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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. ¿Es usted el candidato adecuado para esta oportunidad? Asegúrese de leer la descripción completa a continuación. 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.

pTake your career to the next level with Amaris Consulting as a bValidation Specialist (Test QA) /b. 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. /ppbr/ppbWHAT WOULD YOU NEED? ✍️ /b /pulli+3 years of senior experience in IT validation within GxP environments /liliProven expertise in bVeeva Conformance and Validation Testing /b and bW3C Validation /b /liliStrong knowledge of pharma industry regulations and GxP compliance /liliExperience with LeVA system life cycle documentation (VP, URS, FS, RA, Testing Reports, AAP) /liliDegree in Business Administration, Computer Science or comparable professional experience /lilibEnglish fluency /b and Spanish as mother tongue is highly valued /li /ulpbr/ppb WHAT WILL YOU DO? /b /pulliLead validation activities for global testing applications (BI-AS-ODIN, BI-IT-INMATION) /liliEnsure compliance with validation planning and applicable BI standards before system operation /liliDevelop and maintain system-specific SOPs and SLC documentation /liliManage validation status throughout system lifecycle and post-operation phases /liliCreate and deliver training on Standard Operating Procedures as defined in Validation Plans /liliCoordinate with IT Operations Laboratories teams on Manufacturing Connectivity projects /li /ulpbr/ppb /p /b

At Astek, we are seeking a SAT Tester to collaborate with our partner in the pharmaceutical industry in an international setting 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?

pAbout 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. /ppbr/ppbJob title: /bSales Director, Spain /ppbLocation: /bMadrid, Spain /ppbReporting to: /b General Manager /ppbr/ppbWe are seeking a Sales Director /bto lead our commercial organization and drive the next phase of growth in Spain. /ppThis is a critical leadership role, with full responsibility for sales strategy, execution, and performance across a diverse and growing portfolio. /ppbr/ppbAbout the role /b /ppbr/ppThe Sales Director plays a key role in leading the sales organization and driving sustainable growth across the company’s portfolio. /ppThis 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. /ppYou 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. /ppbr/ppKey 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. /ppbr/ppbSales Strategy Performance /b /pulliDefine and implement sales strategies to achieve and exceed revenue, market share, and profitability objectives. /liliDevelop territory plans and account strategies based on customer insights, market dynamics, and competitor activity. /liliEnsure resources are prioritized effectively to maximize performance in high-potential areas. /liliDrive the transition toward innovative, omnichannel engagement models to expand reach and impact. /liliRegularly review sales performance, adjusting strategy to capture new opportunities and mitigate risks. /li /ulpbr/ppbTeam Leadership Development /b /pulliLead, coach, and develop the sales team to achieve and exceed sales targets. /liliEstablish clear goals and accountability frameworks. /liliBuild a culture of accountability, continuous improvement, and high performance. /liliEnsure sales teams are fully trained and equipped for successful product launchesb. /b /li /ulpbr/ppbCross-Functional Collaboration /b /pulliCollaborate with marketing, medical, market access, and regulatory colleagues to align execution with company strategy. /liliContribute insights from the field to inform broader business planning and decision-making. /li /ulpbr/ppbCompliance Governance /b /pulliEnsure all sales activities adhere to compliance standards, industry codes, and company SOPs. /liliPromote ethical practices and integrity in all customer interactions. /li /ulpbr/ppbr/ppbWhat we are looking for /b /ppbr/pulliBachelor’s degree in life sciences, business, or related field (MBA desirable). /lili10+ years’ experience in pharmaceutical or life sciences sales, with at least 5 years in senior leadership roles. /liliProven experience managing multi-channel sales teams (hospital, primary care and/or private sector). /liliStrong experience in selling products and/or services to private clinics, preferably within ophthalmology or other specialty care areas. /liliExpertise in territory planning, pipeline management, and sales operations. /liliExperience in building and executing omnichannel strategies and improving customer engagement models. /liliProven track record in CRM development, adoption and optimization /liliExperience in product launches and lifecycle management. /liliStrong financial acumen with experience in forecasting, budgeting, and PL responsibility. /li /ulpbr/ppbr/ppIf you are ready to take on a high-visibility leadership role and drive meaningful growth, we would love to hear from you. /ppbr/ppWe are an equal opportunity employer committed to build a working culture that embraces diversity and inclusion. All qualified applicants will be considered. /p

At 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, • 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), • 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 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.

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. 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, • Design and implement REST / GraphQL integrations, • Connect Aprimo with CMS, PIM, and downstream platforms, • Optimize search, indexing, and caching for high performance, • Improve system responsiveness and global scalability, • Implement role-based access controls and permissions, • Ensure compliance with enterprise security and audit standards, • Translate business needs into technical solutions with Product Owners, • Participate in Agile ceremonies (sprint planning, code reviews, retrospectives) 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, • Experience with Aprimo DAM (strong advantage), • Experience integrating with Veeva CRM / Vault, • Knowledge of metadata standards (IPTC, XMP), • Experience with Digital Rights Management (DRM) 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. Take the next step in your career and become a key player in driving change at Amaris Consulting. Apply now to embark on a journey of professional growth and personal fulfillment.

In a few words Position: Data Scientist Location: Madrid (Chamberí area). Want to know more? INSUD PHARMA operates across the entire pharmaceutical value chain, providing specialized knowledge and experience in scientific research, development, manufacturing, sales, and marketing of a wide range of active pharmaceutical ingredients (API), finished dosage forms (FDF), and branded pharmaceutical products, adding value to human and animal health. The activities of INSUD PHARMA are organized into three synergistic business areas: Industrial (Chemo), Branded (Exeltis), and Biotech (mAbxience), with over 9,000 professionals in more than 50 countries, 20 state-of-the-art facilities, 15 specialized R&D centers, 12 commercial offices, and more than 35 pharmaceutical subsidiaries, serving 1,150 customers in 96 countries worldwide. INSUD PHARMA believes in innovation and sustainable development. Ready to be a #Challenger? What are we looking for? We are the Data Science team within AI Labs, the applied AI department at Insud Pharma. We are a team of 30 professionals (AI Engineers, Data Scientists, DevOps Engineers, and Product Managers) working across the full breadth of the company, building products, models, and analytical solutions that directly inform and shape decision-making. We are looking for an Applied Data Scientist with strong technical foundations who is eager to work across diverse and complex problem domains (R&D, drug manufacturing process optimization, clinical trials, and beyond). You will model problems from the ground up—defining the right framing, selecting appropriate methodologies, and owning solutions through rigorous development to full deployment. We are seeking someone curious enough to tackle varied challenges (graph theory, embeddings, neural network forecasting models, causality, Bayesian optimization), rigorous enough to justify every technical and methodological decision, and independent enough to deliver end-to-end impact while taking full ownership of their work. How the team works: AI Labs operates with a startup mindset within Insud Pharma. The department is young, and the culture reflects that: flat, collaborative, and fast-moving. Beyond the Data Science team, you will work alongside AI Engineers, DevOps Engineers, and Product Managers who are equally committed to delivering high-quality work. We hold regular demo days where teams present their work, as well as whiteboard sessions where we tackle problems together. The cross-disciplinary dynamic is genuinely strong. The office is located in central Madrid (Chamberí, near Eloy Gonzalo), well connected and situated in a vibrant part of the city. The challenge! • Collaborate with small, cross-functional teams. Each project is run by a small group — typically a Product Manager, a Data Scientist, an Engineer, and key stakeholders. Iteration is fast, feedback loops are short, and your contribution is visible from day one., • Conduct exploratory data analysis to uncover patterns and insights in large datasets., • Design, implement, and validate machine learning models and statistical methodologies to solve high-impact, real-world business problems., • Translate technical findings into clear narratives, visualizations, and decision frameworks for both technical and non-technical stakeholders, enabling informed and data-driven decisions. What do you need? • Strong understanding of statistics, machine learning, and data mining techniques., • Expertise in Python programming, including proficiency with data science libraries (e.g., NumPy, Pandas, Scikit-learn, TensorFlow…)., • Strong understanding of data preprocessing, feature engineering, and model evaluation techniques., • Proven ability to translate complex technical concepts into clear, actionable insights for non-technical audiences., • Knowledge and experience in causal inference methodologies will be highly valued., • Knowledge of deep learning architectures and natural language processing is beneficial., • Familiarity with Large Language Models (LLMs) and their applications in business contexts is a plus., • Experience with version control systems (e.g., Git) and collaborative development practices., • Clean, maintainable code and familiarity with software engineering best practices., • Familiarity with cloud platforms (e.g., AWS, Azure, Google Cloud) and their machine learning services., • Experience with big data technologies (e.g., Spark, Hadoop) and SQL databases is a plus., • Proficient in Spanish and English in written and verbal communication. Our benefits! ⏰ Flexible start time from Monday to Friday Permanent contract.

Desde 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 Entorno SAP privado Módulos: SD, MM, PP, WM, QA • Foco principal en producción y logística (SD / MM), • Experiencia sólida en implantaciones SAP end-to-end, • Experiencia en entornos industriales, Pharma o Alimentación muy valorable 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. Aplica directamente o escríbeme por LinkedIn para más información.

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

IF YOU ARE INTERESTED, PLEASE SHARE YOUR CV IN ENGLISH LANGUAGE ONLY! Who are we? We are a technology-led healthcare solutions provider. We are driven by our purpose to enable healthcare organizations be future ready. We offer accelerated, global growth opportunities for talent that's bold, industrious, and nimble. With Indegene, you gain a unique career experience that celebrates entrepreneurship, and is guided by passion, innovation, collaboration, and empathy. To explore exciting opportunities at the convergence of healthcare and technology, check out What if we told you that you can move to an exciting role in an entrepreneurial organization without the usual risks associated with it? We understand that you are looking for growth in your career at this point and we would love for you to join us in our journey and grow with us. At Indegene, our roles come with the excitement you require at this stage of your career with the reliability you seek. We believe in creating leaders of tomorrow and mentor our leads to help them grow and nurture them as people managers and account managers. We are a rapidly growing global organization and are scouting for the best talent for this phase of growth. With us, you are at the intersection of two of the most exciting industries of healthcare and technology. We offer global opportunities with fast-track careers while you work with a team that is fueled by purpose. The combination of this will lead to a truly differentiated experience for you. If this excites you, then apply below. 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. 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. Por favor, asegúrese de leer completamente el resumen y los requisitos de esta oportunidad de empleo que se detallan a continuación. 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.

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

Brand/Product roles within skincare, beauty, pharma.

Senior Data Engineer Se anima a todos los posibles solicitantes a que se desplacen y lean la descripción completa del puesto antes de presentar su candidatura. 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.

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 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

Ejecutivo de Compras Farmacéuticas.Haga clic en "Solicitar" a continuación para enviar su candidatura.Asegúrese de que su CV está actualizado y de que ha leído primero las especificaciones del puesto.Liderar la negociación estratégica con laboratorios farmacéuticos y proveedores clave para a

You will act as a trusted legal partner to Commercial, Regulatory, Quality and Operations teams, handling:. Legal support in a regulated pharma environment. We are hiring a Legal Counsel (Commercial & Corporate) to join an international pharmaceutical company based in Madrid.

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.INSUD PHARMA opera en toda la cadena de valor farmacéutica, aportando conocimientos especializados y experiencia en investigaci

En pocas palabras /b /ppbr/ppPosición: Técnico/a Garantía de Calidad /ppLocalización: Azuqueca de Henares.Experiencia: 2 a 4 años en funciones similares.Quieres saber más? /b /ppbr/ppbr/ppINSUD PHARMA opera en toda la cadena de valor farmacéutica, aportando conocimientos especializados y exp

Cuál será tu misión? /b /pulliVisitar farmacias en la zona asignada /liliLanzar, promocionar y gestionar nuestro portfolio de productos /liliMantener y desarrollar la cartera de clientes, así como captar nuevas farmacias /liliEstablecer relaciones comerciales sólidas, acompañando y formando

Te interesaría seguir desarrollándote como.Especialista de Cualificaciones y Calibraciones.Es este el siguiente paso en su carrera? Descubra si es el candidato adecuado leyendo la descripción completa a continuación.TÉCNICO/A DE CUALIFICACIONES Y CALIBRACIONES.Cuáles serán tus funciones princ

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