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Ven a descubrir y ejercer la profesión de cirujano dentista en Francia. Convertirse en cirujano dentista en Francia requiere dominar el idioma, conocer las prácticas profesionales del país y superar el examen de idioma exigido por el Colegio Oficial de Odontólogos.

Descripción de la empresa ¡Prueba la aventura de Dentego en Francia! Dentego, actor imprescindible de la medicina bucodental en Francia, cuenta hoy con más de 100 centros dentales y 2300 empleados dedicados a hacer que la atención sanitaria sea accesible y de calidad para todos. Descripción del empleo Para reforzar nuestro equipo ante una demanda en fuerte crecimiento, nuestra clínica dental busca un(a) Odontólogo(a) a tiempo completo o parcial y completar así su equipo dinámico, concienzudo y familiar. • Tratamientos polivalentes (profilaxis, endodoncia, pequeñas intervenciones quirúrgicas, prótesis, etc.), • Posibilidad de colocar implantes (implantes: ETK o Biotech según los centros; biomateriales: Geistlich), • Posibilidad de tratar casos con alineadores si se cuenta con la formación adecuada (Invisalign y/o Smilers) Requisitos LO QUE LE OFRECE NUESTRA CLÍNICA • Atractiva retrocesión en función de su experiencia y especialidad, • Cartera de pacientes existente, • Auxiliares dentales dedicados, • Personal administrativo formado y polivalente, • Seguro médico y seguro de prevención sanitaria, • Reembolso del 50 % de los gastos de transporte público RAZONES PARA UNIRSE A NOSOTROS • Compañeros con un verdadero sentido de la ética y los valores humanos, • Personal dedicado a la gestión del consultorio (administrativo, material, mantenimiento, etc.), • Plataforma técnica de calidad (equipo radiográfico, cámara 3Shape o Medit, quirófano y motor de implantología), • Intercambio de conocimientos y experiencias entre compañeros, • Seguimiento de la formación continua DPC, • Formación interna y en colaboración con profesionales reconocidos en la profesión, • Programa de integración específico para profesionales junior: experiencia, asesoramiento y formación ¿Tienes un título en odontología de la Unión Europea ? ¿Tienes un nivel básico de francés (A2 / B1) y estás dispuesto a mejorarlo? ¿Te apetece la aventura Dentego ? Postula directamente a esta oferta o contáctanos a nuestra dirección de correo electrónico : _. Información adicional Videos To Watch https://vimeo.com/1119815146

Estoy buscando una persona de confianza para acompañarme a citas médicas en el horario de mañana. Se valorarán referencias y una primera reunión para conocernos.

La visita sería en la ciudad y las horas pueden variar según las citas; agradecería flexibilidad y buena comunicación para coordinar con mi agenda. Requiero que la persona sea puntual, respetuosa y que tenga disponibilidad para acompañarme de forma regular si el servicio funciona bien. Necesito

Busco ayuda para acompañar a una persona mayor a sus citas médicas. Requiere puntualidad, paciencia y capacidad para gestionar agenda, transporte básico y recordatorios de medicación. El servicio incluye coordinar con familiares, ayudar a llenar formularios y acompañar durante la consulta para

Enfermera/o para Clínica Psiquiátrica General Enfermera/o para Clínica Psiquiátrica General Empresa: Clinica Psiquiatrica General Actividad de la Empresa: Psiquiatria Puesto requerido: Enfermera/o Generalista Número de plazas: 3 Lugar físico del centro de trabajo: Juan Jose Lopez Ibor n2 Durac

Mercor in Madrid, Spain is seeking experienced physicians who are native or fluent in Spanish to train and evaluate AI agents on realistic professional medical tasks. You will build workspaces and files, write prompts, and create grading rubrics based on real medicine as practiced in Spain. This remote, part-time role is about 21 hours per week, paid hourly, and runs a pilot from Oct 23 to Nov 19. #J-18808-Ljbffr

We're looking for experienced physicians who are native or fluent in Spanish to help train and evaluate AI agents on realistic professional tasks. What you'll do: You'll work in realistic digital workspaces, with documents, spreadsheets, email, chat and industry tools, to create and review the kinds of tasks you handle in your own job. Your work will include: Building workspaces: reviewing files, memos and records a real team would have for a project or case. Writing tasks: drafting realistic requests in your language that a colleague or client might send, grounded in local practice, regulations and terminology. Defining what good looks like: writing clear grading criteria and checking whether an AI agent's work would meet your professional standard. Reviewing AI work: going through an agent's step-by-step work, spotting mistakes such as wrong calculations, missed details or incorrect local rules, and correcting them. Requirements: Experience in clinical practice Native or fluent in Spanish Bachelor's degree from a recognized institution in Spain Licensed physician in Spain (colegiado), typically after MIR residency, familiar with SNS protocols and Spanish clinical guidelines Details: Remote, about 21 hours per week, hourly, pilot running Oct 23 to Nov 19. #J-18808-Ljbffr

Jobrapido, Pharmarecs seeks Dentists to work in private clinics in Ireland. Vacancies cover General Dentistry, Orthodontics, Oral Surgery (Dental Implants, prosthodontics), Odontopediatrics, and Endodontics. Requires EU dentistry degree, fluent English, and relevant field experience. Masters/postgraduate studies in orthodontics or oral surgery are preferred. Relocation and Ireland registration assistance provided. #J-18808-Ljbffr

Senior Ad Tech Specialist (Temp) Location: Remote, EU time zones Team: Product / Development Contract Type: Contractor Contract Duration: 6 months, with possibility of extension English Level: Professional fluency, C1/C2 mandatory AdTech Experience: Mandatory Reports to: CTO IMPORTANT This is a temporary 6 month contractor position, with the possibility of extension depending on business needs and performance. Professional English proficiency is mandatory for this role. Candidates must also have significant previous experience in programmatic AdTech. This is a senior position and is not suitable for candidates looking to transition into AdTech without prior industry experience. About Refinery89 Refinery89 is a Dutch AdTech company headquartered in Madrid, working with premium publishers around the world to optimize their programmatic advertising performance. Through advanced technology, data, and hands on technical support, we help publishers increase advertising revenue, improve efficiency, and gain greater transparency across their monetization stack. Our international team operates at the intersection of technology, digital advertising, data, and publisher operations. About The Role We are looking for a Senior Ad Tech Specialist to join our Product and Development environment and take ownership of complex technical investigations across live publisher advertising stacks. This is a deeply technical role focused on diagnosing issues, reproducing problems, identifying root causes, validating solutions, and translating findings into clear specifications or fixes that our Development team can act on. You will work directly with live publisher environments, Prebid, Google Ad Manager, Amazon APS, consent frameworks, SSP integrations, browser debugging tools, and the wider programmatic ecosystem. The objective is simple: when something is not behaving as expected, you should be able to determine what is happening, prove why it is happening, and define what needs to happen next. The role also supports Product decisions, roadmap prioritization, and technical go or no go decisions with evidence from real publisher environments. What You Will Do Technical Support and Escalations Own complex technical issues that Operations or Development teams have been unable to resolve. Investigate tag defects, rendering failures, consent issues, bid path problems, and unexpected revenue behavior. Reproduce issues using live publisher inventory and controlled staging environments. Identify root causes and distinguish structural limitations from configuration problems that can be resolved. Produce clear technical specifications or patched tag implementations before handing work over to Development. Live Ad Stack Debugging Investigate publisher implementations directly at browser level. Use Prebid debugging, network requests, browser consoles, HAR files, and consent string inspection to understand what is happening. Validate request ordering, consent propagation, and bidding behavior against the intended configuration. Confirm fixes in live environments before considering an issue resolved. Ad Stack Audits Perform structured audits across publisher monetization stacks. Review areas including Prebid configuration, Google Ad Manager, Amazon APS, CMP and TCF implementation, floor models, ad units, identity solutions, video, SSP health, and bidder performance. Score findings and produce clear action plans prioritized by impact and severity. Ecosystem Monitoring Track technical changes across Google, Amazon APS, Prebid.js, SSP partners, and the IAB Tech Lab. Assess how ecosystem changes may affect the Refinery89 stack and publisher implementations. Translate findings into clear technical recommendations. Escalate decisions when changes require Product or Development involvement. Rollouts and Technical Validation Support phased technical rollouts using clearly defined success metrics. Establish validation criteria and rollback conditions. Test implementations in staging environments before Development handoff. Monitor performance following deployment and validate results against agreed thresholds. Must Have Skills At least 5 years of experience in programmatic advertising technology, preferably within publisher monetization or the supply side. Significant hands on experience diagnosing and debugging live advertising environments. Deep working knowledge of Prebid.js, including configuration, adapters, modules, identity solutions, floors, and debugging. Ability to inspect and understand bidder adapter source code when documentation alone is insufficient. Strong technical knowledge of Google Ad Manager, including line items, pricing rules, AdX, dynamic allocation, GPT implementations, and MCM models. Strong understanding of IAB TCF 2.x and GDPR consent mechanics, including how consent is propagated across Prebid, GAM, and Amazon APS. Understanding of OpenRTB and supply chain transparency standards including ads.txt, sellers.json, and schain. Strong JavaScript knowledge, with the ability to read, modify, and validate production advertising tags. Advanced browser developer tools skills including network inspection, HAR analysis, and console debugging. Ability to write structured technical documentation that a developer can execute without requiring extensive additional explanation. Professional English proficiency at C1/C2 level. Previous professional experience in AdTech is mandatory. THINGS THAT WILL HELP YOU STAND OUT Experience implementing or troubleshooting Amazon APS or TAM. Python or TypeScript experience for internal tooling. Experience with video advertising and outstream environments, including IMA SDK and VAST. Familiarity with identity solutions such as ID5, SharedID, UID2, or EUID. Experience working with Jira and Confluence. Previous exposure to LATAM or Dutch publisher markets. What This Role Is Not This is not a commercial partnerships or sales position. You will not be responsible for commercial negotiations, SSP relationship ownership, or partner outreach. This is also not a traditional campaign management or trafficking position. Day to day ad operations and GAM campaign trafficking are not the primary focus of the role. Who This Role Is For This role could be a strong fit if: You enjoy opening developer tools and understanding exactly what is happening behind an advertising implementation. When an issue cannot immediately be explained, your instinct is to investigate it methodically rather than guess. You are comfortable working across JavaScript, browser behavior, programmatic infrastructure, and publisher configurations. You can move between technical details and the larger business impact of an issue. You value evidence and reproducibility when making technical recommendations. You can clearly communicate complex findings to both technical and non technical colleagues. You are comfortable taking ownership of difficult problems that do not have an obvious answer. INTERVIEW PROCESS Our interview process consists of four stages. Initial Screening A short introductory conversation with our recruitment team to understand your background, experience, English level, AdTech experience, and motivation. Technical Conversation A live technical discussion based around a real Prebid or Google Ad Manager configuration. Written Technical Exercise A practical exercise designed to assess how you investigate, document, and solve complex AdTech problems. Final Conversation A final conversation with the CTO and relevant team members. What We Offer Remote working within compatible EU time zones. A temporary 6 month contractor agreement with the possibility of extension. 50% coverage of the standard Sanitas private health insurance plan. The opportunity to work directly on complex publisher monetization environments and real world programmatic infrastructure. An international team working across AdTech, technology, data, and publisher operations. JOIN REFINERY89 If you have spent years working inside programmatic advertising stacks, enjoy debugging the problems others cannot immediately solve, and want to work closer to Product and Development while remaining deeply connected to real publisher environments, we would love to hear from you. #J-18808-Ljbffr

En Avodent buscamos un/a odontólogo/a con formación de posgrado en prótesis o rehabilitación oral, a jornada parcial o completa, para trabajar en nuestros dos centros de Alcobendas y San Sebastián de los Reyes, a pocos minutos uno de otro. Incorporación lo antes posible. Funciones: Primeras visitas con diagnóstico completo y elaboración de planes de tratamiento integrales. Rehabilitación protésica fija y removible, sobre dientes naturales y sobre implantes: coronas y puentes (CAD-CAM, e.max, zirconio), sobredentaduras y prótesis híbridas. Odontología conservadora y restauradora (composites, reconstrucciones). Férulas de descarga y urgencias. Grado en Odontología (si el título es extranjero, homologado). Colegiado/a en un Colegio Oficial de Odontólogos de España. Experiencia demostrable en primeras visitas y planes de tratamiento integrales. Experiencia en rehabilitación protésica sobre implantes (coronas, puentes, sobredentaduras). Se valorará: Carillas de porcelana o composite. Experiencia con flujo digital CAD-CAM. Experiencia en mantenimiento periodontal e implantológico. Contrato indefinido a jornada parcial o completa, con trabajo en nuestros dos centros según la organización de la agenda. Jornada parcial, en uno de estos dos bloques: lunes y viernes completos, o martes y miércoles completos y jueves por la mañana. Jornada completa: lunes, martes y miércoles de 10:00 a 14:00 y de 16:00 a 20:00; jueves de 10:00 a 14:00; viernes de 10:00 a 13:30 y de 15:30 a 19:00. Salario desde 40.000 € brutos/año a jornada completa (parte proporcional en jornada parcial), más un complemento variable por producción sin límite. Agenda consolidada desde el primer día. * Equipo estable y formación interna en nuestros protocolos y en Gesden. #J-18808-Ljbffr

Tether is seeking a Technical Content Creator to demonstrate the practical power of its peer-to-peer stack. This builder-centric role targets engineers who bridge low-level infrastructure, cryptography, and applications. You will write code, spin up nodes, and record polished demos. Create ongoing visual prototypes that prove decentralized, serverless infra in action, collaborating with core teams across Pear and Bare. #J-18808-Ljbffr

El Instituto de Investigaciones Biomédicas de Córdoba (IMIBIC) busca un técnico/a de laboratorio para la Unidad IMSMI, con foco en preparación de muestras y labores de laboratorio. Se ofrece incorporación estable en Córdoba, España, con desarrollo profesional mediante cursos de formación asociados al puesto. La posición es de 35 horas semanales, contrato indefinido y una retribución de 1.930 euros brutos mensuales, con hasta un 10% de retribución variable ligada a objetivos. #J-18808-Ljbffr

Banc de Sang i Teixits busca un Facultativo/a referente en Hemodonación para coordinar la salud del donante en la División de la Sangre. Colaborará estrechamente con la dirección médica y con los jefes de centro BST para garantizar la seguridad y la calidad del proceso de donación. La persona seleccionada se responsabilizará de coordinar las actividades de sangre total, plasma y plaquetas, leche y redmo, promoviendo buenas prácticas y estándares en toda la red de centros BST. #J-18808-Ljbffr

ICON Strategic Solutions is seeking a Project Planner to support sponsor-dedicated models with ICON’s global expertise and to contribute to the development of treatments that benefit patients worldwide. As an Associate Project Manager, you will help coordinate clinical trials, participate in study design, data collection, and regulatory submissions, and ensure milestones are met through collaboration with cross-functional teams. Travel approximately 10% may be required. #J-18808-Ljbffr

Hospital Universitario de Canarias busca un Facultativo/a Especialista de Área en Cirugía Torácica para un puesto en Tenerife. Se realiza cirugía torácica mayor y robótica, con guardias y atención en consultas externas, en un entorno con tecnología avanzada para la mejor atención al paciente. El candidato debe poseer Licenciatura en Medicina y Cirugía con titulación MIR en Cirugía Torácica. Se valorará experiencia en Cirugía Robótica y en Cirugía Mayor Mínimamente Invasiva, con capacidad de #J-18808-Ljbffr

Senior/Principal Statistical Programmer SAS + R (Remote) Sponsor-dedicated: Working fully embedded within one of our pharmaceutical clients, with the support of Cytel right behind you, you'll be at the heart of our client's innovation. As a Principal Statistical Programmer you will be dedicated to one of our global pharmaceutical clients; a company that is driving the next generation of patient treatment, where individuals are empowered to work with autonomy and ownership. This is an exciting time to be a part of this new program. Position Overview: This position reports to the Director, Biostatistics and Programming in the FSP Services business unit in Cytel. The Principal Statistical Programmer works independently with only concept level instruction and very little supervision, tracks progress, and provides expert technical support to team members. We are looking for a highly experienced senior statistical programmer who will work on clinical development programs on different therapeutic areas and participate in overseeing CRO programmers to ensure that data summaries are delivered in a consistent, high-quality manner. This individual will be responsible for implementing all reporting and analysis activities for the Sponsor clinical trials. As a Principal Statistical Programmer, your responsibilities will include: Generate SDTM, ADaM specifications, datasets, reviewer's guide and define.xml files for multiple studies Develop SAS programs which generate datasets, complex listings, tables (including those with descriptive and standard inferential statistics in collaboration with a Statistician), and complex graphs Deliver high-quality statistical programming results including developing, validating, and maintaining SAS and/or R programs tailored to clinical development programs' needs Participate in overseeing CRO's statistical programming deliverables for multiple clinical studies to ensure high-quality and meet the pre-specified timelines Support the preparation of clinical study reports, regulatory submissions, publications, annual DSUR, and exploratory analyses Understand and follow FDA regulations which affect the reporting of clinical trial data. This includes good clinical practice and guidelines for electronic submissions. Contribute to the creation, maintenance, documentation, and validation of standards for programming tools, outputs, and macros Participate in the development of CRFs, edit check specifications, and data validation plans Provide review and/or author data transfer specifications for external vendor data Collaborate with internal and external functions (e.g. CROs, software vendors, clinical development partners, etc.) to ensure meeting project timelines and goals Provide review and/or author SOPs and/or Work Instructions related to statistical programming practices Here at Cytel we want our employees to succeed and we enable this success through consistent training, development and support. To be successful in this position you will have: At a minimum bachelor's degree in computer science, data science, mathematics, or statistics major preferred 7+ years of experience as a Statistical Programmer on a Biotech/Pharma Clinical Development Biometrics Team or with a similar team and experience supporting drug development, medical device development, or intervention studies Exceptional SAS programming skills and expertise in the development and implementation of statistical programming procedures and processes in a clinical development environment Extensive applied experience of CDISC standards (SDTM, ADaM, and Define.xml), medical terminology, clinical trial methodologies, and FDA/ICH regulation Experience supporting regulatory submissions, interacting with the FDA and/or global regulatory authorities Must be able to work independently Outstanding communication skills (written and verbal) and strong leadership skills Preferred Qualifications (nice to have) Prior work experience with pharmacokinetic data and the neuroscience field, proficiency in languages or tools other than SAS (e.g., R, Python, and Java, Shiny, Markdown, Unix/Linux and git) #LI-KO1 Cytel Inc. is an Equal Employment / Affiliation Employer. Applicants are considered for all positions without regard to race, color, religion, sex, national origin, age, veteran status, disability, sexual orientation, gender identity or expression or any other characteristics protected under or law. #J-18808-Ljbffr

LILT is seeking professional voice talents for an exciting project. We value native speakers with voice acting experience and a high-quality home studio who can deliver clear, natural, and engaging recordings. You should be comfortable with fast turnarounds and may need to provide voice samples or demos. Independent contractor role offering flexible schedule and participation in AI/voice cloning initiatives. #J-18808-Ljbffr

About the job Software Control DSP Engineer ALDIA is a multinational company based in London with presence in some of the main countries of the European Union (England, Sweden, Spain, France and Germany). We specialize in technology and engineering consulting. Our core business focuses on key areas of the Insurance, Finance, Communication, Infrastructure, Multimedia, Entertainment, Automotive, Railways, Wind Turbines and Oil & Gas industries. ALDIA works with its own group of consultants to improve quality, create stability, minimize risks and provide technological and innovative solutions by being part of all phases of the complete life cycle of the processes incorporating the agile methodology in each of them. We are currently looking for SW Control DSP to join our team of consultants in Spain. What are we looking for? Demonstrated experience inDSP and Texas Instrument #J-18808-Ljbffr

DERTOUR DMC Network is seeking a Client Success Manager in Palma to drive digital distribution of accommodation and destination services across our DMC network. You will own the end-to-end client lifecycle, oversee onboarding, go-live activities and ongoing optimization for internal brands and external B2B partners. You will coordinate API integrations with partners like Peakwork, Travelgate and Anixe, monitor data quality and KPIs, translate client needs into scalable solutions, and represent #J-18808-Ljbffr

Dextromedica busca un/a Account Manager de Sistemas Médicos para su delegación de Barcelona. El perfil debe provenir del sector sanitario y contar con experiencia en proyectos de consultoría tecnológica o transformación digital. Ubicación en Barcelona con disponibilidad para viajar por Cataluña; se valorará experiencia en entornos hospitalarios y habilidades de comunicación con clientes y stakeholders. Se requiere al menos 1 año de experiencia y nivel de inglés B2. #J-18808-Ljbffr

Nuestro cliente, una Start-Up delsector Fintech, con el fin de ampliar el equipo de sus oficinas situadas enMadrid, está buscando un CTO. Deseamos conocer perfiles con almenos 5 años de experiencia gestión de equipos tecnológicos compuestos por, almenos, 5 personas. Además la persona deberá tener experiencia programando conJava, Spring framework y arquitectura AWS. Además, estar acostumbrado atrabajar con metodologías agile, en concreto Scrum. Tendrás la oportunidad de dirigir unequipo tecnológico de alto nivel, compuesto por unas 8 personas, y que se prevécrecerá en el futuro. Podrás llevar la compañía al siguiente nivel tecnológico,de la mano de grandes profesionales. Adicionalmente, junto con el equipodirectivo, serás parte activa de las decisiones de futuro. - Ingeniería informática o similar - Experiencia en gestión de equipos tecnológicos - Experiencia trabajando con metodologías ágiles, Scrum. Te ofrecemos la oportunidad de integrarte en una multinacional en continuocrecimiento, donde podrás desarrollar una atractiva carrera profesional yobtener una remuneración competitiva, acorde con tu valía y experienciaprofesional. #J-18808-Ljbffr

Senior/Principal Statistical Programmer SAS + R (Remote) Sponsor-dedicated Working fully embedded within one of our pharmaceutical clients, with the support of Cytel right behind you, you'll be at the heart of our client's innovation. As a Principal Statistical Programmer you will be dedicated to one of our global pharmaceutical clients; a company that is driving the next generation of patient treatment, where individuals are empowered to work with autonomy and ownership. This is an exciting time to be a part of this new program. Position Overview This position reports to the Director, Biostatistics and Programming in the FSP Services business unit in Cytel. The Principal Statistical Programmer works independently with only concept level instruction and very little supervision, tracks progress, and provides expert technical support to team members. We are looking for a highly experienced senior statistical programmer who will work on clinical development programs on different therapeutic areas and participate in overseeing CRO programmers to ensure that data summaries are delivered in a consistent, high-quality manner. This individual will be responsible for implementing all reporting and analysis activities for the Sponsor clinical trials. As a Principal Statistical Programmer, your responsibilities will include: Generate SDTM, ADaM specifications, datasets, reviewer's guide and define.xml files for multiple studies Develop SAS programs which generate datasets, complex listings, tables (including those with descriptive and standard inferential statistics in collaboration with a Statistician), and complex graphs Deliver high-quality statistical programming results including developing, validating, and maintaining SAS and/or R programs tailored to clinical development programs' needs Participate in overseeing CRO's statistical programming deliverables for multiple clinical studies to ensure high-quality and meet the pre-specified timelines Support the preparation of clinical study reports, regulatory submissions, publications, annual DSUR, and exploratory analyses Understand and follow FDA regulations which affect the reporting of clinical trial data. This includes good clinical practice and guidelines for electronic submissions. Contribute to the creation, maintenance, documentation, and validation of standards for programming tools, outputs, and macros Participate in the development of CRFs, edit check specifications, and data validation plans Provide review and/or author data transfer specifications for external vendor data Collaborate with internal and external functions (e.g. CROs, software vendors, clinical development partners, etc.) to ensure meeting project timelines and goals Provide review and/or author SOPs and/or Work Instructions related to statistical programming practices Here at Cytel we want our employees to succeed and we enable this success through consistent training, development and support. To be successful in this position you will have: At a minimum bachelor's degree in computer science, data science, mathematics, or statistics major preferred 7+ years of experience as a Statistical Programmer on a Biotech/Pharma Clinical Development Biometrics Team or with a similar team and experience supporting drug development, medical device development, or intervention studies Exceptional SAS programming skills and expertise in the development and implementation of statistical programming procedures and processes in a clinical development environment Extensive applied experience of CDISC standards (SDTM, ADaM, and Define.xml), medical terminology, clinical trial methodologies, and FDA/ICH regulation Experience supporting regulatory submissions, interacting with the FDA and/or global regulatory authorities Must be able to work independently Outstanding communication skills (written and verbal) and strong leadership skills Preferred Qualifications (nice to have) Prior work experience with pharmacokinetic data and the neuroscience field, proficiency in languages or tools other than SAS (e.g., R, Python, and Java, Shiny, Markdown, Unix/Linux and git) #LI-KO1 Cytel Inc. is an Equal Employment / Affiantive Action Employer. Applicants are considered for all positions without regard to race, color, religion, sex, national origin, age, veteran status, disability, sexual orientation, gender identity or expression, or any other characteristics protected by law. #J-18808-Ljbffr

A leading HR tech firm in Spain is looking for a Sales Engineer to enhance B2B sales in Italy. The ideal candidate should have at least 2 years of experience in tech sales, understand HR processes, and possess advanced English and Italian skills. Responsibilities include delivering presentations, analyzing client needs, and collaborating with the sales team. This role offers an opportunity to grow within a dynamic environment focused on innovative solutions. #J-18808-Ljbffr

Wood Mackenzie seeks an experienced Technical Diligence expert to strengthen its Iberian Power & Renewables practice in Madrid. You will lead advisory engagements on M&A investments, combining deep technical knowledge of transmission and distribution networks with analytical, commercial, and communication skills. You will mentor junior team members and represent WoodMac at industry events, traveling for client meetings as needed. Fluency in Spanish and English is required. #J-18808-Ljbffr

Q-Ready, perteneciente al Grupo Quirónsalud, busca Médicos/as en GUADALAJARA para realizar valoraciones de trabajadores en situación de IT. Se ofrece contratación mercantil y horario de mañanas en jornada de lunes a viernes. El profesional debe estar graduado o licenciado en Medicina con colegiación y disponibilidad para darse de alta como autónomo. Incorporación tras el verano de 2026. Se valorará experiencia en valoraciones y gestión de IT. #J-18808-Ljbffr

Capitole is growing fast, and we want you to be part of the journey! We’re looking for a Tech PO / Business Analyst with +5 years of experience to join our amazing team. Responsibilities: Own the functional and delivery coordination of data platform initiatives for one or more business domains, such as Client Data or Sales Strategy Data. The role connects business stakeholders, Data Owners, Data Stewards, architects, and engineering teams to ensure that data products are well-defined, scalable, documented, trusted, and fit for their intended use. The role also contributes to the continuous improvement of data platform processes, delivery practices, data quality, and platform evolution. Coordinate the end-to-end functional delivery of data platform initiatives, from initial discovery and scope definition through requirements, development coordination, validation, stakeholder acceptance, and handover to the relevant operational owner. Gather and document business and data requirements. Translate requirements into user stories and acceptance criteria in Jira. Understand, analyze, and validate the data structure, data sources, transformations, and business rules. Validate data quality and the consistency of the resulting output. Maintain project and data documentation in Confluence. Collaborate with reporting and analytics teams by providing clear definitions, data context, and requirements for downstream reporting. The role does not own report development, deployment, or adoption. Requirements: Experience as a Tech Product Owner/Business Analyst/System Analystor in a similar role Strong understanding of data, data structures, data models, sources, pipelines, transformations, and data quality. Ability to explain data clearly and validate its meaning and usage with data owners. Ability to translate business needs into clear requirements for data and engineering teams. Experience writing user stories and acceptance criteria in Jira. Familiarity with Databricks, Azure data services, Power BI. Ability to use SQL or equivalent data investigation techniques to explore data, validate requirements, investigate quality issues, etc. Strong communication, coordination, and documentation skills. Proactive and curious mindset, with the ability to ask the right questions and investigate data issues independently. Experience with Agile ways of working, Jira, and Confluence. Why you'll love working with us At Capitole, we believe our people are our greatest strength. That's why we offer: €1,200/year for your professional development (trainings, events, certifications…) Monthly feedback sessions with your team to keep learning and growing Private health insurance fully covered by Capitole Payflow benefits (meal, transport, childcare vouchers) Wellhub subscription Discounts with top brands through Capitole Club Life at Capitole Team buildings every two months (our summer party and Christmas dinner are legendary!) Football, padel, and basketball teams sponsored by Capitole Tech communities where sharing knowledge is part of our DNA And above all… an AMAZING TEAM that you’ll love being a part of! Want to learn more about us? capitole-consulting.com See what our teams are saying about us: Glassdoor Reviews The employee will adhere to information security policies: Will have access to confidential information related to Capitole and the project they are working on. Must comply with the security and internal policies of both the company and the client. Must sign an NDA (Non-Disclosure Agreement) . #J-18808-Ljbffr

Tecdata Engineering busca un Líder Técnico de Data & IA para definir y evolucionar la práctica desde cero, reportando al CTO y liderando iniciativas de Data, ML e IA. El rol combina arquitectura, desarrollo hands-on y interacción con clientes en un entorno internacional híbrido. Se valoran más de 6 años de experiencia, experiencia en Data Engineering/Data Science, y dominio de Python/SQL, con exposición a GCP/AWS/Azure y plataformas como Databricks o Snowflake. #J-18808-Ljbffr

Sulzer is seeking a Senior Application Tendering Engineer to bolster our Spain-based Business Support team. You will craft technical and commercial proposals for configurable equipment and engineering solutions, collaborating with sales, product managers and manufacturing to ensure accurate sizing, pricing and high-quality tenders. In this role you will enable the sales process from leads through negotiation, while maintaining strong stakeholder relationships and driving continuous improvement #J-18808-Ljbffr

Warman O'Brien, partnering with a leading global CRO, seeks an experienced Principal Biostatistician to provide statistical leadership across complex global clinical trials, lead studies and regulatory submissions, and mentor junior statisticians. This fully home-based role supports Poland, Spain, Romania, Bulgaria, Czech Republic or Hungary, offering a competitive salary and comprehensive benefits. You will collaborate with pharma and biotech clients on innovative development programmes. #J-18808-Ljbffr

Perk, a leader in travel and spend management, is seeking a Senior Sales Development Representative to drive the UKI market. You will qualify and engage prospective customers, feed the sales funnel, and collaborate with the sales team to arrange consultations on the account director’s calendar. You will leverage outbound outreach via phone, email and social channels, maintain CRM data, and develop deep knowledge of Perk’s product to articulate value to prospective clients. #J-18808-Ljbffr

Davidson Consulting España busca un Senior IT Project Manager con background técnico para liderar iniciativas tecnológicas en Iberia y Latinoamérica. La posición gestionará proyectos desde su inicio hasta su cierre, dentro de un entorno internacional complejo y con proveedores externos. El candidato debe aportar más de 5 años gestionando proyectos IT en entornos complejos, con un nivel alto de inglés y experiencia en alcance, presupuesto, riesgos y stakeholders. #J-18808-Ljbffr

ODONTOLOGIA GENERALCLINICA DENTAL SANT LLUISBarcelona, BarcelonaDentista / OdontólogoJornadaJornada completa## DescripciónOferta de Empleo: Odontólogo/a GeneralUbicación: Clínica DentalTipo de contrato: Jornada completaIncorporación: InmediataDescripción del puestoBuscamos un/a Odontólogo/a para incorporarse a nuestro equipo en una clínica dental comprometida con la excelencia asistencial y la atención personalizada al paciente.La persona seleccionada desarrollará su actividad clínica en un entorno profesional, colaborativo y con los recursos necesarios para ofrecer un servicio de máxima calidad.Funciones del puestoLa persona seleccionada será responsable de prestar una atención clínica integral a los pacientes, desarrollando las siguientes funciones:• Realización de tratamientos de odontología general.• Diagnóstico, prevención y tratamiento de enfermedades periodontales (periodoncia).• Realización de tratamientos de endodoncia en dientes unirradiculares y multirradiculares.• Ejecución de procedimientos de cirugía oral, incluyendo exodoncias simples y complejas, cirugía preprotésica y otros tratamientos quirúrgicos propios de su ámbito competencial.• Elaboración de diagnósticos y planes de tratamiento personalizados.• Seguimiento clínico y control de la evolución de los tratamientos.• Información y asesoramiento a los pacientes sobre las diferentes opciones terapéuticas y medidas de prevención en salud bucodental.• Cumplimentación y actualización de historias clínicas conforme a la normativa vigente.• Coordinación con el resto del equipo clínico para garantizar una atención integral y de calidad.• Cumplimiento de los protocolos clínicos, de calidad, bioseguridad y protección radiológica establecidos por la clínica.Requisitos• Grado o Licenciatura en Odontología.• Colegiación vigente.• Experiencia mínima de 2 años como odontólogo/a.• Dominio de castellano y catalán, tanto hablado como escrito.• Capacidad para trabajar en equipo, orientación al paciente y excelentes habilidades de comunicación.• Disponibilidad para incorporación inmediata.ENTREVISTA PRESENCIAL PREVIA #J-18808-Ljbffr

EasySalud, grupo de gestión de servicios sanitarios, busca un médico especialista en Cardiología para un hospital privado en Torrevieja (Alicante). Se ofrece contrato laboral o mercantil, jornada completa o parcial, horario a convenir. Las funciones incluyen consulta, urgencias y hospitalización; sin hemodinamia. Requisitos: licenciatura en Medicina y homologación, especialidad MIR o reconocimiento, colegiación y disponibilidad inmediata. #J-18808-Ljbffr

A leading international cleaning solutions company in Granollers is seeking a Project Manager to oversee optimization and improvement projects. The successful candidate will be responsible for project implementation, resource coordination, and performance analysis. Applicants should hold a Bachelor's Degree in Industrial Engineering, possess at least 2 years of Project Management experience, and be fluent in English. Join us to contribute to a cleaner world while enjoying a collaborative work environment. #J-18808-Ljbffr

Capchase is hiring a Tech Generalist to own end-to-end systems—from frontend to backend—with a focus on scalable infrastructure and data-driven decisions. You’ll select the right tools and shape the platform. In a remote-first, distributed team, you’ll collaborate across product and finance domains, design reliable services, and mentor others while delivering visible impact from day one. #J-18808-Ljbffr

North Search te ofrece la oportunidad de unirte como Key Account en Aragón, para construir relaciones a largo plazo con farmacéuticos/as y reforzar la presencia de la empresa y de sus productos OTC, asesorando a nivel científico y de marketing en todo el territorio. La posición es de campo, con responsabilidad de desarrollar planes, colaborar con marketing y ventas, y asegurar el cumplimiento de políticas internas y códigos del sector. #J-18808-Ljbffr

Alfasigma S.p.A. busca un Director de Ventas para gestionar y desarrollar todos los canales comerciales minoristas en España. Este rol es clave para maximizar la rentabilidad a través de inversiones estratégicas y decisiones de producto. Los candidatos deberán tener experiencia en el sector farmacéutico o de bienes de consumo y un enfoque analítico orientado a resultados. La posición ofrece la oportunidad de liderar un equipo dinámico en un entorno competitivo. #J-18808-Ljbffr

Secpre busca un/a Cirujano/a Plástico en Vigo para su servicio de Cirugía Plástica. Se ofrece contrato a tiempo completo y guardias localizadas, con incorporación inmediata y periodo de prueba de 6 meses. Se valorará experiencia en microcirugía y cirugía de la mano, aunque no es excluyente. Es imprescindible tener la titulación de la especialidad o estar homologada por el Ministerio de Sanidad de España. Remuneración competitiva y ambiente laboral positivo. #J-18808-Ljbffr

Field Clinical Specialist, Cardiac Rhythm Management (Northern region) Join to apply for the Field Clinical Specialist, Cardiac Rhythm Management (Northern region) role at Boston Scientific Location Remote – Based in the Northern region of Spain (Asturias, Cantabria, País Vasco, Navarra, La Rioja) About The Role As a Field Clinical Specialist in our Cardiac Rhythm Management (CRM) team, you will play a critical role in supporting Boston Scientific’s mission to advance science for life. You will provide expert clinical and technical support to physicians, CRM Lab staff, and the broader commercial team. This includes hands‑on case coverage, education, and customer engagement to ensure safe, effective, and confident use of CRM devices. Your contributions will directly support clinical success and business growth across your region. Your Responsibilities Will Include Serving as the primary clinical resource for case coverage, basic troubleshooting, and system/software updates. Educating internal and external stakeholders on the clinical use of CRM devices through presentations, demonstrations, and other formats. Attending CRM procedures in hospital labs to support device use and clinical outcomes. Delivering initial and ongoing training to sales representatives and development teams on CRM systems and procedures. Engaging directly with physicians and clinical staff to assess needs, demonstrate product value, and support care goals. Building and maintaining relationships with hospital personnel and decision‑makers to expand CRM adoption and strengthen customer loyalty. Responding to customer feedback and collaborating with internal teams (sales, marketing, tech support) to deliver effective solutions. Required Qualifications Minimum of 1–2 years’ experience in a similar clinical or technical support role, preferably within cardiology. Newly graduated biomedical engineers or life sciences professionals are also encouraged to apply. Strong verbal and written communication skills. Ability to quickly grasp and communicate complex technical and clinical information. Fluent in English (minimum B2 level). Based in, or willing to relocate to, Northern Spain. Willingness to travel extensively across the assigned territory. Preferred Qualifications Previous experience in international markets. Knowledge of the Cardiac Rhythm Management (CRM) market. Proficiency in additional languages. Demonstrated ability to work collaboratively and cross‑functionally in dynamic environments. Self‑motivated with the ability to influence others and manage competing priorities. What We Can Offer To You A permanent contract with a company car and competitive benefits package. Continuous learning and development through upskilling and mentoring. An environment of healthy competition and innovation. A purposeful mission—transforming lives through medical technology. Requisition ID 620497 Seniority level Not Applicable Employment type Full‑time Job function Other Industries Medical Equipment Manufacturing Referrals increase your chances of interviewing at Boston Scientific by 2x #J-18808-Ljbffr

Senior/Principal Statistical Programmer SAS + R (Remote) Sponsor-dedicated: Working fully embedded within one of our pharmaceutical clients, with the support of Cytel right behind you, you'll be at the heart of our client's innovation. As a Principal Statistical Programmer you will be dedicated to one of our global pharmaceutical clients; a company that is driving the next generation of patient treatment, where individuals are empowered to work with autonomy and ownership. This is an exciting time to be a part of this new program. Position Overview: This position reports to the Director, Biostatistics and Programming in the FSP Services business unit in Cytel. The Principal Statistical Programmer works independently with only concept level instruction and very little supervision, tracks progress, and provides expert technical support to team members. We are looking for a highly experienced senior statistical programmer who will work on clinical development programs on different therapeutic areas and participate in overseeing CRO programmers to ensure that data summaries are delivered in a consistent, high-quality manner. This individual will be responsible for implementing all reporting and analysis activities for the Sponsor clinical trials. As a Principal Statistical Programmer, your responsibilities will include: Generate SDTM, ADaM specifications, datasets, reviewer's guide and define.xml files for multiple studies Develop SAS programs which generate datasets, complex listings, tables (including those with descriptive and standard inferential statistics in collaboration with a Statistician), and complex graphs Deliver high-quality statistical programming results including developing, validating, and maintaining SAS and/or R programs tailored to clinical development programs' needs Participate in overseeing CRO's statistical programming deliverables for multiple clinical studies to ensure high-quality and meet the pre-specified timelines Support the preparation of clinical study reports, regulatory submissions, publications, annual DSUR, and exploratory analyses Understand and follow FDA regulations which affect the reporting of clinical trial data. This includes good clinical practice and guidelines for electronic submissions. Contribute to the creation, maintenance, documentation, and validation of standards for programming tools, outputs, and macros Participate in the development of CRFs, edit check specifications, and data validation plans Provide review #J-18808-Ljbffr

Investment Counsellor – Spanish Private Clients Recruit UK are working with a leading global investment management firm that is looking to appoint an Investment Counsellor to join its Dublin-based team. The Opportunity This is an exciting opportunity for an experienced finance professional to develop their career within wealth management, working closely with high-net-worth private clients. You will be responsible for building and maintaining long-term client relationships, providing an exceptional level of service, and helping clients understand their investment strategy and the wider financial markets. The Day-to-Day Build and maintain strong, long-term relationships with high-net-worth private clients. Manage a portfolio of client relationships and act as a key point of contact. Keep clients informed about their portfolios, relevant market developments and investment strategies. Clearly communicate investment decisions and financial information in an engaging and easy-to-understand manner. Work closely with internal investment, research, trading and client service teams. Develop your knowledge of financial markets, investments and portfolio management through ongoing training and development. Your Qualifications 2+ years' experience working with private clients within wealth management, private banking, financial services or a related environment. Strong knowledge of financial markets, investments and broader economic developments, with excellent communication and relationship-building skills. Native Spanish and fluent English language skills are essential. A relevant degree or financial qualification such as QFA, CISI or CFA would be beneficial, but is not essential. What’s on Offer Salary up to €82,000, depending on experience, plus performance-related bonus. Opportunity to work with high-net-worth private clients within a global investment management organisation. Comprehensive training and ongoing professional development. Collaborative and supportive working environment. Dublin-based office with potential hybrid working opportunities, subject to role, tenure and performance. #J-18808-Ljbffr

Sanitas Hospitales selecciona para el servicio de pediatría del Hospital Universitario Sanitas la Zarzuela una plaza de Médico/a Especialista en Pediatría con perfil de cuidados intensivos/neonatos/pediátricos. Contratos laborales indefinidos a jornada completa o parcial, según preferencia y disponibilidad del/la profesional interesado/a. Ofrecemos un entorno hospitalario universitario, con posibilidad de docencia, participación en sesiones clínicas y desarrollo profesional continuo, en un #J-18808-Ljbffr

Private Physician — Live-In Medical Continuity — Riyadh Salary £240,000 per year (gross), accommodation & travel included Private Medical Recruitment for the Gulf | UK & European Trained Specialists Who We Place: Private & Maternity Nurses, Physiotherapists & Osteopaths, Private & Concierge Physicians Job Description We are seeking a UK & European-trained private physician to join a private family in Riyadh, for its live-in medical continuity post. Moving between Riyadh and the family's European addresses is routine, and standards for primary medical care and long-term health oversight never change. When you travel with the family, all local arrangements (visa, licensing and coordination with local clinics) remain with the family's own office and advisers. The family appoints you, and you sign with them directly, once Medical Staff Talent has introduced and verified you. Requirements This post is for a family medicine physician (GP) trained and registered in the UK or Europe, with a record that includes primary medical care and long-term health oversight. A career of 2 years since qualifying is required, with private or one-to-one work counting in your favour. This Riyadh post is limited to clinicians trained and registered in the UK or Europe, and anything else is outside the brief. The family's working language is English, and yours must be fluent, and everything you see in the home remains confidential. Your professional history is verified by us before the introduction takes place, and references are followed up personally. Benefits A gross salary of £240,000 per year, with accommodation and travel included, applies to this Riyadh appointment, reflecting the seniority and discretion of the role. The salary is agreed directly between the family and the clinician; each clinician should take advice from their own tax adviser on whether the income is taxable in their circumstances. Living arrangements within the family's residence in Riyadh are provided by the family. Annual leave is guaranteed in your contract with the family, together with annual flights and a secure, long-term contract. Remuneration, leave and duties are put in writing by the family, and Medical Staff Talent takes no role in the employment. Engagement essentials Availability to begin within six weeks of offer. Live-in and single-status: the role suits clinicians who relocate alone, with full flexibility to travel worldwide with the family at short notice. Medical Staff Talent introduces and verifies clinicians. The engagement is contracted directly between the family and the clinician, and all local arrangements (visa, licensed entity, coordination with local clinics) remain with the family's own office and advisers. #J-18808-Ljbffr

Rockwell Automation is seeking a Cyber Technology Consultant to join our Global Sales and Marketing team. This role delivers presales support and acts as a trusted advisor on SecureOT Platform across Europe. Candidates will have OT cybersecurity experience, pre-sales or consulting background, and the ability to present technical solutions to customers in English; role can be based anywhere in Europe with Rockwell presence. #J-18808-Ljbffr

We are seeking a Hematologist - Medical Director to join our dynamic team. The Medical Director will have overall responsibility for providing medical, scientific, and strategic leadership for the successful planning, execution, and reporting of clinical trials. Additionally, this role acts as the Medpace internal medical expert and will serve as a medical resource for the review, presentation, and interpretation of results in the Clinical Study Report. The Medical Director will also be involved in the development of new clinical projects, including study design, protocol, and project plans as required. We are currently seeking Medical Directors in different locations. All Medical Directors have hybrid WFH flexibility. Responsibilities Provide medical management and expertise for clinical trials; Contribute medical expertise to study reports, regulatory documents, and manuscripts; Manage safety issues in clinical trials and work closely with associates in evaluation and assessment of the trials; Participate in new business development through involvement in proposal and sponsor meetings as requested; Coordinate with other departments in all phases of the studies and trials including feasibility assessments, design processes, educational efforts, management of medical information, and reviewing and editing of medical documents; Follow specific research related protocol and lead others in strict adherence to the policies. Qualifications Must have an M.D. degree or equivalent. Board certification and current medical licensure are preferred; Prior clinical trial research experience preferred; and Previous experience in pharmaceutical-related clinical research is preferred. Travel: up to 20% Medpace Overview Medpace is a full-service clinical contract research organization (CRO) providing phase l-lV clinical development services to the biotechnology, pharmaceutical, and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through the advancement of clinical research. We leverage in-country regulatory and therapeutic expertise across all major therapeutic areas including oncology, cardiology, metabolic, endocrinology, central nervous system, and anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, we employ more than 6,500 people across 40+ countries. Why Medpace? When you join Medpace, you become part of an innovative team that brings cutting-edge therapies to market while building a meaningful and rewarding career focused on scientific excellence and improving patient outcomes around the world through continuous learning and cross-functional collaboration. Purpose-Driven Work Work alongside physicians, scientists, and industry-leading experts committed to advancing the global development of medical therapeutics through clinical research excellence Collaborative Culture Contribute to an interactive team environment that empowers decision making, creative thinking, and continuous learning through open communication and mutual trust. Leadership throughout Medpace is both accessible and approachable Continuous Growth & Development Office based environment with on-site mentors Defined career paths with clear advancement opportunities Industry renowned onboarding and training programs designed to accelerate professional development Ongoing training and continuous learning opportunities throughout your career An environment that encourages employees to influence change, contribute ideas, and grow quickly Other Employee Benefits Competitive compensation programs that recognize and reward performance Comprehensive health, wellness, retirement, and PTO benefits Office based culture with occasional WFH that provides flexibility for eligible positions after training Company-sponsored social events Please note benefits may vary based on country. What to Expect Next A Medpace team member will review your application and if your profile matches our current needs, you will be contacted for an interview. While we review all applications carefully, we are unable to respond to every applicant, and only candidates selected for interviews will be contacted. #J-18808-Ljbffr

RemoteJobsOne is seeking a Biostatistician for a fully remote contractor role open to candidates based in Spain. You will contribute clinical statistics expertise to AI-assisted clinical research, applying your domain knowledge to train next-generation models while working from home. The role emphasizes evaluating statistical outputs, ensuring alignment with the SAP, and communicating results clearly. A MSc/PhD in Biostatistics and experience with SAS or R are preferred. #J-18808-Ljbffr

Kabilio is seeking a hands-on Tech Lead to shape and scale our AI-native Financial Operating System for accounting firms and SMEs in Southern Europe. You will own core platform areas, set technical direction, and mentor a high-impact engineering team while writing production-grade code across the stack. You’ll collaborate closely with the CTO and cross-functional teams to balance speed with quality, improve testing and performance practices, and help define the roadmap as we expand into Spain #J-18808-Ljbffr