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If you are a current Jazz employee please apply via the Internal Career site. Jazz Pharmaceuticals is a global biopharma company whose purpose is to innovate to transform the lives of patients and their families. We are dedicated to developing life-changing medicines for people with serious diseases — often with limited or no therapeutic options. We have a diverse portfolio of marketed medicines, including leading therapies for sleep disorders and epilepsy, and a growing portfolio of cancer treatments. Our patient-focused and science-driven approach powers pioneering research and development advancements across our robust pipeline of innovative therapeutics in oncology and neuroscience. Jazz is headquartered in Dublin, Ireland with research and development laboratories, manufacturing facilities and employees in multiple countries committed to serving patients worldwide. Please visit ___ for more information. Brief Description: Reporting to the Haem/Onc Associate Director Medical Affairs & MSL Manager, the Field Medical Advisor is responsible for the implementation of the local affiliates' Medical Plan and tactics that support the successful commercialization of in-market and future Jazz Pharma products. This is a field and office based, non-promotional role. The incumbent will be one the medical and scientific point of contact for the therapy area. The main areas of responsibility include the tactical implementation of the National Medical Plan, responding reactively to unsolicited requests for information from healthcare professionals, building collaborative relationships with opinion leaders and facilitating the exchange of unbiased scientific information between the medical community and the company through best-in-class medical education. The incumbent is responsible for ensuring all activities are executed in accordance with regulatory and legal frameworks including but not limited to GCP, IFPMA and local regulations as well as Jazz Pharmaceuticals Policies and Healthcare compliance procedures. Essential Functions/Responsibilities Position Self as Scientific Expert and Provision of Medical Information * Provides high quality, balanced and scientific Medical Information to both internal and external customers on request and in a timely manner * Delivers scientific and educational meetings executed in accordance with Jazz and local regulatory and legal frameworks * Provides scientific information to ensure appropriate positioning of Jazz Pharmaceuticals medicines within relevant national and local protocols, guidelines and formularies in order to ensure appropriate access. * Maintains an up-to-date knowledge of the therapy area and Jazz products * Attends appropriate scientific congresses to stay abreast of developments and to support National and local External Expert (EE) activities and Jazz interests * Acquires a broad understanding of local and national protocols and standards of clinical practice and trends in disease management in country Supports company-sponsored and Investigator Initiated Research * Supports the national implementation of Jazz Pharmaceuticals sponsored studies and projects. * Responds to requests for Investigator Initiated Research grants in accordance with Jazz standard operating procedures * Supports the submission and review of Investigator Initiated Research proposals Develop External Relationships * Develop relationships with National and Local External Experts (EE) in his/her area of responsibility, leading to a productive two-way exchange of scientific information and opinion. * Supports national EE advocacy through provision of scientific and clinical information * Develop and maintain a regional database of key strategic contacts for each relevant product and disease area Medical Affairs Planning and Execution * Helps to ensure implementation and execution of country Medical Plan at local/territory * Supports the budget control to enable execution of local Medical Plan * Works in a collaborative manner with cross-functional colleagues • This Field Medical Advisor will support the tactical implementation of the Medical Plan at a national level, but in any case will be its responsible, this responsibility and ownership will be of his/her direct manager and the Medical Advisor of the therapeutical area. The Field Medical Advisor will also act as Medical Scientific Liaison in the regions of Galicia, Asturias and Cantabria, ensuring the territory plan of 2026 plus the 2027 planning of this area is implemented and developed respectively. Responsible for maintaining minimum Company standards * Adhere to the relevant national and local Codes of Practice * Always behave ethically and with integrity * Act as an ambassador for Jazz Pharmaceuticals following company mission and values * Prepare timely reporting according to the company needs Required Knowledge, Skills, and Abilities * Knowledge of specialty Hematology and Oncology market in Spain * Ability to critically analyse complex data * Clear and concise communication and presentation skills * Planning and organization skills * Negotiation skills * Inter-personal relationship building skills/collaboration and teamwork * Good command of spoken and written English Required/Preferred Education and Licenses • Scientific Graduate with a higher qualification (e.g.,PhD, Pharm D, MSc etc.) #LI-SM1 #LI-field Jazz Pharmaceuticals is an equal opportunity/affirmative action employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any characteristic protected by law. The successful candidate will also be eligible to participate in various benefits offerings, including, but not limited to, medical, dental and vision insurance, retirement savings plan, and flexible paid vacation. For more information on our Benefits offerings please click here: ___.

Who We Are Whitewater Group is a leading provider of innovative and sustainable water treatment engineering systems operating in Ireland, UK and across Europe in the Data Centre, Pharma, Power and Industrial sectors. We specialise in designing, installing, commissioning, and maintaining water treatment solutions to meet our clients' specific needs. Our team is dedicated to delivering high-quality, cost-effective engineering solutions that prioritize safety, reliability, and environmental sustainability. Whitewater Group is headquartered in Bray, Co. Wicklow with a satellite office in Naas, Co. Kildare. We also operate from European bases in Spain, Sweden, Italy and UK, with plans for further offices to open in Finland, Denmark and Germany. The Group is experiencing significant growth due to its focus on off-site construction methods (OSM) of delivering turnkey projects, meaning on-site construction time is kept to a minimum. Role: Due to continued expansion, we now seek a Electrical Engineer to work on various projects in Data Centre Sectors. This appointment will provide the successful applicant with the opportunity to further develop their technical skills in this role, you will plan and work on all aspects of design of water treatment solutions. Main Responsibilities • Verify that the technical documentation complies with the applicable quality standards and regulations., • Review with implementation of KKS and ISA regulations., • Develop lists of instruments, signals, and cables, as well as data sheets., • Tabulating technical offers of instrumentation and control systems, • Develop electrical deliverables: wiring diagrams, cable lists, routing layouts, routing, MTOs., • Participate in the design of control systems: PLCs, distributed systems, emergency shutdown systems and monitoring of rotating equipment., • Prepare plans for cable routes, implementation of instruments and boxes. Requirements • Degree in Electrical or Industrial Engineering or Higher Degree Training Cycle, • Experience in industrial projects, especially in sectors such as Oil & Gas (Upstream/Downstream), energy or water treatment., • Knowledge of applicable international standards (IEC, UL, NFPA)., • Experience in FEED phases and detailed engineering., • Minimum level of English B2 (essential for technical documentation and international environments)., • Handling of CAD tools such as AutoCAD Electrical and EPLAN P8., • Experience with documentation of instrumentation equipment connections such as: Control valves, On-Off valves, self-regulating valves. Level, differential pressure, radar, magnetic elements. Flow meters: Vortex, Coriolis, ultrasound, magnetic, positive displacement type. Temperature meters: thermometers, RTDs, multimeters, thermocouples. Pressure, differential pressure, flow and temperature transmitters.

¿Estás preparado/a para diseñar soluciones tecnológicas de alta calidad en la industria farmacéutica? 🔍 ¡Estamos buscando un/una Project Manager apasionado/a y comprometido/a! Tu principal misión dentro de la compañía será la responsabilidad de alcanzar los objetivos del proyecto, funcionalidad, presupuesto, cronograma y alcance de acuerdo con los requerimientos del usuario, normativa farmacéutica, seguridad y medio ambiente. Responsabilidades 📌 • Proponer el equipo del proyecto junto con el cliente y resto de mandos implicados., • Liderar el equipo del proyecto. Delegar responsabilidades a los miembros del equipo de proyecto, en especial a los ingenieros de proyectos y al equipo de delineación., • Establecer métodos y herramientas para la ejecución del proyecto (estructura de proyecto, sistemas CAE, control, etc.) y garantizar la comunicación necesaria dentro de la organización del proyecto y con los responsables de la obra (reuniones con el equipo del proyecto, con los diferentes equipos por disciplina y con el comité de dirección)., • Punto de contacto con el cliente, se asegurará de que sus necesidades se interpreten correctamente y se transfieran al equipo interno del proyecto., • Definir, programar y estimar la duración de las tareas. Seguimiento del cronograma y cumplimiento de los plazos, evitando y anticipando posibles retrasos., • Control de costes durante las diferentes fases del proyecto para mantener el presupuesto dentro de los límites e intentar optimizarlo., • Asegurar informes adecuados para la organización del cliente y para el director operativo., • Garantizar el cumplimiento de las normas, reglamentos de compras y contabilidad., • Garantizar la elaboración del Manual de Procedimiento de Proyecto (PPM) y de las especificaciones de requisitos de usuarios (URS) junto con el cliente., • Generar documentos técnicos para gestionar adecuadamente el proyecto., • Elaboración y presentación de solicitudes de aprobación de costos (CAR) o controles de cambios de proyecto (PCN) al cliente para su aprobación., • Asegurar la preparación para las posibles inspecciones junto con los departamentos de calidad., • Responsable de la entrega del proyecto, incluida la entrega de documentación a la organización. Conocimientos y experiencia 🎓 • Experiencia previa como Project Manager o ingeniero de proyectos en un campo técnico., • Licenciado en ingeniería: química, ciencias de la vida..., • Conocimiento fluido del español y del inglés. Se valorarán idiomas adicionales., • Usuario de Microsoft Office, Microsoft Project, Power Point, Adobe. Competencias 🥇 • Excelentes habilidades de comunicación., • Excelente pensamiento analítico y resolución de problemas., • Capacidad para priorizar tareas y cumplir plazos estrictos., • Excelente conjunto de habilidades de gestión de clientes., • Capacidad para trabajar bajo presión, responsable de múltiples proyectos importantes en paralelo., • Capaz de trabajar en equipo, colaborativo, innovador y responsable., • Se requiere disponibilidad para viajar para visitar clientes. Razones para trabajar en KLINEA 🏆 • Lugar de trabajo: Alcobendas (Madrid), • Incorporación inmediata., • Salario competitivo según su experiencia y habilidades., • Tiempo completo y contrato indefinido., • Horario flexible., • Plan interno de formación y certificaciones., • Actividades de trabajo en equipo., • Un excelente entorno de trabajo con un equipo colaborativo, joven y dinámico. Si la calidad, la eficiencia y el profesionalismo te definen, ¡esta oportunidad es para ti! 🌟

Do you want to be part of a company where you can become a partner? Our cornerstones are customer satisfaction, colleagues and professional development. If you identify with this, keep reading! ABOUT THE JOB We are looking for a Commissioning & Start‑Up (CSU) Manager to join the Corporate PMC team in our Bilbao, Madrid or Barcelona offices. The CSU Manager leads the planning, resourcing of project-specific professionals in the CSU management domain, and execution of pre‑commissioning, commissioning, start‑up, and performance testing to achieve safe, compliant, and right‑first‑time handover to Clients in the context of PMC professional services. This role drives systemization, readiness, and risk management from late construction through operational acceptance, coordinating closely with engineering, construction, HSE, quality, vendors, and the client’s operations/maintenance teams. At IDOM, we offer you the opportunity to participate in national and international projects as part of a team where you will have the support to push your professional boundaries and improve your skills every day. In a multidisciplinary environment you will be exposed to all the latest technologies and best practices. IDOM offers… • Flexible schedule, • Work remotely, one day or two afternoons per week, • Summer Timetable (July and August), • Tax deductible items (restaurant card, medical insurance, travel card, childcare ....), • Life and accident insurance, • Work-life balance, • Long-term career path, • Opportunity to become a partner, • A multicultural and multidisciplinary environment, • Opportunity to take on more responsibility, • Shared commitment, • Strong interpersonal relationships ABOUT YOU Apply if you… • Have a Bachelor’s degree Engineering (Mechanical, Electrical, Instrumentation/Controls, Chemical) or related field., • Have over 8-12 years in commissioning/start‑up on capital projects (energy, chemicals, utilities, data centers, pharma, infrastructure, etc.)., • Proven delivery in owner’s team/PMC or EPC environments, • Demonstrated experience with system completion and turnover to Clients., • Strong knowledge of pre‑commissioning, commissioning, and start‑up methodologies across disciplines, • Competence in P&IDs, cause‑and‑effect matrices, control narratives, and interlock testing., • Experience with completions management systems, • Familiarity with process safety, LOTO/energy isolation, and temporary systems, • Comfort with Power BI / dashboards and digital field tools for progress and punch management., • Are a team player with technical excellence., • Can work independently with a flair for innovation., • Do have an advanced level of English., • Above all, are attracted by a multinational company like IDOM. Key responsabilities: • Governance & Systemization: establish and enforce commissioning standards, systemization structures, and readiness gate checks while maintaining the completions database and driving continuous improvement across the CSU function., • Planning & Readiness: oversee the CSU execution strategy, resourcing, detailed schedules, preservation and energization plans, vendor mobilization, and all readiness requirements to ensure a fully prepared commissioning phase., • System Completion & Turnover: ensure MC verification, punch‑list management, pre‑commissioning activities, energization and fluid introduction safety, functional/start‑up testing, performance testing, and full turnover dossier completion., • HSE, Quality & Risk: champion process and personal safety during CSU, lead PSSRs, manage CSU risk registers and barrier health, and enforce quality standards for testing, calibration, and NCR resolution., • Interfaces & Leadership: coordinate with construction, engineering, operations, contractors, and OEMs while validating competencies and ensuring effective leadership across all CSU‑related scopes., • Controls, Reporting & Documentation: implement progress measurement for completions and punch KPIs, maintain the commissioning database, issue CSU reports, manage change impacts, and support claims prevention through robust documentation., • Operational Handover & Stabilization: ensure operations readiness (procedures, training, spares, CMMS data), support start‑up stabilization, troubleshoot early‑operation issues, and capture lessons learned for corporate improvement. ABOUT US IDOM is an Association of Professionals working in the areas of Engineering, Architecture, and Consulting on projects that contribute to a more sustainable world. The ownership structure of IDOM creates a culture of engagement, to offer the best service for the client, while our people develop both professionally and personally in an environment of technical excellence. IDOM's most important assets are the expertise and experience of our people.Our employees are deeply united, highly qualified, and skilled professionals. We work within a framework of professional liberty and integrity, with a strong commitment to progress, development, quality service, and innovation. Since IDOM’s foundation in 1957, we have grown steadily to become a multidisciplinary and integrated multinational organization, with more than 5,300 people working in over 145 countries. Are you ready to take the next step? As a member of our TEAM, you will have the opportunity for career development at the highest level in an environment of respect and professional integrity. Send us your CV if you share our philosophy and want to be part of our company. We look forward to meeting you!

Do you want to be part of a company where you can become a partner? Our cornerstones are customer satisfaction, colleagues and professional development. If you identify with this, keep reading! ABOUT THE JOB We are looking for a Construction Manager to join the Corporate PMC team in our Bilbao, Madrid or Barcelona offices. The Construction Manager leads the planning and execution of construction activities across PMC projects, ensuring resourcing of project-specific professionals in the construction management and supervision domains, safe delivery, quality, schedule integrity, and cost control in alignment with the corporate PMC governance framework. The role coordinates EPCs/contractors, owners’ teams, PMC project teams and cross‑functional stakeholders to achieve predictable outcomes and successful handover. You will oversee constructability, site readiness, and disciplined execution from mobilization through mechanical completion and commissioning interface. At IDOM, we offer you the opportunity to participate in national and international projects as part of a team where you will have the support to push your professional boundaries and improve your skills every day. In a multidisciplinary environment you will be exposed to all the latest technologies and best practices. IDOM offers… • Flexible schedule, • Work remotely, one day or two afternoons per week, • Summer Timetable (July and August), • Tax deductible items (restaurant card, medical insurance, travel card, childcare ....), • Life and accident insurance, • Work-life balance, • Long-term career path, • Opportunity to become a partner, • A multicultural and multidisciplinary environment, • Opportunity to take on more responsibility, • Shared commitment, • Strong interpersonal relationships ABOUT YOU Apply if you… • Have a Bachelor’s degree in Civil/Mechanical/Electrical/Industrial Engineering, Construction Management or related field, • Have over 8-12 years of construction management experience on capital projects (infrastructure, energy, industrial, pharma, data centers, real estate, etc.), • Have proven delivery in multi‑contractor/EPC environments and complex brownfield/greenfield sites, • Have experience working within a PMC/Owner’s Team governance framework, • Have strong track record in schedule control, field productivity, and quality/HSE performance, • Have strong expertise in construction methodologies, temporary works, heavy‑lift logistics, and proficiency with Primavera P6 / MS Project for field planning., • Have solid understanding of codes/standards, permit‑to‑work systems, and familiarity with systemization/MC, commissioning, and turnover documentation., • Are skilled in Power BI, reporting dashboards, and digital field‑management tools., • Are a team player with technical excellence., • Can work independently with a flair for innovation., • Do have an advanced level of English., • Above all, are attracted by a multinational company like IDOM. Key responsabilities: • Pre‑Construction & Constructability: lead constructability and methodology definition across design, resourcing, mobilization, procurement support, and continuous improvement to ensure execution‑ready project setup., • Execution Planning & Scheduling: oversee the development and control of detailed construction schedules, ensuring alignment of field execution with engineering deliverables, material readiness, commissioning milestones, shutdowns, and high‑risk construction activities., • Field Supervision & Interface Management: coordinate multidisciplinary contractors and site teams while ensuring permit‑to‑work compliance, timely resolution of technical queries, and effective interfaces with commissioning, operations, and external stakeholders., • Safety, Quality & Compliance: drive HSE leadership and quality assurance, ensuring strict adherence to safety rules, inspection standards, regulatory requirements, and effective non‑conformance management., • Progress, Productivity & Cost Control: ensure accurate progress measurement, productivity tracking, validation of contractor claims, optimized resource utilization, and proactive recovery planning to safeguard schedule and cost performance., • Change, Risk & Issues Management: identify and manage construction risks, support disciplined change control, and ensure timely resolution and mitigation of critical issues with clear ownership and follow‑through., • Documentation, Reporting & Handover: ensure complete and accurate field documentation and reporting, while overseeing systemization, MC readiness, and a structured handover to commissioning and operations. ABOUT US IDOM is an Association of Professionals working in the areas of Engineering, Architecture, and Consulting on projects that contribute to a more sustainable world. The ownership structure of IDOM creates a culture of engagement, to offer the best service for the client, while our people develop both professionally and personally in an environment of technical excellence. IDOM's most important assets are the expertise and experience of our people.Our employees are deeply united, highly qualified, and skilled professionals. We work within a framework of professional liberty and integrity, with a strong commitment to progress, development, quality service, and innovation. Since IDOM’s foundation in 1957, we have grown steadily to become a multidisciplinary and integrated multinational organization, with more than 5,300 people working in over 145 countries. Are you ready to take the next step? As a member of our TEAM, you will have the opportunity for career development at the highest level in an environment of respect and professional integrity. Send us your CV if you share our philosophy and want to be part of our company. We look forward to meeting you!

Senior Sales Manager - Expanding Automation Company - Madrid (Hybrid) - English and Spanish speaker We're hiring for an experienced Senior Sales Manager for an expanding automation company. You will be responsible for developing regional sales and BD strategies across industries such as pharma, energy, manufacturing, developing relationships with customers, leading on negotiations and project bidding for automation / process control software solutions. This position is a full time, permanent position, based hybrid in Madrid. It can also be remote, as long as you can visit Madrid fairly often. Budget is between €55,000-€75,000 + bonus. This is an individual contributor position. For this Senior Sales Manager position, I'm interested in speaking to you if you have the following: • Degree in Business, Robotics, Automation, Engineering or similar, • Ideally 3-10 years sales experience in industrial automation software or process control, • Experience selling DCS, PLC, instrumentation or industrial software solutions, • Must be fluent in Spanish and English I welcome your application if you'd like to find out more and if you know someone it would suit, we offer a fantastic referral scheme which I would be happy to discuss. Keywords: Industrial Automation / Sales / Process Control / Manufacturing / PLC By applying to this role you understand that we may collect your personal data and store and process it on our systems. For more information please see our Privacy Notice ()

Drasanvi es una empresa española experta en salud natural y nutrición desde 1993. Líder en el mercado del colágeno y una de las principales marcas de salud y belleza natural, forma parte del grupo farmacéutico internacional Olyos, que integra 4 entidades: Drasanvi (España), EA Pharma (Francia), Stardea (Italia) y W Group (Estados Unidos), además de 4 marcas globales: Drasanvi, Laboratoire des Granions, Eafit y Stardea. El grupo Olyos se distingue por su visión a largo plazo, su fuerte inversión en I+D y su capacidad para lanzar innovaciones de referencia en los mercados en los que opera. Esta solidez y proyección internacional garantizan a nuestros equipos estabilidad y reales oportunidades de desarrollo. Fabricamos y comercializamos soluciones naturales y eficaces para responder a las necesidades de toda la familia: complementos alimenticios, nutrición, alimentos ecológicos y cosmética natural. Controlamos todas las etapas de desarrollo de un producto, desde el diseño y la producción hasta la puesta en el mercado, cumpliendo con las normativas vigentes. Comprometidos con la mejora continua en lo social y medioambiental, nuestra misión es contribuir al bienestar de todos. Con una clara voluntad de crecimiento, seguimos expandiéndonos tanto de forma orgánica como externa. Buscamos un/a Formador/a de producto para la Comunidad de Madrid que impulse el crecimiento de Drasanvi en su zona, potencie el conocimiento en producto de nuestros clientes y capacite a nuestros comerciales sobre todo acerca de nuestros productos. Te incorporarás a un proyecto en fuerte desarrollo, con nuevas gamas de innovación y una estrategia de expansión sólida. Responsabilidades • Realización de formaciones de producto a nuestros comerciales de zona, formándoles sobre los cambios, innovaciones y desarrollos que existan., • Formaciones específicas sobre demanda a nuestros clientes y sus trabajadores acerca de productos de nuestras marcas., • Promover campañas de exposición y muestra de productos en los establecimientos de nuestros clientes., • Presentar propuestas comerciales., • Realizar formaciones de producto y técnicas de introducción al cliente de los comerciales que se incorporen a la compañía., • Formaciones periódicas a través de plataformas de la empresa., • Alcanzar y superar los objetivos de ventas mediante la captación y fidelización de nuevos clientes., • Monitoreo de la competencia y tendencias del sector: Estar al tanto de las tendencias del mercado y la actividad de la competencia para ajustar y mejorar las estrategias de ventas junto con la dirección comercial. Perfil buscado • Mínimo 2 años de experiencia de formación en el canal farmacia, parafarmacia o sectores afines (nutrición, dermocosmética, FMCG)., • Gran capacidad de comunicación, y valorable experiencia en fitoterapia y complementos alimenticios., • Pasión por la salud y la belleza natural, con enfoque en el cliente y resultados., • Capacidad de negociación, autonomía y habilidades de comunicación., • Residencia en Madrid y disponibilidad para viajar. Lo que ofrecemos • Incorporación a una marca líder en colágeno, con proyectos de innovación continua y gran potencial de crecimiento., • Pertenencia al Grupo Olyos, líder europeo con marcas de prestigio, presencia internacional y una cultura de innovación y desarrollo de talento., • Salario atractivo con un potencial de variable por objetivos muy competitivos., • Coche de empresa, gastos de representación y herramientas digitales., • Formación continua y posibilidades de evolución profesional dentro del grupo. Únete a un equipo apasionado, en un entorno en pleno crecimiento, al servicio de la salud y del bienestar natural.

LETI Pharma somos una compañía biofarmacéutica, independiente y de capital familiar. Especializados en alergia e inmunoterapia, salud animal y cuidado integral de la piel, nuestra prioridad es contribuir al aumento de la salud y el bienestar de la sociedad. La innovación y el desarrollo de productos de alto valor nos han llevado a ser una empresa global líder en segmentos especializados de salud y bienestar. Con sede central en Barcelona, y planta productiva y laboratorio de investigación en Madrid, contamos también con filiales en Alemania y Portugal. En LETI Pharma creemos en las personas, por eso promovemos un entorno laboral diverso e integrador, promoviendo la transparencia y la confianza mutua a través de la comunicación abierta. Apostamos por nuestros equipos y su desarrollo personal y profesional. Nos encontramos actualmente en búsqueda de un Pharmacy Sales Representative de nuestra línea de productos de dermatología. Se trata de una posición indefinida para la cobertura de la zona Noroeste de Madrid. Este perfil tendrá como misión la promoción y venta del portfolio de dermatología para alcanzar los objetivos de ventas propuestos por el DNV a través de una venta consultiva, y siguiendo los valores y procedimientos de la compañía. Funciones: • Promocionar los productos del portfolio de dermatología en su cartera de clientes, • Plan de acción anual por zona y cliente, • Adaptación de la estrategia comercial a su zona de trabajo, • Análisis de ventas desde el frontline management, • Cobertura de visitas y frecuencias, • Segmentación de clientes de la zona en múltiples parámetros comerciales, • Colaborar y proponer ideas y acciones al equipo de Marketing, MSLs e I+D, • Implementar la estrategia comercial de la compañía, • Parte activa de lanzamientos de productos al mercado, • Seguimiento de las incidencias técnicas de los productos, gestión de incidencias y de insuficiencias, • Gestión de KOL’s Requisitos: • Conocimiento del mercado de dermatología y de la competencia., • Habilidades comerciales en visita farmacia. Si cuentas con la experiencia requerida en el sector y en posiciones similares, ¡es tu oportunidad! LETI Pharma promueve el desarrollo profesional y personal de todas las personas colaboradoras, asegurando la igualdad de oportunidades en todos los procesos y normativa interna. En esta línea, LETI Pharma no acepta ningún tipo de discriminación por motivos de sexo, edad, raza, religión, origen, procedencia, opinión política, discapacidad o cualquier otro motivo discriminatorio ni cualquier conducta hostil, abusiva u ofensiva o acoso. Así, todas las personas colaboradoras de Leti Pharma serán tratadas de manera justa y con respeto.

Project Manager – PMO | Pharmaceutical CDMO | New Production Site Location: Madrid, Spain - onsite Languages: Spanish (fluent), English (advanced) Ready to lead strategic transformation in pharmaceutical manufacturing? We are launching a state-of-the-art drug product production site and we’re hiring a Project Manager to build and drive our new centralized PMO. This impactful role will standardize project management, accelerate drug launches, and boost cross-functional teamwork across R&D, regulatory, quality, and commercial teams. Responsibilities: • Establish and lead a central PMO for new site ramp-up and innovation projects., • Standardize project governance and best practices across countries and teams., • Manage complex portfolios—clinical trials, tech transfers, CAPEX, and digital projects., • Ensure compliance with ANVISA, EMA, FDA, and GMP regulations., • Collaborate daily with passionate experts across our business. Requirements: • 5+ years in project management (preferably pharma/CDMO/new site launches)., • Skilled at PMO frameworks, stakeholder management & regulatory requirements., • Fluent Spanish and strong English communication., • Strategic, proactive, and passionate about execution excellence. Join our journey and make a real impact on global health and innovation!

Omega CRM is a Merkle & Dentsu company, leader in development of Customer Experience services, with +20 years of experience in the use of Technology applied to Marketing and providing a unique Customer Relationship with mainly focus on Innovation is looking for a PMO & Project Strategy Manager The PMO combines a solid management background with hands-on experience in consulting projects and CRM solution implementation. The ideal candidate will be responsible for overseeing the overall approach and profitability of projects. This role is key to ensuring the viability of each project by optimizing resources (commercial, operational, and technological) and supporting strategic and tactical decision-making. Responsibilities: Project Management and PMO: • Monitor and control the profitability and expectations of multi-client CRM consulting projects, from proposal to closure and delivery., • Manage PMO (Project Management Office) tracking, analyzing deviations between budgeted and actual project costs, and ensuring corrective and preventive measures. A hands-on approach is required., • Coordinate with the commercial team to manage client expectations. Planning and Budgeting: • Collaborate with the technical leadership (CTO) to ensure focus on project efficiency., • Manage and control project budgets, ensuring optimal allocation of resources and personnel. Operational Performance Analysis: • Work with the Operations team to focus on project contribution margin, resource utilization, and process efficiency., • Identify areas for operational improvement and propose solutions to optimize the profitability of the project portfolio. Support to Management and Project Leaders: • Provide advice to management and project leaders for decision-making, acting as a strategic partner and leader., • Collaborate with the Solutions leadership to provide feasibility analysis for new projects and partnership proposals, anticipating financial and implementation risks. Experience: • Proven experience of at least 3–5 years in a role with similar responsibilities in the consulting or technology implementation services sector., • Demonstrated experience in project management and client management., • Valuable: Specific experience in implementing CRM solutions (Salesforce or Microsoft Dynamics 365) or ERP in commercial areas., • Experience in a multi-client PMO environment, with the ability to manage and report on a portfolio of simultaneous projects. Skills: • Advanced Excel / Google Sheets skills (pivot tables, financial models)., • Experience with management software, CRM, and Business Intelligence tools (Power BI or Tableau)., • Knowledge of project management methodologies (PMI, Agile, PRINCE2, etc.)., • Functional knowledge of databases and data governance., • Analytical ability and strategic vision for decision-making., • Strong communication and collaboration skills with multidisciplinary teams., • Demonstrated proactivity, results orientation, and the ability to work under pressure in a project environment., • Drive, change management, and initiative. WHAT DO WE OFFER • Permanent contract., • Flexible Schedule. We make it easy. Balance your professional and personal life., • Certifications plan. Improve your skills and get the official certificate from our main partners., • Home Office. You decide and we support you., • Flexible retribution (public transport ticket, Ticket restaurtant, …)., • Health insurance., • OMEGA in action. Our commitment to a better society is not just an intention, • Professional development: Evolve, grow and get where you want to go. About us Omega CRM, a Merkle Company, is a global digital company specialising in accelerating the Business Experience (BX) of our clients through customer-centric solutions, technology, and data – all enhanced by AI. Together with Merkle, we form the largest Customer Experience Management (CXM) agency in Spain, and as part of the dentsu group, we offer end-to-end solutions that integrate media, creativity, content, technology, and strategy to deliver real business impact. With over 23 years of experience, a team of 580+ professionals from 24 nationalities, and 2,500+ certifications, Omega CRM is a recognised leader in the Salesforce ecosystem in Spain. We operate across key industries including Retail, Healthcare, Pharma, Real Estate, Education, and Non-Profit, delivering omnichannel experiences in Customer Service, eCommerce, Marketing, and Analytics. Client satisfaction is at our core (rating: 4.9/5), and we’ve been recognised with awards such as Salesforce Partner of the Year FY23 and Most Innovative Project (Iberia). At Omega CRM, we believe in growth through people – guided by our values: #Talent, #Flexibility, #Commitment, and #Innovation. We grow #Together.

Omega CRM is a Merkle & Dentsu company, leader in development of Customer Experience services, with +20 years of experience in the use of Technology applied to Marketing and providing a unique Customer Relationship with mainly focus on Innovation is looking for a Client Partner to continue developing interactions with our customers throughout their Customer Journey Map, ensuring to increase their satisfaction and loyalty to the brand. The Client Partner is responsible for managing client interactions throughout their Customer Journey Map, ensuring increased satisfaction and loyalty to the brand. They possess knowledge and experience in the sales process, excelling in lead generation, relationship building, and deal closing. They achieve company goals through effective planning, setting sales targets, performance data analysis, and projecting future performance. They generate leads, build, and nurture client relationships. Additionally, they collaborate with a group of PMs to ensure the evolution and success of the projects under their responsibility at the delivery level. They support the roles involved in the various project stages to meet client and company expectations regarding quality and profitability, identifying potential gaps, anticipating issues related to the team, solution, or client, and proposing the best solutions. • For existing clients, the focus is on continuously offering new ways for the client to gain value from the product/service, leading consultancy sessions for future needs., • Lead the negotiation, preparation, and presentation of commercial offers for assigned accounts and manage communication with the client throughout the presales process, even when other teams are involved., • Share the client’s sales strategy, objectives, and digital transformation roadmap with the PMs of their assigned accounts, paying special attention when multiple PMs are working on one account., • Collaborate with the PM/DM throughout the project, attending progress demos, management committees, and resolving client-related issues., • Manage and negotiate scope expansions related to initial contracts., • Monitor the progress of projects within assigned accounts, paying special attention to potential budget and timeline deviations., • Identify possible Up & Cross-Selling opportunities for the account. Along with the PMs, they work post-project to identify successful and unsuccessful project elements., • Lead the end-of-project retrospective with the client, reviewing the overall experience, evaluating goal achievement, and exploring potential future developments., • Write success stories and send satisfaction surveys to the client., • The Client Lead is familiar with all operational team members: their experience, skills, and professional motivation., • Collaborate with PMs on team allocation for new or ongoing projects, taking into account both project profitability objectives and the best fit for the professional development of the individuals., • Use workload tracking tools and meet periodically with team members to ensure commitment and satisfaction with assignments., • Communicate the needs of the new team. If necessary, they communicate hiring needs to HR., • Aware of project progress and contribute to meeting deadlines, scope, and budget., • Alert operations management about potential delivery deviations and propose and collaborate on risk mitigation plans. Experience and Skills: • Large account management experience., • Experience across cloud and enterprise technology ecosystems (Salesforce is a plus)., • Experience in the education sector and the public sector is a great plus., • At least, 6 years of previous experience in business /technology consulting, • Previous experience in Project Management, • Experience in digital projects, • Experience in international projects., • High level of English. WHAT DO WE OFFER • Permanent contract., • Flexible Schedule. We make it easy. Balance your professional and personal life., • Certifications plan. Improve your skills and get the official certificate from our main partners., • Home Office. You decide and we support you., • Flexible retribution (public transport ticket, Ticket restaurtant, …)., • Health insurance., • OMEGA in action. Our commitment to a better society is not just an intention, • Professional development: Evolve, grow and get where you want to go. About us Omega CRM, a Merkle Company, is a global digital company specialising in accelerating the Business Experience (BX) of our clients through customer-centric solutions, technology, and data – all enhanced by AI. Together with Merkle, we form the largest Customer Experience Management (CXM) agency in Spain, and as part of the dentsu group, we offer end-to-end solutions that integrate media, creativity, content, technology, and strategy to deliver real business impact. With over 23 years of experience, a team of 580+ professionals from 24 nationalities, and 2,500+ certifications, Omega CRM is a recognised leader in the Salesforce ecosystem in Spain. We operate across key industries including Retail, Healthcare, Pharma, Real Estate, Education, and Non-Profit, delivering omnichannel experiences in Customer Service, eCommerce, Marketing, and Analytics. Client satisfaction is at our core (rating: 4.9/5), and we’ve been recognised with awards such as Salesforce Partner of the Year FY23 and Most Innovative Project (Iberia). At Omega CRM, we believe in growth through people – guided by our values: #Talent, #Flexibility, #Commitment, and #Innovation. We grow #Together.

At EVERSANA, we are proud to be certified as a Great Place to Work across the globe. We’re fueled by our vision to create a healthier world. How? Our global team of more than 7,000 employees is committed to creating and delivering next-generation commercialization services to the life sciences industry. We are grounded in our cultural beliefs and serve more than 650 clients ranging from innovative biotech start-ups to established pharmaceutical companies. Our products, services and solutions help bring innovative therapies to market and support the patients who depend on them. Our jobs, skills and talents are unique, but together we make an impact every day. Join us! Across our growing organization, we embrace diversity in backgrounds and experiences. Improving patient lives around the world is a priority, and we need people from all backgrounds and swaths of life to help build the future of the healthcare and the life sciences industry. We believe our people make all the difference in cultivating an inclusive culture that embraces our cultural beliefs. We are deliberate and self-reflective about the kind of team and culture we are building. We look for team members that are not only strong in their own aptitudes but also who care deeply about EVERSANA, our people, clients and most importantly, the patients we serve. We are EVERSANA. Job Description THE POSITION: Medical Communications is part of our integrated commercial services. This position is fundamental to building credibility and strengthening relationships with healthcare providers, patients, and industry clients. The position delivers industry-leading services, which include call center staffing for responding to product information requests, identifying and in-taking of adverse events and/or product quality issues, and medical writing. The role is home office based, (full-time position), ideally located in Poland, Ireland, the UK, Italy, Portugal, Germany or Spain and the job holder must be legally eligible to work in the European Union or in the UK Working hours: US hours, working 9 hour shifts between 2pm and 2am CET Mon-Fri. ESSENTIAL DUTIES AND RESPONSIBILITIES: Our employees are tasked with delivering excellent business results through the efforts of their teams. These results are achieved by: • Translation of English documents into the target language or vice-versa, and delivering these translated responses either on the phone or in writing., • Triage and respond to drug information inquiries from physicians, pharmacists, nurses, other health care professionals, and consumers/patients., • Disseminate drug information either verbally or by written correspondence., • Identify adverse events and product complaints during interactions with customers. Perform intake sufficient to generate initial adverse event and product complaint reports in compliance with EVERSANA-Medical Communications and client SOPs. Fulfill local Regulatory Authority regulations and requirements for post-marketing adverse event reporting. In addition to being fluent in safety terminology, the individual should be able to make accurate assessments regarding what information needs to be obtained and level or depth of information to be collected., • Utilise writing skills for adverse event and product complaint narratives during intake as well as medical inquiry custom responses., • Coordinate processes necessary for responding to quality-related complaints. This process may involve interactions with personnel in the following departments: Quality Assurance, Regulatory Affairs, and the complainant., • Utilise drug information skills to critically evaluate medical literature in researching and developing information for written dissemination to healthcare professionals., • Miscellaneous projects including market and competitive product research, system development, sales training projects, and field liaison support., • Medical Writing, • On-call responsibilities on an as assigned basis., • Customer Services: Maintain and improve customer services associated with activity of the Medical Communications Call Centre., • Place of Work: Home Office or European Hub Office, • Working hours: US hours, working 9 hour shifts between 2pm and 2am CET Mon-Fri., • Metrics: Maintain and contribute toward process improvement which positively impacts metrics associated with activities of the Medical Communications Call Centre; metrics are subject to change annually or more often as deemed necessary., • Travel: In general, this position does not travel; however, the incumbent will need to be able to travel up to 10%. Qualifications MINIMUM KNOWLEDGE, SKILLS AND ABILITIES: • The requirements listed below are representative of the experience, education, knowledge, skill and/or abilities required., • Education: Life Sciences or healthcare degree or equivalent, • Experience and/or Training: Strong clinical background and excellent verbal/written communication skills., • Language: English C1 level is obligatory. In addition to mother tongue fluency in Spanish is essential., • Education: Preferred Pharma D / M Pharma but other degrees such as BSc. or MSc. in Pharmacy also considered., • Experience and/or Training: Call Center, Medical Information, pharmaceutical industry, and clinical experiences including medical writing., • Language skills: fluent English along with Native Spanish., • Technology/Equipment: Computer proficiency in Microsoft Word, Excel, and other Window applications. The utilization of Medical Information Management Systems, Safety Databases, or equivalent., • Positive Attitude and Energy: Exhibits an upbeat attitude, a genuine interest in others, and a sense of humor. Energises others and heightens morale through her/his attitude., • Communication Skills: Possesses the ability to develop and articulate ideas and information that generate understanding and create a climate that motivates and encourages others to participate., • Innovator: Transforms creative ideas into original solutions that positively impact the company’s performance., • Highly Principled: Proves to be a professional of unquestionable integrity, credibility, and character who demonstrates high moral and ethical behavior Additional Information Patient Minded I act with the patient’s best interest in mind. Client Delight I own every client experience and its impact on results. Take Action I am empowered and hold myself accountable. Embrace Diversity I create an environment of awareness and respect. Grow Talent I own my development and invest in the development of others. Win Together I passionately connect with anyone, anywhere, anytime to achieve results. Communication Matters I speak up to create transparent, thoughtful, and timely dialogue. Always Innovate I am bold and creative in everything I do. Our team is aware of recent fraudulent job offers in the market, misrepresenting EVERSANA. Recruitment fraud is a sophisticated scam commonly perpetrated through online services using fake websites, unsolicited e-mails, or even text messages claiming to be a legitimate company. Some of these scams request personal information and even payment for training or job application fees. Please know EVERSANA would never require personal information nor payment of any kind during the employment process. We respect the personal rights of all candidates looking to explore careers at EVERSANA. From EVERSANA’s inception, Diversity, Equity & Inclusion have always been key to our success. We are an Equal Opportunity Employer, and our employees are people with different strengths, experiences, and backgrounds who share a passion for improving the lives of patients and leading innovation within the healthcare industry. Diversity not only includes race and gender identity, but also age, disability status, veteran status, sexual orientation, religion, and many other parts of one’s identity. All of our employees’ points of view are key to our success, and inclusion is everyone's responsibility. Follow us on ___ | ___

In a nutshell 📌 Position: Launch Specialist – New Product Introduction (NPI) Location: INSUD PHARMA Headquarters, Sanchinarro (Madrid) – On-site Experience: 3-5 years in project management, preferably in the pharmaceutical industry or regulated sectors Want to know more? 👇 INSUD PHARMA operates across the entire pharmaceutical value chain, providing specialized knowledge and experience in scientific research, development, manufacturing, sales, and commercialization of a wide range of active pharmaceutical ingredients (APIs), finished dosage forms (FDF), and branded pharmaceutical products, adding value to both human and animal health. INSUD PHARMA’s activity is organized into three synergistic business areas: Industrial (Chemo), Branded (Exeltis), and Biotech (mAbxience), with more than 9,000 professionals in over 50 countries, 20 state-of-the-art facilities, 15 specialized R&D centers, 12 commercial offices, and more than 35 pharmaceutical subsidiaries, serving 1,150 clients in 96 countries worldwide. INSUD PHARMA believes in innovation and sustainable development. Ready to be a #Challenger? 💪 What are we looking for? 🔎 As a Launch Specialist at INSUD PHARMA, you will be the bridge between development and industrialization, ensuring every new product is ready for its first commercial production. Your mission will be to coordinate all key functions to guarantee successful launches, meeting the highest standards of quality, cost, and service. Key Responsibilities: • Manage and maintain launch plans for new products, ensuring milestones, dependencies, and timelines are met., • Coordinate cross-functional teams (Engineering, QA, QC, Production, Supply Chain, Planning, Regulatory Affairs, Finance, etc.) for timely execution of launch activities., • Lead follow-up meetings, facilitating communication and alignment among all stakeholders., • Serve as the operational point of contact for internal and external clients for assigned launches., • Proactively identify risks, constraints, or deviations, and propose mitigation plans., • Manage documentation, progress reports, and ensure data accuracy in the launch database., • Prioritize and sequence activities to maximize speed, service level, and business value., • Capture lessons learned and contribute to continuous improvement of launch processes. The challenge! 🚀 • Coordinate and oversee the execution of multiple launch projects simultaneously., • Ensure delivery ON TIME, IN FULL, AT THE RIGHT COST, and with the HIGHEST QUALITY., • Drive collaboration between departments and operational excellence. What do you need? 🤓 • University degree in Pharmacy, Chemistry, Engineering, Life Sciences, or similar., • 3-5 years of experience in project management, preferably in the pharmaceutical, chemical, or regulated sectors., • Experience coordinating cross-functional teams and managing stakeholders., • Solid knowledge of technology transfer processes, quality assurance, and supply chain., • High level of English (minimum B2); other languages are a plus., • Proficiency in project management tools (MS Project, Excel, etc.)., • Outstanding communication, organizational, analytical, and problem-solving skills. Our benefits! 👏 📜 Permanent contract 🌍 International and dynamic environment 🎓 Professional development plan and continuous training 🍽️ Subsidized canteen at headquarters 🅿️ Free parking 💼 Private health insurance What will the selection process be like? 🕵️ • Initial contact by phone or email., • 1-2 on-site/virtual interviews, • Ongoing communication about your application status. 🔷Think this offer isn’t for you?🔷 Follow us on LinkedIn and Instagram to discover more career opportunities at INSUD PHARMA! #InsudPharma #Challenger #Insuder #InsudTalent COMMITMENT TO EQUAL OPPORTUNITIES The InsudPharma group is aware that business management must align with the needs and demands of society, and therefore assumes the commitment to equal opportunities and treatment between men and women, as stated in the current regulations on the matter - Organic Law 3/2007, and we do not discriminate against any person on the grounds of ethnicity, religion, age, sex, nationality, marital status, affective or sexual orientation, gender identity or expression, disability, or any other personal or social circumstance.

Sobre la Empresa: ¿Qué hacemos en el Grupo Cibernos? Ayudamos a pequeñas y grandes empresas a desarrollar sus ideas innovadoras. Gracias a nuestro bagaje y know-how, nos sabemos adaptar a las necesidades de los clientes de cualquier tipología y en cualquier ámbito del desarrollo tecnológico, ya que se dispone de áreas de conocimiento en todos ellos. Sobre el Rol: Forma parte de nuestra estrategia de expansión El Grupo Cibernos continua su estrategia de expansión, reforzando su catálogo de servicios y soluciones, así como su presencia a nivel nacional, y para ello estamos Reforzando nuestros equipos de Comerciales IT, para ampliar y crear sinergias en el grupo. El candidato/a, se ocupará de: • Identificar oportunidades de negocio y prospectar clientes potenciales con necesidades en el área de SISTEMAS (Infraestructura, comunicaciones, redes, ciberseguridad, servicios cloud, etc), • Comprender las necesidades técnicas de los clientes y ofrecer soluciones adecuadas., • Presentar a los clientes nuestros servicios/productos/soluciones., • Negociar condiciones comerciales y cerrar acuerdos de venta., • Realizar el seguimiento de las ventas y mantener relaciones duraderas con los clientes. Habilidades y competencias necesarias: • Experiencia de al menos 2 años desarrollando nuevo negocio, realizando una venta consultiva para ofrecer la mejor solución de nuestro portfolio., • Aportar experiencia en llevar un offering con propuestas diversas en el ámbito de los sistemas, • Habilidad para establecer relaciones sólidas y generar confianza con los clientes., • Orientación al cliente y capacidad para ofrecer soluciones personalizadas., • Habilidad para negociar y cerrar acuerdos comerciales., • Capacidad para trabajar de manera autónoma y gestionar el ciclo completo de venta., • Conocimientos en técnicas de ventas y habilidades de comunicación efectiva., • Aportar una red de contactos activos en alguno de los sectores en los que queremos crecer: BANCA, SEGUROS, INDUSTRIA, AAPP, ENERGÍA, TELECOMUNICACIONES, PHARMA Ofrecemos: • Contrato Indefinido, • Salario fijo + variable y poder acogerte a un plan de retribución flexible, • Modalidad de trabajo: 2 Teletrabajo y 3 Presenciales (con flexibilidad) 50 años en el mercado IT. Nos distingue nuestra experiencia más de 50 años en el mercado tecnológico. El esfuerzo, el entusiasmo, la pasión y la capacidad de innovar que nos caracterizan, nos llevan a emprender proyectos motivadores que convierten nuestro día a día en un reto.

🚀 Account Manager Enterprise (Data & IA) | Madrid En Tenth Revolution Group, firma especializada en talento tecnológico, estamos colaborando con uno de los principales partners IT españoles - con más de 30 años de trayectoria y oficinas en el centro de Madrid - en la incorporación de un/a Account Manager. ¿Por qué es interesante esta oportunidad? Te unirás a una compañía consolidada, pero con mentalidad ágil, que está liderando proyectos de Data, Cloud e Inteligencia Artificial para grandes organizaciones en España. Tendrás un rol clave en el crecimiento del negocio, con alta visibilidad interna, autonomía real y contacto directo con clientes estratégicos. Tu misión • Liderar ciclos de venta end-to-end en proyectos de consultoría IT (Data, Analytics, Cloud, IA), • Desarrollar y expandir cuentas enterprise en sectores como Financial Services, Retail, Pharma, Industria o Sector Público, • Detectar oportunidades de negocio y transformar necesidades complejas en soluciones de alto valor, • Construir relaciones sólidas con interlocutores C-Level, IT y negocio, • Colaborar con partners tecnológicos en estrategias de co-selling, • Gestionar tu pipeline y forecast de forma estructurada ¿Qué buscamos? • +4/5 años de experiencia en venta consultiva de servicios IT, • Experiencia gestionando cuentas enterprise, • Track record en gestión de ciclos completos de venta, • Background en entornos de Data, Cloud, Analytics o transformación digital, • Perfil con mentalidad consultiva, autonomía y orientación a resultados, • Nivel de inglés suficiente para entorno profesional ¿Qué ofrecemos? • 60k – 80k OTE (fijo + variable), • Oficinas en el centro de Madrid + modelo híbrido (2 días oficina), • Cultura cercana, dinámica y orientada a resultados, • Formación continua en tecnologías punteras Si estás buscando un rol con impacto real, donde puedas gestionar cuentas estratégicas y participar en proyectos de alto nivel en Data e IA, estaremos encantados de contarte más.

Who we are? Xiromed (___) is a vertically integrated generic company focused on delivering high quality & value products to the US and some European markets. Xiromed’s vision is to be a high quality provider of generic pharmaceuticals that bring enhanced value to our patients, customers and the healthcare system. We strive to bring broad based access to drug products across dosage forms, therapeutic areas and market channels. We continue to invest strongly in state of the art infrastructure across technology, manufacturing and quality systems to build a strong and diversified portfolio of offerings. The biggest asset that makes us who we are will always be our people across the organization, who epitomize the passion, leadership, integrity and the culture of success at our company. 👇Responsibility The Alliance Manager plays a key role in coordinating internal activities between global/regional headquarters and European country affiliates to ensure the successful execution of alliance and partnership agreements. The role focuses on information flow, strategic alignment, and operational readiness across EU markets, ensuring that affiliates have the guidance and clarity needed to meet partnership commitments. This position helps drive consistent implementation of alliance objectives throughout Europe while monitoring local needs, risks, and performance. 🕵️Requirements and personal skill Education • Bachelor’s degree in Life Sciences, Business, or related field required., • 2–5 years of experience in the pharmaceutical or biotechnology industry., • Demonstrated experience managing projects or coordinating activities across multiple EU countries is required., • Experience in roles involving internal coordination, project management, affiliate support, commercial operations, or medical operations., • Understanding of the dynamics between global/regional and European country organizations. Skills & Competencies • Strong communication and interpersonal skills, with comfort working across diverse European markets., • Solid project management, prioritization, and follow-through capabilities., • Ability to work effectively within a matrixed, multicultural environment., • Analytical skills to track country performance and interpret data trends., • Cultural awareness and adaptability to various European working styles and regulatory landscapes., • Proficiency in English required; additional European languages are an asset. Key Success Factors • Strong relationship-building skills with EU affiliates and internal functions., • Ability to synthesize country insights into clear, actionable recommendations., • Proactive mindset with an ability to anticipate country needs or operational challenges., • High attention to detail and accountability in driving follow-up., • Adaptability to varying levels of affiliate readiness and market maturity within Europe. Our benefits! 👏 📜 Permanent contract ⏰ Flexible schedule 🏥 Health insurance coverage 🎓 Professional development opportunities Selection process 🕵️ • Initial contact through phone or email., • 1-2 interviews conducted virtually or in person., • Continuous communication about the selection status. 🔷 Not the right fit? 🔷 Follow us on LinkedIn and Instagram for more exciting career opportunities at INSUD PHARMA. Stay connected and be ready for your next challenge! #InsudPharma #Challenger #InsudTalent COMMITMENT TO EQUAL OPPORTUNITY XIROMED promotes gender equality and does not discriminate based on ethnicity, religion, sexual orientation, disability, or any other condition. We foster a diverse, inclusive, and respectful work environment.

El ___ en España busca a una persona para la vacante de TRAINER en nuestras marcas ___, ___ y ___. Buscamos a una persona apasionada por el cuidado de la piel y la belleza, con habilidades comunicativas excepcionales y con capacidad para transmitir conocimientos de manera dinámica, clara y motivadora. La persona seleccionada será responsable de formar a equipos de venta, personal de tiendas y otros perfiles profesionales sobre productos cosméticos, rutinas de cuidado, ingredientes y técnicas de venta. La persona seleccionada se responsabilizará de las siguientes funciones: • Impartir formaciones presenciales y online sobre productos, rutinas cosméticas e ingredientes., • Diseñar, actualizar y presentar materiales formativos con especial agilidad y dominio de PowerPoint., • Realizar sesiones prácticas, role plays y demostraciones de producto. Acompañar a los equipos en el punto de venta para reforzar conocimientos, mejorar la ejecución y animar las ventas., • Detectar necesidades formativas y proponer acciones que mejoren el rendimiento comercial., • Apoyar eventos, lanzamientos y actividades especiales en tienda., • Colaborar con marketing y ventas para asegurar coherencia de mensaje formativo., • Traducir y adaptar materiales formativos (presentaciones, guías, protocolos) del inglés al español y viceversa., • Participar en reuniones internas y externas, incluidas aquellas que requieran comunicación en inglés., • Control de P&L y gestión de presupuestos de las marcas a gestionar, • Spokeperson para las marcas trabajando mano a mano con Trade e E-trade en activaciones orientadas a mejorar el SO de la marca, • Perfil de contacto con EMEA como responsable de la estrategia Retail de la marca La persona seleccionada deberá reunir los siguientes requisitos: • Experiencia de al menos 2 años como formadora en cosmética, dermocosmética o sectores afines., • Experiencia en retail, entendiendo la operativa de tienda, KPIs y la gestión de equipos., • Dominio avanzado de PowerPoint y agilidad para crear materiales visuales profesionales., • Buenas habilidades de comunicación y expresión en público., • Conocimientos sólidos en cuidado de la piel, ingredientes y rutinas cosméticas., • Nivel de inglés: capaz de mantener conversaciones, comprender reuniones y realizar traducciones funcionales de materiales formativos., • Capacidad de organización, autonomía y flexibilidad., • Disponibilidad para viajar, • Carnet de conducir, • Valorable familiaridad con herramientas digitales (Canva, plataformas e-learning, herramientas de gamificación, CRM, etc.)., • Valorable experiencia dinamizando ventas en tiendas o acciones de campo., • Valorable conocimientos adicionales en maquillaje o técnicas de venta., • Valorable formación reglada nivel universitario., • Valorable perfil con conocimiento y presencia en RRSS., • Valorable control de P&L y gestión de presupuestos de las marcas a gestionar. ¿Qué ofrecemos? • Atractivo paquete salarial y de beneficios sociales., • Oportunidades de aprendizaje, desarrollo y crecimiento en empresa multinacional líder en el sector., • Política de teletrabajo y flexibilidad horaria., • Programa de bienestar en el trabajo: seguro médico, seguro de vida, programa fitness, fisioterapia, dermatólogo y nutricionista., • Empresa inclusiva y socialmente responsable: apostamos por la diversidad y buscamos el desarrollo sostenible.

En Logista, tendrás la oportunidad de llegar tan lejos como te propongas. Aprenderás a diario y aportarás valor en un entorno profesional, sólido, diverso, sostenible y tecnológico colaborando con equipos de alto rendimiento. Si buscas dar un salto profesional, vivir nuevas experiencias y estar en constante crecimiento, este es tu lugar. A nosotros nos motiva que consigas éxitos y sobre todo disfrutes del camino ¿y tú? ¿te animas a sumarte a este viaje? Logista es el distribuidor líder a comercios de proximidad en Europa y está esoecualiuzada en la distribución a canales de proximidad. Sirve regularmente a más de 200.000 puntos de venta en España, Francia, Italia, Portugal, Polonia y Países Bajos. Facilita el mejor y más rápido acceso al mercado de una amplia gama de productos de conveniencia, farmacéuticos, recarga electrónica, libros, publicaciones, tabaco y loterías, entre otros. Logista cuenta con un equipo de profesionales altamente cualificados integrado por más de 8.000 empleados directos y 15.000 colaboradores, centrados en dar servicio a sus clientes del modo más eficiente y adaptado a sus necesidades. En concreto, Logista Freight es la filial del Grupo Logista especializada en la gestión del transporte de largo recorrido y carga completa de productos de alto valor y a temperatura controlada, con plena cobertura en la UE y países periféricos. En estos momentos buscamos un Especialista en gestión de cargas de transporte cuya misión principal será gestionar y controlar las operaciones diarias de tráfico: contratación, negociación, asignación, seguimiento, gestión de incidencias y documentación de transporte. Funciones: • Búsqueda proactiva de envíos y venta de cargas, a través de las plataformas disponibles en el mercado., • Tramitación de apertura de nuevos clientes y proveedores., • Seguimiento de los envíos e informar al KAM de su estado., • Identificar nuevas oportunidades de negocio sobre las necesidades de los clientes., • Resolución de incidencias., • Negociación de precios con los transportistas y clientes (SPOT)., • Asegurar que se cumplen en cada etapa de aplicación al puesto, los requisitos de la normativa IFS Logistics, a través de los procedimientos y formaciones que la empresa pone a disposición de los empleados y los cuales minimizan los riesgos de contaminación intencionada o no, de la mercancía., • Asegurar que se cumplen en cada etapa de aplicación al puesto de la mercancía Pharma, los requisitos de la directriz GDP, a través de los procedimientos y formaciones que la empresa pone a disposición de los empleados, y los cuales minimizan los riesgos de alterar las propiedades del medicamento para su consumo humano. Requisitos: • FP de grado superior en Transporte y Logística, Comercio Internacional o estudios relacionados., • Deseable: Maestría en Transporte y Logística, Comercio Internacional o estudios relacionados., • Experiencia previa de 2 años como Gestor de flota, tráfico o comercial., • Deseable: 2-4 años de experiencia en puestos similares (actividad de transporte import – export con España), • Conocimiento del sector del transporte (Deseable), • Microsoft Office., • Visión estratégica., • Capacidad analítica., • Inglés (Mínimo B2) Unirte a Logista significa: • Formar parte de una empresa líder en su sector., • Trabajar con los mejores profesionales y especialistas del mercado., • Apostar por la innovación tecnológica., • Colaborar en un ambiente internacional gracias a nuestra presencia en 7 países europeos., • Tener un aprendizaje continuo, crecimiento y desarrollo profesional., • Mejorar la calidad de vida gracias a los mejores beneficios. Qué te ofrecemos: • Medidas de conciliación: política de teletrabajo, flexibilidad horaria., • Gran ambiente de trabajo., • Estabilidad laboral., • Tarjeta restaurante. Si quieres sumarte al viaje, ¡inscríbete en la oferta! Logista | Your partner along the way, all the way. • Somos una compañía que ofrece igualdad de oportunidades y fomenta la diversidad y el respeto a la diferencia en nuestra empresa. No toleramos ningún tipo de discriminación basada en la raza, el color, la expresión de género, la identidad de género, la etnia, la religión, la clase social, la política, la ciudadanía, la orientación sexual, el estado civil, la discapacidad o cualquier otra causa., • Nos aseguramos de que las personas con discapacidad reciben las adaptaciones necesarias para participar en el proceso de selección, así como para desempeñar las funciones propias su puesto de trabajo. Ponte en contacto con nosotros si necesitas transmitir cualquier petición en este sentido.

Talent Lab PhD 🚀 Your Career Has No Borders. Neither Do We Join our Young Talent Experience and unlock opportunities worldwide Insud Pharma: a dynamic, entrepreneurial, and globally diverse pharma group, redefining what a pharmaceutical company can be and where your career helps shape the future of global health. 👇The ideal candidate Profile -We´re not looking for perfect CVs. We´re looking for bold, curious and driven people. Proactive, high-potential talent with an innovative mindset. -International postgraduate studies with interest in pharma in a multicultural language's environment. -Progressive experience and strong growth ambition -Open to global mobility and new challenges 📌What´s in it for you? 📜Permanent contract for long-term and accelerated growth . 🏥Competitive compensation aligned with your impact and potential. 🎓 Learn from internationally experienced professionals while building the skills that matter. 🏆Hands-on involvement in strategic projects, with personalized mentoring. 🔍Development Areas Our Young Talent Experience offers hands-on learning with international professionals and the chance to work on strategic projects across key pharma areas: Business Development, Data & Digital, Operations, Engineering, Logistics, R+D and more. A real opportunity to grow, learn and make an impact Selection process 🕵️ • Initial contact through phone or email., • 1-2 interviews conducted virtually or in person., • Continuous communication about the selection status. 🔷 Not the right fit? 🔷 Follow us on LinkedIn and Instagram for more exciting career opportunities at INSUD PHARMA. Stay connected and be ready for your next challenge! #InsudPharma #Challenger #InsudTalent COMMITMENT TO EQUAL OPPORTUNITY INSUD PHARMA promotes gender equality and does not discriminate based on ethnicity, religion, sexual orientation, disability, or any other condition. We foster a diverse, inclusive, and respectful work environment.

Job Description: Toxicologist In a few words📌 Position: Toxicologist Location: Madrid Experience: Toxicologist with a Ph.D. in relevant area and extensive experience in preclinical (in vivo) drug efficacy and toxicology studies. EXELTIS is an organization that develops innovative treatments and targets the unmet medical needs of individuals, families and healthcare professionals. It has nearly 4,000 professionals in over 40 countries. A company born from innovation and the desire to offer the highest quality to everyone. Want to know more? 👇 We are seeking a highly qualified Senior Toxicologist with a Ph.D. in Pharmacology or another relevant biomedical discipline and extensive experience in preclinical toxicological assessment of drugs. The ideal candidate will have a solid scientific and biomedical background, be familiar with ICH/OECD regulatory guidelines, and possess expertise in toxicology screening strategies, study design, data interpretation, and human translation of toxicological findings in the context of drug development. This role is suited for someone motivated to contribute to the development of safe medicines for patients in need through strategic and scientific guidance to project teams. Key Responsibilities: • Prepare and review toxicology‑related study protocols, reports, and regulatory documents in compliance with SOPs, GLP regulations, and ICH/OECD guidelines., • Advise the team on all aspects of the toxicological profile of potential candidate drugs and drugs under development, including toxicology screening strategy, experimental study designs, scientific queries, interpretation of study findings, and translation strategy to humans., • Provide strategic toxicology input as a core member of project teams, ensuring alignment of toxicology plans with overall development objectives., • Partner with internal stakeholders and CROs to support the design, conduct and scientific oversight of preclinical toxicology studies in collaboration with other team members., • Analyze, interpret, and review toxicology data, generating high-quality and accurate assessments. Nice to have: • Experience with new approach methodologies (NAMs), including in vitro and alternative models to support toxicology screening and mechanistic understanding., • Prior experience with toxicological assessment of small molecules and peptides (e.g. selection of relevant species, identification of target organs, human translation of findings)., • Familiarity with integrating in vitro and in vivo data into overall non‑clinical safety packages and regulatory submissions. Required Qualifications: • Ph.D. in relevant area, • 5-10 years of experience in preclinical drug toxicology studies (GLP and non-GLP) and translation to humans., • Strong knowledge of ICH/OECD guidelines and regulatory frameworks., • Proven scientific writing and communication skills., • Experience in project management, • Professional proficiency in English Skills: • Organized, flexible, pro-active, and critical thinker., • Excellent attention to detail and time management., • Ability to multitask and manage deadlines., • Eager to learn and develop professionally. Our benefits! 👏 📜 Permanent contract ⏰ Flexible schedule 🔷Meal vouchers 🏥 Health insurance - flexible coverage 🎓 Professional development opportunities Selection process 🕵️ • Initial contact through phone or email., • 1-3 interviews conducted virtually or in person., • Continuous communication about the selection status. 🔷 Not the right fit? 🔷 Follow us on LinkedIn and Instagram for more exciting career opportunities at INSUD PHARMA. Stay connected and be ready for your next challenge! #InsudPharma #Challenger #InsudTalent COMMITMENT TO EQUAL OPPORTUNITY INSUD PHARMA promotes gender equality and does not discriminate based on ethnicity, religion, sexual orientation, disability, or any other condition. We foster a diverse, inclusive, and respectful work environment.

Ejecutivo de Compras Farmacéuticas Ubicación preferente: Murcia | Madrid | Valencia Misión del Puesto Liderar la negociación estratégica con laboratorios farmacéuticos y proveedores clave para asegurar las mejores condiciones comerciales, garantizar el suministro a los almacenes y maximizar la rentabilidad del portafolio, contribuyendo al desarrollo comercial y al servicio óptimo a socios y clientes. Principales Responsabilidades 1. Negociación Estratégica con Laboratorios • Negociar condiciones comerciales anuales con proveedores., • Gestionar rappels, descuentos, aportaciones promocionales y condiciones estructurales., • Establecer acuerdos de colaboración a medio y largo plazo., • Definir políticas de pago, cuotas, devoluciones y puntos de entrega., • Revisar el cumplimiento de cuotas y acuerdos comerciales. 2. Desarrollo Comercial de Proveedores • Impulsar la participación de laboratorios en:, • campañas comerciales, • herramientas promocionales, • acciones dirigidas a la red de farmacias, • Diseñar y gestionar el calendario promocional anual., • Promover nuevas oportunidades de colaboración comercial. 3. Optimización de Margen • Analizar la rentabilidad por proveedor., • Identificar oportunidades de mejora de margen y eficiencia comercial., • Ajustar pricing y condiciones comerciales en función del rendimiento. 4. Gestión del Portafolio de Proveedores • Desarrollar relaciones estratégicas con laboratorios clave., • Detectar oportunidades de crecimiento y nuevas colaboraciones., • Evaluar el rendimiento y potencial de cada proveedor. 5. Análisis Comercial Utilizar datos para mejorar la toma de decisiones comerciales: • Rotación de producto, • Pricing, • Márgenes, • Sell-out, • Efectividad de promociones 6. Coordinación Interna y Representación • Actuar como interlocutor principal entre laboratorios y los diferentes departamentos de la compañía., • Elaborar informes comerciales y seguimiento de proveedores., • Representar a la empresa en ferias del sector y eventos profesionales., • Participar en proyectos transversales con otras áreas de la organización. Perfil Buscado (H/M/D) 3 a 5 años de experiencia en posiciones relacionadas con: • Negociación con proveedores, • Compras estratégicas, • Gestión de cuentas clave (Key Account Management), • Distribución farmacéutica, • Industria farmacéutica, • Gran consumo (FMCG), • Inglés profesional, necesario para la relación con proveedores internacionales.

In few words 📌 Position: PKPD Modelling Scientist Location: Madrid Experience: Basic to initial professional experience in exposure-response modelling applied to drug discovery and/or development. 👇Global Responsibility As a PKPD Modelling Scientist, you will play a pivotal role in shaping drug discovery and development strategies through the application of innovative modelling and simulation approaches. This is a unique opportunity to contribute across all stages of drug discovery and development, from preclinical research and translational science through to clinical development. You will develop and apply a broad range of PK/PD models to generate quantitative insights that guide key project decisions, with a major focus on informing preclinical and clinical study design, dose selection, exposure-response characterization, and translational strategies to support progression into and through the clinic. The role also offers the opportunity to apply advanced mathematical and translational modelling approaches to connect preclinical findings with clinical relevance and development plans. By integrating diverse datasets and performing simulations and quantitative analyses, you will help de-risk development, strengthen evidence-based decision-making, and maximize the probability of clinical success. You will work closely with cross-functional teams, transform complex data into clear and impactful recommendations, and communicate your findings to project teams, internal governance committees. In addition, you will contribute to the development and implementation of innovative technologies, including AI-driven approaches, to accelerate the drug development pipeline and support drug repurposing strategies. Specific Responsibilities • Develop and apply a range of modelling and simulation approaches—including PK/PD, NLME, PBPK, and/or QSP—to support decision-making across preclinical, translational, and clinical drug development programs., • Generate quantitative insights by integrating diverse datasets and performing simulations to guide study design, dose selection and exposure-response assessment in both preclinical and clinical settings., • Drive preclinical-to-clinical translation by combining preclinical PK/PD, biomarker, and disease-model data to predict human pharmacokinetics, pharmacodynamics, efficacious exposure ranges, and clinically relevant dosing strategies., • Prepare and analyze datasets, interpret modelling outputs, and translate results into clear, scientifically grounded recommendations for project teams., • Work closely with cross-functional teams and communicate model-based findings through presentations, technical documentation, and regulatory reports. 🕵️Requirements and personal skills • Education: PhD in pharmacometrics, pharmacokinetics, pharmaceutical science, mathematics, or related field, with a focus on model-based PK/PD approaches., • Languages: Fluent English, knowledge of other languages will be an asset., • Experience (years/area): Basic to initial professional experience in exposure-response modelling applied to drug discovery and/or development., • Specific Knowledge: Industry or academic experience in exposure-response modelling, including PK/PD, NLME, PBPK, and/or QSP, with hands-on expertise in scriptable modelling platforms such as Phoenix, R, NONMEM, or PK-Sim. Understanding of pharmacokinetics, pharmacodynamics, and modelling and simulation principles. Ability to work with biological and clinical datasets and perform quantitative data analysis. Demonstrated willingness to continuously expand expertise in modelling and simulation methodologies, while exploring and applying emerging AI-driven approaches. A strong record of scientific contribution and leadership, evidenced by relevant peer-reviewed publications, is highly desirable., • Personal skills: strong leadership, a high level of strategy and organizational and communication skills are essential. Our benefits! 👏 📜 Permanent contract ⏰ Flexible schedule 🏥 Health insurance coverage 🎓 Professional development opportunities Selection process 🕵️ • Initial contact through phone or email., • 1-2 interviews conducted virtually or in person., • Continuous communication about the selection status. 🔷 Not the right fit? 🔷 Follow us on LinkedIn and Instagram for more exciting career opportunities at INSUD PHARMA. Stay connected and be ready for your next challenge! #InsudPharma #Challenger #InsudTalent COMMITMENT TO EQUAL OPPORTUNITY INSUD PHARMA promotes gender equality and does not discriminate based on ethnicity, religion, sexual orientation, disability, or any other condition. We foster a diverse, inclusive, and respectful work environment.

En Alzamora Carton Packaging, empresa industrial especializada en soluciones de packaging en cartón, queremos incorporar un Técnico/a Comercial para la zona centro (Madrid, Ávila, Segovia y Toledo), con el objetivo de reforzar el equipo comercial y seguir impulsando el crecimiento del negocio. ¿Cuál será tu misión? Serás el/la responsable de desarrollar negocio en tu zona, aportando una visión comercial y técnica para ofrecer soluciones de packaging ajustadas a las necesidades del cliente, acompañando el proceso desde la detección de la oportunidad hasta la entrega final. Tus principales funciones: • Desarrollar e implementar las estrategias comerciales definidas por la Dirección Comercial., • Identificar nuevas oportunidades de negocio mediante prospección activa., • Ampliar y fidelizar la cartera de clientes, ofreciendo soluciones adaptadas a sus necesidades., • Realizar visitas comerciales y de seguimiento, construyendo relaciones de confianza a largo plazo., • Analizar las necesidades del cliente y proponer alternativas de packaging en cartoncillo., • Recoger información técnica necesaria para el departamento de presupuestos (documentación, muestras, especificaciones, etc.)., • Acompañar el proceso del pedido desde su confirmación hasta la entrega final., • Realizar el seguimiento completo de los presupuestos hasta su validación., • Analizar tendencias del mercado y la evolución del sector para anticiparse a las necesidades del cliente., • Cumplir con los objetivos de ventas establecidos. Requisitos: • Formación en áreas comerciales, marketing o técnicas, así como experiencia en venta consultiva B2B., • Experiencia previa en posiciones comerciales, preferiblemente en sectores industriales, packaging o artes gráficas., • Conocimiento del tejido empresarial de la zona centro (Madrid, Ávila, Segovia y Toledo)., • Valorable experiencia comercial en sectores como alimentación, cosmética, pharma, gran consumo o industria., • Habilidades de negociación, orientación a resultados y comunicación efectiva., • Disponibilidad para viajar dentro de la zona asignada. Qué ofrecemos: • Contrato estable a jornada completa, con incorporación a un proyecto sólido y en crecimiento., • Salario compuesto por fijo mensual más variable ligado a objetivos y resultados comerciales., • Formación continua y desarrollo profesional., • Integración en un equipo profesional y colaborativo, con un entorno de trabajo cercano, organizado y orientado a resultados. Formarás parte de una empresa con más de 125 años de historia en el sector del packaging que apuesta por la innovación, la mejora continua y el trabajo en equipo en cada proyecto. Si quieres descubrir más sobre nuestra trayectoria, visita: ___

Desde 1962 desarrollamos productos icónicos de cosmética y peluquería profesional, presentes actualmente en más de 55 países. Hoy somos más de 300 personas trabajando con un objetivo común: seguir creciendo e innovando en el sector de la belleza y el cuidado personal. En este momento queremos impulsar la presencia de nuestra marca Thader Pharma en el canal farmacia, buscamos personas autónomas con perfil comercial que quieran desarrollar la marca en su zona. Si eres una persona con iniciativa, habilidades comerciales, y te motiva desarrollar una marca con gran potencial en farmacia, nos encantará conocerte. Zonas disponibles: • Madrid, • Cataluña, • Islas Baleares, • País Vasco, • Valencia, • Alicante Funciones principales: • Prospectar la zona asignada y analizar clientela potencial (farmacias y parafarmacias)., • Presentar, informar y asesorar sobre los productos de la compañía para introducirlos., • Negociar y cerrar acuerdos comerciales., • Desarrollar y mantener relaciones comerciales con la cartera de clientes., • Ofrecer un excelente servicio postventa para fidelizar a la clientela y reforzar el posicionamiento de la marca., • Participar en campañas, promociones y acciones formativas dirigidas a las farmacias colaboradoras., • Gestionar las tareas administrativas derivadas de la actividad comercial siguiendo los procedimientos internos. Qué ofrecemos: • Colaboración como persona autónoma con atractivo sistema de comisiones por ventas., • Marca consolidada con presencia internacional y gran potencial de crecimiento. Se valorará: • Experiencia previa en farmacias o parafarmacias., • Formación en Comercio, Marketing o Ventas., • Conocimiento del canal farmacia. Si te interesa desarrollar una marca con recorrido dentro del canal farmacia y formar parte de un proyecto en crecimiento, estaremos encantadas y encantados de conocerte.

Buscamos un/a especialista en fotónica o biofotónica con formación universitaria (Grado o Máster en Física, Ingeniería Óptica, Ingeniería Biomédica o similar) para participar en un proyecto de desarrollo e implementación de tecnología fotónica aplicada al ámbito biomédico. La persona seleccionada será responsable de la coordinación técnica y científica del proyecto, colaborando con otros investigadores y departamentos técnicos, así como con socios externos y organismos financiadores. Responsabilidades • Colaborar en el diseño, desarrollo y validación de sistemas o dispositivos basados en tecnologías fotónicas o biofotónicas., • Planificar y ejecutar las etapas del proyecto, gestionando recursos, cronograma y entregables., • Coordinar las actividades de laboratorio: mediciones ópticas, espectroscopía, caracterización de materiales o muestras biológicas., • Elaborar informes técnicos y documentación científica., • Participar en la preparación de publicaciones, patentes o propuestas de financiación., • Colaborar con el equipo multidisciplinar (ingeniería, biotecnología, óptica, análisis de datos). Calificaciones • Grado o Máster en Física, Ingeniería Óptica, Ingeniería Biomédica, Biotecnología o campos afines., • Experiencia demostrable en fotónica, biofotónica o tecnologías ópticas aplicadas., • Capacidad para gestionar proyectos de I+D, coordinar equipos y cumplir hitos técnicos., • Nivel medio/alto de inglés técnico. Habilidades Requeridas • Conocimientos en Medical Device., • Publicaciones o patentes en el ámbito de la fotónica o biofotónica., • Habilidades de comunicación y redacción científica., • Conocimientos en tecnología de Diagnosis In Vitro., • Experiencia en proyectos financiados (Horizon Europe, CDTI, etc.). Rango de Pago y Paquete de Compensación • Modalidad presencial, jornada 40 horas/semana., • 26 días laborales de vacaciones., • Contrato indefinido., • Incorporación a un equipo multidisciplinar con alto nivel técnico., • Participación directa en un proyecto innovador con aplicación real en biomedicina., • Posibilidades de desarrollo profesional y continuidad. Declaración de Igualdad de Oportunidades Comprometidos con la diversidad y la inclusión en el lugar de trabajo.

In a nutshell 📌 Position: Regulatory Affairs Manager - Biosimilars Location: Madrid (on-site) Experience: 5+ years in Regulatory Affairs within biotech/biopharma Want to know more? 👇 INSUD PHARMA operates across the entire pharmaceutical value chain, bringing specialist knowledge and experience in scientific research, development, manufacturing, sales, and commercialization of a broad range of active pharmaceutical ingredients (API), finished dosage forms (FDF), and branded pharmaceutical products, adding value in both human and animal health. Our activities are organized in three synergistic business areas: Industrial (Chemo), Branded (Exeltis), and Biotech (mAbxience), with over 9,000 professionals in more than 50 countries. We are committed to innovation and sustainable development to deliver solutions that positively impact global health. Ready to be a #Challenger at INSUD PHARMA? 💪 What are we looking for? 🔎 We are seeking a Regulatory Affairs Manager to lead the regulatory strategy for our innovative and biosimilar products, ensuring compliance and collaborating with global, cross-functional teams. Key Responsibilities: • Monitor changes in the regulatory landscape, identify their impact, and propose solutions to maintain compliance., • Define regulatory strategy for each product in coordination with Management and Business teams., • Build strong collaborative partnerships with internal and external teams to ensure organizational success and patient safety., • Identify and mitigate regulatory risks, adapting strategies to evolving regulations and Health Authority feedback., • Interpret and communicate legislative changes that affect product registration, manufacturing, or development., • Support the review of license and quality agreements for targeted geographies., • Lead engagement with Health Authorities during Scientific Advice procedures and responses to deficiency letters., • Prepare, review, and approve regulatory submission documents (briefing packages, IBs, INDs, CTAs, MAAs, etc.)., • Manage external consultants and vendors for regulatory activities., • Support product launch activities, ensuring regulatory risks are managed with appropriate action plans., • Organize the regulatory submission schedule and coordinate with Regulatory Affairs teams., • Participate in product plan development, regulatory strategy, and CMC documentation., • Drive digitalization and the use of computerized systems within the department. The challenge! 🚀 • Oversee the preparation and submission of regulatory documentation., • Coordinate regulatory strategy with R&D, QA, QC, and Production teams., • Lead negotiations and presentations with regulatory agencies., • Manage regulatory information and ensure data integrity., • Actively participate in scientific committees and project teams. What do you need? 🤓 • University degree in Health Sciences (preferably Pharmacy; degrees in Chemistry, Biology, Biochemistry, Veterinary or similar will also be considered)., • 5+ years of experience in Regulatory Affairs within biotechnology, biopharma, or biosimilars., • In-depth knowledge of pharmaceutical legislation, GMP, and ICH guidelines., • Fluent in Spanish and English (other languages are a plus)., • Advanced skills in Microsoft Office (Word, Excel, PowerPoint, Project) and regulatory software., • Willingness to travel., • Inspiring, influential, results-oriented with excellent communication skills. Our benefits! 👏 📜 Permanent contract 🎯 Professional development & continuous training 🌍 International and multidisciplinary environment 🏆 Innovative projects with high impact on health What’s the selection process like? 🕵️ • Initial contact by phone or email., • 1–2 interviews (virtual and/or on-site) with HR and technical teams., • Ongoing updates throughout your recruitment process. 🔷 Not the right fit for you? 🔷 Follow us on LinkedIn to stay updated on future opportunities and news from INSUD PHARMA. We’d love to connect! #InsudPharma #Challenger #Insuder #InsudTalent COMMITMENT TO EQUAL OPPORTUNITIES At INSUD PHARMA, we promote gender equality and do not discriminate based on ethnicity, religion, sexual orientation, disability, or any other condition. We firmly believe that diversity and talent drive innovation and growth.

QA Specialist – Qualification & Aseptic Operations | Pharmaceutical Manufacturing Location: Madrid, Spain - onsite Languages: Spanish (fluent), English (advanced) Are you an expert in qualification and aseptic operations? We are seeking a pro-active QA Specialist to ensure the highest standards of compliance, product integrity, and operational excellence at our new state-of-the-art facility. Responsibilities: • Review and approve qualification/validation documents for equipment, utilities, HVAC, water, and production areas., • Maintain compliance with EU Annex 1, aseptic techniques, cleanroom behavior, and contamination control best practices., • Provide QA oversight for commissioning, qualification, and validation (CQV) activities., • Evaluate deviations, CAPAs, and change controls—supporting thorough investigations and root-cause analysis., • Participate in GMP walkthroughs, on-site quality checks, and aseptic observations., • Act as a key QA partner for engineering, production, microbiology, and validation teams—driving qualification excellence., • Champion data integrity and continuous improvement initiatives for sterile manufacturing., • Deliver training and guidance on aseptic behavior and EU Annex 1 expectations. Requirements: • Bachelor’s or higher in Pharmacy, Life Sciences, Engineering, or a related field., • 3+ years’ QA experience in GMP pharma, with strong background in qualification/validation and sterile environments., • Deep understanding of EU Annex 1 and aseptic operations., • Excellent communicator, detail-oriented, and fluent in Spanish and English. Join us and make your mark by advancing quality and safety in pharmaceuticals!

Quality Control Specialist | Pharmaceutical Manufacturing Location: Madrid, Spain - onsite Languages: Spanish (fluent), English (advanced) Are you passionate about quality excellence in pharma? Join our growing team as a Quality Control Specialist and play a vital role in supporting critical QC operations for our state-of-the-art production site. Responsibilities: • Investigate and review deviations, CAPAs, and Out-of-Trend (OOT) events—delivering robust root-cause analysis., • Perform hands-on QC activities—including environmental monitoring, microbiological testing, gas analysis, and water system validation., • Execute and document environmental and water system monitoring in line with GMP and regulatory standards., • Collaborate closely with QA, manufacturing, and engineering teams to drive continuous improvement and uphold high-quality standards., • Ensure all QC work follows SOPs, safety protocols, and the latest compliance requirements. Requirements: • Bachelor’s in Pharmacy, Chemistry, Biology, or related field., • 3+ years of experience in QC roles in pharma/biotech (GMP-regulated)., • Skilled in deviation/CAPA management, EM, water and gas analysis, and microbiology methods., • Detail-oriented, proactive, a clear communicator in Spanish and English. Take your quality career to the next level in a dynamic, innovative environment!

Looking for your next in-house move in Pharma? We are hiring a Legal Counsel (Commercial & Corporate) to join an international pharmaceutical company based in Madrid. If you enjoy being close to the business, negotiating complex agreements, and working in a regulated environment with real ownership — this might be for you. The role You will act as a trusted legal partner to Commercial, Regulatory, Quality and Operations teams, handling: • Drafting and negotiating commercial agreements (distribution, supply, manufacturing, licensing, services, NDAs)., • Corporate governance and cross-border matters., • Legal support in a regulated pharma environment., • Day-to-day GDPR contractual topics., • Coordination with IT on cybersecurity/compliance matters (non-implementation role), • Managing external counsel. Profile • 5+ years’ experience in commercial & corporate law., • Strong negotiation skills and international exposure., • Experience in pharma/life sciences is a plus., • Excellent English (drafting & negotiation)., • Pragmatic, business-oriented mindset. What you’ll get • High visibility and direct impact on business decisions., • International scope., • Strong ownership in a lean, agile structure., • Competitive package aligned with experience. Our commitment We foster a diverse and inclusive working environment, focusing on talent and potential rather than labels. We are firmly committed to equal opportunities and non-discrimination on the basis of race, age, gender, marital status, ideology, nationality, religion, sexual orientation, disability, or any other personal condition.

Job Role: Solution Architect- Power platform Job Location: Spain (occasional travel to office when required) Mode of employment: Contract Manager inputs: Need strong exp with: Power platform, power automate desktop, Power BI, secondary skills on Celonis, AWS Bedrock/Nova Act, Python, Snowflake & Databricks. Pharma domain not mandatory The Solution Architect for Hyperautomation and Process Insights domain will ensure that common architecture decisions support both business and the IS strategy, and that architectures delivered, both logical and physical, are compliant with relevant architecture standards, blueprints and roadmaps. A Solution Architect will understand implications of architecture requirements to ‘As-Is’ architectures and define/update ‘To-Be’ architectures applying architecture guiding principles. As a Solution Architect, the Role is focused on Current Project Portfolios typically over the 0–18-month horizon in the Hyperautomation and Process Insights domain. Typical Accountabilities The role will be accountable to provide solution design support in the below focused domains of architecture and popular technologies. Ø Data (with focus on data pipelines) o Databricks, Snowflake o Python (incl. popular data transformation packages) Ø Task & Process Mining o Causal Ø Front-end and BI Analytics: Power BI o React Ø Workflow & Automation: o Microsoft Power Suite Ø AI/ML: o Python (incl. popular ML packages) o Microsoft Copilot Studio / AI Builder o Agentic AI: AWS Bedrock & Agentcore Accountable for the direction, performance and ongoing health of the current solution architectures within one or more given portfolios. · Accountable for the architecture and design of comprehensive set of solutions that meet business requirements and are aligned to 's Enterprise Architecture, providing subject matter expertise to ensure business opportunities are identified and realised in line with a standard and cost-effective architecture. · The role will guide and support other architects (including third party suppliers) in the development and documentation of IS/IT architectures for complex and business critical projects. · The role will be accountable for driving solution evaluation and selection decisions, buy vs. build decisions, and early- phase project estimates which contribute to the business case. · Lead the effort to ensure that common architecture decisions support the business and IS strategy, and that the architectures delivered are cost effective and compliant with relevant architecture standards, blueprints and roadmaps. · Participate in Architecture Assessments &, Reviews either as Lead Reviewing Architect or as a Subject Matter Expert in the review team. · Contribute to and lead the development of Solution Blueprints ensuring adherence to 's technology standards and principles. · Be accountable for the architecture and design of comprehensive solutions that meet business requirements and are aligned to 's Enterprise Architecture, Education, Qualifications, and Experience · Relevant technical degree or equivalent · Experience demonstrating proficiency in at least one technical domain. · Experience implementing and maintaining business solution architectures under any formal framework for their domain of architecture. · Proven consultancy experience designing end to end solutions that operate across all domains of IT. · Experience developing and leading innovative solutions · Proven experience of leading change and challenging approaches/ideas. · Proven ability to influence across business and IT. · Experience developing and managing relationships with third party suppliers · Experience with policies, procedures and guidelines within a quality, compliant, and secure environment · Experience with large scale solution Justification phase work – product evaluation, business case formulation Skills and Capabilities: · Strong networking skills with good internal/external links · Well developed communication and facilitation skills · Ability to interpret and communicate technical information into business language at all levels of leadership. · Awareness of developments in the marketplace for domain focus and potential impact to IS · Proven business acumen · Understanding of the pharmaceutical/healthcare industry and of competitor activity, on a particular architecture and Information Management · Ability to work well in diverse, multinational teams and proven ability to influence others to achieve positive outcomes · Master's and/or Professional Certification

Position: Events Leader Experience: Minimum 5 years in end-to-end corporate event execution Want to know more? 👇 INSUD PHARMA operates across the entire pharmaceutical value chain, providing specialized knowledge and expertise in scientific research, development, manufacturing, sales, and marketing of a wide range of Active Pharmaceutical Ingredients (APIs), Finished Dosage Forms (FDFs), and branded pharmaceutical products, delivering added value for human and animal health. INSUD PHARMA’s activities are organized into three synergistic areas: Industrial (Chemo), Branded (Exeltis), and Biotech (mAbxience), with over 9,000 professionals in more than 50 countries, 20 state-of-the-art facilities, and a strong commitment to innovation and sustainable development. What are we looking for? 🔎 • Manage the full lifecycle of corporate, sports, and trade events, including international events with over 1,000 participants., • Review briefings and act as the primary client contact for clarifications., • Define objectives and goals for each event aligned with the proposal., • Develop work plans with schedules, budgets, and required resources., • Create creative and technical proposals in collaboration with the creative team., • Select, negotiate with, and coordinate suppliers (venues, catering, audiovisuals, décor)., • Coordinate with internal departments such as Administration, Marketing, and Creative., • Maintain continuous client follow-up according to established protocols., • Organize documentation, prepare and manage budgets, monitor expenses, and optimize costs., • Coordinate comprehensive logistics: space distribution, guest flow, and scheduling., • Resolve issues effectively to ensure excellent client service., • Conduct post-event debriefings, results analysis, and prepare case studies and satisfaction surveys., • Manage invoicing and documentation archiving. The Challenge! 🚀 What do you need? • Degree in Protocol and Event Management; additional training in Advertising, Public Relations, or Audiovisuals is a plus., • Spanish and English, C1 level., • At least 5 years of experience in end-to-end corporate event execution, including international, sports, and trade events., • Strong knowledge of comprehensive event management, supplier negotiation, and sustainability applied to events., • Availability to travel nationally and internationally., • Personal skills: client orientation, speed with quality, adaptability to change, innovation, leadership, teamwork, effective communication, growth mindset, and business focus. COMMITMENT TO EQUAL OPPORTUNITIES INSUD PHARMA promotes gender equality and guarantees non-discrimination based on ethnicity, religion, sexual orientation, disability, or other factors. We value diversity and inclusion as fundamental pillars of our corporate culture. If you want, I can also adapt it into a punchy, recruiter-style English version for LinkedIn, so it reads more like a job posting that attracts candidates quickly. Do you want me to do that?

Algenex es una compañía perteneciente al grupo Insud Pharma, con sede en Tres Cantos, Madrid. Algenex está dedicada a la producción de proteínas recombinantes para el desarrollo de vacunas para salud humana y animal, así como para aplicaciones terapéuticas. Nuestra tecnología patentada de producción se basa en el uso de insectos lepidópteros (___). Descripción del puesto: El Técnico de Garantía de Calidad Documental y de EQMS es responsable de gestionar, mantener y mejorar el sistema de gestión documental y el sistema electrónico de gestión de calidad (EQMS) de la compañía, asegurando el cumplimiento de los requisitos regulatorios y normativos aplicables al sector biotecnológico. Su labor contribuye a garantizar la integridad, trazabilidad y disponibilidad de la documentación de calidad, así como el correcto funcionamiento de los procesos gestionados a través del EQMS. Funciones principales: • Gestionar la creación, revisión, aprobación, distribución y archivo de la documentación del sistema de calidad (procedimientos, instrucciones, registros, libros de registro etc.)., • Administrar y mantener el sistema electrónico de gestión de calidad (EQMS), asegurando su correcto funcionamiento y la actualización de los procesos gestionados en el mismo (gestión de cambios, desviaciones, CAPAs, auditorías, formación, etc.)., • Dar soporte a los usuarios en el uso del EQMS y en la gestión documental, incluyendo la formación y resolución de incidencias., • Participar en la preparación y desarrollo de auditorías internas y externas, proporcionando la documentación requerida y gestionando las acciones derivadas., • Colaborar en la implantación de mejoras en los procesos de gestión documental y en el EQMS., • Asegurar el cumplimiento de los requisitos regulatorios y normativos aplicables (GxP) en materia de gestión documental y calidad., • Elaborar informes y métricas relacionadas con la gestión documental y el desempeño del EQMS. Educación: • Grado universitario en Farmacia, Biología, Biotecnología, Química, Ingeniería o similar., • Se valorarán estudios de postgrado o formación específica en Calidad, Buenas Prácticas de Fabricación (GMP) o Gestión Documental. Formación: • Formación en sistemas de gestión de calidad (GXP)., • Conocimientos sólidos en gestión documental y sistemas electrónicos de gestión de calidad (EQMS)., • Cursos o certificaciones en herramientas informáticas de gestión documental y calidad (por ejemplo, TrackWise, etc.)., • Formación en normativas regulatorias aplicables al sector biotecnológico y farmacéutico. Habilidades: • Capacidad analítica y atención al detalle., • Organización y gestión eficiente de documentos y registros., • Habilidad para trabajar en equipo y colaborar con diferentes departamentos., • Proactividad y capacidad de resolución de problemas., • Buenas habilidades de comunicación oral y escrita., • Manejo avanzado de herramientas informáticas (Microsoft Office,Trackwise Digital System, bases de datos)., • Adaptabilidad a cambios y nuevas tecnologías. Experiencia: • Experiencia de 3-5 años en departamentos de calidad, preferentemente en empresas biotecnológicas, farmacéuticas o afines., • Experiencia en gestión documental, control de versiones, archivo y revisión de procedimientos y registros., • Experiencia en la administración y mantenimiento de sistemas EQMS., • Participación en auditorías internas y externas, gestión de desviaciones, CAPAs y cambios documentales., • Experiencia en la formación de usuarios en procedimientos de calidad y uso de sistemas EQMS ¡Nuestros beneficios! ⏰ Horario de entrada flexible de lunes a viernes (jornada completa). 📜 Contrato indefinido. 🥼 Seguro de vida y accidentes. 🍽️ Ticket restaurante. 💸 Club de Beneficios y Ahorro. 📈 Planes de desarrollo, política de movilidad interna. ⭐ ¡Y muchos más! ¿Cómo será el proceso de selección? ➡️ ¡Estate atento/a a tu teléfono y correo electrónico! Lo primero que probablemente haremos será contactarte a través de uno de estos dos canales. ➡️ ¡Prepárate bien! Continuaremos con una entrevista presencial/virtual según disponibilidad y lo que acordemos; puede haber una o dos entrevistas en el proceso y, dependiendo del tipo de proceso, también puede haber alguna prueba. ➡️ ¡Espera el resultado! Nos importa que te sientas acompañado/a durante todo el proceso de selección y que sepas qué esperar de nosotros, por lo que siempre intentaremos informarte sobre el estado del proceso. COMPROMISO CON LA IGUALDAD DE OPORTUNIDADES Algenex es una empresa comprometida con la igualdad de oportunidades. Celebramos la diversidad y estamos comprometidos con la creación de un entorno inclusivo para todos los empleados, independientemente de su género, etnia, religión, orientación sexual, discapacidad o cualquier otra característica.

¿Te interesaría seguir desarrollándote como Técnico/a de validaciones y cualificaciones de procesos en una multinacional líder del sector farmacéutico, participando en la mejora continua de sus plantas productivas y colaborando con equipos técnicos multidisciplinares? Desde Oxigent Technologies seleccionamos un TÉCNICO/A DE VALIDACIONES Y CUALIFICACIONES DE PROCESOS para incorporarse en una compañía multinacional, ubicada en San Sebastián de los Reyes, Madrid. ¿Cuáles serán tus funciones principales? Realización de validaciones de proceso y de limpieza: • Planificación, ejecución y documentación de estudios de validación para asegurar que los procesos productivos y los procedimientos de limpieza cumplen con los estándares internos y regulatorios. Evaluación de riesgos, definición de criterios de aceptación, seguimiento de resultados y elaboración de informes técnicos conforme a GMP. Aplicación y supervisión de prácticas asépticas: • Implementación y verificación del cumplimiento de las prácticas asépticas en entornos de producción estéril. Formación del personal, monitorización del comportamiento en áreas clasificadas, investigación de desviaciones y propuesta de acciones correctivas/preventivas (CAPA). Conocimiento y ejecución de actividades relacionadas con media fill: • Planificación, coordinación y supervisión de simulaciones de llenado aséptico (media fill) según la normativa vigente. Revisión de protocolos, control de las condiciones de ejecución, análisis de resultados y preparación de la documentación requerida para garantizar el estado de control del proceso. Cualificación de equipos de envasado (OQ y etapas relacionadas): • Participación en las fases de cualificación de equipos (DQ, IQ, OQ y soporte en PQ) para líneas de envasado estéril. Revisión de URS, elaboración y ejecución de protocolos, verificación del cumplimiento de especificaciones técnicas, análisis de desviaciones y generación de informes finales. Colaboración transversal con Producción, Calidad e Ingeniería: • Apoyo técnico en la implementación de mejoras de proceso, gestión de cambios, resolución de desviaciones y optimización del rendimiento de las líneas, asegurando siempre el cumplimiento de las GMP y los estándares regulatorios. Para ello, ¿qué vas a necesitar? • Formación: Ingeniería, Farmacia o similar., • Mínimo 3 años gestionando proyectos similares, con conocimiento de clean utilities, normativa GMP y conocimiento de inyectables y estériles., • Experiencia en validaciones de elaboración de procesos de fabricación, • Nivel fluido de inglés (B2/C1) ¿Qué te ofrecemos? • Contratación indefinida a través de Oxigent., • Salario acorde a la experiencia aportada (entre 45.000 - 50.000 euros brutos anuales), • Horario flexible, • Modelo presencial, • Cheque Formación para desarrollarte en las áreas profesionales que más te interesen., • Seguro médico privado., • Retribución flexible aplicable a seguro médico, restaurante, transporte, guardería y formación., • Aplicación de acceso a gimnasios y actividades deportivas en toda España con descuentos., • ¡Y muchos otros beneficios! ¡Únete al equipo de Oxigent! Empresa comprometida con la sostenibilidad y la igualdad de oportunidades, donde el talento y la tecnología no entienden de género.

In a nutshell 📌 Position: Portfolio Manager Location: Madrid, on site Experience: 2–5 years in pharma, biotechnology, or life sciences Want to know more? 👇 Chemo (INSUD PHARMA) is a global leader in the pharmaceutical industry, driving innovation and expertise across the entire value chain—research, development, manufacturing, and commercialization of products for human and animal health. Present in over 50 countries, Chemo fosters a culture of collaboration, talent development, and bold innovation. Ready to be a #Challenger? 💪 What are we looking for? 🔎 As a Portfolio Manager, you will play a key role in planning, analyzing, and coordinating projects within our development and commercial portfolio, collaborating in a global, cross-functional environment. Your core responsibilities will include: • Assisting in developing and maintaining portfolio plans, including timelines, milestones, and prioritization frameworks, • Preparing strategic materials for governance meetings and portfolio reviews, • Ensuring accurate documentation and communication of portfolio decisions and updates, • Performing portfolio analyses: risk assessments, scenario comparisons, timeline evaluations, and KPIs, • Creating dashboards and regular monitoring reports with digital tools, • Coordinating with R&D, Clinical, Regulatory, Commercial, Manufacturing, and other internal partners to collect information and align strategies, • Supporting multifunctional teams in identifying potential challenges and resource constraints, • Communicating portfolio insights to stakeholders at various levels, • Tracking and highlighting emerging risks, issues, or opportunities within the portfolio, • Assisting with the evaluation of new projects, initiatives, or external collaborations, • Contributing to continuous improvement of portfolio management processes, digital tools, and systems Your challenge! 🚀 • Analyze and present data for strategic decision-making, • Coordinate processes with multidisciplinary global teams, • Optimize communication and information flow, • Identify and propose improvements to portfolio management tools and processes What do you need? 🤓 • Bachelor’s degree in Life Sciences, Engineering, Business, or similar, • Advanced degree (MBA, MSc, PharmD, PhD) is a plus, but not mandatory, • 2–5 years of experience in pharma, biotechnology, or related industries, • Background in portfolio management and/or strategy, • Basic understanding of the drug development lifecycle, regulatory steps, or commercial product management, • Strong analytical and problem-solving skills, • Excellent written and verbal communication and presentation capabilities, • Advanced organizational skills, managing multiple priorities efficiently, • Proficient in Excel, PowerPoint, and portfolio/project management tools (including dashboards, analytics platforms), • Collaborative mindset and ability to work effectively in global, matrixed environments, • Detail-oriented, proactive, and results-driven, • Strong relationship-building skills and eagerness for continuous learning Our benefits! 👏 📜 Permanent, long-term contract 🌱 Continuous training and development 🌍 International and collaborative environment 🎯 Challenging projects with global impact 🚗 Company parking 🍏 Subsidized cafeteria 🩺 Private health insurance What will the Selection Process look like? 🕵️ • Initial contact by phone or email, • 1–2 virtual/on-site interviews with HR and area managers, • Transparent and ongoing communication at every stage 🔷Think this role isn’t for you?🔷 Follow us on LinkedIn and stay tuned for new opportunities—your next challenge may be just around the corner! #ChemoCareers #InsudPharma #Challenger #InsudTalent COMMITMENT TO EQUAL OPPORTUNITY At Chemo (INSUD PHARMA), we are committed to real equality. We do not discriminate by gender, ethnicity, religion, sexual orientation, disability or any other factor. We actively foster an inclusive workplace where everyone’s talent and capabilities make the difference.

In few words 📌 Position: Contracts and Financial Specialist Location: Madrid Experience: Experience in contract and budget management (ideally in pharma/biotech or CRO environment). 👇Global Responsibility The Contracts and Financial Specialist is responsible for supporting the R&D project teams in the end‑to‑end management of contracts and budgets with CROs and other external vendors. This role ensures accurate scoping, timely contract execution, rigorous budget tracking and proactive follow‑up on timelines and invoices, working closely with Project Leaders, Preclinical Project Manager, Toxicologist, DMPK/PD Scientist and internal finance/procurement. Specific Responsibilities • Prepare, review and coordinate work orders, service agreements and contract amendments with CROs and other vendors, ensuring alignment between scientific/operational scope, timelines and budget., • Translate study and project plans into clear financial scopes (units, rates, milestones), in collaboration with scientific and project leads., • Track budgets and actuals for preclinical and clinical projects, monitor variances, and flag risks or deviations early with proposed mitigation options., • Maintain an up‑to‑date overview of all ongoing contracts, milestones, payment schedules and expiry dates, ensuring timely renewals or closures., • Coordinate the internal contract review and approval workflow (project team, legal, finance, procurement), ensuring smooth and timely execution., • Follow up with CROs and vendors on deliverables and milestones linked to payments, verifying that invoices match contractual terms and services performed., • Generate regular financial and contractual status reports for project teams and senior management (e.g. committed vs spent, forecast to completion)., • Support RFP processes (request for proposals) by preparing comparison tables, budget analyses and recommendations from a financial and contractual standpoint., • Contribute to continuous improvement of tools and processes for budget tracking, contract management and vendor follow‑up within the R&D organization. 🕵️Requirements and personal skills • Education: Degree in Business, Economics, Finance, Life Sciences or related field, with, • Languages: Fluent Spanish and English, knowledge of other languages will be an asset., • Experience (years/area): Experience in contract and budget management (ideally in pharma/biotech or CRO environment)., • Personal skills: Highly autonomous, detail‑oriented executor with strong follow‑up, timeline discipline and numerical skills, able to manage multiple projects and vendors while communicating effectively in a multidisciplinary environment. Our benefits! 👏 📜 Permanent contract ⏰ Flexible schedule 🏥 Health insurance coverage 🎓 Professional development opportunities Selection process 🕵️ • Initial contact through phone or email., • 1-2 interviews conducted virtually or in person., • Continuous communication about the selection status. 🔷 Not the right fit? 🔷 Follow us on LinkedIn and Instagram for more exciting career opportunities at INSUD PHARMA. Stay connected and be ready for your next challenge! #InsudPharma #Challenger #InsudTalent COMMITMENT TO EQUAL OPPORTUNITY INSUD PHARMA promotes gender equality and does not discriminate based on ethnicity, religion, sexual orientation, disability, or any other condition. We foster a diverse, inclusive, and respectful work environment.

Omega CRM is a Merkle & Dentsu company, leader in development of Customer Experience services, with +20 years of experience in the use of Technology applied to Marketing and providing a unique Customer Relationship with mainly focus on Innovation is looking for a Salesforce Developer / Admistrator. Responsibilities • Analyze requirements., • Participate in the technical design of projects., • Provide effort estimations for projects., • Work collaboratively with the Omega team and/or the client’s team to help achieve project objectives., • Analyze and optimize application performance., • Identify potential technical risks in the project and propose alternative solutions., • Collaborate with technology providers when required by the project., • Document processes and track system performance metrics., • Validate and test the technical solution against business requirements., • Train end users on the developed functionality and proper use of the software applications., • Implement the latest technological advancements and solutions., • Ensure compliance with the software quality standards established by Omega's Technical Management., • Generate technical documentation for completed projects., • Actively contribute to the training and development of other team members., • Collaborate in Omega’s community of practice by sharing technical knowledge., • Identify potential methodological improvements for the technical team., • Evaluate and recommend products and systems that drive technological innovation. Knowledge / Experience • Degree in Computer Engineering or a similar technology-related field., • At least 2 years of experience as a Salesforce Developer., • Experience developing solutions on Sales Cloud and/or Service Cloud in the Salesforce ecosystem. Experience in other Salesforce clouds is a plus., • Knowledge of development technologies (APEX, Visualforce, LWC, migration tools, SOQL, web services)., • Understanding of both DevOps/Agile (SCRUM) and Waterfall delivery principles, as well as the importance of SDLC (Software Development Life Cycle) and coding methodology principles, is a plus., • Ability to work independently and take ownership of assigned applications., • Excellent spoken and written English., • Any Salesforce certification is a plus. What do we offer • Permanent contract., • Flexible Schedule. We make it easy. Balance your professional and personal life., • Trainings & Certifications. Improve your skills and get the official certificate from our main partners., • Home Office., • Flexible retribution (public transport ticket, Ticket restaurant, …)., • Health insurance., • OMEGA in action. Our commitment to a better society is not just an intention. About us Omega CRM, a Merkle Company, is a global digital company specialising in accelerating the Business Experience (BX) of our clients through customer-centric solutions, technology, and data – all enhanced by AI. Together with Merkle, we form the largest Customer Experience Management (CXM) agency in Spain, and as part of the dentsu group, we offer end-to-end solutions that integrate media, creativity, content, technology, and strategy to deliver real business impact. With over 23 years of experience, a team of 580+ professionals from 24 nationalities, and 2,500+ certifications, Omega CRM is a recognised leader in the Salesforce ecosystem in Spain. We operate across key industries including Retail, Healthcare, Pharma, Real Estate, Education, and Non-Profit, delivering omnichannel experiences in Customer Service, eCommerce, Marketing, and Analytics. Client satisfaction is at our core (rating: 4.9/5), and we’ve been recognised with awards such as Salesforce Partner of the Year FY23 and Most Innovative Project (Iberia). At Omega CRM, we believe in growth through people – guided by our values: #Talent, #Flexibility, #Commitment, and #Innovation. We grow #Together.

IF YOU ARE INTERESTED, PLEASE SHARE YOUR CV IN ENGLISH LANGUAGE ONLY! Who are we? We are a technology-led healthcare solutions provider. We are driven by our purpose to enable healthcare organizations be future ready. We offer accelerated, global growth opportunities for talent that’s bold, industrious, and nimble. With Indegene, you gain a unique career experience that celebrates entrepreneurship, and is guided by passion, innovation, collaboration, and empathy. To explore exciting opportunities at the convergence of healthcare and technology, check out ___ What if we told you that you can move to an exciting role in an entrepreneurial organization without the usual risks associated with it? We understand that you are looking for growth in your career at this point and we would love for you to join us in our journey and grow with us. At Indegene, our roles come with the excitement you require at this stage of your career with the reliability you seek. We believe in creating leaders of tomorrow and mentor our leads to help them grow and nurture them as people managers and account managers. We are a rapidly growing global organization and are scouting for the best talent for this phase of growth. With us, you are at the intersection of two of the most exciting industries of healthcare and technology. We offer global opportunities with fast-track careers while you work with a team that is fueled by purpose. The combination of this will lead to a truly differentiated experience for you. If this excites you, then apply below. IF YOU ARE INTERESTED, PLEASE SHARE YOUR CV IN ENGLISH LANGUAGE ONLY! Job title: Veeva Developer Job Description: Veeva Content Development · Build and maintain CLM (Closed Loop Marketing) presentations for Veeva CRM. · Develop and deploy Approved Emails using Veeva Approved Email and Engage functionalities. · Create and configure digital assets Veeva CLM presentations, Approved Email and Fragments · Troubleshoot and resolve rendering or functionality issues in Veeva presentations and emails. · Familiarity within Veeva CRM and Salesforce · Configure and manage content components, shared resources, and document relationships. · Support user acceptance testing (UAT) and ensure proper deployment in production environments. · Collaborate with stakeholders to optimize workflows and user experience within Veeva CRM. Quality, Compliance & Documentation · Ensure all deliverables follow pharmaceutical compliance, regulatory, and MLR requirements. · Validate content using Veeva preview and testing tools across devices and browsers. · Maintain proper documentation, version control, and audit trail of deployed materials. · Support audits and compliance reviews as required. Collaboration & Project Delivery · Work closely with Brand/Marketing teams to understand campaign objectives and translate them into functional assets. Ideal Profile: · 1 - 3 years of experience of relevant experience. · Strong hands-on experience with Veeva Promo Mats with expertise in HTML5, CSS3, and JavaScript. · Proven experience in developing Veeva CLM presentations, Approved Email and Fragments along with in asset publishing, updating, and lifecycle management within Veeva. · Familiarity with Veeva CRM and Salesforce · Familiarity with responsive email design and cross browser compatibility. · Skilled in the Adobe suite: Photoshop, Illustrator, InDesign, Premier Pro/After Effects in order to make minor artwork amends · Bachelor's degree in design or marketing (or other related field) or equivalent years of experience · Experience within the pharma or healthcare industry would be an advantage · Proficiency in Microsoft Office (Word, PowerPoint and Excel) · Familiarity of working within a project management system such as Jira · Have a detail-oriented mind, be well-organized, and be able to thrive in a deadline-driven environment with strong attention to detail · Should possess good oral and written communication skills and have a collaborative approach Business level written and verbal English is required for this role. EQUAL OPPORTUNITY: Indegene is proud to be an Equal Employment Employer and is committed to the culture of Inclusion and Diversity. We do not discriminate on the basis of race, religion, sex, colour, age, national origin, pregnancy, sexual orientation, physical ability, or any other characteristics. All employment decisions, from hiring to separation, will be based on business requirements, candidate’s merit and qualification. We are an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, colour, religion, sex, national origin, gender identity, sexual orientation, disability status, protected veteran status, or any other characteristics.

Key Responsibilities 1. SFMC Architecture & Development • Lead the build and optimization of journeys in Journey Builder, including multi-branch paths, triggers, decision splits, and event-based orchestration., • Build automations in Automation Studio, including SQL-based segmentation, scheduled automations, and data hygiene processes., • Develop modular, compliant email and content blocks, leveraging AMPscript, SSJS, and data extensions best practices., • Implement and optimize Einstein features and predictive capabilities within SFMC, • Own the final audit and quality validation of campaigns executed by team members, ensuring adherence to defined processes, compliance standards, technical accuracy, and client requirements before deployment. 2. Data & Integration Leadership • Design and maintain data models, data extensions, relational mappings, and business rules aligned with CRM, website, and analytics inputs. o WordPress VIP for personalization, tagging, and behavioral capture feeding MCP o Enterprise Data Lakes, CDPs, or analytics environments • · Ensure data dictionary, taxonomy alignment, and governance across all activation channels. 3. Marketing Cloud Personalization (MCP) • Implement MCP tagging, site wide java scripting, custom scripting (if any) rule sets, decisioning logic, personalization recipes, and identity resolution approaches., • Partner with web and analytics teams to ensure MCP instrumentation is clean, compliant, and aligned to journey logic., • Optimize hybrid (rule-based + algorithmic) MCP experiences based on campaign goals. 4. Cross-Functional Collaboration & Enablement • Work closely with omnichannel strategists, CRM leads, web/CMS teams, and localization leads., • Provide documentation, technical playbooks, and training for marketing, operations, and downstream teams., • Participate in solution design discussions, validation sessions, gap assessment, and technical Q&A. Required Qualifications • 7–10+ years of hands-on SFMC development and architecture experience at scale., • Advanced mastery of Journey Builder, Automation Studio, SQL, AMPscript, SSJS, and SFMC data modeling., • Proven experience with MCP implementation, including tagging, decisioning, and integration with websites (e.g., WordPress VIP)., • Strong familiarity with Veeva CRM data structures and how CRM segments feed omnichannel journeys., • Demonstrated experience supporting pharma or life sciences omnichannel operations., • Comfortable working cross-platform (CRM → SFMC → Web) in complex enterprise ecosystems., • Based in Madrid or already residing in Spain or Japan with ability for regular on-site work., • Language proficiency required in Spanish (for Spain market) EOE: Our client is an Equal Opportunity Employer and Prohibits Discrimination and Harassment of Any Kind: We are committed to the principle of equal employment opportunity for all employees and to providing employees with a work environment free of discrimination and harassment. All employment decisions at our client are based on business needs, job requirements, and individual qualifications, without regard to race, color, religion or belief, national, social or ethnic origin, sex (including pregnancy), age, physical, mental or sensory disability, HIV Status, sexual orientation, gender identity and/or expression, marital, civil union or domestic partnership status, past or present military service, family medical history or genetic information, family or parental status, or any other status protected by the laws or regulations in the locations where we operate. We will not tolerate discrimination or harassment based on any of these characteristics

Who We Are Whitewater Group is a leading provider of innovative and sustainable water treatment engineering systems operating across Ireland, the UK, and Europe in the Data Centre, Pharma, Power, and Industrial sectors. We specialize in designing, installing, commissioning, and maintaining bespoke water treatment solutions for our clients. Headquartered in Bray, Co. Wicklow, Whitewater Group operates from European bases in Spain, Sweden, Finland, and the UK, with plans for further expansion across Europe. The Group is experiencing significant growth driven by its focus on off-site construction methods (OSM), enabling the delivery of turnkey projects while minimizing on-site construction time. The Role Due to continued expansion, we are seeking to strengthen our HR function by hiring a Payroll Coordiantor based in Zaragoza. Reporting into HR, this role is responsible for managing payroll operations and leading HR controlling activities, ensuring accuracy, compliance, and transparency of employee-related costs. While the position sits within HR, it requires close collaboration with the Finance team to ensure proper cost allocation, budgeting alignment, and financial reporting accuracy. This is a critical role at the intersection of HR operations and governance, combining executional precision with analytical capability. What You’ll Do: Payroll Management • Manage end-to-end payroll processing in collaboration with payroll providers in all the countries we develop our business., • Coordinate payroll inputs including new hires, terminations, variable compensation, overtime, bonuses, and benefits., • Ensure compliance with labour regulations, tax regulations, and social security requirements., • Act as the primary liaison with external payroll providers., • Reconcile payroll data and ensure alignment between HR records and payroll outputs., • Maintain payroll documentation and support internal and external audits. HR Controlling & Workforce Cost Management • Monitor, analyse, and report on personnel costs (fixed and variable compensation, benefits, employer contributions)., • Prepare monthly HR cost reports and variance analysis versus budget and forecast., • Support annual workforce budgeting and reforecasting processes in collaboration with Finance., • Maintain accurate headcount and FTE tracking across entities and departments., • Develop and maintain HR dashboards and KPIs (e.g., turnover, absenteeism, workforce cost ratios)., • Ensure strong internal controls and data integrity across HRIS and payroll systems. Cross-Functional Collaboration • Work closely with Finance to ensure accurate cost allocation and reporting of personnel expenses., • Provide workforce cost insights to support decision-making., • Contribute to continuous improvement initiatives across payroll, HR analytics, and reporting processes., • Support broader HR initiatives as required. What we’re Looking For: • Degree in Human Resources, Finance, Business Administration, or a related field., • 5 years of experience in payroll and HR controlling or HR analytics roles., • Strong knowledge of Spanish payroll process and experience in a multi-country environment., • Solid understanding of budgeting, forecasting, and personnel cost analysis., • Advanced Excel skills; experience with HRIS and ERP systems is desirable., • Strong analytical mindset with high attention to detail., • Ability to manage sensitive and confidential information with discretion., • Strong stakeholder management skills and ability to work cross-functionally., • Competitive salary and health& life insurance , pension plan and flex retribution, • Opportunity for career progression within a fast-growing international company., • Exposure to HR operations across multiple European countries., • Hybrid working model combining home office and on-site presence in Zaragoza., • Seniority Level, • Mid-Senior level, • Industry, • Engineering Services, • Employment Type, • Full-time, • Job Functions, • Human Resources, • Finance, • Skills, • English, • Labor and Employment Law, • Human Resources Information Systems (HRIS), • Human Resources (HR), • Payroll, • ADP Payroll, • Payroll Processing, • Payroll Administration, • Payroll Management, • Payroll Taxes

Who are we? We are a technology-led healthcare solutions provider. We are driven by our purpose to enable healthcare organizations be future ready. We offer accelerated, global growth opportunities for talent that’s bold, industrious, and nimble. With Indegene, you gain a unique career experience that celebrates entrepreneurship, and is guided by passion, innovation, collaboration, and empathy. To explore exciting opportunities at the convergence of healthcare and technology, check out ___ What if we told you that you can move to an exciting role in an entrepreneurial organization without the usual risks associated with it? We understand that you are looking for growth in your career at this point and we would love for you to join us in our journey and grow with us. At Indegene, our roles come with the excitement you require at this stage of your career with the reliability you seek. We believe in creating leaders of tomorrow and mentor our leads to help them grow and nurture them as people managers and account managers. We are a rapidly growing global organization and are scouting for the best talent for this phase of growth. With us, you are at the intersection of two of the most exciting industries of healthcare and technology. We offer global opportunities with fast-track careers while you work with a team that is fueled by purpose. The combination of this will lead to a truly differentiated experience for you. If this excites you, then apply below. Role: Lead SFMC Developer IF YOU ARE INTERESTED, PLEASE SHARE YOUR CV IN ENGLISH LANGUAGE ONLY! Job Description: We are seeking an experienced SFMC Lead Developer with deep hands-on expertise across Automation Studio, Journey Builder, complex audience segmentation, Marketing Cloud Personalization (MCP), and enterprise integrations. This role is ideal for someone who is comfortable operating in a pharma environment, with strong data governance sensibilities and the ability to translate business objectives into scalable omnichannel journeys. The ideal candidate will partner closely with platform architects (e.g., CRM, Web, CMS) while leading technical design and building for Salesforce Marketing Cloud programs. This is a hands-on technical role, not purely strategic, requiring someone who can architect, develop, troubleshoot, optimize, and operationalize journeys at scale. Key Responsibilities 1. SFMC Architecture & Development • Lead the build and optimization of journeys in Journey Builder, including multi-branch paths, triggers, decision splits, and event-based orchestration., • Build automations in Automation Studio, including SQL-based segmentation, scheduled automations, and data hygiene processes., • Develop modular, compliant email and content blocks, leveraging AMPscript, SSJS, and data extensions best practices., • Implement and optimize Einstein features and predictive capabilities within SFMC, • Own the final audit and quality validation of campaigns executed by team members, ensuring adherence to defined processes, compliance standards, technical accuracy, and client requirements before deployment. 2. Data & Integration Leadership • Design and maintain data models, data extensions, relational mappings, and business rules aligned with CRM, website, and analytics inputs. o WordPress VIP for personalization, tagging, and behavioral capture feeding MCP o Enterprise Data Lakes, CDPs, or analytics environments • · Ensure data dictionary, taxonomy alignment, and governance across all activation channels. 3. Marketing Cloud Personalization (MCP) • Implement MCP tagging, site wide java scripting, custom scripting (if any) rule sets, decisioning logic, personalization recipes, and identity resolution approaches., • Partner with web and analytics teams to ensure MCP instrumentation is clean, compliant, and aligned to journey logic., • Optimize hybrid (rule-based + algorithmic) MCP experiences based on campaign goals. 4. Cross-Functional Collaboration & Enablement • Work closely with omnichannel strategists, CRM leads, web/CMS teams, and localization leads., • Provide documentation, technical playbooks, and training for marketing, operations, and downstream teams., • Participate in solution design discussions, validation sessions, gap assessment, and technical Q&A. Required Qualifications • 7–10+ years of hands-on SFMC development and architecture experience at scale., • Advanced mastery of Journey Builder, Automation Studio, SQL, AMPscript, SSJS, and SFMC data modeling., • Proven experience with MCP implementation, including tagging, decisioning, and integration with websites (e.g., WordPress VIP)., • Strong familiarity with Veeva CRM data structures and how CRM segments feed omnichannel journeys., • Demonstrated experience supporting pharma or life sciences omnichannel operations., • Comfortable working cross-platform (CRM → SFMC → Web) in complex enterprise ecosystems., • Based in Madrid or already residing in Spain or Japan with ability for regular on-site work., • Language proficiency required in Spanish (for Spain market) EQUAL OPPORTUNITY: Indegene is proud to be an Equal Employment Employer and is committed to the culture of Inclusion and Diversity. We do not discriminate on the basis of race, religion, sex, colour, age, national origin, pregnancy, sexual orientation, physical ability, or any other characteristics. All employment decisions, from hiring to separation, will be based on business requirements, candidate’s merit and qualification. We are an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, colour, religion, sex, national origin, gender identity, sexual orientation, disability status, protected veteran status, or any other characteristics

Who are we? We are a technology-led healthcare solutions provider. We are driven by our purpose to enable healthcare organizations be future ready. We offer accelerated, global growth opportunities for talent that’s bold, industrious, and nimble. With Indegene, you gain a unique career experience that celebrates entrepreneurship, and is guided by passion, innovation, collaboration, and empathy. To explore exciting opportunities at the convergence of healthcare and technology, check out ___ What if we told you that you can move to an exciting role in an entrepreneurial organization without the usual risks associated with it? We understand that you are looking for growth in your career at this point and we would love for you to join us in our journey and grow with us. At Indegene, our roles come with the excitement you require at this stage of your career with the reliability you seek. We believe in creating leaders of tomorrow and mentor our leads to help them grow and nurture them as people managers and account managers. We are a rapidly growing global organization and are scouting for the best talent for this phase of growth. With us, you are at the intersection of two of the most exciting industries of healthcare and technology. We offer global opportunities with fast-track careers while you work with a team that is fueled by purpose. The combination of this will lead to a truly differentiated experience for you. If this excites you, then apply below. Role: Salesforce Marketing Cloud (SFMC) Developer Job Description: We are seeking an experienced SFMC Lead Developer with deep hands-on expertise across Automation Studio, Journey Builder, complex audience segmentation, Marketing Cloud Personalization (MCP), and enterprise integrations. This role is ideal for someone who is comfortable operating in a pharma environment, with strong data governance sensibilities and the ability to translate business objectives into scalable omnichannel journeys. The ideal candidate will partner closely with platform architects (e.g., CRM, Web, CMS) while leading the technical design and building for Salesforce Marketing Cloud programs. This is a hands-on technical role, not purely strategic, requiring someone who can architect, develop, troubleshoot, optimize, and operationalize journeys at scale. Key Responsibilities 1. SFMC Architecture & Development • · Execute the build and optimization of journeys in Journey Builder, including multi-branch paths, triggers, decision splits, and event-based orchestration., • · Build automations in Automation Studio, including SQL-based segmentation, scheduled automations, and data hygiene processes., • · Develop modular, compliant email and content blocks, leveraging AMPscript, SSJS, and data extensions best practices., • · Implement and optimize Einstein features and predictive capabilities within SFMC, • · Own the final audit and quality validation of campaigns executed by team members, ensuring adherence to defined processes, compliance standards, technical accuracy, and client requirements before deployment. 2. Data & Integration • Execute and maintain data models, data extensions, relational mappings, and business rules aligned with CRM, website, and analytics inputs. o WordPress VIP for personalization, tagging, and behavioral capture feeding MCP o Enterprise Data Lakes, CDPs, or analytics environments • · Ensure data dictionary, taxonomy alignment, and governance across all activation channels. 3. Marketing Cloud Personalization (MCP) • · Implement MCP tagging, site wide java scripting, custom scripting (if any) rule sets, decisioning logic, personalization recipes, and identity resolution approaches., • · Partner with web and analytics teams to ensure MCP instrumentation is clean, compliant, and aligned to journey logic., • · Optimize hybrid (rule-based + algorithmic) MCP experiences based on campaign goals. Required Qualifications • · 3–4 years of hands-on SFMC development and architecture experience at scale., • · Advanced mastery of Journey Builder, Automation Studio, SQL, AMPscript, SSJS, and SFMC data modeling., • · Proven experience with MCP implementation, including tagging, decisioning, and integration with websites (e.g., WordPress VIP)., • · Strong familiarity with Veeva CRM data structures and how CRM segments feed omnichannel journeys., • · Demonstrated experience supporting pharma or life sciences omnichannel operations., • · Comfortable working cross-platform (CRM → SFMC → Web) in complex enterprise ecosystems., • · Based in Madrid or already residing in Spain or Japan with ability for regular on-site work., • · Language proficiency required in Spanish (for Spain market) Nice to Have • · Experience with Veeva Vault / Promomats metadata or workflow integration points., • · Familiarity with data lakes, GA/GA4 analytics, and tagging plans for paid/owned channels., • · Understanding of AI-assisted accelerators for segmentation, QA, tagging, or content workflows., • · Exposure to enterprise personalization strategies across web, SFMC, and CRM ecosystems. EQUAL OPPORTUNITY: Indegene is proud to be an Equal Employment Employer and is committed to the culture of Inclusion and Diversity. We do not discriminate on the basis of race, religion, sex, colour, age, national origin, pregnancy, sexual orientation, physical ability, or any other characteristics. All employment decisions, from hiring to separation, will be based on business requirements, candidate’s merit and qualification. We are an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, colour, religion, sex, national origin, gender identity, sexual orientation, disability status, protected veteran status, or any other characteristics.

Who are we? Indegene is a global consultancy at the forefront of driving innovation in the Pharmaceutical and Life Sciences industry, through combining medical and commercial expertise with innovative digital and AI technologies. We enable global healthcare organizations address complex challenges and drive better health and business outcomes by seamlessly integrating analytics, technology, operations, and medical expertise. Find out more at ___ Who are you? We are looking for a seasoned Veeva Developer to support pharmaceutical marketing and commercial operations. The role will be responsible for creating, editing, and managing digital content within the Veeva ecosystem, including CLM presentations and approved email campaigns, while also working with Veeva CRM (Salesforce-based). You must have the ability to partner effectively with brand teams and understand business and customer experience goals, working closely with preferred suppliers and internal cross-functional areas to ensure successful and timely delivery of those projects. This role is ideally suited to a driven individual who is looking for their next step in a digitally focused creative or marketing role. Job Description: Veeva Content Development • Build and maintain CLM (Closed Loop Marketing) presentations for Veeva CRM., • Develop and deploy Approved Emails using Veeva Approved Email and Engage functionalities., • Create and configure digital assets Veeva CLM presentations, Approved Email and Fragments, • Troubleshoot and resolve rendering or functionality issues in Veeva presentations and emails., • Familiarity with Veeva CRM and Salesforce, • Configure and manage content components, shared resources, and document relationships., • Support user acceptance testing (UAT) and ensure proper deployment in production environments., • Ensure all deliverables follow pharmaceutical compliance, regulatory, and MLR requirements., • Validate content using Veeva preview and testing tools across devices and browsers., • Maintain proper documentation, version control, and audit trail of deployed materials., • Work closely with Brand/Marketing teams to understand campaign objectives and translate them into functional assets., • Coordinate with designers, copywriters, and medical reviewers during content development., • Provide effort estimates and support project planning with PM teams., • 4 - 7 years of experience with experience of working and managing a team of Veeva Developers., • Strong hands-on experience with Veeva Promo Mats with expertise in HTML5, CSS3, and JavaScript., • Proven experience in developing Veeva CLM presentations, Approved Email and Fragments along with in asset publishing, updating, and lifecycle management within Veeva., • Familiarity with Veeva CRM and Salesforce, • Familiarity with responsive email design and cross browser compatibility., • Skilled in the Adobe suite: Photoshop, Illustrator, InDesign, Premier Pro/After Effects in order to make minor artwork amends, • Bachelor's degree in design or marketing (or other related field) or equivalent years of experience, • Experience within the pharma or healthcare industry would be an advantage, • Proficiency in Microsoft Office (Word, PowerPoint and Excel), • Familiarity of working within a project management system such as Jira, • Have a detail-oriented mind, be well-organized, and be able to thrive in a deadline-driven environment with strong attention to detail, • Should possess good oral and written communication skills and have a collaborative approach, • Business level written and verbal English is required for this role.

We are looking for a seasoned Veeva Developer to support pharmaceutical marketing and commercial operations. The role will be responsible for creating, editing, and managing digital content within the Veeva ecosystem, including CLM presentations and approved email campaigns, while also working with Veeva CRM (Salesforce-based). You must have the ability to partner effectively with brand teams and understand business and customer experience goals, working closely with preferred suppliers and internal cross-functional areas to ensure successful and timely delivery of those projects. This role is ideally suited to a driven individual who is looking for their next step in a digitally focused creative or marketing role. Job Description: Veeva Content Development · Build and maintain CLM (Closed Loop Marketing) presentations for Veeva CRM. · Develop and deploy Approved Emails using Veeva Approved Email and Engage functionalities. · Create and configure digital assets Veeva CLM presentations, Approved Email and Fragments · Troubleshoot and resolve rendering or functionality issues in Veeva presentations and emails. · Familiarity with Veeva CRM and Salesforce · Configure and manage content components, shared resources, and document relationships. · Support user acceptance testing (UAT) and ensure proper deployment in production environments. · Collaborate with stakeholders to optimize workflows and user experience within Veeva CRM. Quality, Compliance & Documentation · Ensure all deliverables follow pharmaceutical compliance, regulatory, and MLR requirements. · Validate content using Veeva preview and testing tools across devices and browsers. · Maintain proper documentation, version control, and audit trail of deployed materials. · Support audits and compliance reviews as required. Collaboration & Project Delivery · Work closely with Brand/Marketing teams to understand campaign objectives and translate them into functional assets. · Coordinate with designers, copywriters, and medical reviewers during content development. · Provide effort estimates and support project planning with PM teams. · Communicate technical constraints and provide implementation recommendations. Ideal Profile: · 4 - 7 years of experience with experience of working and managing a team of Veeva Developers. · Strong hands-on experience with Veeva Promo Mats with expertise in HTML5, CSS3, and JavaScript. · Proven experience in developing Veeva CLM presentations, Approved Email and Fragments along with in asset publishing, updating, and lifecycle management within Veeva. · Familiarity with Veeva CRM and Salesforce · Familiarity with responsive email design and cross browser compatibility. · Skilled in the Adobe suite: Photoshop, Illustrator, InDesign, Premier Pro/After Effects in order to make minor artwork amends · Bachelor's degree in design or marketing (or other related field) or equivalent years of experience · Experience within the pharma or healthcare industry would be an advantage · Proficiency in Microsoft Office (Word, PowerPoint and Excel) · Familiarity of working within a project management system such as Jira · Have a detail-oriented mind, be well-organized, and be able to thrive in a deadline-driven environment with strong attention to detail · Should possess good oral and written communication skills and have a collaborative approach · Business level written and verbal English is required for this role. Our client is an Equal Opportunity Employer, committed to a workplace free from discrimination and harassment. Employment decisions are based on business needs, job requirements, and individual qualifications without regard to race, color, religion, gender, age, disability, sexual orientation, gender identity, marital status, military service, genetic information, or any other status protected by law.

SAVANA () is an award-winning, international medical company aiming to accelerate health science by putting into the hands of healthcare providers the power to unlock all of the clinical value embedded within existing Electronic Health Records (EHRs) with Artificial Intelligence and Natural Language Processing. Always ensuring maximum privacy and security. Founded in 2014, Savana is an international medical company that has developed a scientific methodology that applies Artificial Intelligence (AI) to unlock all the clinical value embedded within Electronic Health Records' free-text (EHRs). With the largest AI-enabled, multi-language, multi-center research network in the world, Savana generates customized descriptive and predictive, High-quality Deep Real World Evidence research studies. Engineered by doctors for doctors, the company is built following the highest privacy-by-design standards. Savana operantes in more than 160 hospitals, 5 languages, 15 countries and has already improved more than 6 clinical practices with more than 100 employees from 10 nationalities. It constitutes a clinical research ecosystem that aims to advance personalized and precision medicine worldwide. Client Partner - Healthcare Software & Data Solutions at Savana Major Accountabilities where this role is involved: Client Engagement & Relationship Management: • Establish and maintain strong relationships with key decision-makers in healthcare organizations, including hospitals, research institutions, and public health entities., • Address and resolve blockades with hospitals, healthcare providers, health insurance companies and regional/national health systems, among other stakeholders, if data needs for RWE studies are not being covered., • Developing and maintaining a robust sales pipeline through effective lead generation and qualification., • Oversee and optimize (reducing timelines and resources dedication year over year) the entire sales cycle, from lead generation and qualification to contract negotiation and closing, ensuring a seamless and positive customer experience., • Coordinate workflows (considering legal, data privacy, and data transfer aspects) with new or existing clinical data providers, and coordinate internally with other teams, ensuring the required data sources to execute RWE studies are obtained on time. Collaboration with External Stakeholders: • Work closely with industry stakeholders, including healthcare regulators and professional associations, to promote Savana’s solutions and influence industry standards., • Represent Savana at healthcare and industry conferences, workshops, and other events to enhance brand visibility and generate new business leads. Information Security Management System Responsibilities • Ensure familiarity with and adherence to the organization's information security policies and procedures., • Participate in regular information security training sessions to stay updated on potential threats and necessary security measures., • Promptly report any security incidents or vulnerabilities to the designated function within the organization., • Maintain the confidentiality, integrity, and availability of information by following best practices for data handling and protection; including using strong passwords, encrypting sensitive data, regularly updating software, and promptly reporting any security incidents. Quality Management System Responsibilities: • Adhere to Savana’s Quality Management System (QMS) policies, procedures, and applicable laws and regulations., • Participate in and complete assigned training activities., • Identify and report any deviations from controlled processes or regulations., • Work closely with the Quality Team to resolve Corrective and Preventive Actions (CAPA), deviations, and audit findings as deemed applicable., • Contribute to the maintenance and review of Standard Operating Procedure (SOPs) and Application Manuals (AMs) related to team activities as applicable. Skills, Experience and Qualifications required: • More than 5 years’ experience. Experience selling SaaS in the healthcare environment and with health insurance companies., • Good understanding of technology, big data and AI applications in health., • Fluency in both English and Spanish is required. Fluency in either German or French is a plus., • Excellent communication skills and strong leadership capability., • Experience managing international sales and business development teams., • Interested in shaping the future of health, focussing on unmet medical needs., • Ability to communicate with medical departments in the pharma industry., • Willing to work from home and travel., • Ability to work well within a team or alone., • Ability to work in a multinational, multidisciplinary and fast-growing environment., • Maintain one's strategy but adapting it to a changing and even volatile environment., • Patient, flexible attitude, ability to perform under pressure., • Autonomy, creativity, good capacities for analysis and organization of work., • Maintain one's own strategy but adapting it to a changing and even volatile environment. If you are practical, experienced, proactive, independent, articulate, passionate about facilitating the digital transformation of healthcare, fascinated by Artificial Intelligence, the future of medicine and determined to solve healthcare's biggest problems. You are a Savaner. Join us! We offer: • Work with a multidisciplinary team of clinicians, computer engineers, computational linguists, mathematicians, designers, medical Natural Language Processing expert programmers and other disciplines. We are a team of professionals with a common goal: to blend the knowledge of all of us to seek excellence in our purpose. Coming from very different disciplines, we want everyone to learn from everyone, creating a unique entity that moves towards the transformation of health through Artificial Intelligence., • An opportunity to provoke a positive impact. We seek to improve health on the planet through technology and to help people and health institutions. Our employees and collaborators strive to provide our users with the necessary tools and support to achieve a more accessible and egalitarian global health. We care about our environment and we are willing to improve it., • An environment to express yourself as you are and enjoy what you know. We defend individuality to form a richer and more plural "ecosystem". Be yourself and tell us what you have learned and how could we use it together to help us achieve our purpose. If you like what you do, we like to work with you., • Competitive salary conditions, flexible culture and a development framework to growth your career. People are our main asset, so we invest in training and development and recognize and compensate for achievements and valuable work. We trust in the talent and commitment of people and focus on objectives and results, so we are flexible in our way of working, providing a framework to reconcile our personal and professional lives. Details from this job description are not to be used for marketing purposes. Savana does not accept unsolicited resumes from search firms. All resumes submitted by search firms to any employee at Savana via e-mail, the Internet or directly without a valid written search agreement will be deemed the sole property of Savana, and no fee will be paid in the event the candidate is hired by Savana. Medsavana S.L. (“Medsavana”) will process the personal data you provide to us during the selection process (the “Candidate’s Personal Data”) in order to manage your curriculum data and the selection process you are applying to. You can exercise the rights of access, rectification or erasure, restriction of processing, objection, portability, and to object automated individual decisions at the registered office of the company indicated or in the email . For more information, please refer to the privacy policy section on our webpage:

IF YOU ARE INTERESTED, PLEASE SHARE YOUR CV IN ENGLISH LANGUAGE ONLY! Who are we? We are a technology-led healthcare solutions provider. We are driven by our purpose to enable healthcare organizations be future ready. We offer accelerated, global growth opportunities for talent that’s bold, industrious, and nimble. With Indegene, you gain a unique career experience that celebrates entrepreneurship, and is guided by passion, innovation, collaboration, and empathy. To explore exciting opportunities at the convergence of healthcare and technology, check out ___ What if we told you that you can move to an exciting role in an entrepreneurial organization without the usual risks associated with it? We understand that you are looking for growth in your career at this point and we would love for you to join us in our journey and grow with us. At Indegene, our roles come with the excitement you require at this stage of your career with the reliability you seek. We believe in creating leaders of tomorrow and mentor our leads to help them grow and nurture them as people managers and account managers. We are a rapidly growing global organization and are scouting for the best talent for this phase of growth. With us, you are at the intersection of two of the most exciting industries of healthcare and technology. We offer global opportunities with fast-track careers while you work with a team that is fueled by purpose. The combination of this will lead to a truly differentiated experience for you. If this excites you, then apply below. IF YOU ARE INTERESTED, PLEASE SHARE YOUR CV IN ENGLISH LANGUAGE ONLY! Role: Veeva Lead Developer Who are you? We are looking for a seasoned Veeva Developer to support pharmaceutical marketing and commercial operations. The role will be responsible for creating, editing, and managing digital content within the Veeva ecosystem, including CLM presentations and approved email campaigns, while also working with Veeva CRM (Salesforce-based). You must have the ability to partner effectively with brand teams and understand business and customer experience goals, working closely with preferred suppliers and internal cross-functional areas to ensure successful and timely delivery of those projects. This role is ideally suited to a driven individual who is looking for their next step in a digitally focused creative or marketing role. Job Description: Veeva Content Development • Build and maintain CLM (Closed Loop Marketing) presentations for Veeva CRM., • Develop and deploy Approved Emails using Veeva Approved Email and Engage functionalities., • Create and configure digital assets Veeva CLM presentations, Approved Email and Fragments, • Troubleshoot and resolve rendering or functionality issues in Veeva presentations and emails., • Familiarity with Veeva CRM and Salesforce, • Configure and manage content components, shared resources, and document relationships., • Support user acceptance testing (UAT) and ensure proper deployment in production environments., • Ensure all deliverables follow pharmaceutical compliance, regulatory, and MLR requirements., • Validate content using Veeva preview and testing tools across devices and browsers., • Maintain proper documentation, version control, and audit trail of deployed materials., • Work closely with Brand/Marketing teams to understand campaign objectives and translate them into functional assets., • Coordinate with designers, copywriters, and medical reviewers during content development., • Provide effort estimates and support project planning with PM teams., • Communicate technical constraints and provide implementation recommendations. Ideal Profile: • 4 - 7 years of experience with experience of working and managing a team of Veeva Developers., • Strong hands-on experience with Veeva Promo Mats with expertise in HTML5, CSS3, and JavaScript., • Proven experience in developing Veeva CLM presentations, Approved Email and Fragments along with in asset publishing, updating, and lifecycle management within Veeva., • Familiarity with Veeva CRM and Salesforce, • Familiarity with responsive email design and cross browser compatibility., • Skilled in the Adobe suite: Photoshop, Illustrator, InDesign, Premier Pro/After Effects in order to make minor artwork amends, • Bachelor's degree in design or marketing (or other related field) or equivalent years of experience, • Experience within the pharma or healthcare industry would be an advantage, • Proficiency in Microsoft Office (Word, PowerPoint and Excel), • Familiarity of working within a project management system such as Jira, • Have a detail-oriented mind, be well-organized, and be able to thrive in a deadline-driven environment with strong attention to detail, • Should possess good oral and written communication skills and have a collaborative approach, • Business level written and verbal English is required for this role. EQUAL OPPORTUNITY: Indegene is proud to be an Equal Employment Employer and is committed to the culture of Inclusion and Diversity. We do not discriminate on the basis of race, religion, sex, colour, age, national origin, pregnancy, sexual orientation, physical ability, or any other characteristics. All employment decisions, from hiring to separation, will be based on business requirements, candidate’s merit and qualification. We are an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, colour, religion, sex, national origin, gender identity, sexual orientation, disability status, protected veteran status, or any other characteristics.

Mediance es un grupo empresarial en crecimiento especializado en la adquisición y desarrollo de compañías del sector sanitario. El grupo integra empresas que operan en diferentes ámbitos del healthcare, incluyendo la distribución de medicación, producto sanitario y equipamiento médico, así como a la optimización de procesos asistenciales y asesoramiento en la gestión a través del desarrollo de soluciones tecnológicas para el sector. El modelo de Mediance se basa en una estrategia buy & build, mediante la cual el grupo adquiere empresas especializadas y las impulsa mediante servicios centrales que aportan soporte estratégico en áreas como finanzas, recursos humanos, operaciones y tecnología. En este contexto, Mediance busca incorporar un Head of Technology / IT Director que lidere la estrategia tecnológica del grupo, impulsando la integración de sistemas entre las empresas participadas y construyendo una plataforma tecnológica común que permita mejorar la eficiencia operativa y escalar el crecimiento del grupo. Descripción del Puesto: El Head of Technology / IT Director será responsable de definir y ejecutar la estrategia tecnológica del grupo Mediance, con especial foco en la integración de sistemas, la estandarización de herramientas y la digitalización de las empresas participadas. Se trata de un rol con alto impacto estratégico, pero también con un enfoque hands-on, ideal para un perfil con mentalidad de constructor que quiera liderar la transformación tecnológica de un grupo sanitario en crecimiento. La persona seleccionada trabajará de forma transversal con los equipos directivos de las diferentes compañías del grupo, coordinando proveedores tecnológicos y apoyándose en los equipos técnicos existentes en las empresas participadas. Responsabilidades: • Definir la arquitectura tecnológica global del grupo Mediance., • Diseñar el roadmap de digitalización y evolución tecnológica., • Evaluar los sistemas y plataformas existentes en las empresas participadas., • Experiencia en implementaciones mediante APIs o middleware., • Liderar procesos de integración tecnológica tras adquisiciones., • Diseñar e implementar planes de unificación de sistemas., • Estandarizar herramientas y procesos tecnológicos entre compañías., • Seleccionar e implementar sistemas clave para el grupo (ERP, CRM, herramientas financieras, plataformas de reporting y business intelligence)., • Establecer estándares tecnológicos para todas las empresas participadas., • Definir la arquitectura de infraestructura y cloud del grupo., • Diseñar integraciones entre sistemas mediante APIs o middleware., • Garantizar la seguridad y escalabilidad de la plataforma tecnológica., • Seleccionar y coordinar consultoras y partners tecnológicos., • Supervisar proyectos tecnológicos y controlar calidad, tiempos y costes., • Garantizar una ejecución eficiente de las implementaciones., • Asesorar a los equipos técnicos existentes en las compañías del grupo., • Apoyar proyectos tecnológicos específicos en las empresas participadas., • Identificar oportunidades de mejora operativa mediante tecnología., • Definir estándares tecnológicos comunes., • Priorizar iniciativas tecnológicas con impacto en negocio., • Construir progresivamente una función tecnológica central para el grupo. Requisitos: • Entre 10 y 15 años de experiencia en tecnología, sistemas o transformación digital., • Experiencia liderando implementaciones de ERP o sistemas corporativos., • Experiencia en integración de sistemas entre diferentes empresas o unidades de negocio., • Conocimiento de arquitecturas cloud y sistemas empresariales., • Experiencia gestionando proveedores tecnológicos y consultoras., • Capacidad para liderar proyectos tecnológicos complejos con múltiples stakeholders., • Experiencia con Plataformas de Business Intelligence y reporting (Power BI, Tableau, etc.)., • Experiencia en implementaciones mediante APIs o middleware., • Disponibilidad para viajar a nivel nacional, con desplazamientos frecuentes por toda España (viajes semanales) para trabajar de forma presencial con las distintas compañías del grupo. Nice to have: • Experiencia en sectores como healthcare, pharma, distribución sanitaria o entornos industriales., • Experiencia en consultoría tecnológica o transformación digital., • Experiencia trabajando en grupos empresariales o empresas participadas por private equity., • Experiencia en procesos de integración tecnológica tras adquisiciones.

Who are we? Indegene is a global consultancy at the forefront of driving innovation in the Pharmaceutical and Life Sciences industry, through combining medical and commercial expertise with innovative digital and AI technologies. We enable global healthcare organizations address complex challenges and drive better health and business outcomes by seamlessly integrating analytics, technology, operations, and medical expertise. Find out more at ___ Who are you? We are looking for a seasoned Veeva Developer to support pharmaceutical marketing and commercial operations. The role will be responsible for creating, editing, and managing digital content within the Veeva ecosystem, including CLM presentations and approved email campaigns, while also working with Veeva CRM (Salesforce-based). You must have the ability to partner effectively with brand teams and understand business and customer experience goals, working closely with preferred suppliers and internal cross-functional areas to ensure successful and timely delivery of those projects. This role is ideally suited to a driven individual who is looking for their next step in a digitally focused creative or marketing role. Job Description: Veeva Content Development • Build and maintain CLM (Closed Loop Marketing) presentations for Veeva CRM., • Develop and deploy Approved Emails using Veeva Approved Email and Engage functionalities., • Create and configure digital assets Veeva CLM presentations, Approved Email and Fragments, • Troubleshoot and resolve rendering or functionality issues in Veeva presentations and emails., • Familiarity within Veeva CRM and Salesforce, • Configure and manage content components, shared resources, and document relationships., • Support user acceptance testing (UAT) and ensure proper deployment in production environments., • Collaborate with stakeholders to optimize workflows and user experience within Veeva CRM. Quality, Compliance & Documentation • Ensure all deliverables follow pharmaceutical compliance, regulatory, and MLR requirements., • Validate content using Veeva preview and testing tools across devices and browsers., • Maintain proper documentation, version control, and audit trail of deployed materials., • Support audits and compliance reviews as required. Collaboration & Project Delivery • Work closely with Brand/Marketing teams to understand campaign objectives and translate them into functional assets. Ideal Profile: • 1 - 3 years of experience of relevant experience., • Strong hands-on experience with Veeva Promo Mats with expertise in HTML5, CSS3, and JavaScript., • Proven experience in developing Veeva CLM presentations, Approved Email and Fragments along with in asset publishing, updating, and lifecycle management within Veeva., • Familiarity with Veeva CRM and Salesforce, • Familiarity with responsive email design and cross browser compatibility., • Skilled in the Adobe suite: Photoshop, Illustrator, InDesign, Premier Pro/After Effects in order to make minor artwork amends, • Bachelor's degree in design or marketing (or other related field) or equivalent years of experience, • Experience within the pharma or healthcare industry would be an advantage, • Proficiency in Microsoft Office (Word, PowerPoint and Excel), • Familiarity of working within a project management system such as Jira, • Have a detail-oriented mind, be well-organized, and be able to thrive in a deadline-driven environment with strong attention to detail, • Should possess good oral and written communication skills and have a collaborative approach, • Business level written and verbal English is required for this role.

In a few words Position: Data Scientist Location: Madrid (Chamberí area). Want to know more? 👇 INSUD PHARMA operates across the entire pharmaceutical value chain, providing specialized knowledge and experience in scientific research, development, manufacturing, sales, and marketing of a wide range of active pharmaceutical ingredients (API), finished dosage forms (FDF), and branded pharmaceutical products, adding value to human and animal health. The activities of INSUD PHARMA are organized into three synergistic business areas: Industrial (Chemo), Branded (Exeltis), and Biotech (mAbxience), with over 9,000 professionals in more than 50 countries, 20 state-of-the-art facilities, 15 specialized R&D centers, 12 commercial offices, and more than 35 pharmaceutical subsidiaries, serving 1,150 customers in 96 countries worldwide. INSUD PHARMA believes in innovation and sustainable development. Ready to be a #Challenger? What are we looking for? 🔎 We are the Data Science team within AI Labs, the applied AI department at Insud Pharma. We are a team of 30 professionals (AI Engineers, Data Scientists, DevOps Engineers, and Product Managers) working across the full breadth of the company, building products, models, and analytical solutions that directly inform and shape decision-making. We are looking for an Applied Data Scientist with strong technical foundations who is eager to work across diverse and complex problem domains (R&D, drug manufacturing process optimization, clinical trials, and beyond). You will model problems from the ground up—defining the right framing, selecting appropriate methodologies, and owning solutions through rigorous development to full deployment. We are seeking someone curious enough to tackle varied challenges (graph theory, embeddings, neural network forecasting models, causality, Bayesian optimization), rigorous enough to justify every technical and methodological decision, and independent enough to deliver end-to-end impact while taking full ownership of their work. How the team works: AI Labs operates with a startup mindset within Insud Pharma. The department is young, and the culture reflects that: flat, collaborative, and fast-moving. Beyond the Data Science team, you will work alongside AI Engineers, DevOps Engineers, and Product Managers who are equally committed to delivering high-quality work. We hold regular demo days where teams present their work, as well as whiteboard sessions where we tackle problems together. The cross-disciplinary dynamic is genuinely strong. The office is located in central Madrid (Chamberí, near Eloy Gonzalo), well connected and situated in a vibrant part of the city. The challenge! • Collaborate with small, cross-functional teams. Each project is run by a small group — typically a Product Manager, a Data Scientist, an Engineer, and key stakeholders. Iteration is fast, feedback loops are short, and your contribution is visible from day one., • Conduct exploratory data analysis to uncover patterns and insights in large datasets., • Design, implement, and validate machine learning models and statistical methodologies to solve high-impact, real-world business problems., • Translate technical findings into clear narratives, visualizations, and decision frameworks for both technical and non-technical stakeholders, enabling informed and data-driven decisions. What do you need? • Strong understanding of statistics, machine learning, and data mining techniques., • Expertise in Python programming, including proficiency with data science libraries (e.g., NumPy, Pandas, Scikit-learn, TensorFlow…)., • Strong understanding of data preprocessing, feature engineering, and model evaluation techniques., • Proven ability to translate complex technical concepts into clear, actionable insights for non-technical audiences., • Knowledge and experience in causal inference methodologies will be highly valued., • Knowledge of deep learning architectures and natural language processing is beneficial., • Familiarity with Large Language Models (LLMs) and their applications in business contexts is a plus., • Experience with version control systems (e.g., Git) and collaborative development practices., • Clean, maintainable code and familiarity with software engineering best practices., • Familiarity with cloud platforms (e.g., AWS, Azure, Google Cloud) and their machine learning services., • Experience with big data technologies (e.g., Spark, Hadoop) and SQL databases is a plus., • Proficient in Spanish and English in written and verbal communication. Our benefits! ⏰ Flexible start time from Monday to Friday 📜 Permanent contract. 🥼 Life and accident insurance. 🍽️ Ticket restaurant 💻 Training and language learning platform 💆🏻 ♀️ Wellness platform with unlimited free psychologist sessions 🚕 Cabify transportation service for employee use 📈 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! #InsudPharma #Challenger #Insuder #InsudTalent COMMITMENT TO EQUAL OPPORTUNITIES The InsudPharma group is aware that business management must align with the needs and demands of society, and therefore assumes the commitment to equal opportunities and treatment between men and women, as stated in the current regulations on the matter - Organic Law 3/2007, and we do not discriminate against any person on the grounds of ethnicity, religion, age, sex, nationality, marital status, affective or sexual orientation, gender identity or expression, disability, or any other personal or social circumstance.