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Necesitamos incorporar para una de las empresas del GRUPO OZONA en las oficinas de SANTIAGO de COMPOSTELA un (a): ADMINISTRATIVO (A) Los candidatos (as) han de cumplir los siguientes REQUISITOS: • Titulado grado medio o superior en administración, ADE o similar., • Experiencia de al menos 2 años en posiciones administrativas., • Conocimiento de contabilidad y facturación., • Manejo a nivel avanzado de herramientas y paquetes informáticos (Office)., • Conocimiento en el uso y manejo de programas de gestión., • La persona debe tener disponibilidad para desplazarse a la oficina en SANTIAGO DE COMPOSTELA. Habrá posibilidad de algún día de teletrabajo tras la adaptación al puesto y el periodo de formación inicial., • Buscamos una persona confiable, comprometida y motivada, con capacidad para trabajar en equipo, rigurosa, metódica y planificada. Se VALORARÁ: • Experiencia en gestión y presentación de Concursos Públicos. El candidato (a) seleccionado (a), en dependencia de la dirección financiera, se incorporará al departamento de administración y asumirá FUNCIONES administrativas tales como facturación, gestión de proveedores, gestión de cobros, pedidos cliente, altas de proyecto, compras, ventas, apoyo en la gestión de los RRHH, etc. Se OFRECE: • Posición estable, con posibilidades de desarrollo y crecimiento profesional en una empresa consolidada con buen ambiente laboral., • Contrato indefinido con horario flexible y posibilidad de modalidad híbrida de trabajo (presencial + teletrabajo). GARANTIZAMOS ABSOLUTA CONFIDENCIALIDAD A TODOS (AS) LOS (AS) CANDIDATOS (AS)

Position Description FEUGA is seeking a professional specialised in the management of European Research and Innovation programmes to manage a MSCA COFUND project. The position requires solid knowledge of MSCA procedures, obligations and principles, as well as strong management, technical writing, planning and communication skills in multicultural environments. Main Responsibilities 1. Management of the TALENTGAL – MSCA COFUND Programme • Operational implementation of the programme in compliance with Horizon Europe MSCA COFUND requirements., • Coordination with the beneficiary entity and other national and international partners., • Preparation and follow-up of documentation: deliverables, technical and administrative reports., • Monitoring programme progress, risks, milestones and KPIs., • Financial monitoring of the project in accordance with the Horizon Europe Model Grant Agreement., • Preparation of documentation for reporting, audits and mid-term review. 2. Management of MSCA COFUND Calls • Organisation of the evaluation and selection process, ensuring compliance with OTM-R principles and MSCA criteria (mobility, eligibility, international panels, transparent criteria)., • Identification and management of expert evaluators (national and international) and support during the evaluation and redress processes., • Coordination of the publication of TALENTGAL calls on EURAXESS and other dissemination channels. 3. Training, Mobility and Career Development of Researchers • Monitoring of Career Development Plans., • Coordination with supervisors and monitoring committees., • Organisation of secondments and programme-specific training activities. 4. Coordination of the Programme Management Team • Close coordination with the communication manager to ensure coherence between programme implementation and external communication (calls, news, results, etc.)., • Coordination with the knowledge transfer manager to provide information on the progress of researchers’ projects and facilitate the identification of results with potential for valorisation and exploitation., • Ensuring efficient internal information flows among all entities and individuals involved in programme management., • Contribution to the joint planning of tasks, deadlines and milestones within the management team, aligned with MSCA COFUND obligations. RequirementsEducation • University degree (Bachelor or equivalent)., • A Master’s degree, MBA or PhD will be considered an asset. Experience Essential: • Direct experience in the management or coordination of MSCA COFUND programmes (H2020 or Horizon Europe), including interaction with REA, use of SyGMa, management of mandatory deliverables, reporting, verification of MSCA rules (mobility, eligibility) and compliance with OTM-R principles., • Participation in the drafting of MSCA or European R&I proposals., • C1 level of English (spoken and written)., • Strong planning, organisational and prioritisation skills in deadline-driven environments., • Technical writing and communication skills in a scientific-administrative context., • Availability for occasional travel. What We Offer • Full-time contract at FEUGA., • Salary according to experience., • International and highly collaborative professional environment., • Possibility of partial remote work., • Intensive working hours during summer and two days per week throughout the year., • Access to continuous training and professional development opportunities. About FEUGA FEUGA is a private non-profit foundation based in Galicia, Spain, with a permanent office in Brussels. With more than 40 years of experience in innovation management, FEUGA has established itself as a leading organization in the field of knowledge and technology transfer from the Galician University System (SUG) to the industry players and society in general. Its mission is to bring the talent and scientific and technical expertise generated by university research groups closer to the market, in order to foster entrepreneurship, job creation, the competitiveness of the productive sector, and the dynamism of the regional R&D&I system. It is currently partening in more than 40 EU funded projects. At FEUGA, we firmly believe in equal opportunities as the foundation of a more innovative and fair society. We work to build an inclusive and diverse working environment, where everyone can develop and contribute their talent without barriers or discrimination. Our recruitment processes are governed by fairness and transparency, with no distinction based on gender, gender identity or expression, sexual orientation, origin, age, religion or disability. Because only through equality can we continue to foster the knowledge and innovation that drive FEUGA, we would be delighted to have you join us.

Soltel Group continúa creciendo. Somos una compañía IT con un sólido proyecto empresarial con más de 800 profesionales especializados en Ingeniería de Sistemas, Ingeniería de Software, Soporte Tecnológico, Asistencia Técnica, I+D+i y Smart Cities. Abrimos una nueva posición para perfil de Técnicos/as de microinformática en aeropuertos de Santiago, A Coruña y Vigo, en modalidad presencial. ✅ Requisitos • Titulación ◦ Grado Medio (SMR): Técnico/a en Sistemas Microinformáticos y Redes ◦ Grado Superior (ASIR): Técnico/a Superior en Administración de Sistemas Informáticos en Red o titulación equivalente • Experiencia profesional: mínimo 2 años en operación o soporte microinformático, • Idiomas: inglés nivel B1 Conocimientos técnicos: • Sistemas operativos Windows 10 o superior, • Microsoft 365 (Office, Teams, OneDrive, Outlook), • Configuración de correo y redes (VPN, TCP/IP), • Hardware y periféricos (instalación de componentes y drivers), • Dispositivos móviles Android/iOS 🛠️ Funciones principales • Atención y soporte a personas usuarias (presencial y remoto), • Instalación y configuración de equipos y aplicaciones corporativas, • Configuración y soporte de smartphones y tabletas, • Gestión de inventario y control de activos, • Mantenimiento y reparación de hardware, • Soporte básico de red y parcheo, • Soporte de impresión (impresoras, escáneres, plotters), • Traslado y reinstalación de equipos 📍 Ubicación de los puestos A Coruña, Santiago y Vigo. Qué te ofrecemos? Soltel Group te da la oportunidad de: • Trabajar con tecnologías emergentes, • Valoramos tu dedicación y te recompensamos por ello con oportunidades de crecimiento a través de la formación continua., • Participar en el Plan Amigo Todo ello con un trato cercano y profesional. Si te encanta la tecnología y los retos, encajarás bien en Soltel Group. ¡Te esperamos!

We are seeking experienced freelance Clinical Research Nurses to support an Acute Ischaemic Stroke study. This is an ad-hoc role with flexible scheduling, ideal for nurses currently working freelance or supporting multiple clients. Perform clinical trial-related procedures including blood sampling and injections ECG performance (recording only; Qualified nurse with a minimum of 3 years post-registration experience Previous clinical trial experience strongly preferred Valid and current GCP certificate (R3) — candidates in progress or planning to obtain soon will be considered (please confirm at submission) All required immunisations up to date Own car and willingness to travel to patient visits Planet Pharma is an American parented Employment Business/Agency that provides global staffing services with its head-quarters in Chicago and our EMEA regional office located in Central London. We have invested significantly in creating a robust international platform that enables us to work compliantly in 30+ countries with a current network of 2500+ active contractors globally as well as a very strong permanent / direct hire recruitment offering. Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs / Writing. We welcome applications from all suitably qualified candidates regardless of their race, sex, disability, religion/belief, sexual orientation or age.

We are seeking experienced freelance Clinical Research Nurses to support an Acute Ischaemic Stroke study. This is an ad-hoc role with flexible scheduling, ideal for nurses currently working freelance or supporting multiple clients. Perform clinical trial-related procedures including blood sampling and injections ECG performance (recording only; Qualified nurse with a minimum of 3 years post-registration experience Previous clinical trial experience strongly preferred Valid and current GCP certificate (R3) — candidates in progress or planning to obtain soon will be considered (please confirm at submission) All required immunisations up to date Own car and willingness to travel to patient visits Planet Pharma is an American parented Employment Business/Agency that provides global staffing services with its head-quarters in Chicago and our EMEA regional office located in Central London. We have invested significantly in creating a robust international platform that enables us to work compliantly in 30+ countries with a current network of 2500+ active contractors globally as well as a very strong permanent / direct hire recruitment offering. Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs / Writing. We welcome applications from all suitably qualified candidates regardless of their race, sex, disability, religion/belief, sexual orientation or age.

We are seeking experienced freelance Clinical Research Nurses to support an Acute Ischaemic Stroke study. This is an ad-hoc role with flexible scheduling, ideal for nurses currently working freelance or supporting multiple clients. Perform clinical trial-related procedures including blood sampling and injections ECG performance (recording only; Qualified nurse with a minimum of 3 years post-registration experience Previous clinical trial experience strongly preferred Valid and current GCP certificate (R3) — candidates in progress or planning to obtain soon will be considered (please confirm at submission) All required immunisations up to date Own car and willingness to travel to patient visits Planet Pharma is an American parented Employment Business/Agency that provides global staffing services with its head-quarters in Chicago and our EMEA regional office located in Central London. We have invested significantly in creating a robust international platform that enables us to work compliantly in 30+ countries with a current network of 2500+ active contractors globally as well as a very strong permanent / direct hire recruitment offering. Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs / Writing. We welcome applications from all suitably qualified candidates regardless of their race, sex, disability, religion/belief, sexual orientation or age.

We are seeking experienced freelance Clinical Research Nurses to support an Acute Ischaemic Stroke study. This is an ad-hoc role with flexible scheduling, ideal for nurses currently working freelance or supporting multiple clients. Perform clinical trial-related procedures including blood sampling and injections ECG performance (recording only; Qualified nurse with a minimum of 3 years post-registration experience Previous clinical trial experience strongly preferred Valid and current GCP certificate (R3) — candidates in progress or planning to obtain soon will be considered (please confirm at submission) All required immunisations up to date Own car and willingness to travel to patient visits Planet Pharma is an American parented Employment Business/Agency that provides global staffing services with its head-quarters in Chicago and our EMEA regional office located in Central London. We have invested significantly in creating a robust international platform that enables us to work compliantly in 30+ countries with a current network of 2500+ active contractors globally as well as a very strong permanent / direct hire recruitment offering. Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs / Writing. We welcome applications from all suitably qualified candidates regardless of their race, sex, disability, religion/belief, sexual orientation or age.

Somos una compañía IT con un sólido proyecto empresarial con más de 800 profesionales especializados en Ingeniería de Sistemas, Ingeniería de Software, Soporte Tecnológico, Asistencia Técnica, I+D+i y Smart Cities. Abrimos una nueva posición para perfil de Técnicos/as de microinformática en aeropuertos de Santiago, A Coruña y Vigo, en modalidad presencial. ✅ Grado Medio (SMR): Técnico/a en Sistemas Microinformáticos y Redes ◦ Grado Superior (ASIR): Técnico/a Superior en Administración de Sistemas Informáticos en Red Experiencia profesional : mínimo 2 años en operación o soporte microinformático • Idiomas : inglés nivel B1 Conocimientos técnicos: • Sistemas operativos Windows 10 o superior • Microsoft 365 (Office, Teams, OneDrive, Outlook) • Configuración de correo y redes (VPN, TCP/IP) • Hardware y periféricos (instalación de componentes y drivers) • Dispositivos móviles Android/iOS &##Atención y soporte a personas usuarias (presencial y remoto) • Instalación y configuración de equipos y aplicaciones corporativas • Configuración y soporte de smartphones y tabletas • Gestión de inventario y control de activos • Mantenimiento y reparación de hardware • Soporte básico de red y parcheo • Ubicación de los puestos Valoramos tu dedicación y te recompensamos por ello con oportunidades de crecimiento a través de la formación continua. -

We are seeking experienced freelance Clinical Research Nurses to support an Acute Ischaemic Stroke study. This is an ad-hoc role with flexible scheduling, ideal for nurses currently working freelance or supporting multiple clients. Visits will be scheduled well in advance. Study Overview Study Duration: 20 months Visit Duration: Approximately 2 hours per visit Key Responsibilities Conduct patient visits in line with study protocol Perform clinical trial-related procedures including blood sampling and injections Process biological samples, including centrifugation Accurately document study activities in accordance with GCP and protocol requirements Required Clinical Skills Venepuncture Sample processing and centrifugation Subcutaneous injection administration Cannulation ECG performance (recording only; interpretation not required) Port-a-Cath access and de-access Essential Requirements Qualified nurse with a minimum of 3 years post-registration experience At least 1 year of acute clinical experience Previous clinical trial experience strongly preferred Valid and current GCP certificate (R3) — candidates in progress or planning to obtain soon will be considered (please confirm at submission) All required immunisations up to date Own car and willingness to travel to patient visits Flexible availability during weekdays Additional Information This is an ad-hoc role; weekly or monthly hours are not guaranteed initially As additional studies are awarded, opportunities for increased work may become available Candidates must be comfortable working independently and managing schedules across multiple commitments About Planet Pharma: Planet Pharma is an American parented Employment Business/Agency that provides global staffing services with its head-quarters in Chicago and our EMEA regional office located in Central London. We have invested significantly in creating a robust international platform that enables us to work compliantly in 30+ countries with a current network of 2500+ active contractors globally as well as a very strong permanent / direct hire recruitment offering. Our specialist knowledge and close relationships with our clients and the wider industry really makes us unique in our field. Just recently we were recognised by FORBES as the 17th best professional staffing firm, and have won multiple awards from industry accredited bodies for our commitment to excellence and service delivery. We have extensive functional expertise including: Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs / Writing. We are an equal opportunities Recruitment Business and Agency. We welcome applications from all suitably qualified candidates regardless of their race, sex, disability, religion/belief, sexual orientation or age. Please click ‘apply’ or contact Charlotte Fagan (Recruitment Manager) at Planet Pharma for more information: E: T:

Buscas empleo en office, friegaplatos? En Gozón te esperan nuevas oportunidades este enero.