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We are a technology-led healthcare solutions provider. We are driven by our purpose to enable healthcare organizations to be future-ready. We offer accelerated, global growth opportunities for talent that is bold, industrious and nimble. With Indegene, you gain a unique career experience that celebrates entrepreneurship and is guided by passion, innovation, collaboration and empathy. To explore exciting opportunities at the convergence of healthcare and technology, check out if we told you that you can move to an exciting role in an entrepreneurial organization without the usual risks associated with it? We understand that you are looking for growth and variety in your career at this point and we would love for you to join us in our journey and grow with us. At Indegene, our roles come with the excitement you require at this stage of your career with the reliability you seek. We hire the best and trust them from day 1 to deliver global impact, handle teams and be responsible for the outcomes while our leaders support and mentor you. We are a profitable rapidly growing global organization and are scouting for the best talent for this phase of growth. With us, you are at the intersection of two of the most exciting industries of healthcare and technology. We offer global opportunities with fast-track careers while you work with a team that is fueled by purpose. The combination of these will lead to a truly differentiated experience for you. If this excites you, then apply below. Lea el resumen de esta oportunidad para comprender qué habilidades, incluidas las habilidades interpersonales relevantes y el dominio de paquetes de software, se requieren. Content Coordinator – Global Content Operations Location – Spain Remote You will be responsible for: • Act as the primary liaison for content submissions from internal teams and external agencies., • Managing end-to-end content intake, validation, and preparation for submission., • Coordinating across medical, brand, regulatory/legal, and agency teams to ensure timely progression of content., • Monitoring jobs through all workflow stages and resolving blockers or routing issues., • Assist in managing content calendars and supporting campaign execution across channels., • Tracking global content timelines across franchises, identifying potential bottlenecks before SLA breaches, and reporting progress to Commercial Excellence teams., • Acting as a coordination point between content owners, agencies, and DAM librarians to align on quality control expectations and operational workflows., • Supporting onboarding of external agencies on franchise-specific PromoMats processes and ensuring appropriate system access and governance from the start., • Supporting lifecycle management including version control, renewals, expirations, and archival of content assets., • Tracking global-to-local content adaptation across markets and supporting insights that inform content reuse and evolution guidelines., • Maintaining content trackers, dashboards, and SLA-based performance reporting., • Contributing to the continuous improvement of content operations processes, templates, and workflow governance., • Supporting scalable content operations by enabling structured content, reuse, and governance practices that improve global content efficiency across franchises., • Support change management activities related to new processes, templates, or system enhancements., • Identify opportunities to improve operational efficiency and content reuse., • Assist in coordinating Medical, Legal, and Regulatory (MLR) review processes where applicable. Desired Profile (Key Skills) • A seasoned content operations professional with 12+ years of strong experience in pharma or life sciences., • Background in managing large volumes of medical/promotional content within structured, regulated environments., • Deep familiarity with Veeva systems (PromoMats, DAM) and end‑to‑end content lifecycle processes., • Proven ability to coordinate multiple stakeholders across global and local teams., • Strong understanding of claims, references, compliance, and medical review processes., • Highly organized, detail‑oriented, and capable of managing simultaneous submissions under strict timelines., • Comfortable working in a complex global ecosystem with multiple agencies and cross‑functional partners., • Demonstrates strong communication, follow‑up, and operational ownership., • Understanding of structured content, modular content, taxonomy, and metadata frameworks., • Strong project coordination and workflow management capabilities., • Ability to maintain accurate trackers, dashboards, and SLA reporting., • Skilled in content lifecycle management (intake → review → approval → publish → archive)., • Familiarity with global-to-local content adaptation and reuse strategies. Nice to have: (Additional desired qualities) • Any Certifications related to the platform, like Aprimo certification, Veeva Vault Administration Certification, etc. EQUAL OPPORTUNITY Indegene is proud to be an Equal Employment Employer and is committed to the culture of Inclusion and Diversity. We do not discriminate on the basis of race, religion, sex, colour, age, national origin, pregnancy, sexual orientation, physical ability, or any other characteristics. All employment decisions, from hiring to separation, will be based on business requirements, candidate’s merit and qualification. We are an Equal Opportunity Employer. xcskxlj All qualified applicants will receive consideration for employment without regard to race, colour, religion, sex, national origin, gender identity, sexual orientation, disability status, protected veteran status, or any other characteristics.

INSUD PHARMA operates across the entire pharmaceutical value chain, providing specialized knowledge and experience in scientific research, development, manufacturing, sales, and commercialization of a wide range of active pharmaceutical ingredients (APIs), finished dosage forms (FDF), and branded ph

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 phar

Está pensando en solicitar este empleo? No se demore, desplácese hacia abajo y envíe su solicitud lo antes posible para no perder la oportunidad.Posición: Técnico/a Garantía de Calidad.Localización: Azuqueca de Henares.Experiencia: 2 a 4 años en funciones similares.INSUD PHARMA opera en toda

At ASTEK Iberia, we are looking for Senior and Principal Statistical Programmers to support upcoming projects within the Life Sciences industry in a remote model based in Spain. Es esencial asegurarse de que cumple con los requisitos como solicitante para este puesto; por favor, lea atentamente la información a continuación. If you have solid experience in statistical programming and are open to exploring new opportunities, we would be happy to connect. Main responsibilities: • Develop and validate statistical outputs using R (primary language), • Work with CDISC standards, including: ADaM, TFLs (Tables, Figures & Listings), (SDTM experience is also valuable), • Contribute to the production of analysis datasets and study outputs, • Support regulatory submissions (ISS/ISE, when applicable), • Perform quality control (QC) and ensure high-quality deliverables, • Collaborate with cross-functional teams in an international environment Who are you? • 5+ years of experience in Statistical Programming within the Life Sciences / Pharma / CRO environment, • Strong expertise in R programming, • Hands-on experience with CDISC (ADaM, TFLs; SDTM is a plus), • Familiarity with regulatory submissions is highly valued, • Good understanding of clinical trial data and processes, • Fluent in English Nice to Have • Experience with SAS and/or SQL, • Exposure to agile ways of working, • Experience working with large pharmaceutical companies Who are we? Since 2015, Astek Iberia has been accompanying its customers in their development throughout Spain (Madrid, Barcelona, Valencia, Basque Country, Andalusia, Galicia, etc.). Founded in France in 1988, Astek is a global player in engineering and technology consulting, present in five continents and 25 countries. With expertise in a wide range of industrial and service sectors, Astek is an essential partner, supporting its customers in an intelligent deployment of their products and services, and in the implementation of their digital transformation. Today we are more than 8,000 employees, committed every day to promote the complementarity between digital technologies and complex systems engineering. Our style is to have flexible schedules and highly value the well-being of our employees. Why join us? You will grow professionally in a company in constant development and evolution. You will benefit from a personalized follow-up of your professional projects as close as possible to your ambitions. You will make a real contribution to the company's development in real time. You will enjoy 23 days of vacation (in addition to holidays) that you will be able to choose whenever you want. You will join our team: diverse, multicultural and constantly growing. You will have days full of good energy and good atmosphere. ...although you still have a lot to discover! Shall we meet? xcskxlj If you want to participate in the process, apply from here attaching your CV (in English) as detailed as possible and we will tell you more.

Estamos contratando: Medical Writer (Pharma Project) Por favor, asegúrese de leer atentamente los siguientes detalles antes de enviar cualquier solicitud. ¿Tienes formación científica y experiencia creando o revisando contenido en la industria farmacéutica? ¿Te interesa trabajar en un entorno internacional donde la calidad, el rigor científico y el impacto en comunicación son clave? ¡Entonces este rol puede ser para ti! Rol: Medical Writer Buscamos perfiles con background científico que quieran formar parte de un equipo internacional desarrollando y revisando materiales promocionales y educativos en el sector farmacéutico. Trabajarás en estrecha colaboración con equipos médicos, regulatorios y de marketing para asegurar que los contenidos cumplen con los estándares científicos y normativos. Responsabilidades principales Creación y revisión de contenidos • Desarrollo de materiales promocionales y educativos, • Revisión médica y científica de contenidos, • Adaptación de materiales globales a mercados locales Calidad y compliance • Asegurar cumplimiento de normativa (EFPIA y códigos locales), • Garantizar rigor científico y consistencia del mensaje Colaboración transversal • Trabajo con equipos médicos, marketing y regulatory, • Participación en procesos de revisión y aprobación Perfil que buscamos Formación científica (MD, PharmD, PhD o Máster en Life Sciences) Experiencia en Medical Writing o revisión de materiales promocionales Conocimiento de normativa farmacéutica Perfil analítico, organizado y con atención al detalle Buenas habilidades de comunicación y trabajo en equipo Idiomas • Italiano nativo Condiciones • Salario hasta 30k brutos anuales, • Ubicación: preferiblemente Málaga (abierto a toda España), • Proyecto internacional en entorno farmacéutico ¿Te interesa? xcskxlj Si quieres formar parte de un proyecto con impacto en el sector healthcare y trabajar en un entorno global, ¡nos encantará conocerte! Aplica o envía tu CV para más información

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

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

Estamos buscando un Obtenga más información sobre este puesto leyendo los detalles a continuación y luego envíe su solicitud para ser considerado. Key Account Manager para incorporarse a nuestra unidad de Selección de Talento . En esta división ayudamos a las empresas a identificar, atraer y contratar profesionales para reforzar sus equipos, desde posiciones operativas hasta roles de gestión. Tenemos amplia experiencia en la búsqueda de talento especializado en IT, Ingeniería y disciplinas técnicas , y estamos en plena expansión hacia sectores como Pharma & Healthcare y otros mercados estratégicos. Además, disponemos de nuestro Programa de Relocation internacional “Salta Conmigo” , que facilita la incorporación de profesionales procedentes de otros países. ¿Cuál será tu misión como Key Account Manager? Desarrollar nuevas oportunidades de negocio y captar clientes en los sectores objetivo Pharma&Healthcare. Promocionar nuestros servicios de selección (selección directa y outsourcing). Además, tendrás la posibilidad de ofrecer cualquier solución o servicio del ecosistema Cibernos. ¿Contrato indefinido . ~ Horario flexible y trabajo en modalidad híbrida . xcskxlj ~ Jornada intensiva de verano (del 15 de junio al 15 de septiembre). ~22 días laborables de vacaciones al año.

Estamos buscando un Obtenga más información sobre este puesto leyendo los detalles a continuación y luego envíe su solicitud para ser considerado. Key Account Manager para incorporarse a nuestra unidad de Selección de Talento . En esta división ayudamos a las empresas a identificar, atraer y contratar profesionales para reforzar sus equipos, desde posiciones operativas hasta roles de gestión. Tenemos amplia experiencia en la búsqueda de talento especializado en IT, Ingeniería y disciplinas técnicas , y estamos en plena expansión hacia sectores como Pharma & Healthcare y otros mercados estratégicos. Además, disponemos de nuestro Programa de Relocation internacional “Salta Conmigo” , que facilita la incorporación de profesionales procedentes de otros países. ¿Cuál será tu misión como Key Account Manager? Desarrollar nuevas oportunidades de negocio y captar clientes en los sectores objetivo Pharma&Healthcare. Promocionar nuestros servicios de selección (selección directa y outsourcing). Además, tendrás la posibilidad de ofrecer cualquier solución o servicio del ecosistema Cibernos. ¿Contrato indefinido . ~ Horario flexible y trabajo en modalidad híbrida . xcskxlj ~ Jornada intensiva de verano (del 15 de junio al 15 de septiembre). ~22 días laborables de vacaciones al año.

En pocas palabras ¿Es usted el candidato adecuado para esta oportunidad? Asegúrese de leer la descripción completa a continuación. Posición: Operario/a de Producción Galénica - I+D. Localización: Azuqueca de Henares. Experiencia: Valorable al menos 3 años en el desempeño de las funciones descritas. ¿Quieres saber más? INSUD PHARMA opera en toda la cadena de valor farmacéutica, aportando conocimientos especializados y experiencia en investigación científica, desarrollo, fabricación, venta y comercialización de una amplia gama de principios activos farmacéuticos (API), formas farmacéuticas acabadas (FDF) y productos farmacéuticos de marca, 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. INSUD PHARMA cree en la innovación y el desarrollo sostenible. ¿Preparado para ser un #Challenger? ¿Qué buscamos? Incorporamos un/a nuevo/a INSUDER como Operario/a de Producción Galénica - I+D, para incorporarse al equipo en nuestra planta en Azuqueca de Henares. ¡El reto! Realizar pruebas farmacéuticas, biolotes y lotes en entorno GMP y de acuerdo a los procedimientos internos. Registrar, controlar y reportar los resultados. Limpiar equipos y materiales. Formar nuevos trabajadores Mantener los equipos y materiales en buenas condiciones. Realizar ensayos farmacéuticos y lotes de registro para I+D. Evaluar los resultados de las pruebas y procesos y asesorar a los técnicos en los próximos pasos y en las guías de trabajo. Realizar inventario e informar al superior inmediato. Gestión de materiales de planta (controlar stock, envío y recepción de materiales del almacén…). Capacitar a nuevos operadores en los equipos existentes. ¿Qué necesitas? Experiencia previa de al menos 3 años en departamentos de Producción o I+D en una planta de fabricación farmacéutica. Experiencia en ambiente GMP. Idiomas: español fluido Competencias: ~ Atención al detalle y a la calidad, adaptabilidad/flexibilidad, disponibilidad, innovación, comunicación, trabajo en equipo, productividad, autodesarrollo, sentido de urgencia, iniciativa. ¡Nuestros beneficios! Horario rotativo de lunes a viernes; mañanas 06.00 a 14.00, tardes 14.00 a 22.00 y turno partido con posibilidad puntual de realizar noches Contrato indefinido Atractivo paquete salarial (fijo + pluses) Seguro de vida y accidentes Copago en el seguro voluntario de salud Club de Beneficios y Ahorro Planes de desarrollo, política de movilidad interna ¡Muchos más! ¿Cómo será el proceso de Selección? ¡Estate atento/a al teléfono y al correo! Seguramente lo primero que haremos será contactarte por alguna de las dos vías. ¡Prepárate bien! Continuaremos con una entrevista presencial/virtual según la disponibilidad y acordemos, en el proceso puede haber entre una y dos entrevistas y según el tipo de proceso puede haber también algún tipo de prueba. ¡Espera el resultado! Nos preocupamos de que cada proceso de selección os sintáis guiados y sabiendo qué esperar de nosotros, por lo que procuraremos indicaros siempre el estado del proceso. xcskxlj ¿Crees que esta oferta no es para ti? Síguenos en redes sociales como LinkedIn/Instagram y estate atento a cualquier oferta que vayamos sacando, ¡La oportunidad de ser un nuevo Insuder está a la espera!. #InsudPharma #Challenger #Insuder #InsudTalent COMPROMISO CON LA IGUALDAD DE OPORTUNIDADES El grupo InsudPharma es consciente que la gestión empresarial tiene que estar en consonancia con las necesidades y demandas de la sociedad, y por ello asume el compromiso de igualdad de oportunidades y trato entre hombres y mujeres, tal y como se recoge en la normativa vigente en la materia -Ley Orgánica 3/2007, y no discriminamos a ninguna persona por motivos de etnia, religión, edad, sexo, nacionalidad, estado civil, orientación afectiva o sexual, identidad o expresión de género, discapacidad, o cualquier otra circunstancia personal o social.

Ejecutivo de Compras Farmacéuticas.

About Nordic Pharma is a mid-size privately-owned international pharmaceutical company which focuses on the development and commercialization of niche hospital and orphan products to address unmet medical needs. Nordic Pharma’s expertise relies on the development and sales of its own products, but also on partner products acquired at various stages of development. Today, Nordic Pharma has a range of highly specialized proprietary and in-licensed products in the following therapeutic areas: Rheumatology, Women’s Health, Ophthalmology, Pediatrics and Critical Care. Nordic Pharma’s values of Commitment, Ambition, Respect, Reliability, Integrity and Agility describe our culture and standards and guide us in our way of working. ¿Es este el puesto que está buscando? Si es así, siga leyendo para obtener más detalles y no olvide enviar su solicitud hoy mismo. Job title: Sales Director, Spain Location: Madrid, Spain Reporting to: General Manager We are seeking a Sales Director to lead our commercial organization and drive the next phase of growth in Spain. This is a critical leadership role, with full responsibility for sales strategy, execution, and performance across a diverse and growing portfolio. About the role The Sales Director plays a key role in leading the sales organization and driving sustainable growth across the company’s portfolio. This role is responsible for shaping and executing the sales strategy, maximizing revenue and market share, and strengthening customer engagement across channels, while ensuring that all activities are carried out in full compliance with ethical and regulatory standards. You will lead a multi-channel sales organization spanning private clinics (direct sales model), public hospitals (Key Account Management), and primary care/consumer health. Managing a team of professionals, you will have a clear mandate to accelerate growth, enhance customer engagement, and unlock new opportunities. Key priorities include expanding in the private healthcare sector, particularly in specialized areas such as ophthalmology, driving the evolution toward an omnichannel engagement model, advancing the development and adoption of CRM tools and data-driven decision-making, and ensuring strong alignment across Sales, Marketing, and Medical. Sales Strategy & Performance • Define and implement sales strategies to achieve and exceed revenue, market share, and profitability objectives., • Develop territory plans and account strategies based on customer insights, market dynamics, and competitor activity., • Ensure resources are prioritized effectively to maximize performance in high-potential areas., • Drive the transition toward innovative, omnichannel engagement models to expand reach and impact., • Regularly review sales performance, adjusting strategy to capture new opportunities and mitigate risks. Team Leadership & Development • Lead, coach, and develop the sales team to achieve and exceed sales targets., • Establish clear goals and accountability frameworks., • Build a culture of accountability, continuous improvement, and high performance., • Ensure sales teams are fully trained and equipped for successful product launches. Cross-Functional Collaboration • Collaborate with marketing, medical, market access, and regulatory colleagues to align execution with company strategy., • Contribute insights from the field to inform broader business planning and decision-making. Compliance & Governance • Ensure all sales activities adhere to compliance standards, industry codes, and company SOPs., • Promote ethical practices and integrity in all customer interactions. What we are looking for • Bachelor’s degree in life sciences, business, or related field (MBA desirable)., • 10+ years’ experience in pharmaceutical or life sciences sales, with at least 5 years in senior leadership roles., • Proven experience managing multi-channel sales teams (hospital, primary care and/or private sector)., • Strong experience in selling products and/or services to private clinics, preferably within ophthalmology or other specialty care areas., • Expertise in territory planning, pipeline management, and sales operations., • Experience in building and executing omnichannel strategies and improving customer engagement models., • Proven track record in CRM development, adoption and optimization, • Experience in product launches and lifecycle management., • Strong financial acumen with experience in forecasting, budgeting, and P&L responsibility. If you are ready to take on a high-visibility leadership role and drive meaningful growth, we would love to hear from you. We are an equal opportunity employer committed to build a working culture that embraces diversity and inclusion. xcskxlj All qualified applicants will be considered.

Estamos buscando un Obtenga más información sobre este puesto leyendo los detalles a continuación y luego envíe su solicitud para ser considerado. Key Account Manager para incorporarse a nuestra unidad de Selección de Talento . En esta división ayudamos a las empresas a identificar, atraer y contratar profesionales para reforzar sus equipos, desde posiciones operativas hasta roles de gestión. Tenemos amplia experiencia en la búsqueda de talento especializado en IT, Ingeniería y disciplinas técnicas , y estamos en plena expansión hacia sectores como Pharma & Healthcare y otros mercados estratégicos. Además, disponemos de nuestro Programa de Relocation internacional “Salta Conmigo” , que facilita la incorporación de profesionales procedentes de otros países. ¿Cuál será tu misión como Key Account Manager? Desarrollar nuevas oportunidades de negocio y captar clientes en los sectores objetivo Pharma&Healthcare. Promocionar nuestros servicios de selección (selección directa y outsourcing). Además, tendrás la posibilidad de ofrecer cualquier solución o servicio del ecosistema Cibernos. ¿Contrato indefinido . ~ Horario flexible y trabajo en modalidad híbrida . xcskxlj ~ Jornada intensiva de verano (del 15 de junio al 15 de septiembre). ~22 días laborables de vacaciones al año.

SawesPharma #Empleo #CanalFarmacia #Ventas #OportunidadLaboral #DelegadoComercial #Farmacia. Representantes Comerciales para el canal farmacia. Visitar farmacias en la zona asignada.

En pocas palabras Obtenga más información sobre este puesto leyendo los detalles a continuación y luego envíe su solicitud para ser considerado. Posición: Técnico/a Garantía de Calidad Localización: Azuqueca de Henares. Experiencia: 2 a 4 años en funciones similares. ¿Quieres saber más? INSUD PHARMA opera en toda la cadena de valor farmacéutica, aportando conocimientos especializados y experiencia en investigación científica, desarrollo, fabricación, venta y comercialización de una amplia gama de principios activos farmacéuticos (API), formas farmacéuticas acabadas (FDF) y productos farmacéuticos de marca, 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. INSUD PHARMA cree en la innovación y el desarrollo sostenible. ¿Preparado para ser un #Challenger? ¿Qué buscamos? El Técnico/a de Garantía de Calidad que trabajará en el área de Sistemas de Calidad de la planta. ¡El reto! Gestión de las desviaciones de la planta Gestión de OOS/OOT y eventos de calidad de la planta Revisión de investigaciones de las áreas de Operaciones y Laboratoriales Evaluación de impacto de calidad de lotes asociados a desviaciones Evaluación de acciones correctivas/preventivas soportando las demás áreas de la planta de manera a asegurar la recurrencia de desviaciones Evaluación de tendencias de desviaciones de la planta Preparación de Análisis de Riesgos Preparación y/o revisión de PQR Gestión de Controles de Cambios Revisión y/o aprobación de documentación de control de calidad Gestión de PNT Reporte de KPIs Soporte en auditorias externas, inspecciones y auditorias internas Soporte en actividades del sistema de calidad ¿Qué necesitas? Graduado en Química, Farmacia o graduación asociadas a Ciencias Farmacéuticas Máster en Farmacia, Química o titulación científica relacionada con las Ciencias Farmacéuticas Ingles fluido Conocimiento SAP, herramientas de IA ¡Nuestros beneficios! Contrato indefinido Atractivo paquete salarial. Seguro de vida y accidentes. Comedor de empresa (gratuito). Copago en el seguro voluntario de salud. Club de Beneficios y Ahorro. xcskxlj Planes de desarrollo, política de movilidad interna. ¡Muchos más!

Tu nueva empresa Asegúrese de enviar su solicitud rápidamente para maximizar sus posibilidades de ser considerado para una entrevista. Lea la descripción completa del puesto a continuación. Compañía farmacéutica internacional con presencia creciente en el mercado español, especializada en el desarrollo, fabricación y comercialización de medicamentos de alta calidad, especialmente en el ámbito de genéricos complejos y productos biotecnológicos. La organización combina la solidez de un gran grupo industrial con un enfoque ágil y orientado a crecimiento en sus filiales europeas. Tu nuevo rol Como Customer Control / Customer Manager, tu misión será garantizar el control end‑to‑end de los pedidos de cliente, asegurando la calidad del servicio y una gestión analítica y proactiva del forecast, los tiempos de suministro y los hitos clave del ciclo del pedido. Principales responsabilidades: • Seguimiento continuo de pedidos y volúmenes solicitados por cliente., • Monitorización del ciclo completo del pedido: desde la recepción hasta la entrega (envío, tránsito, liberación, entrega de muestras y recogida)., • Identificación de retrasos, desviaciones y puntos críticos en cada fase del proceso., • Gestión, actualización y mantenimiento del forecast por cliente, comparándolo con el Business Plan., • Análisis de desviaciones y medición del nivel de precisión del forecast., • Reclamación proactiva de información pendiente (forecast y pedidos)., • Elaboración de informes de previsiones y seguimiento de servicio., • Experiencia en customer service, customer operations, supply chain o planificación en entornos industriales o farmacéuticos., • Perfil analítico y orientado a procesos y datos., • Experiencia en gestión de forecast, seguimiento de pedidos y control de KPIs de servicio., • Capacidad de organización y coordinación con múltiples clientes y áreas internas., • Conocimiento de entornos regulados (GMP / entorno farmacéutico), valorable., • Experiencia o exposición a serialización, valorable., • Incorporación a un entorno farmacéutico estable y en crecimiento., • Rol con alto impacto operativo y visibilidad transversal., • Participación activa en la mejora continua de procesos de supply y servicio al cliente., • Entorno profesional, estructurado y orientado a la calidad. xcskxlj, • Oportunidades de desarrollo en áreas de Customer, Supply Chain y Operations.

¿Te interesa la Inteligencia Artificial aplicada a casos reales? ¿Quieres participar en la creación de un Agente de IA que ayude a cientos de usuarios en su día a día? Esta es tu oportunidad para aprender y crecer en un entorno corporativo y tecnológico dentro del sector salud. Consulte la descripción del puesto a continuación. Si confía en que tiene las habilidades y la experiencia adecuadas, envíe su solicitud hoy mismo. Otsuka es una multinacional farmacéutica japonesa con 100 años de historia y 34.000 personas en todo el mundo que investigamos, desarrollamos, fabricamos y comercializamos fármacos innovadores para abordar necesidades médicas no cubiertas y productos nutracéuticos para el mantenimiento de la salud diaria. ¿Cuál será tu misión? Colaborarás en un proyecto innovador para diseñar y configurar un Agente de Inteligencia Artificial integrado en Veeva Vault CRM, con el objetivo de dar soporte a los usuarios del sistema. Trabajarás en estrecha colaboración con IT y con áreas de negocio, entendiendo las necesidades reales de los usuarios. Principales funciones • Apoyar en el diseño y configuración de un Agente de Copilot para soporte a usuarios de Veeva Vault CRM., • Analizar preguntas frecuentes e incidencias de usuarios y convertirlas en: casos de uso de Copilot / Flujos de respuesta y knowledge base., • Colaborar con el equipo IT en: uso de Microsoft Copilot (M365) / Integración con documentación y fuentes internas., • Documentar: flujos de soporte / respuestas del agente / casos de uso y mejoras continuas., • Participar en pruebas, ajustes y evolución funcional del agente Copilot. Perfil que buscamos • Estudiante de último curso o recién graduado/a en: Ingeniería Informática / Ingeniería de Software / Ingeniería de Datos / Inteligencia Artificial o similar, • Interés claro en: Microsoft Copilot / Automatización y soporte inteligente, • Capacidad analítica y orientación a resolución de problemas, • Buenas habilidades de comunicación y enfoque usuario, • Nivel medio de inglés (lectura de documentación técnica) Se valorará positivamente • Experiencia académica o personal con: Microsoft Copilot / M365 / Chatbots basados en knowledge base (no ML), • Conocimiento previo de CRM: Veeva Vault CRM (muy valorado) / Salesforce / Dynamics, • Interés por: Entornos regulados / Documentación y trazabilidad, • Nociones de: Power Automate / SharePoint / Teams / OneDrive, • Conocimientos básicos de programación (Phyton recomendado) ¿Qué ofrecemos? • Participar en un proyecto real de IA aplicada con impacto directo en usuarios, • Aprendizaje práctico en Veeva CRM, herramienta líder en el sector pharma, • Acompañamiento y mentoring por parte de profesionales IT y de negocio, • Excelente oportunidad de desarrollo profesional en entornos digitales y de IA, • Buen ambiente de trabajo y aprendizaje continuo Si te motiva la tecnología, la IA y quieres aplicar tus conocimientos en un entorno real, ¡nos encantaría conocerte! Te informamos de que, en cumplimiento de lo establecido en el Reglamento 2016/679 de 27 de abril del Parlamento Europeo y del Consejo y de la Ley Orgánica 3/2018, de 5 de diciembre, de Protección de Datos Personales y garantía de los derechos digitales, al inscribirte a esta oferta y/o enviarnos tu CV, con tus datos personales, éstos serán gestionados durante la realización del proceso de selección al que estás participando. xcskxlj Puedes revisar nuestra política de privacidad a través de así como ejercer tus derechos de acceso, rectificación, portabilidad, cancelación y oposición en cualquier momento accediendo a , o bien a través de comunicación por escrito a la siguiente dirección: Avinguda Diagonal, 615, 08028 Barcelona, a la atención del departamento legal.

Key Responsibilities Envíe su solicitud a continuación después de leer todos los detalles y la información de apoyo sobre esta oportunidad de trabajo. • Acting as the key liaison between the Spanish entity, the external accounting firm, and the Finance & Accounting Department of the parent company in Poland, • Serving as the primary local business partner for all accounting and tax‑related matters, providing expert support to operational and management teams, • Reviewing accounting reports and documentation prepared by the external accounting firm to ensure accuracy and compliance with local regulations and group standards, • Coordinating and supporting the resolution of accounting issues, clarifying discrepancies, and ensuring effective communication between all stakeholders, • Reconciling accounts and preparing financial data for internal reporting and audits, • Advanced proficiency in MS Office, • Experience working with ERP systems (preferably SAP), • Strong knowledge of Spanish accounting regulations and tax compliance, • Fluent Spanish and communicative English (spoken and written), • Excellent organizational and communication xcskxlj skills, with the ability to work independently in a multicultural environment, • Experience in ERP system implementation, • Experience in accounting process migration or transformation projects

En pocas palabras Obtenga más información sobre este puesto leyendo los detalles a continuación y luego envíe su solicitud para ser considerado. Posición: Técnico/a Garantía de Calidad Localización: Azuqueca de Henares. Experiencia: 2 a 4 años en funciones similares. ¿Quieres saber más? INSUD PHARMA opera en toda la cadena de valor farmacéutica, aportando conocimientos especializados y experiencia en investigación científica, desarrollo, fabricación, venta y comercialización de una amplia gama de principios activos farmacéuticos (API), formas farmacéuticas acabadas (FDF) y productos farmacéuticos de marca, 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. INSUD PHARMA cree en la innovación y el desarrollo sostenible. ¿Preparado para ser un #Challenger? ¿Qué buscamos? El Técnico/a de Garantía de Calidad que trabajará en el área de Sistemas de Calidad de la planta. ¡El reto! Gestión de las desviaciones de la planta Gestión de OOS/OOT y eventos de calidad de la planta Revisión de investigaciones de las áreas de Operaciones y Laboratoriales Evaluación de impacto de calidad de lotes asociados a desviaciones Evaluación de acciones correctivas/preventivas soportando las demás áreas de la planta de manera a asegurar la recurrencia de desviaciones Evaluación de tendencias de desviaciones de la planta Preparación de Análisis de Riesgos Preparación y/o revisión de PQR Gestión de Controles de Cambios Revisión y/o aprobación de documentación de control de calidad Gestión de PNT Reporte de KPIs Soporte en auditorias externas, inspecciones y auditorias internas Soporte en actividades del sistema de calidad ¿Qué necesitas? Graduado en Química, Farmacia o graduación asociadas a Ciencias Farmacéuticas Máster en Farmacia, Química o titulación científica relacionada con las Ciencias Farmacéuticas Ingles fluido Conocimiento SAP, herramientas de IA ¡Nuestros beneficios! Contrato indefinido Atractivo paquete salarial. Seguro de vida y accidentes. Comedor de empresa (gratuito). Copago en el seguro voluntario de salud. Club de Beneficios y Ahorro. xcskxlj Planes de desarrollo, política de movilidad interna. ¡Muchos más!

En pocas palabras Obtenga más información sobre este puesto leyendo los detalles a continuación y luego envíe su solicitud para ser considerado. Posición: Técnico/a Garantía de Calidad Localización: Azuqueca de Henares. Experiencia: 2 a 4 años en funciones similares. ¿Quieres saber más? INSUD PHARMA opera en toda la cadena de valor farmacéutica, aportando conocimientos especializados y experiencia en investigación científica, desarrollo, fabricación, venta y comercialización de una amplia gama de principios activos farmacéuticos (API), formas farmacéuticas acabadas (FDF) y productos farmacéuticos de marca, 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. INSUD PHARMA cree en la innovación y el desarrollo sostenible. ¿Preparado para ser un #Challenger? ¿Qué buscamos? El Técnico/a de Garantía de Calidad que trabajará en el área de Sistemas de Calidad de la planta. ¡El reto! Gestión de las desviaciones de la planta Gestión de OOS/OOT y eventos de calidad de la planta Revisión de investigaciones de las áreas de Operaciones y Laboratoriales Evaluación de impacto de calidad de lotes asociados a desviaciones Evaluación de acciones correctivas/preventivas soportando las demás áreas de la planta de manera a asegurar la recurrencia de desviaciones Evaluación de tendencias de desviaciones de la planta Preparación de Análisis de Riesgos Preparación y/o revisión de PQR Gestión de Controles de Cambios Revisión y/o aprobación de documentación de control de calidad Gestión de PNT Reporte de KPIs Soporte en auditorias externas, inspecciones y auditorias internas Soporte en actividades del sistema de calidad ¿Qué necesitas? Graduado en Química, Farmacia o graduación asociadas a Ciencias Farmacéuticas Máster en Farmacia, Química o titulación científica relacionada con las Ciencias Farmacéuticas Ingles fluido Conocimiento SAP, herramientas de IA ¡Nuestros beneficios! Contrato indefinido Atractivo paquete salarial. Seguro de vida y accidentes. Comedor de empresa (gratuito). Copago en el seguro voluntario de salud. Club de Beneficios y Ahorro. xcskxlj Planes de desarrollo, política de movilidad interna. ¡Muchos más!

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

Astek is looking for a Senior Scrum Master to work with our partner in the pharmaceutical sector, supporting agile delivery and fostering high-performing teams while driving digital transformation in an international environment. Envíe su solicitud a continuación después de leer todos los detalles y la información de apoyo sobre esta oportunidad de trabajo. Who are you? We are looking for someone with the following knowledge and experience: • 5–6 years of experience working in Agile environments, with at least 3–4 years as a Scrum Master, • Solid experience applying Scrum principles and facilitating agile ceremonies (Sprint Planning, Daily, Review, Retrospective), • Ex7erience working with multiple Scrum teams simultaneously in complex environments, • Previous experience in large or regulated organizations (pharma, healthcare, finance, etc.), • Experience using agile tools such as Jira and Confluence, • Strong facilitation, coaching, and stakeholder management skills, • Ability to identify and remove impediments and help teams continuously improve, • Experience working with frameworks such as Kanban or scaled environments like SAFe is a plus, • Scrum certifications such as Professional Scrum Master (PSM) or Certified ScrumMaster (CSM) are considered an advantage Who are you? We are looking for someone with the following knowledge and experience: • 5–6 years of experience working in Agile environments, with at least 3–4 years as a Scrum Master, • Solid experience applying Scrum principles and facilitating agile ceremonies (Sprint Planning, Daily, Review, Retrospective), • Experience working with multiple Scrum teams simultaneously in complex environments, • Previous experience in large or regulated organizations (pharma, healthcare, finance, etc.), • Experience using agile tools such as Jira and Confluence, • Strong facilitation, coaching, and stakeholder management skills, • Ability to identify and remove impediments and help teams continuously improve, • Experience working with frameworks such as Kanban or scaled environments like SAFe is a plus, • Scrum certifications such as Professional Scrum Master (PSM) or Certified ScrumMaster (CSM) are considered an advantage Who are we? Since 2015, Astek Iberia has been accompanying its customers in their development throughout Spain (Madrid, Barcelona, Valencia, Basque Country, Andalusia, Galicia, etc.). Founded in France in 1988, Astek is a global player in engineering and technology consulting, present in five continents and 25 countries. With expertise in a wide range of industrial and service sectors, Astek is an essential partner, supporting its customers in an intelligent deployment of their products and services, and in the implementation of their digital transformation. Today we are more than 8,000 employees, committed every day to promote the complementarity between digital technologies and complex systems engineering. Our style is to have flexible schedules and highly value the well-being of our employees. Why join us? You will grow professionally in a company in constant development and evolution. You will benefit from a personalized follow-up of your professional projects as close as possible to your ambitions. You will make a real contribution to the company's development in real time. You will enjoy 23 days of vacation (in addition to holidays) that you will be able to choose whenever you want. You will join our team: diverse, multicultural and constantly growing. You will have days full of good energy and good atmosphere. ...although you still have a lot to discover! Shall we meet? If you want to participate in the process, apply from here attaching your CV (in English) as detailed as possible and we will tell you more. xcskxlj Hay opciones de teletrabajo/trabajo desde casa disponibles para este puesto.

Who are we? Amaris Consulting is an independent technology consulting firm providing guidance and solutions to businesses. With more than 1,000 clients across the globe, we have been rolling out solutions in major projects for over a decade – this is made possible by an international team of 7,600 people spread across 5 continents and more than 60 countries. Our solutions focus on four different Business Lines: Information System & Digital, Telecom, Life Sciences and Engineering. We’re focused on building and nurturing a top talent community where all our team members can achieve their full potential. Amaris is your steppingstone to cross rivers of change, meet challenges and achieve all your projects with success. ¿Está pensando en solicitar este empleo? No se demore, desplácese hacia abajo y envíe su solicitud lo antes posible para no perder la oportunidad. About the Role We’re looking for a hands-on Senior DAM Developer, serving as the single source of truth for digital assets across an international organization. This is a builder role: you will design, develop, and deploy features — not just configure or coordinate. You’ll work closely with Product and business teams in a global, fast-paced environment, delivering real impact from day one. What You’ll Do • Build and deploy custom features inside Aprimo (workflows, metadata models, UI extensions, APIs), • Extend platform capabilities to support global digital use cases, • Improve asset lifecycle management (ingestion → transformation → distribution) Integrations & APIs • Design and implement REST / GraphQL integrations, • Connect Aprimo with CMS, PIM, and downstream platforms, • Ensure real-time asset and metadata synchronization Performance & Scalability • Optimize search, indexing, and caching for high performance, • Improve system responsiveness and global scalability, • Implement monitoring, alerting, and reliability best practices Governance & Security • Implement role-based access controls and permissions, • Ensure compliance with enterprise security and audit standards, • Support digital rights management (DRM) Collaboration • Translate business needs into technical solutions with Product Owners, • Participate in Agile ceremonies (sprint planning, code reviews, retrospectives), • Contribute to continuous improvement of the platform What You Bring Must-Have • 5+ years of hands-on software development experience, • Strong skills in:, • JavaScript (preferred), • Java (nice to have), • Experience customizing/extending:, • DAM or CMS platforms (Aprimo, AEM, Bynder, etc.), • Solid experience with:, • REST APIs / GraphQL / webhooks, • Experience working in cloud environments (AWS, Azure or GCP), • Familiarity with CI/CD pipelines, • Strong ownership, autonomy, and problem-solving mindset, • Fluent English Nice to Have • Experience with Aprimo DAM (strong advantage), • Experience integrating with Veeva CRM / Vault, • Knowledge of metadata standards (IPTC, XMP), • Experience with Digital Rights Management (DRM), • Background in regulated industries (pharma, healthcare, cosmetics) Ideal Profile A developer who can quickly understand an existing platform and start building impactful improvements from day one, with a strong hands-on and delivery-oriented mindset. WHY US? Join our dynamic team of talented individuals and experience a world of growth and opportunities. Here's what we offer: • Rapid growth with a tailored career path and salary evaluation; 70% of our senior leaders started at entry level., • Enhance your skills with our Tech Academy catalog, Udemy E-learning Platform, Language Sessions, webinars, and workshops., • Control your training with an annual personal budget and company-paid certifications., • Enjoy flexible policies, remote work options, and fantastic social benefits like transit and restaurant tickets, kindergarten support, and private health insurance., • Benefit from our WeCare program, supporting employees in critical situations., • Unleash your full potential, both professionally and personally. Amaris Consulting is proud to be an equal-opportunity workplace. We are committed to promoting diversity within the workforce and creating an inclusive working environment. For this purpose, we welcome applications from all qualified candidates regardless of gender, sexual orientation, race, ethnicity, beliefs, age, marital status, disability, or other characteristics. Take the next step in your career and become a key player in driving change at Amaris Consulting. xcskxlj Apply now to embark on a journey of professional growth and personal fulfillment.

Desde Inscríbase rápido, consulte la descripción completa desplazándose hacia abajo para conocer todos los requisitos de este puesto. Hays estamos colaborando con una compañía que busca incorporar un/a SAP Senior Consultant con perfil de Project Lead , para asumir un rol clave en un proyecto SAP estratégico . Buscamos a una persona con experiencia, liderazgo y capacidad para tomar las riendas de un proyecto complejo y hacerlo avanzar con criterio y orden. Tu reto: Ser la figura referente SAP , liderando implementaciones, estabilizando el entorno, resolviendo incidencias críticas y asegurando la correcta adopción por parte del negocio. Responsabilidades Gestión del ciclo completo del proyecto SAP Experiencia en integraciones SAP Toma de requisitos, diseño funcional y técnico Parametrización, validación y documentación Formación a usuarios y soporte evolutivo Gestión y resolución de incidencias Identificación y definición de desarrollos necesarios Coordinación con equipos internos Liderar y pilotar implementaciones SAP de principio a fin Experiencia en post go live Entorno tecnológico Entorno SAP privado Módulos: SD, MM, PP, WM, QA Foco principal en producción y logística (SD / MM) Conocimientos en FI/CO valorables pero no críticos Perfil buscado Experiencia sólida en implantaciones SAP end-to-end Experiencia en entornos industriales, Pharma o Alimentación muy valorable Inglés B2 (no mandatorio) Qué ofrecen Teletrabajo híbrido: flexibilidad Proyecto estable, con alta visibilidad y autonomía Posición con recorrido y peso dentro de la organización Si buscas un reto profesional donde tu experiencia sea realmente decisiva, esta puede ser tu próxima oportunidad. xcskxlj Aplica directamente o escríbeme por LinkedIn para más información.

At Astek, we are seeking a SAT Tester to collaborate with our partner in the pharmaceutical industry in an international setting Siga leyendo para descubrir lo que necesitará para tener éxito en este puesto, incluyendo habilidades, cualificaciones y experiencia. Your mission, should you choose to accept it… • Design and execute System Acceptance Tests (SAT) in GxP environments., • Perform both manual and automated testing., • Ensure traceability between requirements, test cases, and results., • Identify, document, and track defects., • Collaborate with validation teams to ensure compliance with regulatory standards., • Contribute to the testing strategy and the continuous improvement of testing processes. Who are you? We are looking for someone with the following knowledge and experience: • Solid experience in testing and validation within the pharmaceutical industry., • Experience in manual and automated testing., • Knowledge of GxP and the validation lifecycle., • Familiarity with test automation tools (e.g., Selenium, Cypress, or equivalents)., • Experience with CI/CD pipelines., • Knowledge of CSV and validation documentation., • Fluency in English and strong collaboration skills in international teams Who are we? Since 2015, Astek Iberia has been accompanying its customers in their development throughout Spain (Madrid, Barcelona, Valencia, Basque Country, Andalusia, Galicia, etc.). Founded in France in 1988, Astek is a global player in engineering and technology consulting, present in five continents and 25 countries. With expertise in a wide range of industrial and service sectors, Astek is an essential partner, supporting its customers in an intelligent deployment of their products and services, and in the implementation of their digital transformation. Today we are more than 8,000 employees, committed every day to promote the complementarity between digital technologies and complex systems engineering. Our style is to have flexible schedules and highly value the well-being of our employees. Why join us? You will grow professionally in a company in constant development and evolution. You will benefit from a personalized follow-up of your professional projects as close as possible to your ambitions. You will make a real contribution to the company's development in real time. You will enjoy 23 days of vacation (in addition to holidays) that you will be able to choose whenever you want. You will join our team: diverse, multicultural and constantly growing. You will have days full of good energy and good atmosphere. ...although you still have a lot to discover! Shall we meet? xcskxlj If you want to participate in the process, apply from here attaching your CV (in English) as detailed as possible and we will tell you more.

At ¿Todo listo para enviar su solicitud? Por favor, lea la descripción al menos una vez antes de hacer clic en "Solicitar". Astek , we are looking for a Senior IT Project Manager to join a high-impact international initiative with one of our key partners in the pharmaceutical industry . You will be part of a global program with teams distributed across Europe, the US, and China , collaborating with multiple IT and business stakeholders in a highly regulated environment (Pharma R&D). Main Responsibilities Coordinate project timelines, deliverables, and financial activities across multiple R&D IT systems Support the execution of system changes aligned with program objectives Act as a primary point of contact for global stakeholders (EU/US/Asia) Ensure alignment and communication across distributed teams Prepare program-level reports (status, risks, dependencies, progress) Anticipate risks, propose mitigation strategies, and drive resolution Contribute to governance activities and continuous improvement within the program Who You Are 5+ years of experience managing IT projects in international or multicultural environments Experience in Pharma, Life Sciences, Biotech, or regulated environments (highly valued) Project Management certifications ( PMP or PRINCE2 Practitioner ) Solid understanding of Waterfall and Agile methodologies (Scrum, Kanban) Knowledge of ITIL and IT Service Delivery practices Hands-on experience with tools such as ServiceNow (SNOW) , HPSM , Jira Exposure to Release / Change Management processes Excellent communication and stakeholder management skills English C1/C2 (global environment) Availability to travel if required Why Join Us? Grow professionally in a company in constant evolution 100% Remote position Personalized follow-up to support your career path Real impact on projects and company development 23 vacation days (plus local holidays), fully flexible Diverse, multicultural, and growing team Great energy, supportive environment, and people who care …and much more to discover! Interested? Let’s talk! If you'd like to join the process, apply through this offer and attach your English CV . xcskxlj We’ll contact you to share more details about the role and the project.

Cyber Security Engineer, Braine (Belgium), Site Based Aumente sus posibilidades de conseguir una entrevista leyendo la siguiente descripción general de este puesto antes de presentar su candidatura. Cognizant Company is a world leader in delivering digital transformation solutions to Life Sciences. Through our knowledge and expertise in Automation, MES & Digital, we deliver stable manufacturing systems that are optimized to improve operational efficiencies, whilst maintaining compliance. Our specialist engineering teams have the aptitude to deliver and support Pharma architectures and solutions covering all IT, OT and IoT applications, infrastructures and services. About the role: We are seeking an OT Engineer who play a key role in supporting OT Security BAU team within a regulated manufacturing environment. The purpose of the role is to ensure accurate and up-to-date documentation, align procedures across sites, and contribute to overall cyber security governance. The successful candidate will help drive continuous improvement of OT security controls and processes while ensuring compliance with internal standards and regulatory requirements. Responsibilities: • Ensure alignment and harmonization of cyber security procedures across global manufacturing sites., • Contribute to the governance and continuous improvement of OT security controls, including risk assessments and control effectiveness reviews. • Utilize tools such as Veeva or other regulated document management systems to manage documentation workflows in a GMP-compliant manner. • Assist in tracking and reporting progress of ongoing cyber security initiatives and ensuring alignment with the company's cyber security framework and regulatory requirements Requirements: • Strong knowledge of pharmaceutical and manufacturing systems, • Bachelor’s degree (preferred), • Automation Engineering, Information Technology, OT Cyber security, or Automation, • A foundational understanding of engineering or IT principles is essential to interpret and apply OT security standards, compliance frameworks, and technical documentation within regulated manufacturing environments. • Minimum 3 years of experience in OT Cyber security or Automation within GMP-regulated manufacturing., • Hands-on experience with governance processes, SOP development, and regulated documentation systems (e.g., Veeva)., • Familiarity with OT security frameworks (e.g., IEC 62443), network segmentation, and enabling services such as patching, antivirus, and asset inventory., • Demonstrated ability to collaborate cross-functionally with Quality, IT, and Engineering stakeholders, • The position requires an experienced professional capable of operating independently in a regulated environment, ensuring alignment of OT cyber security controls with quality and compliance expectations. Proven knowledge reduces onboarding time and enhances the team’s ability to meet global audit and regulatory requirements. • Proficiency in documentation lifecycle management • Experience with GxP and CFR Part 11 compliance, • Strong written communication and process improvement skills About Cognizant Cognizant (Nasdaq-100: CTSH) is one of the world's leading professional services companies, transforming clients' business, operating and technology models for the digital era. Our unique industry-based, consultative approach helps clients envision, build and run more innovative and efficient businesses. Headquartered in the U.S., Cognizant is ranked 185 on the Fortune 500 and is consistently listed among the most admired companies in the world. xcskxlj Learn how Cognizant helps clients lead with digital at or follow us @Cognizant.

At Oxford Global Resources, we are currently recruiting a Senior Brand Manager with solid experience in pharmaceutical environments for a pharmaceutical client in Barcelona. This is an 8‑month project to cover a leave. Para una comprensión completa de esta oportunidad y de lo que se requerirá para ser un candidato exitoso, siga leyendo. Responsibilities: • Lead global product strategy, marketing, and branding for key Cetaphil ranges., • Develop integrated 360° global activation toolboxes for product and commercial innovations., • Drive cross‑functional global teams throughout all product development phases., • Partner with key markets, scientific teams, and commercial teams to deliver strong global toolboxes and claims., • Manage project budgets, timelines, and governance with strong ownership. Qualifications: • 8–12 years of experience in global or regional Brand/Product roles within skincare, beauty, pharma., • Strong leadership and ability to influence in a global matrix environment., • Proven experience in product innovation, brand building, and digital‑first marketing., • Science‑driven mindset with strong analytical skills and ability to turn insights into action. xcskxlj, • Excellent communication skills, growth mindset, and passion for skincare and science.

Senior Data Engineer ¿Es usted el candidato adecuado para esta oportunidad? Asegúrese de leer la descripción completa a continuación. 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! xcskxlj 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.

¿Te interesaría seguir desarrollándote como Descubra exactamente qué habilidades, experiencia y cualificaciones necesitará para tener éxito en este puesto antes de enviar su solicitud a continuación. Especialista de Cualificaciones y Calibraciones en una empresa líde r del sector pharma ? Desde Oxigent Technologies seleccionamos un/a TÉCNICO/A DE CUALIFICACIONES Y CALIBRACIONES para incorporarse a esta empresa referente en investigación, desarrollo y fabricación de una amplia variedad de principios activos farmacéuticos , con sede central en Madrid . ¿Cuáles serán tus funciones principales? • Participar en la adquisición de nuevos equipos, utilidades e instalaciones y revisar/aprobar la documentación (URS, documentación del proveedor), con el fin de comprobar la correcta ejecución y finalización del trabajo. • Elaborar los documentos de cualificación (DQ, IQ, OQ y PQ) de equipos (producción e I+D) e instalaciones, utilidades (HVAC, Agua Purificada, aire comprimido y nitrógeno) cuando el trabajo lo realice personal interno. • Ejecutar/coordinar, cuando aplique, la realización de las actividades de cualificación (pruebas de ejecución/run test) y liderar cualquier desviación generada durante estas actividades. • Elaborar el plan maestro de validación asociado a las actividades de cualificación y el correspondiente plan de calibración. • Elaborar la documentación de cualificación o calibración (protocolos, análisis de riesgos, evaluación de riesgos, informes, evaluaciones, según sea necesario) y coordinar la ejecución correspondiente o ejecutarla cuando aplique. • Realizar la investigación (análisis de causa raíz) de las desviaciones relacionadas con las utilidades y las instalaciones . Definir, junto con el departamento implicado en la investigación, las acciones apropiadas y las CAPA . • Dar soporte a auditorías e inspecciones externas de acuerdo con el Plan Anual para evaluar la calidad del sistema GMP . CSV (Validación de Sistemas Informáticos): Garantiza que los sistemas informáticos en industrias reguladas (farmacéutica, dispositivos médicos) cumplan estándares de calidad, fiabilidad y requisitos regulatorios (FDA, EMA). Para ello, ¿qué vas a necesitar? 2-3 años de experiencia en departamentos de validaciones y cualificaciones , en plantas de producción. Nivel muy alto de inglés y español ; el conocimiento de otro idioma europeo también es un plus Conocimiento de procesos de fabricación, equipos de producción, instalaciones y utilidades de plantas de fabricación farmacéutica. • Conocimiento de desviaciones, análisis de causa raíz, definición de CAPA. Análisis de tendencias. Conocimiento de análisis de riesgos. Valorable: Conocimiento de procesos de fabricación, equipos de producción, instalaciones y utilidades de plantas de fabricación farmacéutica . ¿Qué te ofrecemos? Contratación indefinida. • Salario acorde a la experiencia aportada ( entre 4 euros brutos anuales ). Horario flexible. Cheque Formación para desarrollarte en las áreas profesionales que más te interesen. Seguro médico privado . Retribución flexible aplicable a seguro médico, restaurante, transporte, guardería y formación. Aplicación de acceso a gimnasios y actividades deportivas en toda España con descuentos. ¡Y muchos otros beneficios! ¡Únete al equipo de Oxigent! xcskxlj Empresa comprometida con la sostenibilidad y la igualdad de oportunidades, donde el talento y la tecnología no entienden de género.

Who are we? We are a technology-led healthcare solutions provider. We are driven by our purpose to enable healthcare organizations be future ready. We offer accelerated, global growth opportunities for talent that’s bold, industrious, and nimble. With Indegene, you gain a unique career experience that celebrates entrepreneurship, and is guided by passion, innovation, collaboration, and empathy. To explore exciting opportunities at the convergence of healthcare and technology, check out if we told you that you can move to an exciting role in an entrepreneurial organization without the usual risks associated with it? We understand that you are looking for growth in your career at this point and we would love for you to join us in our journey and grow with us. At Indegene, our roles come with the excitement you require at this stage of your career with the reliability you seek. We believe in creating leaders of tomorrow and mentor our leads to help them grow and nurture them as people managers and account managers. We are a rapidly growing global organization and are scouting for the best talent for this phase of growth. With us, you are at the intersection of two of the most exciting industries of healthcare and technology. We offer global opportunities with fast-track careers while you work with a team that is fueled by purpose. The combination of this will lead to a truly differentiated experience for you. If this excites you, then apply below. ¿Es este su próximo empleo? Descúbralo leyendo la descripción completa a continuación y no dude en enviar su candidatura. Role: Salesforce Marketing Cloud (SFMC) Developer Job Description: We are seeking an experienced SFMC Lead Developer with deep hands-on expertise across Automation Studio, Journey Builder, complex audience segmentation, Marketing Cloud Personalization (MCP), and enterprise integrations. This role is ideal for someone who is comfortable operating in a pharma environment, with strong data governance sensibilities and the ability to translate business objectives into scalable omnichannel journeys. The ideal candidate will partner closely with platform architects (e.g., CRM, Web, CMS) while leading the technical design and building for Salesforce Marketing Cloud programs. This is a hands-on technical role, not purely strategic, requiring someone who can architect, develop, troubleshoot, optimize, and operationalize journeys at scale. Key Responsibilities 1. SFMC Architecture & Development • · Execute the build and optimization of journeys in Journey Builder, including multi-branch paths, triggers, decision splits, and event-based orchestration., • · Build automations in Automation Studio, including SQL-based segmentation, scheduled automations, and data hygiene processes., • · Develop modular, compliant email and content blocks, leveraging AMPscript, SSJS, and data extensions best practices., • · Implement and optimize Einstein features and predictive capabilities within SFMC, • · Own the final audit and quality validation of campaigns executed by team members, ensuring adherence to defined processes, compliance standards, technical accuracy, and client requirements before deployment. 2. Data & Integration • Execute and maintain data models, data extensions, relational mappings, and business rules aligned with CRM, website, and analytics inputs. o WordPress VIP for personalization, tagging, and behavioral capture feeding MCP o Enterprise Data Lakes, CDPs, or analytics environments • · Ensure data dictionary, taxonomy alignment, and governance across all activation channels. 3. Marketing Cloud Personalization (MCP) • · Implement MCP tagging, site wide java scripting, custom scripting (if any) rule sets, decisioning logic, personalization recipes, and identity resolution approaches., • · Partner with web and analytics teams to ensure MCP instrumentation is clean, compliant, and aligned to journey logic., • · Optimize hybrid (rule-based + algorithmic) MCP experiences based on campaign goals. Required Qualifications • · 3–4 years of hands-on SFMC development and architecture experience at scale., • · Advanced mastery of Journey Builder, Automation Studio, SQL, AMPscript, SSJS, and SFMC data modeling., • · Proven experience with MCP implementation, including tagging, decisioning, and integration with websites (e.g., WordPress VIP)., • · Strong familiarity with Veeva CRM data structures and how CRM segments feed omnichannel journeys., • · Demonstrated experience supporting pharma or life sciences omnichannel operations., • · Comfortable working cross-platform (CRM → SFMC → Web) in complex enterprise ecosystems., • · Based in Madrid or already residing in Spain or Japan with ability for regular on-site work., • · Language proficiency required in Spanish (for Spain market) Nice to Have • · Experience with Veeva Vault / Promomats metadata or workflow integration points., • · Familiarity with data lakes, GA/GA4 analytics, and tagging plans for paid/owned channels., • · Understanding of AI-assisted accelerators for segmentation, QA, tagging, or content workflows., • · Exposure to enterprise personalization strategies across web, SFMC, and CRM ecosystems. EQUAL OPPORTUNITY: Indegene is proud to be an Equal Employment Employer and is committed to the culture of Inclusion and Diversity. We do not discriminate on the basis of race, religion, sex, colour, age, national origin, pregnancy, sexual orientation, physical ability, or any other characteristics. All employment decisions, from hiring to separation, will be based on business requirements, candidate’s merit and qualification. We are an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, colour, religion, sex, national origin, gender identity, sexual orientation, disability status, protected veteran status, or any other characteristics. xcskxlj Hay opciones de teletrabajo/trabajo desde casa disponibles para este puesto.

Take your career to the next level with Amaris Consulting as a Validation Specialist (Test QA). Become part of an international team, thrive in a global group with €800M turnover and 1,000+ clients worldwide, and an agile environment by planning the kickoff and follow up on projects. Join Amaris Consulting, where you can develop your potential and make a difference within the company. Por favor, asegúrese de leer atentamente los siguientes detalles antes de enviar cualquier solicitud. WHAT WOULD YOU NEED? • +3 years of senior experience in IT validation within GxP environments, • Proven expertise in Veeva Conformance and Validation Testing and W3C Validation, • Strong knowledge of pharma industry regulations and GxP compliance, • Experience with LeVA system life cycle documentation (VP, URS, FS, RA, Testing Reports, AAP), • Degree in Business Administration, Computer Science or comparable professional experience, • English fluency and Spanish as mother tongue is highly valued WHAT WILL YOU DO? • Lead validation activities for global testing applications (BI-AS-ODIN, BI-IT-INMATION), • Ensure compliance with validation planning and applicable BI standards before system operation, • Develop and maintain system-specific SOPs and SLC documentation, • Manage validation status throughout system lifecycle and post-operation phases, • Create and deliver training on Standard Operating Procedures as defined in Validation Plans, • Coordinate with IT Operations & Laboratories teams on Manufacturing Connectivity projects WHY US? Join our dynamic team of talented individuals and experience a world of growth and opportunities. Here's what we offer: • Grow rapidly with a tailored career path and salary evaluation. 70% of our senior leaders started at entry level., • Enhance your skills through our Tech Academy catalog, Udemy E-learning Platform, Languages Sessions, webinars, and workshops., • Take charge of your training with an annual personal budget and company-paid certifications., • Enjoy flexible policies, remote work options, and fantastic social benefits like transit and restaurant tickets, kindergarten support, and private health insurance., • Benefit from our WeCare program, supporting employees in critical situations., • Unleash your full potential, both professionally and personally Amaris Consulting is proud to be an equal-opportunity workplace. We are committed to promoting diversity within the workforce and creating an inclusive working environment. xcskxlj For this purpose, we welcome applications from all qualified candidates regardless of gender, sexual orientation, race, ethnicity, beliefs, age, marital status, disability, or other characteristics.

Cognizant is a world leader in delivering digital transformation solutions to Life Sciences. Through our knowledge and expertise in Automation, MES & Digital, we deliver stable manufacturing systems that are optimized to improve operational efficiencies, whilst maintaining compliance. A continuación, encontrará un desglose completo de todo lo que se requiere de los posibles candidatos, así como la forma de presentar su candidatura. ¡Mucha suerte! Our specialist engineering teams have the aptitude to deliver and support Pharma 4.0 architectures and solutions covering all IT, OT and IoT applications, infrastructures and services The AVEVA PI Engineer position offers the opportunity to join a multidisciplinary team that operates across multiple sites, providing support for the PI Historian Operational Service. The AVEVA PI Engineer will be an integral member of the support team, responsible for monitoring the system to ensure continuous production at the manufacturing site. Responsibilities: • Support site vertical integration defined by the Project Manager or Lead Engineer., • Create/Update the configuration and validation documents related to the PI system., • Execute the validation as defined in the change control., • Ensure data integrity and consistency by implementing data quality control, • measures and monitoring data validation processes., • Collaborate within Automation Infra team to manage system upgrades, patches, and, • performance optimizations for the OSIsoft PI system., • Handling and addressing tickets or issues associated with the PI system., • Provide maintenance to the PI system to ensure system availability 24/7., • Stay up-to-date with industry trends, emerging technologies, and regulatory, • requirements related to data engineering and manufacturing systems., • Contribute to continuous improvement initiatives, identifying opportunities to, • enhance data management processes, system performance, and user experience To apply for this PI Software Engineer role, you will need an undergraduate degree in IT, Automation, Science or Engineering, or a related discipline, or equivalent work experience. You will also require the following: • Experience working with the OSIsoft PI system, ideally within the pharmaceutical industry., • Understanding of pharmaceutical manufacturing processes, including batch processing, equipment automation, and data acquisition systems., • Proficiency in data engineering concepts, data integration, and data management best practices., • Ability to multitask, manage multiple projects and prioritize tasks in a busy environment, • Experience with programming languages (e.g., Python, SQL) and scripting is advantageous., • Experience with ticketing systems such as Service Now or similar The Cognizant community: We are a high caliber team who appreciate and support one another. Our people uphold an energetic, collaborative and inclusive workplace where everyone can thrive. • Cognizant is a global community with more than 300,000 associates around the world., • We don’t just dream of a better way – we make it happen., • We take care of our people, clients, company, communities and climate by doing what’s right., • We foster an innovative environment where you can build the career path that’s right for you. About us: Cognizant is one of the world's leading professional services companies, transforming clients' business, operating, and technology models for the digital era. Our unique industry-based, consultative approach helps clients envision, build, and run more innovative and efficient businesses. xcskxlj Headquartered in the U.S., Cognizant (a member of the NASDAQ-100 and one of Forbes World’s Best Employers 2024) is consistently listed among the most admired companies in the world. Learn how Cognizant helps clients lead with digital at

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

Omega CRM Consulting is looking for a ServiceNow developer that would like to collaborate with one of the top global pharmaceutical companies. ¿Está considerando presentar su candidatura para este trabajo? Compruebe todos los detalles en esta descripción del puesto y luego haga clic en "Solicitar". • Responsible for the development, configuration, testing, and general administration of the ServiceNow platform., • Experienced in customizing applications, workflows, dashboards, and Service Portals., • Main duties include incident and request management, access control implementation (ACLs), platform testing and validation, technical support, performance analysis, and process documentation., • Collaborates with cross-functional teams and clients to gather requirements, propose solutions, and ensure alignment with business needs., • Stays up to date with ServiceNow capabilities and best practices. Key Skills & Experience: • 3+ years of experience in ServiceNow development., • Proficient in JavaScript, GlideScript, HTML/XML, and ServiceNow APIs., • Hands-on experience with core modules and custom app development., • Solid understanding of ServiceNow architecture, ITIL processes, and relational databases., • Experience in testing and validating ServiceNow solutions for functionality and performance., • Familiar with Agile methodologies and DevOps practices., • Strong communication skills in English., • Analytical, proactive, and team-oriented mindset. What do We offer • Permanent contract., • Flexible Schedule. We make it easy. Balance your professional and personal life., • Trainings & Certifications. Improve your skills and get the official certificate from our main partners., • Home Office., • Flexible retribution (public transport ticket, Ticket restaurant, …)., • Health insurance., • OMEGA in action. Our commitment to a better society is not just an intention. About us Omega CRM, a Merkle Company, is a global digital company specialising in accelerating the Business Experience (BX) of our clients through customer-centric solutions, technology, and data – all enhanced by AI. Together with Merkle, we form the largest Customer Experience Management (CXM) agency in Spain, and as part of the dentsu group, we offer end-to-end solutions that integrate media, creativity, content, technology, and strategy to deliver real business impact. With over 23 years of experience, a team of 580+ professionals from 24 nationalities, and 2,500+ certifications, Omega CRM is a recognised leader in the Salesforce ecosystem in Spain. We operate across key industries including Retail, Healthcare, Pharma, Real Estate, Education, and Non-Profit, delivering omnichannel experiences in Customer Service, eCommerce, Marketing, and Analytics. Client satisfaction is at our core (rating: 4.9/5), and we’ve been recognised with awards such as Salesforce Partner of the Year FY23 and Most Innovative Project (Iberia). At Omega CRM, we believe in growth through people – guided by our values: #Talent, #Flexibility, #Commitment, and #Innovation. xcskxlj We grow #Together.

Omega CRM is a Merkle & Dentsu company, leader in development of Customer Experience services, with +20 years of experience in the use of Technology applied to Marketing and providing a unique Customer Relationship with mainly focus on Innovation is looking for a Salesforce Technical Lead. Cualquier información adicional que necesite para este trabajo se encuentra en el texto a continuación. Asegúrese de leerla detenidamente y luego envíe su solicitud. MAIN TASKS: Provide support to the sales and functional team in assigned accounts when technical knowledge of the solution is required: Solution design, estimation, and assumptions. Support the PM/DM in technical leadership on the project, bringing comprehensive technical knowledge of the platform and identifying the best solution to meet the project's functional demands. Detect and notify risks in the technical management of project/client profitability. Ensure the smooth progress of the project in terms of Scope, Schedule, and Costs. Alerting and anticipating possible deviations to the Project Manager/Delivery Manager. Ensure the fulfillment of the project's technical objectives. Ensure compliance with the agreed software quality standards with Omega's Technical Management. Supervise the effort estimations of the development and support team during the testing phase of a project. Collaborate with the PM/DM in project demos for the client. Ensure the final delivery of technical documentation for a project. Participate in the development and training of the technical team, advising them to improve their technical skills. Identify possible technical Up & Cross Selling opportunities. Identify possible methodological improvements for the technical team. Collaborate in Omega's community of practice, providing thought leadership, training, and mentoring to other collaborators to develop technical capabilities. REQUIRED EXPERIENCE: 3+ years participating in the full lifecycle of implementations. Experience in projects. Experience in the different modules: Sales Cloud, Service Cloud, Marketing Cloud, Experience with agile methodologies. High level of English. WHAT DO WE OFFER Permanent contract. Flexible Schedule. We make it easy. Balance your professional and personal life. Certifications plan. Improve your skills and get the official certificate from our main partners. Home Office. You decide and we support you. Flexible retribution (public transport ticket, Ticket restaurtant, …). Health insurance. OMEGA in action. Our commitment to a better society is not just an intention Professional development: Evolve, grow and get where you want to go. About us Omega CRM, a Merkle Company, is a global digital company specialising in accelerating the Business Experience (BX) of our clients through customer-centric solutions, technology, and data – all enhanced by AI. Together with Merkle, we form the largest Customer Experience Management (CXM) agency in Spain, and as part of the dentsu group, we offer end-to-end solutions that integrate media, creativity, content, technology, and strategy to deliver real business impact. With over 23 years of experience, a team of 580+ professionals from 24 nationalities, and 2,500+ certifications, Omega CRM is a recognised leader in the Salesforce ecosystem in Spain. We operate across key industries including Retail, Healthcare, Pharma, Real Estate, Education, and Non-Profit, delivering omnichannel experiences in Customer Service, eCommerce, Marketing, and Analytics. Client satisfaction is at our core (rating: 4.9/5), and we’ve been recognised with awards such as Salesforce Partner of the Year FY23 and Most Innovative Project (Iberia). At Omega CRM, we believe in growth through people – guided by our values: #Talent, #Flexibility, #Commitment, and #Innovation. xcskxlj We grow #Together.

IF YOU ARE INTERESTED, PLEASE SHARE YOUR CV IN ENGLISH LANGUAGE ONLY! Si desea conocer los requisitos para este puesto, siga leyendo para obtener toda la información relevante. Who are we? We are a technology-led healthcare solutions provider. We are driven by our purpose to enable healthcare organizations be future ready. We offer accelerated, global growth opportunities for talent that’s bold, industrious, and nimble. With Indegene, you gain a unique career experience that celebrates entrepreneurship, and is guided by passion, innovation, collaboration, and empathy. To explore exciting opportunities at the convergence of healthcare and technology, check out if we told you that you can move to an exciting role in an entrepreneurial organization without the usual risks associated with it? We understand that you are looking for growth in your career at this point and we would love for you to join us in our journey and grow with us. At Indegene, our roles come with the excitement you require at this stage of your career with the reliability you seek. We believe in creating leaders of tomorrow and mentor our leads to help them grow and nurture them as people managers and account managers. We are a rapidly growing global organization and are scouting for the best talent for this phase of growth. With us, you are at the intersection of two of the most exciting industries of healthcare and technology. We offer global opportunities with fast-track careers while you work with a team that is fueled by purpose. The combination of this will lead to a truly differentiated experience for you. If this excites you, then apply below. Role: KAM - Marketing Automation IF YOU ARE INTERESTED, PLEASE SHARE YOUR CV IN ENGLISH LANGUAGE ONLY! Role Overview We are seeking a Project Manager with strong functional and operational understanding of Salesforce Marketing Cloud campaign operations, Veeva CRM workflows, and the end-to-end Closed Loop Marketing (CLM) asset lifecycle within a pharma / life sciences environment. This role focuses on managing delivery, operational governance, and compliance across campaign operations and CLM programs rather than hands-on technical configuration. Key Responsibilities Campaign Operations – SFMC · Manage complete campaign intake and briefing process with marketing stakeholders. · Validate scope, segmentation requirements, and dependencies before campaign build. · Coordinate with data, content, and deployment teams to ensure timely execution. · Oversee QA cycles, proof approvals, and deployment readiness checks. · Ensure alignment to campaign calendars and SLA commitments. · Track campaign performance reporting and ensure insights are shared with business teams. · Identify process improvement opportunities within campaign operations workflow. Veeva CRM Operations · Manage CRM-related operational initiatives impacting field users. · Coordinate updates to customer data, territory alignment, and targeting inputs (as applicable). · Oversee CRM enhancement requests and ensure proper documentation and prioritization. · Align with sales operations to ensure readiness before new deployments. · Monitor CRM adoption metrics and escalate operational challenges. · Act as liaison between business users and technical teams for requirement clarification. CLM Asset Lifecycle Management · Manage end-to-end CLM asset lifecycle: intake → content development → MLR review → approval → deployment → tracking. · Coordinate agency partners and internal teams for timely content creation. · Track MLR submissions, feedback cycles, and approval timelines. · Ensure proper version control and archival of approved materials. · Coordinate field force rollout planning and deployment scheduling. · Monitor asset engagement data and support business performance reviews. · Ensure all documentation supports audit and compliance requirements. Project Governance & Stakeholder Management · Develop project plans, timelines, and milestone tracking. · Maintain RAID logs (Risks, Assumptions, Issues, Dependencies). · Provide structured weekly status reporting and executive updates. · Manage cross-functional stakeholders across Marketing, Medical, Legal, Regulatory (MLR), IT, and Sales Operations. · Drive continuous improvement initiatives across operational workflows. EQUAL OPPORTUNITY: Indegene is proud to be an Equal Employment Employer and is committed to the culture of Inclusion and Diversity. We do not discriminate on the basis of race, religion, sex, colour, age, national origin, pregnancy, sexual orientation, physical ability, or any other characteristics. All employment decisions, from hiring to separation, will be based on business requirements, candidate’s merit and qualification. We are an Equal Opportunity Employer. xcskxlj All qualified applicants will receive consideration for employment without regard to race, colour, religion, sex, national origin, gender identity, sexual orientation, disability status, protected veteran status, or any other characteristics.

INSUD PHARMA opera en toda la cadena de valor farmacéutica, aportando conocimientos especializados y experiencia en investigación científica, desarrollo, fabricación, venta y comercialización de una amplia gama de principios activos farmacéuticos (API), formas farmacéuticas acabadas (FDF) y p

Provide documentation, technical playbooks, and training for marketing, operations, and downstream teams. We are seeking an experienced SFMC Lead Developer with deep hands-on expertise across Automation Studio, Journey Builder, complex audience segmentation, Marketing Cloud Personalization (MCP), an

¡En Grupo Cibernos seguimos creciendo! ¿Le interesa este puesto? Puede encontrar toda la información relevante en la descripción a continuación. Estamos buscando un Key Account Manager para incorporarse a nuestra unidad de Selección de Talento. Sobre nuestra unidad En esta división ayudamos a las empresas a identificar, atraer y contratar profesionales para reforzar sus equipos, desde posiciones operativas hasta roles de gestión. Tenemos amplia experiencia en la búsqueda de talento especializado en IT, Ingeniería y disciplinas técnicas, y estamos en plena expansión hacia sectores como Pharma & Healthcare y otros mercados estratégicos. Además, disponemos de nuestro Programa de Relocation internacional “Salta Conmigo”, que facilita la incorporación de profesionales procedentes de otros países. ¿Cuál será tu misión como Key Account Manager? • Gestionar y potenciar las cuentas activas que ya trabajan con nosotros., • Desarrollar nuevas oportunidades de negocio y captar clientes en los sectores objetivo Pharma&Healthcare., • Promocionar nuestros servicios de selección (selección directa y outsourcing)., • Posicionar a Cibernos como un socio estratégico para la captación de talento., • Además, tendrás la posibilidad de ofrecer cualquier solución o servicio del ecosistema Cibernos. ¿Qué ofrecemos? • Contrato indefinido., • Paquete retributivo compuesto por fijo + bonus anual., • Horario flexible y trabajo en modalidad híbrida., • Jornada intensiva de verano (del 15 de junio al 15 de septiembre). xcskxlj, • 22 días laborables de vacaciones al año. Nos encantaría conocerte y explorar juntos esta oportunidad.

Position: Data ScientistINSUD 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. ¿Está considerando presentar su candidatura para este trabajo? Compruebe todos los detalles en esta descripción del puesto y luego haga clic en "Solicitar". 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. 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. 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.The office is located in central Madrid (Chamberí, near Eloy Gonzalo), well connected and situated in a vibrant part of the city. Each project is run by a small group — typically a Product Manager, a Data Scientist, an Engineer, and key stakeholders. 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. 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.Experience with version control systems (e.g., 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. Flexible start time from Monday to Friday#Permanent contract.#Training and language learning platform#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. xcskxlj Follow us on social media like LinkedIn/Instagram and stay tuned for any offers we may release; 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.

Position: Data ScientistINSUD 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),

En pocas palabras Obtenga más información sobre este puesto leyendo los detalles a continuación y luego envíe su solicitud para ser considerado. Posición: Técnico/a Garantía de Calidad Localización: Azuqueca de Henares. Experiencia: 2 a 4 años en funciones similares. ¿Quieres saber más? INSUD PHARMA opera en toda la cadena de valor farmacéutica, aportando conocimientos especializados y experiencia en investigación científica, desarrollo, fabricación, venta y comercialización de una amplia gama de principios activos farmacéuticos (API), formas farmacéuticas acabadas (FDF) y productos farmacéuticos de marca, 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. INSUD PHARMA cree en la innovación y el desarrollo sostenible. ¿Preparado para ser un #Challenger? ¿Qué buscamos? El Técnico/a de Garantía de Calidad que trabajará en el área de Sistemas de Calidad de la planta. ¡El reto! Gestión de las desviaciones de la planta Gestión de OOS/OOT y eventos de calidad de la planta Revisión de investigaciones de las áreas de Operaciones y Laboratoriales Evaluación de impacto de calidad de lotes asociados a desviaciones Evaluación de acciones correctivas/preventivas soportando las demás áreas de la planta de manera a asegurar la recurrencia de desviaciones Evaluación de tendencias de desviaciones de la planta Preparación de Análisis de Riesgos Preparación y/o revisión de PQR Gestión de Controles de Cambios Revisión y/o aprobación de documentación de control de calidad Gestión de PNT Reporte de KPIs Soporte en auditorias externas, inspecciones y auditorias internas Soporte en actividades del sistema de calidad ¿Qué necesitas? Graduado en Química, Farmacia o graduación asociadas a Ciencias Farmacéuticas Máster en Farmacia, Química o titulación científica relacionada con las Ciencias Farmacéuticas Ingles fluido Conocimiento SAP, herramientas de IA ¡Nuestros beneficios! Contrato indefinido Atractivo paquete salarial. Seguro de vida y accidentes. Comedor de empresa (gratuito). Copago en el seguro voluntario de salud. Club de Beneficios y Ahorro. xcskxlj Planes de desarrollo, política de movilidad interna. ¡Muchos más!

At Por favor, presente su candidatura sin demora si su perfil encaja bien con este puesto, debido al alto nivel de interés. Astek , we are looking for a Senior IT Project Manager to join a high-impact international initiative with one of our key partners in the pharmaceutical industry . You will be part of a global program with teams distributed across Europe, the US, and China , collaborating with multiple IT and business stakeholders in a highly regulated environment (Pharma R&D). Main Responsibilities Coordinate project timelines, deliverables, and financial activities across multiple R&D IT systems Support the execution of system changes aligned with program objectives Act as a primary point of contact for global stakeholders (EU/US/Asia) Ensure alignment and communication across distributed teams Prepare program-level reports (status, risks, dependencies, progress) Anticipate risks, propose mitigation strategies, and drive resolution Contribute to governance activities and continuous improvement within the program Who You Are 5+ years of experience managing IT projects in international or multicultural environments Experience in Pharma, Life Sciences, Biotech, or regulated environments (highly valued) Project Management certifications ( PMP or PRINCE2 Practitioner ) Solid understanding of Waterfall and Agile methodologies (Scrum, Kanban) Knowledge of ITIL and IT Service Delivery practices Hands-on experience with tools such as ServiceNow (SNOW) , HPSM , Jira Exposure to Release / Change Management processes Excellent communication and stakeholder management skills English C1/C2 (global environment) Availability to travel if required Why Join Us? Grow professionally in a company in constant evolution 100% Remote position Personalized follow-up to support your career path Real impact on projects and company development 23 vacation days (plus local holidays), fully flexible Diverse, multicultural, and growing team Great energy, supportive environment, and people who care …and much more to discover! Interested? Let’s talk! If you'd like to join the process, apply through this offer and attach your English CV . We’ll contact you to share more details about the role and the project. xcskxlj Hay opciones de teletrabajo/trabajo desde casa disponibles para este puesto.

Pharma, Life Sciences, Biotech, or regulated environments (highly valued). Great energy, supportive environment, and people who care. Por favor, presente su candidatura sin demora si su perfil encaja bien con este puesto, debido al alto nivel de interés.

Position: Data ScientistINSUD 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. ¿Está considerando presentar su candidatura para este trabajo? Compruebe todos los detalles en esta descripción del puesto y luego haga clic en "Solicitar". 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. 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. 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.The office is located in central Madrid (Chamberí, near Eloy Gonzalo), well connected and situated in a vibrant part of the city. Each project is run by a small group — typically a Product Manager, a Data Scientist, an Engineer, and key stakeholders. 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. 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.Experience with version control systems (e.g., 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. Flexible start time from Monday to Friday#Permanent contract.#Training and language learning platform#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. xcskxlj Follow us on social media like LinkedIn/Instagram and stay tuned for any offers we may release; 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.

Nos encontramos actualmente en búsqueda de un Pharmacy Sales Representative de nuestra línea de productos de dermatología. LETI Pharma promueve el desarrollo profesional y personal de todas las personas colaboradoras, asegurando la igualdad de oportunidades en todos los procesos y normativa inter