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pChemo is seeking a Technical and Quality Department Technician in Madrid. This role involves providing technical support in compliance with industry regulations, managing customer specifications, and overseeing documentation for API products. /ppThe ideal candidate will have a Pharmacy degree, 1-2 years of relevant experience, and strong problem-solving skills. Opportunities for professional development in an international environment are also included. /p #J-18808-Ljbffr

Chemo está buscando un Regulatory Affairs Associate para mercados internacionales en Barcelona. Este puesto requiere al menos 4 años de experiencia en funciones similares, donde se encargará de revisar normas reglamentarias y documentaciones de productos.El candidato ideal tendrá excelentes habilidades de comunicación y será responsable de coordinar la presentación de nuevos productos con licenciatarios. Se espera que gestiones las solicitudes de registro y realices el seguimiento hasta la aprobación.#J-18808-Ljbffr

Position: Supply Digital, Automation AI Analyst /p pLocation: Madrid /p pExperience: 3–5 years of experience in automation, digital solution development, or applied AI /p pChemo is the industrial division of Insud Pharma, a leading company across the pharmaceutical value chain, with strong expert

Location: Madrid Experience: 5+ years in commercial and financial controlling, including solid experience in pricing and margin management Insud Pharma is a global pharmaceutical group operating across the entire value chain, offering specialized expertise and broad 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. Insud Pharma is organized into three synergistic business areas: Industrial (Chemo), Branded (Exeltis) and Biotech (mAbxience), with 10,000 professionals in more than 50 countries, 20 industrial plants, 15 specialized R&D centers, 12 commercial offices and more than 35 pharmaceutical affiliates, serving 1,150 customers in over 110 countries worldwide. At Insud Pharma, we strongly believe in innovation and sustainable development. We are looking for a Commercial & Financial Controller to join our team in Madrid and take on a global, transversal Finance/Controlling role with responsibility for commercial controlling and corporate financial coordination across international entities. This is a high-impact position for a finance professional who enjoys combining analytical depth, business understanding and cross-functional collaboration in a fast-paced multinational environment. What are we looking for? We are seeking a professional with strong expertise in commercial controlling, financial analysis and accounting, who can ensure the reliability, consistency and quality of financial information related to sales, pricing, margins, Capex, R&D investments and structural expenses. The challenge! Analyze sales, pricing, margins and profitability by country, customer and product. Perform price reconciliations in both Tender and Non-Tender environments. Identify deviations versus Budget and Forecast, and propose improvement actions. Execute the monthly consolidated financial closing based on submissions from international entities. Ensure financial accuracy, detect inconsistencies and define corrective actions. Lead Budget and Forecast processes in line with Group requirements. Support entities during financial planning preparation and consolidate financial information. Analyze Capex projects and R&D investments, monitoring commitments and evaluating returns and key financial indicators. Monitor structural costs by department and identify operational deviations, risks and opportunities. Ensure alignment of international entities with Corporate deadlines, policies and ad hoc requirements. Maintain and promote the correct use of finance systems and reporting tools such as SAP, BW, QlikView, BPC and other reporting solutions. Work closely with Corporate Finance, Plant Directors, Commercial Management, R&D, Operations and Controlling teams. Support the implementation and continuous improvement of finance processes and policies. Provide financial validation and constructive challenge on pricing decisions, investment proposals and budget deviations within defined thresholds. Present financial results, key deviations, risks and opportunities to senior management when required. What do you need? University degree in Business Administration, Economics, Engineering or a similar field. Strong experience in Commercial Controlling and financial analysis. At least 3–4 years of specific experience in pricing analysis and margin management, including Tender and Non-Tender environments. Solid and demonstrable accounting background, including financial accounting and reconciliation processes. Deep understanding of industrial and commercial business models. Good understanding of Capex, R&D and cost structures. Advanced Excel and expert use of Office tools. ERP knowledge, preferably SAP. Experience with Business Intelligence tools such as BW, QlikView, BPC and Power BI. Previous broader experience in accounting and finance roles will be highly valued. Experience working in multinational environments. We will also value: Strong leadership and excellent communication and cross-functional influencing abilities. High analytical rigor and attention to detail. Results-oriented mindset and continuous improvement approach. Ability to perform effectively in high-ambiguity environments and manage changing priorities. Strong relationship-building skills across different functions and organizational levels. What we offer A global role within an international pharmaceutical company A strategic position with high visibility and exposure to key business areas Team leadership responsibility in a cross-functional environment Professional development opportunities in a dynamic and challenging setting EQUAL OPPORTUNITIES COMMITMENT At Insud Pharma, we are committed to equal opportunities in all our selection and professional development processes. We promote diverse and inclusive workplaces and ensure non-discrimination on the basis of gender, age, ethnicity, origin, religion, sexual orientation, gender identity, disability or any other personal, physical or social condition. #J-18808-Ljbffr

pChemo, the industrial division of Insud Pharma, is seeking a Supply Digital, Automation AI Analyst in Madrid. You will drive the digital transformation of Supply through scalable, data-driven automation, AI agents, and dashboards using React and FastAPI. /ppThe role requires 3–5 years in automation, digital solutions, or applied AI, with hands-on experience in Python, SQL, and Microsoft ecosystem tools. You will work across multiple data sources to deliver robust digital applications. /p #J-18808-Ljbffr

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. Experiencia, cualificaciones y habilidades interpersonales, ¿tiene todo lo necesario para triunfar en esta oportunidad? Descúbralo a continuación. 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. xcskxlj Benefits, • Flexible start time from Monday to Friday, • Training and language learning platform, • Wellness platform with unlimited free psychologist sessions, • Development plans, internal mobility policyCOMMITMENT 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. #J-18808-Ljbffr

ppPosition: Regulatory Affairs Manager - Biosimilars /p pLocation: Madrid (on-site) /p pExperience: 5+ years in Regulatory Affairs within biotech/biopharma /p pbWant to know more? /b /p pINSUD 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. /p pOur 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. /p h3What are we looking for? /h3 pWe 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. /p h3Key Responsibilities /h3 ul liMonitor changes in the regulatory landscape, identify their impact, and propose solutions to maintain compliance. /li liDefine regulatory strategy for each product in coordination with Management and Business teams. /li liBuild strong collaborative partnerships with internal and external teams to ensure organizational success and patient safety. /li liIdentify and mitigate regulatory risks, adapting strategies to evolving regulations and Health Authority feedback. /li liInterpret and communicate legislative changes that affect product registration, manufacturing, or development. /li liSupport the review of license and quality agreements for targeted geographies. /li liLead engagement with Health Authorities during Scientific Advice procedures and responses to deficiency letters. /li liPrepare, review, and approve regulatory submission documents (briefing packages, IBs, INDs, CTAs, MAAs, etc.). /li liManage external consultants and vendors for regulatory activities. /li liSupport product launch activities, ensuring regulatory risks are managed with appropriate action plans. /li liOrganize the regulatory submission schedule and coordinate with Regulatory Affairs teams. /li liParticipate in product plan development, regulatory strategy, and CMC documentation. /li liDrive digitalization and the use of computerized systems within the department. /li /ul h3Challenge /h3 ul liOversee the preparation and submission of regulatory documentation. /li liCoordinate regulatory strategy with RD, QA, QC, and Production teams. /li liLead negotiations and presentations with regulatory agencies. /li liManage regulatory information and ensure data integrity. /li liActively participate in scientific committees and project teams. /li /ul h3Requirements /h3 ul liUniversity degree in Health Sciences (preferably Pharmacy; degrees in Chemistry, Biology, Biochemistry, Veterinary or similar will also be considered). /li li5+ years of experience in Regulatory Affairs within biotechnology, biopharma, or biosimilars. /li liIn-depth knowledge of pharmaceutical legislation, GMP, and ICH guidelines. /li liFluent in Spanish and English (other languages are a plus). /li liAdvanced skills in Microsoft Office (Word, Excel, PowerPoint, Project) and regulatory software. /li liWillingness to travel. /li liInspiring, influential, results-oriented with excellent communication skills. /li /ul h3Selection Process /h3 ul liInitial contact by phone or email. /li li1–2 interviews (virtual and/or on‑site) with HR and technical teams. /li liOngoing updates throughout your recruitment process. /li /ul h3Equal Opportunity Statement /h3 pAt INSUD PHARMA, we promote gender equality and do not discriminate based on ethnicity, religion, sexual orientation, disability, or any other condition. We firmly believe that diversity and talent drive innovation and growth. /p /p #J-18808-Ljbffr

Buscamos un perfil analítico con sólida base técnica en datos para apoyar al Head de Chemo en la gestión y explotación de información clave para la toma de decisiones. ¿Es este su próximo empleo? Descúbralo leyendo la descripción completa a continuación y no dude en enviar su candidatura. La posición se centrará en la generación, mantenimiento y explotación de datos, trabajando con fuentes tanto internas como externas (IQVIA, agencias regulatorias, CRM, import/export, entre otras), asegurando su calidad, consistencia y disponibilidad. En una primera fase, el rol estará enfocado en el desarrollo y optimización de procesos ETL, integración de fuentes de datos y estructuración de modelos que permitan su análisis eficiente. Progresivamente, la persona evolucionará hacia el desarrollo de aplicaciones, automatización de procesos y construcción de soluciones orientadas al usuario final. El candidato tendrá un papel activo en la generación de insights y en el soporte a la toma de decisiones estratégicas, contribuyendo a mejorar la eficiencia operativa y la capacidad analítica del equipo. • Diseñar, desarrollar y mantener procesos de ETL y automatización de datos., • Integrar, transformar y estandarizar múltiples fuentes de información (mercado, competencia, datos internos)., • Optimizar consultas SQL y estructuras de datos para mejorar rendimiento y escalabilidad., • Construir y mantenerKPIs, benchmarks y dashboards para equipos de Portfolio y BD., • Realizar análisis cuantitativos y estratégicos para la evaluación de nuevas oportunidades de producto., • Monitorizar competidores y tendencias del mercado farmacéutico., • Traducir necesidades de negocio en soluciones técnicas estructuradas y escalables., • Colaborar con equipos técnicos y de negocio en proyectos estratégicos y operativos., • 1–2 años de experiencia en roles de datos, backend o análisis estratégico., • Sólida experiencia enPython y SQL avanzado., • Experiencia en procesos ETL y automatización de flujos de datos., • Familiaridad con Git y entornos colaborativos., • Capacidad analítica y estructuración de problemas complejos., • Habilidad para comunicarse con perfiles no técnicos., • Orientación a negocio y toma de decisiones basada en datos. Se valorará • Experiencia en sector farmacéutico o healthcare., • Conocimiento de datos de mercado (ventas, cuotas, competencia)., • Experiencia con Docker u otras herramientas de despliegue., • Interés en arquitectura de datos moderna y escalabilidad., • Rol híbrido con impacto real en decisiones estratégicas., • Alta exposición a negocio y dirección., • Entorno dinámico donde datos y estrategia van de la mano. xcskxlj, • Oportunidad de crecer hacia un perfil con mayor responsabilidad técnica y estratégica. #J-18808-Ljbffr

La actividad de INSUD PHARMA se organiza en tres áreas de negocio sinérgicas: Industrial (Chemo), Branded (Exeltis) y Biotech (mAbxience), con más de 10.

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. Habilidades, experiencia, cualificaciones... Si tiene el perfil adecuado para esta oportunidad, asegúrese de inscribirse hoy mismo. The activities of INSUD PHARMA are organized into three synergistic business areas: Industrial (Chemo), Branded (Exeltis), and Biotech (mAbxience), with over 9,000 professionals in more than 50 countries, 20 state‑of‑the‑art facilities, 15 specialized R&D centers, 12 commercial offices, and more than 35 pharmaceutical subsidiaries, serving 1,150 customers in 96 countries worldwide. INSUD PHARMA believes in innovation and sustainable development. Ready to be a #Challenger? What are we looking for? We are AI Labs, the applied AI team inside Insud Pharma. 30 people — AI Engineers, Data Scientists, DevOps Engineers, Product Managers — building GenAI and LLM‑powered tools that reach real users across trial design, patient recruitment, monitoring, and site operations. We are seeking a highly skilled DevOps Engineer to join our Applied AI Team. The ideal candidate will have a background in computer engineering and networking, and experience working with Software or Data teams. As a DevOps at AI Labs, you will be tasked with supporting engineers, data scientists and product owners in delivering AI applications across business units within our company, including Regulatory, Business Intelligence, Clinical Trials, and Drug Manufacturing. Your focus will be on building infrastructure for hosting Web, AI, Data Science applications and agents. From data acquisition and infrastructure requirements, through deployment, monitoring, and security. 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. You will work alongside Data Scientists, 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 closely with data scientists, engineers, and product managers to ensure infrastructure requirements are fully understood and meet development goals., • Manage our Cloud Infrastructure in Microsoft Azure and Amazon Web Service., • Support engineers and data scientists with IT related tasks, incl system administration, productionization, and maintenance of AI services., • Investigate, solve, and prevent problems related to our computing infrastructure., • Continuous Integration and Continuous Deployment (CI/CD) pipelines, • Infrastructure as Code (IaC) to automate infrastructure management, • Ensure seamless integration and deployment of code changes from development to production environments. What do you need? • Proficient in Spanish and English in written and verbal communication., • Proven experience in Cloud Infrastructure (AWS, GCP or Azure), with services like AKS/EKS, Azure App container/Lambdas, API Management, Blob Storage/S3, SQL, Azure Monitor/Cloudwatch, AD and Security Center., • General understanding of Linux, Python and Web technologies., • Experience in agile development, including issue tracking software such as Jira., • Knowledge of containerization (Docker), • Knowledge of CI/CD tools, such as Github Actions., • Knowledge of monitoring tools, such as Grafana., • A demonstrated ability to work and collaborate in engineering teams., • Experience in startups or scaleups is a plus. Flexible start time from Monday to Friday Training and language learning platform Wellness platform with unlimited free psychologist sessions Development plans, internal mobility policy. What will the Selection process be like? Stay tuned to your phone and email! The first thing we will likely do is contact you through one of the two channels. Prepare well! We will continue with an in‑person/virtual interview depending on availability and what we agree upon; there may be one or two interviews in the process, and depending on the type of process, there may also be some kind of test. Wait for the result! We care that you feel guided throughout each selection process and know what to expect from us, so we will always try to inform you of the status of the process. Do you think this offer is not for you? Follow us on social media like LinkedIn/Instagram and stay tuned for any offers we may release; the opportunity to be a new Insuder is waiting! 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. #J-18808-Ljbffr

ph3Global Systems Architect /h3 pInsud Pharma operates across the entire pharmaceutical value chain, providing specialized knowledge and expertise in scientific research, development, manufacturing, sales, and marketing of a wide range of active pharmaceutical ingredients (API), finished dosage forms (FDF), and branded pharmaceutical products for both human and animal health. /p pInsud Pharma’s activity is organized into three synergistic business areas: Industrial (Chemo), Branded (Exeltis), and Biotech (mAbxience), with 10,000 professionals in more than 50 countries, 20 industrial plants, 15 specialized RD centers, 12 commercial offices, and more than 35 pharmaceutical subsidiaries, serving 1,150 customers in over 110 countries worldwide. /p h3Responsibilities /h3 ul liDefine, govern, and evolve Insud Pharma’s global systems and applications architecture. /li liDesign, document, and maintain the corporate map of systems, platforms, applications, and integrations. /li liEnsure the coherence, standardization, interoperability, scalability, and efficiency of the technology ecosystem. /li liDefine architecture principles, standards, and criteria for the development, integration, and maintenance of IT solutions. /li liLead architecture governance and contribute to strategic technology decision-making. /li liEnsure alignment between technology initiatives and the Group’s business strategy. /li liCollaborate with Technology Transformation Competence Centers, the Transformation Office, and business teams to translate business needs into sustainable solutions. /li liAssess the impact of new initiatives and projects on the current and future technology ecosystem. /li liEnsure compliance with best practices, security standards, and enterprise architecture frameworks. /li liAdvise on the adoption of new technologies, cloud and hybrid architectures, integration solutions, automation, and artificial intelligence. /li liParticipate in the planning and execution of digital transformation initiatives and technology landscape evolution. /li liOversee integration between the SAP ecosystem and other corporate platforms, including CRMs, regulatory solutions, and industrial applications. /li liOversee the integration of critical plant applications such as V10, EBR, LIMS, Seavision, Aveva, and other industrial solutions with the Group’s core systems. /li /ul h3Qualifications /h3 pEducation /p ul liUniversity degree in Systems Engineering, Computer Science, Telecommunications Engineering, or a related field. /li liA Master’s degree in enterprise architecture, technology, or digital transformation considered a plus. /li /ul pLanguages /p ul liAdvanced level of Spanish and English, both written and spoken. /li /ul pExperience /p ul liMinimum 8 years of experience in systems architecture, enterprise architecture, or complex solution architecture roles. /li /ul pSpecific knowledge /p ul liProven experience in SAP-centric environments and industrial/plant applications such as EBR, LIMS, V10, Seavision, among others. /li liExperience in the design and governance of scalable, secure, and efficient enterprise architectures. /li liExperience integrating core platforms, data solutions, industrial applications, and corporate tools. /li liExperience in environments where legacy and target architectures coexist. /li liKnowledge of enterprise architecture frameworks, security standards, and technology governance best practices. /li liExperience assessing technology impact and defining sustainable solutions aligned with business needs. /li liExperience working in complex and evolving technology ecosystems with multiple transformation initiatives running in parallel. /li /ul h3Preferred Experience /h3 ul liExperience in SAP S/4HANA migration projects. /li liExperience with hybrid architectures and large-scale international digital transformation initiatives. /li liFamiliarity with complementary tools such as Celonis and CRMs such as Salesforce. /li liKnowledge of security best practices and technology governance. /li /ul h3Main Technology Scope /h3 ul liSAP landscape: SAP ECC, SAP S/4HANA, SAP IBP, SAP PPDS, SAP BPC, SAP SuccessFactors, SAP BTP, SAP MDG-MDM /li liPlant Industrial Applications: V10, EBR, LIMS, Seavision, Aveva, ad-hoc simulation tools /li liBusiness Corporate Platforms: Celonis, Salesforce /li liData Analytics Platform: Snowflake, SAP DataSphere, Dataedo /li /ul h3Personal Skills /h3 ul liStrategic thinking: Ability to align technology architecture with business goals. /li liTechnical leadership: Ability to influence and guide multidisciplinary teams. /li liProblem-solving: Ability to analyze complex situations and propose innovative solutions. /li liEffective communication: Ability to translate technical concepts into clear messages for non-technical audiences and support decision-making. /li liCollaboration: Ability to work cross-functionally with different areas of the organization. /li liProactivity and innovation: Ability to identify continuous improvement opportunities and propose innovative solutions. /li /ul pStrategic role with high impact on the Group’s transformation journey. /p pOpportunity to work within a global, complex, and continuously evolving technology ecosystem. /p pInnovative and transformation-driven environment. /p pCross-functional collaboration with technology and business teams at corporate level. /p pProfessional development opportunities within an international company. /p h3EQUAL OPPORTUNITIES COMMITMENT /h3 pAt Insud Pharma, we are committed to equal opportunities and to building a diverse, inclusive, and respectful workplace. All applications will be considered without regard to gender, gender identity or expression, sexual orientation, ethnicity, nationality, religion, age, disability, or any other characteristic protected by applicable law. /p /p #J-18808-Ljbffr

En pocas palabras Inscríbase rápido, consulte la descripción completa desplazándose hacia abajo para conocer todos los requisitos de este puesto.Posición: Pharmaceutical Development Team LeaderLocalización: Azuqueca de HenaresExperiencia: más de 5 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 10.000 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.¿Qué buscamos?Incorporamos un/a Pharmaceutical Development Team Leader para incorporarse en una de nuestras plantas ubicada en Azuqueca de Henares.¡El reto!Dirección integral de proyectos de desarrollo farmacéutico para productos inhalados, desde la evaluación de patentes, selección de APIs y desarrollo de formulaciones hasta la industrialización y transferencia a fabricación comercial. Responsable de la estrategia técnica y regulatoria, gestión de estudios de bioequivalencia, coordinación de equipos multidisciplinares, cumplimiento de estándares ICH, EMA y FDA, y control de presupuestos y plazos de proyecto.Responsabilidades específicas:Planificar, organizar y coordinar las actividades de desarrollo farmacéutico para garantizar el correcto avance de los proyectos. Evaluar y supervisar las actividades de los científicos especializados en formulación y análisis, analizando y valorando los resultados, con el fin de desarrollar formulaciones sólidas y procesos satisfactorios.Actuar como experto técnico para seleccionar la estrategia de formulación adecuada y las actividades de desarrollo de procesos.Realizar búsquedas bibliográficas y extraer información relevante de patentes y publicaciones científicas.Redactar y/o revisar protocolos, informes, registros maestros de lotes, documentos de transferencia técnica y otros documentos clave, de acuerdo con las directrices de la ICH y los requisitos reglamentarios.Elaborar informes de desarrollo de productos, redactar y revisar el resumen general de calidad y otros documentos para respaldar las solicitudes reglamentarias de CMC con vistas a su presentación y para responder a las cartas de deficiencias.Preparar y aprobar la documentación científica para asuntos de calidad y reglamentarios con el fin de respaldar los proyectos asignados a I+D y cumplir con el flujo de aprobación estándar establecido por el sistema de calidad; todo ello de conformidad con las normativas GMP y CFR, el cumplimiento del sistema de calidad y los acuerdos técnicos y contratos con terceros, de modo que los proyectos avancen adecuadamente.Analizar los resultados obtenidos en los estudios de bioequivalencia.Elaborar informes resumidos y presentaciones para su revisión por parte de la dirección.Supervisar, motivar, orientar y desarrollar al equipo.¿Qué necesitas?Formación: Máster en Farmacia; se valorará positivamente un doctorado en Farmacia.Idiomas: Inglés fluido; se valorarán los conocimientos de español.Experiencia (años/área): Más de 5 años de experiencia en proyectos de desarrollo farmacéutico. Se valorará la experiencia en asuntos clínicos y regulatorios. Habilidades de liderazgo demostradas. Experiencia en la gestión de personas. Se valorará la experiencia en la gestión de múltiples proyectos y el conocimiento de los requisitos de la FDA.Conocimientos específicos: Se valorarán los conocimientos sobre el desarrollo de productos para inhalación.Viajes: Disponibilidad para viajar.Habilidades personales: Capacidad de impacto e influencia, buenas habilidades de comunicación y gestión de proyectos, orientación a la calidad y liderazgo de equipos.¡Nuestros beneficios!Jornada completa en horario flexible de entrada de 08:00 a 09:30h y salida en función de la hora de entrada desde las 16:30hContrato indefinidoAtractivo paquete salarial.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. xqysrnh¿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 #InsudTalentCOMPROMISO CON LA IGUALDAD DE OPORTUNIDADESEl 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.

Position: QA Specialist (PRD) – Investigations, CRs, CAPAs & Floor Oversight Location: León (on-site) Experience: At least 3 years' experience in similar roles within the Quality department in pharmaceutical industrial settings Want to find out more? LEONFARMA is part of INSUD PHARMA, a global leader in the pharmaceutical value chain and a benchmark in the research, development, manufacture and marketing of pharmaceutical products that contribute to human and animal health. Our purpose is to transform the industry through innovation, excellence and a commitment to sustainable development. Ready to be a #Challenger at LEONFARMA? What are we looking for? We are looking for a QA Specialist (PRD) – Investigations, CRs, CAPAs & Floor Oversight who is passionate about the industrialisation of new products. General Responsibility Ensure quality oversight of production-related activities in a GMP-regulated manufacturing environment, acting as a key quality partner for operations on the shop floor. The role is responsible for leading and coordinating investigations, change controls and CAPAs, ensuring appropriate risk assessment, impact evaluation and timely closure in compliance with quality and regulatory requirements. In addition, the position provides real-time QA support to production, reinforcing GMP compliance, issue resolution and continuous improvement across daily manufacturing operations. Specific Responsibilities • Lead and manage quality investigations related to deviations associated with production activities., • Perform and support root cause analysis, ensuring robust identification of underlying causes and appropriate documentation of findings., • Evaluate the impact of deviations on product quality, manufacturing processes and GMP/regulatory compliance., • Coordinate cross-functional investigation activities with Production, Engineering, Quality Control, Maintenance and other relevant departments., • Review, assess and approve change requests/change controls, ensuring proper justification, impact assessment and implementation in line with GMP requirements., • Ensure that change controls are adequately evaluated, approved, implemented and closed within established timelines., • Review and approve CAPA plans derived from investigations, audits and inspections, ensuring actions are appropriate and sustainable., • Monitor CAPA implementation and verify effectiveness prior to closure., • Provide routine QA floor oversight through regular presence in production areas, supporting real-time decision-making and compliance with approved procedures., • Support production teams during critical operations, helping resolve GMP issues promptly and reinforcing quality culture on the shop floor. Experience (area) Quality Assurance in GMP-regulated pharmaceutical or biotechnology manufacturing environments, with strong exposure to production-related quality activities. Personal skills • Adaptability to change and flexibility, • Speed without compromising on quality, • Leadership and teamwork, • Effective communication, • Compliance, integrity and sustainability, • Growth mindset, • Business focus Our benefits! Permanent contract Career progression and development within a growing international group Ongoing training and an innovative working environment Subsidised canteen and other employee benefits What will the recruitment process be like? ️ Initial contact by phone or email with our Talent Acquisition team. 1 or 2 face-to-face interviews at our premises in León. Regular updates on the progress of the process. Do you think this role isn't for you? Follow us on LinkedIn and Instagram so you don't miss out on future career opportunities! #Leonfarma #Challenger #InsudPharma #InsudTalent COMMITMENT TO EQUAL OPPORTUNITIES AT LEONFARMA, we believe in and act to promote genuine equality of opportunity. We do not discriminate on the basis of gender, ethnicity, religion, sexual orientation, disability or any other characteristic. We value diversity and talent. We'd love to meet you!

Posición: QA inspector, departamento de garantía de calidad. Incorporamos un/a nuevo/a INSUDER como QA INSPECTOR para incorporarse al equipo de garantía de calidad de nuestra planta situada en León.

Posición: QA inspector, departamento de garantía de calidad. Incorporamos un/a nuevo/a INSUDER como QA INSPECTOR para incorporarse al equipo de garantía de calidad de nuestra planta situada en León.

En pocas palabras Posición: QA inspector, departamento de garantía de calidad. Localización: León. Experiencia: 2-3 años en departamento de garantía de calidad en planta de producción de medicamentos. ¿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. ¿Qué buscamos? Incorporamos un/a nuevo/a INSUDER como QA INSPECTOR para incorporarse al equipo de garantía de calidad de nuestra planta situada en León. ¡El reto! Apoyar al Área de Operaciones (Compounding, Operaciones Asépticas y Envasado) perteneciente a la Unidad de Calidad. Colaborar con los equipos de producción. Trabajar como parte del equipo de producción facilitando la función diaria de producción. Trabajar de forma proactiva asegurando que la fabricación de los lotes se realiza correctamente, de acuerdo con los MBR y los estándares de calidad definidos. Expedición y revisión de cuadernos. Verificación de las autorizaciones de línea. Verificación de los IPC (controles en proceso). Realización de AQL de lotes fabricados. Verificación de muestras de producto de proceso o validación y distribución a los laboratorios correspondientes. Observación de los registros de fabricación de lotes. Apoyo al departamento de Garantía de Calidad y al departamento de Producción en la investigación de incidencias. Seguimiento del proceso/validación del proceso/validación del proceso. Supervisión del comportamiento aséptico de los operarios. Supervisión de las tareas de producción en el área de envasado. Formar a las nuevas incorporaciones en las actividades y funciones específicas del puesto en el que es experto/a. ¿Qué necesitas? Formación: Formación Profesional Superior, estudios universitarios en farmacia, ciencias químicas, biológicas o similar. Idiomas: español, inglés es un plus. Experiencia (años/área): mínimo un año de experiencia en posiciones de producción o en áreas de calidad, preferentemente trabajando directamente en las líneas de fabricación. Conocimiento específico: GMP, ALCOA, Integridad de Datos. ¡Nuestros beneficios! Horario: lunes a viernes rotativo mañana tarde y noche. Contrato indefinido.

Posición: QA inspector, departamento de garantía de calidad.Experiencia: 2-3 años en departamento de garantía de calidad en planta de producción de medicamentos.INSUD PHARMA opera en toda la cadena de valor farmacéutica, aportando conocimientos especializados y experiencia en investigación ci

Posición: QA inspector, departamento de garantía de calidad. Incorporamos un/a nuevo/a INSUDER como QA INSPECTOR para incorporarse al equipo de garantía de calidad de nuestra planta situada en León.

En pocas palabras: Puesto: Operario de Producción.

El grupo InsudPharma es consciente de que la gestión empresarial debe alinearse con las necesidades y demandas de la sociedad, y por ello asume el compromiso con la igualdad de oportunidades y de trato entre hombres y mujeres, tal y como establece la normativa vigente en la materia - Ley Orgánica

Las actividades de INSUD PHARMA se organizan en tres áreas de negocio sinérgicas: Industrial (Chemo), Marca (Exeltis) y Biotecnología (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 comercia

El grupo InsudPharma es consciente de que la gestión empresarial debe alinearse con las necesidades y demandas de la sociedad, y por ello asume el compromiso con la igualdad de oportunidades y de trato entre hombres y mujeres, tal y como establece la normativa vigente en la materia - Ley Orgánica

El grupo InsudPharma es consciente de que la gestión empresarial debe alinearse con las necesidades y demandas de la sociedad, y por ello asume el compromiso con la igualdad de oportunidades y de trato entre hombres y mujeres, tal y como establece la normativa vigente en la materia - Ley Orgánica

Chemo busca un QA Inspector para unirse al departamento de Garantía de Calidad en nuestra planta.

COMPROMISO CON LA IGUALDAD DE OPORTUNIDADES El grupo Insud Pharma 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

Incorporamos un/a nuevo/a INSUDER como QA INSPECTOR para incorporarse al equipo de garantía de calidad de nuestra planta situada en León. En pocas palabras Posición: QA inspector, departamento de garantía de calidad.

Posición: QA inspector, departamento de garantía de calidad. Incorporamos un/a nuevo/a INSUDER como QA INSPECTOR para incorporarse al equipo de garantía de calidad de nuestra planta situada en León.

Chemo busca un Técnico/a de Producción para su planta en Azuqueca de Henares.

pChemo, part of Insud Pharma, is seeking a Jr. Area Manager to drive direct sales in a multinational B2B pharmaceutical environment based in Madrid. You will support growth across countries, manage key accounts, and prepare commercial offers while coordinating with internal teams to ensure high service levels. /ppThe role requires 1–3 years in pharma or related fields, fluency in Spanish and English, and willingness to travel internationally. A Master’s degree is a plus. /p #J-18808-Ljbffr

Chemo busca un/a Pharmaceutical Development Team Leader en Azuqueca de Henares con más de 5 años de experiencia en desarrollo farmacéutico. El candidato liderará actividades de desarrollo y supervisará el equipo, buscando siempre la calidad y el cumplimiento normativo.Se requiere un Máster en Farmacia y se valorará un doctorado. Además, es esencial tener habilidades de comunicación y ser capaz de impactar e influir, siendo el inglés fluido un requisito fundamental.Ofrecemos jornada completa, contrato fijo, un atractivo paquete salarial, seguro de vida y más beneficios.#J-18808-Ljbffr

Local Quality Assurance Manager (GDP) IberiaApplylocations:Barcelonatime type:Full timeposted on:Posted Todayjob requisition id:R-21807Title:Local Quality Assurance Manager (GDP) IberiaCompany:Ipsen Pharma SAAbout Ipsen:Ipsen is a mid-sized global biopharmaceutical company with a focus on transformative medicines in three therapeutic areas: Oncology, Rare Disease and Neuroscience. Supported by nearly 100 years of development experience, with global hubs in the U.S., France and the U.K, we tackle areas of high unmet medical need through research and innovation. Our passionate teams in more than 40 countries are focused on what matters and endeavor every day to bring medicines to patients in 88 countries. We build a workplace that champions human-centric leadership and fosters a culture of collaboration, excellence and impact. At Ipsen, every individual is empowered to be their true selves, grow and thrive alongside the company’s success. Join us on our journey towards sustainable growth, creating real impact on patients and society!For more information, visit us at https://www.Ipsen.Com/and follow our latest news on LinkedIn and Instagram.Job Description:At Ipsen, we believe that patients cannot wait to receive the right treatment, support, and awareness they need. Therefore, our goal is to make a difference by significantly improving the health and quality of life of patients and providing them with effective therapeutic solutions for unmet medical needs through differentiated and innovative medicines in Oncology, Neurosciences, and Rare Diseases.The patient is at the center of everything we do, and we also care about our employees because they are the ambassadors and the ones who truly make a difference. We attract and develop bold, agile, and entrepreneurial people who take full responsibility for their decisions; leaders drawn to the purpose of making a direct impact through their work on people's lives.We offer employees a wealth of rewarding challenges and growth opportunities, and the chance to contribute within a constantly moving organization, an organization that truly changes the game.At Ipsen, we are looking for aLocal Quality Assurance Manager (GDP) Iberia, based in Barcelona, who, under the direction of the Quality Lead Iberia, willact as the Quality Assurance Manager function at Ipsen Commercial Operations Iberia (Spain & Portugal) for Good Distribution Practices (GDP) activities.The Quality Assurance Manager is responsible for the overall management of the Affiliate Quality Management System and quality assurance programs, to foster a strong quality and continuous improvement culture, and thus ensuring that the local license to operate activities meet internal and external requirements (including regulations and Good x Practices), policies and procedures.Your main responsibilities will include:Quality Assurance: Act as the local quality assurance/quality system representative for the Iberian cluster; Establish and maintainIberian cluster Quality Management System and Quality Assurance activities to ensure compliance with all regulatory and GxP requirements; Host/Coordinate audits/inspections on behalf of GDP functions within theIberian cluster; Local supplier assessment and oversight including QTAs maintenance and local audits conduct; Ensure Quality management review and KPIs are established; Maintain qualityassurance activities for GDP programs/activities; Focuses on proactive crisis prevention and supports crisis (QSEB) and CAPA follow-up when needed; Drive and support local and global initiatives on continuous quality improvement; Drives remediation plan when a product quality or GxP process issue is identified; As Product Quality Complaint Manager Iberia, maintain and ensure local Product Complaints and recalls management; To control, in conjunction with local distributor(s), the reception, warehousing and distribution of the Ipsen products; To ensure that distributors comply with Good Distribution Practices (in particular cold chain and transportation); Integrate global/corporate and Iberian cluster, as applicable, quality needs and priorities, including representing the Affiliate at the Ipsen Global Quality Forum; Foster quality cultureby encouraging best practices and a high performing “quality beyond compliance” culture, both from procedural and patient/customer centricity perspectives; Contribute strongly tobuilding quality and compliance through governance and education; Participate on regulatory intelligence process and, where necessary, escalate with technical expertise, assessment and solution proposals; Ensures comprehensive training program covering GDP activities; Ensure the Iberian cluster, self-inspection, GDP audit readiness; business continuity, change control, Deviations and CAPA management systems and activities are in place and implemented to cover GDP processes; Conduct and/or host risk assessments, self-inspections, regulatory inspections, audits, mock-recalls and should the situation arise, to participate in Product Recall Management; Support local product release activities; Facilitate troubleshooting; support any OOS, if applicable; * Quality interface for local Distribution partners; Collaboration with other Departments Proactively advocate for quality processes across functions Proactively identify areas for process improvement and mediate cooperation cross-functionally to effect and implement the Quality System; Contribute towards stakeholder value by providing quality leadership and operational input towards affiliate strategic and tactical activities Strengthen the risk management culture and support the update of the IPSEN Risk register; CommunicationTo respect and apply the company rules (especially the confidentiality ones) and strategy in communication with media, authorities and health professionals; To maintain membershipof societies and professional organisations of interest to the company, according to local legislation and the Group’s guidance; To act with all relevant authorities/entities, with a great sense of public relations, having in perspective an increased efficiency and recognition of Ipsen; To maintain and develop positive and ethical interactions with relevant authorities; * To respect and apply the IPSEN ethical codeWho are we looking for?Requirements:Knowledge & Experience (essential): Experience in a similar position with a proven experience in Maintaining Quality Management System in accordance with GDP and Regulations on Distribution of Medicinal Products. Auditing Host/Coordinate audits/inspections Risk assesment Approximately 1-2 years in similar positionKnowledge & Experience (preferred): Experience in a similar position with a proven experience in Maintaining Quality Management System in accordance with GDP and Regulations on Distribution of Medicinal Products. Auditing Host/Coordinate audits/inspections Risk assesment Approximately 2-3 years in similar positionEducation / Certifications (essential): Degree in Scientific discipline (Pharmacy, Chemistry, or Biological Sciences) with accredited training on GDPsEducation / Certifications (preferred): Master in Pharmaceutical Industry and Postgraduation in Quality, Pharmacovigilance and Regulatory Affairs of the Pharma IndustryLanguage(s) (essential): Expert/fluent communicator in Spanish and English.Language(s) (preferred): Expert/fluent communicator in Portuguese and English.* Knowledge of Portuguese is a valuable assetCompetencies:* Drive Purpose: Puts values and ethics at the forefront of everything; Anchors Ipsen's purpose, mission and commitments to patients and society.* Manage Complexity: Identifies contradictory information/demands/inputs to effectively solve problems; Develops and evaluatesalternative scenario and solutions; Able to identifywhat truly matters and ruthlessly focus/ prioritize on making decisions with real impact. Mindfulness Risk-taking: Methodically assesses, transparently shares, and makes risk-informed decisions; Empowers to takeownership and accountability.* Excellence in execution: Establishes clarity about the goals, accountabilities, timelines, and next steps; can identify/spotopportunities for real impact on patient and society; Able to be focused andperformance-driven with clear KPIs Plans and aligns effectively (steps, resources, timelines etc.) Displays a commitment to best practice sharing and settingWhat do we offer?Joining Ipsen means becoming part of a global biopharmaceutical group focused on innovation and specialized care in three key therapeutic areas: oncology, neurosciences, and rare diseases.Ipsen's Human Resources policy pays special attention to ensuring that all employees have good working conditions, including a flexible working hours model, training and development programs, as well as social benefits and competitive remuneration based on three main principles: internal equality, external competitiveness, and recognition of work.TYPE OF CONTRACTPermanent – Full-timeWe are committed to creating a workplace where everyone feels heard, valued, and supported; where we embrace “The Real Us”. The value we place on different perspectives and experiences drives our commitment to inclusion and equal opportunities. When we include diverse ways of thinking, we make more thoughtful decisions and discover more innovative solutions. Together we strive to better understand the communities we serve. This means we also want to help you perform at your best when applying for a role with us. If you require any adjustments or support during the application process, please let the recruitment team know. This information will be handled with care and will not affect the outcome of your application.#J-18808-Ljbffr

Buscamos un técnico de automatización industrial para realizar el mecanizado, confección de armarios eléctricos, cableado y validación de sistemas en maquinaria. Se ofrece formación y crecimiento.

ppbPosition: /b Technical and Quality Department Technicianbr/bLocation: /b Madridbr/bExperience: /b 1-2 years in the pharmaceutical industry /p pbWant to know more? /b /p pChemo Ibérica is part of Insud Pharma, a fully integrated pharmaceutical group operating across the entire value chain, offering specialized expertise and experience in scientific research, development, manufacturing, sales, and marketing of a wide range of active pharmaceutical ingredients (APIs), finished dosage forms (FDFs), and branded pharmaceutical products, adding value to both human and animal health. /p pInsud Pharma’s activity is organized into three synergistic business areas: Industrial (Chemo), Branded (Exeltis), and Biotech (mAbxience), with 10,000 professionals across more than 50 countries, 20 industrial plants, 15 specialized RD centers, 12 commercial offices, and more than 35 pharmaceutical subsidiaries, serving 1,150 customers in over 110 countries worldwide. At Insud Pharma, we are committed to innovation and sustainable development. /p pWe are looking for an API Technical Quality Technician to provide technical and quality support to the commercial project of the API Division, ensuring agile, accurate, and compliant responses aligned with current pharmaceutical industry regulations across different markets. /p h3What are we looking for? /h3 pWe are looking for a detail-oriented professional with a strong customer focus, problem-solving mindset, and coordination skills, who is eager to grow in an international pharmaceutical environment and provide technical and quality support to customers, manufacturing sites, and internal teams, while helping ensure GDP/GMP compliance in distribution activities coordinated by Chemo Ibérica. /p h3The challenge! /h3 ul liProcess, review, and resolve customer technical requests, escalating them to the relevant manufacturing sites when needed and following them through until the final response is delivered. /li liPrepare and send the required documentation to customers, ensuring quality, traceability, and timely response. /li liManage customer specifications. /li liRecord all information related to technical support provided to customers and API manufacturing sites in the CRM system. /li liManage regulatory documentation related to the activity. /li liProvide support to API manufacturers, both internal and external sites. /li liPropose alternatives and contingency solutions when changes or execution issues arise. /li liFollow up on work related to internal development projects. /li liSupervise, support, and train junior technicians under your responsibility, contributing to their performance and professional development within the department. /li /ul h3QA responsibilities /h3 ul liAssist the GDP Responsible Person in ensuring GDP and GMP compliance, when applicable, across all distribution activities coordinated and carried out by Chemo Ibérica, S.A. and its contractors. /li liMaintain CHIB authorizations and GDP certification. /li liManage commitments with Authorities. /li liSupport Authorities during audits and inspections. /li liEnsure GDP compliance throughout the entire supply chain of active substances and medicinal products under CHIB responsibility, including warehousing activities. /li liMaintain and continuously improve the CHIB Quality System, including: /li ul liPreparation and review of SOPs /li liManagement of deviations, complaints, returns, and rejections /li liTechnical and quality agreements with suppliers and customers /li liFollow-up of supplier qualification/homologation /li /ul liPrepare Quality, Regulatory, Legal, and Import/Export documentation to support CHIB commercial operations. /li liPrepare and approve, when applicable, technical documentation related to applications for own marketing authorizations of medicinal products and DMF files for APIs. /li liSupport other tasks carried out by the Technical Department team. /li /ul h3What do you need? /h3 ul liDegree in Pharmacy. /li liA Master’s degree in the Pharmaceutical Industry will be considered a plus. /li li1-2 years of experience in a similar role within the pharmaceutical industry, especially related to API products, or recent completion of a Master’s in the Pharmaceutical Industry. /li liExperience in the preparation of Drug Master Files (DMF) and/or Certificates of Suitability (CEP). /li liKnowledge of GDP/GMP. /li liKnowledge of Regulatory Affairs procedures and guidelines. /li liFamiliarity with different pharmacopoeias. /li liKnowledge of other languages will be considered a plus. /li liProficiency in Microsoft Office. /li liExperience with CRM tools will be valued. /li /ul h3Personal skills /h3 ul liStrong internal and external customer orientation. /li liHigh problem-solving capacity. /li liPlanning and organizational skills. /li liStrong interpersonal skills. /li liFlexible working hours. /li liContinuous learning and training. /li liProfessional development in an international environment. /li liThe opportunity to join a solid, innovative, and growing company. /li /ul h3Equal Opportunity Commitment /h3 pAt Chemo Ibérica, we are committed to fostering a diverse, inclusive, and equal‑opportunity workplace. All applications will be considered without regard to gender, gender identity or expression, age, ethnic or social origin, nationality, religion, sexual orientation, disability, or any other personal or social condition protected by applicable law. /p /p #J-18808-Ljbffr

Position: QA Specialist (PRD) – Investigations, CRs, CAPAs & Floor Oversight Location: León (on-site) Experience: At least 3 years’ experience in similar roles within the Quality department in pharmaceutical industrial settings Want to find out more? Los candidatos deben tomarse el tiempo de leer atentamente todos los elementos de este anuncio de empleo. Por favor, envíen su solicitud sin demora. LEONFARMA is part of INSUD PHARMA, a global leader in the pharmaceutical value chain and a benchmark in the research, development, manufacture and marketing of pharmaceutical products that contribute to human and animal health. Our purpose is to transform the industry through innovation, excellence and a commitment to sustainable development. Ready to be a #Challenger at LEONFARMA? What are we looking for? We are looking for a QA Specialist (PRD) – Investigations, CRs, CAPAs & Floor Oversight who is passionate about the industrialisation of new products. General Responsibility Ensure quality oversight of production-related activities in a GMP-regulated manufacturing environment, acting as a key quality partner for operations on the shop floor. The role is responsible for leading and coordinating investigations, change controls and CAPAs, ensuring appropriate risk assessment, impact evaluation and timely closure in compliance with quality and regulatory requirements. In addition, the position provides real-time QA support to production, reinforcing GMP compliance, issue resolution and continuous improvement across daily manufacturing operations. Specific Responsibilities • Lead and manage quality investigations related to deviations associated with production activities. • Perform and support root cause analysis, ensuring robust identification of underlying causes and appropriate documentation of findings. • Evaluate the impact of deviations on product quality, manufacturing processes and GMP/regulatory compliance. • Coordinate cross-functional investigation activities with Production, Engineering, Quality Control, Maintenance and other relevant departments. • Review, assess and approve change requests/change controls, ensuring proper justification, impact assessment and implementation in line with GMP requirements. • Ensure that change controls are adequately evaluated, approved, implemented and closed within established timelines. • Review and approve CAPA plans derived from investigations, audits and inspections, ensuring actions are appropriate and sustainable. • Monitor CAPA implementation and verify effectiveness prior to closure. • Provide routine QA floor oversight through regular presence in production areas, supporting real-time decision-making and compliance with approved procedures. • Support production teams during critical operations, helping resolve GMP issues promptly and reinforcing quality culture on the shop floor. Experience (area) Quality Assurance in GMP-regulated pharmaceutical or biotechnology manufacturing environments, with strong exposure to production-related quality activities. Personal skills • Adaptability to change and flexibility • Speed without compromising on quality • Leadership and teamwork • Effective communication • Compliance, integrity and sustainability • Growth mindset • Business focus Our benefits! Permanent contract Career progression and development within a growing international group Ongoing training and an innovative working environment Subsidised canteen and other employee benefits What will the recruitment process be like? Initial contact by phone or email with our Talent Acquisition team. 1 or 2 face-to-face interviews at our premises in León. Regular updates on the progress of the process. Do you think this role isn’t for you? Follow us on Linked In and Instagram so you don’t miss out on future career opportunities! #Leonfarma #Challenger #Insud Pharma #Insud Talent COMMITMENT TO EQUAL OPPORTUNITIES AT LEONFARMA, we believe in and act to promote genuine equality of opportunity. We do not discriminate on the basis of gender, ethnicity, religion, sexual orientation, disability or any other characteristic. xkdbapo We value diversity and talent. We’d love to meet you!

ppbLocation: /b Madrid (Onsite) /p pbExperience: /b 1–3 years of experience /p pbWhat are we looking for? /b /p pWe are looking for a bJr. Area Manager /b to actively participate in the direct sales process in a bB2B pharmaceutical environment /b, contributing to the achievement of commercial targets and supporting business growth across multiple countries. /p pbThe challenge! /b /p ul liParticipate actively in the direct sales process, contributing to the achievement of sales targets. /li liDrive business growth by managing and expanding existing accounts and identifying new business opportunities across different countries. /li liPrepare commercial offers aligned with company strategy. /li liFollow up with clients throughout the full commercial cycle, from offer preparation to execution and post sale support. /li liCoordinate closely with internal departments such as Customer Service, Supply Chain, Regulatory Affairs, Legal, and Project Management to ensure high quality service. /li liSupport and participate in client visits, business reviews, and negotiations. /li liContribute actively to internal processes and crossfunctional initiatives. /li liManage routine account activities with a strong focus on customer satisfaction and service quality. /li liBuild and maintain long term relationships with key clients. /li liAnalyze market data, including pricing, volumes, competitors, and trends, to identify opportunities and support decision making. /li liEnsure continuous follow up of ongoing projects to maximize business opportunities across different accounts and geographies. /li /ul pbWhat do you need? /b /p ul liUniversity degree in bEconomics, Business Administration, Life Sciences /b (such as Biology, Biotechnology, Pharmacy) or related fields. /li liA bMaster’s degree /b will be considered a plus. /li lib1–3 years of experience /b in the pharmaceutical industry, B2B sales, or business related roles. /li liStrong knowledge of bsales strategy /b. /li liFluent bSpanish and English /b. /li liKnowledge of other languages will be considered an asset. /li liWillingness to btravel internationally /b. /li /ul pbWe will value especially: /b /p ul liStrong communication and negotiation skills. /li liHigh customer orientation and business mindset. /li liProactive problem solving mindset, with the ability to anticipate challenges, drive solutions, and coordinate effectively across internal stakeholders. /li liSensitivity to market trends and commercial opportunities. /li liInternational mindset and ability to work in crossfunctional environments. /li liStrong ability to manage multiple priorities simultaneously in dynamic environments. /li liHigh adaptability and flexibility in response to changing business needs and market conditions. /li liResilience and ability to work effectively under pressure while maintaining a results oriented approach. /li /ul pBenefits package from Insud Pharma Group /p pProfessional development in an international environment /p pExposure to a multicultural and crossfunctional business setting /p pbWhat will the selection process look like? /b /p ul liInitial contact by phone or email. /li liInterview process with the team. /li liContinuous communication regarding your application status throughout the process. /li /ul pbDon’t think this role is for you? /b /p pFollow us on LinkedIn to stay up to date with future career opportunities at Chemo and Insud Pharma. /p pbEqual Opportunity Commitment /b /p pAt bChemo /b and bInsud Pharma /b, we are firmly committed to equal opportunities in our selection processes and work environment. We promote an inclusive culture and do not discriminate on the basis of gender, age, ethnic origin, nationality, religion, sexual orientation, gender identity, disability, or any other personal, physical, or social condition. /p /p #J-18808-Ljbffr

Overview Position: Launch Specialist – New Product Introduction (NPI) Por favor, asegúrese de leer atentamente los siguientes detalles antes de enviar cualquier solicitud. Experience: 3-5 years in project management, preferably in the pharmaceutical industry or regulated sectors Want to know more? INSUD PHARMA operates across the entire pharmaceutical value chain, providing specialized knowledge and experience in scientific research, development, manufacturing, sales, and commercialization of a wide range of active pharmaceutical ingredients (APIs), finished dosage forms (FDF), and branded pharmaceutical products, adding value to both human and animal health. INSUD PHARMA’s activity is organized into three synergistic business areas: Industrial (Chemo), Branded (Exeltis), and Biotech (mAbxience), with more than 9,000 professionals in over 50 countries, 20 state-of-the-art facilities, 15 specialized R&D centers, 12 commercial offices, and more than 35 pharmaceutical subsidiaries, serving 1,150 clients in 96 countries worldwide. INSUD PHARMA believes in innovation and sustainable development. What are we looking for? As a Launch Specialist at INSUD PHARMA, you will be the bridge between development and industrialization, ensuring every new product is ready for its first commercial production. Your mission will be to coordinate all key functions to guarantee successful launches, meeting the highest standards of quality, cost, and service. Key Responsibilities • Manage and maintain launch plans for new products, ensuring milestones, dependencies, and timelines are met., • Coordinate cross-functional teams (Engineering, QA, QC, Production, Supply Chain, Planning, Regulatory Affairs, Finance, etc.) for timely execution of launch activities., • Lead follow-up meetings, facilitating communication and alignment among all stakeholders., • Serve as the operational point of contact for internal and external clients for assigned launches., • Proactively identify risks, constraints, or deviations, and propose mitigation plans., • Manage documentation, progress reports, and ensure data accuracy in the launch database., • Prioritize and sequence activities to maximize speed, service level, and business value., • Capture lessons learned and contribute to continuous improvement of launch processes.The challenge!, • Coordinate and oversee the execution of multiple launch projects simultaneously., • Ensure delivery ON TIME, IN FULL, AT THE RIGHT COST, and with the HIGHEST QUALITY., • Drive collaboration between departments and operational excellence.What do you need?, • University degree in Pharmacy, Chemistry, Engineering, Life Sciences, or similar., • 3-5 years of experience in project management, preferably in the pharmaceutical, chemical, or regulated sectors., • Experience coordinating cross-functional teams and managing stakeholders., • Solid knowledge of technology transfer processes, quality assurance, and supply chain., • High level of English (minimum B2); other languages are a plus., • Proficiency in project management tools (MS Project, Excel, etc.)., • Outstanding communication, organizational, analytical, and problem-solving skills. International and dynamic environment Professional development plan and continuous training What will the selection process be like? • Initial contact by phone or email., • 1-2 on-site/virtual interviews, • Ongoing communication about your application status.Think this offer isn’t for you? Follow us on LinkedIn and Instagram to discover more career opportunities at INSUD PHARMA! xcskxlj #InsudPharma #Challenger #Insuder #InsudTalent COMMITMENT TO EQUAL OPPORTUNITIES The InsudPharma group is aware that business management must align with the needs and demands of society, and therefore assumes the commitment to equal opportunities and treatment between men and women, as stated in the current regulations on the matter - Organic Law 3/2007, and we do not discriminate against any person on the grounds of ethnicity, religion, age, sex, nationality, marital status, affective or sexual orientation, gender identity or expression, disability, or any other personal or social circumstance. #J-18808-Ljbffr

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