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Humanizando la Tecnología. Somos una gran empresa con alma de start-up. Por ello buscamos personas inquietas, que les motiven los retos y con ganas de crecer personal y profesionalmente , que se unan a nuestro equipo para tener un impacto positivo en el mundo a través de la tecnología. ¿Como Arquitecto/a Cloud , formarás parte nuestro departamento de Servicios de Infraestructura IT, Infraestructura IT , Gestión y Gobierno de Servicios , equipo altamente especializado en soluciones de infraestructuras de sistemas, virtualización, on-premises y/o Cloud basadas en las soluciones de los principales fabricantes líderes del mercado. Ejecutamos servicios gestionados de Infraestructura en grandes clientes nacionales e internacionales. Además, realizamos proyectos con tecnología punta y con un impacto extraordinario. ¿Diseñar arquitecturas Cloud seguras, escalables y resilientes en Azure y GCP. Liderar proyectos de migración de cargas de trabajo on premise a la nube. o Compute, Networking, Storage, IAM, Policies o Kubernetes (AKS, GKE) o Serverless / Microservicios Supervisar y optimizar la seguridad en ambos entornos: IAM, políticas, WAF, bastionado, Zero Trust. Optimizar el consumo y costes Cloud mediante FinOps. Acompañar al equipo técnico en la implementación y resolución de incidencias complejas. Trabajar con las áreas de Seguridad, Redes y Sistemas en el diseño de soluciones integradas. Preparar documentación técnica, hojas de ruta y presentaciones ejecutivas para dirección. ¿QUÉ ESPERAMOS DE TI? Formación: Ciclo formativo de grado superior o Ingeniería en el área informática o campo relacionado. Idiomas: Deseable nivel alto de inglés Experiencia: más de 5 años en puestos similares, a nivel arquitectura. Conocimientos técnicos elevados y/o experiencia en Conocimientos avanzados en Azure: VNETs, ExpressRoute, Private Endpoints, AKS, App Services. Conocimientos avanzados en GCP: VPCs, GKE, IAM, Cloud Run. Dominio de IaC: Terraform (imprescindible). Experiencia en observabilidad: Azure Monitor, Google Cloud Logging. Gestión de seguridad Cloud y estándares CIS/NIST. ¿Un equipo diverso . Respetamos las diferencias que nos hacen más humanos. Trabajamos en equipo y aprendemos los unos de los otros. Flexibilidad y conciliación . El teletrabajo está en nuestro ADN. Promovemos la flexibilidad horaria, y tenemos jornada intensiva los viernes y los meses de julio y agosto.

Humanizando la Tecnología. Somos una gran empresa con alma de start-up. Por ello buscamos personas inquietas, que les motiven los retos y con ganas de crecer personal y profesionalmente , que se unan a nuestro equipo para tener un impacto positivo en el mundo a través de la tecnología. ¿Como Arquitecto/a Cloud , formarás parte nuestro departamento de Servicios de Infraestructura IT, Infraestructura IT , Gestión y Gobierno de Servicios , equipo altamente especializado en soluciones de infraestructuras de sistemas, virtualización, on-premises y/o Cloud basadas en las soluciones de los principales fabricantes líderes del mercado. Ejecutamos servicios gestionados de Infraestructura en grandes clientes nacionales e internacionales. Además, realizamos proyectos con tecnología punta y con un impacto extraordinario. ¿Diseñar arquitecturas Cloud seguras, escalables y resilientes en Azure y GCP. Liderar proyectos de migración de cargas de trabajo on premise a la nube. o Compute, Networking, Storage, IAM, Policies o Kubernetes (AKS, GKE) o Serverless / Microservicios Supervisar y optimizar la seguridad en ambos entornos: IAM, políticas, WAF, bastionado, Zero Trust. Optimizar el consumo y costes Cloud mediante FinOps. Acompañar al equipo técnico en la implementación y resolución de incidencias complejas. Trabajar con las áreas de Seguridad, Redes y Sistemas en el diseño de soluciones integradas. Preparar documentación técnica, hojas de ruta y presentaciones ejecutivas para dirección. ¿QUÉ ESPERAMOS DE TI? Formación: Ciclo formativo de grado superior o Ingeniería en el área informática o campo relacionado. Idiomas: Deseable nivel alto de inglés Experiencia: más de 5 años en puestos similares, a nivel arquitectura. Conocimientos técnicos elevados y/o experiencia en Conocimientos avanzados en Azure: VNETs, ExpressRoute, Private Endpoints, AKS, App Services. Conocimientos avanzados en GCP: VPCs, GKE, IAM, Cloud Run. Dominio de IaC: Terraform (imprescindible). Experiencia en observabilidad: Azure Monitor, Google Cloud Logging. Gestión de seguridad Cloud y estándares CIS/NIST. ¿Un equipo diverso . Respetamos las diferencias que nos hacen más humanos. Trabajamos en equipo y aprendemos los unos de los otros. Flexibilidad y conciliación . El teletrabajo está en nuestro ADN. Promovemos la flexibilidad horaria, y tenemos jornada intensiva los viernes y los meses de julio y agosto.

Lead and strengthen the accounting function in a growing international digital company At Your New Self (YNS), we are looking for a Financial Controller with a strong technical accounting background to take ownership of the accounting and reporting function. You will work closely with the General Manager, acting as the financial reference within the company and supporting business decision-making in a fast-paced, international environment. Your New Self (YNS) is a B2B2C marketplace in the eHealth industry. Founded 15 years ago, YNS is a profitable company currently undergoing a transformation phase, working on a new strategy to triple sales in the next 10 years. YNS operates in 11 markets in Europe and LATAM and has its headquarters in Barcelona. In 2021, the American Company RealSelf acquired YNS within their geographical expansion plan. RealSelf has its headquarters in NY and operates in the US, Canada, Australia and UK with the same business model as YNS. As a group, we are the leading marketplace in the plastic surgery and aesthetics industry. Our customers are the clinics and doctors, and our consumers are their potential patients. We are transforming the Company, going from an SEO-oriented marketplace to a social media and user-centric one. We are currently working on passionate projects across Product & Tech, MKT, Sales & Operations to grow sales x3 in ten years in a scalable and profitable way. As Financial Controller, you will oversee and take responsibility for the company’s accounting and reporting function, ensuring full compliance with accounting and tax obligations in Spain and across subsidiaries. You are expected to have a strong technical accounting background and be able to review, validate, and guide accounting decisions with rigor and confidence. You will lead the monthly closing process, oversee cash management, and ensure accurate and timely financial reporting for management in Spain and the US. In addition, you will act as the main financial reference for the General Manager, translating financial data into clear insights and providing sound financial judgement to support decision-making. This role is ideal for a strong accounting professional who wants to go beyond bookkeeping, combining technical depth with business understanding in a growing international digital company. As the finance function continues to consolidate and mature, this role is expected to progressively evolve into a broader Head of Finance position over time, for the right candidate. We are the source of truth in the industry with more than 130k reviews, more than 24k forum threads, more than 54k questions to doctors, more than 53k consumer stories and more than 8k articles. As a RealSelf group company, we operate in 15 countries, with more than 110 million users and more than 100k clinics and doctors published on our websites. We work in a startup environment , with agile methodologies, a data-driven mindset, and digital company ways of working. Every person and job counts on the Company's evolution and results. &##Accounting: Oversee and control the accounting: accounting entries, amortizations, provisions, capitalizations, fixed assets, revenue accruals. Oversee and approve the accounting of subsidiaries and the accounting of intercompany invoices (done by local external accountants) Taxes : Oversee the tax obligations of the Company in Spain. Oversee the tax presentation in the subsidiaries. Lead the potential tax breaks. Identify and manage potential tax optimization opportunities. Lead the annual books presentation (Cuentas anuales al registro). Lead the annual audit. Execute the monthly sales report in excel for management and shareholders. Monitor and report financial performance against budget. Cash management : Own the cash management control. Own the currency exchange control. Manage banking relationships. 5+ years of progressive experience in accounting and/or financial controlling roles. ~ Strong technical accounting knowledge with solid exposure to the full accounting cycle. ~3+ years of experience with financial reporting (P&L, Balance Sheet and Cash Flow). ~3+ years of experience in Spanish tax and accounting standards. ~ Advanced Excel skills are a must; Professional fluency in both English and Spanish is required. ~ Remote position. ~ Monday–Thursday: Summer schedule: Intensive working hours on special dates (Noche de reyes, Sant Jordi, Verbena de San Juan, Christmas Eve, etc) ~ Private Health Insurance and the possibility of family memberships at YNS rates and tax exemption. ~ Payroll payment on the 25th of each month. ~ Option to work remotely from another country for limited periods during the year (Easter, Christmas, and summer), subject to company policy. ~ Young, dynamic environment with expertise in B2C2B digital environments. You’ll work in an international environment where things happen quickly because the digital industry is in constant evolution.

Kärcher is a leading German multinational company specializing in cleaning solutions. It stands out in the market thanks to its maximum performance, innovation, and quality. Currently, the company employs over 15,000 people and has a presence in 70 different countries. We continue to grow and improve thanks to the effort, commitment, and dedication of every single person who is part of this great team. Desplácese hacia abajo para encontrar los detalles completos de la oferta de trabajo, incluyendo la experiencia requerida y las funciones y tareas asociadas. Do you want to be a part of the Kärcher world? Now is your opportunity! We are looking for a Project Manager to join our technical team in Granollers. This role will plan, coordinate, and ensure the successful execution of optimization and continuous improvement projects assigned by the Kärcher Spain Technical Service Management. Responsibilities • Assigned Project Management: Directly responsible for the practical implementation of projects (e.g., the launch of OneView)., • Resource Coordination: Organize the necessary resources (technical staff, materials, training) to execute the project, maintaining fluid communication among all internal stakeholders., • Measurement and Monitoring: Actively monitor the progress of the implementation, reporting deviations and proposing immediate corrective actions to ensure the project stays on course., • Analysis and Data: Collect and analyze performance metrics (e.g., repair time, spare part usage) to detect bottlenecks and opportunities for improvement at the workshop level., • Continuous Technical Training: Always stay informed and technically trained regarding the Kärcher product from a technical perspective. Qualifications • Bachelor's Degree in Industrial Engineering, • Desirable +2 years of demonstrable experience in Project Management., • Fluency in English What We Offer The opportunity to work for a company with a highly prestigious and market-leading brand in a stable position, alongside a team that maintains an excellent working environment and prioritizes teamwork and collaboration. Social Benefits • Fixed salary., • 100% subsidized private medical insurance., • Employee discount on brand products., • 1 remote work day per week (after the 6-month onboarding period)., • Subsidized English classes. Do you think you are a good fit? Are you looking for a WOW career path at Kärcher? Apply now and build a cleaner world with us. We are looking forward to meeting you! Together towards a Cleaner World At Kärcher Spain, we are an employer committed to equal opportunities. xcskxlj We seek to attract, develop, and retain the most talented people within a diverse team. We do not discriminate on the grounds of race, color, religion or belief, sex, sexual orientation, identity...

Join Impress – Europe's Leading Health-Tech Innovator! Si los siguientes requisitos del puesto y la experiencia coinciden con sus habilidades, por favor, asegúrese de enviar su solicitud sin demora. We believe everyone deserves a smile they'll love . As the largest Ortho clinic chain in Europe, we combine cutting-edge tech with expert care, revolutionizing invisible orthodontics since 2019. With 140+ clinics across 9 countries and rapid growth, we're improving lives worldwide. The Impress team is passionate about teeth, digitalization, and customer service. We are looking for a Doctor Trainer to accompany and support our doctors in their daily needs across all our clinics. What we offer: • High-end, high-performance technical equipment: ., • Modern, fully renovated dental centers., • Ongoing training., • Support from a general practitioner for procedures not related to orthodontics., • Professional supervision team dedicated to patients, alongside clinical appointments and available 7 days a week via the treatment tracking app., • International network of colleagues (EU & USA)., • Energetic clinical team that listens to each other., • Career path and growth opportunities., • Approve treatment plans cases, review eligibility, approve refinements., • Be the first level of support for the doctors and auxiliaries., • Create the team and the process for smooth support for the front doctors., • Be the liaison between the clinics and the HQ in Barcelona., • Create training and processes., • Train teams on processes and training techniques., • Daily monitor quality reports and NPS and ensure good performance., • Create improvement action plans and implement them., • Daily monitor utilization and efficiency of time of the clinic teams. Organize daily quality checks., • Create and implement procedures on quality monitoring of hygienist, auxiliaries, doctors in the use of tools and compliance with processes., • Solve escalated patient requests and personally work with problem patients via meeting in the clinic, call, video conference or emails., • Engage in marketing and interviews, receipt of influencers, and photoshoots. This may involve videos for social media., • Combine work in the office and in the clinic when clinic requires orthodontic knowledge support., • The work may involve travelling and need to work on weekends., • Graduate in dentistry or orthodontics, registered with the Dental Association., • Solid clinical experience, ideally with aligners and digital technologies., • Experience in supervising or coordinating a medical team., • Proficiency in digital tools and patient tracking software., • Ability to supervise and validate treatment plans and manage complex cases., • Natural leadership, organizational skills, and excellent communication skills., • Focus on patient excellence and continuous improvement. xcskxlj, • Fluent Spanish , professional English ., • Willingness to travel frequently to all of our clinics at an international level.

JOB SUMMARY Asegúrese de presentar su candidatura con toda la información solicitada, tal como se expone en la descripción del puesto a continuación. Coordinate clinical studies execution in clinical sites world-wide . Provide support to principal investigators and their team: on-site trainings, monitoring of sites and clinical data, manage study-related administration and logistics tasks. Ensure that studies and data management are performed in compliance with GCP, Ethical and Regulatory frame. Key Accountabilities • Develop clinical study design., • Write clinical study protocols., • Write study monitoring plan., • Train study team on the relevant part of clinical studies., • Ensure statistical plan is properly performed and followed., • Ensure data management plan is properly performed and followed., • Ensure study risk analysis plans is properly performed., • Ensure that CRFs (case report forms) are well designed, completed and collected., • Prepare documentation to submit project to EC/IRB (ethical Committee) and follow up with them during the study., • Conduct site initiation visits in the clinical sites for the purpose of training site personnel about the protocol, study procedures, patient recruitment, reporting procedures, GCP and regulatory requirements., • Monitor the study throughout its duration. This activity may be done directly or managing the activity or a CRA/CRO., • Ensure that all study close-out activities are performed., • Manage clinical databases and data analysis., • Prepare final clinical study reports., • Develop all activities in compliance with GCP and under an ethical and regulatory frame., • Prepare study documentation for FDA pre-submissions and submissions, and for other regulatory agencies, as required. Mainly with R&D, Regulatory Affairs, and Design Quality and Operations colleagues. Minimum Knowledge & Experience required for the position: Education: • Required: Bachelor's degree (Diplomatura) in Life or Medical Sciences (Medicine, Biology, Pharmacist...), • Degree may be substituted by relevant skills and work experience., • Experience in CRF/e-CRF and other recruitment documentation, • Experience in clinical study monitoring, data management and analysis., • Knowledge of Medical Device Regulatory framework. Mainly CE and FDA., • Knowledge in GCPs., • Knowledge in immunoassay techniques and anlysers., • Knowledge in biostatistics and Data management., • Knowledge of basic software tools (Excel, Word, PowerPoint). Knowledge of SAP., • Attention to detail and accuracy, • Able to apply general scientific methods and theoretical knowledge to tasks within one area of expertise., • Teamwork and interpersonal skills. Flexibility in order to work with, and provide support for a number of people., • Oral and written communication skills., • Time management skills. Excellent organizational and multi-tasking skills., • Thorough knowledge of design control processes and familiarity with quality standards as required., • Excellent analytical skills., • Able to work independently on the project with moderate guidance., • Well organized, able to handle large data sets, and communicate results, problems, and progress to the supervisor, and within the group as required., • Ability to adapt to R&D flexible and changing environment., • Certain troubleshooting ability required. xcskxlj, • Reflects values of Werfen and OEM in the quality of work and working relationship.

JOB SUMMARY Asegúrese de presentar su candidatura con toda la información solicitada, tal como se expone en la descripción del puesto a continuación. Coordinate clinical studies execution in clinical sites world-wide . Provide support to principal investigators and their team: on-site trainings, monitoring of sites and clinical data, manage study-related administration and logistics tasks. Ensure that studies and data management are performed in compliance with GCP, Ethical and Regulatory frame. Key Accountabilities • Develop clinical study design., • Write clinical study protocols., • Write study monitoring plan., • Train study team on the relevant part of clinical studies., • Ensure statistical plan is properly performed and followed., • Ensure data management plan is properly performed and followed., • Ensure study risk analysis plans is properly performed., • Ensure that CRFs (case report forms) are well designed, completed and collected., • Prepare documentation to submit project to EC/IRB (ethical Committee) and follow up with them during the study., • Conduct site initiation visits in the clinical sites for the purpose of training site personnel about the protocol, study procedures, patient recruitment, reporting procedures, GCP and regulatory requirements., • Monitor the study throughout its duration. This activity may be done directly or managing the activity or a CRA/CRO., • Ensure that all study close-out activities are performed., • Manage clinical databases and data analysis., • Prepare final clinical study reports., • Develop all activities in compliance with GCP and under an ethical and regulatory frame., • Prepare study documentation for FDA pre-submissions and submissions, and for other regulatory agencies, as required. Mainly with R&D, Regulatory Affairs, and Design Quality and Operations colleagues. Minimum Knowledge & Experience required for the position: Education: • Required: Bachelor's degree (Diplomatura) in Life or Medical Sciences (Medicine, Biology, Pharmacist...), • Degree may be substituted by relevant skills and work experience., • Experience in CRF/e-CRF and other recruitment documentation, • Experience in clinical study monitoring, data management and analysis., • Knowledge of Medical Device Regulatory framework. Mainly CE and FDA., • Knowledge in GCPs., • Knowledge in immunoassay techniques and anlysers., • Knowledge in biostatistics and Data management., • Knowledge of basic software tools (Excel, Word, PowerPoint). Knowledge of SAP., • Attention to detail and accuracy, • Able to apply general scientific methods and theoretical knowledge to tasks within one area of expertise., • Teamwork and interpersonal skills. Flexibility in order to work with, and provide support for a number of people., • Oral and written communication skills., • Time management skills. Excellent organizational and multi-tasking skills., • Thorough knowledge of design control processes and familiarity with quality standards as required., • Excellent analytical skills., • Able to work independently on the project with moderate guidance., • Well organized, able to handle large data sets, and communicate results, problems, and progress to the supervisor, and within the group as required., • Ability to adapt to R&D flexible and changing environment., • Certain troubleshooting ability required. xcskxlj, • Reflects values of Werfen and OEM in the quality of work and working relationship.

JOB SUMMARY Asegúrese de presentar su candidatura con toda la información solicitada, tal como se expone en la descripción del puesto a continuación. Coordinate clinical studies execution in clinical sites world-wide . Provide support to principal investigators and their team: on-site trainings, monitoring of sites and clinical data, manage study-related administration and logistics tasks. Ensure that studies and data management are performed in compliance with GCP, Ethical and Regulatory frame. Key Accountabilities • Develop clinical study design., • Write clinical study protocols., • Write study monitoring plan., • Train study team on the relevant part of clinical studies., • Ensure statistical plan is properly performed and followed., • Ensure data management plan is properly performed and followed., • Ensure study risk analysis plans is properly performed., • Ensure that CRFs (case report forms) are well designed, completed and collected., • Prepare documentation to submit project to EC/IRB (ethical Committee) and follow up with them during the study., • Conduct site initiation visits in the clinical sites for the purpose of training site personnel about the protocol, study procedures, patient recruitment, reporting procedures, GCP and regulatory requirements., • Monitor the study throughout its duration. This activity may be done directly or managing the activity or a CRA/CRO., • Ensure that all study close-out activities are performed., • Manage clinical databases and data analysis., • Prepare final clinical study reports., • Develop all activities in compliance with GCP and under an ethical and regulatory frame., • Prepare study documentation for FDA pre-submissions and submissions, and for other regulatory agencies, as required. Mainly with R&D, Regulatory Affairs, and Design Quality and Operations colleagues. Minimum Knowledge & Experience required for the position: Education: • Required: Bachelor's degree (Diplomatura) in Life or Medical Sciences (Medicine, Biology, Pharmacist...), • Degree may be substituted by relevant skills and work experience., • Experience in CRF/e-CRF and other recruitment documentation, • Experience in clinical study monitoring, data management and analysis., • Knowledge of Medical Device Regulatory framework. Mainly CE and FDA., • Knowledge in GCPs., • Knowledge in immunoassay techniques and anlysers., • Knowledge in biostatistics and Data management., • Knowledge of basic software tools (Excel, Word, PowerPoint). Knowledge of SAP., • Attention to detail and accuracy, • Able to apply general scientific methods and theoretical knowledge to tasks within one area of expertise., • Teamwork and interpersonal skills. Flexibility in order to work with, and provide support for a number of people., • Oral and written communication skills., • Time management skills. Excellent organizational and multi-tasking skills., • Thorough knowledge of design control processes and familiarity with quality standards as required., • Excellent analytical skills., • Able to work independently on the project with moderate guidance., • Well organized, able to handle large data sets, and communicate results, problems, and progress to the supervisor, and within the group as required., • Ability to adapt to R&D flexible and changing environment., • Certain troubleshooting ability required. xcskxlj, • Reflects values of Werfen and OEM in the quality of work and working relationship.

What You’ll Do Assure that data quality and compliance meet our high standards Monitor data delivery to the product Optimize the existing data tools to streamline data operations Identify data gaps and quality issues from large data sets and provide root cause analysis Collaborate with cross-

Ensure interfaces are scientifically rigorous, communicating confidence levels and scientific context while remaining intuitive for users with varying computational backgrounds Lead usability testing sessions and gather continuous feedback from scientist users Monitor and drive adoption through ta

Ensure interfaces are scientifically rigorous, communicating confidence levels and scientific context while remaining intuitive for users with varying computational backgrounds* Lead usability testing sessions and gather continuous feedback from scientist users* Monitor and drive adoption through ta

Organize the activity of the store: planning, determine collective and individual actions. Support and organize communication with store staff: lead daily briefings and other meetings, set and monitor individual goals, identify areas for improvement. Ensure that the store xcskxlj is perfectly displa

Una organització social a Barcelona cerca un/a Monitor/a per a Centre Ocupacional per atendre persones amb discapacitat física i paràlisi cerebral.

Monitor/a de classes dirigides (Cycling, Tonificació i BodyPump).

Desplácese hacia abajo para encontrar una descripción detallada de este trabajo y lo que se espera de los candidatos.Envíe su solicitud haciendo clic en el botón "Solicitar".In this role you lead planning and forecasting and ensure data integrity in SAC.You monitor actuals vs plan and forecast,

You work closely with PMs to ensure project success, manage scope and budgets, and identify growth opportunities through upselling and cross-selling. Your expertise in sales, negotiation, and account management supports high client satisfaction and loyalty. Monitor project progress, budgets, and tim

You’ll collaborate with cross-functional teams to translate client vision into actionable plans, manage scope, timeline, and budget, and lead customer-facing demos and retrospectives. Experience in Health and Life Sciences. Monitor project documentation and ensure deliverables meet quality standar

Perform risk identifications/assessments and monitor risks via GRC tools; conduct control assessments against Allianz framework. As Information Security Analyst, you support security oversight, governance and risk management across Allianz Technology GDN Spain and the UK. You will help monitor vulne

You’ll set and monitor KPIs, lead forecasting and funding decisions, and embed cash discipline across the organization. This is an opportunity to shape how cash and working capital enable our international logistics business to scale. Define and track working capital KPIs (DSO, DPO) and standardiz

Create, optimize, and maintain SEO-driven content (blogs, landing pages, guides, resources). Apply SEO best practices (on-page, internal linking, search intent, technical hygiene). Monitor content and SEO performance using GA, GSC, Ahrefs/SEMrush/Screaming Frog.

We are seeking talented Bartenders to join our culinary teams across several new restaurant concepts that will be opening in the coming months. Monitor inventory levels, anticipate needs, and coordinate with the Head Bartender to manage stock and place timely orders.

Desplácese hacia abajo para ver todos los requisitos del puesto y las responsabilidades que pueden esperar los candidatos seleccionados.Será el encargado/a de preparar, coordinar e impartir actividades de clases colectivas según los estándares de calidad requeridos por la compañía, constanteme

Estem constituint una BORSA DE TREBALL per a monitors i monitores de suport a alumnes amb Necessitats Específiques de Suport Educatiu (NESE). Es busca MONITOR/A DE SUPORT D'ALUMNES AMB NESE a BALENYÀ.

En VivaGym creemos en un estilo de vida activo, saludable y accesible para todos.Somos una compañía en constante crecimiento, con un equipo dinámico, comprometido y apasionado por ayudar a nuestros socios a alcanzar sus objetivos.Aumente sus posibilidades de llegar a la fase de entrevista leyendo

Newlink Education, empresa dedicada a la organización de estancias formativas en el extranjero, está buscando monitores para acompañar a grupos de adolescentes en sus viajes al extranjero. Se buscan monitores dinámicos, con capacidad de organización y resolución de problemas, responsables, con

Se busca monitor/a de natación con experiencia para impartir clases dinámicas y adaptadas.