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Clinical Quality Assurance & Training Lead – CROVELIS Localización: Madrid Experiencia: 5-7 años en Quality Assurance dentro de clinical research, pharma, biotech o healthcare, con experiencia en liderazgo de calidad o gestión de operaciones clínicas. La oportunidad En CROVELIS buscamos incorporar un/a Clinical Quality Assurance & Training Lead para liderar y desarrollar el sistema de calidad y formación de la compañía. Será una posición clave para impulsar una cultura de calidad, asegurar el cumplimiento regulatorio y acompañar el crecimiento de la organización, garantizando que los procesos, equipos y sistemas estén preparados para afrontar los retos de una compañía innovadora de investigación clínica. ¿Cuál será tu reto? Liderar la estrategia y mejora continua del Quality Management System (QMS) . Garantizar el cumplimiento de estándares GxP, requisitos regulatorios y expectativas de clientes. Definir y monitorizar KPIs de calidad, análisis de tendencias y planes de mejora. Gestionar auditorías internas, externas y preparación ante inspecciones regulatorias. Coordinar CAPAs, desviaciones, cambios y actividades de gestión de riesgos. Liderar el modelo de formación y cualificación de empleados, incluyendo onboarding, SOPs y formación GxP. Supervisar la gestión documental y los sistemas de calidad. Colaborar con equipos internos y proveedores para asegurar la excelencia operativa. ¿Qué buscamos? Formación universitaria en Life Sciences (Farmacia, Biotecnología, Medicina, Química u otras áreas relacionadas). Experiencia sólida en Quality Assurance dentro de clinical research, CRO, pharma o biotech . Experiencia liderando iniciativas de calidad, equipos o proyectos transversales. Conocimiento profundo de GxP, ICH-GCP, auditorías, CAPAs, gestión de riesgos y compliance regulatorio . Experiencia trabajando con sistemas como eQMS, eTMF, CTMS/TMS o DMS . Inglés fluido (oral y escrito). Experiencia en entornos internacionales será valorada. Perfil ideal Buscamos una persona con visión estratégica y capacidad para aterrizar la calidad en procesos prácticos, con habilidades de comunicación, influencia transversal y orientación a la mejora continua. Alguien capaz de combinar conocimiento técnico, liderazgo y mentalidad de crecimiento para ayudar a construir y evolucionar el modelo de calidad de CROVELIS. ¿Por qué CROVELIS? Formarás parte de una compañía de investigación clínica en crecimiento dentro de Insud Pharma , con un entorno innovador donde la calidad, la tecnología y la excelencia operativa son pilares fundamentales para transformar la forma en la que se desarrollan los ensayos clínicos.

Desde la división de Química&Pharma nos encontramos en la búsqueda de un/a Técnico/a Desarrollo Galénico - Inyectables para una empresa del sector industrial con sede en Madrid. ¿Qué harás? Desarrollo farmacéutico de productos inyectables estériles (soluciones, suspensiones, liofilizados, formulaciones peptídicas y complejas), incluyendo estudios de preformulación, optimización y escalado bajo normativa GMP. Diseño, ejecución y transferencia de procesos de fabricación, participando en validaciones, soporte a producción y asegurando el cumplimiento regulatorio e ICH. Gestión y análisis de datos experimentales y documentación técnica, elaborando protocolos, informes, SOPs y batch records, y aplicando metodologías de Quality by Design (QbD) para la mejora continua. Colaboración multidisciplinar y liderazgo de proyectos, con una actitud proactiva, creativa y orientada a la resolución de problemas, asumiendo la responsabilidad y seguimiento integral de los proyectos hasta su finalización. ¿Qué buscamos? Graduado en Farmacia, Química o similar. Nivel de Ingles tanto oral como escrito alto. Se requieren de 1-3 años de experiencia en desarrollo de formulaciones de inyectables. ¿Qué ofrecemos? Contrato indefinido con cliente final. Salario competitivo. Retribución flexible. Banda Salarial; Según experiencia aportada por los candidatos (30k-40k).

¿Te apasiona Regulatory Affairs y quieres contribuir al desarrollo de nuevos tratamientos? En Crovelis , la CRO del grupo Insud Pharma , seguimos creciendo y buscamos incorporar un/a Senior Regulatory Affairs Specialist para unirse a nuestro equipo de Clinical Operations en Madrid . Si tienes experiencia gestionando ensayos clínicos internacionales , trabajando con CTIS , el European Clinical Trials Regulation (EU CTR 536/2014) y procesos regulatorios con la FDA , esta puede ser la oportunidad que estabas esperando. En pocas palabras Posición: Senior Regulatory Affairs Specialist Ubicación: Madrid, España Experiencia: +5 años en Regulatory Affairs dentro de ensayos clínicos ¿Cuál será tu misión? Serás una pieza clave en la estrategia regulatoria de estudios clínicos internacionales, coordinando todas las actividades regulatorias desde el start-up hasta el cierre del estudio y garantizando el cumplimiento de los requisitos regulatorios en Europa y Estados Unidos. Trabajarás de forma transversal con equipos de Clinical Operations, Medical Writing, Pharmacovigilance, Quality, sponsors y autoridades regulatorias, contribuyendo al éxito de proyectos con impacto real en el desarrollo de nuevos medicamentos. ¿Qué buscamos? Buscamos un perfil con experiencia demostrada en: ✅ Regulatory submissions mediante CTIS . ✅ Gestión del ciclo de vida regulatorio de ensayos clínicos. ✅ Preparación de submissions a la FDA (INDs y otras interacciones regulatorias). ✅ Resolución de Requests for Information (RFIs) . ✅ Coordinación con autoridades regulatorias y comités éticos. ✅ Conocimiento sólido de ICH-GCP , normativa europea y regulación internacional. Valoraremos especialmente experiencia en entornos internacionales, CROs y proyectos multicéntricos. ¿Qué encontrarás en Crovelis? ✨ Formar parte de una CRO en pleno crecimiento dentro de un grupo farmacéutico internacional. ✨ Participar en proyectos clínicos estratégicos con alcance global. ✨ Colaborar con equipos multidisciplinares altamente especializados. ✨ Un entorno donde podrás seguir desarrollando tu carrera profesional y asumir nuevos retos. ¿Te interesa? Si buscas un proyecto con impacto internacional y quieres formar parte de un equipo que contribuye al desarrollo de nuevas terapias para los pacientes, nos encantará conocerte . Puedes enviar tu candidatura a través de LinkedIn o compartir esta publicación con alguien a quien pueda interesarle. #Crovelis #InsudPharma #ClinicalResearch #RegulatoryAffairs #ClinicalTrials #LifeSciences #HealthcareJobs #ClinicalOperations #Hiring #InsudTalent En Crovelis promovemos la igualdad de oportunidades y creemos en equipos diversos e inclusivos. Todas las candidaturas serán valoradas exclusivamente en función de su experiencia, competencias y potencial, sin distinción de género, edad, origen, orientación sexual, discapacidad o cualquier otra condición protegida por la legislación vigente.

Responsabilidades: * Creación y gestión del almacén de repuestos en SAP.Creación de OT de preventivos y calibraciones, gestión y cierres técnicos.Gestión de los controles de acceso.Seguimiento de legalizaciones (inspecciones periódicas por OCA y revisiones reglamentarias por empresa autoriza

ppJoin bIQVIA /b and become part of a global team dedicated to delivering high-quality data that supports decision-making across the healthcare industry. /p pIn this role, you will receive training and guidance while learning how to code, validate, and bridge healthcare-related data within IQVIA systems. You will work with large datasets, ensuring data accuracy, consistency, and quality while gaining exposure to industry-leading tools and processes. /p h3Key Responsibilities /h3 ul liLearn and apply data coding and bridging methodologies to integrate incoming healthcare and pharmaceutical data into IQVIA systems. /li liCompare transaction data against reference databases to identify and create accurate matches using both manual and automated processes. /li liPerform data quality checks to identify anomalies, duplicates, missing information, and inconsistencies. /li liSupport the maintenance of data quality standards and governance procedures. /li liCollaborate with colleagues across different teams to ensure data accuracy and reliability. /li liContribute to continuous improvement initiatives related to data management and quality processes. /li liDevelop technical skills in data analysis, data quality, and reporting tools while building expertise in healthcare and pharmaceutical data management. /li /ul h3Main Requirements /h3 ul liRecent graduate in Life Science or related disciplines. /li liInterest in healthcare data, pharmaceutical information, and data quality processes. /li liBasic knowledge of Microsoft Excel. /li liStrong attention to detail and analytical mindset. /li liAbility to work with large datasets and follow established procedures. /li liStrong organizational and communication skills. /li liEnglish language skills required. /li /ul pAt IQVIA, we believe that diversity, inclusion, and belonging empower our mission to accelerate innovation for a healthier world. We create a culture of belonging by valuing the perspectives of all talented employees worldwide and providing them with the opportunity to power smarter healthcare for everyone, everywhere. /p /p #J-18808-Ljbffr

ppReady to play a key role in bringing innovative treatments to patients? Join a global clinical research team where you'll build partnerships with leading investigators, drive the success of clinical trials, and make a real impact on the future of healthcare. /p pWe are looking for a bClinical Research Lead /b to oversee clinical trial sites, support patient enrollment, ensure compliance with regulatory requirements, and deliver an exceptional site and investigator experience. /p h3What You'll Do /h3 ul liManage and support clinical trial sites from start-up through study delivery /li liDrive site performance, patient recruitment, and enrollment success /li liBuild strong relationships with investigators and research institutions /li liEnsure compliance with Good Clinical Practice (GCP) and inspection readiness /li liOversee site monitoring activities and vendor performance /li liSupport feasibility assessments and site selection strategies /li /ul h3What You'll Bring /h3 ul liBachelor's degree in a scientific or health-related field /li li5+ years of experience in Clinical Research, Pharma, Biotech, or CRO environments /li liStrong knowledge of Clinical Trials and GCP /li liExcellent communication and stakeholder management skills /li liAvailability to travel up to 50–75% /li /ul h3Benefits /h3 ul liContribute to cutting-edge clinical research and innovative therapies /li liWork with world‑class investigators and research sites /li liSignificant autonomy and ownership of your studies /li liInternational and collaborative work environment /li liStrong career progression opportunities within a growing global organization /li liCompetitive salary, bonus, and benefits package /li /ul pbApply today and help shape the future of medicine. /b /p /p #J-18808-Ljbffr

A leading executive search firm is seeking a Regulatory Manager to provide regulatory advice and support for pharmaceutical products. The ideal candidate will have a degree in Pharmacy or Life Sciences, 10 years of experience in Regulatory Affairs, and strong knowledge of promotion regulations. This full-time position is based in Madrid, Spain, and involves maintaining marketing authorisations and ensuring compliance with local laws.#J-18808-Ljbffr

A pharmaceutical company in Valencia is seeking an Analytical Development Scientist to execute and document analytical activities for bioanalytical methods. The ideal candidate has a bachelor's degree in sciences, 3-5 years of experience in the pharma industry, and expertise in LC-MS. Responsibilities include reviewing GMP documentation, analyzing samples, and managing analytical projects. This is a full-time position at the mid-senior level.#J-18808-Ljbffr

pADVANZ PHARMA is seeking a Regional Market Access Manager for Madrid and surrounding regions to drive access across biosimilars, generics, and established products. You will engage hospital pharmacists, regional authorities, and decision makers to secure access and reimbursement. /ppThe role focuses on market access strategy, tender processes, and collaboration with Medical, Commercial, and Market Access teams to deliver results in a fast-paced, entrepreneurial environment. /p #J-18808-Ljbffr

ph3Job Title /h3 pindustry principal, Pharma/life science /p h3Location /h3 pLondon, UK / Frankfurt, Germany / Paris, France / Madrid, Spain / Malmo, Sweden (Hybrid, 50% working time at the office) /p h3Employment Type /h3 pFull time /p h3Key Responsibilities /h3 ul liIncrease AVEVA’s penetration and market share within the industry value chain. /li liBuild a strong ecosystem with executive level relationships throughout the customer base and partnerships. /li liSupport specific and numerous sales opportunities with industry specific information and expertise. /li liUnderstand the business drivers, strategic trends and competitive threats and influence in this industry and deliver our response as required to increase the value proposition. /li liCreate value proposition, emerging use cases and collateral for our products, and solution. /li /ul h3Essential Requirements /h3 ul liBachelor’s degree required. Master’s degree preferred. STEM degree highly desired. /li liMinimum of 10+ years direct experience working in industry in charge, with specific experience supporting operations and/or engineering at some level in two or more of these industries/areas. /li liHigh level of business acumen; professional written and oral communication skills; proven ability to deliver executive-level value statements; excellent presentation skills. /li liVisionary, you are a change agent in your organization and a technology early adopter in your industry. /li /ul h3Desired Skills /h3 ul liBackground in software sales highly desired. /li liProven track record of Business Development in an industry vertical. /li liHigh energy and curiosity is highly desired. /li /ul h3Benefits /h3 ul liFlexible benefits fund /li liEmergency leave days /li liAdoption leave /li li28 days annual leave (plus bank holidays) /li liPension /li liLife cover /li liPrivate medical insurance /li liParental leave /li liEducation assistance program /li /ul h3EEO Statement /h3 pAVEVA is an Equal Opportunity Employer. We are committed to being an exemplary employer with an inclusive culture, developing a workplace environment where all our employees are treated with dignity and respect. We value diversity and the expertise that people from different backgrounds bring to our business. AVEVA provides reasonable accommodation to applicants with disabilities where appropriate. If you need reasonable accommodation for any part of the application and hiring process, please notify your recruiter. Determinations on requests for reasonable accommodation will be made on a case‑by‑case basis. /p /p #J-18808-Ljbffr

pRoche Holding AG sucht einen Digital Innovation Board und Portfolio Lead, um die digitale Strategie zu leiten und sicherzustellen, dass das Portfolio effektiv mit den organisatorischen Zielen ausgerichtet ist. Zu den Schlüsselverantwortlichkeiten gehören die Leitung des Digital Innovation Boards, das Management von KPIs und die Gewährleistung der Compliance. /ppDer ideale Kandidat verfügt über mehr als 5 Jahre Erfahrung in der Leitung digitaler Transformationen im Pharma-Bereich und bringt fundierte Kenntnisse im Bereich Governance und Compliance mit. /p #J-18808-Ljbffr

Roche is looking for an experienced Senior Data Product Owner to drive business value through innovative data solutions in Madrid. Maximice sus posibilidades de que su candidatura sea seleccionada asegurándose de que su CV y sus habilidades se ajustan al perfil. This role involves managing the full lifecycle of data products and aligning them with organizational goals, ensuring data compliance and governance. The ideal candidate has over 7 years of experience in agile methodologies, with significant background as a Product Owner in the pharma or healthcare sectors. xcskxlj Strong cloud platform expertise, particularly with AWS, Azure, GCP, or Snowflake, is essential for this position. #J-18808-Ljbffr

pHaleon plc. is seeking an Account Manager to drive sales, distribution, promotion, and profitability within the pharmacy channel. The role includes developing a new omnichannel commercial model and identifying KBDs for the wholesale channel. /ppYou will coordinate with ComEx, Marketing, and Supply to unlock resources, define client-focused strategies, and maximize sell-out for Haleon brands. Strong leadership, planning, and analytical skills are essential for success. /p #J-18808-Ljbffr

pQCS Staffing is seeking a Project Scheduler for a high-impact pharmaceutical project in Madrid. This role involves developing and maintaining project schedules in Primavera P6, integrating inputs from various project phases, and performing critical path analysis. /ppThe ideal candidate will have a degree in Engineering or Project Management and extensive scheduling experience on major capital projects. Strong skills in Primavera P6 and MS Excel are essential. This is an exciting opportunity to shape the future of advanced manufacturing. /p #J-18808-Ljbffr

Project Controls Engineer – Planning, Data Centres A continuación, encontrará un desglose completo de todo lo que se requiere de los posibles candidatos, así como la forma de presentar su candidatura. ¡Mucha suerte! Join to apply for the Project Controls Engineer - Planning, Data Centres role at Turner & Townsend. Turner & Townsend is a global professional services company with over 22,000 people in more than 60 countries. Working with our clients across real estate, infrastructure, energy and natural resources, we transform together delivering outcomes that improve people’s lives. Working in partnership makes it possible to deliver the world’s most impactful projects and programmes as we turn challenge into opportunity and complexity into success. Due to growth and ongoing delivery success with our clients, we have multiple opportunities within Industrial, Science & Technology projects and are looking for Project Controls Professionals with proven experience of delivery to join our team. We encourage applicants at every skill level to apply. You might be an ideal fit for our team even if you don’t have all the required skills. Primary Responsibilities • Lead the schedule development lifecycle for one or more projects, from high‑level planning to detailed execution., • Lead dynamic planning sessions and collaborate with the extended project management team to create schedules., • Develop and manage the Owner’s schedule, ensuring alignment with quality standards., • Verify that contractor schedules and reports contain all relevant scope and escalating when lacking., • Track and summarize schedule performance (e.g., s‑curves, critical and sub‑critical paths, planned vs actual variance, float trend, start finish curves, etc.), providing stakeholders with clear and actionable reports., • Develop and maintain resource‑loaded schedules., • Undertake “what if” / scenario analysis on schedules., • Frequent visits to the construction site to provide team support, nurture relationships and assess the progress of the project., • Promote a culture of continuous improvement, focusing on creating scalable solutions and team development. Qualifications • Engineering degree or equivalent experience in a construction‑related discipline., • Strong knowledge of PMO and project controls with a focus on scheduling and risk management., • Skilled in Primavera P6 and Microsoft Project mandatory., • Skilled in Acumen Fuse and PowerBi is a plus., • Experience in data centre or pharma is a plus., • Competent in Earned Value Management (EVM)., • Fluent in both Spanish and English., • Excellent communication skills, strong attention to detail and adept problem‑solving abilities., • Have a passion for building a global team and fostering employee development. Additional Information Our inspired people share our vision and mission. We provide a great place to work, where each person has the opportunity and voice to affect change. We want our people to succeed both in work and life. To support this we promote a healthy, productive and flexible working environment that respects work‑life balance. Referrals Referrals increase your chances of interviewing at Turner & Townsend by 2x. Seniority level Mid‑Senior level Employment type Full‑time Job function Project Management Industries Construction, Civil Engineering, and Business Consulting and Services Equal Opportunity Statement Turner & Townsend is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees and actively encourage applications from all sectors of the community. Recruitment Policy It is strictly against Turner & Townsend policy for candidates to pay any fee in relation to our recruitment process. No recruitment agency working with Turner & Townsend will ask candidates to pay a fee at any time. Any unsolicited resumes/CVs submitted through our website or to Turner & Townsend personal e‑mail accounts are considered property of Turner & Townsend and are not subject to payment of agency fees. xcskxlj To be an authorised Recruitment Agency/Search Firm for Turner & Townsend, there must be a formal written agreement in place and the agency must be invited, by the Recruitment Team, to submit candidates for review. #J-18808-Ljbffr

Indegene is looking for an Account Director in Madrid to lead client relationships and oversee multiple brands within healthcare and pharma sectors. This role involves strategic oversight of projects worth $4-6 M+ and requires excellent communication skills, experience in client management, and the ability to build collaborative relationships. As an equal opportunity employer, Indegene values diversity and inclusion in its hiring process, offering a dynamic career path in the healthcare technology space.#J-18808-Ljbffr

Advanz Pharma Corp in Madrid is seeking a Regional Access Manager to drive market access strategies across Spain, focusing on biosimilars, generics, and established products. This field-based role collaborates with hospital pharmacists, regional authorities, and tender teams to secure timely access and reimbursement.You will analyze pricing, identify hospital tender opportunities, and work with Medical and Commercial teams to deliver value-based access.#J-18808-Ljbffr

F. Hoffmann-La Roche AG seeks a Senior Data Product Owner in Madrid to drive business value through innovative data solutions. The ideal candidate will lead the vision and roadmap for data products, managing the entire lifecycle from ideation to deployment and ensuring compliance with governance standards.Applicants should have over 7 years of agile experience and a proven track record in the pharma industry. The role includes collaboration with various teams and involvement in mentoring other Data Product Owners.#J-18808-Ljbffr

pHanbai.io en Madrid busca un/a Business Development Representative (BDR) para impulsar el crecimiento comercial. La persona seleccionada se encargará de generar oportunidades de negocio y establecer el primer contacto con farmacias que busquen digitalizarse. /ppEl rol incluye investigar potenciales clientes, realizar prospección activa y colaborar con el equipo comercial. Se ofrece un ambiente cercano y oportunidades de crecimiento dentro de la empresa. /p #J-18808-Ljbffr

ph3Senior Data Product Owner – Digital Operational Excellence (PTE) /h3pWe are looking for a passionate and experienced Data Product Owner to drive business value through innovative data solutions. /ph3Responsibilities /h3ulliDefine Communicate Product Vision: Lead the vision and roadmap for data products, aligning with organizational goals and stakeholder needs. /liliLead Data Product Development: Manage the full lifecycle of data products, from ideation to deployment, leveraging Roche’s IT/OT ecosystems for stable, automated solutions. /liliDrive Value Delivery Prioritization: Develop prioritized product backlogs, guiding teams to deliver scalable, reusable data products that achieve measurable business outcomes. /liliEnsure Governance Compliance: Guarantee data products adhere to Roche’s data quality standards, governance policies, and regulatory requirements (e.g., data privacy, GxP). /liliChampion Collaboration Mentorship: Act as a key liaison between business and technical teams, fostering harmonization and mentoring other Data Product Owners. /li /ulh3Qualifications /h3ulli7+ years of agile experience designing and delivering complex data solutions. /lili4+ years as a Product Owner or Data Analyst, preferably in the pharma or healthcare industry. /liliProven track record of data management on cloud platforms (AWS, Azure, GCP, Snowflake). /liliStrong understanding of data architectures, data modeling, data integration (e.g., data mesh, data warehousing), and SDLC/CSV. /liliExcellent ability to translate business requirements into technical specifications and lead teams in an agile setting. /liliStrong communication, collaboration, and stakeholder management skills. /li /ulh3Equal Opportunity Employment /h3pRoche is an Equal Opportunity Employer. We believe it’s urgent to deliver medical solutions right now – even as we develop innovations for the future. We are proud of who we are, what we do, and how we do it. We are many, working as one across functions, across companies, and across the world. /p /p #J-18808-Ljbffr

A multinational pharmaceutical company based in Barcelona is looking for a Medical Information Manager to drive strategic medical information initiatives. This role involves providing high-quality medical information services, collaborating with healthcare professionals, and supporting local business activities. Candidates should have significant experience in medical information and fluency in Spanish. The position offers an opportunity to make a substantial impact in the medical dermatology field.#J-18808-Ljbffr

pWhitewater Group is seeking a Process Engineer – Water Treatment Systems to design and deliver water treatment solutions for data centres, pharma, municipal and industrial clients. The role involves planning the design, master planning, and coordinating across disciplines with a focus on safety, reliability and sustainability. /ppYou will work in Madrid Getafe with remote options possible; the position offers a permanent full-time contract and opportunities for career progression. /p #J-18808-Ljbffr

Seqirus Spain is seeking a Medical Science Liaison to cover vaccines across Spain. You will operate in a field-based role, delivering scientific information to healthcare professionals and collaborating with Medical Affairs and cross-functional teams.The role requires fluency in English and Spanish, strong communication skills, and willingness to travel up to 50–60% across Spain. A medical or life sciences degree is required, with 3+ years in clinical/education roles in pharma preferred.#J-18808-Ljbffr

ph3Descripción /h3 pDesde Izertis, buscamos ampliar nuestro equipo con la incorporación de un bPerfil Compliance /b para participar en un proyecto estratégico dentro del sector Pharma. /p h3Funciones /h3 ul liRevisión y validación de datos regulatorios antes y después de cada evento farmacéutico realizado, asegurando que toda la información a enviar a las autoridades sanitarias es presentada en tiempo y forma. /li liGestión de documentación contractual. /li liSoporte en reporting y envíos a autoridades. /li liInteracción con equipos internos y cliente. /li /ul h3Requisitos /h3 ul li5 años de experiencia en compliance, operaciones o gestión documental/data. /li liFrancés alto imprescindible (capacidad de trabajar con documentación legal). /li liPerfil muy orientado a detalle, validación de datos y procesos. /li liCapacidad de trabajar con alto volumen de información y bajo presión (deadlines regulatorios). /li liInterés en entornos regulatorios / pharma. /li /ul h3Beneficios /h3 ul liContratación indefinida /li liSalario competitivo adaptado a tu experiencia y expectativas profesionales. /li liPaquete de retribución flexible en el que podrás contratar seguro médico, ticket restaurante, cheque guardería o transporte. /li liClases gratuitas de inglés. /li liAcceso a una amplia página de beneficios (vuelos, hoteles, moda, tecnología, hogar...) /li /ul /p #J-18808-Ljbffr

ADVANZ PHARMA is seeking a Regional Market Access Manager to drive access for biosimilars across Spain, with focus on hospital stakeholders, pricing strategies, and tender management.You will build regional market access plans, manage tenders, engage hospital pharmacists and decision makers, analyze pricing, and collaborate with Medical, Commercial and Market Access teams to secure timely patient access.#J-18808-Ljbffr

pF. Hoffmann-La Roche AG is looking for an IT Strategic Risk Audit Manager in Madrid. This role involves guiding digital transformation while ensuring robust risk management practices. Applicants should have over 15 years of experience in IT risk and audit, ideally in regulated sectors like Pharma or Finance, and expertise in various risk frameworks and GxP principles. /ppThe manager will drive strategic initiatives and manage complex compliance projects. The position requires strong leadership capabilities, excellent risk assessment skills, and familiarity with IT audits. /p #J-18808-Ljbffr

A global leader in pharmaceuticals is seeking an Engineering Project Manager to lead and coordinate projects focused on plant modifications and equipment installations. The ideal candidate should have over 5 years of experience in industrial project management within the pharmaceutical sector, a strong grasp of GMP regulations, and proficiency in both English and Spanish. This role offers the chance to work on international projects in a multicultural team environment. Join us for a rewarding career and apply today.br#J-18808-Ljbffr

ppbProject Scheduler - Spain, Madrid - 12 Months Initial Contract /b /p pLooking to take your career to the next level? We’re recruiting for a high-impact pharmaceutical project located near Madrid. With major capital investment experience driving various facility build projects. This is a unique opportunity for a Project Scheduler to join a global leader in the life sciences market and play a key role in shaping the future of advanced manufacturing. /p h3What You’ll Do /h3 ul liDevelop, baseline and maintain the fully integrated project schedule (Level 1–4) in Primavera P6. /li liDefine and maintain the Work Breakdown Structure (WBS) and activity coding aligned with project controls requirements. /li liIntegrate inputs from Engineering, Procurement, Construction and Commissioning into a consolidated schedule. /li liPerform critical path analysis, identify schedule risks and monitor float trends. /li liTrack schedule progress vs. baseline, identify variances and issue early warnings. /li /ul h3What you’ll need /h3 ul liDegree in Engineering, Project Management or related field. /li liExtensive project scheduling experience, including 5 years on major capital projects (Oil Gas, Energy, Infrastructure, Pharma, etc.). /li liAdvanced Primavera P6 proficiency (mandatory). /li liExperience with Concerto preferred (training available). /li liStrong MS Excel; MS Project desirable; Power BI beneficial. /li /ul pDon’t miss your chance to be part of something extraordinary, apply now and let’s talk! /p /p #J-18808-Ljbffr

AVEVA is looking for an Industry Principal for the Pharma/life science sector, located in Madrid, Spain. The successful candidate will increase AVEVA’s market share by fostering executive relationships and supporting sales opportunities with industry insights. With a strong background in the industry and over 10 years of experience, the candidate will be visionary and become a change agent. The role offers remote flexibility and a comprehensive benefits package, including annual leave and private medical insurance. #J-18808-Ljbffr

pAVEVA is looking for an Industry Principal for the Pharma/life science sector, located in Madrid, Spain. The successful candidate will increase AVEVA’s market share by fostering executive relationships and supporting sales opportunities with industry insights. /ppWith a strong background in the industry and over 10 years of experience, the candidate will be visionary and become a change agent. The role offers remote flexibility and a comprehensive benefits package, including annual leave and private medical insurance. /p #J-18808-Ljbffr

Viseven Group in Madrid is seeking a Head of Product to own and drive the success of the entire products and services portfolio, create synergies across solutions, and increase portfolio value and profitability. You will lead portfolio strategy, lifecycle, and cross-functional collaboration in a multinational environment, balancing innovation with optimization while building a high-performing product organization. xcskxlj Usted podría ser el solicitante perfecto para este trabajo. Lea toda la información asociada y asegúrese de presentar su candidatura. Hybrid work option available. #J-18808-Ljbffr

Chez Roche, vous pouvez être vous-même et être apprécié pour les qualités uniques que vous apportez. Notre culture encourage l'expression personnelle, le dialogue ouvert et les connexions authentiques, où vous êtes valorisé, accepté et respecté pour ce que vous êtes, vous permettant de prospérer tant personnellement que professionnellement. Voici comment nous visons à prévenir, arrêter et guérir les maladies et à garantir à chacun l'accès aux soins de santé aujourd'hui et pour les générations à venir. Rejoignez Roche, où chaque voix compte.La positionAre you a passionate and experienced Data Product Owner ready to drive business value through innovative data solutions? Join Roche's PT Digital and Operational Excellence (PTE) organization as a Senior Data Product Owner!At Roche, our 10-year Pharma vision is centered on delivering new data analytics solutions to scientists across Pharma Technical Operations (PT). PTE is catalyzing PT's digital transformation, activating data citizenship, and building a FAIR data ecosystem. In this role, you will be pivotal in building, maintaining, and sustaining data products that drive operational excellence and enable impactful decision-making for our patients' benefit.In this role, you will:- Define & Communicate Product Vision: Lead the vision and roadmap for data products, aligning with organizational goals and stakeholder needs.- Lead Data Product Development: Manage the full lifecycle of data products, from ideation to deployment, leveraging Roche’s IT/OT ecosystems for stable, automated solutions.- Drive Value Delivery & Prioritization: Develop prioritized product backlogs, guiding teams to deliver scalable, reusable data products that achieve measurable business outcomes.- Ensure Governance & Compliance: Guarantee data products adhere to Roche’s data quality standards, governance policies, and regulatory requirements (e.G., data privacy, GxP).- Champion Collaboration & Mentorship: Act as a key liaison between business and technical teams, fostering harmonization and mentoring other Data Product Owners.Who You Are:- 7+ years of agile experience designing and delivering complex data solutions, including 4+ years as a Product Owner or Data Analyst, preferably in the pharma or healthcare industry.- Proven track record of data management on cloud platforms (AWS, Azure, GCP, Snowflake)- Strong understanding of data architectures, data modeling, data integration (e.G., data mesh, data warehousing), and SDLC/CSV.- Excellent ability to translate business requirements into technical specifications and lead teams in an agile setting.- Strong communication, collaboration, and stakeholder management skills.Qui nous sommesUn avenir plus sain nous pousse à innover. Ensemble, plus de 100 000 employés à travers le monde sont dédiés à faire progresser la science et à garantir à chacun l'accès aux soins de santé aujourd'hui et pour les générations à venir. Nos efforts aboutissent à plus de 26 millions de personnes traitées avec nos médicaments et plus de 30 milliards de tests réalisés avec nos produits de Diagnostique. Nous nous encourageons mutuellement à explorer de nouvelles possibilités, à favoriser la créativité et à conserver nos grandes ambitions, afin de fournir des solutions de santé qui changent des vies et ont un impact mondial.Construisons ensemble un avenir plus sain.Roche est un employeur offrant l'équité en matière d'emploi.#J-18808-Ljbffr

Project Scheduler - Spain, Madrid - 12 Months Initial Contract Es esencial asegurarse de que cumple con los requisitos como solicitante para este puesto; por favor, lea atentamente la información a continuación. Looking to take your career to the next level? We’re recruiting for a high-impact pharmaceutical project located near Madrid. With major capital investment experience driving various facility build projects. This is a unique opportunity for a Project Scheduler to join a global leader in the life sciences market and play a key role in shaping the future of advanced manufacturing. What you’ll do: • Develop, baseline and maintain the fully integrated project schedule (Level 1–4) in Primavera P6., • Define and maintain the Work Breakdown Structure (WBS) and activity coding aligned with project controls requirements., • Integrate inputs from Engineering, Procurement, Construction and Commissioning into a consolidated schedule., • Perform critical path analysis, identify schedule risks and monitor float trends., • Track schedule progress vs. baseline, identify variances and issue early warnings.What you’ll need:, • Degree in Engineering, Project Management or related field., • Extensive project scheduling experience, including 5 years on major capital projects (Oil & Gas, Energy, Infrastructure, Pharma, etc.)., • Advanced Primavera P6 proficiency (mandatory)., • Experience with Concerto preferred (training available). xcskxlj, • Strong MS Excel; MS Project desirable; Power BI beneficial. #J-18808-Ljbffr

Cornerstone OnDemand Ltd. in Madrid invites an experienced Manager Data Science & GenAI to lead AI-driven transformations for Healthcare & Life Sciences clients. Todos los candidatos deben asegurarse de leer atentamente la siguiente descripción del puesto y la información antes de enviar su solicitud. You will shape analytics strategy, design GenAI use cases, and deliver end-to-end projects with measurable impact. You will collaborate with pharma, biotech, and medtech teams, translate business questions into analytical xcskxlj approaches, oversee workstreams, and present insights to senior executives while advancing innovative GenAI #J-18808-Ljbffr

pBETWEEN busca profesional para validar sistemas computarizados (CSV) en su unidad farmacéutica de Madrid. Se ofrece una temporalidad de 6 meses para cubrir proyectos críticos y asegurar cumplimiento regulatorio. /ppSe requiere experiencia en IQ, OQ, PQ, URS y GAMP5, con capacidad de gestionar desviaciones y respaldar auditorías. Se valorará formación continua y apoyo en crecimiento profesional dentro de la empresa. /p #J-18808-Ljbffr

A global B2B marketing firm is seeking an Account Director to manage client relationships and develop account strategies in the Pharma sector. This role involves leading client meetings, ensuring account profitability, and driving revenue growth by capitalizing on new opportunities. The ideal candidate will have a background in Pharma marketing, proven management experience, and excellent communication skills. The position offers competitive compensation, opportunities for career growth, and a supportive work environment.br#J-18808-Ljbffr

Viseven Group in Madrid is seeking a Head of Product to own and drive the success of the entire products and services portfolio, create synergies across solutions, and increase portfolio value and profitability.You will lead portfolio strategy, lifecycle, and cross-functional collaboration in a multinational environment, balancing innovation with optimization while building a high-performing product organization. Hybrid work option available.#J-18808-Ljbffr

Tech Mahindra is seeking a Solution Architect for Pharma Technical Operations to guide strategic architecture across pharma/diagnostics with a focus on business processes, data architecture, and technology strategy. You will collaborate with Product Owners, Scrum Masters, and Architects to map current solutions to future needs and identify opportunities for modernization. The role requires deep Pharma domain expertise, TOGAF certification, and strong leadership to drive enterprise-wide #J-18808-Ljbffr

Turner & Townsend in Madrid is seeking a Cost Manager to oversee cost planning, estimating, and reporting for complex real estate, infrastructure, and industrial projects, acting as day-to-day interface with clients. The role is site-based five days a week; you will lead the cost management team, advise on value engineering, manage procurement, and ensure time, cost, and quality targets are met; fluency in Spanish and English is essential. #J-18808-Ljbffr

pTurner Townsend is looking for a Cost Manager to manage cost planning and project delivery. This role is site-based 5 days a week, responsible for all aspects of cost management while assisting clients and delivering complex projects. Candidates should have over 5 years of experience in the MEP construction sector and a degree in Quantity Surveying. /ppThe company promotes a healthy work-life balance and offers opportunities for professional growth. /p #J-18808-Ljbffr

ALK is seeking an Operational Excellence and Digitalization Specialist to support CI, OPEX, and digital projects within Product Supply Spain. Maximice sus posibilidades de que su candidatura sea seleccionada asegurándose de que su CV y sus habilidades se ajustan al perfil. The role identifies improvement opportunities, coordinates cross‑functional teams, applies Lean methods, and delivers measurable business impact in a regulated pharma environment. xcskxlj Ideal candidate is early in career with a technical background, strong communication, and a desire to grow in CI and project management. #J-18808-Ljbffr

IQVIA LLC in Madrid is seeking a Jr Healthcare Data Coding professional to join their team. You will receive comprehensive training while learning to code and validate healthcare-related data, ensuring accuracy across systems.The ideal candidate is a recent graduate with an interest in healthcare data and strong analytical skills. This role offers exposure to industry-leading tools in a collaborative environment.#J-18808-Ljbffr

Pharma Lex is seeking a Process Excellency and Digital Lead for its Pharmacovigilance services in Madrid. This role focuses on driving process improvements and enhancing operational efficiency through automation and innovative strategies. You will lead change initiatives, support teams in embedding new processes, and contribute to client satisfaction by optimizing service delivery. Ideal candidates will have significant experience in Pharmacovigilance operations and strong analytical skills, ready to make a meaningful impact. #J-18808-Ljbffr

Viseven Group is a leading global B2B MarTech service provider for Pharma and Life Sciences. We seek a results-driven consultant to drive technical discovery, design tailored solutions, deliver demos, and support ROI/TC0 analyses for client proposals.Ideal candidates have 3–5 years in pharma/healthcare, strong stakeholder management, and excellent communication. The role offers hybrid work options and opportunities for professional growth.#J-18808-Ljbffr

A leading healthcare agency in Madrid seeks an Account Director AOR to oversee multiple brands and lead strategic recommendations. This role requires an authoritative presence, exceptional communication skills, and the ability to manage client expectations while fostering relationships across teams. A successful candidate will possess a strong background in healthcare and brand management, contributing actively to the agency’s growth and client satisfaction.#J-18808-Ljbffr

F. Hoffmann-La Roche AG is seeking a Digital Innovation Board and Portfolio Lead in Madrid. This role is critical for aligning the digital portfolio with organizational objectives, managing complexities in governance, and driving performance metrics.The ideal candidate will have over 5 years of experience leading digital transformations in the pharma sector, with strong communication skills and a solid grasp of governance and value realization.#J-18808-Ljbffr

pProclinical Group is looking for a Product Specialist to join a dynamic team in Madrid, Spain. This role focuses on promoting specialty and rare disease products across Spain and Portugal, emphasizing strong relationships with healthcare professionals. /ppThe ideal candidate will possess pharmaceutical sales experience, strong knowledge of the Iberian healthcare system, and excellent communication skills. Responsibilities include building relationships with KOLs, analyzing market trends, and ensuring compliance with regulations. /p #J-18808-Ljbffr

Turner & Townsend is seeking a Senior Quantity Surveyor / Senior Cost Manager to drive cost management on complex projects in Madrid, acting as the day-to-day interface with clients to achieve excellent outcomes. Responsibilities include cost planning, procurement, post-contract cost control, and value engineering while leading cost management activities on medium to large projects. xcskxlj Descubra si esta oportunidad es adecuada para usted leyendo toda la información que sigue a continuación. A strong background in data center, pharma, or oil & gas sectors is preferred. #J-18808-Ljbffr