Trabajos pharma en España

In a few words • Position: Senior Frontend Developer, • Location: Madrid (Chamberí area)., • +4 years of experience 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 AI Labs team, the applied AI department at Insud Pharma. We are a team of 30 professionals (AI Engineers, Data Scientists, Backend Engineers, DevOps Engineers, and Product Managers) working across the full breadth of the company, building products and systems that directly inform and shape decision-making. We are looking for a Senior Frontend Developer with a strong technical foundation and extensive experience in modern frontend technologies, particularly React. You will work on building high-quality interfaces and applications, translating complex business and technical requirements into intuitive, efficient, and scalable user experiences. You will take part in frontend architecture decisions, contribute to the definition and evolution of technical standards, design systems, and component libraries, and collaborate closely with backend, product, and design teams to build robust and maintainable end-to-end solutions. We are seeking someone curious enough to explore new tools, frameworks, and best practices within the frontend ecosystem; rigorous enough to ensure code quality, performance, and accessibility; and autonomous enough to take full ownership of solutions and drive them from concept to production with real impact 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 AI Engineering team, you will work alongside Data Scientists, 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! • Design and develop modern web applications using React and React Native., • Build scalable, reusable, and high-performance user interfaces., • Translate business requirements into high-quality user experiences., • Design and maintain design systems and UI component libraries., • Manage application state efficiently., • Integrate REST APIs and collaborate with backend teams on clear and maintainable contracts., • Optimize application performance (rendering, loading time, bundle size)., • Contribute to frontend architecture decisions (structure, modularity, scalability)., • Apply best practices in accessibility and usability., • Collaborate closely with product, design, and backend teams., • Ensure code quality through testing, code reviews, and best practices., • Contribute to defining technical standards and evolving the frontend stack., • Mentor and support junior developers. What do you need? • Fluency in Spanish and English., • Strong experience with React, React Native and the modern frontend ecosystem., • Solid knowledge of modern JavaScript and TypeScript., • Experience with state management solutions., • Experience integrating and consuming REST APIs., • Strong knowledge of HTML and CSS (responsive design, layouts, best practices)., • Experience with frontend development tools (bundlers, build tools, etc.)., • Familiarity with frontend testing (Jest, React Testing Library, or similar)., • Experience using Git in collaborative environments., • Understanding of software development best practices (clean code, frontend architecture)., • Ability to work autonomously with strong ownership and a product-oriented mindset. 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.

En BETWEEN te ofrecemos las oportunidades que necesitas para alcanzar tus objetivos profesionales. Si quieres desarrollar tus capacidades en IT e Ingeniería, ¡este es tu próximo destino! Damos soporte en una gran variedad de áreas como Firmware, Software, BI, Diseño, Project Management y muchas más. Además, desarrollamos soluciones tecnológicas a medida desde nuestros BETWEEN Labs. Descripción del Puesto: Estamos buscando un/a Coordinador/a de Ingeniería de Proyectos Pharma para unirse a nuestro equipo en Santo Domingo, Colombia. La persona seleccionada será responsable de la gestión integral de proyectos de ingeniería en el sector farmacéutico, asegurando la correcta ejecución del proyecto, el cumplimiento de plazos y presupuestos. Se requiere una sólida experiencia en la gestión de la fase de ingeniería, coordinación de recursos internos y comunicación fluida con el cliente, así como una profunda comprensión de la planificación de la ejecución de proyectos, incluyendo aspectos como HVAC y salas blancas. Salario entre los 45.000€ y 50.000€ en base a experiencia y conocimientos. Proyecto de 18 meses. Al salario se le añadirá alojamiento, transporte y dietas. Responsabilidades Principales: • Liderar y gestionar proyectos de ingeniería desde la concepción hasta la finalización, con un enfoque específico en el sector farmacéutico., • Gestionar la fase de ingeniería del proyecto, asegurando la calidad y el cumplimiento de los estándares y normativas aplicables., • Coordinar eficazmente los recursos internos (equipos de ingeniería, técnicos, etc.)., • Desarrollar y supervisar planes de ejecución detallados, incluyendo cronogramas, presupuestos y asignación de recursos., • Gestionar el alcance del proyecto, controlando cambios y asegurando que las entregas cumplan con los requisitos definidos., • Identificar, evaluar y mitigar los riesgos del proyecto., • Asegurar el cumplimiento de las normativas específicas del sector farmacéutico., • Supervisar y gestionar aspectos técnicos clave de los proyectos, tales como sistemas HVAC (Calefacción, Ventilación y Aire Acondicionado) y el diseño y cálculo de salas blancas., • Gestionar la documentación técnica del proyecto, incluyendo planos, especificaciones, informes y manuales. ¿Qué Ofrecemos? • Seguro Médico: Cobertura con Alan para tu tranquilidad., • Formación Continua: Oportunidades de desarrollo profesional a través de cursos de idiomas, certificaciones, bootcamps y mucho más., • Eventos y Actividades: Participa en una multitud de eventos como BETWEEN Night, Torneo de Pádel, y otras actividades para fomentar la camaradería., • Retribución Flexible: Beneficios adaptados a tus necesidades (restaurante, transporte, guardería)., • Incentivos: Reconocimiento por talento validado o recomendado., • Oportunidad de Crecimiento: Únete a una empresa en expansión con un fuerte enfoque en el desarrollo del talento y la innovación tecnológica. Si cumples con los requisitos y buscas un entorno dinámico donde puedas aplicar tus conocimientos y crecer profesionalmente, te invitamos a formar parte de nuestro equipo en BETWEEN Group. Requisitos: • Ingeniería Mecánica, Química, Industrial, o afín., • Mínimo 10 años de experiencia demostrable en gestión de proyectos de ingeniería en el sector pharma., • Conocimientos avanzados de CYPE enfocados a HVAC y mecánica., • Sólida experiencia en la gestión de la fase de ingeniería, planificación de la ejecución, coordinación de recursos y comunicación con clientes., • Conocimiento intermedio de las áreas de Electricidad, fluidos, paneles, y otros., • Conocimiento básico de las áreas de construcción y obra civil.

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 una posición como Regulatory Affairs para nuestras oficinas ubicadas en Tres Cantos, Madrid. Se trata de una posición de carácter temporal por suplencia y en formato de presencialidad del 100%. Objetivos: • Registro y mantenimiento de autorizaciones de comercialización y distribución de medicamentos, acorde a la legislación aplicable, fuera y dentro de la Unión Europea., • Gestión de proyectos específicos enfocados al registro, mantenimiento y distribución de nuevos medicamentos, en actuales o nuevos mercados. Funciones: • Mantenerse actualizado en la normativa aplicable acorde a la misión del puesto. Comunicar los aspectos relevantes de la misma, a las áreas afectadas de la empresa, según las necesidades., • Coordinación, y realización de trabajos científicos y administrativos complejos a partir de la evaluación de la documentación disponible o que se deba buscar., • Planificación, elaboración, evaluación y mantenimiento de los Expedientes de Registro y la Documentación Técnica de medicamentos de acuerdo a la planificación anual del departamento basada en las prioridades de las Unidades de Negocio., • Participación en la preparación del expediente técnico de los productos, para los que la compañía se declara fabricante y/o responsable de la comercialización; incluyendo los trámites necesarios para su distribución fuera y dentro de la Unión Europea., • Revisión del Material de acondicionamiento a utilizar previo a la comercialización de medicamentos y productos en los diferentes países, cuando se requiera., • Apoyo a Marketing en la información, promoción y publicidad de los productos de la Compañía, cuando se requiera para verificar el cumplimiento de la legislación., • Coordinación y seguimiento de proyectos específicos enfocados al registro, mantenimiento y distribución de nuevos medicamentos, en actuales o nuevos mercados. Requisitos: • Titulado Superior en Farmacia, o en otras Ciencias de la Salud., • Inglés C1, • Buen nivel de ofimática, • Conocimiento de la actual legislación española y europea en registro y distribución de medicamentos., • Conocimiento en registros a nivel europeo y a nivel internacional, • Conocimiento de formatos electrónicos para la preparación y presentación de la documentación requerida de medicamentos y otros productos a las agencias reguladoras; en especial, NeeS/VNeeS y eCTD para medicamentos de uso humano y de uso veterinario. Si estas buscando adquirir experiencia en el área regulatoria en una de las empresas líder en el sector de la inmunología, ¡esta 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.

SAVANA (www.savanamed.com) 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 16 nationalities. It constitutes a clinical research ecosystem that aims to advance personalized and precision medicine worldwide. Client Partner / KAM - Life Science at Savana Major Accountabilities where this role is involved: • Implement Savana’s sales global strategy., • Contribute to Savana’s lead generation activities., • Management of the key accounts: follow up to ensure the highest level of satisfaction understanding their needs and offer good value proposition, seeking for new projects with existing key customers., • Seek for new customers with potential of becoming key accounts., • Build a long-term relationship with the customers., • Develop a trusted advisor relationship with key accounts, customer stakeholders and executive, • sponsors., • Ensure the timely and successful delivery of our solutions according to customer needs and, • objectives., • Clearly communicate the progress of monthly/quarterly initiatives to internal and external, • stakeholders., • Forecast and track key account metrics to the sales department., • Liaise with internal teams and ensure customer satisfaction and loyalty., • Operate according to Security Policies, Procedures and Manuals., • Report any suspect of incident or improvement proposals. Skills, Experience and Qualifications required: • 3 to 5 years’ experience in key account management position at a CRO or pharmaceutical company., • Understanding on technology, big data and AI applications in health is a plus., • Capable of stablishing durable relationships pharma companies., • Experience on account management., • Ability to communicate a technical value proposition., • Innovative mind with the ability to discover and test new value propositions., • Strong understanding of clinical research and market access activities., • Experience with public tenders., • Result oriented., • Fluent in English and Spanish., • Excellent communication skills (verbal and written)., • Interested on shaping the future of health, focussing on unmet medical needs., • Ability to work well within a team or alone., • Ability to work in a multinational, multidisciplinary and fast-growing environment., • Maintain one´s own 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 organisation of work. 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 grow 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 dpo@savanamed.com. For more information, please refer to the privacy policy section on our webpage: https://www.savanamed.com/es/curriculum/

Role Overview We are looking for a highly motivated and experienced Senior Casualty Underwriter to join our team and support the development of our local portfolio. This is an excellent opportunity for a seasoned professional seeking to advance their career in a dynamic and collaborative environment. As a Senior Underwriter, you will assess and underwrite casualty risks, primarily General Liability and Life Sciences, manage client relationships, and support our business growth. You will work closely with our Local and European team, ensuring alignment with underwriting guidelines, risk appetite, and compliance standards. What will you do? • Underwrite General Liability and Products Liability risks, with a focus on Life Sciences clients, • Assess complex exposures including clinical trials, product risks, and international operations, • Structure policy terms, limits, deductibles, and coverage conditions in line with risk profile, • Price risks using underwriting judgment, market benchmarks, and available data, • Manage and grow a portfolio in line with underwriting strategy and profitability targets, • Build and maintain strong broker relationships to generate new business opportunities, • Monitor claims trends and loss experience to inform underwriting decisions, • Collaborate with local and European teams, including reinsurance partners where relevant What are we looking for? • 5+ years of experience in Casualty underwriting, • Strong technical knowledge of General Liability and Products Liability, • Experience underwriting Life Sciences risks (pharma, biotech, medtech, clinical trials), • Commercial mindset with proven broker-facing experience, • Ability to make autonomous underwriting decisions within authority, • Strong communication and negotiation skills, • Fluent in English and Spanish About DUAL Established in 1998, Dual is a leading global MGA with more than 1,500 employees and total premium revenues of USD 3.5 billion. Our global network enables us to provide access to international expertise, knowledge, and developments, so that we can continuously improve our products and services. We work hard to understand our customers' needs to ensure they receive consistently excellent service from DUAL. What do we offer in return? • A career that you define., • A competitive salary, • Benefits package, • Rewarding annual leave, • Birthday off, • Flexibility with hybrid working, • A challenging role at one of the most ambitious underwriting agencies, • Collaboration with specialists and market leaders where your development and growth is central Our culture: People first Our core values dictate how we live and work. We’re a group with independence and people at its heart and we’re a home for talent with a unique culture: the biggest small company in the world. The focus on being a people-first business has always been at the very heart of the group; Our vision was to create an independent business with a unique culture and one that would survive and thrive as a business controlled by the people working for it. And finding the most talented and entrepreneurial people to join the group has been and will continue to be key. Diversity and inclusion At DUAL, we consider our people our chief competitive advantage and, as such, we treat colleagues, candidates, clients and business partners with equality, fairness and respect, regardless of their age, disability, race, religion or belief, gender, sexual orientation, marital status or family circumstances.

🚀 We are hiring | Clinical Project Manager – Crovelis 📍 Madrid | Hybrid 🌍 International environment 🧪 Clinical Research At Crovelis, the CRO division of Insud Pharma, we are continuing to grow and are looking for a Clinical Project Manager to join our team and lead the operational management of international clinical studies. We are looking for someone with solid experience in clinical research and project management, capable of driving studies forward while coordinating multidisciplinary teams and ensuring timelines, quality standards, budgets, and regulatory compliance are successfully met. This is an opportunity to join a dynamic, collaborative, and fast-growing environment where you will have real visibility and impact across global clinical projects. 🔎 What will you do? • Lead and coordinate assigned clinical projects from an operational perspective, • Collaborate cross-functionally with Clinical Operations, Regulatory, Pharmacovigilance, Data Management, Biostatistics, QA and external vendors, • Support study planning, risk management, timelines and budget tracking, • Ensure compliance with ICH-GCP, SOPs and applicable regulations, • Participate in study feasibility, site selection and project oversight activities, • Contribute to stakeholder communication, study reporting and project governance, • Support TMF oversight, audit readiness and study close-out activities, • Work closely with CRAs, CTAs and international teams across multiple regions 🎯 What are we looking for? ✔ 4–5+ years of experience in Clinical Research ✔ Previous experience as Clinical Project Manager or in similar project management roles ✔ Strong understanding of ICH-GCP and clinical trial regulations ✔ International and multicountry study experience highly valued ✔ Excellent communication, coordination and organizational skills ✔ Proactive, solution-oriented and able to work in fast-paced environments ✔ Advanced English level 👏 What do we offer? • Stable opportunity within an international pharmaceutical group, • Exposure to global and high-impact clinical projects, • Collaborative and multidisciplinary environment, • Professional growth and development opportunities If you are looking for your next challenge in Clinical Research and want to be part of a company with an entrepreneurial mindset and international reach, we would love to hear from you. 📩 Feel free to apply or share this opportunity with your network.

🚀 Want to shape the future of Clinical Operations? At CROVELIS (Insud Group), we’re looking for a Clinical Operations Digitalization Manager to lead how we transform the way clinical teams work. This is not a traditional role — it’s a build-from-scratch opportunity to rethink processes, tools, data, and collaboration across Clinical Operations. 💡 If you have a strong background in Clinical Operations (CRA, CTM…) and a passion for: • Artificial Intelligence, • Automation & digital tools, • Innovation applied to real workflows …this could be your next challenge. 🔎 What will you do? • Lead the digitalization strategy for Clinical Operations, • Redesign workflows using AI and automation, • Identify opportunities to improve efficiency, quality, and oversight, • Act as a bridge between Clinical, IT/Digital, and Data teams, • Drive adoption of new tools and ways of working, • Build best practices and foster a culture of innovation 🎯 What are we looking for? • +6 years in Clinical Operations, • Strong understanding of clinical trial processes, • Experience as CRA / CTM or similar, • Interest or experience in AI, automation, and digital tools, • Strategic mindset with hands-on execution, • Fluent English 🌍 Why CROVELIS? We are part of Insud Group, a global healthcare organization committed to innovation and scientific excellence. Here, you’ll have the opportunity to create impact, build new capabilities, and transform how teams operate. 💬 If you’re excited about combining Clinical Operations with digital innovation — let’s talk. #ClinicalOperations #DigitalTransformation #AI #Pharma #Innovation #Hiring

Head of Scientific Strategy & Operations | Executive Leadership | Gene Therapy I’m partnered with a recently funded, high-growth biotechnology company building next-generation gene therapies for neurodegenerative disease, now seeking a Director of Scientific Strategy & Operations to join its executive leadership team in Madrid. This is a rare opportunity to step into a highly visible leadership role at a pivotal stage of company growth helping shape the scientific direction, financing strategy, operational build-out, and long-term expansion of an emerging gene therapy platform. The company is entering an ambitious new phase of development and is looking for an exceptional biotech operator who can bridge world-class science with execution, strategy, and investor engagement. Why This Role? You’ll work directly alongside the CEO and leadership team to: • Drive scientific and operational strategy, • Help execute upcoming financing activities and investor engagement, • Shape the future of a cutting-edge gene therapy pipeline, • Build scalable infrastructure and processes, • Evaluate partnership and licensing opportunities, • Play a central role in the growth of a next-generation biotech company The company is especially interested in individuals with: • ~15+ years’ experience within biotech or large pharma, • Strong gene therapy experience (highly preferred), • Exposure to neurology or neurodegenerative disease programs, • Financing, fundraising, or investor-facing experience, • A hands-on, execution-driven mindset, • Relocation support package included

Study Coordinator – Clinical Trials (Fase III | Salud de la Mujer) 📍 Madrid 🗓 Inicio: Julio 2026 ⏳ 18 meses 💰 57.000€ En Insud Pharma, buscamos incorporar un/a Study Coordinator para un ensayo clínico fase III en el área de salud de la mujer. Formarás parte de un proyecto internacional con impacto real en la vida de las mujeres, dentro de un entorno colaborativo y dinámico. ¿Cuál será tu día a día? • Coordinación de visitas de pacientes y gestión del estudio (site management), • Introducción y validación de datos en eCRF, • Gestión documental (ISF, consentimientos informados, etc.), • Interacción con CRAs y equipo investigador, • Cumplimiento de GCP y protocolo 🎯 ¿Qué buscamos? • Experiencia en clinical trials (Study Coordinator o Data Entry), • Conocimiento de ICH-GCP, • Nivel de inglés medio-alto, • Perfil organizado, proactivo y detallista 💼 ¿Qué ofrecemos? • Contrato de 18 meses, • Salario: 57.000€ brutos anuales (por la totalidad del tiempo), • Proyecto internacional fase III, • Excelente ambiente de trabajo, • Desarrollo y aprendizaje continuo 🚀 Si quieres seguir creciendo en investigación clínica, ¡nos encantará conocerte! 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.

🚀 Clinical Services Specialist | Madrid | +5 años experiencia En CROVELIS, compañía perteneciente al grupo Insud Pharma, seguimos creciendo y buscamos incorporar un/a Clinical Services Specialist para unirse al área de Clinical Operations, con un rol clave en la coordinación de proveedores y servicios asociados a ensayos clínicos y estudios de investigación. 🔎 ¿Cuál será tu impacto? Serás una pieza clave para asegurar la ejecución eficiente de los estudios clínicos, garantizando la correcta gestión de proveedores, el cumplimiento regulatorio y la alineación con los objetivos operativos, contractuales y financieros de cada proyecto. 💡 Responsabilidades principales • Coordinar la relación diaria con proveedores vinculados a ensayos clínicos, • Identificar, evaluar y seleccionar service providers según necesidades del estudio, • Liderar procesos de selección, negociación y contratación de proveedores, • Asegurar la correcta ejecución del Vendor Management Plan junto al Project Manager, • Supervisar presupuestos, facturación, cambios de alcance y pass-through costs, • Coordinar la revisión contractual con Legal y Procurement, • Garantizar el cumplimiento de SOPs, requisitos regulatorios y estándares de calidad, • Colaborar con Data Management & Biostatistics en la evaluación de proveedores de datos, • Apoyar la preparación de auditorías, inspecciones y CAPAs junto a Quality Assurance, • Participar en la implementación y evolución de soluciones de Inteligencia Artificial aplicadas a Clinical Development, • Actuar como representante del sponsor en reuniones, eventos y congresos, • Contribuir a la formación y mentoring de nuevos miembros del equipo 🎯 ¿Qué buscamos? • Formación universitaria en área científica o de ciencias de la salud, • +5 años de experiencia en Clinical Operations y/o gestión de proveedores, • Experiencia en ensayos clínicos y entorno CRO/farma, • Conocimiento de herramientas: EDC, RTSM, eTMF, • Experiencia en negociación, presupuestos y gestión de vendors, • Nivel alto de español e inglés (otros idiomas valorables), • Capacidad analítica, organización y gestión de múltiples proyectos, • Mentalidad colaborativa, flexible y orientada a resultados 🚀 Lo que hace especial este rol Es una posición con alto impacto operativo y estratégico, con exposición transversal a múltiples áreas (Clinical, Data, Legal, QA, Procurement) y participación en iniciativas de innovación como la implementación de Inteligencia Artificial en Clinical Trials. 📩 Si buscas un entorno dinámico, innovador y con impacto real en el desarrollo clínico, esta puede ser tu oportunidad. 🤝 En CROVELIS, dentro del grupo Insud Pharma, promovemos la diversidad, la igualdad de oportunidades y la creación de equipos inclusivos donde cada persona pueda desarrollar su máximo potencial.

🚀 We’re Hiring | Medical Science Liaison – Hematology & Nephrology | Spain MADRID An exciting opportunity to join Medical Affairs organization as a Medical Science Liaison supporting Hematology and Nephrology across key territories in Spain. This role will focus on scientific engagement with the medical community through high-quality education, evidence-based scientific exchange, and strategic collaboration with Key Opinion Leaders and Healthcare Professionals. 🔬 Key Responsibilities: • Develop expertise in Hematology & Nephrology therapeutic areas, • Engage and build strong relationships with KOLs and HCPs, • Deliver compliant scientific exchange and medical education, • Gather actionable medical insights supporting strategy and patient outcomes, • Participate in regional, national & international scientific congresses, • Support Investigator-Initiated Studies and cross-functional medical initiatives 👩 ⚕️ What we’re looking for: • Degree in Pharmacy, Science or Medicine (MD, PhD or PharmD preferred), • 2-3 years of MSL experience within pharma/biopharma, • Experience in hematology, nephrology, rare diseases or specialty care is highly valued, • Strong scientific communication and stakeholder engagement skills, • Ideally based in Madrid, covering Madrid, Cataluña and selected northwest territories This is a fantastic opportunity to join an innovative and science-driven environment within specialty care and rare diseases. Interested or know someone who could be a fit? Feel free to reach out directly. Susagna_sastre@oxfordcorp.com #MSL #MedicalAffairs #Hematology #Nephrology #RareDiseases #PharmaJobs #Biotech #CSLVifor #SpainJobs

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 a nutshell 📌 Position: Launch Specialist (Project Manager) Location: Chemo Headquarters, Sanchinarro (Madrid) – On-site Experience: 3-5 years in project management, preferably in the pharmaceutical industry or regulated sectors Want to know more? 👇 Chemo 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) and finished dosage forms (FDFs), adding value to both human and animal health. As part of Insud Pharma, Chemo is integrated into a global organization with more than 10,000 professionals in over 50 countries, 20 industrial plants, 15 specialized R&D centers, 12 commercial offices, and more than 35 pharmaceutical subsidiaries, serving 1,150 clients in more than 110 countries worldwide. At Chemo, we believe in innovation, operational excellence, 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.

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.

¡Nuestro equipo está creciendo! Por eso, desde Théa Pharma Spain, empresa certificada como Great Place To Work, estamos buscando a un/a Visitador/a Médico/a para para cubrir la zona de Madrid, Ávila y Valladolid. En Théa nos especializamos en la investigación, el desarrollo y la comercialización de productos de oftalmología. Como empresa familiar y con valores, nos centramos en el desarrollo a largo plazo. Creemos que, si tenemos personas con talento y apasionadas en la innovación y mejora constante, no hay obstáculo que se interponga en nuestro camino. Hoy en día, somos más de 2000 personas colaboradoras en todo el mundo, fomentando una cultura diversa, orientada a las personas, colaborativa e inclusiva. La posición En Théa tendrás la oportunidad de desarrollar tu carrera y mejorar la salud ocular del mundo. Si quieres dar tu siguiente paso profesional en un entorno innovador, internacional y multicultural, ¡Théa es para ti! Como DELEGADO/A VISITA MÉDICA tu misión en nuestra compañía será representar a Laboratorios Thea ante nuestros clientes, mediante visitas regulares dentro del territorio de ventas asignado. ¿Cuáles van a ser tus funciones y responsabilidades? • Reportando al Gerente de Zona, serás responsable de detectar, gestionar y satisfacer las necesidades de los clientes asignados, alcanzando los objetivos de ventas establecidos por la compañía mediante un enfoque basado en datos., • Analizar de forma continua los datos de ventas, actividad comercial y evolución del mercado de la zona asignada para identificar oportunidades de crecimiento, riesgos y áreas de mejora., • Mantener actualizada la segmentación de clientes del territorio/zona asignada en función de los cambios de mercado, apoyándose en el análisis de datos del CRM, tendencias de prescripción y necesidades de la marca., • Planificar y priorizar la actividad diaria y las rutas de visita en base al análisis de datos de desempeño, potencial del cliente y retorno de la actividad comercial., • Mantener, analizar y reportar la actividad en el CRM, garantizando la calidad y fiabilidad de la información como herramienta clave para el seguimiento de resultados y la toma de decisiones., • Supervisar y analizar la actividad de los KOL en la zona designada y/o en congresos, reuniones nacionales o internacionales, evaluando su impacto y alineación con la estrategia de la compañía., • Elaborar informes y análisis periódicos sobre resultados, tendencias y acciones comerciales, compartiéndolos con el Gerente de Zona y otros stakeholders., • Colaborar con el resto del equipo de ventas y con otros departamentos relacionados con el negocio, aportando insights basados en datos y contribuyendo al desarrollo de un entorno de trabajo colaborativo, alineado con los valores de la compañía. ¿Qué necesitas para tener éxito? • Valorable formación Universitaria preferiblemente en ciencias de la salud, • Valorable Máster o Posgrado en Ventas., • Conocimiento de informática a nivel usuario: Excel, Word, PowerPoint y Outlook y CRM., • Inglés medio-alto, • Persona proactiva, con habilidades de comunicación, con pensamiento analítico, orientada a resultados, tener persuasión e influencia y con gran facilidad para trabajar con las nuevas tecnologías. ¿Cómo te vamos a cuidar? Trabajamos para poder ofrecerte la mejor experiencia: • Seguro de salud, • Contrato indefinido, • Inversión en formación y desarrollo, • Vehículo de empresa, • Ipad, teléfono móvil, etc., • Tarjeta bancaria de empresa, • …y mucho más! Si has leído hasta aquí, ¿qué esperas para aplicar? ¡Queremos saber más de ti! ¿Quieres saber más? ¡Síguenos en LinkedIn para ver nuestras novedades! Fecha límite inscripción: 14/06/2026 Empleador con igualdad de oportunidades Théa se enorgullece de ser un empleador con igualdad de oportunidades y con una cultura global que acepta la diversidad. Nos comprometemos a proporcionar un entorno libre de discriminación y acoso injustos. No discriminamos por motivos de edad, raza, color, sexo, religión, nacionalidad, discapacidad, embarazo, estado civil, orientación sexual, cambio de sexo, o cualquier otra categoría.

Who We Are Whitewater Group is a leading provider of innovative and sustainable water treatment engineering systems operating in Ireland, the UK and across Europe in the Data Centre, Pharma, Power and Industrial sectors. We specialize 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 Naas Co. Kildare and operates from European bases in Spain, Sweden, Finland, and the UK, with plans for further offices in Germany, Denmark, and Italy. The Group is experiencing significant growth driven by its focus on off-site construction methods (OSM) for delivering turnkey projects, reducing on-site construction time to a minimum. Role Description Imagine working on projects where every decision matters. Where your judgment has real impact, and you can contribute far beyond day-to-day tasks. At Whitewater, we’re looking for a procurement professional who enjoys understanding each scope in depth, navigating complex markets, and bringing a strategic perspective to decision-making. You’ll be involved in managing key packages — equipment, materials, or subcontracts — working closely with engineering, construction, and other teams to make sure everything comes together: cost, quality, and schedule. We’re looking for someone who brings strong judgment, negotiation skills, and a continuous improvement mindset; someone who wants to go deeper, develop expertise in specific scopes, and create real value in every project. Here, you’ll find a collaborative environment with great professionals, where you can learn, contribute, and keep growing while maintaining your autonomy. If this way of working resonates with you… we’d love to meet you. What you’ll do You will lead procurement for critical packages in complex industrial projects (water treatment plant, etc), owning the full lifecycle, from sourcing strategy to contract execution and supplier performance. • Define and execute procurement strategies for key equipment, materials, and services, • Lead end-to-end sourcing: RFQs, negotiations, award, and contract management, • Drive cost, quality, delivery, and risk optimization, • Act as the procurement lead within project teams, influencing key decisions, • Manage supplier relationships, performance, and critical negotiations, • Ensure smooth coordination across Engineering, Construction, QA/QC, HSE, Planning, Legal, and Finance Your impact • Secure competitive, reliable supply solutions for strategic projects, • Mitigate risks through strong contracting and proactive supplier management, • Improve project performance through early involvement and smart sourcing decisions, • Mentor and support junior buyers, raising team capability What we’re looking for • 5+ years in industrial/EPC procurement, • Strong negotiation and contract management skills, • Experience with complex equipment and international suppliers, • Ability to work cross-functionally in demanding project environments, • Fluent English Why join us • Competitive salary + full benefits package, • Hybrid working model, • Flexible hours, • High-impact role with real ownership on strategic projects

¿Quieres liderar la entrada de la IA en el corazón de la industria? Sobre Mesai En Mesai hacemos tecnología con un propósito: transformar las plantas de producción. Somos una SaaS de IA Industrial que analiza procesos productivos en tiempo real para optimizar la producción, reducir el scrap y anticipar averías. En resumen: vendemos eficiencia. El Reto: Business Development Representative (BDR) Part-Time Buscamos a un Hunter puro. No queremos a alguien que envíe secuencias automáticas y espere sentado. Buscamos a alguien con la piel curtida, capaz de levantar el teléfono, saltar gatekeepers y hablar el lenguaje de un Director de Planta o de Operaciones. Tu misión no es solo agendar reuniones; es ser el arquitecto de nuestra maquinaria outbound en un sector poco digitalizado pero con un potencial masivo. Tus Responsabilidades • Ejecución Outbound 100%: Tu canal rey será la llamada en frío. Contactarás con perfiles industriales que viven teléfono en mano., • Cualificación Estratégica: Identificarás empresas de fabricación discreta (alimentación, metalurgia, forja, pharma)., • Generación de Oportunidades: Agendarás reuniones de alta calidad para el CEO, asegurando que el fit sea real., • Documentación de Aprendizaje: No solo llamarás; documentarás qué discursos funcionan mejor para ayudar a escalar el proceso., • Gestión de Pipeline: Uso diario de HubSpot para traquear actividad y asegurar que ningún lead se enfríe. Perfil Ideal Imprescindibles: • Mentalidad Hunter: Disfrutas del reto de la puerta fría y la persistencia telefónica., • Comunicación Directa: Capacidad para hablar "lenguaje de planta" (ahorro, paradas, eficiencia) y no solo "lenguaje SaaS"., • Autonomía Proactiva: Preferimos a alguien que pida perdón antes que permiso., • Resiliencia: Capacidad para recibir "noes" y seguir con la misma energía en la llamada número 35 del día., • Pasión por la IA: Ser un crack explicando el dolor que solucionamos., • Ubicación: Residencia en Madrid para trabajar físicamente con el equipo de Hanbai. Valorable: • Experiencia previa vendiendo a sector industrial o entornos técnicos., • Haber trabajado con herramientas como LinkedIn Sales Navigator. Qué Ofrecemos • Salario: Fijo + Variable (Contrato Part-Time)., • Horario: Mañanas (máxima productividad en el sector industrial)., • Crecimiento: Oportunidad real de pasar a Full-Time en función de los resultados., • Formación: Recibirás entrenamiento específico de alto nivel impartido por Hanbai. ¿Tienes el hambre necesaria para abrir mercado donde otros no se atreven? Inscríbete

I’m currently supporting an exciting international biotech/pharmaceutical company with the search for an Administrative Assistant to join their team based in Madrid. This is a fantastic opportunity for someone early in their career looking to gain further exposure within a global life sciences environment, supporting both Medical Affairs and Commercial teams. 🔹 Location: Madrid (Paseo de la Castellana) 🔹 Hours: Full-time (40 hours/week) The role will involve: ✔ Calendar and meeting coordination ✔ Travel and expense management ✔ Supporting MSL and Sales teams ✔ Office coordination and administration ✔ Presentation/document preparation ✔ Liaising with HR, IT and Finance teams ✔ CRM and reporting support What they’re looking for: • Around 1–3 years of administrative/coordinator experience, • Experience within pharma, biotech, healthcare or life sciences would be highly beneficial, • Fluent Spanish and English, • Strong organisational and communication skills, • Confident using Microsoft Office (especially PowerPoint, Excel and Word), • Immediately available candidates highly preferred Additional experience with SAP, CRM systems, customer service/order management or HCP contract coordination would be a plus. This is a brilliant opportunity for someone looking to build their career within a fast-paced and highly collaborative pharmaceutical environment. ABOUT PLANET PHARMA Planet Pharma is an American parented Employment Business/Agency that provides global staffing services with its head-quarters in Chicago and our EMEA regional office located in Central London. We have invested significantly in creating a robust international platform that enables us to work compliantly in 30+ countries with a current network of 2500+ active contractors globally as well as a very strong permanent / direct hire recruitment offering. Our specialist knowledge and close relationships with our clients and the wider industry really makes us unique in our field. Just recently we were recognised by FORBES as the 17th best professional staffing firm, and have won multiple awards from industry accredited bodies for our commitment to excellence and service delivery. We have extensive functional expertise including: Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs / Writing. We are an equal opportunities Recruitment Business and Agency. We welcome applications from all suitably qualified candidates regardless of their race, sex, disability, religion/belief, sexual orientation or age. www.planet-pharma.com TO APPLY Please click ‘apply’ or contact Hamish Hopkins (Recruitment Consultant III) at Planet Pharma for more information: E: hhopkins@planet-pharma.co.uk T: : +44 20 3953 1459

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. Buscamos incorporar un/a Corporate Communications Manager para contribuir al desarrollo y ejecución de la estrategia de comunicación corporativa de la compañía. La posición tiene como objetivo reforzar el posicionamiento y la reputación corporativa de LETI Pharma, aportar estructura y criterio a la función de comunicación y dar soporte a proyectos corporativos prioritarios en un entorno transversal y de alta exigencia, incluyendo iniciativas vinculadas a ESG / sostenibilidad. Se trata de una posición senior con alto nivel de interacción con Presidencia y con las distintas áreas del negocio. Responsabilidades principales Comunicación corporativa y reputación • Elaborar y desarrollar planes de comunicación corporativa., • Revisar, alinear y mejorar los mensajes corporativos de la compañía., • Redactar y preparar materiales de comunicación corporativa., • Revisar notas de prensa, presentaciones y contenidos elaborados por distintas áreas., • Realizar seguimiento y priorización de temas abiertos del área., • Identificar riesgos reputacionales y proponer ajustes en narrativa y enfoque., • Asegurar la coherencia del posicionamiento corporativo en todos los canales. Relación con medios y visibilidad • Mantener y reforzar la relación con medios de comunicación estratégicos., • Identificar oportunidades informativas y de posicionamiento reputacional., • Detectar temas con potencial noticioso y proponer enfoques relevantes para medios., • Gestionar peticiones de medios y coordinar entrevistas y encuentros., • Organizar acciones de relación con medios., • Analizar la cobertura obtenida y el impacto de las acciones., • Impulsar la visibilidad de la compañía en medios sectoriales, farmacéuticos, generalistas, lifestyle y económicos. Contenidos y soporte editorial • Elaborar borradores y propuestas de contenido corporativo., • Revisar mensajes, textos y documentos preparados por otras áreas., • Dar soporte en la preparación de presentaciones corporativas, argumentarios y materiales clave. ESG / Sostenibilidad • Dar apoyo a la coordinación de la implantación de la estrategia ESG., • Realizar seguimiento de iniciativas y proyectos de sostenibilidad, asegurando orden y trazabilidad., • Colaborar con las áreas implicadas para recopilar información y alinear enfoques., • Identificar oportunidades de posicionamiento reputacional vinculadas a ESG, con un enfoque riguroso y alineado con la realidad del negocio. Trabajo transversal y organización • Colaborar con las unidades de negocio para alinear mensajes y prioridades., • Trabajar de forma coordinada con Presidencia y el resto de áreas., • Actuar como punto de apoyo y coordinación en proyectos transversales., • Aportar estructura, orden y método a la actividad del área., • Calendarizar acciones, hitos y entregables., • Coordinar la relación con agencias y colaboradores externos., • Documentar y mantener actualizada la documentación del área. Requisitos • Titulación universitaria en Periodismo, Comunicación, Publicidad y Relaciones Públicas o similar., • Más de 10 años de experiencia en comunicación corporativa, reputación y relaciones con medios., • Experiencia en sectores regulados (muy valorable)., • Experiencia sólida en relación directa con medios y agenda de contactos relevante., • Español nativo., • Inglés nivel C1. 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.

En pocas palabras 📌 • Posición: Demand Planner, • Localización: Madrid, • Experiencia: 1-3 años de experiencia ¿Quieres saber más? 👇 Exeltis es la división de marca de Insud Pharma, una compañía global con amplia experiencia en toda la cadena de valor farmacéutica, desde la investigación y el desarrollo hasta la fabricación, comercialización y distribución de productos con valor añadido para la salud humana y animal. La actividad de Insud Pharma se organiza en tres áreas de negocio sinérgicas: Industrial (Chemo), Branded (Exeltis) y Biotech (mAbxience), con más de 9.000 profesionales en más de 50 países, 20 instalaciones de última generación, 15 centros especializados de I+D, 12 oficinas comerciales y más de 35 filiales farmacéuticas, que atienden a 1.150 clientes en 96 países de todo el mundo. En Insud Pharma creemos en la innovación y el desarrollo sostenible. ¿Preparado/a para ser un #Challenger? 💪 ¿Qué buscamos? 🔎 Buscamos un/a Demand Planner para Exeltis que asegure una previsión de demanda precisa y alineada globalmente, integrando información de mercados, ventas, marketing y operaciones. Su misión será optimizar inventarios, mejorar el nivel de servicio y garantizar que la producción y el suministro respondan de forma eficiente a las necesidades de cada región, contribuyendo de forma directa a la toma de decisiones en un entorno internacional y dinámico. ¡El reto! 🚀 • Elaborar el forecast global, consolidando previsiones de todas las regiones y filiales mediante modelos estadísticos, análisis histórico y datos de mercado., • Participar activamente en el proceso de S&OP / IBP, presentando análisis, riesgos y oportunidades., • Analizar desviaciones entre forecast y demanda real, identificando causas y proponiendo acciones de mejora., • Colaborar estrechamente con Supply Planning para asegurar la disponibilidad de producto, la capacidad de producción y los planes de suministro., • Gestionar y mantener los datos maestros de planificación en los sistemas, incluyendo lead times, MOQ, ciclos de vida, clasificaciones ABC y otros parámetros clave para una correcta planificación., • Asegurar una adecuada gestión de datos en sistemas, velando por la calidad, consistencia y actualización de la información utilizada en los procesos de demanda y planificación., • Coordinar la planificación del ciclo de vida del producto, incluyendo lanzamientos, discontinuaciones, transiciones y gestión de obsolescencias., • Impulsar la optimización de inventarios globales, equilibrando niveles de stock, reduciendo excesos y evitando roturas., • Integrar variables de mercado como tendencias, estacionalidad, campañas comerciales y factores externos que impacten la demanda., • Coordinarse con equipos globales de ventas, marketing, finanzas, supply chain y operaciones regionales., • Utilizar herramientas avanzadas de forecasting, ERP y analítica para mejorar la precisión de la previsión y la calidad de la planificación. ¿Qué necesitas? 🤓 • Formación en Ingeniería, Economía, Estadística, Supply Chain, Business Analytics o similar., • Entre 1 y 3 años de experiencia en Demand Planning, Supply Chain, Forecasting o S&OP., • Experiencia preferiblemente en entornos globales; también se valorarán perfiles con experiencia local dentro del sector farmacéutico., • Conocimiento de ERP SAP., • Experiencia en gestión de datos en sistemas y mantenimiento de parámetros maestros de planificación., • Manejo de herramientas de forecasting como APO, Anaplan o equivalentes., • Valorable conocimiento de SAP IBP., • Nivel avanzado de Excel., • Nivel alto de inglés para la comunicación con equipos internacionales., • Capacidad para interpretar grandes volúmenes de datos y convertirlos en insights accionables., • Habilidades de comunicación e influencia para interactuar con stakeholders globales., • Pensamiento estratégico y orientación a resultados., • Capacidad para trabajar en entornos multiculturales y con múltiples zonas horarias., • Rigor analítico, atención al detalle y adaptabilidad ante cambios de mercado y prioridades., • Valorable experiencia en sectores con alta complejidad regulatoria o de portafolio. ¡Nuestros beneficios! 👏 • 📜 Contrato indefinido, • 📍 Madrid, • 🚀 Impacto real en decisiones estratégicas, • 🤝 Alta exposición a negocio y dirección, • 📈 Oportunidad de crecimiento en un entorno dinámico ¿Cómo será el proceso de Selección? 🕵️ • Contacto inicial por teléfono o correo electrónico., • Entrevistas con el equipo de selección y/o hiring manager., • Comunicación constante sobre el estado del proceso. 🔷¿Crees que esta oferta no es para ti? 🔷 Síguenos en LinkedIn e Instagram para conocer nuevas oportunidades y mantenerte al día de nuestras vacantes. #InsudPharma #Challenger #Insuder #InsudTalent COMPROMISO CON LA IGUALDAD DE OPORTUNIDADES En Exeltis apostamos por la igualdad de oportunidades y por un entorno de trabajo diverso e inclusivo. Todas las candidaturas serán valoradas sin distinción de género, identidad o expresión de género, edad, etnia, nacionalidad, religión, orientación sexual, discapacidad o cualquier otra condición personal, física o social.

In few words 📌 Position: Quality Assurance Technician Location: Madrid Experience: At least 2 years’ experience in quality assurance or quality systems in distribution center/affiliates and/or manufacturing sites. Specific Knowledge: Experience in cGDPs, cGMPs, Quality for Marketing Affiliate. Quality Assurance and Quality control and/or manufacturing processes. SAP. 👇Global Responsibility Assure compliance of GxP, regulatory and internal standards according to quality policies and applicable requirements within Insud Pharma Group. Management of quality activities in products commercialized in different countries under Exeltis MAs. (Complaints, Deviations, PQRs, Recalls, Quality Agreements, etc). Support to the MAH to compile to the applicable local legislation where the products are marketed. Specific Responsibilities • Reporting to Exeltis Manufacturing Quality Manager., • Ensuring that appropriate Quality systems are established, implemented, and maintained in each market, and appropriate oversight is in place to ensure that local regulatory requirements can be supported in a simple, compliance and continuous improvement manner., • Providing support to MAH in the resolution of serious quality issues and quality management documentation., • Suppliers management: Manage technical quality agreements between Third Partiers and the MAH, establish a good quality management oversight in routine operations, identify risks and propose risk mitigation. Be the key contact between MAH and the different sites involved in the supply chain of the product (Manufacturers, transport companies, distributors. etc)., • Develop and monitor Quality metrics related to third party organization., • Stay current with the applicable regulations and promote Quality across the sites., • Support MAH in the implementation of Quality digitalization strategy. 🕵️Requirements and personal skill • Education: University Degree in Pharmacy or Medium Diploma in Pharmacy or equivalent. Pharmaceutical Industry Master will be a plus., • Languages: Fluent in English and Spanish., • Experience (years/area): At least 2 years’ experience in quality assurance or quality systems in distribution center/affiliates and/or manufacturing sites., • Specific Knowledge: Experience in cGDPs, cGMPs, Quality for Marketing Affiliate. Quality Assurance and Quality control and/or manufacturing processes. Office system., • Travels: Willing to travel occasionally., • Personal skills: Good communication skills, proactivity, energy, good working under pressure, problems-solving, good organizational skills and persistent. 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.

JOB SUMMARY: We are looking for an experienced and highly motivated Account Manager to join our team in the HealthCare sector in Iberia. The successful candidate will be responsible for supporting our team of Account Managers in the Iberia Plastics Market (Pharma, veterinary and OTC) This position requires a strong ability to manage the assigned sales budget, as well as solid customer management skills, ensuring that the company maintains its commitment to quality without losing competitiveness. ACCOUNTABILITIES: • Identify and attract new potential clients within their assigned area or sector., • Maintain and strengthen relationships with existing clients, ensuring loyalty and satisfaction., • Explain the features, benefits, and competitive advantages of the company’s commercial offering., • Prepare commercial proposals, negotiate terms, and close deals., • Ensure the client receives the product or service correctly and resolve any issues that may arise., • Gather information on trends, customer needs, and competitor activity., • Meet sales, margin, and growth objectives set by the company., • Ensure that all terms of the contract are clearly defined and protect the interests of the company., • Collaborate with other departments to align sales strategies with company objectives., • Monitor segment specific trends and competitor developments, producing strategic reports and recommendations for leadership., • Represent the company at key industry events, trade fairs, and strategic customer meetings to strengthen visibility and influence., • Serve as the senior point of escalation for key clients, ensuring operational excellence, service continuity, and rapid issue resolution., • Environmental responsibility. SKILLS AND EXPERIENCE – REQUIRED FOR THE ROLE: • Demonstrated experience (3-5 Years) in Sales, ideally in pharmaceutical packaging (such as vials and their stoppers), showcasing a solid understanding of sales processes., • Familiarity with packaging materials, packaging suppliers, and packaging processes. This includes understanding packaging trends, regulations, and best practices., • Strong investigative skills, with the ability to research new customers, trends, and market conditions., • Proficiency with basic computer programs such as Microsoft Office (Excel, Word, etc.) for tracking data, preparing reports, and communicating with teams and experience with Navision ERP & Salesforce., • High level of accuracy and attention to detail., • Enthusiastic, motivated, and proactive attitude, with the drive to continually improve sales processes and contribute positively to the team., • A background in Chemistry, Health Sciences or related fields is a must., • Language skills: English, Italian/French is a must.

Contrato temporal para cubrir una baja por maternidad, con posibilidad de continuidad posterior mediante otro contrato por sustitución. 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: Desde Algenex, empresa especializada en el desarrollo y la fabricación de proteínas recombinantes para la formulación de medicamentos biológicos, buscamos un/a analista de desarrollo de procesos para nuestra planta en Tres Cantos, Madrid. Responsabilidades generales: El/La analista de desarrollo de procesos será responsable de: • Realizar los experimentos que desarrollen Técnicos especialistas o Científicos del área basados en la purificación de proteínas. Puesta a punto Upstream y Downstream, • Apoyo en la gestión de reactivos, estándares y muestras., • Las técnicas necesarias para los experimentos incluyen, entre otras, uso de equipos de purificación (sistemas FPLC), conocimientos básicos de cromatografía (afinidad, intercambio iónico, hidrofobicidad…), técnicas analíticas como ELISA, Western blot, electroforesis en gel de poliacrilamida con dodecilsulfato de sodio (SDS-PAGE), Bradford y BCA. Responsabilidades específicas: • Realiza de forma individual las tareas de desarrollo asignadas para apoyar el desarrollo del producto, el registro, la liberación de lotes y las actividades previas y posteriores a la presentación de documentación regulatoria., • Realiza las actividades dentro de los plazos establecidos y en cumplimiento con las cGXP, los requisitos regulatorios y las prácticas y procedimientos de la empresa., • Documenta las actividades y los resultados analíticos de forma precisa, oportuna y correcta desde el primer intento., • Se comunica eficazmente con sus compañeros, supervisor y gerencia sobre el estado de las actividades asignadas Requisitos y aptitudes personales: • Formación académica: Ciclo Formativo de grado superior en laboratorio Clínico y Biomédico o en otras diciplinas relacionadas con las ciencias de la vida, graduado en ciencias de la vida., • Experiencia (años/área): Mínimo de 2 años de experiencia relevante en la industria biofarmacéutica/biotecnológica en las áreas de desarrollo analítico, validación analítica o control de calidad., • Conocimientos específicos: Conocimientos de productos biotecnológicos y experiencia en la industria de productos biológicos. Experiencia con péptidos y proteínas., • Experiencia práctica en métodos de purificación de proteínas y técnicas analíticas como ELISA, SDS-PAGE, Western blot y otras técnicas relacionadas con la caracterización de proteínas. ¡Nuestros beneficios! ⏰ Horario de entrada flexible de lunes a viernes (jornada completa). 🥼 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.

Desde la división de Química&Pharma nos encontramos en la búsqueda de un Project Engineer para una empresa del sector industrial con sede en Madrid. ¿Qué harás? • Coordinar iniciativas de inversión, mejoras técnicas y creación o adaptación de instalaciones y equipos dentro del entorno industrial., • Asegurar que las instalaciones, documentación y procesos estén actualizados y alineados con los estándares legales y de calidad del sector., • Dar soporte a las áreas de producción y calidad, solucionando incidencias y promoviendo mejoras en rendimiento, mantenimiento y eficiencia energética., • Se requiere experiencia consolidada en proyectos industriales, preferiblemente farmacéuticos, junto con habilidades de liderazgo, organización, autonomía y trabajo en entornos exigentes. ¿Qué buscamos? • Grado en Ingeniería (Industrial, mecánica, química) ¿Qué ofrecemos? • Contrato indefinido con cliente final., • Salario competitivo, • Retribución flexible.

Descripción del puesto: Buscamos incorporar un/a Director/a Comercial y Técnico/a con sólida experiencia en industrialización, comercialización y despliegue de tecnologías en el mercado. La persona seleccionada liderará el desarrollo estratégico y la ejecución comercial en sectores clave como diagnóstico in vitro, aguas y ámbito clínico. Funciones principales: • Definir y ejecutar la estrategia comercial de la compañía en los mercados objetivo., • Diseñar planes de acción orientados a la captación de nuevos clientes y expansión de negocio., • Identificar oportunidades de mercado y desarrollar propuestas de valor adaptadas a cada segmento., • Liderar negociaciones y cerrar acuerdos para la venta de productos y soluciones tecnológicas., • Coordinar el despliegue técnico y comercial de las soluciones en clientes., • Colaborar con equipos multidisciplinares (I+D, operaciones, marketing) para asegurar la correcta industrialización de productos., • Establecer objetivos comerciales y realizar seguimiento de indicadores de rendimiento. Requisitos: • Experiencia demostrable en puestos similares de dirección comercial y/o técnica., • Conocimiento en industrialización y comercialización de tecnologías., • Experiencia en alguno o varios de los siguientes sectores: diagnóstico in vitro, tratamiento de aguas, sector clínico., • Capacidad para desarrollar estrategias comerciales y planes de ejecución efectivos., • Habilidades de negociación y orientación a resultados., • Perfil analítico, con visión estratégica y capacidad de liderazgo., • Disponibilidad para viajar. Se valorará: • Red de contactos en los sectores mencionados., • Experiencia en entornos internacionales., • Formación técnica o científica (biotecnología, química, ingeniería o similar). Ofrecemos: • Proyecto estratégico con alto impacto en la organización., • Autonomía y capacidad de liderazgo en la toma de decisiones., • Desarrollo profesional en un entorno innovador., • Paquete retributivo competitivo acorde a la experiencia aportada. Si estás interesado/a en liderar el crecimiento comercial y tecnológico en sectores de alto valor, envíanos tu candidatura.

Senior Data Engineer In a few words • Position: Senior Data Engineer – AI Labs at Insud Pharma, • Location: Madrid (hybrid), • Experience: 5+ years in Data Engineering or Analytics Engineering roles About AI Labs at Insud Pharma 👇 AI Labs is Insud Pharma’s transversal team for Artificial Intelligence, Data Science, and Machine Learning, working across the group to deliver production‑ready data and AI solutions with real impact. The team operates across a wide range of areas, including R&D and clinical data, global health and epidemiology, manufacturing and quality, supply chain and operations, and business analytics, partnering closely with business units, and external organizations. AI Labs combines strong engineering standards with pragmatic execution, focusing on building scalable AI‑enabled solutions that move from experimentation to real‑world adoption. Role Context This role will be primarily focused on projects linked to Fundación Mundo Sano, an international organization dedicated to improving health and quality of life for vulnerable communities through research, innovation, and international cooperation (e.g. neglected diseases such as Chagas). The goal of this position is to ensure that data coming from multiple sources becomes available, consistent, reliable, and reusable, enabling dashboards, reporting, and AI/ML use cases. Due to the international nature of the projects, the role may involve occasional travel to Latin America, Africa, or other regions to work closely with local teams and better understand data generation on the ground. Role Objective Build and operate a coherent, well‑structured data foundation for Fundación Mundo Sano projects by owning the data engineering layer end‑to‑end: ingestion, modeling, data quality, availability, monitoring, and data delivery for dashboards and AI enablement. Key Responsibilities • Build and operate data ingestion pipelines (ETL/ELT) from multiple sources (field programs, research datasets, epidemiological surveillance systems, partners, files, APIs)., • Design and maintain data models and curated datasets that standardize entities, metrics, and definitions across projects., • Ensure data quality, reliability, and consistency through automated checks, monitoring, and basic observability., • Decide how data is structured, stored, and versioned to enable long‑term reuse and scalability., • Make data available and easy to consume for dashboards, reporting, and AI/ML use cases., • Proactively guide business and project teams on data best practices, setting standards, shaping requirements, and influencing how data should be collected, structured, and used., • Collaborate closely with stakeholders to translate needs into scalable, maintainable data foundations. Technologies (examples – adapt to actual stack) • Languages: SQL, Python, • Pipelines / orchestration: Airflow, Prefect, Dagster or similar, • Transformations: dbt or equivalent, • Storage: Data warehouse / lakehouse (e.g. Snowflake, BigQuery, Databricks, Synapse), • Data quality / monitoring: Great Expectations, Soda, or similar, • BI / Dashboards: Power BI, Tableau, Looker or similar, • Engineering basics: Git, CI/CD, basic cloud concepts (AWS / Azure / GCP) What we are looking for • A senior, hands‑on Data Engineer with a strong ownership mindset, comfortable building and operating core data structures and pipelines., • 5+ years of experience in Data Engineering or Analytics Engineering roles., • Strong SQL and solid Python, with hands‑on experience building and running ETL/ELT pipelines in production., • Proven experience integrating heterogeneous and diverse data sources (multiple systems, files, APIs, changing schemas, inconsistent identifiers)., • Good understanding of data modeling and analytical data structures, with the ability to standardize entities, metrics, and definitions across projects., • Experience ensuring data quality, reliability, and monitoring, including automated checks and basic observability., • Comfortable making data available for dashboards, reporting, and AI/ML use cases through curated, analytics‑ready datasets., • Able to work proactively with business and project teams, shaping requirements and setting data standards rather than waiting for fully specified inputs., • Spanish as the daily working language; English required for specific projects and international collaboration., • Pragmatic, ownership‑driven mindset, strong communication skills, and motivation to work on social and public‑health impact projects. 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! 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.

🔔 We’re hiring! | Regulatory Affairs Specialist (Dutch speaking) 📍 Remote or Madrid (Hybrid options available) We are currently looking for a Dutch speaking Regulatory Affairs Specialist to join our international team and support regulatory activities for our of our clients with a strong focus on Belgium and the Netherlands. This is a great opportunity to work in a highly collaborative, European environment with strong cross‑functional exposure. 🎯 Key Responsibilities Dutch-specific responsibilities (Belgium & The Netherlands): • Review and approval of promotional materials in Dutch, ensuring compliance with local regulatory requirements, • Monitoring, interpretation, and implementation of new and evolving regulatory regulations, • Regulatory support to multiple departments including General Management, Market Access, Marketing, and Quality General regulatory support (English): • Support with EUDAMED-related activities, • Assistance with Authorised Representative responsibilities, • Collaboration with cross-functional teams across different European countries, • Administrative regulatory support to the Netherlands Manager and European Manager, including:, • Updating regulatory databases, • Managing product registration and notification processes with competent authorities 👤 Profile • Fluent in Dutch and English (mandatory), • Previous experience in Regulatory Affairs, ideally in medical devices, pharma, or life sciencesJunior or post‑trainee profiles are welcome, given the Dutch language requirement, • Good understanding of European regulatory frameworks (EUDAMED knowledge is a plus), • Highly detail-oriented, well organised, and comfortable working in a multi-country, matrix environment, • Strong communication skills and ability to interact with diverse stakeholders 🌍 Why join us? • International exposure across several European markets, • Work in a dynamic and evolving regulatory environment, • Strong cross-functional collaboration, • Key role supporting regulatory compliance and business continuity 💼 What we offer • 💰 Gross annual salary (SBA): €30,000, • 🍽️ Restaurant ticket, • 🏥 Private medical insurance, • 🌐 Language classes, • 🏡 Hybrid or fully remote work model

Join Amaris Consulting and work on strategic business transformation initiatives within regulated environments. You will collaborate closely with business and digital stakeholders to design scalable, market-ready processes that support global product launches and customer experience excellence. 🎯 Your Mission & Impact As a Business Consultant – Business Analysis & Market Rollout, you will act as a trusted advisor coming from the business side, supporting marketing, customer experience, and content teams in defining and optimizing end-to-end processes. Your mission is to translate business needs into clear, scalable process models and rollout strategies that enable successful product launches across multiple markets, while ensuring compliance and operational efficiency. ✅ What We’re Looking For • 7+ years of experience as a Business Consultant or Business Analyst working closely with business and marketing teams., • Strong understanding of Marketing, Customer Experience, and business operations., • Proven experience defining end-to-end business processes, especially content-related processes., • Hands-on experience with market rollouts: defining how products are launched across different markets, phases, and maturity levels (must-have)., • Experience identifying and framing business-driven automation opportunities., • Background in healthcare, pharma, or other regulated industries., • Excellent soft skills: stakeholder management, facilitation, communication, and influence., • Ability to translate business needs into structured processes, requirements, and rollout plans., • Experience working with global and local stakeholders., • Advanced English (written and spoken). 🛠 What You’ll Do Business & Process Consulting • Work closely with business, marketing, and customer experience teams to understand needs and priorities., • Lead workshops to document as-is processes, pain points, and inefficiencies across content and customer-facing activities., • Design to-be end-to-end processes aligned with business strategy, regulatory constraints, and digital capabilities. Market Rollout & Product Launch Strategy • Define market rollout approaches for product launches across multiple markets., • Identify where to launch first based on market maturity, readiness, volume, and regulatory complexity., • Design phased rollout strategies, pilots, and scaling approaches., • Ensure alignment between global process standards and local market realities. Automation & Optimization • Identify steps within business and content processes suitable for automation versus those requiring human or regulatory oversight., • Support the definition of automation roadmaps with clear business value and prioritization., • Act as the business interface with digital and IT teams to ensure solutions truly serve business needs. Stakeholder Engagement • Act as a bridge between business and digital stakeholders., • Facilitate alignment, decision-making, and prioritization discussions., • Provide structured recommendations and trade-off analyses to support leadership decisions. 🚀 Why Join Us? • Career Growth: 70% of our senior leaders started in entry-level positions., • Continuous Learning: Technology Academy, Udemy, certifications, and training budget., • Flexibility & Well-being: Remote options, flexible policies, and the WeCare program., • Meaningful Impact: Work on high-visibility business initiatives in global, regulated environments

En BIGZON seleccionamos SAP MDG PMO / Master Data Governance para incorporarse a una importante compañía multinacional del sector Pharma, con fuerte crecimiento internacional y un ecosistema SAP complejo. Buscamos un perfil senior con experiencia en proyectos SAP relacionados con Master Data Governance y gobierno del dato. FUNCIONES: • Coordinación de iniciativas relacionadas con SAP MDG., • Gestión y seguimiento de proyectos de gobierno del dato maestro., • Interlocución con negocio, áreas funcionales y equipos técnicos., • Coordinación de procesos relacionados con datos maestros y calidad del dato., • Participación en proyectos SAP internacionales y evolutivos. REQUISITOS: • Experiencia en SAP MDG / Master Data Governance., • Experiencia en proyectos SAP complejos., • Conocimiento de procesos de gobierno y calidad del dato., • Experiencia en coordinación y gestión de proyectos., • Nivel alto de inglés., • Perfil autónomo y acostumbrado a entornos exigentes. MODELO DE TRABAJO HIBRIDO, 2-3 días presenciales por semana. Oficinas situadas en la zona de Sanchinarro. SALARIO: En función de experiencia, hasta 95.000€ b/a. En esta GRAN ZONA de trabajo que es BIGZON valoramos la diversidad y la inclusión. Estamos comprometidos a crear un entorno de trabajo en el que todas las personas se sientan valoradas y respetadas. Buscamos a quien comparta estos valores y tenga ganas de trabajar en un ambiente sano, colaborativo y orientado a objetivos. ¡Te esperamos!

Product Manager – Consumer Health Innovation (Marketing) About the Company 🌍 At Exeltis, part of _, we are a global healthcare company present in more than 50 countries, committed to improving people’s lives through innovation, science, and consumer-focused healthcare solutions. We are currently looking for a Product Manager Innovation to join our marketing team and drive the growth and innovation of our consumer health portfolio. Your Mission 🚀 You will be responsible for driving the marketing strategy, innovation pipeline, and growth of Consumer Health products, ensuring strong market positioning, consumer relevance, and commercial success. This role combines brand management, innovation thinking, and go-to-market execution, with a strong focus on understanding consumers, identifying market opportunities, and translating insights into impactful products and campaigns. Key Responsibilities 🔎 • Lead the marketing strategy and innovation roadmap for assigned Consumer Health categories., • Identify consumer insights, market trends, and whitespace opportunities for innovation., • Develop and execute product positioning, value proposition, and brand strategy., • Drive end-to-end product launches in collaboration with cross-functional teams., • Define go-to-market strategies across pharmacy and retail channels., • Work closely with Sales, Trade Marketing, Medical, and Regulatory teams to ensure successful execution., • Manage product lifecycle, ensuring growth, differentiation, and portfolio optimization., • Support development of campaigns, packaging, and communication aligned with consumer needs., • Analyze market performance, KPIs, and competitive landscape to identify growth opportunities., • Collaborate with external agencies and partners to support innovation and activation initiatives. What We Are Looking For 🤓 • Degree in Marketing, Business Administration, Economics, or related fields., • 4–7 years of experience in Product Marketing, Brand Management, or Category Management, ideally within Consumer Health, OTC, or Pharma., • Strong understanding of pharmacy/consumer healthcare retail environment., • Experience in product launches, brand strategy, or innovation projects., • Strong commercial and consumer mindset., • Ability to translate insights into actionable marketing strategies., • Strong project management and cross-functional collaboration skills., • Fluent English required. Key Competencies 💡 • Consumer & customer centricity, • Marketing & brand strategy, • Innovation mindset, • Analytical thinking, • Execution excellence, • Stakeholder management, • Creativity & storytelling, • Business orientation Why Join Us? 💙 This is an opportunity to shape the future of Consumer Health brands within a global healthcare company. At Exeltis, we believe in innovation, agility, and talent as drivers of growth and transformation. Ready to become a #Challenger? 🚀

In few words 📌 Position: Quality Assurance Coordinator Location: Madrid Experience: A minimum of 2-3 years’ experience in similar positions. Essential minimum 2 years’ experience in quality assurance or quality systems in production plants, distribution center and/or affiliates. Experience in cGMPs, cGDPs, Quality for Marketing Affiliate. Quality Assurance and Quality control and/or manufacturing processes. Office system. ISO 13485 for medical devices. 👇Global Responsibility Assure compliance of GxP, regulatory and internal standards according to quality policies and applicable requirements within affiliates/subsidiaries. Management of quality documentation (procedures, reports, etc.). Management of quality technical agreements and their fulfilment. Support to affiliates/subsidiaries Specific Responsibilities • Ensuring that appropriate Quality systems are established, implemented, and maintained in each market in scope, and appropriate oversight is in place to ensure that local regulatory requirements can be supported in a simple, compliance and continuous improvement manner., • Providing support to Quality teams across marketing affiliates/subsidiaries per region in the resolution of serious quality issues and quality management documentation., • Support Quality training program for Exeltis affiliates/subsidiaries., • Third Party quality management oversight: Manage technical quality agreements between Third Partiers and Exeltis, establish a good quality management oversight in routine operations, identify risks and propose risk mitigation., • Develop and monitor Quality metrics related to third party organization and marketing affiliates., • Collect, prioritize, drive and monitor execution of strategic Quality initiatives in affiliates and subsidiaries., • Stay current with the applicable regulations and promote Quality across the organization., • Support Affiliates/Subsidiaries in the implementation of Quality digitalization strategy 🕵️Requirements and personal skills • Education: University Degree in Pharmacy or Medium Diploma in Pharmacy or equivalent. Pharmaceutical Industry Master will be a plus., • Languages: Fluent in English, Spanish will be a plus., • Experience (years/area): A minimum of 2-3 years’ experience in similar positions. Essential minimum 2 years’ experience in quality assurance or quality systems in production plants, distribution center and/or affiliates, • Specific Knowledge: Experience in cGMPs, cGDPs, Quality for Marketing Affiliate. Quality Assurance and Quality control and/or manufacturing processes. Office system. ISO 13485 for medical devices., • Travels: Willing to travel occasionally., • Personal skills: Good communication skills, proactivity, energy, good working under pressure, problems-solving, good organizational skills and persistent. 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 S&You estamos buscando un/a Business Intelligence Manager para incorporarse a una importante compañía internacional del sector biotecnológico y biosimilares ubicada en Madrid. Si tienes experiencia en análisis estratégico de negocio dentro del entorno pharma/biotech y te motiva participar en proyectos globales de alto impacto, esta puede ser una gran oportunidad para ti. 🔍 ¿Cuál será tu misión? Serás responsable de transformar datos en insights estratégicos que permitan impulsar la toma de decisiones comerciales y de negocio a nivel global. Trabajarás de forma transversal con diferentes áreas analizando mercado, competencia, pricing, forecasts y nuevas oportunidades dentro del sector biosimilar y biológico. 💡 Funciones principales ✔️ Análisis del mercado de biosimilares y biológicos: tendencias, competidores y evolución de precios. ✔️ Elaboración de forecasts globales, regionales y locales. ✔️ Desarrollo de business cases, PnL y presentaciones ejecutivas. ✔️ Gestión y optimización de bases de datos y herramientas BI. ✔️ Seguimiento de KPIs comerciales y pipelines estratégicos. ✔️ Automatización y mejora de procesos BI mediante herramientas IA. ✔️ Participación en budget reviews y reporting para dirección. 🎯 ¿Qué buscamos? 🔹 Formación universitaria científica, económica o similar. 🔹 Experiencia mínima de 5 años en posiciones de data analytics dentro de biotech, pharma o MedTech. 🔹 Conocimiento del mercado farmacéutico y biosimilares. 🔹 Experiencia en forecasting y modelización financiera. 🔹 Nivel alto de inglés. 🔹 Dominio de Power BI, Tableau, SQL y Excel avanzado. 🔹 Valorable experiencia en Python, IA y CRM. 🌟 Competencias clave ✔️ Visión analítica y estratégica ✔️ Capacidad de síntesis y organización de información compleja ✔️ Comunicación con interlocución ejecutiva ✔️ Autonomía y orientación a negocio ✔️ Gestión de proyectos ✨ ¿Qué ofrece la compañía? ✔️ Proyecto internacional dentro de una compañía en crecimiento ✔️ Participación en decisiones estratégicas globales ✔️ Entorno innovador y altamente especializado ✔️ Desarrollo profesional dentro del sector biopharma 📩 Si buscas un nuevo reto en un entorno internacional y estratégico dentro del sector biotech, estaremos encantados/as de conocerte.

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., • Proficiency in English is required. Why Join Us: • 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

In a nutshell 📌 Position: OTC Area Manager Location: Madrid Experience: 3+ years of experience in Pharma / Food Supplements in Sales or Business Development roles with a B2B and international scope Want to know more? 👇 Chemo is the industrial division of Insud Pharma, an international pharmaceutical group operating across the entire value chain, from research and development to manufacturing, commercialization, and distribution of pharmaceutical and healthcare products. At Chemo, we work to deliver high-quality solutions in a dynamic, international, and excellence-driven environment, promoting innovation, sustainability, and professional development across our teams. Are you ready to take on a new challenge in a global environment? 💪 What are we looking for? 🔎 We are looking for an OTC Area Manager to lead the development, management, and growth of sales performance for medicines and food supplements within the assigned international region. The selected candidate will be responsible for driving commercial execution, managing distributors and partners, identifying new business opportunities, and ensuring the achievement of sales and profitability targets across the markets under their responsibility. This role will cover the following markets: • Europe: Spain, Italy, Poland, Germany, and Portugal, • LATAM: Mexico, Brazil, Chile, Colombia, and Paraguay The challenge! 🚀 • Define and execute the commercial strategy to achieve sales, market share, and profitability targets across the assigned countries., • Manage and develop distributors, partners, and key accounts within the region., • Ensure the right pricing and promotional execution in line with company strategy., • Monitor sales performance, forecasts, and KPIs, proposing corrective actions when needed., • Identify and develop new business opportunities and market expansion initiatives., • Build a strong understanding of local market dynamics, competition, customer needs, and regulatory frameworks., • Adapt global strategies to local market realities., • Coordinate cross-functionally with Technical, Regulatory, Supply Chain, and Finance teams., • Ensure effective field execution through regular visits, coaching, and performance reviews., • Prepare annual business plans, budgets, and sales forecasts for the region., • Analyze market data and provide regular performance reports to management., • Ensure full compliance with local regulations, quality standards, and company ethical guidelines related to medicines and food supplements. What do you need? 🤓 • University degree in Economics, Pharmacy, Business Administration, or related fields., • MBA or postgraduate studies will be a plus., • 3+ years of experience in the pharmaceutical and/or food supplements business, in Sales or Business Development roles, with a B2B focus., • Proven experience managing international or multi-country markets., • Strong knowledge of the pharmaceutical and food supplements market., • Fluent Spanish and English., • Additional languages will be considered an asset., • Knowledge of sales strategy and customer tools such as CRM or AI tools., • Availability for frequent international travel. We will also highly value the following personal skills: • Strong impact and influence, • Excellent communication skills, • Sensitivity to market evolution, • Strong customer orientation, • International mindset 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 🔷Do you think this opportunity is not for you? 🔷 Follow us on LinkedIn to stay updated on new opportunities at Chemo and Insud Pharma. Your next professional challenge might be closer than you think! EQUAL OPPORTUNITIES COMMITMENT At Chemo, we are committed to equal opportunities and to building a diverse and inclusive workplace. All applications will be considered without discrimination based on gender, age, ethnic origin, nationality, religion, sexual orientation, gender identity, disability, or any other personal or social condition.

🚀 Oportunidad en INSUD PHARMA | Commercial Controlling & Corporate En INSUD PHARMA seguimos creciendo y buscamos incorporar un/a profesional con experiencia en pricing y gestión de márgenes que quiera asumir un rol estratégico, con impacto directo en negocio y exposición internacional. 📍 Localización: Madrid 💡 ¿Qué podrás hacer en este rol? Formarás parte de un entorno global, liderando el Commercial Controlling y coordinando la información financiera entre distintas entidades del grupo. Será una posición clave para asegurar la calidad y el análisis de la información financiera vinculada a ventas, pricing, márgenes, inversiones (Capex y R&D) y costes estructurales. Además: ✔️ Liderarás un equipo de 3-4 controllers ✔️ Trabajarás de forma transversal con Finance, Comercial, Operaciones y R&D ✔️ Tendrás un rol activo en la toma de decisiones y el “challenge” financiero 🎯 Responsabilidades principales • Análisis de ventas, pricing y rentabilidad por país, cliente y producto, • Gestión de procesos de price reconciliation (Tender y Non-Tender), • Seguimiento y análisis de desviaciones vs Budget & Forecast, • Cierres financieros mensuales consolidados, • Participación en procesos de planificación financiera, • Evaluación y seguimiento de inversiones (Capex y R&D), • Monitorización de costes y detección de riesgos y oportunidades, • Presentación de resultados y análisis a senior management 🔎 ¿Qué buscamos? • +3-4 años de experiencia en pricing analysis y margin management, • Base sólida en finanzas y contabilidad, • Experiencia en entornos multinacionales, • Nivel alto de inglés, • Conocimiento de SAP y herramientas de BI (valorable) Y, sobre todo: • Alta capacidad analítica, • Visión de negocio, • Habilidades de comunicación e influencia, • Experiencia liderando equipos 🌍 ¿Qué ofrecemos? ✨ Entorno internacional con alta exposición 👥 Liderazgo de equipo y rol transversal 📈 Participación en decisiones clave de negocio 🚀 Desarrollo profesional en una compañía farmacéutica global Si te interesa o quieres explorar más detalles, estaré encantado/a de comentarlo contigo 📩 #Finance #Controlling #Pharma #Hiring #InsudPharma

SAVANA (www.savanamed.com) 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 16 nationalities. It constitutes a clinical research ecosystem that aims to advance personalized and precision medicine worldwide. Client Partner - Healthcare Software & Data Solutions (German/French-speaking) 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. Accountability Level in Terms of Security of Information Compliance: • Operate according to Security Policies, Procedures and Manuals, • Report any suspect of incident or improvement proposals Skills, Experience and Qualifications required: • More than 10 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 also required., • 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 dpo@savanamed.com. For more information, please refer to the privacy policy section on our webpage: https://www.savanamed.com/es/curriculum/

THE COMPANY Who is Bloom Bloom is a digital agency specialized in women's health. We work with pharmaceutical brands in the US market — helping them build compliant, effective, and genuinely human digital presences across the full funnel, from awareness to prescription and retention. THE ROLE What this position is about Our team brings together specialists across paid media, CRM, influencer, web, and data. As our Senior Omnichannel Specialist, you will be the person who sits across all of them — taking the strategic direction from above and translating it into coherent, personalized experiences for the two audiences that matter most: patients and HCPs. Our salesforce (consisting of 120 sales representatives) sits at the center of both loops, and this person is responsible for making sure data flows in both directions and across both audiences. For patients, that means owning the full DTC journey — from the first paid media impression to the refill — ensuring every channel works in sync and every touchpoint feels intentional. For HCPs, the scope goes further. The brand operates on a connected loop where sales, marketing, digital communication, and data work together to deliver a personalized experience for prescribers. This role sits at the center of that loop, ensuring that what happens in the field informs the digital messages HCPs receive, and that what happens digitally reaches the sales team in a way they can act on. RESPONSIBILITIES What you will do PATIENT JOURNEY • Define activation logic for each patient audience segment across paid media, CRM, influencer, and web — what they see, when, in what channel, and based on what behavior or trigger, • Ensure message coherence across all touchpoints — a woman who sees a paid ad, visits the website, and receives a CRM email should feel like she is in one continuous conversation, • Brief channel specialists with precise journey context. HCP JOURNEY • Bridge the field and digital loops — translate HCP interaction data from the salesforce into actionable digital triggers, and ensure the field team receives relevant digital behavior insights about their HCPs on an ongoing basis, • Coordinate with the US team’s sales operations to improve the quality and flow of data between field interactions and digital activation, • Support the development of digital resources that complement field activity — ensuring what a rep leaves behind and what an HCP sees online are part of the same narrative MEASUREMENT & OPTIMIZATION • Work with the data analyst to define cross-channel KPIs that reflect funnel health across both the patient and HCP loops — not just per-channel performance, • Monitor both journeys regularly — identify where drop-off happens and brief the relevant specialist on what to test and document learnings for the team, • Build and own the monthly omnichannel performance review. CLIENT & TEAM COORDINATION • Lead the omnichannel agenda with the US team — presenting journey logic, collecting feedback, and coordinating regulatory timelines so blockers surface before they become delays, • Keep the whole team aligned through regular channel check-ins and clear documentation of active journeys, audience segments, and activation rules — a single source of truth everyone can refer to WHAT WE ARE LOOKING FOR Requirements MUST HAVE • 5–8 years in digital marketing with a clear focus on omnichannel, full-funnel, or integrated campaign execution, • Experience designing multi-channel user journeys — across both consumer and professional audiences is a strong plus, • Understanding of how sales and marketing data connect — hands-on experience with a sales team as a coordination layer between field and digital teams, • Experience with a sales team — both as a marketing CRM and as a field sales coordination tool, • Solid working knowledge of CRM logic and paid media mechanics — enough to brief specialists and review their work confidently, • Experience in regulated industries — pharma, health, or medtech preferred, • Comfortable reading funnel data and translating it into actionable decisions for channel teams, • Advanced English (C1/C2) — all work is produced in English for a US client and audience [Required], • Available to work US Eastern time hours from Spain[Required] STRONG PLUS • Direct experience in women's health, contraception, or consumer health categories, • Familiarity with US pharmaceutical marketing compliance — OPDP, fair balance, regulatory review processes, • Experience working at the intersection of field sales and digital marketing in a pharma environment, • Background in agency environments managing multiple stakeholders and approval workflows, • Curiosity about AI-driven search and GEO — increasingly relevant for health brands THE PERSON Who we are looking for Someone who naturally thinks in journeys rather than campaigns — and who sees the full picture, not just the digital half of it. In this role, the channel is sometimes a sales rep walking into a doctor's office, and the data from that visit matters as much as the data from a paid media campaign. Someone genuinely comfortable sitting between specialists and between teams. You know how to bring the cross-channel view without overstepping, brief clearly, and build alignment without friction. Someone who finds the constraints of healthcare marketing interesting rather than limiting — and who plans accordingly. WHAT WE OFFER Working at Bloom • A role with real scope — you will own something meaningful and your work will be visible across the agency and the client, • Work that matters — we help women understand and access their healthcare options better, • A clear career path within a growing agency, with real opportunities to evolve as the team grows, • Hybrid work model, • Compensation aligned with your experience level

In few words 📌 Position: Financial Controller Location: On-site role based in Madrid with occasional trips to Sweden Experience: Minimum 4 years of experience in Big 4 and/or the pharmaceutical industry; experience in generic pharma is strongly preferred. 👇Global Responsibility We are looking for a Financial Controller – to support financial performance management across Northern Europe. Based on-site in Madrid and reporting to the FP&A Manager, this role will drive high-quality financial planning, reporting and business insights, ensuring accurate performance tracking and supporting decision-making across the Generics organization. Specific Responsibilities • Own and coordinate the planning cycle for the region (budget, forecast updates, long-range planning where applicable)., • Prepare and deliver monthly management reporting packs (P&L, OPEX, KPIs), ensuring accuracy, timeliness and clarity., • Perform variance analysis vs. budget/forecast/prior year; identify drivers and provide actionable recommendations., • Act as a finance business partner for Northern Europe stakeholders, supporting performance reviews and commercial/operational initiatives., • Support month-end activities from a controlling perspective, liaising with accounting teams to ensure robust accruals and correct performance recognition., • Maintain and improve financial models, dashboards and reporting automation using SAP, SAP BPC and Power BI., • Ensure consistent application of internal controlling standards and contribute to continuous improvement of processes and data quality., • Support ad-hoc analyses (profitability, cost efficiency, scenario analysis) as required by management. 🕵️Requirements and personal skills • Minimum 4 years of experience in Big 4 and/or the pharmaceutical industry; experience in generic pharma is strongly preferred., • Solid controlling/FP&A background with strong analytical and problem-solving skills., • Advanced user of MS Office (especially Excel)., • Hands-on experience with SAP, SAP BPC and Power BI., • High level of English (professional fluency). Nordic languages are not required but a plus., • Strong stakeholder management skills, attention to detail, and ability to work effectively in a fast-paced 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.

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.

La actividad del puesto se centra en ayudar a uno de nuestros clientes líderes a nivel internacional en el sector farmacéutico para que sus equipos, procesos y sistemas cumplan con los requerimientos y especificaciones adecuados a su uso previsto y al marco regulador vigente de la industria farmacéutica. RESPONSABILIDADES: • Preparación de planes maestros de cualificación/validación., • Redacción de protocolos DQ / IQ / OQ / PQ., • Gestión y ejecución de los trabajos de cualificaciones de equipos y procesos., • Evaluación de riesgos del proceso y cumplimiento de la planificación., • Realización de informes. REQUISITOS: • Contar como mínimo con 5 años de experiencia trabajando en entornos GMP y en cualificaciones de equipos y procesos en áreas de laboratorio y de empaque final en la industria farmacéutica., • Conocimiento de las normativas GxP, EMA, FDA y CFR Part 11 y de otros sistemas., • Nivel de Inglés alto: B2/C1 – hablado y escrito., • Habilidades para resolver problemas técnicos, con dotes comunicativos., • Persona rigurosa y eficiente, capaz de trabajar de forma colaborativa en equipos multidisciplinares. ¿QUÉ OFRECEMOS?: • Incorporación a un proyecto estable y de alto impacto dentro del sector farmacéutico., • Participación en entorno GMP con proyectos de validaciones y cualificaciones de alto nivel técnico., • Integración en un equipo especializado y en crecimiento., • Alto nivel de autonomía y desarrollo profesional., • Contrato indefinido., • Buen ambiente de trabajo y cultura corporativa., • Flexibilidad horaria. Si crees que cumples con el perfil solicitado y te interesa nuestra oferta laboral, no dudes en inscribirte. En la entrevista, se concretarán todos los puntos con más detalle. ¡Estaremos encantados de conocerte!

Insud Pharma is a recognised and respected company in the pharmaceutical and healthcare sector with more than 40 years of history and more than 7,000 employees in 50 countries specialising in the research, development, manufacture and marketing of active pharmaceutical ingredients and medicines for human and veterinary use. Chemo, industrial area of the Insud Pharma group, is a world leader in R&D and manufacturing of more than 100 value-added active pharmaceutical ingredients and more than 122 medicines with more than 200 different product presentations. Chemo produces its own active pharmaceutical ingredients (API) as well as finished pharmaceutical products (FDF) covering the main therapeutic groups (Cardiology, Gastroenterology, Central Nervous System, Anti-infectives, Respiratory, Women's Health, Endocrinology, Dermatology and Urology). General Responsibility Lead and oversee the Environmental, Health, Safety (EHS&S) strategy and operations across INSUD PHARMA’s Pharma Fineshed Dosage Form (FDF) manufacturing sites (12 sites), ensuring compliance with legal requirements, corporate standards, and continuous improvement initiatives aligned with the company’s strategic objectives. Specific Responsibilities • Drive the reduction of safety incidents and accidents with focus on key risks (inflammables, electrical, etc.), • Develop the new corporate EHS&S Master Plan 2024-2026., • Define, standardize and ensure the development of corporate EHS&S policies, standards, and guidelines., • Specify, harmonize and oversee the implementation of EHS&S technologies across pharmaceutical and chemical manufacturing sites., • Conduct internal audits, manage corrective action plans and ensure ongoing compliance and continuous improvement., • Identify, benchmark and promote best practices in safety, health, and environmental management., • Lead Operational Excellence and Double Impact projects, integrating EHS&S improvements with operational and cost efficiencies., • Foster a strong EHS&S culture, positioning EHS as a strategic business pillar., • Manage relationships and proceedings with governmental authorities and trade union committees., • Develop, monitor and report on key performance indicators (KPIs) and corporate dashboards for EHS&S performance., • Oversee audits and certifications related to continuous improvement and sustainability standards (ISO14001, ISO45001, Ecovadis, PSCI)., • Ensure legal compliance in EHS&S and provide expert support to manufacturing locations. Requirements and personal skills • Education: Degree in Engineering, Environmental Sciences, Industrial Safety or related fields. MBA will be an asset., • Languages: Fluent English and Spanish. Other languages will be an asset., • Experience (years/area): +10 years of proven experience in similar roles within the pharmaceutical or chemical industry. Have led HSE for a big Manufacturing site. Corporate roles and multi-site experience., • Specific Knowledge: Advanced knowledge of ISO14001, ISO45001, Ecovadis and PSCI standards and certifications. Experience managing internal and external audits, KPI development and corporate dashboard tools., • Travels: Available to travel once per week to the Sites in Spain (León) during the first year and then in addition once per quarter to international sites., • Personal skills:, • Change Management, • Proactivity and initiative, • Ability to collaborate internally with production and maintenance and with with regulatory authorities and unions., • Excellence organizational skills. COMMITMENT TO EQUAL OPPORTUNITIES Insud Pharma is aware that business management has to be in line 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 legislation on the subject - Organic Law 3/2007, and we do not discriminate against any person on 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.

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.

En BIGZON seleccionamos un/a SAP QM Senior Consultant para incorporarse a una importante compañía multinacional del sector Pharma, en pleno crecimiento internacional y con un entorno SAP complejo. Buscamos un perfil senior, autónomo y con sólida experiencia en SAP QM dentro de entornos regulados y de alta exigencia operativa. FUNCIONES: • Participación en proyectos y evolutivos SAP relacionados con el módulo QM., • Análisis y optimización de procesos de calidad dentro de entorno Pharma., • Parametrización y soporte funcional SAP QM., • Interlocución con negocio, usuarios y equipos internacionales., • Participación en integraciones con otros módulos SAP y sistemas corporativos., • Soporte en incidencias, evolutivos y proyectos internacionales. REQUISITOS: • Experiencia sólida en SAP QM como módulo principal., • Experiencia en entornos Pharma, químico, industrial o regulado., • Conocimiento de procesos de calidad, validación y compliance., • Experiencia en SAP ECC y S/4HANA., • Nivel alto de inglés., • Perfil autónomo, resolutivo y acostumbrado a entornos exigentes. MODELO DE TRABAJO HIBRIDO, 2-3 días presenciales por semana. Oficinas situadas en la zona de Sanchinarro. SALARIO: En función de experiencia, hasta 80.000€ b/a. En esta GRAN ZONA de trabajo que es BIGZON valoramos la diversidad y la inclusión. Estamos comprometidos a crear un entorno de trabajo en el que todas las personas se sientan valoradas y respetadas. Buscamos a quien comparta estos valores y tenga ganas de trabajar en un ambiente sano, colaborativo y orientado a objetivos. ¡Te esperamos!

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. 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.

En BIGZON seleccionamos un/a SAP PMO Senior para incorporarse a una importante compañía multinacional del sector Pharma con presencia internacional y un entorno SAP estratégico. Buscamos un perfil senior con amplia experiencia en gestión y coordinación de proyectos SAP complejos en entornos internacionales. FUNCIONES: Coordinación y seguimiento de proyectos SAP internacionales. Gestión de planificación, riesgos, hitos y reporting. Coordinación de equipos funcionales, técnicos y proveedores. Interlocución con negocio y stakeholders internacionales. Seguimiento de rollouts, evolutivos y proyectos de transformación SAP. REQUISITOS: Experiencia sólida como SAP PMO o SAP Project Manager. Experiencia en proyectos SAP complejos y entornos internacionales. Conocimiento de SAP ECC y/o S/4HANA. Experiencia coordinando múltiples proveedores y equipos. Nivel alto de inglés. Perfil muy autónomo y orientado a resultados. UBICACIÓN: Madrid (zona Sanchinarro). Modelo híbrido: 2-3 días presenciales por semana. SALARIO: En función de experiencia, hasta 85.000€ b/a. En BIGZON apostamos por la diversidad y la inclusión. Estamos comprometidos con la creación de entornos de trabajo donde todas las personas se sientan valoradas y respetadas. ¡Te esperamos!

Job Insights: ▸ 10-15 years of business experience including 5 years of omnichannel delivery or operations experience with expertise in digital production (e.g., web development) and campaign management activities in the Healthcare industry; Pharma experience is a bonus ▸ Strong ability to build and manage/grow customer relationships, and navigate complex buying and decision-making environments ▸ Deep understanding of digital marketing tactics (websites, email, paid media, social media, SEO/GEO, mobile apps, etc.) and the technology platforms that enable them ▸ Experience managing multiple large-scale programs with complex and heterogeneous technology landscapes ▸ Strong written and verbal communication skills, with proven ability to communicate with technical and non-technical audiences alike ▸ Robust analytical skills to evaluate operational performance and identify efficiencies or areas for improvement ▸ Excellent project, program, and portfolio management skills in a digital domain, with attention to detail, urgency, and a solution-oriented mindset ▸ Skilled relationship-builder and cross-functional collaborator, able to manage priorities and drive results across internal and external stakeholders ▸ Experience creating detailed reports and delivering presentations to senior audiences ▸ Excellent planning, organizational, and time management skills ▸ Ability to travel EOE: 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.

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., • 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.

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.