the future of healthcare? Do you want to enhance the lives of millions of people? Grifols is a global healthcare company that since 1909 has been working to improve the health and well-being of people around the world. We are leaders in plasma-derived medicines and transfusion medicine and develop, produce and market innovative medicines, solutions and services in more than 110 countries and regions. We believe that diversity adds value to our business, our teams and our culture. We are committed to equal employment opportunities that foster an inclusive environment. Help us lead one of the world’s largest pharmaceutical companies. We are a world leader in plasma-derived medicines with a presence in more than 100 countries, and a growing global team of over 20 000 people. That’s why we need a Operational Excellence Specialist like you. Role Mission To lead and drive continuous improvement, operational excellence, and project management initiatives, promoting process optimization, waste elimination, standardization of best practices, and enhanced operational performance. The successful candidate will act as a key contributor in the planning, coordination, monitoring, and communication of strategic initiatives, ensuring alignment across all involved functions and facilitating the successful execution of transformation and improvement projects that deliver business value. You will work cross-functionally with Operations, Quality, Engineering, Supply Chain, IT, and other business areas to identify improvement opportunities and develop solutions that increase productivity, quality, efficiency, and internal and external customer satisfaction. What Your Responsibilities Will Be Lead and coordinate Biomat workstreams related to the implementation of the new Plasma Logistics Center (PLC). Plan, organize and monitor project activities, ensuring alignment of timelines, milestones, deliverables, resources and dependencies. Coordinate cross-functional teams and stakeholders, facilitating effective communication and collaboration across the organization. Drive process improvement, standardization, digitalization and Operational Excellence initiatives to enhance operational performance. Monitor project progress, identify risks and issues, and ensure appropriate mitigation and follow-up actions. Prepare and communicate project status updates, KPIs, governance materials and executive reports to support decision-making. Ensure compliance with GxP requirements, quality standards and applicable regulatory expectations throughout the project lifecycle. Support change management and project portfolio initiatives, promoting successful implementation and sustainable adoption of new processes and ways of working. Facilitate collaboration between cross-functional teams and help drive alignment, accountability and execution discipline across the project. Support change management activities to enable successful implementation and adoption of the future processes and ways of working. Manage and/or contribute to other projects within the Biomat project portfolio, as required, ensuring alignment with business priorities, operational excellence standards and quality requirements. Contribute to the development of the Operational Excellence strategy and support broader business transformation initiatives. Who You Are To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skills, education, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions). Bachelor's degree in Engineering, Biotechnology, Life Sciences, Business Administration, or a related field. Advanced level of English, Spanish, both written and spoken. 3 to 5 years of experience in Operational Excellence, Continuous Improvement, PMO, Project Management, Process Excellence, or similar roles in industrial or regulated environments. Advanced proficiency in Microsoft Office and project management tools; knowledge of Power BI, Minitab, Tableau, MS Project, Smartsheet, and similar analytical tools is a plus. Proven experience leading cross-functional projects, process improvement initiatives, and organizational transformation programs. Strong knowledge of Lean, Six Sigma, Continuous Improvement methodologies, and project management principles. Experience in project planning, coordination, governance, risk management, and stakeholder management. Knowledge of GMP/GxP regulated environments is a plus. Lean Six Sigma Green Belt, Project Management, or PMO certifications are a plus. Strong analytical, communication, and problem-solving skills, with the ability to manage multiple priorities and influence stakeholders at different organizational levels. What We Offer It is a brilliant opportunity for you, Grifols is fully aware that its employees are one of its major assets. We are committed to maintaining an atmosphere that encourages all our employees to develop their professional careers in an excellent working environment. Information about Grifols is available at If you are interested in joining our company and you have what it takes for such an exciting position, then don’t hesitate to apply! We look forward to receiving your application! Grifols is an equal opportunity employer. Flexible schedule: Monday-Thursday 8:00h – 17:00h and Friday 8:00 - 15:00h (with the same flexible start time). Benefits Package Contract of Employment: Permanent position. Flexibility for U Program: Remote working. Location: Parets del Vallès. Learn more about Grifols

Mollet del Valles (Barcelona), Spain Hybrid Working Global tech company founded in 2011 Our mission is to shape the future through technology The role We are looking for a highly driven, hands‑on Engineering Project Manager / Lead Mechanical Systems Engineer who thrives at the intersection of complex mechanical design, system architecture, and technical leadership. You won't just be managing from afar; you will get your handsdirty, working directly with the physical product and shaping it from end to end. In this role, you will be the bridge between our customers' needs and our engineering realities. You will oversee the entire product lifecycle—from initial customer conceptualization to industrialization—leading multidisciplinary teams and ensuring the successful delivery of complex, multi‑component machines and systems. Key responsibilities End-to-End System Leadership: Take full ownership of the product lifecycle for complex machines and complete systems, maintaining a holistic vision from initial customer contact and concept definition through to final manufacturing. Hands-on Engineering & Problem Solving: Stay deeply involved with the product. Get on the floor, work with prototypes, troubleshoot complex system interactions, and drive technical solutions firsthand. Customer Facing & Requirements Management: Act as the primary technical point of contact for clients. Translate complex customer needs into robust technical specifications and manage expectations throughout the project milestones. Multidisciplinary Team Leadership: Lead, mentor, and synchronize cross‑functional teams (mechanical, hardware, software, quality, and manufacturing) to ensure seamless system integration and alignment. BOM & System Architecture Management: Oversee and manage complex Bills of Materials (BOMs), ensuring accurate tracking of intricate assemblies, cost optimization, and supply chain alignment. Design & Architecture Oversight: Shift focus from designing individual parts to overseeing the macro‑level mechanical architecture. Guide design teams, conduct rigorous system‑level design reviews, and ensure DFM/DFA principles are met. Risk Analysis: Drive proactive risk analysis (DFMEA/PFMEA at the system level) and manage engineering changes with a clear understanding of their impact on the entire machine. Testing, Validation & Industrialization: Lead system‑level testing, analyze performance data, and partner closely with manufacturing to guarantee a smooth transition into mass production. (*) 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. 8+ years of proven experience in product engineering, specifically dealing with complete, complex products, machines, or electro‑mechanical systems (not just isolated parts). Bachelor’s or Master’s degree in Mechanical Engineering, Systems Engineering, or a related technical field. Proven track record of leading multidisciplinary engineering projects and cross‑functional teams. Hands‑on mentality: strong willingness to interact directly with the physical product, prototypes, and manufacturing processes. Expertise in managing complex BOMs and overseeing system‑level architecture (proficiency in 3 D/2 D CAD tools is expected to review and guide, but the daily focus is on system integration). Experience in customer‑facing roles, with strong communication skills to manage technical discussions and negotiations. English advanced level. We are engineering the future #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. Your Role 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. Who You Are 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. 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! Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity! #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. 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 Are 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 5yearsof 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

¿Te gustaría un equipo internacional que trabaja para mejorar el futuro del sector de la salud? ¿Quieres contribuir a mejorar la vida de millones de personas? Grifols es una compañía global del sector de la salud que desde 1909 mejora la salud y el bienestar de las personas en todo el mundo. Somos líderes en medicamentos hemoderivados y medicina transfusional y desarrollamos, producimos y comercializamos medicamentos, soluciones y servicios innovadores en más de 110 países y regiones.Creemos que la diversidad aporta valor a nuestro negocio, a nuestros equipos y a nuestra cultura. Estamos comprometidos con la igualdad de oportunidades y nuestra misión es ofrecer un entorno inclusivo donde las diferencias sumen a nuestra compañía.En el departamento de Validaciones de Instituto Grifols necesitamos incorporar un/a Técnico/a de Validaciones de equipos y procesos, cuya misión principal consistirá en gestionar y ejecutar los proyectos de validación asignados de acuerdo a la normativa vigente con el objetivo de asegurar la validez de los procesos productivos.Tus responsabilidades seránRealizarás la redacción, revisión y aprobación de protocolos e informes de cualificación.Realizarás la redacción, revisión y aprobación de protocolos e informes de validación.Ejecutarás estudios de cualificación y validación.Actualizarás los protocolos de validación a la normativa vigente.Editarás las desviaciones, seguimiento de CAPAs y valoración de controles de cambios.Quién eresPara realizar este trabajo con éxito, una persona debe ser capaz de llevar a cabo las responsabilidades de manera satisfactoria. Los requisitos enumerados a continuación son representativos de los conocimientos, habilidades, formación y/o capacidad requeridos. Se pueden realizar adaptaciones del puesto para que las personas con diversidad funcional puedan realizar las tareas del puesto.Posees un Grado en Ingeniería Técnica o Superior, Licenciatura en Ciencias de la Salud, siendo valorable Máster en Industria FarmacéuticaTienes experiencia de entre 1 y 3 años trabajando en posición similar.Tu nivel de inglés es avanzado (mínimo B2.2).Dominas el paquete Office y tienes conocimientos a nivel usuario de SAP.Posees disponibilidad para viajar de forma puntual.Lo que ofrecemosFormar parte de Grifols significa la oportunidad de trabajar en un entorno de proyección internacional dónde se promueve la igualdad de oportunidades. Significa la oportunidad de desarrollarte profesionalmente, de disponer de formación continua y de integrarte en un equipo de profesionales en el que la aportación individual de cada uno cuenta. Nuestro compromiso es mantener un entorno que favorezca el desarrollo profesional de nuestros empleados en un buen ambiente de trabajo. El capital humano de Grifols es clave tanto en el desarrollo de las actividades como en el proceso de expansión de la compañía. Creemos en el talento diverso y queremos eliminar cualquier barrera que pueda impedir tu participación. Si necesitas algún ajuste en nuestro proceso de selección, por favor, no dudes en informarnos al aplicar. Estamos aquí para ayudarte.Horario flexible:Lunes-Jueves 7-10 a 16-19h y Viernes 8-15h.Contrato de trabajo:Indefinido.Paquete de beneficios.Flexibility for U Program: 1 día de trabajo remoto a la semana.Ubicación:Parets del Vallès.#J-18808-Ljbffr

Te interesa conducir para una empresa con camiones nuevos y trabajo estable? Entonces aplica hoy mismo a Welvaart Logistics SL.Transportamos exclusivamente para una empresa global del sector de venta por catálogo y comercio electrónico.Actualmente estamos buscando empleados a tiempo completo debid

Te interesa conducir para una empresa con camiones nuevos y trabajo estable? Entonces aplica hoy mismo a Welvaart Logistics SL.Transportamos exclusivamente para una empresa global del sector de venta por catálogo y comercio electrónico.Actualmente estamos buscando empleados a tiempo completo debid

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 plann

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 ro

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Des d’Agrupa Global Talent, busquem incorporar un/a.Director/a d’Infraestructures Sanitàries.En dependència directa de la Gerència, serà la persona responsable de planificar, dirigir i supervisar el conjunt d’infraestructures, instal·lacions, equipaments i serveis associats, garantint-ne

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Merck Group in Spain seeks an experienced IT Project Manager to drive application projects that optimize Supply Chain planning, manufacturing, and logistics.You will lead initiatives across the global application landscape, translating priorities into scope, milestones, budgets, and risk controls, a

Una reconocida marca de moda femenina busca un/a Business Development Manager para liderar la expansión internacional.El candidato ideal tendrá más de 5 años de experiencia en el desarrollo de negocio internacional, habilidades de negociación y un dominio fluido de español e inglés.Ofrecemos

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GoodLife Foods is seeking a Senior Group S&OP Manager to develop and implement a group-wide S&OP strategy across 14 factories and six commercial areas.You will lead an international team and report to the Chief Supply Chain Officer, ensuring a financially aligned plan across demand, supply, inventor

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, Spai

Good Life 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 ei

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Somos un líder mundial en medicamentos derivados del plasma con presencia en más de 100 países y un equipo global en crecimiento de más de 20. Te gustaría unirte a un equipo internacional que trabaja para mejorar el futuro del sector de la salud? ¿Quieres contribuir a mejorar la vida de millon

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Manage and lead internal audit activities for a global manufacturing company, focusing on governance, risk, and controls. Report to Director, manage a team, and travel across EMEA.

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Descubra más sobre las tareas diarias, las responsabilidades generales y la experiencia requerida para esta oportunidad desplazándose hacia abajo ahora. Transportamos exclusivamente para una empresa global del sector de venta por catálogo y comercio electrónico. Actualmente estamos buscando empl

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