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Somos Terresis (antigua Magnesitas Navarras), nos dedicamos a la extracción y procesamiento de la magnesita, mineral aplicado en la industria agroalimentaria, ambiental y siderúrgica. En dependencia directa del Produc Manager Visiomag precisamos incorporar un/a Técnico/a de Mantenimiento con el objetivo de reforzar el equipo en el Departamento de SAT . Tus principales funciones a desempeñar serán: Realizar el mantenimiento mecánico, eléctrico y/o neumático preventivo y correctivo de las máquinas de medida, según indicaciones del cliente o del responsable. Realizar el montaje y pruebas de nuevas máquinas de medida, atendiendo a los requerimientos del Product Manager y del responsable Comercial de la zona. Garantizar una buena relación comercial con el cliente, realizando la resolución de las reclamaciones comerciales del cliente asignado, atendiendo sus peticiones, analizando las posibles soluciones y coordinándolas con los departamentos de apoyo y con el comercial. Proponer mejoras en la máquinas y/o pruebas de materiales, analizando su funcionamiento in situ, y realizando informes sobre la toma de medida y la análisis del desgaste de refractarios. Requisitos mínimos: Te ofrecemos la oportunidad de unirte a un equipo joven y dinámico, en un momento clave de crecimiento. Si cumples con los requisitos, ¡no dudes en postularte a esta oferta! Necesario Formación Profesional de Grado Superior en Electromecánica y/o Eléctrica o Grado de ingeniería en ramas similares. Experiencia mínima de 2 años desempeñando funciones similares, valorable sector siderúrgico. Indispensable inglés avanzado . Se realizará prueba. Disponibilidad para realizar viajes nacionales e internacionales. Necesario conocimientos ofimática nivel usuario (Outlook, Excel, Word). Residir en Navarra, Guipúzcoa o Vizcaya. Competencias personales: Persona organizada y autónoma en el desempeño de sus funciones. Alta orientación al cliente y capacidad resolutiva. Buenas habilidades de comunicación y de trabajo en equipo. Ofrecemos: Contrato estable y oportunidades de desarrollo profesional. Salario competitivo y beneficios sociales. Ambiente de trabajo agradable y colaborativo. Formación continua y actualizaciones técnicas.

Career Development Opportunity Are you looking for an opportunity to develop your professional career in a CDMO Manufacturing Operations Department? From day one on, 3PBIOVIAN has been inspired from the people that conforms it, and because of that matter, one of the main values of the company has always been the professional and personal growth of its employees in an international and biotechnological environment. Due to this prioritization, Navarra site of 3PBIOVIAN is currently looking for professionals who want to focus their careers in Scale Up and Manufacturing department USP and DSP both. As 3PBIOVIAN is committed to the continuous, updated and personalized improvement of our personnel´s learning, our Learning and Development department is focused in offering opportunities for professional growth and opting for an environment of trust. The successful candidate will join 3PBIOVIAN, in Navarra, Spain, as part of our Scale Up and Manufacturing department. The candidate will be expected to provide strategic development oversight know-how and technical input in specific tasks and in the group in general. In addition, the candidate will be involved in the manufacturing to obtain products (biomass or recombinant proteins) with the specifications required by our clients, in the execution of the tech transfer processes; as well as contribution to routine laboratory activities. What we´re looking for: Experience in either Manufacturing departments in upstream and/or downstream processes, in the biotechnological industry. People who have performed manufacturing activities in either the Upstream processing or Downstream processing area according to GMP guidelines, ensuring batch execution, evaluating test results, resolving issues and make proposals for resolution. People who assists document preparation (e.g electronic batch records, SOPs) specific to the assigned manufacturing area. Experience in working with bioreactor and filtration systems is desirable. Experience in a GMP environment. Proven initiative and independent thinking to deliver tasks on time, whilst working in a team environment. A person capable to identify technical and scientific problems and discuss possible solutions. Fluency in Spanish, fluency in English is considered a plus. Open to work in shifts. What we offer: A permanent and stable position in a competitive growing company. A competitive time off package with 41 paid days of vacation. Flexible compensation plan, allowing all employees to allocate up to 30% of their gross annual salary to daily services exempt from income taxes (childcare, health insurance, academic training etc.) All new hires who reside outside Navarra are provided with a relocation service and/or assistance. Company benefits club, which allows 3PBIOVIAN employees to obtain exclusive prices and discounts on a multitude of products and services (Booking, FNAC, Rituals, El Corte Inglés etc.) 3PBio is committed to the continuous, updated and personalized improvement of our personnel's learning. To this end, we have Learning & Development department, who is in charge of creating personalized, individualized and differentiating career plans for our employees. The company continues to focus on internal talent and stable employment, focusing on upskilling and reskilling. We offer opportunities for professional growth and take an environment of trust. We encourage the participation of our employees in solidarity events such as charity races, social donations... We have several programs aimed at improving the physical, psychological and emotional well-being of our employees. In this context, we participate in the Corporate Challenge, promote healthy lunches and comfortable and safe work spaces. We have a high-impact work environment with flat hierarchies and short decision-making processes. And so much more! Do you want to know us better? It´s within us.

Career Development Opportunity Are you looking for an opportunity to develop your professional career in a CDMO Manufacturing Operations Department? From day one on, 3PBIOVIAN has been inspired from the people that conforms it, and because of that matter, one of the main values of the company has always been the professional and personal growth of its employees in an international and biotechnological environment. Due to this prioritization, Navarra site of 3PBIOVIAN is currently looking for professionals who want to focus their careers in Scale Up and Manufacturing department USP and DSP both. As 3PBIOVIAN is committed to the continuous, updated and personalized improvement of our personnel´s learning, our Learning and Development department is focused in offering opportunities for professional growth and opting for an environment of trust. The successful candidate will join 3PBIOVIAN, in Navarra, Spain, as part of our Scale Up and Manufacturing department. The candidate will be expected to provide strategic development oversight know-how and technical input in specific tasks and in the group in general. In addition, the candidate will be involved in the manufacturing to obtain products (biomass or recombinant proteins) with the specifications required by our clients, in the execution of the tech transfer processes; as well as contribution to routine laboratory activities. What we´re looking for: Experience in either Manufacturing departments in upstream and/or downstream processes, in the biotechnological industry. People who have performed manufacturing activities in either the Upstream processing or Downstream processing area according to GMP guidelines, ensuring batch execution, evaluating test results, resolving issues and make proposals for resolution. People who assists document preparation (e.g electronic batch records, SOPs) specific to the assigned manufacturing area. Experience in working with bioreactor and filtration systems is desirable. Experience in a GMP environment. Proven initiative and independent thinking to deliver tasks on time, whilst working in a team environment. A person capable to identify technical and scientific problems and discuss possible solutions. Fluency in Spanish, fluency in English is considered a plus. Open to work in shifts. What we offer: A permanent and stable position in a competitive growing company. A competitive time off package with 41 paid days of vacation. Flexible compensation plan, allowing all employees to allocate up to 30% of their gross annual salary to daily services exempt from income taxes (childcare, health insurance, academic training etc.) All new hires who reside outside Navarra are provided with a relocation service and/or assistance. Company benefits club, which allows 3PBIOVIAN employees to obtain exclusive prices and discounts on a multitude of products and services (Booking, FNAC, Rituals, El Corte Inglés etc.) 3PBio is committed to the continuous, updated and personalized improvement of our personnel's learning. To this end, we have Learning & Development department, who is in charge of creating personalized, individualized and differentiating career plans for our employees. The company continues to focus on internal talent and stable employment, focusing on upskilling and reskilling. We offer opportunities for professional growth and take an environment of trust. We encourage the participation of our employees in solidarity events such as charity races, social donations... We have several programs aimed at improving the physical, psychological and emotional well-being of our employees. In this context, we participate in the Corporate Challenge, promote healthy lunches and comfortable and safe work spaces. We have a high-impact work environment with flat hierarchies and short decision-making processes. And so much more! Do you want to know us better? It´s within us.

Career Development Opportunity Are you looking for an opportunity to develop your professional career in a CDMO Manufacturing Operations Department? From day one on, 3PBIOVIAN has been inspired from the people that conforms it, and because of that matter, one of the main values of the company has always been the professional and personal growth of its employees in an international and biotechnological environment. Due to this prioritization, Navarra site of 3PBIOVIAN is currently looking for professionals who want to focus their careers in Scale Up and Manufacturing department USP and DSP both. As 3PBIOVIAN is committed to the continuous, updated and personalized improvement of our personnel´s learning, our Learning and Development department is focused in offering opportunities for professional growth and opting for an environment of trust. The successful candidate will join 3PBIOVIAN, in Navarra, Spain, as part of our Scale Up and Manufacturing department. The candidate will be expected to provide strategic development oversight know-how and technical input in specific tasks and in the group in general. In addition, the candidate will be involved in the manufacturing to obtain products (biomass or recombinant proteins) with the specifications required by our clients, in the execution of the tech transfer processes; as well as contribution to routine laboratory activities. What we´re looking for: Experience in either Manufacturing departments in upstream and/or downstream processes, in the biotechnological industry. People who have performed manufacturing activities in either the Upstream processing or Downstream processing area according to GMP guidelines, ensuring batch execution, evaluating test results, resolving issues and make proposals for resolution. People who assists document preparation (e.g electronic batch records, SOPs) specific to the assigned manufacturing area. Experience in working with bioreactor and filtration systems is desirable. Experience in a GMP environment. Proven initiative and independent thinking to deliver tasks on time, whilst working in a team environment. A person capable to identify technical and scientific problems and discuss possible solutions. Fluency in Spanish, fluency in English is considered a plus. Open to work in shifts. What we offer: A permanent and stable position in a competitive growing company. A competitive time off package with 41 paid days of vacation. Flexible compensation plan, allowing all employees to allocate up to 30% of their gross annual salary to daily services exempt from income taxes (childcare, health insurance, academic training etc.) All new hires who reside outside Navarra are provided with a relocation service and/or assistance. Company benefits club, which allows 3PBIOVIAN employees to obtain exclusive prices and discounts on a multitude of products and services (Booking, FNAC, Rituals, El Corte Inglés etc.) 3PBio is committed to the continuous, updated and personalized improvement of our personnel's learning. To this end, we have Learning & Development department, who is in charge of creating personalized, individualized and differentiating career plans for our employees. The company continues to focus on internal talent and stable employment, focusing on upskilling and reskilling. We offer opportunities for professional growth and take an environment of trust. We encourage the participation of our employees in solidarity events such as charity races, social donations... We have several programs aimed at improving the physical, psychological and emotional well-being of our employees. In this context, we participate in the Corporate Challenge, promote healthy lunches and comfortable and safe work spaces. We have a high-impact work environment with flat hierarchies and short decision-making processes. And so much more! Do you want to know us better? It´s within us.

Career Development Opportunity Are you looking for an opportunity to develop your professional career in a CDMO Manufacturing Operations Department? From day one on, 3PBIOVIAN has been inspired from the people that conforms it, and because of that matter, one of the main values of the company has always been the professional and personal growth of its employees in an international and biotechnological environment. Due to this prioritization, Navarra site of 3PBIOVIAN is currently looking for professionals who want to focus their careers in Scale Up and Manufacturing department USP and DSP both. As 3PBIOVIAN is committed to the continuous, updated and personalized improvement of our personnel´s learning, our Learning and Development department is focused in offering opportunities for professional growth and opting for an environment of trust. The successful candidate will join 3PBIOVIAN, in Navarra, Spain, as part of our Scale Up and Manufacturing department. The candidate will be expected to provide strategic development oversight know-how and technical input in specific tasks and in the group in general. In addition, the candidate will be involved in the manufacturing to obtain products (biomass or recombinant proteins) with the specifications required by our clients, in the execution of the tech transfer processes; as well as contribution to routine laboratory activities. What we´re looking for: Experience in either Manufacturing departments in upstream and/or downstream processes, in the biotechnological industry. People who have performed manufacturing activities in either the Upstream processing or Downstream processing area according to GMP guidelines, ensuring batch execution, evaluating test results, resolving issues and make proposals for resolution. People who assists document preparation (e.g electronic batch records, SOPs) specific to the assigned manufacturing area. Experience in working with bioreactor and filtration systems is desirable. Experience in a GMP environment. Proven initiative and independent thinking to deliver tasks on time, whilst working in a team environment. A person capable to identify technical and scientific problems and discuss possible solutions. Fluency in Spanish, fluency in English is considered a plus. Open to work in shifts. What we offer: A permanent and stable position in a competitive growing company. A competitive time off package with 41 paid days of vacation. Flexible compensation plan, allowing all employees to allocate up to 30% of their gross annual salary to daily services exempt from income taxes (childcare, health insurance, academic training etc.) All new hires who reside outside Navarra are provided with a relocation service and/or assistance. Company benefits club, which allows 3PBIOVIAN employees to obtain exclusive prices and discounts on a multitude of products and services (Booking, FNAC, Rituals, El Corte Inglés etc.) 3PBio is committed to the continuous, updated and personalized improvement of our personnel's learning. To this end, we have Learning & Development department, who is in charge of creating personalized, individualized and differentiating career plans for our employees. The company continues to focus on internal talent and stable employment, focusing on upskilling and reskilling. We offer opportunities for professional growth and take an environment of trust. We encourage the participation of our employees in solidarity events such as charity races, social donations... We have several programs aimed at improving the physical, psychological and emotional well-being of our employees. In this context, we participate in the Corporate Challenge, promote healthy lunches and comfortable and safe work spaces. We have a high-impact work environment with flat hierarchies and short decision-making processes. And so much more! Do you want to know us better? It´s within us.

Desde Fundación Laboral de la Construcción buscamos un/a Responsable de Formación para nuestro centro de Formación ubicado en Huarte, Navarra. Su misión será dirigir la actividad de formación en el área geográfica del Consejo Territorial de Navarra, en coordinación con Gerencia y según la política y Planes marcados por la Dirección de Formación. La Fundación Laboral de la Construcción es una entidad que trabaja desde hace 30 años para impulsar un sector de la construcción innovador y sostenible, liderando su transformación en los ámbitos del empleo, la formación y la seguridad en el trabajo. ¿Cómo será tu día a día? Desarrollar, liderar y supervisar los proyectos de formación a nivel territorial, de acuerdo a la organización y planificación diseñada para alcanzar los objetivos definidos. Controlar el presupuesto del departamento de Formación en su CT y elaborar el presupuesto de los planes de formación dentro de los límites, criterios y presupuestos de cada programa, estableciendo acciones de seguimiento y correctoras que garanticen un cumplimiento de este. Detectar y preparar convocatorias del Gobierno de Navarra susceptibles de convertirse en proyectos de formación. Participar en jornadas y eventos sobre formación al objeto de difundir acciones que la Fundación Laboral de la Construcción ofrece y pone al servicio del sector. Contribuir y asesorar a empresas del sector con el objetivo de la profesionalización del sector a través de la adquisición de conocimientos profesionales. Análisis y evaluación de la calidad de la formación, creando planes de mejora y acciones que permitan corregir posibles desviaciones. Participar en la elaboración y desarrollo de los productos y servicios de formación con el objetivo de responder a las necesidades específicas de las empresas y personas trabajadoras del sector. Colaborar con Sede Social en los proyectos en los que sea requerido, siguiendo sus directrices para alcanzar los objetivos marcados. ¿Cuáles son los requisitos del puesto? Formación mínima requerida: Formación Universitaria relacionada con el sector de la Construcción, Pedagogía o titulaciones afines. Formación en capacitación de Docentes. Necesaria experiencia como responsable en la gestión y desarrollo de planes de formación. Necesaria experiencia en gestión de planes de formación bonificada y subvencionada. ¿Qué te ofrecemos? Contrato Indefinido a jornada completa. Horario: L y J 8:00-16:15h. M y X 8:00-14:00h y 15:30-17:45h. V 8:00-15:00h. En verano jornada intensiva L-V 8:00-15:00h. Flexibilidad de entrada. 1 día de teletrabajo a la semana. Lugar de trabajo: C/ Bideberri, 56 CP. 31620 Huarte (Navarra). Formación continua a cargo de la empresa. Trabajar en una organización centrada en las personas, donde la colaboración y compañerismo son los pilares de nuestro ambiente. La Fundación Laboral de la Construcción es una organización comprometida con la diversidad y la igualdad en todas sus vertientes, y conforme a su compromiso con la igualdad de trato y oportunidades basa sus procesos de selección sobre criterios de adecuación al perfil, siempre desde el punto de vista de competencias, experiencia y cualificación profesional garantizando en todo momento la no discriminación por razón de género, edad, ideología, procedencia cultural, etc.

En Stonhard , llevamos más de 100 años ayudando a empresas de todo el mundo a proteger y mejorar sus espacios industriales y comerciales mediante soluciones de pavimentos y revestimientos de alto rendimiento. Somos líderes globales en la fabricación e instalación de sistemas continuos de resina, epoxi, poliuretano y MMA, diseñados para ofrecer durabilidad, seguridad, resistencia química y facilidad de mantenimiento en entornos exigentes como industria alimentaria, manufactura, logística, automoción y construcción. Lo que nos diferencia es nuestro modelo de servicio integral: acompañamos al cliente desde el diseño de la solución hasta la instalación final, ofreciendo un único punto de contacto y una garantía completa de producto e instalación. Como Territory Manager , tu misión será desarrollar y consolidar la presencia de Stonhard en Navarra, País Vasco y La Rioja, ayudando a clientes industriales y comerciales a encontrar soluciones duraderas, seguras y adaptadas a sus necesidades operativas. No buscamos únicamente vender un producto: buscamos construir relaciones de confianza y convertirte en un socio estratégico para nuestros clientes, entendiendo sus desafíos y aportando soluciones técnicas de alto valor añadido. Tu trabajo tendrá un impacto directo en el crecimiento del negocio, la satisfacción del cliente y el posicionamiento de Stonhard como referente en el mercado. ¿En esta posición combinarás desarrollo de negocio, gestión de proyectos y asesoramiento técnico-comercial. Gestionar y hacer crecer la facturación del territorio, identificando nuevas cuentas y oportunidades de expansión. • Comprender las necesidades del cliente y ofrecer nuestras soluciones de forma consultiva, aportando valor técnico y comercial. • Desarrollar relaciones sólidas con clientes, proyectistas, ingenierías y usuarios finales, interactuando a distintos niveles de decisión. • Participar en la coordinación y seguimiento de proyectos para asegurar una correcta instalación y una excelente experiencia del cliente. • Trabajar para cumplir y superar los objetivos comerciales definidos. • Mantener actualizada la información y referencias de clientes en el sistema. • Elaborar reportes comerciales y participar activamente en reuniones, ferias y formaciones. • Mantenerse actualizado/a sobre tendencias del mercado, soluciones técnicas y oportunidades de desarrollo en el sector industrial y construcción. ¿Qué te ayudará a tener éxito en esta posición? Buscamos una persona con mentalidad comercial, autonomía y capacidad para generar relaciones de largo plazo, para tener éxito en esta posición, deberías de tener: • Experiencia en ventas B2B y desarrollo de negocio en entornos industriales o de la construcción. • Experiencia gestionando cuentas clave y proyectos comerciales complejos. • Capacidad de negociación e interacción con distintos perfiles y niveles organizativos. • Alto nivel de iniciativa, autonomía y orientación a resultados. • Disponibilidad para viajar y trabajar en modalidad home office. • Nivel fluido de español e inglés. ¿En Stonhard creemos en el desarrollo de las personas y en construir relaciones a largo plazo, tanto con nuestros clientes como con nuestros equipos. Un completo programa de formación e inducción acompañado por un consultor senior. • Contrato de sustitución con posibilidades reales de según performance pasar a contrato indefinido. • La oportunidad de desarrollar tu carrera en una empresa líder mundial en su sector. • Autonomía y responsabilidad real sobre tu territorio y clientes. Si buscas una posición donde puedas combinar desarrollo comercial, relación con clientes y soluciones técnicas de alto valor, nos encantará conocerte!

Programador/a PLC – Siemens TIA Portal (Intralogística). Ubicación: Navarra, España (Pamplona). Sector: Ingeniería / Automatización industrial / Intralogística Experiencia requerida: 2–4 años Sobre el proyecto: Estamos buscando incorporar Programadores/as PLC para un proyecto industrial de intralogística en pleno crecimiento en Navarra. Formarás parte de un entorno técnico altamente especializado, participando en el desarrollo, programación y puesta en marcha de sistemas automatizados para procesos logísticos industriales. Responsabilidades principales Programación de PLCs Siemens utilizando TIA Portal . Desarrollo y puesta en marcha de sistemas de automatización industrial. Integración de equipos en líneas de intralogística (transportadores, sistemas de clasificación, etc.). Diagnóstico y resolución de incidencias en planta. Soporte en fase de commissioning y arranque de instalaciones. Colaboración con equipos de ingeniería y puesta en marcha. Ajustes y optimización de programas PLC según necesidades del proyecto. Requisitos Experiencia de 2 a 4 años como Programador/a PLC . Dominio de Siemens TIA Portal . Experiencia en proyectos de automatización industrial. Conocimiento de procesos de puesta en marcha en planta. Capacidad de trabajo en equipo y resolución de problemas técnicos. Nivel de inglés B2. Proceso de selección: Primera entrevista online (Microsoft Teams) Segunda entrevista presencial Vida en K-LAGAN: También queremos que disfrutes plenamente de la experiencia de formar parte de nuestro equipo. Por eso ofrecemos: Actividades de team building Seguimiento y feedback continuo Departamento de carrera y formación con una amplia oferta de cursos profesionales Eventos especiales: Cena de Verano, Cena de Navidad y Día Solidario Día libre por cumpleaños: ¡disfruta de tu día especial como, donde y con quien quieras! Descuentos en gimnasios, guarderías y más

En Nippon Sanso Homecare somos una compañía especializada en terapias respiratorias domiciliarias y atención a pacientes crónicos en su propio entorno. Trabajamos cada día para mejorar la calidad de vida de pacientes con patologías respiratorias, colaborando estrechamente con profesionales sanitarios y centros hospitalarios. Nuestro propósito es claro: cuidar a las personas allí donde más lo necesitan, en su propio hogar , garantizando excelencia asistencial, seguridad y cercanía. Actualmente buscamos incorporar un/a Responsable Asistencial en Navarra para liderar la operativa de la zona y asegurar un servicio de máxima calidad. ¿Cuál será tu misión? Coordinar y supervisar la actividad asistencial y operativa de la zona, liderando al equipo y garantizando la correcta prestación del servicio de Terapias Respiratorias Domiciliarias, así como la gestión de centros de atención propio, taller y almacén. Responsabilidades principales Liderar, coordinar y desarrollar al equipo asistencial y técnico de la zona (planificación, seguimiento, evaluación y feedback). Coordinar la relación operativa y asistencial con hospitales y centros sanitarios de referencia en la zona. Garantizar la correcta prestación del servicio de Terapias Respiratorias Domiciliarias, asegurando calidad asistencial y cumplimiento de protocolos. Supervisar la planificación diaria de rutas, instalaciones, revisiones y retiradas de equipos. Controlar y analizar los principales KPIs operativos (actividad, tiempos de respuesta, incidencias, calidad de servicio, costes). Gestionar y optimizar los recursos materiales (equipos, almacén, taller, vehículos). Asegurar el cumplimiento normativo en materia de calidad, PRL y procedimientos internos. Detectar oportunidades de mejora en procesos y proponer acciones correctivas. Participar en la elaboración y seguimiento del presupuesto de la zona. Gestionar incidencias complejas con pacientes o centros sanitarios, actuando como referente local. Impulsar un clima de trabajo colaborativo, promoviendo la motivación y el compromiso del equipo. ¿Qué buscamos? Titulación universitaria (valorable sanitaria) Experiencia en gestión de equipos (valorable en sector salud) Valorable experiencia en Terapias Respiratorias Domiciliarias Alta capacidad organizativa y orientación a resultados Habilidades de liderazgo, comunicación y desarrollo de personas Perfil analítico, con manejo de Excel, KPIs y seguimiento de indicadores Carné de conducir ¿Qué ofrecemos? Proyecto estable en compañía referente del sector Entorno profesional, colaborativo y orientado a la mejora continua Desarrollo profesional dentro de un grupo sólido Conciliación y horario flexible

¡Únete a nuestro equipo en Fundación Hospitalarias Navarra! Estamos buscando Especialista en psiquiatría para unirse a nuestro equipo multidisciplinar en nuestros Centros de Navarra. ¿Qué necesitas para aplicar? Título oficial de Licenciado en Medicina y Cirugía (homologado por el Ministerio si es de otro país). Especialista en Psiquiatría , homologado o con perspectivas de homologación en España. ¿Qué ofrecemos? Contrato a jornada completa : estabilidad y seguridad laboral. Desarrollo personal y profesional: Participa de nuestros planes de formación y benefíciate de la apuesta que Fundación Hospitalarias Navarra hace por la formación continua, el desarrollo profesional y la investigación. Equipo de guardias : únete a nuestro equipo de guardias localizadas de Psiquiatría Flexibilidad horaria : equilibrio entre tu vida laboral y personal. Buen ambiente de trabajo : un lugar donde te sentirás valorado. Incorporación inmediata : ¡te esperamos con los brazos abiertos! ¿Qué valoramos? Formación y experiencia en psiquiatría. Habilidad y competencias en trabajo en equipo multidisciplinar. Actitud empática con nuestros pacientes y sus familias. Ética profesional en todas tus acciones. ¡Anímate a trabajar en nuestro equipo! FUNDACIÓN HOSPITALARIAS 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

¿Te gustaría afrontar un nuevo desafío profesional? Desde Securitas Seguridad España S.A, buscamos Técnicos/as de Sistemas de Seguridad para unirse a nuestro equipo en Navarra Securitas es la compañía líder global en soluciones de seguridad, con casi un siglo de historia. Más de 336.000 profesionales en todo el mundo estamos transformando la seguridad privada mediante la innovación, la tecnología y un enfoque centrado en las personas. Nuestro propósito, "Ayudamos a hacer de tu mundo un lugar más seguro", guía cada una de nuestras decisiones y describe el impacto positivo de lo que hacemos. Cultivamos un entorno donde las oportunidades profesionales, el éxito compartido y un liderazgo que empodera, son una realidad. Funciones: - Realizar en forma y plazo las asistencias técnicas que le sean asignadas. - Realizar en forma y plazo los mantenimientos que le sean asignados. - Revisar y anotar en el parte de trabajo todos los materiales usados en cada asistencia y/o mantenimiento. - Llevar un inventario al día del material que le es asignado. - Efectuar el seguimiento de reparaciones de materiales con el Encargado/a Técnico/a para poder finalizar las averías o mantenimientos asignados. - Realizar diariamente los partes de asistencia derivados de su actividad. - Enviar el cierre de las asistencias diariamente. - Realizar las guardias 24*7 que le sean asignadas en cuadrante de rotación semanal. - Velar por el correcto estado de las instalaciones en las que interviene. - Comunicar cualquier deficiencia de las instalaciones en las que interviene al Encargado/a Técnico/a. - Velar por la imagen corporativa de la compañía. Ofrecemos: Contrato indefinido. Salario competitivo acorde a la responsabilidad del puesto. Formación continua. Desarrollo profesional en un contexto internacional. Requisitos mínimos: Estudios: Formación Profesional de Grado Medio: Electricidad o Electrónica o similares. Conocimientos técnicos en servicios de mantenimiento e instalación. Manejo y control de sistemas de seguridad. Ofimática a nivel usuario. Experiencia: En puesto similar, al menos 6 meses. Carné de conducir. Requisitos deseados: Estudios: Formación Profesional de Grado Superior: Electricidad o Electrónica o similares. Cursos de acreditación y/o certificación de fabricantes de sistemas de seguridad. Experiencia: Experiencia en trabajos realizados como instaladores y/o mantenedores. Valorable también experiencia en PCI. Se valorará certificado de discapacidad igual o superior al 33%.

¡Únete a nuestro equipo en Fundación Hospitalarias Navarra! Estamos buscando Especialista en psiquiatría para unirse a nuestro equipo multidisciplinar en nuestros Centros de Navarra. ¿Qué necesitas para aplicar? Título oficial de Licenciado en Medicina y Cirugía (homologado por el Ministerio si es de otro país). Especialista en Psiquiatría , homologado o con perspectivas de homologación en España. ¿Qué ofrecemos? Contrato a jornada completa : estabilidad y seguridad laboral. Desarrollo personal y profesional: Participa de nuestros planes de formación y benefíciate de la apuesta que Fundación Hospitalarias Navarra hace por la formación continua, el desarrollo profesional y la investigación. Equipo de guardias : únete a nuestro equipo de guardias localizadas de Psiquiatría Flexibilidad horaria : equilibrio entre tu vida laboral y personal. Buen ambiente de trabajo : un lugar donde te sentirás valorado. Incorporación inmediata : ¡te esperamos con los brazos abiertos! ¿Qué valoramos? Formación y experiencia en psiquiatría. Habilidad y competencias en trabajo en equipo multidisciplinar. Actitud empática con nuestros pacientes y sus familias. Ética profesional en todas tus acciones. ¡Anímate a trabajar en nuestro equipo! FUNDACIÓN HOSPITALARIAS 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

¡Únete a nuestro equipo en Fundación Hospitalarias Navarra! Estamos buscando Especialista en psiquiatría para unirse a nuestro equipo multidisciplinar en nuestros Centros de Navarra. ¿Qué necesitas para aplicar? Título oficial de Licenciado en Medicina y Cirugía (homologado por el Ministerio si es de otro país). Especialista en Psiquiatría , homologado o con perspectivas de homologación en España. ¿Qué ofrecemos? Contrato a jornada completa : estabilidad y seguridad laboral. Desarrollo personal y profesional: Participa de nuestros planes de formación y benefíciate de la apuesta que Fundación Hospitalarias Navarra hace por la formación continua, el desarrollo profesional y la investigación. Equipo de guardias : únete a nuestro equipo de guardias localizadas de Psiquiatría Flexibilidad horaria : equilibrio entre tu vida laboral y personal. Buen ambiente de trabajo : un lugar donde te sentirás valorado. Incorporación inmediata : ¡te esperamos con los brazos abiertos! ¿Qué valoramos? Formación y experiencia en psiquiatría. Habilidad y competencias en trabajo en equipo multidisciplinar. Actitud empática con nuestros pacientes y sus familias. Ética profesional en todas tus acciones. ¡Anímate a trabajar en nuestro equipo! FUNDACIÓN HOSPITALARIAS 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

¡Únete a nuestro equipo en Fundación Hospitalarias Navarra! Estamos buscando Especialista en psiquiatría para unirse a nuestro equipo multidisciplinar en nuestros Centros de Navarra. ¿Qué necesitas para aplicar? Título oficial de Licenciado en Medicina y Cirugía (homologado por el Ministerio si es de otro país). Especialista en Psiquiatría , homologado o con perspectivas de homologación en España. ¿Qué ofrecemos? Contrato a jornada completa : estabilidad y seguridad laboral. Desarrollo personal y profesional: Participa de nuestros planes de formación y benefíciate de la apuesta que Fundación Hospitalarias Navarra hace por la formación continua, el desarrollo profesional y la investigación. Equipo de guardias : únete a nuestro equipo de guardias localizadas de Psiquiatría Flexibilidad horaria : equilibrio entre tu vida laboral y personal. Buen ambiente de trabajo : un lugar donde te sentirás valorado. Incorporación inmediata : ¡te esperamos con los brazos abiertos! ¿Qué valoramos? Formación y experiencia en psiquiatría. Habilidad y competencias en trabajo en equipo multidisciplinar. Actitud empática con nuestros pacientes y sus familias. Ética profesional en todas tus acciones. ¡Anímate a trabajar en nuestro equipo! FUNDACIÓN HOSPITALARIAS 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

Tienes experiencia gestionando establecimientos hoteleros y te motiva liderar un proyecto con.Director/a Operativo/a de Establecimiento Hostelero.Supervisión de la operativa diaria del hostal, restaurante y lavandería.Liderazgo y coordinación del equipo en el día a día.Organización de turnos y

📢Career Development Opportunity📢 Are you looking for an opportunity to develop your professional career in a CDMO Manufacturing Operations Department? From day one on, 3PBIOVIAN has been inspired from the people that conforms it, and because of that matter, one of the main values of the company has always been the professional and personal growth of its employees in an international and biotechnological environment. Due to this prioritization, Navarra site of 3PBIOVIAN is currently looking for professionals who want to focus their careers in Scale Up and Manufacturing department USP and DSP both. As 3PBIOVIAN is committed to the continuous, updated and personalized improvement of our personnel´s learning, our Learning and Development department is focused in offering opportunities for professional growth and opting for an environment of trust. The successful candidate will join 3PBIOVIAN, in Navarra, Spain, as part of our Scale Up and Manufacturing department. The candidate will be expected to provide strategic development oversight know-how and technical input in specific tasks and in the group in general. In addition, the candidate will be involved in the manufacturing to obtain products (biomass or recombinant proteins) with the specifications required by our clients, in the execution of the tech transfer processes; as well as contribution to routine laboratory activities. 🚀 What we´re looking for: • Experience in either Manufacturing departments in upstream and/or downstream processes, in the biotechnological industry., • People who have performed manufacturing activities in either the Upstream processing or Downstream processing area according to GMP guidelines, ensuring batch execution, evaluating test results, resolving issues and make proposals for resolution., • People who assists document preparation (e.g electronic batch records, SOPs) specific to the assigned manufacturing area., • Experience in working with industrial-scale bioreactor and filtration systems is desirable., • Experience in a GMP environment., • Proven initiative and independent thinking to deliver tasks on time, whilst working in a team environment., • A person capable to identify technical and scientific problems and discuss possible solutions., • Fluency in Spanish, fluency in English is considered a plus., • Open to work in shifts. 💊What we offer: • A permanent and stable position in a competitive growing company., • A competitive time off package with 41 paid days of vacation., • Flexible compensation plan, allowing all employees to allocate up to 30% of their gross annual salary to daily services exempt from income taxes (childcare, health insurance, academic training etc.), • All new hires who reside outside Navarra are provided with a relocation service and/or assistance., • Company benefits club, which allows 3PBIOVIAN employees to obtain exclusive prices and discounts on a multitude of products and services (Booking, FNAC, Rituals, El Corte Inglés etc.), • 3PBio is committed to the continuous, updated and personalized improvement of our personnel's learning. To this end, we have Learning & Development department, who is in charge of creating personalized, individualized and differentiating career plans for our employees., • The company continues to focus on internal talent and stable employment, focusing on upskilling and reskilling. We offer opportunities for professional growth and take an environment of trust., • We encourage the participation of our employees in solidarity events such as charity races, social donations..., • We have several programs aimed at improving the physical, psychological and emotional well-being of our employees. In this context, we participate in the Corporate Challenge, promote healthy lunches and comfortable and safe work spaces., • We have a high-impact work environment with flat hierarchies and short decision-making processes., • And so much more! 💥 Do you want to know us better? 🌟It´s within us.

¿Te gustaría iniciarte en el mundo del mantenimiento de robots? O, ¿Tienes experiencia como técnico de postventa? ¿Te gustaría desarrollarte en una importante empresa multinacional? Si te interesa poder optar a un puesto estable, ¡sigue leyendo porque esta oferta te interesa! Nuestro cliente es una importante compañía dedicada a la fabricación de robots industriales y sistemas de soluciones automatizadas de fabricación que, precisa incorporar de manera estable, directamente por empresa a un/a técnico/a de servicio postventa para las instalaciones ubicadas en la zona de Navarra Tus responsabilidades serán las tareas postventa dentro del departamento de servicio: · Mantenimiento de los robots en casa de cliente, en especial robots Kuka. · Resolución de incidencias y reparaciones en equipos/maquinaria. · Asistencia técnica y apoyo al resto de técnicos de campo y clientes. · Puesta en marcha y programación de celdas robotizadas. · Formación a clientes. Tus beneficios : • contratación directa con cliente, • Salario de entre 25.000 y 30.000 euros brutos/anuales en función de experiencia aportada., • Coche de empresa y dietas. Además, trabajarás en una empresa líder en el sector, con muy buen ambiente de trabajo. Requisitos: • Grado Superior en automatización y robótica, mecatrónica, mantenimiento o similar., • Tener disponibilidad para viajar., • Nivel medio de inglés. La empresa busca perfiles que quieran aprendizaje y desarrollo profesional. Valoramos tu actitud, ganas y compromiso y que quieras desarrollarte en el sector, aportar ideas y crecer. Si te interesa la oferta no lo dudes e inscríbete… ¡TE ESTAMOS ESPERANDO!

Somos un grupo empresarial multinacional, diversificado, innovador y sostenible. Contamos con más de cien años de experiencia en la construcción, promoción y desarrollo de grandes proyectos de infraestructuras y servicios en Europa, Oriente Medio y Latinoamérica. Nuestras líneas de negocio más importantes son la construcción y promoción de infraestructuras y servicios en régimen concesional, ejecución de obras de electrificación ferroviaria, transporte ferroviario de mercancías y servicios de mantenimiento, revisión y reparación de maquinaria ferroviaria. Buscamos incorporar un/a Técnico/a de Calidad y Medio Ambiente para nuestra empresa AZVI, con ubicación en Navarra. Requisitos: • Experiencia: mínimo 2 años desempeñando funciones propias del puesto en el sector de la construcción., • Formación: Ciencias Ambientales, Arquitectura Técnica, otras Ingenierías Superiores y/o Técnicas., • Incorporación inmediata y disponibilidad completa. Ofrecemos la posibilidad de incorporación a una empresa y departamento con retos motivadores y en constante expansión, desarrollo profesional y condiciones económicas competitivas.

Trina Tracker, a global leader tracker solutions provider and business unit of Trina Solar is looking for talented multi-cultural professionals to participate in its international growth. Trina Tracker is positioned among the 5 top global tracker companies with projects deployed in more than 40 countries. Pioneers in R+D+I, we design trackers solutions focused to obtain maximum energy yield at a minimum cost. Todos los posibles candidatos deben leer con atención los siguientes detalles de este trabajo antes de presentar una candidatura. As Trina Solar Tracker continues to expand its capacity, improves its technology and enters new markets, Trina Solar Tracker is always looking for people who are hard-working and passionate about solar energy. From research and development to sales and marketing to manufacturing, Trina Solar Trackers looks for people who thrive in exciting, challenging and dynamic work environments to become a part of our dedicated team of professionals and contribute daily to bringing clean, reliable and cost-effective solar energy solutions to customers around the globe. Join us and our mission to promote and develop solar energy as a source of clean, renewable energy for all. For our team in Spain, we are currently looking for a Global Technical Support Technician. Roles and Responsibilities • Development of software, tools and improved calculation procedures to increase the efficiency of engineering teams, costs, etc., • Technology monitoring and implementation of advanced solutions (AI, Automation, etc.) for the analysis of possibilities for improving the work procedures of the rest of the departments., • Support for digitalization at HQ., • Technical support in after sales, problems in installations, consultations on possibilities of adapting current solutions, • Alignment with the technical team to respond to requirements in customer approval processes, • Analysis of calculation methodologies in new products or developments, • Review of potential problems on new developments for evaluation, study and justification before entering the market phase., • Analysis of new technical documentation such as wind tunnels, corrosion studies, etc for the application in the technical justifications., • Preparation, monitoring and management of cybersecurity procedures in accordance with the requirements of European or international regulations. Study of the applicability of specific customer requirements. Lead related certifications., • Preparation, management and update of product assembly manuals., • Participation in tasks to reduce costs and improve the competitiveness of the company's portfolio., • Support to the sales and pre-sales area for the technical defense of solutions in the offers that require it., • Support in the alignment of the different regions to improve shared information and common decision-making., • Support in the development of the development plans of the product management team., • Active dialogue with third parties of a technical nature such as technical advisors, customer technical teams, technical solution providers and other similar parties., • Strictly comply with the environmental standards established in the company., • Strictly comply with the cybersecurity standards established in the company., • Take into account the responsibilities in terms of prevention, which will be indicated in the prevention plan, coinciding with the responsibilities of the interlocutor with the External Prevention Service., • Be responsible for the efficient use of energy and compliance with policies and procedures., • Work actively with the QHSE manager in the monitoring of the company's management system (Quality, Environment, ORP and energy management)., • To keep the management manager (Quality, Environment, ORP and energy management) permanently informed about any aspects or incidents related to quality management, the environment, prevention and energy management., • Be aware of quality and the environment, as well as risk prevention, including relationships and actions with suppliers and subcontractors., • Training in Civil Engineering / Industrial Engineering with a speciality in structural calculation., • 2 years of experience in calculation of steel structures., • Experience Excel + VBA., • Advanced knowledge of programming (C#, Python, JavaScript)., • Experience in using Robot or Sap2000 calculation software., • Fluent English., • Experience in .NET API (VB.NET/C#), AutoLisp, ObjectARX (C++)., • Knowledge in photovoltaic installations., • Knowledge in topography. xcskxlj, • Knowledge in foundation design.

¿Te gustaría iniciarte en el mundo del mantenimiento de robots? O, ¿Tienes experiencia como técnico de postventa? ¿Te gustaría desarrollarte en una importante empresa multinacional? Si te interesa poder optar a un puesto estable, ¡sigue leyendo porque esta oferta te interesa! Nuestro cliente es una importante compañía dedicada a la fabricación de robots industriales y sistemas de soluciones automatizadas de fabricación que, precisa incorporar de manera estable, directamente por empresa a un/a técnico/a de servicio postventa para las instalaciones ubicadas en la zona de Navarra Tus responsabilidades serán las tareas postventa dentro del departamento de servicio: · Mantenimiento de los robots en casa de cliente, en especial robots Kuka. · Resolución de incidencias y reparaciones en equipos/maquinaria. · Asistencia técnica y apoyo al resto de técnicos de campo y clientes. · Puesta en marcha y programación de celdas robotizadas. · Formación a clientes. Tus beneficios : • contratación directa con cliente, • Salario de entre 25.000 y 30.000 euros brutos/anuales en función de experiencia aportada., • Coche de empresa y dietas. Además, trabajarás en una empresa líder en el sector, con muy buen ambiente de trabajo. Requisitos: • Grado Superior en automatización y robótica, mecatrónica, mantenimiento o similar., • Tener disponibilidad para viajar., • Nivel medio de inglés. La empresa busca perfiles que quieran aprendizaje y desarrollo profesional. Valoramos tu actitud, ganas y compromiso y que quieras desarrollarte en el sector, aportar ideas y crecer. Si te interesa la oferta no lo dudes e inscríbete… ¡TE ESTAMOS ESPERANDO!

📢We are looking for a goal-oriented, proactive, and motivated Downstream Technician to join our Manufacturing Operations Department. 🚀 Main Responsibilities: As a DSP Manufacturing Technician, your responsibilities will include: • Achieve the objectives set by the Team Leader and the DSP manufacturing manager., • Prepare, control and develop processes for the production of recombinant proteins, monoclonal antibodies or similar biological molecules in microorganisms., • Comply with good manufacturing practice (GMP), as well as occupational health and safety standards., • Maintain equipment and facilities in perfect state of repair, ensuring that they are operated according to the manuals provided by the manufacturer., • Conduct and/or supervise chromatographic runs, as well as all other manufacturing operations., • Ensure that the necessary material orders are scheduled in the SAP system to meet the production schedule according to the project and the weekly production plan., • Carry out the control and supervision, the stock of materials needed to perform the daily activities., • Prepare, pack, evaluate and unpack chromatography columns, as well as supervise these operations performed by Operators., • Program chromatography methods in UNICORN to ensure the correct execution of DSP processes., • Prepare and ensure the correct preparation of solutions required for the performance of manufacturing activities., • Participate in internal / external audits as required by the Quality Assurance Department., • Participate in the correct transfer of technologies and resources between companies related to 3P Biopharmaceuticals in collaboration with other departments and your manager. Documentary responsibilities: • Perform the incoming documentation of new equipment from the Scaling and Manufacturing DSP area under the supervision of the Team Leader DSP (FAB)., • Ensure the maintenance of up to date technical documentation of the DSP process, as well as all documentation related to assigned tasks., • Record and manage any quality indicators associated with a scaling and manufacturing process. Participate in the investigation of the same together with the Team Leader DSP (FAB)., • Oversee and write SOPs that correspond to the activities carried out in the Scaling and Manufacturing DSP department., • Prepare the documentation related to the quality system associated with the DSP Scale-up and Manufacturing plant: Deviations; Change Controls; Action Plans; Corrective, preventive and improvement actions, etc.). 📚 Assesment criteria: Education: • Advanced Vocational Training or equivalent in related areas (Biology, Biochemistry, Biotechnology, Chemistry, Health, Clinical Laboratory, etc.)., • University Degree or equivalent in related areas (Biology; Biochemistry; Biotechnology; Chemistry; IPPA; Chemical Engineering, etc.)., • Master's Degree in related areas (Biology; Biochemistry; Biotechnology; Chemistry; IPPA, etc.) is valued but not required. Languages: Fluent in Spanish. Intermediate level of English (Level B2 / First Certificate). Between 1 and 2 years of experience in/with: • GMP/GLP regulations, • Chromatographic equipment, • Packed chromatographic columns, • Experience with ÄKTA, • Experience with Unicorn Other requirements: • Open to work in shifts., • Office Software Package: User Level., • Unicorn Software Package: User Level. 💊Why 3PBiovian? • A permanent and stable position in a competitive growing company., • A competitive time off package with 41 paid days of vacation., • Flexible compensation plan, allowing all employees to allocate up to 30% of their gross annual salary to daily services exempt from income taxes (childcare, health insurance, academic training etc.), • All new hires who reside outside Navarra are provided with a relocation service and/or assistance., • Company benefits club, which allows 3PBIOVIAN employees to obtain exclusive prices and discounts on a multitude of products and services (Booking, FNAC, Rituals, El Corte Inglés etc.), • 3PBio is committed to the continuous, updated and personalized improvement of our personnel's learning. To this end, we have Learning & Development department, who is in charge of creating personalized, individualized and differentiating career plans for our employees., • The company continues to focus on internal talent and stable employment, focusing on upskilling and reskilling. We offer opportunities for professional growth and take an environment of trust., • We encourage the participation of our employees in solidarity events such as charity races, social donations..., • We have several programs aimed at improving the physical, psychological and emotional well-being of our employees. In this context, we participate in the Corporate Challenge, promote healthy lunches and comfortable and safe work spaces., • We have a high-impact work environment with flat hierarchies and short decision-making processes., • ...And so much more! 💥Why us? We know it takes people with passion and a shared purpose to manufacture advanced medicines. We specialize in process development and GMP manufacturing of biologics and cell therapy products using microbial and mammalian expression systems. We are with you on your biologics journey, growing with you and supporting you with process and analytical development, preclinical and clinical supply, and commercial production. With a focus on biotechnology applications in both human and animal health sectors, we offer customized solutions that meet the specific needs of all our clients From development to product delivery, we are with you on your biologics journey. We are a leading global CDMO and preferred partner for pharmaceutical and biotech companies. We have what it takes to help you improve lives. 🌟It's within us.

🚀 About VISCOFAN: Viscofan is the world leader in casings production and distribution representing a unique proposal for the meat industry. With presence in more than 110 countries worldwide 🌍, in more than 1,700 customers, more than 1.200M€ turnover and more than 5,000 employees distributed in 18 countries, Viscofan Group leads not only casing market, but also biotechnology innovations delivering significant medical advances 🔎. We are seeking a Business Controller, who wishes to develop his/her professional career in an international, innovative and fast-paced environment, surrounded by a multidisciplinary and highly qualified team. The position will be based in Tajonar (Pamplona, Navarra), involving commuting to the different factories of the Group. 💡 About the role: The main responsibilities will involve: • Business controlling: Supporting decision-making in areas such as Sales and Operations (Purchasing, Logistics, Production, Maintenance, Energy, etc.) in coordination with colleagues in the department (Corporate & Regional Controllers)., • Industrial controlling: Monitoring production costs and analyzing deviations., • Profitability analysis: Conducting profitability analyses for the main business lines., • Consolidated profitability and margin analysis: Providing consolidated analysis of profitability and margins for customers and products., • Subsidiary support: Assisting various Group subsidiaries with incident resolution, defining global criteria, performing specific analysis, coordinating with local CFOs, and providing training, support, and oversight for plant controllers., • Planning management: Overseeing annual budget processes, budget monitoring, forecasting, and integrating operational budgets across various functions (Purchasing, Sales, Production, etc.)., • Global transfer price monitoring: Managing global monitoring of transfer prices., • Functional reporting & analysis: Conducting functional reporting and analytical studies, including a PowerBI dashboard of key management KPIs. You’re going to be a match if you... 🤗 • Hold a Bachelor's Degree in Business Administration, Economics, or a related field. An MBA or Master’s degree in finance is a plus. Chartered Controller Analyst Certification is an advantage., • Have at least 5 years of experience in consulting, auditing, or industrial controlling (preferably in international environments)., • Are proficient in Excel and have good knowledge of SAP FI/CO. Experience with Power BI or similar data visualization tools is an asset., • Possess strong financial knowledge, including corporate operations, taxation, balance sheet analysis, strategic and business planning, and annual audit processes., • Maintain a customer-focused approach., • Are a self-starter and fast learner who enjoys taking initiative., • Demonstrate a high level of curiosity with a solutions-oriented and problem-solving mindset., • Are able to see the big picture while identifying the crucial details that contribute to it., • Are adaptable and agile, capable of thriving in a fast-paced environment and quickly re-prioritizing in response to internal or external changes., • Value teamwork and promote a positive atmosphere, fostering synergies between colleagues and across work teams., • Are not afraid to take risks and have strong communication skills., • Fluency in English is required as we operate in a global environment. 🙌 Perks & Benefits Permanent contract in a growing, agile, and people-oriented company. Professional challenges that will keep you engaged. Competitive salary. Corporate credit card and cell phone. Health insurance discounts. Discounted tickets for kindergarten. Gym discounts. A positive work environment where you'll experience trust, cooperation, enthusiasm, support for risk-taking, accountability, and equity. Viscofan is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. Ready to take the next step in your career? Apply now!

Buscamos incorporar un/a Técnico/a de Calidad y Medio Ambiente para nuestra empresa AZVI, con ubicación en Navarra.

Tienes experiencia gestionando establecimientos hoteleros y te motiva liderar un proyecto con.Director/a Operativo/a de Establecimiento Hostelero.Supervisión de la operativa diaria del hostal, restaurante y lavandería.Liderazgo y coordinación del equipo en el día a día.Organización de turnos y

Tienes experiencia gestionando establecimientos hoteleros y te motiva liderar un proyecto con.Director/a Operativo/a de Establecimiento Hostelero.Supervisión de la operativa diaria del hostal, restaurante y lavandería.Liderazgo y coordinación del equipo en el día a día.Organización de turnos y

📢Career Development Opportunity📢 Are you looking for an opportunity to develop your professional career in a CDMO Manufacturing Operations Department? From day one on, 3PBIOVIAN has been inspired from the people that conforms it, and because of that matter, one of the main values of the company has always been the professional and personal growth of its employees in an international and biotechnological environment. Due to this prioritization, Navarra site of 3PBIOVIAN is currently looking for professionals who want to focus their careers in Scale Up and Manufacturing department USP and DSP both. As 3PBIOVIAN is committed to the continuous, updated and personalized improvement of our personnel´s learning, our Learning and Development department is focused in offering opportunities for professional growth and opting for an environment of trust. The successful candidate will join 3PBIOVIAN, in Navarra, Spain, as part of our Scale Up and Manufacturing department. The candidate will be expected to provide strategic development oversight know-how and technical input in specific tasks and in the group in general. In addition, the candidate will be involved in the manufacturing to obtain products (biomass or recombinant proteins) with the specifications required by our clients, in the execution of the tech transfer processes; as well as contribution to routine laboratory activities. 🚀 What we´re looking for: • Experience in either Manufacturing departments in upstream and/or downstream processes, in the biotechnological industry., • People who have performed manufacturing activities in either the Upstream processing or Downstream processing area according to GMP guidelines, ensuring batch execution, evaluating test results, resolving issues and make proposals for resolution., • People who assists document preparation (e.g electronic batch records, SOPs) specific to the assigned manufacturing area., • Experience in working with industrial-scale bioreactor and filtration systems is desirable., • Experience in a GMP environment., • Proven initiative and independent thinking to deliver tasks on time, whilst working in a team environment., • A person capable to identify technical and scientific problems and discuss possible solutions., • Fluency in Spanish, fluency in English is considered a plus., • Open to work in shifts. 💊What we offer: • A permanent and stable position in a competitive growing company., • A competitive time off package with 41 paid days of vacation., • Flexible compensation plan, allowing all employees to allocate up to 30% of their gross annual salary to daily services exempt from income taxes (childcare, health insurance, academic training etc.), • All new hires who reside outside Navarra are provided with a relocation service and/or assistance., • Company benefits club, which allows 3PBIOVIAN employees to obtain exclusive prices and discounts on a multitude of products and services (Booking, FNAC, Rituals, El Corte Inglés etc.), • 3PBio is committed to the continuous, updated and personalized improvement of our personnel's learning. To this end, we have Learning & Development department, who is in charge of creating personalized, individualized and differentiating career plans for our employees., • The company continues to focus on internal talent and stable employment, focusing on upskilling and reskilling. We offer opportunities for professional growth and take an environment of trust., • We encourage the participation of our employees in solidarity events such as charity races, social donations..., • We have several programs aimed at improving the physical, psychological and emotional well-being of our employees. In this context, we participate in the Corporate Challenge, promote healthy lunches and comfortable and safe work spaces., • We have a high-impact work environment with flat hierarchies and short decision-making processes., • And so much more! 💥 Do you want to know us better? 🌟It´s within us.

Te gustaría desarrollarte profesionalmente como.Técnico/a de Soporte a Coordinación de Proyectos Industriales.Te atrae trabajar dando soporte directo a la coordinación de proyectos para una planta de automoción de referencia como Volkswagen Navarra?.Si buscas un proyecto estable, técnico y con

Buscamos incorporar un/a Técnico/a de Calidad y Medio Ambiente para nuestra empresa AZVI, con ubicación en Navarra. Contamos con más de cien años de experiencia en la construcción, promoción y desarrollo de grandes proyectos de infraestructuras y servicios en Europa, Oriente Medio y Latinoamé

La enfermera/o de Ensayos Clínicos de la UCEC es responsable de proporcionar una atención de enfermería integral y de calidad a los pacientes oncológicos participantes en ensayos clínicos, así como de coordinar las actividades de enfermería asociadas a los estudios, de acuerdo con los protoco

📢 We are looking for a results-driven, dynamic, and self-motivated Quality Control Supervisor Technician to join our Physicochemical Laboratory. 🚀Main responsibilities: As a Quality Control Supervisor Technician, your responsibilities will include: • Ensure GMP activities in the physicochemical laboratory., • Evaluate and review the technical documentation corresponding to the Quality Control of the physicochemical laboratory, as well as the analytical results in routine manufacturing, validation and transfer activities., • Organize and ensure compliance with the weekly program and coordinate human, material and technical resources to ensure its achievement., • Propose process improvements aimed at improving quality, cost, performance, time and safety of workers and the environment., • To train and qualify the analysts to carry out the controls correctly., • Maintain the installations in perfect state of conservation ensuring that they are operated according to the manuals provided by the manufacturer., • Carry out the drafting and supervision of standard operating procedures (SOP's)., • Carry out the resolution of deviations in the laboratory., • Coordinate the release of raw materials and the analysis of intermediates, drug substances and drug products., • Support stability studies agreed with our customers in collaboration with other technicians., • Provide production quality support in case of incidents that may arise., • Approve and close CAPAS (corrective and preventive actions) arising from deviations and applicable efficacy verification., • Check the correct traceability of the materials consumed in the analysis process. 📚 Assesment criteria: Education: • University Degree or equivalent in Chemistry; Biotechnology; Biology or similar., • Master's degree related to the area of study., • PhD in a related area is valued, but not necessary Languages: • Fluent in Spanish. Intermediate level of English (B1 level / First Certificate) At least 4 years of work experience in/with: • Use of techniques such as HPLC, UV and IR Spectrophotometry, UPLC, Fluorescence, DAD, UV-VIS…, • Experience with recombinant proteins, mAbs, Biosimilar, ADCs (desirable)., • Experience with pharmaceutical regulatory guidelines., • Use of Agilent equipment with Empower 3 software. Other requirements: • Open to work in shifts. 💊 Why 3PBiovian? • A permanent and stable position in a competitive growing company., • A competitive time off package with 41 paid days of vacation., • Flexible compensation plan, allowing all employees to allocate up to 30% of their gross annual salary to daily services exempt from income taxes (childcare, health insurance, academic training etc.), • Company benefits club, which allows 3P Biovian employees to obtain exclusive prices and discounts on a multitude of products and services (Booking, FNAC, Rituals, El Corte Inglés etc.), • All new hires who reside outside Navarra are provided with a relocation service and/or assistance., • ...And so much more! 💥Why us? We know it takes people with passion and a shared purpose to manufacture advanced medicines. We specialize in process development and cGMP manufacturing of biologics and cell therapy products using microbial and mammalian expression systems. We are with you on your biologics journey, growing with you and supporting you with process and analytical development, preclinical and clinical supply, and commercial production. With a focus on biotechnology applications in both human an animal health sectors, we offer customized solutions that meet the specific needs of all our clients From development to product delivery, we are with you on your biologics journey. We are a leading global CDMO and preferred partner for pharmaceutical and biotech companies. We have what it takes to help you improve lives. 🌟It's within us.

En Nippon Sanso Homecare somos una compañía especializada en terapias respiratorias domiciliarias y atención a pacientes crónicos en su propio entorno. Trabajamos cada día para mejorar la calidad de vida de pacientes con patologías respiratorias, colaborando estrechamente con profesionales sanitarios y centros hospitalarios. Nuestro propósito es claro: cuidar a las personas allí donde más lo necesitan, en su propio hogar, garantizando excelencia asistencial, seguridad y cercanía. Actualmente buscamos incorporar un/a Responsable Asistencial en Navarra para liderar la operativa de la zona y asegurar un servicio de máxima calidad. ¿Cuál será tu misión? Coordinar y supervisar la actividad asistencial y operativa de la zona, liderando al equipo y garantizando la correcta prestación del servicio de Terapias Respiratorias Domiciliarias, así como la gestión de centros de atención propio, taller y almacén. Responsabilidades principales • Liderar, coordinar y desarrollar al equipo asistencial y técnico de la zona (planificación, seguimiento, evaluación y feedback)., • Coordinar la relación operativa y asistencial con hospitales y centros sanitarios de referencia en la zona., • Garantizar la correcta prestación del servicio de Terapias Respiratorias Domiciliarias, asegurando calidad asistencial y cumplimiento de protocolos., • Supervisar la planificación diaria de rutas, instalaciones, revisiones y retiradas de equipos., • Controlar y analizar los principales KPIs operativos (actividad, tiempos de respuesta, incidencias, calidad de servicio, costes)., • Gestionar y optimizar los recursos materiales (equipos, almacén, taller, vehículos)., • Asegurar el cumplimiento normativo en materia de calidad, PRL y procedimientos internos., • Detectar oportunidades de mejora en procesos y proponer acciones correctivas., • Participar en la elaboración y seguimiento del presupuesto de la zona., • Gestionar incidencias complejas con pacientes o centros sanitarios, actuando como referente local., • Impulsar un clima de trabajo colaborativo, promoviendo la motivación y el compromiso del equipo. ¿Qué buscamos? • Titulación universitaria (valorable sanitaria), • Experiencia en gestión de equipos (valorable en sector salud), • Valorable experiencia en Terapias Respiratorias Domiciliarias, • Alta capacidad organizativa y orientación a resultados, • Habilidades de liderazgo, comunicación y desarrollo de personas, • Perfil analítico, con manejo de Excel, KPIs y seguimiento de indicadores, • Carné de conducir ¿Qué ofrecemos? • Proyecto estable en compañía referente del sector, • Entorno profesional, colaborativo y orientado a la mejora continua, • Desarrollo profesional dentro de un grupo sólido, • Conciliación y horario flexible

📢 Career Development Opportunity 📢 Are you looking for an opportunity to start your professional career in a CDMO Quality Control Department? From day one on, 3PBIOVIAN has been inspired from the people that conforms it, and because of that matter, one of the main values of the company has always been the professional and personal growth of its employees in an international and biotechnological environment. Due to this prioritization, Navarra site of 3PBIOVIAN is currently looking for professionals who want to focus their careers in Quality Control and digital laboratory systems (LIMS). As 3PBIOVIAN is committed to the continuous, updated and personalized improvement of our personnel´s learning, our Learning and Development department is focused in offering opportunities for professional growth and opting for an environment of trust. 🚀 Main Responsibilities: As a Quality Control Intern, your responsibilities will include: • Provide support in the setup and maintenance of the Laboratory Information Management System (LIMS)., • Collaborate in data entry and the creation of inspection plans within the LIMS software., • Support the LIMS technical team in the development and design of the system., • Assist in the preparation of URS (User Requirement Specifications) and technical datasheets., • Provide support in the tasks assigned within the Quality Control department. 📚 What we´re looking for: • Recent graduates in Biology, Biochemistry, Biotechnology, or related fields., • Fluency in Spanish, fluency in English is considered a plus., • Interest in working in a GMP-regulated environment., • Proven initiative and independent thinking to deliver tasks on time, whilst working in a team environment., • No prior professional experience is required, though any prior experience in QC Department or LIMS Software is a plus. 🧠 Valuable knowledge (non‑mandatory): • STARLIMS (LIMS), • JavaScript, • R and SQL programming, • Crystal Reports (labels, certificates and reports), • Understanding of laboratory workflows, • ELN (Electronic Laboratory Notebook) 💊 Why 3PBiovian? At 3PBiovian, we offer a unique opportunity to start your professional career in a cutting-edge, fast-growing sector. Joining us means becoming part of a leading global company at the forefront of the biopharmaceutical industry. Here, you'll gain invaluable experience in a dynamic, high-impact environment. • Flexible working hours during the week and a reduced workday on Fridays (7 hours)., • Special Summer working day of 7 hours during July and August, as well as 7-hour working days during the first week of September and the last week of December., • Learning & Development: We are committed to the continuous and personalized development of our people. Our dedicated Learning & Development department creates tailored career plans, ensuring you receive the tools and support to reach your full potential., • Internal talent focus: We prioritize the growth of our internal talent, offering stability and opportunities for professional advancement in a supportive and trust-based environment., • We actively encourage our employees to engage in charitable events and social causes, such as charity races and donations, making a real difference in our communities., • Employee well-being: We care about the physical, psychological, and emotional health of our employees, offering wellness programs, Corporate Challenges, healthy lunches, and safe, comfortable workspaces., • Join a dynamic and innovative team in an organization that values flat hierarchies and fast decision-making processes, ensuring you have the agility to thrive in your career. 💥 Do you want to know us better? 🌟It´s within us.

📢 We are looking for a results-driven, dynamic, and self-motivated Quality Control Supervisor Technician to join our Physicochemical Laboratory. 🚀Main responsibilities: As a Quality Control Supervisor Technician, your responsibilities will include: • Ensure GMP activities in the physicochemical laboratory., • Evaluate and review the technical documentation corresponding to the Quality Control of the physicochemical laboratory, as well as the analytical results in routine manufacturing, validation and transfer activities., • Organize and ensure compliance with the weekly program and coordinate human, material and technical resources to ensure its achievement., • Propose process improvements aimed at improving quality, cost, performance, time and safety of workers and the environment., • To train and qualify the analysts to carry out the controls correctly., • Maintain the installations in perfect state of conservation ensuring that they are operated according to the manuals provided by the manufacturer., • Carry out the drafting and supervision of standard operating procedures (SOP's)., • Carry out the resolution of deviations in the laboratory., • Coordinate the release of raw materials and the analysis of intermediates, drug substances and drug products., • Support stability studies agreed with our customers in collaboration with other technicians., • Provide production quality support in case of incidents that may arise., • Approve and close CAPAS (corrective and preventive actions) arising from deviations and applicable efficacy verification., • Check the correct traceability of the materials consumed in the analysis process. 📚 Assesment criteria: Education: • University Degree or equivalent in Chemistry; Biotechnology; Biology or similar., • Master's degree related to the area of study., • PhD in a related area is valued, but not necessary Languages: • Fluent in Spanish. Intermediate level of English (B1 level / First Certificate) At least 4 years of work experience in/with: • Use of techniques such as HPLC, UV and IR Spectrophotometry, UPLC, Fluorescence, DAD, UV-VIS…, • Experience with recombinant proteins, mAbs, Biosimilar, ADCs (desirable)., • Experience with pharmaceutical regulatory guidelines., • Use of Agilent equipment with Empower 3 software. Other requirements: • Open to work in shifts. 💊 Why 3PBiovian? • A permanent and stable position in a competitive growing company., • A competitive time off package with 41 paid days of vacation., • Flexible compensation plan, allowing all employees to allocate up to 30% of their gross annual salary to daily services exempt from income taxes (childcare, health insurance, academic training etc.), • Company benefits club, which allows 3P Biovian employees to obtain exclusive prices and discounts on a multitude of products and services (Booking, FNAC, Rituals, El Corte Inglés etc.), • All new hires who reside outside Navarra are provided with a relocation service and/or assistance., • ...And so much more! 💥Why us? We know it takes people with passion and a shared purpose to manufacture advanced medicines. We specialize in process development and cGMP manufacturing of biologics and cell therapy products using microbial and mammalian expression systems. We are with you on your biologics journey, growing with you and supporting you with process and analytical development, preclinical and clinical supply, and commercial production. With a focus on biotechnology applications in both human an animal health sectors, we offer customized solutions that meet the specific needs of all our clients From development to product delivery, we are with you on your biologics journey. We are a leading global CDMO and preferred partner for pharmaceutical and biotech companies. We have what it takes to help you improve lives. 🌟It's within us.

📢We are looking for a goal-oriented, proactive, and motivated Downstream Technician to join our Manufacturing Operations Department. 🚀 Main Responsibilities: As a DSP Manufacturing Technician, your responsibilities will include: • Achieve the objectives set by the Team Leader and the DSP manufacturing manager., • Prepare, control and develop processes for the production of recombinant proteins, monoclonal antibodies or similar biological molecules in microorganisms., • Comply with good manufacturing practice (GMP), as well as occupational health and safety standards., • Maintain equipment and facilities in perfect state of repair, ensuring that they are operated according to the manuals provided by the manufacturer., • Conduct and/or supervise chromatographic runs, as well as all other manufacturing operations., • Ensure that the necessary material orders are scheduled in the SAP system to meet the production schedule according to the project and the weekly production plan., • Carry out the control and supervision, the stock of materials needed to perform the daily activities., • Prepare, pack, evaluate and unpack chromatography columns, as well as supervise these operations performed by Operators., • Program chromatography methods in UNICORN to ensure the correct execution of DSP processes., • Prepare and ensure the correct preparation of solutions required for the performance of manufacturing activities., • Participate in internal / external audits as required by the Quality Assurance Department., • Participate in the correct transfer of technologies and resources between companies related to 3P Biopharmaceuticals in collaboration with other departments and your manager. Documentary responsibilities: • Perform the incoming documentation of new equipment from the Scaling and Manufacturing DSP area under the supervision of the Team Leader DSP (FAB)., • Ensure the maintenance of up to date technical documentation of the DSP process, as well as all documentation related to assigned tasks., • Record and manage any quality indicators associated with a scaling and manufacturing process. Participate in the investigation of the same together with the Team Leader DSP (FAB)., • Oversee and write SOPs that correspond to the activities carried out in the Scaling and Manufacturing DSP department., • Prepare the documentation related to the quality system associated with the DSP Scale-up and Manufacturing plant: Deviations; Change Controls; Action Plans; Corrective, preventive and improvement actions, etc.). 📚 Assesment criteria: Education: • Advanced Vocational Training or equivalent in related areas (Biology, Biochemistry, Biotechnology, Chemistry, Health, Clinical Laboratory, etc.)., • University Degree or equivalent in related areas (Biology; Biochemistry; Biotechnology; Chemistry; IPPA; Chemical Engineering, etc.)., • Master's Degree in related areas (Biology; Biochemistry; Biotechnology; Chemistry; IPPA, etc.) is valued but not required. Languages: Fluent in Spanish. Intermediate level of English (Level B2 / First Certificate). Between 1 and 2 years of experience in/with: • GMP/GLP regulations, • Chromatographic equipment, • Packed chromatographic columns, • Experience with ÄKTA, • Experience with Unicorn Other requirements: • Open to work in shifts., • Office Software Package: User Level., • Unicorn Software Package: User Level. 💊Why 3PBiovian? • A permanent and stable position in a competitive growing company., • A competitive time off package with 41 paid days of vacation., • Flexible compensation plan, allowing all employees to allocate up to 30% of their gross annual salary to daily services exempt from income taxes (childcare, health insurance, academic training etc.), • All new hires who reside outside Navarra are provided with a relocation service and/or assistance., • Company benefits club, which allows 3PBIOVIAN employees to obtain exclusive prices and discounts on a multitude of products and services (Booking, FNAC, Rituals, El Corte Inglés etc.), • 3PBio is committed to the continuous, updated and personalized improvement of our personnel's learning. To this end, we have Learning & Development department, who is in charge of creating personalized, individualized and differentiating career plans for our employees., • The company continues to focus on internal talent and stable employment, focusing on upskilling and reskilling. We offer opportunities for professional growth and take an environment of trust., • We encourage the participation of our employees in solidarity events such as charity races, social donations..., • We have several programs aimed at improving the physical, psychological and emotional well-being of our employees. In this context, we participate in the Corporate Challenge, promote healthy lunches and comfortable and safe work spaces., • We have a high-impact work environment with flat hierarchies and short decision-making processes., • ...And so much more! 💥Why us? We know it takes people with passion and a shared purpose to manufacture advanced medicines. We specialize in process development and GMP manufacturing of biologics and cell therapy products using microbial and mammalian expression systems. We are with you on your biologics journey, growing with you and supporting you with process and analytical development, preclinical and clinical supply, and commercial production. With a focus on biotechnology applications in both human and animal health sectors, we offer customized solutions that meet the specific needs of all our clients From development to product delivery, we are with you on your biologics journey. We are a leading global CDMO and preferred partner for pharmaceutical and biotech companies. We have what it takes to help you improve lives. 🌟It's within us.

📢We are looking for a results-driven, enthusiastic and proactive Upstream Technician to join our Manufacturing Operations Department. 🚀 Main Responsibilities: As a USP Manufacturing Technician, your responsibilities will include: • Ensure the timely compliance with the planning of the USP Scale-Up and Manufacturing department previously made by a Team leader., • Ensure the correct training of the personnel in charge., • Prepare, control and develop processes for the production of recombinant proteins, monoclonal antibodies or similar biological molecules in microorganisms., • Participate in internal / external audits as required by the Quality Assurance Department., • Comply and ensure compliance with GMP standards within the work team., • Record and manage any quality indicators associated with a scale-up and manufacturing process. Participate in the investigation of the same together with the Team Leader USP (FAB)., • Investigate and propose new methods or process innovations to optimize and improve the work in the area., • Ensure proper compliance with regulations and correct completion of current documentation., • Participate in the correct transfer of technologies and resources between companies related to 3P Biopharmaceuticals in collaboration with other departments and their manager., • Perform the entry documentation of new equipment from the USP Scale-up and Manufacturing area under the supervision of the Team Leader USP (FAB)., • Supervise the correct completion of the new equipment entry documentation., • Supervise the correct training of the personnel in charge, if any., • Carry out the distribution and supervision of daily activities., • Write and keep updated the documentation associated with the production processes carried out in the USP area., • Control / monitoring of orders placed in the USP production area using ERP software. 📚 Assesment criteria: Education: Bachelor's degree in Pharmacy; Biology; Biochemistry; Biotechnology; Chemistry; IPPA; Chemical Engineering, cell culture etc . Desirable but not required Master's degree or equivalent in related fields. Languages: Fluent in Spanish. Intermediate level of English (Level B2 / First Certificate). Between 1 and 2 years of experience in/with: • GMP/GLP regulations, • With industrial-scale bioreactors, • Cell Cultures, • Microbiological analysis techniques, • Upstream production positions, • Biotechnology / Biopharmaceutical Sector Other requirements: • Open to work in shifts., • Software package: Office. User level. 💊Why 3PBiovian? • A permanent and stable position in a competitive growing company., • A competitive time off package with 41 paid days of vacation., • Flexible compensation plan, allowing all employees to allocate up to 30% of their gross annual salary to daily services exempt from income taxes (childcare, health insurance, academic training etc.), • All new hires who reside outside Navarra are provided with a relocation service and/or assistance., • Company benefits club, which allows 3PBIOVIAN employees to obtain exclusive prices and discounts on a multitude of products and services (Booking, FNAC, Rituals, El Corte Inglés etc.), • 3PBio is committed to the continuous, updated and personalized improvement of our personnel's learning. To this end, we have Learning & Development department, who is in charge of creating personalized, individualized and differentiating career plans for our employees., • The company continues to focus on internal talent and stable employment, focusing on upskilling and reskilling. We offer opportunities for professional growth and take an environment of trust., • We encourage the participation of our employees in solidarity events such as charity races, social donations..., • We have several programs aimed at improving the physical, psychological and emotional well-being of our employees. In this context, we participate in the Corporate Challenge, promote healthy lunches and comfortable and safe work spaces., • We have a high-impact work environment with flat hierarchies and short decision-making processes., • ...And so much more! 💥Why us? We know it takes people with passion and a shared purpose to manufacture advanced medicines. We specialize in process development and GMP manufacturing of biologics and cell therapy products using microbial and mammalian expression systems. We are with you on your biologics journey, growing with you and supporting you with process and analytical development, preclinical and clinical supply, and commercial production. With a focus on biotechnology applications in both human and animal health sectors, we offer customized solutions that meet the specific needs of all our clients From development to product delivery, we are with you on your biologics journey. We are a leading global CDMO and preferred partner for pharmaceutical and biotech companies. We have what it takes to help you improve lives. 🌟It's within us.

TE MOTIVA PARTICIPAR EN EL LANZAMIENTO DE NUEVOS MODELOS Y ASEGURAR LA CALIDAD DESDE EL PRIMER DÍA?.Ingeniero/a o Técnico/a con FP de Grado Superior en Automoción.Garantizar el control, análisis y seguimiento de las reclamaciones de red durante las fases de lanzamiento de vehículo, asegurando e

En Volkswagen Navarra buscamos un/a.

En Volkswagen Navarra buscamos un/a.

We are looking for a goal-oriented, proactive, and motivated Downstream Technician to join our Manufacturing Operations Department. Habilidades, experiencia, cualificaciones... Si tiene el perfil adecuado para esta oportunidad, asegúrese de inscribirse hoy mismo. Main Responsibilities: As a DSP Manufacturing Technician , your responsibilities will include: • Achieve the objectives set by the Team Leader and the DSP manufacturing manager., • Prepare, control and develop processes for the production of recombinant proteins, monoclonal antibodies or similar biological molecules in microorganisms., • Comply with good manufacturing practice (GMP), as well as occupational health and safety standards., • Maintain equipment and facilities in perfect state of repair, ensuring that they are operated according to the manuals provided by the manufacturer., • Conduct and/or supervise chromatographic runs, as well as all other manufacturing operations., • Ensure that the necessary material orders are scheduled in the SAP system to meet the production schedule according to the project and the weekly production plan., • Carry out the control and supervision, the stock of materials needed to perform the daily activities., • Prepare, pack, evaluate and unpack chromatography columns, as well as supervise these operations performed by Operators., • Program chromatography methods in UNICORN to ensure the correct execution of DSP processes., • Prepare and ensure the correct preparation of solutions required for the performance of manufacturing activities., • Participate in internal / external audits as required by the Quality Assurance Department., • Perform the incoming documentation of new equipment from the Scaling and Manufacturing DSP area under the supervision of the Team Leader DSP (FAB)., • Ensure the maintenance of up to date technical documentation of the DSP process, as well as all documentation related to assigned tasks., • Record and manage any quality indicators associated with a scaling and manufacturing process. Participate in the investigation of the same together with the Team Leader DSP (FAB)., • Oversee and write SOPs that correspond to the activities carried out in the Scaling and Manufacturing DSP department. Education: • Advanced Vocational Training or equivalent in related areas (Biology, Biochemistry, Biotechnology, Chemistry, Health, Clinical Laboratory, etc.)., • University Degree or equivalent in related areas (Biology; Biochemistry; Biotechnology; Chemistry; IPPA; Chemical Engineering, etc.). Between 1 and 2 years of experience in/with: • GMP/GLP regulations, • Chromatographic equipment, • Packed chromatographic columns, • Experience with ÄKTA, • Open to work in shifts., • Office Software Package: User Level., • A permanent and stable position in a competitive growing company., • A competitive time off package with 41 paid days of vacation., • Flexible compensation plan, allowing all employees to allocate up to 30% of their gross annual salary to daily services exempt from income taxes (childcare, health insurance, academic training etc.), • All new hires who reside outside Navarra are provided with a relocation service and/or assistance., • Company benefits club, which allows 3PBIOVIAN employees to obtain exclusive prices and discounts on a multitude of products and services (Booking, FNAC, Rituals, El Corte Inglés etc.), • 3PBio is committed to the continuous, updated and personalized improvement of our personnel's learning. To this end, we have Learning & Development department, who is in charge of creating personalized, individualized and differentiating career plans for our employees., • The company continues to focus on internal talent and stable employment, focusing on upskilling and reskilling. We offer opportunities for professional growth and take an environment of trust., • We encourage the participation of our employees in solidarity events such as charity races, social donations..., • We have several programs aimed at improving the physical, psychological and emotional well-being of our employees. In this context, we participate in the Corporate Challenge, promote healthy lunches and comfortable and safe work spaces., • We have a high-impact work environment with flat hierarchies and short decision-making processes. We know it takes people with passion and a shared purpose to manufacture advanced medicines. We specialize in process development and GMP manufacturing of biologics and cell therapy products using microbial and mammalian expression systems. We are with you on your biologics journey, growing with you and supporting you with process and analytical development, preclinical and clinical supply, and commercial production. With a focus on biotechnology applications in both human and animal health sectors, we offer customized solutions that meet the specific needs of all our clients From development to product delivery, we are with you on your biologics journey. We are a leading global CDMO and preferred partner for pharmaceutical and biotech companies. xcskxlj We have what it takes to help you improve lives. It's within us.

📢We are looking for a results-driven, enthusiastic and proactive Upstream Technician to join our Manufacturing Operations Department. 🚀 Main Responsibilities: As a USP Manufacturing Technician, your responsibilities will include: • Ensure the timely compliance with the planning of the USP Scale-Up and Manufacturing department previously made by a Team leader., • Ensure the correct training of the personnel in charge., • Prepare, control and develop processes for the production of recombinant proteins, monoclonal antibodies or similar biological molecules in microorganisms., • Participate in internal / external audits as required by the Quality Assurance Department., • Comply and ensure compliance with GMP standards within the work team., • Record and manage any quality indicators associated with a scale-up and manufacturing process. Participate in the investigation of the same together with the Team Leader USP (FAB)., • Investigate and propose new methods or process innovations to optimize and improve the work in the area., • Ensure proper compliance with regulations and correct completion of current documentation., • Participate in the correct transfer of technologies and resources between companies related to 3P Biopharmaceuticals in collaboration with other departments and their manager., • Perform the entry documentation of new equipment from the USP Scale-up and Manufacturing area under the supervision of the Team Leader USP (FAB)., • Supervise the correct completion of the new equipment entry documentation., • Supervise the correct training of the personnel in charge, if any., • Carry out the distribution and supervision of daily activities., • Write and keep updated the documentation associated with the production processes carried out in the USP area., • Control / monitoring of orders placed in the USP production area using ERP software. 📚 Assesment criteria: Education: Bachelor's degree in Pharmacy; Biology; Biochemistry; Biotechnology; Chemistry; IPPA; Chemical Engineering, cell culture etc . Desirable but not required Master's degree or equivalent in related fields. Languages: Fluent in Spanish. Intermediate level of English (Level B2 / First Certificate). Between 1 and 2 years of experience in/with: • GMP/GLP regulations, • With industrial-scale bioreactors, • Cell Cultures, • Microbiological analysis techniques, • Upstream production positions, • Biotechnology / Biopharmaceutical Sector Other requirements: • Open to work in shifts., • Software package: Office. User level. 💊Why 3PBiovian? • A permanent and stable position in a competitive growing company., • A competitive time off package with 41 paid days of vacation., • Flexible compensation plan, allowing all employees to allocate up to 30% of their gross annual salary to daily services exempt from income taxes (childcare, health insurance, academic training etc.), • All new hires who reside outside Navarra are provided with a relocation service and/or assistance., • Company benefits club, which allows 3PBIOVIAN employees to obtain exclusive prices and discounts on a multitude of products and services (Booking, FNAC, Rituals, El Corte Inglés etc.), • 3PBio is committed to the continuous, updated and personalized improvement of our personnel's learning. To this end, we have Learning & Development department, who is in charge of creating personalized, individualized and differentiating career plans for our employees., • The company continues to focus on internal talent and stable employment, focusing on upskilling and reskilling. We offer opportunities for professional growth and take an environment of trust., • We encourage the participation of our employees in solidarity events such as charity races, social donations..., • We have several programs aimed at improving the physical, psychological and emotional well-being of our employees. In this context, we participate in the Corporate Challenge, promote healthy lunches and comfortable and safe work spaces., • We have a high-impact work environment with flat hierarchies and short decision-making processes., • ...And so much more! 💥Why us? We know it takes people with passion and a shared purpose to manufacture advanced medicines. We specialize in process development and GMP manufacturing of biologics and cell therapy products using microbial and mammalian expression systems. We are with you on your biologics journey, growing with you and supporting you with process and analytical development, preclinical and clinical supply, and commercial production. With a focus on biotechnology applications in both human and animal health sectors, we offer customized solutions that meet the specific needs of all our clients From development to product delivery, we are with you on your biologics journey. We are a leading global CDMO and preferred partner for pharmaceutical and biotech companies. We have what it takes to help you improve lives. 🌟It's within us.

La enfermera/o de Ensayos Clínicos de la UCEC es responsable de proporcionar una atención de enfermería integral y de calidad a los pacientes oncológicos participantes en ensayos clínicos, así como de coordinar las actividades de enfermería asociadas a los estudios, de acuerdo con los protoco

En virtud de ello, desde COPASA nos comprometemos a proporcionar las mismas oportunidades en el acceso al trabajo y a la promoción profesional, procurando que la objetividad presida los procesos de contratación, selección y promoción profesional y que, tanto el proceso de selección como la eval

En virtud de ello, desde COPASA nos comprometemos a proporcionar las mismas oportunidades en el acceso al trabajo y a la promoción profesional, procurando que la objetividad presida los procesos de contratación, selección y promoción profesional y que, tanto el proceso de selección como la eval

Te gustaría desarrollarte profesionalmente como.Técnico/a de Soporte a Coordinación de Proyectos Industriales.Te atrae trabajar dando soporte directo a la coordinación de proyectos para una planta de automoción de referencia como Volkswagen Navarra?.Si buscas un proyecto estable, técnico y con

We are looking for a goal-oriented, proactive, and motivated Experiencia, cualificaciones y habilidades interpersonales, ¿tiene todo lo necesario para triunfar en esta oportunidad? Descúbralo a continuación. Downstream Technician to join our Manufacturing Operations Department. Main Responsibilities: As a DSP Manufacturing Technician , your responsibilities will include: Achieve the objectives set by the Team Leader and the DSP manufacturing manager. Prepare, control and develop processes for the production of recombinant proteins, monoclonal antibodies or similar biological molecules in microorganisms. Comply with good manufacturing practice (GMP), as well as occupational health and safety standards. Maintain equipment and facilities in perfect state of repair, ensuring that they are operated according to the manuals provided by the manufacturer. Conduct and/or supervise chromatographic runs, as well as all other manufacturing operations. Ensure that the necessary material orders are scheduled in the SAP system to meet the production schedule according to the project and the weekly production plan. Carry out the control and supervision, the stock of materials needed to perform the daily activities. Prepare, pack, evaluate and unpack chromatography columns, as well as supervise these operations performed by Operators. Program chromatography methods in UNICORN to ensure the correct execution of DSP processes. Prepare and ensure the correct preparation of solutions required for the performance of manufacturing activities. Participate in internal / external audits as required by the Quality Assurance Department. Participate in the correct transfer of technologies and resources between companies related to 3P Biopharmaceuticals in collaboration with other departments and your manager. Documentary responsibilities: Perform the incoming documentation of new equipment from the Scaling and Manufacturing DSP area under the supervision of the Team Leader DSP (FAB). Ensure the maintenance of up to date technical documentation of the DSP process, as well as all documentation related to assigned tasks. Record and manage any quality indicators associated with a scaling and manufacturing process. Participate in the investigation of the same together with the Team Leader DSP (FAB). Oversee and write SOPs that correspond to the activities carried out in the Scaling and Manufacturing DSP department. Prepare the documentation related to the quality system associated with the DSP Scale-up and Manufacturing plant: Deviations; Change Controls; Action Plans; Corrective, preventive and improvement actions, etc.). Assesment criteria: Education: Advanced Vocational Training or equivalent in related areas (Biology, Biochemistry, Biotechnology, Chemistry, Health, Clinical Laboratory, etc.). University Degree or equivalent in related areas (Biology; Biochemistry; Biotechnology; Chemistry; IPPA; Chemical Engineering, etc.). Master's Degree in related areas (Biology; Biochemistry; Biotechnology; Chemistry; IPPA, etc.) is valued but not required. Languages: Fluent in Spanish. Intermediate level of English (Level B2 / First Certificate). Between 1 and 2 years of experience in/with: GMP/GLP regulations Chromatographic equipment Packed chromatographic columns Experience with ÄKTA Experience with Unicorn Other requirements: Open to work in shifts. Office Software Package: User Level. Unicorn Software Package: User Level. Why 3PBiovian? A permanent and stable position in a competitive growing company. A competitive time off package with 41 paid days of vacation. Flexible compensation plan, allowing all employees to allocate up to 30% of their gross annual salary to daily services exempt from income taxes (childcare, health insurance, academic training etc.) All new hires who reside outside Navarra are provided with a relocation service and/or assistance. Company benefits club, which allows 3PBIOVIAN employees to obtain exclusive prices and discounts on a multitude of products and services (Booking, FNAC, Rituals, El Corte Inglés etc.) 3PBio is committed to the continuous, updated and personalized improvement of our personnel's learning. To this end, we have Learning & Development department, who is in charge of creating personalized, individualized and differentiating career plans for our employees. The company continues to focus on internal talent and stable employment, focusing on upskilling and reskilling. We offer opportunities for professional growth and take an environment of trust. We encourage the participation of our employees in solidarity events such as charity races, social donations... We have several programs aimed at improving the physical, psychological and emotional well-being of our employees. In this context, we participate in the Corporate Challenge, promote healthy lunches and comfortable and safe work spaces. We have a high-impact work environment with flat hierarchies and short decision-making processes. ...And so much more! Why us? We know it takes people with passion and a shared purpose to manufacture advanced medicines. We specialize in process development and GMP manufacturing of biologics and cell therapy products using microbial and mammalian expression systems. We are with you on your biologics journey, growing with you and supporting you with process and analytical development, preclinical and clinical supply, and commercial production. With a focus on biotechnology applications in both human and animal health sectors, we offer customized solutions that meet the specific needs of all our clients From development to product delivery, we are with you on your biologics journey. We are a leading global CDMO and preferred partner for pharmaceutical and biotech companies. xcskxlj We have what it takes to help you improve lives. It's within us.

We are looking for a goal-oriented, proactive, and motivated Experiencia, cualificaciones y habilidades interpersonales, ¿tiene todo lo necesario para triunfar en esta oportunidad? Descúbralo a continuación. Downstream Technician to join our Manufacturing Operations Department. Main Responsibilities: As a DSP Manufacturing Technician , your responsibilities will include: Achieve the objectives set by the Team Leader and the DSP manufacturing manager. Prepare, control and develop processes for the production of recombinant proteins, monoclonal antibodies or similar biological molecules in microorganisms. Comply with good manufacturing practice (GMP), as well as occupational health and safety standards. Maintain equipment and facilities in perfect state of repair, ensuring that they are operated according to the manuals provided by the manufacturer. Conduct and/or supervise chromatographic runs, as well as all other manufacturing operations. Ensure that the necessary material orders are scheduled in the SAP system to meet the production schedule according to the project and the weekly production plan. Carry out the control and supervision, the stock of materials needed to perform the daily activities. Prepare, pack, evaluate and unpack chromatography columns, as well as supervise these operations performed by Operators. Program chromatography methods in UNICORN to ensure the correct execution of DSP processes. Prepare and ensure the correct preparation of solutions required for the performance of manufacturing activities. Participate in internal / external audits as required by the Quality Assurance Department. Participate in the correct transfer of technologies and resources between companies related to 3P Biopharmaceuticals in collaboration with other departments and your manager. Documentary responsibilities: Perform the incoming documentation of new equipment from the Scaling and Manufacturing DSP area under the supervision of the Team Leader DSP (FAB). Ensure the maintenance of up to date technical documentation of the DSP process, as well as all documentation related to assigned tasks. Record and manage any quality indicators associated with a scaling and manufacturing process. Participate in the investigation of the same together with the Team Leader DSP (FAB). Oversee and write SOPs that correspond to the activities carried out in the Scaling and Manufacturing DSP department. Prepare the documentation related to the quality system associated with the DSP Scale-up and Manufacturing plant: Deviations; Change Controls; Action Plans; Corrective, preventive and improvement actions, etc.). Assesment criteria: Education: Advanced Vocational Training or equivalent in related areas (Biology, Biochemistry, Biotechnology, Chemistry, Health, Clinical Laboratory, etc.). University Degree or equivalent in related areas (Biology; Biochemistry; Biotechnology; Chemistry; IPPA; Chemical Engineering, etc.). Master's Degree in related areas (Biology; Biochemistry; Biotechnology; Chemistry; IPPA, etc.) is valued but not required. Languages: Fluent in Spanish. Intermediate level of English (Level B2 / First Certificate). Between 1 and 2 years of experience in/with: GMP/GLP regulations Chromatographic equipment Packed chromatographic columns Experience with ÄKTA Experience with Unicorn Other requirements: Open to work in shifts. Office Software Package: User Level. Unicorn Software Package: User Level. Why 3PBiovian? A permanent and stable position in a competitive growing company. A competitive time off package with 41 paid days of vacation. Flexible compensation plan, allowing all employees to allocate up to 30% of their gross annual salary to daily services exempt from income taxes (childcare, health insurance, academic training etc.) All new hires who reside outside Navarra are provided with a relocation service and/or assistance. Company benefits club, which allows 3PBIOVIAN employees to obtain exclusive prices and discounts on a multitude of products and services (Booking, FNAC, Rituals, El Corte Inglés etc.) 3PBio is committed to the continuous, updated and personalized improvement of our personnel's learning. To this end, we have Learning & Development department, who is in charge of creating personalized, individualized and differentiating career plans for our employees. The company continues to focus on internal talent and stable employment, focusing on upskilling and reskilling. We offer opportunities for professional growth and take an environment of trust. We encourage the participation of our employees in solidarity events such as charity races, social donations... We have several programs aimed at improving the physical, psychological and emotional well-being of our employees. In this context, we participate in the Corporate Challenge, promote healthy lunches and comfortable and safe work spaces. We have a high-impact work environment with flat hierarchies and short decision-making processes. ...And so much more! Why us? We know it takes people with passion and a shared purpose to manufacture advanced medicines. We specialize in process development and GMP manufacturing of biologics and cell therapy products using microbial and mammalian expression systems. We are with you on your biologics journey, growing with you and supporting you with process and analytical development, preclinical and clinical supply, and commercial production. With a focus on biotechnology applications in both human and animal health sectors, we offer customized solutions that meet the specific needs of all our clients From development to product delivery, we are with you on your biologics journey. We are a leading global CDMO and preferred partner for pharmaceutical and biotech companies. xcskxlj We have what it takes to help you improve lives. It's within us.

Buscamos incorporar un/a Técnico/a de Calidad y Medio Ambiente para nuestra empresa AZVI, con ubicación en Navarra.

We are looking for a goal-oriented, proactive, and motivated Downstream Technician to join our Manufacturing Operations Department. Main Responsibilities: As a DSP Manufacturing Technician , your responsibilities will include: • Achieve the objectives set by the Team Leader and the DSP manufacturing manager., • Prepare, control and develop processes for the production of recombinant proteins, monoclonal antibodies or similar biological molecules in microorganisms., • Comply with good manufacturing practice (GMP), as well as occupational health and safety standards., • Maintain equipment and facilities in perfect state of repair, ensuring that they are operated according to the manuals provided by the manufacturer., • Conduct and/or supervise chromatographic runs, as well as all other manufacturing operations., • Ensure that the necessary material orders are scheduled in the SAP system to meet the production schedule according to the project and the weekly production plan., • Carry out the control and supervision, the stock of materials needed to perform the daily activities., • Prepare, pack, evaluate and unpack chromatography columns, as well as supervise these operations performed by Operators., • Program chromatography methods in UNICORN to ensure the correct execution of DSP processes., • Prepare and ensure the correct preparation of solutions required for the performance of manufacturing activities., • Participate in internal / external audits as required by the Quality Assurance Department., • Participate in the correct transfer of technologies and resources between companies related to 3P Biopharmaceuticals in collaboration with other departments and your manager. Documentary responsibilities: • Perform the incoming documentation of new equipment from the Scaling and Manufacturing DSP area under the supervision of the Team Leader DSP (FAB)., • Ensure the maintenance of up to date technical documentation of the DSP process, as well as all documentation related to assigned tasks., • Record and manage any quality indicators associated with a scaling and manufacturing process. Participate in the investigation of the same together with the Team Leader DSP (FAB)., • Oversee and write SOPs that correspond to the activities carried out in the Scaling and Manufacturing DSP department., • Prepare the documentation related to the quality system associated with the DSP Scale-up and Manufacturing plant: Deviations; Change Controls; Action Plans; Corrective, preventive and improvement actions, etc.). Assesment criteria: Education: • Advanced Vocational Training or equivalent in related areas (Biology, Biochemistry, Biotechnology, Chemistry, Health, Clinical Laboratory, etc.)., • University Degree or equivalent in related areas (Biology; Biochemistry; Biotechnology; Chemistry; IPPA; Chemical Engineering, etc.)., • Master's Degree in related areas (Biology; Biochemistry; Biotechnology; Chemistry; IPPA, etc.) is valued but not required. Languages: Fluent in Spanish. Intermediate level of English (Level B2 / First Certificate). Between 1 and 2 years of experience in/with: • GMP/GLP regulations, • Chromatographic equipment, • Packed chromatographic columns, • Experience with ÄKTA, • Experience with Unicorn Other requirements: • Open to work in shifts., • Office Software Package: User Level., • Unicorn Software Package: User Level. Why 3PBiovian? • A permanent and stable position in a competitive growing company., • A competitive time off package with 41 paid days of vacation., • Flexible compensation plan, allowing all employees to allocate up to 30% of their gross annual salary to daily services exempt from income taxes (childcare, health insurance, academic training etc.), • All new hires who reside outside Navarra are provided with a relocation service and/or assistance., • Company benefits club, which allows 3PBIOVIAN employees to obtain exclusive prices and discounts on a multitude of products and services (Booking, FNAC, Rituals, El Corte Inglés etc.), • 3PBio is committed to the continuous, updated and personalized improvement of our personnel's learning. To this end, we have Learning & Development department, who is in charge of creating personalized, individualized and differentiating career plans for our employees., • The company continues to focus on internal talent and stable employment, focusing on upskilling and reskilling. We offer opportunities for professional growth and take an environment of trust., • We encourage the participation of our employees in solidarity events such as charity races, social donations..., • We have several programs aimed at improving the physical, psychological and emotional well-being of our employees. In this context, we participate in the Corporate Challenge, promote healthy lunches and comfortable and safe work spaces., • We have a high-impact work environment with flat hierarchies and short decision-making processes., • ...And so much more! Why us? We know it takes people with passion and a shared purpose to manufacture advanced medicines. We specialize in process development and GMP manufacturing of biologics and cell therapy products using microbial and mammalian expression systems. We are with you on your biologics journey, growing with you and supporting you with process and analytical development, preclinical and clinical supply, and commercial production. With a focus on biotechnology applications in both human and animal health sectors, we offer customized solutions that meet the specific needs of all our clients From development to product delivery, we are with you on your biologics journey. We are a leading global CDMO and preferred partner for pharmaceutical and biotech companies. We have what it takes to help you improve lives. It's within us.