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¿Te apasiona la comunicación, el marketing y el entorno científico-tecnológico? En ITENE te ofrecemos la oportunidad de realizar tus prácticas en el departamento de Comunicación y Eventos, colaborando en proyectos reales que impactan en la sociedad. 🎯 ¿Qué harás durante tus prácticas? Bajo la supervisión del equipo de comunicación, podrás participar en: • Apoyo en la generación de contenidos para notas de prensa, artículos, guiones de vídeo, newsletters, presentaciones, etc., • Colaboración en campañas de inbound marketing, e-mail marketing, SEO y SEM., • Actualización de contenidos en la web y redes sociales., • Revisión y edición de textos generados por especialistas., • Apoyo en la maquetación visual de materiales gráficos., • Participación en la organización de eventos y ferias., • Elaboración de informes básicos sobre el impacto de las acciones de comunicación. 🧠 ¿Qué buscamos en ti?: • Estudiantes de Grado en Periodismo, Comunicación Audiovisual o Marketing., • Valorable formación complementaria en comunicación digital o diseño gráfico., • Interés por el sector de la innovación, el medio ambiente y la tecnología., • Buen nivel de inglés (mínimo B2)., • Creatividad, proactividad y ganas de aprender. 💼 ¿Qué te ofrecemos?: • Prácticas formativas remuneradas en un entorno profesional y multidisciplinar., • Participación en proyectos reales con impacto en el sector industrial y científico., • Flexibilidad horaria. Todos los viernes tarde libres! (Nos adaptamos a cada alumno para que puedas desarrollar con nosotros tus prácticas, eso si, siempre trabajamos de mañanas!).

En ADAMS Formación buscamos profesores/as altamente cualificados/as y con experiencia en gestión financiera, para la preparación de empleados públicos del grupo A2 de la Administración General del Estado. ¿Cuáles serán tus funciones? • Impartir contenidos formativos de gestión financiera pública, adaptados a los grupos A2., • Facilitar el aprendizaje mediante casos reales, ejercicios prácticos y simulaciones relacionadas con la normativa vigente., • Evaluar de forma continua el progreso del alumnado, aplicando metodologías activas y participativas. Requisitos: • Se valorará ser funcionario/a de carrera o especialista en la materia., • Conocimientos actualizados de la normativa aplicable ¡Si te apasiona enseñar, queremos contar contigo! Únete a Adams Formación.

Kapadi is a full service CRO that focuses on complex oncology indications including immunotherapy and cellular therapies. We know that innovative research requires innovative operations and we've built that into our culture, systems and processes. We have an infrastructure to enhance access to patients and integrated technology to provide higher quality and faster access to results. We are looking for a highly-motivated Clinical Research Associate III - Study Start-Up and Maintenance to help us continue to grow our business and deliver new, life-changing therapies for the cancer patients who need them. As a Clinical Research Associate III - Study Start-Up and Maintenance, you will: Primary liaison between site and project team throughout the study lifecycle- from site identification through close-out related to site start-up support and regulatory document maintenance. Able to respond to site concerns and questions as applicable. Documents activities via communication logs and other required project documents as per SOPs and project plans. Enters data into tracking systems as required to track all observations, ongoing status and assigned action items for resolution. Assists the project team with the creation and finalization of the Clinical Site Activation Plan. Collects, compiles and reviews essential document packages for site activation in accordance with ICH-GCP and/or all applicable local and federal regulatory requirements. Ensures essential documents are sent to the assigned Regulatory specialist for submissions to the FDA and/or for submission for EU and other regions for any type of application (i.e., submissions for the EU via CTIS, submissions of Medical Device trials to IRB/EC and Regulatory Agencies submissions). Performs study regulatory maintenance activities including but not limited to: collection of updated 1572 or equivalent, Informed Consent Form (ICF) updates resulting from amendments and addenda, distribution and IRB/IEC approval of Protocol Amendments etc. Manage, coordinate and perform Central IRB submissions for North America and local CTIS submissions for Europe, including but not limited to: initial submissions, amendment submission, changes of PIs, safety submission, annual reviews etc.. May participate in the identification and selection of investigators and clinical sites and/or may proactively suggest potential sites based on local knowledge of treatment patterns and clinical trial requirement. Understands project scope, budgets, and timelines for the trial and is expected to provide input and manage site-level activities and communication to meet project deliverables and timelines are met.Identifies and communicates out of scope activities, operational efficiencies, and process improvements to the Project Manager. May prepare for and attend Investigator Meetings, Sponsor face to face meetings and global clinical monitoring / project team meetings. As required, collaborates and builds relationships with Sponsor and other affiliates, medical advisors, and local country staff. Completes all assigned training programs and applies learning to job responsibilities. Maintains working knowledge of ICH-GCP guidelines as well as all applicable country and local regulations. Knowledge, skills and abilities: • Demonstrated knowledge of the clinical research and development process in pharmaceutical and/or biotechnology industries., • Demonstrated ability to lead and coordinate study start-up and regulatory activities for large-scale clinical trials., • Strong knowledge of Good Clinical Practice/ICH guidelines and other applicable regulatory requirements. Requirements: • Bachelor’s Degree (or equivalent) level of qualification in Life Sciences, Medicine, Pharmacy, Nursing or equivalent combination of education and experience., • Minimum of 3 years of experience in clinical R&D in pharmaceutical, biotechnology and/or clinical research organization (CRO) businesses, including at least 2 years of experience in a CRO providing clinical research services to pharmaceutical, biotechnology or medical device companies., • 5+ years of experience in a study start-up position.

Company Description Space Robotics Workers (SRW) is focused on developing key technologies for robotics for space and Low-Earth Orbit Destinations. The company offers in-orbit services such as assembly, maintenance, manufacturing, and debris removal, with a goal to facilitate space exploration and innovation. Job Description We are seeking an experienced Design Engineer to join our team in Santander, Spain. This is a full-time, on-site position for a skilled professional with a strong background in designing and simulating mechanical elements of space vehicles. You will play a key role in developing advanced solutions for space applications, working alongside a multidisciplinary team of experts. As a Design and Simulation Engineer, you will be responsible for the design, modelling, and simulation of spacecraft structures and mechanisms. You will utilize advanced CAD and FEA tools to ensure the performance, reliability, and compliance of our products with industry standards. Responsibilities • Design and model mechanical components and assemblies for space vehicles., • Perform finite element analysis (FEA) simulations to validate performance and structural integrity., • Prepare and review technical documentation, including design reports and simulation results., • Collaborate with engineering teams to optimize designs and resolve technical challenges., • Ensure compliance with industry standards and customer requirements., • Contribute to continuous improvement of design and simulation processes. Qualifications • Minimum 3 years of experience in designing and simulating mechanical and thermal elements for space vehicles or related aerospace applications., • Industrial experience in designing pressurised vessels, e.g. submarines, aircraft, habitable modules for space., • Knowledge of Additive Manufacturing applied to space technology., • Knowledge of characterization of materials for Space., • Proficiency in SolidEdge, CATIA, SolidWorks or similar 3D CAD software., • Proficiency in NX Femap with Nastran or similar FEA tools for structural., • Strong understanding of mechanical engineering principles as applied to space systems., • BSc/MSc in Mechanical Engineering, Aerospace Engineering, or a related field., • Fluency in English is desirable., • Thermal analysis and design experience is a desirable asset., • Availability to work on-site in Santander, Spain, in a full-time capacity.

Company Description Space Robotics Workers (SRW) is focused on developing key technologies for robotics for space and Low-Earth Orbit Destinations. The company offers in-orbit services such as assembly, maintenance, manufacturing, and debris removal, with a goal to facilitate space exploration and innovation. Job Description We're looking for a Software Engineer to develop and implement embedded systems software for Space Applications. You'll be one of our first employees, working directly with our founding team to build the foundational Software that controls actuators, sensors, power systems, and data interfaces operating in the extreme environment of space. Responsibilities • Develop flight-ready Software following aerospace software standards (NASA and ECSS standards), • Implement command and data handling (C&DH) software for telemetry, commanding, and health monitoring, • Design state machines and control logic for robotics, autonomous docking sequences, latch mechanisms, and fluid/power transfer operations, • Create bootloaders, firmware update mechanisms, and version control for in-orbit software maintenance, • Develop watchdog timers, error handling, and safe-mode recovery logic, • Write software that is testable, maintainable, and documented to space industry standards, • Develop comprehensive test plans for verification and validation, • Perform unit testing, integration testing, and system-level testing of embedded software, • Conduct hardware-in-the-loop testing with actuators, sensors, and mechanical assemblies, • Participate in environmental testing (thermal vacuum, vibration, radiation) to validate firmware performance, • Participate in design reviews, technical discussions, and system architecture decisions, • Create detailed software specifications, design documents, and interface control documents (ICDs), • Support configuration management and traceability for space-qualified systems Qualifications • 3+ years of professional experience in embedded software development in the space or robotics industry, • Proven experience developing embedded systems software for electromechanical components (motors, actuators, sensors, valves, etc.), • Strong proficiency in Python for scripting, testing, data analysis, and rapid prototyping, • Hands-on experience with Arduino or similar microcontroller development platforms, • Strong understanding of digital electronics, including ADCs, DACs, PWM, encoders, and communication protocols (CAN, SPI, I2C, UART, etc.), • Experience with embedded C/C++ for microcontrollers and embedded processors, • Familiarity with debugging tools including oscilloscopes, logic analyzers, JTAG/SWD debuggers, and multimeters, • Bachelor’s degree in computer engineering, Electrical Engineering, Aerospace Engineering, or equivalent technical field Strongly Preferred • Flight software development experience for space systems (satellites, launch vehicles, landers, or space robotics), • Aerospace software standards knowledge such as NASA or ECSS software engineering standards, • Space-qualified hardware experience with radiation-tolerant processors, FPGAs, or components, • Real-Time Operating Systems (RTOS) experience such as FreeRTOS, VxWorks, or RTEMS, • Motor control experience including brushless DC motors, stepper motors, servo systems, or linear actuators, • Sensor integration experience with IMUs, force/torque sensors, proximity sensors, encoders, or vision systems, • Communication protocols for space or industrial applications (SpaceWire, MIL-STD-1553, Ethernet/IP, Modbus, ROS, Industrail ROS/ROS 2.0), • Familiarity with control theory including PID control, state-space controllers, or model-based control, • Simulation and modeling tools such as MATLAB/Simulink for control system design, • Experience with hardware-in-the-loop (HIL) testing and test automation frameworks, • Knowledge of power electronics and power management systems, • Version control and CI/CD experience with Git, GitLab/GitHub, and automated testing pipelines, • Python libraries experience such as NumPy, SciPy, Matplotlib for data analysis and visualization Personal Attributes • Hands-on problem solver: Comfortable working directly with hardware, debugging in the lab, and troubleshooting complex issues, • Startup mentality: Comfortable with ambiguity, fast pace, and wearing multiple hats in an early-stage environment, • Collaborative: Works effectively across disciplines (mechanical, electrical, software) and with external partners, • Mission-driven: Passionate about advancing space exploration and building sustainable space infrastructure, • Strong communicator: Can document technical work clearly and explain firmware behavior to diverse audiences, • Continuous learner: Stays current with embedded systems technologies and aerospace industry best practices

Position: Chief Operating Officer / SVP Operations You are a senior executive responsible for leading and managing the company’s operational sites to ensure efficiency, safety, quality, and productivity across all locations. Reporting to the Chief Executive Officer (CEO), the COO will provide strategic and hands-on leadership to optimize site performance, drive operational excellence. Responsibilities: • Oversee manufacturing operations (process development → commercial scale GMP) for small molecules/APIs, drug product., • Lead scale-up strategy: from early development to commercial manufacturing, including site expansion, capacity build-out., • Drive operational excellence: supply chain, quality systems (GMP), cost-effectiveness, on‐time delivery., • Partner with R&D/CMC, quality/RA, business development to align manufacturing operations with client expectations and regulatory compliance., • Global mindset: ability to manage international operations, client interfaces (US, Europe, Asia). Required Experience: • 10 - 15+ years in pharmaceutical or biotech manufacturing operations (preferably CDMO/CMO or API/drug product manufacturing)., • Proven scale-up experience (clinical → commercial)., • Experience in a service environment (client-facing CDMO or contract manufacturing)., • Understanding of GMP, CMC, process development, continuous improvement., • Leadership of large teams, cross-functional; P&L responsibility desirable. Core Competencies • Site Operations Management, • Strategic and Operational Planning, • Leadership and Team Development, • Lean / Continuous Improvement, • Financial and Performance Management, • Safety and Compliance, • Cross-Functional Collaboration, • Change Management

PROFESOR/A MÁSTER PREVENCIÓN DE RIESGOS LABORALES. Facultad de Ciencias Sociales y Jurídicas. En la Universidad Católica de Ávila (UCAV), institución centrada en la formación integral del alumno, abrimos una convocatoria para incorporar un/a Profesor/a a nuestro equipo docente e investigador. Buscamos personas con vocación académica y capaces de contribuir en el crecimiento de la Universidad. Apostamos por una enseñanza de calidad, cercana al estudiante, que integra la innovación y la investigación como pilares fundamentales de nuestro modelo educativo. ¿Qué buscamos? • Profesor/a para el Máster de Prevención de Riesgos Laborales. -Acreditación ANECA. -Reconocimiento de sexenios de investigación. -Experiencia docente universitaria y participación en proyectos de innovación. ¿Qué ofrecemos? • Funciones: dirigir trabajos fin de máster., • Salario acorde a la formación y experiencia del/a candidato/a., • Docencia online, • Estabilidad laboral en un entorno que valora el talento y el compromiso. Si deseas formar parte de un proyecto educativo con valores, ¡queremos conocerte!

About MGI MGI Tech Co., Ltd. (MGI), a subsidiary of BGI Group, is committed to enabling effective and affordable healthcare solutions for all. Based on its proprietary technology, MGI produces sequencing devices, equipment, consumables, and reagents to support life science research, medicine, and healthcare. MGI’s multi-omics platforms include genetic sequencing and Liquid Handling. Providing real-time, comprehensive, life-long solutions, its mission is to develop and promote advanced life science tools for future healthcare. Position：DCS Senior Sales Specialist Base：France & Spain Major Responsibilities • Own and drive revene achievement and growth across the assigned region for single-cell, spatial biology and multi-omics solutions, including instruments, consumables., • Develop and execute sales plans, ensuring alignment with broader organizational goals and market conditions., • Identify, qualify, and manage new business opportunities in academic research institutions, core facilities and relevant targeted customer segment., • Lead complex sales cycles, from opportunity identification through negotiation and successful close., • Provide consultative sales support by deeply understanding customer workflows in single-cell, multi-omics, and spatial applications., • Collaborate closely with Field Application Scientists, product management, marketing, and operations to ensure customer success and long-term account retention., • Participate in conferences, trade shows, and customer workshops to promote product portfolio awareness and strengthen brand presence., • Deep understanding of territory management, account strategy and technical/product positioning., • Proactively gather customer feedback and market intelligence to support product development and competitive strategy., • Forecast revenue, manage pipeline health, and deliver accurate reporting to leadership. Maintain accurate records of opportunities, forecasts, and customer interactions in CRM systems. Required • Bachelor’s degree in Life Sciences (Molecular Biology, Genomics, Biotechnology, or related field); advanced degree preferred., • 5+ years of life science sales experience, with at least 2–3 years selling NGS, single-cell, spatial, or multi-omics products., • Demonstrated success managing accounts and closing high-value deals., • Strong technical understanding of sequencing workflows, including single-cell, spatial transcriptomics, library prep, and data-analysis considerations., • Exceptional communication, negotiation, and presentation skills with the ability to influence diverse stakeholders., • Proven ability to work independently, prioritize high-impact opportunities, and manage a complex sales cycle., • Willingness to travel 50% as required., • Working language is English, additional language is benefical., • Hands-on research or industry experience in single-cell sequencing, spatial biology, or advanced NGS applications., • Experience selling capital equipment into genomics, immunology, oncology, or neuroscience markets., • Familiarity with relevant platforms (e.g., 10x Genomics, CosMx/GeoMx, MERFISH, etc.).

Novogene is a leading global provider of genomic services and solutions. Leveraging the latest next-generation sequencing (NGS), bioinformatics expertise, and the largest sequencing capacity in the world, Novogene provides unsurpassed data quality and fast turnaround time to all our customers. We are seeking a proactive and results-driven Inside Sales Representative (NGS background) to expand our business across the Southern Europe. The ideal candidate will be responsible for identifying and prospecting new clients within biotech, biopharma, and pharmaceutical industries, utilising data mining techniques and market research. This is a fantastic opportunity for a motivated individual with a strong background in genomics and sequencing technologies to grow within a leading sequencing provider. Location: Remote working (Spain) Job descriptions: • Proactively identify and engage potential customers through online research, databases, and industry websites., • Utilize Excel and other data analysis tools to compare datasets, track prospects, and refine lead lists., • Conduct outbound cold calls, emails and on site visit to introduce Novogene’s sequencing services to new clients., • Develop and maintain a strong pipeline of potential clients within Iberia & Italy area., • Understand customer needs and effectively communicate how Novogene’s NGS and third-generation sequencing services can support their research and development goals., • Collaborate with the sales and marketing teams to execute targeted outreach campaigns., • Maintain accurate records of client interactions and progress using CRM tools., • Stay up-to-date with advancements in genomics, sequencing technologies, and industry trends., • Provide operational support to Account Managers, including preparing quotations, coordinating administrative tasks, and assisting with follow-up actions to ensure smooth project execution. Your skills and experience: • MSc in Genomics, Molecular Biology, Biotechnology, or a related field., • Strong understanding of next-generation sequencing (NGS) and third-generation sequencing technologies and their applications., • Experience in data mining from websites and databases to identify potential clients., • Outstanding listening, verbal and written English communication skills. Native or business level Spanish speaking is preferred; Italian proficiency is a plus., • Proficiency in Microsoft Excel, including data comparison and analysis., • Excellent communication skills and confidence in cold calling prospective clients., • Self-motivated, driven, and able to work independently in a remote setting., • Previous sales or customer-facing experience in life sciences is a plus but not mandatory. Novogene is an Equal Opportunity Employer that prohibits discrimination and harassment of any kind. Novogene is committed to ensure all qualified applicants will receive consideration for employment without regard to race colour, religion or belief, sex, sexual orientation, gender identity, national origin, disability, or any other legally-protected characteristics. All employment decisions at Novogene are based on business requirements on its positions and skill sets on applicants, The business is committed to providing an inclusive and accessible recruiting experience for candidates with disabilities, or other physical or mental conditions.

We are looking for someone who can: • Contributes to the companies’ performance by providing models, products and services adapted to his portfolio customers’ needs, by finding new customers and by retaining existing customers, within the framework of trade policy., • Structures his business action plan in line with the company’s strategy to achieve revenue and margin target. The prospection area is the Iberian Peninsula Your profile : • Excellent technical knowledge of the products/services offered by the company, the legal framework in which it operates, the sector and its developments, • Mastery of commercial techniques in a scientific environment, • Mastery of major office software, • Mastery of a CRM, • English spoken is required Please feel free to contact me if you are interested

We are seeking several QC Technicians to join the Biologics Lab team of one of Hlx's clients. This role is ideal for those candidates who enjoy hands-on laboratory work, operating under GMP standard, and contributing to high-quality, safe production processes. Responsibilities: • Analytical tests on production materials, • Complete laboratory documentation in line with GMP requirements, • Maintain laboratory equipment, • Support method transfers, method validations and continuous improvement initiatives Experience Required: • Experience in a QC Laboratory environment, in a similarly regulated industry, • Familiarity with GMP guidelines, • Strong attention to detail, documentation accuracy and commitment to quality Candidates must be able to speak fluent Spanish.

At ISPROX, a consultancy specialized in talent acquisition and headhunting, we are supporting our client —a multinational company in the chemical sector, recognized for its innovation in the manufacture and commercialization of industrial and cosmetic specialties— in the search for an R&D Leader for their Personal Care Active Ingredients division. Mission of the position: To lead research and development tasks and functions related to new products, techniques, and laboratory projects, ensuring compliance with quality, environmental, and occupational health and safety standards. Key responsibilities: • Actively participate in new R&D developments., • Plan, monitor, and partly carry out project-related lab work., • Conduct bibliographic research in articles, journals, patents, and other relevant sources., • Develop and optimize synthesis routes and product formulations., • Support the scale-up phase of new products or synthesis processes to production., • Develop analytical methods related to new projects., • Prepare technical laboratory reports and presentations. Requirements: • Degree in Chemistry, Pharmacy, or Biochemistry., • Master’s degree or PhD in Organic Chemistry, or demonstrable equivalent experience., • English level C1., • Proven experience in R&D within the cosmetic industry (laboratory, research, and synthesis design)., • Knowledge of chemical structures and functionality of preservatives and/or multifunctional cosmetic ingredients., • Knowledge of green or natural chemistry will be an advantage., • Skills: self-motivated, decisive, organized, with leadership and communication abilities, and capable of working independently while adapting to change and competing priorities. We offer: An opportunity to join a stable and growing international company with a strong commitment to innovation, flexibility, and employee well-being. • Permanent full-time position (Monday to Friday)., • Flexible working hours and the possibility of remote work., • Attractive and competitive salary package., • Social benefits including free canteen, pension plan, life insurance, flexible remuneration, and a range of wellness initiatives (sports activities, physiotherapy, fresh fruit, and more)., • A collaborative environment with values based on innovation, commitment, credibility, and cooperation.

Note: This is a high-paying part-time job that allows for remote work. Please read the recruitment requirements carefully. Thank you. WHAT YOU NEED to Have • Doctorate PhD or equivalent advanced degree in the subject area, • Published at least 30 papers in SCIE/SSCI/AHCI journals in the past five years, • Thorough understanding of research methodologies and ethical principles within the relevant discipline, • Excellent analytical and critical thinking skills, • Strong written communication skills, with the ability to provide clear, concise, and constructive feedback, • Ability to adhere to deadlines and manage time effectively, • Commitment to maintaining confidentiality and objectivity, • Prior experience as a peer reviewer for academic journals is highly desirable, • Familiarity with online manuscript submission and review systems WHAT YOU WILL DO • Assess Novelty: Evaluate whether the manuscript is original and adds new knowledge or insights to the field of study., • Evaluate Study Design and Methodology: Check whether the study design and methods are appropriate, comprehensive, and clearly described to ensure reproducibility., • Literature Review: Ensure the manuscript thoroughly incorporates and cites relevant, up-to-date research in the field., • Analyse Results and Conclusions: Determine whether results are presented clearly and appropriately, and whether conclusions are supported by the data and significant to the field., • Provide Constructive Feedback: Suggest improvements and highlight any flaws, omissions, or ethical concerns., • Recommend Publication: Based on your evaluation, the journal editor will decide whether the manuscript should be accepted, revised, or rejected.

RESUMEN DEL CANDIDATO/A BUSCADO/A En Premium Research buscamos un/a Investigador/a en Inteligencia Artificial y Machine Learning (PhD) para reforzar nuestro equipo de I+D. La persona seleccionada participará en el diseño, desarrollo y despliegue de modelos avanzados de IA en proyectos de investigación aplicada, principalmente, en el ámbito de la salud (aunque no exclusivamente), trabajando en entornos altamente técnicos, colaborativos y multidisciplinares. DESCRIPCIÓN DEL PUESTO La persona incorporada formará parte del área de Inteligencia Artificial y Machine Learning de Premium Research, contribuyendo activamente a proyectos estratégicos de I+D a nivel nacional y europeo. Su labor abarcará desde el diseño conceptual de modelos y metodologías avanzadas hasta su implementación técnica y validación, colaborando estrechamente con perfiles investigadores, ingenieros y expertos en el ámbito biomédico. Entre sus principales responsabilidades se incluyen: • Diseño, desarrollo y validación de modelos de Machine Learning y Deep Learning aplicados a problemas complejos., • Análisis y procesamiento de grandes volúmenes de datos, incluyendo datos biomédicos y de salud, entre otros., • Desarrollo de pipelines de datos y modelos, desde la fase de investigación hasta su despliegue., • Colaboración en proyectos de I+D+i, incluyendo consorcios europeos y nacionales., • Elaboración de documentación técnica, informes científicos y apoyo a publicaciones científicas cuando proceda., • Trabajo en entornos cloud, DevOps y MLOps para el escalado y mantenimiento de soluciones de IA. Se valorará especialmente la experiencia o especialización en el ámbito de la salud, incluyendo proyectos de bioinformática, biomedicina o salud digital, así como experiencia en dry lab (análisis computacional de datos biomédicos) y, de forma adicional, conocimientos de wet lab, técnicas de laboratorio y procesamiento de muestras, que permitan una comprensión integral del ciclo experimental y su traducción a datos y modelos de IA. El puesto ofrece la oportunidad de integrarse en un entorno investigador de alto nivel, con participación en proyectos punteros financiados en gran parte por la Unión Europea, y con una clara orientación a la excelencia científica y tecnológica. REQUISITOS: Experiencia profesional • Mínimo 3–5 años de experiencia en investigación aplicada, I+D o desarrollo avanzado en Inteligencia Artificial y Machine Learning, en entornos académicos, industriales o mixtos., • Experiencia demostrable en:, • Diseño, desarrollo, entrenamiento y validación de modelos de Machine Learning y Deep Learning., • Análisis y procesamiento de grandes volúmenes de datos y pipelines complejos., • Participación en proyectos de I+D+i, preferentemente a nivel nacional y/o europeo., • Experiencia en el desarrollo de soluciones de IA desde fases de investigación hasta su implementación técnica., • Valorable experiencia previa en proyectos del ámbito de la salud, biomedicina, bioinformática o salud digital, incluyendo trabajo con datos biomédicos. REQUISITOS: Formación Doctorado (PhD) en una de las siguientes áreas o disciplinas afines: • Inteligencia Artificial, • Machine Learning / Data Science, • Bioinformática / Computación, • Matemáticas, Física, • Ingeniería de software Sólida formación en matemáticas y estadística, aplicada al modelado y análisis de datos. CONOCIMIENTO, HABILIDADES Y COMPETENCIAS CLAVE Imprescindibles: • Elevado nivel de matemáticas., • Experiencia avanzada en Machine Learning e Inteligencia Artificial, • Dominio avanzado de Python., • Programación de software., • Nivel avanzado de inglés hablado y escrito., • Modelos supervisados y no supervisados., • Deep Learning y arquitecturas avanzadas., • Capacidad de trabajo autónomo y en equipos multidisciplinares., • Responsabilidad, eficiencia y capacidad de esfuerzo. Deseables: • Conocimientos de ingeniería de software., • Cloud engineering., • DevOps., • Experiencia en entornos cloud (AWS, GCP, Azure u otros)., • Escalado y mantenimiento de soluciones de IA en producción., • Habilidades transversales: comunicación, síntesis, capacidad analítica, etc., • Experiencia en proyectos de salud. CONDICIONES DE TRABAJO Y SALARIO: • Contrato indefinido, con 6 meses iniciales de prueba., • Jornada completa., • 100% teletrabajo desde cualquier punto de España., • Flexibilidad para elegir horario y vacaciones., • Jornada intensiva sólo por las mañanas los meses de julio y agosto., • Disponibilidad para reuniones presenciales cada 1-2 meses y posibles viajes al extranjero 1-2 veces al año., • Puesta a disposición de teléfono de empresa y equipos informáticos de última generación., • Rango salarial orientativo: 32.000 € - 38.000 € euros brutos anuales, en función de la experiencia, formación y capacidades. El puesto incluye un plan de crecimiento y revisión salarial según la progresión del candidato/a. NUESTRA EMPRESA Premium Research es una empresa de base tecnológica especializada en la prestación de servicios de ciencia e innovación y en el desarrollo de proyectos de I+D+i tanto a nivel europeo como nacional. Cuenta con un equipo multidisciplinar con experiencia en biomedicina, nanotecnología, genética, bioinformática y machine learning, y ha participado en proyectos de alto impacto en ámbitos como la salud, la economía circular y smart cities entre otros. En su área de Data Science, Premium Research destaca en la gestión de grandes volúmenes de datos, la bioestadística y el modelado predictivo, además de liderar iniciativas propias de desarrollo de producto e innovación.

The Company Our customer is a technology-based startup with solid funding that is in the midst of expansion. They will hire the selected candidate as an internal and permanent employee. Description of the position We’re looking for a Cloud FinOps Specialist for its global operations in Madrid. He/She will take ownership of cloud financial operations, ensuring efficient, transparent and sustainable scalation. Working Experience & Tech Skills @ Proven experience in FinOps or cloud cost management, ideally with Microsoft Azure. @ Strong understanding of cloud infrastructure, billing models, and optimization techniques. @ Analytical mindset with proficiency in Excel, Power BI, or similar tools. @ Experience with Azure Cost Management, CloudHealth, Cloudability or similar tools would be an asset. @ Familiarity with SaaS metrics, unit economics, and cost-to-serve models (desirable). @ Exposure to startup scaling challenges and rapid cloud growth (desirable). Soft skills @ Comfortable working in a fast-paced, agile startup environment. @ Leadership capabilities. @ Ability to work cross-functionally with different teams (engineering, finance). @ International work experience working with international teams Key Responsibilities @ Own Azure’s FinOps strategy: cost visibility, allocation, and optimization. @ Collaborate with engineering teams to design cost-efficient architectures and promote cloud cost awareness. @ Partner with Finance to forecast cloud expenses, align budgets, and support reporting needs. @ Implement and manage FinOps tools and dashboards. @ Define and enforce governance policies. @ Lead cloud cost reviews, anomaly detection, and savings initiatives. @ Stay current with Azure pricing models, service updates, and best practices. Languages @ Spanish: At least B2-C1. @ English: At least B2-C1. Job location Tres Cantos (Madrid). European Union citizen; otherwise, a valid job permit is mandatory. Salary A very competitive salary package. Working from home 3-4 days a week (but according to the specific needs that may arise from the perspective of project development, department, clients, and/or partners). If you are interested, please apply here or send an email to including in the subject: ‘Cloud FinOps Specialist along with your English CV.

🧬 Are you passionate about clinical research and eager to be part of projects that directly impact people’s health? You will join a strategic project within a leading pharmaceutical company, working closely with medical teams and investigators, and actively participating in all phases of clinical studies, from study start-up to close-out. 🎯 What do we offer? Permanent contract through Manpower to provide services on a project within a top-tier pharmaceutical company. A high-impact project focused on clinical research and the development of innovative medicines. A collaborative environment with continuous training and close interaction with multidisciplinary teams. 🔬 What will your day-to-day look like? You will be responsible for monitoring and following up on clinical studies at assigned investigator sites, ensuring compliance with the protocol, Good Clinical Practices (GCP), and regulatory requirements. Your main responsibilities will include: Conducting study initiation, monitoring (on-site and remote), and close-out visits. Verifying the quality and accuracy of clinical data and the correct management of informed consent. Overseeing adverse event reporting and ensuring ethical and regulatory compliance. Keeping study documentation up to date and preparing visit reports. Providing ongoing support to investigators to ensure proper patient recruitment and follow-up. 🌟 What are we looking for? University degree in health sciences, biology, pharmacy, medicine, or related fields. Previous experience as a Clinical Research Associate or in clinical research (experience in observational or clinical studies is highly valued). Good knowledge of Good Clinical Practices (GCP) and applicable regulations. Strong analytical skills, attention to detail, and a focus on data quality. Good communication skills, autonomy, and the ability to manage multiple sites and tasks. High level of confidentiality, professional ethics, and scientific rigor. 🚀 Apply now and take the next step in your career in clinical research!

The Company Our customer is a technology-based startup with solid funding that is in the midst of expansion. They will hire the selected candidate as an internal and permanent employee. Description of the position We’re looking for an Enterprise AI Program Manager for its global operations in Madrid. As Enterprise AI Program Manager, you will have a direct impact on the company’s innovation strategy, orchestrating generative AI projects from concept through to production deployment. You’ll work closely with technical and business teams to turn technical advances into real-world solutions that deliver value. This role blends strategic vision, technical leadership, and project management in a context where your work will enable AI to be deeply integrated into our enterprise processes and operations. Working Experience @ Strong experience in AI and automation: Minimum 3-5 years leading or developing AI and automation projects (Power Platform or similar). Hands-on experience with generative AI models and preferably knowledge of autonomous agent systems (Copilot Studio, AI Foundry and similar). @ Strategic vision: Ability to identify how AI creates business value. Capable of prioritizing AI initiatives based on impact and aligning AI roadmaps with company goals. @ Team leadership and management: Proven experience coordinating multidisciplinary technical teams and collaborating across departments. Not mandatory but preferred: Knowledge of ethical AI frameworks and experience implementing responsible AI practices. Experience deploying generative AI solutions in production environments. Familiarity with Agentic AI frameworks and autonomous decision-making systems. Experience with Power Platform, Copilot, Azure, or other Microsoft ecosystem tools. Soft skills @ Communication skills: Exceptional ability to communicate complex technical concepts clearly to non-technical audiences. @ Ability to work in a fast-paced, agile startup environment. Key Responsibilities @ Lead end-to-end Agentic AI projects: Coordinate initiatives from concept (use case, scope, feasibility) through production deployment and monitoring. @ Align Enterprise AI initiatives with business strategy: Collaborate with technical and business stakeholders to identify opportunities where AI adds value and competitive advantage. Translate AI capabilities into functional solutions that meet real business needs. @ Ensure cross-functional and governed AI adoption: You will make sure AI is not an isolated effort by a single team, but a capability embedded across the entire organization. @ Agile project management in coordination with our PMO: Plan and manage projects using agile methodologies, setting roadmaps, timelines, and clear milestones. Identify and mitigate risks throughout execution. @ Technical oversight and quality assurance: Validate proposed technical solutions, in coordination with our technology partners and other IT Teams, and ensure best practices in AI development. Review architecture to ensure scalability and maintainability. @ AI governance and ethics: Champion responsible AI practices in coordination with our Security and Compliance Team. Implement policies and controls to ensure AI solutions meet ethical, security, and regulatory standards. Oversee safe operation of autonomous agents, bias mitigation, and data privacy compliance. @ Continuous innovation: Keep the team and company up to date with the latest AI trends. Research and pilot new approaches leading proof-of-concept projects. Propose new AI applications that could become future initiatives and act as an internal evangelist for AI. Languages @ Spanish: At least B2-C1. @ English: At least B2-C1. Job location Tres Cantos (Madrid). European Union citizen; otherwise, a valid job permit is mandatory. Salary A very competitive salary package. Working from home 3-4 days a week (flexibility available). If you are interested, please apply here or send us an email to including in the subject: ‘Enterprise AI Program Manager’ along with your CV in English.

The company Our customer is a technology-based startup with solid funding that is currently undergoing expansion. They will hire the selected candidate as an internal, permanent employee based in Madrid to provide services to their global organization. Description of the position We’re looking for a IT Project Manager for their global operations in Madrid. He/she will join the CIO Technical Project Office, acting as a strategic connector between IT, technical teams, and business stakeholders. As a Project Manager, he/she will be responsible for coordinating strategic projects, ensuring alignment across technical domains, and establishing portfolio management standards. He/she will work closely with senior leadership, engineering, IT, and PMO teams to provide visibility, consistency, and execution across initiatives. And also will be responsible for leading and coordinating some projects within the portfolio. Key Responsibilities and Tasks • Translate strategic vision into actionable projects and oversee their execution., • Align project methodologies, reporting, and governance with global PMO standards., • Define and uphold project management standards across IT initiatives., • Manage the IT project portfolio, including planning, prioritization, and resource allocation., • Monitor progress, risks, and performance across projects., • Facilitate collaboration and communication among stakeholders and teams., • Deliver projects as part of the project delivery team., • Provide tools, guidance, and support to improve project outcomes., • Ensure compliance with internal policies and external regulations., • Promote continuous improvement and a culture of transparency and accountability. Working Experience More than 5 years of hands-on experience in Project Management or a similar role. Tech skills (required) • Proven experience in project management within multinational environments., • Experience working closely with CIOs, PMOs, and cross-functional technical teams., • Knowledge of project governance frameworks and portfolio management tools., • Excellent communication, stakeholder management, and organizational skills., • Strong leadership and team collaboration skills., • Comfortable working in a fast-paced, agile startup environment. Tech skills (preferred) • Experience in startups or scale-ups, especially in tech or SaaS., • Knowledge of MS Project, Planner, Dynamics 365, Jira, ServiceNow, and similar platforms., • Knowledge of PMP, Prince2, and Agile Scrum methodologies., • Understanding IT strategy, architecture, and application of lifecycle management. Soft skills • Global Mindset: Experience working in a multi-national environment or on international teams., • Team Collaboration: Strong interpersonal skills and a team-oriented attitude., • Communication: Clear and concise communicator, both verbally and in writing., • Continuous Learning: Eagerness to stay updated on networking trends and emerging technologies. Education and Training • Bachelor's Degree or vocational training qualification: In information technology, telecommunications, or a related field., • Certifications: Relevant certifications are a plus (PMP, Scrum Master…) Languages • Spanish: At least a medium level is required. B2 level or higher., • English: Excellent Business English required (it is their working language). B2/C1 level. Job conditions • Job location: Tres Cantos (Madrid)., • Work permit: European Union nationality. Otherwise, an EU/Spain work permit is required., • Employment type: Permanent Full Time, as an internal employee., • Salary: Depending on qualifications and experience., • Work from home: Hybrid working model, including the possibility of working from home (70%), but according to the specific needs that may arise from the perspective of project development, department, clients, and/or partners. If you are interested, please apply here or send an email to , including in the subject: ‘Technical Project Manager’, along with your English CV.

Descripción del puesto En Spanglish English Academy, buscamos un/a profesor/a de inglés altamente cualificado/a para unirse a nuestro equipo de clases online. Nuestro objetivo es ofrecer formación de calidad que ayude a los alumnos a alcanzar sus metas, especialmente en la preparación de exámenes oficiales de Cambridge. El puesto tendrá el objetivo de preparar exámenes de Cambridge a nivel B2 y C1 de manera intensiva (6 horas semanales por nivel, dando un total de 45 horas por nivel). Requisitos indispensables • Dominio experto de inglés: C2 acreditable (Cambridge C2 Proficiency/CPE o equivalente)., • Nivel bilingüe en español o mínimo C1 (se evaluará en la entrevista)., • Más de 5 años de experiencia enseñando inglés., • Mínimo 3 años de experiencia preparando exámenes de Cambridge (FCE y CAE obligatoriamente)., • Titulación universitaria relacionada con la enseñanza del inglés o la educación., • Residencia en España., • Experiencia y conocimientos en enseñanza online., • Equipamiento disponible para dar clases online., • (Opción de contratar a autónomos). Calendario y disponibilidad • Incorporación: 7 de enero (aunque hay opción de poder incorporarse el 12 de enero)., • Duración del curso: del 7 de enero al 26 de febrero. Opción a extender el contrato hasta junio gracias a los intensivos bimensuales (según disponibilidad y necesidades. NO ES OBLIGATORIO). Habrá otras dos ediciones más de intensivos en marzo-abril y mayo-junio., • Horario: lunes a jueves de 17:00 a 20:00. Habrá opción de trabajar viernes de tarde y sábados de mañana pagando dichas horas como horas complementarias para hacer Speaking (ESTO ES OPCIONAL). Qué ofrecemos • Trabajo 100% remoto (desde casa) dentro de España., • Mejora en el equipamiento si es necesario., • Vacaciones pagadas en Semana Santa y festivos según calendario académico nacional., • Sueldo muy competitivo, claramente por encima del convenio., • 12 horas semanales garantizadas (habiendo opción a horas complementarias siempre y cuando se quiera), • Descanso de 5-7 minutos en mitad de la jornada de 3 horas totalmente remunerado., • Pago adicional por correcciones de redacciones y preparación de clases.

Responsabilidades Funciones • Firmar y supervisar proyectos de montaje de equipos electrónicos, • Cumplimiento marcado CE • Montaje de equipos eléctricos, • Construcción y programación de prototipos, • Elaborar presupuestos, listas de materiales, • Buscar proveedores • Elaborar documentación, • Diseño 3D, hacer planos y croquis de proyectos Requisitos: • Persona proactiva, con iniciativa, con capacidad para tomar decisiones, y con ganas de trabajar y aprender., • Experiencia montando cuadros eléctricos y cableado de máquinas, • Experiencia con montajes mecánicos en piezas de aluminio y acero inoxidable, • Conocimientos avanzados de AutoCAD, • Capacidad para seguir procedimientos de fabricación, y su control y verificación, • Habilidad para mecanizado (taladro, corte con radial, dremel en plástico metal, etc), • Idealmente con capacidad para programar en plataformas tipo Arduino, ESP32, etc. Estudios mínimos • Ciclo Formativo Grado Medio - Electricidad y Electrónica Experiencia mínima • Inglés - Nivel Avanzado Conocimientos requeridos • AutoCad, • Arduino, • 3D, • Mecanizado, • Cableado, • Presupuestos, • Prototipado, • Montaje conjuntos mecánicos, • Neumática, • Python Valorable experiencia en servicio de soporte técnico Valorable inglés avanzado profesional Documentación Experiencia en montaje eléctrico y cableado de máquinas. Disponibilidad para viajar Carnet de conducir B Jornada completa Sector • Investigación biotecnológica

The Senior Clinical Project Manager reports to the Clinical Operations Manager and is responsible to manage the local and international projects in compliance with contractual requirements, timelines, standard operating procedures and relevant regulations and legislations. He/she leads the internal study team allocated on his/her projects ensuring that all deliverables meet agreed expectations and milestones. Establishes with the study team strategies for achieving the study/investigation commitment. Collaborates with major functional areas to identify and evaluate potential issues on the project and ensures the implementation of timely solutions. Proactively manages project level operational aspects including management of trial timeline, budget, and vendors. Forecasts units/hours/generic resources for monitoring activities and analyzes forecasted and worked activities to ensure adherence to contract and budget identifying/escalating any out of scope. Some of what you'll that: • Proactively manages and coordinates the overall project activities ensuring that the deliverable meet contractual requirements, timelines, and quality standard;, • Leads the clinical project team and the various study team meetings;, • Organizes and prepares kick-of meeting, periodic meeting with Sponsor, Investigators’ meeting and internal project meetings ensuring that meeting minutes are appropriately filed in the Trial Master File;, • Provides efficient updates on study/investigation progress to the Sponsor and to the internal team; Prepares feasibility questionnaires and ensures that the site feasibility and qualification process for identification of qualified investigational sites is conducted as per study/investigation requirements and within timelines;, • Prepares the project plans, study/investigation specific procedure and tools;, • Manages study/investigation IMP/IP/MD (i.e., re-supply/IMP/IP/MD expiration/re-labelling of IMP/IP/MD, etc.)  Manages study/investigation materials (questionnaires, sample kit, etc.) Collaborates effectively with the Regulatory and Submission team to speed up the regulatory process and site contract negotiation;, • Reviews and approves the Investigator’s Folder and Trial Master File prototype;, • Ensures that the monitoring team is trained on study/investigation specific procedures and aspects;, • Ensures that the enrolment curve is on-track and take actions in case of under-performance; Ensures that the monitoring activities are conducted as per monitoring plan requirements;, • Reviews and approves site/remote reports;, • Ensures tracking, follow up and resolution of site issues have been completed in a timely manner; Proposes and guarantees the implementation of action plans that resolve issues and/or improve processes;, • Properly and timely escalates relevant issues according to the relevant procedures;, • Ensures potential study/investigation risks are assessed, managed, and communicated according to the relevant procedures., • Manages the administrative aspects of studies/investigations, including study/investigation budget and interact with the Finance and Administrative Unit in case of extra-budgets are needed; Interacts with the Vendor Manager in evaluating vendors services based on study/investigation requirements;, • Manages the study/investigation vendors and monitor the quality of vendor deliverables, addresses quality issues with the appropriate team member and identifies opportunities to improve the execution of the activities;, • Reviews vendor invoices and ensures that hospital fees are paid as per contractual requirements; Ensures all project level study/investigation documentation is filed in the TMF in accordance with company SOPs/all regulatory requirements and provides oversight to the study/investigation team regarding TMF filing, maintenance and archival procedures;, • Ensures that the site TMFs are checked by the monitoring team according to OPIS and/or Sponsor procedures;, • Keeps track of terminating studies and do the final check of the completeness of TMFs;, • Provides support with proposal development and participates in client presentations and/or bid defense meetings, as required;, • Performs co-monitoring visits with CRAs, if necessary;, • Can conduct Feasibility, Pre-study Visit, Site Initiation Visit, Monitoring Visit or Close out visit as necessary (e.g., back-up or directly allocated to the site), if he/she is compliant with local minimum requirements for monitoring;, • Collaborates in establishing and maintaining SOPs related to his/her activities;, • Collaborates to on-boarding of new associates and act as a mentor of junior staff., • Performs and completes on time all required trainings (training on OPIS and/or Sponsor SOPs, all other applicable trainings) by the assigned due date., • Ensures compliance of his/her study team on completing in due time all required assigned study-specific trainings;, • Ensures that OPIS and Sponsors’ KPI/KQI are respected;, • Ensures daily completion of TRACK system, correct entry of appropriate billable and non-billable time and ensure that the activities are billed on time What you have: • Degree in a scientific field, • At least 7 years of experience as Clinical Project Manager, • Excellent knowledge of ICH-GCP, ISO1455 and techniques for the monitoring of clinical trials, • Able to coordinate all the activities related to the management of local and international projects, monitoring of clinical studies/clinical investigations, guaranteeing the security of information, • Able to work independently under the supervision of the Clinical Operations Manager, • Good ability to manage and coordinate resources, • Excellent knowledge of English language, • Able to oversee the activities of CRAs Who we are: Founded in 1998 in Italy and now operating at an international level, OPIS is a full-service science driven biotech focused CRO providing premium trial management for multi-country clinical trials, including state-of-the-art information technology solutions and innovative approaches to the increasing complexity and variety of current projects. OPIS added value lies in its highly specialized professionals who can assist their clients using their deep know-how and experience to guarantee a top-quality level of Clinical Trial Management and ability to operate in a wide range of fields (medical writing, scientific and statistical consultancy for trial design, regulatory activities, pharmacovigilance, etc.) always contributing to our clients’ challenging achievements. What we offer: We offer a competitive salary with other benefits/bonuses and opportunity to develop your professional career with an expanding and growing company. Please read the information notice on the processing of personal data in the candidates information section of our company website.

Entrenador / Coordinador (Programa Internacional de Fútbol): ¡Vive y Trabaja en el Corazón de un Programa de Fútbol Internacional de Élite! Estamos buscando un Entrenador/Coordinador apasionado/a y responsable para unirse a nuestro programa deportivo internacional de alto rendimiento en Madrid. Esta es una oportunidad única para vivir una experiencia inmersiva, ofreciendo supervisión y apoyo vital a jóvenes deportistas internacionales. Requisitos Imprescindibles: • Nivel de Inglés: Mínimo nivel básico de inglés para una comunicación efectiva con los atletas y el personal., • Experiencia en Fútbol: Experiencia previa demostrable trabajando con clubes y/o organizaciones relacionadas con el fútbol., • Disponibilidad de Lunes a Viernes por las tardes: Horario flexible pero generalmente comprendido entre las 5pm y las 9pm., • Habilidades Interpersonales: Excelentes habilidades de comunicación, empatía y capacidad para trabajar con adolescentes y jóvenes adultos de diversas culturas. Condiciones: • Formar parte de un proyecto deportivo en crecimiento en Madrid., • Ambiente de trabajo joven y motivador., • Horario flexible parcial de lunes a viernes por las tardes compaginable con otras actividades., • Salario competitivo y posibilidad de crecimiento dentro de TFL F.C., • Incorporación inmediata. ¿Te interesa formar parte de nuestro equipo? Si cumples con los requisitos y te apasiona el fútbol y el desarrollo de jóvenes talentos, ¡queremos conocerte! Mándanos tu CV y una breve explicación de por qué crees que tu perfil debería ser valorado por nuestros directores para dicha posición a nuestro email ¡Esperamos tu candidatura!

In a nutshell 📌 Position: Clinical Study Coordinator Location: Madrid, Hibrid Experience: 4+ years in international clinical trial coordination Want to know more? 👇 mAbxience is a global biopharmaceutical company committed to innovation and excellence in the development and manufacturing of biotechnological medicines. We operate with a strong focus on quality, regulatory compliance, and scientific rigor to improve patient outcomes worldwide. What are we looking for? 🔎 • Oversee and ensure the proper execution and follow-up of clinical trials, managing CROs and vendors to meet timelines, quality standards, and regulatory requirements., • Design and manage clinical trial plans, identifying risks and implementing corrective actions., • Coordinate site and investigator selection, budget management, and vendor contracts., • Ensure compliance with GCP, FDA, EMA, ICH guidelines, and internal procedures., • Manage regulatory documentation and submissions, maintaining audit readiness., • Supervise clinical trial monitoring, investigational product handling, and patient recruitment strategies., • Collaborate with pharmacovigilance teams to ensure timely reporting and management of safety events., • Support quality management through monitoring reports, deviation handling, and protocol amendments., • Maintain effective communication with internal teams, CROs, investigators, and regulatory authorities. What do you need? 🤓 • Degree in Health Sciences; Master’s degree is a plus., • Fluent in English and Spanish; additional languages are an asset., • Minimum 4 years’ experience coordinating international clinical trials and managing CROs., • Deep knowledge of international clinical trial regulations (ICH-GCP, FDA, EMA)., • Experience in oncology is a strong plus, • Strong organizational, communication, and interpersonal skills., • Ability to work under pressure and prioritize tasks effectively., • Willingness to travel up to 10%. Our benefits! 👏 • ⏰ Flexible start time from Monday to Friday (full-time)., • 📜 Permanent contract., • 💸 Attractive salary package., • 🥼 Life and accident insurance., • 🍽️ Ticket restaurant, • 💸 Benefits and Savings Club., • 📈 Development plans, internal mobility policy., • ⭐ Many more! What will the Selection process be like? 🕵️ ➡️ Stay tuned to your phone and email! The first thing we will likely do is contact you through one of the two channels. ➡️ Prepare well! We will continue with an in-person/virtual interview depending on availability and what we agree upon; there may be one or two interviews in the process, and depending on the type of process, there may also be some kind of test. ➡️ Wait for the result! We care that you feel guided throughout each selection process and know what to expect from us, so we will always try to inform you of the status of the process. 🔷 Do you think this offer is not for you? 🔷 Follow us on social media like LinkedIn/Instagram and stay tuned for any offers we may release; the opportunity to be a new Insuder is waiting! #mAbxience #ClinicalStudyCoordinator #BiotechCareers COMMITMENT TO EQUAL OPPORTUNITIES mAbxience is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees regardless of gender, ethnicity, religion, sexual orientation, disability, or any other characteristic.

Job Responsibilities 1. Develop new markets, establish and maintain overseas customer relationships, expand the market share of the company's products, understand and collect market information and the situation of competitors in the same industry;, 2. Be responsible for the negotiation and signing of sales contracts, ensure that the contract terms are in line with the company's interests, track the execution of orders, ensure timely delivery and meet customer requirements;, 3. Be responsible for maintaining existing customer relationships, communicating with customers regularly, understanding their needs, providing solutions, handling customer inquiries, complaints and feedback, and ensuring customer satisfaction;, 4. Be familiar with the terms and legal requirements of international trade contracts and be capable of effectively managing contracts and orders; Job Requirements 1.Business or life sciences and related majors; Have a certain foundation of professional knowledge and be able to provide professional support for international market development and customer service. 2.Be suitable for different cultures and environments, be capable of working in a cross-cultural communication environment, be able to communicate and negotiate effectively with international clients, and at the same time have good time management and organizational skills;

We are hiring – Data Scientist (Clinical Data) | Permanent Contract 📍 Enovalife – Consulting firm specialized in pharmaceutical, cosmetics, specialized nutrition 🎯 Experience: 1–3 years 📊 Focus: Clinical trial data Enovalife is a consultancy firm with over 20+ years of experience in supporting Clinical & Medical projects & 7+ years in supporting Data & AI projects dedicated to life sciences companies. Our specialty lies in combining our historical expertise (in clinical and medical R&D) with innovative skills (in data and AI) to provide our clients with tailor-made solutions. In this sense, one of our customer, a french major cosmetics company, wants us to create a team of data experts (partly Data Quality & BI and partly data science). Within this data science team, we are looking for clinical data scientists to join the team in order to provide clinical trial analysis on high-impact, scientifically rigorous projects. Your mission You will work at the intersection of statistics, clinical science, and decision-making, contributing directly to the robustness and credibility of clinical studies. About the Role As a Clinical Data Scientist at Enovalife, you will join our team dedicated to supporting the life sciences industries on their Data & AI activities. You will work on strategic projects aimed at strengthening the scientific robustness of clinical studies and leveraging data from trials. Your role will be key in designing, analyzing, and interpreting complex datasets using advanced statistical methods and Bayesian approaches. Key Responsibilities • Design statistical analysis plans for clinical studies (sample size calculation, experimental design, power calculations)., • Participate in blind review with clinicians and data manager., • Perform statistical analyses (mixed models, ANOVA, regressions, multivariate analyses)., • Develop robust, reproducible scripts in R (tidyverse, lme4, brms) and/or Python., • Ensure quality, traceability, and reproducibility of analyses., • Collaborate with clinical, R&D, and Data Science teams., • Contribute to writing scientific reports and regulatory documentation., • Nice to Have: Implement Bayesian approaches (Gaussian or binomial linear mixed model, MCMC algorithm, ...) for modeling and decision-making. Desired Profile • Master’s degree or PhD in Biostatistics, Applied Statistics, Data Science, or equivalent., • 1–3 years of experience in statistical analysis, ideally in a clinical or cosmetic context., • Strong knowledge of classical and Bayesian statistical methods., • Excellent skills in R (tidyverse, lme4, brms, rstan) or Python (pandas, statsmodels, pymc)., • Familiarity with Git/GitHub and development best practices., • Scientific rigor, critical thinking, attention to detail, and ability to communicate complex concepts clearly.

The Company Our customer is a technology-based startup with solid funding that is in the midst of expansion. Their mission is to scale smart, and they’re building the backbone of our operations on Microsoft Dynamics365. They will hire the selected candidate as an internal and permanent employee Description of the position We’re looking for an ERP Financial Solutions Owner for its global operations in Madrid. We are seeking a skilled and proactive candidate, who thrives in dynamic environments and wants to make a real impact from day one, with deep expertise in Microsoft Dynamics365 Finance and other Financial and Planning tools. Working Experience @ 7+ years hands-on experience in ERP implementation, maintenance, and operations. @ Strong financial literacy and understanding of accounting workflows. @ Proven experience with Microsoft Dynamics365 Finance in multinational environments. Not mandatory but preferred: Experience with Power Platform, Copilot, Azure, or other Microsoft ecosystem tools. Knowledge of project management methodologies (Agile, Waterfall). Familiarity with compliance and audit requirements in financial systems. Familiarity with SaaS business models and subscription billing. Knowledge of data analytics or BI tools (e.g. Power BI). Exposure to startup scaling challenges (e.g. rapid hiring, international expansion). Soft skills @ Excellent communication and problem-solving skills. @ Ability to work in a fast-paced, agile startup environment. Key Responsibilities @ Lead and support implementation projects of Dynamics 365 Finance across multiple regions, in coordination with the PMO, including future potential deployments of additional Finance tools (e.g. Procurement, FP&A) @ Ensure system performance, data integrity, and user adoption across departments. @ Collaborate with finance, product, and tech teams to streamline processes and improve reporting. @ Provide hands-on support, training, and documentation for internal users. @ Translate business needs into functional ERP configurations and enhancements. @ Monitor and optimize workflows, integrations, and automation within the Dynamics ecosystem. @ Stay ahead of regulatory and compliance requirements in international operations. @ Manage vendor/partner activities (Microsoft, other SaaS vendors and System Integrators). @ Develop other Digitalization initiatives around automation and AI in collaboration with the Finance Team. Languages @ Spanish: At least B2-C1. @ English: At least B2-C1. Job location Tres Cantos (Madrid). European Union citizen; otherwise, a valid job permit is mandatory. Salary A very competitive salary package. Working from home 3-4 days a week (flexibility available). If you are interested, please apply here or send us an email to including in the subject: ‘ERP Financial Solution Owner’ along with your CV in English.

En Microomics ayudamos a la comunidad científica y a la industria a descubrir el impacto del microbioma. Somos un CRO especializado en metagenómica, aplicando tecnologías de biología molecular, secuenciación masiva (NGS) y herramientas computacionales para responder a preguntas clave en salud, nutrición y sectores agroalimentarios y medioambientales. Con más de 8 años de crecimiento, sede en Sant Feliu de Llobregat y origen en el Centre for Genomic Regulation (CRG), nos encontramos en plena fase de expansión y buscamos incorporar a nuestro equipo un/a Laboratory Manager de Biología Molecular, que lidere y haga crecer nuestro laboratorio. Misión El/la Laboratory Manager será responsable de la gestión integral del Laboratorio de Biología Molecular, asegurando la excelencia operativa en los proyectos de análisis de microbioma para clientes y en iniciativas internas de I+D. Su misión será: • Garantizar la calidad, eficiencia y cumplimiento normativo del laboratorio., • Dar soporte científico al equipo de laboratorio, contribuyendo a la correcta toma de decisiones experimentales en la operativa diaria., • Impulsar la optimización continua de los flujos de trabajo., • Liderar la definición, mejora y estandarización de PNTs., • Implementar soluciones de automatización que permitan escalar procesos, mejorar la trazabilidad y acompañar el crecimiento de la compañía. ¿Qué buscamos? • Formación en Biología, Biotecnología, Microbiología, Laboratorio Clínico o áreas afines., • Experiencia mínima de 3 años en laboratorios de Biología Molecular y/o NGS., • Se valorará especialmente la experiencia en metagenómica de microbioma, incluyendo extracción de DNA a partir de distintas matrices (biológicas, ambientales, alimentarias, etc.), preparación de librerías, control de calidad y gestión de flujos de trabajo asociados., • Conocimiento avanzado de técnicas de biología molecular y secuenciación., • Experiencia en gestión de calidad, documentación técnica y organización de laboratorio., • Capacidad de liderazgo técnico, coordinación de equipos y toma de decisiones en entornos dinámicos., • Castellano e inglés hablado y escrito correctamente., • Se valorará positivamente conocimiento de catalán. ¿Qué ofrecemos? • Posición presencial en nuestras instalaciones de Sant Feliu de Llobregat., • Jornada completa., • Salario competitivo acorde a la experiencia., • Oportunidad de desarrollo profesional en una empresa en fase de expansión., • Entorno innovador, colaborativo y con impacto real en ciencia y sociedad. Las personas interesadas pueden enviar su CV y carta de presentación a , indicando en el asunto “Laboratory Manager”.

✍️ Buscamos ENGLISH TEACHERS (Remote) para enseñar con WhatsApp voice notes | Posición Full-time en Dudons.com 🚀 Dudons es la primera escuela de inglés que usa notas de voz en WhatsApp para practicar inglés con un profesor. Ayudamos a Profesionales y Ejecutivos en España a mejorar su inglés hablando 15 minutos al día (método flexible y asincrónico). Requisitos ✅ 🧑‍🏫 +3 años de experiencia enseñando inglés 🇬🇧 Nivel nativo / native-level de inglés 👔 Pasión por enseñar a adultos (profesionales y ejecutivos) 🙂 Perfil amable, social y open-minded 📜 CELTA / TEFL / TESOL o equivalente 📱 Cómodo/a trabajando desde el móvil con notas de voz (sin clases en directo) Ofrecemos 👩‍💻 🌍 100% remoto: trabaja desde cualquier lugar, solo con tu teléfono 🕒 Compromiso de 39 horas/semana 📈 Crecimiento real: formación, desarrollo y acompañamiento 🤝 Estabilidad: posición a largo plazo (no somos plataforma, somos empresa) 🧠 Reuniones semanales con el equipo + inversión fuerte en training 🎥 ¿Quieres ver cómo es trabajar con nosotros? ⭐ 4.8 sobre 5 en TrustPilot con más de 400 valoraciones 🔍 Busca en YouTube: “Join our team at Dudons” ➡️ Si esto encaja contigo, aplica aquí. We are excited to meet you! 🚀

Job Title: English Instructor (Part-time, 2-18 teaching hours a week) Company Name: Kids&Us Location: Poblenou, Sant Martí, Sant Andreu Are you passionate about teaching English in a fun, dynamic way while balancing other interests like studying, music, acting, or fitness? If your answer is yes, this job is for you! We are seeking part-time English Teachers for our locations in Poblenou, Sant Martí, and Sant Andreu. These teaching roles offer a schedule ideal for individuals with other commitments. Our goal is to maintain an inclusive and supportive work environment. Key Responsibilities: • Conduct English classes, • Follow a structured curriculum and lesson plans., • Foster a positive and inclusive learning environment that encourages student participation and interaction., • Assess student progress and provide constructive feedback to support their language development. Qualifications: • Minimum C1 or equivalent level of English., • Strong communication skills and the ability to engage students effectively., • Passionate about creating a dynamic and enjoyable learning atmosphere. Preferred Qualifications: • Experience teaching diverse age groups and proficiency levels (optional). Benefits: • Part-time schedule (Monday-Thursday), ideal for balancing other commitments., • Opportunity to make a meaningful impact on students' language skills and growth., • Collaborative and supportive work environment. Additional Information: • Groups: Small groups with a maximum of 8 students., • Schedule: Monday-Friday, • Starting: Immediately If you're enthusiastic about teaching English in a fun environment, we'd love to hear from you!

Due to our ongoing global expansion, we have a great opportunity for a Regulatory Submissions Specialist to join our growing regulatory team in Taiwan, on a fully remote basis. We are looking for someone who can autonomously carry on the work within the scope of their activities and interacts with the Direct Manager to define priorities and manages workload. The Regulatory Submissions Specialist contributes to the management and development of procedures related to the activities in which he/she is involved in and ensures that the outputs of their activities meet the quality standards required by the company. Ensures the timely compilation of activity tracking and attendance systems. What you'll do: • Develops and maintains knowledge of global and local regulatory requirements and industry practice/guidelines for submission activities., • Manages adaptation of master documentation for submission (Informed Consent and any additional patient items such as patient emergency card, patient diary and questionnaires etc…) to local requirements., • Manages activities associated with obtaining initial and amended central authority approvals from Competent Authorities (CAs), Central Ethics Committee (CECs), IRB and any other authorities, • Manages contract and budget negotiation/execution with sites/investigators/other parties involved as applicable., • Prepares the financial agreement/addendum to the financial agreement/loan/assignment letter for an external structure and obtain the Sponsor/OPIS signatures for the shipment to the Site., • Maintains tracking of regulatory, ethics and administrative submission and approval dates. What we are looking for: • Experience with CA and CEC submission, using combined ways of submission, • ICF customization;, • Contracts and budget negotiation,, • CTIS (The Clinical Trials Information System) experience - a new central way how EU submission are being processed, • Minimum 2 years’ experience in a pharmaceutical or Clinical Research Organization, • Good knowledge of ICH / GCP regulations / IRB, • Fluent in English, • Good planning, problem solving and organizational skills What we offer: We offer a competitive salary, bonuses, and other benefits together with the opportunity to develop your professional career with an expanding and growing international company. Please read the information notice on the processing of personal data in the candidates’ information section of our company website. Who we are: OPIS is an International CRO with 25 years of experience in conducting Phase I-IV, non-interventional and medical devices studies on an international level. We always offer state-of-the-art information technology solutions and innovative approaches to the increasing complexity and variety of projects. OPIS extensive expertise covers all phases of drug-related trials, taking care of the Sponsor beyond the therapeutic area, offering also accurate clinical investigations for medical and diagnostic devices. With Global Clinical Research Locations all over the world, OPIS offers a full range of integrated clinical research services as scientific advice, medical writing, trial start-up, monitoring, study management, data management, statistics, pharmacovigilance, medical monitoring, electronic data capture as well as quality assurance and training.

DesignRush.com is a leading B2B marketplace connecting businesses with agencies. We are seeking an experienced SEO Manager with strong leadership skills and in-depth knowledge of search engine optimization. The ideal candidate will have over 7 years of proven experience in SEO. Our platform offers four key values to users: • Agency Rankings: Brands can view qualified agencies based on their expertise, location, clients, and various other factors., • Awards: Agencies and brands can enter their finest work and compete for the best web logo, app, print, packaging, and video design awards., • Marketplace: Businesses can post their projects at no cost and receive proposals from verified agencies., • Trending Brands: Agencies and brands can feature their expertise and achievements via news, interviews, and trends articles to get noticed and recognized as an industry leader. We’re looking for an experienced and results-driven SEO Manager with strong project management skills to lead the growth and optimization of our SEO initiatives, coordinating with the team to drive revenue, engagement, and brand awareness. Goals: • Achieve best-in-class website optimization to maximize visibility and search engine rankings, • Continuously improving SEO-related processes for greater efficiency and scalability, • Establish the company as a category leader in terms of organic traffic and SEO-driven value, • Develop and execute a best-in-class content strategy that drives sustainable growth and authority. We offer GROWTH, job stability, and a work culture that enables our teammates to excel in their careers. This is for a full-time, remote-work-at-home position. DesignRush is seeking to make IMMEDIATE hires. Responsibilities: • Create effective, professional-looking SEO strategies to win new business, • Document and enforce best practices, processes, and checklists, • Create, set up, track, and optimize SEO campaigns, • Create and present weekly and monthly reports on team performance with KPIs, • Improve SEO processes and workflow automation using AI tools and agents Requirements: • Over seven years of SEO experience, including a proven track record of managing large and complex websites., • Extensive knowledge of SEO best practices and tools, • Proven experience in project management, • Excellent English communication skills, • Driven to get results and grow with the team, • Able to work between 6 a.m. and 3 p.m. ET, • Strong knowledge of AI tools, AI agents, and workflows Recruitment steps: • Receive a short questionnaire, • Send back answers + CV, • Have an interview with our Recruiter, • Receive a short test, • Have an interview with the Hiring Manager, • Get feedback We kindly ask for your CV and all correspondence to be in English.

The Company Our customer is a very innovative company which aims to positively impact on the planet and people’s lives, by providing detailed information and insights about daily changes on the surface of the Earth to empower organizations and businesses to make better decisions. They have a startup mindset with a very solid funding fostering a very quick growing process, and you can grow with them! They will hire the selected candidate as an internal and permanent employee Description of the position We’re looking for a Network Engineer for its global operations in Madrid. He/She will be play a critical role in managing and optimizing company’s network infrastructure. Working Experience @ 3–5 years of hands-on experience in network engineering or a similar role. This includes experience in designing and managing enterprise networks (LAN/WAN), configuring network equipment. Tech skills @ Excellent at diagnosing and resolving complex network issues quickly and under pressure. @ Strong understanding of networking protocols and systems. Proficient with TCP/IP, routing (e.g., OSPF, BGP) and switching (VLANs, STP), and experienced with enterprise network hardware (routers, switches, firewalls, APs). @ Hands-on experience with network security devices and concepts. @ Knowledge of ITIL or similar IT service management frameworks. Soft skills @ Experience working in a multi-national environment or on international teams. @ Excellent communication and interpersonal skills. @ Excellent problem-solving and analytical skills. @ Team-oriented attitude. Key Responsibilities @ Manage Network Architecture & Topology Design: Plan and develop the network’s structure (LAN, WAN, Wi-Fi) to meet business needs, ensuring the design is scalable, secure, and well-documented. @ Network Hardware Management: Install, configure, and maintain network devices (switches, routers, firewalls, access points) in the office and data center, keeping all equipment updated and running optimally. @ Performance Monitoring & QoS: Use network monitoring tools to track performance and reliability. Implement Quality of Service policies to prioritize critical traffic, so important data (e.g., voice or video) isn’t delayed or dropped during congestion. @ VLAN Configuration & Segmentation: Set up and manage Virtual LANs to segment network traffic for security and efficiency. @ Connectivity Redundancy: Implement redundant links and failover paths to achieve high availability ensuring the network stays up even if a primary connection or device fails. @ ITIL-Compliant Operations: Follow ITIL processes for network changes and incidents. @ Cross-Team Collaboration: Work closely with other IT teams (cloud, security, workplace) and vendors/partners. Provide network support in projects (such as new software rollouts or office expansions) and ensure external providers meet agreed service levels. @ Documentation & Policy: Maintain up-to-date network documentation, including diagrams, device configurations, IP address inventories, and failover procedures. Develop standard operating procedures for routine tasks and troubleshooting, to facilitate knowledge sharing and consistency. @ Continuous Improvement: Regularly evaluate the network setup for improvements. Stay informed about new networking technologies (SD-WAN, Wi-Fi 6/7, automation tools) and propose upgrades or optimizations that enhance performance, security, or efficiency. @ Management Advisement: Provide recommendations to IT leadership on network capacity planning, infrastructure investments, and design improvements. @ Security & Compliance: Work with the information security team to safeguard the network (ensure firewall rules, VPN access, and intrusion prevention systems are effective). Ensure all network activities comply with company policies and relevant regulations (e.g., data protection laws). Languages @ Spanish: At least B2 @ English: At least C1. Job location Tres Cantos (Madrid). European Union citizen; otherwise, a valid job permit is mandatory. Salary A very competitive salary package. Working from home 3-4 days a week (but according to the specific needs that may arise from the perspective of project development, department, clients, and/or partners). If you are interested, please apply here or send us an email to including in the subject: ‘Network Engineer’ along with your CV in English.

🚀 Are you seeking a challenge in the critical high-tech sector? Do you have experience applying ECSS standards and have you worked on projects with ESA? If the answer is YES, we want to hear from you. We are looking for a Product Assurance (PA) Manager with demonstrable experience in ensuring the reliability and conformity of critical products used in space or defense programs. Key Responsibilities • Develop, maintain, and implement the Product Assurance (PA) Plans for each contract/project, in accordance with ECSS-Q standards and customer requirements., • Ensure the implementation of product assurance processes across all phases: design, manufacturing, integration, testing, and delivery., • Control the traceability of materials, components, and batches, verifying Certificates of Conformity (CoC) and managing FAI/FA (First Article Inspection/Approval)., • Review and approve relevant technical documentation (specifications, test procedures, test reports) to ensure contractual conformity., • Identify, assess, and manage product risks (obsolescence, special processes, critical defects). Essential Requirements • Degree in Engineering (Aerospace, Electronics, Telecommunications, Industrial), Physics, or a related technical field., • Minimum 3-5 years of experience in Product Assurance (PA) or Quality Assurance (QA) roles within the space or defense sector., • Expert knowledge and practical experience with ECSS standards (mandatory)., • Prior experience working on projects funded or governed by entities such as ESA or other European agencies and consortia., • Experience in product assurance environments for critical hardware., • Knowledge of quality management system standards such as ISO 9001 or EN 9100 is a plus. 🛡️ Ready to ensure the future? Apply now and join the mission! ⭐ 🚀¿Buscas un reto en el sector high-tech? ¿Tienes experiencia aplicando normativas ECSS y has trabajado en proyectos con ESA? Si la respuesta es SÍ, queremos conocerte. Estamos buscando un/a Product Assurance Manager con experiencia en asegurar la calidad de productos críticos en programas espaciales o de defensa. Buscamos un perfil con visión técnica, orientación a procesos y enfoque en cumplimiento normativo internacional. Responsabilidades • Elaborar, mantener y aplicar los Planes de Product Assurance (PA) de cada contrato/proyecto, conforme a normas ECSS-Q y requisitos del cliente., • Asegurar la implementación de los procesos de garantía de producto en todas las fases: diseño, fabricación, integración, pruebas, entrega., • Controlar la trazabilidad de materiales, componentes y lotes, verificando certificados de conformidad (CoC) y gestionando FAI/FA (First Article Inspection/Approval)., • Revisar y aprobar la documentación técnica relevante (especificaciones, procedimientos de prueba, informes de ensayos) para garantizar conformidad contractual., • Identificar, evaluar y gestionar riesgos de producto (obsolescencia, procesos especiales, defectos críticos). Requisitos • Titulación en Ingeniería, Física, Matemáticas o similar., • Mínimo 3-5 años de experiencia en funciones de PA en el sector espacial o de defensa., • Conocimiento experto de las normativas ECSS (imprescindible)., • Experiencia previa trabajando en proyectos financiados por ESA u otras entidades europeas., • Experiencia en entornos de aseguramiento de producto para hardware crítico., • Conocimiento en gestión de riesgos y calidad. 🛡️ ¿Listo para asegurar el futuro? ¡Aplica ahora y únete a la misión! ⭐

🔍 ¿Te apasiona el mundo de los Recursos Humanos y estás buscando tu primera experiencia profesional? ¡Esta oportunidad es para ti! En ITENE, centro tecnológico ubicado en el Parque Tecnológico de Paterna, buscamos incorporar a una persona en prácticas para nuestro equipo de Personas y Talento. Si eres estudiante de máster en RRHH, Psicología, Relaciones Laborales o similar, y tienes ganas de aprender rodead@ de un equipo multidisciplinar, ¡te estamos esperando! 🎯 ¿Qué aprenderás con nosotros? • Redacción e inserción de ofertas de empleo., • Contacto con entidades y difusión de ofertas de empleo., • Criba curricular y contacto con candidatos., • Participación en entrevistas e informes., • Apoyo en formación y tareas administrativas del área., • Participación en eventos y ferias de empleo. 📌 Requisitos: • Poder firmar convenio de prácticas (mínimo 4 meses)., • Estar cursando un máster en áreas afines a RRHH, psicología o similares., • Interés real por el área de selección y RRHH., • Inglés B2., • Ganas de crecer, aportar y trabajar en equipo. 💡 ¿Te animas a formar parte de un entorno innovador y dinámico? ¡Déjanos tu candidatura y empieza tu camino en el mundo de los RRHH con nosotros! #PrácticasRRHH #Talento #ITENE #RecursosHumanos #OportunidadProfesional #Paterna #CentroTecnológico

Se busca profesores/estudiantes/universitarios para brindar clases de distintas materias a estudiantes de diferentes niveles educativos (primaria, secundaria, bachillerato o universidad). No se requiere experiencia previa como profesor.

Wall Street Oasis is the largest community focused on careers in finance, with over 1 million registered members and 20 million annual visits.The platform offers valuable resources, insights, and networking opportunities for finance professionals and aspiring candidates.Are you a student passionate

En ADAMS Formación buscamos profesores/as altamente cualificados/as y con experiencia en gestión financiera , para la preparación de empleados públicos del grupo A2 de la Administración General del Estado. Evaluar de forma continua el progreso del alumnado, aplicando metodologías activ

En ADAMS Formación buscamos profesores/as altamente cualificados/as y con experiencia en gestión financiera , para la preparación de empleados públicos del grupo A2 de la Administración General del Estado. Evaluar de forma continua el progreso del alumnado, aplicando metodologías activ

En ADAMS Formación buscamos profesores/as altamente cualificados/as y con experiencia en gestión financiera , para la preparación de empleados públicos del grupo A2 de la Administración General del Estado.

We are currently looking for an experienced Safety Physician to support ongoing and upcoming clinical development projects.This role requires a highly competent professional with strong expertise across Clinical Safety and Pharmacovigilance , contributing both operationally and strategically.Key

These teaching roles offer a schedule ideal for individuals with other commitments. Part-time schedule (Monday-Thursday), ideal for balancing other commitments.

These teaching roles offer a schedule ideal for individuals with other commitments. Part-time schedule (Monday-Thursday), ideal for balancing other commitments.

Buscamos incorporar a nuestra Institución Tutores/as de TFM para el Máster en Psicología General Sanitaria y/o Neuropsicología ¿Te apasiona la docencia y la investigación en el ámbito de la psicología? Buscamos profesionales con experiencia académica y/o clínica para acompañar a nuest

At ISPROX, a consultancy specialized in talent acquisition and headhunting, we are supporting our client —a multinational company in the chemical sector, recognized for its innovation in the manufacture and commercialization of industrial and cosmetic specialties— in the search for an R&D Lead

En ADAMS Formación buscamos profesores/as altamente cualificados/as y con experiencia en gestión financiera , para la preparación de empleados públicos del grupo A2 de la Administración General del Estado.

These teaching roles offer a schedule ideal for individuals with other commitments. Part-time schedule (Monday-Thursday), ideal for balancing other commitments.

These teaching roles offer a schedule ideal for individuals with other commitments. Part-time schedule (Monday-Thursday), ideal for balancing other commitments.

Profesor/a de Economía y Gestión para clases particulares ¿Eres docente o profesional del ámbito económico con vocación por la enseñanza? Únete a nuestra plataforma educativa y forma parte de una red de profesores comprometidos con el aprendizaje de alumnos de distintos niveles: Bachillerat