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Pharmacokinetic Scientist We’re looking for a skilled Pharmacokinetic Scientist to lead key PK activities across our drug development programs. In this role, you’ll design and interpret studies, serve as a principal investigator, guide ADME/DMPK strategy, and play a central role in supporting both internal teams and external partners. Key Responsibilities • Lead assigned studies as Principal Investigator/Study Director, overseeing all PK-related activities., • Design, execute and interpret pharmacokinetic and pharmacodynamic analyses across preclinical and clinical programs., • Conduct non‑compartmental and compartmental analyses using Phoenix WinNonlin., • Prepare protocols and scientific reports describing study objectives, methodology, analysis and results across multiple species and biological matrices., • Analyse and interpret PK data from a broad range of studies (DMPK, ADME, BE/BA, toxicology, SAD/MAD) and refine sampling and dosing strategies., • Provide expert ADME/DMPK input into non‑clinical and clinical study design., • Ensure full compliance with GLP, GCP, SOPs and sponsor protocols., • Engage with clients, support onboarding, contribute to business development, and present study findings directly to sponsors., • MSc or PhD in Pharmacy, Chemistry, Biochemistry, Biology, Biomedicine or a related life science., • Hands-on experience with toxicology studies, bioavailability/bioequivalence, biomarkers and immunogenicity testing., • Advanced proficiency with Phoenix WinNonlin., • Strong understanding of ADME/DMPK regulatory expectations., • Proven ability to work collaboratively in a matrix environment while managing multiple priorities., • Strong interpersonal and communication skills in fluent English., • Proficient with MS Office tools. About Planet Pharma: Planet Pharma is an American parented Employment Business/Agency that provides global staffing services with its head-quarters in Chicago and our EMEA regional office located in Central London. We have invested significantly in creating a robust international platform that enables us to work compliantly in 30+ countries with a current network of 2500+ active contractors globally as well as a very strong permanent / direct hire recruitment offering. Our specialist knowledge and close relationships with our clients and the wider industry really makes us unique in our field. Just recently we were recognised by FORBES as the 17th best professional staffing firm, and have won multiple awards from industry accredited bodies for our commitment to excellence and service delivery. We have extensive functional expertise including: Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs / Writing. We are an equal opportunities Recruitment Business and Agency. We welcome applications from all suitably qualified candidates regardless of their race, sex, disability, religion/belief, sexual orientation or age.

¡ÚNETE A NUESTRO EQUIPO EN BARCELONA! 🌟 Posición: Guía Acompañante de Turistas y Gestor de Reservas Tipo de contrato: Indefinido Jornada laboral: Completa (8:30-17:30) Salario: 18.000€ a 20.000€ brutos anuales ¿Quiénes somos? Somos la delegación en Barcelona de un importante touroperador de Tokio, con un equipo entusiasta y dinámico. Buscamos incorporar a un nuevo miembro para apoyar a nuestros viajeros japoneses y brindarles una experiencia única. Requisitos: • Residencia en Barcelona, • Nivel de japonés Noken 3 o superior, con fluidez en la conversación., • Experiencia en atención al público, preferentemente en el sector turístico., • Actitud sociable, proactiva y capacidad para trabajar en equipo., • Titulación preferible en Estudios de Asia Oriental, Traducción e Interpretación, Turismo, entre otras. Funciones: • Asistencia a los turistas y gestión de su experiencia en Barcelona., • Interpretación de patrimonio y cultura local., • Recogida y acompañamiento de viajeros., • Atención personalizada y gestión de reservas y entradas. Si tienes pasión por la cultura japonesa y el turismo, ¡te estamos esperando! Interesados: Enviar CV en castellano y japonés a: ¡Esperamos conocerte pronto y que te unas a nuestro equipo! 💼✨

🧬CNAG – The Institute The Centro Nacional de Análisis Genómico (CNAG) is a world-leading genomics research institute located in Barcelona. With state-of-the-art genomic analysis capabilities, CNAG supports national and international researchers, as well as clinicians, in their pursuit of cutting-edge research and clinical applications. The CNAG carries out genomic analysis projects of any scale to improve quality of life in collaboration with the Spanish, European and international research community. CNAG is one of the largest genome analysis centers in Europe, with Illumina, Oxford Nanopore Technologies and Pacific Biosciences sequencers, state-of-the-art single-cell equipment, and an extensive computing infrastructure. The operation is certified according to ISO 9001 and ISO 27001 and accredited according to ISO 17025, delivering standardized, high-quality data for research and clinics. The CNAG has more than 130 professionals who participate in major International Genome Initiatives and EU funded projects. The institute is structured into different teams, units and groups, spanning from Bioinformatics, Sequencing, Single-cell, to Corporate Management. 🧬About the Unit/ Team The Biorepository team is a part of the Sequencing unit that provides highly specialized support in next generation genomics to national and international researchers and clinicians and conducts strategic development and implementation of the protocols. It assesses DNA/RNA extraction procedures used by collaborators, evaluates sample suitability for CNAG sequencing applications, and coordinates sample shipments. The biorepository also ensures appropriate sample storage under highly controlled conditions and distributes working aliquots to the Sample Preparation and Long Read Sequencing teams. The contract will be funded by the Carlos III Health Institute through project “PMPER24/00002,” financed by the European Union – NextGenerationEU 🧬The Role The successful candidate will work closely with the Biorepository Manager and team members, and the Head of the Sequencing Unit to maintain, develop, implement, and run protocols within the Biorepository team. Responsibilities: • Sample reception, verification, and LIMS data entry., • DNA and RNA samples quality control., • Preparation of aliquots for sequencing, manually and using automated systems., • Development and implementation of new quality control protocols and integration of new instruments, • Sample data management through CNAG LIMS tools., • Keeping rigorous audit trails of the work carried out, writing and updating documentation such as Standard Operating Procedures (SOPs)., • Recognizing and reporting erroneous protocol outcomes., • Stock and orders management. Professional experience • At least 3 years of work experience in molecular biological laboratory, in particular using: DNA/RNA extraction procedures, DNA/RNA quality control, quantification techniques, gel electrophoresis, PCR and other enzymatic reactions., • At least 1 year of work experience in data base use, especially lab centered (LIMS)., • Experience with liquid handling robots., • Experience with capillary electrophoresis instruments, • Experience in ISO certified/accredited environments. Must Have • Excellent laboratory techniques and able to work very reliably, pay attention to detail and work as part of a team, • Proactive and autonomous attitude, • Capability to work with computers and common software packages, • Automation and instrumentation competence, • The emphasis will be on excellent laboratory practices, • Fluent in English, • Advanced MS Office skills Nice to have • Experience with biobanking or biorepository workflows for sequencing applications, • Knowledge of sample traceability, chain of custody, and documentation., • Experience coordinating sample shipments and logistics., • Familiarity with regulatory or ethical requirements related to biological samples. 🧬Competences • Responsible and reliable working attitude, with willingness to learn., • Good organizational and time-management skills in a supervised laboratory environment., • Ability to follow SOPs, instructions, and established workflows., • Attention to detail and commitment to good laboratory practices., • Ability to recognize routine issues and report them to senior staff., • Ability to work safely in a laboratory, maintaining good housekeeping standards., • Basic understanding of quality procedures and regulatory requirements relevant to the role., • Technical aptitude for working with laboratory instruments and automation., • Ability to record data accurately and maintain clear laboratory documentation., • Ability to communicate observations and results clearly within the team., • Cooperative attitude and ability to work effectively as part of a team. Education and training • Master’s or PhD degree in Molecular Biology, Biochemistry, Biotechnology or a related field. 🧬The Offer • Contract duration: 12 months, • Estimated annual gross salary: Salary is commensurate with qualifications and consistent with our pay scales., • Target start date: March 2026 We provide a highly stimulating environment with state-of-the-art infrastructures, and unique professional career development opportunities. We offer and promote a diverse and inclusive environment and welcome applicants regardless of age, disability, gender, nationality, ethnicity, religion, sexual orientation or gender identity. We are committed to reconciling work and family life for our employees and are offering the opportunity to benefit from flexible working hours. Application Procedure All applications must include: • A complete CV including contact details., • Motivation letter, • Contact details of two referees. All applications must be addressed to – Deadline: Please submit your application by 28/02/2026 🌐 Please, see all our job opportunities in the Career site of CNAG website: ___ sequencing for a better life

🧬Consorcio para la Explotación del Centro Nacional de Análisis Genómico El Centro Nacional de Análisis Genómico (CNAG) es un instituto de investigación en genómica de clase mundial ubicado en Barcelona. Con capacidades de análisis genómico de última generación, el CNAG apoya a investigadores nacionales e internacionales, así como a clínicos, en su búsqueda de investigación de vanguardia y aplicaciones clínicas. El CNAG lleva a cabo proyectos de análisis genómico de cualquier escala para mejorar la calidad de vida, en colaboración con la comunidad científica española, europea e internacional. El CNAG es uno de los mayores centros de análisis genómico de Europa, con secuenciadores de Illumina, Oxford Nanopore Technologies y Pacific Biosciences, equipos de última generación para análisis de célula única, y una infraestructura informática extensa. Su operación está certificada según ISO 9001 e ISO 27001 y acreditada según ISO 17025, ofreciendo datos estandarizados y de alta calidad para investigación y aplicaciones clínicas. El CNAG cuenta con más de 130 profesionales que participan en importantes iniciativas internacionales del genoma y en proyectos financiados por la UE. El instituto está estructurado en diferentes equipos, unidades y grupos, que abarcan desde Bioinformática, Secuenciación y Análisis de Célula Única, hasta Gestión Corporativa. 🧬Acerca de la Unidad/Equipo La Unidad de Secuenciación del CNAG ofrece a los investigadores acceso a métodos de secuenciación de alto rendimiento de última generación para una amplia gama de aplicaciones. Actualmente, operamos varios tipos de secuenciadores de Illumina, así como plataformas de Oxford Nanopore Technologies y Pacific Biosciences. Los miembros de la plataforma de secuenciación incluyen investigadores postdoctorales, ingenieros y técnicos con formación especializada, que conforman un equipo altamente cualificado para llevar a cabo las tareas científicas especializadas que requiere la secuenciación. Han establecido, y continúan desarrollando, numerosas técnicas para analizar la información codificada en los genomas. 🧬Funciones del Puesto La persona seleccionada trabajará en estrecha colaboración con los equipos de la Unidad de Secuenciación y, bajo la supervisión de la Dirección de la Unidad de Secuenciación, apoyará el correcto funcionamiento de los espacios de laboratorio, garantizando la limpieza y el control de la contaminación de acuerdo con los protocolos de laboratorio establecidos y los requisitos de acceso restringido. Este puesto desempeña un papel clave en el mantenimiento de los laboratorios en condiciones que eviten la contaminación de muestras y experimentos, la gestión de suministros básicos de laboratorio, el apoyo a los procedimientos de gestión de residuos y la realización de tareas rutinarias de apoyo operativo conforme a protocolos definidos. 🧬Responsabilidades • Limpieza y mantenimiento de los espacios de laboratorio para garantizar entornos libres de contaminación para el trabajo experimental, de acuerdo con los protocolos internos y los estándares de calidad del laboratorio., • Trabajo en condiciones de acceso restringido, cumpliendo las normas del laboratorio, los requisitos de bioseguridad y las políticas de confidencialidad., • Solicitud, recepción, organización y reposición de consumibles básicos de laboratorio (p. ej., guantes, papel de laboratorio, puntas de pipeta, etanol, material de vidrio y plástico, desinfectantes, detergentes y productos de limpieza)., • Control de los niveles de inventario y notificación de faltantes o inconsistencias al personal responsable., • Autoclavado de instrumentos y materiales de laboratorio siguiendo los procedimientos aprobados de descontaminación y esterilización., • Coordinación de la recogida y eliminación de residuos biológicos y químicos del laboratorio con el personal de mantenimiento del PCB, en cumplimiento de los requisitos de seguridad y normativos., • Mantenimiento del orden en los espacios de laboratorio y comunicación de desviaciones, riesgos o posibles problemas de contaminación al personal sénior., • Apoyo en tareas logísticas y operativas rutinarias necesarias para el correcto funcionamiento diario de los laboratorios. 🧬Experiencia Profesional • Experiencia demostrable en limpieza de laboratorios, oficinas u otros entornos controlados (p. ej., oficinas, laboratorios de investigación, salas blancas, laboratorios clínicos o industriales)., • Experiencia en organización de almacén, gestión de inventarios o logística en entornos técnicos., • Familiaridad con principios básicos de seguridad. 🧬Requisitos Imprescindibles • Alta atención al detalle y fuerte sentido de la responsabilidad en el mantenimiento de entornos con control de contaminación., • Capacidad para seguir con precisión los protocolos internos, las directrices de calidad y los procedimientos de acceso restringido., • Estilo de trabajo fiable, diligente y metódico., • Capacidad para trabajar de forma autónoma y en equipo., • Respeto por los requisitos de confidencialidad y la integridad del laboratorio., • Conocimientos básicos de informática para el control de inventarios, uso de Excel y Word para documentación sencilla y correo electrónico para la comunicación. Se Valorará • Experiencia previa en entornos de laboratorio certificados o acreditados (ISO)., • Familiaridad con autoclaves y procedimientos de esterilización., • Experiencia en la gestión y coordinación de residuos biológicos o químicos. 🧬Competencias • Alta concienciación sobre los riesgos de contaminación y buenas prácticas de laboratorio., • Ejecución constante y cuidadosa de tareas rutinarias., • Buenas habilidades organizativas y de gestión del tiempo en un entorno de laboratorio supervisado., • Disposición para aprender y aplicar procedimientos específicos de calidad y seguridad del laboratorio., • Capacidad para comunicar observaciones o incidencias de forma clara al personal sénior., • Capacidad para interactuar eficazmente con los equipos de mantenimiento e infraestructuras. 🧬Formación y Educación Grado Medio, Bachillerato, formación profesional o formación equivalente. Formación adicional en prácticas de laboratorio, control de la contaminación o seguridad será valorada, aunque no es imprescindible. 🧬La Oferta • Duración del contrato: 12 meses, • Salario bruto anual estimado: acorde a la cualificación y conforme a nuestras escalas salariales, • Fecha prevista de incorporación: 01/03/2026 Ofrecemos un entorno de trabajo altamente estimulante, con infraestructuras de laboratorio de última generación y la oportunidad de contribuir directamente a investigación genómica de alta calidad. Promovemos un entorno diverso e inclusivo y damos la bienvenida a candidaturas independientemente de la edad, discapacidad, género, nacionalidad, origen étnico, religión, orientación sexual o identidad de género. Estamos comprometidos con la conciliación de la vida laboral y familiar y ofrecemos la posibilidad de horarios flexibles cuando sea apropiado. 🧬Procedimiento de Solicitud Todas las candidaturas deberán incluir: • CV completo con datos de contacto, • Carta de motivación, • Datos de contacto de dos personas de referencia Las solicitudes deberán dirigirse a: Fecha límite de presentación: 28/02/2026 Consulta todas nuestras oportunidades laborales en el apartado Careers de la web de CNAG: ___

About us Royal Queen Seeds is one of the world’s leading cannabis seed brands. What started in 2011 as a single website has evolved into a global, digital-first company with brand stores, international reach, and a strong focus on innovation, education, and community. Our digital team is based near Barcelona in a modern, open, and collaborative office environment. We move fast, test constantly, and care deeply about brand, product, and user experience. We collaborate with iconic global figures and cultural leaders — including Mike Tyson — and develop experiences for both direct-to-consumer (B2C) and business-to-business (B2B) audiences. As we enter a new phase of growth, we are redesigning and elevating the RQS experience, and we’re looking for a UX & Design Director to lead this transformation. The role As UX & Design Director, you will own the UX vision, design quality, and visual consistency across B2C and B2B digital experiences, with a strong focus on e-commerce performance, brand storytelling, and scalable design systems. You will work closely with: • Internal teams (Design, Growth, CRM, SEO, Content, Development, B2B), • Senior stakeholders and management This role combines strategic leadership, hands-on design oversight, and operational excellence. You won’t just design, you’ll define standards, guide execution, and ensure quality from concept to live product. Your mission Deliver a modern, conversion-optimized, and brand-driven digital experience across B2C and B2B, by building a strong UX operation, elevating design quality, and aligning user experience with business growth, including high-profile collaborations. What you’ll be responsible for UX & Product Experience (B2C & B2B) • Define and own the global UX vision for RoyalQueenSeeds.com and related B2B digital platforms., • Lead the new website layout implementation., • Review, refine, and elevate UX/UI proposals with quality tweaks, brand alignment, and CRO focus., • Oversee post-implementation QA and UX debugging (layout issues, responsiveness, usability flaws)., • Ensure seamless experiences across homepage, navigation, PDPs, collections, landings, and B2B portals or flows. Design Direction & Brand Consistency • Own the visual language and design system across B2C, B2B, CRM, campaigns, and partnerships., • Ensure brand storytelling is consistently expressed through layout, imagery, and hierarchy., • Supervise logos, imagery, and visual assets across projects, • Act as final design quality gate before implementation. B2B Experience & Marketing Assets • Define UX and visual standards for B2B journeys (wholesale, partners, distributors)., • Oversee design of B2B marketing and sales materials (digital and print)., • Ensure consistency between B2B brand expression and B2C experience, while respecting different user needs. Design Operations & Workflow • Structure and optimize Figma workflows, libraries, and handoffs., • Build scalable processes between design, development, marketing, and B2B teams., • Document UX decisions, standards, and best practices. Leadership & Collaboration • Lead and mentor designers (and potentially grow the design team)., • Collaborate closely with Growth, CRM, SEO, Content, and B2B teams to align UX with performance goals., • Participate in management meetings, presenting progress, risks, and opportunities., • Translate business objectives into clear UX and design priorities. What we’re looking for Experience & Skills • 4+ years of experience in UX/UI, digital design, or product design, with leadership exposure., • Strong background in e-commerce UX., • Excellent command of Figma (components, systems, collaboration workflows)., • Solid understanding of CRO, usability, and performance-driven design., • Strong visual design foundations: typography, layout, hierarchy, branding., • Ability to debug UX/UI issues post-implementation. Soft skills • Ownership mindset: you take responsibility for outcomes, not just deliverables., • Clear communicator, able to give structured, constructive feedback., • Comfortable balancing strategy and hands-on execution., • Proactive, organized, and detail-oriented., • Collaborative leader who elevates others’ work. Languages • Fluent in English, • Spanish is valued What we offer • Permanent contract, • Flexible working hours (Monday–Friday), • Attractive compensation package, • Open, dynamic, and international work environment, • High ownership and real impact on a global brand, • Exposure to cutting-edge marketing, UX, CRO, B2C, B2B, and high-profile collaborations, • Free food, drinks, and fruit at the office 🍎☕ Note: Due to location, access to a car or motorbike is required. Why this role is special You’ll be joining Royal Queen Seeds at a pivotal moment: redefining its digital experience, scaling B2B and B2C platforms, and working on globally visible projects, including collaborations with icons like Mike Tyson. This is not a pixel-pushing role. It’s a strategic UX & Design leadership position with real ownership, real impact, and real reach.

Optimization Scientist Barcelona | Modelo híbrido Desde LHH, acompañamos a una organización líder en su sector en la incorporación de un/a Optimization Scientist para un programa clave de transformación analítica y toma de decisiones avanzadas. El rol se integra en un equipo que trabaja directamente con negocio para abordar retos complejos de planificación, asignación y eficiencia operativa, donde la clave no es solo analizar datos, sino diseñar la mejor decisión posible. Se trata de una posición con alto componente consultivo, que combina pensamiento estructurado, modelado matemático y capacidad para interactuar con distintos stakeholders. Principales responsabilidades Analizar problemáticas complejas de negocio y estructurarlas en modelos de optimización. Traducir reglas operativas y necesidades del cliente en restricciones y objetivos matemáticos. Diseñar y adaptar soluciones de optimización orientadas a impacto real y uso en producción. Evaluar escenarios, sensibilidades y trade-offs para apoyar la toma de decisiones informada. Colaborar con equipos técnicos y de delivery para asegurar la viabilidad y escalabilidad de las soluciones. Comunicar conclusiones y recomendaciones de forma clara a interlocutores técnicos y de negocio. Perfil buscado Formación técnica en Ingeniería, Matemáticas, Investigación Operativa, Informática o disciplinas afines. Experiencia profesional de al menos 3–4 años en proyectos de optimización o modelado matemático aplicado. Sólida capacidad para estructurar problemas complejos y transformarlos en soluciones accionables. Experiencia en programación (preferentemente Python) y uso de librerías de optimización. Buen nivel de inglés, tanto oral como escrito. Se valorará Experiencia con técnicas de optimización clásica y/o metaheurística. Conocimiento de programación matemática y modelado de restricciones. Experiencia previa en consultoría tecnológica o proyectos para cliente. Exposición a entornos cloud y despliegue de soluciones analíticas. ¿Qué ofrece el proyecto? Participación en proyectos estratégicos de alto impacto. Entorno colaborativo, con foco en aprendizaje continuo. Posición estable, con recorrido y visibilidad. Modelo híbrido de trabajo y ubicación en Barcelona. Condiciones alineadas con la experiencia aportada. Si te motiva trabajar en la intersección entre negocio, analítica avanzada y toma de decisiones, desde LHH estaremos encantados de conocerte y ampliar detalles del proyecto.

El Barcelona Brain Health Centre (BBHC) busca incorporar un/a Treballador/a Social Clínic/a – Clinical Patient Navigator per guiar i acompanyar els nous pacients de la unitat de memòria durant les primeres fases del procés de diagnòstic i tractament. Aquesta figura té com a objectiu informar pacients i famílies, facilitar la navegació pel sistema sanitari , gestionar la recollida de consentiments informats per a recerca i assegurar una comunicació fluida entre la Unitat de Memòria de l’Hospital del Mar (HM) i el Brain Health Service (BHS) del BBRC. Responsabilitats principals Proporcionar informació i suport detallat a pacients i famílies en les primeres fases del deteriorament cognitiu. Gestionar consultes telefòniques, resolent preguntes freqüents de baixa complexitat i derivant les més complexes al neuròleg assignat. Facilitar la comprensió del circuit assistencial i orientar pacients i famílies en la navegació pel sistema sanitari i de recerca. Dissenyar i implementar procediments per a l’obtenció de consentiments informats segons les Bones Pràctiques Clíniques (GCP) i els protocols d’estudi. Explicar el paper clau de la recerca i implementar estratègies de reclutament de participants. Garantir el registre prospectiu de dades de salut a les cohorts clíniques de l’Hospital del Mar. Introduir dades retrospectives rellevants a les cohorts clíniques. Identificar candidats/es potencials per a estudis de recerca i registres, contactant-los per proporcionar informació específica. Fer seguiment dels participants inclosos a les cohorts clíniques. Requisits acadèmics i professionals Grau en Treball Social o Infermeria. Mínim 5 anys d’experiència en el sistema sanitari. Experiència en recerca clínica (coordinació d’estudis, CRA/CRO en indústria). Es valorarà coneixement de polítiques d’assaigs clínics, ètica en recerca amb humans i GCP. Capacitat d’ús d’eines de fulls de càlcul (p. ex., Excel) per a tasques bàsiques de gestió de dades; coneixement de plataformes de gestió de dades (p. ex., REDCap) és un plus. Excel·lent comunicació oral i escrita en català, castellà i anglès. Competències personals Habilitats de comunicació. Iniciativa i proactivitat. Capacitat de treballar de manera autònoma i col·laborativa. Capacitat organitzativa. Habilitats interpersonals per a entorns interdisciplinaris. Capacitat de resolució de problemes i orientació a resultats. Interès a formar part d’una organització sense ànim de lucre amb missió social. Oferim Incorporació immediata. Posició a temps complet . Retribució segons experiència i d’acord amb la Política de Recompenses i el Pla de Desenvolupament del BBRC . Pla de compensació flexible (targeta de menjador, assegurança mèdica, guarderia). Vacances: 23 dies laborables proporcionals a la data d’incorporació, més dies addicionals segons el calendari (ponts i dies al març–abril i al desembre). Entorn estimulant amb excel·lents infraestructures i oportunitats úniques de desenvolupament professional. Entorn divers i inclusiu , amb oportunitats d’experiència en recerca multidisciplinària. Procés de selecció Per presentar la candidatura, cal enviar un únic fitxer PDF que inclogui: Carta de motivació , destacant els interessos, l’experiència i la motivació per unir-se a la missió de la Fundació. Currículum Vitae (CV) actualitzat.

Quality Control (QC) Technician – Biologics - Morning Shift 6am-2pmWe are seeking a highly motivated and detail-oriented Quality Control Technician to join our team, specializing in the analysis of biological products. This role involves hands-on laboratory work, project management, and technical oversight in a GMP-regulated environment.Key Responsibilities:Design, supervise, and execute quality control studies for biological products, with a strong focus on chromatography and HPLC techniques.Manage assigned projects, ensuring timely delivery and maintaining direct communication with clients.Oversee the preparation and maintenance of technical documentation, including standard operating procedures (SOPs), certificates of analysis, deviations, OOS reports, and CAPAs.Provide direction and supervision to technical staff, ensuring high-quality experimental execution and compliance with regulatory standards.Requirements:Bachelor’s or Master’s degree in Biochemistry, Biotechnology, Chemistry, or a related field.Minimum of 3 years of hands-on experience with HPLC and chromatography techniques.Proven experience in Quality Control within a pharmaceutical company, with a solid understanding of GMP regulations.Familiarity with electrophoretic techniques, Western Blot, ELISA, and protein quality control is a strong plus.Strong organizational and communication skills.Proficiency in English (written and spoken) is required.About Planet Pharma:Planet Pharma is an American parented Employment Business/Agency that provides global staffing services with its head-quarters in Chicago and our EMEA regional office located in Central London. We have invested significantly in creating a robust international platform that enables us to work compliantly in 30+ countries with a current network of 2500+ active contractors globally as well as a very strong permanent / direct hire recruitment offering.Our specialist knowledge and close relationships with our clients and the wider industry really makes us unique in our field. Just recently we were recognised by FORBES as the 17th best professional staffing firm, and have won multiple awards from industry accredited bodies for our commitment to excellence and service delivery. We have extensive functional expertise including: Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs / Writing.We are an equal opportunities Recruitment Business and Agency. We welcome applications from all suitably qualified candidates regardless of their race, sex, disability, religion/belief, sexual orientation or age.

A MagmaCultura estem compromesos amb la cultura. Som un referent en el desenvolupament i gestió de projectes culturals, educatius i turístics. La nostra passió és promoure el valor de la cultura i fer-la accessible a les persones. El nostre motor principal és la professionalitat, el talent i el compromís del nostre equip expert en gestió cultural. Un dels principals valors de MagmaCultura consisteix en la creació d'un lloc de treball en el qual totes les persones se sentin respectades, representades i incloses en un entorn segur en el qual puguin desenvolupar i impulsar la seva carrera professional amb èxit. Per això mateix, com a institució compromesa amb la cultura i la diversitat, vetllem per la promoció d'un ambient de treball en el qual destaqui la igualtat de gènere i el respecte per motius de raça, ètnia, sexe, orientació sexual o diversitat funcional. T'apassiona l'art, la cultura i la ciència? Tens ganes de formar part d'un projecte innovador i dinamitzar l'experiència del públic? T'estem buscant, envia'ns la teva candidatura! Volem incorporar un/a Educador/ora - Divulgador/ora Cultural per a un prestigiós equipament cultural de Lleida , amb la missió de dinamitzar visites guiades i tallers educatius adaptant els continguts a diferents públics i acostant la cultura d’una manera accessible, rigorosa i inspiradora. Imagina't com serà el teu dia a dia: - Conduir tallers i activitats educatives en l’àmbit de l'art adaptats a cada públic. - Realitzar visites guiades, adaptant i transformant continguts, que despertin la curiositat i el pensament crític. -Preparar l'espai i el material necessaris per a la realització dels diferents tallers i activitats. -Resoldre dubtes i explicar conceptes de manera clara, entenedora i atractiva. - Adaptar els continguts per oferir una experiència educativa única i significativa. Requisits: - Ser una persona amb destacades habilitats comunicatives, orientada al servei, amb capacitat de resolució d'incidències, treball en equip i apassionada per la cultura i l'art. - Formació en Història de l'Art, Història, Belles Arts, Publicitat i Relacions Públiques, Protocol, Turisme, Educació, Humanitats, o equivalents. - Idiomes : català i castellà nadiu/bilingüe, anglès avançat per a fer visites guiades. El coneixent d'altres idiomes serà benvingut i valorat. - Experiència en realització de visites, tallers i/o docència. Valorable posseir experiència en educació en museus, centres culturals o projectes de divulgació científica. - El més importan t: ser una persona amb entusiasme i amb capacitat de fer viure experiències úniques a través de la ciència, l'art i la cultura. Què t'oferim: - Oportunitat d'incorporar-te a un equip líder en la gestió cultural, compromès amb la promoció del valor del patrimoni cultural i fer-lo accessible a les persones. - Formació i aprenentatge continu: creixeràs en un entorn que et convidarà a prendre petites decisions diàriament i on l'aprenentatge també forma part del procés. - Contracte : fixe discontinu. - Jornada i horari laboral: mínim 3 hores/setmanals : tenir disponibilitat dimecres, dijous i divendres de 09:00 h a 14:00 h (horari segons reserves i programació). - Incorporació : març 2026. - Lloc del centre de treball : Lleida.

Are you a Regulatory Affairs professional with solid experience in EU Clinical Trial Regulation (CTR) and submissions via CTIS and AEMPS? At the Barcelonaßeta Brain Research Center (BBRC) – research center of the Pasqual Maragall Foundation – we are looking for a Senior Regulatory Affairs Specialist to lead institutional clinical trial submissions and ensure full regulatory oversight across our research portfolio focused on Alzheimer’s prevention. This role sits within the Clinical Operations Office and acts as the institutional reference for regulatory strategy and compliance. Main responsibilities: Regulatory Strategy & Clinical Trial Submissions Lead regulatory strategy for institutional clinical trials under EU CTR. Prepare and submit dossiers via CTIS , AEMPS , and Ethics Committees (CEIm) . Manage substantial modifications, DSURs, safety notifications, and regulatory updates. Act as primary contact with competent authorities and regulatory bodies. Sponsor Regulatory Oversight Ensure compliance with EU CTR, GCP, GDPR , and national regulations. Support inspection-readiness and regulatory audits. Contribute to regulatory risk assessment and mitigation strategies. Quality & Institutional Compliance Develop and maintain SOPs related to regulatory activities and GCP. Support CAPAs and quality system improvements. Promote harmonization of regulatory processes across research units. Team & Institutional Support Supervise and mentor a junior regulatory profile. Provide internal training on regulatory requirements and updates. Collaborate closely with scientific and clinical operations teams. Requirements Degree in Life Sciences (Pharmacy, Biotechnology, Biomedicine, Biology or related field). Minimum 3–5 years of experience in Regulatory Affairs within clinical trials involving Investigational Medicinal Products (IMPs) in a clinical research institution or pharmaceutical industry setting. Demonstrated experience in the preparation and submission of clinical trial applications under the EU Clinical Trial Regulation (EU CTR) via CTIS . Proven experience interacting directly with AEMPS and Research Ethics Committees (CEIm) . Solid knowledge of ICH-GCP, EU CTR, and Spanish clinical trial regulatory framework . Experience managing substantial modifications, safety notifications, and Development Safety Update Reports (DSURs). Familiarity with EudraCT, RIMS, and other regulatory platforms. Advanced level of English and Spanish; Catalan is an asset. Proficiency in digital tools for document management and regulatory tracking. What we offer Location: Barcelona Contract: Permanent, full-time (38 hours per week) Salary: Commensurate with experience and aligned with the institutional compensation policy Benefits: Flexible benefits scheme including meal vouchers, health insurance and childcare support The opportunity to join a leading European research center focused on the prevention of Alzheimer’s disease and related dementias within a scientifically rigorous and collaborative environment.

¿Quieres impulsar tu carrera en un entorno donde tu talento sí importa? En El Corte Inglés creemos en las personas, en su capacidad para crecer y en el valor de su esfuerzo. Aquí cada día es una oportunidad para aprender, evolucionar y aportar lo mejor de ti en un ambiente dinámico, cercano y lleno de futuro . Imagina un equipo diverso, unido por la vocación de servicio al cliente y la excelencia. Un lugar donde tu trabajo tiene impacto real y donde podrás brillar desde el primer día. ✨ El proyecto que te espera Buscamos a alguien con vocación internacional y pasión por el trato al cliente. Formarás parte de un equipo encargado de: Resolver consultas, incidencias y reclamaciones de clientes internacionales con eficiencia y empatía. Prestar servicio de traducción cuando sea necesario. Colaborar en la organización de eventos para clientes prescriptores y viajes de familiarización. Atender de forma singular a clientes high spenders , ofreciendo una experiencia exclusiva y memorable. Funciones principales Facilitar mapas, folletos y materiales informativos. Orientar a visitantes sobre atracciones turísticas, eventos y servicios locales. Gestionar consultas y resolver incidencias con profesionalidad y amabilidad. Mantener actualizada la información turística y colaborar con otros servicios del sector. Realizar tareas administrativas, incluyendo la gestión del tax free . Nuestros beneficios Queremos que te sientas bien, dentro y fuera del trabajo. Por eso te ofrecemos: Descuentos exclusivos y opciones de financiación. Seguro de vida. Universidad Corporativa y formación continua. Ayudas al estudio para hijos e hijas de empleados. Servicio Médico propio. Plan de retribución flexible. ¿Te encaja? Si este proyecto te inspira, ¡queremos conocerte! Tu experiencia y tu manera de entender el servicio al cliente pueden aportar un gran valor a nuestro equipo. En El Corte Inglés, todas las personas son bienvenidas.

Ready to power up the performance of a fast-growing sales team? We’re European Sales Group , a fast-growing French-founded company based in Barcelona, specialising in outsourced B2B sales. In just 18 months, we’ve built a team of 30+ talented professionals, opened two offices, supported dozens of clients, and we’re just getting started. We’re now looking for our first-ever Sales Enablement Lead/ Sales Trainer (VIE contract) , a key role that will directly shape how our SDR team to ramp, learn, and grow. What you’ll be doing You’ll be the backbone of our Sales organisation, enabling our teams to perform at a higher level & faster. Your missions will include: Owning and delivering onboarding for new SDRs. Designing and rolling out ongoing training modules (prospecting, discovery, objection handling, etc.) Creating enablement assets: playbooks, scripts, toolkits, and frameworks Identifying skill gaps in partnership with the Team Leader SDR Running regular coaching sessions (1:1 and group) Embedding a consistent sales methodology across all teams Tracking enablement impact through clear KPIs and performance metrics Collaborating closely with SalesOps to optimise tools and workflows Accelerating ramp-up time and supporting the continuous development of the team What we’re looking for 2+ years’ experience in B2B sales, ideally including 1 year as a BDR/SDR + 1 year as an AE Strong understanding of the full sales cycle Excellent communication and teaching skills Fluent in French & English (Spanish is a plus) Dynamic, structured, impact-driven mindset Excited to join a fast-growing, entrepreneurial environment ⚡ What’s in it for you A highly strategic role with direct visibility and impact The chance to build a complete enablement program from the ground up Close collaboration with Sales Leadership & SalesOps An international environment in the heart of Barcelona Interested? Apply today and help shape the future of our Sales organisation !

IUL is an international technology company with more than 35 years of experience designing and manufacturing analytical instrumentation for laboratories worldwide.Our core areas of expertise include optics and photonics, electronic and sensor systems, precision mechanics, and AI-based data analysis, applied to microbiology, diagnostics, and quality control. We develop complete instruments that integrate hardware, software, and algorithms, both under our own brand and as an OEM partner for leading global companies.IUL’s R&D activities cover the full product lifecycle, from concept and prototyping to industrialization, production, and successful commercialization in global markets. Our developments are characterized by robust engineering, scientific rigor, and long-term reliability, operating in regulated environments including in vitro diagnostics (IVD).As part of our continued growth, we are expanding our R&D team and are looking for a highly qualified PhD-level scientist or engineer to contribute to the development of next-generation sensing, optoelectronic, and AI-enabled technologies.Academic BackgroundPhD in one of the following fields:PhysicsOpticsElectronicsTelecommunications EngineeringAdditional Training / ExperienceComplementary studies and/or professional experience providing strong expertise in one or more of the competencies listed below.Technical CompetenciesSensorsElectrochemical sensorsPhotomultipliersPhotodiodesImage sensorsPhotonicsBioluminescenceFluorescenceImmunochromatographyRadiometryOpticsInstrumental optical systemsNon-imaging opticsElectronicsSignal acquisition systemsAmperometry and potentiometryAnalog-to-digital converters (ADC)Adjustment and calibrationLow-level software for signal acquisition and processingRegulated EnvironmentsExperience with sanitary devices for in vitro diagnostics (IVD) or other regulated environments is highly valued.What We OfferDirect involvement in the development of real products with global market impact.A technically challenging role with responsibility across the full product lifecycle.Collaboration with a multidisciplinary R&D team combining physics, engineering, mechanics, software, and AI.Long-term professional growth in a stable, industrial R&D environment.

Language Avenue es una escuela de idiomas independiente que se enfoca en la comunicación real y efectiva. Estamos ubicados cerca de la Sagrada Familia. Nuestra metodología de enseñanza es comunicativa, donde la gramática se utiliza como un medio para lograr una meta, y no como el objetivo principal.Estamos buscando un profesor de español ELE para unirse a nuestro equipo en crecimiento en nuestra escuela junto a la Sagrada Familia. Nos comprometemos a ayudar a nuestros estudiantes a alcanzar sus metas y ofrecemos un ambiente de trabajo cómodo, colaborativo y orientado a brindar la mejor experiencia tanto para estudiantes como para empleados.Requisitos:Certificado de profesor de español del Instituto Cervantes (DELE o similar).Experiencia demostrable trabajando con los niveles del MCER (Marco Común Europeo de Referencia).Experiencia en la preparación de exámenes DELE.Disponibilidad en horario de tarde.Residir en BarcelonaCompetencia tecnológica y habilidad para generar confianza en el aula.Ser creativo/a. Inclusión de juegos en el aprendizaje.¡Pasión por la enseñanza!Ofrecemos:Contrato con perspectiva de largo plazo.Alrededor de 12 horas de enseñanza para comenzar por las mañanas y algunas tardes, con posibilidad de aumento.lunes a jueves de 10:00-12:00martes y jueves de 19:00 - 21:00Sueldo: 16,50€-17,00€ la horaUn equipo directivo que colabora contigo (tu voz cuenta)Plus (Opcional):Conocimiento de metodologías como enseñanza comunicativa o enfoques multiculturales.Experiencia en la enseñanza de español para negocios.Experiencia con método AULA PLUS.

Role: QA Oversight Specialist Hlx are partnered with a fast-growing biologics CDMO who are growing their quality capabilities. We are looking for a QA Oversight Specialist, reporting to the Senior Quality Manager . This is a highly visible, hands-on role focused on real-time GMP oversight on the production floor , ensuring product quality and inspection readiness. Focus of Role: To supervise and coordinate Quality Assurance activities within assigned processes, ensuring full compliance with GMP requirements and internal Quality Systems. Key Responsibilities Provide hands-on QA oversight on the production floor to ensure GMP compliance Lead and support deviation management, investigations, and CAPA execution Review and approve batch documentation and critical process parameters Monitor quality KPIs and verify effectiveness of implemented CAPAs Support and participate in internal and external audits, including FDA inspections Ensure GMP training compliance and contribute to continuous improvement initiatives Profile Experience working in a GMP-regulated pharmaceutical manufacturing environment Direct exposure to FDA inspections (very nice to have!) Strong understanding of deviations, CAPA, and quality systems Comfortable spending the majority of time on the production floor Proactive, detail-oriented, and confident working closely with operations

Scientist – Biopharma (Small & Large Molecules)Location: Barcelona area, Spain Shift: Morning shift only (06:00–14:00)OverviewA well‑established CRO operating within a GMP/GLP environment is expanding its biopharma team and seeking a Scientist to support technology transfer and validation activities across both small and large molecule products. This role offers broad analytical exposure within a regulated setting.Candidates currently working at Analyst level and looking to progress into a Scientist role are welcomed. Applicants may come from industry or investigational/research backgrounds.Key ResponsibilitiesDesign, supervise, and execute analytical method transfer and validation studiesPerform and support analytical testing for biologics and small molecule productsEnsure all activities comply with GMP and/or GLP requirementsPrepare, review, and maintain technical documentationCollaborate with internal teams to deliver projects to agreed timelinesRequirementsBachelor’s degree in Chemistry, Biochemistry, Biotechnology, or a related scientific discipline1–2 years’ experience in a pharmaceutical, biotech, or CRO environment (industry or research considered)Strong hands‑on experience with HPLC (essential)Experience with biologics and/or small molecule analytics (both preferred; one considered)Understanding of GMP principles (GLP considered)Clear communication skills and ability to work in a regulated environmentLanguage RequirementsEnglish and Spanish at strong conversational level (English minimum B2)About Planet Pharma: Planet Pharma is an American parented Employment Business/Agency that provides global staffing services with its head-quarters in Chicago and our EMEA regional office located in Central London. We have invested significantly in creating a robust international platform that enables us to work compliantly in 30+ countries with a current network of 2500+ active contractors globally as well as a very strong permanent / direct hire recruitment offering. Our specialist knowledge and close relationships with our clients and the wider industry really makes us unique in our field. Just recently we were recognised by FORBES as the 17th best professional staffing firm, and have won multiple awards from industry accredited bodies for our commitment to excellence and service delivery. We have extensive functional expertise including: Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs / Writing. We are an equal opportunities Recruitment Business and Agency. We welcome applications from all suitably qualified candidates regardless of their race, sex, disability, religion/belief, sexual orientation or age.

Som la firma global de talent: Selecció, headhunting, formació i consultoria d'Eurofirms Group. A Claire Joster creiem en el talent únic de cada persona i sabem que la diversitat aporta valor als equips, impulsant organitzacions més innovadores, creatives i eficients. Per això, com a part d'Eurofirms Group, i d'acord amb la cultura de la nostra empresa People First, treballem per generar entorns laborals inclusius en què cada individu pugui créixer i desenvolupar la seva millor versió. Així mateix, busquem actuar com a agents de canvi per promoure la igualtat d'oportunitats en el nostre entorn, fomentant el respecte i apostant per la diversitat en totes les seves formes. Siguis com siguis i sentis com sentis, a Claire Joster tindràs un lloc per brillar. Per una empresa industrial tecnològicament avançada, especialitzada en fabricació de components per als sectors aeronàutic, espacial i industrial, amb una forta aposta per la qualitat, la millora contínua i l'excel·lència operativa, cerquem incorporar un/a Quality Controller a l'àrea de Producció. L'obectiu principal de la persona que incorpori serà assegurar que els productes fabricats compleixen els requisits del client i els estàndards interns de qualitat, tant en el producte final com durant totes les fases del procés de fabricació. Les funcions principals son: -Implementació del pla de qualitat en projectes i producció -Control de qualitat durant el procés productiu i en producte final -Realització i documentació de mesures, assaigs i inspeccions -Detecció, notificació i seguiment de desviacions de qualitat -Control de qualitat de productes d'entrada (incoming) i de sortida (outgoing) -Revisió de documentació de qualitat i logística (CoC, FAR, notes d'entrega, etc.) -Auditories de processos interns i seguiment d'accions correctives -Gestió d'equips de mesura i control de calibracions -Control de materials peribles i suport a la gestió d'estoc. Requisits de la vacant: -Formació tècnica: FP2, Enginyeria Tècnica Mecànica o similar -Mínim 2 anys d'experiència en una posició similar -Coneixements de metrologia i lectura de plànols -Experiència amb braç de mesura 3D -Coneixement d'assaigs no destructius per materials compòsits -Anglès parlat i escrit -Persona ordenada, metòdica, amb capacitat analítica i bona comunicació. S'ofereix: -Incorporació a un entorn industrial altament tècnic i especialitzat -Projectes amb elevat nivell d'exigència i aprenentatge continu -Col·laboració directa amb Quality Manager, enginyeria i producció -Estabilitat laboral i possibilitats de desenvolupament professional - Horari de flexible de dilluns a divendres - Salari negociable segons les capacitats de cada candidat/a

WOULD YOU LIKE TO JOIN THE GDC BEAUTY GROUP? We are an innovative global beauty group with over 60 years of experience operating with a portfolio of leading brands in the professional cosmetics sector. The company is present in more than 80 countries, with subsidiaries in Italy, Belgium, the United Kingdom, the Dominican Republic, Colombia and the USA. GdC Beauty Group was established following the launch of a strategic plan for sustainable growth, with a clear ambition: to become a leading international beauty group. Our brands are widely recognised for their quality, innovation and strong values. We are currently looking for an International Beauty Trainer to join our team, based at our Barcelona office. The International Beauty Trainer will be responsible for developing and delivering technical and commercial training programs for our international distributors, ensuring consistent brand messaging, product knowledge and professional application standards across all markets. KEY RESPONSIBILITIES Design and deliver technical and commercial training sessions for international distributors, local trainers and sales teams. Train on the correct use of professional cosmetic products, treatment protocols and new product launches. Adapt training content to different markets, cultures and levels of expertise. Ensure correct implementation of brand standards, methodology and values worldwide. Support distributors during international events, trade shows and product launches. Create, update and maintain training materials (presentations, manuals, technical guides and digital content). Monitor and evaluate training effectiveness, proposing continuous improvement actions. Identify training needs in different markets and provide feedback to support business growth. JOB REQUIREMENTS Education in Aesthetics, Cosmetology, Dermocosmetics or related fields. Minimum 3 years of experience as a trainer in professional cosmetics. Strong technical and product knowledge within the professional beauty sector. Willingness to travel internationally on a regular basis. Excellent communication, presentation and teaching skills. Ability to work independently and adapt to multicultural environments. Fluent English is required; additional languages are a strong plus. WHAT WE OFFER Join a solid international group in continuous growth. Work with prestigious professional cosmetic brands. An international role with exposure to multiple markets. Ongoing professional development. Competitive compensation package aligned with experience. A dynamic, collaborative and multicultural working environment. Position based in Barcelona. If you are passionate about professional beauty, training and international environments, and want to be part of a growing global group where knowledge, quality and people matter — we would love to hear from you.

En Grupo Planeta, buscamos incorporar un/a Account Specialist con francés e inglés para el departamento de Marketing de la instrucción de Iberonex perteneciente a la división de Planeta Formación y Universidades. ¿En qué consistirá tu día a día? Supervisión y apoyo en la gestión de las estrategias de PPC (Facebook Ads, Google Ads y LinkedIn Ads). Elaboración de informes y control de dashboards de análisis de inversión, rendimiento de campañas y captación de leads. Seguimiento de la estrategia digital y apoyo en la planificación de acciones para distintos mercados. Apoyo en la ejecución del plan de comunicación y reputación institucional. Colaboración en la elaboración, adaptación y redacción de contenidos alineados con la narrativa y el tono de marca. Creación de contenidos a nivel creativo, incluyendo diseño de piezas gráficas y redacción de copys para campañas digitales. Requisitos: Formación superior (preferiblemente en Marketing, ADE, Economía o similares). Idiomas: Español, Francés e Inglés avanzado. Perfil proactivo, con buena capacidad analítica y orientación a resultados. Conocimiento en la generación de leads y su conversión a venta mediante campañas publicitarias, principalmente en Google y Meta. Experiencia o conocimientos en plataformas de Google Ads, SA360 y Meta Ads. Conocimientos en herramientas de diseño y creación de contenidos, como Canva, Adobe Illustrator u otras herramientas similares. Valorable el conocimiento en otras herramientas digitales como GA4, WordPress, Core Web Vitals, SEMrush, entre otras. ¿Qué ofrecemos? Contrato estable: Indefinido y a jornada completa. Descuentos y promociones exclusivas para nuestros empleados (masters y posgrados, sellos editoriales, coleccionables, Casa del Libro...). Un atractivo paquete de beneficios sociales a través del plan de retribución flexible que incluye: tarjeta transporte, tarjeta restaurante, cheque guardería, seguro médico, etc. Si crees que es tu oportunidad laboral, ¡Te animamos a inscribirte y formar parte de nuestro equipo! En Grupo Planeta ofrecemos igualdad de oportunidades. Nos comprometemos a tratar todas las candidaturas por igual en función de sus capacidades, logros y experiencia independientemente de su raza, nacionalidad, sexo, edad, discapacidad, orientación sexual, identidad de género o cualquier otra clasificación protegida por la ley.

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 posición 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 estructural. Responsabilidades principales Participar en actividades de site start-up, incluyendo revisión de documentación esencial. Elaborar y ejecutar el plan de monitorización del estudio. Realizar visitas de monitorización en los centros participantes (4) asegurando el cumplimiento del protocolo, GCP y requisitos regulatorios. Revisar la correcta cumplimentación de los consentimientos informados y documentación de los investigadores. Verificar datos en eCRF y documentación fuente, asegurando coherencia y completitud. Gestionar desviaciones, queries y acciones correctivas (CAPA), con seguimiento hasta su cierre. Preparar informes de monitorización y documentación asociada dentro de los plazos establecidos. Apoyar en la gestión del TMF. Participar en reuniones de seguimiento con el promotor (BBRC) y colaborar en auditorías e inspecciones regulatorias. Crear materiales de formación sobre el estudio para los distintos centros. Requisitos Grado en Enfermería, Farmacia, Biomedicina, Biología, Biotecnología, Ciencias Biomédicas o similar. Formación acreditada en Buenas Prácticas Clínicas (GCP). Formación específica en monitorización o gestión de ensayos clínicos. Mínimo 2–3 años de experiencia como CRA en ensayos clínicos, incluyendo: Gestión de TMF y documentación esencial. Site start-up y close-out. Revisión de consentimientos y verificación de datos/eCRF. Gestión de queries, desviaciones y CAPA. Competencias personales Autonomía y capacidad de monitorización independiente. 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 correcciones. Capacidad de anticipar riesgos y proponer mejoras. Flexibilidad para trabajar en entornos multicéntricos con recursos limitados.

We are BAA Training, one of the TOP 3 largest independent aviation training centers in Europe. Our people are united by passion for aviation and a desire to ensure efficient training solutions for both pilots and airlines. A comprehensive list of EASA approved training programs and extensive experience on the market allow us to meet the training needs of the global aviation. At the moment we are looking to grow our team of experienced and qualified Flight Instructors for Initial Pilot training in Lleida, Spain. Our instructors: • Provide hands-on flight training to students, both in the air and on the ground. This involves teaching fundamental flying or theory skills; • Clearly and effectively communicate instructions, adapt teaching methods to accommodate different learning styles and individual student needs; • Emphasize and enforce safety standards throughout the training process. Instruct students on emergency procedures and ensure compliance with aviation regulations; • Regularly assess students’ progress through evaluations and provide constructive feedback. Identify areas for improvement and work with students to address weaknesses; • Maintain accurate records of student progress, flight hours and instructional activities. Ensure that all required paperwork is completed and submitted in a timely manner; • Stay current with aviation regulations and ensure that all training activities adhere to applicable laws and standards set by aviation authorities. To be successful you should have: • Valid EASA CPL(A) or ATPL(A) License; • Valid EASA 1st Class Medical Certificate; • Valid Unrestricted FI(A) rating; • ICAO English level 4 or higher; • EU work permit; • More than 200 flight instruction hours. Good to have: • Valid IRI(A) rating; • IRI experience. We offer to you: ✓ A bonus of Type rating training after 2 000 of dual flight training hours performed. ✓ Accommodation options. ✓ Coverage of rating renewals that are directly related to your position. ✓ A health Insurance package after 3 months of working for the Company. ✓ Additional holiday days for seniority after 2 years of working for the Company. ✓ A Wellness Day to take care of yourself and a Birthday day off to celebrate. ✓ An international and multicultural environment in vibrant industry with plenty of challenges to achieve. ✓ We enjoy seeing our employees’ careers growing, so there are plenty of opportunities to progress, we have a bunch of examples to share.

Key Responsibilities: Provide expert troubleshooting for multi-forest Active Directory service issues (DFS, DNS, WINS, LDAP etc) Promote and demote domain controllers Support AD name resolution technologies (DNS, WINS, DHCP, Infoblox) Implement AD security methodologies (JEA, JIT, Delegation models and Tiered Admin model etc) Perform AD schema extensions Create PowerShell scripts Support Azure AD, AAD-DS and other Azure technologies IDAM project delivery & process design Simplification of complex IDAM processes & tools Maintaining security, standards and high availability of AD architecture Design and review any required changes to Active Directory with a specific focus on structure, delegation models, tiering and management. We look forward to receiving your application!

Medical Director, Clinical Development (Global Clinical Lead)Location: Barcelona, Catalonia, SpainARTO are partnered with a global Pharmaceutical company, who are committed to the growth of their portoflio within the Medical Dermatology space. Role OverviewThis role provides global medical and scientific leadership for a late-phase clinical development program. The Medical Director (Clinical Lead) will own clinical strategy and execution across Phase II–III studies, acting as the accountable clinical lead within a cross-functional global team and supporting progression toward registration.Key ResponsibilitiesProvide global medical and scientific leadership for a late-phase (Phase II–III) clinical development program, ensuring delivery against quality, timelines, and strategic objectives.Define and drive the clinical development strategy, including Target Product Profile (TPP), study concepts, and alignment with regulatory and commercial goals.Serve as the clinical lead within global, cross-functional project teams, partnering closely with Clinical Operations, Regulatory Affairs, Safety, Biometrics, and Medical Affairs.Act as the medical accountable lead for late-phase clinical studies, including protocol development, data review and interpretation, and ongoing benefit–risk evaluation.Represent the clinical program in interactions with external stakeholders, including investigators, key opinion leaders, and regulatory authorities as required.Candidate Profile & QualificationsMD required, with board certification or equivalent clinical training; Dermatology background a strong plus.Approximately 5+ years of experience in pharmaceutical or biotechnology clinical development, with exposure to late-phase programs.Demonstrated experience contributing at program level within Clinical Development, beyond single-study execution.Solid scientific grounding in immunology-driven diseases (e.g. dermatology, allergy, inflammatory or immune-mediated indications).Strong understanding of late-phase trial design, clinical data interpretation, and global regulatory expectations.If you think this role would be a good fit for you, please feel free to reach out to me either through DM, or on email -

International School seeks primary school teacher. Functions: ⋅ Develop and implement teaching plans for the transdisciplinary and disciplinary units. ⋅ Attend department meetings and participate in collaborative planning sessions. ⋅ Take part in standardizing assessment tasks. ⋅ Contribute to curriculum research and improvement. ⋅ Stay updated on the PYP scope and sequence. ⋅ Communicate with parents the students’ progress ⋅ Attend to school activities such as festivals and Open Days We are looking for: ⋅ Nativee or C2 level of English ⋅ Teaching experience, PYP or MYP We offer: ⋅ Monday to Friday from 9:00 to 17:00h ⋅ Permanent contract ⋅ Immediate incorporation

Sobre Inetum, Positive digital flow Inetum es líder europeo en servicios digitales. El equipo de Inetum, formado por 28.000 consultores y especialistas, se esfuerza cada día por generar un impacto digital en las empresas, las entidades del sector público y la sociedad. Las soluciones de Inetum tienen como objetivo contribuir al desempeño y la innovación de sus clientes, así como al bien común. Presente en 19 países con una densa red de sitios, Inetum se asocia con los principales editores de software para afrontar los desafíos de la transformación digital con proximidad y flexibilidad. Top Employer Europe 2026 Buscamos un perfil junior orientado a operaciones TI , responsable de la monitorización continua de los servicios críticos de la compañía. Su objetivo es detectar alertas tempranas, validar su relevancia, activar los escalados adecuados y asegurar que ninguna señal de riesgo pasa desapercibida. Este rol es clave para reducir Major Incidents y mejorar la estabilidad operativa. Requisitos mínimos: -Formación técnica (FP, ingeniería o similar). - Conocimientos básicos de ITSM y monitorización. - Inglés operativo para documentación y comunicación con equipos globales. - Conocimientos básicos de redes, Linux/Windows y entornos Cloud (AWS valorado). - Familiaridad con herramientas como Grafana, Datadog, Zabbix, etc. - Atención al detalle, capacidad analítica y comunicación clara con equipos técnicos. Responsabilidades: - Supervisar dashboards y alarmas críticas en tiempo real. - Validar alertas, identificar falsos positivos y notificar a los equipos técnicos. - Realizar y seguir escalados hasta su resolución. - Colaborar con Problem Management y Major Incident Coordination. Registrar alertas revisadas y proponer mejoras. - Contribuir a la optimización de dashboards, umbrales y reglas de monitorización. - Participar en auditorías y revisiones de eficacia. ¿Qué ofrecemos? -Contrato Indefinido -Retribución salarial acorde con la experiencia aportada -Plan de carrera: ofrecemos una atractiva carrera profesional en función de la experiencia y potencial personal dentro de una compañía en continua evolución y con un sólido crecimiento -Plan de formación en competencias tecnológicas de acuerdo con las exigencias de los proyectos y clientes. -Retribución flexible: te ofrecemos una retribución a la carta pudiendo elegir diferentes productos y modelar tú mismo cómo distribuirlos: seguro de salud, tickets de comida, guardería, tarjeta transporte, etc. -Flexibilidad horaria

We are working with an exciting US biotech seeking a strategic, dynamic, and highly organized Medical Director to lead and manage international clinical studies focused on an exciting new IVF/IVM product.. This role will be pivotal in driving the success of global clinical trials and post-market surveillance studies across key markets including Europe, Australia, the Middle East, Latin America, and Asia.The ideal candidate is an infertility specialist medical doctor, self-starter with deep clinical management experience in clinical research, strong leadership capability, and a passion for innovation in reproductive health. Candidates with in vitro maturation (IVM) and a proven track record in clinical operations within pharma or biotech will be strongly preferred.About the RoleThis role will be pivotal in driving the success of global clinical trials and post-market surveillance studies across key markets including Europe, Australia, the Middle East, Latin America, and Asia.ResponsibilitiesImproving product adoption at external partner clinics and study sitesThis work will consist of virtual meetings as well as on-site visits to clinics internationally and in the US, including:Advising PIs on patient selectionAdvising PIs on appropriate application of minimal stimulation protocolTroubleshooting with PIs to improve egg yield and egg qualityWorking with centres to perform best practices in embryo transfersParticipate in publications, conference presentations, and scientific communications to strengthen product credibility.Scientific & Strategic LeadershipWork directly with the CSO to design new clinical studies and trials to further expand product development. Advising and developing protocols for advanced maternal age patientsAdvising and developing protocols for PCOS and hyper responder patientsRefining stimulation and monitoring protocolsImproving company resources for clinics and physiciansDevelopment and design of clinical and research studies QualificationsMedical Degree in Obstetrics/Gynecology and/or reproductive endocrinologistInfertility treatment provider for IVF servicesFor more information on this company and the outstanding opportunity here please forward an up to date CV to

Julius Clinical is looking for an experienced Market Strategy Manager (Inside Sales) in Europe!As an Inside Sales/Market Strategy Manager, you will play a key role in supporting our Business Development team by identifying and seizing new market opportunities. You will proactively gather market intelligence, connect with potential clients, and align Julius Clinical’s unique benefits with market needs. This position is ideal for someone with a university degree, minimum 1-3 years of experience, with strong networking skills and a passion for driving growth in the clinical research sector.Key ResponsibilitiesOrganise and undertake prospection activities (through email, cold-calling, LinkedIn and other relevant channels);Collect and analyze market data including using database search tools to identify potential leads and opportunities;Support Business Development potential leads;Support and arrange client meetings, ensuring both logistical and content preparation;Maintain CRM tool and master lists up to date.What we’re looking forBachelor's degree (biomedical science or related field is a plus);Strong affinity with business development;Knowledge of database search tools;Currently working as Inside Sales or similar role;Strong track record;Entrepreneurial mindset, tenacious; Strong initiative and creativity;Excellent planning and organizational skills;Ability to listen, identify client needs, and pivot accordingly;Proficient in English;Living in Europe.Why Join Us?Be part of an innovative organization that values scientific excellence and client partnerships;Work in an international environment with opportunities to take initiative and shape market strategies and plenty of room to grow your career;Competitive compensation and benefits;Working remote/home based (when living abroad) or 1/2 days per week from our office in the Netherlands;Opportunity to grow into Outside Sales role.Interested?Apply now and help us connect science to better health outcomes worldwide.If you have further questions, you can contact Marjolijn Woudstra (Senior Recruitment Business Partner a.i.) via whatsapp/call: +31 6 28 25 65 82.About Julius ClinicalJulius Clinical is a leading clinical research organization committed to advancing science and improving patient care worldwide. With our headquarters in the Netherlands and a global presence, we combine scientific expertise with operational excellence to deliver high-quality clinical trials.

Senior Statistician – Oncology (EU) We’re supporting an active search for a Senior Statistician to join an oncology clinical development team, working across Phases I–IV . This is a hands-on role with strong exposure to study design, statistical analysis, CRO collaboration, and regulatory interactions. Key highlights: Oncology-focused role across Phases I–IV Protocol & SAP development, analysis design, and oversight Close collaboration with CROs and internal teams Regulatory interaction experience required Bayesian methods experience preferred Location & flexibility: Ideally Spain (hybrid: 2 days WFH) Open to France or Italy with monthly site visits Salary: €75,000–€85,000 base - depending on experience Start: ASAP Shortlisting will be complete at the end of this week, but CVs are still very welcome , with potential for additional hires later in the year. Please share CVs along with current location, notice period, salary expectations, and office attendance flexibility (weekly/monthly) .

Full-time | Remote (CET / GMT preferred) | €40-45k base + equity Reports to: Digital Health Lead About Hyfe Hyfe is a health technology company using AI to turn cough into a continuous, objective health signal. Our technology is used globally in academic research, clinical trials, and pharma-led studies to generate high-quality cough data as a digital biomarker. We work closely with researchers, clinicians, pharma teams, and CROs who care deeply about evidence, rigor, and real-world impact. The Research Partnerships Associate Role This is a science-led partnerships role, designed for someone early in their career with a medical or scientific background who has recently moved, or wants to move, into healthtech. You´ll work with your Hyfe colleagues to build and maintain strong relationships with researchers, key opinion leaders, and industry partners, supporting early conversations, preparing scientific context, and helping turn interest into long-term collaborations. This is not a traditional sales role. It’s about credibility, organisation, and relationship-building in research-driven environments. What You’ll Do Research upcoming studies, funding calls, and institutions where cough monitoring is relevant Build and maintain target lists across academia, pharma, and CROs Support outreach and early conversations with researchers and partners Prepare background research, briefs, decks, and proposals for meetings Join partnership calls with senior team members; support early opportunity qualification Manage and improve our CRM (HubSpot): contacts, pipelines, follow-ups Support Hyfe’s presence at key scientific conferences and run structured follow-up Over time, you’ll take ownership of academic and early research partnerships. What We’re Looking For (Required) A medical, scientific, or technical background (via education or meaningful professional experience) Evidence of ownership and momentum (e.g. a side project, startup experience, independently launched initiative, or sustained project you drove end-to-end) Comfort engaging with research-driven topics and expert audiences Strong written and verbal communication Highly organised, reliable, and detail-oriented Motivated, curious, and comfortable working with autonomy Nice to Have (Not Required) Exposure to academia, clinical research, healthcare, or digital health Experience using CRM, research tools, or automation / AI tools What to Expect Salary: €40-45k base + equity, depending on experience Fully remote within CET / GMT timezones Budget for home work setup Occasional travel for conferences (mainly Europe) Motivated, friendly, “low-ego” colleagues Work on innovation in health/AI How to Apply We’re using LinkedIn Easy Apply. Please ensure your profile clearly shows your scientific or medical background and any experience working with research, healthcare, or technical teams. The next step will be a 30 minute interview with either the Digital Health Lead, or the CEO.

Empresa líder en investigación para terceros busca incorporar un/a Científico/a para el Departamento de Control de Calidad de Productos Biológicos.Bajo la supervisión de la Gerencia del Departamento, serás responsable de garantizar la calidad y cumplimiento normativo en proyectos de análisis de productos biológicos.Funciones principales- Diseño, supervisión y ejecución de estudios de control de calidad de productos biológicos, incluyendo técnicas cromatográficas y HPLC.- Gestión integral de proyectos, asegurando el cumplimiento de plazos y manteniendo comunicación directa con el cliente.- Elaboración y control de documentación técnica (PNT, certificados de análisis, desviaciones, OOS’s, CAPA’s, etc.).- Dirección y supervisión del trabajo experimental del personal técnico asignado.Se ofrece: - Contrato indefinido.- Dos vacantes de lunes a viernes, una en horario de mañanas de 6h a 14h y otra en turno de tarde de 14h a 22h.- Salario fijo entre 31.500€ y 38.000€ en función de la experiencia aportada.- Desarrollo profesional, ambiente colaborativo y una cultura de empoderamiento.- Acceso a la plataforma de beneficios para empleados.Requisitos: - Licenciatura en Bioquímica, Biotecnología, Química o áreas afines.- Experiencia mínima de 3 años en técnicas HPLC y cromatografía.- Experiencia en Control de Calidad en entornos farmacéuticos bajo normativa GMP.- Se valorarán conocimientos en técnicas electroforéticas, Western-Blot, ELISA y control de calidad de proteínas.- Buen dominio del inglés.

A MagmaCultura estem compromesos amb la cultura. Som un referent en el desenvolupament i gestió de projectes culturals, educatius i turístics. La nostra passió és promoure el valor de la cultura i fer-la accessible a les persones. El nostre motor principal és la professionalitat, el talent i el compromís del nostre equip expert en gestió cultural. Un dels principals valors de MagmaCultura consisteix en la creació d'un lloc de treball en el qual totes les persones se sentin respectades, representades i incloses en un entorn segur en el qual puguin desenvolupar i impulsar la seva carrera professional amb èxit. Per això mateix, com a institució compromesa amb la cultura i la diversitat, vetllem per la promoció d'un ambient de treball en el qual destaqui la igualtat de gènere i el respecte per motius de raça, ètnia, sexe, orientació sexual o diversitat funcional. T’apassiona l’art contemporani, la creativitat i la interacció amb el públic? Uneix-te a un equip on la imaginació i l’expressió artística es combinen amb la divulgació cultural. Volem incorporar un/a Mediador/ora Cultural - Educador/ora per a un espai cultural de referència dedicat a la promoció i difusió de l'art contemporani a la ciutat de Barcelona . La teva funció principal serà realitzar visites guiades per a facilitar la comprensió de les obres del centre a les persones visitants, adaptant el contingut segons el públic i procurant garantir la millor experiència possible. Imagina't com serà el teu dia a dia: - Guiar al públic visitant durant el recorregut, proporcionant informació clara i atractiva de les exposicions, com també fomentar la interacció amb les persones generant una experiència dinàmica. - Explicar conceptes relacionats amb l'art i la cultura de manera accessible i enriquidora, adaptant el discurs segons el perfil del públic. - Elaborar informes periòdics sobre el desenvolupament de les activitats i observacions rellevants per a la millora del projecte. Requisits: - Ser una persona amb excel·lents habilitats de comunicació, capaç de captar l'atenció del públic i generar interès. Amb passió per l'art, estar orientada al servei i al treball en equip, i comptar amb capacitat per a resoldre incidències de manera àgil i eficaç. - Formació en Turisme, Publicitat i Relacions Públiques, Humanitats, Comunicació, Història, Història de l'Art, Belles Arts o equivalents. - Idiomes: català i castellà nadius o bilingües, anglès i francès a nivell avançat per a visites guiades. Es valorarà el coneixement d’italià o alemany. - Experiència prèvia en atenció al públic, en visites guiades i/o tallers en qualsevol entorn de mediació cultural i/o educació. - El més important: ser una persona amb entusiasme i amb capacitat de fer viure experiències úniques a través de l'art i la cultura. Què t'oferim: - Oportunitat d'incorporar-te a un equip líder en la gestió cultural, compromès amb la promoció del valor del patrimoni cultural i fer-lo accessible per a les persones. - Formació i aprenentatge continu: creixeràs en un entorn que et convidarà a prendre petites decisions diàriament i on equivocar-te també forma part del procés. - Contracte: indefinit. - Jornada i horari laboral: 30 h/setmanals: Temporada 1: Setmana A: de dimarts a divendres de 14.15 h a 19.00 h. Setmana B: de dimarts a divendres de 14.15 h a 19.00 h, dissabte i diumenge de 9.45 h a 19.00 h. Temporada 2: Setmana A: de dimarts a dijous de 14.45 h a 20.00 h. Setmana B: de dimarts a dijous de 14.45 h a 20.00 h, dissabte de 9.45 h a 20.00 h i diumenge de 9.45 h a 19.00 h. Festius segons el calendari laboral. - Incorporació: immediata. - Lloc de treball: Barcelona.

En tekman education buscamos un/a docente de humanidades para el departamento editorial. Si tienes experiencia en el aula, te apasiona la educación y quieres dar un paso más en tu carrera, esta oportunidad es para ti. ¿Qué es tekman Education? Somos una editorial experta en didáctica de las matemáticas y la lengua. Creamos programas educativos para transformar la educación desde las aulas, apostando por un aprendizaje manipulativo, emocionante y significativo. Desde infantil hasta secundaria, acompañamos a los maestros y profesores para transformar la enseñanza con todo lo necesario para planificar la docencia y llevar a cabo sus clases. ¡Es en el aula donde ocurre la magia! tekman Education es una empresa internacional en continuo crecimiento, con presencia en escuelas de España, México, Chile, Argentina y Ecuador. Actualmente, más de 1 millón de alumnos aprenden con nuestros programas educativos. ¡Y seguimos creciendo! Los valores que nos mueven: Haz que suceda, ¡y disfruta! Nos atrevemos, asumimos riesgos, vamos más allá. Prioriza al cliente Acompañamos a los docentes para seguir creciendo. Juega en equipo ¡Juntos somos mejores! En tekman remamos todos a una. Impacta sin dejar huella Apoyamos acciones para un futuro más verde, diverso y responsable. ¿Cuáles serán tus principales responsabilidades? Formarás parte del equipo de producto editorial, y entre tus tareas destacan: Liderar y gestionar el equipo de autores, revisores y editores de los contenidos de filosofía y lenguas. Planificar y supervisar la creación de materiales educativos, asegurando calidad, rigor académico y adecuación pedagógica. Evaluar y seleccionar contenidos y recursos didácticos innovadores para su integración en el catálogo de la editorial. Gestionar los proyectos editoriales, estableciendo cronogramas, prioridades y control de presupuestos. Colaborar con otros departamentos ( marketing, ventas) para asegurar una presentación atractiva y adecuada de los materiales. ¿Cómo esperamos que sea? Queremos ampliar nuestro equipo incorporando un perfil senior para el área de filosofía y letras, una persona con experiencia como docente de la ESO y le apasione la creación de contenido en el mundo editorial educativo ¿Te reconoces? Grado/Licenciatura en Filología Hispánica, Catalana o Inglesa. Experiencia Mínimo 5 años de experiencia en aula de Educación Secundaria Obligatoria (ESO) y/o Bachillerato en asignaturas de Humanidades. Se valorará experiencia en audiovisual Además, si te consideras que tus puntos fuertes son.. Liderazgo proactivo, con alta capacidad para aportar ideas y visión de futuro. Alta capacidad organizativa y de planificación. Rigor y atención al detalle en la gestión de contenidos. ¿Qué ofrecemos? Contrato estable y jornada completa. Inicio de contrato : A partir de julio 2026 Horario flexible • viernes tarde libre. Jornada intensiva en verano (de julio hasta la tercera semana de agosto). Oficinas modernas en Barcelona 22@, con cultura digital y ambiente joven. Plan de beneficios flexibles y programas de bienestar. Formar parte de una EdTech en pleno crecimiento internacional . ¿Eres la persona que estamos buscando? ¡Únete al equipo y transforma la educación!

At Firmament, we don’t just organize football events, we create unforgettable international football experiences. Young players from Canada and the United States travel to Spain to train, compete and grow through elite programs with FC Barcelona Experience and Atlético de Madrid Experience. Now, we’re building our team, and we’re looking for YOU. We’re searching for high-energy, football-passionate Assistant Coaches to join us during our international football camps. This role is ideal for players who: Live and breathe football Love working with kids Want to learn from top European club methodologies Are responsible, committed and ready for an intense, action-packed week You’ll be involved on and off the pitch, playing a key role in the success of the experience. WHAT YOU’LL DO Support official coaches during training sessions and activities Help young players improve their technique, confidence and game understanding Motivate, guide and take care of the kids at all times Manage group logistics: transfers, schedules and daily activities Ensure players’ safety, well-being and positive experience Act as a role model in attitude, discipline and teamwork Learn and apply the FC Barcelona or Atlético de Madrid football methodology WHO WE’RE LOOKING FOR Full availability for one full week (mandatory) Solid football background (you must know how to play) Passion for football and youth development Comfortable working with children and teenagers English level B2–C1 (mandatory) Fluent Spanish (mandatory) High level of responsibility and maturity Energetic, proactive and team-oriented mindset WHY JOIN US? Work in top-level football environments Learn directly from elite European club methodologies Live a unique international experience Develop coaching, leadership and communication skills Join a young, dynamic and football-driven team Opportunity to collaborate in future international events

We are Impress . We believe everyone deserves a smile they love. Our long-term vision is to disrupt European conventional dentistry and orthodontia. Impress is a European direct-to-consumer teeth-aligner and oral care startup. We provide an affordable and convenient way to straighten teeth with aligners treatment. Within the Human Resources department, we are looking for a Health & Safety Specialist . You will be part of a winning team and passionate about what it does. Are you ready to join us? Responsabilities: Be the point of contact of our sservicio de prevención ajeno in Spain and make sure we comply with all the regulations across all our locations in Spain Prepare risk evaluations for our different workplaces, both the office and the clinics, to propose preventive and control measures and risk reduction Create prevention plans, politics and procedures Adapt our facilities to the current health and safety regulations Prepare the needed technical reports and documentation Manage inspections, audits and follow-up visits Manage the information and training of the employees Collaborate in internal health and safety campaigns What you need to be successful: Master’s Degree in Occupational Risk Prevention +2 years’ experience in a similar role in Occupational Risk Prevention, preferably in a similar company Knowledge of health and safety legislation Spanish and communicative level of English

EAE forma parte de Planeta Formación y Universidades, una de las redes internacionales de instituciones educativas más importantes del mundo. EAE Business School, fundada en 1958, es una escuela de negocios internacional especializada en management, con más de 77.000 directivos y profesionales formados a nivel global. ¿Tienes acreditación ANECA y experiencia docente e investigadora? ¿Quieres impactar en la formación de talento internacional? Este proyecto académico es para ti. ¿En que consistirá tu día a día? Desde EAE Barcelona buscamos ampliar nuestro claustro con docentes especialistas en Supply Chain, Operaciones y Cadena de Suministro Global . Responsabilidades principales: Impartir docencia universitaria en programas de grado y posgrado en el área de Supply Chain y Operaciones. Diseñar, actualizar y ejecutar asignaturas con metodologías activas (casos, simulaciones, proyectos aplicados). Tutorizar Trabajos Fin de Máster (TFM). Integrar contenidos académicos con la realidad empresarial. Participar en actividades académicas, de investigación y desarrollo institucional. Perfil requerido: A. Expertise en Supply Chain & Operaciones Globales (E2E) Dominio estratégico y operativo de Supply Chain End-to-End. Planificación y ejecución: Demanda, S&OP / IBP, Operaciones, Compras y Distribución. Capacidad de análisis cuantitativo y resolución de problemas complejos. B. Data, Digitalización e IA aplicada Experiencia con ERPs y procesos S&OP/IBP orientados a calidad del dato. Analítica operativa: KPIs, dashboards y análisis causa raíz. Aplicación de IA en casos reales de Supply Chain. C. Docencia y metodologías activas Experiencia docente universitaria o en escuelas de negocio. Diseño instruccional y evaluación mediante rúbricas. Enfoque práctico academia–empresa. Requisitos imprescindibles Doctorado finalizado . Acreditación ANECA (Profesor/a Doctor/a Acreditado/a) . Nivel alto de inglés y castellano (docencia bilingüe) . Experiencia profesional relevante en Supply Chain u Operaciones. Disponibilidad para docencia presencial en Barcelona. Se valorará especialmente Producción investigadora activa. Experiencia internacional. Participación en proyectos de innovación educativa o digitalización. ¿Que ofrecemos? Integrarte en una institución académica internacional de alto prestigio. Proyección profesional y académica. Entorno dinámico, multicultural y orientado a excelencia educativa. Participación en programas de impacto global.

We are partnered with a well-funded Causal-AI Pharmaceutical company at the forefront of the next generation of artificial intelligence. They are expanding their research team in Barcelona and are looking for an enthusiastic, curious, and adaptable individual to join them in this highly innovative & dynamic environment. The Role As a Causality Research Scientist, your primary focus will be on fundamental research and its application to complex real-world problems. You will be responsible for developing new ideas, improving foundational methods, and conducting comprehensive data analysis using causal methods. Your work will directly impact observational-longitudinal studies in medicine and chemistry, and you will collaborate closely with field experts. We are looking for a specific kind of researcher. This role is for someone who loves to think, reflect, and then produce. We value deep, critical thinking and the ability to build new ideas independently, not just the ability to execute memorized code. Key Responsibilities • Develop and improve new foundational methods in causal inference. • Conduct comprehensive data analysis on observational-longitudinal studies. • Collaborate with domain experts to translate abstract scientific ideas into concrete results. • Organize and write research for publication in international, peer-reviewed journals. • Engage in the academic community by refereeing, presenting, and discussing new research. What we are looking for: • Are a true problem-solver with a high degree of curiosity and adaptability. • Are passionate about creating the future of AI. • Have a proven ability to transform abstract concepts into concrete, published research. • Are honest, self-aware of your limitations, and capable of managing a full research workload. Required Qualifications • A strong track record in research, evidenced by peer-reviewed publications. • Proficiency in Python. • Knowledge of basic Machine Learning (ML) and Deep Learning (DL) algorithms. Desirable • A research background in Mathematics, Physics, Chemistry, or Biology is highly preferred over a background in Computer Science or AI research. • Strong knowledge of causal reasoning, do-calculus, and related simplification algorithms. • Experience with backend coding.

Emocional Technologies 22 SL Tarragona | Modalidad presencial Sobre Emocional En Emocional.com somos un centro de psicología y formación que combina lo mejor de la tecnología con lo mejor de las personas. Ayudamos a más de 200 empresas y más de 20.000 personas cada día a mejorar su salud mental y emocional. Sobre el proyecto Buscamos coordinadores para incorporarse a un programa donde vamos a garantizar continuidad educativa, conciliación familiar y equidad social a infantes de 1 y 2 años durante el periodo no lectivo (junio–julio), en Tarragona, brindando servicio educativo, comedor, descanso y acogida matinal. Gracias a ello, las familias pueden conciliar trabajo y cuidados y los niños mantienen rutinas seguras y estimulantes en un entorno conocido. Funciones principales Supervisar la implementación del proyecto. Organizar horarios, tareas y distribución de grupos. Garantizar seguridad y funcionamiento del proyecto. Canalizar información, incidencias y comunicación diaria. Control de asistencia y registros del servicio. Requisitos imprescindibles Titulación (imprescindible una de estas): Diploma de Director/a de actividades de tiempo libre infantil y juvenil (Generalitat de Catalunya o de otra CCAA). Certificado de profesionalidad de dirección y coordinación de tiempo libre educativo. CFGS Animación Sociocultural y Turística (TASOC). CFGS Enseñanza y Animación Socioesportiva. Títol del sistema educatiu que inclogui tots els mòduls formatius per obtenir la qualificació professional de direcció i coordinació d'activitats d'educació en el lleure infantil i juvenil, tal com estipula la Direcció General de Joventut. Nivel C1 Catalán Experiencia previa: Se valora la experiencia laboral remunerada ejerciendo funciones de dirección o coordinación en proyectos específicos para la franja de edad 0-3 años. La experiencia debe haberse realizado en los últimos 2 años. Los servicios de voluntariado no puntúan y no se tendrán en cuenta Se valorará especialmente Formación complementaria: Se valora que, además de la titulación mínima exigida (Director de Lleure, TASOC, etc.), el coordinador tenga formación universitaria específica en educación infantil: Grado en Educación Infantil o doble grado (Infantil + Primaria). Qué ofrecemos Participación en un proyecto público de alto impacto social . Colaboración con una entidad referente en intervención psicosocial y salud emocional. Integración en un equipo multidisciplinar especializado . Condiciones profesionales acordes al perfil y al marco del contrato público. Entorno de trabajo comprometido con la calidad técnica y la atención ética a las personas. ¿Te interesa? Envíanos tu DNI, CV con la experiencia de coordinación con niños de 0-3 años, Informe Vida Laboral y Titulación de formación (mínima exigida + complementaria), a: , , y (Asunto: Educador – Tarragona) Fecha límite 12 de Febrero

Pharmacokinetic Scientist We’re looking for a skilled Pharmacokinetic Scientist to lead key PK activities across our drug development programs. In this role, you’ll design and interpret studies, serve as a principal investigator, guide ADME/DMPK strategy, and play a central role in supporting both internal teams and external partners. Key Responsibilities Lead assigned studies as Principal Investigator/Study Director, overseeing all PK-related activities. Design, execute and interpret pharmacokinetic and pharmacodynamic analyses across preclinical and clinical programs. Conduct non‑compartmental and compartmental analyses using Phoenix WinNonlin. Prepare protocols and scientific reports describing study objectives, methodology, analysis and results across multiple species and biological matrices. Analyse and interpret PK data from a broad range of studies (DMPK, ADME, BE/BA, toxicology, SAD/MAD) and refine sampling and dosing strategies. Provide expert ADME/DMPK input into non‑clinical and clinical study design. Ensure full compliance with GLP, GCP, SOPs and sponsor protocols. Engage with clients, support onboarding, contribute to business development, and present study findings directly to sponsors. Stay current with evolving PK methodologies, regulatory guidance and industry best practices to drive continuous improvement. About You MSc or PhD in Pharmacy, Chemistry, Biochemistry, Biology, Biomedicine or a related life science. Hands-on experience with toxicology studies, bioavailability/bioequivalence, biomarkers and immunogenicity testing. Advanced proficiency with Phoenix WinNonlin . Strong understanding of ADME/DMPK regulatory expectations. Proven ability to work collaboratively in a matrix environment while managing multiple priorities. Strong interpersonal and communication skills in fluent English. Proficient with MS Office tools. About Planet Pharma: Planet Pharma is an American parented Employment Business/Agency that provides global staffing services with its head-quarters in Chicago and our EMEA regional office located in Central London. We have invested significantly in creating a robust international platform that enables us to work compliantly in 30+ countries with a current network of 2500+ active contractors globally as well as a very strong permanent / direct hire recruitment offering. Our specialist knowledge and close relationships with our clients and the wider industry really makes us unique in our field. Just recently we were recognised by FORBES as the 17th best professional staffing firm, and have won multiple awards from industry accredited bodies for our commitment to excellence and service delivery. We have extensive functional expertise including: Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs / Writing. We are an equal opportunities Recruitment Business and Agency. We welcome applications from all suitably qualified candidates regardless of their race, sex, disability, religion/belief, sexual orientation or age.

Forvis Mazars is a leader in audit, tax and advisory services, operating worldwide across 100+ countries and territories. Join our 40,000+ strong team to grow your career through global opportunities, diverse projects and continuous learning. We are seeking a highly skilled Microsoft 365 Technical Trainer with a strong focus on M365 Copilot to design, develop, and deliver high‑quality learning content and experiences that accelerate digital upskilling across the global organisation. You will work closely with the Digital Learning Program Manager, SMEs, and instructional designers to shape practical, scenario‑based training that empowers colleagues to confidently adopt Microsoft 365 tools, especially Copilot. Content creation: Develop engaging training materials, including guides, walkthroughs, demos, and interactive activities - for Microsoft 365 applications. Build eLearning modules and digital learning resources following established design and production processes in collaboration with Instructional Dessign. Review, update, and improve existing training materials to reflect new Microsoft 365 features, best practices, and organisational priorities. Stay up to date with Microsoft roadmap updates, Office 365 release notes, and industry learning trends. Work with the Program Manager to maintain a forward‑looking training calendar. Training facilitation: Facilitating (global) training sessions either in classroom sessions or via remote delivery (Webinars) Supporting and collaborating with external providers to support scaling of M365 Copilot adoption and training through online and in-person workshops in Copilot basics, adoption of use-cases, training ambassadors in Copilot, and usage of Copilot studio “full”. Deliver global training sessions - virtually and in‑person - covering Microsoft 365 applications (including Outlook, PowerPoint, Teams, Excel, OneNote, Loop), and digital productivity best practices to support a strong level of digital literacy among users. Creating videos and/or audio segments, where relevant, to demonstrate processes or use of specific Microsoft tools or functionality Monitoring and analysing the feedback received on the delivered training We are looking for an engaging and innovative M365 trainer, with experience in delivering/facilitating technical training programmes to a large audience. Expert across the M365 suite, in particular including: Copilot, Excel, Outlook, Teams, Word, PowerPoint, SharePoint, OneNote, Loop Strong interest in Learning & Development (L&D), experience in delivering/facilitating technical training programs. Experience with training people with a financial services or professional services background Ability to communicate very confidently and effectively in English, both in written and verbal form A second language would be beneficial but not essential (French, Spanish, German…) Able to travel occasionally to team meetings and to support training delivery and/ or workshops across the world.

WOULD YOU LIKE TO JOIN THE GDC BEAUTY GROUP? We are an innovative global beauty group with over 60 years of experience operating with a portfolio of leading brands in the professional cosmetics sector. The company is present in more than 80 countries, with subsidiaries in Italy, Belgium, the United Kingdom, the Dominican Republic, Colombia and the USA. GdC Beauty Group was established following the launch of a strategic plan for sustainable growth, with a clear ambition: to become a leading international beauty group. Our brands are widely recognised for their quality, innovation and strong values. We are currently looking for an International Beauty Trainer to join our team, based at our Barcelona office. The International Beauty Trainer will be responsible for developing and delivering technical and commercial training programs for our international distributors, ensuring consistent brand messaging, product knowledge and professional application standards across all markets. Design and deliver technical and commercial training sessions for international distributors, local trainers and sales teams. Adapt training content to different markets, cultures and levels of expertise. Ensure correct implementation of brand standards, methodology and values worldwide. Create, update and maintain training materials (presentations, manuals, technical guides and digital content). Monitor and evaluate training effectiveness, proposing continuous improvement actions. Identify training needs in different markets and provide feedback to support business growth. Minimum 3 years of experience as a trainer in professional cosmetics. Strong technical and product knowledge within the professional beauty sector. Fluent English is required; Work with prestigious professional cosmetic brands. Ongoing professional development. If you are passionate about professional beauty, training and international environments, and want to be part of a growing global group where knowledge, quality and people matter — we would love to hear from you.

En Emocional.com somos un centro de psicología y formación que combina lo mejor de la tecnología con lo mejor de las personas. Ayudamos a más de 200 empresas y más de 20.000 personas cada día a mejorar su salud mental y emocional. Buscamos coordinadores para incorporarse a un programa donde vamos a garantizar continuidad educativa, conciliación familiar y equidad social a infantes de 1 y 2 años durante el periodo no lectivo (junio–julio), en Tarragona, brindando servicio educativo, comedor, descanso y acogida matinal. Gracias a ello, las familias pueden conciliar trabajo y cuidados y los niños mantienen rutinas seguras y estimulantes en un entorno conocido. Organizar horarios, tareas y distribución de grupos. Control de asistencia y registros del servicio. Diploma de Director/a de actividades de tiempo libre infantil y juvenil (Generalitat de Catalunya o de otra CCAA). Certificado de profesionalidad de dirección y coordinación de tiempo libre educativo. CFGS Animación Sociocultural y Turística (TASOC). CFGS Enseñanza y Animación Socioesportiva. Títol del sistema educatiu que inclogui tots els mòduls formatius per obtenir la qualificació professional de direcció i coordinació d'activitats d'educació en el lleure infantil i juvenil, tal com estipula la Direcció General de Joventut. Nivel C1 Catalán Experiencia previa: Se valora la experiencia laboral remunerada ejerciendo funciones de dirección o coordinación en proyectos específicos para la franja de edad 0-3 años. La experiencia debe haberse realizado en los últimos 2 años. Formación complementaria: Se valora que, además de la titulación mínima exigida (Director de Lleure, TASOC, etc.), el coordinador tenga formación universitaria específica en educación infantil: Grado en Educación Infantil o doble grado (Infantil + Primaria). Participación en un proyecto público de alto impacto social . Colaboración con una entidad referente en intervención psicosocial y salud emocional. Integración en un equipo multidisciplinar especializado . Condiciones profesionales acordes al perfil y al marco del contrato público. Entorno de trabajo comprometido con la calidad técnica y la atención ética a las personas. ¿Envíanos tu DNI, CV con la experiencia de coordinación con niños de 0-3 años, Informe Vida Laboral y Titulación de formación (mínima exigida + complementaria), a: , , Fecha límite 12 de Febrero

Early years / Nursery Teacher with QTS required as soon as possible in Marbella The British International School of Marbella seeks an exceptional, well-qualified Early years / Nursery Teacher to join an innovative and dynamic school. Please send your up to date CV and supporting statemen to penny . kontopyrghou @ hays . com If you have an EU passport for VISA purposes please confirm this when applying. If you have any questions about this position or location please contact Penny Kontopyrghou Senior Business Director who has visited Marbella and placed many teachers there since 2010. Newly qualified Teachers are welcome to apply. The successful candidate will demonstrate a creative and rigorous approach to teaching and have the necessary skills and vision to enhance learning within the school. Suitable candidates for this post will: have recent UK or International experience of teaching primary have UK Qualified Teacher Status (QTS) or equivalent have a proven track record of raising standards a commitment to curriculum innovation be an outstanding teacher be well organised and creates a stimulating learning environment be enthusiastic and demonstrate a positive approach to pupils be a reflective practitioner and continually strives to improve performance consistently apply school policies have a keen interest in the personal development of pupils have experience of being an effective form tutor (or equivalent) demonstrate a willingness to contribute to the extra curricular life of the school Remuneration includes a competitive salary and retention bonus. The school and BSF provide strong opportunities for ongoing professional development. Salaries in Spain- Net salary significantly lower than the UK being under 29,000 EU in Spain Accommodation Costs Housing does vary quite significantly depending on location Closer to school rent is more likely to be within the region of 1000 EUR per month. Those that live more locally to school walk/cycle or take advantage of gaining a bus pass giving them free travel. Smaller villages away from Marbella centre they could well find something for as low as 750 EUR- Car required. To apply Please send your up to date CV and supporting statemen to penny . kontopyrghou @ hays . com

Company Description PhotonExport specializes in Semiconductors, Sputtering Targets, PVD Materials, and advanced Equipment such as PVD, PECVD, Plasma, and Thin Films Deposition. The company offers tailored solutions in vacuum deposition technologies, evaporation materials, and rare earths. With expertise in Thin Film Coating, PhotonExport supports projects ranging from small-scale to industrial-level coating. Additionally, the company provides R&D outsourcing in photonics, nanotechnologies, and thin films, enabling cutting-edge innovation. PhotonExport is dedicated to delivering high-quality materials and equipment, ensuring sustainability, customization, and competitive pricing. Main Tasks Serve as the company’s Technical Manager, coordinating support, service, and quality control activities. Provide technical support to customers and representatives, including troubleshooting, diagnostics, and repair of plasma, vacuum, and coating equipment. Manage and maintain the ISO 9001 quality management system, including process monitoring, documentation control, internal audits, and continuous improvement. Offer technical and commercial support, analyzing quotation requests, preparing technical offers, and assisting the sales team. Conduct quality control of materials and products supplied by the company. Supervise or assist in the installation and commissioning of vacuum and plasma equipment. Perform sputtering target bonding processes (manual or using epoxy/elastomer techniques). Collaborate with suppliers and customers in reviewing drawings, specifications, and technical standards. Key Responsibilities Ensure proper technical execution and full traceability of internal processes. Maintain ISO 9001 compliance and foster a culture of continuous improvement. Deliver high-quality after-sales support and ensure customer satisfaction. Coordinate technical interventions and preventive maintenance of equipment. Guarantee the technical reliability of commercial proposals and quotations. Skills & Qualifications Technical degree or engineering background (preferably in Electrical Engineering, though Electronics, Physics, or related fields are also suitable). Experience in repair, installation, and maintenance of industrial equipment—ideally in high vacuum, plasma, or semiconductor systems. Knowledge of electricity, vacuum technology, and preferably gases, furnaces, MFC valves, and PVD/PECVD coating processes. Highly valued (but not required): practical experience in manual bonding of sputtering targets using indium. Experience with ISO 9001 quality management systems. Intermediate computer skills and excellent documentation and organizational abilities. Strong interpersonal skills and a customer-oriented mindset. Ability to work independently, with initiative and a strong sense of responsibility. Languages: Spanish and English (intermediate to advanced level, spoken and written). Employment Details Type: Full-time position Location: Barcelona, Spain Experience: 10+ years in semiconductors, nanotechnology, vacuum, or thin-film industries

Maths Teacher Wingate School is seeking to recruit an energetic, flexible, and dedicated Maths Teacher to start in September 2026. Additional skills in Further maths would be essential Teaching an additional subject such as Economics or Business would also be desirable.. The successful candidate will embrace the role at our unique school, delivering a balanced and relevant teaching programme based on the British National Curriculum at KS3,KS4 and 5 iGCSE and A Level to a high level. The successful candidate will be expected to: Utilise and develop exciting and stimulating schemes of work in line with new curriculum and syllabus objectives. Organise learning resources and the classroom learning environment. Develop and foster the appropriate skills and social abilities to enable the optimum development of children according to age, ability and aptitude Assess and record progress. Challenge and inspire pupils to deepen their knowledge and understanding. Work in a team of experienced teachers to develop and advance the Maths Department at Wingate School Be a year group tutor.

Pharmacokinetic Scientist We’re looking for a skilled Pharmacokinetic Scientist to lead key PK activities across our drug development programs. In this role, you’ll design and interpret studies, serve as a principal investigator, guide ADME/DMPK strategy, and play a central role in supporting both internal teams and external partners. Key Responsibilities Lead assigned studies as Principal Investigator/Study Director, overseeing all PK-related activities. Design, execute and interpret pharmacokinetic and pharmacodynamic analyses across preclinical and clinical programs. Conduct non‑compartmental and compartmental analyses using Phoenix WinNonlin. Prepare protocols and scientific reports describing study objectives, methodology, analysis and results across multiple species and biological matrices. Analyse and interpret PK data from a broad range of studies (DMPK, ADME, BE/BA, toxicology, SAD/MAD) and refine sampling and dosing strategies. Provide expert ADME/DMPK input into non‑clinical and clinical study design. Ensure full compliance with GLP, GCP, SOPs and sponsor protocols. Engage with clients, support onboarding, contribute to business development, and present study findings directly to sponsors. Stay current with evolving PK methodologies, regulatory guidance and industry best practices to drive continuous improvement. About You MSc or PhD in Pharmacy, Chemistry, Biochemistry, Biology, Biomedicine or a related life science. Hands-on experience with toxicology studies, bioavailability/bioequivalence, biomarkers and immunogenicity testing. Advanced proficiency with Phoenix WinNonlin . Strong understanding of ADME/DMPK regulatory expectations. Proven ability to work collaboratively in a matrix environment while managing multiple priorities. Strong interpersonal and communication skills in fluent English. Proficient with MS Office tools. About Planet Pharma: Planet Pharma is an American parented Employment Business/Agency that provides global staffing services with its head-quarters in Chicago and our EMEA regional office located in Central London. We have invested significantly in creating a robust international platform that enables us to work compliantly in 30+ countries with a current network of 2500+ active contractors globally as well as a very strong permanent / direct hire recruitment offering. Our specialist knowledge and close relationships with our clients and the wider industry really makes us unique in our field. Just recently we were recognised by FORBES as the 17th best professional staffing firm, and have won multiple awards from industry accredited bodies for our commitment to excellence and service delivery. We have extensive functional expertise including: Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs / Writing. We are an equal opportunities Recruitment Business and Agency. We welcome applications from all suitably qualified candidates regardless of their race, sex, disability, religion/belief, sexual orientation or age.

Deutsche Telekom connects millions of people around the world. We are a leading telecommunications company and a trusted companion in a connected world, at home, at work, everywhere. We believe technology should serve people and the planet. We balance innovation with responsibility, combining business success with social and ecological impact. Our goal is simple: connect everyone to the opportunities of now while shaping a sustainable tomorrow. Within Telekom, Products Innovation Experience (PIX) brings this vision to life. Designers, product thinkers and technologists from many disciplines work side by side to create products and services that people love and trust. The heart of PIX is its people. Brave, curious and driven by purpose, they grow and innovate together. We value empowerment and balance, because meaningful innovation begins with people who feel inspired to create. We are looking for a CX Researcher (m / f / d) to join our Design & Customer Experience team and help to ground innovation in deep customer understanding. What We Provide We believe great work happens when people feel trusted, supported and inspired. Our culture combines ambition with humility, bold in what we create and grounded in how we collaborate. Our culture comes to life through: • Value-based innovation culture that unites creativity, responsibility and purpose. • International and diverse team of creative minds collaborating across domains and locations, empowered by Telekom’s world-class capabilities. • Responsible impact through near-term and visionary projects that shape how people and businesses experience technology worldwide. • Creative environment that encourages experimentation and collective problemsolving. • Continuous learning and growth through horizontal and vertical development opportunities. • Caring leaders who empower career development and a positive work environment. • Flexible hybrid setup based in Milan or Barcelona, with collaboration shaped by project and individual needs (up to 50 % onsite, up to 20 % travel). What You’ll Do You enable customer-centric evidence in international fast-moving digital environments, balancing depth and speed to keep decisions grounded and impactful. • Lead quantitative research end to end – design and run studies from early concepts to live products across our markets, translating complex business questions into robust research designs. • Apply advanced methodologies – use segmentation, conjoint, MaxDiff, behavioral analytics and related approaches to uncover customer needs, priorities and tradeoffs. • Collaborate across disciplines – work closely with qualitative research, data science, product and design to integrate quantitative insights into decision-making. • Ensure methodological excellence – guide sampling strategies, survey design and statistical interpretation to maintain high research quality and confidence. • Turn data into direction – synthesize findings into clear stories and actionable recommendations that influence strategic and product decisions. • Grow research maturity – mentor junior researchers and contribute to upskilling teams in data-driven customer understanding. • Evolve research practice – drive innovation in methods, including automation, dashboarding and AI-based analysis. Your Skills As Senior CX Researcher at Telekom, you combine a broad methodological range of research expertise with strategic product knowledge. • Mixed-method research – you know qualitative and quantitative, scientific and pragmatic approaches to evaluate and improve digital product effectively. • Facilitation and communication – when you share insights, dull facts become inspiring stories with high adoption rates • Research leadership – support others in delivering high-quality research and foster continuous learning. • Tool mastery – work confidently with survey platforms and analytical tools such as Quantilope, SPSS, R, Python or Tableau. • Collaborative mindset – partner effectively with design, product, data science and engineering teams, using your familiarity with the challenges of intercultural teams and cross-market product development. Your Profile • Master’s or PhD in Statistics, Behavioral Science, Market Research, Psychology or a related field. • 6+ years of experience in quantitative and or neuroscience research for digital products and services. • Proven track record of influenced key business or product decisions in complex stakeholder environments. • Fluent in English; German or other European languages are a plus.

Our client is an advanced engineering services organization delivering highly specialized R&D solutions for complex, high-performance applications. The company operates at the intersection of applied physics and multidisciplinary engineering, supporting customers in sectors where precision, reliability, and technical rigor are critical. Its work spans the full lifecycle of complex systems, from early concept and design through validation and delivery, leveraging deep expertise in optical systems, instrumentation, and tightly integrated mechanical, electronic, and analytical domains. Projects are typically customer-driven, technically demanding, and executed in parallel within a contract engineering environment. Mission The Engineering Manager is responsible for ensuring predictable, high-quality execution of multiple concurrent R&D projects while leading and developing a highly skilled engineering team. The role exists to translate complex technical scopes into structured execution, align people and resources with delivery commitments, and create the operational stability required for advanced engineering work to succeed. This position has a direct impact on project outcomes, team performance, and customer confidence. Responsibilities Project Execution & Delivery Own end-to-end planning, scheduling, and tracking of multiple parallel customer projects. Translate technical scopes, proposals, and statements of work into executable project plans. Monitor progress against milestones, identifying risks, dependencies, and capacity constraints. Proactively resolve delivery bottlenecks and execution issues. Ensure contractual milestones and technical deliverables are met with consistent quality. People & Team Management Lead the day-to-day operations of a multidisciplinary R&D team of approximately 20 engineers. Conduct regular one-to-one meetings, performance reviews, and development discussions. Support career development in a highly technical, expert-driven environment. Lead hiring, onboarding, and team scaling as required. Foster a collaborative, disciplined, and resilient engineering culture. Process, Coordination & Communication Establish and maintain lightweight but effective project and delivery processes. Run sprint planning, reviews, retrospectives, and cross-project coordination meetings. Maintain clear internal documentation, delivery visibility, and execution metrics. Act as the primary operational interface with customers and internal stakeholders. Coordinate work across optical, mechanical, electronic, analysis, and test disciplines. Shield engineering teams from unnecessary operational noise to preserve technical focus. Operational Leadership Own resource allocation and capacity planning across projects. Lead prioritization and arbitration of competing demands. Drive continuous improvement of execution, delivery, and operational workflows. Required Qualifications Strong engineering background with the ability to deeply understand and challenge technical discussions. Minimum 7+ years of experience in engineering environments, with at least 3–5 years in an engineering leadership role. Proven experience leading multidisciplinary engineering teams in complex technical contexts. Demonstrated ability to plan, execute, and deliver complex R&D or contract engineering projects. Excellent organizational, communication, and stakeholder management skills. Comfortable owning delivery commitments and execution accountability. Pragmatic, structured leadership style with the ability to remain effective under pressure. Preferred Experience Background in optical systems, instrumentation, applied physics, or physics-based engineering. Experience in high-reliability or precision-driven industries. Prior exposure to contract engineering or customer-funded R&D environments. Experience scaling teams or managing rapid changes in project load and priorities.

Language Avenue es una escuela de idiomas independiente que se enfoca en la comunicación real y efectiva. Estamos ubicados cerca de la Sagrada Familia. Nuestra metodología de enseñanza es comunicativa, donde la gramática se utiliza como un medio para lograr una meta, y no como el objetivo principal. Estamos buscando un profesor de español ELE para unirse a nuestro equipo en crecimiento en nuestra escuela junto a la Sagrada Familia. Nos comprometemos a ayudar a nuestros estudiantes a alcanzar sus metas y ofrecemos un ambiente de trabajo cómodo, colaborativo y orientado a brindar la mejor experiencia tanto para estudiantes como para empleados. Requisitos: ~ Certificado de profesor de español del Instituto Cervantes (DELE o similar). ~ Experiencia demostrable trabajando con los niveles del MCER (Marco Común Europeo de Referencia). ~ Experiencia en la preparación de exámenes DELE. ~ Disponibilidad en horario de tarde. ~ Residir en Barcelona ~ Competencia tecnológica y habilidad para generar confianza en el aula. ~ Ser creativo/a. Inclusión de juegos en el aprendizaje. ~¡Pasión por la enseñanza! Ofrecemos: Contrato con perspectiva de largo plazo. Alrededor de 12 horas de enseñanza para comenzar por las mañanas y algunas tardes, con posibilidad de aumento. lunes a jueves de 10:00-12:00 martes y jueves de 19:00 - 21:00 Sueldo: 16,50€-17,00€ la hora Un equipo directivo que colabora contigo (tu voz cuenta) Plus (Opcional): Conocimiento de metodologías como enseñanza comunicativa o enfoques multiculturales. Experiencia en la enseñanza de español para negocios. Experiencia con método AULA PLUS.