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Who We Are Whitewater Group is a leading provider of innovative and sustainable water treatment engineering systems operating in Ireland, the UK and across Europe in the Data Centre, Pharma, Power and Industrial sectors. We specialize in designing, installing, commissioning, and maintaining water treatment solutions to meet our clients' specific needs. Our team is dedicated to delivering high-quality, cost-effective engineering solutions that prioritize safety, reliability, and environmental sustainability. Whitewater Group is headquartered in Naas Co. Kildare and operates from European bases in Spain, Sweden, Finland, and the UK, with plans for further offices in Germany, Denmark, and Italy. The Group is experiencing significant growth driven by its focus on off-site construction methods (OSM) for delivering turnkey projects, reducing on-site construction time to a minimum. Role Description Due to continued expansion, Whitewater is seeking a Pre-Commissioning Engineer (Electrical) to support the delivery of water treatment systems across European projects. This role is focused on electrical pre-commissioning activities, ensuring that electrical systems, control panels, instrumentation, and field devices are correctly installed, tested, and ready prior to energisation and live commissioning. The Pre-Commissioning Engineer will work closely with QA/QC, OSM, automation, and commissioning teams to identify and resolve issues early, helping ensure a smooth transition into commissioning and system start-up. Main Duties and Responsibilities Electrical Pre-Commissioning & Inspections to include: • Carry out detailed electrical pre-commissioning inspections of:, • MCCs, control panels, PLC panels, VSDs, soft starters, • Pumps, motors, actuated valves, instrumentation, and field devices, • Verify installations against P&IDs, electrical schematics, I/O lists, and approved drawings, • Confirm correct installation of power, control, and instrument cabling, • Verify earthing, bonding, labelling, and panel workmanship, • Identify installation or wiring issues and support timely resolution, • Provide clear feedback on electrical readiness to support commissioning planning Testing & Verification to include: • Perform or witness electrical testing to include:, • Insulation resistance testing, • Continuity and earth checks, • Phase rotation and supply verification, • Support loop checks and point-to-point testing in coordination with automation teams, • Confirm systems are safe and suitable for energisation Interface & Coordination • Work closely with:, • QA/QC team, • Automation / PLC engineers, • Commissioning engineers and project teams, • OSM team Documentation • Complete and maintain pre-commissioning checklists and inspection records (ITP’s), • Ensure testing and inspection results are clearly recorded and traceable, • Support the preparation of handover information required for commissioning activities Required Qualifications and Experience • Degree or trade qualification in Electrical Engineering, or an electrical trade-qualified background with experience in industrial systems and automation, or equivalent, • 3+ years’ experience in electrical installation, pre-commissioning, or site-based engineering roles, • Strong understanding of:, • MCCs, control panels, VSDs, motors, and instrumentation, • Ability to read and work from:, • P&IDs, • Electrical schematics, • I/O lists and construction drawings, • Strong attention to detail and safety-focused approach, • Permit to work in the EU Desirable • Experience working on water treatment plants or within water treatment environments, • Exposure to industrial process systems, utilities, or data centre infrastructure, • Previous involvement in commissioning or system start-up activities Benefits • Competitive salary, • Annual bonus, • Pension scheme, • Opportunity for progression within a growing commissioning team

SEARGIN IS HIRING! As a dynamic multinational tech company operating in 50 countries, we drive innovation and create projects that shape the future and greatly enhance the quality of life. You will find our solutions in the space industry, supporting scientists in the development of cancer drugs, and implementing innovative technological solutions for industrial clients worldwide. These are just some of the areas in which we operate! Currently, for the new Seargin project we are looking for SAP EWM Consultant. Location: Barcelona, Spain Employment Type: Contract FTE: Full-time Project: SAP WM → Advanced Embedded EWM migration for a pharma/GMP regulated warehouse (Interquim, Sant Cugat). The project covers full E2E implementation: inbound, internal movements, production supply, dispatch, HU management, and label traceability. Validation (IQ/OQ/PQ) is in scope. S/4HANA 2021 environment. Tasks: • Lead or support AS-IS process analysis and gap assessment vs EWM standard, • Configure and test EWM processes: inbound (transfer orders, HU creation, RF confirmation), internal storage, production supply, order picking, dispatch, • Design and configure HU management and Packing Instructions to replace manual Z-transactions, • Support functional specification writing (FDS) and user acceptance testing, • Collaborate with ABAP developers on custom developments (label printing, interfaces), • Participate in IQ/OQ/PQ validation activities alongside QA team, • Provide knowledge transfer and end-user training, • Support hyper-care period post Go-Live Must have: • SAP WM experience: minimum 3 years, • SAP EWM experience: minimum 3 years (Embedded or Decentralised), • Minimum one full E2E SAP EWM deployment (go-live experience required), • Strong knowledge of EWM inbound / outbound processes, HU management, RF Framework, • Experience with GMP / pharma / regulated environments preferred, • Familiarity with 21 CFR Part 11 and/or EU GMP Part II is a strong asset, • Fluent English (working language); Spanish is a plus Nice to have: • Experience with SAP QM integration in WM/EWM context, • Knowledge of Zebra label printing integration, • Experience with LabVantage or other LIMS systems, • SAP S/4HANA certification, • Experience with IQ/OQ/PQ validation processes Discover the Power of IT Excellence. Apply! To learn more about Seargin, please visit our web page: www.seargin.com

At ASTEK Iberia, we are looking for a highly skilled AI Specialist to join a global initiative focused on transforming how content is created, managed, and delivered across multiple channels across a large-scale consumer healthcare organization. This role sits at the intersection of AI, cloud engineering, and marketing technology, driving end-to-end AI solutions from concept to production. 💪 Main responsibilities: • Design and deliver end-to-end AI-powered solutions to automate content generation and management, • Build and deploy scalable applications using Microsoft Azure AI services, • Integrate LLMs, image and video generation models into real business workflows, • Develop and maintain data pipelines to connect AI models with enterprise systems, • Lead initiatives from POC to MVP to enterprise-scale deployment, • Collaborate with cross-functional teams (Product, Marketing, IT), • Ensure AI governance, compliance, and performance monitoring 👀 Who are you? 8+ years of experience in software development, with strong exposure to AI/ML engineering Hands-on experience with: • Azure AI Foundry, • Azure AI Search, • Azure Document Intelligence, • Azure Cognitive Services Strong experience with: • LLMs (prompting, fine-tuning, RAG), • Generative AI (image/video) Solid background in: • Python + one additional language (e.g. TypeScript), • API design & microservices, • Cloud-native architectures Experience building and scaling production-grade AI systems Knowledge of data pipelines and MLOps practices English fluent ⭐ Nice to have • Experience in marketing tech / content platforms, • Exposure to regulated industries (pharma, healthcare, etc.), • Familiarity with tools like SAP, Veeva, Adobe Experience Cloud, • Azure certifications 💼 Who are we? Since 2015, Astek Iberia has been accompanying its customers in their development throughout Spain (Madrid, Barcelona, Valencia, Basque Country, Andalusia, Galicia, etc.). Founded in France in 1988, Astek is a global player in engineering and technology consulting, present in five continents and 25 countries. With expertise in a wide range of industrial and service sectors, Astek is an essential partner, supporting its customers in an intelligent deployment of their products and services, and in the implementation of their digital transformation. Today we are more than 8,000 employees, committed every day to promote the complementarity between digital technologies and complex systems engineering. Our style is to have flexible schedules and highly value the well-being of our employees. Why join us? 🚀 You will grow professionally in a company in constant development and evolution. 📏 You will benefit from a personalized follow-up of your professional projects as close as possible to your ambitions. 📈 You will make a real contribution to the company's development in real time. 🏝️ You will enjoy 23 days of vacation (in addition to holidays) that you will be able to choose whenever you want. 🌍 You will join our team: diverse, multicultural and constantly growing. 🔋 You will have days full of good energy and good atmosphere. ..although you still have a lot to discover! 😄 ☎️ Shall we meet? 📧 If you want to participate in the process, apply from here attaching your CV (in English) as detailed as possible and we will tell you more.

At Astek, we are looking for an experienced SAP Functional ERP Consultant to join a leading organization in the pharma & diagnostics sector, supporting large-scale global transformation programs and ERP deployments. 💪 Your mission, should you choose to accept it… • Lead and coordinate end-to-end (E2E) integrations across define, build, test, and deployment phases, • Act as a key contact between business, SAP, and technical teams, ensuring alignment and connectivity readiness, • Gather, validate, and review functional requirements, mappings, and solution design documentation, • Ensure all integrations are properly documented, tracked, and included in deployment backlogs, • Align timelines, manage stakeholders, and support testing phases (SAT, DET, DIL) focusing on critical processes, • Maintain integration knowledge (E2E repository) and perform impact analysis on downstream systems, • Support cutover, hypercare, and handover to operations, ensuring monitoring and incident readiness 👀 Who are you? • Proven experience working in SAP ERP environments, • Strong background in system integrations and middleware technologies, • Experience in global deployment projects and complex system landscapes, • Solid project management skills (SAFE framework is a plus), • Strong business analysis and documentation review capabilities, • Excellent stakeholder management and communication skills, • Experience in pharma and/or diagnostics is highly valued 💼 Who are we? Since 2015, Astek Iberia has been accompanying its customers in their development throughout Spain (Madrid, Barcelona, Valencia, Basque Country, Andalusia, Galicia, etc.). Founded in France in 1988, Astek is a global player in engineering and technology consulting, present in five continents and 25 countries. With expertise in a wide range of industrial and service sectors, Astek is an essential partner, supporting its customers in an intelligent deployment of their products and services, and in the implementation of their digital transformation. Today we are more than 8,000 employees, committed every day to promote the complementarity between digital technologies and complex systems engineering. Our style is to have flexible schedules and highly value the well-being of our employees. Why join us? 🚀 You will grow professionally in a company in constant development and evolution. 📏 You will benefit from a personalized follow-up of your professional projects as close as possible to your ambitions. 📈 You will make a real contribution to the company's development in real time. 🏝️ You will enjoy 23 days of vacation (in addition to holidays) that you will be able to choose whenever you want. 🌍 You will join our team: diverse, multicultural and constantly growing. 🔋 You will have days full of good energy and good atmosphere. ...although you still have a lot to discover! 😄 ☎️ Shall we meet? 📧 If you want to participate in the process, apply from here attaching your CV (in English) as detailed as possible and we will tell you more.

About Traverse Health Traverse Health is a real-world evidence provider from the EU, operating in emerging markets. We develop cutting-edge digital solutions for the healthcare and life-science industry. By connecting healthcare organizations with the pharmaceutical and biotech industries, we maximize the potential of patient data to support smarter healthcare decisions and improve patient outcomes. Our services and solutions cater to pharmaceutical, biotech, and medical device companies, healthcare providers, CROs, health insurance providers, healthtech, drug discovery, and beyond. The Role We are looking for a Proposals & Business Development Analyst or Associate to join our commercial team. You will work at the front end of our business — shaping how we present Traverse Health to pharma and biotech clients and directly contributing to new business generation. Your core focus will be developing proposals, requests for proposals, pricing formation and pitch materials — translating scientific and commercial contexts into compelling narratives that win business. This role is for someone who enjoys structured thinking, works well with ambiguity, and wants real exposure to the life sciences and RWE space early in their career. Join us if start up environment is what you are looking for — to build together and grow fast. What You Will Do • Lead and coordinate the end-to-end development of RFP and unsolicited proposals, ensuring alignment with client needs and Traverse Health's capabilities, • Prepare high-quality pitch decks, capability presentations, and business development materials for pharma and biotech clients, • Collaborate with scientific, data, and technical teams to accurately represent our RWE study designs, digital registry solutions, and analytical methodologies in client-facing materials, • Contribute to the development and maintenance of proposal templates, case studies, and a reusable content library, • Assist in the preparation of client meetings, conferences, and follow-up communications, • Support project scoping discussions and budget estimation for new engagements What We Are Looking For Required: • 1–2 years of experience in a Big 4 consulting firm (healthcare or life sciences practice), pharmaceutical company, healthtech, or related environment, • Demonstrated experience contributing to the formation of Requests for Proposals (RFPs), proposals, or pitches in a professional setting, • Excellent written and verbal communication skills in English — you can translate complex ideas into clear, compelling narratives, • Strong proficiency in PowerPoint and ability to create visually clear, well-structured presentations, • Highly organised, detail-oriented, and able to manage multiple workstreams and deadlines simultaneously, • Comfortable working independently in a distributed, international team Preferred: • Understanding of real-world evidence, health economics, or clinical research concepts, • Familiarity with pharmaceutical drug development and regulatory pathways, • Familiarity with procurement and tender submission platforms such as SAP Ariba, Coupa, Jaggaer, or similar — experience navigating vendor portals used by large pharma and biotech companies is a plus, • Experience working with clients or stakeholders across multiple countries and cultures, • Additional European language Spanish is a plus, • University degree in Mathematics, Statistics, Economics, Engineering, or another quantitative discipline — we are looking for a structured thinker who is comfortable with numbers and logical reasoning, not just communication Alternative Profiles We Welcome We recognise that great talent does not always follow a linear path. We also encourage applications from: • MBA students or recent MBA graduates seeking part-time or project-based engagement (minimum 3 days per week) while completing their programme — ideally based in or near Barcelona, Madrid, • Candidates transitioning from academic research (PhD or MSc in life sciences, epidemiology, public health, or health economics) who have developed strong analytical and communication skills and are looking to apply them in a commercial context, • Consultants from strategy, market access backgrounds who want to move closer to data and evidence generation What We Offer • Direct exposure to senior leadership and real commercial decisions from day one, • The opportunity to work on cutting-edge RWE projects across Europe, MENA, and emerging markets, • A collaborative, international team that values intellectual curiosity and initiative over hierarchy, • Flexible working arrangements — remote-first within Europe, with preference for Barcelona-based candidates, • In person meetings and all company field trips, • Competitive compensation commensurate with experience, • The chance to grow with a company at an exciting stage of its development

INSUD PHARMA es un grupo farmacéutico internacional con presencia en toda la cadena de valor, desde la investigación y el desarrollo hasta la fabricación y comercialización, apostando por la innovación y el crecimiento sostenible. InsudPharma #Challenger #Insuder #InsudTalent. En INSUD PHARMA p

Join Rephine Barcelona: Leading Life Sciences Quality Worldwide At Rephine, we set the standard for quality assurance and GxP compliance in the Life Sciences industry. With offices in Barcelona, the UK, and China, India, we support the Pharmaceutical, Biotech, and Medical Device supply chains globally. Who We're Looking For: Are you passionate about consulting in the Pharma and Life Sciences sector? Do you thrive in dynamic environments, eager to take on multiple projects and drive real impact? If you're excited by the challenge of enhancing quality and compliance in a global company, we want you as our next Computer System Validation Senior Consultant in Barcelona. Your Role: As a CSV L2 Consultant, you will take an active role in delivering high-impact validation projects, with a focus on ERP systems and other critical computerized systems in regulated environments. You will be part of innovative projects, ensuring compliance, efficiency, and quality across the lifecycle. Key Responsibilities: Lead CSV Projects: • Take ownership of ERP and other computerized system validations (IQ, OQ, PQ), preparing and reviewing critical documentation (VMP, URS, SOPs)., • Ensure compliance with EU GMP Annex 11, FDA 21 CFR Part 11, GAMP 5, and Data Integrity guidelines. ERP & System Expertise: • Work hands-on with ERPs, eDMS, eQMS, LIMS, laboratory systems, SCADA, EBRs, pharmacovigilance, and maintenance systems., • Assess system compliance and performance to optimize regulatory readiness and operational efficiency. Audits & Compliance Assessments: • Perform supplier audits and compliance checks, focusing on Annex 11, 21 CFR Part 11, and global regulations., • Identify risks, provide actionable recommendations, and ensure corrective measures are implemented. International Project Engagement: • Contribute to projects across Spain, Europe, and China, adapting to diverse regulatory environments., • Represent Rephine on-site with clients, ensuring seamless collaboration and delivering high-quality results. Project Delivery & Client Success: • Manage timelines and ensure all deliverables, including documentation and test execution, are completed on schedule., • Maintain clear communication with stakeholders and provide progress updates regularly. Why This Role Could Excite You: • Take a leading role in ERP validation projects while expanding your CSV expertise., • Work with international teams and cutting-edge systems in a fast-paced consulting environment., • Be recognized as an L2 expert contributing to both client success and Rephine’s high standards. What You Bring: • A Bachelor’s degree in Chemistry or Engineering., • Solid experience in the pharmaceutical industry, GxP compliance, and computerized systems validation., • Strong multitasking skills and experience in managing multiple consulting projects to meet client needs., • Fluency in Spanish and English, with excellent communication skills., • Since client sites are often not easily accessible by public transportation, a valid driver’s license and willingness to travel by car are required. Is This Role for You? Ask yourself: • Are you excited about working with clients to tackle their most critical challenges?, • Can you maintain a sense of ownership and connection to the Rephine team, even when managing demanding client-facing responsibilities?, • Do you have the adaptability to move between technical tasks, regulatory compliance, and client interaction with ease?, • Are you ready to learn and grow in a role that exposes you to a wide range of systems and industries? If your answer is "yes" to these questions, then this opportunity at Rephine is your chance to make a significant impact while growing your career in CSV consulting. Why Choose Rephine? We believe in rewarding talent and commitment with a comprehensive benefits package designed to support your personal and professional growth: • Competitive Compensation: A salary that reflects your experience, along with additional vacation days and other benefits., • Work-Life Balance: Take advantage of our hybrid work model, flexible hours, and a shorter workday on Fridays, allowing you to maintain a healthy balance between work and personal life., • Global Exposure: Work with a multicultural team across multiple countries, providing opportunities to expand your professional network and gain international experience., • Dynamic Work Environment: Join a young, enthusiastic team where your contributions are valued, and your ideas can shape the future of the company., • Flexible Salary Options: Benefit from salary sacrifice schemes and more flexibility in managing your compensation package., • Opportunities for Growth: We provide a nurturing environment where your career can grow beyond expectations. Whether you're looking for new challenges or leadership opportunities, Rephine is committed to your continuous development., • Drive Digital Transformation: Participate in projects where you can use the latest technologies to optimize manufacturing and quality processes. For over 20 years, Rephine has been at the forefront of improving manufacturing quality processes for leading Life Sciences companies. We’re evolving rapidly and looking for passionate professionals eager to grow with us. Ready to embark on this journey? Visit our career site to learn more and apply in English.

En pocas palabras 📌 • Posición: Junior Demand Planner, • Localización: Madrid, • Experiencia: 1-3 años de experiencia ¿Quieres saber más? 👇 Exeltis es la división de marca de Insud Pharma, una compañía global con amplia experiencia en toda la cadena de valor farmacéutica, desde la investigación y el desarrollo hasta la fabricación, comercialización y distribución de productos con valor añadido para la salud humana y animal. La actividad de Insud Pharma se organiza en tres áreas de negocio sinérgicas: Industrial (Chemo), Branded (Exeltis) y Biotech (mAbxience), con más de 9.000 profesionales en más de 50 países, 20 instalaciones de última generación, 15 centros especializados de I+D, 12 oficinas comerciales y más de 35 filiales farmacéuticas, que atienden a 1.150 clientes en 96 países de todo el mundo. En Insud Pharma creemos en la innovación y el desarrollo sostenible. ¿Preparado/a para ser un #Challenger? 💪 ¿Qué buscamos? 🔎 Buscamos un/a Demand Planner para Exeltis que asegure una previsión de demanda precisa y alineada globalmente, integrando información de mercados, ventas, marketing y operaciones. Su misión será optimizar inventarios, mejorar el nivel de servicio y garantizar que la producción y el suministro respondan de forma eficiente a las necesidades de cada región, contribuyendo de forma directa a la toma de decisiones en un entorno internacional y dinámico. ¡El reto! 🚀 • Elaborar el forecast global, consolidando previsiones de todas las regiones y filiales mediante modelos estadísticos, análisis histórico y datos de mercado., • Participar activamente en el proceso de S&OP / IBP, presentando análisis, riesgos y oportunidades., • Analizar desviaciones entre forecast y demanda real, identificando causas y proponiendo acciones de mejora., • Colaborar estrechamente con Supply Planning para asegurar la disponibilidad de producto, la capacidad de producción y los planes de suministro., • Gestionar y mantener los datos maestros de planificación en los sistemas, incluyendo lead times, MOQ, ciclos de vida, clasificaciones ABC y otros parámetros clave para una correcta planificación., • Asegurar una adecuada gestión de datos en sistemas, velando por la calidad, consistencia y actualización de la información utilizada en los procesos de demanda y planificación., • Coordinar la planificación del ciclo de vida del producto, incluyendo lanzamientos, discontinuaciones, transiciones y gestión de obsolescencias., • Impulsar la optimización de inventarios globales, equilibrando niveles de stock, reduciendo excesos y evitando roturas., • Integrar variables de mercado como tendencias, estacionalidad, campañas comerciales y factores externos que impacten la demanda., • Coordinarse con equipos globales de ventas, marketing, finanzas, supply chain y operaciones regionales., • Utilizar herramientas avanzadas de forecasting, ERP y analítica para mejorar la precisión de la previsión y la calidad de la planificación. ¿Qué necesitas? 🤓 • Formación en Ingeniería, Economía, Estadística, Supply Chain, Business Analytics o similar., • Entre 1 y 3 años de experiencia en Demand Planning, Supply Chain, Forecasting o S&OP., • Experiencia preferiblemente en entornos globales; también se valorarán perfiles con experiencia local dentro del sector farmacéutico., • Conocimiento de ERP SAP., • Experiencia en gestión de datos en sistemas y mantenimiento de parámetros maestros de planificación., • Manejo de herramientas de forecasting como APO, Anaplan o equivalentes., • Valorable conocimiento de SAP IBP., • Nivel avanzado de Excel., • Nivel alto de inglés para la comunicación con equipos internacionales., • Capacidad para interpretar grandes volúmenes de datos y convertirlos en insights accionables., • Habilidades de comunicación e influencia para interactuar con stakeholders globales., • Pensamiento estratégico y orientación a resultados., • Capacidad para trabajar en entornos multiculturales y con múltiples zonas horarias., • Rigor analítico, atención al detalle y adaptabilidad ante cambios de mercado y prioridades., • Valorable experiencia en sectores con alta complejidad regulatoria o de portafolio. ¡Nuestros beneficios! 👏 • 📜 Contrato indefinido, • 📍 Madrid, • 🚀 Impacto real en decisiones estratégicas, • 🤝 Alta exposición a negocio y dirección, • 📈 Oportunidad de crecimiento en un entorno dinámico ¿Cómo será el proceso de Selección? 🕵️ • Contacto inicial por teléfono o correo electrónico., • Entrevistas con el equipo de selección y/o hiring manager., • Comunicación constante sobre el estado del proceso. 🔷¿Crees que esta oferta no es para ti? 🔷 Síguenos en LinkedIn e Instagram para conocer nuevas oportunidades y mantenerte al día de nuestras vacantes. #InsudPharma #Challenger #Insuder #InsudTalent COMPROMISO CON LA IGUALDAD DE OPORTUNIDADES En Exeltis apostamos por la igualdad de oportunidades y por un entorno de trabajo diverso e inclusivo. Todas las candidaturas serán valoradas sin distinción de género, identidad o expresión de género, edad, etnia, nacionalidad, religión, orientación sexual, discapacidad o cualquier otra condición personal, física o social.

SEARGIN IS HIRING! As a dynamic multinational tech company operating in 50 countries, we drive innovation and create projects that shape the future and greatly enhance the quality of life. You will find our solutions in the space industry, supporting scientists in the development of cancer drugs, and implementing innovative technological solutions for industrial clients worldwide. These are just some of the areas in which we operate! Currently, for the new Seargin project we are looking for ABAP Consultant (SAP WM/EWM) to join project for our client from pharma industry. Location: Barcelona Employment Type: contract FTE: full-time Working mode: hybrid Responsibilities: • Develop ABAP objects according to technical specifications from the Senior ABAP Lead, • Implement label printing enhancements: reprint reason recording, label preview, audit trail logging, unique label ID (FR.01–FR.09), • Support Zebra printer integration for HU labels at inbound, production, and dispatch stages, • Develop and unit-test interface components (LabVantage / LIMS stock status updates), • Build enhancements for EWM inbound/outbound processes and internal movements, • Participate in code reviews and apply GxP data integrity principles (ALCOA+), • Prepare technical documentation for validation (IQ/OQ/PQ) artefacts, • Support functional testing, bug fixing, and hyper-care activities Requirements: • ABAP WM/EWM development: minimum 3 years, • Label / printout development: minimum 3 years (Zebra/ZPL, SmartForms or Adobe Forms), • Interface development: minimum 3 years (IDocs, BAPIs, or REST/SOAP), • Minimum one full E2E SAP deployment (go-live experience required), • Solid understanding of SAP EWM or WM module from a development perspective, • Ability to follow technical specifications and coding standards set by team lead Nice to have: • Experience in pharma or regulated industry ABAP projects, • Familiarity with 21 CFR Part 11 requirements for software development, • Experience with SAP EWM RF Framework, • Knowledge of LabVantage or LIMS integration patterns, • Spanish or Catalan language skills Discover the Power of IT Excellence. Apply! To learn more about Seargin, please visit our web page: www.seargin.com

At ASTEK Iberia, we are currently looking for a Veeva Vault Application Integrator to join a dynamic digital innovation team in the pharmaceutical sector. You will join a team responsible for ensuring the performance, integration, and compliance of Veeva Vault applications supporting key business functions such as R&D, Quality, Regulatory, and Medical Affairs. 💪 Main responsibilities: • Act as the main point of contact between IT and business stakeholders, • Manage incidents, service requests, and system evolutions, • Ensure system validation and compliance, especially during releases, • Maintain and enforce platform governance processes, • Perform data loading activities using Vault Loader / TMF Transfer, • Contribute to integration with enterprise systems (identity, data flows, etc.), • Support ongoing build and deployment projects 👀 Who are you? • Proven experience with Veeva Vault applications, • Veeva Vault certification (mandatory), • Experience working in regulated environments (pharma, life sciences, etc.), • Strong understanding of IT security and architecture principles, • Ability to translate business needs into system configurations, • Fluent in French and English (written & spoken) 📍 Location • Toulouse (France) or Remote from Spain. 💼 Who are we? Since 2015, Astek Iberia has been accompanying its customers in their development throughout Spain (Madrid, Barcelona, Valencia, Basque Country, Andalusia, Galicia, etc.). Founded in France in 1988, Astek is a global player in engineering and technology consulting, present in five continents and 25 countries. With expertise in a wide range of industrial and service sectors, Astek is an essential partner, supporting its customers in an intelligent deployment of their products and services, and in the implementation of their digital transformation. Today we are more than 8,000 employees, committed every day to promote the complementarity between digital technologies and complex systems engineering. Our style is to have flexible schedules and highly value the well-being of our employees. Why join us? 🚀 You will grow professionally in a company in constant development and evolution. 📏 You will benefit from a personalized follow-up of your professional projects as close as possible to your ambitions. 📈 You will make a real contribution to the company's development in real time. 🏝️ You will enjoy 23 days of vacation (in addition to holidays) that you will be able to choose whenever you want. 🌍 You will join our team: diverse, multicultural and constantly growing. 🔋 You will have days full of good energy and good atmosphere. ..although you still have a lot to discover! 😄 ☎️ Shall we meet? 📧 • If you want to participate in the process, apply from here attaching your CV (in English) as detailed as possible and we will tell you more.

SEARGIN IS HIRING! As a dynamic multinational tech company operating in 50 countries, we drive innovation and create projects that shape the future and greatly enhance the quality of life. You will find our solutions in the space industry, supporting scientists in the development of cancer drugs, and implementing innovative technological solutions for industrial clients worldwide. These are just some of the areas in which we operate! Currently, for the new Seargin project we are looking for a SAP ABAP Consultant. Location: Barcelona, Spain Employment Type: contract FTE: full-time Requirements: • ABAP WM/EWM development: minimum 3 years, • Label / printout development: minimum 3 years (Zebra/ZPL, SmartForms or Adobe Forms), • Interface development: minimum 3 years (IDocs, BAPIs, or REST/SOAP), • Minimum one full E2E SAP deployment (go-live experience required), • Solid understanding of SAP EWM or WM module from a development perspective, • Ability to follow technical specifications and coding standards set by team lead Nice to have: • Experience in pharma or regulated industry ABAP projects, • Familiarity with 21 CFR Part 11 requirements for software development, • Experience with SAP EWM RF Framework, • Knowledge of LabVantage or LIMS integration patterns, • Spanish or Catalan language skills Responsibilities: • Develop ABAP objects according to technical specifications from the Senior ABAP Lead, • Implement label printing enhancements: reprint reason recording, label preview, audit trail logging, unique label ID (FR.01–FR.09), • Support Zebra printer integration for HU labels at inbound, production, and dispatch stages, • Develop and unit-test interface components (LabVantage / LIMS stock status updates), • Build enhancements for EWM inbound/outbound processes and internal movements, • Participate in code reviews and apply GxP data integrity principles (ALCOA+), • Prepare technical documentation for validation (IQ/OQ/PQ) artefacts, • Support functional testing, bug fixing, and hyper-care activities Discover the Power of IT Excellence. Apply! To learn more about Seargin, please visit our web page: www.seargin.com

SEARGIN IS HIRING! As a dynamic multinational tech company operating in 50 countries, we drive innovation and create projects that shape the future and greatly enhance the quality of life. You will find our solutions in the space industry, supporting scientists in the development of cancer drugs, and implementing innovative technological solutions for industrial clients worldwide. These are just some of the areas in which we operate! Currently, for the new Seargin project we are looking for a SAP ABAP Consultant. Location: Barcelona, Spain Employment Type: contract FTE: full-time Requirements: • ABAP WM/EWM development: minimum 3 years, • Label / printout development: minimum 3 years (Zebra/ZPL, SmartForms or Adobe Forms), • Interface development: minimum 3 years (IDocs, BAPIs, or REST/SOAP), • Minimum one full E2E SAP deployment (go-live experience required), • Solid understanding of SAP EWM or WM module from a development perspective, • Ability to follow technical specifications and coding standards set by team lead Nice to have: • Experience in pharma or regulated industry ABAP projects, • Familiarity with 21 CFR Part 11 requirements for software development, • Experience with SAP EWM RF Framework, • Knowledge of LabVantage or LIMS integration patterns, • Spanish or Catalan language skills Responsibilities: • Develop ABAP objects according to technical specifications from the Senior ABAP Lead, • Implement label printing enhancements: reprint reason recording, label preview, audit trail logging, unique label ID (FR.01–FR.09), • Support Zebra printer integration for HU labels at inbound, production, and dispatch stages, • Develop and unit-test interface components (LabVantage / LIMS stock status updates), • Build enhancements for EWM inbound/outbound processes and internal movements, • Participate in code reviews and apply GxP data integrity principles (ALCOA+), • Prepare technical documentation for validation (IQ/OQ/PQ) artefacts, • Support functional testing, bug fixing, and hyper-care activities Discover the Power of IT Excellence. Apply! To learn more about Seargin, please visit our web page: www.seargin.com

Who We Are Whitewater Group is a leading provider of innovative and sustainable water treatment engineering systems operating in Ireland, the UK and across Europe in the Data Centre, Pharma, Power and Industrial sectors. We specialize in designing, installing, commissioning, and maintaining water treatment solutions to meet our clients' specific needs. Our team is dedicated to delivering high-quality, cost-effective engineering solutions that prioritize safety, reliability, and environmental sustainability. Whitewater Group is headquartered in Naas Co. Kildare and operates from European bases in Spain, Sweden, Finland, and the UK, with plans for further offices in Germany, Denmark, and Italy. The Group is experiencing significant growth driven by its focus on off-site construction methods (OSM) for delivering turnkey projects, reducing on-site construction time to a minimum. Role Description Due to continued expansion, Whitewater is seeking a Pre-Commissioning Engineer (Electrical) to support the delivery of water treatment systems across European projects. This role is focused on electrical pre-commissioning activities, ensuring that electrical systems, control panels, instrumentation, and field devices are correctly installed, tested, and ready prior to energisation and live commissioning. The Pre-Commissioning Engineer will work closely with QA/QC, OSM, automation, and commissioning teams to identify and resolve issues early, helping ensure a smooth transition into commissioning and system start-up. Main Duties and Responsibilities Electrical Pre-Commissioning & Inspections to include: • Carry out detailed electrical pre-commissioning inspections of:, • MCCs, control panels, PLC panels, VSDs, soft starters, • Pumps, motors, actuated valves, instrumentation, and field devices, • Verify installations against P&IDs, electrical schematics, I/O lists, and approved drawings, • Confirm correct installation of power, control, and instrument cabling, • Verify earthing, bonding, labelling, and panel workmanship, • Identify installation or wiring issues and support timely resolution, • Provide clear feedback on electrical readiness to support commissioning planning Testing & Verification to include: • Perform or witness electrical testing to include:, • Insulation resistance testing, • Continuity and earth checks, • Phase rotation and supply verification, • Support loop checks and point-to-point testing in coordination with automation teams, • Confirm systems are safe and suitable for energisation Interface & Coordination • Work closely with:, • QA/QC team, • Automation / PLC engineers, • Commissioning engineers and project teams, • OSM team Documentation • Complete and maintain pre-commissioning checklists and inspection records (ITP’s), • Ensure testing and inspection results are clearly recorded and traceable, • Support the preparation of handover information required for commissioning activities Required Qualifications and Experience • Degree or trade qualification in Electrical Engineering, or an electrical trade-qualified background with experience in industrial systems and automation, or equivalent, • 3+ years’ experience in electrical installation, pre-commissioning, or site-based engineering roles, • Strong understanding of:, • MCCs, control panels, VSDs, motors, and instrumentation, • Ability to read and work from:, • P&IDs, • Electrical schematics, • I/O lists and construction drawings, • Strong attention to detail and safety-focused approach, • Permit to work in the EU Desirable • Experience working on water treatment plants or within water treatment environments, • Exposure to industrial process systems, utilities, or data centre infrastructure, • Previous involvement in commissioning or system start-up activities Benefits • Competitive salary, • Annual bonus, • Pension scheme, • Opportunity for progression within a growing commissioning team

IF YOU ARE INTERESTED, PLEASE SHARE YOUR CV IN ENGLISH LANGUAGE ONLY! Who are we? We are a technology-led healthcare solutions provider. We are driven by our purpose to enable healthcare organizations be future ready. We offer accelerated, global growth opportunities for talent that’s bold, industrious, and nimble. With Indegene, you gain a unique career experience that celebrates entrepreneurship, and is guided by passion, innovation, collaboration, and empathy. To explore exciting opportunities at the convergence of healthcare and technology, check out www.careers.indegene.com What if we told you that you can move to an exciting role in an entrepreneurial organization without the usual risks associated with it? We understand that you are looking for growth in your career at this point and we would love for you to join us in our journey and grow with us. At Indegene, our roles come with the excitement you require at this stage of your career with the reliability you seek. We believe in creating leaders of tomorrow and mentor our leads to help them grow and nurture them as people managers and account managers. We are a rapidly growing global organization and are scouting for the best talent for this phase of growth. With us, you are at the intersection of two of the most exciting industries of healthcare and technology. We offer global opportunities with fast-track careers while you work with a team that is fueled by purpose. The combination of this will lead to a truly differentiated experience for you. If this excites you, then apply below. Role: Lead SFMC Developer IF YOU ARE INTERESTED, PLEASE SHARE YOUR CV IN ENGLISH LANGUAGE ONLY! Job Description: We are seeking an experienced SFMC Lead Developer with deep hands-on expertise across Automation Studio, Journey Builder, complex audience segmentation, Marketing Cloud Personalization (MCP), and enterprise integrations. This role is ideal for someone who is comfortable operating in a pharma environment, with strong data governance sensibilities and the ability to translate business objectives into scalable omnichannel journeys. The ideal candidate will partner closely with platform architects (e.g., CRM, Web, CMS) while leading technical design and building for Salesforce Marketing Cloud programs. This is a hands-on technical role, not purely strategic, requiring someone who can architect, develop, troubleshoot, optimize, and operationalize journeys at scale. Key Responsibilities 1. SFMC Architecture & Development • Lead the build and optimization of journeys in Journey Builder, including multi-branch paths, triggers, decision splits, and event-based orchestration., • Build automations in Automation Studio, including SQL-based segmentation, scheduled automations, and data hygiene processes., • Develop modular, compliant email and content blocks, leveraging AMPscript, SSJS, and data extensions best practices., • Implement and optimize Einstein features and predictive capabilities within SFMC, • Own the final audit and quality validation of campaigns executed by team members, ensuring adherence to defined processes, compliance standards, technical accuracy, and client requirements before deployment. 1. Data & Integration Leadership • Design and maintain data models, data extensions, relational mappings, and business rules aligned with CRM, website, and analytics inputs., • Lead integrations between SFMC and: o Veeva CRM (triggers, segmentation, report extraction) o WordPress VIP for personalization, tagging, and behavioral capture feeding MCP o Enterprise Data Lakes, CDPs, or analytics environments • · Ensure data dictionary, taxonomy alignment, and governance across all activation channels. 1. Marketing Cloud Personalization (MCP) • Implement MCP tagging, site wide java scripting, custom scripting (if any) rule sets, decisioning logic, personalization recipes, and identity resolution approaches., • Partner with web and analytics teams to ensure MCP instrumentation is clean, compliant, and aligned to journey logic., • Optimize hybrid (rule-based + algorithmic) MCP experiences based on campaign goals. 1. Cross-Functional Collaboration & Enablement • Work closely with omnichannel strategists, CRM leads, web/CMS teams, and localization leads., • Provide documentation, technical playbooks, and training for marketing, operations, and downstream teams., • Participate in solution design discussions, validation sessions, gap assessment, and technical Q&A. Required Qualifications • 7–10+ years of hands-on SFMC development and architecture experience at scale., • Advanced mastery of Journey Builder, Automation Studio, SQL, AMPscript, SSJS, and SFMC data modeling., • Proven experience with MCP implementation, including tagging, decisioning, and integration with websites (e.g., WordPress VIP)., • Strong familiarity with Veeva CRM data structures and how CRM segments feed omnichannel journeys., • Demonstrated experience supporting pharma or life sciences omnichannel operations., • Comfortable working cross-platform (CRM → SFMC → Web) in complex enterprise ecosystems., • Based in Madrid or already residing in Spain or Japan with ability for regular on-site work., • Language proficiency required in Spanish (for Spain market) EQUAL OPPORTUNITY: Indegene is proud to be an Equal Employment Employer and is committed to the culture of Inclusion and Diversity. We do not discriminate on the basis of race, religion, sex, colour, age, national origin, pregnancy, sexual orientation, physical ability, or any other characteristics. All employment decisions, from hiring to separation, will be based on business requirements, candidate’s merit and qualification. We are an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, colour, religion, sex, national origin, gender identity, sexual orientation, disability status, protected veteran status, or any other characteristics.

INSUD PHARMA operates across the entire pharmaceutical value chain, providing specialized knowledge and experience in scientific research, development, manufacturing, sales, and marketing of a wide range of active pharmaceutical ingredients (API), finished dosage forms (FDF), and branded pharmaceuti

Workday Implementation Specialist | HR Tech & Pharma 💊 En Shakers colaboramos con una empresa farmacéutica internacional de referencia para incorporar un/a Workday Implementation Specialist que lidere la implementación de Workday de principio a fin. Un proyecto de 9 meses de alto impacto estratégico con visibilidad directa sobre la transformación digital del área de People. El reto Serás la figura clave para orquestar la implementación de Workday desde el diseño hasta el go-live, gestionando cada etapa del proyecto: planificación, seguimiento, gestión de riesgos y comunicación con stakeholders. Coordinarás las integraciones de Workday con otros sistemas corporativos, actuando como punto de contacto esencial entre equipos técnicos, el departamento de People y dirección. Requisitos • Workday: Mínimo 5 años liderando proyectos de implementación end-to-end, • Integraciones: Experiencia sólida en definición, diseño y coordinación de integraciones con Workday (APIs, conectores y middleware), • HR/People: Conocimiento profundo de procesos clave como nóminas, onboarding, gestión de talento y offboarding, • Gestión de proyectos: Capacidad demostrada para planificar, priorizar, gestionar riesgos y cumplir plazos en proyectos complejos Se valora • Experiencia con otras soluciones HCM como SAP SuccessFactors, • Certificaciones oficiales de Workday, • Experiencia en el sector farmacéutico o de salud, • Inglés fluido para coordinación con equipos internacionales ¿Por qué este proyecto? • Liderazgo de una transformación digital estratégica en el área de People de una farmacéutica global, • Visibilidad directa con dirección y stakeholders de alto nivel, • Empresa con cultura colaborativa e inclusiva, comprometida con la sostenibilidad, • Proyecto freelance, 100% remoto Si esto encaja con tu perfil o con alguien de tu entorno, ¡aplica o comparte! Nos ponemos en contacto enseguida 🙌 #Workday #HRTech #WorkdayImplementation #HRIS #HCM #PeopleOps #Pharma #FreelanceTech #Barcelona #Shakers

IF YOU ARE INTERESTED, PLEASE SHARE YOUR CV IN ENGLISH LANGUAGE ONLY! Who are we? We are a technology-led healthcare solutions provider. We are driven by our purpose to enable healthcare organizations be future ready. We offer accelerated, global growth opportunities for talent that’s bold, industrious, and nimble. With Indegene, you gain a unique career experience that celebrates entrepreneurship, and is guided by passion, innovation, collaboration, and empathy. To explore exciting opportunities at the convergence of healthcare and technology, check out www.careers.indegene.com What if we told you that you can move to an exciting role in an entrepreneurial organization without the usual risks associated with it? We understand that you are looking for growth in your career at this point and we would love for you to join us in our journey and grow with us. At Indegene, our roles come with the excitement you require at this stage of your career with the reliability you seek. We believe in creating leaders of tomorrow and mentor our leads to help them grow and nurture them as people managers and account managers. We are a rapidly growing global organization and are scouting for the best talent for this phase of growth. With us, you are at the intersection of two of the most exciting industries of healthcare and technology. We offer global opportunities with fast-track careers while you work with a team that is fueled by purpose. The combination of this will lead to a truly differentiated experience for you. If this excites you, then apply below. Role: Lead SFMC Developer IF YOU ARE INTERESTED, PLEASE SHARE YOUR CV IN ENGLISH LANGUAGE ONLY! Job Description: We are seeking an experienced SFMC Lead Developer with deep hands-on expertise across Automation Studio, Journey Builder, complex audience segmentation, Marketing Cloud Personalization (MCP), and enterprise integrations. This role is ideal for someone who is comfortable operating in a pharma environment, with strong data governance sensibilities and the ability to translate business objectives into scalable omnichannel journeys. The ideal candidate will partner closely with platform architects (e.g., CRM, Web, CMS) while leading technical design and building for Salesforce Marketing Cloud programs. This is a hands-on technical role, not purely strategic, requiring someone who can architect, develop, troubleshoot, optimize, and operationalize journeys at scale. Key Responsibilities 1. SFMC Architecture & Development • Lead the build and optimization of journeys in Journey Builder, including multi-branch paths, triggers, decision splits, and event-based orchestration., • Build automations in Automation Studio, including SQL-based segmentation, scheduled automations, and data hygiene processes., • Develop modular, compliant email and content blocks, leveraging AMPscript, SSJS, and data extensions best practices., • Implement and optimize Einstein features and predictive capabilities within SFMC, • Own the final audit and quality validation of campaigns executed by team members, ensuring adherence to defined processes, compliance standards, technical accuracy, and client requirements before deployment. 1. Data & Integration Leadership • Design and maintain data models, data extensions, relational mappings, and business rules aligned with CRM, website, and analytics inputs., • Lead integrations between SFMC and: o Veeva CRM (triggers, segmentation, report extraction) o WordPress VIP for personalization, tagging, and behavioral capture feeding MCP o Enterprise Data Lakes, CDPs, or analytics environments • · Ensure data dictionary, taxonomy alignment, and governance across all activation channels. 1. Marketing Cloud Personalization (MCP) • Implement MCP tagging, site wide java scripting, custom scripting (if any) rule sets, decisioning logic, personalization recipes, and identity resolution approaches., • Partner with web and analytics teams to ensure MCP instrumentation is clean, compliant, and aligned to journey logic., • Optimize hybrid (rule-based + algorithmic) MCP experiences based on campaign goals. 1. Cross-Functional Collaboration & Enablement • Work closely with omnichannel strategists, CRM leads, web/CMS teams, and localization leads., • Provide documentation, technical playbooks, and training for marketing, operations, and downstream teams., • Participate in solution design discussions, validation sessions, gap assessment, and technical Q&A. Required Qualifications • 7–10+ years of hands-on SFMC development and architecture experience at scale., • Advanced mastery of Journey Builder, Automation Studio, SQL, AMPscript, SSJS, and SFMC data modeling., • Proven experience with MCP implementation, including tagging, decisioning, and integration with websites (e.g., WordPress VIP)., • Strong familiarity with Veeva CRM data structures and how CRM segments feed omnichannel journeys., • Demonstrated experience supporting pharma or life sciences omnichannel operations., • Comfortable working cross-platform (CRM → SFMC → Web) in complex enterprise ecosystems., • Based in Madrid or already residing in Spain or Japan with ability for regular on-site work., • Language proficiency required in Spanish (for Spain market) EQUAL OPPORTUNITY: Indegene is proud to be an Equal Employment Employer and is committed to the culture of Inclusion and Diversity. We do not discriminate on the basis of race, religion, sex, colour, age, national origin, pregnancy, sexual orientation, physical ability, or any other characteristics. All employment decisions, from hiring to separation, will be based on business requirements, candidate’s merit and qualification. We are an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, colour, religion, sex, national origin, gender identity, sexual orientation, disability status, protected veteran status, or any other characteristics.

Senior Purchasing Specialist – Chemical Additives La persona incorporada será responsable de la gestión de compras internacionales y desarrollo de proveedores de aditivos químicos y materias primas para diferentes sectores industriales como Plastics, Coatings, Pharma, Food y Agro, trabajando estrechamente con fabricantes y proveedores internacionales, principalmente en China e India. Funciones: • Gestión integral de compras internacionales de aditivos químicos y materias primas para sectores como Plastics, Coatings, Pharma, Food y Agro., • Gestión y negociación directa con proveedores internacionales, principalmente fabricantes y proveedores estratégicos en China e India., • Búsqueda, homologación y desarrollo de nuevos proveedores de Specialty Chemicals, asegurando competitividad, calidad y continuidad de suministro., • Negociación de precios, condiciones comerciales, contratos, lead times y planificación de compras, optimizando costes y niveles de stock., • Seguimiento de mercados internacionales, tendencias de precios y evolución de materias primas químicas y aditivos industriales., • Coordinación transversal con departamentos de ventas, supply chain, regulatory, calidad y logística para asegurar el correcto abastecimiento y desarrollo de negocio., • Participación activa en la definición de la estrategia de compras y portfolio de productos, identificando nuevas oportunidades y representadas para el mercado europeo. Perfil: • Formación superior en Química, Ingeniería Química, ADE, Comercio Internacional o similar, valorándose especialmente conocimiento técnico relacionado con Specialty Chemicals y aditivos químicos., • Experiencia consolidada en compras internacionales dentro del sector químico, especialmente en aditivos y materias primas para Plastics, Coatings, Pharma, Food, Agro o sectores afines., • Experiencia en negociación y gestión de proveedores internacionales, principalmente en China e India, así como en búsqueda y homologación de nuevos fabricantes., • Conocimiento de mercados internacionales de materias primas químicas, dinámica de precios, supply chain y procesos de importación internacional., • Nivel alto de inglés para negociación y gestión diaria con proveedores internacionales., • Perfil analítico, negociador y orientado a negocio, con capacidad para trabajar en entornos internacionales y multiculturales.

About Traverse Health Traverse Health is a real-world evidence provider from the EU, operating in emerging markets. We develop cutting-edge digital solutions for the healthcare and life-science industry. By connecting healthcare organizations with the pharmaceutical and biotech industries, we maximize the potential of patient data to support smarter healthcare decisions and improve patient outcomes. Our services and solutions cater to pharmaceutical, biotech, and medical device companies, healthcare providers, CROs, health insurance providers, healthtech, drug discovery, and beyond. The Role We are looking for a Proposals & Business Development Analyst or Associate to join our commercial team. You will work at the front end of our business — shaping how we present Traverse Health to pharma and biotech clients and directly contributing to new business generation. Your core focus will be developing proposals, requests for proposals, pricing formation and pitch materials — translating scientific and commercial contexts into compelling narratives that win business. This role is for someone who enjoys structured thinking, works well with ambiguity, and wants real exposure to the life sciences and RWE space early in their career. Join us if start up environment is what you are looking for — to build together and grow fast. What You Will Do • Lead and coordinate the end-to-end development of RFP and unsolicited proposals, ensuring alignment with client needs and Traverse Health's capabilities, • Prepare high-quality pitch decks, capability presentations, and business development materials for pharma and biotech clients, • Collaborate with scientific, data, and technical teams to accurately represent our RWE study designs, digital registry solutions, and analytical methodologies in client-facing materials, • Contribute to the development and maintenance of proposal templates, case studies, and a reusable content library, • Assist in the preparation of client meetings, conferences, and follow-up communications, • Support project scoping discussions and budget estimation for new engagements What We Are Looking For Required: • 1–2 years of experience in a Big 4 consulting firm (healthcare or life sciences practice), pharmaceutical company, healthtech, or related environment, • Demonstrated experience contributing to the formation of Requests for Proposals (RFPs), proposals, or pitches in a professional setting, • Excellent written and verbal communication skills in English — you can translate complex ideas into clear, compelling narratives, • Strong proficiency in PowerPoint and ability to create visually clear, well-structured presentations, • Highly organised, detail-oriented, and able to manage multiple workstreams and deadlines simultaneously, • Comfortable working independently in a distributed, international team Preferred: • Understanding of real-world evidence, health economics, or clinical research concepts, • Familiarity with pharmaceutical drug development and regulatory pathways, • Familiarity with procurement and tender submission platforms such as SAP Ariba, Coupa, Jaggaer, or similar — experience navigating vendor portals used by large pharma and biotech companies is a plus, • Experience working with clients or stakeholders across multiple countries and cultures, • Additional European language Spanish is a plus, • University degree in Mathematics, Statistics, Economics, Engineering, or another quantitative discipline — we are looking for a structured thinker who is comfortable with numbers and logical reasoning, not just communication Alternative Profiles We Welcome We recognise that great talent does not always follow a linear path. We also encourage applications from: • MBA students or recent MBA graduates seeking part-time or project-based engagement (minimum 3 days per week) while completing their programme — ideally based in or near Barcelona, Madrid, • Candidates transitioning from academic research (PhD or MSc in life sciences, epidemiology, public health, or health economics) who have developed strong analytical and communication skills and are looking to apply them in a commercial context, • Consultants from strategy, market access backgrounds who want to move closer to data and evidence generation What We Offer • Direct exposure to senior leadership and real commercial decisions from day one, • The opportunity to work on cutting-edge RWE projects across Europe, MENA, and emerging markets, • A collaborative, international team that values intellectual curiosity and initiative over hierarchy, • Flexible working arrangements — remote-first within Europe, with preference for Barcelona-based candidates, • In person meetings and all company field trips, • Competitive compensation commensurate with experience, • The chance to grow with a company at an exciting stage of its development

About Traverse Health Traverse Health is a real-world evidence provider from the EU, operating in emerging markets. We develop cutting-edge digital solutions for the healthcare and life-science industry. By connecting healthcare organizations with the pharmaceutical and biotech industries, we maximize the potential of patient data to support smarter healthcare decisions and improve patient outcomes. Our services and solutions cater to pharmaceutical, biotech, and medical device companies, healthcare providers, CROs, health insurance providers, healthtech, drug discovery, and beyond. The Role We are looking for a Proposals & Business Development Analyst or Associate to join our commercial team. You will work at the front end of our business — shaping how we present Traverse Health to pharma and biotech clients and directly contributing to new business generation. Your core focus will be developing proposals, requests for proposals, pricing formation and pitch materials — translating scientific and commercial contexts into compelling narratives that win business. This role is for someone who enjoys structured thinking, works well with ambiguity, and wants real exposure to the life sciences and RWE space early in their career. Join us if start up environment is what you are looking for — to build together and grow fast. What You Will Do • Lead and coordinate the end-to-end development of RFP and unsolicited proposals, ensuring alignment with client needs and Traverse Health's capabilities, • Prepare high-quality pitch decks, capability presentations, and business development materials for pharma and biotech clients, • Collaborate with scientific, data, and technical teams to accurately represent our RWE study designs, digital registry solutions, and analytical methodologies in client-facing materials, • Contribute to the development and maintenance of proposal templates, case studies, and a reusable content library, • Assist in the preparation of client meetings, conferences, and follow-up communications, • Support project scoping discussions and budget estimation for new engagements What We Are Looking For Required: • 1–2 years of experience in a Big 4 consulting firm (healthcare or life sciences practice), pharmaceutical company, healthtech, or related environment, • Demonstrated experience contributing to the formation of Requests for Proposals (RFPs), proposals, or pitches in a professional setting, • Excellent written and verbal communication skills in English — you can translate complex ideas into clear, compelling narratives, • Strong proficiency in PowerPoint and ability to create visually clear, well-structured presentations, • Highly organised, detail-oriented, and able to manage multiple workstreams and deadlines simultaneously, • Comfortable working independently in a distributed, international team Preferred: • Understanding of real-world evidence, health economics, or clinical research concepts, • Familiarity with pharmaceutical drug development and regulatory pathways, • Familiarity with procurement and tender submission platforms such as SAP Ariba, Coupa, Jaggaer, or similar — experience navigating vendor portals used by large pharma and biotech companies is a plus, • Experience working with clients or stakeholders across multiple countries and cultures, • Additional European language Spanish is a plus, • University degree in Mathematics, Statistics, Economics, Engineering, or another quantitative discipline — we are looking for a structured thinker who is comfortable with numbers and logical reasoning, not just communication Alternative Profiles We Welcome We recognise that great talent does not always follow a linear path. We also encourage applications from: • MBA students or recent MBA graduates seeking part-time or project-based engagement (minimum 3 days per week) while completing their programme — ideally based in or near Barcelona, Madrid, • Candidates transitioning from academic research (PhD or MSc in life sciences, epidemiology, public health, or health economics) who have developed strong analytical and communication skills and are looking to apply them in a commercial context, • Consultants from strategy, market access backgrounds who want to move closer to data and evidence generation What We Offer • Direct exposure to senior leadership and real commercial decisions from day one, • The opportunity to work on cutting-edge RWE projects across Europe, MENA, and emerging markets, • A collaborative, international team that values intellectual curiosity and initiative over hierarchy, • Flexible working arrangements — remote-first within Europe, with preference for Barcelona-based candidates, • In person meetings and all company field trips, • Competitive compensation commensurate with experience, • The chance to grow with a company at an exciting stage of its development

Workday Implementation Specialist | HR Tech & Pharma 💊 En Shakers colaboramos con una empresa farmacéutica internacional de referencia para incorporar un/a Workday Implementation Specialist que lidere la implementación de Workday de principio a fin. Un proyecto de 9 meses de alto impacto estratégico con visibilidad directa sobre la transformación digital del área de People. El reto Serás la figura clave para orquestar la implementación de Workday desde el diseño hasta el go-live, gestionando cada etapa del proyecto: planificación, seguimiento, gestión de riesgos y comunicación con stakeholders. Coordinarás las integraciones de Workday con otros sistemas corporativos, actuando como punto de contacto esencial entre equipos técnicos, el departamento de People y dirección. Requisitos • Workday: Mínimo 5 años liderando proyectos de implementación end-to-end, • Integraciones: Experiencia sólida en definición, diseño y coordinación de integraciones con Workday (APIs, conectores y middleware), • HR/People: Conocimiento profundo de procesos clave como nóminas, onboarding, gestión de talento y offboarding, • Gestión de proyectos: Capacidad demostrada para planificar, priorizar, gestionar riesgos y cumplir plazos en proyectos complejos Se valora • Experiencia con otras soluciones HCM como SAP SuccessFactors, • Certificaciones oficiales de Workday, • Experiencia en el sector farmacéutico o de salud, • Inglés fluido para coordinación con equipos internacionales ¿Por qué este proyecto? • Liderazgo de una transformación digital estratégica en el área de People de una farmacéutica global, • Visibilidad directa con dirección y stakeholders de alto nivel, • Empresa con cultura colaborativa e inclusiva, comprometida con la sostenibilidad, • Proyecto freelance, 100% remoto Si esto encaja con tu perfil o con alguien de tu entorno, ¡aplica o comparte! Nos ponemos en contacto enseguida 🙌 #Workday #HRTech #WorkdayImplementation #HRIS #HCM #PeopleOps #Pharma #FreelanceTech #Barcelona #Shakers

Key Responsibilities: • Sales Target Achievement: Lead market sales targets for products like nab-paclitaxel (e.g., Abraxane generic) and injectables. Identify market opportunities and competitive challenges, gather primary market data, and develop marketing strategies and plans., • Distributor Management: Manage distributors, track performance, conduct regular field visits with their KAMs across regions. Identify strengths and weaknesses, and guide distributors to gain higher market share., • Value Assessment & Redistribution: Evaluate distributor value across all marketing functions (access, promotion, distribution, payment collection) to lay the foundation for renegotiating profit-sharing terms., • Market Mapping: Research and map the value chain and drivers of the Spanish hospital and retail markets. Deliver a "Hospital & Clinic Map for nab-paclitaxel in Spain" and a list of purchasing groups (Central de Compras) with their coverage scope., • Resource & Demand Mining: Continuously build distributor networks and identify unmet clinical and retail needs. Requirements: 1. Legal & Compliance • Fluent English (working language); native or C2 Spanish., • Background in pharmacy, bioscience, or related fields preferred., • No record of industry violations. Familiar with AEMPS compliance requirements. 1. Experience & Tender Expertise (Critical) • 10+ years of sales experience in pharmaceutical marketing, including 5+ years of tender experience in the Spanish pharma industry (especially prescription/injectable drugs) ., • Familiar with Spain's national healthcare tender process (e.g., SERMAS, regional bidding rules)., • Independently led provincial or national pharmaceutical tender projects in Spain – proficient in bid document preparation, pricing strategy, and compliance review., • Oncology product marketing experience (especially injectable cytotoxics) strongly preferred. 1. Local Network • Established contacts within Spain's public healthcare system (hospital pharmacy departments, procurement bodies, health authorities) and major pharmaceutical distributors. 1. End-to-End Capability • Able to drive new product launches and coordinate supply chain (import customs clearance, warehousing, distribution). 1. Cross-Cultural Adaptability • Basic cross-cultural communication skills; understands and accommodates the working rhythm and expectations of a Chinese headquarters.

Join Rephine Barcelona: Leading Life Sciences Quality Worldwide At Rephine, we set the standard for quality assurance and GxP compliance in the Life Sciences industry. With offices in Barcelona, the UK, and China, India, we support the Pharmaceutical, Biotech, and Medical Device supply chains globally. Who We're Looking For: Are you passionate about consulting in the Pharma and Life Sciences sector? Do you thrive in dynamic environments, eager to take on multiple projects and drive real impact? If you're excited by the challenge of enhancing quality and compliance in a global company, we want you as our next Computer System Validation Senior Consultant in Barcelona. Your Role: As a CSV L2 Consultant, you will take an active role in delivering high-impact validation projects, with a focus on ERP systems and other critical computerized systems in regulated environments. You will be part of innovative projects, ensuring compliance, efficiency, and quality across the lifecycle. Key Responsibilities: Lead CSV Projects: • Take ownership of ERP and other computerized system validations (IQ, OQ, PQ), preparing and reviewing critical documentation (VMP, URS, SOPs)., • Ensure compliance with EU GMP Annex 11, FDA 21 CFR Part 11, GAMP 5, and Data Integrity guidelines. ERP & System Expertise: • Work hands-on with ERPs, eDMS, eQMS, LIMS, laboratory systems, SCADA, EBRs, pharmacovigilance, and maintenance systems., • Assess system compliance and performance to optimize regulatory readiness and operational efficiency. Audits & Compliance Assessments: • Perform supplier audits and compliance checks, focusing on Annex 11, 21 CFR Part 11, and global regulations., • Identify risks, provide actionable recommendations, and ensure corrective measures are implemented. International Project Engagement: • Contribute to projects across Spain, Europe, and China, adapting to diverse regulatory environments., • Represent Rephine on-site with clients, ensuring seamless collaboration and delivering high-quality results. Project Delivery & Client Success: • Manage timelines and ensure all deliverables, including documentation and test execution, are completed on schedule., • Maintain clear communication with stakeholders and provide progress updates regularly. Why This Role Could Excite You: • Take a leading role in ERP validation projects while expanding your CSV expertise., • Work with international teams and cutting-edge systems in a fast-paced consulting environment., • Be recognized as an L2 expert contributing to both client success and Rephine’s high standards. What You Bring: • A Bachelor’s degree in Chemistry or Engineering., • Solid experience in the pharmaceutical industry, GxP compliance, and computerized systems validation., • Strong multitasking skills and experience in managing multiple consulting projects to meet client needs., • Fluency in Spanish and English, with excellent communication skills., • Since client sites are often not easily accessible by public transportation, a valid driver’s license and willingness to travel by car are required. Is This Role for You? Ask yourself: • Are you excited about working with clients to tackle their most critical challenges?, • Can you maintain a sense of ownership and connection to the Rephine team, even when managing demanding client-facing responsibilities?, • Do you have the adaptability to move between technical tasks, regulatory compliance, and client interaction with ease?, • Are you ready to learn and grow in a role that exposes you to a wide range of systems and industries? If your answer is "yes" to these questions, then this opportunity at Rephine is your chance to make a significant impact while growing your career in CSV consulting. Why Choose Rephine? We believe in rewarding talent and commitment with a comprehensive benefits package designed to support your personal and professional growth: • Competitive Compensation: A salary that reflects your experience, along with additional vacation days and other benefits., • Work-Life Balance: Take advantage of our hybrid work model, flexible hours, and a shorter workday on Fridays, allowing you to maintain a healthy balance between work and personal life., • Global Exposure: Work with a multicultural team across multiple countries, providing opportunities to expand your professional network and gain international experience., • Dynamic Work Environment: Join a young, enthusiastic team where your contributions are valued, and your ideas can shape the future of the company., • Flexible Salary Options: Benefit from salary sacrifice schemes and more flexibility in managing your compensation package., • Opportunities for Growth: We provide a nurturing environment where your career can grow beyond expectations. Whether you're looking for new challenges or leadership opportunities, Rephine is committed to your continuous development., • Drive Digital Transformation: Participate in projects where you can use the latest technologies to optimize manufacturing and quality processes. For over 20 years, Rephine has been at the forefront of improving manufacturing quality processes for leading Life Sciences companies. We’re evolving rapidly and looking for passionate professionals eager to grow with us. Ready to embark on this journey? Visit our career site to learn more and apply in English.

INSUD PHARMA operates across the entire pharmaceutical value chain, providing specialized knowledge and experience in scientific research, development, manufacturing, sales, and marketing of a wide range of active pharmaceutical ingredients (API), finished dosage forms (FDF), and branded pharmaceuti

AI search & content specialist: About this role This position will act as the internal subject-matter expert on SEO, GEO, and AI-driven discovery. Scilife is looking for a strategic, AI-forward content professional to lead our content presence across both traditional SEO and ai-powered search channels. As search behavior rapidly evolves with users increasingly turning to tools like ChatGPT, Perplexity, Google AI overviews, and Gemini for answers — we need a specialist who can ensure Scilife is visible, authoritative, and trusted in these new discovery surfaces. This role goes beyond traditional SEO. You will own our answer engine optimization (AEO) and generative engine optimization (GEO) strategy, shaping quarterly roadmaps that align content initiatives with broader business goals. You will develop and implement strategies that improve Scilife’s visibility within AI-generated results, answer engines, and entity-based discovery systems, aligning both content and technical structure to support AI-native search experiences. The goal is to make Scilife the go-to brand cited by AI tools when life sciences professionals search for quality management solutions. You will create structured, authoritative, AI-readable content that positions Scilife as a thought leader and drives organic brand recall across both human and machine audiences. This role is responsible to: • Own organic growth strategy across traditional search and AI-driven discovery (Google AI Overviews, LLMs, answer engines)., • Define and evolve GEO best practices to ensure brand visibility and citation in generative responses., • Establish standards for structured content (schema, summaries, FAQs, entities, metadata) optimized for AI consumption., • Translate shifts in search behavior (zero-click, AI summaries) into clear priorities and roadmaps that balance traditional SEO and GEO., • Work cross-functionally with different teams to align SEO with companywide business goals and objectives., • Responsible for growing new user acquisition and hitting core KPIs across traditional SEO, GEO and AEO., • Extensive knowledge of current SEO/GEO best practices with strong technical SEO/GEO background experience, • Utilize research tools to perform keyword gap analysis to support and prioritize keyword and content strategies., • Ability to monitor ongoing SEO site health and maintenance reports while translating insights into actionable tasks and projects, • Familiarity with SEO tools (Google Search Console, Semrush, etc.), • Ability to lead multiple projects simultaneously with strong prioritization skills, • Champion data-driven testing initiatives to identify opportunities and scale acquisition efficiently, • Develop analysis that provides conclusions into customer behavior and communicates those conclusions clearly with key stakeholders., • Provide insight-driven reporting that explains what happened, why it happened, and what to do next., • Evaluate and adapt strategies based on shifts in AI-generated search visibility and user interaction patterns. AEO / GEO & AI visibility • Develop and execute an answer engine optimization (AEO) and generative engine optimization (GEO) strategy to increase Scilife’s brand presence and citation frequency in AI-powered tools (ChatGPT, Perplexity, Google AI overviews, Gemini, Copilot, etc.)., • Conduct competitive benchmarking to understand how scilife appears vs. Competitors (e.g., Qualio, Mastercontrol, Greenlightguru, Veeva, etq) across AI-generated responses., • Identify and close content gaps that prevent Scilife from being surfaced by LLMs as the recommended eQMS solution for life sciences companies., • Implement structured data, FAQ schemas, and authoritative content formats optimized for AI parsing and citation., • Monitor brand mentions and citations in ai tools and establish a reporting framework to track LLM visibility over time. Content strategy & creation • Plan and execute a multi-channel content strategy aligned with AEO/GEO goals and broader marketing objectives., • Create high-quality, authoritative content (articles, whitepapers, landing pages, use cases, FAQs, glossaries) that establishes Scilife as a definitive source of truth in the eQMS and quality management space., • Optimize the existing content library for AI readability: clear structure, direct answers, entity coverage, and factual depth., • Manage the content calendar and ensure a consistent publishing cadence across the blog, website, and newsletters., • Collaborate with the design team and external contributors to deliver polished, on-brand content assets. Traditional SEO & search visibility • Maintain and improve organic search rankings through keyword research, on-page seo, and internal linking strategies., • Monitor search performance metrics and produce regular reports with actionable insights using tools such as google search console, semrush, or ahrefs., • Ensure all content is SEO-friendly, up-to-date, and aligned with current search intent and user behavior. Collaboration & process • Work closely with the brand manager, knowledge manager, and marketing teams to align content with business priorities., • Coordinate content approvals across stakeholders in a timely and organized manner., • Stay ahead of ai search trends, platform changes, and industry best practices, and proactively share insights with the broader team. Required skills & experience Core requirements • 4+ years of experience in content marketing, SEO, or digital content roles., • Demonstrated understanding of AEO / GEO concepts and how LLMs source and cite information., • Strong SEO fundamentals: keyword research, on-page optimization, technical SEO basics, and schema markup., • Excellent English writing and editing skills; ability to produce clear, authoritative, and engaging B2B content., • Proficiency with SEO analytics tools (google search console, semrush, or similar)., • Analytical mindset with the ability to translate data into content decisions and strategy. Nice to have • Experience with marketing automation tools (hubspot preferred)., • Experience in B2B SaaS, life sciences, or regulated industries (pharma, medtech, biotech)., • Familiarity with structured data, json-ld, and schema.org vocabulary., • Experience using AI tools (ChatGPT, Perplexity, Claude, etc.) As part of content research or production workflows., • Experience with Jira or similar project management and ticketing tools., • Comfort working in a fast-paced, international, and remote-first environment., • Experience of search planning fundamentals across Paid and Organic channels., • Familiarity with core PPC marketing principles and tools such as Google and Meta Ads Core competencies Candidates will be assessed against the following competencies during the hiring process and in periodic performance evaluations: • Strategic thinking, • AI & tech curiosity, • Content excellence, • Data-driven, • Creativity, • Collaborative, • Attention to detail, • Getting things done, • Communication, • Adaptability, • Time management, • Innovation Candidates will also be assessed against scilife’s core company values: • Healthy inside-out, • Outside of the box, • Driven by evidence, • All hearts and ears Why join Scilife? Scilife helps life science companies digitize, automate, and scale their quality and compliance processes. Our eQMS platform supports organizations worldwide in staying audit-ready while enabling innovation. We are in the early stages of an ambitious AI-first transformation. As our AI Search & Content Specialist, you will play a key role in shaping how Scilife brand appears in high-intent industry conversations, how we build topical authority, and how we position Scilife as a category-relevant voice in the future of quality management. You will join a collaborative, international, and fast-evolving company environment, working closely with the Brand team as well as cross-functional partners across marketing, sales, and customer successes teams. This is a role for someone who enjoys combining strategic thinking with hands-on execution, and who is excited by the opportunity to build new capabilities in a space that is still taking shape. At Scilife, you will find a team that values curiosity, ownership, fresh thinking, and meaningful collaboration. We care deeply about building work that is thoughtful, relevant, and impactful — and we are looking for someone who is energized by that kind of environment. If you are excited by the intersection of content, SEO, AI, and category building — and motivated by the chance to shape a capability that is still emerging — this role offers the opportunity to make a visible, strategic impact from day one. What we offer • Fully remote work within Europe with flexible hours., • Competitive compensation., • Collaborative, international team culture., • Continuous learning and professional development., • The chance to play a defining role in an emerging area of strategic importance for the company., • More info about benefits at Scilife.

We’re looking for a Senior Technical Project Manager to lead complex R&D delivery initiatives for a global pharmaceutical client. Pharmaceutical/life sciences experience and familiarity with regulated environments (GxP, 21 CFR Part 11). Lead high-impact digital transformation initiatives in pharma

Workday Implementation Specialist | HR Tech & Pharma 💊 En Shakers colaboramos con una empresa farmacéutica internacional de referencia para incorporar un/a Workday Implementation Specialist que lidere la implementación de Workday de principio a fin. Un proyecto de 9 meses de alto impacto estratégico con visibilidad directa sobre la transformación digital del área de People. El reto Serás la figura clave para orquestar la implementación de Workday desde el diseño hasta el go-live, gestionando cada etapa del proyecto: planificación, seguimiento, gestión de riesgos y comunicación con stakeholders. Coordinarás las integraciones de Workday con otros sistemas corporativos, actuando como punto de contacto esencial entre equipos técnicos, el departamento de People y dirección. Requisitos • Workday: Mínimo 5 años liderando proyectos de implementación end-to-end, • Integraciones: Experiencia sólida en definición, diseño y coordinación de integraciones con Workday (APIs, conectores y middleware), • HR/People: Conocimiento profundo de procesos clave como nóminas, onboarding, gestión de talento y offboarding, • Gestión de proyectos: Capacidad demostrada para planificar, priorizar, gestionar riesgos y cumplir plazos en proyectos complejos Se valora • Experiencia con otras soluciones HCM como SAP SuccessFactors, • Certificaciones oficiales de Workday, • Experiencia en el sector farmacéutico o de salud, • Inglés fluido para coordinación con equipos internacionales ¿Por qué este proyecto? • Liderazgo de una transformación digital estratégica en el área de People de una farmacéutica global, • Visibilidad directa con dirección y stakeholders de alto nivel, • Empresa con cultura colaborativa e inclusiva, comprometida con la sostenibilidad, • Proyecto freelance, 100% remoto Si esto encaja con tu perfil o con alguien de tu entorno, ¡aplica o comparte! Nos ponemos en contacto enseguida 🙌 #Workday #HRTech #WorkdayImplementation #HRIS #HCM #PeopleOps #Pharma #FreelanceTech #Barcelona #Shakers

At ASTEK Iberia, we are looking for a highly skilled AI Specialist to join a global initiative focused on transforming how content is created, managed, and delivered across multiple channels across a large-scale consumer healthcare organization. This role sits at the intersection of AI, cloud engineering, and marketing technology, driving end-to-end AI solutions from concept to production. 💪 Main responsibilities: • Design and deliver end-to-end AI-powered solutions to automate content generation and management, • Build and deploy scalable applications using Microsoft Azure AI services, • Integrate LLMs, image and video generation models into real business workflows, • Develop and maintain data pipelines to connect AI models with enterprise systems, • Lead initiatives from POC to MVP to enterprise-scale deployment, • Collaborate with cross-functional teams (Product, Marketing, IT), • Ensure AI governance, compliance, and performance monitoring 👀 Who are you? 8+ years of experience in software development, with strong exposure to AI/ML engineering Hands-on experience with: • Azure AI Foundry, • Azure AI Search, • Azure Document Intelligence, • Azure Cognitive Services Strong experience with: • LLMs (prompting, fine-tuning, RAG), • Generative AI (image/video) Solid background in: • Python + one additional language (e.g. TypeScript), • API design & microservices, • Cloud-native architectures Experience building and scaling production-grade AI systems Knowledge of data pipelines and MLOps practices English fluent ⭐ Nice to have • Experience in marketing tech / content platforms, • Exposure to regulated industries (pharma, healthcare, etc.), • Familiarity with tools like SAP, Veeva, Adobe Experience Cloud, • Azure certifications 💼 Who are we? Since 2015, Astek Iberia has been accompanying its customers in their development throughout Spain (Madrid, Barcelona, Valencia, Basque Country, Andalusia, Galicia, etc.). Founded in France in 1988, Astek is a global player in engineering and technology consulting, present in five continents and 25 countries. With expertise in a wide range of industrial and service sectors, Astek is an essential partner, supporting its customers in an intelligent deployment of their products and services, and in the implementation of their digital transformation. Today we are more than 8,000 employees, committed every day to promote the complementarity between digital technologies and complex systems engineering. Our style is to have flexible schedules and highly value the well-being of our employees. Why join us? 🚀 You will grow professionally in a company in constant development and evolution. 📏 You will benefit from a personalized follow-up of your professional projects as close as possible to your ambitions. 📈 You will make a real contribution to the company's development in real time. 🏝️ You will enjoy 23 days of vacation (in addition to holidays) that you will be able to choose whenever you want. 🌍 You will join our team: diverse, multicultural and constantly growing. 🔋 You will have days full of good energy and good atmosphere. ..although you still have a lot to discover! 😄 ☎️ Shall we meet? 📧 If you want to participate in the process, apply from here attaching your CV (in English) as detailed as possible and we will tell you more.

At Astek, we are looking for an experienced SAP Functional ERP Consultant to join a leading organization in the pharma & diagnostics sector, supporting large-scale global transformation programs and ERP deployments. 💪 Your mission, should you choose to accept it… • Lead and coordinate end-to-end (E2E) integrations across define, build, test, and deployment phases, • Act as a key contact between business, SAP, and technical teams, ensuring alignment and connectivity readiness, • Gather, validate, and review functional requirements, mappings, and solution design documentation, • Ensure all integrations are properly documented, tracked, and included in deployment backlogs, • Align timelines, manage stakeholders, and support testing phases (SAT, DET, DIL) focusing on critical processes, • Maintain integration knowledge (E2E repository) and perform impact analysis on downstream systems, • Support cutover, hypercare, and handover to operations, ensuring monitoring and incident readiness 👀 Who are you? • Proven experience working in SAP ERP environments, • Strong background in system integrations and middleware technologies, • Experience in global deployment projects and complex system landscapes, • Solid project management skills (SAFE framework is a plus), • Strong business analysis and documentation review capabilities, • Excellent stakeholder management and communication skills, • Experience in pharma and/or diagnostics is highly valued 💼 Who are we? Since 2015, Astek Iberia has been accompanying its customers in their development throughout Spain (Madrid, Barcelona, Valencia, Basque Country, Andalusia, Galicia, etc.). Founded in France in 1988, Astek is a global player in engineering and technology consulting, present in five continents and 25 countries. With expertise in a wide range of industrial and service sectors, Astek is an essential partner, supporting its customers in an intelligent deployment of their products and services, and in the implementation of their digital transformation. Today we are more than 8,000 employees, committed every day to promote the complementarity between digital technologies and complex systems engineering. Our style is to have flexible schedules and highly value the well-being of our employees. Why join us? 🚀 You will grow professionally in a company in constant development and evolution. 📏 You will benefit from a personalized follow-up of your professional projects as close as possible to your ambitions. 📈 You will make a real contribution to the company's development in real time. 🏝️ You will enjoy 23 days of vacation (in addition to holidays) that you will be able to choose whenever you want. 🌍 You will join our team: diverse, multicultural and constantly growing. 🔋 You will have days full of good energy and good atmosphere. ...although you still have a lot to discover! 😄 ☎️ Shall we meet? 📧 If you want to participate in the process, apply from here attaching your CV (in English) as detailed as possible and we will tell you more.

At Astek, we are looking for an experienced SAP Functional ERP Consultant to join a leading organization in the pharma & diagnostics sector, supporting large-scale global transformation programs and ERP deployments. 💪 Your mission, should you choose to accept it… • Lead and coordinate end-to-end (E2E) integrations across define, build, test, and deployment phases, • Act as a key contact between business, SAP, and technical teams, ensuring alignment and connectivity readiness, • Gather, validate, and review functional requirements, mappings, and solution design documentation, • Ensure all integrations are properly documented, tracked, and included in deployment backlogs, • Align timelines, manage stakeholders, and support testing phases (SAT, DET, DIL) focusing on critical processes, • Maintain integration knowledge (E2E repository) and perform impact analysis on downstream systems, • Support cutover, hypercare, and handover to operations, ensuring monitoring and incident readiness 👀 Who are you? • Proven experience working in SAP ERP environments, • Strong background in system integrations and middleware technologies, • Experience in global deployment projects and complex system landscapes, • Solid project management skills (SAFE framework is a plus), • Strong business analysis and documentation review capabilities, • Excellent stakeholder management and communication skills, • Experience in pharma and/or diagnostics is highly valued 💼 Who are we? Since 2015, Astek Iberia has been accompanying its customers in their development throughout Spain (Madrid, Barcelona, Valencia, Basque Country, Andalusia, Galicia, etc.). Founded in France in 1988, Astek is a global player in engineering and technology consulting, present in five continents and 25 countries. With expertise in a wide range of industrial and service sectors, Astek is an essential partner, supporting its customers in an intelligent deployment of their products and services, and in the implementation of their digital transformation. Today we are more than 8,000 employees, committed every day to promote the complementarity between digital technologies and complex systems engineering. Our style is to have flexible schedules and highly value the well-being of our employees. Why join us? 🚀 You will grow professionally in a company in constant development and evolution. 📏 You will benefit from a personalized follow-up of your professional projects as close as possible to your ambitions. 📈 You will make a real contribution to the company's development in real time. 🏝️ You will enjoy 23 days of vacation (in addition to holidays) that you will be able to choose whenever you want. 🌍 You will join our team: diverse, multicultural and constantly growing. 🔋 You will have days full of good energy and good atmosphere. ...although you still have a lot to discover! 😄 ☎️ Shall we meet? 📧 If you want to participate in the process, apply from here attaching your CV (in English) as detailed as possible and we will tell you more.

Join Rephine Barcelona: Leading Life Sciences Quality Worldwide At Rephine, we set the standard for quality assurance and GxP compliance in the Life Sciences industry. With offices in Barcelona, the UK, and China, India, we support the Pharmaceutical, Biotech, and Medical Device supply chains globally. Who We're Looking For: Are you passionate about consulting in the Pharma and Life Sciences sector? Do you thrive in dynamic environments, eager to take on multiple projects and drive real impact? If you're excited by the challenge of enhancing quality and compliance in a global company, we want you as our next Computer System Validation Senior Consultant in Barcelona. Your Role: As a CSV L2 Consultant, you will take an active role in delivering high-impact validation projects, with a focus on ERP systems and other critical computerized systems in regulated environments. You will be part of innovative projects, ensuring compliance, efficiency, and quality across the lifecycle. Key Responsibilities: Lead CSV Projects: • Take ownership of ERP and other computerized system validations (IQ, OQ, PQ), preparing and reviewing critical documentation (VMP, URS, SOPs)., • Ensure compliance with EU GMP Annex 11, FDA 21 CFR Part 11, GAMP 5, and Data Integrity guidelines. ERP & System Expertise: • Work hands-on with ERPs, eDMS, eQMS, LIMS, laboratory systems, SCADA, EBRs, pharmacovigilance, and maintenance systems., • Assess system compliance and performance to optimize regulatory readiness and operational efficiency. Audits & Compliance Assessments: • Perform supplier audits and compliance checks, focusing on Annex 11, 21 CFR Part 11, and global regulations., • Identify risks, provide actionable recommendations, and ensure corrective measures are implemented. International Project Engagement: • Contribute to projects across Spain, Europe, and China, adapting to diverse regulatory environments., • Represent Rephine on-site with clients, ensuring seamless collaboration and delivering high-quality results. Project Delivery & Client Success: • Manage timelines and ensure all deliverables, including documentation and test execution, are completed on schedule., • Maintain clear communication with stakeholders and provide progress updates regularly. Why This Role Could Excite You: • Take a leading role in ERP validation projects while expanding your CSV expertise., • Work with international teams and cutting-edge systems in a fast-paced consulting environment., • Be recognized as an L2 expert contributing to both client success and Rephine’s high standards. What You Bring: • A Bachelor’s degree in Chemistry or Engineering., • Solid experience in the pharmaceutical industry, GxP compliance, and computerized systems validation., • Strong multitasking skills and experience in managing multiple consulting projects to meet client needs., • Fluency in Spanish and English, with excellent communication skills., • Since client sites are often not easily accessible by public transportation, a valid driver’s license and willingness to travel by car are required. Is This Role for You? Ask yourself: • Are you excited about working with clients to tackle their most critical challenges?, • Can you maintain a sense of ownership and connection to the Rephine team, even when managing demanding client-facing responsibilities?, • Do you have the adaptability to move between technical tasks, regulatory compliance, and client interaction with ease?, • Are you ready to learn and grow in a role that exposes you to a wide range of systems and industries? If your answer is "yes" to these questions, then this opportunity at Rephine is your chance to make a significant impact while growing your career in CSV consulting. Why Choose Rephine? We believe in rewarding talent and commitment with a comprehensive benefits package designed to support your personal and professional growth: • Competitive Compensation: A salary that reflects your experience, along with additional vacation days and other benefits., • Work-Life Balance: Take advantage of our hybrid work model, flexible hours, and a shorter workday on Fridays, allowing you to maintain a healthy balance between work and personal life., • Global Exposure: Work with a multicultural team across multiple countries, providing opportunities to expand your professional network and gain international experience., • Dynamic Work Environment: Join a young, enthusiastic team where your contributions are valued, and your ideas can shape the future of the company., • Flexible Salary Options: Benefit from salary sacrifice schemes and more flexibility in managing your compensation package., • Opportunities for Growth: We provide a nurturing environment where your career can grow beyond expectations. Whether you're looking for new challenges or leadership opportunities, Rephine is committed to your continuous development., • Drive Digital Transformation: Participate in projects where you can use the latest technologies to optimize manufacturing and quality processes. For over 20 years, Rephine has been at the forefront of improving manufacturing quality processes for leading Life Sciences companies. We’re evolving rapidly and looking for passionate professionals eager to grow with us. Ready to embark on this journey? Visit our career site to learn more and apply in English.

En pocas palabras 📌 • Posición: Junior Demand Planner, • Localización: Madrid, • Experiencia: 1-3 años de experiencia ¿Quieres saber más? 👇 Exeltis es la división de marca de Insud Pharma, una compañía global con amplia experiencia en toda la cadena de valor farmacéutica, desde la investigación y el desarrollo hasta la fabricación, comercialización y distribución de productos con valor añadido para la salud humana y animal. La actividad de Insud Pharma se organiza en tres áreas de negocio sinérgicas: Industrial (Chemo), Branded (Exeltis) y Biotech (mAbxience), con más de 9.000 profesionales en más de 50 países, 20 instalaciones de última generación, 15 centros especializados de I+D, 12 oficinas comerciales y más de 35 filiales farmacéuticas, que atienden a 1.150 clientes en 96 países de todo el mundo. En Insud Pharma creemos en la innovación y el desarrollo sostenible. ¿Preparado/a para ser un #Challenger? 💪 ¿Qué buscamos? 🔎 Buscamos un/a Demand Planner para Exeltis que asegure una previsión de demanda precisa y alineada globalmente, integrando información de mercados, ventas, marketing y operaciones. Su misión será optimizar inventarios, mejorar el nivel de servicio y garantizar que la producción y el suministro respondan de forma eficiente a las necesidades de cada región, contribuyendo de forma directa a la toma de decisiones en un entorno internacional y dinámico. ¡El reto! 🚀 • Elaborar el forecast global, consolidando previsiones de todas las regiones y filiales mediante modelos estadísticos, análisis histórico y datos de mercado., • Participar activamente en el proceso de S&OP / IBP, presentando análisis, riesgos y oportunidades., • Analizar desviaciones entre forecast y demanda real, identificando causas y proponiendo acciones de mejora., • Colaborar estrechamente con Supply Planning para asegurar la disponibilidad de producto, la capacidad de producción y los planes de suministro., • Gestionar y mantener los datos maestros de planificación en los sistemas, incluyendo lead times, MOQ, ciclos de vida, clasificaciones ABC y otros parámetros clave para una correcta planificación., • Asegurar una adecuada gestión de datos en sistemas, velando por la calidad, consistencia y actualización de la información utilizada en los procesos de demanda y planificación., • Coordinar la planificación del ciclo de vida del producto, incluyendo lanzamientos, discontinuaciones, transiciones y gestión de obsolescencias., • Impulsar la optimización de inventarios globales, equilibrando niveles de stock, reduciendo excesos y evitando roturas., • Integrar variables de mercado como tendencias, estacionalidad, campañas comerciales y factores externos que impacten la demanda., • Coordinarse con equipos globales de ventas, marketing, finanzas, supply chain y operaciones regionales., • Utilizar herramientas avanzadas de forecasting, ERP y analítica para mejorar la precisión de la previsión y la calidad de la planificación. ¿Qué necesitas? 🤓 • Formación en Ingeniería, Economía, Estadística, Supply Chain, Business Analytics o similar., • Entre 1 y 3 años de experiencia en Demand Planning, Supply Chain, Forecasting o S&OP., • Experiencia preferiblemente en entornos globales; también se valorarán perfiles con experiencia local dentro del sector farmacéutico., • Conocimiento de ERP SAP., • Experiencia en gestión de datos en sistemas y mantenimiento de parámetros maestros de planificación., • Manejo de herramientas de forecasting como APO, Anaplan o equivalentes., • Valorable conocimiento de SAP IBP., • Nivel avanzado de Excel., • Nivel alto de inglés para la comunicación con equipos internacionales., • Capacidad para interpretar grandes volúmenes de datos y convertirlos en insights accionables., • Habilidades de comunicación e influencia para interactuar con stakeholders globales., • Pensamiento estratégico y orientación a resultados., • Capacidad para trabajar en entornos multiculturales y con múltiples zonas horarias., • Rigor analítico, atención al detalle y adaptabilidad ante cambios de mercado y prioridades., • Valorable experiencia en sectores con alta complejidad regulatoria o de portafolio. ¡Nuestros beneficios! 👏 • 📜 Contrato indefinido, • 📍 Madrid, • 🚀 Impacto real en decisiones estratégicas, • 🤝 Alta exposición a negocio y dirección, • 📈 Oportunidad de crecimiento en un entorno dinámico ¿Cómo será el proceso de Selección? 🕵️ • Contacto inicial por teléfono o correo electrónico., • Entrevistas con el equipo de selección y/o hiring manager., • Comunicación constante sobre el estado del proceso. 🔷¿Crees que esta oferta no es para ti? 🔷 Síguenos en LinkedIn e Instagram para conocer nuevas oportunidades y mantenerte al día de nuestras vacantes. #InsudPharma #Challenger #Insuder #InsudTalent COMPROMISO CON LA IGUALDAD DE OPORTUNIDADES En Exeltis apostamos por la igualdad de oportunidades y por un entorno de trabajo diverso e inclusivo. Todas las candidaturas serán valoradas sin distinción de género, identidad o expresión de género, edad, etnia, nacionalidad, religión, orientación sexual, discapacidad o cualquier otra condición personal, física o social.

En INSUD PHARMA promovemos la igualdad de oportunidades y la no discriminación. INSUD PHARMA es un grupo farmacéutico internacional con presencia en toda la cadena de valor, desde la investigación y el desarrollo hasta la fabricación y comercialización, apostando por la innovación y el crecimi

AI search & content specialist: About this role This position will act as the internal subject-matter expert on SEO, GEO, and AI-driven discovery. Scilife is looking for a strategic, AI-forward content professional to lead our content presence across both traditional SEO and ai-powered search channels. As search behavior rapidly evolves with users increasingly turning to tools like ChatGPT, Perplexity, Google AI overviews, and Gemini for answers — we need a specialist who can ensure Scilife is visible, authoritative, and trusted in these new discovery surfaces. This role goes beyond traditional SEO. You will own our answer engine optimization (AEO) and generative engine optimization (GEO) strategy, shaping quarterly roadmaps that align content initiatives with broader business goals. You will develop and implement strategies that improve Scilife’s visibility within AI-generated results, answer engines, and entity-based discovery systems, aligning both content and technical structure to support AI-native search experiences. The goal is to make Scilife the go-to brand cited by AI tools when life sciences professionals search for quality management solutions. You will create structured, authoritative, AI-readable content that positions Scilife as a thought leader and drives organic brand recall across both human and machine audiences. This role is responsible to: • Own organic growth strategy across traditional search and AI-driven discovery (Google AI Overviews, LLMs, answer engines)., • Define and evolve GEO best practices to ensure brand visibility and citation in generative responses., • Establish standards for structured content (schema, summaries, FAQs, entities, metadata) optimized for AI consumption., • Translate shifts in search behavior (zero-click, AI summaries) into clear priorities and roadmaps that balance traditional SEO and GEO., • Work cross-functionally with different teams to align SEO with companywide business goals and objectives., • Responsible for growing new user acquisition and hitting core KPIs across traditional SEO, GEO and AEO., • Extensive knowledge of current SEO/GEO best practices with strong technical SEO/GEO background experience, • Utilize research tools to perform keyword gap analysis to support and prioritize keyword and content strategies., • Ability to monitor ongoing SEO site health and maintenance reports while translating insights into actionable tasks and projects, • Familiarity with SEO tools (Google Search Console, Semrush, etc.), • Ability to lead multiple projects simultaneously with strong prioritization skills, • Champion data-driven testing initiatives to identify opportunities and scale acquisition efficiently, • Develop analysis that provides conclusions into customer behavior and communicates those conclusions clearly with key stakeholders., • Provide insight-driven reporting that explains what happened, why it happened, and what to do next., • Evaluate and adapt strategies based on shifts in AI-generated search visibility and user interaction patterns. AEO / GEO & AI visibility • Develop and execute an answer engine optimization (AEO) and generative engine optimization (GEO) strategy to increase Scilife’s brand presence and citation frequency in AI-powered tools (ChatGPT, Perplexity, Google AI overviews, Gemini, Copilot, etc.)., • Conduct competitive benchmarking to understand how scilife appears vs. Competitors (e.g., Qualio, Mastercontrol, Greenlightguru, Veeva, etq) across AI-generated responses., • Identify and close content gaps that prevent Scilife from being surfaced by LLMs as the recommended eQMS solution for life sciences companies., • Implement structured data, FAQ schemas, and authoritative content formats optimized for AI parsing and citation., • Monitor brand mentions and citations in ai tools and establish a reporting framework to track LLM visibility over time. Content strategy & creation • Plan and execute a multi-channel content strategy aligned with AEO/GEO goals and broader marketing objectives., • Create high-quality, authoritative content (articles, whitepapers, landing pages, use cases, FAQs, glossaries) that establishes Scilife as a definitive source of truth in the eQMS and quality management space., • Optimize the existing content library for AI readability: clear structure, direct answers, entity coverage, and factual depth., • Manage the content calendar and ensure a consistent publishing cadence across the blog, website, and newsletters., • Collaborate with the design team and external contributors to deliver polished, on-brand content assets. Traditional SEO & search visibility • Maintain and improve organic search rankings through keyword research, on-page seo, and internal linking strategies., • Monitor search performance metrics and produce regular reports with actionable insights using tools such as google search console, semrush, or ahrefs., • Ensure all content is SEO-friendly, up-to-date, and aligned with current search intent and user behavior. Collaboration & process • Work closely with the brand manager, knowledge manager, and marketing teams to align content with business priorities., • Coordinate content approvals across stakeholders in a timely and organized manner., • Stay ahead of ai search trends, platform changes, and industry best practices, and proactively share insights with the broader team. Required skills & experience Core requirements • 4+ years of experience in content marketing, SEO, or digital content roles., • Demonstrated understanding of AEO / GEO concepts and how LLMs source and cite information., • Strong SEO fundamentals: keyword research, on-page optimization, technical SEO basics, and schema markup., • Excellent English writing and editing skills; ability to produce clear, authoritative, and engaging B2B content., • Proficiency with SEO analytics tools (google search console, semrush, or similar)., • Analytical mindset with the ability to translate data into content decisions and strategy. Nice to have • Experience with marketing automation tools (hubspot preferred)., • Experience in B2B SaaS, life sciences, or regulated industries (pharma, medtech, biotech)., • Familiarity with structured data, json-ld, and schema.org vocabulary., • Experience using AI tools (ChatGPT, Perplexity, Claude, etc.) As part of content research or production workflows., • Experience with Jira or similar project management and ticketing tools., • Comfort working in a fast-paced, international, and remote-first environment., • Experience of search planning fundamentals across Paid and Organic channels., • Familiarity with core PPC marketing principles and tools such as Google and Meta Ads Core competencies Candidates will be assessed against the following competencies during the hiring process and in periodic performance evaluations: • Strategic thinking, • AI & tech curiosity, • Content excellence, • Data-driven, • Creativity, • Collaborative, • Attention to detail, • Getting things done, • Communication, • Adaptability, • Time management, • Innovation Candidates will also be assessed against scilife’s core company values: • Healthy inside-out, • Outside of the box, • Driven by evidence, • All hearts and ears Why join Scilife? Scilife helps life science companies digitize, automate, and scale their quality and compliance processes. Our eQMS platform supports organizations worldwide in staying audit-ready while enabling innovation. We are in the early stages of an ambitious AI-first transformation. As our AI Search & Content Specialist, you will play a key role in shaping how Scilife brand appears in high-intent industry conversations, how we build topical authority, and how we position Scilife as a category-relevant voice in the future of quality management. You will join a collaborative, international, and fast-evolving company environment, working closely with the Brand team as well as cross-functional partners across marketing, sales, and customer successes teams. This is a role for someone who enjoys combining strategic thinking with hands-on execution, and who is excited by the opportunity to build new capabilities in a space that is still taking shape. At Scilife, you will find a team that values curiosity, ownership, fresh thinking, and meaningful collaboration. We care deeply about building work that is thoughtful, relevant, and impactful — and we are looking for someone who is energized by that kind of environment. If you are excited by the intersection of content, SEO, AI, and category building — and motivated by the chance to shape a capability that is still emerging — this role offers the opportunity to make a visible, strategic impact from day one. What we offer • Fully remote work within Europe with flexible hours., • Competitive compensation., • Collaborative, international team culture., • Continuous learning and professional development., • The chance to play a defining role in an emerging area of strategic importance for the company., • More info about benefits at Scilife.

Who We Are Whitewater Group is a leading provider of innovative and sustainable water treatment engineering systems operating in Ireland, the UK and across Europe in the Data Centre, Pharma, Power and Industrial sectors. We specialize in designing, installing, commissioning, and maintaining water treatment solutions to meet our clients' specific needs. Our team is dedicated to delivering high-quality, cost-effective engineering solutions that prioritize safety, reliability, and environmental sustainability. Whitewater Group is headquartered in Naas Co. Kildare and operates from European bases in Spain, Sweden, Finland, and the UK, with plans for further offices in Germany, Denmark, and Italy. The Group is experiencing significant growth driven by its focus on off-site construction methods (OSM) for delivering turnkey projects, reducing on-site construction time to a minimum. Role Description Due to continued expansion, Whitewater is seeking a Pre-Commissioning Engineer (Electrical) to support the delivery of water treatment systems across European projects. This role is focused on electrical pre-commissioning activities, ensuring that electrical systems, control panels, instrumentation, and field devices are correctly installed, tested, and ready prior to energisation and live commissioning. The Pre-Commissioning Engineer will work closely with QA/QC, OSM, automation, and commissioning teams to identify and resolve issues early, helping ensure a smooth transition into commissioning and system start-up. Main Duties and Responsibilities Electrical Pre-Commissioning & Inspections to include: • Carry out detailed electrical pre-commissioning inspections of:, • MCCs, control panels, PLC panels, VSDs, soft starters, • Pumps, motors, actuated valves, instrumentation, and field devices, • Verify installations against P&IDs, electrical schematics, I/O lists, and approved drawings, • Confirm correct installation of power, control, and instrument cabling, • Verify earthing, bonding, labelling, and panel workmanship, • Identify installation or wiring issues and support timely resolution, • Provide clear feedback on electrical readiness to support commissioning planning Testing & Verification to include: • Perform or witness electrical testing to include:, • Insulation resistance testing, • Continuity and earth checks, • Phase rotation and supply verification, • Support loop checks and point-to-point testing in coordination with automation teams, • Confirm systems are safe and suitable for energisation Interface & Coordination • Work closely with:, • QA/QC team, • Automation / PLC engineers, • Commissioning engineers and project teams, • OSM team Documentation • Complete and maintain pre-commissioning checklists and inspection records (ITP’s), • Ensure testing and inspection results are clearly recorded and traceable, • Support the preparation of handover information required for commissioning activities Required Qualifications and Experience • Degree or trade qualification in Electrical Engineering, or an electrical trade-qualified background with experience in industrial systems and automation, or equivalent, • 3+ years’ experience in electrical installation, pre-commissioning, or site-based engineering roles, • Strong understanding of:, • MCCs, control panels, VSDs, motors, and instrumentation, • Ability to read and work from:, • P&IDs, • Electrical schematics, • I/O lists and construction drawings, • Strong attention to detail and safety-focused approach, • Permit to work in the EU Desirable • Experience working on water treatment plants or within water treatment environments, • Exposure to industrial process systems, utilities, or data centre infrastructure, • Previous involvement in commissioning or system start-up activities Benefits • Competitive salary, • Annual bonus, • Pension scheme, • Opportunity for progression within a growing commissioning team

Key Responsibilities: • Sales Target Achievement: Lead market sales targets for products like nab-paclitaxel (e.g., Abraxane generic) and injectables. Identify market opportunities and competitive challenges, gather primary market data, and develop marketing strategies and plans., • Distributor Management: Manage distributors, track performance, conduct regular field visits with their KAMs across regions. Identify strengths and weaknesses, and guide distributors to gain higher market share., • Value Assessment & Redistribution: Evaluate distributor value across all marketing functions (access, promotion, distribution, payment collection) to lay the foundation for renegotiating profit-sharing terms., • Market Mapping: Research and map the value chain and drivers of the Spanish hospital and retail markets. Deliver a "Hospital & Clinic Map for nab-paclitaxel in Spain" and a list of purchasing groups (Central de Compras) with their coverage scope., • Resource & Demand Mining: Continuously build distributor networks and identify unmet clinical and retail needs. Requirements: 1. Legal & Compliance • Fluent English (working language); native or C2 Spanish., • Background in pharmacy, bioscience, or related fields preferred., • No record of industry violations. Familiar with AEMPS compliance requirements. 1. Experience & Tender Expertise (Critical) • 10+ years of sales experience in pharmaceutical marketing, including 5+ years of tender experience in the Spanish pharma industry (especially prescription/injectable drugs) ., • Familiar with Spain's national healthcare tender process (e.g., SERMAS, regional bidding rules)., • Independently led provincial or national pharmaceutical tender projects in Spain – proficient in bid document preparation, pricing strategy, and compliance review., • Oncology product marketing experience (especially injectable cytotoxics) strongly preferred. 1. Local Network • Established contacts within Spain's public healthcare system (hospital pharmacy departments, procurement bodies, health authorities) and major pharmaceutical distributors. 1. End-to-End Capability • Able to drive new product launches and coordinate supply chain (import customs clearance, warehousing, distribution). 1. Cross-Cultural Adaptability • Basic cross-cultural communication skills; understands and accommodates the working rhythm and expectations of a Chinese headquarters.

SEARGIN IS HIRING! As a dynamic multinational tech company operating in 50 countries, we drive innovation and create projects that shape the future and greatly enhance the quality of life. You will find our solutions in the space industry, supporting scientists in the development of cancer drugs, and implementing innovative technological solutions for industrial clients worldwide. These are just some of the areas in which we operate! Currently, for the new Seargin project we are looking for SAP EWM Consultant. Location: Barcelona, Spain Employment Type: Contract FTE: Full-time Project: SAP WM → Advanced Embedded EWM migration for a pharma/GMP regulated warehouse (Interquim, Sant Cugat). The project covers full E2E implementation: inbound, internal movements, production supply, dispatch, HU management, and label traceability. Validation (IQ/OQ/PQ) is in scope. S/4HANA 2021 environment. Tasks: • Lead or support AS-IS process analysis and gap assessment vs EWM standard, • Configure and test EWM processes: inbound (transfer orders, HU creation, RF confirmation), internal storage, production supply, order picking, dispatch, • Design and configure HU management and Packing Instructions to replace manual Z-transactions, • Support functional specification writing (FDS) and user acceptance testing, • Collaborate with ABAP developers on custom developments (label printing, interfaces), • Participate in IQ/OQ/PQ validation activities alongside QA team, • Provide knowledge transfer and end-user training, • Support hyper-care period post Go-Live Must have: • SAP WM experience: minimum 3 years, • SAP EWM experience: minimum 3 years (Embedded or Decentralised), • Minimum one full E2E SAP EWM deployment (go-live experience required), • Strong knowledge of EWM inbound / outbound processes, HU management, RF Framework, • Experience with GMP / pharma / regulated environments preferred, • Familiarity with 21 CFR Part 11 and/or EU GMP Part II is a strong asset, • Fluent English (working language); Spanish is a plus Nice to have: • Experience with SAP QM integration in WM/EWM context, • Knowledge of Zebra label printing integration, • Experience with LabVantage or other LIMS systems, • SAP S/4HANA certification, • Experience with IQ/OQ/PQ validation processes Discover the Power of IT Excellence. Apply! To learn more about Seargin, please visit our web page: www.seargin.com

IF YOU ARE INTERESTED, PLEASE SHARE YOUR CV IN ENGLISH LANGUAGE ONLY! Who are we? We are a technology-led healthcare solutions provider. We are driven by our purpose to enable healthcare organizations be future ready. We offer accelerated, global growth opportunities for talent that’s bold, industrious, and nimble. With Indegene, you gain a unique career experience that celebrates entrepreneurship, and is guided by passion, innovation, collaboration, and empathy. To explore exciting opportunities at the convergence of healthcare and technology, check out www.careers.indegene.com What if we told you that you can move to an exciting role in an entrepreneurial organization without the usual risks associated with it? We understand that you are looking for growth in your career at this point and we would love for you to join us in our journey and grow with us. At Indegene, our roles come with the excitement you require at this stage of your career with the reliability you seek. We believe in creating leaders of tomorrow and mentor our leads to help them grow and nurture them as people managers and account managers. We are a rapidly growing global organization and are scouting for the best talent for this phase of growth. With us, you are at the intersection of two of the most exciting industries of healthcare and technology. We offer global opportunities with fast-track careers while you work with a team that is fueled by purpose. The combination of this will lead to a truly differentiated experience for you. If this excites you, then apply below. Role: Lead SFMC Developer IF YOU ARE INTERESTED, PLEASE SHARE YOUR CV IN ENGLISH LANGUAGE ONLY! Job Description: We are seeking an experienced SFMC Lead Developer with deep hands-on expertise across Automation Studio, Journey Builder, complex audience segmentation, Marketing Cloud Personalization (MCP), and enterprise integrations. This role is ideal for someone who is comfortable operating in a pharma environment, with strong data governance sensibilities and the ability to translate business objectives into scalable omnichannel journeys. The ideal candidate will partner closely with platform architects (e.g., CRM, Web, CMS) while leading technical design and building for Salesforce Marketing Cloud programs. This is a hands-on technical role, not purely strategic, requiring someone who can architect, develop, troubleshoot, optimize, and operationalize journeys at scale. Key Responsibilities 1. SFMC Architecture & Development • Lead the build and optimization of journeys in Journey Builder, including multi-branch paths, triggers, decision splits, and event-based orchestration., • Build automations in Automation Studio, including SQL-based segmentation, scheduled automations, and data hygiene processes., • Develop modular, compliant email and content blocks, leveraging AMPscript, SSJS, and data extensions best practices., • Implement and optimize Einstein features and predictive capabilities within SFMC, • Own the final audit and quality validation of campaigns executed by team members, ensuring adherence to defined processes, compliance standards, technical accuracy, and client requirements before deployment. 1. Data & Integration Leadership • Design and maintain data models, data extensions, relational mappings, and business rules aligned with CRM, website, and analytics inputs., • Lead integrations between SFMC and: o Veeva CRM (triggers, segmentation, report extraction) o WordPress VIP for personalization, tagging, and behavioral capture feeding MCP o Enterprise Data Lakes, CDPs, or analytics environments • · Ensure data dictionary, taxonomy alignment, and governance across all activation channels. 1. Marketing Cloud Personalization (MCP) • Implement MCP tagging, site wide java scripting, custom scripting (if any) rule sets, decisioning logic, personalization recipes, and identity resolution approaches., • Partner with web and analytics teams to ensure MCP instrumentation is clean, compliant, and aligned to journey logic., • Optimize hybrid (rule-based + algorithmic) MCP experiences based on campaign goals. 1. Cross-Functional Collaboration & Enablement • Work closely with omnichannel strategists, CRM leads, web/CMS teams, and localization leads., • Provide documentation, technical playbooks, and training for marketing, operations, and downstream teams., • Participate in solution design discussions, validation sessions, gap assessment, and technical Q&A. Required Qualifications • 7–10+ years of hands-on SFMC development and architecture experience at scale., • Advanced mastery of Journey Builder, Automation Studio, SQL, AMPscript, SSJS, and SFMC data modeling., • Proven experience with MCP implementation, including tagging, decisioning, and integration with websites (e.g., WordPress VIP)., • Strong familiarity with Veeva CRM data structures and how CRM segments feed omnichannel journeys., • Demonstrated experience supporting pharma or life sciences omnichannel operations., • Comfortable working cross-platform (CRM → SFMC → Web) in complex enterprise ecosystems., • Based in Madrid or already residing in Spain or Japan with ability for regular on-site work., • Language proficiency required in Spanish (for Spain market) EQUAL OPPORTUNITY: Indegene is proud to be an Equal Employment Employer and is committed to the culture of Inclusion and Diversity. We do not discriminate on the basis of race, religion, sex, colour, age, national origin, pregnancy, sexual orientation, physical ability, or any other characteristics. All employment decisions, from hiring to separation, will be based on business requirements, candidate’s merit and qualification. We are an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, colour, religion, sex, national origin, gender identity, sexual orientation, disability status, protected veteran status, or any other characteristics.

SEARGIN IS HIRING! As a dynamic multinational tech company operating in 50 countries, we drive innovation and create projects that shape the future and greatly enhance the quality of life. You will find our solutions in the space industry, supporting scientists in the development of cancer drugs, and implementing innovative technological solutions for industrial clients worldwide. These are just some of the areas in which we operate! Currently, for the new Seargin project we are looking for SAP EWM Teach Lead. Location: Barcelona, hybrid Employment Type: B2B FTE: full-time Requirements: • EWM team Lead (+5 years),, • Multiple E2E SAP EWM deployments in team lead role,, • At least one E2E SAP EWM deployment in Pharma,, • Spanish language Responsibilities: • Leading the functional design and implementation of the SAP EWM solution replacing the current SAP WM module at Ferrer's Interquim site (Sant Cugat)., • End-to-end delivery of warehouse management processes including raw material receipt and labelling, location management across multiple warehouse types, supply to production and fractionation areas, semi-finished and finished product handling, repackaging order management, and outbound processes (picking, preparation, labelling)., • As-is analysis against written requirements (RFPURSWM), produces the functional design, ensures FDA compliance requirements are addressed, and oversees the implementation of GS1 label management in SAP., • Coordinating with the SAP EWM consultants, ABAP team, and client stakeholders, and is responsible for the quality of functional deliverables including training manuals and the support plan. Discover the Power of IT Excellence. Apply! To learn more about Seargin, please visit our web page: www.seargin.com

Senior Purchasing Specialist – Chemical Additives La persona incorporada será responsable de la gestión de compras internacionales y desarrollo de proveedores de aditivos químicos y materias primas para diferentes sectores industriales como Plastics, Coatings, Pharma, Food y Agro, trabajando estrechamente con fabricantes y proveedores internacionales, principalmente en China e India. Funciones: • Gestión integral de compras internacionales de aditivos químicos y materias primas para sectores como Plastics, Coatings, Pharma, Food y Agro., • Gestión y negociación directa con proveedores internacionales, principalmente fabricantes y proveedores estratégicos en China e India., • Búsqueda, homologación y desarrollo de nuevos proveedores de Specialty Chemicals, asegurando competitividad, calidad y continuidad de suministro., • Negociación de precios, condiciones comerciales, contratos, lead times y planificación de compras, optimizando costes y niveles de stock., • Seguimiento de mercados internacionales, tendencias de precios y evolución de materias primas químicas y aditivos industriales., • Coordinación transversal con departamentos de ventas, supply chain, regulatory, calidad y logística para asegurar el correcto abastecimiento y desarrollo de negocio., • Participación activa en la definición de la estrategia de compras y portfolio de productos, identificando nuevas oportunidades y representadas para el mercado europeo. Perfil: • Formación superior en Química, Ingeniería Química, ADE, Comercio Internacional o similar, valorándose especialmente conocimiento técnico relacionado con Specialty Chemicals y aditivos químicos., • Experiencia consolidada en compras internacionales dentro del sector químico, especialmente en aditivos y materias primas para Plastics, Coatings, Pharma, Food, Agro o sectores afines., • Experiencia en negociación y gestión de proveedores internacionales, principalmente en China e India, así como en búsqueda y homologación de nuevos fabricantes., • Conocimiento de mercados internacionales de materias primas químicas, dinámica de precios, supply chain y procesos de importación internacional., • Nivel alto de inglés para negociación y gestión diaria con proveedores internacionales., • Perfil analítico, negociador y orientado a negocio, con capacidad para trabajar en entornos internacionales y multiculturales.

En pocas palabras 📌 • Posición: Junior Demand Planner, • Localización: Madrid, • Experiencia: 1-3 años de experiencia ¿Quieres saber más? 👇 Exeltis es la división de marca de Insud Pharma, una compañía global con amplia experiencia en toda la cadena de valor farmacéutica, desde la investigación y el desarrollo hasta la fabricación, comercialización y distribución de productos con valor añadido para la salud humana y animal. La actividad de Insud Pharma se organiza en tres áreas de negocio sinérgicas: Industrial (Chemo), Branded (Exeltis) y Biotech (mAbxience), con más de 9.000 profesionales en más de 50 países, 20 instalaciones de última generación, 15 centros especializados de I+D, 12 oficinas comerciales y más de 35 filiales farmacéuticas, que atienden a 1.150 clientes en 96 países de todo el mundo. En Insud Pharma creemos en la innovación y el desarrollo sostenible. ¿Preparado/a para ser un #Challenger? 💪 ¿Qué buscamos? 🔎 Buscamos un/a Demand Planner para Exeltis que asegure una previsión de demanda precisa y alineada globalmente, integrando información de mercados, ventas, marketing y operaciones. Su misión será optimizar inventarios, mejorar el nivel de servicio y garantizar que la producción y el suministro respondan de forma eficiente a las necesidades de cada región, contribuyendo de forma directa a la toma de decisiones en un entorno internacional y dinámico. ¡El reto! 🚀 • Elaborar el forecast global, consolidando previsiones de todas las regiones y filiales mediante modelos estadísticos, análisis histórico y datos de mercado., • Participar activamente en el proceso de S&OP / IBP, presentando análisis, riesgos y oportunidades., • Analizar desviaciones entre forecast y demanda real, identificando causas y proponiendo acciones de mejora., • Colaborar estrechamente con Supply Planning para asegurar la disponibilidad de producto, la capacidad de producción y los planes de suministro., • Gestionar y mantener los datos maestros de planificación en los sistemas, incluyendo lead times, MOQ, ciclos de vida, clasificaciones ABC y otros parámetros clave para una correcta planificación., • Asegurar una adecuada gestión de datos en sistemas, velando por la calidad, consistencia y actualización de la información utilizada en los procesos de demanda y planificación., • Coordinar la planificación del ciclo de vida del producto, incluyendo lanzamientos, discontinuaciones, transiciones y gestión de obsolescencias., • Impulsar la optimización de inventarios globales, equilibrando niveles de stock, reduciendo excesos y evitando roturas., • Integrar variables de mercado como tendencias, estacionalidad, campañas comerciales y factores externos que impacten la demanda., • Coordinarse con equipos globales de ventas, marketing, finanzas, supply chain y operaciones regionales., • Utilizar herramientas avanzadas de forecasting, ERP y analítica para mejorar la precisión de la previsión y la calidad de la planificación. ¿Qué necesitas? 🤓 • Formación en Ingeniería, Economía, Estadística, Supply Chain, Business Analytics o similar., • Entre 1 y 3 años de experiencia en Demand Planning, Supply Chain, Forecasting o S&OP., • Experiencia preferiblemente en entornos globales; también se valorarán perfiles con experiencia local dentro del sector farmacéutico., • Conocimiento de ERP SAP., • Experiencia en gestión de datos en sistemas y mantenimiento de parámetros maestros de planificación., • Manejo de herramientas de forecasting como APO, Anaplan o equivalentes., • Valorable conocimiento de SAP IBP., • Nivel avanzado de Excel., • Nivel alto de inglés para la comunicación con equipos internacionales., • Capacidad para interpretar grandes volúmenes de datos y convertirlos en insights accionables., • Habilidades de comunicación e influencia para interactuar con stakeholders globales., • Pensamiento estratégico y orientación a resultados., • Capacidad para trabajar en entornos multiculturales y con múltiples zonas horarias., • Rigor analítico, atención al detalle y adaptabilidad ante cambios de mercado y prioridades., • Valorable experiencia en sectores con alta complejidad regulatoria o de portafolio. ¡Nuestros beneficios! 👏 • 📜 Contrato indefinido, • 📍 Madrid, • 🚀 Impacto real en decisiones estratégicas, • 🤝 Alta exposición a negocio y dirección, • 📈 Oportunidad de crecimiento en un entorno dinámico ¿Cómo será el proceso de Selección? 🕵️ • Contacto inicial por teléfono o correo electrónico., • Entrevistas con el equipo de selección y/o hiring manager., • Comunicación constante sobre el estado del proceso. 🔷¿Crees que esta oferta no es para ti? 🔷 Síguenos en LinkedIn e Instagram para conocer nuevas oportunidades y mantenerte al día de nuestras vacantes. #InsudPharma #Challenger #Insuder #InsudTalent COMPROMISO CON LA IGUALDAD DE OPORTUNIDADES En Exeltis apostamos por la igualdad de oportunidades y por un entorno de trabajo diverso e inclusivo. Todas las candidaturas serán valoradas sin distinción de género, identidad o expresión de género, edad, etnia, nacionalidad, religión, orientación sexual, discapacidad o cualquier otra condición personal, física o social.

Nuestro cliente, Kern Pharma (www.kernpharma.com), que forma parte del grupo empresarial y familiar, Grupo Indukern. Desarrolla, fabrica y comercializa productos farmacéuticos en seis líneas de negocio: genéricos, consumer, biosimilares, Gynea, Finisher e internacional & producción para terceros. El Sistema de Gestión de la Calidad Integral de Kern Pharma, en el que se enmarca su actividad, es una muestra más de su compromiso con la salud y la calidad de vida de las personas y con la sostenibilidad. Gracias a sus valores de compromiso, honestidad y afán de superación y al equipo humano que forma la compañía, ha alcanzado posiciones de referencia dentro del sector con tan solo 26 años de historia. Dado su momento de expansión, necesita incorporar un/a para su sede central ubicada en Terrassa: Leader de Desarrollo Galénico Su misión, reportando al Responsable de Desarrollo, y lidereando un equipo de personas, será la gestión de proyectos de desarrollo y escalado industrial de nuevas formulaciones, garantizando la calidad, productividad y cumplimiento regulatorio. Sus principales funciones serán: • Diseñar y desarrollar nuevas formulaciones y productos, incluyendo estudios de preformulación y desarrollo bajo criterios QbD., • Liderar el escalado e industrialización de formulaciones y la elaboración de lotes clínicos y de validación., • Gestionar y desarrollar al equipo de Desarrollo Galénico, impulsando la mejora continua y el crecimiento profesional., • Coordinarse con áreas clave (analítica, IP, negocio, clínica, farmacocinética) para asegurar el avance de los proyectos., • Garantizar la correcta documentación en entorno GMP y el cumplimiento de normas de calidad, PRL y medio ambiente., • Participar en la definición de presupuestos, inversiones y proyectos estratégicos de mejora. Estamos pensando en un perfil con estudios universitarios en Farmacia, química, Biología o áreas afines, y que pueda aportar al menos 5 años de experiencia en la industria farmacéutica dentro del desarrollo galénico con nivel fluido de inglés, dominio de Office y familiaridad con entornos GMP, además de capacidad de liderazgo, organización, visión técnica y orientación a la mejora continua.

Nuestro cliente, Kern Pharma (www.kernpharma.com), que forma parte del grupo empresarial y familiar, Grupo Indukern. Desarrolla, fabrica y comercializa productos farmacéuticos en seis líneas de negocio: genéricos, consumer, biosimilares, Gynea, Finisher e internacional & producción para terceros. El Sistema de Gestión de la Calidad Integral de Kern Pharma, en el que se enmarca su actividad, es una muestra más de su compromiso con la salud y la calidad de vida de las personas y con la sostenibilidad. Gracias a sus valores de compromiso, honestidad y afán de superación y al equipo humano que forma la compañía, ha alcanzado posiciones de referencia dentro del sector con tan solo 26 años de historia. Dado su momento de expansión, necesita incorporar un/a para su sede central ubicada en Terrassa: Leader de Desarrollo Galénico Su misión, reportando al Responsable de Desarrollo, y lidereando un equipo de personas, será la gestión de proyectos de desarrollo y escalado industrial de nuevas formulaciones, garantizando la calidad, productividad y cumplimiento regulatorio. Sus principales funciones serán: • Diseñar y desarrollar nuevas formulaciones y productos, incluyendo estudios de preformulación y desarrollo bajo criterios QbD., • Liderar el escalado e industrialización de formulaciones y la elaboración de lotes clínicos y de validación., • Gestionar y desarrollar al equipo de Desarrollo Galénico, impulsando la mejora continua y el crecimiento profesional., • Coordinarse con áreas clave (analítica, IP, negocio, clínica, farmacocinética) para asegurar el avance de los proyectos., • Garantizar la correcta documentación en entorno GMP y el cumplimiento de normas de calidad, PRL y medio ambiente., • Participar en la definición de presupuestos, inversiones y proyectos estratégicos de mejora. Estamos pensando en un perfil con estudios universitarios en Farmacia, química, Biología o áreas afines, y que pueda aportar al menos 5 años de experiencia en la industria farmacéutica dentro del desarrollo galénico con nivel fluido de inglés, dominio de Office y familiaridad con entornos GMP, además de capacidad de liderazgo, organización, visión técnica y orientación a la mejora continua.

Nuestro cliente, Kern Pharma (www.kernpharma.com), que forma parte del grupo empresarial y familiar, Grupo Indukern. Desarrolla, fabrica y comercializa productos farmacéuticos en seis líneas de negocio: genéricos, consumer, biosimilares, Gynea, Finisher e internacional & producción para terceros. El Sistema de Gestión de la Calidad Integral de Kern Pharma, en el que se enmarca su actividad, es una muestra más de su compromiso con la salud y la calidad de vida de las personas y con la sostenibilidad. Gracias a sus valores de compromiso, honestidad y afán de superación y al equipo humano que forma la compañía, ha alcanzado posiciones de referencia dentro del sector con tan solo 26 años de historia. Dado su momento de expansión, necesita incorporar un/a para su sede central ubicada en Terrassa: Leader de Desarrollo Galénico Su misión, reportando al Responsable de Desarrollo, y lidereando un equipo de personas, será la gestión de proyectos de desarrollo y escalado industrial de nuevas formulaciones, garantizando la calidad, productividad y cumplimiento regulatorio. Sus principales funciones serán: • Diseñar y desarrollar nuevas formulaciones y productos, incluyendo estudios de preformulación y desarrollo bajo criterios QbD., • Liderar el escalado e industrialización de formulaciones y la elaboración de lotes clínicos y de validación., • Gestionar y desarrollar al equipo de Desarrollo Galénico, impulsando la mejora continua y el crecimiento profesional., • Coordinarse con áreas clave (analítica, IP, negocio, clínica, farmacocinética) para asegurar el avance de los proyectos., • Garantizar la correcta documentación en entorno GMP y el cumplimiento de normas de calidad, PRL y medio ambiente., • Participar en la definición de presupuestos, inversiones y proyectos estratégicos de mejora. Estamos pensando en un perfil con estudios universitarios en Farmacia, química, Biología o áreas afines, y que pueda aportar al menos 5 años de experiencia en la industria farmacéutica dentro del desarrollo galénico con nivel fluido de inglés, dominio de Office y familiaridad con entornos GMP, además de capacidad de liderazgo, organización, visión técnica y orientación a la mejora continua.

Omega CRM Consulting is looking for a Power Platform Technical Consultant that would like to collaborate with one of the top global pharmaceutical companies. The Power Platform Technical Consutlant primarily focuses on hands-on Power Platform delivery for squad use cases, including solution assessment, build, integration, ALM, and coordination with IT on technical and licensing dependencies. In addition, the role may support broader enablement topics such as citizen development guidance, governance contribution, training, and platform evolution, but these are supporting expectations rather than the core purpose of the role. Responsibilities Low-Code Development • Design and build scalable low-code solutions using Power Platform (PowerApps, Power Automate, Power BI) for the use cases managed by the squad., • Create reusable components, templates, and patterns for common business needs., • Develop complex workflows and integrations that connect business processes, while contributing to use case assessment and helping determine the most suitable Power Platform approach based on business value, technical feasibility, and governance constraints., • Ensure solutions follow best practices for performance, security, and maintainability, while supporting the delivery process through testing, deployment, and handover as needed. Supporting Expectations – Citizen Developer Guidance • Empower Champions and Citizen Developers to build their own solutions safely., • Provide guidance, coaching, and technical support to non-technical builders., • Create training materials, documentation, and self-service resources., • Review and quality-assure solutions built by Citizen Developers. Supporting Expectations – Governance, Compliance & Security Contribution • Contribute to governance frameworks for low-code development in alignment with enterprise standards., • Work within defined security rules, DLP policies, and environment management practices, in coordination with IT and platform owners where applicable., • Ensure compliance with enterprise standards, regulatory requirements, data protection expectations, and relevant Responsible AI principles when solutions include AI-enabled capabilities., • Promote best practices across the organisation and provide visibility on platform usage where relevant to the role. Platform Administration & Optimisation • Support Power Platform environments, connectors, and related licensing topics in collaboration with the IT partner., • Optimise platform performance and work with the IT partner to help resolve technical issues, recognising that technical configuration and licensing decisions remain IT-owned and that this role can influence them only indirectly., • Support feature scouting by evaluating new Power Platform features and capabilities relevant to squad delivery needs., • Coordinate with IT on platform updates, integrations, technical dependencies, licensing considerations, and enterprise alignment. Integration & Scalability • Design integrations between Power Platform and enterprise systems (SharePoint, Dataverse, APIs)., • Ensure solutions can scale from tactical fixes to enterprise-grade applications when needed., • Bridge low-code solutions with broader ScaleOS and automation capabilities., • Identify whether a use case should be solved with Power Platform, require additional enterprise integration, or transition from low-code to pro-code development. Must-Have Competencies • Expert-level experience with Microsoft Power Platform (PowerApps, Power Automate, Power BI)., • Strong understanding of Dataverse, SharePoint, and Microsoft 365 ecosystem., • Experience designing and implementing Power Platform governance and security., • Proficiency in building complex workflows, custom connectors, and integrations., • Knowledge of Power Platform ALM (Application Lifecycle Management) and DevOps practices., • Understanding of API integrations and data connectivity patterns. Supporting Expectations / Nice to Have • Microsoft certifications (PL-100, PL-200, PL-400, PL-600)., • Experience with Copilot Studio and AI Builder., • Background in traditional software development (.NET, JavaScript)., • Experience with Power Platform Center of Excellence (CoE) toolkit., • Knowledge of other low-code platforms (Appian, OutSystems, Mendix)., • Experience in regulated environments (pharma, healthcare, life sciences), with awareness of compliance, data protection, and Responsible AI expectations. Core Enabling Skills • Ability to provide practical guidance to Citizen Developers when needed., • Strong communication skills to translate technical concepts for business users., • Patient and supportive approach when working with non-technical colleagues., • Proactive problem-solver with a service-oriented mindset., • Ability to balance governance requirements with business agility needs., • Ability to provide practical judgment during use case assessment and to advise stakeholders across the delivery process, while keeping hands-on solution development as the primary focus of the role. What do We offer • Permanent contract., • Flexible Schedule. We make it easy. Balance your professional and personal life., • Trainings & Certifications. Improve your skills and get the official certificate from our main partners., • Home Office., • Flexible retribution (public transport ticket, Ticket restaurant, …)., • Health insurance., • OMEGA in action. Our commitment to a better society is not just an intention. About us Omega CRM, a Merkle Company, is a global digital company specialising in accelerating the Business Experience (BX) of our clients through customer-centric solutions, technology, and data – all enhanced by AI. Together with Merkle, we form the largest Customer Experience Management (CXM) agency in Spain, and as part of the dentsu group, we offer end-to-end solutions that integrate media, creativity, content, technology, and strategy to deliver real business impact. With over 23 years of experience, a team of 580+ professionals from 24 nationalities, and 2,500+ certifications, Omega CRM is a recognised leader in the Salesforce ecosystem in Spain. We operate across key industries including Retail, Healthcare, Pharma, Real Estate, Education, and Non-Profit, delivering omnichannel experiences in Customer Service, eCommerce, Marketing, and Analytics. Client satisfaction is at our core (rating: 4.9/5), and we’ve been recognised with awards such as Salesforce Partner of the Year FY23 and Most Innovative Project (Iberia). At Omega CRM, we believe in growth through people – guided by our values: #Talent, #Flexibility, #Commitment, and #Innovation. We grow #Together.

AI search & content specialist: About this role This position will act as the internal subject-matter expert on SEO, GEO, and AI-driven discovery. Scilife is looking for a strategic, AI-forward content professional to lead our content presence across both traditional SEO and ai-powered search channels. As search behavior rapidly evolves with users increasingly turning to tools like ChatGPT, Perplexity, Google AI overviews, and Gemini for answers — we need a specialist who can ensure Scilife is visible, authoritative, and trusted in these new discovery surfaces. This role goes beyond traditional SEO. You will own our answer engine optimization (AEO) and generative engine optimization (GEO) strategy, shaping quarterly roadmaps that align content initiatives with broader business goals. You will develop and implement strategies that improve Scilife’s visibility within AI-generated results, answer engines, and entity-based discovery systems, aligning both content and technical structure to support AI-native search experiences. The goal is to make Scilife the go-to brand cited by AI tools when life sciences professionals search for quality management solutions. You will create structured, authoritative, AI-readable content that positions Scilife as a thought leader and drives organic brand recall across both human and machine audiences. This role is responsible to: • Own organic growth strategy across traditional search and AI-driven discovery (Google AI Overviews, LLMs, answer engines)., • Define and evolve GEO best practices to ensure brand visibility and citation in generative responses., • Establish standards for structured content (schema, summaries, FAQs, entities, metadata) optimized for AI consumption., • Translate shifts in search behavior (zero-click, AI summaries) into clear priorities and roadmaps that balance traditional SEO and GEO., • Work cross-functionally with different teams to align SEO with companywide business goals and objectives., • Responsible for growing new user acquisition and hitting core KPIs across traditional SEO, GEO and AEO., • Extensive knowledge of current SEO/GEO best practices with strong technical SEO/GEO background experience, • Utilize research tools to perform keyword gap analysis to support and prioritize keyword and content strategies., • Ability to monitor ongoing SEO site health and maintenance reports while translating insights into actionable tasks and projects, • Familiarity with SEO tools (Google Search Console, Semrush, etc.), • Ability to lead multiple projects simultaneously with strong prioritization skills, • Champion data-driven testing initiatives to identify opportunities and scale acquisition efficiently, • Develop analysis that provides conclusions into customer behavior and communicates those conclusions clearly with key stakeholders., • Provide insight-driven reporting that explains what happened, why it happened, and what to do next., • Evaluate and adapt strategies based on shifts in AI-generated search visibility and user interaction patterns. AEO / GEO & AI visibility • Develop and execute an answer engine optimization (AEO) and generative engine optimization (GEO) strategy to increase Scilife’s brand presence and citation frequency in AI-powered tools (ChatGPT, Perplexity, Google AI overviews, Gemini, Copilot, etc.)., • Conduct competitive benchmarking to understand how scilife appears vs. Competitors (e.g., Qualio, Mastercontrol, Greenlightguru, Veeva, etq) across AI-generated responses., • Identify and close content gaps that prevent Scilife from being surfaced by LLMs as the recommended eQMS solution for life sciences companies., • Implement structured data, FAQ schemas, and authoritative content formats optimized for AI parsing and citation., • Monitor brand mentions and citations in ai tools and establish a reporting framework to track LLM visibility over time. Content strategy & creation • Plan and execute a multi-channel content strategy aligned with AEO/GEO goals and broader marketing objectives., • Create high-quality, authoritative content (articles, whitepapers, landing pages, use cases, FAQs, glossaries) that establishes Scilife as a definitive source of truth in the eQMS and quality management space., • Optimize the existing content library for AI readability: clear structure, direct answers, entity coverage, and factual depth., • Manage the content calendar and ensure a consistent publishing cadence across the blog, website, and newsletters., • Collaborate with the design team and external contributors to deliver polished, on-brand content assets. Traditional SEO & search visibility • Maintain and improve organic search rankings through keyword research, on-page seo, and internal linking strategies., • Monitor search performance metrics and produce regular reports with actionable insights using tools such as google search console, semrush, or ahrefs., • Ensure all content is SEO-friendly, up-to-date, and aligned with current search intent and user behavior. Collaboration & process • Work closely with the brand manager, knowledge manager, and marketing teams to align content with business priorities., • Coordinate content approvals across stakeholders in a timely and organized manner., • Stay ahead of ai search trends, platform changes, and industry best practices, and proactively share insights with the broader team. Required skills & experience Core requirements • 4+ years of experience in content marketing, SEO, or digital content roles., • Demonstrated understanding of AEO / GEO concepts and how LLMs source and cite information., • Strong SEO fundamentals: keyword research, on-page optimization, technical SEO basics, and schema markup., • Excellent English writing and editing skills; ability to produce clear, authoritative, and engaging B2B content., • Proficiency with SEO analytics tools (google search console, semrush, or similar)., • Analytical mindset with the ability to translate data into content decisions and strategy. Nice to have • Experience with marketing automation tools (hubspot preferred)., • Experience in B2B SaaS, life sciences, or regulated industries (pharma, medtech, biotech)., • Familiarity with structured data, json-ld, and schema.org vocabulary., • Experience using AI tools (ChatGPT, Perplexity, Claude, etc.) As part of content research or production workflows., • Experience with Jira or similar project management and ticketing tools., • Comfort working in a fast-paced, international, and remote-first environment., • Experience of search planning fundamentals across Paid and Organic channels., • Familiarity with core PPC marketing principles and tools such as Google and Meta Ads Core competencies Candidates will be assessed against the following competencies during the hiring process and in periodic performance evaluations: • Strategic thinking, • AI & tech curiosity, • Content excellence, • Data-driven, • Creativity, • Collaborative, • Attention to detail, • Getting things done, • Communication, • Adaptability, • Time management, • Innovation Candidates will also be assessed against scilife’s core company values: • Healthy inside-out, • Outside of the box, • Driven by evidence, • All hearts and ears Why join Scilife? Scilife helps life science companies digitize, automate, and scale their quality and compliance processes. Our eQMS platform supports organizations worldwide in staying audit-ready while enabling innovation. We are in the early stages of an ambitious AI-first transformation. As our AI Search & Content Specialist, you will play a key role in shaping how Scilife brand appears in high-intent industry conversations, how we build topical authority, and how we position Scilife as a category-relevant voice in the future of quality management. You will join a collaborative, international, and fast-evolving company environment, working closely with the Brand team as well as cross-functional partners across marketing, sales, and customer successes teams. This is a role for someone who enjoys combining strategic thinking with hands-on execution, and who is excited by the opportunity to build new capabilities in a space that is still taking shape. At Scilife, you will find a team that values curiosity, ownership, fresh thinking, and meaningful collaboration. We care deeply about building work that is thoughtful, relevant, and impactful — and we are looking for someone who is energized by that kind of environment. If you are excited by the intersection of content, SEO, AI, and category building — and motivated by the chance to shape a capability that is still emerging — this role offers the opportunity to make a visible, strategic impact from day one. What we offer • Fully remote work within Europe with flexible hours., • Competitive compensation., • Collaborative, international team culture., • Continuous learning and professional development., • The chance to play a defining role in an emerging area of strategic importance for the company., • More info about benefits at Scilife.

SEARGIN IS HIRING! As a dynamic multinational tech company operating in 50 countries, we drive innovation and create projects that shape the future and greatly enhance the quality of life. You will find our solutions in the space industry, supporting scientists in the development of cancer drugs, and implementing innovative technological solutions for industrial clients worldwide. These are just some of the areas in which we operate! Currently, for the new Seargin project we are looking for SAP EWM Teach Lead. Location: Barcelona, hybrid Employment Type: B2B FTE: full-time Requirements: • EWM team Lead (+5 years),, • Multiple E2E SAP EWM deployments in team lead role,, • At least one E2E SAP EWM deployment in Pharma,, • Spanish language Responsibilities: • Leading the functional design and implementation of the SAP EWM solution replacing the current SAP WM module at Ferrer's Interquim site (Sant Cugat)., • End-to-end delivery of warehouse management processes including raw material receipt and labelling, location management across multiple warehouse types, supply to production and fractionation areas, semi-finished and finished product handling, repackaging order management, and outbound processes (picking, preparation, labelling)., • As-is analysis against written requirements (RFPURSWM), produces the functional design, ensures FDA compliance requirements are addressed, and oversees the implementation of GS1 label management in SAP., • Coordinating with the SAP EWM consultants, ABAP team, and client stakeholders, and is responsible for the quality of functional deliverables including training manuals and the support plan. Discover the Power of IT Excellence. Apply! To learn more about Seargin, please visit our web page: www.seargin.com

Consultor/a Funcional SAP S/4HANA O2C En Vortech PCI Group buscamos un/a Consultor/a Funcional SAP S/4HANA O2C para incorporarse a un proyecto en una compañía referente del sector alimentación. Buscamos una persona con experiencia en procesos Order to Cash, muy cercana a áreas de Customer Service, Order Management y Administración Comercial, que pueda ayudar a estabilizar la operativa diaria tras una migración a SAP S/4HANA. La posición combina soporte funcional, acompañamiento a usuarios y análisis de incidencias en procesos de pedidos, entregas, facturación, pricing, EDI/OCR y condiciones comerciales. ¿Cuál será tu rol? • Dar soporte funcional al equipo de Customer Service / Order Management., • Analizar incidencias relacionadas con pedidos, entregas, facturación y pricing., • Acompañar a usuarios de negocio en el uso de SAP S/4HANA., • Gestionar y hacer seguimiento de tickets con equipos IT/SAP., • Participar en pruebas, validaciones y mejoras de procesos., • Revisar flujos de entrada de pedidos por EDI/OCR., • Apoyar en procesos de facturación, abonos y condiciones comerciales., • Documentar procesos y formar usuarios/key users., • Actuar como nexo entre negocio, equipo local y equipos SAP/globales. No buscamos un perfil puramente técnico ni orientado solo a la parametrización. Buscamos una persona funcional, práctica y hands-on, con capacidad para trabajar cerca de usuarios y resolver problemas del día a día. ¿Qué buscamos? • Experiencia en SAP S/4HANA o SAP SD., • Conocimiento de procesos Order to Cash., • Experiencia en Customer Service, Order Management, Sales Administration o Administración Comercial., • Experiencia con pedidos, entregas, facturación, abonos/incidencias y pricing., • Conocimiento de EDI, IDocs, OCR o flujos automatizados de entrada de pedidos., • Capacidad para dar soporte funcional a usuarios de negocio., • Experiencia con tickets, pruebas, documentación o formación a usuarios., • Inglés funcional., • Español bilingüe o nativo., • Disponibilidad para modelo híbrido con presencialidad en Murcia/Alcantarilla. Valoraremos especialmente • Experiencia en alimentación, gran consumo, retail, distribución, industria o pharma., • Experiencia con gran distribución y acuerdos comerciales., • Conocimiento de condiciones fuera de factura, rappels, descuentos o promociones., • Experiencia con herramientas como Esker u otras soluciones OCR., • Conocimiento de Vistex o soluciones de Trade Promotion Management., • Participación en migraciones, rollouts o estabilizaciones post go-live de SAP S/4HANA., • Experiencia como key user, power user, business process expert o consultor/a funcional cercano/a a negocio. Modalidad • Modelo híbrido con presencialidad en la zona de Murcia/Alcantarilla., • Entorno SAP S/4HANA tras proceso de migración global., • Proyecto muy cercano a negocio y a procesos operativos reales., • Impacto directo en procesos críticos de Customer Service y Order to Cash. ¿Por qué puede interesarte? Es una oportunidad para trabajar en un entorno SAP S/4HANA con impacto directo en procesos clave de negocio: pedidos, facturación, pricing, EDI/OCR, acuerdos comerciales y soporte a usuarios. Si tienes experiencia en SAP S/4HANA, SAP SD, Order to Cash, Customer Service, Order Management, facturación, pricing o EDI, y te interesa un rol funcional muy cercano a negocio, queremos conocerte.