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Bring more to life. Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology? At Radiometer, one of Danaher’s 15+ operating companies, our work saves lives—and we’re all united by a shared commitment to innovate for tangible impact. You’ll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher’s system of continuous improvement, you help turn ideas into impact – innovating at the speed of life. At Radiometer, life comes first. Our vision is to improve global healthcare with reliable, fast, and easy patient diagnoses. We’re a team that celebrates diverse ideas and continuous improvement. Here, you’ll find a place to grow and make a real impact, with your unique perspective driving us forward in improving patient care. At Radiometer, our vision is to improve global healthcare with reliable, fast, and easy patient diagnoses. We're seeking a Medical Information Advisor to join Radiometer's Global Medical Affairs team. This position drives critical medical and scientific initiatives both internally and externally, supporting our existing product portfolio while helping define the future of point-of-care technologies in acute and emergency healthcare environments. Based remotely in Spain with up to 25% travel to Copenhagen, Denmark, and various international locations. Part of our CMSS (Clinical, Medical Safety and Surveillance) Department, you'll report directly to our Senior Director of Medical Affairs. Your responsibilities will span leading medical initiatives across the organization, facilitating cross-functional collaboration in development projects, creating scientific and promotional materials, and building relationships with internal experts and Key External Experts (KEE) in hospitals globally. If you're energized by applying your medical and clinical expertise while engaging extensively with diverse stakeholders and are passionate about building an exceptional Medical Affairs organization, we'd love to hear from you. In this role, you will have the opportunity to: Lead Medical Information Strategy: Apply your Medical Affairs expertise to shape and execute the global medical information strategy, owning the development, quality, and lifecycle of scientific content and MAPSS assets while aligning cross-functional stakeholders on strategic priorities. Act as the Scientific and Clinical Expert: Serve as a trusted subject matter expert in acute and emergency diagnostics, translating complex clinical evidence into clear, actionable insights that inform Medical Affairs, Marketing, and product development decisions. Drive High-Impact Scientific Communications: Lead publication planning and execution, transforming clinical performance data into peer-reviewed evidence and compelling medical materials that strengthen scientific credibility and support global adoption. Build and Activate Global Expert Networks: Develop and manage strategic relationships with KOLs and KEEs, leading engagement processes, supporting IIS initiatives, and enabling high-value scientific collaborations that expand external impact. Represent Medical Affairs Internally and Externally: Play a visible role at scientific conferences and industry forums, delivering impactful presentations and ensuring consistent, compliant communication of medical insights across global stakeholders. The essential requirements of the job include: Advanced Credentials with Relevant Industry Experience: Hold an advanced degree in Life Sciences (PhD, PharmD, MSc, or equivalent) combined with a minimum of 5 years of experience in Medical Affairs, Medical Information, or related roles within the IVD, medical device, pharma or healthcare industry, with strong exposure to clinical applications. Strong Expertise in Medical Information and Processes: Demonstrate in-depth knowledge of medical information tools, processes, and compliance requirements, with hands-on experience developing, reviewing, and managing scientific and medical content in a regulated environment. Exceptional Scientific Communication Skills: Exhibit outstanding written and verbal communication in English, with proven ability to translate complex scientific data into clear, impactful messages for both expert and non-expert audiences. Solid Clinical and Technical Understanding: Bring strong familiarity with IVD technologies and their application in clinical settings, particularly in acute or hospital-based workflows, enabling meaningful scientific contribution and credible stakeholder engagement. Effective Cross-Functional Collaboration and Execution: Show the ability to work effectively across Medical Affairs, Clinical, Marketing, and external stakeholders, managing multiple priorities while maintaining high standards of quality, compliance, and execution. It would be a plus if you also possess previous experience in: Technical/Scientific knowledge /experience in Clinical Chemistry is desirable. Experience in Acute and Emergency care spaces is desirable At Radiometer, we believe in designing a better, more sustainable workforce. We recognize the benefits of flexible, remote working arrangements for eligible roles and are committed to providing enriching careers, no matter the work arrangement. This position is eligible for a remote work arrangement in which you can work remotely from your home. Additional information about this remote work arrangement will be provided by your interview team. Explore the flexibility and challenge that working for Radiometer can provide. #LI-Remote #LI-VF1 Join our winning team today. Together, we’ll accelerate the real-life impact of tomorrow’s science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life. For more information, visit _.

Tu nueva empresa Compañía del sector farmacéutico con un fuerte enfoque en calidad, cumplimiento GMP y desarrollo de nuevos proyectos para clientes internacionales, que requiere de la incorporación de un/a técnico/a a HSE/ PRL. Tu nuevo puesto Garantizar la implantación, seguimiento y mejora continua de los sitemas de HSE en planta química-farmacéutica, asegurando el cumplimiento de la legislación, políticas corporativas y los estándares de seguridad de proceso. Entre tus principales funciones: • Liderar y participar en análisis de riesgos de proceso (HAZOP, What If, FMEA, LOPA, Bow Tie)., • Evaluar modificaciones de instalaciones mediante procedimientos de Management of Change (MOC)., • Colaborar en la definición de medidas de protección frente a riesgos ATEX, incendios y explosiones., • Garantizar la correcta gestión de sustancias peligrosas, inflamables, tóxicas y corrosivas., • Participar en estudios de seguridad y cumplimiento de normativa Seveso cuando aplique., • Desarrollar, implantar y supervisar el Plan de PRL., • Realizar evaluaciones de riesgos en áreas productivas, laboratorios, almacenes y servicios auxiliares., • Investigar accidentes, incidentes y casi accidentes, definiendo acciones correctivas y preventivas., • Coordinar actividades empresariales (CAE) con contratistas y empresas externas., • Impartir formación e información en materia de PRL a empleados y colaboradores., • Participar activamente en auditorías internas y externas. Qué necesitarás para encajar con el puesto • Grado universitario en Ingeniería Química, Química, Ciencias Ambientales, Farmacia, otras titulaciones afines., • Máster en PRL con las tres especialidades (Seguridad en el Trabajo, Higiene Industrial y Ergonomía y Psicosocilogía aplicada). Qué obtendrás a cambio • Incorporación a una empresa consolidada y en crecimiento dentro del sector farmacéutico., • Participación en proyectos innovadores con clientes internacionales., • Desarrollo profesional en un entorno altamente especializado en calidad., • Horario flexible de lunes a viernes. Tu siguiente paso Si estás interesado en esta oferta, haz click en "aplicar ahora" para enviar una copia actualizada de tu CV, o llámanos ahora.

The InsudPharma group is aware that business management must align with the needs and demands of society, and therefore assumes the commitment to equal opportunities and treatment between men and women, as stated in the current regulations on the matter - Organic Law 3/2007, and we do not discrimina

Adragos Pharma in Barcelona is looking for an IT Operations Support professional, focusing on Microsoft 365 administration and cybersecurity support.Recuerde revisar su CV antes de enviar la solicitud.Además, asegúrese de leer todos los requisitos relacionados con este puesto.This hybrid role offe

Buscamos un/a Account Directo con experiencia en ventas consultivas dentro del sector Healthcare/Pharma, orientado/a tanto a la captación de nuevas oportunidades como al desarrollo y fidelización de cuentas estratégicas.La posición combina un enfoque Hunter + Farmer, acompañando al cliente desd

Ambit Iberia is looking for a MES Senior Systems Engineer to enhance Manufacturing Execution Systems within a global pharmaceutical environment.You will ensure stable operations, continuous improvement, and compliance of MES applications while collaborating with IT and business stakeholders.Your rol

ph3Are you ready to shape the future of healthcare products? /h3 pJoin 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 bProduct Management /b and bAgile methodologies /b to define product strategy, maximize business value and deliver high quality solutions. /p pAt ERNI, you are never just a number. Even if you work on an external project, you will feel part of the team and always supported. /p h3How do we make this happen? /h3 pWith people. Besides your team and manager, you will have several support figures like a godparent, who will help you with the practical and administrative aspects of daily life during your first 6 months. /p pAnd the second most important person after you, your mentor, who will guide you through your entire onboarding and career at ERNI. You will have regular 1:1 meetings with them, and recurrently, you will work on your development plan to define your short-, medium-, and long-term goals. /p pAt ERNI, we highly value experience and technical knowledge. As a senior profile, you will have the space to continue growing, whether by deepening your technical skills or having greater influence on project decisions, with autonomy and the opportunity to share knowledge with other experts. And if you are interested in mentoring, there is also space for that: supporting other ERNIans while still focusing on the technical excellence that sets us apart. /p h3What you will bring /h3 ul liMore than 7 years of experience as Product Owner or Product Manager managing complex digital products. /li liStrong experience defining product roadmaps, backlog prioritization and Agile delivery using Scrum, Kanban or SAFe. /li liExperience working with cross functional teams including engineering, UX and business stakeholders. /li liExperience with Jira, Confluence, Miro and product management tools in global organizations. /li liAdvanced English level and excellent communication and stakeholder management skills. /li /ul pYou will be responsible for leading the product vision, roadmap and backlog while working closely with engineering, UX, architecture and business teams. You will prioritize features, coordinate stakeholders, facilitate product refinement sessions and ensure each delivery provides maximum value for users and the business. /p h3What if the project ends? /h3 pWe work on a wide variety of projects, technologies, and sectors, allowing you to keep growing in different environments. If a project ends or you feel ready for a new challenge, we will find another one that aligns with your professional development. /p pWe ask you to be available for key meetings. Need to leave for a doctor’s appointment or to pick up your child from school? No problem. We trust you to deliver quality work within your 40-hour workweek. /p pOur model is hybrid: we usually go to the office 2 days a week, though this depends on the project and team, but we love seeing each other’s faces; the best stories always happen in the office! /p pYou will also enjoy: /p h3And the salary? /h3 pWe will discuss it during the first call. If it is important to you, feel free to ask! /p /p #J-18808-Ljbffr

pFusion Consulting is seeking a Senior IT Project Manager to lead the implementation of Extended Warehouse Management (EWM) systems in Barcelona, Spain. This pivotal role involves managing complex projects, ensuring compliance with stringent pharmaceutical regulations and delivering transformational solutions. /ppThe ideal candidate will have over 8 years of project management experience, with proven skills in SAP EWM and a strong understanding of the pharmaceutical sector. Fusion Consulting offers a dynamic work environment focused on innovation and excellence. /p #J-18808-Ljbffr

pSARIA Food Pharma is hiring a Business Development Manager to scale the biomedical collagen portfolio. You will lead strategy development and execution, prioritise opportunities, and build key customer partnerships across Europe. /ppThe role requires extensive travel and strong life science knowledge. Ideal candidates have 10+ years in medical device sales or business development within biological materials, with fluency in English and Spanish preferred. /p #J-18808-Ljbffr

pRed - The Global SAP Solutions Provider is seeking a Power Apps Developer to design, develop and enhance Microsoft Power Platform solutions for a global pharma client. This remote, Europe-based role focuses on delivering scalable applications that improve processes and digital transformation across the organization. /ppYou will collaborate with business stakeholders to translate requirements into effective technical solutions, following best practices for Power Apps, Power Automate, Dataverse, and /p #J-18808-Ljbffr

ph3Overview /h3 pbGlobal OT Process Control Architect /b – Own and drive the standardization, architecture, and lifecycle management of the global process control and OT infrastructure landscape (ISA‑95 Levels 1–2) across manufacturing sites. Ensure scalable and reliable control and infrastructure solutions, support sites to deploy and sustain these standards, improve reliability, reduce complexity, and minimize vendor dependency. This role is based in Spain, Turkey or Slovenia. /p h3Where You’ll Make a Difference /h3 ul liDefine and govern vendor-agnostic global standards and reference architectures/best practices across Level 1–2 Industrial Control Systems (PLC/HMI/SCADA/DCS). /li liEstablish and maintain standard URS/FRS frameworks for process control and OT systems to support consistent design, vendor engagement, and lifecycle management across sites. /li liDrive harmonization standardization of Industrial Control Systems across Taste with expertise and knowledge. /li liReduce reliance on proprietary vendor ecosystems and build a knowledge base including approved vendors and technologies, standard configurations and architectures, reusable design patterns. /li liEnsure compliance with industrial standards and laws (ISA‑95, ISA‑99 / IEC 62443 / NIS2). /li liAct as technical authority for process control and OT infrastructure across all sites. /li liIdentify and prioritize control system and infrastructure modernization opportunities. /li liSupport sites in implementing global standards during control system upgrades (PLC/DCS migrations), SCADA/historian deployments, and infrastructure modernization (networks, servers). /li liSupport commissioning, testing (FAT/SAT), and validation of OT systems. /li liCapture lessons learned from sites and continuously refine global standards. /li liProvide remote support for complex control system troubleshooting, control architecture design decisions, and stability and reliability issues at Levels 1–2. /li liDrive consistent execution across sites through close collaboration with engineering and operations teams. /li /ul h3Key Success Metrics /h3 ul liAdoption rate of global control and OT infrastructure standards. /li liReduction in site‑vendor dependency. /li liImproved reliability and uptime of process control systems. /li liReduced variability in control architectures across sites. /li liLower lifecycle cost and complexity of OT systems. /li /ul h3Qualifications /h3 ul liDegree in Automation Engineering, Process Control, or related field. /li li8+ years in batch process industries (biotech, food ingredients, specialty chemicals, pharma). /li liHands‑on experience with PLC/DCS systems, SCADA/HMI platforms, industrial networks and OT infrastructure. /li liExperience driving/supporting global deployments. /li liExcellent analytical, documentation, and communication skills. /li liAbility to lead cross‑functional initiatives and drive compliance. /li liSolid understanding of industrial communication protocols (PROFINET, PROFIBUS, Modbus, Ethernet/IP, OPC). /li liFull professional proficiency in English. /li /ul h3How You Stand Out /h3 ul liStrategic capability – Designed and deployed global OT standards. /li liArchitecture thinking – Strong grasp of ISA‑95 L1–L2 system architecture. /li liExecution at scale – Proven multi‑site rollout success. /li liVendor independence mindset – Reduced dependency / unified platforms. /li /ul h3Benefits /h3 ul liBecome a part of a global leader driving innovation in Taste. /li liWork on cutting‑edge automation and digitalization projects. /li liCollaborate with diverse, talented teams across multiple disciplines. /li liShape our OT team with your expert knowledge and vision. /li liOpportunities for continuous learning and professional growth. /li liMake a tangible impact on safety, quality and operational excellence. /li liJoin a culture that values creativity, integrity, and collaboration. /li /ul h3Equality, Diversity Inclusion /h3 pAt IFF we value the diverse mosaic of ethnicity, national origin, race, age, sex, veteran status, religion, gender identity expression, sexual orientation and disability. We strive for an inclusive workplace that allows each of our colleagues to bring their authentic self to work. /p /p #J-18808-Ljbffr

pERNI seeks an experienced Product Owner/Manager to shape product vision, define roadmaps and backlog while collaborating with engineering, UX and business stakeholders. Hybrid model: office 2 days a week, 40-hour workweek, with focus on delivering maximum value. /ppYou will drive healthcare digital products and partner with global teams, benefiting from career growth, language courses, and professional certifications support. /p #J-18808-Ljbffr

ph3Experteer Overview /h3 pIn this role you will define and lead Lubrizol’s global strategic roadmap for nutraceutical actives, shaping portfolio and investment decisions. You will drive growth across regions, applications, and partnerships, balancing core optimization with next‑gen innovation. You’ll translate market intelligence into actionable pipelines and robust business cases, steering cross‑functional teams from concept to commercialization. This is a high‑impact role with global scope and a clear focus on market leadership in nutraceuticals. /p h3Key Responsibilities /h3 ul liDefine global strategic roadmap and segment prioritization for nutraceutical actives /li liShape portfolio through disciplined management and investment strategies /li liIdentify new growth platforms across geographies, applications, technologies, and partnerships /li liLead market intelligence to uncover trends, unmet needs, and growth opportunities /li liTranslate insights into innovation pipelines, partnerships, and commercial playbooks /li liBuild finance‑aligned business cases with clear ROI and value capture /li liCoordinate cross‑functional execution to scale from concept to commercialization /li liDrive global marketing initiatives across commercial, BD, and technical teams /li liRepresent the company with customers, industry bodies, and partners to strengthen thought leadership /li /ul h3Qualifications /h3 ul liBachelor’s degree in Business, Marketing, Life Sciences, or related field /li liMinimum 10 years in strategic marketing, business leadership, or innovation‑driven roles /li liProven track record in defining and executing global growth strategies /li liExperience in nutraceuticals, food, pharma, or related regulated industries /li liStrong understanding of nutraceutical value chains, regulatory environments, and innovation ecosystems /li liDemonstrated ability to lead and influence cross‑functional, global teams /li liStrong financial acumen with experience building investment cases and driving ROI /li liExcellent communication, stakeholder management, and strategic thinking skills /li /ul h3Benefits /h3 ul liCompetitive salary with performance‑based bonus plans /li liComprehensive medical, dental vision coverage /li liPaid holidays, vacation, and parental leave /li liFlexible work environment /li liLearning and development opportunities /li liCareer and professional growth /li /ul pSr. Global Strategic Marketing Manager - Nutraceuticals • Gava, ES /p /p #J-18808-Ljbffr

ph3Job Title /h3 pbGroup FPA Senior Analyst /b /p h3Location /h3 pBarcelona, Spain – Hybrid /p h3Job Description /h3 pWe are seeking a highly motivated and detail-oriented Group FPA Senior Analyst to join our finance team. The successful candidate will play a critical role in financial analysis, supporting budgeting and forecasting processes, and driving data‑driven decision‑making while ensuring data quality across various financial systems. /p h3Key Responsibilities /h3 ul liMonthly performance PL reporting and analysis, including automated reporting solutions (PowerBI implementation), regional performance insights, trend analysis, and run‑rate tracking. /li liOversee monthly Group OPEX and non‑core items management, ensuring cost transparency and control through variance analysis against budget, YoY performance assessment, run‑rate tracking, and monitoring against financial targets. /li liHeadcount reporting and KPI tracking, ensuring data accuracy and providing workforce insights to support organizational and financial planning. /li liLead Group personnel cost planning, forecasting, and analysis, including headcount, salary costs, variable compensation, STI outlook and achievement tracking, and other workforce cost drivers. /li liLead and support financial analyses, scenario modeling, and cross‑functional projects to drive strategic decision‑making, business performance, process improvements, and innovation initiatives. Assess AI projects. /li liSupport annual budget and latest outlook processes, and contribute to the development of Executive Committee and Board of Directors presentations. /li liSupport quarterly and year‑end financial landing, ensuring robust forecast accuracy, clear variance insights, and alignment with internal commitments and external expectations. /li /ul h3Skills Qualifications /h3 ul liBachelor’s degree in Finance, Accounting, Economics, or a related field. /li li7‑10 years of experience in FPA, corporate finance, or related fields. /li liProven experience in financial planning and analysis, preferably within a corporate environment (Cosmetic, Consumer Goods, or Pharma‑related). /li liStrong analytical skills with the ability to interpret complex financial data. /li liAdvanced proficiency in financial systems and tools, including expert‑level Excel and sophisticated financial modeling capabilities. /li liDemonstrated project management expertise and ability to lead cross‑functional initiatives and deliver high‑quality outcomes under tight timelines. /li liExcellent communication and presentation skills. /li liHigh attention to detail and strong organizational skills. /li liAbility to work collaboratively in a multinational team environment and manage multiple priorities. /li /ul h3What We Offer /h3 pJoining Galderma as a Group FPA Senior Analyst offers a unique opportunity to be part of a dynamic and successful company. You will have direct exposure to top management and be involved in strategy and financial planning. The role is strategic and vital to shaping the future of the company. /p h3Application Process /h3 ul liIf your application is successful, you will be invited for a first virtual conversation with the recruiter. /li liA virtual conversation with the hiring manager. /li liFinal panel conversation with the extended team. /li /ul h3Our People Make a Difference /h3 pAt Galderma, we value diverse perspectives and foster a supportive, collaborative environment that allows employees to thrive and excel in what they do. /p /p #J-18808-Ljbffr

ph3Global Lead - Market Research /h3pLocation: Barcelona, Spain. /ppThe Global Lead – Market Research (MR) is responsible for providing market and customer insights through the execution of market research that will help drive key strategic and tactical decisions across Sanofi with a focus on the Pharma portfolio (GenMed and Speciality Care). As a member of the Insights and Analytics (IA) team, this individual will be an integral strategic partner to Sanofi Commercial leadership, leading the development and application of cutting‑edge market research methodologies to achieve the full potential of the expanding portfolio. /ph3Responsibilities /h3ulliDesign and execute a Market Research strategy with methodologies aligned to business goals, efficiency, and cost parameters. /liliDrive innovative use of insights to inform marketing decisions, from high‑level strategic tradeoffs to operational execution. /liliDeliver strategic, audience‑tailored insights that empower Vaccine Asset Commercial teams. /liliProvide strategic guidance and ad‑hoc support to Sanofi Commercial teams and the IA organization. /liliActively contribute to brand planning by grounding commercial/brand strategy in market research insights. /liliPartner with other support functions (forecasting, analytics, competitive intelligence) to deliver integrated insights. /liliBuild strong agency partnerships to ensure reliable, high‑quality research and seamless process flow. /liliStay current on emerging market research methodologies and vendors. /liliSpecialize across multiple therapy areas, collaborating with peer Leads to avoid duplication of effort. /liliParticipate in commercial meetings, proactively surfacing business questions that market research can address. /liliPresent market research insights to Senior Leadership. /liliSelect the right vendor for each project based on business objectives. /liliEnsure all projects comply with relevant policies, including procurement and SOPs. /liliCoordinate vendors throughout the research process, contributing business/brand expertise to fieldwork materials and reports. /liliSign off on final fieldwork materials and reports, incorporating input from all relevant stakeholders. /liliCreate engaging, innovative deliverables (e.g., avatar presentations) with clear calls to action for stakeholders. /liliLead and develop market research team members as needed. /li /ulh3Education Requirements /h3ulliBachelor’s degree required. /liliAdvanced degree (MBA, MS, MD, PhD) preferred. /li /ulh3Skills and Competencies /h3ulliMinimum of 7+ years of experience in pharmaceutical market research; equivalent combination of education and/or consulting experience may be considered. /liliStrong understanding of all types of market research methodologies, with experience conducting both quantitative and qualitative research from end-to-end, including strong quantitative analytical skills, data analysis and statistics. /liliStrong strategic thinking ability, with deep understanding of the life sciences industry. /liliDemonstrated ability to drive to deadlines, balance competing priorities, and ensure high quality. /liliExperience leading and developing high‑functioning teams. /liliExperience across global, regional, local roles strongly preferred. /liliKnowledge and experience with pharmaceutical data sources (e.g., prescription and sales data, patient claims data, promotional audits) preferred. /liliProduct launch experience preferred. /liliExperience working directly within or partnering with related functions including new product planning, marketing, value access preferred. /liliEffectively and confidently communicate to various audiences, including senior leadership. /liliSynthesize complex ideas to simple and develop brand implications from market research findings. /liliStrong learning agility and high degree of curiosity. /liliStrong focus on detail, accuracy, and ability to solve problems through analytical reasoning. /liliStrong work ethic and personal motivation. /liliAbility to think strategically in an ambiguous environment and flex and pivot as the business requires. /liliDemonstrated EQ and leadership skills. /li /ulh3Benefits and Salary /h3pSalary range: €49,600.00 – €66,133.00. Final compensation will be determined based on demonstrated experience, skills, location, and other relevant factors. /ppEmployees may be eligible to participate in Company employee benefit programs. /ph3Equal Opportunity Statement /h3pAt Sanofi, we provide equal opportunities to all regardless of race, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, ability, or gender identity. /p /p #J-18808-Ljbffr

pFagron Genomics, nabij Barcelona, zoekt een Medical Sales Representative voor de regio Noord. Je brengt het productgamma bij artsen, bouwt langetermijnrelaties op en levert deskundig advies voor personalized behandeltrajecten. /ppJe beschikt over een wetenschappelijke diploma en sterke commerciële vaardigheden, hebt ervaring in pharma, en woont bij voorkeur in de tewerkstellingsregio. Een bedrijfswagen, laptop en gsm zijn inbegrepen in het pakket. /p #J-18808-Ljbffr

pGalderma seeks a Materials Scientist to join our Barcelona team. You will analyze and optimize materials used across products and packaging, applying deep technical expertise to ensure performance and compatibility. /ppThe role requires collaboration with Product Science, MST, and Quality, translating complex findings into clear documentation and presentations while working in a regulated dermatology environment. /p #J-18808-Ljbffr

ph3Overview /h3pIn this role you will provide statistical expertise to cross‑functional teams within a leading multinational pharma company based in Barcelona. You will lead teams of statisticians and programmers, plan and execute statistical analyses for drug development, and ensure data analysis quality. You will also oversee statistical work outsourced to external providers, contributing to high‑impact decisions across development programs. This is a hands‑on, collaborative, impact‑driven position with global reach and a strong focus on data integrity and methodological rigor. /ph3Compensaciones / Beneficios /h3ulliProvide statistical expertise to cross‑functional teams /liliLead teams of statisticians and programmers /liliPlan studies and execute statistical analyses for drug development /liliEnsure the accuracy and quality of data analysis and interpretation /liliOversee statistical work outsourced to external providers /li /ulh3Responsabilidades /h3ulliPhD or MS in Biostatistics, Statistics, or Mathematics or similar /lili2+ years of experience as a Statistician in Pharma, Biotech, CRO, Research Center, Hospital or a similar field /liliDesirable experience in statistical programming (SAS and/or R) /liliExcellent communication skills and ability to work both independently and in teams /liliFluent English (written and spoken) /li /ul /p #J-18808-Ljbffr

ph3Job Function /h3 pData Analytics Computational Sciences /p h3Job Sub Function /h3 pData Science /p h3Job Category /h3 pPeople Leader /p h3Locations /h3 pBarcelona, Spain; Madrid, Spain /p h3Job Description /h3 pJohnson Johnson Innovative Medicine (JJ IM), a pharmaceutical company of Johnson Johnson, is recruiting for an Associate Director, Product Mastering. The primary location is Madrid, Spain, and the secondary location is Barcelona. /p h3Position Summary /h3 pThe Associate Director, Product Mastering is responsible for maintaining and governing an end-to-end mastering capability for product‑related data, from compounds in Therapeutic Discovery through regulatory and commercialization and loss of exclusivity. The role ensures that product master data—including compounds, formulations, investigational products, clinical identifiers, regulatory submissions, and commercial brand hierarchies—is trusted, harmonized, and semantically consistent across the entire RD to Commercial continuum. The AD will work cross‑functionally within RD, Data Science, and support the development of ontologies and knowledge graphs to connect and contextualize product information across silos, enabling advanced analytics, AI/ML, regulatory compliance, and interoperability. /p h3Key Responsibilities – End‑to‑End Product Mastering Strategy /h3 ul liHelp develop and execute a data management strategy covering the full product lifecycle: from discovery through commercialization and LOE. /li liEnsure a single, authoritative source of truth through stewardship of all product‑related master data, harmonized across functions and systems. /li liIdentify gaps, redundancies, and opportunities for automation, external data partnerships, and standards alignment. /li /ul h3Governance Standards /h3 ul liEstablish stewardship and governance models for product master data across RD, Supply Chain and Commercial. /li liDefine and enforce standards for product hierarchies and data model extensions. /li liPartner with Regulatory Affairs, Clinical Operations, Supply Chain, and Commercial to ensure product mastering supports submission, labeling, and compliance needs. /li /ul h3Integration Collaboration /h3 ul liCollaborate with Knowledge Management, Data Products, and Metadata/Cataloging teams to ensure product master data is discoverable, connected, and reusable across the enterprise. /li liAlign with parallel MDM domains (e.g., patient, site, account) to ensure cross‑domain consistency and best practices. /li /ul h3Quality, Performance Communication /h3 ul liMonitor dashboards and track KPIs for product master data quality, timeliness, and traceability across the lifecycle. /li liProvide governance dashboards and reports to RD and Commercial leadership. /li liCommunicate the vision, progress, and value realization of product mastering to senior executives and cross‑functional stakeholders. /li /ul h3Qualifications – Education /h3 ul liBachelor or Master’s in life sciences, regulatory sciences, informatics, data science, or related field. Advanced degree preferred. /li /ul h3Skills Expertise /h3 ul li5+ years of experience in pharma/biotech RD or commercial functions, with significant exposure to product lifecycle and regulatory data. /li liDemonstrated expertise in master data management, data governance, and data stewardship. /li liKnowledge of ontology development and knowledge graph applications. /li liProven track record of integrating product data across discovery, development, clinical, regulatory, and commercial domains. /li liStrong understanding of product data standards (e.g., IDMP), with hands‑on experience with metadata management. /li liAbility to connect scientific, regulatory, and commercial perspectives into a unified product mastering framework. /li liStrong leadership, communication, and cross‑functional collaboration skills. /li liAbility to influence and drive adoption of product mastering practices across functions. /li /ul h3Required Skills /h3 pNone specified. /p h3Preferred Skills /h3 pAdvanced Analytics, Budget Management, Compliance Management, Critical Thinking, Cross‑Functional Collaboration, Data Analysis, Data Privacy Standards, Data Quality, Data Reporting, Data Savvy, Data Science, Data Visualization, Developing Others, Digital Fluency, Inclusive Leadership, Leadership, Strategic Thinking, Team Management. /p /p #J-18808-Ljbffr

ppCompensation: Executive-level salary + meaningful equity participation /p pWe are partnering with an ambitious, science-driven biotech based in Barcelona to appoint a Chief Scientific Officer who will define, lead, and own the company’s scientific strategy from discovery through early clinical development. This is a pivotal executive role for a senior scientific leader who combines deep technical credibility with strategic foresight and decisive leadership. /p pAs CSO, you will be entrusted with shaping the long‑term scientific vision, translating cutting‑edge research into robust development programmes, and building a high‑performing scientific organisation capable of delivering value at pace. /p h3Key Responsibilities /h3 ul liSet and own the scientific vision and RD strategy, aligned with corporate and investor objectives /li liLead discovery, preclinical, and translational activities, ensuring scientific excellence and disciplined execution /li liAct as the scientific authority internally and externally, representing the company to investors, partners, and key opinion leaders /li liBuild, mentor, and scale a world‑class scientific team, fostering a culture of accountability, innovation, and rigor /li liDrive decision-making across pipeline prioritisation, resource allocation, and risk management /li liOversee scientific governance, data integrity, and readiness for regulatory interactions /li liPartner closely with the CEO and Board to support fundraising, partnering, and long‑term growth strategy /li /ul h3Candidate Profile /h3 ul liPhD or MD/PhD in a relevant scientific discipline /li liProven leadership experience at executive or senior RD leadership level within biotech or pharma /li liStrong track record of advancing programmes from discovery through IND‑enabling / early clinical stages /li liDemonstrated ability to operate in fast‑paced, capital‑efficient environments /li liStrategic thinker with the confidence to make high‑impact scientific and organisational decisions /li liExcellent communicator, capable of influencing at Board and investor level /li /ul h3Why Join /h3 ul liOpportunity to shape the scientific direction of a high‑potential biotech at a critical stage of growth /li liSignificant ownership and influence at executive leadership level /li liWork from Barcelona — one of Europe’s leading life science hubs, offering exceptional quality of life /li liCompetitive executive compensation with meaningful equity upside /li /ul h3Next Steps /h3 pThis role is being handled on a confidential basis. For an initial discussion, please apply or contact our retained search team directly. /p h3Seniority level /h3 ul liExecutive /li /ul h3Employment type /h3 ul liFull‑time /li /ul h3Job function /h3 ul liResearch /li /ul /p #J-18808-Ljbffr

ph3Role Overview /h3pGalderma is seeking a Group Head of Internal Audit to lead its global internal audit function and provide independent, forward‑looking assurance to Executive Management and the Board Audit Finance Committee. /ppThe Group Head of Internal Audit is responsible for designing and delivering a risk‑based global internal audit strategy, ensuring the effectiveness of governance, risk management and internal controls across Galderma’s worldwide operations. The role goes beyond traditional assurance to act as a strategic partner to leadership, identifying emerging risks, driving control maturity and providing insight during periods of transformation, growth and increased regulatory scrutiny. /ph3Key Responsibilities /h3ulliDefine and own Galderma’s global internal audit strategy aligned with enterprise risks, growth priorities and regulatory requirements. /liliLead the annual enterprise risk assessment and translate results into a rolling, multi‑year audit plan. /liliOversee the end‑to‑end execution of internal audits across all Galderma entities worldwide. /liliEnsure high‑quality audit execution, clear issue articulation and pragmatic, value‑adding recommendations. /liliUphold consistent methodologies, quality standards and reporting globally. /liliProvide clear, concise and timely reporting to the Group CFO, Executive Committee and Audit Finance Committee. /liliElevate systemic issues, emerging risks and control weaknesses with independence and sound judgment. /liliBuild strong, trusted relationships with senior leadership while preserving audit objectivity. /liliOwn governance over audit findings and remediation plans. /liliAggregate and trend audit themes to strengthen the Group’s overall control environment. /liliProvide forward‑looking insight on strategic initiatives without compromising independence. /liliBuild and lead a high‑performing global internal audit team. /liliDrive innovation through data analytics, automation and modern audit practices. /li /ulh3Experience Qualifications /h3ulli15+ years of experience in internal audit, external audit, risk or control leadership roles. /liliProven leadership of a global internal audit function or equivalent senior assurance role. /liliStrong understanding of governance, internal control frameworks and listed‑company requirements. /liliExperience in regulated, complex and international environments (pharma, medical devices, life sciences, consumer healthcare or similar). /liliProfessional qualification such as CIA, CPA, ACCA or equivalent preferred. /liliFluent in English; additional languages are an asset. /li /ulh3Leadership Personal Attributes /h3ulliHigh integrity and strong ethical compass. /liliExecutive presence with the confidence to challenge constructively. /liliAnalytical, independent and commercially minded. /liliAble to balance rigorous assurance with pragmatic business insight. /liliTrusted, discreet and resilient in sensitive situations. /li /ul /p #J-18808-Ljbffr

pAdvanced Resource Managers Ltd is seeking an experience Project Manager with a pharmaceutical or life sciences consulting background to lead QMS implementation projects in Barcelona. The role focuses on delivering end-to-end QMS implementations for global pharma, biotech and medical device clients, coordinating multi-disciplinary teams and ensuring compliance with GMP/GxP standards. /ppA hybrid Barcelona-based work arrangement is preferred, with occasional travel required for on-site client /p #J-18808-Ljbffr

OGYX | High-Throughput Organ-on-a-Chip Platform CEO & Co-Founder Opportunity | Deeptech BioEngineering | Drug Discovery Are you looking for an entrepreneurial opportunity at the intersection of microfluidics, advanced in-vitro models and drug discovery, with the chance to build a high-impact deep-tech spin-off? OGYX is developing a cost-effective, robust and user-friendly microfluidic Organ-on-a-Chip platform designed for high-throughput in-vitro assays in research, drug development and toxicology. Backed by Leitat and a strong technical team, the project is now seeking an entrepreneurial CEO to lead the creation of the spin-off and drive its commercial and strategic development. As CEO & Co-Founder, you will lead the venture-building journey together with the scientific and technical team, shaping the business model, early market traction and fundraising strategy of a company with the potential to become a preferred platform provider in the Organ-on-a-Chip market. About OGYX Drug discovery still relies heavily on animal models and conventional in-vitro systems, both of which often fail to accurately replicate human physiology. This results in poor predictive power, major development inefficiencies and growing ethical and regulatory pressure to reduce animal testing. Organ-on-a-Chip technologies offer a promising alternative, but current solutions face important limitations: they often compromise essential 2D/3D co-culture features, require peripheral equipment, or are not well suited for multiplexed high-throughput readouts and scalable production. OGYX addresses this challenge with a microfluidic OoC plate designed for high-throughput screening, compatible with 2D/3D co-cultures and organoids, and readable with standard multi-well plate readers. Its design combines biological relevance, usability and manufacturability in a single platform. Why OGYX Novel Organ-on-a-Chip plate combining high-throughput screening with human-relevant 2D/3D co-culture capabilities Patent published in 2024: WO2024033549 Technology designed for scalable production and ease of adoption Gravity-driven microfluidics, avoiding peripheral flow equipment Membrane-free design, reducing complexity and cost Compatible with standard plate readers through a design-for-detection approach Validated models already demonstrated in intestine, cartilage and tendon, with additional models under development including liver and kidney Early industry validation and feedback through collaborations with Leitat and ReadyCell / MedTech Barcelona The current microfluidic plate validation stage is TRL 7 Clear roadmap for spin-off creation, beta testing and commercial operation Current Founding Team Pooya Azizian – Future CTO Joan Marc Cabot – Principal Investigator & Advisor Head of Diagnostic Devices Group The project combines strong technical expertise in microfluidics and OoC systems with institutional backing and venture support from Leitat. Your Role as CEO & Co-Founder (Next 6 Months) You will lead OGYX through a critical transition phase focused on: Spin-off creation and shareholder structuring Defining the go-to-market strategy for CROs, biotech, pharma and research groups Validating the business model and pricing logic across standard plates, customized plates and modelling services Structuring early commercial traction and beta-testing strategy Leading private fundraising efforts Building partnerships with CROs, biotech companies and pharmaceutical players Building engagement with regulatory agencies. Supporting the strategic roadmap toward upscaling, product launch and new application development The Offer Relevant equity as CEO & Co-Founder upon company incorporation €6,000 stipend during the validation phase (3 monthly instalments of €2,000) Opportunity to access a participative loan of up to €50,000 to finance the first phases of the project Access to The Collider venture-building programme, including: Mentors and specialists in biotech, IP, go-to-market and fundraising Support in spin-off creation and shareholder structuring Access to experts in life sciences and industrial strategy International exposure through The Collider ecosystem (4YFN, Mobile World Congress, corporate & investor networks) Coworking space in Barcelona (Tech Barcelona – Pier 01) Two years of post-incorporation venture-builder support, including in-kind services, community access and portfolio perks This Opportunity Is for You If You are an entrepreneur with experience in biotech, life sciences, deep tech or scientific instrumentation Previous experience as founder or co-founder Strong network in pharmaceutical sector You understand the dynamics of drug discovery, CROs, pharma or advanced research tools Experience in B2B sales, fundraising and strategic partnerships Familiarity with platform business models and technology transfer is a strong plus You are comfortable bridging science, product and business strategy Eligible to work in Spain Fluent in English and Spanish, Catalan is a plus.

ppJoin to apply for the bQualification Validation Specialist /b role at bQbD Group /b /p pQbD Group team offers knowledge tailored (software) solutions in development, clinical, regulatory compliance, production and distribution for companies active in Pharma, ATMP and Medical Devices/IVD. We are always looking for the next QbD’er in bProcess validation. /b /p h3What do we expect from you as a Qualification and Validation Specialist? /h3 ul liProvide quality and validation oversight to ensure that validation, qualification and other life cycle activities are consistent with company validation policies, procedures and federal regulations; /li liSupport process validations (IQ/OQ/PQ) and cleaning validation; /li liIdentify critical areas for improvement and prioritize and execute the initiatives. /li liPerform or support nonconformance / CAPA root cause investigations, defining action plans and driving these to completion; /li liProceed according to the company’s quality policy in all business activities; /li liProvide advice to improve the quality policies and validation procedures; /li liProvide coaching, training and guidance on validations; /li liImplement controls to ensure data integrity and traceability of Quality records; /li liAct as a subject matter expert during internal and external audits (e.g. FDA). /li /ul h3Who are we looking for? /h3 ul liYou have an academic background related to areas such as pharmacy, chemistry, biology, engineering and related fields. /li liYou have at least 2 years of experience in qualifications/validations within validation departments in the pharmaceutical sector, medical devices, biotechnology… /li liYou have experience in qualification/validation documentation management: VP, URS, IQ, OQ, PQ. /li liYou have experience in complete processes of validations: protocols and validation reports. /li liYou have an advanced level of English: you should be able to write technical documentation in English. Spoken English will also be an advantage as you will be joining a multinational company. /li liYou have user-level computer skills: word processing, spreadsheet and database. /li liYou have a strong ability to self-manage and love working in a team. Rigour and proactivity are highly desirable. /li liYou have excellent communication skills. /li liYou are an autonomous person with the ability to adapt. /li liYou are able to adapt to high quality standards, data integrity, GMP. /li liA btrue QbD’er /b can be recognized by the following qualities: /li libResilient /b: Your strong and positive attitude helps you overcome any challenge /li libHungry for knowledge /b: You are always open to learning /li libNo non-sense mentality /b: you can be straightforward in a respectful way /li libInnovative /b: You are constantly looking for new and better solutions /li lib(Not too) serious /b: your job is serious, but you don’t take yourself too serious. /li /ul h3What’s in it for you? /h3 ul liQbD Group offers you an battractive and competitive salary package /b, that will be tailored to individual needs, considering legal requirements and local laws and regulations. /li liJoin us to build a bsustainable career /b, where job security is ensured, and lasting, meaningful connections are formed. /li liAs we’re a bknowledge-based company /b, you’re guaranteed to embark on a continuous journey of learning and development. /li liBe part of our global success story. As an baward-winning company /b we value everyone’s contribution and celebrate achievements together /li /ul h3Our promise to you: /h3 ul liAs an bambitious and pioneering company /b, we want to offer you the best possible environment to thrive within the life sciences. /li liMoreover, we aim to create a bjoyful community /b where you dare to be and can be yourself. Because the best way to grow is by growing together as unique individuals. /li liIn short … We stand for? bJPEG /b: bJ /boy in bP /bartnership, going for the bE /bxtra mile to bG /bet things done! /li /ul pInterested? Send us your CV and motivation letter and who knows, we might welcome you soon in our QbD family! /p h3Seniority level /h3 pAssociate /p h3Employment type /h3 pFull-time /p h3Job function /h3 pConsulting, Project Management, and Science /p h3Industries /h3 pPharmaceutical Manufacturing and Business Consulting and Services /p /p #J-18808-Ljbffr

ph3Senior IT Project Manager - EWM in Pharma /h3 pFull-time /p pSwiss Delivery Excellence: Transforming Life Science Consulting Worldwide. /p pFusion Consulting is a globally leading Business and IT boutique consultancy specialized in the Life Sciences industry, partnering with leading companies in pharma, healthcare, and animal health. /p pWith over 450 employees and 25 offices worldwide, our mission is to revolutionize our clients' business transformation challenges and set new industry standards through innovative solutions. /p pFocused on S4HANA, Data Cloud, and innovative technologies, Fusion Consulting brings unparalleled expertise and commitment to excellence to every project we undertake. /p pGrounded in our commitment to fast and intelligent decision-making, our client-first and open-hearted approach defines our ethos. With unwavering support and an entrepreneurial spirit, our global teamwork transcends boundaries and turns shared visions into reality. /p pWe are seeking an experienced Senior IT Project Manager to lead the implementation and optimisation of Extended Warehouse Management (EWM) systems within our pharmaceutical operations. This is a pivotal role that combines technical expertise with strategic project leadership, requiring a professional who can navigate complex regulatory environments whilst delivering transformational warehouse management solutions. /p h3Responsibilities /h3 ul liLead the planning, execution, and closure of EWM system implementation projects, ensuring delivery within scope, budget, and timeline constraints. /li liManage stakeholder communications across multiple departments and external partners, maintaining transparency and managing expectations throughout the project lifecycle. /li liDevelop comprehensive project plans, including resource allocation, risk mitigation strategies, and contingency measures specific to pharmaceutical operations. /li liOversee the configuration, testing, and deployment of EWM solutions, ensuring compliance with pharmaceutical regulatory requirements (GxP, GDP). /li liDirect and mentor project teams, fostering collaboration and accountability whilst maintaining high standards of technical excellence. /li liAnalyse business requirements and translate them into technical specifications, working closely with IT architects and warehouse operations teams. /li liManage project budgets, procurement processes, and vendor relationships to optimise cost-effectiveness. /li liFacilitate change management activities, ensuring smooth transition and user adoption of new systems. /li /ul h3Required Experience and Skills /h3 ul liMinimum 8 years' experience in IT project management, with at least 5 years leading EWM or warehouse management system implementations. /li liProven expertise in SAP EWM systems, including configuration, customisation, and deployment. /li liStrong knowledge of pharmaceutical industry operations, regulatory frameworks (GxP, GDP), and compliance requirements. /li liDemonstrated ability to manage complex, multi-phase projects with budgets exceeding €1 million. /li liExcellent people skills and proven track record of leading high-performing teams. /li liAdvanced proficiency in project management methodologies (Agile, Waterfall, or hybrid approaches). /li liStrong analytical and problem-solving capabilities with meticulous attention to detail. /li liProficiency in project management tools (MS Project, Jira, or equivalent). /li liExcellent written and verbal communication skills in English; ability to present to senior stakeholders. /li /ul h3Desirable Skills and Experience /h3 ul liSAP EWM or change management certification, or equivalent professional qualification. /li liExperience with warehouse automation technologies, system integration, and API management. /li liFluency in English language. /li liBackground in pharmaceutical manufacturing, distribution, or supply chain environments. /li /ul /p #J-18808-Ljbffr

pCencora is seeking an Innovation and CGT Business Developer in Barcelona to drive growth for our advanced therapies unit. You will listen to client needs, craft tailored cell and gene therapy solutions, and build strong relationships with stakeholders globally. /ppIdeal candidates have 3+ years in pharma business development, a relevant degree, and strong English; Master’s/MBA is a plus. This hybrid role emphasizes strategic partnerships and regulatory compliance within Alcura’s CGT framework. /p #J-18808-Ljbffr

ppBiorce is a pioneering Healthtech company dedicated to revolutionizing drug development through the power of AI. We are passionate about accelerating medical advancements and improving patient outcomes. /p pOur team comprises seasoned clinical research professionals, data scientists, and AI experts, working collaboratively to bridge the gap between cutting‑edge technology and real‑world clinical needs. /p pWith an unwavering commitment to revolutionize healthcare, we envision a world where all patients benefit from accelerated and cost‑effective access to treatments. /p h3About the role /h3 pAt Biorce, we’re transforming how the pharmaceutical industry designs and executes clinical trials. Our AI‑driven platform, AIKA, helps global pharma, biotech, and CROs accelerate molecule‑to‑market timelines, reduce protocol amendments, and build smarter, more inclusive trials. /p pWith operations in Europe and the U.S., and ambitious growth targets ahead, we’re building a world‑class commercial organisation to redefine what “AI for Clinical Trials” means. Our mission is to reduce timelines, prevent avoidable errors, and help life‑science organisations bring treatments to patients faster. As we scale globally, strategic partnerships with regulators, healthcare providers, and technology ecosystems are critical to expanding our impact and credibility. /p h3Key Responsibilities /h3 h3Strategic Partnership Development /h3 ul liDefine and execute Biorce’s global partnership strategy aligned with product, regulatory, and commercial priorities /li liIdentify, qualify, and prioritize strategic partners across regulators, healthcare systems, and technology ecosystems /li liBuild long‑term, scalable partnership frameworks rather than one‑off commercial deals /li /ul h3Regulatory Public Partnerships /h3 ul liLead partnerships and collaborations with regulatory authorities, public institutions, and policy‑shaping bodies /li liSupport regulatory alignment initiatives, pilot programmes, sandboxes, and innovation frameworks /li liWork closely with internal clinical, regulatory, and legal teams to ensure credibility and compliance /li /ul h3Healthcare System Partnerships /h3 ul liEstablish strategic relationships with hospitals, clinics, and healthcare networks for clinical research enablement /li liNegotiate partnership models covering data access, workflow integration, pilots, and long‑term collaboration /li liEnable Biorce’s technology to be embedded into real‑world clinical and research environments /li /ul h3Technology SaaS Alliances /h3 ul liNegotiate and manage partnerships with complementary SaaS providers (CRO tech stack, data platforms, AI tools) /li liDesign integration, co‑selling, and co‑marketing frameworks where appropriate /li liEnsure partnerships create measurable product, commercial, or strategic leverage /li /ul h3Negotiation Deal Ownership /h3 ul liOwn end‑to‑end partnership negotiations, including commercial terms, scope, governance, and KPIs /li liBalance speed, strategic value, and risk in complex, multi‑stakeholder negotiations /li /ul h3Internal Alignment Execution /h3 ul liAct as the internal owner of strategic partnerships post‑signature, ensuring value realization /li liAlign partnership outcomes with product roadmap, sales strategy. Collaborate with Legal, Product, and Commercial teams to structure agreements that scale globally /li /ul h3Who We’re Looking For /h3 pA hands‑on, executive‑level negotiator with deep regulatory and ecosystems fluency. This person should be able to build long‑term, scalable frameworks with hospitals, SaaS providers, and public bodies, ensuring Biorce's technology becomes deeply embedded in real‑world clinical environments. /p h3Requirements /h3 bMust‑haves /b ul liProven executive‑level experience in strategic partnerships, business development, or alliances within Healthtech, Biotech, or Clinical Research. /li liDeep regulatory fluency and experience navigating healthcare systems, hospitals, and public bodies. /li liExceptional negotiation skills with a track record of closing complex, multi‑stakeholder deals. /li liFamiliarity with the clinical trial tech stack (data, EDC, eCOA, eTMF, CTMS, RWD, etc.). /li /ul bNice‑to‑Haves /b ul liAn existing network of contacts within global regulatory agencies or major healthcare networks is a strong plus. /li liExperience building SaaS integration or co‑marketing frameworks. /li /ul h3Compensation /h3 pBase salary: $250,000 – $325,000 USD annually (U.S.) /p pIn addition to base salary, this role is eligible for a competitive performance‑based bonus and equity package. /p pActual compensation will be determined based on several factors, including experience, expertise, skills, geographic location, and overall fit for the role. /p pBiorce is committed to providing competitive compensation and equal pay for equal work. /p h3Why Join Us /h3 ul liA dynamic work environment with an international team, where collaboration and diversity thrive. /li liWork alongside top talent, united by a shared purpose and committed to making a real impact. /li liComprehensive private health coverage to ensure your physical and mental well‑being. /li liHybrid work model offering flexibility to balance your professional and personal life. /li liCompany events to celebrate achievements and enjoy time together. /li liGet equipped with a MacBook to enhance your productivity and work experience. /li liOur office is pet‑friendly! You’ll likely be greeted by a few wagging tails upon arrival. /li /ul /p #J-18808-Ljbffr

ppLocation: Barcelona, ES Remote, ES /p pJob ID: 10056 /p h3SAP EWM Consultant - fully remote possible /h3 pYour new home base at Körber is the bKörber Supply Chain Consulting /b team. /p pA smoothly running supply chain of goods - end-to-end - is what makes today’s world go round. Here is your chance to become part of this challenge. At Körber Supply Chain Consulting we work with our customers to envisage and implement their supply chains for tomorrow. We work with best-in-class software companies like SAP and turn our customers end-to-end supply chain vision into reality. We bring to the table supply-chain intelligence and advanced digital expertise gained in many projects. We ensure a seamless integration in the overall IT landscape of our customers, even down to driving automation technology on the hardware level. If you like software engineering and consulting, applied to real life problems in warehousing, transport management, yard management and manufacturing execution, you don’t need to look further. /p h3Your role in our team /h3 ul liRecording and qualification of technical requirements from tenders and workshops at the customer's site /li liDevelopment of IT solution concepts and documentation in specifications and business blueprints /li liRealization of solution concepts with the focus on SAP EWM and connected SAP modules /li liCreation of test cases, support of tests at the customer, cutover and change management activities /li liConducting trainings /li liQualified support for solutions implemented at our customers /li /ul h3Your profile /h3 ul liCompleted vocational training and/or university degree in information technology, supply chain management, logistics, natural sciences or similar /li liAnalytical skills and IT affinity /li liAt least 2 years experiences as an SAP EWM Consultant /li liWillingness to travel /li liConversationally confident in English, other foreign language advantageous /li liDesirable: located in Barcelona or surroundings /li liExciting challenges in national and international SAP implementation projects in different industries /li liTaking on responsibility and the opportunity to make a difference from day one. Compatibility of work, family and free time through flexible working hours, mobile working - also from home /li liWorking in an environment with a good team spirit, solidarity, and mutual support /li liPersonal development opportunities in a growing team /li liFlat hierarchies and short communication channels /li liOngoing training and further education /li liPersonal mentoring and individual development opportunities /li /ul pWe value diversity and therefore welcome all applicants - regardless of gender, nationality, ethnic or social origin, religion/belief, disability, age, sexual orientation and identity, and any other protected status. /p /p #J-18808-Ljbffr

ph3Perfil /h3 pNos encontramos en la búsqueda de un perfil de Pharma Operations Specialist con visión transversal de negocio y potencial para evolucionar hacia posiciones de mayor responsabilidad dentro de la organización para una empresa del sector farmacéutico. /p h3Responsabilidades y requisitos /h3 pBuscamos profesionales con experiencia en entornos farmacéuticos regulados y capacidad para coordinar diferentes áreas operativas, mejorar procesos y contribuir activamente al crecimiento del negocio. /p pRequisitos: /p ul liExperiencia real en entorno farmacéutico regulado. /li liCapacidad para trabajar de forma transversal con áreas como Supply Chain, Logistics, Quality, Regulatory, Finance y Customer Operations. /li liExperiencia en mejora de procesos, SOPs, reporting y KPIs. /li liInglés profesional alto. /li liPerfil analítico, estructurado y orientado a la mejora continua. /li liMentalidad de ownership y potencial de crecimiento hacia posiciones de liderazgo operativo. /li /ul h3Formas de valor añadido /h3 ul liExperiencia con medicamentos de ensayo clínico (IMP). /li liExperiencias en entornos CRO, Sponsor o Clinical Supply. /li liCadena de frío, trazabilidad y gestión de incidencias. /li liHerramientas de reporting, automatización e IA aplicada a operaciones. /li /ul h3Beneficios /h3 ul liIncorporación a una compañía en crecimiento dentro del sector farmacéutico. /li liEntorno internacional. /li liParticipación en proyectos estratégicos y de mejora de operaciones. /li liExposición transversal a diferentes áreas del negocio. /li liPlan de desarrollo con recorrido hacia posiciones de mayor responsabilidad operativa. /li liFormación continua y desarrollo profesional. /li /ul pSalario 30‑35 k + 12 % variable. /p pEs una excelente oportunidad para profesionales que quieran dar un paso más allá de la ejecución operativa y participar activamente en la construcción y optimización de procesos dentro de una organización internacional y en crecimiento. /p /p #J-18808-Ljbffr

ph3Overview /h3pJoin our expert team to work on a Data Analytics project, contributing to the development of scalable cloud data platforms and modern data pipelines. You will apply your knowledge of AWS, Snowflake, dbt, Apache Airflow, Python and SQL to deliver high‑quality data solutions that support analytics initiatives. /ph3Responsibilities /h3pYou will be responsible for designing, developing and maintaining scalable ETL and ELT pipelines using AWS services, building reliable workflows with Apache Airflow, optimizing data models in Snowflake and dbt, implementing data quality and monitoring practices, and collaborating with analysts and data teams to deliver trusted datasets for analytics and business intelligence. /ph3Qualifications /h3ulliStrong experience with Python and SQL. /liliHands‑on experience with AWS data services, Snowflake, dbt, and Apache Airflow. /liliKnowledge of data warehousing, data modeling, and cloud‑based architectures. /liliExperience working with Git and CI/CD practices. /liliExperience building and maintaining ETL/ELT pipelines. /li /ulh3Benefits /h3ulliCertification coverage and reward for technical achievements up to €1,500. /liliPrivate health insurance. /liliFull coverage for sick leave. /liliFree emotional, legal and family support. /liliGym discounts or sports compensation. /liliFlexible remuneration options: meals, transport, childcare, etc. /liliReferral bonuses up to €6,000 per candidate and €5,000 per client. /lili23 working days of vacation. /liliFree language courses: English, Spanish, Catalan and German. /li /ulh3Work Model /h3pHybrid: usually 2 days a week in office, but depends on project and team. Flexible with key meetings and a 40‑hour work week. Availability for key meetings is required, while time off for personal matters is accepted. Trust is placed in delivering quality work within the standard work week. /p /p #J-18808-Ljbffr

pAizon, a fast-growing SaaS provider in life sciences, seeks an Artificial Intelligence Intern in Barcelona. You will collaborate with AI and Data Consulting teams, analyze complex data, and help deploy scalable AI solutions across GMP workflows. /ppIdeal candidates have a quantitative background, Python skills, and familiarity with ML libraries. English proficiency is required, and you’ll join an internationally focused team with strong growth prospects. /p #J-18808-Ljbffr

pTamarind Intelligence is seeking an experienced packaging engineer to help deliver secure enterprise software solutions in the pharmaceutical sector. You will manage end-to-end software packaging, ensure quality and traceability, and automate deployments using PowerShell, Intune, SCCM and related packaging technologies. /ppJoin an international team in a hybrid Barcelona-based role, collaborating with IT and business stakeholders. /p #J-18808-Ljbffr

pMorgan Philips Group is seeking a statistics leader in Barcelona to provide statistical expertise, lead teams of statisticians and programmers, and plan analyses for drug development. You will ensure data integrity and oversee outsourced statistical work with a hands-on, collaborative approach and global reach. /ppThe role requires a PhD or MS in Biostatistics/Statistics/Mathematics, 2+ years of pharma/biotech statistics experience, and strong communication skills in English. /p #J-18808-Ljbffr

pHuxley is seeking an Omnichannel Consultant to enhance a leading international pharma project focused on global oncology and rare diseases. This role involves strategic design and execution of omnichannel customer journeys for healthcare professionals in a collaborative, international atmosphere. /ppApplicants should have over 5 years of experience in omnichannel marketing, proficiency in HCP engagement, and strong familiarity with digital tools. The position combines mostly remote work with occasional on-site visits in Barcelona. /p #J-18808-Ljbffr

pGalderma is seeking a hands-on Statistician for its new Global Capability Center in Barcelona. The successful candidate will support our Product Science and Manufacturing Science Technology teams through advanced statistical analysis to ensure product quality and optimize processes. /ppThe ideal candidate will have a Master's or PhD in a related field, along with significant experience in pharma or advanced manufacturing. Join us to influence decisions on manufacturing challenges with high impact and collaborate across diverse teams. /p #J-18808-Ljbffr

ph3Experteer Overview /h3 pIn this role, you will shape global value, access and pricing strategies for Neurology indications, with a focus on NMOSD. You’ll operate within the GVAP team to impact launch and lifecycle decisions across key EU markets, collaborating with multiple functions to drive patient access. You’ll translate science into payer value, influence global and local payer dialogues, and support evidence generation and RWE plans. This is a high-visibility position that contributes to advancing transformative therapies in rare neurological diseases. /p h3Compensaciones / Beneficios /h3 ul liLead development of a clear NMOSD value proposition across cross‑functional partners /li liEnsure evidence generation plans and RWE are integrated to support payer value and access /li liSupport GMMA Commercial in NMOSD lifecycle management through governance milestones /li liDevelop and implement global market access and pricing strategies with country partners /li liAssess pricing and reimbursement risks and mitigation actions for Neurology in priority markets /li liCreate strategic value, access, and pricing materials for NMOSD to aid local PU0026R submissions and negotiations /li liUpdate the global NMOSD reimbursement dossier and align cross‑functional readiness for Neurology /li liRepresent GVAP in cross‑functional forums and keep local teams informed of strategy /li liLead the Neurology payer working group to share evidence and best practices /li liIncorporate patient perspectives to inform payer negotiations and access strategies /li /ul h3Responsabilidades /h3 ul liExtensive leadership experience in market access and pricing for rare diseases/Neurology /li liAbility to translate scientific data into payer value stories for senior stakeholders /li liExperience developing evidence‑based value solutions with EU payers or US commercial customers /li liGraduate‑level degree (PhD, PharmD, Biomedical Sciences, business, economics) or equivalent /li liMore than 6 years in drug development and/or commercialization in pharma/biotech /li liKnowledge of payer needs in national/regional markets and familiarity with cost‑effectiveness contexts (UK, Canada, Nordics preferred) /li liStrong communication skills for cross‑functional and leadership audiences /li /ul pLocation: Barcelona, Kingdom Of Spain, ES /p /p #J-18808-Ljbffr

pGracia101 Talent Solutions is assisting a leading global pharmaceutical company in finding an IT Commercial Tech Project Manager in Barcelona. This role focuses on leading IT projects that support product launches and digital initiatives while ensuring compliance with industry standards. /ppThe ideal candidate will have over 7 years of experience in IT Project Management, particularly in Pharma or Life Sciences, and must possess excellent stakeholder management skills. /p #J-18808-Ljbffr

ph3The Position /h3 pReport to: Product Knowledge Manager /p h3Key Responsibilities /h3 ul liWork closely with our product team to understand product features. /li liAssist in creating product content for knowledge sharing. /li liCollaborate with subject matter experts to create training materials and other product documentation. /li liReview and edit existing documentation for accuracy, clarity, and adherence to style guides. /li liSupport activities related to product readiness throughout the product development life cycle. /li liParticipate in the deployment of new versions and features within the platform, which includes training planning, weekly reviews, impact analysis, and managing deadlines. /li liAssist in preparing reports and presentations on product features. /li liWork with product designers to understand and contribute to the user experience design process. /li /ul h3Working Smarter with AI /h3 ul liUse AI tools as part of your daily workflow to accelerate drafting, editing, research, and reviewing of product content and training documentation. /li liConstantly look for room for improvement in both the quality and the speed of your tasks, treating AI as a partner for raising that bar. /li liApply good judgment and quality control when using AI, ensuring outputs are accurate, clear, and compliant with our standards. /li /ul h3Qualifications (Must-Have) /h3 ul liDegree or Professional Training related to Computer Science, Engineering, or English. /li li0-3 years of professional experience. /li liWritten and oral English advanced. /li liCommunication skills and comfort with customer-facing tasks. /li liCuriosity about and comfort using AI tools to improve the quality and efficiency of your work, with a mindset of continuous improvement. /li liWilling to comply with and follow all regulations required when working in a highly regulated environment, such as ISO standards and GMP regulations. /li /ul h3Qualifications (Nice-Have) /h3 ul liGood understanding of pharma manufacturing environments. /li liExperience with technical documentation. /li liGood understanding of Industry 4.0 concepts and principles, and cloud platforms (AWS, SaaS). /li liFamiliarity with agile development methodologies is a plus. /li liStrong interest in product knowledge and the technical aspects of product development. /li /ul h3The Human We’re Looking For /h3 ul liProficient in spoken and written English. /li liCapable of working with a dynamic product that is ever-changing and evolving rapidly. /li liStrong analytical and creative problem-solving skills. /li liEager to embrace new tools and ways of working, including AI, to keep raising the quality and speed of your work. /li liTeam player, collaborative, innovative, and a get-things-done mindset. /li liAbility to understand business requirements and translate them into technical requirements. /li liYou take ownership and feel responsible for the product as a whole. /li liCommitment to quality. /li liYou take responsibility for the success of the project. /li /ul h3Benefits /h3 ul liUnique opportunity to join our company as it scales with excellent market traction and huge potential to grow globally. /li liCompetitive Salary (according to your experience/skills). /li liEquity, bonuses, and generous stock options. /li liFlexible schedule - Intensive Fridays. /li liLanguage one-to-one training courses. /li liCompetitive healthcare plans and benefits – Medical Dental Insurance. /li liInternal training and certifications plan. /li liFlexible Remuneration Options. /li liCareer plan and scheduled salary reviews. /li liTeam-building activities. /li liTop‑notch "tech pack" – We are Mac lovers! /li liAn open and collaborative work environment with a young and dynamic team and a very international culture. /li liAn opportunity for personal and professional growth, supported by stellar investors and the exciting challenges that come with joining a company at the start of its growth trajectory. /li /ul h3Equal Opportunity Employment /h3 pWe are dedicated to maintaining an inclusive workplace in which all employees are treated with respect and are able to contribute meaningfully to society. Our organization brings together professionals from diverse backgrounds, representing more than 28 nationalities, and we take pride in being an equal‑opportunity employer. Employment decisions are based exclusively on qualifications, merit, and business requirements. Applicants who require assistance or accommodation due to a disability may contact us at . /p /p #J-18808-Ljbffr

ppCan you imagine helping deliver secure enterprise software solutions in the pharmaceutical sector? /ppJoin our expert team to work on a Pharma project, contributing to the development of enterprise software packaging and distribution solutions. You will apply your knowledge of PowerShell, Microsoft Intune, SCCM and packaging technologies to deliver secure, reliable and standardized software deployments while collaborating with international teams. /ph3Responsibilities /h3ulliManage software packaging requests from end to end. /liliCreate and maintain enterprise software packages while ensuring quality and traceability. /liliAutomate processes using scripting. /liliDeploy applications through Microsoft Endpoint Management technologies. /liliProvide third‑level support and collaborate with cross‑functional teams to continuously improve the packaging service. /li /ulh3Qualifications /h3ulliStrong experience with software packaging technologies such as MSI, MSIX and Intunewin. /liliSolid knowledge of PowerShell, Ansible and PSADT for automation. /liliHands‑on experience with Microsoft SCCM and Intune for enterprise software deployment. /liliExperience working with Agile, ITIL or similar methodologies and collaborating with technical and business stakeholders. /liliProfessional English level C1 or higher. /li /ulh3Benefits /h3ulliCertifications covered and reward for technical achievements up to 1,500 €. /liliPrivate health insurance. /liliFull coverage for sick leave. /liliFree emotional, legal and family support. /liliGym discounts or sports compensation. /liliFlexible remuneration: meals, transport, childcare, etc. /liliReferral bonuses up to 6,000 € per candidate and 5,000 € per client. /lili23 working days of vacation. /liliFree language courses: English, Spanish, Catalan and German. /li /ulh3Working Model /h3pWe ask you to be available for key meetings. The model is hybrid: we usually go to the office 2 days a week, though this depends on the project and team. We trust you to deliver quality work within your 40‑hour workweek. /ph3Additional Information /h3pIf a project ends or you feel ready for a new challenge, we will find another one that aligns with your professional development. Salary will be discussed during the first call. /p /p #J-18808-Ljbffr

ppAt SARIA Food Pharma, our activities are characterized by connected value chains, decades of shared market expertise and a unifying spirit of innovation to continuously develop our people and our products /ppVan Hessen, Devro and Bioiberica use animal raw materials to create their wide range of products, which are ubiquitous and universal, but anything but ordinary. With a complementary portfolio of casings for the sausage industry that includes natural and collagen-based casings, Devro and Van Hessen are leading product experts in their industry. The global life science company Bioiberica produces active ingredients for humans, animals and plants, from starting material it receives from Van Hessen. /ppWe create the added layer of value with our products and services, improve the well-being of all by taking life science further and combine our attention to detail with the extraordinary, because it all matters. /ph3About the role /h3pThe new role of Business Development Manager will lead the development execution of the strategy to scale the biomedical collagen portfolio, leveraging the capabilities of the division and the strengths of our Bioiberica Devro business units. /ph3Responsibilities: /h3ulliIdentifying developing new business opportunities whilst enhancing existing customer partnerships /liliDevelop and execute strategic business plans to identify, target, and penetrate new accounts /liliConduct analysis on technical financial viability of proposed projects /liliManage sales budget, review pricing, and establish models for margin optimisation /liliMonitoring market dynamics, competitive activity and emerging opportunities /liliDesign, build, and manage commercial contracts, to maximize value for both sides /liliEstablish partnerships with KOLs (Key Opinion Leaders) and academic institutions to enhance the awareness of our Biomedical tissue portfolio /liliEnsure all commercial activities comply with strict regulatory guidelines regarding animal derived materials, including ISO 22442 and relevant local regulations /li /ulh3About you: /h3ulliLife science bachelor's degree, preferred in Biomedical Engineering, Biological Sciences, Veterinary Science /liliA Masters in Business Administration is an advantage /liliAdvanced English and Spanish (not mandatory) language skills /liliMore than 10 years' experience in medical device sales/ key account management/ business development in the field of biological materials or similar type of pharma portfolio. /liliFamiliarity with regulatory and compliance requirements for the sourcing and use of animal derived tissues in medical devices /liliAbility to work independently to build strong customer relationships /liliBuilds effective networks relationships across the various operations and contributes to effective integration of entities /liliCollaborative and internal partnership approach with key departments (Regulatory Affairs, RD, Finance, Marketing) /liliWillingness to travel extensively Europe/ USA/ Australia in support of customers to manufacturing /li /ulh3What's next? /h3pIf this sounds like a role that you would be interested in, then we would love to hear from you. To apply, please email a copy of your CV, along with a cover letter explaining the key attributes that you could bring to the role. /ppWe value the support recruitment agencies provide, however we are unable to accept speculative CV’s from agencies we are not already engaged with. /pp*Please note, closing dates are subject to change and, at time of high volume of applications, this may be brought forward. /ph3Equality and diversity at SARIA Food Pharma: /h3pWe value diversity and are committed to an inclusive working environment in which all employees are respected and supported regardless of gender, age, ethnic origin, religion, sexual orientation, disability, or social background. We expressly welcome applications from people with a wide range of perspectives and experiences. Our goal is to ensure equal opportunities and actively combat discrimination – both in the application process and in everyday working life. /p /p #J-18808-Ljbffr

ppAt Grup Montaner, a consultancy specialized in talent acquisition and development, we are partnering with a bleading European distributor of specialty chemicals. /b With several decades of experience, a strong international presence, sustained growth, and an established network of world-class manufacturing partners, our client is recognized as a key player in the industry. /p pWe are currently looking to hire btwo Industry Managers: one for the Food Pharma division and another for Personal Care. /b These are strategic positions offering significant business impact and the opportunity to drive the growth of high-potential business units. /p pWe are seeking professionals who are eager to lead the development of their business area by defining the commercial strategy for their market and becoming the trusted partner for both customers and international manufacturers. /p pIf you enjoy identifying new business opportunities, building strategic relationships, developing markets, and introducing innovative solutions to the industry, this is an excellent opportunity to take your career to the next level. /p h3bYour Mission /b /h3 pAs Industry Manager, you will be responsible for driving the growth of your business unit across Spain and Portugal, enjoying a high degree of autonomy to develop the market, define your commercial strategy, and build long-term partnerships with customers and international manufacturing partners. /p pYou will work closely with an international portfolio of specialized manufacturers, representing their products and technologies in the market, identifying new business opportunities, and developing high-value applications for customers. You will be supported by well-established Regulatory, Technical Laboratory, and Inside Sales teams, allowing you to focus on strategic business development and commercial growth. /p h3bKey Responsibilities /b /h3 ul liLead the growth of the Food Pharma or Personal Care business unit by defining and executing the commercial strategy for your market. /li liIdentify and develop new business opportunities through a technical, consultative sales approach. /li liBuild long-term strategic relationships with industrial customers, becoming their trusted business partner. /li liRepresent leading international manufacturers, working collaboratively to develop the market and introduce innovative technologies and solutions. /li liMonitor market trends, identify new applications, and uncover growth opportunities within your industry. /li liManage relationships with international suppliers and collaborate on market development strategies. /li liWork closely with Regulatory, Laboratory, and Inside Sales teams to deliver tailored solutions that meet customer needs. /li liManage medium-to-long-term sales cycles, providing both technical and commercial follow-up until business opportunities are successfully converted. /li liConduct regular face-to-face customer visits across Spain and Portugal (bapproximately 3-5 visits per week /b). /li liRepresent the company at trade shows, conferences, and industry events. /li /ul h3bWhat We’re Looking For /b /h3 ul liUniversityb degree in Chemistry, Pharmacy, Biotechnology, Food Technology, or a related scientific discipline. /b /li liPrevious experience within the specialty chemicals distribution industry, raw materials distribution, or manufacturing for the Food Pharma or Personal Care sectors. /li liProven experience in B2B business development, identifying new opportunities, and managing industrial customers. /li liFor the Food Pharma position, candidates with more than five years of experience and an established network within the industry will be highly valued. /li liFor the Personal Care position, we are looking for professionals with industry experience and strong potential for further growth and development. /li liExperience working with international manufacturers or suppliers. /li /ul h3bWhat the Company Offers /b /h3 ul liThe opportunity to join a leading European specialty chemicals distributor with a strong track record, international presence, and sustained growth. /li liThe chance to lead the development of a high-potential business unit with significant autonomy and strategic responsibility. /li liAccess to a well-established portfolio of leading international manufacturing partners, actively contributing to market development and the introduction of innovative solutions. /li liFull-time permanent position. /li liFlexible hybrid working model, with bone office day per week in Barcelona. /b /li liOngoing technical training in collaboration with international manufacturers and specialized organizations. /li liA structured onboarding program during your first months. /li liCompany car for both business and personal use. /li liPrivate health insurance. /li liCompany mobile phone and all necessary work equipment. /li liBetween 28 and 30 days of annual leave. /li liExcellent working environment, collaborative culture, and regular salary reviews. /li libFor candidates with 5-10 years /b of experience: fixed annual gross salary between €65,000 and €75,000, depending on experience, plus a performance-based bonus of 0% to 20% of the annual gross salary. /li libFor candidates with 2-5 years /b of experience: fixed annual gross salary between €40,000 and €50,000, depending on experience, plus a performance-based bonus of 0% to 20% of the annual gross salary. /li /ul p*Please note that professional references and employment history verification will be requested during the recruitment process. /p /p #J-18808-Ljbffr

pSYou España busca un Pharma Operations Specialist para coordinar áreas operativas y liderar iniciativas de mejora en un entorno regulado. El candidato debe aportar visión transversal de negocio y capacidad de crecer hacia posiciones de liderazgo operativo. /ppSe valorará experiencia en SOPs, reporting y KPIs, inglés profesional alto y perfil analítico. La posición ofrece exposición internacional y desarrollo dentro de un sector farmacéutico en crecimiento. /p #J-18808-Ljbffr

ppbReady to build scalable cloud data platforms that power analytics and business intelligence?? /b /ppJoin our expert team to work on a Data Analytics project, contributing to the development of scalable cloud data platforms and modern data pipelines. You will apply your knowledge of AWS, Snowflake, dbt, Apache Airflow, Python, and SQL to deliver reliable, high quality data solutions that support analytics initiatives. /ppAt ERNI, you are never just a number. Even if you work on an external project, you will feel part of the team and always supported. /ph3How do we make this happen? /h3pWith people. Besides your team and manager, you will have several support figures like a godparent, who will help you with the practical and administrative aspects of daily life during your first 6 months. /ppAnd the second most important person after you, your mentor, who will guide you through your entire onboarding and career at ERNI. You will have regular 1:1 meetings with them, and recurrently, you will work on your development plan to define your short-, medium-, and long-term goals. /ppAt ERNI, we highly value experience and technical knowledge. As a senior profile, you will have the space to continue growing, whether by deepening your technical skills or having greater influence on project decisions, with autonomy and the opportunity to share knowledge with other experts. /ppAnd if you are interested in mentoring, there is also space for that: supporting other ERNIans while still focusing on the technical excellence that sets us apart. /ph3What You Will Bring /h3ulliStrong experience with Python and SQL. /liliHands on experience with AWS data services, Snowflake, dbt, and Apache Airflow. /liliKnowledge of data warehousing, data modeling, and cloud based architectures. /liliExperience working with Git and CI/CD practices. /liliExperience building and maintaining ETL/ELT pipelines. /li /ulpYou will be responsible for designing, developing, and maintaining scalable ETL and ELT pipelines using AWS services while building reliable workflows with Apache Airflow. You will optimize data models in Snowflake and dbt, implement data quality and monitoring practices, and collaborate with analysts and data teams to deliver trusted datasets for analytics and business intelligence. /ph3What if the project ends? /h3pWe work on a wide variety of projects, technologies, and sectors, allowing you to keep growing in different environments. If a project ends or you feel ready for a new challenge, we will find another one that aligns with your professional development. /ph3Our working model /h3pWe ask you to be available for key meetings. Need to leave for a doctor’s appointment or to pick up your child from school? No problem. We trust you to deliver quality work within your 40-hour workweek. /ppOur model is hybrid: we usually go to the office 2 days a week, though this depends on the project and team, but we love seeing each other’s faces; the best stories always happen in the office! /ph3You Will Also Enjoy /h3ulliWe cover your certifications and reward technical achievements up to €1,500. /liliPrivate health insurance. /liliFull coverage for sick leave. /liliFree emotional, legal, and family support. /liliGym discounts or sports compensation. /liliFlexible remuneration: meals, transport, childcare, etc. /liliReferral bonuses: up to €6,000 per candidate and €5,0 00 per client. /lili23 working days of vacation. /liliFree language courses: English, Spanish, Catalan and German. /li /ulh3And the salary? /h3pWe will discuss it during the first call. If it is important to you, feel free to ask! /p /p #J-18808-Ljbffr

Experteer Overview As part of the international EMEA Marketing Communications team, you will design and execute multi-channel campaigns to drive engagement and growth for assigned product lines. You will translate objectives into customer journeys, optimize channel mix, and partner with internal and external teams to deliver high-impact campaigns and events. You will manage campaigns in CRM, measure performance, and drive continuous improvements. This role offers exposure to a regulated industry and opportunities to leverage new technologies. Compensaciones / Beneficios • Develop and execute integrated marketing communication plans for assigned product lines, customer segments, and strategic initiatives across EMEA • Translate business and marketing objectives into customer-centric engagement strategies, defining the optimal channel mix, messaging, and customer journey • Design and deliver multi-channel campaigns leveraging email marketing, digital nurturing, webinars, social media, paid media, third-party media, and events • Partner with Marketing Program Managers to define campaign objectives, success metrics, KPIs, and optimization plans • Collaborate with internal marketing partners and external agencies to ensure high-quality, on-time campaign execution • Lead international events planning including booth layout, promo plan, budget management and stakeholder coordination • Build audience segmentation, communication frameworks, and assets ensuring consistent brand experience • Manage campaign setup and execution within CRM and marketing platforms with compliant tracking Responsabilidades • Bachelor in Marketing • Minimum 2-3 years of experience in marketing communications, digital marketing, campaign management, or event marketing • Solid understanding of email marketing, marketing automation, social media, digital advertising, webinars, events, lead nurturing, and customer engagement • Experience managing activities and projects with multiple stakeholders and external partners • Strong analytical mindset for interpreting campaign data and taking action • Hands-on experience with CRM systems and marketing platforms; familiarity with Canva or Adobe Creative Cloud is a plus • Experience in a regulated industry (life sciences/healthcare/medical devices/pharma) is a plus • Strong written and verbal communication skills in English Requisitos principales • company pension scheme • company bonus • private healthcare • medical and life insurance • remote work option • career development opportunities

pMCR International en Barcelona busca un Gerente de Unidad de Negocio que lidere la estrategia y ejecución del plan de negocio. Necesitarás más de 8 años de experiencia en la industria farmacéutica y habilidades destacadas en liderazgo y planificación estratégica. /ppEl candidato ideal tendrá un título universitario en áreas relevantes y será responsable de gestionar el crecimiento del portafolio, desarrollar estrategias comerciales y coordinar equipos multidisciplinarios para asegurar el cumplimiento de objetivos. /p #J-18808-Ljbffr

ppAre you ready to start your career in pharmaceutical marketing and make a difference for people living with brain disorders? /p pJoin Lundbeck as a Brand Assistant Trainee and gain hands‑on experience supporting marketing initiatives across Spain and Portugal within our Psychiatry Business Unit. /p h3Your new role /h3 pAs a Brand Assistant Trainee, you will support the Marketing team in the execution of projects and initiatives that help bring innovative treatments to healthcare professionals and patients across Iberia. /p pYou will have the opportunity to learn about brand management, market insights, omnichannel engagement, congresses and events, while collaborating with experienced colleagues from Marketing, Medical Affairs, Sales and Market Access. /p pThis is a unique opportunity to gain exposure to the pharmaceutical industry and develop your skills in an international and purpose‑driven environment. /p h3Your future team /h3 pYou will become part of the Psychiatry Business Unit in Iberia, working from our Barcelona office in a collaborative and cross‑functional environment. /p pOur team values curiosity, teamwork and continuous learning. You will work closely with experienced professionals who are passionate about improving brain health and committed to helping you grow throughout your internship experience. /p h3What you bring to the team /h3 ul liFinal‑year student or recent graduate in Health Sciences, Pharmacy, Biology, Biotechnology, Business Administration or a related field. /li liPortuguese proficiency at C1 level or native speaker (mandatory). /li liEnglish proficiency at B2 level or above. /li liAvailability to formalize an internship agreement with a university or educational institution. /li liCuriosity, initiative and willingness to learn. /li liStrong communication and collaboration skills. /li /ul h3Our promise to you /h3 pAt Lundbeck, we offer more than an internship. We offer the opportunity to learn from experienced professionals, contribute to meaningful projects and gain valuable exposure to the pharmaceutical industry while developing your professional skills in an international environment. /p pWe are committed to creating a workplace where everyone can grow, contribute and bring their unique perspective. /p h3Practical information /h3 ul liLocation: Barcelona, Spain /li liInternship agreement required /li liMorning schedule (5 hours per day) /li /ul h3Equal Opportunity Commitment /h3 pAt Solutia GHS, we ensure that all our recruitment and selection processes are conducted based on objective criteria, assessing candidates solely on their skills, experience, and talent. /p pWe promote equal opportunities and do not tolerate any form of discrimination based on sex, gender, age, origin, race, religion, sexual orientation, gender identity, disability, or any other personal or social circumstance. /p pFurthermore, our compensation policy is governed by the principle of pay equity for the performance of the same functions, reinforcing our commitment to a diverse, inclusive, and respectful working environment. /p /p #J-18808-Ljbffr

Alcura, a Cencora-owned company in Barcelona, is seeking a GDP Deputy Director responsible for ensuring compliance with Good Distribution Practices across the supply chain. The role includes managing quality systems, regulatory audits, and liaising with health authorities. Candidates should have a Pharmacy degree, experience in quality management, and advanced knowledge of Spanish and English. The position offers a full-time role with opportunities for professional growth within the organization.br#J-18808-Ljbffr

ph3Senior IT Project Manager - Enterprise Platforms Supply Chain in Pharma /h3 h3Overview /h3 pFusion Consulting is a globally leading Business and IT boutique consultancy specialized in the Life Sciences industry. We partner with leading companies in pharma, healthcare and animal health to revolutionize their business transformation challenges. /p pWith over 450 employees and 25 offices worldwide, Fusion’s focus on S/4HANA, Data Cloud and innovative technologies brings unparalleled expertise to every project. /p h3Key Responsibilities /h3 ul liLead end-to-end delivery of global enterprise platform implementations and enhancements, including Supply Chain operations. /li liManage third‑party vendors and system integrators delivering cloud‑based solutions. /li liDrive global rollout activities: planning, testing, validation, training, deployment and hyper‑care. /li liEnsure compliance with GxP requirements, CSV methodologies and quality standards. /li liCoordinate business, IT, Quality and vendor stakeholders across multiple regions and functions. /li liManage project scope, budget, timelines, risks, dependencies and governance activities. /li liFacilitate steering committees and provide executive‑level reporting. /li liSupport organisational change management and user adoption activities. /li /ul h3Required Skills Experience /h3 ul li5+ years of IT Project Management experience within pharmaceutical, biotech or other regulated industries. /li liStrong background in Computer System Validation (CSV) and delivery of GxP‑regulated systems. /li liExperience supporting Supply Chain, Manufacturing, Planning, Quality or other operational business functions. /li liDemonstrated experience leading global platform deployments and rollouts across multiple sites and regions. /li liPMP, Prince2, Agile or equivalent project management certification. /li liStrong stakeholder management skills with the ability to work effectively across business and technical teams. /li liExcellent communication, governance and project delivery capabilities. /li liHands‑on, execution‑oriented approach with a strong focus on achieving project outcomes. /li /ul h3Preferred Experience /h3 ul liFamiliarity with enterprise platforms such as SAP, planning solutions, SaaS platforms or supply‑chain applications. /li /ul h3Benefits /h3 ul liCompetitive salary and benefits package reflecting your impact. /li liAnnual budget for professional development and regular workshops and training. /li liRecognition and reward schemes including referral and loyalty benefits. /li liGlobal mobility support: visas, permits, international assignments. /li liLocal perks tailored to your country of residence. /li /ul /p #J-18808-Ljbffr