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PMO – Digital Industrial & QA Solutions | Pharmaceutical Industry 📍 Barcelona Area, Spain (Hybrid) 💼 Full-Time Opportunity 🏭 Pharmaceutical Manufacturing Environment We are seeking an experienced PMO – Digital Industrial & QA Solutions to support strategic digital transformation initiatives within a leading pharmaceutical organization. This role will play a key part in the successful delivery of critical Manufacturing, Laboratory, and Quality Systems projects, working cross-functionally with QA, QC, Manufacturing, Engineering, and IT teams. Key Responsibilities ✅ Support governance, planning, and execution of strategic projects ✅ Track project plans, milestones, deliverables, and dependencies ✅ Manage risks, issues, and change requests ✅ Prepare Steering Committee materials and project status reports ✅ Monitor KPIs, budgets, resource allocation, and project progress ✅ Coordinate activities with internal stakeholders and external vendors ✅ Ensure compliance with GxP requirements, validation processes, and audit expectations ✅ Maintain project documentation and governance standards Desired Experience ✔ PMO, Project Coordinator, or Project Management experience in the pharmaceutical, biotech, or life sciences industry ✔ Experience supporting digital transformation initiatives ✔ Strong understanding of GxP-regulated environments ✔ Knowledge of Manufacturing, Laboratory, or Quality Systems ✔ Experience with governance, reporting, and stakeholder management ✔ Excellent communication and organizational skills Preferred Systems Experience • PAS-X (MES), • LIMS / LES, • Veeva QMS, • LabWare, • Werum / Körber, • Quality and Manufacturing digital platforms Ideal Candidate You are a proactive and detail-oriented PMO professional who thrives in complex, regulated environments and enjoys coordinating multiple stakeholders, vendors, and technical teams to ensure successful project delivery. 📩 Interested? Apply now or contact me directly for a confidential discussion. #PMO #ProjectManagement #Pharma #LifeSciences #DigitalTransformation #MES #PASX #LIMS #LES #Veeva #QualitySystems #Manufacturing #GxP #Pharmaceuticals #BarcelonaJobs #Hiring #ProjectCoordinator #PMOJobs #OxfordGlobalResources

En Rubió llevamos más de 55 años trabajando para que todas las personas tengan acceso a nuestros medicamentos, independientemente de la prevalencia, contribuyendo así a mejorar su calidad de vida. Uno de nuestros principales rasgos diferenciales es nuestra apuesta por la producción propia, junto con una inversión sostenida en I+D, lo que nos permite seguir creciendo de forma alineada con nuestro propósito: generar un impacto positivo en la sociedad y el medio ambiente. Reconocidos como #GreatPlaceToWork en los últimos años, seguimos apostando por el crecimiento y la incorporación de nuevo talento, en un entorno dinámico, colaborativo y comprometido con la excelencia dentro de la industria farmacéutica. Actualmente, buscamos incorporar un/a Manager de Procurement dentro del área de Compras para nuestra sede en Castellbisbal. ¿Cuál será tu rol? La persona seleccionada será responsable de liderar la creación y desarrollo del área de Procurement, diseñando e implementando la estrategia de compras de la compañía. Su misión será evolucionar el modelo actual hacia un enfoque estratégico orientado a la gestión por categorías, creación de valor y optimización del impacto en la cuenta de resultados (P&L), alineando las políticas de compra con criterios de sostenibilidad, RSC y ESG. Funciones principales • Diseñar y desarrollar el departamento de procurement, estableciendo la estrategia global de compras., • Definir el nivel de madurez del área, evolucionando desde un modelo de purchasing operativo hacia un enfoque estratégico de procurement y value integration., • Desarrollar e implementar estrategias de gestión por categorías, analizando su perímetro de gestión y ciclo de vida., • Gestionar las categorías de compras directas (materias primas, materiales de acondicionamiento, semielaborados y producto acabado)., • Gestionar las compras indirectas relacionadas con operaciones industriales., • Analizar y optimizar el pool de proveedores, racionalizando la base de suministro., • Establecer relaciones de partnership con proveedores estratégicos., • Identificar posibles debilidades en la cadena de suministro y desarrollar planes de contingencia y proveedores alternativos., • Diseñar e implementar políticas de compras y código de conducta para proveedores., • Desarrollar herramientas de seguimiento y evaluación de proveedores, incluyendo scorecards y métricas de rendimiento., • Gestionar el presupuesto de compras considerando tanto volumen (Q) como valor económico (P). ¿Qué requisitos buscamos? • Titulación universitaria en Ingeniería, ADE, Económicas o similar., • Experiencia mínima de 3 a 5 años en un puesto similar dentro del área de compras o procurement., • Experiencia previa en entornos industriales (valorable)., • Conocimiento de GMP’s (valorable)., • Manejo imprescindible de SAP., • Nivel alto de inglés., • Capacidad para cuestionar el status quo e impulsar procesos de cambio., • Perfil analítico, orientado a resultados y a la mejora continua., • Capacidad de trabajo en equipo y liderazgo transversal., • Persona honesta, con capacidad para gestionar el cambio y generar impacto en la organización. ¿Qué ofrecemos? • Contratación estable., • Jornada partida con viernes intensivo., • Horario flexible de entrada., • 2 días de teletrabajo a la semana., • Jornada intensiva en verano., • Beneficios sociales: catering subvencionado, mutua de salud, seguro de vida, club de descuentos y otros beneficios adicionales. Si crees que encajas con el perfil y quieres formar parte de un equipo comprometido con la excelencia y la innovación, ¡te estamos buscando! Si quieres saber más sobre nosotros, visita nuestra web: _ Nuestro Compromiso con la Igualdad: Laboratorios Rubió es un Empleador de Igualdad de Oportunidades. Creemos que las mejores ideas e innovaciones provienen de un equipo diverso de talentos, antecedentes y experiencias. Esta creencia guía nuestro enfoque hacia el reclutamiento, desarrollo y retención de nuestros empleados, asegurando que todos tengan la oportunidad de alcanzar su máximo potencial, independientemente de raza, color, sexo/género, incluidos embarazo, identidad y expresión de género, origen nacional, religión, orientación sexual, discapacidad, edad, estado civil, estatus de ciudadanía, estatus de veterano o cualquier otra clasificación protegida bajo la ley aplicable. Diversidad e Inclusión como propósito: La diversidad y la inclusión no son solo políticas en Laboratorios Rubió; son los pilares de nuestro ethos corporativo. Nos esforzamos por crear una cultura inclusiva donde cada empleado y empleada se sienta valorado, respetado y escuchado. Estamos comprometidos a fomentar un ambiente donde se alienten opiniones y perspectivas diversas y donde cada empleado pueda contribuir a su máximo potencial. Apoyamos activamente las iniciativas de equidad de diversidad e inclusión y estamos dedicados a hacer adaptaciones razonables, para personas calificadas con discapacidades y para aquellos con creencias religiosas, de acuerdo con la ley aplicable.

En BESIDE apostamos por el mejor talento dentro del sector tecnológico e industrial. Contamos con una unidad de Selección Especializada en perfiles de Ingeniería para incorporarse en la plantilla de nuestros clientes. Trabajamos con un amplio rango de empresas, que nos permitirá encontrarte el puesto que más se ajuste a tus necesidades e intereses profesionales. Te podrás incorporar en las empresas más innovadoras, ofreciéndote proyectos punteros dentro de las ramas de I+D, automoción, pharma, diseño de maquinaria, desarrollo de producto, etc. Buscamos un/a Ingeniero de Software Embebido. Funciones • Desarrollo de firmware en C/C++ para microcontroladores de 32 bits en entornos bare-metal y RTOS, asegurando respuesta determinista en tiempo real., • Implementación de control de motor e inversor mediante lógica PWM y gestión de rampas de aceleración/desaceleración., • Desarrollo de algoritmos de detección de obstáculos por análisis de consumo de corriente, sin sensores externos., • Gestión de protocolos de comunicación industrial (CAN-bus, RS485/Modbus, I²C) para integración con sistemas domóticos y periféricos digitales., • Implementación de sistemas de diagnóstico, registro de errores y rutinas de autocalibración de recorrido (autoaprendizaje). Requisitos • Experiencia en desarrollo de firmware con C/C++ para microcontroladores de 32 bits., • Conocimientos de programación bare-metal y/o RTOS., • Experiencia en control de motores e inversores mediante PWM., • Conocimientos de protocolos de comunicación industrial: CAN-bus, RS485/Modbus, I²C., • Capacidad para desarrollar algoritmos de análisis de señal (corriente) para detección de obstáculos., • Experiencia en implementación de sistemas de diagnóstico, logging de errores y rutinas de autocalibración.

En BETWEEN te ofrecemos las oportunidades que necesitas para alcanzar tus objetivos profesionales. Si quieres desarrollar tus capacidades en IT e Ingeniería ¡este es tu próximo destino! Damos soporte en una gran variedad de áreas como Firmware, Software, BI, Diseño, Project Management y muchas más. Además, desarrollamos soluciones tecnológicas a medida desde nuestros BETWEEN Lab s En Between Technology, buscamos un/a Ingeniero/a de Control - Programador/a PLC para unirse a nuestro equipo en Terrassa. Como parte de nuestro compromiso continuo con la innovación y la excelencia, estamos interesados en profesionales altamente cualificados que tengan una sólida experiencia en sistemas de control y programación de PLC, especialmente en entornos relacionados con Siemen s. La posición está enfocada en la programación y puesta en marcha de maquinaria relacionada con procesos de liofilización, carga y descarga, trabajando sobre instalaciones distribuidas globalmen te.Formarás parte de un equipo técnico de aproximadamente 9 personas, organizado por tecnologías, colaborando en entornos dinámicos y altamente especializad os.El rol inclu • ye:Programación de PLCs (Siemens principalmente) y configuración de, • HMIPuesta en marcha y soporte en casa de clie, • nteParticipación en intervenciones técnicas sobre maquinaria industr, • ialCoordinación con equipos internaciona les Requis • itosFormación técnica en Ingeniería (Electrónica, Eléctrica, Automatización o similar) o FP superior equivale, • nte.Experiencia mínima de 3 años en programación de PLCs, principalmente Siemens (TIA Port, • al).Experiencia en puesta en marcha y soporte técnico en casa de cliente, idealmente en entornos industria, • les.Valorable experiencia en maquinaria del sector pharma / procesos de liofilización, carga y desca, • rga.Conocimientos en configuración de HMI y sistemas de control industr, • ial.Nivel de inglés medio-alto para trabajar en entorno internacio, • nal.Disponibilidad para viajar a nivel internacional (hasta un 40%, con estancias máximas de 3 seman, • as).Carnet de condu cir.

En BETWEEN te ofrecemos las oportunidades que necesitas para alcanzar tus objetivos profesionales. Si quieres desarrollar tus capacidades en IT e Ingeniería ¡este es tu próximo destino! Damos soporte en una gran variedad de áreas como Firmware, Software, BI, Diseño, Project Management y muchas más. Además, desarrollamos soluciones tecnológicas a medida desde nuestros BETWEEN Lab En Between Technology, buscamos un/a Ingeniero/a de Control - Programador/a PLC para unirse a nuestro equipo en Terrassa. Como parte de nuestro compromiso continuo con la innovación y la excelencia, estamos interesados en profesionales altamente cualificados que tengan una sólida experiencia en sistemas de control y programación de PLC, especialmente en entornos relacionados con Siemens. La posición está enfocada en la programación y puesta en marcha de maquinaria relacionada con procesos de liofilización, carga y descarga, trabajando sobre instalaciones distribuidas globalmente. Formarás parte de un equipo técnico de aproximadamente 9 personas, organizado por tecnologías, colaborando en entornos dinámicos y altamente especializad os. El rol incluye: • Programación de PLCs (Siemens principalmente) y configuración de HMI, • Puesta en marcha y soporte en casa de cliente, • Participación en intervenciones técnicas sobre maquinaria industrial, • Coordinación con equipos internacionales Requisitos • Formación técnica en Ingeniería (Electrónica, Eléctrica, Automatización o similar) o FP superior equivalente., • Experiencia mínima de 3 años en programación de PLCs, principalmente Siemens (TIA Portal)., • Experiencia en puesta en marcha y soporte técnico en casa de cliente, idealmente en entornos industriales., • Valorable experiencia en maquinaria del sector pharma / procesos de liofilización, carga y descarga., • Conocimientos en configuración de HMI y sistemas de control industrial, • Nivel de inglés medio-alto para trabajar en entorno internacional., • Disponibilidad para viajar a nivel internacional (hasta un 40%, con estancias máximas de 3 semanas), • Carnet de conducir., • Capacidad de adaptación y disponibilidad para cierta flexibilidad horaria en función de intervenciones de servicio.

Uno de nuestros principales rasgos diferenciales es nuestra apuesta por la producción propia, junto con una inversión sostenida en I+D, lo que nos permite seguir creciendo de forma alineada con nuestro propósito: generar un impacto positivo en la sociedad y el medio ambiente.Actualmente, buscamos

Uno de nuestros principales rasgos diferenciales es nuestra apuesta por la producción propia, junto con una inversión sostenida en I+D, lo que nos permite seguir creciendo de forma alineada con nuestro propósito: generar un impacto positivo en la sociedad y el medio ambiente.Actualmente, buscamos

DISPROQUIMA in Terrassa, Spain, is seeking a Pharma & DS Applications Lab Manager for its Terrassa offices. The role involves providing technical support to customers and the sales team on formulation of pharmaceutical dosage forms across Spain and subsidiaries. You will lead development of new applications, conduct compatibility and stability studies, and create prototypes for trade shows and dedicated projects within the Pharma & Dietary Supplements laboratory. #J-18808-Ljbffr

At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters. A healthier future. It's what drives us to innovate. To continuously advance science and ensure everyone has access to the healthcare they need today and for generations to come. Creating a world where we all have more time with the people we love. That's what makes us Roche. At Roche Global Regulatory Affairs we strive to be the world's best Regulatory organization, championing patient access to the world's best diagnostics. Our team is tasked with regulatory projects as well as overarching regulatory topics with specific focus in Companion Diagnostics. You can expect an open-minded work environment, where you will be working closely with colleagues in other departments and other counties. • You oversee regulatory document and submission compilation, which includes the development of submission/product registration dossiers of more complex products/programs. You develop and manage parts of comprehensive global regulatory submissions and registration plans., • You interface with external management. You understand the structure, key roles and responsibilities of external customers/stakeholders and communicate timely and effectively the needs of external customers/stakeholders. You build effective and enduring external relationships and apply effective stakeholder management practices. You contribute to audits by supporting preparation, execution and follow up, • You lead the organization to adapt to the evolving regulatory environment and requirements. You have an understanding of external environmental changes, precedents, to navigate complex situations and influence strategies and decision making. You have the ability to interpret and apply understanding of the regulators' thinking to projects and apply strategies to the different needs of different regions without significant guidance. You proactively create unique/innovative regulatory strategies and influencing approaches to avoid regulatory obstacles and accelerate worldwide approvals, • You effectively partner with external and internal stakeholders to understand and provide best solutions. You take initiative to address problems or opportunities and involve collaborators for best solutions. You develop relationships that significantly influence the current and future direction for Roche and our products., • You have courage to make decisions even outside of scope/comfort zone and proactively initiate activities independently. You embrace good decision making principles, • You model VAAC Leadership and agility. You identify opportunities to develop VACC competency. You act with integrity, courage, passion and honor commitments and contribute to an inclusive environment, • You are able to pull people together around a common goal and seek to understand and build on different perspectives to enhance outcomes. You address and resolve conflict by creating an atmosphere of openness and trust. You bring out the best in people and teams, • You have a Bachelor’s / Master degree in Life Science, Data Science or related subject or equivalent experience. Advanced degree preferred, • You have 3-5 years experience with PhD degree, 5-7 with Masters degree and 6-8 years with Bachelor degree in the field of IVDs/Medical devices/Pharma/Biopharmaceutical with significant experiences in Regulatory Affairs, • You have demonstrated experience and knowledge of Daily Management and Continuous Improvement best practices, • You have knowledge of the European, US, China and other international regulations and demonstrated ability to adequately interpret and implement quality standards considered an advantage, • You have demonstrated the ability to manage more complex work and/or at parts of global projects You are local to Indianapolis, Penzberg, or Sant Cugat. No relocation benefits are available for this position. The expected salary range for this position based on the primary location of Indiana is $106,100 and $197,000. Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors permitted by law. A discretionary annual bonus may be available based on individual and Company performance. This position also qualifies for the benefits detailed at the link provided below. Where pay transparency applies, details are provided based on the primary posting location. For this role, the primary location is Indianapolis. If you are interested in additional locations where the role may be available, we will provide the relevant compensation details later in the hiring process. Who we are A healthier future drives us to innovate. Together, more than 100'000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact. Let's build a healthier future, together. Roche is an equal opportunity employer. It is our policy and practice to employ, promote, and otherwise treat any and all employees and applicants on the basis of merit, qualifications, and competence. The company's policy prohibits unlawful discrimination, including but not limited to, discrimination on the basis of Protected Veteran status, individuals with disabilities status, and consistent with all federal, state, or local laws. If you have a disability and need an accommodation in relation to the online application process, please contact us by completing this form Accommodations for Applicants. #J-18808-Ljbffr

At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters. The Position Are you passionate about driving scientific strategies that transform clinical practice and improve patients' lives? We are looking for a Medical Affairs Lead to define and execute the comprehensive medical strategy for Roche Diagnostics Spain. In this high-impact role, you will serve as the primary liaison between the scientific community, international expert networks, and Roche’s global medical teams. Your mission will be to lead evidence generation, shape the scientific positioning of our diagnostic solutions, and act as a key internal strategic partner—ensuring that science and clinical excellence guide our business decisions. Your Main Responsibilities - Integrated Medical Strategy & Leadership: Develop and execute integrated medical plans across key therapeutic areas, aligning local priorities in Spain with Roche’s global medical strategy. - KOL Engagement & Scientific Partnerships: Lead engagement with a broad national network of Key Opinion Leaders (KOLs) and Tier-1 international experts. You will foster long-term scientific partnerships and capture high-quality clinical insights to inform strategic decision-making. - Evidence Generation & Early Adoption: Drive the generation of required medical evidence (both company-sponsored and Investigator-Initiated Studies) in alignment with strategic priorities, enabling the early adoption of Roche’s technologies into clinical practice guidelines and consensus statements. - Medical Education & Capability Building: Design and deliver medical education and training programs for field teams, enhancing scientific communication, technical accuracy, and engagement effectiveness. - Cross-Functional Strategic Partnership: Provide scientific leadership and influence decision-making across internal stakeholders (Marketing, Market Access, Sales, and Medical), ensuring accuracy, regulatory compliance, and alignment with the overall medical strategy. Who You Are We are looking for a candidate with a strong scientific background, business acumen, and proven leadership through influence. - Education: Degree in Life Sciences (MD, MSc, PhD). - Professional Experience: 2 to 5 years of experience in evidence generation and project management within the healthcare sector (Medtech, IVD, or Pharma). - Capabilities & Core Skills: - Strategic Mindset: Ability to translate complex scientific data into actionable value propositions. - Leadership & Drive: Results-oriented with a strong commitment to operational excellence. - Effective & Assertive Communication: Skilled in tailoring complex technical messages for diverse audiences—from scientific boards to senior management. - Collaboration & Teamwork: Strong interpersonal skills for cross-functional collaboration within a matrix organization. - Languages: High level of English and Spanish (essential for daily interaction with global medical teams and international networks). - Location: Sant Cugat, Barcelona. What is here for You? - Real Impact on Healthcare: A high-visibility role where your strategic input and evidence generation projects directly contribute to transforming diagnostic solutions and personalized healthcare. - Global Exposure: Direct collaboration with global leadership teams, cross-border projects, and international expert panels. - Culture of Innovation & Development: A dynamic, flexible, and collaborative environment that fosters continuous learning, autonomy, and professional growth. Who we are A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact. Let’s build a healthier future, together. Roche is an Equal Opportunity Employer.

At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters. The Position Who We Are At Roche Diagnostics Solutions (RDS), our mission is clear: to diagnose earlier, develop faster, and personalize treatment because every patient is unique. Within Development Services & Integration (DSI), we maximize value in product development by delivering efficient services and integrated solutions that enable standardization, increase efficiency, and ensure compliance. We see ourselves and our partners as a team that can only reach its full potential together. Driven by this collaborative spirit, our expertise, and an enterprise mindset, we create an environment where ideas grow and new ways of doing things are realized—accelerating the DIA strategy and delivering competitive products to patients faster. The Opportunity The Digital Innovation and Operational Services Chapter is a global team in R&D that focuses on internal improvement: increasing productivity, efficiency, and the ability of the R&D organization to collaborate across its global organizational interfaces. Our work involves reducing the complexity of our systems, harmonizing processes, tools, and business practices, and building connections across geographical and organizational silos. To support our digitalization journey, we are looking for a talented and driven Data and Automation Engineer with a passion for eliminating wasteful and mundane tasks through innovative technology. In this role, you will be instrumental in enabling our organization’s transformational transition to Agentic AI by establishing a robust and scalable data foundation. You will bridge the gap between technical data engineering and business process analysis, ensuring our internal R&D and enterprise systems operate in a seamless, automated, and data-driven ecosystem. As part of a global team, you will collaborate with experts coming from IT, business processes, and R&D science backgrounds to build solutions that enhance the productivity of our internal tool service and support teams, while maintaining the highest standards of data integrity, privacy, and security. Key Responsibilities Data Insights & Solution Delivery Support efforts to utilize the power of accumulated R&D data in tool data sources, promote / enable the standardization of data in our internal tool ecosystem. Support the ownership of data products for central data analytics. Data Modernization: Support our digitalisation strategy by driving the migration of data from legacy systems to modern architectures to ensure scalability and performance. Agentic AI Readiness: Combine technical knowledge in Agentic AI and Data Architecture to build a foundation that supports intelligent agents and advanced automation. Business Process Analysis and Requirements Engineering: Act as a bridge between technical teams and business units to analyze, map, and define requirements for specific use cases in support of digitalisation initiatives and the evolution of DSI-owned tools. Collect input from R&D scientists and engineers to support your assessments. Strategic Insights: Generate and communicate data-driven insights and visualizations to support high-level strategic business decisions. Compliance & Validation: Ensure compliance in risk management, data and systems in collaboration with respective experts. Global Collaboration: Participate in global teams across our R&D organization in support of digitalisation initiatives, working with scientists, engineers, and IT professionals in Spain, the US, Germany, and Switzerland to bring value to our organization on a global scale. Operate with limited guidance: Develop and maintain an awareness of the Roche organization and key organizational drivers as well as the relevant processes, customers, and products. Work within existing procedures to perform a range of assignments related to own projects / scope. Solves complex problems by analyzing possible solutions using experience, judgment, and precedents. Fulfill responsibilities with a limited to moderate level of guidance and direction. Basic Qualifications Education: Bachelor’s or Master’s degree in Computer Science, Data Engineering, Software Engineering, or a related technical field. Experience: 3-5+ years of professional experience in data engineering, automation, or a similar technical role. Technical Skills: Experience in programming languages such as Python or JavaScript or C#. Experience with SQL and NoSQL database management. Familiarity with ETL/ELT processes and data integration tools. Language: Excellent command of English (written and spoken) for effective collaboration in a global environment. German language skills are a plus. Global Flexibility: Ability to support a flexible schedule that periodically accommodates collaboration across multiple time zones (primarily CET and PST), ensuring effective communication with global stakeholders and project teams. Travel: Occasional travel, up to 1 week, 1-2 times per year to other Roche sites in US and Europe. Desired Skillsets & Experience Industry Knowledge: Experience working in the Diagnostics industry or other highly regulated environments (e.g., Pharma, MedTech). Regulatory Context Exposure: Exposure to Design Control, formal system engineering / product development processes Enterprise Platforms: Familiarity with SAP S/4HANA environments, HR/Learning systems like Workday or Cornerstone, specifically regarding data extraction and workflow automation. R&D Tools: Familiarity with electronic Lab Notebook, LIMS systems, equipment / asset management systems. AI & Automation: Hands-on experience with LLMs, Agentic AI frameworks, or building conversational AI interfaces (Chatbots). Cloud Architecture: Knowledge of cloud-based data warehouses (e.g., Snowflake) and cloud providers (AWS, Azure, or GCP). Communication: Ability to translate complex technical findings into actionable business insights for non-technical stakeholders. Who You Are You are a proactive problem-solver who thrives in a multicultural environment. You are not just a coder; you are a "thinker" who understands the business impact of data. You are comfortable navigating ambiguity and are committed to continuous learning in the rapidly evolving landscape of AI and automation, supporting our colleagues to speed up their engineering and science. Discover how our benefits and rewards will enable you to do your best work, every day. Let’s thrive together in a culture built on trust, collaboration, respect, and high performance. Who we are A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact. Let’s build a healthier future, together. Roche is an Equal Opportunity Employer.

Uno de nuestros principales rasgos diferenciales es nuestra apuesta por la producción propia, junto con una inversión sostenida en I+D, lo que nos permite seguir creciendo de forma alineada con nuestro propósito: generar un impacto positivo en la sociedad y el medio ambiente.Reconocidos como #Gre

Ambit Iberia in Sant Cugat del Vallès is seeking a DevOps Engineer to support automation and modernization of infrastructure.

In this role, you will design and develop scalable automation solutions, CI/CD pipelines, and Infrastructure as Code (IaC) frameworks, working closely with Infrastructure, Platform, Operations, and Development teams to drive a more efficient, secure, and software-defined operating model.Design and i

Omega CRM Consulting seeks an IT Security & Legal Compliance Specialist to collaborate with a top global pharmaceutical company. You will support Microsoft Purview IRM, improve policies, and maintain auditable processes across Legal, Compliance, HR, and IT Security.

Omega CRM Consulting, a Merkle Company, is seeking an IT Security & Legal Compliance Specialist to support global operations around Microsoft Purview Insider Risk Management and related data privacy governance. You will optimize policies, coordinate with Legal, Compliance, HR, and IT Security, and e

Pharma & DS Applications Lab Manager. We are currently recruiting a new Pharma & DS Applications Lab Manager in Terrassa, Spain. Pharma & DS Applications Lab Manager.

Experiencia demostrada en Pharma comercial (must). Business Analyst Senior – Sector Pharma (Tableau / Power BI). En knowmad mood buscamos un Business Analyst Senior con amplia experiencia en analítica de datos y un profundo entendimiento del sector Pharma comercial (omnichannel, ventas y finanzas

Kern Pharma busca un Facilitador/a de Calidad para sus oficinas de Terrassa, para gestionar y asegurar el sistema de calidad en áreas científico-técnicas, farmacovigilancia, clínica, planta piloto y laboratorio.Se requiere formación universitaria en el sector salud y experiencia en laboratorios

A pharmaceutical company in Sant Cugat del Vallès is seeking a Quality Trainee to provide quality control services across the Spanish, Portuguese, and Italian markets. Key responsibilities include ensuring compliance with GMP/GDP standards, drafting SOPs for the Quality Department, and monitoring p

Business Analyst Senior – Sector Pharma (Tableau / Power BI). En knowmad mood buscamos un Business Analyst Senior con amplia experiencia en analítica de datos y un profundo entendimiento del sector Pharma comercial (omnichannel, ventas y finanzas). Vacante 1– Business Analyst Senior (Tableau).

Grifols in Sant Cugat del Vallès is seeking a Quality Systems Specialist to join our global quality team.

Join a leading global pharmaceutical company as an IT EDP Data Migration System Lead.

Kern Pharma es una compañía farmacéutica, familiar y nacional. Todos los que formamos parte de Kern Pharma tenemos la oportunidad de sentir que somos parte importante de esta gran familia, creando nuevas ideas y soluciones con el propósito de construir nuestra propia historia, en donde compartir

Kern Pharma es una compañía farmacéutica, familiar y nacional. Todos los que formamos parte de Kern Pharma tenemos la oportunidad de sentir que somos parte importante de esta gran familia, creando nuevas ideas y soluciones con el propósito de construir nuestra propia historia, en donde compartir

Kern Pharma cuenta con el compromiso de establecer prácticas que integren la igualdad real de oportunidades entre mujeres y hombres, sin discriminar directa o indirectamente por razón de género.

Kern Pharma busca un/a Analista de Licitaciones para sus oficinas de Terrassa.

Kern Pharma, ubicada en Terrassa, busca un/a Técnico/a de Producción para su área de Acondicionado Sólidos.

ROMACO TECPHARM selecciona para su centro de trabajo ubicado en RUBI, UN/A DELINEANTE-PROYECTISTA OFICINA TECNICA.Se responsabilizará del diseño de piezas y maquinaria, así como del seguimiento del Proyecto asignado bajo la supervisión del Responsable de Oficina Técnica.Deberá aportar conocimi

SYNTEGON is seeking a motivated Design Engineer in Terrassa, Spain, to support customer-specific projects in the pharmaceutical process business.

Kern Pharma en Terrassa busca un/a Maintenance Manager para dirigir el área técnica de mantenimiento de su planta farmacéutica.

Syntegon que opera mundialmente en proyectos GMP de consultoría, ingeniería, construcción y equipo de proceso integrado.Atendemos a la industria de ciencias de la vida, hospitales y centros de investigación, así como soluciones con tecnologías de vacío para sectores energéticos y aeroespacia

Syntegon que opera mundialmente en proyectos GMP de consultoría, ingeniería, construcción y equipo de proceso integrado.Atendemos a la industria de ciencias de la vida, hospitales y centros de investigación, así como soluciones con tecnologías de vacío para sectores energéticos y aeroespacia

Buscamos un/a Commercial Excellence Manager para formar parte del equipo de Leo Pharma y liderar una de las palancas estratégicas clave de la organización dentro del área de Commercial Excellence.

Máyla Pharma busca un/a Director Nacional de Ventas para liderar la estrategia comercial a nivel nacional y acelerar el crecimiento de la compañía en Consumer Healthcare.

Are you ready to shape the future of healthcare products? ðºJoin our expert team to work on a healthcare solution, contributing to the development of innovative digital products that improve the experience of people living with chronic conditions.You will apply your knowledge of Product Management

With offices in Barcelona, the UK, and China, we provide unparalleled support to global Pharmaceutical, Biotech, and Medical Device supply chains. About the Role We are seeking an experienced Project Manager to join our QMS Department and lead the implementation of Quality Management Systems for cli

Are you passionate about building scalable Angular applications with modern frontend architectures?? ð§ª️Join our expert team to work on an international enterprise platform, contributing to the development of data-intensive business applications and complex user workflows.You will apply your k

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. Asegurar una atención profesional, ágil y alineada con los estándares de LETI Pharma. LETI Pharma promueve e

Inventory Planner & Procurement Specialist.La persona seleccionada será responsable de garantizar la disponibilidad de materiales y productos, optimizando los niveles de inventario y asegurando un suministro eficiente para los mercados de España y Portugal.Será una posición clave para coordinar

Would you like to start a new professional adventure as a Global Automation Implementation Project Lead in one of our opportunities in the pharmaceutical industry in Barcelona? Your missions? • Lead the planning, coordination, and execution of global automation projects, from initiation to s

Todo ello para nuestra marca Pfeiffer orientada hacia soluciones de alto vacío (sectores de pharma, equipamiento médico, laboratorios, etc.

Participa en un innovador proyecto para cliente del.Weighing & Dispensing Product Owner.En ALTEN tenemos claro que el éxito de nuestros proyectos se debe a las personas que forman nuestro equipo.Weighing & Dispensing Product Owner.Quieres construir hoy el mundo de mañana? ¡Sigue leyendo!.GxP) o g

Todo ello para nuestra marca Pfeiffer orientada hacia soluciones de alto vacío (sectores de pharma, equipamiento médico, laboratorios, etc.