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Location: Barcelona and surrounding areaWorking model: Hybrid - 4 days remote, 1 day per week in our Barcelona officeOffice: KPS Iberia, C/ Pau Claris 162-164, 08037 Barcelona About KPS KPS is a global consulting and technology company delivering digital transformation and e-commerce solutions for leading international clients. At KPS Iberia, you will work in an international and agile environment on complex digital platforms and business-critical technology solutions. We are looking for an experienced Senior Tech Lead / Full-Stack & DevOps Engineer to join KPS Iberia and work on complex, end-to-end digital and e-commerce platforms for major international clients. This is a hands‑on technical leadership role. We are looking for someone who combines strong software engineering expertise with proven experience leading and coordinating developers, driving technical execution and ensuring successful delivery. The role combines architecture, technical project leadership and hands‑on engineering. You will work closely with developers, guide technical decisions, and actively contribute to the implementation of technical solutions. Your Responsibilities Understand, analyse and evaluate existing software/system architectures. Proactively identify and propose technical improvements and necessary adaptations. Make architecture decisions and help shape scalable and sustainable technical solutions. Provide hands‑on support in the implementation of technical solutions. Take responsibility for technical project leadership. Coordinate developers and ensure effective collaboration within the team. Support the team in resolving technical challenges and maintaining high engineering quality. Communicate technical concepts and decisions clearly to both technical and non-technical stakeholders. Your Profile Several years of experience as an Architect, Senior Architect, Tech Lead or in a comparable technical leadership role. Very strong frontend expertise, particularly with JavaScript, Node.Js and React. Experience in backend development, ideally with Java. Ability to understand, assess and further develop software/system architectures. Solid experience with Cloud Systems (AWS, Azure and/or GCP). A strong hands‑on mentality and willingness to actively contribute to technical solutions. Good understanding of DevOps practices and modern software delivery processes (Docker, Kubernetes, Terraform, CloudFormation, Pulumi or similar, CI/CD pipelining etc.). Experience coordinating developers and leading technical workstreams ideally in an international environment. Strong communication skills in English, as our projects are international and conducted in English. Nice to have Knowledge of container technologies and modern deployment processes. Experience in complex e-commerce, SaaS or digital platform environments. Experience with AI-assisted development, agentic coding or modern AI engineering tools. Good knowledge of security best practices, IAM, secrets management and OWASP principles. What We Offer Architectural responsibility in complex digital and e-commerce projects. The opportunity to shape technical solutions for major international clients. A role combining architecture, technical leadership and hands‑on engineering. An international and collaborative working environment. Modern technologies and agile ways of working. The opportunity to work closely with experienced developers, architects and business stakeholders. Clear opportunities to further develop your architecture and technical leadership career. A hybrid working model with four remote days and one day per week at our Barcelona office. Employment under a Spanish employment contract. #J-18808-Ljbffr

Time Out Group in Barcelona seeks a Senior Programmatic & Ad Tech Specialist to optimize our global ad tech stack (GAM, Prebid) and maximize SSP revenue across markets. This hybrid role blends audience monetization, partner management, and privacy compliance. You will own SSP and demand-partner relationships, monitor eCPMs, manage first-party data strategies, and troubleshoot programmatic delivery with DevTools. Fluent English required; based in Spain with 1 day per week in the Barcelona office. #J-18808-Ljbffr

Computational Scientist - Deep Tech Newton Colmore is proud to be working with a venture that sits at the intersection of AI, biology, and advanced process engineering.We are assisting them in their search for a computational scientist to play a foundational role in the development of their data-rich product. This is a rare opportunity to join a highly ambitious, venture-backed team transforming complex industrial processes into intelligent, predictable, and controllable systems.The successful candidate will help build the modelling and machine learning capabilities that underpin a platform that aims to transform how process data is viewed and utilised. The position offers significant autonomy, technical ownership, and a clear path for growth. As a computational scientist, you will own the development of advanced computational models spanning mechanistic process understanding, machine learning, digital twin technology, and real-time predictive intelligence. Working closely with a multidisciplinary team of scientists and engineers, you will apply cutting-edge mathematics, modelling, and AI techniques to solve complex industrial challenges with real-world impact. The role will also provide an opportunity to build novel predictive models using advanced sensor technology, then looping the data back to the engineering and science teams to ensure that constant iterations and alterations can be made. We are looking for candidates with strong mathematics fundamentals, ideally applying them within a highly complex scientific and engineering field.This will be complemented by experience with working on digital twin technology, simulation platform sand predictive process models. Any additional experience with industrial monitoring applications and/or chemical manufacturing would be highly advantageous. In their pursuit of hiring outstanding engineers and scientists, the company are offering a competitive package with share options and the potential to help with relocation (case by case basis).This mixed with direct access to the founders, and investors, it could be a great destination for the next part of your career, working on something that is aiming to be truly transformational. #J-18808-Ljbffr

Get notified about new Pediatra jobs in Spain.Pamplona, Chartered Community of Navarre, Spain 1 month agoPamplona, Chartered Community of Navarre, Spain 2 months agoPSICOLOGO EXPERTO EN NEURODESARROLLO ROQUETAS DE MARGreater Barcelona Metropolitan Area 1 year agoPamplona, Chartered Community of Navarre, Spain Be an early applicant 1 week agoMETGES/SSES ESPECIALISTES MEDICINA FAMILIAR I COMUNITÀRIA CAP BARCELONETA (TELETREBALL 1 DIA SETMANAL)Colmenar Viejo, Community of Madrid, Spain Be an early applicant 5 hours agoMEDICO COLABORADOR (VARIAS ESPECIALIDADES)Madrid, Community of Madrid, Spain 1 week agoIbiza, Balearic Islands, Spain 1 month agoTres Cantos, Community of Madrid, Spain 3 days ago#J-18808-Ljbffr

Westlake offers you the potential to enrich your work life and career experience in an entrepreneurial environment. We work together to enhance peoples' lives through our products and presence in the communities in which we operate.Ingeniero/a de Servicios Técnicos y Desarrollo Descripción del puestoComo Tech Services & Development Engineer (f/m/d), serás responsable del desarrollo técnico y la mejora de compuestos plásticos para aplicaciones altamente reguladas. Liderarás proyectos de desarrollo de producto, calificarás materias primas y actuarás como referente técnico para los equipos internos y los clientes.Qué harás en el puestoImpulsar la innovación en ingeniería de plásticosLiderar el desarrollo de nuevos compuestos plásticos de PVC y otros materiales poliméricos como XLPE, siliconas y compuestos con poliolefinas y la optimización de formulaciones existentes para aplicaciones altamente reguladas, equilibrando rendimiento, calidad y coste.Gestionar proyectos técnicos de principio a finAsumir la responsabilidad de proyectos de desarrollo de producto desde los ensayos de laboratorio hasta la validación industrial y el escalado a producción.Colaborar con clientes y equipos comercialesActuar como referente técnico de confianza, apoyar pruebas en cliente, resolver retos técnicos y transformar las necesidades del cliente en soluciones innovadoras.Contribuir a la calidad y el rendimiento del productoCalificar nuevas materias primas, mantener especificaciones técnicas, gestionar reclamaciones internas y de clientes, prestar soporte técnico continuado al cliente durante todas las etapas del desarrollo y asegurar que los productos cumplan con los más altos estándares del sector y de los clientes.Trabajar de forma transversalColaborar estrechamente con Producción, Supply Chain, Comercial, QHSE, proveedores y clientes para impulsar la mejora continua y una industrialización de producto exitosa.Liderar la excelencia técnicaCoordinar actividades de laboratorio, supervisar a técnico/s de laboratorio y aportar soporte experto en rendimiento de producto, ensayos y resolución de incidencias.Qué buscamosFormación en Ciencia de Materiales, Química, Ingeniería o una disciplina técnica relacionada, o experiencia equivalente en el sector.Experiencia en tecnologías de fabricación y procesado de plásticos, idealmente incluyendo PVC, extrusión e inyección.Experiencia o conocimientos técnicos en polímeros como XLPE, siliconas, poliolefinas y otros materiales termoplásticos.Conocimientos en formulaciones de polímeros y métodos de ensayo de materiales; se valorará especialmente la experiencia en formulación de PVC.Sólidas habilidades de gestión de proyectos y de interlocución con diferentes áreas, con clara orientación al cliente.Capacidad para comunicar contenidos técnicos de forma clara y eficaz a interlocutores internos y externos.Perfil proactivo, organizado y orientado a soluciones, con motivación por la innovación y la mejora continua.Dominio del español y buen nivel de inglés, mínimo B1.Qué ofrecemosUna gran oportunidad para contribuir a la excelencia operativa y generar un impacto significativo en el desempeño en materia de seguridad, salud, calidad y medioambiente.Oportunidades de desarrollo profesional.Entorno de trabajo internacional.Paquete retributivo competitivo.Amplio paquete de beneficios, que incluye seguro médico privado, plan de pensiones, bonus e iniciativas de conciliación de la vida laboral y personal, entre otros.Westlake is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to any characteristics protected by applicable legislation.Westlake is a global manufacturer and supplier of materials and innovative products that enhance life every day. Headquartered in Houston, with operations in Asia, Europe and North America, we provide the building blocks for vital solutions — from housing and construction, to packaging and healthcare, to automotive and consumer.For more information, visit the company's web site at www.Westlake.Com.Westlake (NYSE: WLK) is a global diversified industrial company that manufactures and supplies essential products that enhance the daily lives of people around the globe. Our products, now under a One Westlake brand, supply the necessary building blocks for everyday products across housing and infrastructure, packaging and healthcare, and automotive and consumer goods. Consumers gain the benefits of materials Westlake produces in products such as food packaging, medical devices, soaps and detergents, car interiors, fashion, toys, shoes, furniture, electronics, siding, stone veneer, windows, outdoor living, roofing, and pipe & fittings. Westlake is proud to contribute to driving a sustainable future through the creation of essential products that are Enhancing Your Life Every Day.To view other career opportunities at Westlake and our family of companies, visit https://westlaketalent.Com#J-18808-Ljbffr

Seeking a qualified EU-trained dentist for a full-time position in a modern Dutch dental clinic. Offers relocation assistance, language training, and a salary of €4500-€6500 monthly.

Clinical Operations Manager 2 (COM2) The COM 2 is a regional role that provides expertise across all aspects of clinical site management and/ or study management for assigned Phase I – IV studies. The COM 2 operates in line with Good Clinical Practices (ICH-GCP), applicable regulatory and legal requirements and Bayer’s standard operating procedures. The COM 2 may be assigned work packages in areas of study start-up, site management and study management on a regional level. Either one or a combination of these work packages may be allocated to the position holder according to expertise, skill set and capacity requirements in a flexible way. The COM 2 must acquire knowledge and adequate training for work packages assigned and become proficient in independently executing assigned responsibilities. STUDY MANAGEMENT Lead and oversee all operational aspects of site management on a regional or study level from protocol feasibility to study archive. Serve as the representative for site management on the core study team. Contribute to the development of the protocol, study overview, monitoring strategy and Risk Based Quality Management with regards to monitoring and operational aspects. Responsible and accountable for developing the monitoring plan and the study-specific training plan. Key contributor in the development of recruitment and retention strategies and tools. Act as key study contact for assigned countries. Responsible for overall deliverables regarding timelines, budget, and quality in assigned countries. Ensure participating country commitment aligns with study commitments. Provide the information required to effectively monitor and manage study activities, ensuring all relevant IT systems are updated with precise and current data. Oversee monitoring activities and ensure sponsor oversight through monitoring report review and co-monitoring visits. SITE MANAGEMENT Act as primary contact for investigational sites. Verify site qualification, ensure the Investigator, and site staff meet all aspects of study delivery and commitments from site selection through close out. Train the Investigator and site staff on study protocol, relevant systems and operational aspects of study conduct. Monitor trial conduct in compliance with the study protocol, ICH-GCP and applicable regulatory requirements on time and quality. Ensure completeness of the Investigator Site File. Prepare and conduct onsite and/or remote monitoring activities according to monitoring plan, including complete reporting and follow up. CLINICAL CUSTOMER ENGAGEMENT Cultivate and sustain customer relations with clinical trial sites, ensure effective communication, drive fit for purpose processes and work towards enhancing overall site satisfaction and engagement. Establish and develop strong professional relationships with clinical investigators to expand/ maintain clinical research partnership opportunities. Cross functional collaboration to ensure alignment of priorities and deliver the portfolio. Influence and challenge internal and external factors to improve clinical research delivery. STUDY START-UP Lead study start-up activities in collaboration with local team. Provide input on site activation strategy. Collect and perform quality review of essential documents on country level such as IRB/IEC approvals, financial disclosure, CVs/medical licenses, etc. Compile and submit submission dossier (country dependent). Obtain any required approvals for relevant site documents (e.G., informed consent, financial disclosures). Prepare and distribute site start up documentation including Investigator Site File. Ensure timely filing of study documents at country and site level in Trial Master File (TMF). Ensure awareness of related local regulations and support maintenance of country intelligence. Provide study status monitoring and systems support (e.G. act as technical expert) Coordinate site and vendor payments. QUALITY Proactively identify and communicate issues, taking appropriate action to prevent the recurrence of identified deviations. Ensure timely and comprehensive resolution of issues that may affectcompliance or the quality of study related activities or data. Maintain corrective action and preventative action plans (CAPAs) at country level. Contribute to the preparation, conduct, and follow-up of Site Audits and Regulatory Inspections to ensure a successful outcome. Oversee completeness of country/site level eTMF and conduct QC for accuracy, completeness, and adherence to ICH/GCP and Bayer QSDs. SKILLS & QUALIFICATIONS: Healthcare related Bachelor’s Degree or equivalent with minimum 4 years of monitoring and site management experience. Or have a combination of education and minimum 8 years of monitoring and site management experience. Experience in Spain. Languages: Effective written and verbal English and Spanish communication skills. Fundamental project management skills, Decision making, Issue resolution Home based in Spain Location: Spain Application Period: 15 días Reference Code: 891581 Division: Pharmaceuticals Location: Spain : Cataluña : Barcelona Functional Area: Clinical Development & Operations Position Grade: VS 1.2 Employment Type: Regular Work Time: Regular Contact Us Address Telephone E-Mail Av. Baix Llobregat, 3, 08970 Sant Joan Despí,Barcelona, Espanya +34 93 495 69 99 Job Segment: Operations Manager, Compliance, Clinical Research, Medical Research, Operations, Legal, Healthcare

Lead a team of developers in the design, development, and delivery of new features and enhancements for the Secure GPT service, ensuring the timely delivery of high-quality features that meet acceptance criteria and align with the product vision. Define and prioritize user stories based on business value and user needs, and manage the product backlog to reflect the latest priorities and business objectives. Develop new functions and enhancements around Secure GPT API usage while identifying opportunities for improvement in API Operations processes, particularly in observability automation and customer service delivery. Take ownership of service issues and incidents, troubleshooting and resolving API-related issues to ensure seamless user experience and high service availability, and serving as a point of escalation for stakeholders seeking assistance. Ensure compliance with security, regulatory requirements, and data privacy standards related to the Secure GPT service. Communicate effectively with stakeholders to gather feedback, provide updates, and align on product direction, collaborating with the broader Secure GPT international team to deliver exceptional customer service to internal stakeholders. About The Job Main missions Your Responsibilities Include Lead a team of developers in the design, development, and delivery of new features and enhancements for the Secure GPT service, ensuring the timely delivery of high-quality features that meet acceptance criteria and align with the product vision. Define and prioritize user stories based on business value and user needs, and manage the product backlog to reflect the latest priorities and business objectives. Develop new functions and enhancements around Secure GPT API usage while identifying opportunities for improvement in API Operations processes, particularly in observability automation and customer service delivery. Take ownership of service issues and incidents, troubleshooting and resolving API-related issues to ensure seamless user experience and high service availability, and serving as a point of escalation for stakeholders seeking assistance. Ensure compliance with security, regulatory requirements, and data privacy standards related to the Secure GPT service. Communicate effectively with stakeholders to gather feedback, provide updates, and align on product direction, collaborating with the broader Secure GPT international team to deliver exceptional customer service to internal stakeholders. Expected Skills & Experience Experience Bachelor's or Master's degree in Computer Science, Software Engineering, or a related field 7+ years of experience as a software engineer, with at least 3-5 years in a lead or senior role Proven track record of successfully leading the delivery of complex software projects Experience in managing and mentoring a team of software engineers Technical Skills JavaScript/TypeScript development (Node.Js) for the backend Github / DevOps experience Experience in API operations and management Competence in monitoring resources on Azure Knowledge of Infrastructure as Code (IaC) Terraform and/or Bicep for automatic infra deployment Expertise in software design patterns, architecture principles, and development methodologies Familiarity with agile software development practices and tools (e.G., Scrum, Kanban, Git, CI/CD) Experience with cloud-based technologies and platforms (e.G., AWS, Azure, GCP) Strong understanding of software testing, debugging, and performance optimization techniques Soft Skills English : Independent user (C1) Ability to travel / ability to be relocated for short periods in other countries (France/Spain/Portugal) Leadership: Ability to inspire and motivate a team, provide guidance, and make decisions Excellent communication and interpersonal skills, with the ability to effectively collaborate with cross-functional teams Strong problem-solving and critical thinking abilities, with a focus on delivering innovative solutions Ability to prioritize tasks, manage multiple projects, and adapt to changing business requirements Demonstrated leadership skills, with the ability to motivate and inspire a team Commitment to continuous learning and professional development What We Offer We bring together the expertise, cultural diversity and creativity of over 8,000 employees worldwide and we’re committed to equal opportunities in all aspects of employment (gender, LGBT+, disabled persons, or people of different origins) and to promoting Diversity & Inclusion by creating a work environment where all employees are treated with dignity and respect, and where individual differences are valued. About The Entity AXA is becoming a sustainable tech-led company and at AXA Group Operations we are one of the major catalysts for this transformation. We set the tone by triggering and empowering the evolution of our insurance business model through technology and innovation, driving its concrete implementation globally at speed, with a high quality of advisory and execution. We are present across 17 countries with committed, highly qualified teams. We leverage technology, data, sourcing, security and investment allocation in a global way, but also achieve economies of scale and synergies when necessary. At AXA Group Operations, we want to be recognized in three fields of action: State-of-the-art Data Technology to drive customer experience State-of-the-art Procurement & Sourcing to drive efficiency and better manage risks High-Performing Global Team for stronger partnerships with AXA entities About AXA As a world-leading insurance company, we act for human progress by protecting what matters. With 153,000 employees in 54 countries working for 105 million customers, we’ve created a truly dynamic and vibrant community. Inclusion and diversity link closely with our values, and together we’re nurturing a culture of respect, for each other, for our customers and the communities around us. Join AXA and you’ll feel like you belong, are included and can thrive. You’ll be able to shape the way you work and truly grow your potential as you seek out new opportunities, push boundaries and benefit people in critical moments of their lives. This is your chance to build the tomorrow you want. Know you can. #J-18808-Ljbffr

Se busca un consultor de talento junior para gestionar procesos de selección, entender vacantes, generar insights de mercado y colaborar en la detección de oportunidades comerciales, con formación y acompañamiento constante.

Seeking a certified caregiver for temporary coverage. Responsibilities include elder care. Must have official certification and experience in the elderly sector. Knowledge of ACP and Catalan language required.

Medical Staff Talent is seeking a UK/Europe-trained private physician for a confidential placement in Dubai with travel to London or Marbella as required. The physician will work for a private family, with duties defined directly by the family and they must maintain registration and clinical standards. The role requires at least 5 years of clinical experience, fluent English, and willingness to travel internationally. #J-18808-Ljbffr

Description Summary: Develops or contributes to the development of the organization's products once human trials begin. Participates in international product teams to define and implement development policy and programs that best support the product strategy and future positioning of the organization. Purpose: Operational public disclosure of clinical trial information into clinical trial registries and posting of clinical trial result summaries on company owned and public international websites based on internal rules and external guidelines, obligations, and legislations for the entire Bayer product portfolio, including regular updates and maintenance of the disclosed information according to internal and external requirements. Contribute to the development and continuous update of Bayer's disclosure processes for clinical trial information based on cross functional internal requirements and the rapidly changing external legal and regulatory requirements, industry commitments and obligations. Disclose information on Bayer's Clinical Trials at high level quality by fully complying to the related Quality Assurance processes Key tasks: Manage the public disclosure of clinical trial information, ensuring timely and accurate posting of trial summaries on international and company websites in accordance with internal rules, external guidelines, and global legislation. Provide up to date and consistent Clinical Trial Posting data on required company owned and public websites. Formal quality control of publicly disclosed clinical trial information according to the QA process established. Contribute to the ongoing development and optimization of Bayer’s disclosure processes, adapting to evolving legal,regulatory, and industry requirements. Position holder directly interacts with study and product teams, Nuclei, SM teams, RegAff and other CD&O / MA / PV and CH managers and teams. Skills & Qualifications: Education: Bachelor’s degree in Business Administration, Life Sciences, or a related discipline. Understanding of global legislations, regulations and guidelines, i.E. ICH/GCP regulations. Understanding of drug development process over different development phases. IT Skills at user level and quick learner in IT processes and systems. Strong skills in English language, both oral and written (fluent speaking mandatory). Project management: Proven ability to lead and manage cross-functional teams to setup and deliver complex projects in an agile and outcome-focused manner. Exhibit agility and accountability in managing tasks and responsibilities. Be self-organized in prioritizing work, ensuring timely delivery of high quality results. Solution-oriented mindset, capable of identifying issues and implementing effective solutions in a timely manner. Communication skills: Excellent verbal and written communication skills and ability to explain complex topics in a simplifiedway. Collaboration: Proven ability to collaborate with internal and external stakeholders without hierarchical authority and withaccountability to make decisions. Strong ability to self-organize, pro-actively drive improvement, trouble-shooting, inclusive mindset and strong display of DSO behaviors. Application Period: 15.10.2026 - 30.10.2026 Reference Code: 892730 Division: Pharmaceuticals Location: Spain : Cataluña : Barcelona Functional Area: Clinical Development & Operations Position Grade: VS 1.1 Employment Type: Regular Work Time: Full Time Contact Us Address Telephone E-Mail Av. Baix Llobregat, 3, 08970 Sant Joan Despí,Barcelona, Espanya +34 93 495 69 99 Job Segment: QA, Quality Assurance, Clinical Research, Medical Research, Clinic, Quality, Technology, Healthcare

Seeking Dentists (General Practitioners, Orthodontists, Prosthodontists) to relocate to private practices in Ireland. Requires a Bachelor in Dental Surgery and advanced English.

Asinsa, empresa lider desde hace 35 años en prestación de servicios sanitarios. Con sede en Barcelona capital trabajamos en varios sectores de sanidad privada: especialidades médicas en nuestro centro, reconocimientos de salud laboral y visitas de asistencia médica domiciliaria. Actualmente contamos con un equipo estable de más de 35 profesionales sanitarios, realizando diferentes turnos y horarios con mucha flexibilidad horaria.Contrato laboral indefinido.20 o 40 horas semanales repartidas en guardiasSalario bruto anual: Base convenio+Pluses visitas realizadas+ Productividad (Aprox. 25.000€ para el contrato de 20h/ 50.000€ para el contrato de 40h)Gastos Km a cargo de la empresaHorariosFlexibilidad horaria:Turnos de 7 a 15h y/o de 15 a 23h a repartir en guardias con otros compañerosTurnos de 21 a 07h a repartir en guardias con otros compañeros (plus nocturnidad)título homologadopermiso de trabajo vigenteBeneficiosEspecial flexibilidad horariaPluses por incentivosPosibilidad de vehículo de empresa (se valorará especialmente vehícuo propio))#J-18808-Ljbffr

Médico/a de urgencias - TelemedicinaTeladoc Health International somos la marca líder en el mundo en asistencia sanitaria virtual. Nuestros servicios abarcan todo el espectro de necesidades de atención médica, desde simples hasta complejas. Conectamos a nuestros usuarios con la atención primaria, salud mental y experta.La persona que se incorpore orientará y dará consejo médico a los pacientes de servicios catalogados como alta complejidad a través de medios telemáticos, gestionando el recurso médico correspondiente en caso necesario, de acuerdo a las directrices del cliente y los estándares marcados por Teladoc Health International.FuncionesAtender a los pacientes a partir de una escucha activa del motivo de la consulta.Realizar una entrevista estructurada.Determinar médicamente la gravedad y el nivel asistencial requerido.Dar consejo y orientación médica al paciente siendo posible la prescripción farmacológica.Activar el recurso adecuado a la situación clínica y adaptarlo según la disponibilidad. En caso de no disponer del recurso necesario contactar con otros servicios de emergencias.Realizar seguimiento del paciente hasta la llegada del recurso, en caso necesario.Cumplimentar de forma adecuada el caso del paciente en el sistema.Reportar las incidencias al supervisor.Cumplir con los estándares de calidad establecidos siguiendo el código ético médico.Conocer, mantenerse actualizado y actuar de acuerdo a los protocolos internos de gestión y los acuerdos pactados con las compañías siguiendo las políticas para cumplir con la ética de Teladoc Health International.#J-18808-Ljbffr

Desde Omnicom Media Spain, buscamos incorporar a nuestro Tech and Data Strategy Lead en la unidad de TRKNN en Madrid o Barcelona, desempeñando un papel clave conectando personas, datos y tecnología. Liderarás la estrategia de clientes e impulsarás la madurez digital de todo tipo de clientes, identificando de forma sistemática palancas y soluciones técnicas en Google Marketing Platform y Google Cloud. Principales funciones y responsabilidades: Preventa y estrategia comercial: liderar la actividad de preventa para nuevas oportunidades de negocio, propuestas comerciales, análisis de oportunidades y cross-selling/upselling con clientes actuales en España. Empaquetado de soluciones y estrategia tecnológica: definir estrategias de venta y empaquetar soluciones (incrementalidad, marcos de medición, estrategias de datos first-party, privacidad y stacks tecnológicos). Consultoría estratégica y workshops: realizar evaluaciones de madurez en Tech & Data y liderar workshops estratégicos con clientes clave para resolver retos de negocio complejos en un ecosistema cada vez más centrado en la privacidad. Key Account Management y Customer Success: ser el principal punto de contacto (POC) del cliente y liderar iniciativas de Customer Success para las cuentas estratégicas más importantes de España. Gestión de proyectos y operaciones: actuar como Project Manager en implementaciones técnicas de gran envergadura y gestionar las operaciones de Google Funds, así como la alineación de la relación con Google España. Liderazgo y desarrollo de equipos: guiar, mentorizar y desarrollar a los consultores de TRKKN para impulsar su crecimiento individual y alcanzar los objetivos de negocio de la compañía. Innovación en la industria: mantenerte al día de las tendencias del sector, los cambios en privacidad y las mejores prácticas en Tech & Data Strategy, compartiendo conocimiento con los equipos de servicio de TRKKN para impulsar la mejora continua. Partnerships y colaboraciones: construir relaciones sólidas con Omnicom Media Spain y Google, e identificar nuevas oportunidades de negocio. Requisitos y competencias deseadas: Amplia experiencia en desarrollo de negocio en consultoría de Tech & Data Strategy, preferiblemente en el sector del marketing digital (stack de Google GMP) y la tecnología cloud. Trayectoria demostrada en preventa, elaboración de propuestas comerciales e impulso del crecimiento de negocio con clientes medianos y grandes. Dominio de Google Analytics, Google Tag Manager y las herramientas de GMP Ads (Campaign Manager 360, Search Ads 360 y Display & Video 360). Experiencia práctica en gestión de Google Funds, demostrando su capacidad para aprovechar el ecosistema y los recursos de Google. Sólidas habilidades de gestión de cuentas y de proyectos. Sobre nosotros En Omnicom Media estamos comprometidos con la diversidad e inclusión, fomentando un entorno en el que las personas colaboran y se respetan, donde las diferencias son valoradas y en el que todo nuestro talento tiene las mismas oportunidades, independientemente de cualquier condición. Omnicom Media , la división de medios de Omnicom (OMC), la mayor red global de medios del mundo. Integra las agencias de OMD, Initiative, PHD Media, UM y Hearts United , conectando estrategia, datos, tecnología, inteligencia, commerce, contenido e innovación para impulsar el crecimiento de las marcas. Con más de 40.000 especialistas en más de 70 mercados, combina la escala y las capacidades globales con la especialización y cercanía de sus agencias. En España, Omnicom Media reúne a más de 1.200 profesionales, trabaja para más de 300 anunciantes y gestiona más de 1.600 M€ de inversión publicitaria, con una cuota cercana al 29%. En 2026 ha liderado el nuevo negocio del sector y cuenta con reconocimientos de Great Place to Work, SCOPEN y Actualidad Económica, que reflejan una cultura basada en el talento, la colaboración, la confianza y el desarrollo profesional, bajo un propósito compartido: crecer haciendo crecer. #J-18808-Ljbffr

Seeking a senior full-stack engineer to develop and implement features, taking ownership of product areas and driving projects from research to delivery.

IRB Barcelona is seeking a highly motivated and talented Postdoctoral Fellow to participate in cutting edge research line of the Quantitative Stem Cell Dynamics lab led by Alejo Rodriguez-Fraticelli.The lab focuses on implementing cutting-edge single-cell technologies to discover new druggable susceptibilities in leukaemia and other blood malignancies. The goal is to identify new targets to prevent drug-resistance and relapse in these terrible diseases.We are looking for a wet lab candidate with a strong background in cancer biology, epigenetic analysis and/or stem cell research. Knowledge of single-cell sequencing, clonal analysis, biostatistics, and/or genomics will be appreciated but is not required for this position and the candidates will be trained in all appropriate skills for this project.The position is for 2 years, with the potential to extend this contract up to 2 additional years. This level of support makes this an excellent opportunity for candidates looking to transition to an independent research-focused position.KEY RESPONSIBILITIESIndependently design and test biological hypotheses.Plan, perform and interpret experiments.Collaborate with a multidisciplinary research team, tapping into the expertise of fellow researchers and external collaborators.Contribute to a culture of scientific excellence, efficiency, and teamwork.Contribute to other lab projects and to the maintenance of protocols and laboratory resources in the group.Critically analyze analytical results, participate in scientific discussions and in preparation of diverse forms of scientific communication (seminars and conferences).Participate in the project activities: meetings, presentations, visits to other labs, collaboration, exchange of data sets, preparing project reports/deliverables.Perform excellent research according to the high standards of the lab and the IRB Barcelona.YOU HAVEPhD in a relevant Life Sciences field.At least one publication as first-author in a top-ranked journal (ranked Q1 in a life sciences field)Experience in hematological malignancies, including ex vivo and in vivo experiments.Demonstrated ability to design and conduct experiments independently, particularly in the area of single-cell genomics (at the very least, single-cell RNAseq).Excellent communication skills and the ability to collaborate effectively.Strong organizational and multitasking skills.Attention to detail and accuracy.Proficiency in English (both written and spoken).Highly motivated, enthusiastic and collaborative person.Willing to keep on learning.Ability to work independently in a demanding research environment.YOU MIGHT ALSO HAVEFamiliarity with acute myeloid leukemia models, including patient derived materials.Experience with CRISPR screening techniques.Experience with computational data analysis of single-cell genomics data.Ability to secure additional funding, such as grant-writing or fellowship-writing skills.WHAT WE OFFER:To be a part a part of something meaningful: We are a biomedical research centre that tirelessly works to achieve a society free of diseases. Our mission is to carry out research of excellence to cure cancer and other diseases linked to ageing.Good Working conditions:Employed in compliance with Spanish legislation and regulations under a full-time contract. Employees receive the benefits of the Spanish Social Security system covering sickness, maternity/paternity leave and injuries at work.Competitive salary: commensurate with experience and qualifications.International Environment: Nearly 90 Postdoctoral researchers (more than a half non-Spanish nationals) are currently working at IRB Barcelona.Multidisciplinary Research: Research of excellence at the unique interface between biology, chemistry, and structural and computational biology.Training and Career: Postdoctoral researchers joining IRB Barcelona gain access to the Institute’s advanced research training and career development opportunities, all within in a competitive international environment. Courses and workshops on themes of particular interest to postdocs are offered regularly by the Institute.Relocation & Visa Assistance: Trained staff provides support on visa paperwork, administrative requirements, and practical information on living and working in Barcelona, etc.Social Life: We like to have fun. We promote several activities, like a Football League, an annual skiing trip, a Mountaineering Club, a Running Club and "Cool-off sessions", where members meet informally for drinks, snacks and scientific discussions.Fairness: Our recruitment is open, transparent and merit-based, and all applicants compete on the same terms. We are an Equal Opportunity Employer and all qualified applicants are considered for employment without regard to race, colour, religion, age, sex, sexual orientation, gender identity, nationality, ethnic origin or disability.HOW TO APPLY & SELECTION PROCESS:Deadline for applications: 31/10/2026 (If no suitable candidate is found, the deadline will be extended)Number of positions available: 1Selection process:Pre-selection: Will be based on CV, motivation letter &experience.Interviews: Short-listed candidates will be interviewed.Job offer: Will be sent to the successful candidate after the interview.IRB BARCELONA endorses the Requirements and Principles of the European Charter for Researchers, the Code of Conduct for the Recruitment of Researchers, and Open, Transparent, Merit-based recruitment promoted by the European Commission and follows Equal Opportunities policies.On 9 December, 2014, IRB Barcelona was awarded the "HR Excellence in Research" logo. This recognition reflects the commitment of the Institute to the continuous improvement of its human resources policies in line with the Charter & Code. The Institute works to ensure fair and transparent recruitment and appraisal procedures.Please check our Recruitment Policy.Note: The strengths and weaknesses of the applications will be provided upon request.ABOUT IRB BARCELONA,Created in 2005 by the Generalitat de Catalunya (Government of Catalonia) and the University of Barcelona, IRB Barcelona is a Severo Ochoa Centre of Excellence—a seal that was awarded in 2011.The institute is devoted to conducting research of excellence in biomedicine and to transferring results to clinical practice, thus improving people’s quality of life, while simultaneously promoting the training of outstanding researchers, technology transfer, and public communication of science. Its 27 laboratories and 9 core facilities address basic questions in biology and are orientated to diseases such as cancer, metastasis, Alzheimer’s, diabetes, and rare conditions.IRB Barcelona is an international centre that hosts 500 members and 45 nationalities. It is located in the Barcelona Science Park. IRB Barcelona forms part of the Barcelona Institute of Science and Technology (BIST) and the “Xarxa de Centres de Recerca de Catalunya” (CERCA).#J-18808-Ljbffr

Join our global team dedicated to innovation and initiative, where physical walls and different time zones don’t limit, but encourage, collaboration. Where all contributions and new ideas are explored with an open mind and work is driven by our shared values: be courageous, be accountable, be honest, be inclusive and elevate others. Job Description Summary The Clinical Site Payment Associate Manager will be part of the team responsible for managing and advancing Investigator Payments. The successful candidate will possess end-to-end knowledge of the clinical site payment process and consistently provide customer-oriented support. Key Responsibilities Process investigator and site payments in compliance with applicable procedures, regulations, contracts, and country-specific requirements. Compile and review data from multiple sources, including but not limited to study budgets, EDC, and CTMS systems. Review site invoices, when required, and investigate, resolve, and respond to any issues or findings. Perform reconciliations and prepare accurate payment accruals and forecasts. Develop and maintain standard reports. Drive process, system, and reporting improvements, including evaluating opportunities for the adoption of Artificial Intelligence within Clinical Payments. Identify, assess, and manage operational and financial risks related to site payments. Collaborate effectively with internal and external stakeholders. Create, maintain, and/or collect process, project, and financial documentation as required. Education and Experience Bachelor's degree or higher in Business, Finance, Accounting, or a related field. Minimum of 5 years of experience in clinical payments. Knowledge, Skills, and Abilities Proficiency in English, both written and verbal. Strong financial, analytical, critical-thinking, problem-solving, and multitasking skills. Strong attention to detail. Ability to analyse data efficiently and present practical solutions and recommendations. Ability to work effectively in a global environment. Ability to quickly learn and adapt to new systems and processes. Strong customer-oriented mindset and service approach. Ability to collaborate effectively with cross-functional internal and external teams. Good knowledge of and experience with MS Office, financial systems, EDC, and CTMS platforms. Contract Type Regular Salary Range The final offer will be determined within the applicable location-specific range and will depend on the candidate’s confirmed work location, relevant experience, skills, qualifications, internal equity, and role scope. 45-65k Euro (Italy, Spain) Germany : 60-85K Euro gross annually. About Alira Health Alira Health is a global advisory firm providing consulting and research and clinical development services whose mission is to humanize healthcare and life sciences, in partnership with patients, through innovative technologies and expert guidance. From development to medical care, we complement the expertise of our Pharma, Biotech, and MedTech clients with a full spectrum of services across their entire solutions lifecycle. With offices around the world, Alira Health provides a vibrant and creative environment with benefits that include professional development, global travel, flexible work programs and more. We welcome your passion and drive, talent and entrepreneurial spirit, sense of service and teamwork. We are an integrated team of over 800 scientists, strategists, economists, clinicians, and biostatisticians representing over 30 nationalities. This broad global perspective and cultural richness has a direct impact on providing innovative solutions for our clients that lead to higher standards of care and an improved patient experience. #J-18808-Ljbffr

START Center for Cancer Research (START) is the world's largest network of Phase I clinical trial centers, dedicated exclusively to oncology research. Since its inception, START has provided hope to cancer patients across global communities by offering access to cutting-edge clinical trials in the United States and Europe. About the Role We are seeking a highly analytical and collaborative Clinical Business Operations Manager, to serve as the critical link between Clinical Operations and Finance. This strategic role ensures that all clinical trial activities are accurately documented, reconciled, and translated into revenue-generating transactions while maintaining the highest standards of data integrity and compliance. The successful candidate will oversee the accuracy of clinical research operational data, support billing dispute resolution, drive cross-functional collaboration, and help ensure that services performed within clinical trials are properly captured, validated, invoiced, and ultimately collected. This position is ideal for a professional with experience in both clinical research operations and healthcare revenue cycle processes who enjoys solving complex problems, improving processes, and working across multidisciplinary teams. Key Responsibilities Ensure the accuracy, integrity, and reconciliation of clinical research data across CTMS and related systems. Serve as the primary resource for sponsor and CRO billing inquiries, invoice disputes, and revenue-related investigations. Collaborate with Clinical Operations, Research Nursing, Pharmacy, Regulatory, Finance, and Revenue Cycle teams to support accurate documentation, billing, and revenue capture. Investigate and resolve operational, clinical, and financial discrepancies to minimize revenue leakage and ensure compliance. Monitor study-level invoicing, payments, aging accounts, and revenue performance, identifying risks and escalation needs. Develop and track key performance indicators (KPIs) related to data quality, billing accuracy, and operational effectiveness. Lead reconciliation, audit, and process improvement initiatives to enhance data quality, operational efficiency, and financial performance. Provide operational insights and reporting to support decision-making, forecasting, and continuous improvement efforts. Act as a liaison between internal stakeholders, sponsors, and CROs to ensure alignment, issue resolution, and successful study execution. Key Requirements Qualifications & Experience Bachelor's degree in Business Administration, Healthcare Administration, Finance, Health Sciences, or a related field. 3+ years of experience in Clinical Research Operations, Clinical Research Finance, Healthcare Revenue Cycle, Healthcare Operations, or related areas. Experience working with Clinical Trial Management Systems (CTMS), preferably OnCore. Proven ability to reconcile data across multiple systems and resolve operational discrepancies. Experience working in a regulated healthcare or clinical research environment. Preferred Qualifications Experience in Phase I Oncology Clinical Research. Knowledge of sponsor billing, clinical trial revenue processes, and study financial workflows. Experience partnering with sponsors, CROs, and finance teams. Professional certifications such as CCRP, CRA, ACRP, or equivalent clinical researchcredentials. Key Competencies Strong analytical, problem-solving, and root-cause analysis skills. High attention to detail with a commitment to data accuracy and integrity. Excellent communication and stakeholder management skills. Ability to collaborate across clinical, operational, financial, and external partner teams. Strong organizational, project management, and prioritization abilities. Continuous improvement mindset with experience using KPIs to drive performance. Understanding of compliance, risk management, and regulatory requirements. Why Join START? At START, you will have the opportunity to contribute directly to groundbreaking oncology research while helping ensure operational excellence and financial sustainability. If you are passionate about data integrity, operational excellence, clinical research, and revenue optimization, we invite you to join our mission of advancing cancer treatment and improving patient outcomes worldwide. #J-18808-Ljbffr

ALDIA, a multinational technology and engineering consultancy, is seeking a Software Control DSP Engineer to join its Spain team. The role focuses on DSP control algorithms and TI platform integration to deliver robust automotive, industrial, or telecom solutions. The ideal candidate has hands-on experience with DSP development, TI DSP components, and a practical approach to software in embedded environments while collaborating with multinational consultants. #J-18808-Ljbffr

Seeking a Laboratory Technician for High Throughput Experimentation Unit to support research in chemistry, focusing on rapid exploration of chemical reaction space via parallel execution and analysis of microscale reactions.

"Delivering innovative digital magazine content on every device in every country" We are seeking a Senior Dev Ops Engineer to join our Barcelona office. ZINIO powers some of the largest digital content distributors in the market. Newsstands, retailers, media service providers, inflight entertainment and libraries offering incremental revenue, auditable paid circulation, and valuable brand exposure for publishers worldwide. ZINIO solves the logistical challenges of a complex digital ecosystem and unlocks new revenue and subscription opportunities for publishers from managed apps & newsstands through to fulfillment services, APIs & content readers. About the Role: The Senior Dev Ops Engineer will design, operate, secure, and improve our infrastructure and production systems. The role combines Dev Ops, Site Reliability Engineering, and infrastructure security, with a focus on automation, observability, scalability, reliability, and secure operations. Working closely with development and infrastructure teams, you will automate processes, improve deployment and recovery, investigate technical issues, and contribute to reliable and secure systems. What you will do: Manage and improve infrastructure across cloud and internal environments. Design and maintain production systems that meet defined availability, scalability, and reliability requirements. Automate infrastructure provisioning, configuration, deployments, and operational processes. Manage servers, applications, containers, networking, and infrastructure services. Develop and maintain Infrastructure as Code and configuration management practices. Develop and maintain CI/CD pipelines and deployment processes. Define and maintain deployment, rollback, disaster recovery, and business continuity procedures. Implement monitoring, logging, alerting, and observability practices. Define and monitor SLOs, SLIs, and system performance metrics. Investigate production incidents, identify root causes, and implement corrective actions. Conduct capacity planning, scalability testing, and performance analysis. Work with development teams to improve application reliability, performance, and operational readiness. Identify and address infrastructure and application security risks. Implement security controls across infrastructure, cloud services, networks, applications, and deployment pipelines. Manage access controls, secrets, credentials, certificates, and other security mechanisms. Support vulnerability management, security hardening, patching, and security incident response. Maintain technical documentation, operational procedures, and runbooks. Contribute to improvements in infrastructure architecture, reliability, security, and operational processes. What you will bring: Experience in Dev Ops, Site Reliability Engineering, Systems Engineering, Infrastructure Engineering, or a related technical field. Experience administering and troubleshooting Linux-based systems. Knowledge of networking, HTTP, DNS, TLS/SSL, load balancing, and common infrastructure components. Experience with cloud platforms, including AWS or equivalent. Experience designing, implementing, or operating production systems with defined availability and scalability requirements. Experience automating technical and operational processes using Python, Go, Type Script, Bash, or another suitable programming language. Experience with Infrastructure as Code and configuration management tools such as Terraform, Open Tofu, and/or Ansible. Experience with Docker and containerized environments. Experience with CI/CD pipelines and automated deployment processes. Experience with monitoring, logging, alerting, and observability platforms. Experience investigating production incidents, including troubleshooting and root cause analysis. Knowledge of infrastructure and cloud security principles, including authentication, authorization, secrets management, and network security. Experience with vulnerability management, security hardening, WAFs, firewalls, or access controls. Experience with web servers and reverse proxies such as Varnish, Nginx, or Apache. Knowledge of load balancing, caching, CDNs, and distributed systems. Ability to communicate technical information clearly and maintain technical documentation. Ability to investigate technical problems, evaluate solutions, and implement appropriate changes. Experience with AWS security services, SIEM/security monitoring, or security automation is an additional qualification. What we offer: Competitive Compensation: Enjoy a competitive salary package, with annual salary reviews based on performance. Collaborative Environment: Work alongside a highly skilled, multicultural team. Dynamic Growth: Play a key role in driving the future of a fast-evolving company in the tech and content delivery space. Work Flexibility: Enjoy flexible working hours with a hybrid model, balancing in-office and remote work. Comprehensive Benefits: Attractive benefits package, including health insurance, meal cards, and transportation perks. Continuous Development: Access ongoing learning and professional growth opportunities. Remote work from abroad (up to 1 month per year), depending on destination and policy. Office Perks: Fresh fruit, tea, coffee, and a vibrant office environment. We are an equal opportunity employer committed to building a diverse and inclusive workplace. We welcome applications from people of all backgrounds and are committed to a fair recruitment process where employment decisions are based on skills, experience, qualifications, and the requirements of the role. #J-18808-Ljbffr

ANYbotics is a fast-growing tech company dedicated to shaping the future of mobile robotics across multiple industries. Join our highly talented and motivated team of more than 200 people and work on cutting-edge robot technology. The Opportunity As Technical Program Manager, you will lead the delivery of one of ANYbotics’ most strategically important robot platform programs, bringing engineering, operations and commercial teams together around a clear and credible path to market. You will carry delivery accountability against the agreed specification, schedule and product-cost targets, providing one clear and credible view of the program. Working closely with Product and Engineering, you will translate agreed product and technical decisions into an executable plan across mechanical and electrical engineering, software, industrialization, supply chain, certification, quality, service and launch readiness. This is a highly visible, hands-on leadership role. You will combine strong technical understanding with excellent program judgement, moving comfortably between detailed engineering discussions and executive-level decisions. You will bring clarity where information is incomplete, identify emerging risks and create the momentum needed to make difficult trade-offs at the right time. You will operate as a senior individual contributor, focusing on one major program at a time and leading through influence rather than direct authority. You will work closely with functional leaders and named workstream owners, while having the opportunity to strengthen how ANYbotics runs complex product development and help shape our broader program-management capability as the company grows. Market & Our Technology ANYbotics is pioneering autonomous robotic platforms for industrial inspection and operations in challenging environments. From explosion-proof systems in oil and gas to agile robotic platforms for power, utilities, mining, metals and other industrial settings, our technology is built for environments where safety, reliability and uptime are critical. Our product combines advanced robotics, mechanical and electrical systems, embedded software, autonomy, inspection payloads, analytics and integrations into an end-to-end industrial solution. Bringing a new robot platform to market requires hardware and software development, industrialization, supply chain, certification, quality and customer readiness to progress together. This creates a distinctive program-management challenge. Long hardware lead times must be balanced with iterative software development, ambitious product goals, demanding certification requirements and complex make-or-buy decisions. Strong technical program leadership is essential to turning this complexity into reliable execution. About us ANYbotics is a leading robotics company specialising in advanced autonomous systems. With a successful Series B financing round closed and strong momentum in the market, we are entering an important phase of growth and international expansion. Our mission is to transform industrial inspection and operations through world-class robotics. We combine deep robotics expertise with real customer deployments in demanding industrial environments. This is an opportunity to join at a stage where the technology is proven, the ambition is high, and the decisions made now will have a major impact on the company’s future. Your Contributions Lead an integrated robot platform program from charter through development, industrialization, launch, early-life reliability and handover, delivering against agreed specification, schedule and product-cost targets Own the integrated program plan against the agreed scope, including the baseline, milestones, dependencies, critical path, COGM targets and delivery gates Align work across hardware, software, industrialization, supply chain, certification, quality, verification and validation, service and launch readiness, maintaining one credible view of progress for senior stakeholders Work through functional leaders and named workstream owners to establish clear responsibilities, identify capability gaps and secure credible delivery commitments Identify risks and cross-functional trade-offs early, bringing forward practical options with their technical, cost and schedule implications, together with a clear recommendation Drive evidence-based program reviews and consolidated delivery readiness across quality, certification, service and launch, adapting the plan early when assumptions or technical evidence change Partner with Product and Engineering to translate agreed requirements into an executable delivery plan, including the certification and country sequencing needed to support launch Work with the CTO and Operations on make-or-buy decisions, industrialization and external-partner execution, ensuring clear interfaces, commitments and acceptance criteria Your Profile Significant experience leading complex technical programs in robotics, autonomous systems, industrial technology, automotive, aerospace, medical devices or another advanced hardware environment Proven experience shipping a certified, volume-manufactured mechatronic product and leading it through development, industrialization and commercial launch Strong engineering foundation in mechanical, electrical, mechatronic, robotics, systems engineering or a similarly relevant discipline Technical depth to understand system architecture, challenge senior technical specialists and recognise system-level risks without needing to design every solution personally Strong command of program-planning methods, critical-path management, structured product-development processes and disciplined change control Practical experience across product cost, industrialization, manufacturing, supply chain, quality, certification and external technology or manufacturing partners Proven ability to influence senior technical and business stakeholders, resolve competing viewpoints and create alignment without relying on direct authority Decisive, resilient and highly organised, with the judgement and communication skills to operate effectively in a fast-moving environment and make progress with incomplete information Bonus Points Direct experience delivering industrial robots, autonomous machines or other complex mechatronic systems Experience with products operating in safety-critical, hazardous or highly regulated environments Experience developing a new product through platform reuse, architectural evolution or a tightly controlled derivative program Experience with international product certification, including CE, UL or comparable market-access requirements Experience transferring products from prototype or internal production into serial production with an EMS, ODM or other external manufacturing partner We offer you a very exciting and dynamic work environment, the opportunity to become part of a fast-growing company and an ambitious team that is on a mission to change the industrial inspection market, a chance to leverage your experience and bring in your own ideas, a fair market salary, an attractive employee stock ownership plan, and a job in the city of Zurich. Agency Policy: We are not currently partnering with external search firms or recruitment agencies. Any profiles or resumes submitted to ANYbotics employees without a prior written agreement will be considered public disclosure and the property of ANYbotics, involving no liability or fee for subsequent hiring.

Is this you?Titan Operating System S.L. (Titan OS), the Barcelona-based technology, entertainment, and advertising company is looking for you!Our platform combines content discovery and advertising technology in one solution, helping leading TV brands unlock greater value. Titan OS powers devices from major brands including Philips, AOC and JVC, reaching millions of viewers across Europe and LATAM. Titan OS is also powering free premium FAST Channels on selected SONY Android TVs.Over the last two years, Titan OS has grown revenue 10x and attracted leading investors, including Highland Europe and Mangrove.At TitanOS, we live by three core values:Make things happen – We take ownership, move fast, and deliver impact.No ego – We collaborate with respect and humility to reach shared goals.Show genuine passion – We love what we do and never stop learning.Culture and environment are at the heart of our ethos. If the above resonates with you, keep reading because we believe you could be a perfect addition to our incredible team!Role overview:We are looking for an entrepreneurial and performance-driven DSP Partnership Director to lead the implementation, optimization, and measurement of performance campaigns across CTV in the European market.The ideal candidate combines strong technical expertise in CTV advertising and DSPs with a deep understanding of performance marketing, data-driven audience targeting, and campaign optimization. This person will play a key role in ensuring campaigns meet their performance objectives, translating insights into actionable improvements, and driving continuous growth.Key responsibilities:Lead and manage the end-to-end implementation of performance campaigns on CTV, leveraging relevant DSP platforms operating in the European market.Define and activate data segments and audience targeting strategies to maximize campaign relevance and performance.Monitor campaign delivery and performance against agreed KPIs, proactively identifying opportunities to optimize targeting, bidding, budgets, and campaign execution.Take ownership of the percentage of campaigns achieving their agreed performance KPIs, driving continuous improvement in campaign effectiveness.Develop performance reports, analyze campaign results, and translate data into actionable insights and learnings to improve future campaign performance.Establish best practices for campaign implementation, optimization, measurement, and reporting across CTV performance campaigns.What makes you a great fit:10+ years of professional experience in digital advertising, programmatic media, performance marketing, or a related field.At least 3 years of hands-on experience managing the implementation of CTV performance campaigns using one or more relevant DSP platforms in the European market.Strong understanding of the CTV advertising ecosystem, programmatic buying, audience segmentation, and performance optimization.Proven ability to analyze campaign data, identify performance drivers, and implement optimization strategies.Experience in performance reporting, campaign measurement, and translating results into actionable recommendations.An entrepreneurial mindset, with a proactive, solution-oriented approach and the ability to thrive in a fast-paced environment.Excellent communication and stakeholder management skills.Fluent in English.University degree in Marketing, Business, Advertising, Data Analytics, or a related field.Reasons to apply:Centrally located office in the heart of Barcelona, with public transportation nearbyCompetitive compensationPrivate health insuranceFriendly, diverse, and international work environmentOpportunity to work outside of your comfort zone and develop professionally in an exciting and fast-growing CTV industry.Change the future of TV! A unique opportunity to join a well-funded, high-growth company in the early stages to help shape a product/business that will impact millions.#J-18808-Ljbffr

In Materialise’s Staff department, we believe that meaningful impact starts with people and their expertise. If you’re passionate about shaping a strong, effective, and forward-looking organization, you’ll love being a part of this team. Through the knowledge and dedication of these teams, we’re creating value every day and building the foundation for long-term success. We are looking for a Functional Analyst for the Microsoft Dynamics 365 Finance and Operations platform to help transform the company's financial and operational processes using modern technologies. You will join a cross-functional team working on the implementation and optimization of business solutions in the field of finance, logistics, and resource management. If you have experience working with D365 F&O and strive to influence strategic processes, this role is for you. What You Will Do Gather information from and collaborate with different types of stakeholders (finance, procurement, warehouse, IT) Understand strategic business needs and plans for growth Gather and document detailed business requirements and transform them into user stories, including acceptance criteria Create, document, and maintain solution designs Execute standard and advanced configuration of the system, giving demos/prototypes to business users Prepare functional gap design documents Test new configurations and customizations — ensuring the provided functionality is in line with existing flows and satisfies stakeholders' needs and requirements Organize key user validation process, support for end-to-end user acceptance testing Users' consultancy and support; handle tickets asa second-level support engineer Follow the Change and Release management process Prepare release notes Manage tasks (AzureDevOps/Jira) Your profile Upper-intermediate English 3 years' experience with Microsoft Dynamics 365 Finance&Operations implementation and support Extensive experience in Microsoft Dynamics 365 Finance&Operations implementation projects Strong knowledge of standard D365 functionalities and most of the business processes listed below: Accounting policy (General Ledger, account structure, period close, etc.) Accounts payable Accounts receivable Manufacturing accounting Inventory accounting (closing and adjustment, inventory revaluation, inventory counting, inventory posting etc.) Cost accounting Tax accounting (understanding of business process flows) Subscription billing (nice to have) Electronic reporting Experience in supply chain management flows is a plus Experience working in an integrated environment (and understanding of the approach of working with it) Experience with AzureDevops/Jira UML/BPMN knowledge is a plus Experience in preparing user stories, user manuals, and release notes Able to adapt requirements to both technical and business languages Experience with the preparation of different types of products and project documentation Experience with organizing validation activities (user acceptance testing) A technical background is an advantage Logical and analytical thinking Independent research on solutions A critical thinker, detail-oriented, and self-organized What’s Waiting For You Work that matters The technology we build at Materialise pushes the boundaries. You’ll find pride in building something that matters, whether you designed it, printed it, or shipped it. No matter your role, we unlock new possibilities to build a better and healthier world every day. At Materialise, we expect you to think about the customer, not just the task. You push for better solutions and care about the difference your work makes. A people-centered space When you join Materialise, you join a group of colleagues invested in you, not just your work. From your own team to a department across the world, you’ll find a sense of belonging with people who help without being asked, challenge you, and have your back. At the same time, we expect you to invest in the people around you — not just your own work — to make the group stronger than the sum of its parts. An environment of trust As a company of innovators, we know how crucial autonomy is in your work. When we hire you, we trust in your expertise, giving you space to organize your tasks, work flexibly, and make your own calls. At Materialise, we expect you to deliver on that trust and keep your commitments. A career ready to build When you see opportunities for your career to grow at Materialise, we encourage you to go for them. People shape a fulfilling career at their own pace here. At Materialise, we expect you to take initiative in your own development. Don’t wait for someone else to plan your career. Step into the space and make it count. Make a difference in our Staff department. #J-18808-Ljbffr

Agilent Technologies is seeking an experienced SAP Tax Technology professional to drive design, implementation, and optimization of indirect tax solutions across a global SAP landscape. You will bridge Tax, Business Partners, and IT to architect scalable, automated tax solutions using SAP ECC, S/4HANA, and DRC. The role emphasizes end-to-end SAP project delivery, cross-functional collaboration, and global compliance initiatives, with a focus on VAT, GST, and other transactional taxes. #J-18808-Ljbffr

Responsibilities Serve as a statistical department resource Conduct training sessions and enhance skills of existing personnel Collaborate with the sponsor and review project work produced by other statisticians Manage multiple projects and ensure timely completion Requirements Experience mentoring biostatisticians on job skills Experience preparing Statistical Analysis Plans (SAPs) Knowledge of SAS annotated case report forms (CRFs) and SAS database design Ability to oversee training plans or materials for Biostatistics associates Proven statistical programming skills Experience conducting quality control of project deliverables #J-18808-Ljbffr

Biorce is seeking a Technical Talent Acquisition Partner to scale our engineering, AI, data science, and product teams from our Austin hub. You will own the full recruitment lifecycle, partner with hiring managers, and build pipelines in a fast‑growth Healthtech AI company. You should be fluent in English, experienced in sourcing for senior technical roles, and comfortable operating in a high‑velocity environment, using LinkedIn Recruiter, ATS, and other tools to outpace competition. #J-18808-Ljbffr

At TRKKN, we are driven by the excitement of taking our client's data-driven businesses to new heights. As the leading European Google partner and reseller of Google Cloud & Google Marketing Platform, we act as a catalyst for cutting-edge digital marketing solutions. Our team is diverse, international, inspiring, and operates in a fast-growing digital & technological environment. This provides the ideal and dynamic work environment for individuals with a hunger for growth, responsibility, and the desire to shape their future. With Google in close proximity, the learning and development opportunities at TRKKN are limitless. With over 25 nationalities, 20+ languages, and 240+ Trakkies on board, we’re taking our business global, and our story doesn't end here! How will you make an impact: As the Tech and Data Strategy Lead (f/m/d) in Spain, you will play a central role in connecting people, data, and technology. You will lead client strategy, drive digital maturity for all type of clients by systematically identifying levers and technical solutions across the Google Marketing Platform and Google Cloud. Your key responsibilities will include: Pre-Sales & Commercial Strategy: Lead pre-sales activity for new business opportunities, commercial proposals, opportunity analysis, and cross-selling/upselling for existing clients in Spain. Solution Packaging & Tech Strategy: Define sales strategies and package solutions (incrementality, measurement frameworks, 1st party data strategies, privacy, and tech stacks). Strategic Consulting & Workshops: Conduct Tech & Data Maturity Assessments and lead Strategy Workshops for key clients to solve complex business challenges in an evolving privacy-centric ecosystem. Key

Seeking a Principal Engineer/Tech Lead & Systems Architect in Barcelona with 15+ years of experience in web development, PHP, and JavaScript frameworks, to lead complex engineering projects.

Seeking a Gerocultor/Caregiver with experience in elder care for a long-term full-time position at a nursing home. Responsibilities include assisting residents with daily needs and participating in activities.

Sponsor Dedicated Global Sr CTM - Home Based in SPAIN. Vendor experience Syneos Health is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at every point across the drug development and commercialization continuum, helping them navigate complexity, anticipate change and accelerate progress. Our Clinical Solutions team members act with a drug development mindset, applying their years of experience and deep expertise to truly understand customer needs and represent those in the solutions we shape. Whether you join us in a Functional Service Provider partnership or a Full-Service environment, you’ll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals. We are agile and driven to deliver – for one another, our customers, and, most importantly, for those in need. Discover what your 25,000 future colleagues already know: Why Syneos Health: We are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program. We are committed to building an inclusive culture – where you can authentically be yourself. Central to this is our purpose – Driven to Deliver – which captures the passion of our colleagues to show up each day and shape solutions that have the ability to dramatically impact someone’s life. We are continuously building the company we all want to work for and our customers want to work with. Why? Because we know that when we bring together smart colleagues from across the world, we can shape the future of healthcare, driving impact for customers and defining the pace of patient progress.Job ResponsibilitiesProtocol Development: Support the development and review of the Clinical Study Blueprint (CSB) and Protocol, and all Amendments and/or Administrative Changes Budget: Manage the execution of the CDAs; support Project Managers in the creation of overall study budget (working with the contract/budget analyst); support site contract amendments and negotiation; manage invoices Countryand Site Feasibility and Selection: assist in development of Investigator Site Selection Plan; attend country and siteselection Jams; Assist with creation ofFeasibility Questionnaire; assist with Site Selection and Green Light Letters, if applicable Site/Country Contracts and Budgets: stay informed of progress with CDAs, CSA and site budgets; support sites forcontract amendments; assist with negotiationfor site contracts Financial/Payment Management: oversight of site payments and vendor payments, if applicable Study Budget Financial Reconciliation: draft and facilitate the Clinical Study Budget review Clinical Study Timelines: Support the planning for the clinical study timelines, finalization and update of clinical study timelines; and manage the study team to meet all timelines Study Team Training: Assist/support in the creation/finalization of Study Specific Training (TA training, Compound, Study Design, Vendors, Eligibility, etc); Facilitate training sessions; Assign training as appropriate; assist with creation/finalization of Study Monitor Training materials Site Training: Assist Project manager in planning for the Investigator Meeting; creation of and collection of slides from all functional areas to create the final master deck for the IM; presenting at theIM, filing documentation of training Data Management and Closeout: Review updates to Data Managemet Plan; Interim/Final Db Lock Preparation (drive study DBL completeness); Interim/Final Database Lock Preparation (Responsible for study DBL completeness) Plans: Site Selection Plan, Study-Specific Issue Management Plan, Vendor Oversight Plan, TMF Artifact Map and Plan Clinical Supplies: Assess and review of materials by external vendors (lab kits, ePRO devices, eConsent tablets, etc); Investigational Product: responsible for overall study reconciliation of IP Vendor Oversight: Assist with selection of vendors; Create and manageVendor Oversight Plan for each vendor; review vendor contracts, work orders and Change Orders; day to day oversight ofvendors Establish Review Committees: creating charter, assisting with member selection, contracting as needed, updating Annual Plan Site Closure Strategy: develop site closure plan Patient Recruitment Strategy: assist Project Managers in development of patient recruitment strategy and plan; develop recruitment materials; drive strategies for needing new sites Trial Master File: support customization of study/country/site specific docs; upload documents,reference Master File Index; oversight of TMF health; TMF reconciliation; TMF archival; quarterly TMF review Risk Management: initial Risk Assessment and Mitigation Plan (RAMP) and maintain throughout study; responsible for Issue Management throughout the study; quarterly Issues reviewICF and Study Specific Language: responsible for building the study specific ICF incorporating appropriate study specific language and safety language CTA submissions and approvals: responsible for assisting with agency responses Meetings: Clinical Study Team meetings, conducting vendor meetings; responsible for agendasand meeting minutes Clinical Trial Management System: Keep CTMS updated at study levelQualificationsBachelor’s degree or RN in a related field or equivalent combination of education, training, and experience 5 years or more of experience as CTM, managing multiple countries, for regional or global trials Proven vendor management experience. Global study management experience. Experience in Oncology clinical trials. Strong experience reviewing and overseeing study plans and study-related documentation. Demonstrated ability to lead and align teams in the achievement of project milestones Demonstrated capability of working in an international environment. Demonstrated expertise in site management and monitoring (clinical or central)Preferred experience with risk-based monitoring Demonstrates understanding of clinical trial management financial principles and budget management Knowledge of Good Clinical Practice/ICH Guidelines and other applicable regulatory requirements Must demonstrate good computer skills Strong conflict resolution skills Demonstrated ability to apply problem solving techniques to resolve complex issues and apply a risk management approach to identifying and mitigating potential threats to the successful conduct of a clinical research project. Demonstrates critical thinking to determine the cause and appropriate solution in the identification of issues Moderate travel may be required, approximately 20%Additional InformationTasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description. The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. Further, nothing contained herein should be construed to create an employment contract. Occasionally, required skills/experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees. The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job.Discover what our Syneos Health colleagues already know: work here matters everywhere. Work alongside the brightest minds in the biopharmaceutical industry taking down walls and removing barriers to speed our customers’ delivery of important therapies to patients. We are strategic thinkers who actively seek different perspectives, whether across offices or across oceans. Because we solve some of the toughest challenges facing the most prestigious healthcare companies today, you'll gain exposure and be supported with comprehensive resources including emerging technologies, data, science and knowledge sharing. The diversification and breadth of Syneos Health creates a multitude of career paths and employment opportunities. We’re a growing, global company dedicated to advancing our talent past their initial role. Discover what our 29,000 employees already know: work here matters everywhere. We work hard, and smart, all in the name of getting much-needed therapies to those who need them most. Selecting us as an employer secures a career in which you’re guaranteed to: Partner with the most diverse team of experts in the industry. From the top down, our people are inspiring. Everyone has a voice and is encouraged to use it. Work in specialized Syneos Health teams that are therapeutically or functionally aligned for expert collaboration. We assemble clinical teams where everyone, from CRAs to senior management, is skilled in the same therapeutic area or customer teams. With this structure, everyone on your team speaks the same language and can deliver unique insights into the therapeutic environment and patient population. We are partners with purpose. We integrate seamlessly with our customers and do what’s best for their success. Our people provide the brilliant ideas, valuable insights and endless energy that accelerates the impact of life changing therapies worldwide.#J-18808-Ljbffr

Se busca médico/a de urgencias con especialización en Medicina de Familia o Interna para un hospital en Barcelona. Se ofrece salario bruto anual de 80.000€, turnos de 12 horas y colegiación obligatoria.

Company Description At Docplanner Group, we’re on a mission to help people live longer, healthier lives. As the world’s largest healthcare platform, each month, we connect 24 million patients with 280k doctors across 13 countries (through brands like ZnanyLekarz, Doctoralia, MioDottore, DoktorTakvimi, and jameda). Our marketplaces, SaaS and AI tools simplify daily tasks and help doctors, clinics and hospitals work more efficiently, so they can focus on what really matters: caring for their patients. Learn more about our products here: pro.Doctoralia.Es Why join us? Real impact – We help doctors help patients. Your work truly makes a difference. At scale, yet agile – 3,000+ employees, but still fast, flexible, and hands-on. Shape the future, sustain growth – Make a difference now and build for long-term success. Job Description How will you make an impact? Job Purpose As Patient Care Regional Manager, you will be the people manager and operational lead for Patient Care teams in your assigned European markets. You will own team performance, quality reviews, and day-to-day operations — while working closely with Country Managers and the Global Patient Care Head to align on priorities and ensure service consistency across markets. You will be the missing link between global standards and local execution: someone who can read data, give direct feedback, run a tight operational cadence, and genuinely develop the people on your team. Key Responsibilities People Management Own performance reviews, 1:1s, and development conversations for direct reports across your markets Manage absence, availability, and team sizing for your region Lead hiring decisions and internal mobility within the Patient Care team Build a culture of direct feedback and consistent follow-through Operational Performance Track and own regional KPIs: response SLA, first-contact resolution, CSAT, and quality scores Run quality review and moderation programs — calibration sessions, rubric definition, feedback loops Identify performance trends using dashboards and reports; translate them into concrete actions Own escalation protocols for complex patient cases Cross-functional Collaboration Partner with Country Managers to align on priorities, workload, and service commitments Work with the Product/PATS team on tooling rollouts, workflow automation, and process improvements Contribute to the monthly Patient Voice reporting — classified ticket analysis, actionable issue surfacing Act as regional interface for global policy rollouts and operational changes Qualifications What will help you thrive? Must-haves 5+ years in customer support, patient experience, or service operations — with at least 2 years managing people Experience managing teams across multiple countries in Europe (not just one market) Strong people instincts: direct, empathetic, consistent — someone teams trust and grow under Data-driven: comfortable with dashboards, pulling operational reports, and making decisions from numbers Experience running quality review or moderation programs (calibration, rubric design, scoring) Fluency in English mandatory Proficiency in project management tools (e.G., Jira, Notion, or similar) Nice to have Background in healthtech, marketplace, or two-sided platforms Experience working with AI-assisted support tools or automation workflows Familiarity with Intercom, Zendesk, or equivalent support tooling SQL knowledge or comfort querying data independently Experience onboarding a new org structure or consolidating teams Strong plus — Spanish, Italian, Polish, or German language speaker. What To Expect From Our Hiring Process Intro Chat A first call with our Talent Partner to explore mutual fit around relevant skills, value alignment, and motivation. Hiring Manager Interview A deeper conversation about your background, aspirations, and experience with your Hiring Manager and your potential manager in this role. Take this chance to ask anything on your mind—it’s just as much about making sure we’re the right fit for you, too. Business Case A take-home exercise incl. a few days' preparation time, designed to understand how you approach real-life problems. You’ll then walk us through your approach in a collaborative discussion with the hiring manager and the team to discuss your thoughts and findings. Additional/ Final Interview (Optional) A final conversation with another senior stakeholder from our Global Team. Why You’ll Love It Here Global Benefits Healthcare insurance – so you can focus on what matters. Wellness that works for you – from gym memberships to mental health support, we’ve got you covered. Time off that counts – whether it’s a vacation, your birthday, or just a day to recharge, we believe in balance. Local Perks Depending on your location, you will be entitled to local benefits like meal vouchers (ticket restaurant), transport allowances, or extended parental leave. Career Growth We’re growing, and so can you! You’ll find lots of chances to learn, develop, and explore new paths—whether within your team or through cross-functional projects. A Truly Global Team Work with talented people from all over the world in a diverse and inclusive environment. Flexibility That Works for You Remote work and flexible hours aren’t just buzzwords here. While the extent of flexibility depends on your role and team, we value results over rigid schedules. Prefer an office setting? You're welcome at any of our hubs in Barcelona, Warsaw, Curitiba, Rio de Janeiro, Mexico City, Bogotá, Munich, Rome or Bologna. What We Believe In Focus on results – we're here to make an impact. Think like an owner – take responsibility, drive outcomes. Keep it simple, keep it lean – smart solutions over complexity. Be respectful and radically honest – openness builds trust. Learn and be curious – growth is part of the job. We are committed to building a team that represents a variety of backgrounds, perspectives, and skills. We welcome applicants from all walks of life, regardless of gender, disability, or background, and are dedicated to fostering an inclusive workplace where everyone feels valued and empowered to contribute. Please note: At this time, we are not able to sponsor visas for this position. To apply, you must already have the legal right to work in your country of residence or the location of the role. #J-18808-Ljbffr

Medical Scientist (m/f/x), Nephrology & Patient Blood Management Location: Barcelona Contract: permanent The Opportunity We are looking for a Medical Scientist, Nephrology & Patient Blood Management (PBM) to join our Medical Affairs organization in Spain. This is an exciting opportunity for a scientific professional who wants to work at the intersection of medical strategy, evidence generation, stakeholder engagement and healthcare innovation. In this role, you will translate scientific evidence, real‑world data and stakeholder insights into meaningful Medical Affairs strategies, helping to identify unmet needs, close evidence and care gaps, and ultimately improve outcomes for patients within nephrology and Patient Blood Management. We will prioritize candidates based in Barcelona. However, exceptional candidates located elsewhere in Spain will also be considered, provided they can meet the requirements of our hybrid working model. The Role As Medical Scientist, you will act as a trusted scientific partner, combining scientific credibility with strategic thinking and strong stakeholder engagement. Your key responsibilities will include: Provide scientific leadership across nephrology, rare kidney diseases and Patient Blood Management, including areas such as coagulation and iron. Build and maintain trusted relationships with Key Opinion Leaders (KOLs), healthcare professionals and other relevant external stakeholders. Translate scientific developments, stakeholder perspectives and emerging evidence into actionable medical insights and strategic recommendations. Identify unmet medical needs, evidence gaps and opportunities to advance patient care. Contribute to evidence-generation activities, including Investigator-Initiated Studies (IIS), research collaborations and real‑world evidence initiatives. Support the development and execution of Medical Affairs plans in close partnership with internal and external stakeholders. Develop and support congress strategies, scientific communications, medical education initiatives and scientific exchange. Explore the use of real‑world evidence, data analytics and AI-enabled approaches to strengthen Medical Affairs insights and decision-making. Collaborate closely with colleagues across Commercial, Market Access, Regulatory and Clinical Development to support aligned, patient‑centric medical strategies. Success in this role means turning scientific insights into strategic action, influencing medical and organizational decisions, building trusted external partnerships, and helping to close evidence and care gaps through science and innovation. Your Qualifications To be successful in this role, you bring: An MD, PhD, PharmD or equivalent advanced scientific qualification. 3–5+ years of relevant experience within Medical Affairs, Medical Science Liaison, Clinical Research or a related pharmaceutical industry role. Previous experience within nephrology, cardio‑renal diseases, coagulation, iron, rare diseases or specialty care. Experience supporting scientific exchange, evidence generation, Investigator‑Initiated Studies and medical education initiatives. Demonstrated ability to collaborate effectively with cross‑functional partners, including Commercial, Market Access, Regulatory and Clinical Development. Familiarity with the Spanish healthcare environment. Excellent communication, scientific exchange and stakeholder engagement skills. A strategic mindset with the ability to translate complex scientific information and stakeholder insights into meaningful actions. Fluency in Spanish and English. What We Offer We want you to feel supported professionally and personally while making a meaningful contribution to patients and healthcare. The opportunity to contribute to Medical Affairs strategies that can make a tangible difference for patients. A highly scientific role combining external engagement, evidence generation and strategic Medical Affairs work. The opportunity to collaborate with leading scientific experts and multidisciplinary teams in an international environment. Exposure to evolving approaches in real‑world evidence, data analytics and AI‑enabled Medical Affairs. Opportunities for professional development and continued growth within an international organization. A collaborative, purpose‑driven working environment focused on science, innovation and patient impact. A hybrid working model. The role requires at least three working days per week either in the office or engaging with external stakeholders in the field, together with occasional travel and in‑person collaboration according to business needs. About CSL Vifor CSL Vifor is a global partner of choice for pharmaceuticals and innovative, leading therapies in iron deficiency and nephrology. We specialize in strategic global partnering, in‑licensing and developing, manufacturing and marketing pharmaceutical products for precision healthcare, aiming to help patients around the world lead better, healthier lives. Headquartered in St. Gallen, Switzerland, CSL Vifor also includes the joint company Vifor Fresenius Medical Care Renal Pharma (with Fresenius Medical Care). The parent company, CSL, headquartered in Melbourne, Australia, employs 32,000 people and delivers its lifesaving therapies to people in more than 100 countries. To learn more about CSL, CSL Behring, CSL Seqirus and CSL Vifor visit and CSL Plasma at Our Benefits For more information on CSL benefits visit How CSL Supports Your Well‑being | CSL . You Belong at CSL. At CSL, Inclusion and Belonging is at the core of our mission and who we are. It fuels our innovation day in and day out. By celebrating our differences and creating a culture of curiosity and empathy, we are able to better understand and connect with our patients and donors, foster strong relationships with our stakeholders, and sustain a diverse workforce that will move our company and industry into the future. To learn more about inclusion and belonging visit Equal Opportunity Employer CSL is an Equal Opportunity Employer. If you are an individual with a disability and need a reasonable accommodation for any part of the application process, please visit CSL is an Equal Opportunity Employer. If you are an individual with a disability and need a reasonable accommodation for any part of the application process, please click here. Privacy Notice CSL Global Privacy Notice for Job Applicants and Candidates #J-18808-Ljbffr

Plastic Surgeon – Wellness Kliniek Group Wellness Kliniek is growing! Are you a Plastic Surgeon with a love for aesthetic procedures? We have a job opening! Full‑time or part‑time. With over 25 years of experience and more than 150,000 satisfied patients, Wellness Kliniek is one of Europe's leading centers for cosmetic surgery. Our team strives every day to fulfill our mission: “More happy patients!”. You can find the list of procedures on our website As Plastic Surgeon, you work on an independent basis in an infrastructure provided by BIRAND SA. You are responsible for the medical process: your consultations, surgeries and the follow‑up of your patients. You will work according to ISO certified quality standards and protocols, in collaboration with a passionate team of experts in cosmetic surgery. Your responsibilities A cosmetic plastic surgeon at Wellness Kliniek is responsible for performing plastic surgery procedures; from consultations to follow‑up care, with the highest degree of safety and professionalism. Each surgeon provides ethical care, up‑to‑date knowledge, and collaboration with a medical team, for optimal patient outcomes. Along with the medical team, you guarantee continuity of care. This is you in a nutshell You are knowledgeable and experienced in aesthetic plastic surgery. You are registered as a plastic surgeon. You are language proficient, and preferably speak several languages. You highly value customer friendliness and friendly collegiality. A positive and professional attitude with a focus on quality and aesthetic results. What we offer You will work in a private clinic with a good reputation, with more than 150,000 satisfied patients. We have been operating for more than 25 years and guarantee quality care with an internationally recognized ISO Quality Label. Your work environment consists of an enthusiastic and driven team, within a modern clinic with secretarial support and skilled nurses. The medical team consists of national and international surgeons and anesthetists. The Wellness Kliniek in Genk, Belgium is managed by BIRAND NV, powered by Spronken Group, an established name in the healthcare sector best known for their quality, innovation and specialist expertise in cosmetic plastic surgery and orthopedic devices. If you are interested in this vacancy, please contact us. Your interest will be kept strictly confidential. We would like to invite you for a visit. Seniority level Executive Employment type Full‑time Job function Health Care Provider Industries Wellness and Fitness Services, Hospitals and Health Care, and Medical Practices #J-18808-Ljbffr

IC Resources in Barcelona, Spain seeks an experienced High-Speed Systems Engineer to take technical ownership of a next-generation hardware platform. You’ll work across system architecture, lab debugging, and collaboration with FPGA and software teams to deliver a complete system. The role combines hands-on hardware work with technical leadership, mentoring a growing engineering team, and driving critical decisions to ensure high-performance outcomes. #J-18808-Ljbffr

Concierge Physician position for a Royal Household in Doha with a tax-free package of £180,000 – £213,333. It requires full registration in the UK or Europe, 5+ years post-qualification clinical experience, and strict NDA compliance, with excellent English. Private accommodation, relocation support and comprehensive medical insurance are included. The QCHP licensing process is outlined before commitment; the appointment is madeby the Royal Household/appointing entity, with annual flights home #J-18808-Ljbffr

En nuestro hospital de tercer nivel en Barcelona queremos incorporar un/a cardiólogo/a con el objetivo de trabajar en equipo, crecer profesionalmente y participar en una cardiología completa y muy activa. Contamos con un servicio con cirugía cardíaca, hemodinámica, electrofisiología, TAC coronario y RMN cardíaca, además de una planta de cardiología con telemetría, lo que permite desarrollar una actividad clínica muy variada. La actividad incluirá: Atención a pacientes hospitalizados en planta de cardiología Pruebas de esfuerzo Ofrecemos flexibilidad de jornada (40h, 30h o 20h) y retribución según convenio + incentivos. Contrato indefinido desde el inicio. No es imprescindible título vía MIR o convalidado, aunque se valorará positivamente. Es importante para nosotros encontrar un buen profesional con ganas de integrarse en un equipo cercano y comprometido con la calidad asistencial. #J-18808-Ljbffr

GE Vernova invites applications for ROC Technical Lead in its Wind Remote Operations Center in Barcelona. The role focuses on monitoring offshore wind assets, remote diagnostics, and coordinating with site teams to resolve issues and optimise performance.The position requires a engineering degree, wind industry experience, SCADA tool familiarity, and the ability to travel up to 20% with willingness to relocate to Barcelona. Fluency in English is essential.

Desde Antal International estamos en la búsqueda de un/a Óptico/a Optometrista para incorporarse a un importante proyecto dentro del sector óptico en Centro Comercial Garbera (San Sebastián).Funciones principalesRealización de exámenes visuales completos.Adaptación y seguimiento de lentes de contacto.Asesoramiento personalizado al cliente.Recomendación de soluciones ópticas adaptadas a cada necesidad del paciente.Participación activa en las actividades del punto de venta.Condiciones laboralesContrato indefinido.Jornada completa de 40 horas semanales.Salario competitivo. Horario intensivo rotativo.Tres sábados al mes: uno libre, uno intensivo y uno ampliado.Qué se ofreceProyecto estable dentro de una compañía referente del sector óptico.Entorno dinámico en uno de los principales centros comerciales de la zona.Formación continua.Pago de colegiación.Variable individual.Oportunidades de crecimiento y desarrollo profesional.RequisitosTitulación en Óptica y Optometría.Experiencia previa como Óptico/a Optometrista.Orientación al cliente y vocación por la salud visual.Capacidad de trabajo en equipo.Ubicación: CC Garbera, San Sebastián, España.Tipo de puesto: Jornada completa | Contrato indefinido.

Founded in 1912, Real Club de Golf El Prat is one of the most prestigious private golf clubs in Spain and Europe. Located just outside Barcelona, the Club enjoys an exceptional natural environment and holds internationally recognized sustainability certifications. It has hosted the Spanish Open on numerous occasions and most recently welcomed the Estrella Damm Catalunya Championship on the DP World Tour . Renowned for its exclusive atmosphere, world-class facilities, and commitment to excellence and innovation, the Club is now seeking an Operations Director to play a key strategic role in ensuring that all services and facilities consistently operate at the highest standards. Reporting directly to the General Manager , the Operations Director will be fully responsible for the operational management of the Club House and all supporting departments that contribute to the daily experience of members, guests and visitors. The primary objective of the role is to ensure operational excellence through effective team leadership, implementation of operational processes and service standards, facility management, and continuous improvement across all Club services. This is a strategic leadership position within the organisation, acting as the General Manager’s key operational partner and contributing actively to the continued development and evolution of the Club. Key Responsibilities Operations Management Lead the day-to-day operations of the Club House, facilities and member services. Ensure an outstanding experience for members, guests and visitors. Oversee the efficient operation of all operational departments. Identify opportunities for continuous improvement and operational excellence. Lead, develop and motivate a multidisciplinary team of approximately 45 professionals , including: Reception Locker Rooms Maintenance Food & Beverage General Services Promote a culture of excellence, accountability and member-focused service throughout the organisation. Operational Excellence Develop and implement operational procedures and protocols. Ensure operational processes are consistently executed. Establish and maintain service quality standards. Define, monitor and report operational KPIs and quality metrics. Ensure compliance with all operational procedures. Facilities Management Plan and oversee preventive and corrective maintenance programmes. Coordinate external suppliers and contractors. Supervise facility improvement projects and capital investments. Ensure the Club’s facilities remain in outstanding condition at all times. Member Experience Maintain a visible presence throughout the Club. Build strong relationships with members and visitors. Handle operational incidents promptly and effectively. Resolve complaints with professionalism and efficiency. Act as a brand ambassador for the Club. Cross-Functional Coordination Work closely with: General Management Sports Director Operational Coordinators Maintenance Teams External Service Providers Ensure effective communication and collaboration across all operational areas. Objectives During the First 12 Months The successful candidate will be expected to: Professionalise the Club’s daily operations. Implement standardised operational procedures. Introduce management dashboards and operational KPIs. Improve member and visitor satisfaction. Foster a culture of continuous improvement. Efficiently execute facility investment and improvement projects. Candidate Profile We are seeking an experienced operations executive with a strong track record of leading customer-focused organisations where service excellence is a key competitive advantage. Professional Experience Minimum of 5–7 years’ experience in senior operational leadership positions. Proven experience managing large, multidisciplinary teams. Strong background in organisations recognised for exceptional customer service and operational excellence. Experience in environments comparable to Real Club de Golf El Prat will be highly valued. Previous experience in one or more of the following sectors is particularly desirable: Golf clubs Five-star hotels Luxury resorts Premium sports facilities High-end hospitality or restaurant groups International experience will be considered a significant advantage. Core Competencies The ideal candidate will demonstrate: Strong leadership and people management skills. Outstanding customer orientation and service mindset. Excellent organisational and planning abilities. Proactive approach with a strong focus on continuous improvement. Strong analytical and problem‑solving capabilities. Excellent communication, reporting and cross-functional coordination skills. High standards, attention to detail and operational discipline. Ability to thrive in dynamic, fast-paced operational environments. Requirements Professional level of English, with the ability to communicate confidently with international members and visitors. Additional languages will be considered an asset. Flexibility to work weekends and public holidays whenever required by the Club’s operations. What We Offer The opportunity to join one of Spain’s most prestigious sporting institutions. A strategic leadership role with significant influence over the Club’s future development. The opportunity to lead the transformation and continuous improvement of a world-class private members’ club. A highly professional environment committed to excellence, innovation and outstanding member experience. #J-18808-Ljbffr

Clinical Monitoring Analyst (Cluepoints) - Remote London, United KingdomBudapest, HungaryReading, Berkshire, United KingdomBloemfontein, South AfricaDublin, IrelandCenturion, South AfricaBarcelona, SpainSofia, BulgariaMadrid, SpainFull timeR This unique role within IQVIA lends itself to a Lead programmer on Cluepoints called Centralized Monitoring Analyst (CMA) with strong communication and organisation skills. Having experience with SAS programming is necessary.This role is part of a sponsor dedicated project where you will be working with the client directly to manage deliveries. The CMA contributes to the execution of the Centralized Monitoring process by performing the setup, programming and refresh(es) of the Centralized Monitoring platform, according to the study-specific Centralized Monitoring Plan (CMP). Supports the Centralized Monitoring Lead (CML) in the development of the fit-for purpose CM strategy by contributing to the identification of the relevant CM elements to be implemented for the study (Quality Tolerance Limits (QTL), Key Risk Indicators, data visualizations and Data Quality Assessments) Setup/Program QTL, KRI and Data Quality Assessments according to the study CMP Refresh the Centralized Monitoring Platform at predefined frequency to enable signal identification Generate and maintain the Centralized Monitoring Platform specifications document and file it in eTMF Review and understanding of protocol is key Understand the data sources for the study, the data transfer specifications and the data structure Execute and document peer-review of CM platform setup done by other CMA colleagues Experience: At least 3 years relevant experience in the area of pharmaceutical research and development or related field preferably in centralized Monitoring, data management, and/or biostatistics 2-3 years SAS experience including macro language Knowledge/ experience working on Cluepoints Ability to work in an autonomous way and engage with relevant stakeholders to execute activities related to study level centralized monitoring process. Ability to understand basic statistical analysis concepts and to interpret their outcome. Ability to maintain confidentiality of data and information during interactions with staff at all levels Ability to work with limited close supervision. Demonstrated communication, interpersonal, organizational and problem-solving skills High levels of initiative, drive and commitment. Prior experience in a Data Management related field is required Experience with relational databases, preferably Clinical Data Management and EDC Systems Experience communicating with all levels of personnel and participating in collaborative work team (locally and globally). Advanced knowledge of federal regulations, Good Clinical Practice, and Good Clinical Data Management Practices. Excellent command, both verbal and written, of English This role is not eligible for UK visa sponsorship IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. ... (company culture and EEO statements omitted for brevity) #J-18808-Ljbffr

Hybrid Sales Representative in Barcelona for a global tech leader. Responsibilities include articulating partner program value, responding to inquiries, providing product information, detecting business opportunities, and processing campaign data.

Mobile unit officer for teleassistance service, providing direct care, emergency response, and administrative support to users in their homes. Requires a driving license, basic training/experience, and high Catalan proficiency.

OverviewKeysight is at the forefront of technology innovation, delivering breakthroughs and trusted insights in electronic design, simulation, prototyping, test, manufacturing, and optimization. Our ~16, employees create world-class solutions in communications, 5G, automotive, energy, quantum, aerospace, defense, and semiconductor markets for customers in over countries. Learn more about what we do.Our award-winningculture embraces a bold vision of where technology can take us and a passion for tackling challenging problems with industry-first solutions. We believe that when people feel a sense of belonging, they can be more creative, innovative, and thrive at all points in their careers.Keysight's Network & Security Operations Business Unit is expanding across the European government market. We're seeking a highly motivated and experienced Technical Business Development Lead to drive growth and market presence across European government agencies, defence organisations, and public-sector bodies.You will focus on understanding customer mission-critical priorities, building deep relationships with government decision-makers across your region, and positioning Keysight as a trusted technology partner in European government markets. You'll help government agencies and public-sector bodies modernise their networks, strengthen cyber resilience for critical infrastructure, and navigate complex data sovereignty and regulatory requirements—and you'll do it by translating technical requirements into compelling business solutions aligned with EU and national policy mandates.You'll engage with national defence ministries, cybersecurity agencies (ANSSI in France, BSI in Germany), NATO-affiliated organisations, and EU agencies developing critical infrastructure and digital sovereignty programmes. Your technical depth in networking and cybersecurity will enable you to engage credibly with customer technical teams, while your business development acumen allows you to align solutions with government mission objectives, EU regulatory requirements, and competitive procurement environments.You'll collaborate internally with Sales Leadership, Solutions Engineering, and Product teams, and externally with European defence primes, channel partners, systems integrators, and government stakeholders across multiple countries. Your ability to navigate multi-country regulatory complexity, cultural nuances, and government procurement processes—backed by strong technical credibility—will unlock growth opportunities across the EU.This is an individual-contributor, technical business development role—it does not carry people-management responsibility.Location: Based in Germany, France, Spain, or Italy (with 50% regional and cross-European travel) ResponsibilitiesMarket Development & Customer RelationshipsBuild and nurture strategic relationships with government executives, technical leaders, and decision-makers across key accounts in your region and across Europe; position yourselfas a trusted advisor who understands both their technical challenges and mission objectives.Identify and qualify government opportunities through market research, customer engagement, and competitive intelligence; develop account strategies that articulate business value aligned with EU and national regulatory priorities (data sovereignty, NIS2, CRA, national security frameworks).Lead customer engagement on complex opportunities—from initial discovery through technical validation and proposal—leveraging your technical credibility and understanding of EU regulatory requirements to unlock conversations and accelerate deal progression.Represent Keysight at EU conferences, industry events, and government briefings; build visibility and thought leadership across European government markets.Pipeline Development & Sales GrowthPartner with Regional Sales Management to identify growth opportunities and systematically build qualified pipeline across European government agencies, defence organisations, and EU-funded programmes in your region.Support strategic capture efforts, competitive positioning, and complex deal strategy; participate in account planning and technical win development across multiple European countries.Track pipeline health, forecast accurately, and drive consistent progress on key opportunities; communicate business development momentum and market trends to leadership.Develop and articulate competitive positioning against incumbent and emerging competitors; ensure consistenttechnical messaging across sales organisation.Regulatory & Market IntelligenceStay current on EU and national government procurement processes, cybersecurity mandates, and compliance frameworks (NIS2 Directive, EU Cyber Resilience Act, national frameworks like ANSSI and BSI standards) and translate implications into business strategy.Serve as internal point of contact for regulatory, standards, and compliance questions related to European government opportunities; flag emerging policy changes, procurement trends, and funding programmes that impact sales strategy.Provide market feedback to Product Management and Sales Leadership on customer priorities, competitive threats, regulatory impacts, and technology gaps; help shape go-to-marketstrategy for European government markets.Cross-Functional EnablementPartner with Solutions Engineering to develop compelling technical demonstrations, proof-of-concepts, and architecture discussions tailored to European regulatory requirements and government priorities.Collaborate with Marketing on EU-level campaigns, events, and thought leadership; participate in webinars, white papers, and customer briefings that build brand credibility in European government markets.Foster relationships with European channel partners, systems integrators, and defence primes; work collaboratively toidentify co-selling opportunities and expand market reach across multiple countries.Work with customer success and professional services teams to ensure smooth deployments and drive adoption, creating reference customers for future European sales.Technical Business StrategyDraw on deep technical expertise to understand customer challenges and translate requirements into winning solutions; partner with Solutions Engineering to develop technically sound proposals aligned with government security frameworks and data sovereignty mandates.Maintain current knowledge of European and national technology priorities, emerging threats, and mission-critical capabilities (network security, cloud modernisation, zero trust, observability, critical infrastructure protection) and how Keysight solutions address them.Provide technical credibility in customer engagements, architecture discussions, and proof-of-concept planning; ensure solutions are technically robust and aligned with EU and national security standards (ANSSI, BSI, Common Criteria, FIPS, national accreditation schemes). QualificationsBachelor's degree in Engineering, Computer Science, Information Technology, Cybersecurity, or a related technical field.10+ years driving business growth and customer success in enterprise technology markets (infrastructure, cybersecurity, or related domains).5+ years in customer-facing technical business development, with proven track record of building strategic relationships, winning complex deals, and accelerating pipeline growth with enterprise and government clients.Demonstrated experience supporting European government agencies, defence organisations, or public-sector customers across multiple countries.Prior experience working with European defence primes, subprimes, and systems integrators in government engagements.Strong technical foundation in enterprise networking and cybersecurity concepts (routing, switching, network security architectures, cloud networking, network monitoring, threat detection, application delivery).Ability to deliver executive-level presentations and engage credibly with both technical and non-technical stakeholders.Strong communication, relationship-building, and cross-cultural collaboration skills suited to working across multiple European markets.Professional fluency in English required; professional fluency inGerman and/or French strongly preferred.Ability to travel approximately 50% within your country and across Europe as business needs require.Understanding of European government procurement frameworks and processes (e.G., EU tendering regulations, national procurement schemes).Preferred QualificationsPrior experience working within a government agency, government contractor, or technology vendor in a business development or strategic account role, building relationships and pipeline within government markets.Working knowledge of Zero Trust architecture, NIS2 Directive, EU Cyber Resilience Act (CRA), national cybersecurity frameworks (ANSSI in France, BSI in Germany), and product certifications (Common Criteria, FIPS, USGv6).Familiarity with EU and national public procurement processes and frameworks (e.G., PRACE, EDA initiatives).Experience supporting large European systems integrators, defence primes, and strategic channel partners.Existing eligibility for national security clearance in Germany, France, Spain, or Italy, or ability to obtain one.Track record of establishing market presence and capturing new logos in competitive government environments.What We're Looking ForWe're seeking a hungry and motivated professional who thrives in a strategic market-building environment. You're entrepreneurial, relationship-focused, and energised by establishing presence in new European government markets. You combine genuine technical credibility with strong business development instincts—you can speak authoritatively about technology challenges but your real passion is understanding customer priorities, navigating complex government dynamics, and winning deals. You understand multi-country government procurement complexity, EU regulatory requirements, and mission-critical needs. You're driven to help European public-sector organisations modernise their infrastructure, enhance data sovereignty, and strengthen cyber resilience. You're comfortable owning outcomes—from identifying opportunities to closing deals to ensuring customer success across borders.Careers Privacy Statement*Keysight is an Equal Opportunity Employer.*

Job DescriptionMar Recruitment, consultora de selección especializada en los sectores marítimo y logístico, busca incorporar un/a Director General a una compañía de referencia, con una sólida trayectoria y una posición consolidada en el sector marítimo, para liderar la siguiente etapa de crecimiento y desarrollo de la organización.La compañía es un grupo empresarial con una sólida trayectoria y una posición consolidada en el sector marítimo, desarrollando actividades que abarcan diferentes áreas de la cadena de valor vinculada al entorno portuario, logístico y de servicios. En el marco de su plan estratégico, afronta una nueva etapa orientada al crecimiento, la consolidación de su liderazgo y el desarrollo de nuevas oportunidades de negocio.El retoBuscamos un líder con una sólida visión estratégica, una marcada orientación al negocio y capacidad para impulsar el desarrollo económico y comercial de la organización.La posición requiere una mirada amplia y transversal, capaz de comprender el conjunto de las actividades del Grupo, identificar nuevas oportunidades de crecimiento, generar valor a largo plazo y liderar la evolución de la compañía en un entorno cada vez más competitivo. Buscamos un profesional con capacidad para combinar estrategia y ejecución, impulsando tanto el crecimiento de los negocios actuales como el desarrollo de nuevas oportunidades.Será fundamental aportar una visión global de empresa, con una fuerte orientación a resultados, capacidad de liderazgo y profundo conocimiento de las operaciones y dinámicas propias del sector marítimo. Se valorará especialmente la capacidad para entender el negocio más allá de una única actividad, aportando una visión corporativa que permita identificar sinergias, optimizar recursos y potenciar el crecimiento de todas las áreas de la organización.Principales responsabilidadesDefinir e implementar la estrategia global de crecimiento del Grupo.Liderar el desarrollo económico, comercial y corporativo de la organización.Identificar y desarrollar nuevas oportunidades de negocio, alianzas estratégicas e iniciativas de expansión.Impulsar la rentabilidad y la creación de valor en las distintas actividades de la compañía.Supervisar y coordinar las diferentes áreas de negocio, garantizando la alineación con los objetivos estratégicos.Liderar y desarrollar los equipos directivos, promoviendo una cultura de alto rendimiento.Garantizar la excelencia operativa y la eficiencia organizativa.Representar a la compañía ante clientes, instituciones, organismos públicos y otros grupos de interés.Liderar procesos de transformación, innovación y mejora continua.RequirementsExperiencia consolidada en posiciones de Dirección General, CEO o funciones ejecutivas de máxima responsabilidad.Sólida visión estratégica y capacidad para convertir oportunidades en crecimiento sostenible.Fuerte orientación al desarrollo de negocio, expansión comercial y generación de resultados.Experiencia liderando organizaciones complejas y gestionando diferentes líneas de actividad.Capacidad para identificar oportunidades de mercado y desarrollar nuevas fuentes de ingresos.Amplio conocimiento de gestión empresarial, financiera y comercial.Profundo conocimiento del sector marítimo y de sus operaciones, con capacidad para comprender, gestionar e impulsar las diferentes actividades que lo conforman.Capacidad para combinar visión estratégica y conocimiento operativo, entendiendo tanto la realidad del negocio como sus oportunidades de desarrollo.Excelente capacidad de liderazgo, negociación, influencia y toma de decisiones.Perfil dinámico, emprendedor y orientado a la ejecución.Se valorará especialmenteExperiencia en procesos de crecimiento, expansión y diversificación empresarial.Capacidad para combinar visión estratégica con una sólida comprensión operativa.Experiencia desarrollando relaciones institucionales y comerciales de alto nivel.Capacidad para generar sinergias entre distintas actividades y detectar oportunidades de desarrollo dentro del ecosistema marítimo y portuario.Experiencia liderando organizaciones en entornos de cambio, crecimiento y transformación.BenefitsLa oportunidad de liderar una organización sólida, con una reconocida trayectoria y un ambicioso proyecto de crecimiento.Participación directa en la definición y ejecución de la estrategia futura de la compañía.Alto nivel de autonomía y capacidad real de impacto en la toma de decisiones.Proyecto profesional de largo recorrido dentro de una organización en plena evolución.Paquete retributivo competitivo acorde con la experiencia y responsabilidad de la posición.ConfidencialidadEste proceso se desarrolla bajo los más estrictos criterios de confidencialidad. La identidad de la compañía será revelada únicamente a aquellos profesionales que avancen en las distintas fases de selección.RequirementsCertificado de Competencia como Capitán hasta 500 GT (mínimo). Certificaciones STCW 2010 vigentes aplicables a remolcadores. Libreta de embarque en vigor. Buen dominio del Ingles y Español (oral y escrito). Sólidos conocimientos de terminología marítima. Residencia en la provincia de Barcelona.