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Our client is a highly regarded fintech delivering web-native collaboration and workflow technology to investment operations teams across the global financial markets. They're already trusted by hundreds of financial institutions worldwide, and the platform supports critical functions such as securities settlements, corporate actions and collateral management. The business operates with the backing of a major financial market infrastructure provider, while retaining the pace and mindset of a modern fintech. The Role As a Software Engineer, you’ll join a small, highly capable engineering team shaping the future of a mission-critical platform. You’ll design and build new capabilities that improve how financial institutions operate, working end-to-end across the development lifecycle. Engineers here are full-stack generalists who value clean design, quality engineering and a strong DevOps culture. You’ll collaborate closely with colleagues in an agile environment, gaining exposure to all parts of the system and having real influence over technical decisions. What You’ll Do Design, develop and maintain server-side Java applications Contribute from requirements through to production deployment Build reliable, scalable solutions in collaboration with your team Participate in code reviews, testing and continuous integration Support operational excellence through DevOps practices What You’ll Bring 3–5+ years’ experience in server-side Java development Strength in at least three areas such as web technologies, messaging, data modelling, security, concurrency or performance tuning A strong focus on testing, reliability and quality Experience working in small, productive Agile/Scrum teams Working knowledge of SQL and relational databases (e.G. Postgres) Clear communication skills and a desire to keep learning Nice to Have Experience in a scale-up or fast-growth environment Exposure to cloud platforms, Kubernetes or DevOps tooling A Computer Science degree or related background You’ll be encouraged to contribute proactively, support your teammates and help shape a growing fintech that values diversity, inclusion and continuous improvement. Important Details Spain - Remote Visits to Madrid quarterly and the occasional visit to the UK would be required (Additional costs covered via the Employer). Initial contract would be via Deel (when the team is established the business will look to incorporate in Spain). Salary Range: €55,000-70,000 inclusive of benefits. Please note we are looking for high performing mid level engineers with 3-5yrs experience that would still benefit from mentoring.

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.

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

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 Med Tech 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 Gmb H, a wholly owned subsidiary of Artivion, Inc. Lotzenäcker 23, 72379 Hechingen

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.

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.

Camarera/o de Pisos - Barceló Punta Umbría Beach ResortApplylocations: Barceló Punta Umbría Beach Resort, Huelva, Españatime type: Part timeposted on: Posted Todayjob requisition id: JR11175Barceló Group is a family-owned company founded in 1931 by Simón Barceló in Mallorca (Spain). Our expansion to the world's major destinations, along with our clear growth strategy, has allowed us to position ourselves as the 2nd largest chain in Spain and one of the top 30 in the world in terms of the number of rooms.Our commitment to ensuring the satisfaction of our visiting guests and the well-being of our entire team has been rewarded with the "Best Hotel Management Company in the World" award at the latest edition of the World Travel Awards, considered the Oscars of the international tourism sector.Currently, Barceló Hotel Group has 270 urban and resort hotels with 4 and 5 stars, totaling over 60,000 rooms distributed in 24 countries. These hotels are marketed under four brands that allow us to provide our guests with a clear differentiating value in terms of both quality and service: ### Royal Hideaway Luxury Hotels Resorts ### Barceló Hotels Resorts ### Occidental Hotels Resorts ### Allegro HotelsAll of the above, combined with a clear spirit of sustainable improvement, enables us to look towards the future with optimism, always backed by the strength and international presence that have characterized the Barceló Group throughout its more than 90 years of business trajectory. Do you want to be part of our story? Join our team!# What will you do?Limpieza y puesta a punto de las habitaciones y las áreas comunes del Hotel. Para ello debe seguir los procedimientos y técnicas establecidos por la dirección que garanticen la higiene del establecimiento y el perfecto estado de uso de las instalaciones. Funciones: • Preparar el material necesario para desarrollar su trabajo: productos, utensilios, maquinaria, etc. • Limpiar y arreglar las habitaciones y zonas comunes del alojamiento, comprobando el buen estado de las instalaciones y el mobiliario. Para ello tendrá que hacer uso del parte de ocupación y realizar todas las tareas que implica la limpieza: hacer la cama, ventilar la habitación, colocar ropas, reponer los objetos de aseo, documentos, complementos y artículos del minibar, y supervisar el estado de la habitación para comprobar que no hay desperfectos. • Atender al cliente mientras permanezca alojado y procesar los objetos perdidos. Deberá tener en cuenta sus quejas y reclamaciones, satisfacer sus peticiones cuando esté en su mano hacerlo y controlar los objetos que puedan dejarse olvidados según el protocolo establecido. • Recoger y limpiar los materiales propios de su trabajo, enviando a lavandería la ropa sucia y rellenando los partes necesarios.# What are we looking for?• Formación: ESO. • Experiencia: deseable en puesto similar. • Idiomas: deseable inglés. • Se valorarán conocimientos en: hostelería. • Orientación al cliente. • Trabajo en equipo. • Preocupación por el orden y la calidad. • Motivación y responsabilidad. • Capacidad de organización.# Your benefits:You will have the opportunity to work in a flexible, collaborative, and responsible work environment, surrounded by the best colleagues. Why limit yourself to one location when you can move between countries and work in different areas of the company? At Barceló Hotel Group, we offer you geographical mobility and the chance to gain knowledge about various products and services throughout your career.* We understand that a committed and experienced team is essential for growth. That's why we have specific career plans available in different areas of the company, which you can join.*You will have access to the best training programs in the market, tailored to your position within the company. Additionally, because we strongly believe in personal development, we provide a wide range of open training activities through our Barceló Campus e-learning platform. * We invite you to explore Barceló Responsible, our Corporate Responsibility brand. This initiative encompasses numerous actions related to social, economic, and environmental development in all the locations where our company operates. We want you to join us in our commitment to building a better future!As one of our greatest challenges is ensuring your happiness, being part of the Barceló Hotel Group team comes with additional advantages and benefits, including:1. Exclusive discounts on hotels and travel for you, your family, and friends. 2. Access to a health insurance policy with numerous advantages and special conditions for the Barceló group. 3. Ongoing discounts with various companies related to leisure and free time. 4. Special offers with product and service companies. 5. Exclusive agreements with different training and business schools# Contract type:Fixed-Term (duración determinada)br#J-18808-Ljbffr