Entrenador/a de Fútbol – Niños y Jóvenes - Tusclasesparticulares - Almería

Descripción del puesto ¿Te gustaría formar parte de una empresa internacional líder en Formación Profesional? Buscamos Docente de Higiene Bucodental para nuestro centro de Almería. Si tienes pasión por la enseñanza y buscas un proyecto estable, ¡esta es tu oportunidad! ¿Cuál será tu misión? • Impartir docencia dinámica y de calidad en los módulos de Higiene Bucodental., • Planificar y diseñar sesiones formativas con un enfoque práctico., • Realizar el seguimiento continuo y tutorización del alumnado., • Colaborar con el equipo académico en la mejora de los programas. ¿Qué buscamos en ti? • Formación: Diplomado/a-Graduado/a en Odontología., • Requisito imprescindible: Máster en Profesorado, CAP o, en su defecto, experiencia docente de un año completo previa al curso 2008/09., • Experiencia: No se requiere experiencia previa., • Competencias: Excelentes habilidades de comunicación, empatía, perfil resolutivo y competencia digital básica. ¿Qué te ofrecemos? ✅ Estabilidad: Contrato indefinido en jornada parcial de mañanas con incorporación en Septiembre para el Curso 2026/27. ✅ Conciliación: Amplio periodo vacacional. ✅ Beneficios: Seguro médico, tarjeta restaurante y cheques guardería a través de nuestro modelo de retribución flexible. ✅Desarrollo: Descuento en nuestro catálogo formativo para tu crecimiento continuo. ¡Trabaja en Davante! Davante es una empresa líder en formación profesional con el compromiso de ofrecer a las personas herramientas que les permitan mejorar sus habilidades y acceder a nuevas oportunidades laborales. Con presencia en España, Portugal e Italia, nos dedicamos a proporcionar formación de calidad que responde a las necesidades del mercado actual. Si quieres crecer profesionalmente y formar parte de un equipo apasionado por la educación, ¡Estamos deseando conocerte! Información básica sobre protección de datos: Los datos personales facilitados serán tratados por Davante Education, S.L como Responsable del tratamiento con la finalidad de gestionar el proceso de selección. Para ejercer sus derechos de acceso, rectificación, supresión y demás derechos reconocidos en la ley puede enviar un correo electrónico a dpo@davante.es

Se busca profesores/estudiantes/universitarios para brindar clases de distintas materias a estudiantes de diferentes niveles educativos (primaria, secundaria, bachillerato o universidad).Arte y materias artísticas.Photoshop, programación, etc.Evaluar el nivel de conocimiento del estudi

Empresa de formación On line busca un/a profesor/a para venta de cursos en inglés, con los siguientes requerimientos técnicos:.

pIt'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. /ppbr/ppbWe are hiring a /b /ppbClinical Research Associate III – Home-Based in Spain (Spanish speaking candidates in France are also welcome) /b /ppbr/ppbYour Strength /b /ppbr/pulliMinimum of 4 years of advanced experience in clinical research monitoring /liliIn-depth knowledge of regulations and guidelines related to clinical trials involving human subjects (e.g., ISO 14155, GCP, MDR, EU, FDA) /liliAbility to independently manage 10–15 study sites from start-up through close-out /liliExcellent communication skills for site interaction, training, and issue resolution /liliStrong collaboration and mentorship abilities, with a passion for supporting and guiding junior team members /liliHands-on experience with monitoring systems, source data verification, and compliance tracking /liliStrong organizational skills with the ability to manage multiple priorities in a dynamic environment /liliWillingness to travel regularly for site visits and investigator meetings across France and Spain /liliBased 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) /liliFluent communication in English and Spanish (Catalan is preferred, French optional) /li /ulpbr/ppbYour Contribution /b /pulliIndependently manage all phases of clinical trial site activities, including site identification, initiation, monitoring, and close-out /liliConduct monitoring visits in accordance with study protocols, GCP, and applicable regulatory requirements /liliAct as the primary contact for investigational sites, ensuring compliance and providing ongoing support /liliBuild and maintain strong relationships with investigators, study coordinators, and site personnel /liliIdentify study risks, recommend solutions, and ensure timely resolution of site-related issues /liliPerform source data verification and data review to ensure patient safety, protocol compliance, and data integrity /liliConduct site training, initiation visits, and support audit and inspection readiness /liliCollaborate closely with Clinical Operations, Data Management, Medical Affairs, and other cross-functional teams /liliSupport investigator meetings, coordinator meetings, and deliver presentations or training sessions when required /liliMentor junior CRAs and contribute to process improvements and best practices /liliParticipate in CAPA activities, quality initiatives, audits, and continuous improvement efforts /li /ulpbr/ppbOur Strength /b /ppbr/pulliA mission-driven company focused on saving lives /liliInternational and collaborative MedTech environment /liliHybrid working model with flexibility /liliOpportunities for growth and professional development /liliInnovative products and meaningful clinical impact /li /ulpbr/ppbContact /b /ppApply now and join the Artivion team. We look forward to receiving your application documents in bEnglish /b through our online application system. /ppbBrian Russo /b /ppbr/ppT: /ppJOTEC GmbH, a wholly owned subsidiary of Artivion, Inc. /ppLotzenäcker 23, 72379 Hechingen /p pbr/p

STEM PhD Expert Location: Remote (U.S. / UK / Canada / Europe) Engagement Type: Hourly Contract Compensation: $70–$75/hour About the Opportunity This opportunity is for STEM PhD experts interested in contributing to advanced AI research and evaluation projects involving state-of-the-art large language models (LLMs). The role involves applying deep subject matter expertise to develop challenging, domain-specific problems and create high-quality data that helps improve the reasoning, accuracy, and problem-solving capabilities of next-generation AI systems. Required Qualifications • PhD in a STEM discipline from a university in the United States, United Kingdom, Canada, or Europe., • Expertise in a relevant field, including:, • Mathematics, • Biology, • Chemistry, • Physics, • Computer Science, • Statistics, • Economics, • Or a closely related STEM discipline, • Deep subject matter expertise with the ability to develop complex, research-level problems within your domain., • Strong analytical and critical-thinking skills., • Exceptional attention to detail and commitment to technical accuracy., • Excellent written and verbal communication skills., • Excellent proficiency in English., • Ability to work independently in a remote environment. Responsibilities • Develop challenging, domain-specific problems based on your area of expertise., • Create high-quality reference solutions and explanations., • Review and evaluate AI-generated responses for accuracy, reasoning, and technical quality., • Identify errors and opportunities to improve AI-generated outputs., • Apply advanced subject matter expertise to help improve the reasoning capabilities of large language models., • Contribute high-quality data to support the development and evaluation of next-generation AI systems. Compensation • Competitive compensation of $70–$75/hour., • Weekly payments., • Independent contractor engagement. Application Process • Upload Resume, • Complete a 20–30 Minute AI Interview Based on Your Resume and Expertise, • Submit Application

Job Purpose The S. A. L. T. (Sea and Land Taste) Host/Coordinator bridges the gap between the ship’s culinary execution and guest engagement. This role blends luxury hospitality hosting, culinary storytelling, laboratory operations management, and destination integration to deliver a seamless, immersive cultural and dining experience for guests. Key Responsibilities Guest Engagement & Culinary Storytelling Mandatory Restaurant Presence: Host and conduct table rounds in the S. A. L. T. Kitchen every evening for at least two hours during dinner service. Pre-Service Prep: Attend all menu briefings 15 minutes prior to opening to master details on ingredient sourcing, preparation techniques, and regional narratives. Table Hosting: Provide warm welcomes, offer curated menu recommendations, and share the S. A. L. T. philosophy without exceeding 5 minutes per table to maintain guest comfort. Post-Service Retention: Actively promote upcoming menus, shore experiences, and program activities to departing guests. S. A. L. T. Lab & Financial Operations: Manage daily operations, cleanliness, and readiness of the S. A. L. T. Lab. Act as the primary liaison between the Chef de Cuisine, Bartender, and Kitchen Stewards. Oversee inventory control, ordering processes via onboard systems (Fidelio), breakage reporting, and equipment maintenance. Coordinate recipe and program collateral distribution with the Media and Broadcast teams. Shore Experiences & Destination Integration: Escort, support, and serve as an auxiliary host during S. A. L. T. culinary shore excursions. Collaborate with the Shore Concierge to actively promote destination-based culinary experiences. Compliance, Safety & Leadership Maintain absolute compliance with USPH (United States Public Health) standards and sanitation regulations. Collaborate with the Cruise Director, Executive Chef, and F&B leadership to align programming with the ship's daily schedule. Participate in all mandatory ship safety drills, environmental compliance training, and emergency duties. Qualifications & Requirements Certifications: Valid STCW 95 certification; must be physically and medically fit for sea duty. Culinary Background: Professional kitchen training or culinary education experience; recipe testing and development experience is highly valued. Soft Skills: Strong public speaking, presentation skills, and the ability to confidently convey complex culinary narratives. Administrative Skills: Experience with budget management, inventory control, cost-control systems, and proficiency in MS Office (Word, Excel, Power Point). Onboard systems experience (Fidelio) is preferred. Experience: Prior experience conducting cooking demonstrations is preferred. Strong worldwide destination and culinary culture knowledge is required. Traits: High moral integrity, discretion, and a commitment to luxury hospitality standards.

Buscamos docente universitario con acreditación ANECA para impartir clases en el Máster de Profesorado (MAES) de forma online. Se requiere experiencia docente y especialización en Matemáticas, Física, Biología o Tecnología.

At Artivion, we manufacture high-quality products and solutions for the treatment of aortic diseases. Clinical Research Associate III – Home-Based in Spain (Spanish speaking candidates in France are also welcome) 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., 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 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) 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 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 Hybrid working model with flexibility Opportunities for growth and professional development We look forward to receiving your application documents in English through our online application system.