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Al Parc Sanitari Sant Joan de Déu cerquem incorporar un/a metge/essa especialista en geriatria, amb l’objectiu de continuar oferint una atenció integral, personalitzada i de qualitat als nostres pacients. • Tipus de contracte: Indefinit, • Dedicació: jornada completa (100% jornada), • Salari: segons conveni SISCAT i experiència aportada., • Ubicació: Sant Boi de Llobregat, • Possibilitats de desenvolupament professional dins de l’organització. Institució sanitària de referència amb una àmplia cartera de serveis i dispositius assistencials., • Treball multidisciplinari orientat a una atenció integral i centrada en la persona., • Diferents beneficis socials centrats en les persones, amb especial èmfasi en el benestar emocional, la conciliació efectiva i un entorn on el professional se senti cuidat i acompanyat, amb oportunitats sòlides de desenvolupament professional. Tot això dins d’un projecte amb propòsit i compromís social, propi de Sant Joan de Déu. La posició està inicialment vinculada a la Unitat d’Aguts de Geriatria (UGA) , participant en l’atenció i seguiment de pacients geriàtrics amb necessitats assistencials complexes. • Valoració geriàtrica integral del pacient., • Diagnòstic, tractament i seguiment de patologies agudes i reaguditzacions., • Coordinació amb equips multidisciplinaris per garantir una atenció centrada en la persona., • Planificació de l’alta i coordinació amb altres recursos assistencials per assegurar la continuïtat de les cures., • Participació en activitats de millora contínua, docència i recerca. A més, atès que el Parc Sanitari Sant Joan de Déu disposa de múltiples dispositius i àmbits assistencials, valorarem conjuntament altres oportunitats professionals dins de la institució que puguin ajustar-se millor al perfil i als interessos de la persona candidata. • Titulació de Grau o Llicenciatura en Medicina., • Especialitat en Geriatria via MIR o homologada a Espanya., • Capacitat de treball en equip i orientació cap a una atenció centrada en la persona. #J-18808-Ljbffr

Stark Future SL is seeking a Market Registration & Compliance Manager to design, implement, and own end-to-end vehicle registration across markets. You will ensure compliance with country-specific frameworks, work with cross-functional teams, and oversee registration as a service tied to product delivery. You will build and lead a team to deliver ready-to-ride experiences, managing external partners and driving continuous process improvements in regulatory operations. #J-18808-Ljbffr

Assurance Quality Product, Process Quality and work with Engineering to develop standards. Our guidelines will include component specification, quality assurance, delivery time, pricing, and sustainability policy. Define Final vehicle process quality assurance and implement auditplanning.

Eres un/a comercial nata/o o quieres aprender a serlo? ¿Te gustaría tener un horario flexible para adaptarlo a tus necesidades? ¿Quieres trabajar en una empresa que se preocupa por tu formación y crecimiento?¡Estás en el lugar adecuado!Si quieres ganar más, emprende una carrera como Asesor In

Oxigent Technologies is seeking a Protection Engineer to participate in testing, commissioning and configuring protection and control systems in electrical substations near Lisbon, Portugal.

Stark is seeking an experienced Senior Android Engineer to own the architecture and technical direction of the Android application, balancing quality, performance, and speed. You will take end-to-end ownership of mobile features from definition and design through development, release, and monitoring, while collaborating with product managers, designers, and stakeholders. The role requires 5+ years of Android leadership, strong Kotlin/Jetpack Compose skills, and a data-driven, quality-focused #J-18808-Ljbffr

Medicina Intensiva (UCI) per a una cobertura temporal de 3 mesos. El/la professional s’integrarà al Servei de Medicina Intensiva, formant part d’un equip multidisciplinari orientat a oferir una atenció de qualitat als pacients crítics. Especialitat en Medicina Intensiva via MIR o titulació h

Bunge is seeking a Global SAP Controlling Lead to manage the SAP CO functional domain in Sant Just Desvern. This role includes overseeing significant operational plans, leading global design workshops, and ensuring best practice adoption. The ideal candidate should have a Bachelor’s degree along with 11-15 years of relevant experience in finance, and be skilled in SAP CO and stakeholder management. #J-18808-Ljbffr

Synthon in Spain seeks a Project Manager R&D to lead planning and prioritization of Operations within R&D according to global roll-out priorities. You will coordinate with heads of R&D, manage resources, and ensure efficient multi-project scheduling across SHIS and SBV. The role requires a Master’s in Pharmaceutical Industry, a Bachelor’s in Pharmacy or related field, and at least 5 years as a PM in pharma R&D, with strong planning, communication, and stakeholder management skills. #J-18808-Ljbffr

Almirall Hermal GmbH sucht eine Senior Managerin/senior Manager für Market Access Institutional Projects in Sant Feliu de Llobregat. Sie koordinieren transversale Projekte mit Behörden, wissenschaftlichen Gesellschaften und Patientenverbänden und stärken externe Partnerschaften. Sie bringen einen Masterabschluss im Gesundheitsbereich, mindestens 7 Jahre relevante Erfahrung und exzellente Kommunikationsfähigkeit mit. Hohe Teamorientierung, Eigeninitiative und strategisches Denken sind gefragt. #J-18808-Ljbffr

Stark Future SL in Sant Boi de Llobregat seeks an International Grants and Subsidies Manager responsible for managing funding projects, from strategic identification and proposal writing to reporting and compliance. The ideal candidate will have a minimum of 5 years' experience in managing grants, strong project management skills, and excellent communication in English and Spanish. The role offers competitive salary and benefits, including subsidized meals, gym access, and 30 days of paid vacation. #J-18808-Ljbffr

• Ownership of product strategy, roadmap, and complete lifecycle for IoT devices in the rail domain incl. creation and maintenance of product requirement documents, • Coordination of new device developments and re‑designs together with the lead engineer and system integration engineer, • End‑to‑end thinking across device and IoT platform: identify domain‑specific requirements and translate them into both product streams, • Translation of market, customer, and domain requirements into technical requirements and features, • Prioritization of functions and development tasks in alignment with device engineering and management, • Direct interaction with customers, technical consultants and sales to understand rail market needs and feed them into product development (IoT devices and IoT platform), • Technical evaluation of concepts, variants, and supplier solutions, • Accompanying certification and testing activities from a product perspective (e.g., rail compliance, ATEX, EMC), • Monitoring of product performance, field feedback, and quality KPIs, • Initiation and steering of product improvements and redesigns based on data and feedback, • Completed degree in electrical engineering, mechatronics, industrial engineering, or comparable, • 3+ years of experience in technical product management, systems engineering, or development of IoT or industrial products, • Solid understanding of electronics, sensors, firmware, and mechanics, • Experience with product roadmaps, requirements management, and development processes, • Ability to think across domains: device, platform, customer value, • Experience working with external development partners and suppliers, • Strong analytical, communicative, and organizational skills, • Fluent in English (written and spoken), German and/or Spanish are a plus, • Experience in the rail sector or understanding of rail‑specific standards and certifications (e.g., EN 50155, EN 45545) is nice to have, • Knowledge of standards, certifications (in particular certifications for explosive‑sensitive environments), and quality management (e.g., ATEX, CE, EMC), • Experience working with platform teams or cross‑product responsibility, • Background in logistics, asset tracking, or telematics #J-18808-Ljbffr

You will support the execution of direct tax compliance and transfer pricing activities for assigned entities, ensuring compliance with local legislation and OECD guidance. Bunge Iberica SA in Sant Just Desvern is seeking a Direct Tax & Transfer Pricing Specialist to join our European Finance and Ta

Stark Future SL in Sant Boi de Llobregat, Barcelona area, seeks a driven Quality & Supplier Manager to lead QMS implementation, ISO/TS compliance, and supplier governance for premium electric motorcycles. You will align with engineering and production to ensure COP, regulatory approvals, and Lean/JIT practices, while driving continuous improvement and environmental, health, and safety standards. #J-18808-Ljbffr

Almirall, S.A in Sant Feliu de Llobregat is seeking a QA Senior Manager to maintain and improve the GVP Quality Management System, ensuring compliance with ICH, EU GVP modules, and pharmacovigilance regulations. You will lead audits, inspections, and QA activities with internal and external partners, fostering continuous improvement while coordinating with safety teams. Fluent English and strong regulatory expertise are required. #J-18808-Ljbffr

Stark Future SL, based in Sant Boi de Llobregat, Barcelona, seeks a Buyer or Senior Buyer for our Electronics purchasing team. You will manage supplier relationships, review BOMs, and secure components while balancing lead times and cost in a fast-growing electric motorcycle company. The role requires 3+ years of sourcing electronics and strong negotiation, with English fluent. Spanish is a plus; role based at Barcelona HQ with cross-functional collaboration with Engineering. #J-18808-Ljbffr

Neuraxpharm is seeking a Supply Chain Manager based in Sant Joan Despí (hybrid). You will lead end-to-end planning, production, procurement, inventory and logistics to ensure product availability and customer satisfaction across the CNS portfolio. The role requires a degree in engineering or business, at least 5 years in pharmaceutical supply chain, strong SAP experience and leadership of planning teams. Fluency in English and Spanish is expected; occasional travel may be required. #J-18808-Ljbffr

A leading electric motorcycle manufacturer based in Sant Boi de Llobregat is looking for a motivated Purchasing Category Manager to lead the EMS and PCBA Category. This role involves strategic sourcing of high-performance electronics, building relationships with global suppliers, and managing cost and quality targets. The ideal candidate will have a minimum of 5 years of sourcing experience, expertise in high-tech electronics sectors, and a strong commitment to sustainability. Join a fast-growing team passionate about innovation. #J-18808-Ljbffr

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

Schneider Electric in Sant Boi de Llobregat is seeking a Project Manager for Modular Data Centers to lead global cross-functional teams through design, procurement, production, testing and commissioning of modular data center solutions. The role focuses on delivering high-quality projects on time and within budget, applying CPP and PMI-based processes to optimize cost, quality, lead-time and business performance. #J-18808-Ljbffr

Bunge is seeking a Middle Office and BI Analyst to design, build and maintain Tableau dashboards for risk and financial analytics. You will translate complex business needs into clear visualizations, promote BI best practices, and support data-driven decision-making across the organization. Location ideally Barcelona, Spain, with a fixed-term contract. Fluent English required, and experience with SQL, Python, and automation is a plus. #J-18808-Ljbffr

Stark Future SL is seeking a seasoned Consolidation & Internal Controls Specialist to lead the general ledger and multi-entity consolidation across the group. You will ensure IFRS/Spanish GAAP compliance, strengthen internal controls, and support strategic financial decisions through accurate reporting. Join a fast-growing, sustainability-driven manufacturing firm based in Sant Boi de Llobregat, Barcelona region, offering a dynamic team and clear pathways to leadership within a multinational #J-18808-Ljbffr

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

Stark builds the world’s most powerful electric motorcycles. From the VARG MX to the road‑legal VARG EX & SM, our bikes have won world championships and are engineered to outperform anything with a combustion engine. We’re based in Sant Boi, Barcelona, growing fast (77% year‑on‑year), and building a team that will take us even further. Our mission is to lead the way towards a sustainable motorcycle industry, reducing plastic and CO2 pollution, by building sustainable products superior to traditional technology in terms of Performance, Emotion and Design. We are seeking a highly skilled and detail‑oriented Consolidation & Internal Controls Specialist to join our finance team in a dynamic and fast‑paced manufacturing company. This role is responsible for overseeing accuracy, integrity, and timeliness of the company’s general ledger accounting and financial consolidation processes across all business units and legal entities. The ideal candidate will play a critical role in financial reporting, compliance, and supporting strategic decision‑making through accurate consolidated financial statements. • Daily, monthly, and year‑end closing activities for the general ledger., • Ensure timely and accurate recording of all financial transactions in compliance with internal policies and accounting standards (e.g., IFRS/Spanish GAAP)., • Maintain and reconcile balance sheet accounts, resolve discrepancies, and ensure account accuracy., • Coordinate with various departments (e.g., procurement, manufacturing, sales, logistics) to ensure completeness and correctness of journal entries., • Prepare the monthly and annual consolidation of multiple subsidiaries., • Prepare consolidated financial statements in accordance with applicable accounting standards., • Prepare consolidated annual report in accordance with applicable accounting standards., • Maintain and improve the consolidation system/tools (e.g., SAP BPC, HFM, OneStream)., • Ensure adherence to internal controls and accounting policies., • Support implementation and continuous improvement of financial controls and processes., • Collaborate with other departments to continuously improve financial processes and information flows., • Support CFO and Financial Controller on budgeting, forecasting, and financial analysis initiatives as required., • Bachelor’s degree in accounting, finance, or related field., • Minimum 3-5 years of progressive experience in accounting and financial consolidation roles, preferably within the manufacturing industry., • Strong understanding of consolidation principles and multi‑entity accounting., • Proficiency with ERP systems; experience in Microsoft Dynamics is preferable., • Advanced level of Microsoft Office (Excel and Word mostly)., • Solid knowledge of IFRS and ES GAAP., • Excellent analytical, organizational, and problem‑solving skills., • Strong communication and leadership abilities with experience managing a team., • Experience in a multinational company or in a shared service center environment., • Understanding of cost accounting and manufacturing supply chain financials is a plus., • The chance to work on a product people are genuinely passionate about., • A fast‑growing company with real momentum., • A creative, international team based in Barcelona., • Competitive salary and benefits package., • Direct access to riders, race teams, and the product – this is not a remote‑from‑the‑product role., • Subsidized lunch in our in‑house restaurant., • Free access to our in‑house gym (including weekends)., • 30 days of paid vacation. We don’t just accept difference—we celebrate it, support it, and thrive on it for the benefit of our employees, our products, and our community. We are committed to creating an inclusive environment where everyone, regardless of gender identity, sexual orientation, race, religion, age, neurodiversity, or disability, feels a true sense of belonging. Diverse teams make better decisions and a culture of equity is a prerequisite for innovation. Accessibility: If you require any reasonable adjustments during the application or interview process (such as assistive technology, extra time, or a specific format), please let us know at We are here to support you. We encourage applications from under‑represented groups and are excited to see how your unique perspective can help us grow. #J-18808-Ljbffr

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

Al Parc Sanitari Sant Joan de Déu , som una institució referent que combina l’atenció hospitalària, sociosanitària, salut mental i recerca. Disposem d’un hospital general amb alta complexitat, equipat amb tecnologia d’última generació i un entorn multidisciplinari enfocat en l’atenció integral i humanitzada. El/la professional s'integrarà en un equip assistencial orientat a l'excel·lència clínica, desenvolupant activitat tant en l'àmbit de les consultes externes com en l'activitat hospitalària i quirúrgic a, amb especial interès en professionals que puguin assumir cirurgia ORL, inclosa l'activitat relacionada amb la població pediàtrica. • Atenció especialitzada en Otorinolaringologia a consultes externes., • Valoració, diagnòstic, tractament i seguiment de patologies pròpies de l'especialitat., • Activitat hospitalària vinculada al servei d'ORL., • Participació en activitat quirúrgica de l'especialitat., • Realització i interpretació de proves diagnòstiques pròpies de l'ORL., • Atenció i seguiment de pacients adults i pediàtrics segons les necessitats assistencials del servei., • Participació en sessions clíniques i activitats assistencials del servei., • Coordinació amb altres professionals i especialitats per garantir una atenció integral al pacient., • Contribució a la millora contínua de la qualitat assistencial i de l'experiència del pacient., • Contractació segons necessitats assistencials del servei., • Jornada flexible, amb horaris de matí i tarda per adaptar-se a l'activitat assistencial., • Retribució segons conveni SISCAT., • Activitat assistencial combinant consulta externa, activitat hospitalària i quirúrgica., • Possibilitat de desenvolupament professional en un hospital de referència., • Integració en un equip multidisciplinari orientat a la qualitat assistencial., • Programa de Benestar SJD T-Cuida: beneficis socials, programa formatiu i activitats de promoció del benestar., • Bon ambient de treball en una organització referent en l'àmbit sanitari i social., • Participació en activitats docents, formatives i de millora contínua., • Títol d’especialista en Otorinolaringologia via MIR o homologat., • Capacitat de treball en equip, responsabilitat i orientació a la qualitat assistencial., • Es valorarà experiència prèvia, participació en recerca o docència i coneixement d’anglès aplicat. #J-18808-Ljbffr

Stark builds the world's most powerful electric motorcycles. From the VARG MX to the road-legal VARG EX & SM, our bikes have won world championships and are engineered to outperform anything with a combustion engine. Stark builds the world's most powerful electric motorcycles. From the VARG MX to the road-legal VARG EX & SM, our bikes have won world championships and are engineered to outperform anything with a combustion engine. We're based in Sant Boi, Barcelona, growing fast (77% year-on-year), and building a team that will take us even further. If you want to work on a product that people are genuinely obsessed with, this is it. Stark will become the global market leader in premium motorcycles. Building premium motorcycles requires innovation and we need your help to make us succeed. Our mission is to lead the way towards a sustainable motorcycle industry, by reducing plastic and CO2 pollution. This will be achieved by building sustainable products that are superior to traditional technology in terms of Performance, Emotion and Design. We are seeking a highly skilled and detail-oriented consolidation & internal controls Specialist to join our finance team in a dynamic and fast-paced manufacturing company. This role is responsible for overseeing the accuracy, integrity, and timeliness of the company’s general ledger accounting and financial consolidation processes across all business units and legal entities. The ideal candidate will play a critical role in financial reporting, compliance, and supporting strategic decision-making through accurate consolidated financial statements. • Daily, monthly, and year-end closing activities for the general ledger., • Ensure timely and accurate recording of all financial transactions in compliance with internal policies and accounting standards (e.g., IFRS/Spanish GAAP)., • Maintain and reconcile balance sheet accounts, resolve discrepancies, and ensure account accuracy., • Coordinate with various departments (e.g., procurement, manufacturing, sales, logistics…) to ensure completeness and correctness of journal entries., • Prepare the monthly and annual consolidation of multiple subsidiaries., • Prepare consolidated financial statements in accordance with applicable accounting standards., • Prepare consolidated annual report in accordance with applicable accounting standards., • Maintain and improve the consolidation system/tools (e.g., SAP BPC, HFM, OneStream)., • Ensure adherence to internal controls and accounting policies., • Support implementation and continuous improvement of financial controls and processes., • Collaborate with other departments to continuously improve financial processes and information flows., • Support CFO and Financial Controler on budgeting, forecasting, and financial analysis initiatives as required., • Bachelor’s degree in accounting, finance, or related field., • Minimum of 5 years of progressive experience in accounting and financial consolidation roles, preferably within the manufacturing industry., • Strong understanding of consolidation principles and multi-entity accounting., • Proficiency with ERP systems. Experience in Microsoft Dynamics is preferable., • Advanced level of Microsoft Office package (Excel and Word mostly), • Solid knowledge of IFRS and ES GAAP., • Excellent analytical, organizational, and problem-solving skills., • Strong communication and leadership abilities with experience managing a team., • Experience in a multinational company or working in a shared service center environment., • Understanding of cost accounting and manufacturing supply chain financials is a plus., • The chance to work on a product people are genuinely passionate about, • A fast-growing company with real momentum, • A creative, international team based in Barcelona, • Competitive salary and benefits package, • Direct access to riders, race teams, and the product — this is not a remote-from-the-product role, • Subsidized lunch in our in-house restaurant, • Free access to our in-house gym (including weekends!), • 30 days of paid vacation At Stark, we don't just accept difference—we celebrate it, we support it, and we thrive on it for the benefit of our employees, our products, and our community. We are committed to creating an inclusive environment where everyone, regardless of gender identity, sexual orientation, race, religion, age, neurodiversity, or disability, feels a true sense of belonging. We believe that diverse teams make better decisions and that a culture of equity is a prerequisite for innovation. Accessibility: If you require any reasonable adjustments during the application or interview process (such as assistive technology, extra time, or a specific format), please let us know at We are here to support you. We encourage applications from underrepresented groups and are excited to see how your unique perspective can help us grow. Stark Future is on a mission to revolutionize the motorcycle industry by leading the shift toward sustainability, drastically reducing CO₂ and plastic pollution. Through cutting-edge design and unmatched performance, we delivers emotionally powerful, timelessly beautiful premium electric motorcycles that surpass traditional technology. Guided by a philosophy of innovation, quality, and user-focused simplicity, Stark combines bold ambition with a relentless pursuit of excellence. Our brand’s iconic gold logo symbolizes its full-circle approach to sustainability and its uncompromising drive to be number one. #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

Select how often (in days) to receive an alert: Date: Sep 29, 2026 Location: Sant Just Desvern, B, ES, 08960 City : Barcelona State : Barcelona (ES-B) Country : Spain (ES) Requisition Number : 48289 Overview: The Business Technology Partner (BTP) Regional Lead EMEA & APAC is a key strategic liaison bridging Bunge Technology (BT) with regional business leaders across Europe, Asia, Australia, and New Zealand. This pivotal regional role focuses on understanding and shaping business strategy, primarily identifying and driving transformational programs (e.g., Digital Platforms, Advanced Analytics) under the Global Business Solutions team. The BTP will operate as a strategic thought partner, providing insights, challenging assumptions, and actively contributing to strategic discussions to drive business value and transformation impact across diverse business models, maturity levels, and regulatory environments. This role requires exceptional business acumen, a strong understanding of transformation technologies, and superior relationship-driven leadership skills, fostering a strategic partnership that extends beyond a traditional technology interface. The BTP Regional Lead EMEA & APAC will report directly to the Business Technology Partner Director. Main Accountabilities: • Business Acumen : Develop a deep understanding of the diverse regional business models, strategic objectives, market trends, and regulatory environments across EMEA & APAC, spanning Origination & Sustainability (upstream) and Downstream value chains (food, feed, and fuel)., • Solution Identification: Proactively identify, shape, and challenge opportunities to leverage advanced business technologies for transformational programs (e.g., Digital Platforms, Advanced Analytics), enhancing business processes, customer experience, and achieving regional strategic objectives, under the Global Business Solutions team., • Roadmap Contribution: Actively contribute to the development and evolution of regional and global business technology roadmaps, ensuring regional priorities are seamlessly integrated with global capabilities, with a strong emphasis on value creation and transformational impact, aligning with business strategy and industry best practices., • Stakeholder Management: Cultivate and maintain strong, strategic relationships with senior regional business leaders across, • Origination & Sustainability and Downstream value chains, acting as a key connection between regional business and the BT organization. Ensure effective communication and collaborative partnership with global and regional technology teams and diverse stakeholders across EMEA & APAC., • Program Guidance & Oversight: Provide strategic guidance and oversight for transformation programs within the region, collaborating closely with dedicated or matrixed Project Managers (as the portfolio grows) to ensure successful delivery against budgets, resources, and timelines. This role focuses on strategic enablement rather than direct project execution., • Value Realization: Lead the establishment of clear metrics to track the business impact, value creation, and transformational outcomes of regional technology investments, ensuring direct alignment with strategic business objectives., • Communication: Serve as a critical communication bridge and trusted thought partner between senior regional business leaders and the BT organization, proactively facilitating strategic discussions, conveying insights, and ensuring transparency regarding transformation program status, challenges, and successes. Knowledge and Technical Competencies: • Deep understanding of diverse regional business processes and advanced technology solutions for transformation programs (e.g., Digital Platforms, Advanced Analytics)., • Knowledge of digital transformation methodologies (agile, lean, DevOps)., • Familiarity with enterprise architecture, cloud computing, data analytics, and emerging technologies relevant to large-scale transformation., • Ability to translate complex regional business needs into strategic technology requirements and vice-versa., • Strong communication, interpersonal, analytical, and problem-solving skills, with a proven ability to challenge and influence. Education and Experience: • Bachelor's degree in Business Administration, Information Technology, or a related field with 7-10 years of experience in a technology-focused role, ideally with experience in business partnership and solution delivery., • An equivalent combination of education and experience demonstrating in-depth knowledge of business technology partnership and a basic understanding of related disciplines will also be considered., • Relevant industry experience is a plus., • Strong understanding of Agile methodologies is preferred., • Experience managing small to medium sized budgets and resources. At Bunge (NYSE: BG), our purpose is to connect farmers to consumers to deliver essential food, feed and fuel to the world. As a premier agribusiness solutions provider, our team of ~34,000 dedicated employees partner with farmers across the globe to move agricultural commodities from where they’re grown to where they’re needed—in faster, smarter, and more efficient ways. We are a world leader in grain origination, storage, distribution, oilseed processing and refining, offering a broad portfolio of plant-based oils, fats, and proteins. We work alongside our customers at both ends of the value chain to deliver quality products and develop tailored, innovative solutions that address evolving consumer needs. With 200+ years of experience and presence in over 50 countries, we are committed to strengthening global food security, advancing sustainability, and helping communities prosper where we operate. Bunge has its registered office in Geneva, Switzerland and its corporate headquarters in St. Louis, Missouri. Learn more at Bunge.com. Every day our people exemplify these values, which represent Bunge at its core: We Are One Team – Collaborative, Respectful, Inclusive We Lead The Way – Agile, Empowered, Innovative We Do What’s Right – Safety, Sustainability, With Integrity If this sounds like you, join us! We value and invest in people who believe in our purpose and are excited to live it every day – people who are #ProudtoBeBunge Job Segment: Information Technology, IT Architecture, Agricultural, Cloud, Agribusiness, Technology, Agriculture #J-18808-Ljbffr

Neuraxpharm is looking for people who want to make a difference and improve patients’ lives within the CNS area. We want individuals who will go the extra mile and make great things happen. Being part of this team does not mean you are just working for a company, but for a cause! Neuraxpharm is looking for a Corporate Strategy & portfolio specialist based in Barcelona (hybrid role). As part of the Strategy & Portfolio team, ssupport portfolio strategy and growth by assessing current and future product opportunities, leading forecasting, generating market and competitive insights, coordinating cross-functional and country stakeholders, and leveraging AI-driven analytics to support strategic decision-making, portfolio management, and planning processes. • Assess and provide support to the analysis and selection of the current and future portfolio within the group, • Lead forecasting and act as coordinator between areas and countries, evaluating product opportunities, leveraging AI tools to enhance analytical quality, efficiency, and decision-making, • Analyze market and competitive data to assess potential opportunities and provide insights for key decisions, • Provide analytic support in the markets and interface with country commercial teams to provide data driven strategic guidance, • Prepare reports and presentations summarizing market insights and trends, • Lead and coordinate the annual review of the business cases of the pipeline projects, together with the local commercial experts and corporate teams, • Support the smaller countries and new affiliates in their portfolio expansion, identifying opportunities of portfolio products to be launched, • Database maintenance to help the group portfolio management, • Give support in key strategic processes (Budget & MRP planning, etc.) with cross-functional teams, • Minimum 3-5 years’ experience in Business and Strategy Consulting, Pharmaceutical industry-related experience preferable, • Demonstrated experience in in-depth data analysis, • Proven experience in forecasting, financial and commercial modelling, and product opportunity evaluation in the pharmaceutical industry, combined with practical experience leveraging AI tools (e.g., Claude, ChatGPT, Copilot) to enhance analysis, insight generation, and decision-making., • Language: Fluent English is mandatory, Spanish & German are valuable, • Ability to work independently is required, • Critical thinking, consistent organized, result-oriented, efficiency and cooperative, ability for international teamwork and communication skills, • Proficient technology skills (Microsoft Excel, Microsoft PowerPoint, etc.) are required, • Financial knowledge will be valued. Neuraxpharm is a leading European specialty pharmaceutical company focused on the treatment of the central nervous system (CNS), including both psychiatric and neurological disorders. It has a unique understanding of the CNS market built over 40 years. Neuraxpharm is constantly innovating, with new products and solutions to address unmet patient needs and is expanding its portfolio through its pipeline and acquisitions. The company has c. 1,000 employees and develops and commercializes CNS products through a direct presence in more than 20 countries in Europe, two in Latin America, one in the Middle East, one in Australia, and globally via partners in more than 50 countries. Neuraxpharm is backed by funds advised by Permira. Neuraxpharm manufactures many of its pharmaceutical products at Neuraxpharm Pharmaceuticals (formerly Laboratories Lesvi) in Spain. Be part of the team where you can count on us to deliver: • Individual Professional development in a leading European pharmaceutical company with an ambitious international growth strategy., • Attractive remuneration according to the experience and skills provided., • An inspiring leadership team that drives performance., • An inclusive culture promoting diversity across the teams that will inspire you every day with a passionate, a dynamic, a result focused and an expert&excellent team! At Neuraxpharm’s we ensure an inclusive, diverse, safe and respectful work environment for everyone in its organization. As we care for our people as much as we do for our patients, we are committed to guaranteeing a healthy, inclusive and equal opportunity workplace that enables employees to develop their professional potential, while ensuring their individual and collective satisfaction. We are guided by a Diversity & Inclusion policy to ensure a business culture based on the principles of diversity, equality and inclusion. Our policy complies with European legal regulations and includes the necessary standards, processes and measures to be taken in the event of discrimination or harassment against any employee of the company. We embrace and promote different cultures, gender identities, seniorities, ages and mindsets within the workplace, to bring different perspectives, styles and experiences to our business. #J-18808-Ljbffr

Gestor/a de Proyectos - Sector Asesoría.

Al Parc Sanitari Sant Joan de Déu cerquem incorporar un/a metge/ssa especialista en Radiodiagnòstic per unir-se al nostre equip de diagnòstic per la imatge. Cerquem una persona amb iniciativa, orientació a la qualitat i ganes de participar en projectes de millora i docència. • Supervisar els estudis i elaborar informes d’ecografia, radiologia convencional (RX), tomografia computada (TC) i ressonància magnètica (RM)., • Valorar i supervisar la idoneïtat i indicació de les sol·licituds de proves diagnòstiques., • Implicar-se en la formació interna del personal de l’àrea de Diagnòstic per la Imatge., • Liderar noves àrees d’investigació i docència en aquest àmbit de coneixement., • Garantir l’eficiència en l’ús dels recursos materials disponibles., • Col·laborar en les activitats docents i de formació contínua de la Unitat., • Dedicació: Jornada Completa. Horari compactat consistent en un dia de 08:00-21:00 hores i 3 dies de 08:00-16:20 hores, essent un dia curt de teletreball. Possibilitat d´activitat extra. Sense guàrdies., • Remuneració: Segons Conveni SISCAT., • Entorn de treball col·laboratiu, amb possibilitats de desenvolupament professional, recerca i docència., • Programa de Benestar SJD T-Cuida: Beneficis socials, programa formatiu, activitats lúdiques i esportives..., • Grau/Llicenciatura en Medicina i Cirurgia amb especialitat via MIR en Radiodiagnòstic., • Experiència prèvia en equips interdisciplinaris., • Habilitats de treball en equip, capacitat organitzativa, adaptació/flexibilitat i comunicació amb impacte i influència., • Experiència en recerca i docència., • Coneixements d’anglès #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.

Al Parc Sanitari Sant Joan de Déu , som una institució referent que combina l’atenció hospitalària, sociosanitària, salut mental i recerca. Disposem d’un hospital general amb alta complexitat, equipat amb tecnologia d’última generació i un entorn multidisciplinari enfocat en l’atenció integral i humanitzada. • Valoració i maneig de pacients amb patologia ORL en consulta externa., • Realització de procediments diagnòstics i terapèutics propis de l’especialitat., • Activitat quirúrgica en les principals àrees de la disciplina (otologia, rinologia, laringologia, cirurgia de cap i coll, etc.)., • Atenció de patologia urgent d’Otorinolaringologia., • Suport en l’atenció multidisciplinària amb altres serveis clínics., • Participació en sessions docents, activitats formatives i iniciatives de millora contínua del servei., • Integració a un equip consolidat i altament qualificat d’Otorinolaringologia., • Activitat clínica variada: consulta externa i quiròfan., • Possibilitat de formació continuada, sessions clíniques i participació en projectes de recerca., • Substitució de llarga durada i condicions competitives segons conveni SISCAT., • Horari de Dilluns a Divendres (4 matins i 1 tarda)., • Bon clima laboral i organització compromesa amb el desenvolupament professional i el benestar del personal., • Títol d’especialista en Otorinolaringologia via MIR o homologat., • Capacitat de treball en equip, responsabilitat i orientació a la qualitat assistencial., • Es valorarà experiència prèvia, participació en recerca o docència i coneixement d’anglès aplicat. #J-18808-Ljbffr

WE ARE HIRING! Supply Chain Manager Neuraxpharm is looking for people who want to make a difference and improve patients’ lives within the CNS area. We want individuals who will go the extra mile and make great things happen. Neuraxpharm is looking for a Supply Chain Manager in our Neuraxpharm Pharmaceuticals (Laboratorios Lesvi) based in Sant Joan Despí, Barcelona (hybrid role). To lead and continuously improve the end-to-end Supply Chain operations of the manufacturing site, ensuring seamless alignment between market demand, production capabilities and supply priorities of Neuraxpharm Pharmaceuticals. The role is responsible for Demand Planning, Production Planning, Procurement, Inventory Management, Logistics, Artwork Coordination and New Product Launches, ensuring reliable product availability, operational excellence and customer satisfaction while optimizing inventory, costs and working capital. • Lead, motivate and develop the Planning & Logistics team, fostering a high-performance culture focused on accountability, collaboration and continuous improvement., • Own and oversee the end-to-end planning and logistics processes, including Demand Planning, Production Planning, Procurement, Inventory Management, Artwork Coordination and New Product Launch activities., • Ensure alignment between commercial demand forecasts, production capacity and supply priorities to guarantee service levels and business continuity., • Drive inventory optimization by defining, monitoring and approving key planning parameters, balancing product availability, operational efficiency and working capital objectives., • Monitor supplier performance through relevant KPIs, ensuring service reliability and implementing corrective and preventive actions when required., • Lead cross-functional collaboration with Manufacturing, Quality, Regulatory Affairs, Finance, Commercial and Global Supply Chain teams to ensure successful execution of business priorities., • Identify, prioritize and implement process improvements and digitalization initiatives across planning, logistics and supply chain processes to increase efficiency, accuracy and scalability., • Manage and control the department budget, ensuring cost discipline, resource optimization and achievement of financial targets., • Support business growth through effective supply chain risk management, proactive issue resolution and successful implementation of new products and strategic initiatives., • Ensure compliance with GMP requirements, company policies and applicable regulatory standards within all supply chain activities., • Bachelor's Degree in Engineering, Business Administration or a related field. A Master's Degree in Integrated Logistics, Supply Chain Management or Operations Management will be considered an advantage., • Minimum of 5 years of experience in Supply Chain Management within the pharmaceutical, chemical or food industry, ideally complemented by at least 8 years leading Planning and Logistics teams in a pharmaceutical manufacturing environment., • Solid experience managing end-to-end supply chain processes, including Demand Planning, Production Planning, Procurement, Inventory Management, Logistics and S&OP., • Strong knowledge of SAP (MM, PP and SD modules), production planning tools such as Ortems, APO or similar solutions, and advanced Microsoft Excel., • Proven ability to plan, implement, monitor and control supply chain activities while balancing service levels, inventory optimization and cost efficiency., • Strong analytical thinking and problem-solving skills, with the ability to identify risks, make data-driven decisions and drive continuous improvement initiatives., • Excellent communication and stakeholder management skills, with the ability to collaborate effectively across Operations, Quality, Regulatory Affairs, Finance, Commercial and Global Supply Chain functions., • Demonstrated leadership capabilities, including team development, performance management and empowerment of high-performing teams., • Results-oriented mindset, high attention to detail, customer focus and the ability to perform effectively in a dynamic and demanding environment., • Fluent in English and Spanish., • Availability to travel occasionally (less than 10%). Neuraxpharm is a leading European specialty pharmaceutical company focused on the treatment of the central nervous system (CNS), including both psychiatric and neurological disorders. It has a unique understanding of the CNS market built over 35 years. Neuraxpharm is constantly innovating, with new products and solutions to address unmet patient needs and is expanding its portfolio through its pipeline and acquisitions. The company has c. 1,000 employees and develops and commercializes CNS products through a direct presence in more than 20 countries in Europe, two in Latin America, one in the Middle East, one in Australia, and globally via partners in more than 50 countries. Neuraxpharm is backed by funds advised by Permira. Neuraxpharm manufactures many of its pharmaceutical products at Neuraxpharm Pharmaceuticals (formerly Laboratories Lesvi) in Spain. • Individual Professional development in a leading European pharmaceutical company with an ambitious international growth strategy., • Attractive remuneration according to the experience and skills provided., • An inspiring leadership team that drives performance., • An inclusive culture promoting diversity across the teams that will inspire you every day with a passionate, a dynamic, a result focused and an expert & excellent team! Have a look at what Neuraxpharm culture represents and what makes us a great place to work: www.neuraxpharm.com WE COUNT ON YOU, YOU COUNT ON US At Neuraxpharm’s we ensure an inclusive, diverse, safe and respectful work environment for everyone in its organization. As we care for our people as much as we do for our patients, we are committed to guaranteeing a healthy, inclusive and equal opportunity workplace that enables employees to develop their professional potential, while ensuring their individual and collective satisfaction. We are guided by a Diversity & Inclusion policy to ensure a business culture based on the principles of diversity, equality and inclusion. Our policy complies with European legal regulations and includes the necessary standards, processes and measures to be taken in the event of discrimination or harassment against any employee of the company. We embrace and promote different cultures, gender identities, seniorities, ages and mindsets within the workplace, to bring different perspectives, styles and experiences to our business. #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.

Stark builds the world’s most powerful electric motorcycles. From the VARG MX to the road-legal VARG EX & SM, our bikes have won world championships and are engineered to outperform anything with a combustion engine. We’re based in Sant Boi, Barcelona, growing fast (77% year-on-year), and our mission is to lead the way towards a sustainable motorcycle industry by reducing plastic and CO2 pollution. We are looking for a Buyer or Senior Buyer to join our Electronics purchasing team at Stark HQ in Sant Boi de Llobregat, Barcelona. This is a strategic role that needs a real understanding of the global electronics ecosystem: navigating semiconductor cycles, managing relationships with top-tier manufacturers, and spotting technical opportunities in our designs. You will report to the Electronics & Electromechanics Purchasing Manager and act as the bridge between Engineering and the market. We are hiring at Buyer and Senior Buyer level. As a guide, Buyers bring 3+ years of sourcing experience, and Senior Buyers 7+ years with ownership of a commodity, supplier portfolio or major negotiations. Apply with the experience you have and we will shape the scope around you. Navigate the global EMS, component manufacturer and distributor landscape to secure the best partners Be the internal expert on semiconductor trends, memory market volatility and supply/demand shifts Review designs and BOMs to find alternative components (pin-to-pin or functional equivalents) with better lead times or cost Build strong relationships with major component manufacturers and global distributors Run RFIs, RFPs and RFQs, and negotiate Master Purchase Agreements that protect our agility Drive cost reduction and total-cost-of-ownership models without compromising technical integrity Support Engineering early in design to ensure design-for-availability 3+ years of sourcing electronic components and assemblies (7+ for Senior Buyer) An electronics engineering or technical degree, or strong electronics manufacturing experience Knowledge of global semiconductor players (TI, ST, NXP, Analog Devices, Rohm, Infineon, Murata and others) and distribution Ability to read a schematic or BOM and spot diversification or optimisation opportunities Strong negotiation skills, from NRE costs to volume rebates and buffer stock agreements Fluent English is a must; Spanish is a plus A product people are genuinely passionate about, and a company with real momentum A creative, international team based in Barcelona Competitive salary and benefits package Subsidised lunch in our in-house restaurant and free access to our gym 30 days of paid vacation At Stark, we celebrate difference. We are committed to an inclusive environment where everyone feels a true sense of belonging, and we encourage applications from underrepresented groups. If you need any adjustments during the application or interview process, contact #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

Synthon is looking for an experienced Application Technician who, together with colleagues will be responsible for the management, continuity, optimization and further development of our Document Management System (DMS), Quality Management System (QMS) and Learning Management System (LMS). You will act as the primary point of contact and application owner for these systems, ensuring they support business processes effectively and comply with quality and regulatory requirements. You will work closely with business stakeholders, IT colleagues and external vendors, taking a leading role in application improvements, upgrades, validation activities and implementation projects. • Own and manage the DMS, QMS and LMS application landscape throughout its lifecycle., • Ensure application availability, performance, reliability and compliance., • Coordinate and manage upgrades, releases, patches and system changes., • Lead the resolution of complex incidents and perform root cause analyses and take preventive measures., • Manage relationships with external vendors and monitor service levels and performance., • Act as the key liaison between business stakeholders, IT teams and suppliers., • Translate business requirements into functional solutions and drive continuous improvement initiatives., • Manage user access, permissions and security in accordance with company policies., • Develop and maintain application documentation, procedures and training materials., • Provide guidance and knowledge sharing to end users and colleagues., • Alternatively, HQ Nijmegen, the Netherlands. Your profile • Bachelor’s degree (BSc) in IT, Information Management, Computer Science or a related field., • Minimum of 5 years of relevant experience in application management, functional management or a comparable role., • Experience with DMS, QMS, LMS or other regulated business‑critical applications., • Experience with vendor management and project‑based work., • Experience in the pharmaceutical sector is an advantage. Good command of the Spanish and English language, both excellent verbal and written communication skills. • As an Application Manager, you act with a strong sense of ownership, taking responsibility for the availability and continuous improvement of your application landscape., • You are committed to delivering reliable, compliant and business‑focused solutions., • You possess strong analytical skills and can translate complex technical and functional issues into practical improvements., • You are comfortable working with stakeholders at different organizational levels and can effectively balance business priorities, compliance requirements and technical considerations., • You are proactive, results‑oriented and capable of managing multiple priorities in a dynamic environment., • Your strong communication skills, structured way of working and continuous improvement mindset enable you to successfully drive change and optimize application performance. Pharmaceutical and biopharmaceutical #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

Únete a nosotros como Supervisor de Operaciones de Manufactura y asume la responsabilidad de la ejecución integral de la producción. Liderarás equipos, coordinarás recursos e impulsarás mejoras de rendimiento que impactan directamente en la calidad, seguridad y eficiencia. • Supervisar las operaciones diarias de manufactura y garantizar la ejecución consistente de los estándares de calidad y seguridad, • Establecer prioridades de producción, asignar personas y equipos, y resolver obstáculos mediante escalación efectiva, • Monitorear KPIs, abordar desviaciones e implementar acciones de mejora para optimizar la productividad y los costos, • Colaborar con los equipos de mantenimiento, suministro y calidad para estabilizar flujos de trabajo y mejorar el rendimiento, • Orientación al cliente — nivel avanzado; alinear las prioridades de producción con las necesidades de clientes internos y externos, • Orientación a resultados — nivel avanzado; establecer objetivos claros y responsabilizar a los equipos por su cumplimiento, • Habilidades de influencia — nivel avanzado; lograr consenso entre funciones para resolver problemas e implementar cambios, • Integración de automatización — nivel intermedio; aprovechar la tecnología para mejorar la eficiencia de procesos y reducir el esfuerzo manual, • Mejora continua — nivel intermedio; identificar oportunidades y liderar iniciativas que aumenten la productividad, • Metodología Lean — nivel intermedio; aplicar principios lean para eliminar desperdicios y optimizar operaciones, • Rendimiento operacional de manufactura — nivel intermedio; monitorear métricas e impulsar acciones para cumplir objetivos de producción, • Optimización de procesos de manufactura — nivel intermedio; analizar flujos de trabajo para mejorar tiempos de ciclo y calidad de salida, • Capacidad de liderazgo comprobada con un historial de motivación de equipos en entornos de manufactura dinámicos, • Sólidas habilidades de resolución de problemas y confianza para tomar decisiones independientes dentro de directrices establecidas, • Excelentes habilidades de comunicación que fomentan la colaboración y alineación entre turnos y departamentos, • Mentalidad orientada a resultados con enfoque en eliminar obstáculos y entregar resultados medibles, • Liderar un trabajo significativo que impacta directamente en el rendimiento de la planta y el éxito del negocio, • Cultura de equipo colaborativa que valora el aprendizaje continuo y la colaboración, • Oportunidades de desarrollo profesional para hacer crecer tus capacidades de liderazgo, • Reconocimiento y visibilidad por los resultados que entregas ¿Listo para liderar con impacto? ¡Postúlate hoy y construyamos algo grandioso juntos! Schneider Electric es un Empleador de Igualdad de Oportunidades. Nuestra política es proporcionar igualdad de oportunidades en el empleo y el avance en áreas de reclutamiento, contratación, capacitación, transferencia y promoción a todas las personas calificadas, independientemente de raza, religión, color, género, discapacidad, origen nacional, ascendencia, edad, estado militar, orientación sexual, estado civil o cualquier otra característica o conducta legalmente protegida. #J-18808-Ljbffr

Synthon-Hispania seeks a Project Manager R&D to lead planning and prioritization of R&D operations in alignment with global roll outs. You will coordinate requirements with heads of R&D, manage multiproject plans with the Global Director, and optimize processes for efficiency. You will oversee manpower, equipment, scheduling, and reporting to upper management, driving Lean improvements and tool development across SHIS and SBV, while ensuring cGMP compliance and safety regulations. #J-18808-Ljbffr

Bunge Iberica SA is seeking a Business Technology Partner Regional Lead EMEA & APAC to bridge BT with regional business leaders. Ideal candidates bring a strong business acumen, excellence in stakeholder management, and a proven record in Agile environments.