Profesor/a de Inglés (C1) - Valladolid - Nortempo - Valladolid

Ubicación: Palencia | Vigo | Incorporación inmediata | Posición estable ¿Qué buscamos? Un/a Docente para formación en energía fotovoltaica ,l a persona que se incorpore será responsable de la planificación, impartición y evaluación de los contenidos teóricos y prácticos del curso En Magtel , aplicamos soluciones innovadoras al diseño, construcción y mantenimiento de infraestructuras en diversos sectores. Nuestro compromiso es mejorar la eficiencia en el uso de recursos naturales, contribuyendo a una sociedad más sostenible y con mayor calidad de vida. ¿Qué harás en tu día a día? Planificar y estructurar los contenidos del curso conforme al programa formativo establecido. Impartir clases teóricas y prácticas relacionadas con la instalación, mantenimiento de paneles solares, así como módulo de electricidad. Acompañar y tutorizar al alumnado durante el proceso de aprendizaje, resolviendo dudas técnicas y fomentando un entorno inclusivo y participativo. Evaluar el progreso del alumnado mediante pruebas, ejercicios y seguimiento individualizado. Velar por el uso correcto de los materiales, herramientas y equipos técnicos durante las sesiones prácticas. Cumplimentar la documentación académica requerida (actas, informes, asistencia, etc.). Coordinarse con el equipo de formación y seguimiento del proyecto Formación y Requisitos Formación técnica en energías renovables- fotovoltaica. Experiencia profesional demostrable en instalaciones eléctricas y montaje de paneles solares. Experiencia docente o formativa (valorable Certificado de Profesionalidad de Docencia de la Formación Profesional para el Empleo o equivalente). Conocimientos actualizados sobre normativas y estándares técnicos del sector. Capacidad para trabajar con colectivos en riesgo de exclusión o en procesos de mejora de empleabilidad. Preferiblemente autónomo. Conocimientos específicos Paquete office a nivel usuario experto. Carné de conducir. Se valorará experiencia con personas del tercer sector. ¿Qué ofrecemos? Incorporación a una empresa sólida y en crecimiento Plan de Retribución Flexible : accede a productos y servicios con ventajas fiscales

It's a good feeling to know you're doing your best with purpose every day. At Artivion, we manufacture high-quality products and solutions for the treatment of aortic diseases. Together with surgeons worldwide, we save lives. In doing so, we rely on the strengths of each and every employee. Your strength counts, too: As an important link in the chain, you make a contribution to saving lives together with us. Bring your strengths and let us grow together. We are hiring a Clinical Research Associate III – Home-Based in Spain (Spanish speaking candidates in France are also welcome) Your Strength • Minimum of 4 years of advanced experience in clinical research monitoring, • In-depth knowledge of regulations and guidelines related to clinical trials involving human subjects (e.g., ISO 14155, GCP, MDR, EU, FDA), • Ability to independently manage 10–15 study sites from start-up through close-out, • Excellent communication skills for site interaction, training, and issue resolution, • Strong collaboration and mentorship abilities, with a passion for supporting and guiding junior team members, • Hands-on experience with monitoring systems, source data verification, and compliance tracking, • Strong organizational skills with the ability to manage multiple priorities in a dynamic environment, • Willingness to travel regularly for site visits and investigator meetings across France and Spain, • Based in Spain (candidates from France may be considered in case a candidate lives nearby the Spain/France border and eager to do cross border monitoring), • Fluent communication in English and Spanish (Catalan is preferred, French optional) Your Contribution • Independently manage all phases of clinical trial site activities, including site identification, initiation, monitoring, and close-out, • Conduct monitoring visits in accordance with study protocols, GCP, and applicable regulatory requirements, • Act as the primary contact for investigational sites, ensuring compliance and providing ongoing support, • Build and maintain strong relationships with investigators, study coordinators, and site personnel, • Identify study risks, recommend solutions, and ensure timely resolution of site-related issues, • Perform source data verification and data review to ensure patient safety, protocol compliance, and data integrity, • Conduct site training, initiation visits, and support audit and inspection readiness, • Collaborate closely with Clinical Operations, Data Management, Medical Affairs, and other cross-functional teams, • Support investigator meetings, coordinator meetings, and deliver presentations or training sessions when required, • Mentor junior CRAs and contribute to process improvements and best practices, • Participate in CAPA activities, quality initiatives, audits, and continuous improvement efforts Our Strength • A mission-driven company focused on saving lives, • International and collaborative MedTech environment, • Hybrid working model with flexibility, • Opportunities for growth and professional development, • Innovative products and meaningful clinical impact Contact Apply now and join the Artivion team. We look forward to receiving your application documents in English through our online application system. Brian Russo T: +41 435 08 39 01 JOTEC GmbH, a wholly owned subsidiary of Artivion, Inc. Lotzenäcker 23, 72379 Hechingen www.artivion.com

It's a good feeling to know you're doing your best with purpose every day. At Artivion, we manufacture high-quality products and solutions for the treatment of aortic diseases. Together with surgeons worldwide, we save lives. In doing so, we rely on the strengths of each and every employee. Your strength counts, too: As an important link in the chain, you make a contribution to saving lives together with us. Bring your strengths and let us grow together. We are hiring a Clinical Research Associate III – Home-Based in Spain (Spanish speaking candidates in France are also welcome) Your Strength • Minimum of 4 years of advanced experience in clinical research monitoring, • In-depth knowledge of regulations and guidelines related to clinical trials involving human subjects (e.g., ISO 14155, GCP, MDR, EU, FDA), • Ability to independently manage 10–15 study sites from start-up through close-out, • Excellent communication skills for site interaction, training, and issue resolution, • Strong collaboration and mentorship abilities, with a passion for supporting and guiding junior team members, • Hands-on experience with monitoring systems, source data verification, and compliance tracking, • Strong organizational skills with the ability to manage multiple priorities in a dynamic environment, • Willingness to travel regularly for site visits and investigator meetings across France and Spain, • Based in Spain (candidates from France may be considered in case a candidate lives nearby the Spain/France border and eager to do cross border monitoring), • Fluent communication in English and Spanish (Catalan is preferred, French optional) Your Contribution • Independently manage all phases of clinical trial site activities, including site identification, initiation, monitoring, and close-out, • Conduct monitoring visits in accordance with study protocols, GCP, and applicable regulatory requirements, • Act as the primary contact for investigational sites, ensuring compliance and providing ongoing support, • Build and maintain strong relationships with investigators, study coordinators, and site personnel, • Identify study risks, recommend solutions, and ensure timely resolution of site-related issues, • Perform source data verification and data review to ensure patient safety, protocol compliance, and data integrity, • Conduct site training, initiation visits, and support audit and inspection readiness, • Collaborate closely with Clinical Operations, Data Management, Medical Affairs, and other cross-functional teams, • Support investigator meetings, coordinator meetings, and deliver presentations or training sessions when required, • Mentor junior CRAs and contribute to process improvements and best practices, • Participate in CAPA activities, quality initiatives, audits, and continuous improvement efforts Our Strength • A mission-driven company focused on saving lives, • International and collaborative MedTech environment, • Hybrid working model with flexibility, • Opportunities for growth and professional development, • Innovative products and meaningful clinical impact Contact Apply now and join the Artivion team. We look forward to receiving your application documents in English through our online application system. Brian Russo T: +41 435 08 39 01 JOTEC GmbH, a wholly owned subsidiary of Artivion, Inc. Lotzenäcker 23, 72379 Hechingen www.artivion.com

Recognized English teaching certification (TESOL / TEFL / TESL – CELTA or equivalent preferred). English proficiency at CEFR C2 (or equivalent) is required.

It's a good feeling to know you're doing your best with purpose every day.At Artivion, we manufacture high-quality products and solutions for the treatment of aortic diseases.Together with surgeons worldwide, we save lives.In doing so, we rely on the strengths of each and every employee.Your strengt