Trabajos compliance en Barcelona - Page 2Crear alertas

Are you ready to join a world leader in the exciting and dynamic fields of the Pharmaceutical and Medical Device industries? PQE Group has been at the forefront of these industries since 1998, with 40 subsidiaries and more than 2000 employees in Europe, Asia and the Americas. We are currently seeking a GMP Analytical Lab Consultant - Maintenance & Qualification to support Quality Control laboratory activities within a GMP environment. The role involves managing qualification, calibration, maintenance, and troubleshooting of chemical laboratory instrumentation, ensuring compliance and proper performance of QC equipment. Responsibilities include, but are not limited to: • Perform Periodic Qualification (IQ, OQ, PQ) of Chemical Quality Control laboratory instrumentation, including: HPLC, UPLC, GC, balances, pH meters, Karl Fischer titrators, AAS, UV-Vis, IR spectrophotometers, climatic chambers, DSC, TGA, TOC analyzers., • Author and execute IQ, OQ, and PQ protocols and generate final qualification reports., • Monitor equipment performance, calibration status, and daily functionality checks to ensure GMP compliance., • Coordinate and manage relationships with vendors and external suppliers., • Plan and schedule qualification, calibration, and maintenance activities., • Oversee activity planning and procurement of kits and consumables., • Execute preventive maintenance and troubleshooting activities on laboratory instruments. Preventive Maintenance & Troubleshooting – HPLC • Detector diagnostics and troubleshooting, • Flow cell cleaning and lamp replacement, • Pump diagnostics and replacement of seals, pistons, and fittings, • Diagnosis of mechanical faults (arms, needle, injector systems), • Replacement of tubing, fittings, frits, filters, gaskets, and capillaries, • Cleaning of solvent inlet filters (dip sticks), • System flushing to remove precipitates and contamination, • Leak detection and seal integrity checks, • Diagnosis and replacement of syringes, septa, O-rings, injectors, and liners Required Qualifications: • Degree in scientific disciplines, • Experience of working in GMP environment, • Strong knowledge of analytical laboratory instrumentation and qualification processes (IQ/OQ/PQ)., • Spanish native, english at least B2 Next Steps Upon receiving your application, if a match is found, the Recruiting department will contact you for an initial HR interview. If there's a positive match, a technical interview with the Hiring Manager will be arranged. In the case of a positive outcome coming from Hiring Manager interview, recruiter will contact you for further steps or to discuss our proposal. Alternatively, if the outcome is negative, we will contact you to halt the recruitment process. Working at PQE Group As a member of the PQE team, you will be part of a challenging, multicultural company that values collaboration and innovation. PQE Group gives you the opportunity to work on international projects, improve your skills and interact with colleagues from all corners of the world. If you are looking for a rewarding and exciting career, PQE Group is the perfect place for you. Apply now and take the first step towards an amazing future with us.

¡Desarrolla tu liderazgo en Laboratorios Ordesa y forma parte de una organización con propósito, visión estratégica e innovación constante! ___ es una compañía referente en el sector de la nutrición especializada, con una sólida trayectoria y en pleno crecimiento. Apostamos por la innovación, el rigor científico y el compromiso con la salud a través de soluciones nutricionales de alto valor para todas las etapas de la vida. Formar parte de Ordesa significa incorporarse a un entorno con grandes oportunidades de desarrollo profesional, donde las personas y el propósito marcan la diferencia. ¿CUÁL SERÁ TU NUEVO RETO? Estamos buscando un/a Regulatory Manager para coordinar y gestionar el cumplimiento regulatorio del portafolio de Ordesa a nivel nacional e internacional, liderando al equipo de Especialistas de Regulatory. Tu misión será estratégica: asegurar la planificación, presentación y mantenimiento de registros, la revisión de etiquetado y del material de marketing y comunicación, la vigilancia normativa y la relación con autoridades distribuidores y proveedores, en alineación con los objetivos del negocio. ¿CUÁLES SERÁN TUS PRINCIPALES FUNCIONES? • Definición y gestión de la estrategia regulatoria para el registro, autorización y mantenimiento de los productos (solicitudes, renovaciones, variaciones y control de caducidades)., • Garantía de cumplimiento normativo mediante la revisión de formulaciones, etiquetado, claims y materiales promocionales, así como la vigilancia regulatoria y comunicación de impactos internos., • Interlocución y coordinación externa e interna, gestionando la relación con Autoridades Sanitarias, asociaciones y consultores, y dando soporte regulatorio a I+D, Calidad, Operaciones, Marketing y Comercial., • Liderazgo del área de Regulatory, incluyendo la coordinación de actividades de vigilancia (nutri/cosmeto/farmacovigilancia) y la gestión y desarrollo del equipo de especialistas. ¿QUÉ BUSCAMOS EN TI? • Experiencia: mínimo 5 años en registros sanitarios y compliance regulatorio en entornos internacionales, y mínimo haber trabajado 1 año en laboratorio farmacéutico o equivalente según Real Decreto 842/2010. Experiencia previa liderando equipos y gestionando relaciones con Autoridades Sanitarias., • Formación: Grado en Farmacia (preferente) u otros grados en Ciencias de la Salud (Biología, Química, Biotecnología, Ciencia y Tecnología de los Alimentos). Además, debes tener formación específica en legislación alimentaria, complementos alimenticios, productos sanitarios, cosméticos y/o medicamentos., • Valorable Máster/Posgrado en Asuntos Regulatorios., • Habilidades digitales avanzadas., • Idiomas: nivel de inglés alto., • Disponibilidad para viajar. ¿QUÉ TE OFRECEMOS? Un entorno donde tu liderazgo genera impacto real, con productos de base científica, equipos cercanos y profesionales, y oportunidades concretas de crecimiento en una compañía que impulsa el talento. ¿Estás preparado/a para dar un salto en tu carrera y liderar con nosotros/as? 👇 ¡Nos encantaría conocerte!

🌟 Join Impress – Europe’s Leading Health-Tech Innovator! We believe everyone deserves a smile they’ll love 😁. As the largest Ortho clinic chain in Europe, we combine cutting-edge tech with expert care, revolutionizing invisible orthodontics since 2019. With 140+ clinics across 9 countries 🌍 and rapid growth, we’re improving lives worldwide. The Impress team is passionate about teeth, digitalization, and customer service. We are looking for a Doctor Trainer to accompany and support our doctors in their daily needs across all our clinics. What we offer: • High-end, high-performance technical equipment: ., • Modern, fully renovated dental centers., • Ongoing training., • Support from a general practitioner for procedures not related to orthodontics., • Professional supervision team dedicated to patients, alongside clinical appointments and available 7 days a week via the treatment tracking app., • International network of colleagues (EU & USA)., • Energetic clinical team that listens to each other., • Career path and growth opportunities., • Special discounts on aligner treatments for you and your family. In this role, you will: • Approve treatment plans cases, review eligibility, approve refinements., • Be the first level of support for the doctors and auxiliaries., • Create the team and the process for smooth support for the front doctors., • Be the liaison between the clinics and the HQ in Barcelona., • Create training and processes., • Train teams on processes and training techniques., • Daily monitor quality reports and NPS and ensure good performance., • Create improvement action plans and implement them., • Daily monitor utilization and efficiency of time of the clinic teams. Organize daily quality checks., • Create and implement procedures on quality monitoring of hygienist, auxiliaries, doctors in the use of tools and compliance with processes., • Solve escalated patient requests and personally work with problem patients via meeting in the clinic, call, video conference or emails., • Engage in marketing and interviews, receipt of influencers, and photoshoots. This may involve videos for social media., • Combine work in the office and in the clinic when clinic requires orthodontic knowledge support., • The work may involve travelling and need to work on weekends., • Your hard work and drive to succeed will deliver nothing less than impressive results. What you need to be successful: • Graduate in dentistry or orthodontics, registered with the Dental Association., • Solid clinical experience, ideally with aligners and digital technologies., • Experience in supervising or coordinating a medical team., • Proficiency in digital tools and patient tracking software., • Ability to supervise and validate treatment plans and manage complex cases., • Natural leadership, organizational skills, and excellent communication skills., • Focus on patient excellence and continuous improvement., • Fluent Spanish, professional English., • Willingness to travel frequently to all of our clinics at an international level.

Amaris is looking for a Data Manager with strong experience in clinical data management for CRO environments. The position focuses on supervising data management activities to ensure the smooth progress and quality of clinical projects. 🔥 Your Responsibilities • Act as the main point of contact for all data management topics and participate in project/study meetings, • Contribute to the selection of subcontractors by preparing specifications and evaluating proposals, • Participate in study design, including data management sections in protocols and CRF specifications, • Oversee outsourced data management activities, ensuring compliance with cost, timelines, and data quality, • Validate deliverables such as data management plans, validation plans, transfer specifications, eCRF completion guides, and coding instructions, • Test eCRF before production deployment and after each protocol amendment, • Implement targeted quality control of data based on risk assessment, • Monitor progress of data management steps (entry, cleaning, coding, external data transfers, SAE reconciliation, etc.), • Approve SDTM specifications and verify SDTM packages as needed, • Regularly assess subcontractor service quality, establish action plans for deviations, and discuss corrective measures, • Participate in data review meetings and validate associated reports, • Ensure responsibility for database lock and unlock, verifying all prerequisites, • Provide statisticians with data for statistical analysis, • Verify the presence of all data management documentation in the Trial Master File (TMF) 🎯 Your Qualifications • Experience in clinical data management for CROs (5–10 years), • Proficiency with industry-standard data management tools and software, • Academic background in Life Sciences, Pharmacy, or related field, • English fluent. French is a plus., • You demonstrate strong analytical and problem-solving skills, • You demonstrate excellent communication skills 💡 What You’ll Get From Us • An international community bringing together 110+ different nationalities, • An environment where trust has a central place: 70% of our key leaders started their careers at the first level of responsibilities, • A robust training system with our internal Academy and 250+ available modules, • A vibrant workplace that frequently gathers for internal events (afterworks, team buildings, etc.), • At Mantu, sustainability is part of everything we do. You’ll have the opportunity to turn your ideas into action and make a tangible impact. Every day, our teams bring our ESG commitments to life, from reducing our footprint to driving positive change within our communities. Through our WeCare Together program, you’ll be empowered to design and lead projects that create real social or environmental impact, with the company’s full support. Amaris Consulting is proud to be an equal-opportunity workplace. We are committed to promoting diversity within the workforce and creating an inclusive working environment. For this purpose, we welcome applications from all qualified candidates regardless of gender, sexual orientation, race, ethnicity, beliefs, age, marital status, disability, or other characteristics.

Revlon, a leading multinational cosmetics company, is seeking an Analytical Chemist to join the R&D team in Barcelona, reporting to the Global Manager of Analytical Services. This is a temporary position lasting 9 months and requiring full on-site presence. The role focuses on executing analytical testing for raw materials and finished products, ensuring compliance with established specifications and methods, while supporting multiple R&D projects in a dynamic environment. Key responsibilities: • Perform routine and non-routine analyses of raw materials and finished products following established methods and specifications, • Execute analytical techniques, including chromatography and wet chemistry, ensuring accurate data generation and interpretation, • Support investigations related to non-conformities, product issues, or alternative raw materials, • Develop, validate, and improve analytical methods in line with regulatory and GMP standards, • Prepare and review technical documentation, including reports, protocols, and validation documents, • Provide analytical support to cross-functional teams across multiple projects, • Supervise, maintain, and troubleshoot laboratory instrumentation, • Ensure proper maintenance, cleanliness, and organization of laboratory equipment and workspace, • Train and support junior team members when required, • Present results and findings in a clear and structured manner Requirements: Technical skills • Degree in Chemistry or related scientific field (Higher Vocational Training also considered with strong experience), • Around 3 years of experience as an analytical chemist in an industrial environment, such as cosmetics, chemicals, food, or pharmaceuticals, • Hands-on experience with chromatographic techniques (LC/GC), ideally with OpenLab software, • Experience in potentiometric titrations and general wet chemistry techniques, • Advanced level of English and Spanish, • Strong Excel and general Office skills Core competencies • Ability to manage multiple projects simultaneously and prioritize effectively, • Strong organizational skills and attention to detail, • Ability to work in a dynamic and changing environment, • Team-oriented profile with strong communication skills

Si, como nosotros, trabajas mejor cuando se confía en ti, súmate a nuestro equipo >> En Elis apostamos por las personas, les damos responsabilidades y las acompañamos en su crecimiento. Formarás parte de un grupo internacional con más de 75 años de historia, líder en su sector y comprometido con la economía circular. Don’t choose Elis si buscas rutina. Pero si te motiva optimizar compras, negociar con proveedores y generar impacto real en la eficiencia del negocio, sigue leyendo 👇 🎯 Tu misión Serás responsable de gestionar las compras indirectas de bienes y servicios para la compañía, asegurando las mejores condiciones de coste, calidad y servicio, y garantizando el cumplimiento de los procedimientos y estándares del grupo. 🔧 ¿Qué harás? ➢ Gestionar la compra de bienes y servicios indirectos necesarios para la compañía. ➢ Solicitar, analizar y comparar ofertas de proveedores para identificar la mejor opción. ➢ Participar en negociaciones con proveedores de complejidad media. ➢ Gestionar pedidos, contratos y seguimiento de entregas para distintos centros. ➢ Actuar como interlocutor entre proveedores y centros operativos. ➢ Participar en procesos de evaluación y homologación de proveedores. ➢ Colaborar en proyectos de racionalización de proveedores y optimización de contratos. ➢ Analizar consumos, desviaciones de precio y oportunidades de ahorro. ➢ Elaborar reporting periódico y seguimiento de KPIs de compras. ➢ Garantizar el cumplimiento de procedimientos de compras, compliance y estándares de grupo. 👤 ¿A quién buscamos? ➢ Formación universitaria en ADE, Ingeniería o similar ➢ 2-4 años de experiencia en compras o gestión de proveedores ➢ Experiencia previa en compras indirectas o entorno similar ➢ Excel nivel intermedio ➢ Nivel de inglés para entorno profesional ➢ Perfil analítico, organizado y con capacidad de negociación 🎁 ¿Qué ofrecemos? ➢ Contrato indefinido en un grupo sólido y en crecimiento ➢ Un rol con impacto directo en la optimización de compras y costes ➢ Desarrollo profesional dentro de un entorno internacional ➢ Salario competitivo y beneficios sociales 👉 ¿Te interesa el reto? Únete a Elis y forma parte de un equipo que impulsa la eficiencia y la mejora continua en nuestras operaciones. ELIS MANOMATIC, S.A.U. te informa que es la entidad responsable del tratamiento de tus datos personales con el fin de valorar tu candidatura para vacantes presentes o futuras a cubrir en nuestra organización. Para más información sobre el tratamiento de tus datos o sobre cómo ejercer sus derechos de derechos de acceso, rectificación, supresión, limitación, portabilidad y oposición, puedes acceder a nuestro portal web en el apartado política de privacidad. ELIS MANOMATIC, S.A.U. no discriminará directa o indirectamente a los candidatos y candidatas en los procesos de selección, por razones de sexo, estado civil, edad, origen racial o étnico, condición social, religión o convicciones, ideas políticas, orientación sexual, afiliación o no a un sindicato, así como por razón de lengua Que ELIS MANOMATIC, S.A.U. se compromete a actuar bajo el principio de igualdad de trato y de oportunidades entre todo el personal que realicen el mismo trabajo. ELIS MANOMATIC, S.A.U. se dispone a adoptar medidas que eviten cualquier forma de discriminación entre hombres y mujeres. En los procesos de selección, realizarán iniciativas para contratar mujeres en áreas donde la presencia femenina esté subrepresentada o dar preferencia a la contratación de mujeres en igualdad de condiciones.

Admissions Assistant (Part-Time) Location: Carrer Montevideo, 31 Barcelona, Spain | 20 hours/week Schedule: Monday to Friday from 10am to 2pm The Position The AESA International School System is seeking a highly organized, professional, and results-driven Admissions & Enrollment Assistant to support both our Barcelona campus and our online school, AESA Prep International. This is not a clerical role. It is a structured, revenue-focused position that combines relationship management, sales discipline, data tracking, and operational precision. You will report to the Director of Operations and play a key role in driving sustainable enrollment growth. About AESA The AESA International School System comprises a global network of schools and affiliated academic programs. We offer students the opportunity to receive a great education that prepares them for success at university. Some of our students learn through face-to-face instruction at our campuses in Spain and the United States. Other students—from all over the world—learn through our innovative online school and its partners. Role Overview The Admissions Assistant manages the full admissions pipeline—from first inquiry through enrollment—for both on-campus and online programs. This role is ideal for someone who enjoys building relationships, creating and refining structured processes, and tracking measurable results. Key Responsibilities: Admissions Pipeline Management • Respond to all new inquiries within one business day, • Qualify prospective families and students, • Schedule and coordinate campus tours and virtual meetings, • Track applicants through every stage of the funnel, • Maintain accurate CRM and admissions records, • Ensure no qualified lead is left without a defined next step Conversion Focus • Drive inquiry-to-enrollment conversion rates, • Monitor funnel performance and identify bottlenecks, • Support achievement of enrollment targets, • Track enrollment completion, • Contribute to admissions forecasting Family Experience • Serve as primary point of contact for prospective families, • Deliver a polished, responsive, and professional experience, • Provide timely follow-up and clear communication, • Coordinate initial onboarding once a student enrolls Administrative & Compliance Support • Prepare enrollment agreements and documentation, • Ensure complete and compliant student files, • Coordinate with finance regarding deposits and tuition plans, • Maintain organized digital records Reporting & KPIs • Maintain weekly admissions dashboard, • Track conversion rates, lead sources, response times, and enrollments, • Provide structured weekly reports to the Director of Operations Candidate Qualifications Required • Impeccable written and verbal communication skills in English and Spanish, • High level of organization and follow-through, • Comfort working with data, dashboards, and CRM systems, • Professional demeanor with international families, • Sales mindset without being pushy Preferred • Full proficiency in Catalan and/or any other major world languages, • Experience in education, international schools, or admissions, • Experience in a structured sales or customer acquisition role, • Familiarity with CRM tools Performance Expectations Success in this role is measured by: • One business day response rate to new inquiries, • Conversion from qualified lead to tour/demo, • Conversion from offer to deposit, • Enrollment growth, • Accuracy and completeness of admissions files, • Weekly KPI reporting discipline Schedule & Growth Opportunity • 20 hours per week at AESA's Barcelona campus: Monday to Friday, 10am to 2pm Strong performance may lead to expanded responsibilities, increased hours, and long-term growth into a senior admissions or other operations role Compensation Competitive compensation commensurate with experience. How to Apply Please submit the following documents to : • CV and cover letter explaining why you are interested in enrollment-driven education roles, • Recommendation letter and/or professional references

MEDICAL AFFAIRS Ophthalmology En Salvat buscamos incorporar un perfil de Medical Affairs Ophthalmology, dispuesto a marcar la diferencia. ¿Quiénes somos? Somos Grupo Farmacéutico Salvat, fundada en Barcelona en 1955 y llevamos 70 años contribuyendo a crear una vida más saludable y feliz con productos emblemáticos como Cristalmina, Cetraxal, Monolitum y Salvacolina. 🌍 Presencia internacional. Operamos en + de 60 países, con plantas de producción en Barcelona, Madrid y Miami. 🔧 Innovación y capacidades. Contamos con I+D propia, innovamos y desarrollamos soluciones en las áreas terapéuticas de oftalmología, otorrinolaringología y gastroenterología, además de abordar el ámbito de la salud en Consumer Health y ofrecer servicios CDMO, donde ambicionamos ser un player relevante. 🏅 Excelencia certificada. Estamos orgullosamente certificados por la FDA y reconocidos con calificación excelente en el Plan Profarma del Ministerio de Industria. Esto respalda nuestro compromiso con la excelencia y ética empresarial. 🚀 Proyecto New Salvat. Estamos inmersos en un ambicioso proyecto transformador que busca crear un Salvat más fuerte, más ágil y competitivo. Si te gustan los retos y quieres disfrutar dejando una huella positiva, Salvat es tu lugar. 🤝 Nuestra cultura. Vivimos nuestros valores AACT (Ambición, Accoountability, Colaboración y Transparencia) en el día a día, creemos en el potencial de las personas y fomentamos entornos de donde cada persona pueda crecer y dar su mejor versión. ¿Qué buscamos? El Medical Affairs Ophthalmology será responsable de proporcionar soporte médico-científico en el desarrollo y ejecución de planes médicos en el área de oftalmología. Reportando al Head of Medical Affairs, este rol representa el enlace clave entre las áreas médico-científica y comercial, asegurando la integración de la evidencia clínica y las actividades operativas y estratégicas de la compañía. Tus principales responsabilidades serán: • Soporte Médico-Científico:, • Apoyo médico a los equipos internos, incluidas las áreas de marketing, ventas, (tanto en la elaboración de materiales como en establecer estrategias conjuntas para las diferentes áreas terapéuticas y los diferentes productos), regulatorio (en la elaboración de documentación necesaria) e I+D (en la valoración de posibles proyectos a desarrollar., • Preparar materiales médicos basados en evidencia científica, • Relaciones con KOLs:, • Establecer y mantener relaciones sólidas con líderes de opinión clave y otros profesionales de la salud, • Facilitar reuniones científicas y grupos de discusión para recopilar información del mercado, • Generar proyectos de valor con Sociedades Científicas en el área terapéutica de oftalmología., • Estudios clínicos:, • Apoyar la implementación de ensayos clínicos, estudios observacionales y generación de datos en práctica clínica (RWE), • Colaborar en la revisión y aprobación de protocolos de investigación y publicaciones científicas, • Compliance:, • Garantizar el cumplimiento de la normativa de buenas prácticas en todas en todas las actividades médicas realizadas, • Participar en la formación y capacitación del equipo sobre normativas y buenas prácticas clínicas, • Estrategia médica:, • Contribuir al desarrollo de planes médicos estratégicos alineados con los objetivos de la compañía, • Revisión y análisis de publicaciones científicas / guías de manejo clínico y monitorizar las tendencias en el campo médico relevante, • Patient Advocacy:, • Colaboración estrecha con asociaciones de pacientes para promover un entendimiento profundo de sus necesidades Perfil ideal • Formación universitaria en ciencias de la salud (preferiblemente Medicina, Farmacia o Biomedicina), • Experiencia mínima de 5 años en departamento médico, imprescindible experiencia en el área de oftalmología, • Capacidad de para mediar y construir relaciones con los diferentes stakeholders (internos y externos), • Habilidades de comunicación efectiva, • Dominio del inglés para la implicación en proyectos internacionales Habilidades: Con habilidades técnicas y conocimientos en el área de Medical Affairs (o similar) , buscamos: • Con experiencia en Oftalmología, • con capacidad de Autocrítica,, • Ganas de Superación y de Aprendizaje constantemente, Proactividad,, • Capacidad de esfuerzo y de trabajo,, • Capacidad de búsqueda de soluciones alternativas a las adversidades., • Motivación ¿Qué te ofrecemos? • Formar parte de una empresa sólida e innovadora, en un momento de transformación y crecimiento., • Un entorno colaborativo donde se valora tu iniciativa y tus ideas., • Oportunidades de desarrollo profesional real, participando en procesos clave del área y trabajando bajo estándares GMP., • Paquete de beneficios y aprendizaje continuo en un entorno regulado., • Horario Flexible y jornada intensiva los viernes y en verano. ¿Quieres formar parte de este proyecto transformador? Aplica para más información ¡Vamos a construir juntos el futuro de Salvat!

We're currently partnering with a leading global consumer health business to find an experienced Global Regulatory Operations Medicine Manager to join their dynamic Regulatory Affairs team. This is an exciting opportunity to lead end-to-end regulatory operations across a diverse portfolio of over-the-counter (OTC) and consumer health products. You’ll be working at the heart of a fast-paced, innovation-driven environment, driving dossier strategy, managing global submissions, and collaborating closely with cross-functional teams across markets. Responsibilities: • Lead Regulatory Submissions: Oversee the planning, preparation, and timely submission of regulatory documentation (e.g., eCTD Modules 1–5) for product registrations, variations, renewals, and withdrawals, ensuring accuracy and compliance., • Coordinate Stakeholder Engagement: Serve as the primary regulatory contact for designated product categories (e.g., analgesics), fostering effective communication with internal teams and external partners., • Maintain Dossier Integrity: Manage the creation and upkeep of core product dossiers, ensuring alignment with current regulatory requirements and submission timelines., • Ensure Documentation Readiness: Supervise the organisation and electronic archiving of regulatory records to support accessibility and inspection readiness., • Collaborate Across Functions: Work cross-functionally with Regulatory Strategy, R&D, Pharmacovigilance, Quality, and Marketing to ensure regulatory alignment throughout the product lifecycle. Requirements: • Degree in Pharmacy, Life Sciences, or a closely related field (Bachelor’s or Master’s level)., • At least 5 years of hands-on experience in regulatory affairs within the pharmaceutical or healthcare sector., • Strong command of international regulatory guidelines (e.g., EMA, ICH, and national health authorities)., • Solid track record in preparing and submitting eCTD dossiers, including CMC M3 content development., • Highly organised with excellent attention to detail and ability to manage multiple regulatory projects simultaneously.

Are you ready to join a world leader in the exciting and dynamic fields of the Pharmaceutical and Medical Device industries? PQE Group has been at the forefront of these industries since 1998, with 40 subsidiaries and more than 2000 employees in Europe, Asia and the Americas. We are seeking a Cleaning Validation Specialist to support cleaning validation activities within a GMP-regulated pharmaceutical manufacturing environment. Responsibilities include, but are not limited to: • Support the planning and execution of cleaning validation activities for manufacturing equipment and facilities., • Assist in the preparation and review of validation protocols and reports., • Participate in sampling activities and support analysis of validation data., • Collaborate with Manufacturing, Quality Assurance, and Engineering teams to ensure compliance with GMP requirements., • Support risk assessments and validation strategies related to equipment cleaning processes., • Contribute to investigations, deviations, and CAPA actions associated with cleaning validation., • Maintain and organize validation documentation according to regulatory and internal quality standards., • Assist in preparing documentation for internal audits and regulatory inspections. Required Qualifications: • Bachelor’s or Master’s degree in Pharmaceutical Sciences, Biotechnology, Chemistry, Chemical Engineering, or Life Sciences., • Minimum 1 year of experience in the pharmaceutical, biotechnology, or related regulated industry (internships or academic projects are also considered)., • Basic understanding of GMP principles and pharmaceutical manufacturing environments., • Strong attention to detail and good analytical skills., • Ability to work collaboratively in cross-functional teams., • Fluent in English and Spanish Next Steps Upon receiving your application, if a match is found, the Recruiting department will contact you for an initial HR interview. If there's a positive match, a technical interview with the Hiring Manager will be arranged. In the case of a positive outcome coming from Hiring Manager interview, recruiter will contact you for further steps or to discuss our proposal. Alternatively, if the outcome is negative, we will contact you to halt the recruitment process. Working at PQE Group As a member of the PQE team, you will be part of a challenging, multicultural company that values collaboration and innovation. PQE Group gives you the opportunity to work on international projects, improve your skills and interact with colleagues from all corners of the world. If you are looking for a rewarding and exciting career, PQE Group is the perfect place for you. Apply now and take the first step towards an amazing future with us.

SOLTI is an academic research group that performs clinical trials of excellence in oncology. Currently, SOLTI is comprised of over 550 renowned research professionals distributed over a broad network of more than 100 leading hospitals in Spain, Portugal, France and Ireland. SOLTI focuses its efforts on developing cutting-edge clinical trials with novel targeted therapeutics including innovative translational research, fostering the participation in international networks and promoting excellence in the management of cancer among their members. We are currently seeking a Clinical Research Associate to join our Clinical Operations Team. Main responsibilities: • Plan and conduct site visits and prepare site visit reports within the specified timelines in accordance with the Clinical Monitoring Plan., • Perform site management and ensure thorough follow-up and resolution of action items., • Oversee trial medication at the site by meticulously reviewing study accountability logs., • Guarantee the proper collection and dispatch of biosamples as per protocol., • Collaborate with the clinical project team in managing trial documentation., • Provide assistance for audit/inspection activities as necessary., • Ensure compliance with the protocol, Good Clinical Practices (GCPs), and clinical trial regulations., • Maintain consistent communication with the PM/CTM and report any pertinent issues concerning the assigned trial sites. Requirements and skills: • BSc in Life Science field (Pharmacy, Biology, Nursing, etc.)., • MSc in Clinical Trials Monitoring., • Minimum 1 year of professional experience as CRA in a CRO, Pharmaceutical Industry or collaborative groups. Breast cancer clinical trials experience will be an asset., • Advanced English level., • Advanced knowledge of GCPs and clinical trials legislation., • Proficiency in MS Office. This is a full-time position (38h/week) based in Barcelona (Spain). What we offer: Explore the opportunity of joining an organization engaged in cutting-edge projects with significant social impact. We offer a full-time position based in Barcelona with the possibility of working from home up to 3 days a week with a flexible work schedule and additional benefits. If your background and experience align with the requirements of this position, we encourage you to apply and explore this exciting opportunity with us. SOLTI is an employer committed to Equal Opportunities regardless of sex, gender, sexual orientation, race, age, origin or disability. Get to know us at:

At Qurv, we are driving a paradigm shift in computer vision applications across automotive, XR, and robotics by developing mass-deployable infrared image sensors that enable machines to see better and further, unlocking new functionalities. We are seeking an Equipment & Maintenance Engineer who will be responsible for the uptime and reliability of our automated wet chemistry tools and vacuum deposition systems. The role focuses on preventive maintenance, rapid troubleshooting, spare parts management, and support with new equipment installations. Key Responsibilities • Maintenance: Perform scheduled and emergency maintenance on glovebox, automated wafer handlers and spin coaters, wet chemistry delivery systems, pumps, and high vacuum material deposition equipment., • Inventory: Own the spare parts inventory, track usage, manage reordering, and ensure critical components are always available to minimise downtime., • Installations: Support vendors and engineers with the installation, hook-up, and qualification of new equipment., • Safety: Ensure compliance with Spanish health and safety regulations, including Ley de Prevención de Riesgos Laborales., • Documentation: Record maintenance activities, inventory levels, and equipment performance. About you • Hands-on problem solver with a proactive attitude., • Highly organised and attentive to spare parts, inventory management, and maintenance scheduling., • Able to work independently in a fast-paced R&D or production environment., • Strong attention to detail and safety standards. Qualifications Mandatory • Technical degree in Engineering, Mechatronics, or a related field., • Experience with gloveboxes, including maintenance, leak checking, and sensor calibration., • Experience with vacuum systems, including pumps, gauges, valves, and leak detection., • Experience with fluid handling and chemical delivery systems., • Experience with automated wet tools, including robotic wafer handlers and spin coaters., • Experience with thermal and E-beam evaporators., • Background in machine automation, including PLCs, HMIs, and electrical troubleshooting., • Cleanroom experience., • Strong knowledge of Spanish occupational health and safety regulations and PRL requirements. What it is like to work with us • Opportunity to work with cutting-edge technology in a deep tech startup environment., • Dynamic and multidisciplinary team., • Flexible benefits scheme through Cobee., • Wellbeing support, including private health insurance with Sanitas and Wellhub membership., • Relocation support if required. How to apply Send your CV and a brief cover letter in English to with the subject line “Equipment Maintenance Application”. We have team members from multiple countries and are committed to promoting an inclusive environment for all employees and candidates. Come and join us.

Empresa alimentaria referente internacional en su sector en plena fase de expansión internacional Misión: Dirigir, coordinar y organizar la actividad productiva de su planta, asegurando el cumplimiento de la normativa y estándares internos, asegurando la adherencia productiva al planning productivo y necesidades de cliente en los plazos previstos y según el nivel de calidad exigido. Funciones y responsabilidades: • Asegurar el cumplimiento de normativas de seguridad, calidad y medio ambiente en todos los procesos productivos., • Supervisar y distribuir de manera efectiva las cargas de trabajo entre las diferentes secciones y turnos, garantizando un ambiente de trabajo motivador y colaborativo., • Fomentar la formación continua del equipo, su motivación y promover un entorno de trabajo que impulse el logro de los objetivos., • Analizar las causas raíz de los problemas del departamento, trabajando con otros responsables para implementar soluciones efectivas., • Velar por el buen estado de la maquinaria e instalaciones, asegurando un mantenimiento adecuado en colaboración con el Departamento de Mantenimiento e Ingeniería., • Realizar análisis para proponer mejoras, optimizar la eficiencia y reducir tiempos de inactividad., • Gestionar y organizar la documentación relacionada con los procesos productivos. Asegurar el cumplimiento de las políticas del sistema de compliance penal en todas las operaciones, colaborando con el equipo de análisis de peligros. Se requiere: • Formación universitaria en ingeniería., • Experiencia mínima de 5 años como Responsable de Producción., • Conocimientos en técnicas de organización de la producción y gestión de costes industriales., • Conocimientos de metodologías de lean manufacturing y mejora continua., • Formación en Prevención de Riesgos Laborales., • Competencias: Capacidad de Liderazgo, capacidad de planificación, organización y gestión de equipos, capacidad de motivación y desarrollo de personas, habilidades en comunicación, capacidad de trabajo en equipo, orientación a calidad, servicio y mejora continua, capacidad de análisis y toma de decisiones, orientación a objetivos, flexibilidad y capacidad de desarrollar trabajo efectivo en escenarios de presión. Se ofrece: • Incorporación inmediata., • Contrato indefinido., • Retribución salarial acorde al perfil y experiencia aportada., • Oportunidades para el crecimiento profesional dentro de un equipo internacional., • Plan de compensación flexible; seguro de salud, guardería, transporte y comida, y seguro para para mascotas.

🔹 Opportunity – Technical Lead 🔹 📌 About the role We are looking for a Tech Lead / Lead Engineer to provide technical leadership and strategic direction for AI and Machine Learning solutions. This is a critical, enterprise-level role focused on designing and scaling reusable AI products that deliver measurable business value across complex, multi-tenant environments and multiple operating companies. You will play a critical role in balancing cost, risk, and time-to-value, ensuring scalable, reusable, and enterprise-grade AI solutions that can be leveraged across multiple operating companies. 🚀 Key Responsibilities Technical Leadership & Architecture • Define and drive technical strategy and architecture for AI/ML solutions., • Lead the design of reusable AI products adopted across multiple business units., • Provide hands-on technical leadership across multiple squads, ensuring consistency and quality., • Develop and evolve technical blueprints, enabling early value delivery and industrialization of AI products., • Define the technical direction for AI/ML platforms, including:, • Generative AI abstraction layers, • ML development and runtime platforms, • MLOps pipelines and CI/CD practices, • Lead technical governance frameworks, including:, • Key Design Decision (KDD) processes, • Architecture standards and reusable components, • Apply a data-driven approach to risk identification and mitigation., • Maintain an “always-on” view of the AI ecosystem, including:, • Generative AI models, • Third-party platforms and tooling, • Evaluate cost-benefit trade-offs of AI technologies and implementation approaches., • Work closely with:, • AI Engineering Lead, • AI Labs (London & Barcelona), • CTO, CDIO, Cloud & Data Platform teams, • Build architectural consensus across enterprise stakeholders., • Optimize internal adoption of AI products, treating colleagues as customers., • Reduce friction in discovery, onboarding, and usage of AI solutions., • Foster a strong AI engineering community across the Group., • Partner with People & Culture to support AI Academy learning initiatives., • Promote a culture of continuous learning and improvement. 🧠 Required Experience & Skills • 15+ years in enterprise software engineering within complex environments., • Proven experience providing hands-on technical leadership across multiple teams., • Strong background in:, • AI / Machine Learning solutions, • ML engineering and MLOps, • Cloud-based architectures and platforms (AWS), • Experience with:, • CI/CD pipelines for data science and ML, • Third-party AI platforms and tools, • Designing scalable, reusable systems 🌟 Key Competencies • Strategic and analytical mindset with strong business-to-technology translation skills, • Ability to simplify complex technical topics for senior stakeholders, • Excellent communication, leadership, and influencing skills, • Strong focus on value delivery, ROI, and pragmatism, • Forward-thinking, innovative, and continuously curious This position is Hybrid (2 per week to the office). English is required (C1 level). . Why join this project? 🤝 People first – inclusive, diverse, and international culture. 🚀 Work with cutting-edge technology on global-scale products. 📈 Clear opportunities for career progression and continuous development. 😁 Collaborative teams with a strong sense of belonging. 🎓 Access to learning resources and development programs. 💰 Competitive compensation. 🩺 Private health insurance & benefits (according to region). ⚡ Flexible working environment and hybrid model. 🏋️ Wellness and mental-health initiatives. 🥳 Team-building activities and global community events. ✨ Want to know more about us? Click ___ and discover all the details. 🔍 Find out what people are saying about us on ___. 💬 We know that not every candidate will meet 100% of the requirements. If your profile doesn’t match perfectly but you believe you can add value, we would still love to hear from you! 👉 Ready for the challenge? Apply now and be part of a global digital leader driving innovation and transformation. Empowering People, Unlocking Innovation. The employee will adhere to information security policies: -Will have access to confidential information related to Capitole and the project they are working on. -Must comply with the security policies and internal policies of the company and the client. -Must sign an NDA.

Are you a Data Architect / Data Product Architect seeking a new interesting challenge? 🔍 If your answer is yes, it’s your lucky day so keep reading — it can be just what you're looking for! 👀 WHAT WILL YOU DO? ✍️ We are looking for a dynamic, proactive and talented person to join our team and perform the following tasks: • Work closely with Data Product Owners to translate business requirements into scalable and efficient data models and architectures aligned with product strategy and outcomes., • Collaborate with business units, data engineers, data scientists, analysts and domain SMEs to align data products with operational goals., • Define and evolve the enterprise data architecture framework, standards and principles, including data modelling, metadata, security, reference data and data quality., • Maintain and govern logical and physical data models, ensuring consistency and alignment across data products., • Drive adoption of data mesh and data product thinking across data teams and domain owners., • Promote data governance best practices, ensuring compliance with data privacy, security and regulatory requirements., • Ensure discoverability, interoperability, observability, lineage and monitoring of all data products., • Ensure all architectural initiatives align with the broader enterprise data strategy., • Maintain and continuously improve current‑state and target‑state data architecture documentation. WHAT TOOLS WILL YOU USE? 💻 • Conceptual, logical and physical data modelling, • Data modelling tools such as Erwin and ER Studio, • Data and integration architectures (APIs, event‑driven, batch processing), • Data lakes, data warehousing, data management and data mesh, • Cloud data platforms (AWS, Databricks, Snowflake), • Data catalog and data quality tools, • Enterprise architecture frameworks and standards, • Agile, waterfall and hybrid delivery methodologies WHAT ARE WE LOOKING FOR? 🧐 • Extensive experience in data modelling from conceptual to physical levels, • Strong expertise in data and integration architecture, including service‑oriented and event‑driven approaches, • Solid experience working with large project and product teams and senior stakeholders, • Familiarity with AWS cloud services and modern data platforms such as Databricks and Snowflake, • Experience with data governance, metadata management and data quality practices, • In‑depth knowledge of sound systems design principles and best practices, • Good understanding of software engineering best practices, including security and performance, • Experience owning solutions and presenting architecture designs in architecture review boards, • Fluent English Good to have: ✅ • Strong stakeholder management skills in complex enterprise environments, • Experience supporting cross‑functional data product initiatives, • Background in regulated or large‑scale data environments WHERE AND WHEN? 📅 • Workplace: Barcelona (hybrid model), • Work Schedule: Business hours WHAT CAN WE OFFER YOU? 🤝 • Permanent contract 📋 – We offer indefinite contracts from the first day., • Pay and benefits 💸 – Competitive salary and a flexible compensation plan adapted to your needs (Ticket Restaurant, Childcare Ticket, Transport Ticket and Health Insurance)., • Work from home 🏚️ – Monthly financial support for your working‑from‑home expenses, plus a welcome bonus in the first month to help you set up your workplace 👨 💻, • Opportunity knocks 👍🏻 – Career development plan and annual performance‑based compensation reviews., • Learn as you grow 📚 – Fantastic onboarding program and access to robust learning platforms., • Bring your buddy 👫 – Referral bonus through our BYB Scheme., • Connect globally 🌏 – Work with multicultural teams from all over the world., • Benefit from being a TCSer 🎟️ – Corporate discounts and exclusive benefits.

We’re looking for an International Purchasing Specialist for Travel to play a key role in the unification of our international travel project and to ensure a seamless, high-quality travel experience for employees across International 1 (ES, PT, IT, CH, BE, NL, LUX, DK, SE, FI). Role Overview This role combines project implementation, strategic purchasing, and long-term travel management. You will lead the rollout of a unified self-booking tool, establish harmonized travel policies, and later take ownership as Team Lead for Travel International 1. Key Responsibilities • Lead and support the implementation of a unified self-booking tool and travel policies across International 1, • Collaborate with international stakeholders to ensure smooth adoption, • Support and train users during the transition phase, • Monitor user experience and continuously improve travel processes, • Take ownership of all International 1 travel initiatives as Team Lead, • Negotiate hotel and travel supplier agreements to optimize costs and service quality, • Manage vendor relationships and escalations, • Analyze travel reports to identify trends and cost-saving opportunities, • Ensure ongoing support and policy compliance for all travelers, • Bachelor’s degree in Business Administration, Supply Chain Management, or a related field (preferred), • Experience in international purchasing, travel management, or similar roles, • Solid understanding of travel-related topics, • Strong negotiation and vendor management skills, • Analytical mindset with experience in data analysis and reporting, • Excellent communication and interpersonal skills in multicultural environments, • Proactive, adaptable, and comfortable working in a fast-paced setting Feel free to apply

Avania are hiring - Quality Manager (based in either Spain, Netherlands, Germany or United Kingdom) As a Quality Manager at Avania, you will play a pivotal role in strengthening and scaling our Quality Management approach—moving beyond post-activity QA checks to proactively partnering with the business on risk management, standards, and consistent execution The Quality Manager role will support regional regulatory monitoring, audit execution, and operational governance oversight across European jurisdictions. The Quality Manager will independently execute and support internal and external audits, monitor applicable regional regulatory updates, assess operational impact, support maintenance of regulatory applicability mapping, and provide structured quality oversight The Quality Manager role ensures continuity of European Quality oversight, sustained inspection readiness, and consistent application of the Quality Management System across EU operation You'll collaborate closely with cross-functional and global stakeholders to ensure our QMS aligns with applicable regulatory expectations Working with a small, high-impact team and periodic travel as needed, this position offers an opportunity to take meaningful ownership, help reduce single points of failure, and drive quality compliance in a practical, business-enabling way. What you'll be doing • Support regional regulatory monitoring, audit execution, and operational governance oversight across European jurisdictions., • Lead interactions with external auditors of Notified Bodies as appropriate, ensuring the right materials, SMEs, and narratives are in place—and escalating to leadership when needed, • Lead and host client audits and support ongoing audit readiness activities, including preparation, coordination, and follow-up to ensure timely, thorough responses and sustained compliance, • Drive inspection readiness efforts by maintaining a proactive state of preparedness across processes, documentation, and teams, • Partner with cross-functional stakeholders to shift quality from primarily "after-the-fact" assurance to upfront quality management, including risk-based thinking, setting minimum standards, and advising on compliant execution, • Support quality-related system work as needed, including contributing to computer system validation activities (e.g., user requirements, risk assessments, test scripts) and helping improve how systems are adopted and maintained Candidates who offer a combination of the skills, knowledge and experience listed below are encouraged to apply to our Quality Manager role . With our continued growth we are hiring talent to join us on our journey and grow with us. What we're looking for • Proven experience in both operations and quality management within a CRO/clinical research or other regulated environment, with a strong focus on maintaining inspection-ready systems and compliant processes, • Experience interpreting and applying relevant regulations and standards (e.g., EU/UK requirements such as MDR/MHRA, where applicable), translating requirements into clear, workable internal expectations., • Strong working knowledge of quality management systems (QMS) and a practical, proactive approach to quality—able to identify risk, set standards up front, and influence teams before issues arise (not just audit after the fact)., • Confident decision-maker who knows when to escalate and when to independently move work forward—comfortable operating in a lean team without being a single point of failure., • Hands-on mindset with the willingness to balance strategy and execution, including rolling up your sleeves to support audit preparation, documentation, CAPAs, and day-to-day quality activities., • Excellent stakeholder management and communication skills, able to partner effectively with cross-functional teams and represent Quality in a client-facing environment when required., • A seasoned, mature quality professional who is motivated by accountability, continuous improvement, and collaborative teamwork—not someone looking for a "quiet" role with minimal engagement. What you'll need • Proven experience in both operations and Quality Management within a CRO, clinical research, or regulated life sciences environment, with strong ownership of a Quality Management System (QMS) and governance activities., • Working knowledge of applicable regulations and standards relevant to clinical research and quality (e.g., EU regulatory environment such as MDR/MHRA awareness, and notified body audit expectations); able to translate requirements into practical, implementable QMS controls., • Hands-on audit experience, including hosting and leading client audits and supporting audit readiness activities; ability to confidently interface with auditors and drive timely, effective responses to observations., • Experience conducting and delivering billable audits (e.g., site audits), including planning/scheduling, execution, and clear, defensible report writing; comfortable operating in a delivery-focused model with limited client interaction., • Ability to shift from "QA after the fact" to proactive Quality Management—supporting upfront risk management, setting minimum standards, and influencing consistent ways of working across teams and locations., • Experience with or willingness to learn computer system validation (CSV) activities, such as user requirements, risk assessments, and test script development., • Strong decision-making and judgment, with the ability to operate independently, escalate appropriately, and reduce single-point-of-failure dependencies in a small team environment., • Excellent stakeholder management and communication skills, able to collaborate effectively across functions and geographies and build credibility with operations and project teams., • Willingness to travel periodically as needed to support audits and key quality activities What we offer We offer a collaborative, hands-on quality environment where you can make a direct impact on inspection readiness, audit outcomes, and the evolution from traditional QA to proactive quality management. You'll work closely with a small, global team and partner cross-functionally with operational stakeholders to strengthen processes, risk management, and consistent compliance across locations. Depending on your region, the role includes meaningful exposure to client and notified body audits, with periodic on-site presence and manageable travel as needed. We provide a clear, structured interview process which will include recruiter conversation, an in-depth technical interview with the hiring manager, and a virtual coffee with the team We look forward to receiving your application!

AP QA Specialist (Aseptic Processing) - FDA Readiness Contract: 2 months, 40 hours/week Start: Immediate (FDA readiness deadline: June) Level: Mid-Senior Specialist About the Role A leading pharmaceutical manufacturer is seeking an experienced AP QA Specialist to support critical aseptic processing readiness activities ahead of an upcoming FDA milestone. This role requires a hands‑on specialist capable of delivering rapid, compliant results within a fast‑paced remediation environment. Key Responsibilities Aseptic Process Compliance & Review • Conduct a retrospective review of 2024-2025 media fills on BS3 and IWK3, mapping operators to interventions and confirming compliance., • Review all authorized aseptic interventions and verify appropriateness of related mitigation measures., • Update risk assessments for direct and indirect product-contact surfaces in aseptic processes., • Conduct an impact assessment supporting the justification of current Preventive Maintenance (PM) acceptance criteria., • Perform a risk‑based evaluation of validated interventions, defining worst‑case scenarios., • Review IWK3 and BS3 set‑up processes, defining the validated sequence and the point at which equipment achieves Grade A readiness for EM sampling., • Update assessment of personnel monitoring limits across aseptic operations., • Review management of quality alarms in SCADA, ensuring proper acknowledgement, justification, root cause analysis, and QA oversight. Requirements • 5+ years in aseptic processing, sterile manufacturing, or pharmaceutical QA., • In‑depth understanding of EU Annex 1 and FDA aseptic guidance., • Proven experience with media fills, interventions, equipment readiness, and risk‑based decision making., • Ability to join mid‑stream and deliver results quickly., • Strong communication, analytical, and documentation skills.

Business Analyst (Data Governance) Summary Location: Barcelona (Hybrid) OR Prague (Hybrid) Day Rate: Negotiable Duration: Until end of August 2026 (with a potential view to extend) Availabilty: ASAP About the Client My client is the air transport industry's IT provider, delivering solutions for airlines, airports, aircraft, and governments. Their technology powers more seamless, safe, and sustainable air travel. They are looking to hire an experienced Business Analyst to support a Data Governance Implementation Project. About the Role Job Summary: The Business Analyst – Data Governance Implementation will play a key role in establishing and operationalizing data governance capabilities across the organization. This role partners with data owners, data stewards, IS teams, finance and business stakeholders to analyse current data processes, define governance requirements, support the implementation of data standards, and ensure alignment with enterprise data strategy. The ideal candidate combines strong analytical skills with experience in data management, process design, and stakeholder facilitation. Key Responsibilities: Data Governance Program Support • Support the rollout of data governance frameworks, policies, and standards. • Collaborate with stakeholders to define and document data ownership, stewardship, and accountability models. • Assist in establishing data quality processes, controls, and monitoring mechanisms. Business Requirements & Process Analysis • Conduct structured requirements gathering for data governance tools, workflows, and processes. • Map current-state vs. target-state data processes and identify gaps., • Translate business needs into functional specifications for master data and data governance platforms (e.g., Dataedo, Collibra, Informatica, Alation). Data Quality & Metadata Management • Identify critical data elements (CDEs) and define associated metadata and quality rules., • Support profiling, cleansing, and remediation activities in collaboration with data stewards., • Document and maintain business glossaries, data dictionaries, and lineage information. Stakeholder Engagement & Change Management • Act as a liaison between business stakeholders and technical teams., • Facilitate workshops, interviews, and decision-making sessions with data owners and SMEs., • Drive awareness and adoption of data governance practices through training, communication, and user support. Tool & Platform Implementation • Contribute to the configuration and onboarding of data governance tools., • Validate technical solutions against business requirements, performing functional testing and UAT as needed., • Help design dashboards and reports for data quality, compliance, and governance KPIs. What we are looking for Required Skills & Experience: • Bachelor’s degree in Business, Information Systems, Data Management, or related field., • 3–5+ years of experience as a Business Analyst, Data Analyst, or similar role., • Hands-on experience with data governance concepts (data quality, metadata, stewardship, lineage)., • Strong skills in process mapping, business requirements documentation, and stakeholder coordination., • Working knowledge of SQL, data modelling, and data profiling tools (a plus). Nice to Have: • Experience with enterprise data governance platforms (e.g., Collibra, Informatica, Alation)., • Familiarity with data management frameworks (e.g., DAMA-DMBOK)., • Background in regulatory/ compliance-driven environments (GDPR, BCBS239, HIPAA, etc.)., • Strong communication skills with the ability to simplify complex data topics. Key Competencies: • Analytical problem-solving, • Process-oriented thinking, • Stakeholder management, • Attention to detail, • Documentation excellence, • Data literacy and governance mindset

🏢 About the company OMODA Motors, part of the Chery Group, is an international automotive brand expanding in Europe. Our European headquarters is in Barcelona, leading the brand’s development across the region. 📍 Work arrangement This position is based fully on-site (no remote) at our EU HQ office (Cornella, Barcelona). 💡 Why join us? • Join the European operations of a fast-growing global automotive brand., • Play a critical role in building and stabilizing inbound logistics operations for OEM production., • Be directly involved in production-driven logistics and pull-based material supply systems., • Work in a dynamic, international manufacturing environment., • Take ownership of warehouse standards, 3PL coordination and inventory excellence., • Long-term development opportunities within a global automotive group. 🔧 Key responsibilities • Manage end-to-end inbound logistics operations for imported KD parts and European local parts, including inland transportation from ports, inbound receiving, warehousing and delivery to the production line. Act as the OEM representative to ensure stable material flow and prevent production line stoppages., • Define, implement and continuously optimize warehouse operational standards and SOPs. Supervise and guide 3PL logistics teams on-site to ensure compliance with safety, quality and efficiency requirements. Drive disciplined on-site (Gemba) management with a strong hands-on approach., • Design inventory strategies and safety stock levels based on production demand, lead time and supply risks. Plan and optimize warehouse zoning, location management and internal logistics flow. Execute cycle counts and annual physical inventories to ensure inventory accuracy of at least 99.5%. Prevent obsolete and excess inventory and continuously improve inventory health., • Manage material delivery schedules based on OEM production plans and takt time. Ensure proper execution of pull-based material supply systems, including Kanban, sequencing and batch management. Oversee material preparation, kitting and line-side delivery to guarantee timely and accurate supply to production., • Monitor real-time inventory and in-transit status with high sensitivity to potential shortages. Proactively identify risks, initiate contingency actions and coordinate cross-functional teams to drive issue resolution until full closure., • Manage inspection, return and handling processes for defective or non-conforming parts. Coordinate supplier claims related to logistics and warehouse quality issues. ✅ Requirements • Bachelor’s degree or above in Logistics, Industrial Engineering or related fields., • 5+ years of experience in automotive manufacturing logistics or warehouse management., • Proven hands-on experience coordinating directly with OEM production lines., • Strong understanding of automotive pull-based material supply systems and production-driven logistics models., • Proficient in WMS and ERP systems, especially SAP PP/MM modules., • Native-level Spanish and fluent business English, capable of reading BOMs, SOPs and conducting effective communication., • Strong problem-solving skills, high resilience and the ability to work effectively under pressure., • Hands-on, detail-oriented work style with a strong focus on on-site execution., • Fluent in English and Spanish. Chinese is a plus. 🎁 What we offer • Competitive opportunity within a global automotive OEM group., • High-impact role directly linked to production stability., • International working environment., • Long-term career development opportunities., • Salary: Negotiable.

Howden es una empresa que apuesta por el talento y ofrece oportunidades de desarrollo profesional para todos aquellos que quieran embarcarse en esta aventura laboral que comenzó hace ya mas de 15 años. Tras nuestro crecimiento continuo y la consolidación de nuevas adquisiciones, Howden ha superado los 108 millones en comisiones y 1.200 millones en primas, posicionándose entre los principales brókers a nivel nacional. Misión: Asegurar una gestión experta y estratégica de las carteras de clientes del área de Employee Benefits, proporcionando asesoramiento especializado en seguros colectivos (vida, salud, expatriados, ahorro y otros beneficios para empleados). La persona seleccionada contribuirá al crecimiento sostenible del área, a la retención y fidelización de clientes y al diseño de soluciones de bienestar corporativo adaptadas a las necesidades de cada organización. Funciones del Puesto: • Proporcionar asesoramiento integral en pólizas colectivas de vida, salud, accidentes, viaje, expatriados y otros beneficios., • Realizar revisiones periódicas de coberturas, condiciones y primas, identificando mejoras y alternativas en el mercado., • Identificar oportunidades de crecimiento en clientes actuales y potenciales., • Participar en la captación de nuevos clientes y en la preparación de propuestas, estudios de riesgos y presentaciones comerciales., • Gestionar de forma directa la interlocución con compañías aseguradoras en materia de Employee Benefits., • Colaborar con áreas técnicas, administración y equipos territoriales para garantizar un servicio coherente, ágil y centrado en el cliente., • Impulsar mejoras en procesos, productos y condiciones., • Asumir la responsabilidad integral sobre la calidad y correcta prestación del servicio a la cartera de clientes asignada, velando por que todas las actividades involucradas propias y de otras áreas (administración, facturación, Compliance, etc.) se ejecuten de manera adecuada y en los plazos establecidos. Coordinar de forma proactiva y transversal con los equipos internos para garantizar una experiencia de servicio consistente, eficiente y satisfactoria Requisitos: Formación universitaria superior. Experiencia mínima de 4–5 años en correduría de seguros gestionando soluciones de Employee Benefits Conocimiento sólido del mercado asegurador y de productos de vida, salud, accidentes, expatriados y planes de ahorro. Competencias en comunicación, negociación, análisis y orientación al servicio. ¿Qué ofrecemos? • Contrato laboral indefinido, • Retribución fija, a acordar en función de experiencia y formación del candidato, • Plan de carrera, con opciones reales de promoción, • Formación inicial y continua a cargo de la empresa, con apoyo al desarrollo profesional., • Herramientas necesarias para el desempeño, • Flexibilidad horaria con posibilidad de teletrabajo 2 días a la semana, • Retribución flexible (detallar más: seguro médico, cheque restaurante…)

Are you passionate about optimising industrial facilities and leading maintenance excellence? We are looking for a Maintenance Manager to join an international pharmaceutical company, with an API manufacturing plant located in the Barcelona area. If you enjoy improving equipment reliability, driving continuous improvement and participating in technical projects within a demanding industrial environment, this could be your next professional challenge. 💡 Your mission You will play a key role in ensuring the proper operation of the facilities by leading the planning and optimisation of maintenance processes in a chemical plant. ⚙️ Your main responsibilities will include: • Managing the plant’s CMMS (Computerised Maintenance Management System)., • Supervising the maintenance team., • Designing and implementing the preventive maintenance plan., • Ensuring compliance with the statutory maintenance plan., • Coordinating the equipment calibration programme., • Creating departmental SOPs (Standard Operating Procedures)., • Collaborating with Engineering on the design and commissioning of new installations., • Participating in FAT/SAT activities and technical improvement projects. 👤 What we are looking for • Bachelor’s or Master’s degree in Engineering., • At least 3 years of experience in maintenance within an industrial or chemical environment., • Strong organisational, planning and resource optimisation skills., • High level of English. 🎯 What we offer • Stable project within an international pharmaceutical company., • Location: Barcelona area., • Flexible working hours, Monday to Friday., • Competitive salary, according to experience.

At Gracia101 we're seeking a SAP Architect for one of our clients based in Barcelona. In this role, you will collaborate closely with other architects, cross-functional teams, and business stakeholders to shape the technology strategy. You will have the opportunity to work on a variety of initiatives across multiple business units in an international context. Key Responsibilities: • Define and communicate the technology vision for product-related business capabilities, including product lifecycle management, portfolio management, regulatory compliance, and product safety., • Work with senior business stakeholders to understand strategy, requirements, objectives, and constraints., • Develop a technology strategy and roadmap that leverages current investments while introducing innovative solutions to improve operational efficiency, reduce costs, and enhance user experiences. Ensure the architecture remains adaptable to evolving business needs., • Design a high-level solution architecture, covering all necessary components and addressing people, process, technology, and data. Ensure functional and non-functional requirements are met, including performance, scalability, reliability, and security., • Establish and promote design principles and standards. Evaluate technology options to recommend the optimal approach, deciding whether to reuse existing solutions or develop new ones., • Incorporate sustainability principles into the architecture, prioritizing environmentally responsible IT practices. Qualifications: • Experience in IT consulting, including functional and technical advisory, and software architecture design., • Strong understanding of digital technologies and IT systems., • Deep knowledge of product-related business processes and capabilities., • Hands-on experience with ERP systems, such as SAP, PLM, or environmental health & safety modules., • Familiarity with the SAP ecosystem., • Bachelor’s or Master’s degree in IT, product innovation, manufacturing, or related fields., • Proven ability to manage stakeholders and understand business requirements.

At Quaker Houghton, we are experts in the development, production and application of industrial process fluids, lubricants and coatings for the manufacturing industry. We have been an integral part in the growth of the world’s largest industrial and manufacturing companies from aerospace and automotive to primary metal and energy. Today, we have a global presence, with our corporate headquarters located in Conshohocken, PA. Quaker Houghton is a global publicly traded company with a unique collaborative culture that supports career growth for its colleagues and offers competitive compensation and benefit programs. About the Job An excellent opportunity to join the EMEA EHS team in a position where you will be able to engage with production, office and lab teams to promote our EHS standards to ensure sustainability and the drive for continuous improvement. Safety is the core of our culture. You will be key in the effort to engage with all company staff operating within the Barberà del Vallès site to ensure adherence to Environment, Health and Safety (EHS). Work with your key stakeholders to identify priorities and create an EHS focused environment where staff feel comfortable raising concerns and helping to minimize any EHS risks. Participate in different European projects that drive innovation and exceed customer expectations. What’s in it For You? • Excellent onboarding and training programs as part of our QH University platform., • Competitive compensation policy., • Attractive Wellbeing, CSR, Sustainability, Women Inclusion & Diversity programs., • Health insurance, Pension plan and other additional benefits, • Mobile phone, laptop., • Vacation days as per "Convenio Colectivo General de la Industria Química" additional to the local official holidays, • 2 annual days paid volunteering leave to dedicate to the cause of your choice., • Joining an international team where empowered decision making and innovative initiatives are expected. What will you do? • Serve as the focal point for support and implementation of the corporate EHS programs and software systems., • Lead and/or participate in incident investigations, near misses and hazard identifications and ensure appropriate root causes are identified and corrective actions are implemented in line with corporate requirements. Perform EHSQ audits/inspections and ensure appropriate corrective actions are developed and implemented on a timely basis., • Provide support of appropriate occupational hygiene related policies and programs., • Support implementation of the Company’s EHS management systems strategy (ISO14001 and 45001), • Provide EHS knowledge, guidance, coaching and training to establish a positive progressive EHS culture. Act as a key resource for EHS training requirements., • Become the technical expert to implement the Corporate EHS online training system, • Serve as a technical resource in the coordination of emergency preparedness on the site., • Work closely with the Regional EHS Manager, Local/Regional Engineering, site operations and the external firms to effectively identify and manage loss prevention issues., • Coordinate with Operations/Engineering personnel work around MOC processes., • Coordinate with Local/Regional Engineering on any facility construction/demolition projects, • Supervise EHS consultants and contractors hired to perform EHS services such as EHS legal compliance audit, samples collection, noise measurements, air emissions, industrial hygiene testing, fit testing, etc., • Interact with regulatory agencies during compliance inspections. Responds to written correspondence and inquiries from outside regulatory agencies, • Analyze and interpret regulatory requirements and permit conditions that apply to Quaker Houghton operations (manufacturing locations and chemical management activities) and work closely with plant management to address EHS requirements and concerns., • Coordinate with other members of EHS department at EMEA, specially from the other Spanish facilities. What do we look for? • Experience: In the range of 3-5 years experience in the environmental, health and safety discipline with a strong focus on safety required. Ideally within a manufacturing environment in the chemical, oil & gas, food or similar sector., • Education: Bachelor's degree is a must. Advance certification, additional specialized environment and safety education is desired but not required., • Technical skills:, • Solid technical and regulatory expertise in relevant environmental, health and safety regulatory requirements., • Knowledge of and some implementation experience with applicable industry standards including but not limited to ISO 14001 and ISO 45001, Responsible Care, etc., • Solid technical and regulatory expertise in relevant regional and national product safety/stewardship regulatory requirements and associated management systems and programs., • Process risk management best practices., • Best practice knowledge related to unsafe acts and at risk behaviors., • Incident investigation experience, root cause analysis and corrective action management., • Language: Spanish & English language skills; written and spoken at high level., • IT skills: MS OFFICE, MS TEAMS, O365 and ability to learn new IT systems., • Location: Ideally Vallès area, Barcelona., • Soft skills:, • Autonomous & proactive., • Good communication skills, written and verbal & listening., • Good practical problem solving with acute attention to detail., • Strong team player, passionate about delivering success. Who are we? We are the global leader in industrial process fluids present in 40+ countries continually improving and innovating so the world’s steel, aluminum, automotive, aircraft, machinery and industrial parts manufacturers can stay ahead in a changing world. Throughout our 100+ locations, our chemists, engineers and industry experts partner with our customers to continually improve their operations so they can run even more efficiently, even more effectively, whatever comes next. Our values: • Live Safe, • Exceed Customer Expectations, • Drive Results, • Embrace Diversity, • Do Great Things Together, • Act with integrity Our core values embody who we are as a company, guide our decisions and inspire us. Our commitment to these values, in words and actions, builds a safer, stronger Quaker Houghton. They are the fundamental beliefs that guide our internal conduct and our relationship with the outside world.

Técnico/a Jurídico – Área Legal & Compliance Ubicación: Barcelona / modalidad presencial con horario de jornada intensiva. ¿Qué buscamos? En FIATC Seguros queremos incorporar a un/a Técnico/a Jurídico de entre 2 y 4 años de experiencia para reforzar nuestro equipo del Área Jurídica. Buscamos una persona con base sólida en derecho contractual y cumplimiento normativo, con ganas de aprender, aportar criterio y crecer en un entorno dinámico y cercano al negocio. ¿Cuál será tu misión? Dar soporte jurídico al conjunto de la organización, participando activamente en la revisión contractual y en el aseguramiento del cumplimiento normativo, contribuyendo a minimizar riesgos legales y reforzar la seguridad jurídica de la compañía. Funciones principales • Revisión, redacción y negociación de contratos (proveedores, colaboradores, acuerdos de confidencialidad, prestación de servicios, etc.), • Asesoramiento jurídico interno a diferentes áreas de negocio (comercial, operaciones, proveedores, etc.), • Colaboración en la adaptación normativa (protección de datos, normativa sector asegurador, etc.), • Elaboración de informes jurídicos y notas técnicas, • Apoyo en proyectos transversales del área jurídica Requisitos • Grado en Derecho, • Máster de Acceso a la Abogacía, • Valorable especialización en compliance / derecho empresarial, • Experiencia de 2 a 4 años en funciones similares en empresas o en despacho, • Valorable conocimiento: protección de datos y/o entorno asegurador, • Nivel alto de castellano y catalán (valorable inglés) ¿En quién pensamos? • Persona rigurosa y estructurada, con atención al detalle, • Capacidad de análisis y criterio jurídico, • Proactividad y ganas de aprender, • Buena capacidad de comunicación, • Orientación a soluciones ¿Qué ofrecemos? • Incorporación a una compañía sólida y en crecimiento, • Entorno colaborativo y cercano al negocio, • Desarrollo profesional dentro del área jurídica, • Exposición a distintas áreas de la compañía, • Condiciones competitivas + beneficios sociales

We are looking for Supply Chain & Packaging Engineer for our team in Barcelona area to work in one of the most important Tier 1 in the automotive sector to design and implement efficient Supply Chain and Packaging solutions for industrial projects, ensuring safety, quality, customer service and cost optimization from the design phase through start of production. Missions: • Design the complete Supply Chain and Packaging scheme (physical and information flows, stock levels, layouts and logistics means)., • Define and control logistics budgets, packaging investments and project KPIs., • Coordinate with plants, suppliers and cross-functional teams during AVP, development, ramp-up and production phases., • Ensure compliance with standards, safety policies, Lean principles and risk management., • Participate in the selection and technical validation of logistics and packaging suppliers., • Provide on-site support to plants during start of production and ramp-up phases. Requirements: • Engineering background with experience in industrial logistics, supply chain or packaging, preferably in the automotive or industrial sector., • Solid understanding of Lean Manufacturing, Supply Chain principles and mechanical engineering basics (ability to work with 3D viewer software)., • High level of English and Spanish., • Availability to travel, • Location: Near to Barcelona. We offer: • Permanent contract., • Competitive salary package., • Global projects., • Career development and training. BCNC GROUP () is an engineering and technology firm with operations in Spain, UK, Germany, France and Sweden. We work with the most prestigious R&D Centers and multinationals in Europe helping them to develop and implement their strategic programs.

Haier HVAC Europe is a leading provider of Heating, Ventilation, and Air Conditioning solutions across the continent. Due to our sustained growth and commitment to digital excellence, we are seeking a Taxonomy & Content Management Specialist to join our Team. Position Summary In this position, you will play a critical role in maximizing the value of our digital assets. You will be responsible for the end-to-end management of corporate knowledge, leveraging advanced technologies to streamline information sharing across our European operations. Role and Responsibilities • Curate and organize corporate content to ensure the highest standards of quality and accessibility., • Define and manage document management frameworks, including tagging schemes and classification structures., • Oversee technical documentation from initial release to end-of-life, ensuring compliance and accuracy., • Partner with Engineering, Marketing, and Senior Leadership to validate content and address knowledge gaps. Skills and Qualifications • University Degree in Library and Information Science, Documentation, Philosophy, or a related field with a focus on content categorization., • Minimum of 3 years in a corporate environment or the publishing sector, with a proven track record in organizing complex content structures., • Strong "hands-on" approach with the ability to manage end-to-end processes. Exceptional written communication skills and the ability to interact effectively with senior stakeholders., • Professional fluency in English (written and spoken) is essential. Total Rewards • Competitive salary and flexible compensation plan (Restaurants, Transport, and Childcare)., • Private Medical Insurance., • Intensive Fridays (Short Fridays), • Fresh fruit, coffee, and drinks in the office., • Opportunities for continuous learning and career progression in a fast-growing organization. Employee discounts on Haier products. Haier Europe is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, religion, national or ethnic origin, sex, sexual orientation, gender identity or expression, age, disability, or other characteristics protected by law.

Company Description IOMED operates a Data Space Platform powered by AI designed to activate healthcare data for secondary use while ensuring compliance with data protection. Utilizing Natural Language Processing, the platform processes both structured and unstructured clinical data, enabling transformation into an interoperable OMOP Common Data Model without data leaving a hospital’s in-house systems, thanks to its Federated Data Model. IOMED’s innovative approach bridges the gap between raw clinical data and standardized formats for meaningful analysis in Data Spaces. With a focus on data security, IOMED's mission is to be a trusted ally for healthcare organizations, fostering the future of data-driven healthcare. Role Description The core of your role will be to provide analytical insights about the data we work with. To this aim, you will design and develop ways of analyzing and visualizing relevant aspects of our datasets, with the final objective of ensuring their quality. As a Quality Analyst, you will be working in a very dynamic environment, which means that you must have a strong problem-solving ability, organization skills, and be proactive. We are looking for sharp analytical minds, who are able to develop innovative solutions to reason about different types of data. In technical terms, you should be able to implement these solutions in code entirely, from database queries to visualizations. Main Responsibilities • Validate and verify datasets across different stages of the data lifecycle to ensure consistency and reliability., • Identify anomalies, unexpected patterns, and inconsistencies in structured and unstructured data., • Design, execute, and maintain data validation checks and quality controls., • Investigate data issues such as missing values, abnormal distributions, inconsistencies between sources, or unexpected pipeline outputs., • Create, document, and manage data quality incidents, ensuring proper tracking and follow-up until resolution., • Perform root cause analysis in collaboration with Data Engineers, Data Scientists, and clinical teams., • Monitor recurring quality problems and propose preventive improvements., • Document validation procedures, findings, and quality standards. Knowledge & Skills • Degree in Data Science, Computer Science, Statistics, Health Informatics, or a related field., • Strong SQL skills and confidence working with large datasets., • Ability to explore data and detect inconsistencies through analytical reasoning., • Understanding of data pipelines and ETL processes., • Good knowledge of statistics., • Proficiency on the use of testing and expectation frameworks., • Knowledge of data visualization methods and tools., • Python for exploratory analysis or validation scripting is a plus., • Experience with healthcare or clinical datasets is a strong plus., • Professional proficiency in English. Soft Skills • In terms of personality, we are looking for someone who enjoys working in a wide range of areas and adapts quickly to new situations., • Excellent communication skills and the ability to work in a team., • To be comfortable with changes and able to adapt quickly to new tools and methodologies., • The ability to identify issues, analyze them, and find creative solutions is critical., • Efficiently managing time and prioritizing tasks. What can we offer? • Competitive salary., • Permanent contract., • Flexible remuneration with restaurant tickets, transport tickets, nursery, training, and medical insurance., • Flexible schedule and hybrid working model., • 28 days of vacations per year., • A warm, transparent and supportive team, with a huge emphasis on work-life balance., • The opportunity to make your mark in e-health and AI.

At ___, we are building the DPDF (Dynamic Portable Document Format) ecosystem. This project moves beyond standard text processing to create a new paradigm of digital text that evaluates documents for pragmatic honesty, logical fallacies, and cognitive biases. We are redefining how humans interact with written documents by introducing conversational agents grounded in Grice’s Cooperative Principle and Theory of Mind. About the Role We are seeking a Computational Linguist to join our team at Indeep Artificial Intelligence (IAI) who is as comfortable with formal semantics as they are with high-performance software engineering. You will be responsible for the "Brain" of the DPDF format: the engine that ingests raw text and outputs a structured, multi-layered pragmatic analysis. You are not just a user of Large Language Models (LLMs); you are an architect who can programmatically constrain, evaluate, and chain them to perform complex linguistic "surgeries" on documents. We also need someone with a strong startup attitude. In practice, this means: • A builder mindset: You don’t just “request” features; you build them. You thrive in an environment where the codebase is evolving and the problem space is undefined., • Versatility: You are willing to wear the hat of a researcher one hour and a DevOps engineer the next, ensuring that your linguistic pipelines are performant, scalable, and secure., • You are precision-obsessed: In a project focused on honesty and clarity, your code and prompts must be the gold standard of precision. This role is for someone energised by wearing multiple hats and making an impact without needing a detailed playbook. If that sounds like you, we’d be excited to hear from you. Key Responsibilities Corpus Building & Annotation • Design, build, and curate annotated corpora of domain-specific documents, including insurance contracts, legal texts, and grant applications., • Define and maintain annotation schemas for pragmatic, semantic, and structural features, ensuring inter-annotator reliability., • Oversee and quality-control annotation workflows, including work performed by external annotators or domain experts. Pragmatic Analysis Engine • Develop and implement the core logic that classifies text according to Gricean Maxims (Quality, Quantity, Relation, Manner) and identifies Epistemic Traps., • Design and implement software functions for granular document evaluation, automated Pragmatic Tagging, and real-time text editing and simplification., • Build proprietary linguistic metrics. Advanced Prompt Engineering & LLM Orchestration • Architect complex LLM orchestration pipelines, including Chain-of-Thought (CoT) & ReAct, programmatic prompting, few-shot, and meta-prompting., • Manage LLM hallucinations through RAG (Retrieval-Augmented Generation) and semantic validation layers. Linguistic Analysis Pipeline Design • Design and refine the linguistic analysis pipelines powering our TRIC scoring system (Truthfulness, Relevance, Informativeness, Clarity) and its Grice’s maxim-based feedback engine., • Translate pragmatic and discourse-level linguistic theory into concrete, implementable feature specifications., • Maintain and evolve linguistic rule sets, ontologies, and concept taxonomies across document types and target languages (initially Italian, Spanish, and English). Evaluation Frameworks & LLM Judging • Develop rigorous evaluation frameworks to assess the quality, accuracy, and consistency of LLM-generated outputs., • Design and implement LLM-as-judge pipelines, including prompt design, evaluation rubrics, and inter-rater calibration against human expert baselines., • Conduct systematic error analysis to identify failure modes in model outputs and translate findings into actionable improvement cycles. Cross-functional Collaboration • Work closely with the product team to inform model fine-tuning, feature engineering, and retrieval pipeline design with linguistic expertise., • Collaborate with the product and compliance teams to ensure linguistic outputs meet regulatory and accessibility requirements. Qualifications Required • PhD or MSc in Computational Linguistics, NLP, or Computer Science with a strong NLP focus. A solid STEM foundation is non-negotiable., • Expert-level proficiency in Python. Hands-on experience with NLP libraries (HuggingFace, spaCy, NLTK) and LLM frameworks (LangChain, LlamaIndex, or equivalent)., • Deep understanding of pragmatics and semantics. Ability to translate abstract principles, such as the Cooperative Principle, into code-based constraints., • Proven experience managing LLM outputs through RAG pipelines and semantic validation layers., • Demonstrated ability to design and implement complex prompting strategies for LLMs, including evaluation and judging pipelines., • Ability to design validation tests for linguistic models, ensuring high inter-rater reliability between AI and human expert baselines., • Hands-on experience building and curating annotated corpora, including annotation schema design and quality control., • C2-level proficiency in English. Qualifications Preferred • Experience with readability metrics and automated text quality assessment (e.g., Flesch-Kincaid, Gulpease)., • Background in legal, insurance, or scientific/grant document processing., • Experience designing inter-annotator agreement studies and applying relevant metrics., • Working proficiency in Italian and/or Spanish., • Familiarity with EU AI Act requirements or regulatory NLP applications. What We Offer • €50,000–€80,000 yearly gross salary depending on demonstrable experience and depth of expertise., • Employee Stock Ownership Plans (ESOPs)., • A role at the intersection of cutting-edge NLP research and real-world product impact., • Early-stage team member at a high-potential EIC-funded startup. How to Apply Submit your CV and a brief cover letter explaining your linguistic expertise and why you’re excited about this role through LinkedIn. Applications will be reviewed on a rolling basis, so apply now to join the innovative team at Indeep AI!

Job Responsibilities • Coordinate the economic substance of companies within the area of responsibility (coordinate communication with management, shareholders and UBO, office and staff issues, communication, business profile, etc.), • Giving support in preparing everything needed for opening and setting up of new companies (including rent of office space, bank accounts, staff (UBO), legal documentation, business plan, etc.), • Communication with banks: preparation documents for opening new bank accounts, where required, assistance with responding to compliance or KYC dept., preparation of requested documents, • Coordinate routine legal support of legal entities within the area of responsibility, • Organize the documents for legal entities of the group, • Participation in substance improvement/creation for existing companies, • Oversee the processes for substance (such as online presence), • Languages: fluency in English, others are nice to have (Spanish, Russian, etc) Required Soft Skills • Excellent communication skills both verbal and written, • Self-starter and self-motivated with a passion to learn and grow, • Proactive and able to identify issues, legal risks, and potential liabilities, • Attention to details, • Bachelor’s degree in Law will be a plus, • Experience in opening and further support of new Legal Entities in min. 2 counties, • Experience in collaboration with banks and EMIs including opening accounts in various financial institutions, • Understanding of ordinary bank practices and requirements What we offer From your first day: • Competitive salary based on experience and skills, • Full day (8h), • Free daily lunches and snacks, • No dress code policy, • Free Parking Space, • Shared knowledge and internal training, • Team buildings and Corporate parties dedicated to your achievements, • Private health insurance, • Up to 50% coverage on sports membership, • Up to 50% coverage of mental health services, • 50% coverage on language lessons (English or Spanish).

🛰️ Indra Space – Leading the Next Generation of Space Systems 🌌 At Indra Space, we are on a mission to redefine the European space industry by delivering high-performance small satellite solutions for LEO missions. Our ambition? To become a leading company in end-to-end satellite systems, driving innovation in:• 🚀 Position, Navigation & Timing (PNT) 🚀 Secure Communications 🚀 Earth Observation & ISR 🚀 Space Domain Awareness (SDA) and Space Traffic Management (STM) 🚀 Science & space exploration As the Space Business Unit of Indra Group, we combine cutting-edge technology with a full value chain approach—from satellite design and integration to ground segment and operations. With the integration of Deimos and strategic participation in Hispasat and Hisdesat, we are scaling Europe’s space autonomy and contributing to flagship programs like IRIS², Galileo, EGNOS, and Copernicus. 🔍 What We’re Looking For We are seeking an experienced GNSS Systems Engineer with strong background in engineering best practices, particularly during conception, specification and design phases. 📌 Key Responsibilities • Apply systems engineering methodologies throughout conception, specification and design phases., • Manage and maintain system requirements using tools such as DOORS or similar., • Use project tracking tools such as JIRA to follow system and engineering workflows.• Analyse and understand GNSS system concepts, GNSS signals, performance aspects, and RF interference detection and geolocation., • Perform radiofrequency-related analysis, including link budgets and RF/baseband subsystem evaluation., • Manage workflows related to engineering instrumentation., • Use MBSE tools such as Capella or Enterprise Architect for architectural modelling and system design., • Produce high-quality technical documentation across complex technical systems., • Ensure compliance with ESA ECSS or related engineering standards. 🎯 Requirements • Experience in systems engineering best practices, especially in early lifecycle phases (conception, specification, design)., • Proficiency with requirements management tools such as DOORS (Advanced level)., • Experience using tracking tools like JIRA., • Strong understanding of GNSS concepts, signals, performances, and RF interference detection/geolocation (4–5 years)., • Solid knowledge of radiofrequency engineering, including link budgets and RF/baseband subsystems., • Experience with MBSE tools such as Capella, Enterprise Architect, etc., • Ability to understand and manage complex technical systems and produce detailed technical documentation., • Familiarity with ESA ECSS standards or similar., • High level of English (verbal and written). ⭐ Optional / Nice-to-Have • Prior experience in defence and security environments., • Experience in global navigation satellite systems (GNSS) domains (Advanced, 4–5 years)., • Experience working in GEO & Location domains (GNSS/WiFi/cellular/RF). 🌟 What We Offer 🌍 Work Your Way: Flexible hours so you can balance life and work effortlessly. 🤝 Open Culture: Direct communication and a friendly environment where your voice matters. 🚀 Innovation at Its Core: Be part of groundbreaking projects with global impact. 💡 People First: A collaborative team that supports and celebrates your success. 📈 Career Acceleration: Continuous feedback and annual reviews to help you grow. 🔒 Stability You Can Trust: Long-term projects in a leading company with a future vision. 🌐 Global Reach: Your work will influence major international initiatives. ✈️ Mobility Opportunities: Explore projects across Spain and beyond. 🎓 Lifelong Learning: Access Open University programs and 3,000+ Udemy for Business courses. ✨ Your next big opportunity is here. Ready to make an impact? Apply today!

WHO ARE WE? Sateliot is a Barcelona-based Startup in the New Space sector, becoming the first satellite telecommunications operator that will provide global and continuous connectivity to all the elements that will make up the massive Internet of Things (IoT) universe under the 5G protocol. In order to do so, Sateliot is launching a constellation of last generation nanosatellites, located at low altitude that act as mobile towers. Sateliot is the perfect complement for large telecommunications companies by providing them with the necessary infrastructure where terrestrial technologies do not arrive. YOUR MISSION Sateliot is seeking an experienced Principal Antenna Product Engineer to lead the end-to-end development of an advanced antenna array for space applications. The successful candidate will take full ownership of the product lifecycle—from concept definition through design, simulation, prototyping, fabrication, testing, qualification, and flight readiness. This role requires deep expertise in antenna engineering for the space environment, including materials selection, lightweight and semi-rigid structures, and deployable antenna systems. The ideal candidate combines strong analytical rigor with first-principles thinking, and a pragmatic, goal-oriented approach focused on delivering flight-ready hardware within program constraints. Antenna design must be carried out in tight coordination with mechanical and thermal constraints, ensuring structural integrity, thermal stability, and manufacturability from the earliest design phases. The candidate will work closely with a senior mechanical engineer to ensure seamless RF-structural integration and optimized system performance. YOUR MAIN FUNCTIONS Technical Leadership & Product Ownership • Lead the architectural definition and technical roadmap of advanced antenna arrays for space applications., • Own the antenna system from concept to design for manufacture, qualification, testing and flight readiness., • Translate mission and system requirements into robust antenna design solutions., • Apply first-principles thinking to challenge assumptions and drive optimal, physics-based solutions., • Design high-performance antenna arrays (e.g., phased arrays, reflectarrays, patch arrays, deployable architectures)., • Perform full-wave electromagnetic simulations (CST, HFSS, FEKO or equivalent)., • Design antennas considering:, • Mechanical constraints (stiffness, launch loads, vibration, deployment reliability), • Thermal constraints (thermal gradients, expansion, cycling, distortion effects), • Mass optimization and structural integrity, • Manufacturability and assembly constraints, • Optimize radiation performance, efficiency, bandwidth, polarization, and thermal stability. Select and qualify materials considering: • Radiation tolerance, • Thermal cycling, • Outgassing (ECSS/NASA compliance), • Vacuum compatibility, • Lead the development of lightweight, semi-rigid antenna structures., • Contribute to or drive deployable antenna concepts and structural integration strategies., • Collaborate closely with the senior mechanical engineer to co-design RF and structural elements from early concept stages., • Oversee prototype development, including PCB-based RF structures, waveguide assemblies, and hybrid solutions., • Define fabrication tolerances, inspection criteria, and manufacturing workflows., • Ensure the design is optimized for repeatability, scalability, and production efficiency., • Interface with suppliers and manufacturing partners., • Define and execute RF validation campaigns (anechoic chamber, near-field/far-field measurements)., • Support environmental qualification (vibration, thermal vacuum, shock, radiation)., • Correlate EM simulations with structural and thermal behaviour., • Analyse test data rigorously and implement corrective design improvements., • Deliver test requirements and test reports., • Work closely with the senior mechanical engineer to ensure fully integrated RF-mechanical-thermal co-design., • Interface with systems, thermal, manufacturing, and mission engineering teams., • Support system integration and mission readiness reviews. REQUIREMENTS • Master’s or PhD in Electrical Engineering, Electromagnetics, RF Engineering, or related field., • 8+ years of experience in antenna design, • Proven experience delivering antenna systems from concept through qualification., • Strong understanding of space environmental constraints and compliant materials., • Experience with lightweight, semi-rigid, and/or deployable antenna structures., • Demonstrated ability to design antennas considering mechanical, thermal, and manufacturing constraints., • Expertise in electromagnetic simulation tools (HFSS, CST, FEKO or similar)., • Hands-on experience with antenna measurement and RF validation., • Attitude of the person:, • Need to have a “can do attitude”. Think outside the box and be able to push boundaries of physics., • Task oriented focused to close out actions ASAP., • Focused on time to market. NICE TO HAVE Preferred Qualification • Antenna design for space qualified systems, • Experience with phased arrays and beam-steering architectures., • Experience in LEO/MEO/GEO satellite missions., • Experience in S-band, L-band, Ka-band, or other satellite communication bands., • First-principles thinker with strong electromagnetic intuition., • Pragmatic and goal-oriented, capable of delivering robust solutions under program constraints., • Strong awareness of mechanical, thermal, and manufacturing realities., • End-to-end product ownership mindset., • Analytical and systematic problem-solving capability., • Cross-disciplinary collaboration skills., • Hands-on engineering attitude with attention to detail nd quality., • Clear technical communication and leadership abilities. WHAT YOU’LL FIND WHEN WORKING AT SATELIOT: You will be part of one the fastest-growing start-ups in Spain with global reach along getting into the challenging world of New Space & Telecommunication. Our culture is based on embracing openness by welcoming multicultural talent, being respectful with everybody and being open to exchange ideas. We are also committed to a healthy lifestyle by helping our team balance their work and personal life and also by providing them facilities for healthy habits. We are a driven team with big goals, that seek for people who are genuinely passionate about their work and that also want to keep learning and getting better personally and professionally! WHAT DO WE OFFER? • Full time permanent Contract, • Hybrid Work Model 💻, • Schedule flexibility, • Flat and transparent organizational structure, • Buddy Program to help you with your integration during your first month 🫂, • Flexible compensation package: Tax benefits with ticket restaurant, transportation and kindergarten, training programs.💰, • We promote good physical and mental health, with a Health insurance, Fresh fruit in the office and the possibility of sharing the cost of bicycle transport or gyms.🏋🏻, • Work in a dynamic, multidisciplinary and multicultural environment that will allow you to boost your professional career 🌍, • To be part of a strong, international, friendly and motivated team, where you can progress both personal and professionally 🪴, • The chance to be part of one of the most exciting and disruptive space projects in Europe 🚀

The Global Product Sustainability Engineer – Packaging is a senior individual contributor responsible for driving Werfen’s global packaging sustainability, compliance, and strategic transformation initiatives. This position leads the development, implementation, and oversight of packaging-related regulatory compliance programs, sustainability frameworks, and cross-functional efforts required to meet worldwide packaging requirements. This role provides deep subject‑matter expertise on packaging regulations (PPWR, EPR, AGEC Law, ESPR), packaging materials, recyclability, reuse, labeling, design optimization, and compliance documentation. As Werfen expands its global packaging obligations—the position ensures readiness, governance, and risk mitigation across Technology Centers (TCs), manufacturing sites, and affiliate markets. The position must excel in influencing without authority, coordinating diverse global teams, engaging suppliers, ensuring data accuracy, and shaping Werfen’s long‑term packaging strategy. This position will report to the Global Product Sustainability Sr. Manager under the corporate sustainability leadership. Key Accountabilities Regulatory Compliance & Stewardship • Lead global compliance for packaging regulations including: EU Packaging & Packaging Waste Regulation (PPWR - material restrictions, recyclability, recycled content thresholds, technical documentation, EU Authorized Representative requirements), Extended Producer Responsibility (EPR - requirements across EU Member States, UK, U.S. states, APAC, and emerging markets), French AGEC Law & national reuse targets, mandatory annual declarations on packaging mass, weight, recyclability, and reuse metrics., • Develop and support Werfen packaging compliance documentation including Declarations of Conformity (DoCs), technical files, testing evidence, and supplier attestations., • Ensure packaging types used across Werfen products are registered appropriately with EU Authorized Representatives and competent authorities., • Support audits, inspections, and reporting for governmental bodies, packaging producer responsibility organizations, and sustainability frameworks. Packaging Strategy, Governance & COE Enablement • Lead creation of a global packaging governance model, advancing the foundation for a Packaging Center of Excellence (COE) to support Werfen’s sustainability, compliance, and innovation goals., • Develop strategic roadmaps addressing packaging redesign, reusable systems, sustainable alternatives, • Oversee global packaging data collection and validation across Werfen, including: Packaging type, weight, material composition, recyclability, recycled content, and country‑specific reporting fields, • Establish standardized templates, processes, and repositories to ensure accurate and consolidated reporting across business units., • Serve as the global subject-matter expert for packaging sustainability across R&D, Operations, Supply Chain, QA/RA, Manufacturing, Procurement, and Affiliate teams., • Provide guidance to packaging engineering teams on design requirements, testing, validation, labeling, and compliance readiness., • Lead engagement with packaging suppliers on recyclability, recycled content, documentation, and engineering constraints., • Identify opportunities for packaging optimization (weight reduction, material substitution, consolidated packaging types, circularity)., • Promote reuse initiatives, recycled content targets, and alternatives to high-impact packaging materials., • Develop and deliver periodic program reports and dashboards to track progress, risks, and milestones., • Prepare and present regular updates to senior leadership and executive sponsors, driving decision-making and transparency. Networking/Key relationships • Global sustainability teams, • Technology centers, • Cross-functional stakeholders (Global Supply Chain & Logistics, Procurement, R&D, QA/RA, Operations, Supply Chain, Marketing, IT) Minimum Knowledge & Experience required for the position: • Education: Bachelor’s degree or higher in Packaging Engineering, Materials Science, Sustainability, Mechanical/Chemical Engineering, Environmental Science, or related field, Master’s or Ph.D. preferred., • Experience: Minimum 7–10 years in packaging sustainability, packaging engineering, product stewardship, or regulatory compliance., • Demonstrated expertise in global packaging regulations, especially PPWR, EPR, AGEC, ESPR, recyclability standards, and packaging data/reporting systems., • Experience working in regulated industries (medical devices, IVD, pharma, life sciences) strongly preferred., • Professional certifications in packaging, sustainability, environmental management, or program leadership., • Experience with digital product compliance, digital product passports, and sustainability tools., • Deep knowledge of packaging materials, sustainability principles, and regulatory frameworks., • Strong analytical, data management, and program management skills., • Excellent communication and cross-functional leadership., • Ability to influence without authority and drive alignment across global teams. • International travel required (<20% of average time)

PLEASE NOTE: please attach your resume in English Position Overview: Following a recent acquisition, this Legal Counsel role is a pivotal member of our legal team, responsible for comprehensively leading and managing all legal affairs for our Spanish operations. This includes providing dedicated support for key strategic initiatives in Spain and championing Group-level compliance within the Spanish entity. The role will also extend to supporting new company establishment and business rollout efforts in Portugal. This position requires strong independent project-managing abilities, robust legal research and analytical skills, and excellent communication abilities to effectively collaborate with internal teams, group headquarters, and external stakeholders including governmental departments. Work Place: Barcelona, Spain Responsibilities: Comprehensive Spain Legal Operations : • Draft, review, negotiate, and finalize a wide range of contracts, agreements, and other legal documents essential for the company’s business operations in Spain, including but not limited to commercial agreements, vendor contracts, partnership agreements, and potentially leases or construction agreements as relevant to the business., • Organize and manage the contract approval matrix and ensure systematic archiving of legal documents for the Spanish entity., • Conduct legal research and manage legal risks in relation to the company’s operations in Spain (both offline and online, if applicable)., • Independently manage and handle comprehensive legal projects and advisory related to Spanish regulatory requirements, including but not limited to importation/exportation compliance, product labeling/marking (if applicable), advertising compliance, data protection (GDPR), employment law, and consumer protection requirements., • Develop, implement, and monitor compliance programs and policies for the Spanish entity, ensuring adherence to local laws (e.g., Spanish Companies Act, GDPR, anti-bribery laws) and Group-level compliance standards., • Act as a key legal partner supporting the Group's establishment strategies and business rollout in Portugal., • Oversee the protection of the company’s intellectual property rights (trademarks, copyrights, patents, etc.) in Spain and support regional IP strategies., • Liaise effectively with external legal counsel in Spain, Portugal, and other relevant jurisdictions and government agencies to ensure smooth operations and compliance with legal obligations., • Participate in and, where appropriate, conduct legal training sessions to enhance the legal knowledge and compliance awareness of internal teams in Spain. Qualifications: • Bachelor's degree or above in Law (LLB, LLM, or JD preferred) from a recognized university., • Eligibility to practice law in Spain; alternatively, qualification in another civil law jurisdiction with substantial experience in Spanish law., • Minimum of 5 year of relevant legal experience, ideally with a combination of law firm and in-house counsel experience, preferably within a multinational corporation. Experience in [mention specific industry if relevant, e.g., tech, retail, manufacturing] is a plus., • Strong legal research and analytical skills, with the ability to independently manage projects, interpret, and apply complex legal provisions relevant to Spain and Portugal., • Solid understanding of Spanish contract law, commercial law, corporate law, data privacy (GDPR), and relevant industry regulations. Desired Skills: • Experience working in a transnational corporation and familiarity with navigating matrix organizations., • Excellent command of English and Spanish (both written and spoken) is a must. Proficiency in Portuguese would be an advantage., • Proven ability to work independently, take ownership of assigned tasks, and manage multiple priorities in a fast-paced environment., • Creative and pragmatic thinker with the ability to provide innovative yet practical legal solutions to complex business challenges., • Positive attitude, commercially astute, and results-oriented approach, with a strong commitment to the company's values and mission., • Proficient in legal software and technology tools, as well as Microsoft Office suite.

🚀 Buscamos Senior Architect HRIS 📍 Ubicación: Barcelona – Híbrido (2 días presencial) 🔎 Desde Capitole estamos acompañando a uno de nuestros clientes del sector asegurador, líder a nivel global con presencia en más de 30 países. Para este desafío, buscamos un/a Senior Architect con experiencia en sistemas HRIS a gran escala, arquitectura cloud e integración de datos. 🎯 ¿Cuál es el desafío? El cliente está redefiniendo su ecosistema de People Tech a nivel internacional — simplificando, convergiendo y haciendo más eficiente la gestión de personas en múltiples países. Vas a ser quien diseñe la arquitectura objetivo y trace el roadmap de transformación. Impacto real, escala global, decisiones que duran años. ✨ Vas a trabajar en: 🏗️ Análisis de la arquitectura HRIS actual en entorno multi-país 🎯 Definición de la arquitectura objetivo funcional y técnica 🔗 Diseño de patrones de integración seguros entre sistemas HR 🗺️ Elaboración del roadmap de transformación con estimación de impactos 🤝 Colaboración con equipos de IT, negocio, seguridad y compliance 🎓 ¿Qué buscamos? ✅ Experiencia como Enterprise o Solution Architect en proyectos HRIS multi-país a gran escala ✅ Sólido conocimiento del mercado de soluciones HRIS (Workday, SAP SuccessFactors u otros) ✅ Dominio de arquitectura cloud, APIs y patrones de integración de datos ✅ Capacidad para trabajar con stakeholders de negocio, IT, seguridad y compliance simultáneamente ✅ Inglés fluido — el proyecto es 100% internacional ✅ Experiencia elaborando blueprints de arquitectura y roadmaps de transformación 🌟 Se valorará especialmente: ⭐ Experiencia con integraciones de soluciones AI/ML en entornos HR ⭐ Conocimiento de estándares de seguridad y compliance en entornos corporativos globales ⭐ Background en sector asegurador o financiero 💙 ¿Por qué unirte a Capitole? 📘 1.200 € al año en formación. 🏥 Seguro médico privado gratuito. 🔹 Retribución flexible en transporte, guardería y tickets restaurante. 🏋️ Acceso a +10K gimnasios por toda España con Wellhub (Gymforless). 🎉 Eventos, team buildings y afterworks cada dos meses. ⚽ ¡Patrocinamos nuestro equipo de fútbol si te animás a jugar! 🔧 Comunidades tecnológicas internas para crecer juntos. 👉 Conocé más sobre nosotros: ✨ ¿Quieres saber más? Haz clic___ y descubre todos los detalles. 🔍 Descubre lo que dicen sobre nosotros en ___ 🎥 ¿Te gustaría conocer más sobre nuestra cultura? Mira este video 👉 ___ ¿Te animás a este desafío? 🚀 Empowering People, Unlocking Innovation ¡Apuntate y conocenos! 🙌 El empleado/a se adherirá a las políticas de seguridad de la información. Tendrá acceso a información confidencial relativa a Capitole y al proyecto. Deberá cumplir las políticas internas de la empresa y cliente, y firmar un NDA.

An international construction company is looking for a Mechanical Site Engineer to join one of the most iconic large-scale stadium redevelopment projects in Europe, currently under construction in Barcelona. This is a unique opportunity to be part of a high-profile international project that will redefine sports and entertainment infrastructure, working within a dynamic and multicultural environment. Key Responsibilities: • Supervise MEP site activities and ensure compliance with project specifications, • Coordinate with subcontractors and multidisciplinary teams, • Monitor installation quality, progress, and safety requirements, • Review technical drawings and resolve site issues, • Support commissioning and handover phases Requirements: • Degree in Mechanical Engineering or related field, • 2–5 years of experience as MEP Site Engineer or similar role, • Experience in construction projects (stadiums, airports, hospitals, or complex buildings preferred), • Strong coordination and problem-solving skills, • Experience working in international environments is a plus, • Fluent English and Spanish required

At Alstom, we understand transport networks and what moves people. From high-speed trains, metros, monorails, and trams, to turnkey systems, services, infrastructure, signalling and digital mobility, we offer our diverse customers the broadest portfolio in the industry. Every day, 80,000 colleagues lead the way to greener and smarter mobility worldwide, connecting cities as we reduce carbon and replace cars. Could you be the full-time Railway Depot Manager / Responsable de Garantia Ferroviaria in Vilanova, Barcelona we’re looking for? Your future role Take on a new challenge and apply your maintenance expertise in a new cutting-edge field. You’ll work alongside young and proactive teammates. You'll be responsible of leading and coordinating all warranty – related activities at rolling stock maintenance depots. Day-to-day, you’ll work closely with teams across the business (external clientes and suppliers), ensure the proper execution of warranty tasks, including fault diagnosis, issue resolution, spare parts management and compliance with contractual obligations and much more. You’ll specifically take care of managing the warranty activities at the customers depot, but also lead the internal warranty team, including planning and development. We’ll look to you for: • Oversee fault diagnosis, issue resolution, repair validation and repair logs accuracy. To restore train availability., • Coordinate with the rest of the waranty team and project team to ensure fleet availability., • Maintain strong relationships with the customer (train operator and or train maintenance) and rest of depot stakeholders., • Prepare and participate in the regular Service Affecting Failures SAFs meeting with the customer., • Coordination with external train Suppliers (subsystems) involved in warranty activities., • Oversee consignment spare parts stock to ensure availability (as per contract)., • Prepare and support internal process audits, • Ensure compliance with safety and environmental standards (EHS) in all warranty related activities (including visitor coming on behalf of Alstom). All about you We value passion and attitude over experience. That’s why we don’t expect you to have every single skill. Instead, we’ve listed some that we think will help you succeed and grow in this role: • University degree or Technical Engineering in Mechanical, Electrical, Electronic Engineering or similar., • 10 years of experience in the railway sector., • Knowledge in: project warranty execution, troubleshooting, commissioning, and EHS., • General knowledge of railway products and maintenance systems. Railway safety (preferred)., • Spanish mandatory and English level B2 is valuable. Things you’ll enjoy Join us on a life-long transformative journey – the rail industry is here to stay, so you can grow and develop new skills and experiences throughout your career. You’ll also: Enjoy stability, challenges and a long-term career free from boring daily routines Work with new security standards for warranty Collaborate with transverse teams and helpful colleagues Contribute to innovative projects Steer your career in whatever direction you choose across functions and countries Benefit from our investment in your development, through award-winning learning Benefit from a fair and dynamic reward package that recognises your performance and potential, plus comprehensive and competitive social coverage (life, medical, pension) You don’t need to be a train enthusiast to thrive with us. We guarantee that when you step onto one of our trains with your friends or family, you’ll be proud. If you’re up for the challenge, we’d love to hear from you! Important to note As a global business, we’re an equal-opportunity employer that celebrates diversity across the 70+ countries we operate in. We’re committed to creating an inclusive workplace for everyone.

🏢 About the company OMODA Motors, part of the Chery Group, is an international automotive brand expanding in Europe. Our European headquarters is in Barcelona, leading the brand’s development across the region. 📍 Work arrangement This position is based fully on-site (no remote) at our EU HQ office (Cornella, Barcelona). 💡 Why join us? • Join the legal team of a fast-growing global automotive company., • Play a key role in supporting EU business operations and ensuring legal compliance., • Gain exposure to cross-border legal matters in a dynamic international environment., • Work closely with business teams and external law firms across Europe., • Contribute to building a strong legal and compliance framework for EU operations., • Long-term career development opportunities within a global group. 🔧 Key responsibilities • Provide legal support and advice on business operations in EU., • Draft, review, and negotiate contracts, agreements, and other legal documents., • Handle legal disputes, claims, and litigation, coordinating with external law firms when necessary., • Provide guidance on labor law, data protection (GDPR), and corporate governance matters., • Conduct legal risk assessments and deliver solutions to mitigate potential risks., • Prepare regular legal reports and updates for management., • Support training sessions to enhance legal awareness within the company., • Support the other legal and compliance requirements of company. ✅ Requirements • Bachelor’s degree or above in Law; admission to practice law in Spain preferred., • 3+ years of legal experience, preferably in the automotive or manufacturing industries., • Strong knowledge of Spanish Civil law, labor law, commercial law, Catalan law, and requirements., • Experience in GDPR and corporate governance frameworks., • Fluent in Spanish and English; Chinese is a plus., • Excellent legal drafting, negotiation, and analytical skills., • Strong communication and problem-solving skills with business-oriented thinking., • Ability to work independently and manage multiple cases in a fast-paced environment. 🎁 What we offer • Opportunity to work in a global automotive group., • Exposure to international legal operations., • Multicultural working environment., • Long-term career development opportunities., • Salary: Negotiable.

At Revlon, the multinational cosmetic leader, we are looking for a Packaging Technical Specialist to join a dynamic, international environment and provide global support across all product categories. This role focuses on the management and maintenance of Bills of Materials (BOMs) and technical packaging specifications, and on coordinating compatibility testing between packaging materials and product formulas to ensure compliance with functional, regulatory, and quality standards. The position requires close collaboration with Packaging Development, Design, Formulation, Procurement, Quality, Production, and Innovation Operations teams, ensuring technical documentation is accurate and aligned with internal processes and external regulations. Key Responsibilities • Draft and maintain technical specifications and datasheets for primary packaging (jars, bottles, tubes) and secondary packaging (labels, folding cartons)., • Create, build, and update Bills of Materials (BOMs) and SKU structures., • Maintain active communication with suppliers to coordinate and implement packaging changes., • Ensure alignment between formulation and packaging components., • Coordinate and support packaging–formula compatibility testing with formulation and packaging testing teams., • Support packaging quality control activities and define standards for new components., • Provide quality-related information required to approve new packaging materials., • Update logistics data to reflect newly created product references., • Maintain and update project trackers in close collaboration with the Innovation Operations team, ensuring real-time visibility of milestones, deliverables, and cross-functional progress. Education and knowledge: • Bachelor’s degree in Packaging Engineering, Industrial Engineering, Chemical Engineering, or equivalent., • Knowledge of packaging materials and technologies., • Proficient in Excel., • Fluent in Spanish and English. Experience: • 1–3 years of experience in packaging-related roles., • Project Management experience would be a plus., • Experience in cosmetics, pharmaceutical, or consumer goods industries is a plus. Competencies: • Good communication, negotiation, and interpersonal skills., • Ability to collaborate effectively across cross-functional teams., • Strong analytical and problem-solving skills., • Attention to detail., • Ability to work under tight timelines and manage multiple priorities., • Organized and methodical.

Role Summary: We are seeking a diligent and detail-oriented Claims Executive to join our dynamic team. The individual will be responsible for managing and processing claims related to the shipment of goods, ensuring the efficient and fair resolution of issues while maintaining high levels of customer satisfaction. Employment Type: Permanent Reports to: General Counsel, Legal & Claims Location: Barcelona, Spain Role and Responsibilities: Claims Management • Receive, review, and process claims submitted by customers for damaged, lost, or delayed shipments., • Conduct thorough investigations to determine the validity and extent of claims., • Coordinate with relevant departments such as logistics, operations, and customer service to gather necessary information and documentation., • Assess the liability and calculate the compensation for valid claims based on company policies and regulations., • Prepare detailed claim reports and maintain accurate records of all claim activities., • Ensure timely resolution of claims in compliance with legal requirements and company standards., • Receive, review, and process claims submitted by customers for damaged, lost, or delayed shipments., • Conduct thorough investigations to determine the validity and extent of claims., • Coordinate with relevant departments such as logistics, operations, and customer service to gather necessary information and documentation., • Assess the liability and calculate the compensation for valid claims based on company policies and regulations., • Prepare detailed claim reports and maintain accurate records of all claim activities., • Ensure timely resolution of claims in compliance with legal requirements and company standards., • Handle claims for the various X-Press Feeders commercial hubs – Asia, Europe, Americas. This includes claims from/against customers, vessel owners, and terminals., • Report claims to and/or liaise with P&I clubs, correspondents, and surveyors., • Manage charterparty disputes and ensure time bars with customers, owners and terminals are adhered to., • Assist hubs with urgent requirements on carriage of cargos/LOI or other matters in consultation with the P&I club. Off-Hire Claims • Coordinate with LMs/operation managers to prepare off-hire statements and send them to owners within the timeline prescribed in the CP., • Follow up on recovery and closure of off-hire claims. Damage Reports • Handle container damage reports from customers and stevedore damage reports from vessel owners. Claim Updates • Provide daily updates to Europe and Americas hubs in respect of claim handling for incidents involving owned vessels., • Prepare bi-monthly updates for Fleet Management claims., • Manage claims involving subsidiary chartered vessels, such as crane breakdowns, stevedore damage, and claims from/against customers. CP Check • Perform CP checks against the fixture recap before the signature., • Communicate effectively with customers to provide updates on the status of their claims., • Address customer inquiries and concerns promptly and professionally., • Negotiate settlement agreements with customers when necessary to resolve disputes amicably., • Provide guidance to customers on the claim submission process and required documentation. Reporting and Analysis • Generate regular reports on claim activities, outcomes, and trends for management review., • Analyze claim data to identify areas for improvement and cost-saving opportunities., • Provide insights and recommendations based on claim analysis to support strategic decision-making. Requirements: Education and Experience • Bachelor’s degree in business administration, logistics, or a related field., • Minimum of 3-5 years of experience in claims handling, preferably within the shipping or logistics industry., • Familiarity with international shipping regulations and insurance practices. Skills and Competencies • Analytical Skills: Ability to assess complex situations and make informed decisions., • Communication Skills: Excellent verbal and written communication skills to interact with customers and internal teams effectively., • Detail-Oriented: Strong attention to detail to ensure accurate documentation and thorough investigations., • Problem-Solving: Ability to resolve disputes and negotiate settlements professionally., • Organizational Skills: Ability to manage multiple claims simultaneously and prioritize tasks efficiently., • Technical Proficiency: Proficient in using claims management software and Microsoft Office Suite (Word, Excel, PowerPoint). Personal Attributes • Integrity: High ethical standards and a commitment to fairness and transparency., • Resilience: Ability to handle challenging situations calmly and professionally., • Customer-Focused: Dedication to providing excellent service and ensuring customer satisfaction., • Team Player: Ability to work collaboratively with colleagues across different departments. Join our team and be part of an exciting journey towards personal and professional growth to make a real impact on global trade. If you are interested in the career opportunity, we invite you to apply today. We regret that only shortlisted candidates will be contacted. Attention to recruitment agencies: X-Press Feeders/Eastaway operates with a preferred supplier list (PSL) for recruitment purposes. As such, we will not be considering or accepting unsolicited applications from non-PSL agencies for the role currently available. We kindly request that you refrain from submitting applications on behalf of your clients. Thank you for your understanding and cooperation.

Hola Consultores, S.L. es una empresa especializada en la provisión de Servicios TIC e Ingeniería para la gestión empresarial, ofreciendo soluciones diseñadas a medida de las necesidades de nuestros clientes. 📍PARA BARCELONA Buscamos un/a Customer Service Specialist con francés y español para incorporarse a un proyecto fintech internacional. La persona seleccionada dará soporte a usuarios de una plataforma de inversión, garantizando una experiencia de cliente excelente y cumpliendo con los estándares regulatorios. Esta posición es ideal para perfiles junior con ganas de desarrollarse en áreas como operaciones, atención al cliente o compliance dentro del sector fintech. Responsabilidades • Gestionar consultas de clientes a través de email y canales escritos, • Asistir a usuarios con acceso a cuentas, pagos y consultas sobre su cartera, • Identificar incidencias y escalar casos complejos a los equipos correspondientes, • Garantizar el cumplimiento de procedimientos internos y normativas Requisitos • Nivel fluido o nativo de francés y español (imprescindible), • Atención al detalle y capacidad organizativa, • Actitud proactiva y ganas de aprender, • Capacidad para trabajar en equipo en un entorno internacional Se valorará • Experiencia previa en atención al cliente, • Interés en fintech, inversiones o servicios financieros, • Conocimiento básico de KYC o compliance Qué ofrecemos • Formación inicial completa, • Experiencia en entorno fintech regulado, • Exposición a áreas como operaciones, producto y compliance, • Ambiente internacional y dinámico, • Oportunidades reales de crecimiento Nos enorgullece ser una empresa 2.0 innovadora donde las personas son el centro de nuestra atención. La ética, transparencia, imparcialidad e independencia son valores fundamentales en nuestra filosofía, y también estamos comprometidos con la igualdad de género. Nos esforzamos por garantizar oportunidades equitativas para hombres y mujeres en todas las áreas de nuestro trabajo. Además, estamos firmemente a favor de la igualdad en todas sus formas y promovemos un entorno inclusivo donde cada individuo, independientemente de su género, religión, orientación sexual, etnia o cualquier otra característica, sea valorado y respetado. Si tu perfil se ajusta al puesto y estás emocionado en formar parte de nuestro equipo, ¡nos encantaría saber de ti!

Glovo is part of the Delivery Hero Group, the world’s pioneering local delivery platform, our mission is to deliver an amazing experience—fast, easy, and to your door. We operate in around 70 countries worldwide. Headquartered in Berlin, Germany. Delivery Hero has been listed on the Frankfurt Stock Exchange since 2017 and is part of the MDAX stock market index. Job Description • Manage a team based in Barcelona but also coordinate each legal PoC in each country where we are running our business (i.e. 22 countries), • Be part of the Legal leadership team, • Evaluate the People/Labour risks associated with the business and ensure appropriate procedures to mitigate them are implemented balancing business needs., • Assist the People department in adapting the business/Strategy needs to local regulations., • Take a strategic and medium/long term view of risk and compliance with Labour and People regulations creating awareness on the best practices among Glovo employee Qualifications • 8+ years of working experience as in-house legal counsel or in a reputed law firm., • Qualified Law Bachelor Degree in Spain, with a Master in Labour Law preferable., • Excellent English & Spanish speaking, • A 360º proven expertise / knowledge of labour law and People matters related., • Expertise in analysis and implementation of strategy balancing business needs., • Leadership and excellent people management skills. Proven ability to work and lead cross-functional teams in multinational context., • Proven experience working with the senior management., • Strong analytical skills, critical thinking, high impactful scope, results oriented, fast execution., • Excellent communication and presentation skills., • Hardworking, problem solver, organized, energetic, proactive., • Tech or industry experience as a plus. Additional Information Individuals representing diverse profiles, and abilities, encompassing various genders, ethnicities, and backgrounds, are less likely to apply for this role if they do not possess solid experience in 100% of these areas. Even if it seems you don't meet our musts don't let it stop you, we are all about finding the best talent out there! Skills can be learned, and embracing diversity is invaluable. We Believe Driven Talent Deserves 🌟 An enticing equity plan that lets you own a piece of the action. 💪 Top-notch private health insurance to keep you at your peak. 🍔 Monthly Glovo credit to satisfy your cravings! 💳 Discounts on transportation, food, and even kindergarten expenses. 🏊 Discounted gym memberships to keep you energized. 🏖️ Extra time off, the freedom to work from home two days a week, and the opportunity to work from anywhere for up to three weeks a year! 👪 Enhanced parental leave, and office-based nursery. 🧠 Online therapy and wellbeing benefits to ensure your mental well-being. Here at Glovo, we thrive on diversity, we believe it enhances our teams, products, and culture. We know that the best ideas come from a mashup of brilliant diverse minds. This is why we are committed to providing equal opportunities to talent from all backgrounds – all genders, racial/diverse backgrounds, abilities, ages, sexual orientations and all other unique characteristics that make you YOU. We will encourage you to bring your authentic self to work, fostering an inclusive environment where everyone feels heard. Feel free to note your pronouns in your application (e.g., she/her/hers, he/him/his, they/them/theirs, etc). So, ready to take the wheel and make this the ride of your life? Delve into our culture by taking a peek at our ___ and check out our ___ and ___!

R&D Manager - Medical Devices (High‑Risk Class III) - Freelance (6 Months) Location: Barcelona, Spain (On‑Site) Contract: 6‑month freelance contract with the possibility of a permanent offer Industry: High‑Risk Medical Devices About the Role We are seeking an experienced R&D Manager to lead the development of high‑risk Class III medical devices-specifically balloon catheters, vascular stents, or comparable interventional products. You will manage a multidisciplinary team of engineers and drive projects from early‑stage feasibility through design, verification, qualification, and transfer to manufacturing. Spanish language skills are not required. Full‑time on‑site presence in Barcelona is essential. Key Responsibilities R&D Leadership & Team Management • Lead and mentor a team of R&D engineers, providing technical direction, workload prioritization, and performance development., • Oversee daily engineering activities including design iterations, prototyping, test planning, and documentation., • Establish and enforce robust engineering processes aligned with global regulatory expectations. Design & Development of High‑Risk Devices • Own the full design life cycle, from concept development and feasibility testing through to final design freeze., • Drive detailed engineering work for balloon catheters, stents, or similar interventional devices, including:, • Balloon forming and bonding processes, • Stent design, coatings, and mechanical performance, • Catheter shaft architecture and material selection, • Tolerance analysis, DFM/A, material characterisation, • Lead Verification & Validation (V&V) strategy, including test method development, equipment qualification, and protocol/report generation. Qualification & Industrialisation • Manage design qualification, including performance testing, biocompatibility considerations, sterilisation validation input, and packaging qualification., • Oversee transfer of designs into manufacturing / scale‑up, collaborating with process engineering and suppliers. Project & Stakeholder Management • Act as project owner for multiple R&D programmes, managing timelines, budgets, risk registers, and resource allocation., • Coordinate with Quality, Regulatory, Clinical, and Operations teams to ensure coherent project execution., • Present project updates to leadership, aligning on strategy, risks, and technical decisions. Regulatory & Compliance (FDA and MDR) • Ensure all R&D activities adhere to Design Control requirements under 21 CFR 820 and EU MDR., • Lead or contribute to core regulatorydeliverables, including:, • Design History File (DHF), • Risk Management File (ISO 14971), • Design Inputs/Outputs, • Verification/Validation documentation, • Support regulatory submissions through technical report preparation and cross‑functional input. Required Experience • Minimum 3 years' experience in R&D management within the medical device sector., • Proven hands‑on experience with high‑risk Class III devices, preferably balloon catheters or stents., • Demonstrated ability to lead engineering teams and manage complex technical projects., • Strong understanding of Design Controls, Risk Management, V&V, and qualification activities., • Proficiency with FDA 21 CFR 820, EU MDR, ISO 13485, and ISO 14971., • Excellent organisational and communication skills., • Ability to work full‑time on site in Barcelona.

Are you ready to join a world leader in the exciting and dynamic fields of the Pharmaceutical and Medical Device industries? PQE Group has been at the forefront of these industries since 1998, with 40 subsidiaries and more than 2000 employees in Europe, Asia and the Americas. We are seeking a Senior Regulatory Affairs & Pharmacovigilance Specialist to support both local and international regulatory and PV activities. The role combines hands-on regulatory work with pharmacovigilance oversight, ensuring compliance across Spain and LATAM markets. Key Responsibilities Regulatory Affairs (RA): • Analyze EU regulatory strategies and provide recommendations to clients, • Author full technical dossiers (Modules 1–5) from scratch, • Manage variations, renewals, labeling updates, and Health Authority interactions, • Support regulatory activities in LATAM markets, • Support PV activities and reporting obligations in Spain and EU, • Ensure compliance with local and international safety regulations, • Assist in signal detection, risk management, and safety documentation, • Coordinate with global PV teams to align processes and reporting Requirements • 4–5 years of experience in Regulatory Affairs and/or Pharmacovigilance in pharma or consultancy, • Strong knowledge of EU and Spanish regulations, • Experience in global or corporate regulatory/PV environments, • Fluency in Spanish and English (C1–C2); Nice-to-Have knowledge of Italian and/or Portuguese, • Experience with LATAM regulatory/PV activities, • Exposure to Medical Devices, Veterinary, Cosmetics, or Food Supplements, • Strong interest in or experience with pharmacovigilance systems and processes Next Steps Upon receiving your application, if a match is found, the Recruiting department will contact you for an initial HR interview. If there's a positive match, a technical interview with the Hiring Manager will be arranged. In the case of a positive outcome coming from Hiring Manager interview, recruiter will contact you for further steps or to discuss our proposal. Alternatively, if the outcome is negative, we will contact you to halt the recruitment process. Working at PQE Group As a member of the PQE team, you will be part of a challenging, multicultural company that values collaboration and innovation. PQE Group gives you the opportunity to work on international projects, improve your skills and interact with colleagues from all corners of the world. If you are looking for a rewarding and exciting career, PQE Group is the perfect place for you. Apply now and take the first step towards an amazing future with us.

Are you ready to join a world leader in the exciting and dynamic fields of the Pharmaceutical and Medical Device industries? PQE Group has been at the forefront of these industries since 1998, with 40 subsidiaries and more than 2000 employees in Europe, Asia and the Americas. We are looking for a Process Validation Specialist to support validation activities related to aseptic filling operations within a GMP-regulated pharmaceutical manufacturing environment. Responsibilities include, but are not limited to: • Support the planning and execution of process validation activities related to filling operations., • Assist in the preparation and review of validation documentation, including protocols and reports., • Participate in Process Performance Qualification (PPQ) activities and other validation lifecycle activities., • Support data collection and analysis during validation runs and routine manufacturing., • Collaborate with Manufacturing, Quality Assurance, and Engineering teams to ensure GMP compliance., • Contribute to investigations, deviations, and CAPA actions related to filling processes., • Assist with risk assessments and continuous improvement initiatives for manufacturing processes., • Support preparation of documentation for internal audits and regulatory inspections. Required Qualifications: • Bachelor’s or Master’s degree in Pharmaceutical Sciences, Biotechnology, Chemical Engineering, Life Sciences, or a related field., • Minimum 1 year of experience in the pharmaceutical, biotechnology, or related regulated industry (internships or thesis projects are also considered)., • Basic knowledge of GMP and pharmaceutical manufacturing processes., • Strong organizational and analytical skills., • Ability to work effectively in cross-functional teams., • Fluent in English and Spanish Next Steps Upon receiving your application, if a match is found, the Recruiting department will contact you for an initial HR interview. If there's a positive match, a technical interview with the Hiring Manager will be arranged. In the case of a positive outcome coming from Hiring Manager interview, recruiter will contact you for further steps or to discuss our proposal. Alternatively, if the outcome is negative, we will contact you to halt the recruitment process. Working at PQE Group As a member of the PQE team, you will be part of a challenging, multicultural company that values collaboration and innovation. PQE Group gives you the opportunity to work on international projects, improve your skills and interact with colleagues from all corners of the world. If you are looking for a rewarding and exciting career, PQE Group is the perfect place for you. Apply now and take the first step towards an amazing future with us.

Are you ready to join a world leader in the exciting and dynamic fields of the Pharmaceutical and Medical Device industries? PQE Group has been at the forefront of these industries since 1998, with 40 subsidiaries and more than 2000 employees in Europe, Asia and the Americas. We are currently seeking an experienced Commissioning, Qualification & Validation (CQV) Consultant in Barcelona. This role will focus on the qualification and validation of equipment and systems in biotechnological production facilities. Responsibilities include, but are not limited to: • Execute commissioning, qualification, and validation activities for pharmaceutical/biotech equipment and systems., • Prepare, review, and execute C&Q and validation documentation (URS, DQ, IQ, OQ, PQ protocols, test scripts, and summary reports)., • Collaborate with cross-functional teams (Engineering, QA, Validation, Manufacturing) to ensure compliance with GMP, regulatory guidelines, and project timelines., • Review technical documentation, P&IDs, FAT/SAT protocols, and vendor manuals., • Identify, troubleshoot, and document deviations, ensuring timely resolution., • Ensure all activities meet GMP, FDA, EMA, and ICH requirements., • Provide project updates and progress reports to stakeholders. Required Qualifications: • Bachelor’s degree in Engineering, Life Sciences, or related field., • At least 1 year of experience in IQ/OQ/PQ protocol development and execution and C&Q for pharmaceutical/biotech facilities, including construction of production plants, • Strong knowledge of GMP, FDA, and EU regulations., • Excellent analytical, problem-solving, and communication skills., • Ability to work independently and collaboratively in a project environment., • Spanish native, English fluent (at least B2) Next Steps Upon receiving your application, if a match is found, the Recruiting department will contact you for an initial HR interview. If there's a positive match, a technical interview with the Hiring Manager will be arranged. In the case of a positive outcome coming from Hiring Manager interview, recruiter will contact you for further steps or to discuss our proposal. Alternatively, if the outcome is negative, we will contact you to halt the recruitment process. Working at PQE Group As a member of the PQE team, you will be part of a challenging, multicultural company that values collaboration and innovation. PQE Group gives you the opportunity to work on international projects, improve your skills and interact with colleagues from all corners of the world. If you are looking for a rewarding and exciting career, PQE Group is the perfect place for you. Apply now and take the first step towards an amazing future with us.

EBRO SUV is looking for an enthusiastic Vehicle Data Control Administrative professional to join our Vehicle Lifecycle Data Control team. This profile will play a key role in coordinating and managing engineering changes related to vehicle components and systems, ensuring all updates are properly assessed, validated, documented, and communicated across the organization. The position requires a highly organized and detail-oriented individual with strong collaboration skills and a solid understanding of automotive processes and data management systems. Key Responsibilities: • Monitor and control change data for vehicle components and systems, ensuring compliance with EBRO system standards., • Ensure proper documentation, approval, and communication of all product changes across departments such as R&D, Quality, Purchasing, Manufacturing, and After-Sales., • Maintain accurate configuration control and product data records within PLM or change management systems., • Collaborate with cross-functional teams to support the smooth implementation of approved design changes into production., • Contribute to the continuous improvement of change management methodologies, tools, and documentation standards., • Ensure all engineering changes comply with homologation and regulatory requirements. Required Skills, Qualifications and Experience: • Intermediate or Higher Technical Certificate in Business Administration or related field., • 1–3 years of experience in product change management, configuration management, or engineering coordination within the automotive or industrial sector., • Solid understanding of vehicle systems, components, and manufacturing processes., • Experience with PLM and change management systems (e.g., Siemens Teamcenter, Windchill, ENOVIA) and SAP., • Strong organizational, analytical, and documentation skills., • Fluent in English (written and spoken); Chinese is a plus., • Ability to collaborate effectively with cross-functional and international teams. We are one of the most challenging projects in the Automotive Industry today in Spain, relaunching an iconic brand in the market. We are looking for talented people who share this mission and want to create a positive impact by joining a dynamic and forward-thinking team.

About Our Organization: Dow Jones is a global provider of news and business information, delivering content to consumers and organizations around the world across multiple formats, including print, digital, mobile and live events. Dow Jones has produced unrivaled quality content for more than 130 years and today has one of the world's largest news-gathering operations globally. It is home to leading publications and products including the flagship Wall Street Journal, America's largest newspaper by paid circulation; Barron's, MarketWatch, Mansion Global, Financial News, Investor's Business Daily, Factiva, Dow Jones Risk & Compliance, Dow Jones Newswires, OPIS and Chemical Market Analytics. Dow Jones is a division of News Corp (Nasdaq: NWS, NWSA; ASX: NWS, NWSLV). About the Team: Our Technology team drives the evolution of our Technology, Engineering, Data, Product and User Experience functions. With a keen focus on delivering cutting-edge solutions, we shape the digital landscape for our customers, readers, and users. From revolutionizing visuals to optimizing tools and harnessing the power of data, mobile, video, and social platforms, our team is committed to providing a seamless and immersive experience across all touchpoints. Collaborating closely with our newsrooms and strategic partners, we spearhead the development of groundbreaking products and technologies. About the Role: You will implement digital tagging and measurement for Dow Jones portfolio of Digital products, including websites, mobile apps and connected device apps. You will work with product, engineering, design, analytics, marketing, and business team members to capture the data needed to lead our decisions. You will: • Following Dow Jones standards, design analytics tracking specifications for Dow Jones digital products and platforms, including web, mobile apps, off-platform, and connected device (OTT) platforms, • Partner with internal and external development teams to test and deploy new tracking solutions while monitoring and optimizing existing integrations, • Be a Data Steward for usage data., • Manage tag management systems and data collection tools., • Work with data collection and analytics vendors to get the most out of systems and services., • Run end-to-end testing, QA, QC, and debugging of analytics code using various tools (Observepoint, Adobe Debugger, Charles or Firebug, etc)., • Confirm the quality of the data collected in analytics tools (Adobe, Piano, Google Analytics) and databases (BigQuery, Athena, Snowflake) with SQL, • Keep documentation up to date. You have: • College degree or technical degree in computing, business data management, analytics, digital marketing or equivalent experience. Advanced degrees welcome., • Up to 2 years of experience in a technology role, in a data intensive environment., • Minimum 1-2 years of SQL experience and understanding of data configuration and databases., • Understanding of digital products, tracking and data collection processes, and platforms., • Experience with Adobe Analytics, Tealium, or Google Analytics a plus., • Up to 2 years working with data; with a focus on data quality, identifying data issues, sources., • Experience in media industry and understanding of industry key metrics., • Familiarity with technical project implementation, including all phases from requirements, development, quality assurances, and launch., • Focus on data quality., • Web development knowledge, specifically an ability to be hands on with HTML, CSS, JavaScript, and Web Services, • Analytical thought process to identify what data may be needed to measure user engagement with products., • Experience creating detailed technical documentation with an understanding of marketing and operations management and processes. Our Benefits • Comprehensive Healthcare Plans for you and your family (paid by Dow Jones), • Extra paid Time Off (30 days of holidays/year), • Possibility to work remotely for 3 months/year (desplazamiento program) or one week of remote work per quarter, • Meal benefit with Pluxee (171€/month on top of your salary), • Retirement Plans (Dow Jones will pay 2% of a members Pensionable Salary and match employee contribution up to a maximum of 3 %)., • Comprehensive Insurance Plans, • Well-being Resources (200 USD allowance per quarter, Classpass, etc.), • Family Care Benefits & Caregiving Support, • Subscription Discounts, • Employee Referral Program