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Job Title: Senior Software Test Engineer - Lingo About Lingo At Lingo, we’re building the future of personal health insights through always-on biosensor data, real-time analytics, and personalized recommendations. Our platform ingests millions of readings daily, delivering clinically relevant insights to consumers and partners across the globe. As we expand across multiple regions, software quality and verification are mission-critical to ensuring our systems are scalable, secure, compliant, and able to support innovation across product, engineering, and R&D. The Opportunity We are seeking a Senior Software Test Engineer to lead verification and validation efforts across our cloud, web, and mobile platforms within a regulated medical device environment. This role is based in our hub in Barcelona, Spain, and plays a critical role in ensuring product quality, regulatory compliance, and scalable delivery across our digital health ecosystem. This is an exciting opportunity for someone with deep experience in software verification, quality engineering, and test automation who is passionate about building quality into the software lifecycle and enabling teams to deliver high-confidence releases. What you’ll do • Lead end-to-end software verification and validation activities across cloud, web, and mobile platforms., • Translate product, system, and technical requirements into effective manual and automated test strategies, plans, and cases., • Design, build, and scale robust test automation frameworks across API, web, and mobile layers., • Drive an automation-first testing approach by identifying automation opportunities and improving coverage, reliability, and execution speed., • Integrate automated testing into CI/CD pipelines to support fast, reliable, and scalable software delivery., • Ensure traceability between requirements, risks, and test cases in alignment with regulated development practices., • Define and execute functional, integration, system, and regression testing strategies., • Develop and maintain verification artifacts, including plans, protocols, and reports, in compliance with FDA 21 CFR, ISO 13485, IEC 62304, and related standards., • Support risk management activities including defect triage, impact assessments, and root-cause investigations., • Partner closely with engineers, product managers, architects, and quality teams to ensure requirements are testable and quality is embedded early in the development lifecycle., • Participate in design reviews to verify that design inputs and outputs meet quality and regulatory expectations., • Mentor other engineers on automation best practices, engineering discipline, and continuous improvement across testing frameworks, tools, and processes. Required Qualifications • Bachelor’s degree in software engineering, Computer Science, or a related field, or equivalent practical experience., • 6+ years of experience in software test engineering, verification, or quality engineering., • 2+ years of experience in regulated software development environments such as medical devices, digital health, or similar industries., • Strong expertise in software verification and validation, including defect management, requirements traceability, and risk-based testing., • Demonstrated experience designing and implementing automated testing across API, web, mobile, or similar platforms., • Experience working within modern CI/CD ecosystems such as GitHub Actions, Azure Pipelines, or similar tooling., • Strong programming or scripting skills in languages such as Python, JavaScript, or TypeScript for test automation and tooling., • Excellent analytical, communication, and documentation skills, with a collaborative and quality-focused mindset. Preferred Qualifications • Experience in medical devices or other regulated environments., • Hands-on experience with frameworks such as Playwright, Cypress, REST Assured, Jest, or similar tools., • Experience with BDD automated testing and integration with Jira test management tools such as Xray or Zephyr., • Understanding of cloud-native systems, APIs, microservices, and distributed architectures., • A builder mindset, with the ability to continuously improve frameworks, tooling, and quality processes., • Exposure to compliance standards such as HIPAA and GDPR., • Experience with end-to-end testing involving both software and connected hardware components., • Ownership mentality, with a focus on driving quality across the full system rather than only individual test cases. Lingo Culture Customer-first, quality-driven, growth-minded, and united. At Lingo, Senior Software Test Engineers play a key role in building trust in our products by ensuring software is verified rigorously, released responsibly, and designed to meet the needs of users in a highly regulated environment.

Descripció de l’oferta vacant 🏫 Centre: Escola Universitària Mediterrani (EUM) – Universitat de Girona Ubicació: Barcelona Departament: Empresa Àrea de coneixement: Màrqueting, Direcció Comercial i Gestió de Serveis Tipus de contractació: Temps parcial 📚 Assignatura a impartir: La vacant docent correspon al Grau en Màrqueting: • _ – 6 ECTS Aquesta assignatura aprofundeix en les particularitats del màrqueting de les empreses industrials, també conegut com a màrqueting B2B, i del màrqueting de serveis. S’hi treballen la satisfacció, la qualitat percebuda i l’experiència de client com a elements clau de la gestió empresarial, amb una orientació eminentment aplicada i connectada amb situacions reals de mercat. L’assignatura té com a objectiu proporcionar a l’estudiantat eines per entendre i desenvolupar estratègies comercials en l’àmbit B2B i en el sector serveis, definir estratègies de gestió de clients i força de vendes, dissenyar models d’avaluació de l’experiència de client i obtenir dades rellevants en entorns digitals per a la presa de decisions de màrqueting. Continguts principals de l’assignatura: • Introducció al màrqueting industrial i de serveis., • Diferències entre B2B i B2C., • Màrqueting transaccional i màrqueting relacional., • Màrqueting de serveis: captació, fidelització, innovació i ús de tecnologies digitals., • Experiència de client, Customer Journey Map, Customer Experience Management, satisfacció, qualitat percebuda i NPS., • Gestió de la qualitat, qualitat total, models, normes i auditoria de qualitat., • Màrqueting industrial, gestió de clients B2B, força de vendes i estratègies de segmentació, posicionament, diferenciació, producte, preu, distribució i comunicació. Horari de classe: Dimarts i Divendres de 16:00 a 19:00 Semestre: primer semestre del curs acadèmic 2026/2027 (setembre - gener) Modalitat: docència presencial Idioma d’impartició: català i/o castellà 👩 🏫 Requisits mínims: • Titulació universitària en Màrqueting, Administració i Direcció d’Empreses, Economia, Investigació i Tècniques de Mercat, Direcció Comercial, Relacions Internacionals, Enginyeria Industrial amb especialització en gestió comercial, o àmbits afins., • Experiència docent en màrqueting B2B, màrqueting de serveis, direcció comercial, gestió de clients, força de vendes, customer experience, qualitat de servei o consultoria empresarial., • Coneixement de metodologies docents aplicades, aprenentatge basat en casos, treball en equip i activitats orientades a la resolució de problemes empresarials., • Competència per impartir docència en català (Nivell C1) i castellà (Nivell C1)., • Coneixement suficient d’anglès per integrar bibliografia, terminologia i recursos docents en aquesta llengua., • Disponibilitat per impartir docència presencial a l’EUM. Es valorarà: • Doctorat., • Acreditació AQU o ANECA., • Experiència docent universitària prèvia., • Experiència professional en entorns B2B, empreses de serveis, direcció comercial, consultoria de màrqueting, CRM, gestió de qualitat, customer experience o transformació digital de la funció comercial., • Coneixement d’eines digitals aplicades al màrqueting, CRM, analítica de clients, gestió de dades online, social listening, automatització comercial o business intelligence., • Experiència en la direcció o formació d’equips comercials i força de vendes., • Participació en projectes de recerca, transferència o innovació vinculats al màrqueting, la gestió de clients, la qualitat de servei, l’experiència de client o la direcció comercial., • Nivell C1 de català. 📊 Barem de valoració del CV – 100 punts • Titulació acadèmica adequada: 10 punts, • Doctorat: 10 punts, • Acreditació AQU o ANECA: 10 punts, • Experiència docent universitària: 20 punts, • Experiència professional rellevant en màrqueting B2B, màrqueting de serveis, direcció comercial o customer experience: 15 punts, • Recerca, publicacions o transferència vinculades a l’àmbit de l’assignatura: 15 punts, • Competències digitals i docents, incloent-hi l’ús de Moodle o plataformes similars: 10 punts, • Innovació docent, aprenentatge basat en casos o coneixement aplicat a l’empresa: 5 punts, • Català C1: 5 punts Candidatures i procés de selecció Les persones candidates hauran d’enviar el seu CV, l’acreditació dels nivells lingüístics i una breu proposta docent de l’assignatura abans del 5 de juliol de 2026. El procediment de selecció constarà de les fases següents: Fase 1 – Recepció de candidatures Les candidatures es rebran fins al 5 de juliol de 2026. Fase 2 – Avaluació de candidatures Totes les candidatures rebudes dins del termini establert seran valorades d’acord amb el barem de CV inclòs en aquesta convocatòria. Fase 3 – Entrevista Les tres persones candidates amb millor puntuació que hagin obtingut una valoració superior a 50 punts en la fase d’avaluació seran preseleccionades per a una entrevista. L’EUM valora l’excel·lència acadèmica, la rellevància professional, la innovació docent, la diversitat i la inclusió. Animem a presentar candidatura a professionals compromesos amb l’aprenentatge actiu, l’orientació al client, la perspectiva internacional, la pràctica ètica i la construcció d’un entorn d’aprenentatge respectuós.

Contexto El Barcelonaβeta Brain Research Center (BBRC) es un centro de referencia en la investigación de la prevención de la enfermedad de Alzheimer y el estudio de funciones cognitivas en el envejecimiento sano y patológico. Fundado por la Fundació Pasqual Maragall en colaboración con la Universitat Pompeu Fabra, el BBRC tiene como misión aportar soluciones innovadoras para descifrar y prevenir los cambios biológicos y la disfunción cognitiva asociados a enfermedades neurodegenerativas .El centro forma parte del Parc de Recerca Biomèdica de Barcelona (PRBB), en un entorno multidisciplinario y colaborativo, con acceso a instalaciones científicas de última generación, incluyendo escáner 3T MR, espacios para ensayos clínicos y EEG, así como un ecosistema internacionalmente estimulante para la investigación traslacional . Descripción de la posici ón Buscamos un CRA freelance para el proyecto DED PET, que pueda dar soporte a la monitorización completa del estudio desde la fase de Start-Up hasta el Close-Out, gestionando el seguimiento de manera ágil y autónoma sin necesidad de incorporación estructur al. Responsabilidades princip • ales Participar en actividades de site start-up, incluyendo revisión de documentación esen • cial.Elaborar y ejecutar el plan de monitorización del est, • udio.Realizar visitas de monitorización en los centros participantes (4) asegurando el cumplimiento del protocolo, GCP y requisitos regulato, • rios.Revisar la correcta cumplimentación de los consentimientos informados y documentación de los investigad, • ores.Verificar datos en eCRF y documentación fuente, asegurando coherencia y complet, • itud.Gestionar desviaciones, queries y acciones correctivas (CAPA), con seguimiento hasta su ci, • erre.Preparar informes de monitorización y documentación asociada dentro de los plazos establec, • idos.Apoyar en la gestión del, • TMF.Participar en reuniones de seguimiento con el promotor (BBRC) y colaborar en auditorías e inspecciones regulato, • rias.Crear materiales de formación sobre el estudio para los distintos cen tros. Requ • isitos Grado en Enfermería, Farmacia, Biomedicina, Biología, Biotecnología, Ciencias Biomédicas o s • imilar.Formación acreditada en Buenas Prácticas Clínicas, • (GCP).Formación específica en monitorización o gestión de ensayos cl, • ínicos.Mínimo 2–3 años de experiencia como CRA en ensayos clínicos, incl, • uyendo:Gestión de TMF y documentación es, • encial.Site start-up y clo, • se-out.Revisión de consentimientos y verificación de dato, • s/eCRF.Gestión de queries, desviaciones y CAPA. Competencias pe • rsonales Autonomía y capacidad de monitorización indep • endiente.Planificación eficiente del calendario de, • visitas.Atención al detalle en datos y documentación, • esencial.Interacción efectiva con investigadores, coordinadores, técnicos y, • sponsor.Comunicación pedagógica de requerimientos y corr, • ecciones.Capacidad de anticipar riesgos y proponer, • mejoras.Flexibilidad para trabajar en entornos multicéntricos con recursos l imitados.

🏋️ ♂️ Buscamos Entrenador/a Personal a Domicilio para formar parte de Hominem Curatio. En Hominem Curatio creemos que el ejercicio puede cambiar vidas. Y no hablamos solo de mejorar la forma física. Trabajamos en los hogares de personas mayores ayudándoles a recuperar movilidad, autonomía, seguridad y confianza en sí mismos. Nuestro trabajo combina entrenamiento basado en evidencia científica con algo imprescindible: cercanía, empatía y trato humano. Aquí no vienes solo a dirigir entrenamientos. Vienes a generar un impacto real. ¿Qué conseguirás con tu trabajo? • Ayudar a prevenir caídas y pérdida de movilidad, • Mejorar la autonomía y calidad de vida de las personas mayores, • Acompañar procesos de recuperación física y emocional, • Devolver independencia… y muchas veces ilusión Porque cuando el ejercicio tiene propósito, los resultados van mucho más allá del cuerpo. 📍 Zona de trabajo: Barcelona 🏡 Trabajo a domicilio 🕓 Jornada parcial de 20h semanales ⭐Horario: lunes a viernes de 10:00 a 14:00 y de 16:00 a 20:00 (Según sesión) 💰 Salario aproximado: 13.000€ brutos/año + plus de transporte 📈 Posibilidad de ampliar horas según disponibilidad ¿Qué buscamos? • Graduados/as en Ciencias de la Actividad Física y del Deporte (o similar), • Entrenadores/as personales con vocación de ayuda, • Personas empáticas, cercanas y con sensibilidad hacia las personas mayores, • Capacidad para adaptar el ejercicio a cada situación y necesidad, • Ganas de aprender, aportar valor y trabajar con propósito. Valoraremos especialmente: • Formación o experiencia en geriatría, • Experiencia en entrenamiento adaptado o poblaciones especiales Requisito imprescindible: • Vehículo propio y distintivo/etiqueta ambiental para poder circular., • Si sientes que tu profesión puede ser mucho más que entrenar en un gimnasio y quieres formar parte de un proyecto humano con impacto real, queremos conocerte. 📩 Envíanos tu candidatura o comparte esta oferta con alguien que encaje.

Docente PRL Sector Automoción y Aeroespacial (Barcelona) En Bureau Veritas Business School estamos buscando un/a docente especializado/a en Prevención de Riesgos Laborales para impartir dos acciones formativas presenciales dirigidas a estudiantes universitarios que participan en proyectos de innovación tecnológica relacionados con la automoción y el sector aeroespacial. Cursos a impartir 🚗 PRL aplicada a baterías de litio en proyectos de automoción • Riesgos asociados a baterías de litio., • Manipulación segura de componentes., • Riesgo eléctrico., • Almacenamiento y actuación ante emergencias., • Medidas preventivas en entornos de fabricación y ensamblaje. 🚀 PRL aplicada a proyectos aeroespaciales • Riesgos asociados al uso y manipulación de sustancias explosivas y pirotécnicas., • Prevención en actividades de fabricación y ensamblaje., • Seguridad en ensayos y pruebas., • Medidas de protección y actuación ante emergencias., • Normativa y buenas prácticas del sector. Requisitos ✅ Formación técnica relacionada con Ingeniería Industrial, Aeroespacial, Química, Automoción, Seguridad Industrial o similar. ✅ Experiencia profesional en alguno de los siguientes ámbitos: • Automoción., • Baterías de litio., • Seguridad industrial., • Aeroespacial., • Explosivos o pirotecnia., • Prevención de Riesgos Laborales. ✅ Valorable experiencia docente. Condiciones: 📍 Modalidad: Presencial. 📍 Ubicación: Barcelona. 📅 Fechas: Sábados de septiembre. ⏱️ Duración: 16 horas por curso (32 horas totales). Si cuentas con experiencia en estas áreas y te interesa colaborar con nosotros como docente, nos encantará conocerte.

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. About the role We are currently seeking a Senior Clinical Trial Assistant (Sr CTA) to take ownership of the operational coordination of assigned studies and contribute with increasing autonomy throughout the study lifecycle. Reporting to the Clinical Operations Development Manager (CODM), you will be part of the Clinical Operations team, playing a key role in ensuring the smooth execution of clinical trials. While you will collaborate with the Regulatory & CTA team when needed, your primary focus will be on clinical operations. Key Responsibilities • Coordinate the day-to-day operations of assigned studies, including TMF maintenance, logistics and milestone tracking., • Maintain and organize the Trial Master File (TMF), ensuring documentation is accurate, complete and up to date., • Monitor and update study milestones, enrollment data and site activity in the CTMS, proactively identifying delays or inconsistencies., • Reconcile data across CTMS, eTMF and IRT systems, flagging discrepancies early., • Support logistics related to central labs, IRT systems and study materials., • Assist CRAs with site documentation and operational follow-up., • Actively participate in study team meetings, contributing with a clear operational perspective., • Collaborate on regulatory submissions (CTIS), EC/RA notifications and site contract management as required., • Support the onboarding of junior CTAs and contribute to keeping operational SOPs updated. What You Bring • 3–5 years of experience as a CTA in clinical trials., • Hands-on experience with eTMF, CTMS and CTIS., • Solid knowledge of ICH-GCP and EU CTR., • Ability to manage multiple studies simultaneously and effectively prioritize in a fast-paced environment., • A proactive mindset with the ability to work independently and take initiative., • Proficiency in written English; spoken English is a plus. Spanish required. What Will Set You Apart • Experience in a CRO or other fast-paced clinical research environments., • Proven ability to identify and improve operational processes., • Strong collaboration skills and adaptability to evolving priorities., • Experience mentoring or training colleagues. What We Offer Join an organization committed to impactful, cutting-edge research: • A role with autonomy to manage your studies and grow your operational expertise., • Exposure to a diverse portfolio of studies, sponsors and investigators., • Career development opportunities towards broader clinical roles., • A collaborative team environment within a meaningful phase of transformation. In addition, we provide: • Full-time position (38 hours/week) based in Barcelona., • Hybrid work model: up to 3 days remote per week., • Flexible working hours to support work-life balance., • Meal voucher (Ticket Restaurant)., • Free English classes for professional development., • Complimentary coffee and fresh fruit in the office., • 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: www.gruposolti.org

Descripció de l’oferta vacant 🏫 Centre: Escola Universitària Mediterrani (EUM) – Universitat de Girona Ubicació: Barcelona Departament: Empresa Àrea de coneixement: Màrqueting i Direcció Comercial Tipus de contractació: Temps parcial 📚 Assignatura a impartir: La vacant docent correspon al Grau en Màrqueting: • _ – 6 ECTS Aquesta assignatura aprofundeix en el paper estratègic del preu dins del màrqueting mix i en la seva incidència en el posicionament, la rendibilitat i la competitivitat de les empreses. S’hi treballen els principals mètodes de fixació de preus, l’anàlisi de costos, la demanda, el valor percebut, la competència, les estratègies de preus en entorns digitals i internacionals, així com la presa de decisions orientada al mercat. Horari de classe: dilluns i dimarts de 16:00 a 19:00 Semestre: 1r semestre del curs acadèmic 2026/2027 (setembre - gener) Modalitat: docència presencial Idioma d’impartició: català i/o castellà 👩 🏫 Requisits mínims: • Titulació universitària en Màrqueting, Administració i Direcció d’Empreses, Economia, Investigació i Tècniques de Mercat, Direcció Comercial o àmbits afins., • Experiencia docent en màrqueting, estratègia de preus, direcció comercial, vendes, revenue management, consultoria comercial o àrees relacionades., • Coneixement de metodologies docents innovadores, aprenentatge aplicat i treball amb casos pràctics., • Nivell C1 de català: obligatori., • Disponibilitat per impartir docència presencial a l’EUM. Es valorarà: • Doctorat., • Acreditació AQU o ANECA., • Experiència docent universitària prèvia., • Experiència professional en estratègia de preus, direcció comercial, màrqueting estratègic, revenue management, consultoria o gestió de producte., • Coneixement d’eines digitals aplicades a l’anàlisi de mercat, pricing, CRM, business intelligence o analítica comercial., • Nivell C1 de castella., • Nivell C2 d’anglès acreditat., • Participació en projectes de recerca, transferència o innovació vinculats al màrqueting, la direcció comercial, el comportament del consumidor o l’estratègia empresarial. 📊 Barem de valoració del CV – 100 punts • Titulació acadèmica adequada: 10 punts, • Doctorat: 10 punts, • Acreditació AQU o ANECA: 10 punts, • Experiència docent universitària: 20 punts, • Experiència professional rellevant en màrqueting, pricing o direcció comercial: 15 punts, • Recerca, publicacions o transferència vinculades a l’àmbit de l’assignatura: 15 punts, • Competències digitals i docents, incloent-hi l’ús de Moodle o plataformes similars: 10 punts, • Innovació docent, aprenentatge aplicat o transferència de coneixement: 5 punts, • Anglès C2: 5 punts Candidatures i procés de selecció Les persones candidates hauran d’enviar el seu CV, l’acreditació dels nivells lingüístics i una breu proposta docent de l’assignatura abans del 5 de juliol de 2026. El procediment de selecció constarà de les fases següents: Fase 1 – Recepció de candidatures Les candidatures es rebran fins al 5 de juliol de 2026. Fase 2 – Avaluació de candidatures Totes les candidatures rebudes dins del termini establert seran valorades d’acord amb el barem de CV inclòs en aquesta convocatòria. Fase 3 – Entrevista Les tres persones candidates amb millor puntuació que hagin obtingut una valoració superior a 50 punts en la fase d’avaluació seran preseleccionades per a una entrevista. L’EUM valora l’excel·lència acadèmica, la rellevància professional, la innovació docent, la diversitat i la inclusió. Animem a presentar candidatura a professionals compromesos amb l’aprenentatge actiu, la perspectiva internacional, la pràctica ètica i la construcció d’un entorn d’aprenentatge respectuós.

Who are we? AESA Prep Academy of Barcelona is an international, American high school that offers grades 9 to 12. Our campus forms part of the AESA International School System, with schools in Texas and online. We are an international school accredited by Cognia and the Generalitat of Catalonia. https://aesaprepbarcelona.com/ Our team currently consists of a group of education professionals, all with different nationalities and backgrounds, working to provide an impactful and positive learning experience to all our high school students. We are seeking a teacher who is passionate about education and committed to the success of our students and our organization. The person joining our team is proactive, organized, works well on a diverse team, and has a positive attitude. What would you do? • Give face-to-face lessons in small classes., • Plan, evaluate, and revise curriculum, course content, course materials and instructional methods., • Prepare course materials such as syllabi, homework assignments, activities and experiments., • Evaluate student performance and share continuous feedback with the coordinator(s), parents and other relevant stakeholders., • Maintain student attendance, grades, and other required records., • Record student performance through our learning management system. Minimum Requirements: • Bachelor’s degree or equivalent in the field of Mathematics and a teaching certification, or advanced degree in the field of Mathematics., • At least 2-3 years of teaching experience., • C1 proficiency level in English (written and verbal)., • Excellent creative, communication, and presentation skills., • Engaging personality and dynamic teaching style. Preferred Requirements: • Advanced degree in the field of Mathematics and a teaching certification., • 5+ years of teaching experience., • C2 proficiency level in English (written and verbal)., • Excellent creative, communication, and presentation skills., • Engaging personality and dynamic teaching style. What do we offer? • Competitive salary, • Professional development opportunities, • Friendly working environment, • Opportunities for career advancement within the organization Schedule: Monday to Friday, from 9am until 4pm. All applications must be sent directly to: jpinho@aesaprepbarcelona.com with a motivation letter. Important: The candidate must have residency in Barcelona, Spain. Applications not following the above instructions will be automatically disregarded.

PAULSON es una firma de inversión inmobiliaria especializada en el mercado residencial de obra nueva en España. A través de su división de Lending financia a promotores y proyectos de desarrollo residencial de obra nueva en España mediante préstamos y líneas de crédito con garantía hipotecaria. Con más de 120 operaciones firmadas y más de 170 millones de euros invertidos, la firma combina criterio técnico propio y relación directa con el promotor a lo largo de toda la vida del préstamo. Misión del puesto El/la Project Monitoring Analyst se integrará en el área de Project Monitoring de la firma y reportará directamente al Head of Project Monitoring, a quien trasladará de forma periódica el estado y el avance de las obras del portfolio. Será responsable de supervisar y analizar el avance técnico y económico de los proyectos financiados por la firma, asegurando el cumplimiento de plazos, presupuestos y estándares de calidad. Realizará visitas a obra para verificar los avances reales. Actuará como puente entre la firma y el promotor y garantizará que las disposiciones del préstamo se ajusten al avance de obra real verificado. Responsabilidades principales · Revisar y validar los avances de obra y certificaciones del promotor/constructor. · Realizar visitas periódicas a las obras para verificar el estado de ejecución. · Analizar desviaciones en costes, plazos y/o calidad y proponer medidas correctivas. · Coordinarse con equipos técnicos externos e internos. · Preparar informes de Project Monitoring para el Comité de Inversiones y el equipo de análisis. · Validar las certificaciones de obra y las facturas asociadas a cada disposición mensual del préstamo, asegurando que cada disposición se corresponde con el avance de obra realmente ejecutado y verificado en campo. · Colaborar con el resto del equipo en los procesos de Due Diligence técnica previa a nuevas financiaciones. · Monitorizar riesgos técnicos, urbanísticos y de construcción que puedan afectar a la inversión. Formación y experiencia · Formación en Arquitectura, Arquitectura Técnica, Ingeniería Civil o similar. · Experiencia mínima de 3 a 5 años en Project Monitoring, Project Management, consultoría técnica o dirección de obra. Conocimientos técnicos · Conocimiento sólido de normativa urbanística y de construcción en España. · Conocimiento de las fases del proyecto de promoción inmobiliaria y su documentación. · Habilidad para el análisis de presupuestos de obra y lectura de certificaciones. · Dominio alto de Excel para el control financiero de promociones y obras. Movilidad · Disponibilidad para viajar y carnet de conducir. Se valorará · Experiencia trabajando con promotores, fondos o entidades financieras. · Nivel alto de inglés. Competencias clave · Criterio técnico para evaluar la viabilidad y el avance real de la obra frente a lo certificado. · Rigor analítico y crítico en el control de costes, plazos y desviaciones presupuestarias. · Capacidad para vincular el avance físico de la obra con las disposiciones y los hitos del préstamo. · Visión de riesgo orientada a proteger la inversión (técnico, urbanístico y de construcción). · Comunicación clara. · Autonomía, capacidad de organización y disposición para el trabajo de campo.

MSCA candidate Do you want to develop your career understanding the role of polyP in cancer and neurodegenerative diseases? We are seeking a suitable candidate to apply for a Marie Skłodowska-Curie Actions Postdoctoral Fellowship in the September 2026 call. What we offer: An innovative research project combining molecular biology, cell biology, biochemistry, microscopy, and disease-relevant cellular models, in a dynamic and international scientific environment with access to state-of-the-art facilities. We will provide scientific guidance, institutional support, and feedback throughout the application process — and strong support for career development, training, and networking. We are a research group based in Barcelona, Spain, led by Josep Clotet and devoted to the study of polyphosphate (polyP) — a polymer of inorganic phosphate present in all living organisms whose roles in mammalian cells are still poorly understood, with emerging links to cancer, neurodegeneration, inflammation, and protein homeostasis. Find our latest relevant contributions: NAR 2026. _ Methods 2025. _ Cell Rep 2021. _ Full publication list: _ We are looking for a candidate with: A PhD in biology, biochemistry, biotechnology, neuroscience, cancer biology, molecular medicine, or a related field. A strong interest in fundamental mechanisms of disease. Experience in cell culture, molecular biology, microscopy, protein analysis, or omics approaches. Good communication skills and the ability to work independently and collaboratively. A competitive scientific track record appropriate to apply to MSCA. Interested candidates should send a CV, a brief motivation letter, and the contact details of two referees to: jjimenez@uic.es Please include in the subject line: MSCA 2026 – polyP project Applications reviewed on a rolling basis — apply as soon as possible and no later than July 22nd. #PostdocPositions #MSCA2026 #CancerResearch #Biochemistry #Neuroscience #OpenPosition #Barcelona

Faculty Recruitment – 2026/2027 Academic Year At ESIC Barcelona, we are expanding our faculty for the 2026–2027 academic year and are seeking to recruit PhD holders accredited by ANECA or AQU who are interested in teaching in our official undergraduate degree programmes, as an affiliated centre of Universitat Rovira i Virgili. Essential eligibility requirements To be considered for this recruitment process, candidates must meet both of the following requirements: • Hold a PhD degree., • Hold current accreditation by ANECA or AQU. Please note that only candidates who meet and can provide evidence of both requirements — PhD degree and ANECA or AQU accreditation — will proceed in the selection process. Applications that do not meet these essential requirements will not be considered further. We are particularly interested in academic and professional profiles in the following areas: Marketing Area Strategic and operational marketing Market research and consumer behaviour Branding, commercial communication and brand management Digital marketing, social media, SEO/SEM and e-commerce Customer experience, CRM and customer loyalty Business and Management Area Strategic management and business administration Business organisation and operations management Entrepreneurship, innovation and new business models Finance, management control and economic analysis Human resources, leadership and talent management Data and Technology Area Data analytics, business intelligence and dashboards Artificial intelligence applied to business and marketing Databases, information systems and ERP Programming, automation and web technologies Digital transformation, fintech, blockchain and digital business We will also positively value profiles linked to humanities, ethics, sociology and critical thinking applied to business, technology and digital society. Selected candidates will join a university project clearly focused on training professionals capable of understanding and leading the challenges of marketing, business management, the digital economy, data and technology. We will especially value: Ability to teach in English Previous university teaching experience Research track record Strong links with the professional and business environment Capacity to apply active, practice-oriented teaching methodologies connected to the realities of companies and organisations Interested candidates who meet the essential eligibility requirements may apply for the position and attach their CV, together with evidence of their PhD degree and ANECA or AQU accreditation, to be considered in the selection process. Equal Opportunities Statement ESIC is committed to equal opportunities and diversity. More information: _ Personal Data Processing ESIC University and ESIC Business & Marketing School, acting under joint responsibility, will process your application. Subsequently, only the entity offering the specific vacancy will process your personal data in order to assess your suitability for the position. Your data will be processed exclusively for the stated purpose during the active recruitment process for the vacancy to which you apply, or—if your application is unsolicited—for a maximum period of 24 months. The interested entity may verify the authenticity and accuracy of the data and documents you submit. This may include consultations with issuing bodies, companies or third parties you list as references, as well as analysis of information you have made publicly available on LinkedIn, other professional social networks, search engines, excluding access to personal social networks, and professional information shared during the interview process. You may consult further information on this data processing and exercise your rights of access, rectification, deletion and other applicable rights as explained in the: _

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. Currently we’re looking for a Clinical Project Manager to join our Clinical Operations Team. Main responsibilities: • Responsible for planning, coordinating, and leading all activities and stakeholders involved in a clinical trial to ensure the delivery of project objectives within the agreed timelines, maintaining high-quality data and adhering to the study budget., • Coordinate operational activities and communication with the Sponsor, Collaborative Groups, and other third parties (e.g., CRO) involved in the projects under your responsibility., • Participate in the development and negotiation of the clinical trial budget., • Manage the study budget throughout the trial and ensure timely billing of achieved milestones., • Perform project setup in the CTMS and ensure it is kept updated by all project team members., • Develop, maintain, and ensure compliance with SOPs and regulations for all study plans., • Ensure the availability and maintenance of all essential documents in accordance with ICH GCP throughout the study., • Support and assist CRAs with project-specific matters. Ensure all study stakeholders receive proper training throughout the study., • Perform vendors selection and management., • Collaborate in the evaluation and selection of study sites., • Review Protocol, ICF and other patient facing documents., • Review and approve monitoring reports., • Coordinate regulatory submissions and site activations across multiple countries, ensuring alignment with local requirements and global study timelines., • Support Risk-Based Quality Management (RBQM) and centralized monitoring activities in collaboration with the clinical operations team. Requirements and skills: • Healthcare/Life Sciences degree., • Minimum 1-2 years of professional experience as PM or CTM/CRM in clinical trials within pharmaceutical industry, CRO or Collaborative Group, preferably including international or multi-country studies. Experience in oncology clinical trials is strongly preferred., • Desirable previous experience as CRA., • Desirable Project Management training., • Budget management know how., • Advanced understanding of GCPs and clinical trial legislation., • Familiarity with Project Management tools, CTMS and eTMF systems; experience with remote or centralized monitoring tools is an asset., • Advanced English level. This is a full-time position (38h/week). Primary base in Barcelona (Spain), with hybrid-remote flexibility for candidates within Spain. What we offer: Join a team driving investigator-initiated oncology research with real potential to influence clinical practice globally. As a Global Clinical Project Manager at SOLTI, you will lead complex, multi-country trials from setup to close-out — with the autonomy and visibility that only an academic sponsor can offer. We offer a hybrid work model (up to 3 days remote per week), flexible schedule, a central Barcelona office, access to international conferences and scientific events, a collaborative and expert team environment and a competitive benefits package. 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: www.gruposolti.org

Context El Barcelonaβeta Brain Research Center (BBRC) és un centre de recerca dedicat a la prevenció de la malaltia d’Alzheimer i a l’estudi de les funcions cognitives afectades durant l’envelliment saludable i patològic. Creat l’any 2012 per la Fundació Pasqual Maragall, amb el suport de la Universitat Pompeu Fabra, el BBRC desenvolupa una recerca d’excel·lència orientada a comprendre els mecanismes biològics i cognitius associats a les malalties neurodegeneratives i a impulsar estratègies per prevenir-les. La Fundació Pasqual Maragall treballa per aconseguir un futur sense Alzheimer. La recerca que es duu a terme al BBRC se centra principalment en la prevenció i la detecció precoç de la malaltia, gràcies a la participació voluntària de milers de persones que contribueixen als nostres estudis científics. El BBRC compta amb el reconeixement HR Excellence in Research (HRS4R) atorgat per la Comissió Europea, que acredita el compromís del centre amb els principis de la Carta Europea de l’Investigador i el Codi de Conducta per a la Contractació de Personal Investigador. Per a més informació, podeu visitar: www.fpmaragall.org, www.barcelonabeta.org Sobre la posició El BBRC cerca un/a Infermer/a de Recerca Clínica (Clinical Research Nurse) amb interès per la recerca clínica, excel·lents habilitats interpersonals i capacitat per treballar en un entorn multidisciplinari format per professionals de la salut i la recerca. La persona seleccionada reportarà clínicament a la Coordinació de l’Equip d’Infermeria i, en els aspectes organitzatius i de gestió, a la Responsable de Clinical Operations. La seva missió serà garantir l’execució dels procediments clínics establerts en els diferents protocols de recerca, vetllant en tot moment per la seguretat, el benestar, la dignitat i la confidencialitat de les persones participants. Principals responsabilitats Les funcions s’adaptaran als requeriments específics de cada protocol de recerca i inclouran, entre d’altres: • Contactar amb potencials participants dels estudis., • Realitzar procediments i valoracions clíniques, incloent mesures antropomètriques, constants vitals i electrocardiogrames., • Gestionar mostres biològiques: extracció, processament, emmagatzematge i registre., • Donar suport a l’equip mèdic durant la realització de puncions lumbars., • Fer el seguiment dels participants per garantir el seu benestar i el compliment dels protocols., • Completar i mantenir actualitzats els quaderns de recollida de dades (CRF)., • Actualitzar les bases de dades dels estudis., • Recollir i registrar la informació requerida segons cada protocol., • Actuar davant situacions d’emergència seguint els procediments establerts., • Aplicar els coneixements clínics i les competències infermeres per proporcionar una atenció de qualitat a les persones participants en els projectes de recerca. Requisits Formació i experiència • Grau en Infermeria., • Col·legiació vigent., • Coneixements de Microsoft Office (Word i Excel)., • Nivell intermedi d’anglès, especialment en comprensió lectora i redacció., • Es valorarà coneixement de terminologia mèdica i de recerca clínica., • Es valorarà experiència prèvia en investigació clínica o assajos clínics., • Competències personals, • Capacitat per treballar de manera efectiva en equips multidisciplinaris., • Excel·lents habilitats de comunicació i relació interpersonal., • Orientació a les persones participants i sensibilitat envers les seves necessitats., • Capacitat d’organització, planificació i priorització de tasques., • Flexibilitat i adaptabilitat davant les necessitats del servei., • Atenció al detall i rigor en l’execució dels procediments., • Motivació per formar part d’una organització sense ànim de lucre amb una clara missió social. Què oferim • Incorporació immediata., • Contracte indefinit., • Jornada completa de 38 hores setmanals., • Retribució segons experiència i d’acord amb la política retributiva del centre., • Model de treball presencial en un entorn científic de referència., • Programa de retribució flexible (tiquet restaurant, assegurança mèdica i tiquet guarderia)., • 23 dies laborables de vacances anuals, de manera proporcional a la data d’incorporació., • Dies addicionals establerts pel calendari corporatiu., • Entorn de treball innovador, multidisciplinari i orientat a l’excel·lència científica., • Oportunitats de desenvolupament professional i formació contínua. Al BBRC promovem la diversitat, la igualtat d’oportunitats i la inclusió. Valorem les candidatures independentment de l’edat, el gènere, la discapacitat, la nacionalitat, l’origen ètnic, la religió, l’orientació sexual o la identitat de gènere. Procés de candidatura Les persones interessades han d’enviar la seva candidatura en un únic document PDF a talent@barcelonabeta.org, indicant a l’assumpte: Infermer/a de Recerca Clínica (Clinical Research Nurse) La candidatura haurà d’incloure: • Carta de motivació explicant l’interès per la posició i per la missió de la Fundació., • Currículum vitae actualitzat.

At Adalvo, we're not just a company - we're a team of passionate people driven by our mission to consistently deliver high-quality products and services to our partners. We are positive, fast and always on target, we are Adalvo! 🎯 🚀 We are looking for an enthusiastic VP, R&D to join our dynamic Portfolio team. If you're someone who thrives in a fast-paced environment and loves tackling new challenges, then this is the perfect opportunity for you. SUMMARY OF POSITION The Vice President of R&D will be responsible for overseeing the development of innovative pharmaceutical products and the advancement of the company's pipeline. Will be responsible for providing scientific leadership, strategic direction, and operational oversight of the R&D function. The VP of R&D will work collaboratively with cross-functional teams to drive the development of new therapeutics and ensure successful product development from preclinical development through regulatory approval. ORGANIZATION STRUCTURE This position will report to the Chief Scientific Affairs Officer and will support the department, as necessary. RESPONSIBILITIES Primary responsibilities of this role include the following: • Provide scientific leadership to guide the development of innovative pharmaceutical products and ensure alignment with the company's strategy., • Develop and implement R&D strategies to advance the company's pipeline and achieve key business objectives., • Oversee the preclinical and clinical development of new therapeutics, including the design and execution of clinical trials, and the submission of regulatory filings., • Ensure the timely delivery of high-quality, scientifically sound, and innovative drug candidates for development., • Establish and maintain relationships with key opinion leaders, academic institutions, and industry partners to advance the company's R&D agenda., • Manage and develop a high-performing R&D team, providing mentoring, guidance, and coaching to promote career growth and development., • Ensure compliance with all relevant regulations and industry standards., • Manage R&D budgets, resource allocation, and timelines, ensuring effective use of resources and alignment with corporate goals., • Represent the company at scientific conferences and events, maintaining a strong external presence in the scientific community., • Identify and develop formulation technologies applicable to potential product candidates., • Manage the R&D teams in the execution of the pharmaceutical development program for generics and 505(B2), • Provide scientific and technical expertise in the development of solid oral dosage form, topicals, injectables for EU and US market, • Responsible for the development strategy, planning and implementation of the company’s research programs, • Develop and budget resource forecasts related to the company’s research programs, • Work together with peers on key functions of Adalvo: Intellectual Property, Business Intelligence, PMO and Regulatory Affairs., • Provides guidance, mentoring, and development of staff; ensures the team has appropriate skills, capabilities, and resources to meet current and future business needs. QUALIFICATIONS • PhD in a relevant scientific discipline (e.g., pharmacology, chemistry, biology, or related field)., • Minimum of 10 years of experience in the pharmaceutical industry, with a track record of successfully leading drug development programs from preclinical through clinical stages., • Strong scientific acumen and expertise in drug discovery and development, with a deep understanding of relevant regulatory requirements and industry standards., • Proven ability to develop and implement R&D strategies that align with corporate objectives and drive pipeline advancement., • Strong leadership skills, with experience managing and developing high-performing R&D teams., • Excellent communication and interpersonal skills, with the ability to effectively collaborate with cross-functional teams and build relationships with key stakeholders., • Demonstrated ability to work in a fast-paced, dynamic environment with a sense of urgency and the ability to prioritize effectively., • Strong analytical and problem-solving skills, with the ability to make data-driven decisions and manage complex projects and timelines., • Understanding of GMP and QSR regulations and guidance applicable to the development of products, • Experience with EMA and FDA understanding of regulatory requirements, • Proven track record of successful product development, • Experience and knowledge across a broad range of different pharmaceutical technologies, • Proven ability to manage multiple projects at operational level, • Experience in leading multicultural team, • Experience with GLP-1 solutions CORE COMPETENCIES • Target Driven, • Attention to details, • Ambitious, responsible, • Enthusiastic, proactive, • Teamwork spirit, also able to perform alone, • Analytical thinking, problem solving capacity, • Well organized, • Good communication skills, • Optimistic Why join us? 🎯 Exciting Challenges: Every day brings new opportunities to learn and grow. 🎯 Supportive Environment: We foster a culture of collaboration, where your ideas are valued, and your voice is heard. 🎯Career Development: We're committed to helping you reach your full potential through ongoing training and development opportunities. 🎯Recognizing Excellence: We recognize and appreciate hard work and dedication by offering competitive compensation packages and employee rewards programs that acknowledge contributions and achievements. 🎯Fun and Inclusive Culture: We believe in celebrating our successes and building strong connections within our team. Ready to Ignite Your Passion? If you're ready to take the next step in your career and join a business committed to consistently deliver high-quality products and services, then we want to hear from you! Send us your resume today! Please be informed that only selected candidates will be contacted.

Descripción de empleo 🏫 Centre: Escola Universitària Mediterrani (EUM) – University of Girona Location: Barcelona Department: Business Area of knowledge: Accounting Employment type: Part-time 📚 Subject to teach: The vacant teaching position corresponds to the Bachelor’s Degree in International Business Management (GIBM): • Introduction to Accounting and Accounting Statements – 6 ECTS (1GM) This course introduces the basic principles of financial accounting and its role as an information system for decision-making. It covers the preparation, structure, and interpretation of the main financial statements and their use in analyzing a firm's economic and financial position. Class Schedule: Fridays from 10:30 to 13:20 Semester: First semester of the 2026/2027 academic year (September-February). On-campus teaching. Teaching language: English. 👩 🏫 Minimum requirements: • University degree in Accounting, Finance, Business Administration, or related fields., • Professional or teaching experience in accounting, financial statements, auditing, or corporate finance., • Knowledge of innovative teaching methodologies and applied quantitative learning., • C2 level of English: mandatory., • C2 level of Spanish: mandatory., • Availability for on-campus teaching at EUM. Will be valued: • PhD or Doctorate., • AQU or ANECA accreditation., • Previous university teaching experience., • Experience teaching quantitative subjects to business students., • Professional experience in accounting, auditing, financial management, or consultancy., • C1 level of Catalan., • Participation in research, transfer or innovation projects related to statistics, analytics, decision-making or quantitative business methods. 📊 CV assessment scale – 100 points • Suitable academic degree: 10 points, • PhD or Doctorate: 10 points, • AQU or ANECA accreditation: 10 points, • University teaching experience: 20 points, • Relevant professional experience in accounting: 15 points, • Research, publications or transfer related to the subject area: 15 points, • Technological and digital teaching competencies, including Moodle or similar platforms: 10 points, • Teaching innovation, applied quantitative learning or knowledge transfer: 5 points, • Catalan C1: 5 points Applications and selection process Candidates must submit their CV, proof of language proficiency, and a brief teaching proposal for the subject, no later than 28 June 2026. The selection procedure will consist of the following phases: Phase 1 – Receipt of applications Applications will be received until 28 June 2026. Phase 2 – Evaluation of applications All applications received within the established deadline will be evaluated according to the CV assessment scale included in this vacancy. Phase 3 – Interview The three highest-ranking candidates who achieve a score above 50 points in the evaluation phase will be shortlisted for an interview. EUM values academic excellence, professional relevance, teaching innovation, diversity and inclusion. We welcome applications from candidates committed to active learning, international perspectives, ethical practice and a respectful learning environment.

¿Te interesa formar parte de un centro tecnológico de excelencia donde podrás contribuir y añadir valor tecnológico a empresa e instituciones, centrándote en la investigación, el desarrollo y la innovación industrial (I+D+2i)? ¿Quieres trabajar en un entorno puntero con todas las innovaciones tecnológicas a tu alcance? Leitat es un centro tecnológico de referencia a nivel estatal y europeo. Con más de 100 años de historia, cuenta con un equipo de más de 400 profesionales, expertos en investigación aplicada, servicios técnicos y gestión de iniciativas tecnológicas y de innovación. Leitat aporta valor social, industrial, económico y sostenible, ofreciendo soluciones integrales en múltiples sectores y ámbitos: salud y biomedicina, desarrollo de nuevos materiales, producción eco-sostenible, sistemas de prevención de salud laboral, revalorización de residuos y aprovechamiento de recursos naturales; interconectividad y digitalización de la industria, energía verde y maximización de la eficiencia energética. Leitat desarrolla proyectos de I+D+i para empresas e instituciones, así como lidera proyectos de investigación con financiación competitiva tanto en el marco de la Unión Europea como del Ministerio de Ciencia e Innovación. Actualmente buscamos un/a Investigador/a Junior en Evaluación de Riesgos Químicos, para unirse en el grupo de Human & Environmental Health & Safety (HEHS). El grupo HEHS se enfoca en ofrecer soporte tecnológico a diferentes sectores industriales en distintos niveles; para garantizar que sus productos, tecnologías y procesos sean seguros para la salud humana y para el medioambiente, así como proporcionar plataformas tecnológicas para añadir valor a sus productos. Tus principales funciones serán: • Ejecución de tareas (combinando trabajo de ordenador y trabajo experimental) para los proyectos en los que el grupo está actualmente involucrado., • Evaluación de la exposición/liberación de materiales/sustancias que presentan potenciales riesgos para la salud humana en diferentes escenarios. Generando datos que serán utilizados en modelos de evaluación de exposición, para fines de evaluación de riesgos para la salud humana o recopilando datos de diferentes bases de datos existentes, analizándolos y seleccionándolos para su integración en modelos de evaluación de riesgos, • Análisis crítico e interpretación de los resultados obtenidos, mediante modelos o metodologías experimentales, tanto para fines de divulgación como para la redacción de informes técnicos., • Presentación de resultados en conferencias nacionales e internacionales y en reuniones de proyectos. ¿Qué esperamos de ti? • Master/ Licenciatura/ Grado en Química, ciencia de (nano)materiales, materiales avanzados o similar., • Conocimiento y experiencia en Nanotecnología, Nanoseguridad y/o áreas relacionadas., • Conocimiento de metodologías para evaluar la exposición/ impacto/ riesgo de materiales y otras sustancias (e.g., metales, sustancias orgánicas, microplasticos, PFAs, etc.) en la salud humana., • Experiencia en técnicas analíticas, análisis e interpretación de datos/resultados experimentales., • Motivación e interés por ampliar conocimientos en áreas afines como pueden ser herramientas digitales para evaluar riesgo y modelos predictivos que permiten el diseño seguro en el desarrollo de nuevos materiales. Idiomas: Español e Inglés. Se valorará disponer de certificado de discapacidad. Triunfaras en la posición si posees experiencia en tratamiento de datos, técnicas analíticas y facilidad en la comunicación y descripción de resultados. ¿Cómo es trabajar en LEITAT? Estarás ubicado/a en la sede de Barcelona, (Cambra de comerç) trabajarás en un entorno atractivo, siendo parte de un ecosistema de innovación único con tecnologías de vanguardia y laboratorios altamente equipados. Te ofrecemos jornadas de trabajo flexible para que puedas conciliar tu vida personal y tu desarrollo profesional. Además, podrás disfrutar de catering subvencionado en nuestros centros, seguro médico y tendrás un contrato indefinido, recibiendo una retribución acorde con tu experiencia, formación y desarrollo. Estamos orgullosos de ofrecer este tipo de beneficios que apoyan los objetivos y el bienestar de los miembros de nuestros equipos. Asimismo, apoyamos la igualdad de oportunidades y la diversidad. ¡Nos esforzamos cada día por ser un lugar de trabajo más inclusivo adaptado a todos los colectivos! Si eres una persona con excelentes habilidades interpersonales y de comunicación, con una alta capacidad para lograr tus objetivos en los plazos establecidos y capaz de trabajar de manera independiente y en equipo, no lo dudes, inscríbete a nuestra oferta. ¡ Nos encantaría saber de ti! ¡En LEITAT estamos deseando conocerte!

¿Te interesa formar parte de un centro tecnológico de excelencia donde podrás contribuir y añadir valor tecnológico a empresa e instituciones, centrándote en la investigación, el desarrollo y la innovación industrial (I+D+2i)? ¿Quieres trabajar en un entorno puntero con todas las innovaciones tecnológicas a tu alcance? Leitat es un centro tecnológico de referencia a nivel estatal y europeo. Con más de 100 años de historia, cuenta con un equipo de más de 400 profesionales, expertos en investigación aplicada, servicios técnicos y gestión de iniciativas tecnológicas y de innovación. Leitat aporta valor social, industrial, económico y sostenible, ofreciendo soluciones integrales en múltiples sectores y ámbitos: salud y biomedicina, desarrollo de nuevos materiales, producción eco-sostenible, sistemas de prevención de salud laboral, revalorización de residuos y aprovechamiento de recursos naturales; interconectividad y digitalización de la industria, energía verde y maximización de la eficiencia energética. Leitat desarrolla proyectos de I+D+i para empresas e instituciones, así como lidera proyectos de investigación con financiación competitiva tanto en el marco de la Unión Europea como del Ministerio de Ciencia e Innovación. Actualmente buscamos un/a Investigador/a principal en Fotónica para liderar la estrategia científica y tecnológica en proyectos avanzados de I+D en el ámbito de la fotónica y visión. Serás el responsable del diseño, ejecución y seguimiento de los proyectos de investigación, definiendo el contenido técnico, elaborando los presupuestos de ejecución; coordinando y planificando los trabajados de los investigadores bajo tu responsabilidad. Trabajarás principalmente en proyectos relacionados con el desarrollo y aplicación de sensores de diferentes tipos (optoelectrónicos, optofluídicos, basados en fibras ópticas, etc) aplicados a diferentes sectores productivos (industria, energía, salud, alimentación, etc). Los proyectos son variables, desde contratos privados con relación directa con el cliente hasta proyectos de colaboración con otras entidades. La posición combina visión estratégica, liderazgo técnico y gestión de innovación, coordinando iniciativas de alto impacto en entornos científicos e industriales. • Liderar proyectos avanzados de I+D en tecnologías ópticas y fotónicas., • Gestionar cartera de proyectos, clientes y propuestas nacionales/europeas., • Coordinar equipos multidisciplinares de investigación e ingeniería., • Supervisar planificación técnica, calidad, riesgos y presupuestos., • Impulsar actividades de transferencia tecnológica, comunicación científica e impacto. ¿Qué esperamos de ti? Buscamos un/a graduado/a con máster/doctorado en fotónica, en física, o ingeniería física, principalmente. También se valorarán aquellos que presenten una experiencia como investigador avanzado y experiencia en diseñar proyectos para la industria. Por otro lado, es importante tener la capacidad contrastada para la captación de recursos para desarrollar la actividad de I+D y liderar proyectos consorciados con otras entidades nacionales o internacionales. Tener experiencia en la gestión de personas y/o equipos multidisciplinares. Deberás aportar capacidades y habilidades en: • Liderazgo de equipos y gestión de personas, • Capacidad para conceptualizar soluciones innovadoras, • Experiencia en dirección de proyectos (Agile), • Gestión de riesgos, calidad y presupuestos, • Excelentes habilidades de comunicación y presentación, • Capacidad para liderar reuniones técnicas complejas Ingles competencia profesional, Castellano, valorable catalán. Se valorará disponer de certificado de discapacidad. ¿Cómo es trabajar en LEITAT? Estarás ubicado/a en nuestra sede de DFactory (Zona Franca de Barcelona, trabajarás en un entorno atractivo, siendo parte de un ecosistema de innovación único con tecnologías de vanguardia y laboratorios altamente equipados. Te ofrecemos jornadas de trabajo flexible para que puedas conciliar tu vida personal y tu desarrollo profesional. Además, podrás disfrutar de catering subvencionado en nuestros centros, seguro médico y tendrás un contrato indefinido recibiendo una retribución acorde con tu experiencia, formación y desarrollo. Estamos orgullosos de ofrecer este tipo de beneficios que apoyan los objetivos y el bienestar de los miembros de nuestros equipos. Asimismo, apoyamos la igualdad de oportunidades y la diversidad. ¡Nos esforzamos cada día por ser un lugar de trabajo más inclusivo adaptado a todos los colectivos! Si eres una persona con excelentes habilidades interpersonales y de comunicación, con una alta capacidad para lograr tus objetivos en los plazos establecidos y capaz de trabajar de manera independiente y en equipo, no lo dudes, inscríbete a nuestra oferta. ¡ Nos encantaría saber de ti! ¡En LEITAT estamos deseando conocerte!

Empresa de base tecnológica en expansión, dedicada a la distribución online de productos especializados dirigidos a profesionales de laboratorio. Como parte de nuestro crecimiento, hemos creado una nueva posición en el equipo de Customer Service, con el objetivo de reforzar nuestro compromiso con la excelencia en la atención al cliente, impulsar nuestra proyección internacional y seguir desarrollando nuestra presencia en laboratorios de control de calidad. ¿Qué harás en tu día a día? • Gestionarás la relación con nuestros clientes, que incluyen empresas de los sectores farmacéutico, cosmético, alimentario, así como centros de investigación y universidades., • Validarás y gestionarás pedidos recibidos a través de nuestra web, manteniendo una comunicación fluida con clientes y proveedores para asegurar un servicio eficaz y de calidad., • Representarás a la empresa en ferias y congresos, ayudando a consolidar nuestra imagen de marca y a detectar nuevas oportunidades de negocio. ¿Qué buscamos en ti? • Persona resolutiva, empática, con atención al detalle, y con facilidad para trabajar en equipo., • Con capacidad para comunicarse con clientes y proveedores de forma amable, profesional y efectiva., • Formación en ciencias, como química, bioquímica, biología o similares., • Dominio fluido de castellano, catalán e inglés.Se valorará muy positivamente el conocimiento de otros idiomas (nivel C1/C2). Nuestra propuesta • Disfrutarás formando parte de una empresa tecnológica, financieramente estable, líder en su sector y con un ambicioso plan de crecimiento., • Excelente ambiente de trabajo, horario flexible, posibilidad de teletrabajo, formación continua y otros beneficios sociales., • Nuestras oficinas están ubicadas en Barcelona, en una zona bien comunicada y con todos los servicios a tu alrededor.

Assessor/a Genètic/a - Desenvolupa la teva carrera en un entorn clínic d'alt nivell T'agradaria desenvolupar-te en un entorn hospitlaari de referència? A la Unitat de Genètica Clínica de l'Hospital Universitari de Bellvitge, busquem incorporar un/a assessor/a genètic/a per a cobrir una baixa per maternitat a partir de l'1 de setembre de 2026. Què faràs? • Avaluar el risc de malalties genètiques en individus i famílies., • Indicar i interpretar proves genètiques amb criteri clínic., • Informar sobre herència, opcions reproductives i implicacions familiars., • Acompanyar en la presa de decisions informades i en l'adaptació emocional., • Coordinar-se amb equips multidisciplinars., • Contribuir a docència, divulgació i projecte de recerca., • Garantir el registre i la traçabilitat clínica dels casos. Requisits • Titulació universitària (grau/llicenciatura o equivalent)., • Màster en assessorament genètic reconegut per EBMG (o acreditació equivalent)., • Experiència mínima d'1 any en consell genètic. Es valorarà • Formació en genètica clínica, psicologia clínica i comunicació tècnica. Què t'oferim • Entorn assistencial multidisciplinari i d'alta complexitat tècnica., • Participació en investigació i projectes innovadors., • Retribució i dedicació segons III Acord de la Mesa Sectorial de l'ICS. T'interessa? Envian's la teva candidatura i forma part d'un equip compromés amb la medicina personalitzada i el futur de la genètica clínica.

Percassi es un grupo empresarial capaz de anticiparse a las tendencias del mercado mirando más allá de las fronteras italianas. Sus actividades se concentran principalmente en tres áreas de negocio: Retail, Real Estate y Atalanta Bergamasca Calcio. El negocio de franquicia desarrolla y gestiona muchas marcas icónicas y prestigiosas, con una oferta diversificada: Nike, Jordan, Victoria's Secret, Bath & Body Works, LEGO®, Garmin, Oakley, K-way, Womo, Bullfrog, Armani Exchange, Saint Laurent y Starbucks. Visítenos en: www.percassi.com Como nuestro/a Jefe/a de Sección ( COACH) en la tienda Nike Paseo de Gracia, en Barcelona , tu misión consistirá en ser el enlace entre el consumidor y la marca proporcionando el más alto nivel de servicio y transmitir inspiración al cliente compartiendo la historia de marca. Responsabilidades del puesto: Utilizar habilidades excepcionales de atención al cliente, técnicas de venta y conocimiento del producto para conectar a los clientes con el producto adecuado e impulsar las ventas Gestionar transacciones o situaciones de atención al cliente más complejas Proporcionar experiencia en una o más áreas o funciones (envío y recepción, tareas de caja y atención al cliente) Buscar formación y educación continuas para seguir desarrollando su experiencia Ayudar a los/as responsables a llevar a cabo programas formales de incorporación y formación para los/as empleados/as Colaborar en la prevención de pérdidas mediante un servicio proactivo de atención al cliente Ayudar a coordinar el trabajo de otros miembros del equipo Puede tener responsabilidades de apertura y cierre de tienda Requisitos del puesto: Título de bachillerato o equivalente 3 años de experiencia en venta al por menor Conocimientos básicos de informática, incluido Microsoft Office Capacidad para trabajar fines de semana y festivos según sea necesario Te ofrecemos: Contrato indefinido Jornadas de trabajo de 5 o 6 días semanales, a elección del/a trabajador/a Descuentos de empleado/a en marcas del grupo Percassi Un sistema variable basado en el desempeño de la tienda en relación con los objetivos comerciales Posibilidad de crecimiento en NIKE y en las diferentes marcas de Percassi PERCASSI se compromete a garantizar la Igualdad de Oportunidades y presta especial atención a la igualdad de género y a la integración de personas con discapacidad en la empresa. Todos los puestos vacantes están también abiertos a solicitudes de miembros de las Categorías Protegidas L.68/99. Los datos serán procesados exclusivamente para los fines y según los métodos informados en la política de privacidad disponible en el sitio web https://www.percassi.it/privacy-policy-candidati/

No se requiere experiencia previa como profesor.

Faculty Recruitment – 2026/2027 Academic Year At ESIC Barcelona, we are expanding our faculty for the 2026–2027 academic year and are seeking to recruit PhD holders accredited by ANECA or AQU who are interested in teaching in our official undergraduate degree programmes, as an affiliated centre of Universitat Rovira i Virgili. Essential eligibility requirements To be considered for this recruitment process, candidates must meet both of the following requirements: • Hold a PhD degree., • Hold current accreditation by ANECA or AQU. Please note that only candidates who meet and can provide evidence of both requirements — PhD degree and ANECA or AQU accreditation — will proceed in the selection process. Applications that do not meet these essential requirements will not be considered further. We are particularly interested in academic and professional profiles in the following areas: Marketing Area Strategic and operational marketing Market research and consumer behaviour Branding, commercial communication and brand management Digital marketing, social media, SEO/SEM and e-commerce Customer experience, CRM and customer loyalty Business and Management Area Strategic management and business administration Business organisation and operations management Entrepreneurship, innovation and new business models Finance, management control and economic analysis Human resources, leadership and talent management Data and Technology Area Data analytics, business intelligence and dashboards Artificial intelligence applied to business and marketing Databases, information systems and ERP Programming, automation and web technologies Digital transformation, fintech, blockchain and digital business We will also positively value profiles linked to humanities, ethics, sociology and critical thinking applied to business, technology and digital society. Selected candidates will join a university project clearly focused on training professionals capable of understanding and leading the challenges of marketing, business management, the digital economy, data and technology. We will especially value: Ability to teach in English Previous university teaching experience Research track record Strong links with the professional and business environment Capacity to apply active, practice-oriented teaching methodologies connected to the realities of companies and organisations Interested candidates who meet the essential eligibility requirements may apply for the position and attach their CV, together with evidence of their PhD degree and ANECA or AQU accreditation, to be considered in the selection process. Equal Opportunities Statement ESIC is committed to equal opportunities and diversity. More information: _ Personal Data Processing ESIC University and ESIC Business & Marketing School, acting under joint responsibility, will process your application. Subsequently, only the entity offering the specific vacancy will process your personal data in order to assess your suitability for the position. Your data will be processed exclusively for the stated purpose during the active recruitment process for the vacancy to which you apply, or—if your application is unsolicited—for a maximum period of 24 months. The interested entity may verify the authenticity and accuracy of the data and documents you submit. This may include consultations with issuing bodies, companies or third parties you list as references, as well as analysis of information you have made publicly available on LinkedIn, other professional social networks, search engines, excluding access to personal social networks, and professional information shared during the interview process. You may consult further information on this data processing and exercise your rights of access, rectification, deletion and other applicable rights as explained in the: _

At Today School, a well-established English academy in Barcelona with over 40 years of excellence in teaching, we believe that education should be exciting and rewarding—for both students and teachers. Collaborate with dedicated Directors of Studies and peer teachers while accessing ongoing profes

Si los siguientes requisitos del puesto y la experiencia coinciden con sus habilidades, por favor, asegúrese de enviar su solicitud sin demora. Plaça disponible: Professor de les següents matèries de l’ESO:. La satisfacció de contribuir al futur dels nostres joves.

Nonetheless, areas identified for particular reinforcement include, but are not limited to: molecular biology, genomics, and omics; digital agriculture, AI, and data sciences; advanced sensing, phenotyping, and precision agriculture; and social sciences, governance, and legal studies. Agrotecnio is

At Adalvo, we're not just a company - we're a team of passionate people driven by our mission to consistently deliver high-quality products and services to our partners. We are positive, fast and always on target, we are Adalvo! 🎯 🚀 We are looking for an enthusiastic VP, R&D to join our dynamic Portfolio team. If you're someone who thrives in a fast-paced environment and loves tackling new challenges, then this is the perfect opportunity for you. SUMMARY OF POSITION The Vice President of R&D will be responsible for overseeing the development of innovative pharmaceutical products and the advancement of the company's pipeline. Will be responsible for providing scientific leadership, strategic direction, and operational oversight of the R&D function. The VP of R&D will work collaboratively with cross-functional teams to drive the development of new therapeutics and ensure successful product development from preclinical development through regulatory approval. ORGANIZATION STRUCTURE This position will report to the Chief Scientific Affairs Officer and will support the department, as necessary. RESPONSIBILITIES Primary responsibilities of this role include the following: • Provide scientific leadership to guide the development of innovative pharmaceutical products and ensure alignment with the company's strategy., • Develop and implement R&D strategies to advance the company's pipeline and achieve key business objectives., • Oversee the preclinical and clinical development of new therapeutics, including the design and execution of clinical trials, and the submission of regulatory filings., • Ensure the timely delivery of high-quality, scientifically sound, and innovative drug candidates for development., • Establish and maintain relationships with key opinion leaders, academic institutions, and industry partners to advance the company's R&D agenda., • Manage and develop a high-performing R&D team, providing mentoring, guidance, and coaching to promote career growth and development., • Ensure compliance with all relevant regulations and industry standards., • Manage R&D budgets, resource allocation, and timelines, ensuring effective use of resources and alignment with corporate goals., • Represent the company at scientific conferences and events, maintaining a strong external presence in the scientific community., • Identify and develop formulation technologies applicable to potential product candidates., • Manage the R&D teams in the execution of the pharmaceutical development program for generics and 505(B2), • Provide scientific and technical expertise in the development of solid oral dosage form, topicals, injectables for EU and US market, • Responsible for the development strategy, planning and implementation of the company’s research programs, • Develop and budget resource forecasts related to the company’s research programs, • Work together with peers on key functions of Adalvo: Intellectual Property, Business Intelligence, PMO and Regulatory Affairs., • Provides guidance, mentoring, and development of staff; ensures the team has appropriate skills, capabilities, and resources to meet current and future business needs. QUALIFICATIONS • PhD in a relevant scientific discipline (e.g., pharmacology, chemistry, biology, or related field)., • Minimum of 10 years of experience in the pharmaceutical industry, with a track record of successfully leading drug development programs from preclinical through clinical stages., • Strong scientific acumen and expertise in drug discovery and development, with a deep understanding of relevant regulatory requirements and industry standards., • Proven ability to develop and implement R&D strategies that align with corporate objectives and drive pipeline advancement., • Strong leadership skills, with experience managing and developing high-performing R&D teams., • Excellent communication and interpersonal skills, with the ability to effectively collaborate with cross-functional teams and build relationships with key stakeholders., • Demonstrated ability to work in a fast-paced, dynamic environment with a sense of urgency and the ability to prioritize effectively., • Strong analytical and problem-solving skills, with the ability to make data-driven decisions and manage complex projects and timelines., • Understanding of GMP and QSR regulations and guidance applicable to the development of products, • Experience with EMA and FDA understanding of regulatory requirements, • Proven track record of successful product development, • Experience and knowledge across a broad range of different pharmaceutical technologies, • Proven ability to manage multiple projects at operational level, • Experience in leading multicultural team, • Experience with GLP-1 solutions CORE COMPETENCIES • Target Driven, • Attention to details, • Ambitious, responsible, • Enthusiastic, proactive, • Teamwork spirit, also able to perform alone, • Analytical thinking, problem solving capacity, • Well organized, • Good communication skills, • Optimistic Why join us? 🎯 Exciting Challenges: Every day brings new opportunities to learn and grow. 🎯 Supportive Environment: We foster a culture of collaboration, where your ideas are valued, and your voice is heard. 🎯Career Development: We're committed to helping you reach your full potential through ongoing training and development opportunities. 🎯Recognizing Excellence: We recognize and appreciate hard work and dedication by offering competitive compensation packages and employee rewards programs that acknowledge contributions and achievements. 🎯Fun and Inclusive Culture: We believe in celebrating our successes and building strong connections within our team. Ready to Ignite Your Passion? If you're ready to take the next step in your career and join a business committed to consistently deliver high-quality products and services, then we want to hear from you! Send us your resume today! Please be informed that only selected candidates will be contacted.

At Adalvo, we're not just a company - we're a team of passionate people driven by our mission to consistently deliver high-quality products and services to our partners. We are positive, fast and always on target, we are Adalvo! 🎯 🚀 We are looking for an enthusiastic VP, R&D to join our dynamic Portfolio team. If you're someone who thrives in a fast-paced environment and loves tackling new challenges, then this is the perfect opportunity for you. SUMMARY OF POSITION The Vice President of R&D will be responsible for overseeing the development of innovative pharmaceutical products and the advancement of the company's pipeline. Will be responsible for providing scientific leadership, strategic direction, and operational oversight of the R&D function. The VP of R&D will work collaboratively with cross-functional teams to drive the development of new therapeutics and ensure successful product development from preclinical development through regulatory approval. ORGANIZATION STRUCTURE This position will report to the Chief Scientific Affairs Officer and will support the department, as necessary. RESPONSIBILITIES Primary responsibilities of this role include the following: • Provide scientific leadership to guide the development of innovative pharmaceutical products and ensure alignment with the company's strategy., • Develop and implement R&D strategies to advance the company's pipeline and achieve key business objectives., • Oversee the preclinical and clinical development of new therapeutics, including the design and execution of clinical trials, and the submission of regulatory filings., • Ensure the timely delivery of high-quality, scientifically sound, and innovative drug candidates for development., • Establish and maintain relationships with key opinion leaders, academic institutions, and industry partners to advance the company's R&D agenda., • Manage and develop a high-performing R&D team, providing mentoring, guidance, and coaching to promote career growth and development., • Ensure compliance with all relevant regulations and industry standards., • Manage R&D budgets, resource allocation, and timelines, ensuring effective use of resources and alignment with corporate goals., • Represent the company at scientific conferences and events, maintaining a strong external presence in the scientific community., • Identify and develop formulation technologies applicable to potential product candidates., • Manage the R&D teams in the execution of the pharmaceutical development program for generics and 505(B2), • Provide scientific and technical expertise in the development of solid oral dosage form, topicals, injectables for EU and US market, • Responsible for the development strategy, planning and implementation of the company’s research programs, • Develop and budget resource forecasts related to the company’s research programs, • Work together with peers on key functions of Adalvo: Intellectual Property, Business Intelligence, PMO and Regulatory Affairs., • Provides guidance, mentoring, and development of staff; ensures the team has appropriate skills, capabilities, and resources to meet current and future business needs. QUALIFICATIONS • PhD in a relevant scientific discipline (e.g., pharmacology, chemistry, biology, or related field)., • Minimum of 10 years of experience in the pharmaceutical industry, with a track record of successfully leading drug development programs from preclinical through clinical stages., • Strong scientific acumen and expertise in drug discovery and development, with a deep understanding of relevant regulatory requirements and industry standards., • Proven ability to develop and implement R&D strategies that align with corporate objectives and drive pipeline advancement., • Strong leadership skills, with experience managing and developing high-performing R&D teams., • Excellent communication and interpersonal skills, with the ability to effectively collaborate with cross-functional teams and build relationships with key stakeholders., • Demonstrated ability to work in a fast-paced, dynamic environment with a sense of urgency and the ability to prioritize effectively., • Strong analytical and problem-solving skills, with the ability to make data-driven decisions and manage complex projects and timelines., • Understanding of GMP and QSR regulations and guidance applicable to the development of products, • Experience with EMA and FDA understanding of regulatory requirements, • Proven track record of successful product development, • Experience and knowledge across a broad range of different pharmaceutical technologies, • Proven ability to manage multiple projects at operational level, • Experience in leading multicultural team, • Experience with GLP-1 solutions CORE COMPETENCIES • Target Driven, • Attention to details, • Ambitious, responsible, • Enthusiastic, proactive, • Teamwork spirit, also able to perform alone, • Analytical thinking, problem solving capacity, • Well organized, • Good communication skills, • Optimistic Why join us? 🎯 Exciting Challenges: Every day brings new opportunities to learn and grow. 🎯 Supportive Environment: We foster a culture of collaboration, where your ideas are valued, and your voice is heard. 🎯Career Development: We're committed to helping you reach your full potential through ongoing training and development opportunities. 🎯Recognizing Excellence: We recognize and appreciate hard work and dedication by offering competitive compensation packages and employee rewards programs that acknowledge contributions and achievements. 🎯Fun and Inclusive Culture: We believe in celebrating our successes and building strong connections within our team. Ready to Ignite Your Passion? If you're ready to take the next step in your career and join a business committed to consistently deliver high-quality products and services, then we want to hear from you! Send us your resume today! Please be informed that only selected candidates will be contacted.

Descripción de empleo 🏫 Centre: Escola Universitària Mediterrani (EUM) – University of Girona Location: Barcelona Department: Business Area of knowledge: Accounting Employment type: Part-time 📚 Subject to teach: The vacant teaching position corresponds to the Bachelor’s Degree in International Business Management (GIBM): • Introduction to Accounting and Accounting Statements – 6 ECTS (1GM) This course introduces the basic principles of financial accounting and its role as an information system for decision-making. It covers the preparation, structure, and interpretation of the main financial statements and their use in analyzing a firm's economic and financial position. Class Schedule: Fridays from 10:30 to 13:20 Semester: First semester of the 2026/2027 academic year (September-February). On-campus teaching. Teaching language: English. 👩 🏫 Minimum requirements: • University degree in Accounting, Finance, Business Administration, or related fields., • Professional or teaching experience in accounting, financial statements, auditing, or corporate finance., • Knowledge of innovative teaching methodologies and applied quantitative learning., • C2 level of English: mandatory., • C2 level of Spanish: mandatory., • Availability for on-campus teaching at EUM. Will be valued: • PhD or Doctorate., • AQU or ANECA accreditation., • Previous university teaching experience., • Experience teaching quantitative subjects to business students., • Professional experience in accounting, auditing, financial management, or consultancy., • C1 level of Catalan., • Participation in research, transfer or innovation projects related to statistics, analytics, decision-making or quantitative business methods. 📊 CV assessment scale – 100 points • Suitable academic degree: 10 points, • PhD or Doctorate: 10 points, • AQU or ANECA accreditation: 10 points, • University teaching experience: 20 points, • Relevant professional experience in accounting: 15 points, • Research, publications or transfer related to the subject area: 15 points, • Technological and digital teaching competencies, including Moodle or similar platforms: 10 points, • Teaching innovation, applied quantitative learning or knowledge transfer: 5 points, • Catalan C1: 5 points Applications and selection process Candidates must submit their CV, proof of language proficiency, and a brief teaching proposal for the subject, no later than 28 June 2026. The selection procedure will consist of the following phases: Phase 1 – Receipt of applications Applications will be received until 28 June 2026. Phase 2 – Evaluation of applications All applications received within the established deadline will be evaluated according to the CV assessment scale included in this vacancy. Phase 3 – Interview The three highest-ranking candidates who achieve a score above 50 points in the evaluation phase will be shortlisted for an interview. EUM values academic excellence, professional relevance, teaching innovation, diversity and inclusion. We welcome applications from candidates committed to active learning, international perspectives, ethical practice and a respectful learning environment.

Descripción de empleo 🏫 Centre: Escola Universitària Mediterrani (EUM) – University of Girona Location: Barcelona Department: Business Area of knowledge: Accounting Employment type: Part-time 📚 Subject to teach: The vacant teaching position corresponds to the Bachelor’s Degree in International Business Management (GIBM): • Introduction to Accounting and Accounting Statements – 6 ECTS (1GM) This course introduces the basic principles of financial accounting and its role as an information system for decision-making. It covers the preparation, structure, and interpretation of the main financial statements and their use in analyzing a firm's economic and financial position. Class Schedule: Fridays from 10:30 to 13:20 Semester: First semester of the 2026/2027 academic year (September-February). On-campus teaching. Teaching language: English. 👩 🏫 Minimum requirements: • University degree in Accounting, Finance, Business Administration, or related fields., • Professional or teaching experience in accounting, financial statements, auditing, or corporate finance., • Knowledge of innovative teaching methodologies and applied quantitative learning., • C2 level of English: mandatory., • C2 level of Spanish: mandatory., • Availability for on-campus teaching at EUM. Will be valued: • PhD or Doctorate., • AQU or ANECA accreditation., • Previous university teaching experience., • Experience teaching quantitative subjects to business students., • Professional experience in accounting, auditing, financial management, or consultancy., • C1 level of Catalan., • Participation in research, transfer or innovation projects related to statistics, analytics, decision-making or quantitative business methods. 📊 CV assessment scale – 100 points • Suitable academic degree: 10 points, • PhD or Doctorate: 10 points, • AQU or ANECA accreditation: 10 points, • University teaching experience: 20 points, • Relevant professional experience in accounting: 15 points, • Research, publications or transfer related to the subject area: 15 points, • Technological and digital teaching competencies, including Moodle or similar platforms: 10 points, • Teaching innovation, applied quantitative learning or knowledge transfer: 5 points, • Catalan C1: 5 points Applications and selection process Candidates must submit their CV, proof of language proficiency, and a brief teaching proposal for the subject, no later than 28 June 2026. The selection procedure will consist of the following phases: Phase 1 – Receipt of applications Applications will be received until 28 June 2026. Phase 2 – Evaluation of applications All applications received within the established deadline will be evaluated according to the CV assessment scale included in this vacancy. Phase 3 – Interview The three highest-ranking candidates who achieve a score above 50 points in the evaluation phase will be shortlisted for an interview. EUM values academic excellence, professional relevance, teaching innovation, diversity and inclusion. We welcome applications from candidates committed to active learning, international perspectives, ethical practice and a respectful learning environment.

Te interesa formar parte de un.I+D+2i)? ¿Quieres trabajar en un entorno puntero con todas las innovaciones tecnológicas a tu alcance?.Leitat es un centro tecnológico de referencia a nivel estatal y europeo.Con más de 100 años de historia, cuenta con un equipo de más de 400 profesionales, exper

Clinical Research Manager | MedTech and IVD Location: Spain, Portugal or UK (Remote with occasional in‑person activities) Employment Type: Full‑time Role Summary We are seeking an experienced Clinical Research Manager to lead and coordinate clinical studies for medical devices and in vitro diagnostics. The role covers the full clinical lifecycle, from early study design and start‑up through execution and close‑out, in compliance with GCP, ISO standards, and applicable European and local regulations. You will act as a key interface between sponsors, study sites, and internal teams, ensuring high‑quality delivery, regulatory compliance, and effective project and people management. This role also includes mentoring and development responsibilities for junior team members and consultants. Key Responsibilities You will: • Lead and manage Clinical Investigations and Performance Studies for medical devices and IVDs from start‑up to close‑out, • Ensure studies are conducted in compliance with GCP, ISO 14155, ISO 20916, EU regulations, and local requirements, • Contribute to protocol, CRF, ICF, and study documentation design and review, • Coordinate submissions to Ethics Committees and Competent Authorities, • Oversee site initiation, monitoring activities, and ongoing site management, • Maintain close communication with investigators, study coordinators, sponsors, and internal stakeholders, • Monitor project progress against timelines, quality metrics, and budgets, • Identify project risks and implement mitigation strategies in collaboration with the project team, • Act as the primary daily point of contact for sponsors, • Develop, maintain, and oversee Trial Master Files and eTMFs, • Prepare and present project status updates to internal and external stakeholders, • Negotiate contracts with study sites, vendors, and service providers, • Manage project finances according to sponsor contracts and approved budgets, • Provide input into proposals, budgets, and bid defense activities, • Ensure adherence to QMS procedures and contribute to continuous improvement initiatives, • Participate in Management Review activities as required People Development and Team Responsibilities You will also: • Support onboarding of new team members by providing guidance, tools access, and structured induction, • Coordinate and follow initial training plans for assigned employees or consultants, • Conduct periodic performance evaluations and development discussions, • Review training effectiveness and contribute to continuous professional development planning, • Support definition and follow‑up of individual training and growth plans Requirements Must‑Have • 1–3 years of professional experience as a Clinical Project Manager or Clinical Research Manager in medical devices or IVDs, • Solid working knowledge of GCP and clinical research standards, • Bachelor’s degree in Life Sciences, • Advanced written and verbal English (C1–C2 level or equivalent), • Ability to manage multiple projects and stakeholders in an international environment, • Availability for remote work with occasional in‑person activities Nice to Have • Master’s degree in Life Sciences, • PhD or advanced scientific training in a medical or related discipline, • Experience with ISO 14155 and or ISO 20916, • Fluency in additional EU languages, • Experience supporting audits or inspections Why Join MDx CRO At MDx CRO, you will join a highly specialised and rapidly growing organisation recognised across the MedTech and IVD sector. We offer a professional, collaborative environment where expertise is valued and continuous development is encouraged. You will benefit from: • Exposure to complex and meaningful clinical projects, • A high level of autonomy and responsibility, • Close collaboration with senior regulatory and clinical experts, • Opportunities for professional and career growth About MDx CRO MDx CRO is a leading Contract Research Organisation specialising in in vitro diagnostics and medical devices. We support clients through regulatory strategy, clinical research, and quality assurance, enabling safe and effective technologies to reach patients worldwide. Our Principles • Make it POSSIBLE, • Make it WIN‑WIN, • Keep IMPROVING, • Keep GROWING, • Keep it DIVERSE Our Vision To democratise access to world‑class regulatory and clinical strategies, ensuring safer and more effective medical technologies for all. Our Mission We pioneer emerging technologies and navigate uncharted territories to redefine the future of the medical sector. Grow with Us If you are looking to take ownership of clinical projects and grow within a specialised and expert‑driven CRO, we would be pleased to hear from you.

Role Overview: The i2CAT Foundation in Barcelona is seeking high-potential postdoctoral candidates to co-develop competitive proposals for the 2026 MSCA Postdoctoral Fellowships. As a premier European hub for applied research, our center focuses on generating social and economic impact in the sectors of Telecommunications (6G), Cybersecurity, Connected Mobility, and GovTech. Scientific Director Dr. Xavier Costa and Dr. Josep Escrig will serve as the supervisors for this fellowship to oversee the researcher's scientific progress and professional integration. Fellows will gain access to state-of-the-art facilities, including Europe's first 6G space laboratory, and receive dedicated proposal-writing support from our European Project Officers. The following research pillars represent the directions we consider most promising for the evolution of autonomous digital workers. These are intended as a strategic starting point; candidates are not required to address all of them and are highly encouraged to propose variations or entirely new research directions that align with their specific expertise and vision for the future of Agentic AI. Research Pillar I:Multi-Agentic AI through Continual Learning and LLM Adaptation This pillar investigates how LLM-powered and new generations of agents can move beyond "frozen" pre-trained weights to become truly adaptive lifelong learners. You will explore Just-In-Time Reinforcement Learning (JitRL), a breakthrough approach that modulates a model's frozen prior toward an optimal posterior without expensive gradient updates or catastrophic forgetting . By leveraging non-parametric memory and adjusting action logits through the , agents can learn from live environmental feedback in real-time . Research will utilize state-of-the-art benchmarks like MEAL (Multi-agent Environments for Adaptive Learning) to ensure these adaptive agents maintain stable cooperation even as their surroundings and roles evolve . Research Pillar II: Quantum Multi-Agentic AI and Entanglement-Based Coordination Scaling multi-agent swarms currently faces a "communication wall" where message overhead grows quadratically with each new agent . This research line aims to shatter that wall by using Quantum Entanglement as a shared substrate for coordination, effectively bypassing the need for explicit message-passing . Through Entangled Quantum Multi-Agent Reinforcement Learning (eQMARL), you will design agents whose cognitive states are physically correlated, allowing for instantaneous state alignment upon quantum measurement . This framework enables constructive interference of compatible plans while incompatible ones are canceled out, allowing massive drone swarms or 6G network slices to synchronize with zero latency . Pillar III: Social Multi-Agentic AI and Cross-Stakeholder Trust This pillar explores the social intelligence required for Multi-Agentic AI systems where independent agents, belonging to different companies or stakeholders, must collaborate despite having different interests. You will investigate mechanisms for Indirect Reciprocity and Reputation Systems, allowing "digital strangers" to build trust and find human-like "win-win" collaborations in decentralized environments. By integrating mathematical Game Theory and negotiation mechanisms, you will develop protocols that lead agents toward a stable Nash Equilibrium, ensuring fair and efficient outcomes in complex environments such as GovTech participation platforms or multi-provider 6G network slices. By joining us, you can expect: • We practice a 4-1 hybrid model (4 days remotely, 1 day at the office) to balance face-to-face collaboration with deep-focus remote work. We embrace a hybrid model, but we truly encourage our team to soak up the in-office experience. There's a unique energy and collaboration in our new space that you simply can't replicate through a screen., • Enjoy core hours flexibility: as long as you're online for our team syncs between 10:00 and 15:00, you can design the rest of your day to fit your rhythm., • Early-Finish Fridays: We believe in a long weekend. Every Friday throughout the year is an intensive 6.5-hour workday, so you can kick off your personal time by mid-afternoon., • Intensive summer schedule: To help you enjoy the sun and balance family life during school holidays, we switch to a 7-hour workday from June 22nd to September 4th., • You get 27 paid vacation days per year, well above the legal minimum, giving you over five full weeks to recharge whenever you need them. You are asked to enjoy at least 12 vacation days during summer., • We will work so that you have a career plan to promote your growth and development. Application Details and Deadlines i2CAT provides a premier environment for researchers holding a PhD with up to 8 years of experience who meet the MSCA mobility rules. • Supervisors: Dr. Josep Escrig and Dr. Xavier Costa, • Mobility Rule: Candidates must not have resided or carried out their main activity in Spain for more than 12 months in the 36 months (1 year of the last 3 years) immediately before the call deadline., • Key Dates: Call opens April 9, 2026; Deadline September 9, 2026., • Contact: Interested candidates are invited to contact and with a CV and a brief research interest statement to begin co-developing a competitive proposal. Requirements: MUST HAVE: • PhD degree at the time of application., • Compliance with the MSCA mobility rule: candidates must not have resided or carried out their main activity in Spain for more than 12 months during the 36 months immediately before the call deadline., • Relevant scientific publications in Artificial Intelligence or related areas., • Previous participation in research projects at national, European, or international level. NICE TO HAVE: • PhD in Artificial Intelligence or a closely related field., • Strong publication record in Artificial Intelligence., • Publications in Agentic AI, Multi-Agent Systems, LLM-based agents, autonomous agents, or related topics., • Previous experience leading or coordinating research activities, work packages, or research projects.

Estamos creciendo y abrimos plaza para un arquitecto o arquitecta. Arquitecto +1 año de titulación. Y si tu primer trabajo como arquitecto fuese enseñar a proyectar?.

Te interesa formar parte de un.I+D+2i)? ¿Quieres trabajar en un entorno puntero con todas las innovaciones tecnológicas a tu alcance?.Leitat es un centro tecnológico de referencia a nivel estatal y europeo.Con más de 100 años de historia, cuenta con un equipo de más de 400 profesionales, exper

PAULSON es una firma de inversión inmobiliaria especializada en el mercado residencial de obra nueva en España. A través de su división de Lending financia a promotores y proyectos de desarrollo residencial de obra nueva en España mediante préstamos y líneas de crédito con garantía hipotecaria. Con más de 120 operaciones firmadas y más de 170 millones de euros invertidos, la firma combina criterio técnico propio y relación directa con el promotor a lo largo de toda la vida del préstamo. Misión del puesto El/la Project Monitoring Analyst se integrará en el área de Project Monitoring de la firma y reportará directamente al Head of Project Monitoring, a quien trasladará de forma periódica el estado y el avance de las obras del portfolio. Será responsable de supervisar y analizar el avance técnico y económico de los proyectos financiados por la firma, asegurando el cumplimiento de plazos, presupuestos y estándares de calidad. Realizará visitas a obra para verificar los avances reales. Actuará como puente entre la firma y el promotor y garantizará que las disposiciones del préstamo se ajusten al avance de obra real verificado. Responsabilidades principales · Revisar y validar los avances de obra y certificaciones del promotor/constructor. · Realizar visitas periódicas a las obras para verificar el estado de ejecución. · Analizar desviaciones en costes, plazos y/o calidad y proponer medidas correctivas. · Coordinarse con equipos técnicos externos e internos. · Preparar informes de Project Monitoring para el Comité de Inversiones y el equipo de análisis. · Validar las certificaciones de obra y las facturas asociadas a cada disposición mensual del préstamo, asegurando que cada disposición se corresponde con el avance de obra realmente ejecutado y verificado en campo. · Colaborar con el resto del equipo en los procesos de Due Diligence técnica previa a nuevas financiaciones. · Monitorizar riesgos técnicos, urbanísticos y de construcción que puedan afectar a la inversión. Formación y experiencia · Formación en Arquitectura, Arquitectura Técnica, Ingeniería Civil o similar. · Experiencia mínima de 3 a 5 años en Project Monitoring, Project Management, consultoría técnica o dirección de obra. Conocimientos técnicos · Conocimiento sólido de normativa urbanística y de construcción en España. · Conocimiento de las fases del proyecto de promoción inmobiliaria y su documentación. · Habilidad para el análisis de presupuestos de obra y lectura de certificaciones. · Dominio alto de Excel para el control financiero de promociones y obras. Movilidad · Disponibilidad para viajar y carnet de conducir. Se valorará · Experiencia trabajando con promotores, fondos o entidades financieras. · Nivel alto de inglés. Competencias clave · Criterio técnico para evaluar la viabilidad y el avance real de la obra frente a lo certificado. · Rigor analítico y crítico en el control de costes, plazos y desviaciones presupuestarias. · Capacidad para vincular el avance físico de la obra con las disposiciones y los hitos del préstamo. · Visión de riesgo orientada a proteger la inversión (técnico, urbanístico y de construcción). · Comunicación clara. · Autonomía, capacidad de organización y disposición para el trabajo de campo.

Who are we? AESA Prep Academy of Barcelona is an international, American high school that offers grades 9 to 12. Our campus forms part of the AESA International School System, with schools in Texas and online. We are an international school accredited by Cognia and the Generalitat of Catalonia. https://aesaprepbarcelona.com/ Our team currently consists of a group of education professionals, all with different nationalities and backgrounds, working to provide an impactful and positive learning experience to all our high school students. We are seeking a teacher who is passionate about education and committed to the success of our students and our organization. The person joining our team is proactive, organized, works well on a diverse team, and has a positive attitude. What would you do? • Give face-to-face lessons in small classes., • Plan, evaluate, and revise curriculum, course content, course materials and instructional methods., • Prepare course materials such as syllabi, homework assignments, activities and experiments., • Evaluate student performance and share continuous feedback with the coordinator(s), parents and other relevant stakeholders., • Maintain student attendance, grades, and other required records., • Record student performance through our learning management system. Minimum Requirements: • Bachelor’s degree or equivalent in the field of Mathematics and a teaching certification, or advanced degree in the field of Mathematics., • At least 2-3 years of teaching experience., • C1 proficiency level in English (written and verbal)., • Excellent creative, communication, and presentation skills., • Engaging personality and dynamic teaching style. Preferred Requirements: • Advanced degree in the field of Mathematics and a teaching certification., • 5+ years of teaching experience., • C2 proficiency level in English (written and verbal)., • Excellent creative, communication, and presentation skills., • Engaging personality and dynamic teaching style. What do we offer? • Competitive salary, • Professional development opportunities, • Friendly working environment, • Opportunities for career advancement within the organization Schedule: Monday to Friday, from 9am until 4pm. All applications must be sent directly to: with a motivation letter. Important: The candidate must have residency in Barcelona, Spain. Applications not following the above instructions will be automatically disregarded.

Who are we? AESA Prep Academy of Barcelona is an international, American high school that offers grades 9 to 12. Our campus forms part of the AESA International School System, with schools in Texas and online. We are an international school accredited by Cognia and the Generalitat of Catalonia. https://aesaprepbarcelona.com/ Our team currently consists of a group of education professionals, all with different nationalities and backgrounds, working to provide an impactful and positive learning experience to all our high school students. We are seeking a teacher who is passionate about education and committed to the success of our students and our organization. The person joining our team is proactive, organized, works well on a diverse team, and has a positive attitude. What would you do? • Give face-to-face lessons in small classes., • Plan, evaluate, and revise curriculum, course content, course materials and instructional methods., • Prepare course materials such as syllabi, homework assignments, activities and experiments., • Evaluate student performance and share continuous feedback with the coordinator(s), parents and other relevant stakeholders., • Maintain student attendance, grades, and other required records., • Record student performance through our learning management system. Minimum Requirements: • Bachelor’s degree or equivalent in the field of Mathematics and a teaching certification, or advanced degree in the field of Mathematics., • At least 2-3 years of teaching experience., • C1 proficiency level in English (written and verbal)., • Excellent creative, communication, and presentation skills., • Engaging personality and dynamic teaching style. Preferred Requirements: • Advanced degree in the field of Mathematics and a teaching certification., • 5+ years of teaching experience., • C2 proficiency level in English (written and verbal)., • Excellent creative, communication, and presentation skills., • Engaging personality and dynamic teaching style. What do we offer? • Competitive salary, • Professional development opportunities, • Friendly working environment, • Opportunities for career advancement within the organization Schedule: Monday to Friday, from 9am until 4pm. All applications must be sent directly to: with a motivation letter. Important: The candidate must have residency in Barcelona, Spain. Applications not following the above instructions will be automatically disregarded.

Apply state-of-the-art research in NLP, LLMs, and generative AI to production systems. Collaborate with engineering and product teams to turn research into practical solutions. Stay at the frontier of AI by evaluating new research and integrating findings.

Clinical Research Manager | MedTech and IVD Location: Spain, Portugal or UK (Remote with occasional in‑person activities) Employment Type: Full‑time Role Summary We are seeking an experienced Clinical Research Manager to lead and coordinate clinical studies for medical devices and in vitro diagnostics. The role covers the full clinical lifecycle, from early study design and start‑up through execution and close‑out, in compliance with GCP, ISO standards, and applicable European and local regulations. You will act as a key interface between sponsors, study sites, and internal teams, ensuring high‑quality delivery, regulatory compliance, and effective project and people management. This role also includes mentoring and development responsibilities for junior team members and consultants. Key Responsibilities You will: • Lead and manage Clinical Investigations and Performance Studies for medical devices and IVDs from start‑up to close‑out, • Ensure studies are conducted in compliance with GCP, ISO 14155, ISO 20916, EU regulations, and local requirements, • Contribute to protocol, CRF, ICF, and study documentation design and review, • Coordinate submissions to Ethics Committees and Competent Authorities, • Oversee site initiation, monitoring activities, and ongoing site management, • Maintain close communication with investigators, study coordinators, sponsors, and internal stakeholders, • Monitor project progress against timelines, quality metrics, and budgets, • Identify project risks and implement mitigation strategies in collaboration with the project team, • Act as the primary daily point of contact for sponsors, • Develop, maintain, and oversee Trial Master Files and eTMFs, • Prepare and present project status updates to internal and external stakeholders, • Negotiate contracts with study sites, vendors, and service providers, • Manage project finances according to sponsor contracts and approved budgets, • Provide input into proposals, budgets, and bid defense activities, • Ensure adherence to QMS procedures and contribute to continuous improvement initiatives, • Participate in Management Review activities as required People Development and Team Responsibilities You will also: • Support onboarding of new team members by providing guidance, tools access, and structured induction, • Coordinate and follow initial training plans for assigned employees or consultants, • Conduct periodic performance evaluations and development discussions, • Review training effectiveness and contribute to continuous professional development planning, • Support definition and follow‑up of individual training and growth plans Requirements Must‑Have • 1–3 years of professional experience as a Clinical Project Manager or Clinical Research Manager in medical devices or IVDs, • Solid working knowledge of GCP and clinical research standards, • Bachelor’s degree in Life Sciences, • Advanced written and verbal English (C1–C2 level or equivalent), • Ability to manage multiple projects and stakeholders in an international environment, • Availability for remote work with occasional in‑person activities Nice to Have • Master’s degree in Life Sciences, • PhD or advanced scientific training in a medical or related discipline, • Experience with ISO 14155 and or ISO 20916, • Fluency in additional EU languages, • Experience supporting audits or inspections Why Join MDx CRO At MDx CRO, you will join a highly specialised and rapidly growing organisation recognised across the MedTech and IVD sector. We offer a professional, collaborative environment where expertise is valued and continuous development is encouraged. You will benefit from: • Exposure to complex and meaningful clinical projects, • A high level of autonomy and responsibility, • Close collaboration with senior regulatory and clinical experts, • Opportunities for professional and career growth About MDx CRO MDx CRO is a leading Contract Research Organisation specialising in in vitro diagnostics and medical devices. We support clients through regulatory strategy, clinical research, and quality assurance, enabling safe and effective technologies to reach patients worldwide. Our Principles • Make it POSSIBLE, • Make it WIN‑WIN, • Keep IMPROVING, • Keep GROWING, • Keep it DIVERSE Our Vision To democratise access to world‑class regulatory and clinical strategies, ensuring safer and more effective medical technologies for all. Our Mission We pioneer emerging technologies and navigate uncharted territories to redefine the future of the medical sector. Grow with Us If you are looking to take ownership of clinical projects and grow within a specialised and expert‑driven CRO, we would be pleased to hear from you.

Buscamos Profesores/Coaches de Tenis y Pádel – Clases Particulares (Todos los niveles y edades) Descripción del puesto: Estamos en búsqueda de profesores y coaches de tenis y pádel apasionados, responsables y con experiencia para impartir clases particulares a alumnos de todas las edades y niveles (infantil, juvenil y adultos). Las clases se ofrecerán en diferentes zonas y horarios, con posibilidad de adaptarse a la disponibilidad del profesor. Funciones: Impartir clases particulares de tenis y/o pádel. Adaptar la enseñanza al nivel y objetivos de cada alumno. Realizar seguimiento del progreso de los alumnos. Fomentar un ambiente positivo, motivador y profesional. Requisitos: Experiencia previa como profesor o coach de tenis o pádel (mínimo 1 año). Formación acreditada (Titulación oficial de monitor o entrenador, o experiencia demostrable). Capacidad para trabajar con alumnos de distintas edades y niveles. Buena presencia y habilidades comunicativas. Vehículo propio o disponibilidad para desplazarse (según zona de trabajo). Se valorará conocimiento de inglés u otros idiomas. Se ofrece: Flexibilidad horaria y autonomía para organizar tus clases. Buenas condiciones económicas por clase impartida. Posibilidad de aumentar progresivamente el número de alumnos. Entorno profesional, dinámico y en crecimiento. Soporte en la gestión de agenda y nuevos alumnos. Ubicación: Varias zonas disponibles. Indica tu área de disponibilidad.

¡Únete a Nuestro Equipo de Profesores Particulares! ¿Te apasiona la enseñanza? ¿Quieres compartir tus conocimientos y apoyar a estudiantes de todas las edades? ¡Esta es tu oportunidad! Estamos en búsqueda de profesores particulares en todas las áreas para impartir clases individuales a domicilio y, según la demanda, online. ¿Qué Buscamos? Profesionales con experiencia docente o sólidos conocimientos en su área. Aptitud para trabajar con alumnos de todas las edades y niveles (primaria, secundaria, universidad y adultos). Capacidad para adaptar la enseñanza a las necesidades y ritmo del estudiante. Áreas de Enseñanza Ciencias: Matemáticas, Física, Química, Biología Idiomas: Inglés, Francés, Alemán, Español para extranjeros, entre otros Arte y Música: Pintura, Dibujo, Instrumentos musicales Tecnología: Programación, Ofimática, Diseño gráfico Apoyo escolar: Refuerzo de materias y preparación para exámenes Ofrecemos: Horarios flexibles según tu disponibilidad. Libertad para elegir las zonas donde impartes clases. Posibilidad de dictar clases online si prefieres trabajar desde casa. Remuneración competitiva y puntual. Formar parte de una comunidad educativa comprometida con la enseñanza personalizada. Requisitos: *RESIDENTES EN ESPAÑA* Nativos de la lengua española o diploma C2 para No nativos. Experiencia en enseñanza (formal o informal) o en la materia que deseas impartir. Actitud proactiva, responsable y paciente. ¡Haz la diferencia en la educación de nuestros estudiantes y construyamos juntos un futuro mejor!

At the i2CAT Space Communications Unit, we don't just research the future; we build it.We are looking for a Head of Innovation with a strategic mindset to lead the intersection between advanced research and market reality.Your challenge will be to transform the center's technical capabilities into s

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Gracias a nuestra plataforma de gestión de clientes, podrás aceptar o descartar solicitudes de trabajos en tu área, enviando presupuestos solo a los clientes que más te interesen. Conocimientos previos para desarrollar funciones de Profesor/a de inglés nativo. Solicitudes de nuevos trabajos y c

El profesor contesta dudas y corrige el proyecto en base a una rúbrica hecha a medida. En Editeca, escuela online especializada en formación BIM, buscamos profesores colaboradores externos para impartir clases online. El profesor graba vídeos en su casa u oficina bajo nuestra metodología.

El profesor contesta dudas y corrige el proyecto en base a una rúbrica hecha a medida. En Editeca, escuela online especializada en formación BIM, buscamos profesores colaboradores externos para impartir clases online. El profesor graba vídeos en su casa u oficina bajo nuestra metodología.

Solicitudes de nuevos trabajos y clientes en tu zona, que necesitan Profesor/a particular de matemáticas. Gracias a nuestra plataforma de gestión de clientes, podrás aceptar o descartar solicitudes de trabajos en tu área, enviando presupuestos solo a los clientes que más te interesen. Conocimie