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Fundación Hospitalarias es una institución sin ánimo de lucro con más de 140 años de historia, comprometida con la atención integral, la dignidad de la persona y la innovación en el ámbito de la salud y salud mental. Con un equipo de profesionales que supera las 9.000 personas en España, trabajamos a través de una red de más de 200 centros en los que priman nuestros valores hospitalarios centrados en el cuidado y atención a la persona, y donde el trato humano y nuestra sensibilidad por cada una de ellas son la clave de lo que nos diferencia. En la Fundación Hospitalarias Barcelona Nord, con más de 65 años de trayectoria en atención intermedia y salud mental, estamos viviendo un momento histórico: la apertura del CAIIB (Centro de Atención Integrada Intermedia de Barcelona), un proyecto pionero que redefine el modelo asistencial en Catalunya. Este nuevo centro nace con la vocación de ser un referente en innovación, calidad y humanización, integrando tecnología de última generación y un enfoque multidisciplinar único. Formar parte de nuestro equipo significa ser protagonista desde el inicio en la construcción de un proyecto transformador para la salud y el bienestar de las personas. Si te motiva la innovación y la práctica clínica de excelencia, súmate como Médico/a Internista a este proyecto pionero. 🎯Funciones principales • Realizar la valoración clínica integral de pacientes con patologías complejas en hospitalización intermedia., • Coordinar el seguimiento diagnóstico y terapéutico, ajustando tratamientos según la evolución del paciente., • Colaborar estrechamente con especialistas de diferentes áreas, garantizando un enfoque interdisciplinar., • Elaborar informes clínicos y asegurar una adecuada comunicación con familiares y profesionales de referencia., • Participar en la definición, implementación y mejora continua de protocolos asistenciales basados en la evidencia., • Favorecer la incorporación de herramientas tecnológicas y metodologías innovadoras en la práctica clínica. 💯Requisitos • Grado en Medicina y valorable especialidad Medicina Interna/Título homologado en España., • Experiencia en atención hospitalaria, preferentemente en hospitales de agudos o intermedios., • Conocimientos actualizados en patologías prevalentes en la atención intermedia., • Habilidades de liderazgo clínico, comunicación efectiva y trabajo en equipo multidisciplinar., • Interés por proyectos innovadores, investigación clínica o docencia (se valorará positivamente)., • Compromiso con la calidad, la humanización y la mejora continua de la asistencia sanitaria. 🔝¿Qué ofrecemos? • Contrato laboral estable bajo el Convenio SISCAT., • Proyecto innovador y en expansión, con posibilidades de crecimiento., • Incorporación a un equipo cercano, comprometido y multidisciplinar., • Acceso a formación continua y desarrollo profesional. Aquí tu talento suma, tu vocación se potencia y tu compromiso marca la diferencia. La Fundació Hospitalàries Barcelona Nord está comprometida con la diversidad, la inclusión, la igualdad de trato y oportunidades y con la lucha contra la discriminación en cualquiera de sus formas, por lo que esta oferta está dirigida a cualquier persona que reúna los requisitos exigidos, independientemente de su condición.

MIVI Salud busca incorporar un Enfermero para formar parte de nuestro equipo en el Institut del Dolor de Sant Cugat (Cataluña). Buscamos un profesional con experiencia en quirófano, áreas intervencionistas o Unidades del Dolor, que quiera formar parte de un entorno profesional, dinámico y especializado, trabajando junto a especialistas de referencia en el tratamiento del dolor. ¿Cuáles serán tus funciones? • Recepción, preparación y valoración básica del paciente antes del procedimiento., • Canalización de vías venosas., • Preparación y control del material necesario para procedimientos intervencionistas., • Asistencia al equipo médico durante las técnicas de la Unidad del Dolor., • Realización de funciones de enfermería instrumentista y circulante., • Control de la esterilidad y mantenimiento del campo quirúrgico., • Monitorización y vigilancia del paciente durante los procedimientos y la sedación., • Registro de la actividad clínica y cumplimentación de la documentación sanitaria., • Gestión, control y reposición de material sanitario y medicación., • Coordinación con el equipo sanitario y no sanitario., • Información al paciente sobre cuidados posteriores al procedimiento., • Cumplimiento de los protocolos de seguridad y calidad asistencial. ¿Qué experiencia mínima buscamos? • Será especialmente valorable contar con experiencia en:, • Experiencia en quirófano o áreas intervencionistas., • Manejo de paciente monitorizado., • Experiencia en esterilidad e instrumentación., • Capacidad de trabajar en procedimientos de ritmo dinámico., • Experiencia en Unidad del Dolor., • Experiencia en CMA., • Experiencia con sedación., • Manejo de escopia/arco en C. Buscamos una persona responsable, organizada, resolutiva y con capacidad de trabajo en equipo, con orientación a la atención y seguridad del paciente. ¿Qué ofrecemos? • Contrato por sustitución de baja médica., • Horario de lunes a jueves de 15:00 a 21:00 h y 2 viernes al mes de 15:00 a 21:00 h., • Incorporación inmediata a un equipo especializado y multidisciplinar., • Entorno profesional y colaborativo., • Trabajo junto a especialistas con amplia experiencia en el ámbito del tratamiento del dolor. Si eres enfermero y cuentas con experiencia en el ámbito intervencionista, quirúrgico o en una Unidad del Dolor, nos gustaría conocerte. Únete a MIVI Salud y forma parte de un equipo comprometido con la excelencia asistencial y el cuidado del paciente.

Buscamos incorporar un/a profesional de enfermería en nuestra sede de Cerdanyola del Vallès para dar soporte a la ejecución de estudios clínicos, formando parte de un equipo multidisciplinar. Las responsabilidades serán: · Gestión y seguimiento de las personas voluntarias participantes en los estudios. · Apoyo en la ejecución de estudios clínicos (administración de cuestionarios, seguimiento del protocolo, etc.). · Realización de extracciones sanguíneas. · Gestión y procesamiento de muestras biológicas (etiquetado, centrifugado, alicuotado, etc.). · Tareas administrativas asociadas a los estudios (contacto con laboratorios, gestión de datos, etc.). · Análisis básico de datos. · Colaboración en la difusión de los estudios clínicos. Requisitos: - Grado en Enfermería, valorable doble Grado en Nutrición y Enfermería. - Experiencia de al menos un año en las funciones descritas. Ofrecemos: - Contrato estable. - Jornada de 10 horas/semanales en turno de mañana. - Horario: de lunes a viernes, en la franja de 8:00 a 12:00 h (2 o 3 días semanales, según necesidades del proyecto) - BS: 30K/año - Paquete de retribución flexible (seguro médico, transporte, ticket restaurante, formación, guardería y alquiler de coches) y otros beneficios como la plataforma de Bienestar y la plataforma de Cashback. - Desarrollo profesional y formación: · Cursos de Eurecat Academy · Sesiones temáticas semanales · Participación en formación especializada · Formación en idiomas (inglés, catalán y castellano)

Overview In this role, you lead medical safety and risk management for Roche-branded products, overseeing the full safety lifecycle from premarket to postmarket. You act as the medical authority across R&D, quality, and vigilance, informing Safety Board decisions and ensuring regulatory alignment. You’ll translate clinical insights into safety evaluations and help optimize interfaces between customer issue resolution and medical safety. This position offers high-impact work in a global, collaborative environment aimed at safer, smarter healthcare solutions. Compensaciones / Beneficios • competitive compensation packages, • equal opportunity employer, • family-friendly career paths, • flexible working arrangements, • sustainability-focused culture, • healthy lifestyle benefits Responsabilidades, • Perform comprehensive medical risk analyses (Health Hazard Evaluations, Medical Risk/Safety Assessments) and contribute to Safety Board discussions, • Handle regulatory inquiries related to adverse event reporting and product recalls across international authorities, • Prepare internal and external medical safety evaluations and expert opinions for Diagnostics across Core Lab, Molecular Lab, Near Patient Care, and Diabetes Care, • Plan and conduct internal trainings to optimize CIR and Medical Safety workflows, • Represent Medical Safety in Safety Board processes and provide medical assessments to inform board decisions, • Maintain and update procedural documents, guidelines, and SOPs/GSPs within scope Requisitos principales, • MD or equivalent; medical licence preferred, • hands-on clinical experience, • familiarity with EU IVDR (2017/746) and US IVD regulations; experience with medical devices/software preferred (EU MDR, 2017/745), • strong knowledge of EN ISO 14971 and TR 24971, • interpersonal, negotiation, analytical, adaptable, decisive, • fluent in English, • collaborative mindset, • effective negotiation, • analytical thinking, • EU IVDR and US IVD regulatory knowledge, • medical device and medical device software awareness, • risk management standards EN ISO 14971, TR 24971

Overview In this role you lead end-to-end study start-up and site activation for clinical trials, ensuring regulatory compliance and timely delivery. You will oversee EC/CA submissions, monitor CRO performance, and serve as the clinical trial expert for site personnel. Collaborating with global and local teams, you create key study documents and ensure quality and audit readiness. This position offers impact through shaping study launches and upholding Roche’s commitment to accessible healthcare. Responsabilidades • Lead end-to-end study start-up activities, including site selection, activation, and qualification assessments, • Manage Ethics Committee (EC) and Competent Authority (CA) submissions, ensuring regulatory compliance, • Provide CRO oversight and monitor external partner deliverables and milestones, • Act as primary contact for assigned study sites, training site personnel and providing technical assistance, • Develop critical study documentation (informed consent, patient guides, EC/CA submissions), • Collaborate cross-functionally with global, local, and virtual teams to achieve business goals and operational excellence, • Adhere to regulations, SOPs, and maintain audit/inspection readiness, • Validate product performance claims and provide data for regulatory submissions, • Work in local and global study teams while exhibiting diversity and cultural awareness, • Build and maintain strong cross-functional relationships Requisitos principales, • Typically 3–5 years of experience, • Bachelor in scientific discipline or related field (or equivalent experience), • Awareness of Roche organization and processes related to own discipline, • Provides informal guidance to new team members, • Strong problem-solving using analysis and judgment, • Ability to explain complex information clearly, • cross-functional collaboration, • communication, • cultural awareness, • IVDR, • Study Start-Up, • EC/CA submissions

Overview In this role you lead end-to-end study start-up and site activation for clinical trials, ensuring regulatory compliance and timely delivery. You will oversee EC/CA submissions, monitor CRO performance, and serve as the clinical trial expert for site personnel. Collaborating with global and local teams, you create key study documents and ensure quality and audit readiness. This position offers impact through shaping study launches and upholding Roche’s commitment to accessible healthcare. Responsabilidades • Lead end-to-end study start-up activities, including site selection, activation, and qualification assessments, • Manage Ethics Committee (EC) and Competent Authority (CA) submissions, ensuring regulatory compliance, • Provide CRO oversight and monitor external partner deliverables and milestones, • Act as primary contact for assigned study sites, training site personnel and providing technical assistance, • Develop critical study documentation (informed consent, patient guides, EC/CA submissions), • Collaborate cross-functionally with global, local, and virtual teams to achieve business goals and operational excellence, • Adhere to regulations, SOPs, and maintain audit/inspection readiness, • Validate product performance claims and provide data for regulatory submissions, • Work in local and global study teams while exhibiting diversity and cultural awareness, • Build and maintain strong cross-functional relationships Requisitos principales, • Typically 3–5 years of experience, • Bachelor in scientific discipline or related field (or equivalent experience), • Awareness of Roche organization and processes related to own discipline, • Provides informal guidance to new team members, • Strong problem-solving using analysis and judgment, • Ability to explain complex information clearly, • cross-functional collaboration, • communication, • cultural awareness, • IVDR, • Study Start-Up, • EC/CA submissions

Merck Group in Spain (Catalunya) seeks a Senior AI/ML Platform Engineer and Technical Lead to build and evolve our AI/ML platform powering enterprise capabilities. You will lead a team of engineers, aligning priorities and delivering high-quality output while coordinating with Cloud, Security, and Governance teams. Ideal candidates have 8+ years in software/platform engineering, 2+ years in production LLM ops, and strong cloud-native experience across AWS/Azure with Python, Docker, IaC, and #J-18808-Ljbffr

Overview In this role, you lead medical safety and risk management for Roche-branded products, overseeing the full safety lifecycle from premarket to postmarket. You act as the medical authority across R&D, quality, and vigilance, informing Safety Board decisions and ensuring regulatory alignment. You’ll translate clinical insights into safety evaluations and help optimize interfaces between customer issue resolution and medical safety. This position offers high-impact work in a global, collaborative environment aimed at safer, smarter healthcare solutions. Compensaciones / Beneficios • competitive compensation packages, • equal opportunity employer, • family-friendly career paths, • flexible working arrangements, • sustainability-focused culture, • healthy lifestyle benefits Responsabilidades, • Perform comprehensive medical risk analyses (Health Hazard Evaluations, Medical Risk/Safety Assessments) and contribute to Safety Board discussions, • Handle regulatory inquiries related to adverse event reporting and product recalls across international authorities, • Prepare internal and external medical safety evaluations and expert opinions for Diagnostics across Core Lab, Molecular Lab, Near Patient Care, and Diabetes Care, • Plan and conduct internal trainings to optimize CIR and Medical Safety workflows, • Represent Medical Safety in Safety Board processes and provide medical assessments to inform board decisions, • Maintain and update procedural documents, guidelines, and SOPs/GSPs within scope Requisitos principales, • MD or equivalent; medical licence preferred, • hands-on clinical experience, • familiarity with EU IVDR (2017/746) and US IVD regulations; experience with medical devices/software preferred (EU MDR, 2017/745), • strong knowledge of EN ISO 14971 and TR 24971, • interpersonal, negotiation, analytical, adaptable, decisive, • fluent in English, • collaborative mindset, • effective negotiation, • analytical thinking, • EU IVDR and US IVD regulatory knowledge, • medical device and medical device software awareness, • risk management standards EN ISO 14971, TR 24971

In this role you lead end-to-end study start-up and site activation for clinical trials, ensuring regulatory compliance and timely delivery. Bachelor in scientific discipline or related field (or equivalent experience). Lead end-to-end study start-up activities, including site selection, activation,

You act as the medical authority across R&D, quality, and vigilance, informing Safety Board decisions and ensuring regulatory alignment. This position offers high-impact work in a global, collaborative environment aimed at safer, smarter healthcare solutions. Perform comprehensive medical risk analy

Overview As Senior AI/ML Platform Engineer and Technical Lead, you will steer the AI/ML platform that powers intelligent capabilities across the organization. You’ll lead a team of engineers, setting objectives and ensuring high-quality, timely delivery. You will synchronize platform sub-functions with enterprise standards, collaborating with Cloud, Cybersecurity, and Governance teams to maintain governance. Your work shapes scalable, well-governed engineering that advances the company’s mission in science and technology. You’ll tackle complex operational challenges and drive real impact across products and platforms. Compensaciones / Beneficios • culture of inclusion and belonging, • opportunities for growth, • diverse and inclusive team, • global collaboration, • focus on innovation, • employee development Responsabilidades, • Lead a team of professional engineers and set objectives, • Prioritize inputs from diverse internal and external sources to solve platform challenges, • Act as technical liaison across Cloud, Cybersecurity, Governance, and adjacent teams, • Define team responsibilities, engineering standards, and platform governance practices, • Ensure quality, accuracy, and timeliness of the team's outputs, • Influence enterprise-standard alignment and best practices across related teams Requisitos principales, • 8 or more years in software or platform engineering, • >=2 years in production LLM operations (LLMOps), • Hands-on with LLM/API gateway tech (LiteLLM or comparable), • Experience with multi-provider cloud AI platforms (Azure OpenAI, Azure AI Foundry, AWS Bedrock), • Cloud-native experience on AWS/Azure (containers, secrets, databases, networking, load balancing), • Production-grade Python backend development; Rust a plus, • Infrastructure-as-code and CI/CD tooling (Docker, Azure DevOps, Terraform/CloudFormation), • leadership, • cross-functional collaboration, • problem solving, • LLMOps, • LLM/API gateway technologies, • Azure OpenAI

As Senior AI/ML Platform Engineer and Technical Lead, you will steer the AI/ML platform that powers intelligent capabilities across the organization.You’ll lead a team of engineers, setting objectives and ensuring high-quality, timely delivery.You will synchronize platform sub-functions with enter

Overview As Senior AI/ML Platform Engineer and Technical Lead, you will steer the AI/ML platform that powers intelligent capabilities across the organization. You’ll lead a team of engineers, setting objectives and ensuring high-quality, timely delivery. You will synchronize platform sub-functions with enterprise standards, collaborating with Cloud, Cybersecurity, and Governance teams to maintain governance. Your work shapes scalable, well-governed engineering that advances the company’s mission in science and technology. You’ll tackle complex operational challenges and drive real impact across products and platforms. Compensaciones / Beneficios • culture of inclusion and belonging, • opportunities for growth, • diverse and inclusive team, • global collaboration, • focus on innovation, • employee development Responsabilidades, • Lead a team of professional engineers and set objectives, • Prioritize inputs from diverse internal and external sources to solve platform challenges, • Act as technical liaison across Cloud, Cybersecurity, Governance, and adjacent teams, • Define team responsibilities, engineering standards, and platform governance practices, • Ensure quality, accuracy, and timeliness of the team's outputs, • Influence enterprise-standard alignment and best practices across related teams Requisitos principales, • 8 or more years in software or platform engineering, • >=2 years in production LLM operations (LLMOps), • Hands-on with LLM/API gateway tech (LiteLLM or comparable), • Experience with multi-provider cloud AI platforms (Azure OpenAI, Azure AI Foundry, AWS Bedrock), • Cloud-native experience on AWS/Azure (containers, secrets, databases, networking, load balancing), • Production-grade Python backend development; Rust a plus, • Infrastructure-as-code and CI/CD tooling (Docker, Azure DevOps, Terraform/CloudFormation), • leadership, • cross-functional collaboration, • problem solving, • LLMOps, • LLM/API gateway technologies, • Azure OpenAI

Enterprise Application Software. Inside Presales Collaboration Tech Consultant with Italian Description - Job Summary This role is responsible for building strong relationships with key customers and stakeholders, advising and influencing their strategic decisions, and tackling unique customer issue

Somos un grupo de centros médicos especializados en el tratamiento integral del aparato locomotor, líder del sector rehabilitación del Barcelonès Nord. Con presencia en Badalona, Barcelona, Santa Coloma de Gramenet, El Masnou y Esplugues de Llobregat. Nacimos hace 40 años con el propósito de proporcionar asistencia médica de máxima calidad y asesoramiento en servicios de rehabilitación. Hemos atendido a más de 200.000 pacientes durante toda nuestra trayectoria. Nuestra esencia es el compromiso con nuestros pacientes y la mejora constante en nuestros procesos por tal de proporcionar la mejor calidad asistencial posible. Actualmente buscamos a un/a Médico/a Rehabilitador/a, quien será responsable de la evaluación, diagnóstico y tratamiento integral de pacientes con afecciones físicas, neuromusculares y funcionales, así como de la planificación y supervisión de programas de rehabilitación orientados a mejorar la calidad de vida y la funcionalidad de los pacientes. Asimismo, deberá trabajar de manera coordinada con un equipo multidisciplinario de profesionales de la salud. • Titulación de Medicina y Especialidad en Medicina Física y Rehabilitación (imprescindible ambos homologados)., • Habilitación profesional vigente para ejercer., • Disponibilidad en Badalona y alrededores., • Buen horario que facilita la conciliación entre vida personal y profesional., • Retribución competitiva acorde con la experiencia y el perfil profesional., • Entorno de trabajo estable, con oportunidades de desarrollo y crecimiento., • Cultura organizativa orientada a la mejora continua y la excelencia asistencial. #J-18808-Ljbffr

Si eres enfermero y cuentas con experiencia en el ámbito intervencionista, quirúrgico o en una Unidad del Dolor,.

Trabajo junto a especialistas con amplia experiencia en el ámbito del tratamiento del dolor. Recepción, preparación y valoración básica del paciente antes del procedimiento. Asistencia al equipo médico durante las técnicas de la Unidad del Dolor.

Buscamos incorporar un/a profesional de enfermería en nuestra sede de Cerdanyola del Vallès para dar soporte a la ejecución de estudios clínicos, formando parte de un equipo multidisciplinar.Gestión y seguimiento de las personas voluntarias participantes en los estudios.Apoyo en la ejecución d

Buscamos incorporar un/a profesional de enfermería en nuestra sede de Cerdanyola del Vallès para dar soporte a la ejecución de estudios clínicos, formando parte de un equipo multidisciplinar.

Chez Roche, vous pouvez être vous-même et être apprécié pour les qualités uniques que vous apportez. Notre culture encourage l'expression personnelle, le dialogue ouvert et les connexions authentiques, où vous êtes valorisé, accepté et respecté pour ce que vous êtes, vous permettant de prospérer tant personnellement que professionnellement. Voici comment nous visons à prévenir, arrêter et guérir les maladies et à garantir à chacun l'accès aux soins de santé aujourd'hui et pour les générations à venir. Rejoignez Roche, où chaque voix compte. The position As a Clinical Site Manager specialising in IVDR and Study Start-Up, you will be responsible for designing, planning, coordinating, and conducting all activities involved in initiating, monitoring, and completing clinical research studies at assigned sites. You will work independently to ensure studies are delivered, recorded, and reported in accordance with protocols, standard operating procedures, and global regulatory guidelines. Key Accountabilities The key accountabilities for this position include, but are not limited to: • Lead end-to-end study start-up activities, driving site selection, activation, and qualification assessments to ensure clinical trials launch efficiently and are compliance-ready., • Manage Ethics Committee (EC) and Competent Authority (CA) submissions, ensuring all trial documentation is available, local contracts, Ethics Committee and Competent Authority approvals meet stringent regulatory requirements., • Provide robust CRO oversight, monitoring external partner deliverables, tracking milestones, and escalation of any issues., • Act as the primary contact and clinical trial expert for assigned study site personnel, for execution of the study - including training and coordinating certification of study site personnel, and provide technical assistance, as necessary., • Develop critical study documentation, including informed consent documents, patient instruction guides, and key documents for EC/CA submissions, • Collaborate cross-functionally with global, local, and virtual teams, demonstrating diversity, cultural awareness, and fostering strong, collaborative relationships with cross-functional team members, internal stakeholders, and external partners to achieve business goals and ensure operational excellence. Responsibilities The following are responsibilities for the individuals in this position: • Adhere to regulations, guidelines and standard operating procedures, and ensure ongoing audit/inspection readiness., • Validate product performance claims, supply data for critical regulatory submissions, define the functional and clinical utility of our products, and obtain the opinions and input regarding our products from laboratories or customers., • Work in local and global study teams, including virtual teams and exhibit diversity and cultural awareness., • Build and maintain strong, collaborative relationships with cross-functional team members. Who you are • Typically has a minimum of 3-5 years of experience., • Bachelors Degree in scientific discipline or related field required, or equivalent combination of education and work experience, experience in a clinical laboratory, clinical study coordination is a plus, • Awareness of the Roche organisation and key organisational drivers as well as the relevant processes, customers and products related to own discipline, • Provides informal guidance to new team members, • Solves potentially complex problems by analysing possible solutions using experience, judgement and precedents, • Explains complex information to others in straightforward situations Where pay transparency applies, details are provided based on the primary posting location. For this role, the primary location is Sant Cugat del Vallès. If you are interested in additional locations where the role may be available, we will provide the relevant compensation details later in the hiring process. Un avenir plus sain nous pousse à innover. Ensemble, plus de 100 000 employés à travers le monde sont dédiés à faire progresser la science et à garantir à chacun l'accès aux soins de santé aujourd'hui et pour les générations à venir. Nos efforts aboutissent à plus de 26 millions de personnes traitées avec nos médicaments et plus de 30 milliards de tests réalisés avec nos produits de Diagnostique. Nous nous encourageons mutuellement à explorer de nouvelles possibilités, à favoriser la créativité et à conserver nos grandes ambitions, afin de fournir des solutions de santé qui changent des vies et ont un impact mondial. Construisons ensemble un avenir plus sain. Roche est un employeur offrant l'équité en matière d'emploi. #J-18808-Ljbffr

Work Your Magic with us! Ready to explore, break barriers, and discover more? We know you’ve got big plans – so do we! Our colleagues across the globe love innovating with science and technology to enrich people’s lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That's why we are always looking for curious minds that see themselves imagining the unimaginable with us. As a Senior AI/ML Platform Engineer and Technical Lead, you will be at the heart of building and evolving the AI/ML platform that powers intelligent capabilities across the organisation. In this role, you will lead a team of professional engineers: setting clear objectives, supporting their development, and being accountable for the quality, accuracy, and timeliness of the team's output. You will solve complex, operationally important engineering challenges by filtering and prioritising inputs from a wide range of internal and external sources, drawing on an in-depth understanding of how platform sub-functions work together. Acting as a key technical liaison across Cloud, Cybersecurity, Governance, and adjacent engineering teams, you will ensure the platform remains aligned with enterprise standards and emerging best practices. Your decisions will be guided by resource availability and organisational objectives, and you will contribute to defining team responsibilities, engineering standards, and platform governance practices that raise the quality bar across closely related teams. • 8 or more years of relevant industry experience in software or platform engineering, including at least 2 years working with large language model operations (LLMOps) in a production environment., • Hands-on experience with LLM/API gateway technologies such as LiteLLM or comparable solutions, and with multi-provider integration across major cloud AI platforms including Azure OpenAI, Azure AI Foundry, and AWS Bedrock., • Practical experience with cloud-native technologies on AWS and/or Azure, including container orchestration (such as ECS Fargate), secrets management, relational and non-relational databases, networking, and load balancing., • Proficiency in developing production-grade backend services using Python and asynchronous programming frameworks; experience with Rust is a plus., • Experience with infrastructure-as-code and CI/CD tooling, including containerisation with Docker, pipeline automation with Azure DevOps, and cloud provisioning frameworks such as Terraform or CloudFormation., • Familiarity with observability and monitoring tools used in AI/ML environments, such as CloudWatch, Prometheus, Grafana, or LLM-specific evaluation tooling., • Experience with identity and access management technologies, including Entra ID, JWT, OIDC, SSO, API keys, and related IAM methods., • Demonstrated ability to lead professional engineers, set team priorities, and drive platform quality — balancing hands‑on technical depth with team accountability and a focus on scalable, well‑governed engineering. We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We believe that this variety drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress! #J-18808-Ljbffr

To be considered for our Registered Dental Hygienist position, you must: Have a Registered Dental Hygienist’s license Have a valid CPR card Be Laser certified Be meticulous about oral health and the health of your patients. Registered Dental Hygienist (RDH) duties include: Providing dental health education about tooth care and diet Removing plaque and calculus by scaling and polishing teeth Taking impressions and/or dental radiographs of teeth Applying prophylactic/antibacterial materials, fissure sealants, and topical fluorides to help prevent tooth decay Carrying out screening and monitoring procedures We are following all guidelines with proper use of PPE to keep our patients and team safe. We are looking to fill this position immediately. Apply today! Benefits: Dental, 401k, PTO, Bonuses Compensation: $50-$55/hour

Se busca técnico/a de QA con experiencia en GMP y planta productiva para supervisar el cumplimiento normativo, gestionar incidencias y mejorar procesos en la industria farmacéutica.

Inside SW Tech Advisor with Italian language Description - Inclusion at HP At HP, we believe in the power of ideas.We use ideas to put technology to work for everyone.And we believe that ideas thrive best in a culture of teamwork.That is why everyone-at every level, in every function-is encouraged t

Sener Aeroespacial y Defensa busca un/a Technical Project Manager para su centro de Cerndayola (Barcelona). Dirigirás proyectos complejos de diseño, desarrollo y fabricación de equipos electrónicos y RF para misiones de vuelo, asegurando alcance, calendario y presupuesto.Reportarás a Dirección de Programas y Operaciones, gestionarás riesgos, coordinarás equipos multidisciplinares y mantendrás comunicación estrecha con clientes internacionales; se valora experiencia PMP y nivel alto de inglés.#J-18808-Ljbffr

BETWEEN se encuentra en Sabadell, España, y busca un Engineering Project Manager / Project Leader para liderar la gestión técnica de proyectos en entornos industriales del sector automoción. La persona seleccionada será el principal interlocutor técnico con el cliente, coordinando equipos multidisciplinares y asegurando el cumplimiento de objetivos técnicos, de calidad y de planificación. Entre tus funciones estarán diseñar y desarrollar componentes mecánicos en 2D y 3D con CATIA V5, realizar #J-18808-Ljbffr

¿Te apasiona el mundo de la producción y buscas una oportunidad para demostrar tus habilidades en un entorno dinámico? ¡Esta es tu ocasión! Una reconocida empresa del sector químico-farmacéutico/a ubicada en Cerdanyola del Vallès, está buscando personas entusiastas y comprometidas para unirse a su equipo como operario/a de producción. Funciones: Entre las funciones que desempeñarás en este puesto, se incluyen: - Estuchado automático de productos farmacéuticos. - Encapsulado. - Manipulación de máquinas de lavado. - Manipulación de viales y ampollas. - Envasado manual de productos. - Etiquetado de los empaques. - Realizar controles de calidad cada media hora, asegurándote de que los productos cumplen con las especificaciones requeridas. . En Adecco creemos en la igualdad de oportunidades y apostamos por el Talento Sin Etiquetas Requisitos Experiencia previa en el sector Valorable formación en fabricación de productos farmacéuticos ¿Qué ofrecemos? Horario fijo de lunes a viernes: - Turno de mañana de 06:00 a 14:00 - Turno de tarde: 13:55 a 21:55 Salario: 12,46€b/h Contrato inicial a través de Adecco.

JOB DESCRIPTIONThe IGTP is seeking to recruit a Laboratory Technician to carry out tasks associated with the Biobank Fluid Node.MAIN RESPONSIBILITIES- Collecting and registering biological samples and associated data according to researchers’ requests and Biobank needs.- Performing specific technical procedures of the Fluid Node: obtaining and fractionating serum, plasma, cells, and other biological samples.- Performing and collaborating in Biobank procedures: preparation, processing, preservation, and distribution of samples.- Assisting in the management of sample and service requests.- Maintenance and quality control of laboratory equipment and materials.- Ensure adherence to the requirements and procedures established within the Quality Management System (QMS).- Actively participate in and collaborate with the ISCIII Biobank Platform.QUALIFICATIONS AND EXPERIENCIE- Holding a Higher Technician degree in Clinical and Biomedical Laboratory or a similar qualification.- Demonstrated intermediate level of English.- Proven previous experience in handling human samples.- Willingness to work in the area of document management.- Ability to work effectively as part of a team.- Immediate availability.- Previous experience in processing blood samples and other derivatives will be an asset.- Previous experience with databases, records, and information management software will be an asset.- Previous experience in handling frozen samples will be an asset.- Previous experience in biobanking and/or research support services will be an asset.WHAT WE OFFER- Open-ended contract (Ley de la ciencia 14/2011).- Full-time working schedule.- Date of incorporation: estimated start date: 25th September 2026- Gross remuneration according to the candidate’s qualifications and experience.- Gross annual remuneration inherent to the square objected to this call, will be fixed based on the experience provided and the skills of the candidate, distributed in 12 payments.- Flexible payment (childminding vouchers).- 23 days holiday and 5 days for personal matters.- Training capsules by the company.- Be part of an excellent multidisciplinary research centre with the HRS4R badge.- Location on the Can Ruti Campus, a first-class translational research environment in the Barcelona area, in a very stimulating scientific environment. The IGTP offers a supportive, friendly and collaborative ecosystem to promote professional development and help you achieve your research goals.FOR MORE INFORMATIONhttps://www.Germanstrias.Org/en/technology-services/biobank/DEADLINE FOR APPLICATIONSThe call for applications will close on 14/09/2026#J-18808-Ljbffr

Buscas trabajo en ayuda a la dependencia? Este mes de agosto surgen nuevas oportunidades para cuidadores en Sabadell.

Hospital universitario a 15 km de Barcelona y bien comunicado ofrece incorporar a un/a:Bajo la dependencia de la Dirección Asistencial Médica y del jefe clínico de Neurología, sus ámbitos de responsabilidad serán:- Actividad asistencial en consultas de Neurología general y, puntualmente, en l

Se requiere titulación de Gerocultor/a, Auxiliar de Enfermería o similar, y se valora experiencia previa en residencias.

ALBA is the Spanish synchrotron light source, a large research infrastructure operating ten beamlines, complementary facilities, and an Electron Microscopy Center, this last in partnership with other institutions. Currently constructing multiple more beamlines, expanding the Electron Microscopy Center, and integrating advanced data analytics, it sums up a wide range of infrastructures geared toward finding solutions to societal challenges.Located in Cerdanyola del Vallès (Barcelona, Catalonia, Spain), it is funded by the Spanish Government (Ministerio de Ciencia e Innovación) and the Catalan Government (Generalitat de Catalunya, Departament de Recerca i Universitats). The synchrotron light produced by 3 GeV electrons is used by thousands of researchers to analyse and understand the properties and functionality of matter, spanning a wide variety of fields, such as catalytic research, health, energy production/storage, environmental research, communication technologies, or cultural heritage.Our highly motivated staff works in a multidisciplinary work environment with an atmosphere formed by lived diversity, inclusion and respect for our colleagues. One of the goals of our gender equality plan is to reach parity within the Consortium’s different divisions and offices, and several actions have been taken to encourage applications from women mostly in scientific, engineer and technical job positions.Located close to Barcelona in a natural park and well connected by car and public transportation, with excellent connectivity to the world and an employer who understands the importance of life-work balance.Facing an upgrade to ALBA II, a 4th generation facility, which will increase dramatically brightness and coherent flux, ALBA is in a phase of growth and dynamics. Being a part of the ALBA team will promote your career and will give you the opportunities to explore new territories.For more information, you can take a look on our history watching this video: Be the person in charge of the technical management, including maintenance of the Catalysis/Battery/Chemistry/Materials-science laboratories. You will mainly develop the activities at these laboratory premises. Provide the technical support and scientific services offered by the Catalysis/Battery/Chemistry/Materials-science laboratories to laboratory users which includes support for experiment setup and sample preparation to users or beamline staff. Identify any safety hazards within the lab operation, develop mitigation strategies using ALBA’s safety resources, and ensure the implementation of all risk mitigation procedures in the daily work. This also includes Update of inventories, lab protocols and Operator Instruction sheets (OIS). Keep the stock products and carry out the purchase orders required for the correct functioning of the laboratory.* And any other similar and reasonable task or function in accordance with the responsibilities that may be assigned by Management, if applicableRequirementsThe requirements for participation must be met on the date of the deadline for the submission of applications and will be accredited by means of the CV attached to it, without prejudice to the power of the selection body to require the contribution of the originals of the certifications accrediting the qualifications, training and work experience invoked in the CV.Applications that do not present the aforementioned or required documentation during the selection procedure will not be accepted.The successful candidate must:Hold an advanced professional training course ("ciclo formativo de grado superior") on laboratory techniques,or a degree in chemistry or material sciences,or must be able to demonstrate an extensive experience of at least 2 years as a laboratory technician in these areas.Everyone who meets the requirements will be admitted for the selective process. This position is reserved for those candidates having the legal status of person with disabilities, with a degree of disability equal or greater than 33%. In case of one or more admitted applicants with this status of disability, these candidates will be evaluated at first. In the event that no candidate with the status of disability is finally selected for the position, the selection process shall continue and the rest of the applicants will be evaluated.Selection Process DevelopmentThe selection will be carried out through the competition-opposition system.As a first phase, an analysis of the curriculum will be carried out (assessment of previous experience and / or scientific history, degree, training and other professional information relevant to the position). Career breaks or variations in the chronological order of CVs will be regarded as an evolution of a career, and consequently, as a contribution to the professional development.The assessment of the CV in the competition phase will be scored up to 40 points, which will consider the following aspects:- Experience in working in scientific and/or industry specific laboratory, proven knowledge of standard laboratory techniques and associated equipments (GloveBox, Vacuum Oven, Gas mixing, Gas handling) (15points)- Advanced proficiency, by training or proven practice in general software, office applications and purchasing specific applications (10points)- Experience or training of standard health and safety protocols in a laboratory setting (10points)- Experience in maintaining in autonomy necessary stock of consumables for operating a laboratory (5points)The best rated candidates, at least two if possible, will be invited to an interview where the technical competence, knowledge, skills and professional experience linked to the position will be assessed, with a total score of 60 points. A minimum of 30 points must be obtained out of a total of 60 points to be eligible.Provided they meet the minimum requirements and have ranked among the top five after the assessment of the CV phase, at least one person from the underrepresented gender in the division/office will be interviewed.The interview will include at least:- Theoretical and practical knowledge in at least one of the following fields : battery, chemistry, catalysis, 2D materials and associeted laboratory techniques (20points)- English level allowing to interact with international teams (generally English speaking only) (10points)- Self assessment of working in autonomy and organizing profile described tasks (10points)- Good interpersonal and communication skills (5 points)- Ability to work in a multidisciplinary team. (5 points)- Vision of the position (5 points)- Motivation for applying (5 points)The merits will be accredited by means of the CV attached to the application. The selection board may require accreditation by additional documentation, originals or certified copies confirming the experience invoked in the CV.In case of a tied final score, the position will be awarded to the person who belongs to the most underrepresented gender in the corresponding Division and subsidiarily to the overall company.If necessary, alternates of the members of the selection board will be appointed by the president of the selection process, and the change will be published in the announcement.The resolution of the selection procedure will be carried out within a maximum period of six months from the deadline for submitting applications for participation.The selection process may be declared vacant if the selection board considers not to have found eligible candidates for the position although they might meet the requirements to participate in the selection process specified in the offer.Other informationPermanent contract.Base salary range € 28,801 – € 33,140 gross per year.The base salary offered will be determined according to the selected candidate's qualifications, relevant professional experience, competencies and overall suitability for the position.Additional remuneration:- Annual productivity bonus (approximately 4% of the base salary), subject to the applicable internal policy and performance evaluation.ALBA also offers an attractive employment conditions, including flexible working arrangements and professional development opportunities.The Selection Board is composed by the following members: Francois Fauth, Marta Avila Perez, Edmundo Fraga, Alexander Missyul, Manuel Valvidares#J-18808-Ljbffr

Carrerasresearch is seeking a Predoctoral Researcher for the 3D chromatin organization group led by Dr. Biola M. Javierre. This position offers an opportunity to work on innovative research within the Josep Carreras Leukaemia Research Institute, focusing on the role of regulatory elements in hematological malignancies.Ideal candidates will possess a Master’s degree in Bioinformatics or Biomedical Sciences, with strong expertise in computational biology and a motivation for a research career. The role involves collaboration in a dynamic environment, contributing to critical research aimed at fighting cancer.#J-18808-Ljbffr

IGTP Retreat is seeking a Laboratory Technician to perform tasks within the Biobank Fluid Node. You will collect and register samples, fractionate serum/plasma/cells, and handle processing and distribution under a quality management system.Collaboration with researchers and ISCIII Biobank Platform is essential. The role requires a Higher Technician degree in clinical/biomedical labs, experience with human samples, and immediate availability.#J-18808-Ljbffr

Redarbor es la #1 compañía HR Tech en Latam. Ayudamos a 55 millones de personas al mes a encontrar un trabajo mejor y a más de 150.000 empresas a reclutar y retener el mejor talento. Somos líderes en Sites y App’s de empleo con nuestros sites de empleo Computrabajo (líder en Latinoamérica), OCC en México e Infojobs y Catho en Brasil, y Software de RRHH en Latinoamérica (Pandapé y Genomawork). • 2013 fundada, • +1.100 colaboradores, • HR Tech 1# en Latam y 2# grupo de sites de empleo con más tráfico en el mundo, • El Software de RH (SaaS) líder en Latinoamérica con más de 10.000 productos activos, • Somos una de las mejores empresas para trabajar en España y la 9ª mejor para trabajar en Europa Buscamos a una persona con mentalidad hunter y experiencia en ventas de soluciones ATS o HR Tech, capaz de liderar la apertura y desarrollo del mercado español, generando nuevas oportunidades de negocio y construyendo la estructura comercial necesaria para escalar el crecimiento. Durante el primer año, su principal misión será abrir grandes cuentas, acelerar el crecimiento comercial y liderar un equipo de SDRs orientado a la generación de oportunidades. A medida que los resultados se consoliden, será responsable de diseñar y desarrollar una estructura de Key Account Managers (KAMs) que permita escalar el negocio y maximizar el valor de los clientes captados. Buscamos una persona que disfrute vendiendo, prospectando y negociando. Un perfil ejecutor, orientado a resultados y con mentalidad emprendedora. Alguien que prefiera estar delante del cliente generando ingresos. • Identificar, prospectar y cerrar oportunidades en empresas medianas y grandes., • Construir relaciones estratégicas con directores de RRHH, CEOs y decisores clave., • Desarrollar nuevas oportunidades comerciales mediante estrategias outbound y networking., • Liderar negociaciones complejas y ciclos de venta consultiva., • Alcanzar y superar los objetivos de captación y facturación., • Gestionar y desarrollar un equipo de SDRs orientado a la generación de pipeline., • Definir metodologías, procesos y métricas comerciales., • Establecer una cultura de alta exigencia y orientación a resultados., • Colaborar estrechamente con Marketing y Customer Success para maximizar la conversión., • Contratar y desarrollar talento comercial conforme evolucione el negocio., • Más de 8 años de experiencia en ventas B2B., • Experiencia demostrable vendiendo soluciones ATS o HR Tech., • Historial de apertura y cierre de grandes cuentas., • Experiencia liderando equipos comerciales enfocados en prospección y generación de demanda., • Capacidad para trabajar en entornos de alto crecimiento y cambio constante., • Experiencia en compañías SaaS de crecimiento acelerado., • Conocimiento profundo del ecosistema de Talent Acquisition., • Experiencia construyendo equipos comerciales desde cero., • Experiencia en mercados internacionales., • Contrato Indefinido + flexibilidad horaria + día libre en tu CUMPLEAÑOS + 24 y 31 de diciembre, • Salario: se concretará en función de la experiencia, conocimientos y trayectoria de la persona seleccionada, garantizando siempre la coherencia con nuestra política de equidad interna., • 23 días laborables de VACACIONES, • Premiamos la antigüedad con días adicionales de vacaciones por cada 2 años cumplidos y hasta un máximo de 5 días., • Jornada intensiva: navidad, Semana Santa, Julio y agosto, • Jornada intensiva en el día de cumpleaños de los hij@s para poder compartir más tiempo en este día tan especial para ellos., • Teletrabajo - Modalidad híbrida: 2 días en oficina y 3 en casa., • 100% Teletrabajo: 5 semanas al año + Navidad y semana santa + puentes específicos + 2 semanas de agosto., • Plan de formación: cursos presenciales + formación online para realizar formaciones específicas desde casa y de forma ilimitada., • Presupuesto individual para certificaciones y eventos., • Gimnasio: subvención del 70% de tu cuota., • Fisio: subvención del 50% del coste del fisioterapeuta al mes. En REDARBOR trabajamos para promover una cultura inclusiva, que busca la equidad y valora las diferentes perspectivas. Esto se traduce en género, religión, personas con discapacidad, LGBTQ+, etnia y diversidad de experiencias. #J-18808-Ljbffr

Se busca un médico o médica para prestar servicio en centros logísticos en Barberà del Vallès (Barcelona). La oferta permite compaginar la actividad profesional con un proyecto temporal dentro de una compañía de ámbito internacional. Se ofrece un contrato temporal a jornada parcial de 25 horas semanales, con turno fijo de noche, de lunes a viernes, en horario de 01:00 a 06:00 horas. El entorno de trabajo es dinámico, dentro de un centro logístico de gran actividad, y existe la posibilidad de que surjan nuevas necesidades en el centro para proyectos posteriores. Las funciones principales incluyen la atención médica a los trabajadores del centro, la valoración de incidencias sanitarias durante el turno nocturno, la prestación de primeros auxilios y asistencia urgente, el registro de las actuaciones realizadas y la coordinación con los equipos de salud laboral. También se apoya en actividades preventivas y de promoción de la salud. Se requiere licenciatura o grado en Medicina, colegiación en vigor, disponibilidad para trabajar en horario nocturno y vehículo propio para el desplazamiento. Se valora experiencia previa en entornos asistenciales, salud laboral, urgencias o medicina del trabajo.

Una empresa farmacéutica en crecimiento busca un/a Técnico de Calidad para unirse a su equipo en Montcada i Reixac. Las funciones incluyen verificar el cumplimiento de los estándares de calidad y realizar inspecciones de productos. Se requiere un mínimo de 2 años en control de calidad y dominio de GMP. Ofrecen un ambiente dinámico y proyectos desafiantes con horarios rotativos tras un periodo de formación.#J-18808-Ljbffr

Carrerasresearch in Badalona, Spain is seeking a motivated researcher to study the organization of DNA in hematopoietic cells. The role involves investigating regulatory elements in cell maturation and diseases.The candidate should possess a Master’s degree in Bioinformatics or related fields and have strong communication skills. The position offers a full-time predoctoral contract with flexible work options, a vacation allowance, and a chance to work in a collaborative environment at the Josep Carreras Leukaemia Research Institute.#J-18808-Ljbffr

SERMEF busca un/a Médico/a Rehabilitador/a para la evaluación, diagnóstico y tratamiento integral de pacientes con afecciones físicas y neuromusculares, coordinando programas de rehabilitación y mejoras funcionales.

Colaborar con otras áreas de la empresa para garantizar la calidad de la información financiera. Analizar cuentas contables y realizar conciliaciones de balances. Supervisar la correcta aplicación de los procedimientos financieros y de control interno.

You will partner with Inside Account Executives and Presales, act as a subject matter expert, and nurture relationships to create opportunities, manage the pipeline, and forecast accurately. Hewlett Packard Enterprise seeks an Inside Sales Consultant to drive growth across defined solution areas in

Buscamos Psicólogo/a en Montcada i Reixac y alrededores.

Sener Aeroespacial y Defensa busca un/a Technical Project Manager para su centro de Cerndayola (Barcelona). Dirigirás proyectos complejos de diseño, desarrollo y fabricación de equipos electrónicos y RF para misiones de vuelo, asegurando alcance, calendario y presupuesto. Reportarás a Dirección de Programas y Operaciones, gestionarás riesgos, coordinarás equipos multidisciplinares y mantendrás comunicación estrecha con clientes internacionales; se valora experiencia PMP y nivel alto de inglés. #J-18808-Ljbffr

HP seeks an Inside Sales Consultant for the UK Market to drive sales growth across multiple HP solutions.

Hospital universitario a 15 km de Barcelona y bien comunicado ofrece incorporar a un/a: Bajo la dependencia de la Dirección Asistencial Médica y del jefe clínico de Neurología, sus ámbitos de responsabilidad serán: • Actividad asistencial en consultas de Neurología general y, puntualmente, en la consulta especializada EAIA de trastornos cognitivos., • Actividad asistencial en la respuesta a interconsultas de pacientes atendidos en Urgencias y hospitalización., • Actividad asistencial en la realización de ecodoppler de TSA, si se dispone de la formación adecuada., • Participación en la docencia de residentes. Licenciado/a en Medicina y Cirugía con la especialidad vía MIR u homologada. • Experiencia laboral en Neurología., • Formación en patología neuromuscular., • Formación en la realización de ecodoppler TSA. El/la profesional deberá tener las siguientes competencias: • Integridad., • Capacidad de trabajo en equipo., • Habilidades de comunicación y relación interpersonal., • Atención Centrada en la Persona., • Rigor y búsqueda de la mejora continua., • Horario flexible, distribuido en días a convenir, en horario de mañana y tarde. #J-18808-Ljbffr

CIMWORKS es una empresa tecnológica especializada en la digitalización integral de los procesos industriales, con un enfoque end‑to‑end que abarca desde el diseño y la ingeniería hasta la producción y la operación en planta.Su propuesta de valor se basa en habilitar la continuidad digital,

Desde la división de Life Sciences de LHH Recruitment Solutions estamos buscando un/a Técnico/a de Garantía de Calidad (QA) para incorporarse en reconocido laboratorio en plena fase de crecimiento.

Technical Sales Engineer for the Iberian Peninsula, based in Sabadell.