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Hemos abierto un proceso de selección de un Junior Accountant para incorporarse en nuestro equipo de Servicios Compartidos de Finanzas para EMEA, esta posición de reportará directamente al Accounting & Reporting Manager.

A leading automation company in Sant Quirze del Vallès is seeking an experienced IS Vendor and Contract Manager to oversee global vendor partnerships.

We are looking for a Medical Manager Immunology to join our Medical Affairs team. In this role, you will help shape and execute the Medical Affairs strategy within Immunology, providing scientific and medical expertise across the organization. You will work closely with internal and external stakeholders to generate and communicate scientific insights, support clinical research activities and build meaningful scientific engagement with healthcare professionals and key opinion leaders. This is an opportunity to combine strong scientific expertise with strategic thinking and cross-functional collaboration to support better outcomes for patients.Salary Range: €53,300.00 - €98,900.00Key ResponsibilitiesSupport the development, implementation and execution of Medical Affairs plans within Immunology, aligned with the overall therapeutic area and product strategy.Provide high-quality and timely responses to medical and scientific enquiries in accordance with applicable standards, including the development of standard response documents for frequently asked questions where appropriate.Provide medical and scientific input into the development and execution of clinical trial and clinical research activities.Support the initiation and oversight of clinical studies and research activities within the therapeutic area.Contribute to the country strategy for Non-Interventional Studies (NIS) and Investigator-Initiated Trials (IITs).Build and maintain high-quality scientific dialogue with Key Opinion Leaders (KOLs), healthcare professionals and relevant external stakeholders.Coordinate the medical review and approval of locally developed medical and promotional materials.Ensure medical materials provided by global or regional teams are appropriately tailored to local stakeholder needs and reviewed and approved according to applicable guidelines.Generate and communicate relevant medical insights to cross-functional partners, including Pharmacovigilance, Regulatory Affairs, Market Access, Quality Assurance, Commercial and Brand teams.Collaborate cross-functionally to ensure medical and scientific perspectives are incorporated into relevant business and therapeutic-area activities.Identify and assess risks within the area of responsibility, develop appropriate mitigation plans and support the implementation and monitoring of internal controls.Ensure activities are conducted in accordance with applicable Ethics & Compliance requirements.Report technical complaints, adverse events and special case scenarios related to Novartis products within 24 hours of receipt.Support the distribution of marketing samples where applicable.What You’ll Bring to the RoleEssential RequirementsRelevant scientific, medical or healthcare educational background.Experience within Medical Affairs, medical/scientific functions or a related pharmaceutical environment.Strong scientific knowledge and the ability to interpret and communicate complex medical and clinical information.Experience engaging with healthcare professionals and other scientific stakeholders.Ability to translate scientific and medical insights into meaningful input for Medical Affairs strategy and activities.Strong cross-functional collaboration skills and the ability to work effectively with Medical, Regulatory, Pharmacovigilance, Market Access, Quality and Commercial colleagues.Strong communication and stakeholder-management capabilities.High standards of ethics, compliance and scientific integrity.Desirable RequirementsPrevious experience or scientific expertise within Immunology.Experience supporting clinical studies, Non-Interventional Studies or Investigator-Initiated Trials.Experience working in a matrixed, cross-functional pharmaceutical environment.Key Measures of SuccessHigh-quality and timely delivery of Medical Affairs activities.Successful execution of annual medical objectives and plans.Quality and impact of medical and scientific stakeholder engagement.Effective generation and communication of medical insights across the organization.Strong cross-functional collaboration.Full adherence to applicable Ethics & Compliance requirements.Benefits & RewardsAt Novartis, we’re committed to reimagining medicine together - and rewarding the people who make it happen.Expected Annual Base Salary Range for role: 53,300.00 - 76,100.00 - 98,900.00 EUR AnnualThe base salary offered is determined based on gender-neutral objectives, such as relevant skills, competencies and experience in accordance with the Novartis pay setting policy and upon joining Novartis will be reviewed periodically.In addition to your base salary, you may be eligible for a performance-based bonus depending on certain performance parameters.The rewards of being part of our team go far beyond base pay and incentives.We also offer a variety of competitive benefits in kind to help you thrive personally and professionally, such as insurance plans, retirement plans, wellbeing resources and global recognition programs.In addition, we provide flexible and hybrid working options, where possible, and minimum 14 weeks paid parental leave.You may be eligible for a company vehicle or a car allowance in accordance with the applicable local Novartis policies and guidelines.Pay equity is a fundamental principle of our employment policy and reflects our commitment to create a diverse, equitable and inclusive environment that treats all employees with dignity and respect, as outlined in our Code of Ethics.Read our brochure to learn more about our global total rewards offering: https://www.Novartis.Com/sites/novartis_com/files/novartis-life-handbook.PdfSkills DesiredClinical Research, Clinical Trials, Drug Development, Health Sciences, Immunology, Internal Medicine, Medical Information, Patient Care, Stakeholder EngagementImproving the lives of people living with disease takes more than innovative science. It takes a focus on the needs of people and a community committed to meeting them. It takes a team of people like you. Working together. Learning together. Thriving together. Discover how you can join us in changing people’s lives.#J-18808-Ljbffr

Overview Join Sevensense by ABB as an experienced Robotic Applications Engineer within the Robotic Systems team to bridge product development and real-world deployments. You’ll work across Sant Quirze del Vallès (Barcelona) and Zurich, collaborating with project, support, and R&D teams to diagnose field issues, improve performance, and validate new features. You’ll contribute hands-on with robotic platforms and help drive customer success and product evolution. This role offers autonomy, teamwork, and a chance to shape the future of robotics in a fast-moving, innovation-driven environment. Compensaciones / Beneficios • Lunch Allowance / Cantine, • Company Mobile Phone, • Employee Parking, • Benefits Platform, • Learning & Training, • Career Development Responsabilidades, • Provide expert technical guidance during integration, commissioning and operation of deployed systems, • Investigate field issues and perform root-cause analysis with R&D to deliver scalable solutions, • Develop tools and software adaptations to improve diagnostics and integration, • Collect and analyze field feedback to identify product gaps and drive development, • Work hands-on with robotic platforms to validate features and verify fixes, • Collaborate across project, support and customer-facing teams to ensure customer success Requisitos principales, • 3+ years of industrial experience in robotics, autonomous systems, or related fields, • Strong Python software engineering and debugging skills, • Experience with Linux-based systems and networking fundamentals, • Familiarity with localization, mapping, navigation, perception, or AMRs, • Experience with ROS/ROS2, • Proven ability to perform root-cause analysis and drive resolution across multidisciplinary teams, • Strong communication and collaboration skills across engineering, project, and customer-facing teams, • Willingness to travel occasionally to customer sites, • Fluent in English (spoken and written), • Initiative, • Ownership, • Autonomy, • Python programming, • Linux and networking fundamentals, • ROS/ROS2

You will design and govern integrations across SAP S/4HANA, SAP IBP, APO PP/DS, and related modules, leading cross-functional deployments from requirements to hypercare while collaborating with validation, compliance. Merck Healthcare is seeking an experienced SAP solution architect to own the end-t

Salary Range: €70,100.00 - €130,300.00 Band Level 6 Job Description Summary #LI-Hybrid Location: Barcelona, SpainYou will play a pivotal role in safeguarding and strengthening Novartis’ Technical Operations by providing independent, strategic assurance across manufacturing and supply. As Director, Internal Audit, TechOps, you will lead complex, high‑impact audit and advisory engagements that shape how risks are identified, mitigated, and managed across end‑to‑end operations. Partnering closely with senior and executive stakeholders, you will bring deep operational insight, sound judgment, and a forward‑looking mindset to influence better outcomes, advance audit innovation, and help ensure we continue to deliver quality medicines to patients worldwide.Key ResponsibilitiesOversee and provide overall direction for complex, risk‑based audit and advisory engagements across manufacturing and supply operationsEnsure audit scopes address end‑to‑end Technical Operations risks, including quality, compliance, technology, and third‑party modelsSupport audit planning and audit program development by identifying key Manufacturing & Supply risks and acting as a technical reference to ensure audit coverage remains risk‑based, relevant, and aligned to business prioritiesReview audit findings and reports to ensure technical accuracy, clarity, and evidence‑based conclusionsDrive pragmatic, value‑adding recommendations that strengthen controls and enable measurable operational improvementAct as a trusted advisor to senior leaders, maintaining independence while fostering constructive, credible partnershipsProvide direct line management to Senior Managers, setting clear strategic direction, overseeing performance and development, and ensuring consistent, high‑quality delivery of risk‑focused audit and advisory engagements across Technical OperationsCoach and develop auditors through hands‑on guidance, feedback, and knowledge‑sharing in Manufacturing and SupplyAdvance digital, data‑driven, and artificial intelligence‑enabled audit practices in collaboration with enablement teamsPlease be advised that this role has a global travel requirement circa 25%.Essential RequirementsDegree in technical or scientific discipline related to manufacturing, supply chain, logistics, or production planningSubstantial experience within internal audit functions in highly regulated industries, preferably pharmaceuticals, biotechnology, or medical devicesStrong practical knowledge of end‑to‑end processes in manufacturing operations, supply chain management, quality systems, and external manufacturing modelsProven experience leading audit and advisory engagements, managing senior stakeholders, and delivering high‑impact outcomesSolid understanding of pharmaceutical regulations and standards, including Good Manufacturing Practice (GMP), Good Distribution Practice (GDP), and global health authority requirements such as FDA, EMA, and other international regulatory bodiesDemonstrated ability to operate in complex environments, influence senior leaders, and communicate audit conclusions with confidence and tactStrong people management experience, with a track record of leading, developing, and motivating high‑performing teams.Fluency in English (written and verbal) is required; additional languages are an advantageDesirable RequirementsProfessional internal audit or supply chain certification, such as Certified Internal Auditor or Certified Supply Chain ProfessionalExperience applying data analytics or artificial intelligence‑enabled tools within internal audit or regulated operating environmentsCommitment to Diversity and InclusionNovartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.Skills DesiredBuilding High Performance TeamCompliance And Controls (Inactive)Critical ThinkingE2E Process View (Inactive)Effective Communications (Inactive)Financial AccountingFinancial And Management Reporting (Inactive)People DevelopmentProblem SolvingProcess OptimizationImproving the lives of people living with disease takes more than innovative science. It takes a focus on the needs of people and a community committed to meeting them. It takes a team of people like you. Working together. Learning together. Thriving together. Discover how you can join us in changing people’s lives.Novartis is aware of employment scams which make false use of our company name or leader’s names or recruiter’s names to defraud job seekers. Novartis does not make job offers without interview and never asks candidates for money. If you have encountered a job posting or been approached with a job offer that you suspect may be fraudulent, we strongly recommend you do not respond, send money or personal information. Novartis is not responsible for any claims, losses, damages, or expenses resulting from scams.In the context of China Cross-Border Data Transfer (CBDT) policy, if you need to apply for a position in China, please go to the local Recruiting System TaleNov.#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.Si sus habilidades, experiencia y cualificaciones coinciden con las de esta descripción del puesto, no demore su solicitud.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 RoleAre you ready to shape the future of Data & AI? Join our team as an AI Engineerand play a key role within our Data & AI Organization (MDAO)- a highly engaged team of data enthusiasts, engineers, and AI specialists. Our mission is to design, build, and run analytics solutions that deliver actionable insights to address business challenges and provide strategic data products to our partners across the Enabling Functions, including Finance, HR, Procurement, Legal, and many more. As an AI Engineer, you will design and implement reliable analytics pipelines and enterprise-grade agentic workflows, integrating LLMs, predictive models, and multi-agent frameworks to deliver scalable AI solutions across our business functions. You will ensure model reliability, reproducibility, and performance at enterprise scale within our modern technology ecosystem, utilizing platforms such as AWS, Palantir Foundry and Snowflake. Embedding explainability, transparency, and security into every AI solution and using Agentic Engineering tools to multiply the delivery is a core expectation of this role. You will work closely with Product Owners, Data Engineers, and fellow Data Scientists in agile, cross-functional Product-Oriented Delivery Teams (PODs), supporting business teams in consuming AI outputs through APIs, dashboards, and embedded analytics. You will actively contribute to building internal AI literacy by sharing knowledge, mentoring peers, and piloting innovative approaches.A genuine curiosity for the latest developments in AI and data science will be essential, soyou will continuously identify opportunities to experiment, measure impact, and drive the field forward within our organization.If you are curious and ambitious about taking on this challenge, we encourage you to apply today!Who You AreUniversity degree in Mathematics, Physics, Computer Science, or a related field.5+ years of experience in data science, data engineering, application design, analytics, or visualization within a global organization.Experience working with Finance, HR, and/or Procurement data and core business processes.Excellent programming skills in Python and SQLStrong foundation in machine learning, statistics, predictive modeling, and NLP combined with practical experience developing LLM-powered applicationsFamiliarity with vector stores, reranking techniques and LLM observability tooling such as (Langfuse, LangSmith, or similar)Experience in using agentic engineering tools such as Claude Code, OpenAI Codex, or OpenCode effectively and responsibly within enterprise software development workflowsExperience working with cloud and enterprise data platforms such as AWS, Palantir Foundry or Snowflake and frameworks like Apache Spark, polars, DuckDB or dbt for data transformation. MLOps & DevOps experience, including MLflow, CI/CD and DockerContinuously up-to-date with digital trends, emerging technologies, and the evolving AI landscape.Excellent communication and presentation skills in English; German language skills are 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! xqysrnh Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

Salary Range: €63,600.00 - €118,000.00 Location: Barcelona (Gran Via), Spain Relocation Support: This role is based in Barcelona (Gran Via), Spain. Novartis is unable to offer relocation support for this role. Please only apply if this location is accessible for you. Imagine leading global clinical studies that have the potential to transform patient outcomes around the world. As a Senior Study Leader at Novartis, you will be at the heart of clinical trial execution, partnering with cross-functional experts to drive complex studies from planning through delivery. This is an opportunity to shape study strategy, champion operational excellence, empower high-performing global teams, and help bring innovative medicines closer to patients. If you thrive in a collaborative, fast-paced environment and are passionate about delivering world-class clinical research, we would love to hear from you. • Lead global clinical studies from planning through delivery, ensuring quality, timeline, and budget objectives are achieved., • Co-lead cross-functional clinical trial teams to drive collaboration, accountability, and study execution excellence., • Develop operational strategies, study timelines, and risk mitigation plans to enable successful study outcomes., • Partner with internal experts and external vendors to deliver high-quality clinical trial activities., • Monitor study progress, proactively resolve issues, and maintain inspection readiness throughout the study lifecycle., • Foster an inclusive, high-performing team culture that promotes learning, innovation, and continuous improvement., • Drive operational excellence through process improvements and the consistent application of agile ways of working., • Bachelor's degree in Life Sciences, Healthcare, or another clinically relevant discipline., • Significant experience leading clinical studies within pharmaceutical, biotechnology, or contract research organisations., • Strong knowledge of international clinical research regulations, quality standards, and health authority requirements., • Proven ability to lead cross-functional teams within complex global matrix environments., • Excellent project management, planning, and risk management skills with a track record of delivery., • Strong communication, stakeholder engagement, negotiation, and problem-solving capabilities. At Novartis, we’re committed to reimagining medicine together - and rewarding the people who make it happen. Expected Annual Base Salary Range for role: €63,600 to € 118,000. The base salary offered is determined based on gender-neutral objectives, such as relevant skills, competencies and experience in accordance with the Novartis pay setting policy and upon joining Novartis will be reviewed periodically. In addition to your base salary, you may be eligible for a performance-based bonus depending on certain performance parameters. The rewards of being part of our team go far beyond base pay and incentives. We also offer a variety of competitive benefits in kind to help you thrive personally and professionally, such as insurance plans, retirement plans, wellbeing resources and global recognition programs. In addition, we provide flexible and hybrid working options, where possible, and minimum 14 weeks paid parental leave. Read our brochure to learn more about our global total rewards offering: https://www.novartis.com/sites/novartis_com/files/novartis-life-handbook.pdf Note: Benefits and compensation may vary by country and are subject to local legal requirements, including provisions of collective bargaining agreements where applicable. A full overview of your compensation package, including any relevant collective bargaining agreement details applicable to your role based on your employment location and Novartis employer entity, will be communicated separately to you during the application process. Novartis is committed to building an outstanding, inclusive work environment and diverse teams' representative of the patients and communities we serve. Improving the lives of people living with disease takes more than innovative science. It takes a focus on the needs of people and a community committed to meeting them. It takes a team of people like you. Working together. Learning together. Thriving together. Discover how you can join us in changing people’s lives. #J-18808-Ljbffr

Overview In this role you own the end-to-end technical architecture for global supply chain planning within a regulated manufacturing setting. You translate business strategy into a multi-year technology roadmap and bridge process owners with enterprise architecture. You design and govern integrations across SAP S/4HANA, SAP IBP, and SAP APO PP/DS, connecting planning with MES, third-party systems, and reporting. You drive sound trade-offs, ensure compliance and cybersecurity, and lead cross-functional deployments to scale planning solutions. Responsabilidades • Define and govern end-to-end planning architecture across SAP planning tools, • Translate business strategy into multi-year tech roadmap for global supply chain planning, • Design and govern integrations between SAP planning systems, MES, and external tools, • Lead cross-functional deployments from requirements to hypercare, • Engage with stakeholders including validation, compliance, and cybersecurity to ensure standard delivery, • Challenge proposals to avoid unnecessary complexity and communicate trade-offs clearly Requisitos principales, • 8+ years leading or supporting large-scale transformation and portfolio prioritization, • Deep hands-on knowledge of SAP Planning Suite (IBP, APO PP/DS, enhanced PP-DS) and satellite modules (PP-PI, MM-PUR), • Experience with SAP Integration Suite, BTP, and Business Data Cloud, • Proven project management across planning, governance, risk, and cross-functional delivery, • Experience in regulated manufacturing environments (GxP, validation, cybersecurity), • Strong ability to communicate complex topics to non-technical audiences, • Clear communication with non-technical stakeholders, • Facilitating workshops and design reviews, • Cross-functional collaboration and stakeholder coordination, • SAP S/4HANA, • SAP IBP, • SAP APO PP/DS

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. At the heart of a multi-year digital transformation, you will own the end-to-end technical architecture for global supply chain planning, shaping how demand, supply, and production planning systems evolve across a complex, regulated manufacturing environment. In this pivotal role, you will translate business strategy into a pragmatic, multi-year technology roadmap, bridging the gap between supply chain process owners and enterprise architecture. You will design and govern integrations across SAP S/4HANA, SAP IBP, and SAP APO PP/DS, connecting planning platforms with manufacturing execution systems, third-party solutions, and reporting environments. Acting as the senior technical authority for planning architecture, you will define solution proposals, validate business cases, and lead cross-functional deployments from requirements through to hypercare. You will partner with business process owners, Centers of Excellence, validation, compliance, and cybersecurity stakeholders to ensure every change is delivered to the right standard. Beyond delivery, you will challenge proposals that introduce unnecessary complexity, represent planning technology interests in cross-functional architecture forums, and guide stakeholders at all levels through technical trade-offs with clarity and confidence. • You bring substantial experience as an SAP solution architect or senior SAP consultant, with deep hands‑on knowledge of the SAP Planning Suite, including SAP IBP, APO PP/DS, enhanced PP/DS, and key satellite modules such as PP‑PI and MM‑PUR, as well as integration technologies including SAP Integration Suite, Business Technology Platform, and Business Data Cloud., • You have 8 or more years of experience leading or supporting large‑scale business transformation and strategic portfolio prioritization, with a track record of delivering integrated planning solutions across enterprise applications., • You combine strong knowledge of demand, supply, and production planning processes with the solution‑architecture judgment to design scalable, enterprise‑aligned integrations between planning, manufacturing execution, and reporting systems., • You have proven project management experience across the full delivery lifecycle, including planning, governance, stakeholder coordination, risk and issue management, and cross‑functional program delivery., • You have worked in a regulated manufacturing environment, such as biopharma, pharmaceutical, or medical technology, and are comfortable navigating GxP validation, compliance, and cybersecurity requirements., • You communicate complex technical topics clearly to non‑technical stakeholders and are confident facilitating workshops, design reviews, and decision‑making sessions with senior business and IT audiences., • A degree in computer science, information systems, engineering, supply chain technology, or a related discipline, or equivalent professional experience, combined with experience working alongside software vendors, systems integrators, or enterprise platform partners in complex environments. Location: Spain 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

Novartis in Sabadell seeks a Senior Change Management Specialist to drive enterprise technology adoption across global programs. You'll own end-to-end change strategy, engage senior sponsors, and shape adoption outcomes.Lead change management using Prosci/ADKAR, map stakeholders, measure adoption KPIs, and design integrated programs blending communications, training and reinforcement. AI transformation experience is a plus.

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 5 yearsof 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 managementknowledge 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!

Overview In this role you own the end-to-end technical architecture for global supply chain planning within a regulated manufacturing setting. You translate business strategy into a multi-year technology roadmap and bridge process owners with enterprise architecture. You design and govern integrations across SAP S/4HANA, SAP IBP, and SAP APO PP/DS, connecting planning with MES, third-party systems, and reporting. You drive sound trade-offs, ensure compliance and cybersecurity, and lead cross-functional deployments to scale planning solutions. Responsabilidades • Define and govern end-to-end planning architecture across SAP planning tools, • Translate business strategy into multi-year tech roadmap for global supply chain planning, • Design and govern integrations between SAP planning systems, MES, and external tools, • Lead cross-functional deployments from requirements to hypercare, • Engage with stakeholders including validation, compliance, and cybersecurity to ensure standard delivery, • Challenge proposals to avoid unnecessary complexity and communicate trade-offs clearly Requisitos principales, • 8+ years leading or supporting large-scale transformation and portfolio prioritization, • Deep hands-on knowledge of SAP Planning Suite (IBP, APO PP/DS, enhanced PP-DS) and satellite modules (PP-PI, MM-PUR), • Experience with SAP Integration Suite, BTP, and Business Data Cloud, • Proven project management across planning, governance, risk, and cross-functional delivery, • Experience in regulated manufacturing environments (GxP, validation, cybersecurity), • Strong ability to communicate complex topics to non-technical audiences, • Clear communication with non-technical stakeholders, • Facilitating workshops and design reviews, • Cross-functional collaboration and stakeholder coordination, • SAP S/4HANA, • SAP IBP, • SAP APO PP/DS

Sabadell is seeking a DesignOps Senior Specialist to optimize design operations across DD&IT, overseeing tools, Figma enterprise operations, licensing, and vendor relationships.

En ASTEK Iberia buscamos un/a SAP CAR & Retail Planning Lead Consultant con experiencia en SAP CAR, SAP AMR y SAP UDF para incorporarse a uno de nuestros clientes del sector Retail, participando en iniciativas estratégicas relacionadas con la planificación de la distribución, la optimización de procesos y la evolución de soluciones SAP. • Liderar iniciativas de evolución, mejora e implantación relacionadas con SAP CAR, SAP AMR y SAP UDF., • Analizar y optimizar procesos de planificación de la distribución en entornos Retail., • Realizar análisis funcionales y técnicos de nuevos requerimientos de negocio., • Participar en actividades de discovery, investigación y validación de nuevas funcionalidades SAP., • Diseñar y proponer soluciones para necesidades de negocio complejas., • Realizar pruebas funcionales, prototipos y validaciones de soluciones., • Coordinar iniciativas transversales que involucren distintos departamentos y equipos., • Colaborar estrechamente con las áreas de Distribución y Gestión Comercial de Producto para transformar necesidades de negocio en soluciones SAP., • Definir, analizar y validar KPIs relacionados con los procesos de planificación., • Analizar integraciones entre SAP CAR y otros módulos o sistemas corporativos., • Trabajar conjuntamente con equipos backend y frontend durante todo el ciclo de vida de las iniciativas., • Revisar y comprender código para analizar soluciones existentes e identificar posibles incidencias, sin necesidad de desempeñar funciones de desarrollo., • Participar en el diseño y seguimiento de soluciones técnicas desde una perspectiva funcional., • Garantizar la calidad de las soluciones y de los entregables., • Actuar como referente funcional dentro del equipo., • Experiencia profesional trabajando con SAP., • Experiencia y conocimientos en SAP CAR., • Conocimientos de SAP AMR (Assortment Management for Retail)., • Conocimientos de SAP UDF (Unified Demand Forecast)., • Experiencia en procesos de planificación de la distribución., • Perfil híbrido funcional y técnico., • Capacidad para leer y comprender código y colaborar eficazmente con equipos técnicos., • Experiencia en análisis funcionales, actividades de discovery y definición de soluciones., • Capacidad para investigar nuevas funcionalidades SAP y validarlas mediante pruebas de concepto., • Conocimientos de integración entre SAP y otros sistemas corporativos., • Capacidad para trabajar de forma autónoma, tomar la iniciativa y liderar proyectos de principio a fin., • Perfil analítico, resolutivo y orientado a la búsqueda de soluciones., • Comodidad trabajando tanto con áreas de negocio como con equipos tecnológicos., • Nivel alto o fluido de inglés, tanto hablado como escrito., • Experiencia con SAP SD y/o SAP MM., • Conocimiento de procesos de compras y distribución., • Experiencia previa en compañías del sector Retail., • Conocimiento o experiencia con SAP S/4HANA., • Experiencia trabajando con equipos multidisciplinares., • Participación en proyectos internacionales. Desde 2015, Astek Iberiaacompaña a sus clientes en su desarrollo en toda España (Madrid, Barcelona, Valencia, País Vasco, Andalucía, Galicia, entre otras regiones). Fundada en Francia en 1988, Astek es una compañía global de consultoría en ingeniería y tecnología, presente en cinco continentes y en 25 países. Con experiencia en una amplia variedad de sectores industriales y de servicios, Astek es un socio estratégico que acompaña a sus clientes en el despliegue inteligente de productos y servicios, así como en la implementación de sus procesos de transformación digital. Actualmente contamos con más de 8.000 profesionales comprometidos cada día con la integración y complementariedad entre las tecnologías digitales y la ingeniería de sistemas complejos. Apostamos por la flexibilidad horaria y damos una gran importancia al bienestar de nuestros empleados. Crecerás profesionalmente en una empresa en constante desarrollo y evolución. Disfrutarás de un acompañamiento personalizado en tus proyectos profesionales, alineado con tus aspiraciones. Tendrás la oportunidad de contribuir de forma real al crecimiento de la compañía. Dispondrás de 23 días laborables de vacaciones, además de los festivos, para disfrutar cuando prefieras. Formarás parte de un equipo diverso, multicultural y en continuo crecimiento. Trabajarás en un entorno dinámico, positivo y con muy buen ambiente. ... ¡aunque todavía te queda mucho por descubrir! #J-18808-Ljbffr

As Investment Projects Sourcing Manager in Technical Sourcing, you lead end-to-end sourcing for complex technical investments across global sites, shaping cost, quality, and delivery. Lead end-to-end sourcing for complex technical investment projects across multiple sites and regions. Experience lea

Overview As Senior Cloud Data & AI Architect, you design and govern cloud-native architectures enabling scalable data, analytics, AI/GenAI, and agentic AI across the healthcare portfolio. You partner with Data & AI, Security, Platform, and cross-functional teams to set standards and reference architectures on AWS, Snowflake, and Palantir Foundry. You lead AI/ML capabilities, including MLOps, model monitoring, and risk controls, with a strong focus on security, governance, and cost management. You translate business priorities into scalable, compliant data and AI solutions and mentor engineers on automation and IaC practices. This role offers impact at scale within a mission-driven healthcare context, Responsabilidades • Design end-to-end cloud architectures on AWS and connected data platforms such as Snowflake and Palantir Foundry, • Define and govern reusable patterns for data ingestion, storage, processing, analytics, and AI/ML workflows, • Lead architecture of AI/ML and GenAI capabilities, including MLOps, model monitoring, and risk controls, • Embed security, privacy, data governance, resilience, and cost management into solution designs, • Evaluate platform and integration choices to improve performance, scalability, and total cost of ownership, • Promote architecture standards and best practices; create reference architectures, design documents, roadmaps, and runbooks; mentor engineers on automation and infrastructure as code, • Collaborate with cross-functional Healthcare teams to translate business priorities into scalable, secure, and compliant data and AI solutions, • Define reusable architecture patterns for agentic AI solutions, including agent orchestration, retrieval-augmented generation, tool integration, human-in-the-loop controls, evaluation, observability, and governance Requisitos principales, • Bachelor’s degree in computer science, information technology, engineering, or a related field, • 6+ years of experience in cloud architecture or a closely related technical role, • Hands-on experience designing solutions on AWS (IAM, storage, compute, serverless, data, security), • Experience with Snowflake or Palantir Foundry, • Experience designing and delivering AI/ML or GenAI infrastructure (data pipelines, deployment, monitoring, governance), • Knowledge of data governance, privacy, security, and regulated-data considerations (PII/PHI, GxP), • Proficiency in Python and SQL, plus Terraform or CloudFormation, • Experience with GenAI and agentic AI, including LLM architecture, RAG, agent orchestration, tool integration, evaluation, monitoring, and responsible-AI controls, • Cross-functional collaboration, • Mentoring and leadership, • Strong communication and stakeholder management, • AWS (IAM, storage, compute, serverless, data, security), • Snowflake, • Palantir Foundry

Merck Healthcare seeks an experienced global business process expert to lead Order to Cash and SAP ERP governance.

Noucor, compañía químico-farmacéutica, busca un Direct Category Buyer para liderar la estrategia de compras de packaging farmacéutico y servicios de CMO, alineada a las necesidades del negocio.Serás responsable de negociar con proveedores, gestionar categorías estratégicas y asegurar el cump

Merck Healthcare in Spain is seeking a Senior Business Process Architect to drive data-driven transformation across planning, logistics, and sustainability within our supply chain. You will connect business priorities with data, analytics, technology, and AI to shape roadmaps, build business cases, and govern a broad program. You will influence product owners, architects, and engineering teams, translating strategic objectives into measurable delivery while leveraging cloud platforms and ERP #J-18808-Ljbffr

Overview In this role you will lead engineering projects within the Engineering Function, coordinating the design team to ensure technical compliance. You will oversee mechanical, hardware, and software development per project specs, and define the design plan and system architecture. You will release modules to production, verify them via simulation and virtual commissioning, and manage system integration and final validation. You will support manufacturing, update BOMs, and drive Design to Cost while promoting knowledge sharing. You will ensure a smooth R&D handover and lead a team with clear objectives, contributing to Volpak’s packaging machinery impact. Responsabilidades • Lead projects within Engineering to meet technical requirements and coordinate the design team, • Oversee Mechanical, Hardware, and Software development per specifications, • Define and manage design plan, system architecture, and module breakdown, • Release modules into production and verify via simulation and virtual commissioning, • Manage system integration, verification, and final design validation, • Support manufacturing and assembly, update BOM as needed, • Review and approve final engineering documentation, • Drive Design to Cost and promote knowledge sharing, • Ensure smooth handover from R&D to the organization, • Lead and support the team with clear objectives and development plans Requisitos principales, • Bachelor in Mechanical Engineering (or related), • Master’s in Engineering or Management, • At least 7 years of experience in mechanical design, • Knowledge of modern 3D CAD systems integrated with PLM, • Good knowledge of pneumatics, • Familiar with basic ERP functions, • Electrical and Software engineering knowledge, • Background in the packaging machine sector preferred, • leadership, • cross-functional collaboration, • clear communication, • 3D CAD with PLM, • pneumatics, • ERP basics

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.Cualquier información adicional que necesite para este trabajo se encuentra en el texto a continuación. Asegúrese de leerla detenidamente y luego envíe su solicitud.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 AreYou 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! xqysrnh Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

Jobtailor in Spain seeks a PPC Campaign Manager to lead high-performing PPC deployments for Dutch clients. You will tailor platform features to client objectives and use analytics to sharpen strategy and ROI.The role requires a blend of technical skill and client interaction across teams. With 2+ years in client-facing roles and fluency in Dutch and English, you'll navigate GDPR considerations and the local market landscape while coordinating with internal departments to ensure a cohesive,

Incorporació: Inici 1 de juliol de 2026 Resum: Operari/ària de neteja viària Funcions a realitzar: Empresa ubicada a Mollet, cerca Operari/ària de neteja viària per al servei de neteja viària i recollida de residus de Mollet del Vallès. Població: Mollet del Vallès Tipus de contracte: Eventu

Overview En Magna, como Comprador/a, gestionarás compras de materiales de producción para proveedores nacionales e internacionales, asegurando precio, calidad y servicio. Colaborarás con equipos globales para optimizar costes y apoyar iniciativas estratégicas. Tu rol impulsa la cadena de suministro y la calidad en proyectos de automoción. Esta posición ofrece desarrollo profesional en un entorno dinámico e innovador con impacto directo en la eficiencia y competitividad de la empresa. Compensaciones / Beneficios • Catering subvencionado, • Fisioterapeuta in-house (75% subvencionado), • Horario flexible, • Ayuda a los estudios, • Idiomas in-company (inglés, francés y más), • Eventos deportivos y actividades healthy Responsabilidades, • Negociación con proveedores, • Análisis de precios y condiciones, • Negociación de cargos y optimización de costes, • Búsqueda y evaluación de nuevos proveedores, • Cumplimiento de requisitos de calidad y auditorías SQA, • Gestión de ofertas: solicitud, seguimiento y adjudicación, • Interlocución directa con proveedores, • Coordinación con departamentos internos, • Seguimiento de homologación de muestras y preseries, • Gestión de modificaciones, • Estrategia corporativa, • Apoyo a iniciativas globales para generar sinergias, • Aseguramiento de calidad y capacidad en la cadena de suministro, • Target Costing y análisis de escandallos, • Creación y actualización de archivos de coste de producto Requisitos principales, • Grado en Ingeniería Industrial o Técnica, • +3 años de experiencia en funciones similares, • Experiencia en automoción (3–5 años), • Inglés fluido C1, • Valorable otros idiomas, • Capacidad de negociación, • Orientación a resultados, • Buena comunicación y coordinación, • Gestión de compras y negociación con proveedores, • Análisis de precios y costes, • Gestión de la cadena de suministro

Overview In this role you ensure high-quality, compliant requirements for clinical trial systems that support a global data repository. You bridge clinical operations and IT to improve specification governance, traceability, and data platform reliability. You will lead workshops, identify gaps, and translate complex rules into precise, actionable documentation. This position offers cross-functional impact in a regulated, global setting with opportunities to shape data-driven clinical trial execution. Responsabilidades • Review, improve, and create Functional Requirement Specifications to align business intent with technical feasibility, • Identify gaps, resolve ambiguities, and simplify complex business rules, • Facilitate structured requirement reviews with cross-functional stakeholders, • Drive improvements to documentation standards, traceability, and requirement governance, • Influence reliability and scalability of data platforms underpinning clinical trial operations Requisitos principales, • 5+ years as a Business Analyst in complex, cross-functional environments, • 3+ years of hands-on experience with clinical trial data and processes, • Experience facilitating requirement workshops and stakeholder reviews, • Practical experience with data platforms, system integrations, and APIs, • Experience in regulated environments with Good Practice standards (validation, traceability, change control), • Degree in Information Technology, Life Sciences, Business, or related field, or equivalent, • AI literacy and ability to assess AI-driven tools responsibly, • facilitation and workshop leadership, • strong analytical mindset, • attention to detail, • functional requirements specification, • data platforms, • system integrations

Novartis Farmacéutica, S.A. in Barcelona is seeking an Operations Senior Project Manager to shape global resource planning and budgeting. You will partner with Site Management and Monitoring leadership to drive strategic planning, budget control, and data-driven decisions.Build agile models to ensure capabilities are available where needed. The role requires strong collaboration across functions, budget management, and experience coordinating complex initiatives in a global environment.

€26,000 Gross Annual Base SalaryUsted podría ser el solicitante perfecto para este trabajo. Lea toda la información asociada y asegúrese de presentar su candidatura.Up to €4,000 Gross Annual Performance BonusTotal On-Target Earnings (OTE): Up to €30,000 Gross per YearAbout The RoleAre you passionate about sales, digital marketing, and helping businesses grow?Location: Barcelona, SpainWork Model: Hybrid (Office + Remote)Employment Type: Full-time (39h/week)Your ResponsibilitiesManage and onboard a portfolio of new business clients.Build strong relationships with customers in the German market.Conduct consultative outbound sales activities.Understand clients' business objectives and recommend tailored digital advertising solutions.Guide customers through the onboarding journey and ensure a seamless experience.Identify upselling and cross-selling opportunities.Monitor account performance and provide optimization recommendations.Collaborate with internal teams to deliver an outstanding customer experience.Maintain accurate CRM records and customer documentation.RequirementsNative or fluent German (C1/C2).Good level of English (B2 or higher).Previous experience in Sales, Account Management, Customer Success, or Digital Marketing is an advantage.Excellent communication and negotiation skills.Goal-oriented with a passion for sales.Strong relationship‑building abilities.EU Citizenship or a valid Spanish work permit is preferred.What We Offer€26,000 Gross Annual Base SalaryUp to €4,000 Gross Annual Performance BonusHybrid working modelPaid trainingCareer growth opportunitiesInternational work environmentModern office in BarcelonaOngoing learning and developmentEmployee referral programStart your next international career in Barcelona and help businesses grow while advancing your own career! xqbhyrx Hay opciones de teletrabajo/trabajo desde casa disponibles para este puesto.

Lead the delivery and evolution of a SaaS platform for clinical study design, protocol authoring, and feasibility analysis, bridging R&D business stakeholders, IT, and vendors.

En trentia estamos colaborando con un Grupo industrial internacional, proveedor del sector de automoción, que busca incorpora un/a Procurement Engineer para su centro de Terrassa (Barcelona). La posición reporta a la Global Technical Procurement Manager.Tu misión será gestionar la compra de bienes y servicios técnicos para las operaciones industriales y asegurar que la calidad de los proveedores responde a los requisitos de los clientes. Es un puesto que une la ingeniería de compras con el desarrollo de la calidad de proveedores, con proyección hacia el liderazgo de compras en proyectos.Buscar y seleccionar el panel de proveedores adecuado para cumplir los objetivos de rentabilidad, calidad y plazo de entrega.Gestionar proveedores y hacer benchmarking.Lanzar solicitudes de oferta (RFQ) y analizar costes.Estar al día de las tecnologías e investigar métodos alternativos de fabricación.Dar soporte en las auditorías de cliente del área de compras.Calidad de proveedores en fase de desarrolloHomologar nuevos proveedores.Gestionar el APQP de productos nuevos o modificados y su aprobación o reaprobación (PPAP).Definir y mantener las especificaciones de compra.Calidad de proveedores en fase de serieHacer seguimiento del desempeño de los proveedores.Desarrollar con ellos planes de mejora continua.Gestionar las no conformidades de proveedor y analizar sus informes 8D.Realizar auditorías SCA y recualificaciones de proveedores.Con al menos 3 años de experiencia en fase de desarrollo, asumirás el rol de PPL en los proyectos asignados: participación en el DVP del producto, control del calendario de compras por hitos para cumplir plazo y presupuesto, seguimiento de los hitos APQP e interlocución entre el jefe de proyecto y el equipo de Compras, con reporting a la Global Technical Procurement Manager.Al menos 3 años de experiencia en calidad de proveedores (SQA) y/o ingeniería de compras. Lo ideal, 5 años o más.Nivel avanzado de inglés (C1), para trabajar a diario en un entorno internacional.Grado o titulación superior en Ingeniería, preferiblemente Mecánica.Conocimiento de ISO 9001 e IATF 16949.Experiencia como auditor/a de segunda parte, y en especial la acreditación VDA 6.3.Conocimiento de procesos de fabricación y de producto: laminación de aluminio o acero, mantas aislantes (needlemat, cerámica y troquelado), recubrimientos (cataforesis, Zn-Ni), soldadura, estampación progresiva, e inyección o extrusión de plástico.CompetenciasNegociación.Liderazgo transversal con ingeniería, calidad, proyectos y proveedores.Comunicación eficaz.Organización y gestión del tiempo.Trabajo en equipo.ModalidadHíbrido: tres días a la semana en el centro de Terrassa (Barcelona) y dos de teletrabajo. El puesto requiere disponibilidad para viajar en torno a un 15-20 % del tiempo.Incorporación a un grupo industrial internacional del sector de automoción.Plan de crecimiento hacia Purchasing Project Leader.

We are currently looking for a Plant Manager Responsible for two manufacturing facilities within the Group, Balsareny and Parets.

Job descriptions may display in multiple languages based on your language selection.What we offer: At Magna, you can expect an engaging and dynamic environment where you can help to develop industry-leading automotive technologies. We invest in our employees, providing them with the support and resources they need to succeed. As a member of our global team, you can expect exciting, varied responsibilities as well as a wide range of development prospects. Because we believe that your career path should be as unique as you are.Group SummaryThe Mechatronics, Mirrors and Lighting group specializes in automotive technologies that are driving the future of mobility. Combining a deep systems knowledge to develop unique vehicle access experiences, intelligent visions systems and advanced automotive lighting technologies, MML's expertise light the path to innovation, safety and styling.Job Responsibilities¡Buscamos un/a Supervisor/a de Producción a cuarto turno para unirse a nuestro equipo! Si te apasiona la mejora continua, liderar equipos y marcar la diferencia en un entorno industrial dinámico, esta oportunidad es para ti.Tu misión Serás responsable de asegurar —y superar— los objetivos de las líneas asignadas, liderando y colaborando con los equipos de la Focus Factory y otras áreas de la organización. Identificarás oportunidades de mejora, impulsarás planes de acción y garantizarás la implantación de estándares que eleven el rendimiento. Además, tendrás un papel clave en el desarrollo del equipo a tu cargo.Asegurar la máxima calidad del producto acabado mediante el cumplimiento de estándares y la monitorización de KPIs.Cumplir los objetivos de producción y costes, impulsando la eficiencia operativa.Fabricar la cantidad establecida por la Focus Factory, optimizando recursos.Mantener equipos motivados y comprometidos.Promover e implementar mejoras continuas (incluyendo yc, A3).Garantizar el cumplimiento de las normas de Seguridad y Salud, liderando los comunicados de riesgo.A quién buscamosFormación Superior, preferentemente del ámbito industrial.Experiencia mínima de 3 años en gestión operacional (valorable en electrónica).Experiencia de 3 a 5 años en automoción.Disponibilidad Cuarto Turno (3 semanas de Lunes a Sábado de Mañana y una semana de descanso- 3 semanas de Noche de Domingo a Viernes y una semana de descanso - 3 semanas de Tarde de Lunes a Sábado y una semana de descanso) Se valorará formación o experiencia en: Robots, atornilladores, averías. Verificación EOL: conexión / programación / funcionamiento. Cámaras, PLCs, resolución de errores de máquina. Liderazgo de equipos, herramientas Lean (5S, TPM, SMED, Six Sigma), A3. Disponibilidad para trabajar en turno rotativo (mañana/tarde/noche) y posibilidad de cuarto turno.Además, qué te ofrecemos:Catering subvencionadoServicio de fisioterapeuta in-house (subvencionado al 75%)Horario flexibleAyudas a la formaciónIdiomas in-company (Inglés, Francés y más)Eventos deportivos y actividades healthy para toda la compañíaAwareness, Unity, EmpowermentAt Magna, we believe that a diverse workforce is critical to our success. That’s why we are proud to be an equal opportunity employer. We hire on the basis of experience and qualifications, and in consideration of job requirements, regardless of, in particular, color, ancestry, religion, gender, origin, sexual orientation, age, citizenship, marital status, disability or gender identity. Magna takes the privacy of your personal information seriously. We discourage you from sending applications via email or traditional mail to comply with GDPR requirements and your local Data Privacy Law.AI-Assisted Screening Disclosure As part of our commitment to a fair, consistent, and efficient recruitment process, we may use artificial intelligence (AI) tools to assist in the initial screening of applications submitted through our Workday system. These tools help identify qualifications and experience that align with the role requirements. Please note that AI is used solely to support our recruiters. Final decisions are always made by the hiring manager and the hiring team. Importantly, no applicant data is shared externally through these AI tools. All information remains securely within our systems and is handled in accordance with our privacy and data protection policies. Under conditions defined by applicable law, you may have the right to request an explanation of how AI is used to support decision-making. If you have any questions or concerns about this process, feel free to contact our Talent Attraction team.Worker Type: Regular / Permanent Group: Magna Mechatronics, Mirrors & LightingWe see a future where everyone can live and move without limitations. That’s why we are developing technologies, systems and concepts that make vehicles safer and cleaner, while serving our communities, the planet and, above all, people. In the right environment, your ideas can turn into industry-changing automotive technologies and improve the lives of people around the world. Let's create the future of mobility, together.Learn more about us: Sustainability Innovation Interview-Tips#J-18808-Ljbffr

Lead cross‑functional project teams to ensure successful project execution. Monitor project performance and adjust schedule, cost or resources as needed. Manage project‑related administrative activities including quotations and purchase requests.

We are Covestro. We are curious. We are courageous. We are colorful. We refine chemical material solutions with game-changing products. Let us empower you to push boundaries. Join us and our 18.000 colleagues now and together we will make the world a brighter place.HSEQ TechnicianMisión del puestoDentro del departamento de HSEQ, dar soporte a la implantación, mantenimiento y mejora continua de los sistemas de gestión de HSEQ de los centros de Parets del Vallés y Santa Margarida dels Monjos, promoviendo una cultura preventiva sólida, garantizando el cumplimiento legal y colaborando en la consecución de los objetivos de seguridad, medio ambiente y calidad.Principales funciones y responsabilidadesDesarrollar e implementar la estrategia, metas y objetivos de HSEQ de la organización, en alineación con los objetivos generales.Fomentar una cultura de mejora continua, responsabilidad y compromiso con los estándares HSEQ.Dar soporte a la implementación, mantenimiento y mejora del sistema de gestión HSEQ y de la documentación derivada, garantizando que sean comprendidos y aplicados en toda la organización.Contribuir al mantenimiento de las certificaciones.Seguimiento de los indicadores clave de rendimiento (KPIs) para medir el progreso e impulsar la mejora continua.Asegurar el cumplimiento de la legislación y requisitos aplicables, así como los estándares corporativos y procedimientos internos.Desarrollar mejores prácticas de HSEQ, asegurando que las operaciones, procesos y prácticas de la organización cumplen con los requisitos aplicables.Impulsar la reducción de incidentes, riesgos e impactos ambientales.Identificar riesgos potenciales para la salud y seguridad de los trabajadores y el medio ambiente para proponer medidas para el control y reducción.Participar en las auditorías e inspecciones periódicas para evaluar el cumplimiento de los estándares y políticas de HSEQ.Seguimiento de las acciones correctivas derivadas de los hallazgos para subsanar deficiencias y mejorar el desempeño.Promover campañas de sensibilización y comunicación en materia de HSEQ.Desarrollar programas de formaciones destinados a informar y capacitar a los trabajadores sobre los requisitos de HSEQ, así como las prácticas de trabajo seguras y la protección ambiental.Soporte en la investigación de accidentes, incidentes y cuasi accidentes para determinar sus causas raíz, implantar acciones correctivas que eviten su repetición y fomentar una cultura de notificación, aprendizaje y mejora continua.Coordinar la vigilancia y control de la salud de los trabajadores para garantizar que se realice acorde con los riesgos de cada puesto de trabajo.Colaborar y participar en la elaboración de los planes de autoprotección, las actuaciones en casos de emergencia/contraincendios, primeros auxilios y documentación derivada de Accidentes graves.Apoyar, coordinar y dar soporte a las actividades preventivas.Realizar inspecciones periódicas en planta para verificar el cumplimiento de los requisitos de seguridad y medio ambiente.Colaborar en la evaluación de riesgos, gestión de contratistas y coordinación de actividades empresariales.Identificar oportunidades de mejora en procesos, instalaciones y comportamientos.Participar en proyectos de mejora continua orientados a incrementar la seguridad, calidad, eficiencia y sostenibilidad de las operaciones.Dar soporte y asesoramiento a los distintos departamentos para garantizar la integración de los principios HSEQ en las actividades diarias.Requisitos (formación, conocimientos y experiencia)Licenciatura/Grado en Ciencias Químicas, Ciencias Ambientales, Ingeniería Química o similar.Máster en Prevención de Riesgos Laborales.Entre 2 y 5 años de experiencia en puestos de HSE en entornos industriales, químicos, de fabricación o sectores relacionados.Inglés: nivel B2 o superior.¿Qué ofrecemos?Contrato indefinido con una retribución competitiva en el rango de 55.000 – 60.000 € brutos anuales, en función de la experiencia y conocimientos aportados, además de un bonus variable vinculado a los resultados de la compañía.Flexibilidad y conciliación, con horario flexible de entrada, jornada intensiva los viernes y durante el periodo de verano.Modelo de trabajo híbrido, con posibilidad de realizar 2 días de teletrabajo por semana y 27 días laborables de vacaciones.Paquete de beneficios sociales, que incluye plan de pensiones, seguro de salud con condiciones especiales, seguro de vida, compensación por comida y retribución flexible en guardería, transporte y seguro médico para familiares.Contact Uswww.Covestro.ComCovestro welcomes applications from all individuals, regardless of racial or ethnic origin, skin color, nationality, religion, philosophy, gender, age, physical characteristics, marital status, disability, appearance, sexual orientation and sexual identity. We are committed to treating all applicants fairly and avoiding discrimination.#J-18808-Ljbffr

ERP (Dynamics 365 Business Central / NAV) y su ecosistema de herramientas complementarias. Participarás en el diseño de la arquitectura funcional, planificarás y desplegarás las aplicaciones de negocio de la compañía, centrándose sobre todo en el ERP Business Central. Amplio dominio técnico

Grifols Site Procurement Senior Specialist in Parets del Vallès leads site-level procurement activities, ensuring continuity, cost control, and compliant operations. You will collaborate with Manufacturing, Quality, Supply Chain, and Finance to execute sourcing, RFx, and contract management within the site scope. The role requires strong stakeholder partnership, regulatory knowledge, and an analytical mindset to optimize spend, supplier performance, and change controls while supporting P2P #J-18808-Ljbffr

Novartis in Sabadell seeks a Senior Change Management Specialist to drive enterprise technology adoption across global programs. You’ll own end-to-end change strategy, engage senior sponsors, and shape adoption outcomes. Lead change management using Prosci/ADKAR, map stakeholders, measure adoption KPIs, and design integrated programs blending communications, training and reinforcement. AI transformation experience is a plus. #J-18808-Ljbffr

Directs AI search and visibility strategy to maximize content discoverability on AI and traditional search platforms, optimizing content for machine readability and performance.

€41,900.00 - €77,700.00 Senior Change Management Specialist responsible for driving change and adoption for enterprise technology initiatives. The role owns end-to-end change and adoption strategies, ensuring smooth transitions, strong stakeholder engagement, and sustained user adoption across complex global programs. Success is measured not only by delivery of the change plan but by achieving meaningful business adoption and user outcomes. • Build and maintain strong relationships with senior stakeholders, sponsors, and cross-functional partners to drive successful change adoption., • Develop and execute stakeholder engagement strategies, including stakeholder mapping, influence assessments, and readiness planning., • Lead and apply change management methodologies (e.g., Prosci, ADKAR) to support business, technology, and AI-driven transformation initiatives., • Facilitate case-for-change discussions, change impact assessments and stakeholder workshops to identify adoption challenges and opportunities., • Define, monitor, and report adoption KPIs, leveraging data, user feedback, and sentiment analysis to optimize change outcomes., • Design and deliver integrated adoption programs that combine communications, training, engagement, and reinforcement activities., • Anticipate resistance and adoption risks, implementing proactive mitigation and enablement strategies to improve business readiness., • Establish sustainable change management practices by developing playbooks, standards, and knowledge-sharing initiatives that strengthen organizational capability., • 7+ years of experience in change management, transformation, organizational adoption, or related roles within complex global organizations., • Strong expertise in applying change management frameworks such as Prosci, including stakeholder management and impact assessment methodologies., • Proven track record of leading change initiatives for digital, technology, or AI-enabled transformations and product launches., • Excellent facilitation and presentation skills with experience leading executive-level workshops and large-scale engagement sessions., • Strong analytical capabilities, including experience interpreting adoption metrics, user insights, and performance data to drive decision-making., • Demonstrated ability to influence stakeholders and deliver results within matrixed, multicultural, and cross-functional environments., • Excellent verbal and written communication skills in English, with the ability to tailor messaging for diverse audiences., • Passion for AI and emerging technologies, with experience leveraging or advocating AI-enabled tools to enhance change and adoption outcomes. Novartis is unable to offer relocation support for this role: please only apply if this location is accessible for you. Expected Annual Base Salary Range for role: €41,900.00 to €77,700 The base salary offered is determined based on gender-neutral objectives, such as relevant skills, competencies and experience in accordance with the Novartis pay setting policy and upon joining Novartis will be reviewed periodically. In addition to your base salary, you may be eligible for a performance-based bonus depending on certain performance parameters. The rewards of being part of our team go far beyond base pay and incentives. We also offer a variety of competitive benefits in kind to help you thrive personally and professionally, such as insurance plans, retirement plans, wellbeing resources and global recognition programs. In addition, we provide flexible and hybrid working options, where possible, and minimum 14 weeks paid parental leave. Pay equity is a fundamental principle of our employment policy and reflects our commitment to create a diverse, equitable and inclusive environment that treats all employees with dignity and respect, as outlined in our Code of Ethics. Read our brochure to learn more about our global total rewards offering: https://www.novartis.com/sites/novartis_com/files/novartis-life-handbook.pdf Note: Benefits and compensation may vary by country and are subject to local legal requirements, including provisions of collective bargaining agreements where applicable. A full overview of your compensation package, including any relevant collective bargaining agreement details applicable to your role based on your employment location and Novartis employer entity, will be communicated separately to you during the application process. Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. • Business Value Creation, • Change Management, • Consulting, • Decision Making, • Digital Capabilities, • Influencing Skills, • Information Technology (IT) Infrastructure, • Information Technology Management, • IT Governance, • Stakeholder Engagement, • System Integration, • Technology Use #J-18808-Ljbffr

Overview In this role, you will architect and operate a cloud-native platform that powers intelligent, autonomous AI applications across a global enterprise. You’ll own the platform strategy, design multi-tenant Kubernetes environments, and drive end-to-end delivery with a focus on security, reliability, and scalable operations. You’ll mentor engineers and collaborate with cross-functional teams to turn complex AI and MLOps needs into reusable platform patterns. This is a mission-driven opportunity to shape how agentic AI drives impact in healthcare and life sciences. Compensaciones / Beneficios • high-autonomy engineering culture, • flexible working models, • global, diverse environment, • opportunity to impact life-changing R&D, • culture of inclusion and belonging, • career development across a global company Responsabilidades, • Own the platform architecture, technical roadmap and ADRs within the broader agentic AI strategy, • Design, build and operate the multi-tenant Kubernetes platform using Amazon EKS, Terraform, Helm, Kustomize, Argo CD and Argo Workflows, • Build repeatable onboarding, promotion, recovery and decommissioning capabilities through Azure DevOps and GitOps, • Implement identity and tenant isolation across OIDC, Kubernetes RBAC and impersonation, AWS workload identity and secrets management, • Design secure integrations with models, tools, MCP/A2A services and other enterprise platforms, • Own operational readiness, including SLOs, telemetry, agent and LLM tracing, evaluation, capacity, cost, incident response, upgrades, backup/restore and rollback, • Develop and review production Python, Terraform modules, Helm charts and pipeline templates, • Establish technical standards, documentation and reusable platform patterns, and mentor other engineers Requisitos principales, • University degree in Computer Science, Engineering, or equivalent, • 8+ years of relevant experience building secure, scalable, resilient cloud-native backend systems at enterprise scale, • Experience in architecting complex cloud-native solutions and in guiding teams in their implementation, • Hands-on experience designing and operating production Kubernetes platforms, preferably Amazon EKS, • Strong AWS platform engineering experience across EKS, ECR, IAM/workload identity, VPC/private connectivity, ALB/WAF, Route 53, Secrets Manager, CloudWatch and S3, • Strong Infrastructure as Code and GitOps experience using Terraform, Helm, Kustomize, Argo CD and Git, • Experience building and governing CI/CD pipelines, preferably with Azure DevOps, • Strong production Python experience, including boto3, API integration, automated testing and operational automation, • Experience with OIDC/OAuth2/JWT, least-privilege access, tenant isolation, Kubernetes RBAC and secure secrets management, • Practical experience building or operating GenAI or agentic systems, including tool integration, state and memory, evaluation, observability and failure handling, • Understanding of MCP and A2A, particularly authentication, authorization, service boundaries and enterprise governance, • Business-fluent English (written and spoken), • Strong sense of ownership and accountability, • Curious and eager to learn; comfortable with evolving tech, • Collaborative, cross-functional teamwork in international settings, • Kubernetes platform design and operation (EKS), • AWS services: EKS, ECR, IAM, VPC, Route 53, Secrets Manager, CloudWatch, S3, • Terraform, Helm, Kustomize, Argo CD, Argo Workflows

Cronoshare es una plataforma online para profesionales que quieren encontrar nuevos clientes. Buscamos Profesor/a de natación en Sabadell y alrededores. Pertenecer a la red de profesionales de Cronoshare no tiene coste y recibirás nuevos clientes según tus preferencias, de forma personalizada. Requisitos: • Conocimientos previos para desarrollar funciones de Profesor/a de natación., • Organización, buena relación con el cliente y gestión de tiempo., • Profesionalidad y proactividad. Qué ofrecemos: • Solicitudes de nuevos trabajos y clientes en tu zona, que necesitan Profesor/a de natación., • Gestión propia de los clientes y márgenes comerciales., • Sin intermediarios: tú fijas tus tarifas y horarios. ¿Cómo funciona Cronoshare? Gracias a nuestra plataforma de gestión de clientes, podrás aceptar o descartar solicitudes de trabajos en tu área, enviando presupuestos solo a los clientes que más te interesen. No pagarás suscripciones ni tarifas mensuales, además tampoco tienes que abonar comisiones por cada cliente que consigas gracias a nosotros. Para conseguir nuevos clientes, solo tienes que incurrir en una pequeña inversión y podrás acceder a estas solicitudes. Empieza a hacer crecer tu actividad comercial o negocio. Si eres freelance, autónomo o pyme, te esperamos.

IT Project Manager for Merck Group in Spain to lead global application projects in Supply Chain, manufacturing, and logistics, managing scope, budget, and risks.

Overview In this role you ensure high-quality, compliant requirements for clinical trial systems that support a global data repository. You bridge clinical operations and IT to improve specification governance, traceability, and data platform reliability. You will lead workshops, identify gaps, and translate complex rules into precise, actionable documentation. This position offers cross-functional impact in a regulated, global setting with opportunities to shape data-driven clinical trial execution. Responsabilidades • Review, improve, and create Functional Requirement Specifications to align business intent with technical feasibility, • Identify gaps, resolve ambiguities, and simplify complex business rules, • Facilitate structured requirement reviews with cross-functional stakeholders, • Drive improvements to documentation standards, traceability, and requirement governance, • Influence reliability and scalability of data platforms underpinning clinical trial operations Requisitos principales, • 5+ years as a Business Analyst in complex, cross-functional environments, • 3+ years of hands-on experience with clinical trial data and processes, • Experience facilitating requirement workshops and stakeholder reviews, • Practical experience with data platforms, system integrations, and APIs, • Experience in regulated environments with Good Practice standards (validation, traceability, change control), • Degree in Information Technology, Life Sciences, Business, or related field, or equivalent, • AI literacy and ability to assess AI-driven tools responsibly, • facilitation and workshop leadership, • strong analytical mindset, • attention to detail, • functional requirements specification, • data platforms, • system integrations

Overview En Magna, como Comprador/a, gestionarás compras de materiales de producción para proveedores nacionales e internacionales, asegurando precio, calidad y servicio. Colaborarás con equipos globales para optimizar costes y apoyar iniciativas estratégicas. Tu rol impulsa la cadena de suministro y la calidad en proyectos de automoción. Esta posición ofrece desarrollo profesional en un entorno dinámico e innovador con impacto directo en la eficiencia y competitividad de la empresa. Compensaciones / Beneficios • Catering subvencionado, • Fisioterapeuta in-house (75% subvencionado), • Horario flexible, • Ayuda a los estudios, • Idiomas in-company (inglés, francés y más), • Eventos deportivos y actividades healthy Responsabilidades, • Negociación con proveedores, • Análisis de precios y condiciones, • Negociación de cargos y optimización de costes, • Búsqueda y evaluación de nuevos proveedores, • Cumplimiento de requisitos de calidad y auditorías SQA, • Gestión de ofertas: solicitud, seguimiento y adjudicación, • Interlocución directa con proveedores, • Coordinación con departamentos internos, • Seguimiento de homologación de muestras y preseries, • Gestión de modificaciones, • Estrategia corporativa, • Apoyo a iniciativas globales para generar sinergias, • Aseguramiento de calidad y capacidad en la cadena de suministro, • Target Costing y análisis de escandallos, • Creación y actualización de archivos de coste de producto Requisitos principales, • Grado en Ingeniería Industrial o Técnica, • +3 años de experiencia en funciones similares, • Experiencia en automoción (3–5 años), • Inglés fluido C1, • Valorable otros idiomas, • Capacidad de negociación, • Orientación a resultados, • Buena comunicación y coordinación, • Gestión de compras y negociación con proveedores, • Análisis de precios y costes, • Gestión de la cadena de suministro

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

Salary Range: €41,900.00 - €77,700.00 Job Description Summary Senior Change Management Specialist responsible for driving change and adoption for enterprise technology initiatives. The role owns end-to-end change and adoption strategies, ensuring smooth transitions, strong stakeholder engagement, and sustained user adoption across complex global programs. Success is measured not only by delivery of the change plan but by achieving meaningful business adoption and user outcomes. • Build and maintain strong relationships with senior stakeholders, sponsors, and cross-functional partners to drive successful change adoption., • Develop and execute stakeholder engagement strategies, including stakeholder mapping, influence assessments, and readiness planning., • Lead and apply change management methodologies (e.g., Prosci, ADKAR) to support business, technology, and AI-driven transformation initiatives., • Facilitate case-for-change discussions, change impact assessments and stakeholder workshops to identify adoption challenges and opportunities., • Define, monitor, and report adoption KPIs, leveraging data, user feedback, and sentiment analysis to optimise change outcomes., • Design and deliver integrated adoption programs that combine communications, training, engagement, and reinforcement activities., • Anticipate resistance and adoption risks, implementing proactive mitigation and enablement strategies to improve business readiness., • Establish sustainable change management practices by developing playbooks, standards, and knowledge-sharing initiatives that strengthen organisational capability., • 7+ years of experience in change management, transformation, organisational adoption, or related roles within complex global organisations., • Strong expertise in applying change management frameworks such as Prosci, including stakeholder management and impact assessment methodologies., • Proven track record of leading change initiatives for digital, technology, or AI-enabled transformations and product launches., • Excellent facilitation and presentation skills with experience leading executive-level workshops and large-scale engagement sessions., • Strong analytical capabilities, including experience interpreting adoption metrics, user insights, and performance data to drive decision-making., • Demonstrated ability to influence stakeholders and deliver results within matrixed, multicultural, and cross-functional environments., • Excellent verbal and written communication skills in English, with the ability to tailor messaging for diverse audiences., • Passion for AI and emerging technologies, with experience leveraging or advocating AI-enabled tools to enhance change and adoption outcomes., • Novartis is unable to offer relocation support for this role: please only apply if this location is accessible for you. Expected Annual Base Salary Range for role: €41,900.00 to €77,700 The base salary offered is determined based on gender-neutral objectives, such as relevant skills, competencies and experience in accordance with the Novartis pay setting policy and upon joining Novartis will be reviewed periodically. In addition to your base salary, you may be eligible for a performance-based bonus depending on certain performance parameters. The rewards of being part of our team go far beyond base pay and incentives. Read our brochure to learn more about our global total rewards offering: https://www.novartis.com/sites/novartis_com/files/novartis-life-handbook.pdf Note: Benefits and compensation may vary by country and are subject to local legal requirements, including provisions of collective bargaining agreements where applicable. A full overview of your compensation package, including any relevant collective bargaining agreement details applicable to your role based on your employment location and Novartis employer entity, will be communicated separately to you during the application process. • We also offer a variety of competitive benefits in kind to help you thrive personally and professionally, such as insurance plans, retirement plans, wellbeing resources and global recognition programs., • In addition, we provide flexible and hybrid working options, where possible, and minimum 14 weeks paid parental leave. Pay equity is a fundamental principle of our employment policy and reflects our commitment to create a diverse, equitable and inclusive environment that treats all employees with dignity and respect, as outlined in our Code of Ethics. Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. Business Value Creation, Change Management, Consulting, Decision Making, Digital Capabilities, Influencing Skills, Information Technology (IT) Infrastructure, Information Technology Management, IT Governance, Stakeholder Engagement, System Integration, Technology Use Improving the lives of people living with disease takes more than innovative science. It takes a focus on the needs of people and a community committed to meeting them. It takes a team of people like you. Working together. Learning together. Thriving together. Discover how you can join us in changing people's lives. In the context of China Cross-Border Data Transfer (CBDT) policy, if you need to apply for a position in China, please go to the local Recruiting System TaleNov. #J-18808-Ljbffr

Se busca Técnico Electromecánico de Mantenimiento Industrial para realizar mantenimiento preventivo y correctivo, diagnosticar y solucionar averías, supervisar equipos y participar en mejoras continuas.Se requiere FP y experiencia industrial.Se ofrece contratación indefinida, salario de 34.