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Almirall seeks a QA GVP Specialist to support maintenance and improvement of the Pharmacovigilance Quality System in line with ICH, EU GVP, and applicable regulations. The role involves audits, inspections readiness, and coordinating outsourced QA activities across corporate and affiliate levels. Degree in Life Sciences with knowledge of pharmacovigilance regulations, data management, and statistics is required. Proficiency in English and IT systems is essential for success. #J-18808-Ljbffr

Estudi 6 Gestió Socioeducativa cerca un/a tallerista per impartir un taller de "Consciencia Postural" al Casal Cívic de Sant Vicenç dels Horts.Les sessions són els dimarts de 9:30 a 10:30 i començaran el 29/09/2026 fins al 15/12/2026, a Sant Vicenç dels Horts.La feina ofereix experiència en i

MOLINS invites you to join its Group Internal Control team as a Group Internal Control Specialist, reporting to the Group Internal Control Director. You will support the implementation, monitoring and continuous improvement of the Group Internal Control framework across geographies, driving consistent practices. This role involves coordinating with Local Internal Control teams, reviewing assessments, and contributing to reports and dashboards. #J-18808-Ljbffr

The Project Lead Global Data Trending Solution Cloud provides operational and functional leadership for initiatives related to the cloud evolution of GDTS, data integration, analytical capability definition, and the coordination of data-driven use cases within the BI Dataland environment. This role combines project leadership, systems analysis, data management, and stakeholder coordination to transform complex business, quality, and technology needs into executable plans and sustainable solutions. The successful candidate will work independently in a regulated and highly complex environment, creating clarity where requirements are ambiguous and connecting business, IT, data teams, suppliers, key users, and support teams throughout the initiative lifecycle. • Plan, coordinate and follow up GDTS Cloud initiatives using a structured, practical and results-oriented project management approach, • Manage priorities, dependencies, risks, issues, decisions, milestones and next steps transparently, • Prepare roadmaps, status summaries, executive materials, decision logs and progress documentation, • Facilitate workshops, refinement sessions, follow-up meetings and cross-functional alignment, • Analyse current and future processes related to GDTS Cloud, Continued Process Verification, reporting, dashboards and data consumption, • Translate business and quality needs into functional, technical and data requirements, including acceptance criteria and assumptions, • Define and document data flows, interfaces, system dependencies, transformation rules, controls and validation points, • Work with data sources, ingestion, cleansing, mapping, contextualisation, metadata, data quality, audit trail and traceability, • Support the connection between GDTS Cloud and BI Dataland-type ecosystems, including data products, downstream consumers and analytical reporting, • Coordinate multidisciplinary teams and suppliers, resolve blockers constructively and follow up commitments against agreed quality criteria, • Contribute to transition, training, handover, operational support and long-term solution sustainability, • Degree or equivalent professional experience in information technology, systems analysis, data management, engineering or a related discipline, • Senior experience in IT or data project management, functional analysis or systems analysis, including end-to-end delivery from discovery through transition and support, • Experience coordinating multidisciplinary teams and working with global stakeholders, suppliers, business functions and technical teams, • Practical knowledge of cloud data ecosystems, data lakes, data integration, data quality, metadata, interfaces, reporting and analytical consumption, • Experience working in regulated or GxP environments, with attention to validation, audit trail, traceability and compliant documentation, • High autonomy, ownership and the ability to operate effectively with limited supervision, • Strong analytical thinking and the ability to structure complex or ambiguous information, • Clear written, verbal and executive communication, adapted to technical and business audiences, • Disciplined organisation, documentation and follow-up, with a strong focus on decisions and delivery, • Familiarity with BI Dataland or equivalent enterprise data platforms is desirable, • Professional working English. German or Spanish is an additional asset depending on stakeholder needs, • GDTS Cloud use cases are clearly defined, prioritised and traceable, • Decisions concerning data, interfaces, models, reporting and ownership are documented and approved by the relevant stakeholders, • Teams work with a common structure for priorities, actions, risks and dependencies, • Deliverables support scalable, reusable and governed cloud solutions aligned with the BI Dataland ecosystem, • Executive communication remains clear, concise and supported by disciplined documentation The job title used in this advertisement may differ from the official contractual title. We are continuously working to design the best experience for you. Here are some examples of how we will take care of you: • Flexible working conditions, • Life and accident insurance, • Health insurance at a competitive price, • Investment in your learning and development, • Gym membership discounts Boehringer Ingelheim is a biopharmaceutical company active in both human and animal health. As one of the industry's top investors in research and development, the company focuses on developing innovative therapies that can improve and extend lives in areas of high unmet medical need. Independent since its foundation in 1885, Boehringer takes a long-term perspective, embedding sustainability along the entire value chain. Our approximately 54,300 employees serve over 130 markets to build a healthier and more sustainable tomorrow. Learn more at With us, you can develop your own path in a company with a culture that knows our differences are our strengths - and break new ground in the drive to make millions of lives better. Here, your development is our priority. Supporting you to build a career as part of a workplace that is independent, authentic and bold, while tackling challenging work in a respectful and friendly environment where everyone is valued and welcomed. Alongside, you have access to programs and groups that ensure your health and wellbeing are looked after - as we make major investments to drive global accessibility to healthcare. By being part of a team that is constantly innovating, you'll be helping to transform lives for generations. Want to learn more? Visit #J-18808-Ljbffr

Cuál es tu misión?Dar soporte al responsable de Producción en la planificación, coordinación, resolución y dirección del equipo de la fábrica, con el fin de cumplir con las necesidades de producción planificadas con los recursos materiales y humanos disponibles. Interactuar en el entorno de

Conocimientos altos en normativas de auditoría y cumplimiento (SCIIF, IFRS, Normas de auditoría, etc. Participará en la ejecución del plan anual de auditoría interna mediante la realización de auditorías financieras, operativas y de cumplimiento, contribuyendo a identificar oportunidades de m

En Admon Talent estamos buscando un/a Technical Product Owner para empresa tecnológica con oficinas en Sant Cugat del Vallès. Buscamos un/a profesional con marcado perfil técnico, a la que le guste entender cómo funciona el software en profundidad, analizarlo, probarlo y pensar continuamente cómo mejorarlo. Te convertirás en el referente técnico y funcional del producto, trabajando muy cerca con el equipo de ID y participando directamente en su evolución. Diseñar nuevas funcio... #J-18808-Ljbffr

The Medical Writing Senior Manager is responsible for leading the development, coordination, and delivery of high‑quality clinical and regulatory documents that support Almirall’s R&D programs. This role ensures scientific accuracy, regulatory compliance, and alignment with strategic and global submission objectives across therapeutic areas. The position collaborates cross‑functionally with clinical development, regulatory affairs, patient safety, biostatistics, and external partners to ensure timely, efficient, and effective communication of scientific data. The role also drives innovation through the informed use of AI/GenAI technologies and strengthened process governance with external vendors. Lead the planning, writing, and review of clinical and regulatory documents including protocols, investigator brochures, clinical study reports, paediatric documentation, responses to HA questions, and submission dossiers. Ensure consistency, clarity, and scientific integrity across all documents in compliance with ICH guidelines, GCP, and global regulatory requirements. Work closely with cross‑functional teams to gather scientific input and ensure alignment on messaging and content. Provide strategic input into document planning, dossier strategy, and global regulatory submission planning. Review and edit documents prepared internally or by external vendors to ensure scientific accuracy and adherence to standards. Contribute to the development and maintenance of medical writing standards, templates, guidance documents, and SOPs. Mentor and guide junior medical writers, fostering capability development and high‑quality output. Evaluate and implement AI/GenAI‑enabled authoring tools to enhance efficiency, consistency, and document quality. Establish guardrails, quality controls, and best practices for safe, compliant, and high‑quality use of AI‑generated content. Support change‑management activities, internal training, and workflow integration of AI/GenAI capabilities within the medical writing team. Manage external medical writing vendors, including selection, contracting, oversight, and performance review. Ensure robust process governance, quality standards, and clear communication channels with external partners. Advanced degree in Life Sciences (PhD, PharmD, MD, MSc or equivalent experience). Minimum 8 years of experience in medical writing within the pharmaceutical or biotech industry. Proven track record in authoring and managing clinical and regulatory documents for global submissions. Experience working with external vendors and overseeing outsourced activities. Fluent in English. Strong understanding of ICH guidelines, GCP, CTD requirements, and global regulatory frameworks. Knowledge of AI/GenAI tools and practical experience integrating them into document workflows is highly desirable. Proficiency with document management systems, authoring tools, and structured content management approaches. Strong communication skills and ability to work in dynamic cross‑functional environments. Excellent attention to detail, strategic thinking, and ability to manage multiple priorities. Strong influencing capacities, and vendor‑management capabilities. #J-18808-Ljbffr

Energy/ Utilities Expert Procurement Strategic Purchaser Descripción del puesto Eres una parte importante de nuestro futuro. ¡Esperamos ser también parte de su futuro! En B. Braun, protegemos y mejoramos la salud de las personas en todo el mundo. Tú apoyas esta visión, aportando experiencia y compartiendo la innovación, la eficiencia y la sostenibilidad como valores. Por eso nos gustaría seguir desarrollando nuestra empresa contigo. Teniendo en cuenta tu futuro, estamos haciendo una contribución conjunta a la atención médica en todo el mundo, con confianza, transparencia y reconocimiento. Eso es Sharing Expertise. Energy/ Utilities Expert Procurement Strategic Purchaser Empresa: B. Braun Medical, S.A. U. Ubicación del puesto: Rubí, Barcelona, Spain Área funcional: Compras Modelo de trabajo: Híbrido ID de la demanda: 12142 Location: Europe Department: Global Indirect Procurement Reporting line: Direct reporting line to the Director Global Category Cluster We are looking for a Global Category Manager (m/f/d) for Utilities for our global indirect procurement organization at the earliest possible date. The Utilities & Sterilization Services department is responsible for the strategic procurement of external services and products in the areas of energy supply (including electricity, gas, steam) and sterilization services. We act as a proactive business partner to internal functions and production sites, aiming to achieve optimal results across the dimensions of quality, supply security, sustainability, innovation, risk, and cost. The key to successful procurement lies in cross-functional and global collaboration, as well as a deep understanding of technical requirements and regulatory frameworks. • Development and implementation of a global category strategy within the overall global energy procurement strategy, • Representation of procurement towards external business partners and senior management, • Monitoring of markets, as well as analysis of innovation and technology trends, • Negotiation and conclusion of energy contracts with a strong focus on risk and cost optimization, • Monitoring regulatory developments in energy markets and deriving required actions, • Collaboration with internal stakeholders (e.g., sustainability team, facility management, finance), • Responsibility for CSRD-relevant procurement measures including PPAs, ESG integration, and reporting support, • Degree in business administration, engineering, energy economics, or comparable, • Several years of experience in strategic energy procurement, • Solid knowledge of energy markets (electricity and gas), • Experience with PPAs and sustainability strategies, • Strong understanding of end-to-end procurement processes, • Fluency in English and Spanish; German is an advantage, • Proficiency with digital tools and MS Office, • SAP knowledge is a plus, • Strong strategic mindset and analytical skills, • Excellent communication and negotiation skills, • High level of initiative and responsibility, • Team player with intercultural competence, • Affinity for sustainability and innovation B. Braun Medical, S.A. U.|Soledad Barragán López #J-18808-Ljbffr

SOPREMA Iberia busca un Director/a de Prescripción para impulsar la prescripción de soluciones técnicas, liderar el equipo y generar negocio mediante relaciones con promotores, arquitectos e ingenierías.

PROMAN Spain busca un Responsable de Compras y Supply Chain para optimizar el flujo de materiales desde proveedores hasta el cliente final. Liderarás la planificación de compras, la gestión de pedidos y la coordinación de importaciones, con foco en eficiencia y coste. Se valorará experiencia en comercio internacional, manejo de ERP y conocimiento de Incoterms. Ofrecemos incorporación estable, desarrollo profesional y salario competitivo, según experiencia. #J-18808-Ljbffr

ASSOCIATE DIRECTOR, REGULATORY AFFAIRSBewerbenremote type: R&D & Medical Affairslocations: SANT FELIU DE LLOBREGATtime type: Full timeposted on: Vor 4 Tagen ausgeschriebenjob requisition id: Warum Almirall?Wir gestalten die Zukunft der medizinischen Dermatologie, indem wir uns auf unerfüllte Bedürfnisse von Patient:innen konzentrieren und Menschen den Raum geben, eigenständig zu denken, Verantwortung zu übernehmen und Wirkung zu erzielen, die wirklich zählt.Unser Anspruch ist klar: das Leben von Patient:innen zu verbessern, indem wir auf echte Bedürfnisse eingehen. Wir arbeiten mit Präzision, handeln mutig, halten die Dinge einfach und richten unsere Innovation dort aus, wo sie wirklich einen Unterschied macht.Als Top Employer in Spanien seit 2008 und in Deutschland seit 2025 investieren wir kontinuierlich in ein Umfeld, in dem Menschen wachsen und vorankommen können.Wenn du Dinge anders angehst, bist du hier richtig.POSITION SUMMARY / MISSIONThe Associate Director, Regulatory Affairs is responsible for leading regulatory strategies and operations to support the development, registration, and lifecycle management of Assigned Almirall’s pharmaceutical products across global markets. This role ensures regulatory compliance, drives submission excellence, and provides strategic input into cross-functional development plans. The position collaborates closely with internal stakeholders and health authorities to enable timely approvals and maintain regulatory integrity throughout the product lifecycle.CORE RESPONSIBILITIESDefine and implement global regulatory strategies for development and marketed products Lead the preparation and submission of regulatory dossiers (e.g., CTA, MAA, variations, renewals) in alignment with regional requirements Provide regulatory guidance to cross-functional teams including Clinical, CMC, Safety, and Market Access Manage interactions with health authorities and respond to regulatory queries Ensure compliance with applicable regulations, guidelines, and internal procedures Monitor regulatory changes and assess impact on Almirall’s portfolio and operations Support due diligence and licensing activities from a regulatory perspective Contribute to the development and maintenance of regulatory systems, tools, and SOPs Represent Regulatory Affairs in internal governance and decision-making forumsREQUIRED EDUCATION AND EXPERIENCEBachelor’s degree in Life Sciences or Pharmacy; advanced degree preferred Minimum 8 years of experience in Regulatory Affairs within the pharmaceutical industry Proven track record in global regulatory submissions and interactions with health authorities Fluent in EnglishPREFERRED SKILLS AND COMPETENCIESStrong knowledge of EU, US and international regulatory frameworks Excellent project management and organizational skills Strategic thinking and problem-solving capabilities Effective communication and stakeholder management skills Ability to work in cross-functional and multicultural environments #J-18808-Ljbffr

Linde Material Handling es una empresa global líder en soluciones intralogísticas. Buscamos un profesional para coordinar pricing y la gestión de recambios, trabajando estrechamente con el Service Director y con soporte centralizado en Alemania. La función implica negociar con proveedores, alinear precios, gestionar proyectos y desarrollar campañas de marketing y branding, con foco en datos para impulsar decisiones estratégicas en un entorno internacional y multilingüe. #J-18808-Ljbffr

Almirall in Sant Feliu de Llobregat is seeking a Director of Computational Discovery to lead the strategic, scientific and operational direction of computational discovery activities, including Bioinformatics and Molecular modelling, with a focus on disease understanding and target identification.

At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters. At Roche, we are passionate about transforming patients’ lives and we are fearless in both decision and action - we believe that good business means a better world. We commit ourselves to scientific rigor, unassailable ethics, and access to medical innovations for all. In this exciting and challenging position as Milestone & Change Support Senior Specialist, you will play a key role in advising and supporting the R&D units of Diagnostics in the planning, tracking, and preparation of product development documentation for design control and regulatory requirements. You work in a cross-functional team distributed across multiple locations involved in global product development projects. Furthermore, you will be in continuous exchange with our internal stakeholders across multiple functions to optimize processes and support offerings. The Milestone & Change Support Team is part of a global team in R&D that focuses on internal improvement: increasing productivity, efficiency, and the ability of the R&D organization to collaborate across its global organizational interfaces. Perfection is our passion, and relieving the workload of R&D units while boosting our customers' effectiveness and efficiency is our mission. Excellence and customer orientation define our identity. We support each other unconditionally, but we are also not afraid to handle tasks independently and proactively. Through our high focus, we accelerate and optimize internal processes, easing the burden on the organization. You share responsibility for the proactive creation, implementation, monitoring, and improvement of quality of product documentation under the quality management standards. Your goal is to achieve project milestones without corrective actions and to ensure IVDR-compliant recertification of our products. You make a decisive contribution to keeping our product portfolio at a continuously IVDR-compliant documentation standard. You share responsibility for providing all types of resources to actively support stakeholders regarding project/product documentation, actively contributing to the continuous development of our standards and tools. You are responsible for implementing and maintaining applicable regulations on occupational health and environmental safety, quality management, Roche guidelines, legal requirements, and regulatory demands. Education: University degree, preferably in a technical, scientific, or business discipline - preferably in Chemistry, Biology, or Pharmaceutical sciences. Experience: 5+ years of relevant professional experience in diagnostic product development, document management, and compliant documentation of R&D products. Language Skills: Excellent written and verbal English AND German Language skills are required. You should have comprehensive knowledge of quality management systems, ISO 13485, IVDR, and/or MDR 2017/745/EU, as well as practical experience with post-market surveillance and vigilance processes and product change management. You are confident and proficient in using common office applications and document management systems. A high level of service orientation and customer focus come naturally to you, as do utmost care and reliability. Interdisciplinary thinking and strong negotiation skills are among your strengths. You possess strong self-organizational skills, are willing to work independently with minimal guidance, and like to drive things forward proactively. As a senior specialist, you may be asked to coach or mentor more junior employees or lead initiatives. A confident demeanor, excellent communication skills, and the ability to build a shared understanding set you apart. You have a strong drive and ability for teamwork and thoroughly enjoy working with intercultural and international teams. Occasional multi-day travel to other Roche sites (e.g. Germany, Switzerland) may be required. To support the global nature of our work (e.g. collaboration between the US and Europe), customer and stakeholder meetings periodically require participation in meetings during the early evening hours (e.g. 1900). A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact. Let’s build a healthier future, together. Roche is an Equal Opportunity Employer. We believe it’s urgent to deliver medical solutions right now – even as we develop innovations for the future. We are passionate about transforming patients’ lives. We are courageous in both decision and action. And we believe that good business means a better world. That is why we come to work each day. We commit ourselves to scientific rigor, unassailable ethics, and access to medical innovations for all. We do this today to build a better tomorrow. We are proud of who we are, what we do, and how we do it. We are many, working as one across functions, across companies, and across the world. We are Roche. #J-18808-Ljbffr

PRINCIPAL INVESTIGATOR, PROJECT LEADERApplylocations: SANT FELIU DE LLOBREGATtime type: Full timeposted on: Posted 30+ Days Agojob requisition id: POSITION SUMMARY / MISSIONThe Principal Investigator, Project Leader leads scientific strategy and execution for a discovery or development project, integrating biology, chemistry, translational, and clinical inputs to advance assets through key milestones. The role frames hypotheses, designs experiments, interprets data, and guides cross-functional teams to make decisive, data-driven choices.This position fosters scientific excellence, collaboration, and external visibility through publications and conferences while ensuring robust documentation, IP awareness, and compliance with EHS and ethical standards.CORE RESPONSIBILITIES• Define scientific strategy and deliverables for assigned project(s); maintain clear objectives and go/no-go criteria.• Design and oversee experimental plans; interpret results and steer decision making.• Lead cross-functional teams (e.g., biology, chemistry, DMPK, tox, CMC) and manage external collaborations.• Present findings to governance; maintain rigorous documentation and data integrity.• Contribute to publications, patents, and scientific engagement with KOLs and partners.• Manage budgets/timelines; identify risks and implement mitigations.REQUIRED EDUCATION AND EXPERIENCE• PhD in a relevant scientific discipline with strong postdoctoral/industry experience.• 6–8+ years in drug discovery/development with demonstrated project leadership.• Track record of impactful scientific contributions and cross-functional collaboration.• Strong communication, data interpretation, and strategic thinking skills.PREFERRED SKILLS AND COMPETENCIES• Experience progressing assets through IND-enabling and early clinical stages.• Publications and conference presence in relevant therapeutic area.• Experience managing CROs/academic collaborations.Discovery Project Leader -responsible in building the scientific breakthrough for novel therapeutic treatments and leading cross-functional teamsWhy work with Almirall?We are a people-centric company where employees are at their best, patients and customer are at the heart of every decision, and our focus and agility allow us to deliver greater impact for all.Additionally, for the 17th year in a row, we have been certified as Top Employer Spain, and also Top Employer Germany for the first time.This strengthens our commitment to create a unique work environment that helps our employees to develop their skills to fullest and grow both professionally and as individuals.We are delighted to have a great team that is proactive, innovative, and eager to transform the world of people with skin conditions.We are proud of each one of our employees, their development, and growth: they are the success of the company.Our purpose"Transform the patients' world by helping them realize their hopes & dreams for a healthy life".*Our values Care: we listen & empathize, we value diverse perspectives & backgrounds and we help each other succeed.* Courage: we challenge the status quo, we take full ownership and we learn from our success & failures.* Innovation: we put the patient and customer at the center, we create novel solutions and we empower entrepreneurial mindsets.* Simplicity: we act decisively and avoid over-analysis, we understand why before we act and we are agile & keep things simple.At Almirall, it’s all about people!#wearealmirall**### About us. Uncommon by Nature.For more than 80 years, we have combined science and purpose to advance medical dermatology—turning research into solutions that improve patients’ lives.Uncommon by Nature is who we are. A way of thinking and working that prioritises relevance over size, combines long‐term ambition with the drive to deliver impact now, and challenges what’s expected to raise standards in medical dermatology.### Why work here? A pivotal momentAlmirall is at a pivotal moment, shaped by clear strategic direction, bold scientific ambition and the capabilities to redefine what’s possible in medical dermatology.Joining now means becoming part of a company that has placed R&D at its core from day one. As the only fully integrated pharmaceutical company in the Western Hemisphere dedicated exclusively to medical dermatology, we cover the full value chain — from discovery and development to manufacturing and commercialization.Let’s shape what comes next. #J-18808-Ljbffr

KION Group AG seeks an SAP Inhouse Consultant (PP) to drive standardization and process improvements across Europe. The role involves detailing process steps, coordinating global key users, and managing new SAP PP requirements with a focus on cross-regional alignment.

Se busca persona para mantenimiento en Sant Vicenç dels Horts, en una empresa de transporte frigorífico. Las tareas incluyen comprobar el estado de los equipos mediante pruebas y mediciones, realizar mantenimiento preventivo y reparar averías cuando sea necesario para que la actividad siga funcio

Almirall, S.A. è alla ricerca di un Associate Director, Regulatory Affairs per guidare strategie regolatorie globali e operazioni di sviluppo e lifecycle management dei prodotti farmaceutici, con contatti continuativi con le autorità sanitarie a livello globale. La posizione è basata a Sant Feliu de Llobregat (Spagna) e richiede almeno 8 anni in Regulatory Affairs, laurea in Scienze della Vita o Farmacia ed eccellente padronanza dell’inglese; è preferita una laurea avanzata. #J-18808-Ljbffr

Coordinador técnico regional para Linde Material Handling, liderando equipos de expertos y brindando soporte técnico especializado en intralogística.

STILL cerca un Consulente SAP Inhouse (EWM) per Operations ITS EMEA, in un contesto internazionale. Definirai processi, standardizzerai attività e supporterai regioni e siti per estensioni di scope, con attenzione a efficienza e trasparenza. Richiesta laurea o titolo equivalente, 5 anni di esperienza in SAP EWM, forte capacità di analisi dei processi e ottima conoscenza dell’inglese; disponibilità a viaggiare e a lavorare in contesti multicountry è essenziale. #J-18808-Ljbffr

¿Buscas trabajo en transporte, logística y almacén? Este mes de septiembre surgen nuevas oportunidades para carretilleros en Molins de Rei. ¡Inscríbete gratis hoy mismo!

• Liderar y coordinar al equipo de QA SAP, promoviendo la colaboración, el desarrollo profesional y la consecución de objetivos de calidad., • Definir y supervisar la estrategia de pruebas para proyectos SAP, asegurando el cumplimiento de estándares y buenas prácticas., • Gestionar el ciclo de vida de las pruebas mediante herramientas especializadas, asegurando la trazabilidad y el seguimiento de los resultados., • Impulsar la definición y evolución de los marcos de automatización de pruebas., • Colaborar con equipos multidisciplinares para identificar, analizar y resolver incidencias relacionadas con la calidad del software., • Realizar el seguimiento de indicadores clave de calidad, elaborando informes y proponiendo acciones de mejora., • Aportar mentoría y soporte al equipo, fomentando una cultura de aprendizaje continuo., • Titulación universitaria en Informática, tecnologías de la Información o áreas afines., • Experiencia sólida liderando equipos de QA y participando en proyectos de implantación SAP., • Experiencia en automatización de pruebas y definición de estrategias de testing., • Capacidad demostrable para gestionar múltiples prioridades y trabajar con plazos exigentes., • Excelentes habilidades de comunicación, colaboración y liderazgo., • Capacidad analítica, orientación al detalle y resolución de problemas., • Experiencia con SAP Solution Manager o SAP Cloud ALM (muy positivo)., • Conocimientos y experiencia con Tricentis Tosca (muy positivo)., • Certificaciones relacionadas con testing de software, automatización o metodologías de calidad (muy positivo). #J-18808-Ljbffr

ASSOCIATE DIRECTOR, REGULATORY AFFAIRSPresenta candidaturaremote type: R&D & Medical Affairslocations: SANT FELIU DE LLOBREGATtime type: Full timeposted on: Offerta pubblicata 2 giorni fajob requisition id: Stiamo costruendo il futuro della dermatologia medica concentrandoci sui bisogni ancora insoddisfatti dei pazienti e dando alle persone lo spazio per pensare in modo indipendente, assumersi responsabilità e generare un impatto che conta davvero.Il nostro purpose è semplice: trasformare la vita dei pazienti rispondendo a bisogni reali. Lavoriamo con rigore, agiamo con coraggio, teniamo le cose semplici e orientiamo l’innovazione dove può davvero fare la differenza.Riconosciuti come Top Employer in Spagna dal 2008 e in Germania dal 2025, continuiamo a investire in un ambiente in cui le persone possono crescere e andare avanti.Se pensi in modo diverso, qui è il posto giusto per te.POSITION SUMMARY / MISSIONThe Associate Director, Regulatory Affairs is responsible for leading regulatory strategies and operations to support the development, registration, and lifecycle management of Assigned Almirall’s pharmaceutical products across global markets. This role ensures regulatory compliance, drives submission excellence, and provides strategic input into cross-functional development plans. The position collaborates closely with internal stakeholders and health authorities to enable timely approvals and maintain regulatory integrity throughout the product lifecycle.CORE RESPONSIBILITIESDefine and implement global regulatory strategies for development and marketed products Lead the preparation and submission of regulatory dossiers (e.g., CTA, MAA, variations, renewals) in alignment with regional requirements Provide regulatory guidance to cross-functional teams including Clinical, CMC, Safety, and Market Access Manage interactions with health authorities and respond to regulatory queries Ensure compliance with applicable regulations, guidelines, and internal procedures Monitor regulatory changes and assess impact on Almirall’s portfolio and operations Support due diligence and licensing activities from a regulatory perspective Contribute to the development and maintenance of regulatory systems, tools, and SOPs Represent Regulatory Affairs in internal governance and decision-making forumsREQUIRED EDUCATION AND EXPERIENCEBachelor’s degree in Life Sciences or Pharmacy; advanced degree preferred Minimum 8 years of experience in Regulatory Affairs within the pharmaceutical industry Proven track record in global regulatory submissions and interactions with health authorities Fluent in EnglishPREFERRED SKILLS AND COMPETENCIESStrong knowledge of EU, US and international regulatory frameworks Excellent project management and organizational skills Strategic thinking and problem-solving capabilities Effective communication and stakeholder management skills Ability to work in cross-functional and multicultural environments #J-18808-Ljbffr

Draxton Central Services in Sant Vicenç dels Horts is seeking a Machining Technology Engineer to design and industrialize machining processes, fixtures and tooling for new products. You will work with engineering teams, plants and suppliers from design through validation to deliver robust, cost-efficient solutions. The role reports to the Machining Technology Leader and requires hands-on expertise in machining, CNC programming and process optimization, with an emphasis on continuous improvement #J-18808-Ljbffr

Se buscan dos personas para realizar verificaciones en el sector de automoción en Martorell, con incorporación para días puntuales. El contrato es temporal y de jornada completa, con 8 horas diarias de lunes a viernes en turno de mañana, entre las 08:00 y las 16:00 horas, respetando los descansos que marca la ley. Las tareas principales consisten en revisar piezas de automoción, clasificarlas según los defectos detectados y realizar el retrabajo de parachoques, además de otras funciones habituales del puesto. Es un trabajo dinámico y práctico, centrado en el control de calidad y el acabado de los componentes. Se valorará la atención al detalle y la capacidad para seguir las indicaciones del proceso, así como el ritmo constante en un entorno de producción. La persona seleccionada se incorporará a un equipo con tareas bien definidas y supervisión cercana.

Almirall Hermal GmbH in Sant Feliu de Llobregat seeks a Principal Investigator, Project Leader to steer scientific strategy and execution across discovery and development programs. You will integrate biology, chemistry, translational and clinical inputs, frame hypotheses, design experiments, interpret data, and guide cross-functional teams to data-driven go/no-go decisions. We value strong communication, robust documentation, and a track record of leading ambitious projects from concept to near #J-18808-Ljbffr

Fistrek en Cataluña busca un Consultor SAP MM-FI con experiencia en SAP S/4HANA para liderar la adecuación del SCIIF y la integración entre los módulos MM y FI.

Trabajo en el sector alimentario en Gelida para operario/a de líneas de producción.

Lear Corporation is seeking an EHS Specialist for the Martorell JIT facility to coordinate Environmental, Health, and Safety programs and promote a proactive safety culture. You will collaborate with employees, supervisors, and site leadership to reduce workplace risks and drive continuous improvement across operations. The role requires a Master’s degree in Safety or related field and 4+ years of manufacturing EHS experience, with strong knowledge of relevant regulations and incident #J-18808-Ljbffr

El verificador de piezas y calidad desempeña un papel fundamental en los procesos de manufactura, asegurando que todos los componentes cumplan con los estándares de calidad establecidos antes de pasar a las siguientes etapas de la cadena de producción. La persona seleccionada trabajará en estrec

Almirall Hermal GmbH sucht einen QA GVP Quality Assurance Specialist zur Unterstützung des Qualitätsmanagementsystems für Pharmakovigilanz. Sie arbeiten eng mit dem GVP Senior Manager zusammen und unterstützen Audits, Inspektionen und die Vorbereitung von Behördenprüfungen in Europa. Ihre Aufgaben umfassen die Mitwirkung bei der Planung und Durchführung risikobasierter Auditprogramme, die Erstellung und Pflege relevanter SOPs sowie die Koordination ausgelagerter QA-Aktivitäten im #J-18808-Ljbffr

¿Buscas trabajo en industria y producción? Este mes de septiembre surgen nuevas oportunidades para operarios en Gelida. ¡Inscríbete gratis hoy mismo!

QA SPECIALISTApplyremote type: Industrial Operationslocations: SANT FELIU DE LLOBREGAT: SANT ANDREU DE LA BARCAtime type: Full timeposted on: Posted 3 Days Agotime left to apply: End Date: July 31, 2026 (20 days left to apply)job requisition id: We’re building the future of medical dermatology by focusing on unmet patient needs and giving people the space to think independently, take ownership and make an impact that matters.Our purpose is simple: to transform patients’ lives by addressing real needs. We work with care, act with courage, keep things simple and focus our innovation where it makes a difference.Recognised as a Top Employer in Spain since 2008 and in Germany since 2025, we continue to invest in an environment where people can grow and move forward.If you care differently, you belong here.MissionTo support the maintenance, development and continuous improvement of the Almirall GVP Quality Management System ensuring compliance with applicable regulations and guidelines.Responsibilities1. To support the QA GVP Senior manager in maintaining the Quality System for Pharmacovigilance activities in accordance with Almirall policies, ICH guidelines, EU GVP modules, and other relevant regulatory requirements with the support of the Almirall Corporate Patient Safety department.2. To cooperate in the setting up of the GVP risk-based audit plan and program and in performing (or coordinating and overseeing when outsourced) audits on a regular basis.3. To report the audit observations arising from audits (or any other quality issue) to applicable management and follow-up on the significant findings until completion.4. To help in the preparation and management of inspection by Competent Authorities and audits by third parties to Almirall by developing an inspection readiness plan.5. To drat the procedures applicable to QA Drug Safety and any other key documents ensuring that they are aligned and compliant with the applicable regulation.6. To contribute in selecting, coordinating and overseeing the outsourced QA activities applicable to pharmacovigilance (e.g. audits, mock inspections, training).9. To support the Pharmacovigilance audits to the Almirall Pharmacovigilance system including processes, partners and CROs at both corporate and affiliate level.EducationLife Sciences degreeSpecific expertise- Knowledge of drug safety, data management, and statistics.- IT systems skills.- Awareness of EU and non-EU regulations applicable to pharmacovigilance.- Training in Quality Assurance, specifically R&D areas.- Proficiency in English languageCENTRO: R&D - Sant Feliu de LLobregatTIPO DE CONTRATO: TemporalGRUPO PROFESIONAL: 6HORARIO: Central FlexQA R&D & CPD - GVP Quality Assurance Specialist #J-18808-Ljbffr

QA SPECIALISTPassa a contenuto principaleQuesto sito web utilizza cookie Questo sito web utilizza cookie propri e di terzi allo scopo di offrire funzionalità di social network e ricavare statistiche. Puoi impostare le tue preferenze per rifiutare o accettare i cookie qui. Per ulteriori informazioni, consulta la nostra Politica sui cookie.# Lavora con noiQA SPECIALIST page is loaded## QA SPECIALISTPresenta candidaturaremote type: Industrial Operationslocations: SANT FELIU DE LLOBREGAT: SANT ANDREU DE LA BARCAtime type: Full timeposted on: Offerta pubblicata 3 giorni fatime left to apply: Data fine: 31 luglio 2026 (20 giorni rimanenti per candidarsi)job requisition id: Stiamo costruendo il futuro della dermatologia medica concentrandoci sui bisogni ancora insoddisfatti dei pazienti e dando alle persone lo spazio per pensare in modo indipendente, assumersi responsabilità e generare un impatto che conta davvero.Il nostro purpose è semplice: trasformare la vita dei pazienti rispondendo a bisogni reali. Lavoriamo con rigore, agiamo con coraggio, teniamo le cose semplici e orientiamo l’innovazione dove può davvero fare la differenza.Riconosciuti come Top Employer in Spagna dal 2008 e in Germania dal 2025, continuiamo a investire in un ambiente in cui le persone possono crescere e andare avanti.Se pensi in modo diverso, qui è il posto giusto per te.MissionTo support the maintenance, development and continuous improvement of the Almirall GVP Quality Management System ensuring compliance with applicable regulations and guidelines.Responsibilities1. To support the QA GVP Senior manager in maintaining the Quality System for Pharmacovigilance activities in accordance with Almirall policies, ICH guidelines, EU GVP modules, and other relevant regulatory requirements with the support of the Almirall Corporate Patient Safety department.2. To cooperate in the setting up of the GVP risk-based audit plan and program and in performing (or coordinating and overseeing when outsourced) audits on a regular basis.3. To report the audit observations arising from audits (or any other quality issue) to applicable management and follow-up on the significant findings until completion.4. To help in the preparation and management of inspection by Competent Authorities and audits by third parties to Almirall by developing an inspection readiness plan.5. To drat the procedures applicable to QA Drug Safety and any other key documents ensuring that they are aligned and compliant with the applicable regulation.6. To contribute in selecting, coordinating and overseeing the outsourced QA activities applicable to pharmacovigilance (e.g. audits, mock inspections, training).9. To support the Pharmacovigilance audits to the Almirall Pharmacovigilance system including processes, partners and CROs at both corporate and affiliate level.EducationLife Sciences degreeSpecific expertise- Knowledge of drug safety, data management, and statistics.- IT systems skills.- Awareness of EU and non-EU regulations applicable to pharmacovigilance.- Training in Quality Assurance, specifically R&D areas.- Proficiency in English languageCENTRO: R&D - Sant Feliu de LLobregatTIPO DE CONTRATO: TemporalGRUPO PROFESIONAL: 6HORARIO: Central FlexQA R&D & CPD - GVP Quality Assurance Specialist #J-18808-Ljbffr

Almirall, S.A. cerca un IT Business Process Manager per il team R&D Data Science a Sant Feliu de Llobregat. Ruolo di punto di contatto tra DS, bioinformatica e AI Engineering per allineare le applicazioni DS interne ed esterne, guidando consegna e adozione. Richiesta forte background scientifico, almeno 5 anni in ambiente R&D Pharma e competenze in infrastrutture cloud, pipeline DS e conformità. Ruolo chiave per accelerare insight e innovazione. #J-18808-Ljbffr

Are you looking for a stable opportunity with strong growth potential in the mobility industry? We would love to get to know you and tell you more about our project. We are an industrial company specialized in manufacturing components for electric, hybrid and internal combustion vehicles. Backed by a team of 4,000 people across 6 countries, we operate 13 production plants and 3 engineering centers, serving more than 100 customers worldwide. Are you motivated by the opportunity to contribute to new industrial projects and define machining processes from the design stage through to implementation? At Draxton Central Services , located in Sant Vicenç dels Horts , we are looking to incorporate a Machining Technology Engineer . The person joining us will have the opportunity to transform ideas into real industrial solutions, defining machining processes, fixtures and tooling that are key to the manufacturing of our products. They will participate in projects from the initial design phase through final validation, collaborating with engineering teams, plants and suppliers to develop efficient, robust solutions focused on continuous improvement. The position will report to the Machining Technology Leader . • You will define and develop machining processes, fixtures and tooling required to industrialize new products, ensuring robust, efficient and competitive solutions., • You will participate from the early stages of projects, providing technical expertise to ensure feasibility, cost optimization, and achievement of quality and timing targets., • You will collaborate with engineering teams, plants and suppliers in the design and implementation of manufacturing solutions, driving innovation and continuous improvement., • You will evaluate investments, processes, technologies and equipment, identifying opportunities to increase efficiency and strengthen project competitiveness., • You will develop machining standards, criteria and best practices, promoting standardization and knowledge sharing across the organization., • You will provide technical support to plants and engineering teams, helping solve manufacturing challenges and build capabilities in machining technologies., • Degree in Engineering., • Minimum of three years of experience in industrial environments related to machining processes, ideally within the automotive industry., • Solid knowledge of machining processes, CNC programming and chip-removal manufacturing technologies., • Ability to interpret technical requirements and contribute to the development and industrialization of new products and processes., • Advanced level of English, enabling effective communication in technical environments and collaboration with a wide range of stakeholders., • Permanent contract within a solid and growing company., • Full-time position with flexible start and finish times, plus Friday afternoons off., • Up to 6 remote working days per month., • 30 vacation days per year., • Training plans and professional development opportunities., • Participation in global projects and collaboration with multicultural and diverse teams., • Direct collaboration with leading manufacturers in the industry and exposure to a wide variety of products., • You will participate in actions that contribute to the advancement and innovation of the sector., • You will be part of an environment that promotes diversity and inclusion., • You will contribute to a more sustainable future by focusing on reducing the carbon footprint and enhancing the circular economy. Are you motivated by this project and feel you’re a good fit for this position? #J-18808-Ljbffr

Roche Diagnostics Solutions (CSI) seeks a Senior Product Owner to shape the product vision, own the backlog, and translate business needs into clear priorities for delivery. You will work with C#/.NET and Rust engineers, Scrum Masters, QA, and architects to ensure outcomes align with business goals and feasibility. You will translate requirements, drive prioritization, manage dependencies, and report status to keep teams aligned and delivering value in an agile environment. #J-18808-Ljbffr

MOLINS, a group focused on sustainable and innovative construction solutions, is seeking a Group Internal Control Specialist to support the Group Internal Control framework across geographies. You will work with Internal Control, Internal Audit, and external auditors to monitor, improve, and standardize controls and reporting. The role involves coordinating with local control functions, applying group requirements, and contributing to dashboards and annual planning while leveraging data #J-18808-Ljbffr

Liderar la estrategia comercial y la ejecución de ventas del negocio de Pintura Decorativa, gestionando los diferentes segmentos de clientes y mercados mediante la aplicación de las herramientas y metodologías comerciales de Jotun. Será responsable de planificar, ejecutar y hacer seguimiento de

Empresa iVascular Sede Sant Vicenç dels Horts, España Profesión/ Función I+D.

iVascular, parte del grupo LVD Biotech, busca un Lead Quality Assurance para unirse al equipo clínico en Sant Vicenç dels Horts (Barcelona). Serás responsable de garantizar la eficacia del SGC, cumplimiento normativo, gestión de riesgos y la calidad de nuestros dispositivos médicos. Se requiere 6 años de experiencia en calidad, dominio de ISO 13485/14644 e inglés avanzado. Ofrecemos contrato indefinido, salario competitivo y beneficios en un entorno global e innovador. #J-18808-Ljbffr

Responsable de Filiales Europa Barcelona | Viajes internacionales frecuentes | Canal Farmacia ¿Te apasiona liderar negocios internacionales y desarrollar equipos en diferentes mercados? En MartiDerm buscamos incorporar un/a Responsable de Filiales Europa , una posición estratégica desde la que l

Almirall, S.A. cerca un Senior Manager per dirigere progetti istituzionali nel Market Access, coordinando attività trasversali con medical affairs, access e partner esterni per avanzare le iniziative dermatologiche. La posizione richiede almeno 7 anni nel settore farmaceutico, laurea e Master in Health Policy o equivalente; ottime capacità di comunicazione, gestione stakeholder e lavoro in contesto matrix. #J-18808-Ljbffr

Valorable experiencia con CMS Playtech, conocimientos del sector iGaming, experiencia en diseño digital o desarrollo front-end, conocimientos de PHP, MySQL o Python, así como experiencia en entornos digitales de alto tráfico. Si te apasionan los entornos digitales, la experiencia de usuario y qui

Chez Roche, vous pouvez être vous-même et être apprécié pour les qualités uniques que vous apportez. Notre culture encourage l'expression personnelle, le dialogue ouvert et les connexions authentiques, où vous êtes valorisé, accepté et respecté pour ce que vous êtes, vous permettant de prospérer tant personnellement que professionnellement. Voici comment nous visons à prévenir, arrêter et guérir les maladies et à garantir à chacun l'accès aux soins de santé aujourd'hui et pour les générations à venir. Rejoignez Roche, où chaque voix compte. Who We Are At Roche, we are passionate about transforming patients’ lives and we are fearless in both decision and action - we believe that good business means a better world. We commit ourselves to scientific rigor, unassailable ethics, and access to medical innovations for all. What Awaits You: In this exciting and challenging position as Milestone & Change Support Specialist, you will play a key role in advising and supporting the R&D units of Diagnostics in the planning, tracking, and preparation of product development documentation for design control and regulatory requirements. You work in a cross-functional team distributed across multiple locations involved in global product development projects. Furthermore, you will be in continuous exchange with our internal stakeholders across multiple functions to optimize processes and support offerings. Your Team The Milestone & Change Support Team is part of a global team in R&D that focuses on internal improvement: increasing productivity, efficiency, and the ability of the R&D organization to collaborate across its global organizational interfaces. Perfection is our passion, and relieving the workload of R&D units while boosting our customers' effectiveness and efficiency is our mission. Excellence and customer orientation define our identity. We support each other unconditionally, but we are also not afraid to handle tasks independently and proactively. Through our high focus, we accelerate and optimize internal processes, easing the burden on the organization. Your Responsibilities: • You share responsibility for the proactive creation, implementation, monitoring, and improvement of quality of product documentation under the quality management standards., • Your goal is to achieve project milestones without corrective actions and to ensure IVDR-compliant recertification of our products, • You make a decisive contribution to keeping our product portfolio at a continuously IVDR-compliant documentation standard, • You share responsibility for providing all types of resources to actively support stakeholders regarding project/product documentation, actively contributing to the continuous development of our standards and tools, • You are responsible for implementing and maintaining applicable regulations on occupational health and environmental safety, quality management, Roche guidelines, legal requirements, and regulatory demands Who You Are: • Education: University degree, preferably in a technical, scientific, or business discipline - preferably in Chemistry, Biology, or Pharmaceutical sciences, • Experience: 3+ years of relevant professional experience in diagnostic product development, document management, and compliant documentation of R&D products., • Language Skills: Excellent written and verbal English AND German Language skills are required, • Preferred candidates have knowledge of quality management systems, ISO 13485, IVDR, and/or MDR 2017/745/EU, as well as practical experience with post-market surveillance and vigilance processes and product change management, • You are confident and proficient in using common office applications and document management systems, • A high level of service orientation and customer focus come naturally to you, as do utmost care and reliability, • Interdisciplinary thinking and strong negotiation skills are among your strengths, • You possess strong self-organizational skills, are willing to work independently with minimal guidance, and like to drive things forward proactively., • A confident demeanor, excellent communication skills, and the ability to build a shared understanding set you apart, • You have a strong drive and ability for teamwork and thoroughly enjoy working with intercultural and international teams, • Occasional multi-day travel to other Roche sites (e.g. Germany, Switzerland) may be required. To support the global nature of our work (e.g. collaboration between the US and Europe), customer and stakeholder meetings periodically require participation in meetings during the early evening hours (e.g. 1900) Un avenir plus sain nous pousse à innover. Ensemble, plus de 100 000 employés à travers le monde sont dédiés à faire progresser la science et à garantir à chacun l'accès aux soins de santé aujourd'hui et pour les générations à venir. Nos efforts aboutissent à plus de 26 millions de personnes traitées avec nos médicaments et plus de 30 milliards de tests réalisés avec nos produits de Diagnostique. Nous nous encourageons mutuellement à explorer de nouvelles possibilités, à favoriser la créativité et à conserver nos grandes ambitions, afin de fournir des solutions de santé qui changent des vies et ont un impact mondial. Construisons ensemble un avenir plus sain. Roche est un employeur offrant l'équité en matière d'emploi. #J-18808-Ljbffr

Seeking a hairdresser assistant for a hair and beauty salon in Palma de Cervelló. Responsibilities include assisting stylists and performing auxiliary tasks like hair washing.

Location: Barcelona, Spain Function: Worldwide Litigation and Government Investigations This is a hybrid position, requiring at least three days per week on-site work. HP seeks an experienced litigation lawyer to manage a significant portfolio of litigation and investigations across Europe, the Middle East and Africa. Based in Barcelona, the Litigation Manager, EMEA will manage a diverse portfolio of disputes, advise on significant legal and business risks, and develop strategies that protect HP’s interests and support its business objectives. The role involves a broad range of litigation and investigations, which may include commercial, intellectual property, competition, consumer protection, privacy, employment, securities, and regulatory matters. It requires strong litigation judgment, experience handling complex disputes, and the ability to work across jurisdictions, legal disciplines, and business functions. As a member of HP’s Worldwide Litigation and Government Investigations team, this lawyer will partner closely with regional and country counsel, legal subject matter experts, business leaders, and outside counsel to deliver coordinated, effective representation. This is an individual contributor position with substantial autonomy and responsibility for litigation strategy, outcomes, and budgets. The lawyer will lead matters, direct outside counsel, and coordinate cross-functional teams, while escalating significant risks and strategic decisions as appropriate. Candidate must have the right to live and work in Barcelona. • Lead litigation and dispute strategy. Take responsibility for EMEA matters from threatened claims and early case assessment through proceedings, trial, appeal, settlement, and implementation of outcomes. Develop and execute strategies grounded in the facts, applicable law, business priorities, and potential financial and reputational exposure., • Manage a broad portfolio. Handle disputes across substantive areas, including commercial and contractual claims, intellectual property and licensing disputes, competition, consumer, privacy, employment, securities, and regulatory matters, working with relevant specialists., • Lead investigations and responses to government inquiries. Direct or support internal and government investigations, regulatory inquiries, competition and other enforcement matters, including preparation for and response to dawn raids and compulsory information requests, in coordination with Ethics and Compliance, Employment, Privacy, and other relevant teams., • Provide substantive litigation counsel. Assess claims and defenses, identify evidentiary strengths and gaps, evaluate procedural options, and guide decisions on litigation posture, settlement, and escalation. Review and shape significant submissions, witness preparation, and advocacy., • Coordinate cross-border matters. Work with litigation colleagues and local counsel to align strategy across jurisdictions, address related proceedings, and anticipate the broader implications of regional decisions., • Advise business and legal leaders. Communicate clear assessments of exposure, likely outcomes, available options, and recommended actions. Translate complex issues into practical advice and elevate significant developments promptly., • Direct outside counsel. Direct outside counsel. Select and manage external legal teams, establish strategy, staffing, budgets, and performance expectations, critically evaluate advice, and ensure high-quality, efficient representation., • Manage financial exposure and spend. Develop and oversee matter budgets, maintain reliable forecasts, evaluate settlement economics, and provide timely assessments to support reserves, disclosures, and internal reporting., • Lead factual and evidentiary development. Work with business teams, witnesses, Discovery and Solutions, and outside counsel to develop the factual record, preserve and collect relevant information, prepare witnesses, and ensure that litigation positions are supported by the available evidence., • Prevent and reduce disputes. Identify recurring issues and lessons from litigation and investigations, and recommend changes to business practices, contracts, policies, or training., • Strengthen the global litigation function. Contribute to knowledge sharing, consistent matter management, process improvements, and the effective use of legal technology and AI., • Law degree and professional qualification to practice law in a relevant jurisdiction., • At least five years of post-qualification experience handling litigation and investigations at a law firm, global company, or both, including meaningful responsibility for strategy, major case decisions, outside counsel direction, and resolution of complex matters., • Demonstrated experience leading or playing a substantial role in litigation strategy and handling matters through multiple stages of contested proceedings, including significant written submissions, hearings, trial, appeal, or settlement, with sound judgment about when to defend, negotiate, or resolve a dispute., • Experience managing matters across EMEA jurisdictions and coordinating local counsel and internal stakeholders., • Ability to handle a varied docket, develop command of unfamiliar subject matter, and work effectively with specialist lawyers., • Strong analytical, written advocacy, negotiation, and communication skills., • Ability to advise senior stakeholders with clarity, exercise independent judgment, and make practical recommendations under uncertainty., • Experience managing outside counsel, legal budgets, forecasts, and financial exposure, while balancing competing priorities., • Excellent written and spoken English and the ability to work effectively in a multinational environment., • In-house experience with a global technology or other multinational company., • Experience with intellectual property and licensing disputes, including patent or competition-related matters., • Experience with government investigations, regulatory enforcement, and complex cross-border disputes., • Familiarity with litigation reserves and disclosure processes, electronic discovery, and legal matter management systems., • Proficiency in additional European languages. Legal Full time No shift premium (Spain) HP, Inc. provides equal employment opportunity to all employees and prospective employees, without regard to race, color, religion, sex, national origin, ancestry, citizenship, sexual orientation, age, disability, or status as a protected veteran, marital status, familial status, physical or mental disability, medical condition, pregnancy, genetic predisposition or carrier status, uniformed service status, political affiliation or any other characteristic protected by applicable national, federal, state, and local law(s). Please be assured that you will not be subject to any adverse treatment if you choose to disclose the information requested. This information is provided voluntarily. The information obtained will be kept in strict confidence. For more information, review HP’s EEO Policy or read about your rights as an applicant under the law here: “Know Your Rights: Workplace Discrimination is Illegal” #J-18808-Ljbffr