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Take your career to the next level with Amaris Consulting as a Validation Specialist (Test QA). Become part of an international team, thrive in a global group with €800M turnover and 1,000+ clients worldwide, and an agile environment by planning the kickoff and follow up on projects. Join Amaris Consulting, where you can develop your potential and make a difference within the company. WHAT WOULD YOU NEED? ✍️ • +3 years of senior experience in IT validation within GxP environments, • Implementation of CSV, • Proven expertise in Veeva Conformance and Validation Testing and W3C Validation, • Strong knowledge of pharma industry regulations and GxP compliance, • Experience with LeVA system life cycle documentation (VP, URS, FS, RA, Testing Reports, AAP), • Degree in Business Administration, Computer Science or comparable professional experience, • English fluency and Spanish 👉 WHAT WILL YOU DO? 👈 • Lead validation activities for global testing applications (BI-AS-ODIN, BI-IT-INMATION), • Ensure compliance with validation planning and applicable BI standards before system operation, • Develop and maintain system-specific SOPs and SLC documentation, • Manage validation status throughout system lifecycle and post-operation phases, • Create and deliver training on Standard Operating Procedures as defined in Validation Plans, • Coordinate with IT Operations & Laboratories teams on Manufacturing Connectivity projects 🚀 WHY US? 🚀 Join our dynamic team of talented individuals and experience a world of growth and opportunities. Here's what we offer: • Grow rapidly with a tailored career path and salary evaluation. 70% of our senior leaders started at entry level., • Enhance your skills through our Tech Academy catalog, Udemy E-learning Platform, Languages Sessions, webinars, and workshops., • Take charge of your training with an annual personal budget and company-paid certifications., • Enjoy flexible policies, remote work options, and fantastic social benefits like transit and restaurant tickets, kindergarten support, and private health insurance., • Benefit from our WeCare program, supporting employees in critical situations., • Unleash your full potential, both professionally and personally Amaris Consulting is proud to be an equal-opportunity workplace. We are committed to promoting diversity within the workforce and creating an inclusive working environment. For this purpose, we welcome applications from all qualified candidates regardless of gender, sexual orientation, race, ethnicity, beliefs, age, marital status, disability, or other characteristics.

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.

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

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.

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

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.

Study Coordinator – Clinical Trials (Fase III | Salud de la Mujer) 📍 Madrid 🗓 Inicio: Julio 2026 ⏳ 18 meses 💰 57.000€ En Insud Pharma, buscamos incorporar un/a Study Coordinator para un ensayo clínico fase III en el área de salud de la mujer. Formarás parte de un proyecto internacional con impacto real en la vida de las mujeres, dentro de un entorno colaborativo y dinámico. ¿Cuál será tu día a día? • Coordinación de visitas de pacientes y gestión del estudio (site management), • Introducción y validación de datos en eCRF, • Gestión documental (ISF, consentimientos informados, etc.), • Interacción con CRAs y equipo investigador, • Cumplimiento de GCP y protocolo 🎯 ¿Qué buscamos? • Experiencia en clinical trials (Study Coordinator o Data Entry), • Conocimiento de ICH-GCP, • Nivel de inglés medio-alto, • Perfil organizado, proactivo y detallista 💼 ¿Qué ofrecemos? • Contrato de 18 meses, • Salario: 57.000€ brutos (por la totalidad del tiempo), • Proyecto internacional fase III, • Excelente ambiente de trabajo, • Desarrollo y aprendizaje continuo 🚀 Si quieres seguir creciendo en investigación clínica, ¡nos encantará conocerte! COMMITMENT TO EQUAL OPPORTUNITIES The InsudPharma group is aware that business management must align with the needs and demands of society, and therefore assumes the commitment to equal opportunities and treatment between men and women, as stated in the current regulations on the matter - Organic Law 3/2007, and we do not discriminate against any person on the grounds of ethnicity, religion, age, sex, nationality, marital status, affective or sexual orientation, gender identity or expression, disability, or any other personal or social circumstance.

Proyecto y equipo Oportunidad para incorporarse a través de Tenth Revolution Group en un proyecto estratégico para una compañía global líder del sector pharma Trabajarás en un entorno internacional y 100% en inglés, participando en la gestión end-to-end de datos Salesforce y colaborando con stakeholders globales para asegurar reporting fiable, calidad de datos y automatización de procesos analíticos. El rol tendrá alta exposición a negocio y trabajará estrechamente con equipos globales en iniciativas relacionadas con CRM, reporting y mejora continua de procesos de datos. Responsabilidades / Funciones • Gestionar end-to-end datos de Salesforce utilizando SQL para extracción, validación y limpieza de datasets., • Garantizar calidad, consistencia y fiabilidad de datos para reporting y toma de decisiones., • Analizar estructuras y flujos de datos dentro de Salesforce para detectar inconsistencias y problemas de calidad., • Diseñar y mantener queries SQL y pipelines de datos para reporting recurrente, KPIs y análisis ad-hoc., • Colaborar con stakeholders para traducir necesidades de negocio en dashboards, reporting y modelos de datos., • Explicar estructura de datos, definición de KPIs y reporting a equipos de negocio., • Impulsar automatización y mejora de procesos relacionados con extracción y reporting de datos., • Inglés B2+ / C1 imprescindible (trabajo 100% en inglés). Ubicación + Modelo de Trabajo • 📍 Barcelona / alrededores, • 🏠 Modelo remoto — 80–90% remote, • Salario Atractivo y Competitivo segun experiencia del candidato

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

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

Study Coordinator – Clinical Trials (Fase III | Salud de la Mujer) 📍 Madrid 🗓 Inicio: Julio 2026 ⏳ 18 meses 💰 57.000€ En Insud Pharma, buscamos incorporar un/a Study Coordinator para un ensayo clínico fase III en el área de salud de la mujer. Formarás parte de un proyecto internacional con impacto real en la vida de las mujeres, dentro de un entorno colaborativo y dinámico. ¿Cuál será tu día a día? • Coordinación de visitas de pacientes y gestión del estudio (site management), • Introducción y validación de datos en eCRF, • Gestión documental (ISF, consentimientos informados, etc.), • Interacción con CRAs y equipo investigador, • Cumplimiento de GCP y protocolo 🎯 ¿Qué buscamos? • Experiencia en clinical trials (Study Coordinator o Data Entry), • Conocimiento de ICH-GCP, • Nivel de inglés medio-alto, • Perfil organizado, proactivo y detallista 💼 ¿Qué ofrecemos? • Contrato de 18 meses, • Salario: 57.000€ brutos (por la totalidad del tiempo), • Proyecto internacional fase III, • Excelente ambiente de trabajo, • Desarrollo y aprendizaje continuo 🚀 Si quieres seguir creciendo en investigación clínica, ¡nos encantará conocerte! COMMITMENT TO EQUAL OPPORTUNITIES The InsudPharma group is aware that business management must align with the needs and demands of society, and therefore assumes the commitment to equal opportunities and treatment between men and women, as stated in the current regulations on the matter - Organic Law 3/2007, and we do not discriminate against any person on the grounds of ethnicity, religion, age, sex, nationality, marital status, affective or sexual orientation, gender identity or expression, disability, or any other personal or social circumstance.

Omega CRM is a Merkle & Dentsu company, leader in development of Customer Experience services, with +20 years of experience in the use of Technology applied to Marketing and providing a unique Customer Relationship with mainly focus on Innovation is looking for a Senior Salesforce Developer. Responsibilities • Requirements analysis., • Participate in the technical design of projects., • Perform effort estimations for projects., • Work in coordination with the rest of the Omega team and/or the client to contribute to achieving project objectives., • Analyze and improve application performance., • Identify potential technical risks within the project and propose alternative solutions., • Collaborate with technology providers when required by the project., • Document processes and monitor system performance metrics., • Validate and test the technical solution against business requirements., • Train end users on the developed project functionality and proper use of the software., • Implement the latest technological advances and solutions., • Comply with software quality standards agreed upon with Omega’s Technical Management., • Produce technical documentation for completed projects., • Actively contribute to the training of other team members., • Collaborate within Omega’s community of practice by sharing technical knowledge., • Identify potential methodological improvements for the technical team. Knowledge / Experience • Degree in Computer Engineering or a similar technology-related field., • At least 3 years of experience as a Salesforce Developer., • Experience developing solutions on Sales Cloud and/or Service Cloud in the Salesforce ecosystem. Experience in other Salesforce clouds is a plus., • Knowledge of development technologies (APEX, Visualforce, LWC, migration tools, SOQL, web services)., • Understanding of both DevOps/Agile (SCRUM) and Waterfall delivery principles, as well as the importance of SDLC (Software Development Life Cycle) and coding methodology principles, is a plus., • Ability to work independently and take ownership of assigned applications., • Excellent spoken and written English., • Any Salesforce certification is a plus. 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.

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.

Take your career to the next level with Amaris Consulting as a Validation Specialist (Test QA). Become part of an international team, thrive in a global group with €800M turnover and 1,000+ clients worldwide, and an agile environment by planning the kickoff and follow up on projects. Join Amaris Consulting, where you can develop your potential and make a difference within the company. WHAT WOULD YOU NEED? ✍️ • +3 years of senior experience in IT validation within GxP environments, • Implementation of CSV, • Proven expertise in Veeva Conformance and Validation Testing and W3C Validation, • Strong knowledge of pharma industry regulations and GxP compliance, • Experience with LeVA system life cycle documentation (VP, URS, FS, RA, Testing Reports, AAP), • Degree in Business Administration, Computer Science or comparable professional experience, • English fluency and Spanish 👉 WHAT WILL YOU DO? 👈 • Lead validation activities for global testing applications (BI-AS-ODIN, BI-IT-INMATION), • Ensure compliance with validation planning and applicable BI standards before system operation, • Develop and maintain system-specific SOPs and SLC documentation, • Manage validation status throughout system lifecycle and post-operation phases, • Create and deliver training on Standard Operating Procedures as defined in Validation Plans, • Coordinate with IT Operations & Laboratories teams on Manufacturing Connectivity projects 🚀 WHY US? 🚀 Join our dynamic team of talented individuals and experience a world of growth and opportunities. Here's what we offer: • Grow rapidly with a tailored career path and salary evaluation. 70% of our senior leaders started at entry level., • Enhance your skills through our Tech Academy catalog, Udemy E-learning Platform, Languages Sessions, webinars, and workshops., • Take charge of your training with an annual personal budget and company-paid certifications., • Enjoy flexible policies, remote work options, and fantastic social benefits like transit and restaurant tickets, kindergarten support, and private health insurance., • Benefit from our WeCare program, supporting employees in critical situations., • Unleash your full potential, both professionally and personally Amaris Consulting is proud to be an equal-opportunity workplace. We are committed to promoting diversity within the workforce and creating an inclusive working environment. For this purpose, we welcome applications from all qualified candidates regardless of gender, sexual orientation, race, ethnicity, beliefs, age, marital status, disability, or other characteristics.

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

Study Coordinator – Clinical Trials (Fase III | Salud de la Mujer) 📍 Madrid 🗓 Inicio: Julio 2026 ⏳ 18 meses 💰 57.000€ En Insud Pharma, buscamos incorporar un/a Study Coordinator para un ensayo clínico fase III en el área de salud de la mujer. Formarás parte de un proyecto internacional con impacto real en la vida de las mujeres, dentro de un entorno colaborativo y dinámico. ¿Cuál será tu día a día? • Coordinación de visitas de pacientes y gestión del estudio (site management), • Introducción y validación de datos en eCRF, • Gestión documental (ISF, consentimientos informados, etc.), • Interacción con CRAs y equipo investigador, • Cumplimiento de GCP y protocolo 🎯 ¿Qué buscamos? • Experiencia en clinical trials (Study Coordinator o Data Entry), • Conocimiento de ICH-GCP, • Nivel de inglés medio-alto, • Perfil organizado, proactivo y detallista 💼 ¿Qué ofrecemos? • Contrato de 18 meses, • Salario: 57.000€ brutos (por la totalidad del tiempo), • Proyecto internacional fase III, • Excelente ambiente de trabajo, • Desarrollo y aprendizaje continuo 🚀 Si quieres seguir creciendo en investigación clínica, ¡nos encantará conocerte! COMMITMENT TO EQUAL OPPORTUNITIES The InsudPharma group is aware that business management must align with the needs and demands of society, and therefore assumes the commitment to equal opportunities and treatment between men and women, as stated in the current regulations on the matter - Organic Law 3/2007, and we do not discriminate against any person on the grounds of ethnicity, religion, age, sex, nationality, marital status, affective or sexual orientation, gender identity or expression, disability, or any other personal or social circumstance.

Omega CRM Consulting is looking for a Veeva System Lead that would like to collaborate with one of the top global pharmaceutical companies. Description • Manage system throughout its whole lifecycle and complete its Compliance documentation, • Coordinating and scheduling backup/recovery & Performing Disaster Recovery Testing, • Service Level Agreement, Mean Time to Resolve, Audit trail, Access & identity monitoring, • Coordinating (but not performing) server, database patches and resolving vulnerabilities, • Coordinating software management:, • Patching / Packaging / Testing / License management / Small enhancements/configuration changes, • Interfacing/Coordinate with multiple areas of the business and IT (Functional Areas & Infrastructure):, • Interfaces to IT SME, IT Capability leads and to other internal stakeholders (e.g. HR, Finance) as well as external stakeholders (vendors, academia, healthcare companies, etc.). Interfaces to/SPOC for the broader IT organization acting in a coordination role., • Performing Incident, Problem for issue resolution and Change Management, • Working with IT Infrastructure to remediate replace migrate or decommission systems (Including legacy systems and coordinating System Archiving) or infrastructure items Skills & Experience • Must have at least 5 years experience in Salesforce or Veeva CRM platforms., • Experience for the following technology/platform experience is a plus, • Vault CRM, JIRA, Confluence, Jenkins, AWS, Azure, ServiceNow, API, • A demonstrated understanding of Operational Excellence ITIL v3.0 or higher Fundamentals Certification Nice to have: • Must be bachelor’s degree in IT or similar, • Must be customer oriented, well organized and methodical, • Must have excellent communication skills both written & verbal, • Must be able to work successfully on a team, • Must have Excellent English speaking, reading & writing skills, • other languages such as German, Japanese, Mandarin, Spanish a plus, • must be able to present information effectively, • Must have demonstrated understanding and experience with Infrastructure topics such as databases, servers, cloud systems, networking etc 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.

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.

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.

En pocas palabras 📌 Posición: Data Analyst Localización: Madrid Experiencia: 2–3 años ¿Quieres saber más? 👇 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. ¿Te interesa un rol donde puedas combinar datos, estrategia y negocio con impacto real en la toma de decisiones? Esta oportunidad puede ser para ti 💪 En INSUD buscamos un/a Data Analyst para apoyar al Head of Portfolio Management y al Director de BD & Portfolio en la identificación, análisis y priorización de nuevas oportunidades de producto, tanto en genéricos como en productos innovadores. Tendrás un papel clave en la generación de insights estratégicos, contribuyendo directamente al desarrollo del pipeline y al crecimiento del negocio. ¿Qué buscamos? 🔎 Una persona analítica, con sólida base técnica en datos y orientación a negocio, capaz de transformar información compleja en insights accionables. ¡El reto! 🚀 • Diseñar y mantener procesos de ETL y automatización de datos., • Integrar, transformar y estandarizar información de mercado, competencia y datos internos., • Optimizar consultas SQL y estructuras de datos., • Construir y mantener KPIs, benchmarks y dashboards para Portfolio y BD., • Realizar análisis estratégicos y cuantitativos para evaluar oportunidades de producto., • Monitorizar competidores y tendencias del mercado farmacéutico., • Traducir necesidades de negocio en soluciones técnicas escalables., • Colaborar con equipos técnicos y de negocio en proyectos estratégicos. ¿Qué necesitas? 🤓 • 2–3 años de experiencia en roles de datos, backend o análisis estratégico., • Experiencia sólida en Python y SQL avanzado., • Experiencia en procesos ETL y automatización de flujos de datos., • Familiaridad con Git y entornos colaborativos., • Alta capacidad analítica y orientación a negocio., • Capacidad para comunicarte con perfiles no técnicos. Se valorará especialmente ✅ • Experiencia en farma o healthcare., • Conocimiento de datos de mercado: ventas, cuotas y competencia., • Experiencia con Docker u otras herramientas de despliegue., • Interés en arquitectura de datos moderna y escalabilidad., • Conocimientos de arquitectura de proyecto., • Conocimientos de HTML. ¡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 email., • Entrevistas con el equipo de selección y Hiring Manager., • Comunicación y seguimiento durante el proceso. 🔷¿Crees que esta oferta no es para ti? 🔷 Síguenos en LinkedIn e Instagram para conocer nuevas oportunidades. #InsudPharma #Challenger #Insuder #InsudTalent COMPROMISO CON LA IGUALDAD DE OPORTUNIDADES En INSUD PHARMA promovemos la igualdad de oportunidades y la no discriminación. Valoramos todas las candidaturas sin distinción de género, origen étnico, religión, orientación sexual, discapacidad, edad u otra condición personal o social protegida por la legislación vigente.

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.

Omega CRM is a Merkle & Dentsu company, leader in development of Customer Experience services, with +20 years of experience in the use of Technology applied to Marketing and providing a unique Customer Relationship with mainly focus on Innovation is looking for a Senior Salesforce Developer. Responsibilities • Requirements analysis., • Participate in the technical design of projects., • Perform effort estimations for projects., • Work in coordination with the rest of the Omega team and/or the client to contribute to achieving project objectives., • Analyze and improve application performance., • Identify potential technical risks within the project and propose alternative solutions., • Collaborate with technology providers when required by the project., • Document processes and monitor system performance metrics., • Validate and test the technical solution against business requirements., • Train end users on the developed project functionality and proper use of the software., • Implement the latest technological advances and solutions., • Comply with software quality standards agreed upon with Omega’s Technical Management., • Produce technical documentation for completed projects., • Actively contribute to the training of other team members., • Collaborate within Omega’s community of practice by sharing technical knowledge., • Identify potential methodological improvements for the technical team. Knowledge / Experience • Degree in Computer Engineering or a similar technology-related field., • At least 3 years of experience as a Salesforce Developer., • Experience developing solutions on Sales Cloud and/or Service Cloud in the Salesforce ecosystem. Experience in other Salesforce clouds is a plus., • Knowledge of development technologies (APEX, Visualforce, LWC, migration tools, SOQL, web services)., • Understanding of both DevOps/Agile (SCRUM) and Waterfall delivery principles, as well as the importance of SDLC (Software Development Life Cycle) and coding methodology principles, is a plus., • Ability to work independently and take ownership of assigned applications., • Excellent spoken and written English., • Any Salesforce certification is a plus. 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.

In a nutshell 📌 Position: Regulatory Affairs Manager - Biosimilars Location: Madrid (on-site) Experience: 5+ years in Regulatory Affairs within biotech/biopharma Want to know more? 👇 INSUD PHARMA operates across the entire pharmaceutical value chain, bringing specialist knowledge and experience in scientific research, development, manufacturing, sales, and commercialization of a broad range of active pharmaceutical ingredients (API), finished dosage forms (FDF), and branded pharmaceutical products, adding value in both human and animal health. Our activities are organized in three synergistic business areas: Industrial (Chemo), Branded (Exeltis), and Biotech (mAbxience), with over 9,000 professionals in more than 50 countries. We are committed to innovation and sustainable development to deliver solutions that positively impact global health. Ready to be a #Challenger at INSUD PHARMA? 💪 What are we looking for? 🔎 We are seeking a Regulatory Affairs Manager to lead the regulatory strategy for our innovative and biosimilar products, ensuring compliance and collaborating with global, cross-functional teams. Key Responsibilities: • Monitor changes in the regulatory landscape, identify their impact, and propose solutions to maintain compliance., • Define regulatory strategy for each product in coordination with Management and Business teams., • Build strong collaborative partnerships with internal and external teams to ensure organizational success and patient safety., • Identify and mitigate regulatory risks, adapting strategies to evolving regulations and Health Authority feedback., • Interpret and communicate legislative changes that affect product registration, manufacturing, or development., • Support the review of license and quality agreements for targeted geographies., • Lead engagement with Health Authorities during Scientific Advice procedures and responses to deficiency letters., • Prepare, review, and approve regulatory submission documents (briefing packages, IBs, INDs, CTAs, MAAs, etc.)., • Manage external consultants and vendors for regulatory activities., • Support product launch activities, ensuring regulatory risks are managed with appropriate action plans., • Organize the regulatory submission schedule and coordinate with Regulatory Affairs teams., • Participate in product plan development, regulatory strategy, and CMC documentation., • Drive digitalization and the use of computerized systems within the department. The challenge! 🚀 • Oversee the preparation and submission of regulatory documentation., • Coordinate regulatory strategy with R&D, QA, QC, and Production teams., • Lead negotiations and presentations with regulatory agencies., • Manage regulatory information and ensure data integrity., • Actively participate in scientific committees and project teams. What do you need? 🤓 • University degree in Health Sciences (preferably Pharmacy; degrees in Chemistry, Biology, Biochemistry, Veterinary or similar will also be considered)., • 5+ years of experience in Regulatory Affairs within biotechnology, biopharma, or biosimilars., • In-depth knowledge of pharmaceutical legislation, GMP, and ICH guidelines., • Fluent in Spanish and English (other languages are a plus)., • Advanced skills in Microsoft Office (Word, Excel, PowerPoint, Project) and regulatory software., • Willingness to travel., • Inspiring, influential, results-oriented with excellent communication skills. Our benefits! 👏 📜 Permanent contract 🎯 Professional development & continuous training 🌍 International and multidisciplinary environment 🏆 Innovative projects with high impact on health What’s the selection process like? 🕵️ • Initial contact by phone or email., • 1–2 interviews (virtual and/or on-site) with HR and technical teams., • Ongoing updates throughout your recruitment process. 🔷 Not the right fit for you? 🔷 Follow us on LinkedIn to stay updated on future opportunities and news from INSUD PHARMA. We’d love to connect! #InsudPharma #Challenger #Insuder #InsudTalent COMMITMENT TO EQUAL OPPORTUNITIES At INSUD PHARMA, we promote gender equality and do not discriminate based on ethnicity, religion, sexual orientation, disability, or any other condition. We firmly believe that diversity and talent drive innovation and growth.

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.

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

Omega CRM Consulting is looking for a Veeva System Lead that would like to collaborate with one of the top global pharmaceutical companies. Description • Manage system throughout its whole lifecycle and complete its Compliance documentation, • Coordinating and scheduling backup/recovery & Performing Disaster Recovery Testing, • Service Level Agreement, Mean Time to Resolve, Audit trail, Access & identity monitoring, • Coordinating (but not performing) server, database patches and resolving vulnerabilities, • Coordinating software management:, • Patching / Packaging / Testing / License management / Small enhancements/configuration changes, • Interfacing/Coordinate with multiple areas of the business and IT (Functional Areas & Infrastructure):, • Interfaces to IT SME, IT Capability leads and to other internal stakeholders (e.g. HR, Finance) as well as external stakeholders (vendors, academia, healthcare companies, etc.). Interfaces to/SPOC for the broader IT organization acting in a coordination role., • Performing Incident, Problem for issue resolution and Change Management, • Working with IT Infrastructure to remediate replace migrate or decommission systems (Including legacy systems and coordinating System Archiving) or infrastructure items Skills & Experience • Must have at least 5 years experience in Salesforce or Veeva CRM platforms., • Experience for the following technology/platform experience is a plus, • Vault CRM, JIRA, Confluence, Jenkins, AWS, Azure, ServiceNow, API, • A demonstrated understanding of Operational Excellence ITIL v3.0 or higher Fundamentals Certification Nice to have: • Must be bachelor’s degree in IT or similar, • Must be customer oriented, well organized and methodical, • Must have excellent communication skills both written & verbal, • Must be able to work successfully on a team, • Must have Excellent English speaking, reading & writing skills, • other languages such as German, Japanese, Mandarin, Spanish a plus, • must be able to present information effectively, • Must have demonstrated understanding and experience with Infrastructure topics such as databases, servers, cloud systems, networking etc 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.

En pocas palabras 📌 Posición: Data Analyst Localización: Madrid Experiencia: 2–3 años ¿Quieres saber más? 👇 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. ¿Te interesa un rol donde puedas combinar datos, estrategia y negocio con impacto real en la toma de decisiones? Esta oportunidad puede ser para ti 💪 En INSUD buscamos un/a Data Analyst para apoyar al Head of Portfolio Management y al Director de BD & Portfolio en la identificación, análisis y priorización de nuevas oportunidades de producto, tanto en genéricos como en productos innovadores. Tendrás un papel clave en la generación de insights estratégicos, contribuyendo directamente al desarrollo del pipeline y al crecimiento del negocio. ¿Qué buscamos? 🔎 Una persona analítica, con sólida base técnica en datos y orientación a negocio, capaz de transformar información compleja en insights accionables. ¡El reto! 🚀 • Diseñar y mantener procesos de ETL y automatización de datos., • Integrar, transformar y estandarizar información de mercado, competencia y datos internos., • Optimizar consultas SQL y estructuras de datos., • Construir y mantener KPIs, benchmarks y dashboards para Portfolio y BD., • Realizar análisis estratégicos y cuantitativos para evaluar oportunidades de producto., • Monitorizar competidores y tendencias del mercado farmacéutico., • Traducir necesidades de negocio en soluciones técnicas escalables., • Colaborar con equipos técnicos y de negocio en proyectos estratégicos. ¿Qué necesitas? 🤓 • 2–3 años de experiencia en roles de datos, backend o análisis estratégico., • Experiencia sólida en Python y SQL avanzado., • Experiencia en procesos ETL y automatización de flujos de datos., • Familiaridad con Git y entornos colaborativos., • Alta capacidad analítica y orientación a negocio., • Capacidad para comunicarte con perfiles no técnicos. Se valorará especialmente ✅ • Experiencia en farma o healthcare., • Conocimiento de datos de mercado: ventas, cuotas y competencia., • Experiencia con Docker u otras herramientas de despliegue., • Interés en arquitectura de datos moderna y escalabilidad., • Conocimientos de arquitectura de proyecto., • Conocimientos de HTML. ¡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 email., • Entrevistas con el equipo de selección y Hiring Manager., • Comunicación y seguimiento durante el proceso. 🔷¿Crees que esta oferta no es para ti? 🔷 Síguenos en LinkedIn e Instagram para conocer nuevas oportunidades. #InsudPharma #Challenger #Insuder #InsudTalent COMPROMISO CON LA IGUALDAD DE OPORTUNIDADES En INSUD PHARMA promovemos la igualdad de oportunidades y la no discriminación. Valoramos todas las candidaturas sin distinción de género, origen étnico, religión, orientación sexual, discapacidad, edad u otra condición personal o social protegida por la legislación vigente.

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

Senior Data Engineer In a few words • Position: Senior Data Engineer – AI Labs at Insud Pharma, • Location: Madrid (hybrid), • Experience: 5+ years in Data Engineering or Analytics Engineering roles About AI Labs at Insud Pharma 👇 AI Labs is Insud Pharma’s transversal team for Artificial Intelligence, Data Science, and Machine Learning, working across the group to deliver production‑ready data and AI solutions with real impact. The team operates across a wide range of areas, including R&D and clinical data, global health and epidemiology, manufacturing and quality, supply chain and operations, and business analytics, partnering closely with business units, and external organizations. AI Labs combines strong engineering standards with pragmatic execution, focusing on building scalable AI‑enabled solutions that move from experimentation to real‑world adoption. Role Context This role will be primarily focused on projects linked to Fundación Mundo Sano, an international organization dedicated to improving health and quality of life for vulnerable communities through research, innovation, and international cooperation (e.g. neglected diseases such as Chagas). The goal of this position is to ensure that data coming from multiple sources becomes available, consistent, reliable, and reusable, enabling dashboards, reporting, and AI/ML use cases. Due to the international nature of the projects, the role may involve occasional travel to Latin America, Africa, or other regions to work closely with local teams and better understand data generation on the ground. Role Objective Build and operate a coherent, well‑structured data foundation for Fundación Mundo Sano projects by owning the data engineering layer end‑to‑end: ingestion, modeling, data quality, availability, monitoring, and data delivery for dashboards and AI enablement. Key Responsibilities • Build and operate data ingestion pipelines (ETL/ELT) from multiple sources (field programs, research datasets, epidemiological surveillance systems, partners, files, APIs)., • Design and maintain data models and curated datasets that standardize entities, metrics, and definitions across projects., • Ensure data quality, reliability, and consistency through automated checks, monitoring, and basic observability., • Decide how data is structured, stored, and versioned to enable long‑term reuse and scalability., • Make data available and easy to consume for dashboards, reporting, and AI/ML use cases., • Proactively guide business and project teams on data best practices, setting standards, shaping requirements, and influencing how data should be collected, structured, and used., • Collaborate closely with stakeholders to translate needs into scalable, maintainable data foundations. Technologies (examples – adapt to actual stack) • Languages: SQL, Python, • Pipelines / orchestration: Airflow, Prefect, Dagster or similar, • Transformations: dbt or equivalent, • Storage: Data warehouse / lakehouse (e.g. Snowflake, BigQuery, Databricks, Synapse), • Data quality / monitoring: Great Expectations, Soda, or similar, • BI / Dashboards: Power BI, Tableau, Looker or similar, • Engineering basics: Git, CI/CD, basic cloud concepts (AWS / Azure / GCP) What we are looking for • A senior, hands‑on Data Engineer with a strong ownership mindset, comfortable building and operating core data structures and pipelines., • 5+ years of experience in Data Engineering or Analytics Engineering roles., • Strong SQL and solid Python, with hands‑on experience building and running ETL/ELT pipelines in production., • Proven experience integrating heterogeneous and diverse data sources (multiple systems, files, APIs, changing schemas, inconsistent identifiers)., • Good understanding of data modeling and analytical data structures, with the ability to standardize entities, metrics, and definitions across projects., • Experience ensuring data quality, reliability, and monitoring, including automated checks and basic observability., • Comfortable making data available for dashboards, reporting, and AI/ML use cases through curated, analytics‑ready datasets., • Able to work proactively with business and project teams, shaping requirements and setting data standards rather than waiting for fully specified inputs., • Spanish as the daily working language; English required for specific projects and international collaboration., • Pragmatic, ownership‑driven mindset, strong communication skills, and motivation to work on social and public‑health impact projects. Our benefits! ⏰ Flexible start time from Monday to Friday 📜 Permanent contract. 🥼 Life and accident insurance. 🍽️ Ticket restaurant 💻 Training and language learning platform 💆🏻 ♀️ Wellness platform with unlimited free psychologist sessions 🚕 Cabify transportation service for employee use 📈 Development plans, internal mobility policy. ⭐ Many more! COMMITMENT TO EQUAL OPPORTUNITIES The InsudPharma group is aware that business management must align with the needs and demands of society, and therefore assumes the commitment to equal opportunities and treatment between men and women, as stated in the current regulations on the matter - Organic Law 3/2007, and we do not discriminate against any person on the grounds of ethnicity, religion, age, sex, nationality, marital status, affective or sexual orientation, gender identity or expression, disability, or any other personal or social circumstance.

In a nutshell 📌 Position: Regulatory Affairs Manager - Biosimilars Location: Madrid (on-site) Experience: 5+ years in Regulatory Affairs within biotech/biopharma Want to know more? 👇 INSUD PHARMA operates across the entire pharmaceutical value chain, bringing specialist knowledge and experience in scientific research, development, manufacturing, sales, and commercialization of a broad range of active pharmaceutical ingredients (API), finished dosage forms (FDF), and branded pharmaceutical products, adding value in both human and animal health. Our activities are organized in three synergistic business areas: Industrial (Chemo), Branded (Exeltis), and Biotech (mAbxience), with over 9,000 professionals in more than 50 countries. We are committed to innovation and sustainable development to deliver solutions that positively impact global health. Ready to be a #Challenger at INSUD PHARMA? 💪 What are we looking for? 🔎 We are seeking a Regulatory Affairs Manager to lead the regulatory strategy for our innovative and biosimilar products, ensuring compliance and collaborating with global, cross-functional teams. Key Responsibilities: • Monitor changes in the regulatory landscape, identify their impact, and propose solutions to maintain compliance., • Define regulatory strategy for each product in coordination with Management and Business teams., • Build strong collaborative partnerships with internal and external teams to ensure organizational success and patient safety., • Identify and mitigate regulatory risks, adapting strategies to evolving regulations and Health Authority feedback., • Interpret and communicate legislative changes that affect product registration, manufacturing, or development., • Support the review of license and quality agreements for targeted geographies., • Lead engagement with Health Authorities during Scientific Advice procedures and responses to deficiency letters., • Prepare, review, and approve regulatory submission documents (briefing packages, IBs, INDs, CTAs, MAAs, etc.)., • Manage external consultants and vendors for regulatory activities., • Support product launch activities, ensuring regulatory risks are managed with appropriate action plans., • Organize the regulatory submission schedule and coordinate with Regulatory Affairs teams., • Participate in product plan development, regulatory strategy, and CMC documentation., • Drive digitalization and the use of computerized systems within the department. The challenge! 🚀 • Oversee the preparation and submission of regulatory documentation., • Coordinate regulatory strategy with R&D, QA, QC, and Production teams., • Lead negotiations and presentations with regulatory agencies., • Manage regulatory information and ensure data integrity., • Actively participate in scientific committees and project teams. What do you need? 🤓 • University degree in Health Sciences (preferably Pharmacy; degrees in Chemistry, Biology, Biochemistry, Veterinary or similar will also be considered)., • 5+ years of experience in Regulatory Affairs within biotechnology, biopharma, or biosimilars., • In-depth knowledge of pharmaceutical legislation, GMP, and ICH guidelines., • Fluent in Spanish and English (other languages are a plus)., • Advanced skills in Microsoft Office (Word, Excel, PowerPoint, Project) and regulatory software., • Willingness to travel., • Inspiring, influential, results-oriented with excellent communication skills. Our benefits! 👏 📜 Permanent contract 🎯 Professional development & continuous training 🌍 International and multidisciplinary environment 🏆 Innovative projects with high impact on health What’s the selection process like? 🕵️ • Initial contact by phone or email., • 1–2 interviews (virtual and/or on-site) with HR and technical teams., • Ongoing updates throughout your recruitment process. 🔷 Not the right fit for you? 🔷 Follow us on LinkedIn to stay updated on future opportunities and news from INSUD PHARMA. We’d love to connect! #InsudPharma #Challenger #Insuder #InsudTalent COMMITMENT TO EQUAL OPPORTUNITIES At INSUD PHARMA, we promote gender equality and do not discriminate based on ethnicity, religion, sexual orientation, disability, or any other condition. We firmly believe that diversity and talent drive innovation and growth.

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.

About us For more than 25 years, our global network of passionate technologists and pioneering craftspeople has delivered cutting-edge technology and game-changing consulting to companies on the brink of AI driven digital transformation. Since 2001, we have grown into a full service digital consulting company with 6000+ professionals working on a worldwide ambition. Driven by the desire to make a difference, we keep innovating. Fuelling the growth of our company with our knowledge worker culture. When teaming up with Xebia, expect in-depth expertise based on an authentic, value-led, and high quality way of working that inspires all we do. At Xebia, we put ‘People First’—committed to attracting diverse talent and fostering an inclusive, respectful workplace where everyone is valued for their contributions. We welcome all individuals and evaluate solely on the quality of their work and teamwork. About the role We’re looking for a Senior Technical Project Manager to lead complex R&D delivery initiatives for a global pharmaceutical client. This role combines strategic delivery leadership, technical depth, and multi-vendor coordination across AI/ML platforms, data engineering, scientific applications, and HPC environments. What You’ll Do • Lead large cross-functional programs across engineering, data, infrastructure, and platform teams, • Drive end-to-end delivery from planning through launch and operational handoff, • Manage dependencies, risks, governance checkpoints, and stakeholder communications, • Coordinate distributed teams and external vendors in hybrid Agile/Waterfall environments, • Partner closely with engineering teams on architecture, cloud, and platform delivery decisions, • Use Jira, Confluence, Gemini Pro, and Atlassian AI to improve delivery forecasting and reporting What We’re Looking For • 8+ years of technical project/program management experience, • Strong background in Agile delivery, dependency management, and stakeholder leadership, • Experience with cloud platforms (GCP preferred), AI/ML systems, data platforms, and HPC environments, • Pharmaceutical/life sciences experience and familiarity with regulated environments (GxP, 21 CFR Part 11), • Excellent communication, escalation management, and executive reporting skills Nice to Have • PMP, Scrum, PRINCE2, or cloud certifications, • Experience with Kubernetes, CI/CD, MLOps, or scientific computing workflows, • Track record delivering large-scale platform transformations and multi-vendor programs Why Join Us • Lead high-impact digital transformation initiatives in pharma R&D, • Work on cutting-edge AI/ML, cloud, and scientific computing platforms, • Gain executive visibility and influence strategic delivery decisions, • Help shape AI-powered project management practices at scale

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

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.

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.

About us For more than 25 years, our global network of passionate technologists and pioneering craftspeople has delivered cutting-edge technology and game-changing consulting to companies on the brink of AI driven digital transformation. Since 2001, we have grown into a full service digital consulting company with 6000+ professionals working on a worldwide ambition. Driven by the desire to make a difference, we keep innovating. Fuelling the growth of our company with our knowledge worker culture. When teaming up with Xebia, expect in-depth expertise based on an authentic, value-led, and high quality way of working that inspires all we do. At Xebia, we put ‘People First’—committed to attracting diverse talent and fostering an inclusive, respectful workplace where everyone is valued for their contributions. We welcome all individuals and evaluate solely on the quality of their work and teamwork. About the role We’re looking for a Senior Technical Project Manager to lead complex R&D delivery initiatives for a global pharmaceutical client. This role combines strategic delivery leadership, technical depth, and multi-vendor coordination across AI/ML platforms, data engineering, scientific applications, and HPC environments. What You’ll Do • Lead large cross-functional programs across engineering, data, infrastructure, and platform teams, • Drive end-to-end delivery from planning through launch and operational handoff, • Manage dependencies, risks, governance checkpoints, and stakeholder communications, • Coordinate distributed teams and external vendors in hybrid Agile/Waterfall environments, • Partner closely with engineering teams on architecture, cloud, and platform delivery decisions, • Use Jira, Confluence, Gemini Pro, and Atlassian AI to improve delivery forecasting and reporting What We’re Looking For • 8+ years of technical project/program management experience, • Strong background in Agile delivery, dependency management, and stakeholder leadership, • Experience with cloud platforms (GCP preferred), AI/ML systems, data platforms, and HPC environments, • Pharmaceutical/life sciences experience and familiarity with regulated environments (GxP, 21 CFR Part 11), • Excellent communication, escalation management, and executive reporting skills Nice to Have • PMP, Scrum, PRINCE2, or cloud certifications, • Experience with Kubernetes, CI/CD, MLOps, or scientific computing workflows, • Track record delivering large-scale platform transformations and multi-vendor programs Why Join Us • Lead high-impact digital transformation initiatives in pharma R&D, • Work on cutting-edge AI/ML, cloud, and scientific computing platforms, • Gain executive visibility and influence strategic delivery decisions, • Help shape AI-powered project management practices at scale

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.

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 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

Omega CRM is a Merkle & Dentsu company, leader in development of Customer Experience services, with +20 years of experience in the use of Technology applied to Marketing and providing a unique Customer Relationship with mainly focus on Innovation is looking for a Salesforce Client Lead (Health & Life Sciences) to continue developing interactions with our customers throughout their Customer Journey Map, ensuring to increase their satisfaction and loyalty to the brand. The Client Lead is responsible for managing client interactions throughout their Customer Journey Map, ensuring increased satisfaction and loyalty to the brand. They possess knowledge and experience in the sales process, excelling in lead generation, relationship building, and deal closing. They achieve company goals through effective planning, setting sales targets, performance data analysis, and projecting future performance. They generate leads, build, and nurture client relationships. Additionally, they collaborate with a group of PMs to ensure the evolution and success of the projects under their responsibility at the delivery level. They support the roles involved in the various project stages to meet client and company expectations regarding quality and profitability, identifying potential gaps, anticipating issues related to the team, solution, or client, and proposing the best solutions. • For existing clients, the focus is on continuously offering new ways for the client to gain value from the product/service, leading consultancy sessions for future needs., • Lead the negotiation, preparation, and presentation of commercial offers for assigned accounts and manage communication with the client throughout the presales process, even when other teams are involved., • Share the client’s sales strategy, objectives, and digital transformation roadmap with the PMs of their assigned accounts, paying special attention when multiple PMs are working on one account., • Collaborate with the PM/DM throughout the project, attending progress demos, management committees, and resolving client-related issues., • Manage and negotiate scope expansions related to initial contracts., • Monitor the progress of projects within assigned accounts, paying special attention to potential budget and timeline deviations., • Identify possible Up & Cross-Selling opportunities for the account. Along with the PMs, they work post-project to identify successful and unsuccessful project elements., • Lead the end-of-project retrospective with the client, reviewing the overall experience, evaluating goal achievement, and exploring potential future developments., • Write success stories and send satisfaction surveys to the client., • The Client Lead is familiar with all operational team members: their experience, skills, and professional motivation., • Collaborate with PMs on team allocation for new or ongoing projects, taking into account both project profitability objectives and the best fit for the professional development of the individuals., • Use workload tracking tools and meet periodically with team members to ensure commitment and satisfaction with assignments., • Communicate the needs of the new team. If necessary, they communicate hiring needs to HR., • Aware of project progress and contribute to meeting deadlines, scope, and budget., • Alert operations management about potential delivery deviations and propose and collaborate on risk mitigation plans. Experience and Skills: • Large account management experience in the health sector., • Experience with IQVIA OCE or Veeva solutions is a plus., • Experience in Salesforce ecosystem., • At least, 6 years of previous experience in business /technology consulting, • Previous experience in Project Management, • Experience in digital projects, • Experience in international projects., • High level of English. Other European languages is a plus. WHAT DO WE OFFER • Permanent contract., • Flexible Schedule. We make it easy. Balance your professional and personal life., • Certifications plan. Improve your skills and get the official certificate from our main partners., • Home Office. You decide and we support you., • Flexible retribution (public transport ticket, Ticket restaurtant, …)., • Health insurance., • OMEGA in action. Our commitment to a better society is not just an intention, • Professional development: Evolve, grow and get where you want to go. 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.

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.

Our client is a digital platform that enables brands to connect directly with consumers through omnichannel promotional campaigns. Its main focus is to facilitate the collection of first-party data and enhance direct communication between brands and shoppers. This is achieved through personalized promotions, refunds, and other mechanics that strengthen the brand-shopper relationship. We offer Digital Marketing (Strategies to improve the online presence of brands), Omnichannel Promotions (Campaigns that integrate multiple channels to maximize reach), Data Collection (Gathering and analyzing consumer data to optimize marketing strategies) and Direct Communication (Tools to establish direct and personalized contact with customers). Due to its growth plans, it is seeking for its subsidiary in Spain (Barcelona or Madrid) a: BUSINESS DEVELOPER - FMCG (All sectors, including food, beverages, beauty, household, alcoholic beverages, pharma…) Are you a proactive, results-oriented individual with a passion for digital Mar Tech solutions in Consumer Goods industry? We are looking for you! Our client is reinventing direct-to-consumer promotions for the Fast-Moving Consumer Goods sector; we are seeking to hire a Business Developer in Spain to drive the growth and strengthen market presence. Main Responsibilities: • Conduct research and analyze the consumer goods sector to detect trends and business opportunities that add value to the company., • Seek out and establish contact with potential clients, namely major international and local producers or exclusive distributors of famous brands, and other relevant industry players, presenting our direct-to-consumer promotion solutions., • Build and maintain strong relationships with potential and existing clients, understanding their needs and offering tailored value propositions., • Deliver sales presentations, negotiate terms, and close mutually beneficial agreements., • Work closely with product team to align strategies and ensure competitive and effective proposals., • Study competitors to identify unique advantages and adjust business development strategies accordingly., • Monitor the progress of sales opportunities, keep records updated, and present results reports to management., • Attend fairs, conferences, and related events in the food and beverage sector to expand your network and identify new opportunities. Requirements: Previous experience in business development, sales or similar roles within the food and beverage sector, either in agency or FMCG Company. Excellent communication and negotiation skills, both in Spanish and English. Knowledge of the Fast-Moving Consumer Goods market and industry trends.

🚨 Buscamos Medical Writer con experiencia en mercado UK 🚨 Seguimos ampliando equipo para un proyecto internacional dentro del sector farmacéutico y necesitamos perfiles con experiencia en el entorno healthcare del Reino Unido. 📌 Requisitos imprescindibles: ✔ Experiencia trabajando con materiales dirigidos a healthcare professionals en UK ✔ Conocimiento sólido de la normativa ABPI (Association of the British Pharmaceutical Industry) ✔ Experiencia en creación y/o revisión de materiales promocionales y científicos para pharma ✔ Nivel de inglés alto (C1/C2) ✔ Capacidad de trabajo en entornos internacionales y multidisciplinares ⚠ Muy importante: Buscamos profesionales con exposición previa al mercado UK y familiarizados con sus requisitos regulatorios y de comunicación dentro de la industria farmacéutica. ⏰ Jornada PART TIME – 24 horas semanales, salario acorde con el número de horas. 🏠 Modalidad: 100% remoto 🌍 Proyecto internacional para compañía farmacéutica líder del sector.

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 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.

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.