Trabajos monitor en Benetússer - Page 5Crear alertas

En Econocom Servicio buscamos un/a Cloud Engineer con experiencia en la administración de entornos Azure que quiera formar parte de un equipo dedicado al cloud público y la automatización. ¿Configurar y administrar servicios Azure, realizando despliegues controlados y asegurando que cumplen las buenas prácticas definidas por el equipo. Automatizar tareas operativas y repetitivas mediante scripts o herramientas de automatización (Terraform, CloudFormation, Ansible), para mejorar la eficiencia y reducir errores manuales. Participar en el mantenimiento y evolución de Infraestructura como Código (IaC), colaborando en la creación de módulos reutilizables, pruebas y validaciones antes de los despliegues. Monitorizar el rendimiento y el estado de los servicios cloud, creando dashboards, alertas y métricas que permitan detectar incidencias de forma proactiva. Proponer mejoras de observabilidad, integrando logs, métricas y trazas en herramientas como CloudWatch, Azure Monitor, Grafana o similares. Apoyar en iniciativas FinOps, revisando consumos, detectando recursos infrautilizados, etiquetando correctamente los recursos y sugiriendo ajustes para optimizar costes. Colaborar en la implementación de políticas de seguridad y cumplimiento, aplicando controles básicos (IAM, políticas, roles, seguridad en redes, gestión de secretos, etc.). Dar soporte técnico en incidencias relacionadas con la infraestructura cloud, investigando, documentando y aplicando soluciones bajo supervisión del equipo. ~ Actualizar y mantener la documentación técnica, garantizando que los procedimientos estén correctamente registrados. Requisitos mínimos: Experiencia mínima de 5 años en la administración de entornos de Cloud Público principalmente Azure. Amplios conocimientos en infraestructura como código (IaC), servicios Cloud, herramientas de automatización, Terraform, Kubernetes, etc. Valorable: conocimientos en AWS. Contrato indefinido. Ubicación: Barcelona o Valencia. Horario flexible de Lunes a Viernes. Modelo híbrido de teletrabajo (80%). Vales comida. Desarrollo profesional y plan de formación a cargo de la empresa. ¡Grupo Econocom es el primer integrador digital en Europa que combina los servicios y la financiación para la transformación digital de grandes y medianas empresas y organizaciones públicas. Como parte del grupo, Econocom Servicios cuenta con 850 colaboradores y 70 millones de facturación en 2022 en España. Sus servicios de TI se estructuran entorno a cinco grandes ejes: Service desk innovation Advanced Managed Services Econocom Cloud, Public Cloud, Hybrid Cloud Managed Security Services

En Econocom Servicio buscamos un/a Cloud Engineer con experiencia en la administración de entornos Azure que quiera formar parte de un equipo dedicado al cloud público y la automatización. ¿Configurar y administrar servicios Azure, realizando despliegues controlados y asegurando que cumplen las buenas prácticas definidas por el equipo. Automatizar tareas operativas y repetitivas mediante scripts o herramientas de automatización (Terraform, CloudFormation, Ansible), para mejorar la eficiencia y reducir errores manuales. Participar en el mantenimiento y evolución de Infraestructura como Código (IaC), colaborando en la creación de módulos reutilizables, pruebas y validaciones antes de los despliegues. Monitorizar el rendimiento y el estado de los servicios cloud, creando dashboards, alertas y métricas que permitan detectar incidencias de forma proactiva. Proponer mejoras de observabilidad, integrando logs, métricas y trazas en herramientas como CloudWatch, Azure Monitor, Grafana o similares. Apoyar en iniciativas FinOps, revisando consumos, detectando recursos infrautilizados, etiquetando correctamente los recursos y sugiriendo ajustes para optimizar costes. Colaborar en la implementación de políticas de seguridad y cumplimiento, aplicando controles básicos (IAM, políticas, roles, seguridad en redes, gestión de secretos, etc.). Dar soporte técnico en incidencias relacionadas con la infraestructura cloud, investigando, documentando y aplicando soluciones bajo supervisión del equipo. ~ Actualizar y mantener la documentación técnica, garantizando que los procedimientos estén correctamente registrados. Requisitos mínimos: Experiencia mínima de 5 años en la administración de entornos de Cloud Público principalmente Azure. Amplios conocimientos en infraestructura como código (IaC), servicios Cloud, herramientas de automatización, Terraform, Kubernetes, etc. Valorable: conocimientos en AWS. Contrato indefinido. Ubicación: Barcelona o Valencia. Horario flexible de Lunes a Viernes. Modelo híbrido de teletrabajo (80%). Vales comida. Desarrollo profesional y plan de formación a cargo de la empresa. ¡Grupo Econocom es el primer integrador digital en Europa que combina los servicios y la financiación para la transformación digital de grandes y medianas empresas y organizaciones públicas. Como parte del grupo, Econocom Servicios cuenta con 850 colaboradores y 70 millones de facturación en 2022 en España. Sus servicios de TI se estructuran entorno a cinco grandes ejes: Service desk innovation Advanced Managed Services Econocom Cloud, Public Cloud, Hybrid Cloud Managed Security Services

Company: Global Responsibility: Lead the assigned pharmaceutical formulation projects within the R&D department, planning, coordinating and supervising the activities of the projects assigned and report their progress to the R&D Manager, other departments and customers. Be responsible for formulation and process development activities associated with the pharmaceutical projects assigned. Develop the required document formulation and process development strategies for polymeric, biopolymeric, and hybrid drug delivery systems, particularly long-acting injectables (LAIs) and other controlled-release platforms. Analyze the status of patents that affect products under development and the results obtained in the clinical studies; coordinate, schedule, monitor, review and validate the proper sequence of the pharmaceutical development plan, batches for bioequivalence or clinical development and registration, reports and people involved, deciding, advising and reporting on the way forward in the development, deviations and modifications of pharmaceutical forms, according to SOP's, the ICH, EMEA and FDA guidance. Critically interpret analytical, preclinical, and clinical data to support development narratives, product characterization summaries, and manufacturing control justifications within the regulatory framework. Provide scientific rationale for biomaterial selection, formulation design, process parameters, and stability testing strategies in accordance with CMC principles. Ensure that the products and processes developed are suitable for a successful scale-up to commercial manufacturing. Interact with raw material vendors to select the suitable quality for API, excipients and container closure systems to be used for development and manufacturing. Plan, organize and coordinate the activities of pharmaceutical and analytical development to ensure the proper progress of the projects assigned. Design, direct and/or follow pre-formulation (compatibility studies), formulation development, process development, process optimization / scale-up on assigned projects. • Design and oversee the development of polymeric and biopolymeric formulations, ensuring reproducibility, scalability, and compliance with regulatory and industry standards., • electrospinning, electrospraying, emulsification), emphasizing data integrity and regulatory relevance for dossier inclusion or technology transfer., • Provide trouble shooting and optimization of formulations, process performance and technical performance in cooperation with the production department., • Prepare product development reports, write and review quality overall summary and other documents to support CMC regulatory submissions for filing and answering to deficiency letters., • Prepare the scientific documentation for quality and regulatory affairs to support the projects assigned and to meet the standard approval flow established by the quality system; all in accordance to GMP and CFR regulations, compliance with quality system and technical agreements and contracts with third parties so that projects progress properly., • Review and interpret results from analytical characterization (TGA, DSC, SEM, vibrational spectroscopy, mechanical testing, rheology, release profiles, etc.) Prepare summary reports and presentations for review by management., • Ensure good relationships and collaboration with all other teams involved in the development, QA, Patents, Medical, Regulatory Affairs, etc., • Ensure good relationships and efficient follow up and tracking of development activities outsourced to third party organizations. PhD in Pharmaceutical Sciences is a plus. • Fluent in English, basic knowledge of Spanish, knowledge of other languages will be an asset., • Experience (years/area): +5 years of experience in leading formulation R&D projects in the pharmaceutical sector. Experience in managing multiple projects and experience with FDA requirements desirable. • Impact and influence, good communication and project management skills, leadership., • Valid driver's license and own vehicle required.

Company: Global Responsibility: Lead the assigned pharmaceutical formulation projects within the R&D department, planning, coordinating and supervising the activities of the projects assigned and report their progress to the R&D Manager, other departments and customers. Be responsible for formulation and process development activities associated with the pharmaceutical projects assigned. Develop the required document formulation and process development strategies for polymeric, biopolymeric, and hybrid drug delivery systems, particularly long-acting injectables (LAIs) and other controlled-release platforms. Analyze the status of patents that affect products under development and the results obtained in the clinical studies; coordinate, schedule, monitor, review and validate the proper sequence of the pharmaceutical development plan, batches for bioequivalence or clinical development and registration, reports and people involved, deciding, advising and reporting on the way forward in the development, deviations and modifications of pharmaceutical forms, according to SOP's, the ICH, EMEA and FDA guidance. Critically interpret analytical, preclinical, and clinical data to support development narratives, product characterization summaries, and manufacturing control justifications within the regulatory framework. Provide scientific rationale for biomaterial selection, formulation design, process parameters, and stability testing strategies in accordance with CMC principles. Ensure that the products and processes developed are suitable for a successful scale-up to commercial manufacturing. Interact with raw material vendors to select the suitable quality for API, excipients and container closure systems to be used for development and manufacturing. Plan, organize and coordinate the activities of pharmaceutical and analytical development to ensure the proper progress of the projects assigned. Design, direct and/or follow pre-formulation (compatibility studies), formulation development, process development, process optimization / scale-up on assigned projects. • Design and oversee the development of polymeric and biopolymeric formulations, ensuring reproducibility, scalability, and compliance with regulatory and industry standards., • electrospinning, electrospraying, emulsification), emphasizing data integrity and regulatory relevance for dossier inclusion or technology transfer., • Provide trouble shooting and optimization of formulations, process performance and technical performance in cooperation with the production department., • Prepare product development reports, write and review quality overall summary and other documents to support CMC regulatory submissions for filing and answering to deficiency letters., • Prepare the scientific documentation for quality and regulatory affairs to support the projects assigned and to meet the standard approval flow established by the quality system; all in accordance to GMP and CFR regulations, compliance with quality system and technical agreements and contracts with third parties so that projects progress properly., • Review and interpret results from analytical characterization (TGA, DSC, SEM, vibrational spectroscopy, mechanical testing, rheology, release profiles, etc.) Prepare summary reports and presentations for review by management., • Ensure good relationships and collaboration with all other teams involved in the development, QA, Patents, Medical, Regulatory Affairs, etc., • Ensure good relationships and efficient follow up and tracking of development activities outsourced to third party organizations. PhD in Pharmaceutical Sciences is a plus. • Fluent in English, basic knowledge of Spanish, knowledge of other languages will be an asset., • Experience (years/area): +5 years of experience in leading formulation R&D projects in the pharmaceutical sector. Experience in managing multiple projects and experience with FDA requirements desirable. • Impact and influence, good communication and project management skills, leadership., • Valid driver's license and own vehicle required.

Company: Global Responsibility: Lead the assigned pharmaceutical formulation projects within the R&D department, planning, coordinating and supervising the activities of the projects assigned and report their progress to the R&D Manager, other departments and customers. Be responsible for formulation and process development activities associated with the pharmaceutical projects assigned. Develop the required document formulation and process development strategies for polymeric, biopolymeric, and hybrid drug delivery systems, particularly long-acting injectables (LAIs) and other controlled-release platforms. Analyze the status of patents that affect products under development and the results obtained in the clinical studies; coordinate, schedule, monitor, review and validate the proper sequence of the pharmaceutical development plan, batches for bioequivalence or clinical development and registration, reports and people involved, deciding, advising and reporting on the way forward in the development, deviations and modifications of pharmaceutical forms, according to SOP's, the ICH, EMEA and FDA guidance. Critically interpret analytical, preclinical, and clinical data to support development narratives, product characterization summaries, and manufacturing control justifications within the regulatory framework. Provide scientific rationale for biomaterial selection, formulation design, process parameters, and stability testing strategies in accordance with CMC principles. Ensure that the products and processes developed are suitable for a successful scale-up to commercial manufacturing. Interact with raw material vendors to select the suitable quality for API, excipients and container closure systems to be used for development and manufacturing. Plan, organize and coordinate the activities of pharmaceutical and analytical development to ensure the proper progress of the projects assigned. Design, direct and/or follow pre-formulation (compatibility studies), formulation development, process development, process optimization / scale-up on assigned projects. • Design and oversee the development of polymeric and biopolymeric formulations, ensuring reproducibility, scalability, and compliance with regulatory and industry standards., • electrospinning, electrospraying, emulsification), emphasizing data integrity and regulatory relevance for dossier inclusion or technology transfer., • Provide trouble shooting and optimization of formulations, process performance and technical performance in cooperation with the production department., • Prepare product development reports, write and review quality overall summary and other documents to support CMC regulatory submissions for filing and answering to deficiency letters., • Prepare the scientific documentation for quality and regulatory affairs to support the projects assigned and to meet the standard approval flow established by the quality system; all in accordance to GMP and CFR regulations, compliance with quality system and technical agreements and contracts with third parties so that projects progress properly., • Review and interpret results from analytical characterization (TGA, DSC, SEM, vibrational spectroscopy, mechanical testing, rheology, release profiles, etc.) Prepare summary reports and presentations for review by management., • Ensure good relationships and collaboration with all other teams involved in the development, QA, Patents, Medical, Regulatory Affairs, etc., • Ensure good relationships and efficient follow up and tracking of development activities outsourced to third party organizations. PhD in Pharmaceutical Sciences is a plus. • Fluent in English, basic knowledge of Spanish, knowledge of other languages will be an asset., • Experience (years/area): +5 years of experience in leading formulation R&D projects in the pharmaceutical sector. Experience in managing multiple projects and experience with FDA requirements desirable. • Impact and influence, good communication and project management skills, leadership., • Valid driver's license and own vehicle required.

Se necesita monitor para actividad extraescolar de patinaje en colegio de Valencia (zona Avda del Puerto) El horario es viernes de 15.

Plataforma de clases particulares selecciona profesores/as y entrenadores/as de natación para impartir clases individuales a alumnos de distintas edades (niños, adolescentes y adultos) Buscamos profesionales comprometidos, con experiencia en enseñanza de natación, y que deseen colaborar , gestionando sus propios horarios y zonas de trabajo. Responsabilidades Impartir clases particulares de natación adaptadas al nivel y objetivos del alumno. Realizar un seguimiento del progreso del alumno y adaptar la metodología según necesidades individuales. Garantizar la seguridad y el correcto desarrollo de cada sesión. Coordinar directamente con el alumno o sus tutores aspectos logísticos (horarios, lugar, necesidades específicas). Requisitos Experiencia demostrable en la enseñanza de natación (mínimo 1 año). Formación relacionada (TAFAD, CAFYD, título de monitor/a de natación, socorrismo acuático u otros títulos oficiales). Capacidad para trabajar con diferentes rangos de edad. Excelente trato interpersonal y habilidades pedagógicas. Se valorará positivamente: Certificados en primeros auxilios y RCP Experiencia con necesidades educativas especiales Disponibilidad de material propio (recomendable, no obligatorio) Ofrecemos Colaboración flexible con gestión autónoma del horario y tarifas. Acceso a una red de alumnos a través de una plataforma consolidada en clases particulares. Soporte continuo en la gestión de clases y alumnos. Posibilidad de crecimiento y desarrollo profesional dentro de la comunidad de profesionales. Cómo postular Envía tu CV

Monitor and report team performance.Give agents feedback on their individual and motivate team members.Keep track of each agent’s training.Participate in the recruitment process close to HR Department.Make sure processes and procedures are up to date and adhered to take overflow calls / tickets.Ta

Lead, mentor, and develop a team of 17-20 customer support agents to ensure high performance and professional growth.Take full ownership of critical performance metrics such as SLA adherence, Net Promoter Score (NPS), Average Handle Time (AHT).Monitor and analyze team performance, providing timely f

Spanish-speaking Content Reviewer.In this role, you’ll play a key part in reviewing and handling.From privacy claims and fraud to defamation and falsification, you’ll be on the front line of.On-site or Remote (only within Greece).Monitor digital activity and ensure compliance with platform.

Valorable formación o interés en el ámbito de la animación sociocultural, monitor/a de tiempo libre o refuerzo escolar. Organizar y dinamizar actividades de tiempo libre y juegos educativos. Apoyar a los niños en la realización de sus tareas escolares (primaria, ESO, etc.

No es necesario tener experiencia previa, pero se valorará formación como entrenador/a, monitor/a deportivo o experiencia en fútbol base. Motivar a los estudiantes y fomentar valores deportivos como la disciplina, el respeto y el esfuerzo.

Nuestros/as monitores/as realizan fundamentalmente las siguientes. Estudios mínimos: Ciclo Formativo Grado Medio o formación de monitor de tiempo libre.

Nuestros monitores/as realizan fundamentalmente las siguientes funciones:. Estudios mínimos: Ciclo Formativo Grado Medio o formación de monitor de tiempo libre.

Es indispensable contar con el Certificado de Monitor de pilates en máquina. Se requiere un/a monitor/a de pilates con experiencia en el manejo de máquinas.

Se busca monitor/a para el transporte escolar, comedor y patios.