Trabajos pharma en SalamancaCrear alertas

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).

Turner- is seeking a Clean Utilities professional for Pharma/Life Sciences construction projects based in Madrid or Salamanca. Ideal candidates should hold a degree in Industrial Engineering, possess strong communication skills in Spanish and English, and have a minimum of 2 years' experience in ind

Estabilidad laboral en proyectos como ingeniero de soporte en el sector farmacéutico.

p strong¿Te apasiona Regulatory Affairs y quieres contribuir al desarrollo de nuevos tratamientos? /strong /ppEn strongCrovelis /strong, la CRO del grupo strongInsud Pharma /strong, seguimos creciendo y buscamos incorporar un/a strongSenior Regulatory Affairs Specialist /strong para unirse a nuestro equipo de strongClinical Operations /strong en strongMadrid /strong. /ppbr/ppSi tienes experiencia gestionando strongensayos clínicos internacionales /strong, trabajando con strongCTIS /strong, el strongEuropean Clinical Trials Regulation (EU CTR 536/2014) /strong y procesos regulatorios con la strongFDA /strong, esta puede ser la oportunidad que estabas esperando. /ppbr/pp En pocas palabras /pullistrongPosición: /strong Senior Regulatory Affairs Specialist /lilistrongUbicación: /strong Madrid, España /lilistrongExperiencia: /strong +5 años en Regulatory Affairs dentro de ensayos clínicos /li /ulpbr/p

The role requires at least 8 years in pharma with 5+ in Market Access/HEOR in Spain, deep experience with pricing & reimbursement, HTA submissions, and leadership of high‑performance teams.

Roche is seeking a Digital Innovation Board and Portfolio Lead who is pivotal in driving digital transformations and ensuring compliance. The role demands extensive experience in managing digital portfolios and aligning them with strategic objectives. Qualified candidates will have a strong background in the pharmaceutical industry, excellent executive communication skills, and a passion for innovative technologies. If you believe you can bridge the gap between functions and influence cross-functional teams, we want to hear from you. #J-18808-Ljbffr

Rho is hiring a Clinical Team Lead for a permanent, remote role with occasional travel to sites and client meetings. You will oversee end-to-end clinical execution on moderate projects, lead CRA/IHCRA teams, and ensure regulatory compliance across sites.Ideal candidates bring 5+ years in clinical research within CRO/pharma, strong GCP knowledge, and proven leadership. You will collaborate with data management, regulatory, and safety teams to drive study success.

Consultant to implement Quality Management Systems in Life Sciences, tailoring solutions for clients. Requires pharmaceutical/life science background and client-facing experience. Offers hybrid work.

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

Especialista de producción farmacéutica para cumplir operaciones del plan de producción asegurando Buenas Prácticas de Manufactura en Sant Joan Despí.

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

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.br#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

Develop and execute international market access strategies for specialty care indications, focusing on pricing, reimbursement, and evidence generation.

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 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! 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, Gx P) 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 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. #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

pAdvanz 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. /ppYou will analyze pricing, identify hospital tender opportunities, and work with Medical and Commercial teams to deliver value-based access. /p #J-18808-Ljbffr

Purchasing Technician role at Insud Pharma in Madrid, focusing on evaluating and selecting API suppliers for R&D, ensuring quality and compliance, and developing purchasing strategies.

pSimon-Kucher in Madrid is seeking a Manager Data Science (Gen)AI to lead analytics initiatives for pharma, biotech, and healthcare clients. You will shape AI-enabled strategies, design end-to-end data pipelines, and deploy GenAI solutions that drive measurable growth. /ppYou will work across data engineering, modelling, and client teams, translating business questions into impactful AI use cases while communicating complex results clearly to non-technical stakeholders. /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

IQVIA in Madrid seeks a Regulatory Program Manager who will provide business support to GRA and lead cross‑functional teams to align product and regulatory strategies. You will own regulatory plans, manage global submissions across NA/EMEA/APJ, develop reports, and ensure timely delivery of regulatory deliverables in a large matrix environment. A BS in pharma and 5+ years in R&D are expected. #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

pINSUD PHARMA in Madrid is seeking a Regulatory Affairs Manager to lead regulatory strategy for biosimilars and innovative products. You will collaborate with global teams to ensure compliance and timely submissions, focusing on lifecycle strategies and Health Authority interactions. /ppRequires 5+ years in regulatory affairs within biotech/biopharma, strong knowledge of GMP/ICH guidelines, and fluency in Spanish and English. /p #J-18808-Ljbffr

Planet Pharma is seeking a Director of Clinical Project Management in Pontevedra, Spain. This strategic role oversees global outsourced clinical trials from Phases I to III while ensuring compliance with regulatory standards and budget management. The adecuado candidate will have extensive experience in managing CROs and leading high-performing teams. You'll play a vital role in aligning clinical programs with corporate development goals and driving operational excellence through cross-functional leadership. #J-18808-Ljbffr

ph3Operational Excellence and Digitalization Specialist /h3 pThe Operational Excellence Technician supports the execution of Continuous Improvement (CI), Operational Excellence (OPEX), and Digitalization initiatives within the Product Supply area at ALK Spain. The role contributes to the site’s performance by identifying improvement opportunities, coordinating multidisciplinary teams, implementing Lean methodologies, and delivering bquantifiable economic impact /b (e.g., waste reduction, efficiency increase, digital workflows). /p h3Position Purpose /h3 pThe role is ideal for someone early in their career, with a technical/engineering background, enthusiasm for continuous improvement, strong communication skills, and a desire to grow in CI and Project Management within a regulated pharmaceutical environment. The position aims to transform manual/paper processes into digital solutions. /p h3Key Responsibilities /h3 ul liOperational Excellence: Identify and execute CI opportunities (waste, throughput, standardization), lead problem‑solving/CI workshops, reduce scrap, increase OEE (bottleneck analysis, downtime categorization), and optimize processes. /li liData dashboards: Collect/analyze operational data, define KPIs, ensure data integrity, build visual management and dashboards for TIER routines, document data sources and calculations. /li liDigitalization: Translate needs into requirements, help create dashboards/automations, support existing IT systems, and improve digital standards and data structures. /li liProject management: Coordinate cross‑functional tasks (Operations, Product Supply, QC, QA, Procurement), plan and track projects, manage risks/stakeholders, prepare documentation, and apply change management. /li liBenefits tracking: Prioritize CI pipeline, quantify financial impact, and track baselines/targets/realization. /li /ul h3Required Qualifications /h3 ul liBachelor’s degree in a technical field. /li li2–5 years of experience in Continuous Improvement, Operational Excellence, Digitalization, Manufacturing, Engineering, Quality, or related fields; preferable in production and/or laboratory environments. /li liStrong communicator; able to coordinate multidisciplinary teams. /li liProactive, analytical, strong problem‑solver. /li /ul h3Nice to Have /h3 ul liExperience with SAP, LIMS, Microsoft Teams. /li liExperience with Power BI (reporting, dashboards). /li liExperience with Minitab for statistical analysis, or other statistical tools. /li liAdvanced Excel skills (pivot tables, formulas, data analysis). /li liExperience with Power Automate (workflow automation). /li liFamiliarity with project management methodologies. /li liUnderstanding of GMP or regulated environments (pharma, biotech, medical devices). /li liBasic knowledge of digitalization and data management concepts. /li /ul h3Core Competencies /h3 ul libCommunication: /b Able to engage and align cross‑functional stakeholders. /li libProblem‑solving: /b Structured, analytical, fact‑based approach. /li libInitiative enthusiasm: /b Positive attitude, proactive, eager to learn. /li libTeamwork: /b Ability to work with multiple departments and profiles. /li libContinuous Improvement mindset: /b Curiosity to challenge and improve current processes. /li libAdaptability: /b Comfortable working in changing environments and learning new tools. /li liReports to Product Supply VP; collaborates with Operations Project Manager; works across Product Supply, QA, Procurement; no direct reports. /li /ul h3What We Offer /h3 ul liCareer growth in OpEx and Project Management in a leading pharma company. /li liImpactful projects with measurable results; strong learning in Lean/CI/digital. /li liCollaborative environment; benefits per ALK policy (up to 1 day/week remote). /li liInternational exposure to global teams. /li /ul h3Location /h3 pbLocation: /b Madrid, Spain (on‑site; up to 1 day/week remote)br/bTravel: /b Up to 10%br/bDepartment: /b Operations (Product Supply)br/bReporting to: /b Reports directly to Product Supply Vice President, but working in close collaboration with Operations Project Managerbr/bEmployment Type: /b Full‑timebr/bContract type: /b Permanentbr/bSchedule: /b Flexible /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

pRhythm Pharmaceuticals Inc. is seeking a Hospital Affairs Lead in Madrid, Spain. This role involves owning sales responsibility and developing partnerships with key stakeholders to enhance the care programs for rare MC4R pathway diseases. /ppCandidates should have at least 5 years of relevant sales experience in the pharma/biotech sector, with a strong track record in building relationships and successful product launches. Fluent Spanish and English communication skills are essential. /p #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.

pViseven 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. /ppIdeal 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. /p #J-18808-Ljbffr

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

pActual Talent, la consultora de adquisición de talento del grupo Actual, busca un Strategic Account Manager Senior para colaborar con laboratorios farmacéuticos líderes. Serás el principal nexo entre cliente y equipos internos. /ppSe requiere al menos 5 años en ventas complejas en sanidad o farmacéutica, grado universitario y inglés profesional. La posición ofrece modalidad híbrida y un entorno dinámico con alto grado de autonomía y proyección internacional. /p #J-18808-Ljbffr

Collaborate with QA-R&D Head to ensure R&D activities comply with internal SOPs, GMP, and EMEA/FDA legislation. Responsibilities include implementing quality systems, writing procedures, and auditing.

pKrka is seeking a Brand Manager to join its team in Madrid. The role involves developing brand marketing strategies, executing campaigns, and engaging with key stakeholders. /ppThe ideal candidate has a bachelor’s or master’s degree and at least 3 years of experience in the pharmaceutical sector. Proficiency in Spanish and English is essential, along with strong digital skills. The position will require some travel in the field. /p #J-18808-Ljbffr

F. 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 Gx P principles. The 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. #J-18808-Ljbffr

pTurner Townsend in Madrid is recruiting a MEP Project Manager to lead pharma/life science construction projects onsite, overseeing strategy, cost controls, and scheduling, while ensuring governance and timely decisions. /ppYou will coordinate consultants, designers and contractors, drive risk management, and align site activity with project standards for transparent reporting and quality delivery. /p #J-18808-Ljbffr

pRoche in Madrid is seeking a Data Scientist to lead, develop and deploy AI-driven data solutions in Pharma RD. You will balance hands-on coding with strategic content leadership and help accelerate healthcare innovation. /ppThe role requires 5+ years in data science, expertise in Python and R, and experience with multi-agent AI frameworks. You will collaborate across functions, own medium-scale projects, and help define the technical roadmap. /p #J-18808-Ljbffr

Proclinical 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.The 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.

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

Experteer Overview In this role you will lead cost management for complex construction projects, acting as the day-to-day interface with clients to drive successful outcomes. You will work within a multi-disciplinary team to deliver cost planning, procurement, and post‑contract cost control across data center and other critical projects. You’ll contribute to value engineering and final accounts while mentoring the cost management team. This is an opportunity to shape project economics for high‑impact programs and collaborate with senior stakeholders to improve value and performance. Compensaciones / Beneficios • Provide estimates and cost planning across concept, programming and detailed levels; present final cost plans • Support feasibility studies and prepare procurement reports • Manage procurement activities including pre-qualification, bid lists, bid analysis, bid reports, and contract documentation • Oversee post‑contract cost variances and change control; escalate major changes • Perform cost checks and valuations on large projects, ensuring timely, accurate reporting • Produce monthly post‑contract cost reports and present to clients • Contribute to value engineering; negotiate and settle final accounts • Liaise with clients and other consultants throughout project stages • Provide leadership to the cost management team when needed and ensure delivery of responsibilities • Identify opportunities to develop new business with existing clients and contribute to marketing efforts • Suggest improvements to cost management procedures, templates, and tools Responsabilidades • Minimum of 8 years' experience preparing cost estimates • Experience in Data center, Pharma, Oil and Gas preferred • Fluent in English • Strong technical proficiency in all cost management areas: pre‑contract, post‑contract and final accounts • Solid understanding of civils, structural and architectural aspects relevant to construction • Experience leading cost management on medium to large, high‑complexity projects • Experience advising on value management, value engineering, and life cycle costing • Excellent presentation, verbal and written communication skills • Strong organizational ability; team player and multi-tasking Requisitos principales • healthy, productive and flexible working environment • work-life balance • equal opportunity employer • inclusive environment • opportunity to affect change • diverse and collaborative culture

Lead and grow strategic projects for clients in the pharma and healthcare sectors, managing accounts, developing teams, and providing actionable recommendations.

ppExperteer Overview En Accenture Technology, buscarás contribuir a implementaciones SAP QM en entornos farmacéuticos, ayudando a transformar procesos y cumplir GMP/GxP. Te integrarás en un equipo global que trabaja con clientes internacionales y equipos multifuncionales para entregar soluciones escalables. Liderarás diseño, configuración y soporte de pruebas y puesta en producción, asegurando integración con PP, MM y WM/EWM. Esta oportunidad ofrece impacto en proyectos internacionales y la posibilidad de influir en la calidad y la conformidad regulatoria. Forma parte de una cultura de innovación, diversidad y desarrollo profesional. /p h3Compensaciones / Beneficios /h3 ul liParticipar en implementaciones, rollouts y mejoras de SAP QM en entornos Pharma /li liAnalizar requisitos y traducirlos en soluciones funcionales SAP QM alineadas a GMP /li liConfigurar procesos SAP QM: calidad, inspección, notificaciones y gestión de lotes /li liSoportar pruebas, formación de usuarios y soporte de go-live en proyectos internacionales /li liActuar como consultor funcional SAP QM, diseñando, configurando y documentando procesos QM /li liAsegurar cumplimiento con normativas farmacéuticas (GxP, GMP) y estándares de calidad dentro de SAP /li liColaborar con equipos multifuncionales (PP, MM, WM/EWM) para asegurar integración de procesos /li liProporcionar guía y soporte funcional a usuarios clave en entornos angloparlantes /li /ul h3Responsabilidades /h3 ul liMínimo 3 años de experiencia en implementaciones SAP QM /li liExperiencia comprobable en la industria farmacéutica /li liNivel alto de inglés, fluidez en conversación /li liDisponibilidad para viajar /li liResidencia en España y permiso de trabajo válido en España (implícito en disponibilidad para viajar) /li /ul h3Requisitos principales /h3 ul liSeguro médico, de vida y accidentes /li liProgramas de bienestar /li liRetribución flexible /li liFormación y certificaciones /li liFlexibilidad horaria y días libres /li liDesarrollo de carrera e itinerario formativo /li /ul /p #J-18808-Ljbffr

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.El 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.

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

ph3Operational Excellence and Digitalization Specialist /h3 pThe Operational Excellence Technician supports the execution of Continuous Improvement (CI), Operational Excellence (OPEX), and Digitalization initiatives within the Product Supply area at ALK Spain. The role contributes to the site’s performance by identifying improvement opportunities, coordinating multidisciplinary teams, implementing Lean methodologies, and delivering bquantifiable economic impact /b (e.g., waste reduction, efficiency increase, digital workflows). /p h3Position Purpose /h3 pThe role is ideal for someone early in their career, with a technical/engineering background, enthusiasm for continuous improvement, strong communication skills, and a desire to grow in CI and Project Management within a regulated pharmaceutical environment. The position aims to transform manual/paper processes into digital solutions. /p h3Key Responsibilities /h3 ul liOperational Excellence: Identify and execute CI opportunities (waste, throughput, standardization), lead problem‑solving/CI workshops, reduce scrap, increase OEE (bottleneck analysis, downtime categorization), and optimize processes. /li liData dashboards: Collect/analyze operational data, define KPIs, ensure data integrity, build visual management and dashboards for TIER routines, document data sources and calculations. /li liDigitalization: Translate needs into requirements, help create dashboards/automations, support existing IT systems, and improve digital standards and data structures. /li liProject management: Coordinate cross‑functional tasks (Operations, Product Supply, QC, QA, Procurement), plan and track projects, manage risks/stakeholders, prepare documentation, and apply change management. /li liBenefits tracking: Prioritize CI pipeline, quantify financial impact, and track baselines/targets/realization. /li /ul h3Required Qualifications /h3 ul liBachelor’s degree in a technical field. /li li2–5 years of experience in Continuous Improvement, Operational Excellence, Digitalization, Manufacturing, Engineering, Quality, or related fields; preferable in production and/or laboratory environments. /li liStrong communicator; able to coordinate multidisciplinary teams. /li liProactive, analytical, strong problem‑solver. /li /ul h3Nice to Have /h3 ul liExperience with SAP, LIMS, Microsoft Teams. /li liExperience with Power BI (reporting, dashboards). /li liExperience with Minitab for statistical analysis, or other statistical tools. /li liAdvanced Excel skills (pivot tables, formulas, data analysis). /li liExperience with Power Automate (workflow automation). /li liFamiliarity with project management methodologies. /li liUnderstanding of GMP or regulated environments (pharma, biotech, medical devices). /li liBasic knowledge of digitalization and data management concepts. /li /ul h3Core Competencies /h3 ul libCommunication: /b Able to engage and align cross‑functional stakeholders. /li libProblem‑solving: /b Structured, analytical, fact‑based approach. /li libInitiative enthusiasm: /b Positive attitude, proactive, eager to learn. /li libTeamwork: /b Ability to work with multiple departments and profiles. /li libContinuous Improvement mindset: /b Curiosity to challenge and improve current processes. /li libAdaptability: /b Comfortable working in changing environments and learning new tools. /li liReports to Product Supply VP; collaborates with Operations Project Manager; works across Product Supply, QA, Procurement; no direct reports. /li /ul h3What We Offer /h3 ul liCareer growth in OpEx and Project Management in a leading pharma company. /li liImpactful projects with measurable results; strong learning in Lean/CI/digital. /li liCollaborative environment; benefits per ALK policy (up to 1 day/week remote). /li liInternational exposure to global teams. /li /ul h3Location /h3 pbLocation: /b Madrid, Spain (on‑site; up to 1 day/week remote)br/bTravel: /b Up to 10%br/bDepartment: /b Operations (Product Supply)br/bReporting to: /b Reports directly to Product Supply Vice President, but working in close collaboration with Operations Project Managerbr/bEmployment Type: /b Full‑timebr/bContract type: /b Permanentbr/bSchedule: /b Flexible /p /p #J-18808-Ljbffr

Designs and maintains automated Windows infrastructure across hybrid cloud environments, leads troubleshooting, and mentors teams on automation best practices for pharma innovation.

Supervisará los montajes mecánicos en obra, asegurando el cumplimiento de especificaciones y estándares. Gestionará contratistas y liderará un equipo técnico.

Drives regional market access for ADVANZ PHARMA in Spain, focusing on biosimilars and hospital stakeholders. Develops strategies, manages tenders, and builds relationships with healthcare authorities.

pALK is seeking an Operational Excellence and Digitalization Specialist to support CI, OPEX, and digital projects within Product Supply Spain. The role identifies improvement opportunities, coordinates cross‑functional teams, applies Lean methods, and delivers measurable business impact in a regulated pharma environment. /ppIdeal candidate is early in career with a technical background, strong communication, and a desire to grow in CI and project management. /p #J-18808-Ljbffr