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COMSER is looking for a Qualification and Validation Technician for the GMP Compliance Services area.We are a company that provides services to the pharmaceutical industry. Our purpose is to help and streamline the industrialization of new medicines that improve people's quality of life. Our focus is on injectable medicines that need to be manufactured in an aseptic environment. What do we offer? • Career plan with personalized professional development in the pharmaceutical sector. In a growing company with many opportunities., • Being part of a multidisciplinary team, where scientific and engineering profiles stand out; where your creative proposals will be valued., • Being the direct interlocutor with our clients during the execution of projects., • Good and young work environment. What will your main functions be? • Design and develop equipment or process validation protocols according to GMP and in accordance with the client's user requirements., • Execution and review of the protocols, with subsequent analysis of the results., • Continuous improvement of the validation documentation and updating of standards adaptable to each project What do we expect from you? That you have a scientific-technical university education (chemical sciences, pharmacy, biology, chemical engineering or similar) and/or training acquired in the development of your usual profession. • That you are an analytical, planned, resolute, results-oriented and dynamic person., • Knowledge of GMP regulations, aseptic manufacturing and the lyophilization technique is a plus., • Availability to travel (national and international)., • Full professional level of English (written and spoken)., • Own vehicle for travel to client sites. At COMSER, we value and respect diversity. We firmly believe that having a diverse team is key to success and innovation. That's why we offer equal opportunities to all candidates, regardless of their gender, age, race, religion, sexual orientation, disability, or any other characteristic. If you believe you fit the profile and are interested in starting a new professional project, do not hesitate to apply for the offer and contact us. We want to meet you!

At Intracon, we are a dynamic collective of companies specializing in Marketing & Sales, HR Consulting, and Corporate Events. Our team embodies innovation, influence, intrepidness, incisiveness, and ingenuity. We are currently looking for a HR Services Business Development Manager. In this multifaceted role, you will be responsible for overseeing and executing HR policies and practices. Additionally, you will manage and develop external HR services at Intracon Consulting, ensuring client satisfaction, service quality, and business growth. This is a unique opportunity for an HR professional with experience in both commercial and operational roles to contribute to a thriving organization. You will join a collaborative, innovative team and play a key role in supporting internal operations and external client relations. We are IN, are you IN? 💼 Main Responsibilities: Reporting to the Managing Director and Executive Director, and working closely with a team of five, you will focus on: External Client Management & Business Development • Oversee consultant onboarding, Statement of Work (SOW) agreements, service proposals, and fee negotiations., • Manage monthly financial and budget closing processes for outsourcing and human resources services provided to external clients, including margin analysis and cost control., • Maintain strong client relationships to ensure satisfaction and alignment with project objectives., • Implement retention strategies and ensure effective communication between consultants and clients., • Identify new business opportunities and expand relationships with the clients. Participate in the development of commercial proposals, ensuring project viability and profitability., • Gather information to enhance the value proposition and differentiation of consulting services. 🎓 Background & Skills: • Bachelor's degree in Human Resources, Business Administration, or related fields., • Experience in both internal HR management and external client service coordination., • Strong interpersonal, negotiation, and leadership skills., • Fluency in English and Spanish. Additional languages are a plus., • Ability to adapt quickly to new challenges and manage multiple responsibilities. 🔎 About the Role: • Dedication: Full-time, • Work Model: Hybrid, combining in-office and telework., • Location: Sant Cugat del Vallès (Barcelona). ➡️ What We Offer: • Flexible work arrangements: including a hybrid model tailored to leadership roles 🏠🏢, • Professional development opportunities: we support your growth through interesting training opportunities 📚, • Opportunities for career advancement: by leading a well-established business to the next level 🚀, • Commitment to Sustainability: We are proud to hold the Biosphere certification and implement responsible policies and practices daily. Through our CSR committee, we also engage in significant global sustainability initiatives. ♻️, • Updated and Useful Technology and Tools: We prioritize efficiency and clarity. In addition to working with agile methodologies, we utilize advanced tools such as ClickUp for project management and AI for various applications. 🛠️, • Free language courses with native-speaker teachers 💬, • Fun & well-being activities including team-building events and regular corporate sports activities 🎾, • Intracon benefits: discounts on health insurance, gym memberships, and more 🏷️, • Employee recognition programs, including bonuses for bringing business leads, acknowledgments for positive client reviews, and celebrations for work anniversaries 🎉, • Well-connected office surrounded by green spaces 🌳, • Office perks, including free coffee/tea, sodas and snacks ☕🍪 As an equal opportunity employer, we value diversity and inclusion in all aspects of our work. Please note: Due to the volume of applications received, only shortlisted candidates will be contacted. However, we thank all applicants for their interest in joining us!

¡Únete a Technotex Quality Fabrics y potencia tu carrera en Marketing! En Technotex Quality Fabrics nos dedicamos a la fabricación y comercialización de tejidos técnicos textiles de alta calidad. Contamos con una amplia gama de productos destinados a diversos sectores, como la industria médica, de seguridad, entre otros. Diseñamos productos que cumplen con estándares específicos de durabilidad, resistencia y funcionalidad. Estamos buscando talento en prácticas con pasión por el marketing, dispuesto a aprender y contribuir a proyectos reales que marcan la diferencia. Lo que harás con nosotros: • Participar en la creación y gestión de campañas de marketing digital., • Dar apoyo en la gestión de redes sociales y en la generación de contenido creativo., • Colaborar en el seguimiento de ventas online y estrategias de comunicación digital., • Contribuir al control de stock y apoyo en la producción de productos para reforzar la estrategia comercial. Requisitos: • Ganas de aprender y asumir nuevos retos., • Actitud proactiva, creativa y comprometida., • Estudios en Marketing Si te interesa, ¡únete a nosotros y comienza tu carrera en un entorno real y profesional! TECHNOTEX se siente orgulloso de ser un lugar de trabajo con igualdad de oportunidades. Celebramos la diversidad y nos comprometemos a crear un entorno inclusivo. Esta contratación está abierta a todos los perfiles. #WECARE #PEOPLE #THETEXTILECOMPANY

CREN PHARMA CONSULTING selecciona: Posición: Técnico de planta piloto GMP para lotes clínicos (AEMPS: Medicamentos en investigación) (Quality Engineer / Specialist for GMP Pilot Plant). Ubicación: Cerdanyola, Barcelona. Estamos buscando un/a profesional junior con un mínimo de 2-3 años de experiencia en el sector farmacéutico para unirse a una compañía especializada en Drug Delivery Systems (DDS), enfocada en la investigación y desarrollo de formulaciones inyectables de liberación controlada, dispositivos médicos y Drug Device Combination Products a terceros. Sus instalaciones cuentan con laboratorios de desarrollo farmacéutico y desarrollo analítico, así como una planta piloto GMP autorizada por la AEMPS para fabricación de lotes clínicos. La empresa desarrolla proyectos de Drug Delivery Systems desde las primeras fases de investigación hasta los ensayos clínicos de fase 1 y 2. Funciones principales: • Perfil técnico que gestione el cumplimiento de la normativa GMP y la política de calidad en entorno de producción de lotes clínicos (I+D) con participación en el desarrollo de nuevos productos/procesos, en un ambiente de colaboración interdepartamental., • Gestionar y asistir en la cualificación y recualificación de salas blancas y equipos de producción, (aisladores flexibles, liofilizador, autoclave, estufas, cabinas de pesadas, etc..) con asistencia de los departamentos de Calidad y Mantenimiento/Ingeniería., • Dependencia del responsable de Desarrollo Galénico., • Redacción de procedimientos normalizados PPNNT de equipos, aparatos y procesos asignados a la planta piloto., • Definición y redacción de los requerimientos de usuario cuando exista compra de equipamientos o aparatos., • Asistencia en la planificación de actividades y fabricaciones en Planta Piloto., • Colaboración con el departamento de Calidad en la investigación y resolución de incidencias y desviaciones (CAPA´s) así como en inspecciones de la AEMPS., • Gestión de Almacén GMP (stock, caducidades, supervisión de registros)., • Seguimiento y revisión de las condiciones ambientales de salas GMP (SCADA), • Contribución a proyectos de I+D, fabricación de lotes pilotos y clínicos., • No tiene asignado personal a su cargo y tendrá mucha interacción con personal externo ligado a la cualificación, mantenimiento e ingenieria de la planta., • Interactuar con los Departamentos de Desarrollo Analítico, Desarrollo Galénico, Garantía de Calidad y Mantenimiento / Ingeniería., • Promover la cultura de mejora continua y fiabilidad técnica de la planta. Requisitos: • Mínimo 2 – 3 años de experiencia en industria farmacéutica, preferiblemente formas estériles,, • Licenciado / Grado en Farmacia o titulación superior equivalente que asegure la cualificación adecuada, como Licenciatura / Grado en Ingeniería., • Valorable máster en Farmacia Industrial y Galénica., • Experiencia en entornos GMP (Anexo I) y desarrollo industrial en el ámbito farmacéutico., • Experiencia en HVAC, cualificación de equipos y en fabricación de productos inyectables y procesos asépticos., • Se valorará experiencia en formulación y desarrollo de productos inyectables, • Idiomas: castellano, inglés (medio-alto). Francés, valorable. Se ofrece: • Incorporación inmediata., • Proyecto internacional con fuerte componente técnico y estratégico., • Cultura colaborativa, sostenible e innovadora., • Formaciones internas y externas definidas por su responsable y Garantía de Calidad., • Jornada partida, 40 h semanales, flexibilidad de entrada y salida., • Retribución: 35.000 – 50.000 € brutos anuales, según experiencia., • Facilidad de aparcamiento en la zona, plazas reservadas de la empresa limitadas según orden de llegada., • Cantina en la empresa (no catering) y restaurantes en la zona., • Posibilidad de algún día de teletrabajo pactado con su responsable en función de las actividades presenciales de planta piloto. Contacto: Interesados/as pueden enviar su candidatura a

Tucai Group is considered one of the leading manufacturers of flexible connection hoses and valves for gas, water, and fuel applications, with globally recognized certifications. The mission of the Customer Service role is to serve our national and international customers in their sales and after-sales activities and experience. THE ROLE Key responsibilities: • Insert customer orders in the ERP systems and manage order confirmations to customers., • Receive and respond to customer enquiries, emails and phone calls. Send invoices and shipment related documents. Send rappel reports to customers. Send samples, commercial documents, catalogues, etc., • Receive customer claims and insert them in the internal app. Transfer and manage with involved departments all information from customers and send back information to customers regarding the status of related claims. Manage credit and replacements., • Carry out the internal processes to ship orders to customers: send internal order to logistic dpt. when goods are produced and ready to be shipped. Work as a team and coordinate with our international plants., • Create and maintain updated customer files in ERP system, keep customer data permanently updated (customer contacts, shipping address, price list). Follow internal procedure to open new customers (Financial approval process and risk assignment), • Insert sales forecast received from customers into ERP system., • Negotiate with customers in case of incidents or needs. WE ARE LOOKING FOR A CANDIDATE WITH: • Middle degree in technical, economics, or any related field., • A minimum of 5 years’ experience in Customer Service within an international company., • Experience with EDI and/or Microsoft 365 or similar. Good command of Ms.Office., • Fluent English is a must for daily communication. French or another European language is a plus., • Willing to travel occasionally., • The role is for a very committed person with high standards of quality, a dynamic personality and a strong customer orientation., • Due to limited public transportation options, applicants must have a car. WHAT CAN WE OFFER YOU? • Full-time and permanent contract, • Flexible hours (7:30/9:15 to 16:30/18:30), short days on Fridays and in August., • You can work from home 1 or 2 days per week depending on your tasks and schedule., • Food vaucher and flexible benefits., • Salary according to experience and profile.

Leanbio is a leading Biopharmaceutical CDMO offering end-to-end services in the field of recombinant proteins, mRNA and pDNA. With over a decade of expertise, we have a proven track record in development and manufacturing of therapeutic molecules such as antibodies, Fab fragments, ADCs, enzymes, complex proteins, mRNA and pDNA. Leanbio has already worked with over 100 candidates over these years, some already in late clinical stages. Leanbio is expanding its development and manufacturing capabilities with a new GMP site in Barcelona with over 4,000 sqm. and three manufacturing areas: one for mammalian expression systems up to 2000L, another for microbial and yeast up to 1000L, and a third are for mRNA up to 50L. The new facility includes state-of-the-art development laboratories, oustanding Quality control rooms and warehouse. Leanbio is a global service provider for the development and manufacturing of biologics. Our commitment to excellence is evident in everything we do: • Prioritizing customer satisfaction., • Providing cutting-edge end-to-end services., • Utilizing state-of-the-art facilities., • Offering extensive expertise in biologics. We are looking for a new person to join the QC as an analyst to work in our brand new facilities in Sant Quirze del Vallès: MAIN RESPONSIBILITIES: • Perform routine and non-routine physicochemical analyses of raw materials, intermediates, and finished products using techniques such as:HPLC (High-Performance Liquid Chromatography), Karl Fischer titration (moisture determination), FTIR / IR (identification of materials), Loss on Drying (LOD), Potentiometric titrations, Residue on Ignition (ROI), pH, conductivity, osmolality, TOC, etc., • Carry out sampling and analysis of water systems, including:Water for Injection (WFI), • Support environmental monitoring activities, including:surface and air sampling in classified areas., • Ensure strict adherence to GMP and ALCOA++ data integrity principles, maintaining complete, accurate, and traceable documentation., • Document all activities clearly and contemporaneously in lab notebooks, logbooks, or electronic systems (e.g., LIMS), in compliance with internal SOPs., • Participate in quality system activities, such as investigation of OOS / OOT results reporting of deviations and support in CAPA implementation., • Maintain and calibrate laboratory equipment, performing routine checks and informing of any malfunction or need for maintenance., • Follow safety protocols and contribute to keeping the lab in a clean condition at all times., • Collaborate with cross-functional teams, including QA, production, and validation, when needed. REQUIREMENTS: • Advanced Training in Laboratory Analysis and Control with 2–5 years of experience in Quality Control in a GMP-regulated pharmaceutical environment., • Practical experience in physicochemical testing including HPLC, Karl Fischer, IR, Loss on Drying, potentiometric titrations, and Residue on Ignition., • Skilled in sampling and analysis of pharmaceutical water systems (WFI, Purified Water) following USP/EP methods., • Familiarity with environmental monitoring in cleanroom environments is an asset., • Strong knowledge of ALCOA++ principles and GMP documentation practices., • Experience with quality systems (OOS, deviations, CAPAs, change control)., • Proactive team player with good organizational skills and the ability to work independently., • Fluent in Spanish with basic to intermediate English communication skills (reading/writing preferred).

We are Applus+, one of the world's leading companies in testing, inspection and certification, with a presence in more than 70 countries on 5 continents and a team of more than 25,000 people. You can consult our projects on the website: During recent years we have experienced great development thanks to our human team who we consider to be a key and strategic piece in the development of this company. Would you like to be part of the project? We are currently looking for a Category Buyer responsible for executing sourcing strategie for IT Equipment & Services to deliver cost savings, improve quality and risk mitigation. What will your day to day be like? Category Management: • Develop and implement IT Services & Equipment strategies for aligned with the company’s objectives., • Identify trends, opportunities, and potential risks, • Lead end-to-end procurement processes, including tendering, negotiating, catalogues and contract management., • Collaborate with internal stakeholders to understand project requirements and ensure procurement strategies meet business needs., • Develop a supplier base that supports the company’s growth, quality, and innovation objectives., • Ensure all contracts comply with company policies, legal requirements, and risk management standards., • Drive cost reduction initiatives while maintaining quality and service levels., • Develop total cost of ownership (TCO) models to evaluate and optimize procurement decisions., • Work closely with IT team, finance, operations, and project management teams to align procurement activities with project timelines and budget constraints., • Identify and mitigate risks, including supply chain disruptions, financial instability, and compliance issues., • Implement best practices in procurement processes and contribute to the continuous improvement of the procurement function., • Keep abreast of industry best practices and innovations in IT procurement, • Support the standardization of procurement processes and cataloguing. He or She leads the creation and usage of the catalogues for the categories for which he/she is responsible Requirements: • University degree in Business, Economics, or a related field (or equivalent experience)., • 3 years of experience in procurement, purchasing, or supply chain operations preferred, • Specialized in procurement of Consultancy & Services, experience in international environment, SAP ARIBA experience is an important plus., • Familiarity with procurement software and ERP systems (e.g., SAP, Oracle, or similar), • Proficiency in MS Office Suite (especially Excel for data management and reporting), • Proficiency in English, Spanish and French (nice to have), other European Language is welcome Applus+ is a company that offers equal opportunities. We are committed to treating all applicants equally based on their abilities, achievements, and experience regardless of race, national origin, sex, age, disability, sexual orientation, gender identity, or any other classification protected by law.

Are you interested in being part of a technological center of excellence where you can contribute and add technological value to companies and institutions, focusing on research, development and industrial innovation (R+D+2i)? Do you want to work in a leading environment with all the technological innovations within your reach? Leitat is a technological center of reference at national and European level. With more than 100 years of history, it has a team of more than 400 professionals, experts in applied research, technical services and management of technological and innovation initiatives. Leitat provides social, industrial, economic and sustainable value, offering integral solutions in multiple sectors and fields: health and biomedicine, development of new materials, eco-sustainable production, occupational health prevention systems, waste revaluation and use of natural resources; interconnectivity and digitalization of industry, green energy and maximization of energy efficiency. Leitat develops R+D+i projects for companies and institutions, as well as leads research projects with competitive funding both within the framework of the European Union and the Ministry of Science and Innovation. We are currently looking for a Senior Researcher Energy Storage & Data Science: As a Senior Researcher in our energy storage group, you will play a key role in leading research and innovation activities within national and Horizon Europe (HE) projects. Your work will focus on advancing methodologies for battery testing, data analysis, and digital tools for energy storage applications. You will drive collaboration with academic, industrial, and institutional partners, while providing technical leadership and guidance to project teams. This position offers an excellent opportunity to contribute to shaping the future of sustainable energy through cutting-edge European projects, while mentoring junior colleagues and strengthening our research capabilities. Key Responsibilities: • Lead research tasks in national and European projects related to battery testing, modeling, and energy storage system optimization., • Guide the development and application of digital tools, AI/ML models, and advanced data analysis methodologies for energy storage research., • Coordinate project deliverables, ensuring quality, and timely completion., • Act as a key technical contact with external project partners, representing the organization in European consortia and research networks., • Contribute to the preparation of proposals for competitive funding calls and support strategic project acquisition., • Provide mentorship and technical guidance to junior researchers and engineers., • Disseminate research outcomes through publications, presentations, and stakeholder engagement. What do we expect from you? Qualifications • Master’s or PhD in Electrical Engineering, Power Electronics, Data Science or a related field., • Demonstrated experience (3+ years) in R&D, particularly within national or European-funded projects., • Coding and data science expertise (Python, C++, MATLAB), with applied knowledge of AI/ML., • Experience in digitalization and advanced analytics for energy systems is a plus., • Strong track record in research outputs (e.g., publications, conference contributions, patents)., • Excellent communication skills and ability to collaborate effectively within multicultural and multidisciplinary teams. Fluent in Spanish and English, oral and written. You will succeed in this position if you bring: • Experience in data science, statistical modeling, and predictive analytics., • Strong proficiency in Python, R, or MATLAB for data processing, AI, and ML modeling., • Knowledge of battery SOH modeling, failure prediction, or degradation analysis is a plus (but not required)., • Strong analytical mindset and ability to work with cross-functional teams., • Familiar with statistical methods and experimental design principles., • Excellent communication and collaboration skills., • Basic knowledge of battery chemistry, mainly at the cell level, is highly recommended., • Ability and motivation to learn battery characterization skills, with a willingness to acquire these skills at our center. What is it like to work at LEITAT? You will be located at the headquarters in Barcelona and will work in an attractive environment, being part of a unique innovation ecosystem with cutting-edge technologies and highly equipped laboratories. We offer flexible working hours so that you can reconcile your personal life and your professional development. In addition, you will enjoy subsidized catering in our centers, medical insurance and you will have a permanent contract with a salary commensurate with your experience, training and development. We are proud to offer these types of benefits that support the goals and well-being of our team members. We also support equal opportunities and diversity - we strive every day to be a more inclusive workplace adapted to all groups! If you are a person with excellent interpersonal and communication skills, with a high capacity to achieve your goals within the established deadlines and able to work independently and as part of a team, do not hesitate, sign up for our offer. We would love to hear from you! At LEITAT we look forward to meeting you!

We are Applus+ Laboratories, the division of the Applus+ Group that provides testing, certification, and product development engineering services. The Marketing Team provides transversal support to the entire division, both nationally and internationally. We are currently looking for a B2B Content & SEO Specialist (native-level English) to join our team on a stable basis. Goals • Own and optimize all multilingual website content to ensure consistency, accuracy, and alignment with business goals, • Drive organic traffic and lead generation through SEO-focused content strategies tailored to B2B industrial audiences, • Streamline content creation workflows to efficiently manage high-volume, multi-language content production What you will do • Manage and maintain website content, including service pages, product descriptions, and articles, ensuring regular updates, • Develop and execute global content strategies aligned with business goals and SEO best practices, • Optimize content for on-page SEO, including keywords, metadata, structure, and internal linking, • Create multi-format content (text, infographics, and so on) tailored to different buyer personas and customer journey stages, • Use CMS platforms (Magnolia, Wordpress, Shopify) and SEO (Semrush, Ahrefs) and AI tools (Copilot, Deepl) to enhance content quality and efficiency, • Collaborate with cross-functional teams to ensure brand consistency and contribute to marketing and communication projects Requirements • At least 3 years of experience in B2B content creation, preferably in industrial or technical sectors, • Native-level English (or at least C2 Proficiency) and excellent Spanish communication skills, • Strong writing, editing, and storytelling skills with attention to detail, • Solid understanding of SEO principles and experience with tools like Semrush or Ahrefs, • Proficiency in CMS platforms (Magnolia, WordPress) and familiarity with web publishing workflows, • Experience using AI tools for content generation and editing, • Ability to manage multiple projects and deadlines across different languages and markets, • Passion for technology and innovation We offer • Full-time permanent contract, • Flexible working hours, • Flexible compensation plan (medical insurance, transportation, childcare and restaurants), • Employees’ parking, • Canteen with reduced prices Are you passionate about content creation and SEO? if you want to take the step towards your next professional challenge… this is the company for you! Applus+ Laboratories is an equal opportunity employer. We are committed to evaluating all applications equally based on skills, achievements, and experience, regardless of race, nationality, gender, age, disability, sexual orientation, gender identity, or any other classification protected by law.

¿Quieres formar parte de la experiencia Exceltic, una empresa con estrategia centrada en las personas? ¿Tienes inquietud por conocer el sector técnico y tecnológico? ¡Ésta es tu oportunidad!👇 En Exceltic estamos en búsqueda activa de un/a Supply Quality Assurance para incorporarse de manera estable en nuestro equipo. ✅Tus funciones se centrarán en: • Proporcionar a la planta y al cliente toda la documentación necesaria, por ejemplo, IATF 16949, ANPQP, PPAP, FMEA y los sistemas de informes de calidad de Lear., • Preparar la documentación para mediciones internas y externas en forma de gráficos MOS, por ejemplo, RPPM, DPPM, etc., para la evaluación y el seguimiento del rendimiento de la calidad., • Comunicar y coordinar, a través de gráficos MOS e información de calidad 8D, entre todos los departamentos internos., • Prestar apoyo en la preparación y el mantenimiento de la documentación y los sistemas con el fin de cumplir con la norma TS 16949., • Garantizar que el FMEA y el plan de control se revisen y actualicen periódicamente cuando surjan 8D, cambios en los productos o procesos o problemas de calidad (por ejemplo, FCPA), al tiempo que se informa de los cambios a todo el personal pertinente., • Coordinar la respuesta de SQTS al estado «enviado para cierre». Realizar actualizaciones semanales de MOS de los proveedores. 🔎¿Qué buscamos? • Licenciatura/Grado en Ciencias, relacionada con Calidad, Organización, Ingeniería o equivalente., • Gestión de proyectos., • Herramientas estadísticas., • 2 años de experiencia laboral en calidad/fabricación (ingeniería, calidad) o experiencia en el sector automovilístico., • Certificación IATF 16949., • Certificación ISO 14001., • Habilidades para resolver problemas 8D., • Inglés fluido. 🙌Ofrecemos: 1.Posición estable. 2.Contrato indefinido. 3.Plan de retribución flexible (seguro médico, ticket transporte, restaurante y guardería). 4.Plan de formación. 5.Horario flexible 💫Vivir la experiencia Exceltic significa: · Participar en proyectos punteros en donde puedas desarrollar tus habilidades. · Percibir un salario competitivo en función de aportación. · Disfrutar de un plan de retribución flexible. · Equilibrar tu vida personal y profesional. · Formar parte de un equipo en el que te sientas escuchado/a y en donde puedas aportar nuevas ideas. Acerca de nosotros... Somos una empresa de servicios de ingeniería y consultoría tecnológica. Desarrollamos nuestra actividad en distintos sectores (Ferroviario, Aeronáutico, Espacio, Defensa, Energía, Automoción, Industria, Tecnologías de la Información y Telecomunicaciones). También proporcionamos servicios de auditoría técnica y formación especializada. A día de hoy contamos con una sólida cartera de clientes multinacionales en los distintos sectores y una de las ofertas más completas del mercado. En la familia Exceltic Somos más de 550 miembros y contamos con oficinas en Madrid, Barcelona y Bilbao y con proyectos en los cinco continentes. ¡Únete a nuestro equipo!

Leanbio is a leading Biopharmaceutical CDMO offering end-to-end services in the field of recombinant proteins, mRNA and pDNA. With over a decade of expertise, we have a proven track record in development and manufacturing of therapeutic molecules such as antibodies, Fab fragments, ADCs, enzymes, complex proteins, mRNA and pDNA. Leanbio has already worked with over 100 candidates over these years, some already in late clinical stages. Leanbio is expanding its development and manufacturing capabilities with a new GMP site in Barcelona with over 4,000 sqm. and three manufacturing areas: one for mammalian expression systems up to 2000L, another for microbial and yeast up to 1000L, and a third are for mRNA up to 50L. The new facility includes state-of-the-art development laboratories, oustanding Quality control rooms and warehouse. Leanbio is a global service provider for the development and manufacturing of biologics. Our commitment to excellence is evident in everything we do: • Prioritizing customer satisfaction., • Providing cutting-edge end-to-end services., • Utilizing state-of-the-art facilities., • Offering extensive expertise in biologics. We are looking for a new person to join the QA as a Specialist to work in our brand new facilities in Sant Quirze del Vallès: MAIN RESPONSIBILITIES: • To build, with the Head of Quality Assurance oversight, the Quality Management System creating and/or approving Standard Operating Procedures to support GMP manufacturing activities., • To build and manage the Documentation Management System and associated training., • To lead the supplier qualification program, approving new suppliers and managing supplier status during its life cycle., • To review Technical Agreements between the company and suppliers/clients., • To review batch documentation for release purposes., • To support facility, utilities and equipment qualification activities, approving protocols and final reports as well as managing related change control records. REQUIREMENTS: • Bachelor’s degree in a Science field with proven experience in GMP Quality Assurance roles., • In-depth knowledge managing Quality Management Systems (deviations, CAPA, change controls, audits and supplier qualification)., • Experience in batch release activities acting as QP deputy will be a plus., • Experience in facilities, utilities and equipment qualification., • Outstanding problem-solving and decision-making skills., • Team player, excellent verbal and written comunication skills (both Spanish and English) and strong analytical and organizatonal skills.

Our client is Valmet (), a leading global developer and supplier of process technologies, automation, and services for different industries. They are leaders in the pulp, paper, and energy industries, but with their automation systems and flow control solutions, they have presence in a lot more industries. Given the growth plan that they have for the upcoming years, we’re looking for a: After Sales Manager We are looking for a dynamic After Sales Manager to lead Valmet’s Service Center and support the development of their Flow Control Sales team. The position is based in Sant Cugat del Vallès, Barcelona, and covers the Spanish market. T his role is responsible for ensuring the effective delivery and continuous improvement of after-sales services, while promoting customer satisfaction, operational reliability, and compliance with safety, quality, and sustainability standards. The main tasks will be: • Collaborate closely with Sales and Services teams to propose value-added services and tailored solutions for existing customers., • Develop and recommend plans to enhance service performance by reviewing current results and identifying areas for improvement., • Oversee and establish the operational framework and provide guidance aligned with the service strategy. Responsible for budget management and policy recommendations and implementation., • Proactively seek new service business opportunities, engage with customers, and implement service agreements., • Lead, direct, evaluate, and develop a team of service employees to ensure adherence to agreed service standards., • Maintain an up-to-date Installed Base for the country and conduct proper follow-up with customers to support service and maintenance development., • Promote and enforce the company’s Health, Safety, and Environmental policies. We are looking for an After Sales Manager with a degree in engineering, business administration, or a related field, and at least 5 years of experience in after-sales management or service operations within industrial sectors. The candidate must have experience in developing service plans, managing budgets, overseeing service teams, and ensuring compliance with safety, quality, and environmental standards. Knowledge in contract management and customer service processes is required. They offer a dynamic role where you can impact the company’s success while growing your skills. Benefits include flexible hours, hybrid work, bonuses, medical insurance, and ongoing training.

Where will you work? We are a well-established international company in the healthcare and wellness sector, committed to improving lives through innovation, quality, and care. With a collaborative culture and a strong focus on employee well-being, we offer a dynamic environment where your work truly makes a difference. What will you do? Key Responsibilities • You will act as the first point of contact for any accounting incidents, escalating when necessary., • You will ensure compliance with HQ procedures, internal policies, and accounting principles., • You will manage Record to Report activities., • You will execute daily transactions and journal entries in line with SSC policies., • You will handle the month-end close for assigned entities, including reconciliations, accruals, allocations, and variance analyses., • You will manage fixed assets processes, including additions, disposals, leases, and depreciation schedules., • You will prepare ad-hoc financial reports and ensure their accuracy and compliance., • You will identify and propose improvements in accounting workflows and tools., • You will collaborate on finance transformation initiatives to enhance integration and automation., • You will maintain the integrity of accounting systems and internal controls under your responsibility. Who are we looking for? • 3-5 years of experience in general accounting or finance, ideally within a shared services environment., • Fluent in German and English (Spanish a plus)., • Proficient in SAP FI and Microsoft Office., • Strong analytical mindset, attention to detail, and sense of ownership., • Excellent communicator and team player in multicultural settings. What do we offer? • Competitive salary package with permanent contract., • Hybrid work model with flexible hours., • Ongoing career development in a leading multinational., • Collaborative, supportive team culture and continuous learning opportunities., • Wellness programs and internal mobility, gym, cantine. To stay up to date on available vacancies, we invite you to visit our website: ___ or join our WhatsApp channel through the following link: ___ To stay up to date on available vacancies, we invite you to visit our website: or join our WhatsApp channel through the following link:

Leanbio is a leading Biopharmaceutical CDMO offering end-to-end services in the field of recombinant proteins, mRNA and pDNA. With over a decade of expertise, we have a proven track record in development and manufacturing of therapeutic molecules such as antibodies, Fab fragments, ADCs, enzymes, complex proteins, mRNA and pDNA. Leanbio has already worked with over 100 candidates over these years, some already in late clinical stages. Leanbio is expanding its development and manufacturing capabilities with a new GMP site in Barcelona with over 4,000 sqm. and three manufacturing areas: one for mammalian expression systems up to 2000L, another for microbial and yeast up to 1000L, and a third are for mRNA up to 50L. The new facility includes state-of-the-art development laboratories, oustanding Quality control rooms and warehouse. Leanbio is a global service provider for the development and manufacturing of biologics. Our commitment to excellence is evident in everything we do: • Prioritizing customer satisfaction., • Providing cutting-edge end-to-end services., • Utilizing state-of-the-art facilities., • Offering extensive expertise in biologics. We are looking for a new person to join the QC as a Bioassay analyst to work in our brand new facilities in Sant Quirze del Vallès: MAIN RESPONSIBILITIES: • Perform cell proliferation methods and others bioassays to verify the potency of biotechnology products, according to to USP, EP, and internal methodologies., • Cell bank production, caracterization and release management., • Maintain detailed and contemporaneous records in laboratory notebooks, logbooks, or electronic systems (LIMS)., • Participate in quality system activities including investigation of OOS/OOT microbiological results, deviation reporting, and support in CAPA implementation., • Maintain laboratory equipment calibration and functionality and promptly report any malfunctions or maintenance needs., • Follow all biosafety and safety protocols contributing to maintaining a clean, organized, and compliant laboratory environment., • Collaborate effectively with QA, production, validation, and other cross-functional teams to support quality assurance and compliance. REQUIREMENTS: • Advanced training in bioassays analysis with 2 to 5 years of proven experience in Quality Control within a GMP-regulated pharmaceutical environment., • Practical expertise in bioassays used in biotechnology, including cell proliferation assay, following USP and EP methods., • Skilled in cell culture. Strong knowledge of ALCOA++ data integrity principles and GMP documentation practices., • Experienced in managing quality systems including Out of Specification (OOS) investigations, deviation reporting, CAPA implementation, and change control., • Proactive team player with strong organizational skills and the ability to work independently while ensuring strict compliance with regulatory requirements., • Fluent in Spanish with basic to intermediate English communication skills (reading and writing preferred).

Around the world, approximately 3,900 Balluff employees work daily on high-quality sensor, identification and image processing solutions, including network technology and software for all automation requirements. That is why, as a globally positioned family business, we always offer you the best conditions. Work with us to ensure our customers' success and let's advance innovations together!! We are looking for passionate and results-oriented team players to start as soon as possible as Business Administration Support Iberia Tasks & Responsibilities: Office Management • Manage office supplies and coordinate with vendors, • Manage the company fleet, • Oversee maintenance, IT support, and general facility issues, • Greet and assist visitors and customers, • Coordinate insurance policies, • Coordinate internal communications and team updates, • Prepare business reports and presentations on sales performance and KPIs, • Organize management meetings, including scheduling, minute-taking, and tracking follow-up actions, • Support office events and social initiatives, • Coordinate travel management incl. visa requirements, organize trips for all employees on special occasions, such as team meetings., • Improve process regarding direct debit., • Provide finance support such assisting with basic accounting tasks, checking travel/personal expenses and credit card transfers., • Invoice processing. Send invoices by post/email., • Main contact and coordination with suppliers and SSC (Shared Service Centre)/ Accounting EMEA, • Monitor budgets and flag overspending, • Process invoices using SAP, • Organize and process refunds, • Put Payroll onto banking for approval, • Manage and process staff expenses, • Contact dunning Level 1 customers, • Support with necessary documentation to yearly Audit working with accounting department and Audit company Your skills and competencies: • Degree in ADE or finance related field, • Several years of professional experience in a comparable position, • Excellent interpersonal and communication skills., • Ability to work collaboratively in a team environment., • Detail-oriented with strong organizational and time management skills., • Fluency in Spanish and English is required., • Experience using SAP and Microsoft Office will be highly valuated. What we offer: • One year fixed-term contract 📄, • Private health insurance with Axa 🩺, • Hybrid remote-office work (2 days WFH) 🏡, • Flexible work schedule ⏰, • 27 days of holidays per year 🌴, • Access to continuous training 💻, • Language lessons 👩🏽 🏫 You want to make a difference with us? Then we look forward to receiving your application! If you are interested, please apply to: enclosing your CV.

Join Our Team as a HS Specialist & QE Administrative! At Falck, we are dedicated to maintaining the highest standards of Quality, Health, Safety, and Environment. We are looking for a proactive and detail-oriented HS Specialist & QE Administrative to contribute to our commitment to excellence and safety. If you are passionate about ensuring compliance, promoting a safe working environment, and driving continuous improvement, we want to hear from you! About the Role: As a HS Specialist & QE Administrative, you will play a crucial role in supporting the implementation and maintenance of our integrated management systems. You will be responsible for monitoring preventive actions, managing documentation, and contributing to our environmental initiatives, ensuring our operations meet all regulatory and internal standards. Your Responsibilities will include: Health and Safety (HS): • Monitoring of preventive and corrective actions in occupational risk prevention., • Collaboration in the implementation, maintenance and monitoring of occupational health and safety procedures., • Support for tasks in the area (health surveillance, stations visits, monitoring of labour accidents, etc.)., • Support on HS Kpi’s follow-up and reporting to territorial ops. team and DK Safety office. Quality and Environment (QE): • Collection and follow-up of KPIs related to quality and environment (e.g., waste management, energy/water consumption, air emissions, customer satisfaction, etc.)., • Waste management data follow-up: Monitoring of the correct waste management and related information., • Follow-up of GHG emissions., • Promote continuous improvements in QHSE matters. QHSE Administrative Tasks: • Support in daily documentation and operational management regarding Health and safety (HS), Quality and Environment (QE)., • Support in the use, maintenance, and management of quality and environmental programs., • Administrative support in the department's various tasks (report writing, document preparation, activity logging, legal requirements follow-up, use of external QHSE platforms, etc.). Requirements: • CFGS (Higher Level Training Cycle) / University Degree / Master’s Degree., • Minimum of 2 years of experience in a similar role., • English level B2-C1. Valued Qualifications: • Integrated Management Systems: Occupational Risk Prevention (HS), Quality, and Environment, • Office Level - Advanced, • Knowledge in environmental aspects, waste management. GHG emissions and Carbon footprint concept., • Preferably with previous experience in international companies. Conditions: • Flexible Hours: Entry between 7:00 AM and 9:00 AM and exit between 3:30 PM and 5:30 PM from Monday to Thursday. Intensive 6-hour workday on Fridays., • Vacation: 30 working days., • Opportunities for growth and development. Apply now and become a part of our team! #QHSE #specialist #administrative #FalckSpain #JoinFalck #Enviromental

¿Tienes experiencia en el análisis de productos biológicos en entornos regulado por las GMP?, ¿te gustaría incorporarte en una organización de investigación para terceros que ofrece servicios de bioanálisis y análisis de CMC a la industria de las ciencias de la vida, cuyas instalaciones están situadas en Cerdanyola del Vallès? Esta oportunidad te va a interesar. Podrás formar parte de una plantilla de más de 250 empleados, incorporándote en el equipo de Control de Calidad de Productos Biológicos y Terapias Avanzadas. Concretamente re responsabilizarás de las siguientes funciones: • Diseño, supervisión y ejecución de estudios de control de calidad de productos biológicos, incluyendo cromatografía y HPLC. Se requiere al menos 3 años de experiencia con estas técnicas., • Gestión de los proyectos asignados, cumpliendo los plazos y estableciendo una comunicación directa con el cliente., • Gestión de la documentación técnica asociada a los estudios (procedimientos estándar, certificados de análisis, desviaciones, etc.)., • Dirección y supervisión del trabajo experimental del personal técnico a cargo. Requisitos: • Grado en Bioquímica, Biotecnología, Química o afín., • Experiencia en métodos de HPLC., • Imprescindible experiencia en control de calidad en empresas farmacéuticas y entornos GMP., • Se valorará el conocimiento de técnicas electroforéticas, Western-Blot, ELISA y control de calidad de proteínas., • Buen nivel de inglés. Se ofrece: • Contrato indefinido, • Horario de lunes a viernes de 6h a 14h, • Salario fijo entre 31.500€ y 34.500€ en función de la experiencia aportada, más bonus por consecución de objetivos., • Desarrollo profesional, ambiente colaborativo y una cultura de empoderamiento., • Acceso a la plataforma de beneficios para empleados.

Our client is Valmet (), a leading global developer and supplier of process technologies, automation, and services for different industries. They are leaders in the pulp, paper, and energy industries, but with their automation systems and flow control solutions, they have presence in a lot more industries. Given the growth plan that they have for the upcoming years, we’re looking for a: Inside Sales Engineer Working in the Flow Control business line, the person will be responsible for improving customer performance by providing customized solutions, focusing on results, and taking a proactive approach to support their success and enhance their operations. The position can be based either in Madrid or Barcelona, offering flexibility for the right candidate. The main tasks will be: • Generate opportunities and quotations by responding promptly to customer inquiries with accurate and competitive proposals., • Work with the Indian Hub or Project Quotation Team to optimize the quotation process., • Review and adjust quotations to meet technical requirements., • Provide detailed product and service information to customers and the sales team., • Support sales and distribution channels to drive business growth., • Assist in resolving customer claims efficiently., • Collaborate with engineers and product management to customize solutions for customers., • Process and validate orders with factories and sub-suppliers., • Advise existing customers on product selection and share feedback with internal teams., • Work with the Account Manager to identify and engage new customers., • Participate in internal projects and training programs., • Ensure compliance with Valmet's quality, health, safety, and environmental standards. We are looking for a candidate with an M.Sc. or B.Sc. in an engineering field and experience in a similar position. Experience in flow control and a background related to valves will be valued. Because we work in a global matrix organization, the ideal candidate should have demonstrated success in a similar environment and possess strong communication skills, both written and verbal, in Spanish and English. We place great value on personal qualities, particularly a combination of autonomy, proactivity, and initiative. The ideal candidate will be a team player, committed to quality, results-driven, and customer-oriented. They offer a challenging position in a dynamic organization and the opportunity to influence the direction and success of the company. As part of their engaged and enthusiastic team, you will have the opportunity to develop your skills and reach your full potential. The benefits they offer include flexible working hours, a hybrid working model, a bonus plan, medical insurance, and training and development opportunities.

En LAINCO, buscamos a un/a Quality Control Analist para nuestro departamento de Quality Control, cuya misión principal será controlar la calidad de nuestros productos para garantizar sus especificaciones finales a los clientes. FUNCIONES Y RESPONSABILIDADES En dependencia directa del/la Quality Control Manager, algunas de sus principales funciones serán: • Realizar el muestreo de materias y productos de acuerdo con las instrucciones que se le faciliten, tanto productos de la sección de agrícola como de farmacia., • Realizar análisis de M/P, Producto intermedio y P/A de las divisiones de FA y AG, que en cada momento se le indiquen. Estos análisis pueden ser de tipo físico, químico y microbiológico., • Realizar el Control de Calidad de material de envasado, verificando tamaño, impresión, texto, materiales, etc., • Realizar análisis microbiológicos., • Anotar y registrar los datos., • Muestreo para estabilidades., • Control y gestión de la caducidad de las materias primas y productos., • Gestión del control de stocks de reactivos y materiales para tener siempre disponible ¿QUÉ ESPERAMOS DE TI? Buscamos a una persona con capacidad para trabajar en equipo, proactiva, con iniciativa y compromiso con la empresa. Un perfil dinámico, ordenado, metódico y eficiente, con capacidad para asimilar de forma rápida los conceptos y la forma de trabajo. EXPERIENCIA Y FORMACIÓN • Formación de Grado Superior de Laboratorio de Análisis y Control de Calidad., • Posibilidad de trabajar a turnos rotativos de mañana (5:55h. a 14h.) y tarde (13:55h. a 22h.) o fijo de tardes., • Experiencia de mínimo 3 años en una posición similar trabajando con HPLC’S., • Valorable conocimientos de SAP e informática nivel usuario avanzado., • Experiencia en industria farmacéutica, realizando el trabajo en un entorno de cumplimiento de Buenas Prácticas de Laboratorio y normativa GMP’S., • Valorable experiencia en análisis microbiológicos., • Carné de conducir y vehículo propio. ¿QUÉ OFRECEMOS? • Te ofrecemos la posibilidad de participar en el crecimiento y expansión de la empresa a nivel nacional e internacional., • Contrato indefinido., • Remuneración atractiva y pack de beneficios sociales.

🎯 ¡Buscamos QA Manual & Automatización – Especialista en Medios de Pago! 📍 Ubicación: Sant Cugat del Vallès (Barcelona) – Modalidad presencial 4 días/semana Somos una empresa de consultoría especializada en IT, ingeniería y digital. Desde nuestra creación en 2007, hemos apostado por una filosofía que combina rendimiento y bienestar laboral. Esta visión ha sido compartida por más de 2.500 Extianeses/as en Francia y a nivel internacional, y ha sido reconocida durante 13 años consecutivos con el sello Great Place to Work®, alcanzando en 2024 y 2025 el primer puesto en el ranking Best Workplaces France. En Extia decimos: "Primero quién, luego qué", ¡así que vamos allá! Desde Extia, estamos buscando perfiles de QA Manual & Automatización con experiencia en dispositivos TPV y medios de pago, para incorporarse a un proyecto estable en uno de nuestros clientes líderes del sector, ubicado en Sant Cugat del Vallès. ✅ ¿Qué buscamos? • Experiencia en entornos QA manual sobre dispositivos de pago / medios de pago., • Conocimientos en herramientas como:, • XRay y Cucumber, • Jira, • Confluence, • Robot Framework, • Appium, • Familiaridad con protocolos de comunicación ISO8583., • Valorable nivel medio de inglés o francés (no obligatorio)., • Personas comprometidas, que busquen estabilidad laboral a largo plazo. 🧑 💻 Modalidad de trabajo • Presencial en las oficinas del cliente de lunes a jueves. 🚀 ¿Por qué unirte a Extia? • Entorno de trabajo colaborativo, cercano y con foco en las personas, "Primero quién, luego qué"., • Proyecto estable en un entorno tecnológico avanzado., • Formación continua y plan de desarrollo profesional., • Ticket restaurante y seguro médico premium. Si tienes experiencia en QA manual y te apasiona el mundo de los pagos, ¡queremos conocerte! Aplica aquí.

💡 ¿Y si tu próximo paso profesional te colocara en el centro de los proyectos que están transformando la industria? ⚙️ Imagina ser una pieza clave en garantizar que los procesos, productos o soluciones cumplan con los más altos estándares de calidad, innovación y rendimiento. En TRIGO, no buscamos solo experiencia. Buscamos personas con actitud, compromiso y ganas de dejar huella en lo que hacen. Bajo nuestro lema QUALITY IS OUR MINDSET, nuestro propósito es permitir a las personas viajar con total tranquilidad y confianza, asegurando que cada método de transporte cumpla con los más altos estándares de calidad y seguridad. ¿Te atreves a dar el siguiente paso? TÉCNICO/A DE CALIDAD 📍 Estabilidad garantizada: incorporación en septiembre (incorporación directa en cliente). ⏳Horarios rotativos de mañana tarde y noche (cada dos semanas) + opción cuarto turno de fines de semana. 💼 Modalidad presencial. ¿Por qué trabajar con nosotros? 🔹Innovación constante: aquí cada día plantea nuevos desafíos, nuevas ideas y nuevas soluciones. 🔹Crecimiento real: te acompañamos a crecer desde dentro con formación y promociones internas. 🔹Cultura colaborativa: trabajamos en equipo, celebramos los logros juntos y aprendemos de los errores. Tu misión 🚧 Como Técnico/a de Calidad, serás quien verifique y valide los productos en entornos de automoción, asegurando el cumplimiento de los requisitos del cliente y gestionando no conformidades. Los retos a los que te enfrentarás: • Colaborarás en los estudios de capacidad requeridos interna o externamente., • Verificarás y validarás los productos y muestras fabricados frente al plan de control y los requisitos de cliente., • Realizarás los ensayos y estudios requeridos para producto o proceso., • Validarás el producto y proceso en los arranques de producción y cambios de referencia., • Revisarás documentación continua del producto fabricado, así como de los rechazos generados en su turno (pasando regularmente por las líneas de producción activas en su turno)., • Tomarás decisiones sobre el producto retenido por producción e identificarás el producto no conforme., • Darás soporte documental y formativo al personal de producción en la detección de posibles defectos subjetivos, transmitiendo criterios basados en la experiencia de reclamaciones de cliente. Qué te hará triunfar en el puesto: ✅ Formación en Ingeniería Mecánica, Industrial o similar. ✅ 3 años de experiencia en diseño, calidad o similares. ✅ Conocimiento práctico de entornos industriales. Así será tu proceso de selección: • 📞 Llamada breve para alinear tus expectativas y conocerte (15 min)., • 💻 Entrevista online con el equipo de Talent Acquisition (40 min)., • 🏢 Validación técnica presencial con el equipo de operaciones/responsables de departamento para conocer cómo es el día a día (45 min). Porque sabemos que lo que haces importa, hazlo en un lugar donde de verdad deje huella. Inscríbete y sigamos formando juntos el #TeamTRIGO. En TRIGO fomentamos la igualdad de oportunidades y la diversidad. Todas las candidaturas serán evaluadas sin discriminación por razones de género, origen, orientación sexual, discapacidad u otras circunstancias.

Conócenos En ZITRO somos referentes en la industria del juego a nivel mundial. Desde nuestra creación en 2007, no hemos parado de crecer y expandirnos por todo el mundo. ¿Nuestro secreto? Una apuesta constante por la innovación tecnológica, la investigación y el desarrollo... y, sobre todo, un equipo humano excepcional con el que trabajar codo con codo. ¿Te animas? 👉 Conócenos mejor: ___ 👉 Conócenos mejor: Tu día a día en Zitro Si estás buscando una posición técnica, dinámica y retadora en el área de Quality Control, ¡has llegado al lugar correcto! Formarás parte de un equipo que valora los pequeños detalles, el trabajo metódico y la calidad del producto por encima de todo. Una persona con perfil analítico, proactivo y resolutivo, con ganas de crecer, marcará la diferencia. Tus principales tareas serán: • Soporte técnico de segundo nivel: resolución de incidencias, instalación de software y configuración remota de equipos., • Seguimiento y aplicación de los procedimientos establecidos para el control de calidad de nuestros productos instalados., • Soporte técnico ocasional en inglés a clientes o equipos en EE.UU. ¿Qué necesitas para unirte a nuestro team? • Formación técnica: CFGS en Administración de Sistemas Informáticos en Red, Telecomunicaciones o similares., • Conocimientos en entorno Linux y bases de datos MySQL/SQL., • Experiencia previa mínima de un año en soporte técnico (incidencias N1 y N2)., • Capacidad de aprendizaje, atención al detalle, comodidad trabajando en equipo y en resolución de problemas. Pensamos en una persona proactiva y con buenas habilidades comunicativas., • Nivel alto de inglés imprescindible (hablado)., • Conocimientos de sistemas de ticketing (JIRA). Nuestra propuesta • Contrato fijo que brinda estabilidad profesional., • Oportunidades reales de desarrollo y crecimiento., • Horario flexible de lunes a jueves y jornada continuada los viernes. Turnos rotativos: • Turno de mañana preferente: 7:00 a 15:15 h (presencial)., • Turno de tarde una vez al mes: 13:45 a 22:00 h (opción de teletrabajo)., • Guardias rotativas: una semana al mes con disponibilidad nocturna (de 22:00 a 7:00 h de lunes a viernes) y disponibilidad completa en fin de semana para emergencias. Beneficios: • Contrato indefinido, que te da estabilidad y confianza en tu desarrollo., • Fantástico ambiente laboral, cercano y colaborativo., • Ticket restaurante., • Seguro de salud y de vida., • Retribución flexible (tickets guardería, etc.)., • Eventos internos, team buildings y afterworks que te permitirán disfrutar también fuera del trabajo., • Nivel de responsabilidad, • Algo de responsabilidad, • Sector, • Proveedores de entretenimiento, • Tipo de empleo, • Jornada completa, • Funciones laborales, • Tecnología de la información, • Aptitudes, • Sistema de seguimiento de incidentes, • JIRA, • MySQL, • Linux, • Sistema de seguimiento de errores, • SQL

Perfil técnico que gestione el cumplimiento de la normativa GMP y la política de calidad en entorno de producción de lotes clínicos (I+D) con participación en el desarrollo de nuevos productos/procesos, en un ambiente de colaboración interdepartamental. Licenciado / Grado en Farmacia o titulac

Our client is Valmet (), a leading global developer and supplier of process technologies, automation, and services for different industries. They are leaders in the pulp, paper, and energy industries, but with their automation systems and flow control solutions, they have presence in a lot more industries. Given the growth plan that they have for the upcoming years, we’re looking for a: Inside Sales Engineer Working in the Flow Control business line, the person will be responsible for improving customer performance by providing customized solutions, focusing on results, and taking a proactive approach to support their success and enhance their operations. The position can be based either in Madrid or Barcelona, offering flexibility for the right candidate. The main tasks will be: • Generate opportunities and quotations by responding promptly to customer inquiries with accurate and competitive proposals., • Work with the Indian Hub or Project Quotation Team to optimize the quotation process., • Review and adjust quotations to meet technical requirements., • Provide detailed product and service information to customers and the sales team., • Support sales and distribution channels to drive business growth., • Assist in resolving customer claims efficiently., • Collaborate with engineers and product management to customize solutions for customers., • Process and validate orders with factories and sub-suppliers., • Advise existing customers on product selection and share feedback with internal teams., • Work with the Account Manager to identify and engage new customers., • Participate in internal projects and training programs., • Ensure compliance with Valmet's quality, health, safety, and environmental standards. We are looking for a candidate with an M.Sc. or B.Sc. in an engineering field and experience in a similar position. Experience in flow control and a background related to valves will be valued. Because we work in a global matrix organization, the ideal candidate should have demonstrated success in a similar environment and possess strong communication skills, both written and verbal, in Spanish and English. We place great value on personal qualities, particularly a combination of autonomy, proactivity, and initiative. The ideal candidate will be a team player, committed to quality, results-driven, and customer-oriented. They offer a challenging position in a dynamic organization and the opportunity to influence the direction and success of the company. As part of their engaged and enthusiastic team, you will have the opportunity to develop your skills and reach your full potential. The benefits they offer include flexible working hours, a hybrid working model, a bonus plan, medical insurance, and training and development opportunities.

We are Applus+, one of the world's leading companies in testing, inspection and certification, with a presence in more than 70 countries on 5 continents and a team of more than 25,000 people. You can consult our projects on the website: During recent years we have experienced great development thanks to our human team who we consider to be a key and strategic piece in the development of this company. Would you like to be part of the project? We are currently looking for a Consultancy and Services Category Buyer responsible for executing sourcing strategies to deliver cost savings, improve quality and risk mitigation. What will your day to day be like? Category Management: • Develop and implement Consultancy and Services strategies for aligned with the company’s objectives., • Identify trends, opportunities, and potential risks, • Lead end-to-end procurement processes, including tendering, negotiating, catalogues and contract management., • Collaborate with internal stakeholders to understand project requirements and ensure procurement strategies meet business needs., • Develop a supplier base that supports the company’s growth, quality, and innovation objectives., • Ensure all contracts comply with company policies, legal requirements, and risk management standards., • Drive cost reduction initiatives while maintaining quality and service levels., • Develop total cost of ownership (TCO) models to evaluate and optimize procurement decisions., • Work closely with IT team, finance, operations, and project management teams to align procurement activities with project timelines and budget constraints., • Identify and mitigate risks, including supply chain disruptions, financial instability, and compliance issues., • Implement best practices in procurement processes and contribute to the continuous improvement of the procurement function., • Keep abreast of industry best practices and innovations in IT procurement, • Support the standardization of procurement processes and cataloguing. He or She leads the creation and usage of the catalogues for the categories for which he/she is responsible Requirements: • University degree in Business, Economics, or a related field (or equivalent experience)., • 3 years of experience in procurement, purchasing, or supply chain operations preferred, • Specialized in procurement of Consultancy & Services, experience in international environment, SAP ARIBA experience is an important plus., • Familiarity with procurement software and ERP systems (e.g., SAP, Oracle, or similar), • Proficiency in MS Office Suite (especially Excel for data management and reporting), • Proficiency in English, Spanish and French (nice to have), other European Language is welcome Applus+ is a company that offers equal opportunities. We are committed to treating all applicants equally based on their abilities, achievements, and experience regardless of race, national origin, sex, age, disability, sexual orientation, gender identity, or any other classification protected by law.

The Siegfried Group is a global life science company with a network of 13 sites in Europe, the USA and Asia. Siegfried offers contract development and manufacturing of active pharmaceutical ingredients, intermediates, and drug products and has sales more than CHF 1.3 billion Swiss Franks. Siegfried Holding AG employs over 3,900 people and is listed on the SIX Swiss Exchange (SIX: SFZN). Are you a Senior Manager Business Applications (SAP Data Migration) looking for a new challenge in a dynamic CDMO Pharmaceutical Industry in our Barberà del Vallès site? Reporting to the Head Data Intelligence and SAP-Basis, you will be responsible for replacing the existing system to migrate data, selecting and evaluating data migration designs, governing scalable data migration architectures and standards across SAP programs. Your role: • Technical and functional lead for SAP data migration and master data projects, including architectural transition from R/3 (ECC 6.0) to the S/4HANA landscape., • Convert business needs and design scalable, compliant data migration solutions and roadmaps, ensuring end-to-end consistency and auditability across all Siegfried sites., • Design and govern scalable data migration architectures and standards to ensure quality, compliance, and consistency across SAP programs., • Select and evaluate data migration (e.g., SAP Data Services, LSMW) and master data tools to ensure reusability, compliance, and fit-for-purpose solutions., • Coordination and management of external consulting resources in term of project management, • Conduct internal trainings on data migration and master data, promoting best practices and knowledge sharing. Your profile: • Educational background in Information Technology or equivalent qualification., • Led at least one complex data migration project to SAP S/4HANA., • At least 7 years experience in delivering services related to data migration, transformation, and support for mergers, acquisitions, and divestitures, • Served as an enterprise architect or advisor, guiding customers in building IT roadmaps using SAP products and services., • Experience with Data Management solutions (e.g., MDG, ILM) or SAP Industry Solutions is an added advantage, • Experience with SQL is a plus., • Solution-oriented with strong communication skills., • Willingness to work on a broad range of topics in the area of SAP Master data ., • Resilient team player with high flexibility., • Fluent in Spanish and English, both written and spoken. Working at Siegfried Siegfried's work environment is dynamic and international. With a highly professional and motivated team, the company operates in a future-oriented business field. Siegfried possesses a unique culture that leverages cultural differences to create a competitive advantage. Siegfried places highest priority on providing a flexible, diverse and discrimination-free working environment in which employees can develop personally and professionally, advance innovation and deliver superior performance. We strive to provide a work environment where employees can take on challenging jobs and associated responsibilities that best serve their personal and technical development and can benefit from the success of our company. The company regulations in respect of compensation and career development opportunities apply to all Siegfried sites. Additional conditions of employment are governed by location-specific circumstances, legislation and customs. Who we are In the Midst of People’s Lives – Across the Globe The Siegfried Group is one of the world’s leading Custom Development and Manufacturing Organizations (CDMOs) developing and producing active pharmaceutical ingredients (API), intermediates and finished dosage forms. As our core competence, we successfully integrate chemical and pharmaceutical capabilities into a single business model. The Siegfried name stands for highest quality, efficiency, flexibility and safety. Present in Europe, Asia and North America, we serve a broad global customer base from major international pharmaceutical companies down to small biologic-pharmaceutical organizations. For them we develop and produce product innovations on a large scale to finished products. We integrate our offer seamlessly into the customers’ value chain. Our comprehensive services range from early-stage Research & Development services such as synthesis, scale-up, formulation development, stability studies and method development all the way through to manufacturing services, ranging from preclinical R&D material for clinical trial purposes to commercial production. We are able to produce about 200 of the approximately 1500 registered drug substances used in medicine. Moreover, we produce 20 percent of global demand for caffeine. Consequently, nearly 1 billion individuals come into contact with Siegfried products.

Are you a highly skilled Supply Chain professional seeking a new challenge? We are currently looking for a talented individual to join our team as a Supply Chain Manager . This role will involve leading and managing the procurement, storage, and distribution of materials and products. You will be responsible for developing and implementing strategies to optimize supply chain operations, ensuring cost-effectiveness and efficiency. In this position, you will also be responsible for : • Managing supplier relationships and negotiating contracts., • Developing and executing sourcing strategies to secure high-quality raw materials and consumables., • Overseeing the storage, handling, and distribution of materials and products., • Minimum 5+ years of experience in supply chain, procurement, or warehouse management within the bio-pharmaceutical or life sciences industry., • Proven ability to develop and execute sourcing strategies for biopharmaceutical raw materials and consumables., • Strong knowledge of warehouse operations, stock control, and logistics., • Regulatory compliance knowledge, including GMP and GDP., • Strong problem-solving and data analysis skills. Requirements : • Bachelor's degree in Supply Chain Management, Business Administration, or related field., • A competitive salary and benefits package. Keyword : SupplyChainManager #J-18808-Ljbffr

Opportunity Overview Join a fast-growing multinational retail company as a General Manager, overseeing store operations across Europe. About Our Client A rapidly expanding multinational retail organization. Job Description The Role The General Manager reports directly to the European Director of Store Operations. The role focuses on executing the business formula, driving organizational growth, and fostering company culture. The General Manager is fully responsible for P&L, expansion, and store operations. They will collaborate closely with Area Managers and central departments such as Real Estate, Operations, Logistics, Buying, and HR. Responsibilities: • Operational Management, • Ensure correct implementation of the business formula, policies, and methods., • Collaborate with Area Managers and central departments., • Maintain high standards in store operations, including stock, cleanliness, and process adherence., • Oversee the opening of new stores without compromising quality., • Achieve sales targets and operational excellence., • Ensure leadership aligns with company values and competencies., • Manage HR functions such as recruitment, training, coaching, and absence management., • Strategy and Policy, • Contribute to sales formula and policy development from local and national perspectives., • Monitor competition and recommend strategic actions., • People Management, • Lead the team towards organizational growth and proactively address future challenges., • Provide constructive feedback and support employee development., • Encourage employee participation in idea generation and learning., • Create a stimulating work environment for continuous development., • Mentor and coach employees to enhance their skills and competencies., • Manage staffing, recruitment, and retention within the department., • Set an example through clear and effective communication., • Results Orientation, • Develop annual plans and monitor operational KPIs such as turnover and wages., • University degree in Business Management or related field., • 5-10 years of leadership experience with P&L responsibility at a national level., • Experience as a Sales Manager/Director in retail discount sector. An excellent opportunity for professional development within a dynamic company. #J-18808-Ljbffr

Are you interested in being part of a technological center of excellence where you can contribute and add technological value to companies and institutions, focusing on research, development and industrial innovation (R+D+2i)? Do you want to work in a leading environment with all the technological innovations within your reach? Leitat is a technological center of reference at national and European level. With more than 100 years of history, it has a team of more than 400 professionals, experts in applied research, technical services and management of technological and innovation initiatives. Leitat provides social, industrial, economic and sustainable value, offering integral solutions in multiple sectors and fields: health and biomedicine, development of new materials, eco-sustainable production, occupational health prevention systems, waste revaluation and use of natural resources; interconnectivity and digitalization of industry, green energy and maximization of energy efficiency. Leitat develops R+D+i projects for companies and institutions, as well as leads research projects with competitive funding both within the framework of the European Union and the Ministry of Science and Innovation. We are currently looking for a Senio r Researcher Energy Storage & Data Science: As a Senior Researcher in our energy storage group, you will play a key role in leading research and innovation activities within national and Horizon Europe (HE) projects. Your work will focus on advancing methodologies for battery testing, data analysis, and digital tools for energy storage applications. You will drive collaboration with academic, industrial, and institutional partners, while providing technical leadership and guidance to project teams. This position offers an excellent opportunity to contribute to shaping the future of sustainable energy through cutting-edge European projects, while mentoring junior colleagues and strengthening our research capabilities. Key Responsibilities: • Lead research tasks in national and European projects related to battery testing, modeling, and energy storage system optimization., • Guide the development and application of digital tools, AI/ML models, and advanced data analysis methodologies for energy storage research., • Coordinate project deliverables, ensuring quality, and timely completion., • Act as a key technical contact with external project partners, representing the organization in European consortia and research networks., • Contribute to the preparation of proposals for competitive funding calls and support strategic project acquisition., • Provide mentorship and technical guidance to junior researchers and engineers. Qualifications • Master’s or PhD in Electrical Engineering, Power Electronics, Data Science or a related field., • Demonstrated experience (3+ years) in R&D, particularly within national or European-funded projects., • Coding and data science expertise (Python, C++, MATLAB), with applied knowledge of AI/ML., • Experience in digitalization and advanced analytics for energy systems is a plus., • Strong track record in research outputs (e.g., publications, conference contributions, patents)., • Excellent communication skills and ability to collaborate effectively within multicultural and multidisciplinary teams. Fluent in Spanish and English, oral and written. You will succeed in this position if you bring: • Experience in data science, statistical modeling, and predictive analytics., • Strong proficiency in Python, R, or MATLAB for data processing, AI, and ML modeling., • Knowledge of battery SOH modeling, failure prediction, or degradation analysis is a plus (but not required)., • Strong analytical mindset and ability to work with cross-functional teams., • Familiar with statistical methods and experimental design principles., • Excellent communication and collaboration skills., • Basic knowledge of battery chemistry, mainly at the cell level, is highly recommended. You will be located at the headquarters in Barcelona and will work in an attractive environment, being part of a unique innovation ecosystem with cutting-edge technologies and highly equipped laboratories. We offer flexible working hours so that you can reconcile your personal life and your professional development. In addition, you will enjoy subsidized catering in our centers, medical insurance and you will have a permanent contract with a salary commensurate with your experience, training and development. We are proud to offer these types of benefits that support the goals and well-being of our team members. We also support equal opportunities and diversity - we strive every day to be a more inclusive workplace adapted to all groups! If you are a person with excellent interpersonal and communication skills, with a high capacity to achieve your goals within the established deadlines and able to work independently and as part of a team, do not hesitate, sign up for our offer. We would love to hear from you! At LEITAT we look forward to meeting you!

• Specialist healthcare company based in Barcelona Specialist healthcare company based in Barcelona, part of a larger international pharmaceutical group. The company focuses on clinically backed, innovative solutions in the gastrointestinal, respiratory, and pediatric areas. With a strong international presence through B2B partnerships, it is currently undergoing a strategic transformation-refining its focus, accelerating execution, and fostering a high-performance culture. Job Description Key Responsibilities Execution & Performance • Drive the successful implementation of the Company's strategic goals through disciplined use of the Group's Operating System., • Translate high-level objectives into executable plans across departments (Operations, Regulatory, Medical, Marketing, Finance, and Commercial)., • Establish clear performance metrics, tracking systems, and accountability mechanisms. Leadership & Culture • Build and sustain a positive, high-performing, and collaborative office culture., • Ensure staff are engaged, empowered, and aligned to the company's goals and values. Operational Oversight • Oversee day-to-day operations and ensure smooth interdepartmental coordination., • Proactively identify bottlenecks or misalignments and resolve them swiftly., • Fire-fight critical issues with urgency and strategic clarity. Group Integration • Serve as a key operational liaison between the CEO and the Barcelona team-ensuring that strategic direction, execution progress, and cultural alignment flow effectively across geographies. Experience • Minimum 8 years of experience in general management, operations, or cross-functional leadership., • Industry experience in pharmaceuticals, consumer health, or similarly regulated environments Skills & Attributes • Strong executional discipline and a solutions-oriented mindset., • High emotional intelligence with the ability to lead through influence., • Comfortable working under pressure and managing competing priorities., • Excellent communication and interpersonal skills., • Committed to building a values-driven, high-trust environment. Languages • English: Fluent (spoken and written at a high level - required) This is a unique opportunity to join a nimble, entrepreneurial healthcare company at a moment of strategic clarity and operational focus. You will play a key leadership role in shaping the company's trajectory, culture, and performance-working alongside a globally-minded team that values ownership, speed, and impact. #J-18808-Ljbffr

About Us Based in Barcelona and Treviso, INDIBA Group stands at the forefront of global leadership in Aesthetics, Beauty, Rehabilitation, Sports, Intimate Health, Pharma, and Animal Health solutions, standing on a rich 40-year history of scientific innovation. Our cutting-edge 448 kHz frequency technology is the cornerstone of our world-renowned therapies, empowering individuals to enhance their lives and accelerate recovery from injuries across various sectors. With the integration of K-LASER, a global leader in medical lasers, we’ve propelled our commitment to advancing treatments, embracing new technologies, and expanding our global presence in medical research. Revitalizing lives is what we do and what our teams are working on to achieve daily. What are we looking for? We are looking for a senior leader to oversee the Medical Affairs & Training Department for INDIBA Group. This strategic role combines regulatory and clinical responsibilities with scientific communication and training leadership. The ideal candidate will bring deep medical expertise, strong stakeholder engagement capabilities, and the ability to align and transform clinical insights into business value while supporting company positioning. Which will be your responsabilities? • Lead the development, maintenance, and strategic use of clinical evidence to support product registration and ensure compliance with global medical device regulations., • Oversee the preparation of clinical documentation, including trial protocols, regulatory submissions, and reports to health authorities and notified bodies., • Supervise clinical trials and post-market surveillance, maintaining strong relationships with key opinion leaders (KOLs) and investigators to support research and product positioning., • Act as a key medical representative in audits, inspections, and quality reviews requiring scientific justification or expertise., • Provide scientific support and strategic guidance across internal departments including Commercial, Marketing, R&D, Regulatory and Quality., • Guide the development of scientific materials, publications, and congress contributions to reinforce K-LASER and INDIBA's position in the medical community., • Lead the Training team to ensure delivery of consistent, high-quality programs aligned with the latest clinical data, approved product claims, and corporate objectives., • Monitor emerging clinical trends and innovations to inform product development and positioning., • Ensure the effectiveness of the medical vigilance system in collaboration with relevant departments. What do you need to be a succesful candidate? • Minimum of 10 years’ experience in Pharmaceutical Laboratory, Medical Devices company or regulatory consultancy, in areas such as Medical / Scientific Department, Clinical Research, Medical Writing, Scientific marketing or equivalent., • Experience in writing clinical reports (expert reports, review reports, clinical, pharmacological, pharmacovigilance, phase III / IV studies, or similar) is essential., • Academic background: Degree in Health Sciences (Medicine, Pharmacy, Human Biology or Biomedical Science). Master's or post-graduate studies aimed at the Pharmaceutical, Cosmetic and/or Aesthetic and Rehabilitation Medicine Industry as well cinical trial monitoring will be valued., • Good command of Clinical research methodology., • Fluent Spanish & English language skills in both verbal and written communication. Fluency in another language will be a plus. What we offer? • Full-time and permanent contract., • Location: Sant Cugat del Vallés., • Hybrid work model, • Attractive remuneration package., • Fringe benefits., • Multinational and flexible environment. #J-18808-Ljbffr

Somos la firma global de talento: Selección, headhunting, formación y consultoría de Eurofirms Group.En Claire Joster creemos en el talento único de cada persona y sabemos que la diversidad aporta valor a los equipos, impulsando organizaciones más innovadoras, creativas y eficientes.Por eso, co

En dependencia directa del/la Quality Control Manager, algunas de sus principales funciones serán:. Quality Control, cuya misión principal será controlar la calidad de nuestros productos para garantizar sus especificaciones finales a los clientes.

Únete a Technotex Quality Fabrics y potencia tu carrera en Marketing!.

Tienes experiencia en el análisis de productos biológicos en entornos regulado por las GMP?, ¿te gustaría incorporarte en una organización de investigación para terceros que ofrece servicios de bioanálisis y análisis de CMC a la industria de las ciencias de la vida, cuyas instalaciones está

Quality Control, cuya misión principal será controlar la calidad de nuestros productos para garantizar sus especificaciones finales a los clientes. En dependencia directa del/la Quality Control Manager, algunas de sus principales funciones serán:.

Experienced in managing quality systems including Out of Specification (OOS) investigations, deviation reporting, CAPA implementation, and change control. The new facility includes state-of-the-art development laboratories, oustanding Quality control rooms and warehouse. Participate in quality syste

Quieres formar parte de la experiencia Exceltic, una empresa con estrategia centrada en las personas?.Tienes inquietud por conocer el sector técnico y tecnológico?.En Exceltic estamos en búsqueda activa de un/a.Tus funciones se centrarán en:.Proporcionar a la planta y al cliente toda la document

Desde nuestra creación en 2007, no hemos parado de crecer y expandirnos por todo el mundo.Nuestro secreto? Una apuesta constante por la innovación tecnológica, la investigación y el desarrollo.Si estás buscando una posición.Formarás parte de un equipo que valora los pequeños detalles, el tra

To build, with the Head of Quality Assurance oversight, the Quality Management System creating and/or approving Standard Operating Procedures to support GMP manufacturing activities. The new facility includes state-of-the-art development laboratories, oustanding Quality control rooms and warehouse.

Buscamos QA Manual & Automatización – Especialista en Medios de Pago!.Sant Cugat del Vallès (Barcelona) – Modalidad.Somos una empresa de consultoría especializada en IT, ingeniería y digital.Desde nuestra creación en 2007, hemos apostado por una filosofía que combina.Esta visión ha sido c

Tienes experiencia en el análisis de productos biológicos en entornos regulado por las GMP?, ¿te gustaría incorporarte en una organización de investigación para terceros que ofrece servicios de bioanálisis y análisis de CMC a la industria de las ciencias de la vida, cuyas instalaciones está

Quieres formar parte de la experiencia Exceltic, una empresa con estrategia centrada en las personas?.Tienes inquietud por conocer el sector técnico y tecnológico?.En Exceltic estamos en búsqueda activa de un/a.Tus funciones se centrarán en:.Proporcionar a la planta y al cliente toda la document

The new facility includes state-of-the-art development laboratories, oustanding Quality control rooms and warehouse. Participate in quality system activities including investigation of OOS/OOT microbiological results, deviation reporting, and support in CAPA implementation. Collaborate effectively w

To build, with the Head of Quality Assurance oversight, the Quality Management System creating and/or approving Standard Operating Procedures to support GMP manufacturing activities. The new facility includes state-of-the-art development laboratories, oustanding Quality control rooms and warehouse.

Desde nuestra creación en 2007, no hemos parado de crecer y expandirnos por todo el mundo.Nuestro secreto? Una apuesta constante por la innovación tecnológica, la investigación y el desarrollo.Si estás buscando una posición.Formarás parte de un equipo que valora los pequeños detalles, el tra

To build, with the Head of Quality Assurance oversight, the Quality Management System creating and/or approving Standard Operating Procedures to support GMP manufacturing activities. Bachelor’s degree in a Science field with proven experience in GMP Quality Assurance roles. In-depth knowledge mana

Buscamos QA Manual & Automatización – Especialista en Medios de Pago!.Sant Cugat del Vallès (Barcelona) – Modalidad.Somos una empresa de consultoría especializada en IT, ingeniería y digital.Desde nuestra creación en 2007, hemos apostado por una filosofía que combina.Esta visión ha sido c