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Posición: Operario/a de Producción de Planta Química Experiencia: muy valorable 1 año de experiencia al menos en las funciones descritas ¿Insud Pharma es una compañía reconocida y respetada en el sector farmacéutico y de la salud con más de 40 años de historia con más de 7.000 empleados en 50 países especializada en la investigación, desarrollo, fabricación y comercialización de principios activos farmacéuticos y medicamentos de uso humano y veterinario. Chemo, área industrial del grupo Insud Pharma, es un líder mundial en I+D y fabricación de más de 100 ingredientes farmacéuticos activos de valor agregado y más de 122 medicamentos con más de 200 presentaciones de producto diferentes. Chemo produce sus propios principios activos (API), así como productos farmacéuticos terminados (FDF) abarcando los principales grupos terapéuticos (Cardiología, Gastroenterología, Sistema Nervioso Central, Antiinfecciosos, Respiratorio, Salud de la Mujer, Endocrinología, Dermatología y Urología). ¿Incorporamos un/a Operario/a de Planta Química con un contrato temporal en nuestra planta química de Alcalá de Henares. ¡Realizar y registrar todas las fases del proceso productivo controlando los equipos de fabricación y producción, realizando controles en proceso de acuerdo con las guías de fabricación y procedimientos aplicables. Control de la maquinaria específica del área (depuradora, reactores u otras según proceda) Registro de la información según hojas de ruta/fabricación Control de materiales, mezclas y productos necesario para la fabricación del medicamento Almacén y control de mercancía Formación FPI/FPII en planta química o similar Español escrito y hablado fluido. Se valorará conocimiento de otros idiomas Disponibilidad para trabajar en turno rotativo de lunes a viernes (mañanas 06.00 a 14.00 / tardes 14.00 a 22.00 y noches 22.00 a 06.00) Experiencia de al menos 1 año en un entorno químico o muy similar desarrollando funciones descritas MUY VALORABLE POSIBILIDAD INCORPORACIÓN INMEDIATA ¡Horario de turno rotativo de lunes a viernes (mañanas 06.00 a 14.00 / tardes 14.00 a 22.00 y noches 22.00 a 06.00) &##Contrato temporal inicialmente &##Continuaremos con una entrevista presencial/virtual según la disponibilidad y acordemos, en el proceso puede haber entre una y dos entrevistas y según el tipo de proceso puede haber también algún tipo de prueba. ➡️¡Síguenos en redes sociales como LinkedIn/Instagram y estate atento a cualquier oferta que vayamos sacando, ¡La oportunidad de ser un nuevo Insuder está a la espera!. #El grupo InsudPharma es consciente que la gestión empresarial tiene que estar en consonancia con las necesidades y demandas de la sociedad, y por ello asume el compromiso de igualdad de oportunidades y trato entre hombres y mujeres, tal y como se recoge en la normativa vigente en la materia -Ley Orgánica 3/2007, y no discriminamos a ninguna persona por motivos de etnia, religión, edad, sexo, nacionalidad, estado civil, orientación afectiva o sexual, identidad o expresión de género, discapacidad, o cualquier otra circunstancia personal o social.

Posición: Operario/a de Producción de Planta Química Experiencia: muy valorable 1 año de experiencia al menos en las funciones descritas ¿Insud Pharma es una compañía reconocida y respetada en el sector farmacéutico y de la salud con más de 40 años de historia con más de 7.000 empleados en 50 países especializada en la investigación, desarrollo, fabricación y comercialización de principios activos farmacéuticos y medicamentos de uso humano y veterinario. Chemo, área industrial del grupo Insud Pharma, es un líder mundial en I+D y fabricación de más de 100 ingredientes farmacéuticos activos de valor agregado y más de 122 medicamentos con más de 200 presentaciones de producto diferentes. Chemo produce sus propios principios activos (API), así como productos farmacéuticos terminados (FDF) abarcando los principales grupos terapéuticos (Cardiología, Gastroenterología, Sistema Nervioso Central, Antiinfecciosos, Respiratorio, Salud de la Mujer, Endocrinología, Dermatología y Urología). ¿Incorporamos un/a Operario/a de Planta Química con un contrato temporal en nuestra planta química de Alcalá de Henares. ¡Realizar y registrar todas las fases del proceso productivo controlando los equipos de fabricación y producción, realizando controles en proceso de acuerdo con las guías de fabricación y procedimientos aplicables. Control de la maquinaria específica del área (depuradora, reactores u otras según proceda) Registro de la información según hojas de ruta/fabricación Control de materiales, mezclas y productos necesario para la fabricación del medicamento Almacén y control de mercancía Formación FPI/FPII en planta química o similar Español escrito y hablado fluido. Se valorará conocimiento de otros idiomas Disponibilidad para trabajar en turno rotativo de lunes a viernes (mañanas 06.00 a 14.00 / tardes 14.00 a 22.00 y noches 22.00 a 06.00) Experiencia de al menos 1 año en un entorno químico o muy similar desarrollando funciones descritas MUY VALORABLE POSIBILIDAD INCORPORACIÓN INMEDIATA ¡Horario de turno rotativo de lunes a viernes (mañanas 06.00 a 14.00 / tardes 14.00 a 22.00 y noches 22.00 a 06.00) &##Contrato temporal inicialmente &##Continuaremos con una entrevista presencial/virtual según la disponibilidad y acordemos, en el proceso puede haber entre una y dos entrevistas y según el tipo de proceso puede haber también algún tipo de prueba. ➡️¡Síguenos en redes sociales como LinkedIn/Instagram y estate atento a cualquier oferta que vayamos sacando, ¡La oportunidad de ser un nuevo Insuder está a la espera!. #El grupo InsudPharma es consciente que la gestión empresarial tiene que estar en consonancia con las necesidades y demandas de la sociedad, y por ello asume el compromiso de igualdad de oportunidades y trato entre hombres y mujeres, tal y como se recoge en la normativa vigente en la materia -Ley Orgánica 3/2007, y no discriminamos a ninguna persona por motivos de etnia, religión, edad, sexo, nacionalidad, estado civil, orientación afectiva o sexual, identidad o expresión de género, discapacidad, o cualquier otra circunstancia personal o social.

Posición: Operario/a de Producción de Planta Química Experiencia: muy valorable 1 año de experiencia al menos en las funciones descritas ¿Insud Pharma es una compañía reconocida y respetada en el sector farmacéutico y de la salud con más de 40 años de historia con más de 7.000 empleados en 50 países especializada en la investigación, desarrollo, fabricación y comercialización de principios activos farmacéuticos y medicamentos de uso humano y veterinario. Chemo, área industrial del grupo Insud Pharma, es un líder mundial en I+D y fabricación de más de 100 ingredientes farmacéuticos activos de valor agregado y más de 122 medicamentos con más de 200 presentaciones de producto diferentes. Chemo produce sus propios principios activos (API), así como productos farmacéuticos terminados (FDF) abarcando los principales grupos terapéuticos (Cardiología, Gastroenterología, Sistema Nervioso Central, Antiinfecciosos, Respiratorio, Salud de la Mujer, Endocrinología, Dermatología y Urología). ¿Incorporamos un/a Operario/a de Planta Química con un contrato temporal en nuestra planta química de Alcalá de Henares. ¡Realizar y registrar todas las fases del proceso productivo controlando los equipos de fabricación y producción, realizando controles en proceso de acuerdo con las guías de fabricación y procedimientos aplicables. Control de la maquinaria específica del área (depuradora, reactores u otras según proceda) Registro de la información según hojas de ruta/fabricación Control de materiales, mezclas y productos necesario para la fabricación del medicamento Almacén y control de mercancía Formación FPI/FPII en planta química o similar Español escrito y hablado fluido. Se valorará conocimiento de otros idiomas Disponibilidad para trabajar en turno rotativo de lunes a viernes (mañanas 06.00 a 14.00 / tardes 14.00 a 22.00 y noches 22.00 a 06.00) Experiencia de al menos 1 año en un entorno químico o muy similar desarrollando funciones descritas MUY VALORABLE POSIBILIDAD INCORPORACIÓN INMEDIATA ¡Horario de turno rotativo de lunes a viernes (mañanas 06.00 a 14.00 / tardes 14.00 a 22.00 y noches 22.00 a 06.00) &##Contrato temporal inicialmente &##Continuaremos con una entrevista presencial/virtual según la disponibilidad y acordemos, en el proceso puede haber entre una y dos entrevistas y según el tipo de proceso puede haber también algún tipo de prueba. ➡️¡Síguenos en redes sociales como LinkedIn/Instagram y estate atento a cualquier oferta que vayamos sacando, ¡La oportunidad de ser un nuevo Insuder está a la espera!. #El grupo InsudPharma es consciente que la gestión empresarial tiene que estar en consonancia con las necesidades y demandas de la sociedad, y por ello asume el compromiso de igualdad de oportunidades y trato entre hombres y mujeres, tal y como se recoge en la normativa vigente en la materia -Ley Orgánica 3/2007, y no discriminamos a ninguna persona por motivos de etnia, religión, edad, sexo, nacionalidad, estado civil, orientación afectiva o sexual, identidad o expresión de género, discapacidad, o cualquier otra circunstancia personal o social.

Position: Launch Specialist – New Product Introduction (NPI) INSUD PHARMA Headquarters, Sanchinarro (Madrid) – On-site Experience: 3-5 years in project management, preferably in the pharmaceutical industry or regulated sectors INSUD PHARMA operates across the entire pharmaceutical value chain, providing specialized knowledge and experience in scientific research, development, manufacturing, sales, and commercialization of a wide range of active pharmaceutical ingredients (APIs), finished dosage forms (FDF), and branded pharmaceutical products, adding value to both human and animal health. INSUD PHARMA’s activity is organized into three synergistic business areas: Industrial (Chemo), Branded (Exeltis), and Biotech (mAbxience), with more than 9,000 professionals in over 50 countries, 20 state-of-the-art facilities, 15 specialized R&D centers, 12 commercial offices, and more than 35 pharmaceutical subsidiaries, serving 1,150 clients in 96 countries worldwide. INSUD PHARMA believes in innovation and sustainable development. As a Launch Specialist at INSUD PHARMA, you will be the bridge between development and industrialization, ensuring every new product is ready for its first commercial production. Your mission will be to coordinate all key functions to guarantee successful launches, meeting the highest standards of quality, cost, and service. Coordinate cross-functional teams (Engineering, QA, QC, Production, Supply Chain, Planning, Regulatory Affairs, Finance, etc.) Manage documentation, progress reports, and ensure data accuracy in the launch database. Coordinate and oversee the execution of multiple launch projects simultaneously. Ensure delivery ON TIME, IN FULL, AT THE RIGHT COST, and with the HIGHEST QUALITY. 3-5 years of experience in project management, preferably in the pharmaceutical, chemical, or regulated sectors. ~ Solid knowledge of technology transfer processes, quality assurance, and supply chain. ~ High level of English (minimum B2); Proficiency in project management tools (MS Project, Excel, etc.). ~ Permanent contract &##Professional development plan and continuous training &##Private health insurance 1-2 on-site/virtual interviews ~ 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.

Applied AI Consultant – Remote working in Italy, France or Spain - Management Consultancy, Life Sciences – Competitive salary and package The Company A leading life sciences service provider and consultancy are looking to grow their management consultancy team focussed on strategy and transformation projects A fantastic opportunity to work with Pharma, Med Tech, and Investors on interesting consultancy projects at a corporate, business unit, and individual product level Great team with lots of opportunities for progression and involvement in the wider business The Role Work with consultant team on client projects within pharmaceutical, biotech and med tech companies. Take lead in building AI agents using LLMs such as OpenAI or Anthropic Claude and build interactive dashboards using Power BI and/or Streamlit. Be part of a small growing team within an established consultancy who want to be at the forefront of innovation. You will have: 2–5 years of experience in applied AI, data engineering, or a consulting-adjacent technical role Strong Python skills (data processing, API integration, modular design) Solid experience working with REST APIs and structured data (e.g., JSON) Hands-on experience with LLM APIs in real-world projects Experience in prompt engineering, structured outputs, tool-use patterns, and error handling Practical knowledge of MCP server design and implementation Ability to manage multiple concurrent projects with a structured, autonomous mindset Strong communication skills, able to clearly present technical work to business audiences What should you do next? To discuss this role further or to find out about other roles I’m currently working on, please get in touch or hit apply to submit your current CV. We look forward to hearing from you. Unless otherwise stated, if applying for a job within the European Union, you must ensure that you are already authorised to work there. Carrot Recruitment acts as an Employment Business and an Employment Agency on behalf of our client in recruitment for this role. We are an Equal Opportunity Employer and do not discriminate against any employee or applicant for employment because of race, colour, sex, age, national origin, religion, sexual orientation, gender identity and/or expression. If there are any arrangements or adjustments we can make to assist you at interview then please let us know and we'll be more than happy to assist.

SAP BTP Developer 6+ months Remote opportunity The reason I am contacting you is because one of our key partners has now a new opportunity for a SAP BTP Developer to start ASAP on a 6 + months contract Remote and English speaker. Node.js Development: Proficiency in designing, developing, and maintaining backend systems using Node.js. Strong understanding of asynchronous programming, event-driven architectures, and RESTful APIs. JavaScript/TypeScript: Advanced knowledge of JavaScript and/or TypeScript for creating robust and scalable backend solutions Familiarity with modern frameworks or libraries such as Express.js for API development. SAP BTP Expertise Hands-on experience with SAP Business Technology Platform (BTP), particularly focused on: CAP (Cloud Application Programming) Model for efficient service-based application design. Development on SAP Cloud Foundry or SAP Kyma. Experience with SAP HANA Cloud for data modeling and backend integration. Understanding of BTP-specific security, roles, and authorization management. Understanding of pharma-critical temperature monitoring processes and standards, such as: Compliance with Good Automated Manufacturing Practices (GAMP) for pharma solutions. Knowledge of FDA or EMA guidelines for temperature-sensitive pharma product transport. Chain of custody and chain of identity integration within monitoring solutions. If you are interested, please contact Adrian a Gomez on or apply here.

Portfolio Manager Experience: 2–5 years in pharma, biotechnology, or life sciences Chemo (INSUD PHARMA) is a global leader in the pharmaceutical industry, driving innovation and expertise across the entire value chain—research, development, manufacturing, and commercialization of products for human and animal health. Present in over 50 countries, Chemo fosters a culture of collaboration, talent development, and bold innovation. As a Portfolio Manager, you will play a key role in planning, analyzing, and coordinating projects within our development and commercial portfolio, collaborating in a global, cross-functional environment. Performing portfolio analyses: risk assessments, scenario comparisons, timeline evaluations, and KPIs Creating dashboards and regular monitoring reports with digital tools Coordinating with R&D, Clinical, Regulatory, Commercial, Manufacturing, and other internal partners to collect information and align strategies Supporting multifunctional teams in identifying potential challenges and resource constraints Assisting with the evaluation of new projects, initiatives, or external collaborations Contributing to continuous improvement of portfolio management processes, digital tools, and systems Analyze and present data for strategic decision-making Coordinate processes with multidisciplinary global teams Bachelor’s degree in Life Sciences, Engineering, Business, or similar ~ Advanced degree (MBA, MSc, PharmD, PhD) is a plus, but not mandatory ~Basic understanding of the drug development lifecycle, regulatory steps, or commercial product management ~ Proficient in Excel, PowerPoint, and portfolio/project management tools (including dashboards, analytics platforms) ~ Collaborative mindset and ability to work effectively in global, matrixed environments ~ Permanent, long-term contract &##Continuous training and development &##Challenging projects with global impact &##Private health insurance 1–2 virtual/on-site interviews with HR and area managers ~ Transparent and ongoing communication at every stage &##

About Xebia With over 20 years of experience, our global network of passionate technologists and pioneering craftsmen deliver cutting-edge technology and game-changing consulting to companies on the brink of transformation. Since 2001, we have grown from a Java company into a full-service digital consulting company with 5,500+ professionals working on a worldwide ambition. We are organized in complementary service lines – teams with a tremendous amount of knowledge and experience within a particular field, such as Agile, DevOps, Data and AI, Cloud, Software Technology, Functional Programming, Intelligent Automation, and Microsoft. We help the world's top 250+ companies and category leaders overcome digital challenges, embrace innovation, adopt new technology, and implement new business models. In addition to high-quality consulting, we also provide offshoring and nearshoring services. We're seeking a Scientific Product Manager (SPM) to lead the strategy, roadmap, and delivery of GenAI products across scientific domains. Lead cross-functional execution (engineering, data science, design, scientific stakeholders) in an Agile environment BS/MS (PhD preferred) in bioinformatics, biology, or related field ~5+ years' relevant experience, including product management for software products ~ Experience in pharma, biotech, or digital health preferred ~ Familiarity with data analysis (Python, R, or MATLAB a plus)

With over 20 years of experience, our global network of passionate technologists and pioneering craftsmen deliver cutting-edge technology and game-changing consulting to companies on the brink of transformation. Since 2001, we have grown from a Java company into a full-service digital consulting company with 4500+ professionals working on a worldwide ambition. We are organized in complementary chapters – teams with a tremendous amount of knowledge and experience within a particular field, such as Agile, DevOps, Data and AI, Cloud, Software Technology, Functional Programming, Low Code, and Microsoft. We help the world’s top 250 companies and category leaders overcome digital challenges, embrace innovation, adopt new technology, and implement new business models. In addition to high-quality consulting, we also provide offshoring and nearshoring services. The Scientific Product Manager (SPM) owns the strategy, roadmap, and delivery of scientific workspace products across multiple domains. Lead discovery to delivery execution with engineering, design, data science, and scientific stakeholders in an Agile environment Drive dependency management, trade-off decisions, and release planning across multiple concurrent initiatives Partner with engineering on validation and testing strategies for deployments in customer environments, including workflow realism and data constraints Define go-to-market readiness with stakeholders: documentation, training needs, enablement, and rollout strategy iterate to improve usability, performance, and scientific value delivered Bachelor’s or Master’s degree in bioinformatics, biology, or a related scientific discipline plus at least 5 years of relevant experience (PhD preferred) Product management experience shipping software products, ideally across complex workflows and multiple user personas Experience in pharma, biotech, and or digital health environments Working knowledge of data analysis and experimentation; Python, R, or MATLAB beneficial Excellent communication and collaboration skills in cross-functional, global teams Experience working in Agile or Scrum environments

With over 20 years of experience, our global network of passionate technologists and pioneering craftsmen deliver cutting-edge technology and game-changing consulting to companies on the brink of transformation. Since 2001, we have grown from a Java company into a full-service digital consulting company with 4500+ professionals working on a worldwide ambition. We are organized in complementary chapters – teams with a tremendous amount of knowledge and experience within a particular field, such as Agile, DevOps, Data and AI, Cloud, Software Technology, Functional Programming, Low Code, and Microsoft. We help the world’s top 250 companies and category leaders overcome digital challenges, embrace innovation, adopt new technology, and implement new business models. In addition to high-quality consulting, we also provide offshoring and nearshoring services. The Scientific Product Manager (SPM) owns the strategy, roadmap, and delivery of scientific workspace products across multiple domains. Lead discovery to delivery execution with engineering, design, data science, and scientific stakeholders in an Agile environment Drive dependency management, trade-off decisions, and release planning across multiple concurrent initiatives Partner with engineering on validation and testing strategies for deployments in customer environments, including workflow realism and data constraints Define go-to-market readiness with stakeholders: documentation, training needs, enablement, and rollout strategy iterate to improve usability, performance, and scientific value delivered Bachelor’s or Master’s degree in bioinformatics, biology, or a related scientific discipline plus at least 5 years of relevant experience (PhD preferred) Product management experience shipping software products, ideally across complex workflows and multiple user personas Experience in pharma, biotech, and or digital health environments Working knowledge of data analysis and experimentation; Python, R, or MATLAB beneficial Excellent communication and collaboration skills in cross-functional, global teams Experience working in Agile or Scrum environments

With over 20 years of experience, our global network of passionate technologists and pioneering craftsmen deliver cutting-edge technology and game-changing consulting to companies on the brink of transformation. Since 2001, we have grown from a Java company into a full-service digital consulting company with 4500+ professionals working on a worldwide ambition. We are organized in complementary chapters – teams with a tremendous amount of knowledge and experience within a particular field, such as Agile, DevOps, Data and AI, Cloud, Software Technology, Functional Programming, Low Code, and Microsoft. We help the world’s top 250 companies and category leaders overcome digital challenges, embrace innovation, adopt new technology, and implement new business models. In addition to high-quality consulting, we also provide offshoring and nearshoring services. The Scientific Product Manager (SPM) owns the strategy, roadmap, and delivery of scientific workspace products across multiple domains. Lead discovery to delivery execution with engineering, design, data science, and scientific stakeholders in an Agile environment Drive dependency management, trade-off decisions, and release planning across multiple concurrent initiatives Partner with engineering on validation and testing strategies for deployments in customer environments, including workflow realism and data constraints Define go-to-market readiness with stakeholders: documentation, training needs, enablement, and rollout strategy iterate to improve usability, performance, and scientific value delivered Bachelor’s or Master’s degree in bioinformatics, biology, or a related scientific discipline plus at least 5 years of relevant experience (PhD preferred) Product management experience shipping software products, ideally across complex workflows and multiple user personas Experience in pharma, biotech, and or digital health environments Working knowledge of data analysis and experimentation; Python, R, or MATLAB beneficial Excellent communication and collaboration skills in cross-functional, global teams Experience working in Agile or Scrum environments

With over 20 years of experience, our global network of passionate technologists and pioneering craftsmen deliver cutting-edge technology and game-changing consulting to companies on the brink of transformation. Since 2001, we have grown from a Java company into a full-service digital consulting company with 4500+ professionals working on a worldwide ambition. We are organized in complementary chapters – teams with a tremendous amount of knowledge and experience within a particular field, such as Agile, DevOps, Data and AI, Cloud, Software Technology, Functional Programming, Low Code, and Microsoft. We help the world’s top 250 companies and category leaders overcome digital challenges, embrace innovation, adopt new technology, and implement new business models. In addition to high-quality consulting, we also provide offshoring and nearshoring services. The Scientific Product Manager (SPM) owns the strategy, roadmap, and delivery of scientific workspace products across multiple domains. Lead discovery to delivery execution with engineering, design, data science, and scientific stakeholders in an Agile environment Drive dependency management, trade-off decisions, and release planning across multiple concurrent initiatives Partner with engineering on validation and testing strategies for deployments in customer environments, including workflow realism and data constraints Define go-to-market readiness with stakeholders: documentation, training needs, enablement, and rollout strategy iterate to improve usability, performance, and scientific value delivered Bachelor’s or Master’s degree in bioinformatics, biology, or a related scientific discipline plus at least 5 years of relevant experience (PhD preferred) Product management experience shipping software products, ideally across complex workflows and multiple user personas Experience in pharma, biotech, and or digital health environments Working knowledge of data analysis and experimentation; Python, R, or MATLAB beneficial Excellent communication and collaboration skills in cross-functional, global teams Experience working in Agile or Scrum environments

Stratence Partners is expanding its Tier-1 Commercial Transformation platform globally. We are appointing several Senior Vice Presidents across Europe, North America, the Middle East, and APAC to accelerate growth in Commercial Transformation, Strategy Optimization, Pricing Excellence, and Commercial Effectiveness. These roles combine revenue origination and executive-level delivery within a structured, IP-driven, governance-led platform. All engagements are designed to institutionalize capabilities within client organizations and deliver measurable financial impact. Mandate Senior Vice Presidents will: Originate and close Tier-1 enterprise Commercial Transformation mandates Engage C-suite and Boards on revenue, margin, growth, and performance architecture Structure strategic, pricing, and commercial governance programs Lead executive-level end-to-end delivery from diagnostic through blueprint and implementation Build long-term strategic client partnerships Platform & Methodology All programs operate within Stratence’s structured Commercial Transformation framework, including: Codified strategic, pricing, and commercial governance methodology Proprietary intellectual property, structured models, and scalable frameworks Data management and applied data science supporting monetization and decision architecture Execution solutions embedded into commercial workflows, AI-powered Structured capability transfer to institutionalize client ownership Clear return on investment with measurable EBIT and margin impact Structured delivery aligned with defined governance, account discipline, and economic rigor Recognized expertise across Pharma, MedTech, Oil & Gas, Chemicals, Industrial, Utilities, Financial Services, Tech & Telco, and Transport & Logistics Profile 25+ years of senior consulting experience, ideally combined with executive operational responsibility Background in commercial transformation and profit-growth optimization at enterprise scale Demonstrated record of originating and closing enterprise-level advisory mandates Experience leading strategic, pricing, revenue architecture, or commercial governance initiatives Established C-suite relationships International experience across Europe, North America, the Middle East, or APAC Comfortable combining revenue generation with structured delivery leadership Engagement Structure Dedicated, institutional support for marketing, positioning, and business development Uncapped earnings potential directly linked to revenue originated and delivered Executive participation in delivery supported by structured Tier-1 resources and platform capabilities Established platform credibility with leading Tier-1 organizations, enabling long-term strategic partnerships Defined account ownership with clear governance discipline and transparent revenue recognition Clear progression path from Senior Vice President to Partner based on performance, client impact, and platform contribution Engagement will proceed with selected profiles meeting the stated requirements.

In a nutshell Position: Portfolio Manager Location: Madrid, on site Experience: 2–5 years in pharma, biotechnology, or life sciences Want to know more? Chemo (INSUD PHARMA) is a global leader in the pharmaceutical industry, driving innovation and expertise across the entire value chain—research, development, manufacturing, and commercialization of products for human and animal health. Present in over 50 countries, Chemo fosters a culture of collaboration, talent development, and bold innovation. Ready to be a #Challenger? What are we looking for? As a Portfolio Manager, you will play a key role in planning, analyzing, and coordinating projects within our development and commercial portfolio, collaborating in a global, cross-functional environment. Your core responsibilities will include: Assisting in developing and maintaining portfolio plans, including timelines, milestones, and prioritization frameworks Preparing strategic materials for governance meetings and portfolio reviews Ensuring accurate documentation and communication of portfolio decisions and updates Performing portfolio analyses: risk assessments, scenario comparisons, timeline evaluations, and KPIs Creating dashboards and regular monitoring reports with digital tools Coordinating with R&D, Clinical, Regulatory, Commercial, Manufacturing, and other internal partners to collect information and align strategies Supporting multifunctional teams in identifying potential challenges and resource constraints Communicating portfolio insights to stakeholders at various levels Tracking and highlighting emerging risks, issues, or opportunities within the portfolio Assisting with the evaluation of new projects, initiatives, or external collaborations Contributing to continuous improvement of portfolio management processes, digital tools, and systems Your challenge! Analyze and present data for strategic decision-making Coordinate processes with multidisciplinary global teams Optimize communication and information flow Identify and propose improvements to portfolio management tools and processes What do you need? Bachelor’s degree in Life Sciences, Engineering, Business, or similar Advanced degree (MBA, MSc, PharmD, PhD) is a plus, but not mandatory 2–5 years of experience in pharma, biotechnology, or related industries Background in portfolio management and/or strategy Basic understanding of the drug development lifecycle, regulatory steps, or commercial product management Strong analytical and problem-solving skills Excellent written and verbal communication and presentation capabilities Advanced organizational skills, managing multiple priorities efficiently Proficient in Excel, PowerPoint, and portfolio/project management tools (including dashboards, analytics platforms) Collaborative mindset and ability to work effectively in global, matrixed environments Detail-oriented, proactive, and results-driven Strong relationship-building skills and eagerness for continuous learning Our benefits! Permanent, long-term contract Continuous training and development International and collaborative environment Challenging projects with global impact Company parking Subsidized cafeteria Private health insurance What will the Selection Process look like? ️ Initial contact by phone or email 1–2 virtual/on-site interviews with HR and area managers Transparent and ongoing communication at every stage Think this role isn’t for you? Follow us on LinkedIn and stay tuned for new opportunities—your next challenge may be just around the corner! #ChemoCareers #InsudPharma #Challenger #InsudTalent COMMITMENT TO EQUAL OPPORTUNITY At Chemo (INSUD PHARMA), we are committed to real equality. We do not discriminate by gender, ethnicity, religion, sexual orientation, disability or any other factor. We actively foster an inclusive workplace where everyone’s talent and capabilities make the difference.

Company Description BrandLink is a MarTech and loyalty platform helping FMCG and consumer goods brands build direct, data-driven relationships with shoppers through personalized, omnichannel promotions. Using advanced receipt-scanning technology and first-party data, BrandLink enables brands to run effective direct-to-consumer campaigns, optimize trade marketing investments, and improve promotional efficiency across both online and offline retail environments. After successfully launching programs with international FMCG brands, BrandLink is now expanding its presence in Spain with a clear ambition to scale across Southern Europe. Role Description The Country Manager – Spain (Southern Europe Growth) is a senior, director-level role with full ownership of the Spanish market and a clear growth path toward leading Southern Europe (Portugal, Italy, France) . This role combines commercial leadership, business development, market strategy, and execution . You will act as the country owner for Spain, working closely with the founders and product team to scale BrandLink’s commercial presence and shape the regional growth strategy. Work format: This role is remote-friendly within Spain , with flexibility to work remotely and periodic travel for client meetings, industry events, and key business activities. Occasional presence in Málaga or other key locations may be required. Key Responsibilities Own and develop BrandLink’s business in Spain, including market strategy, revenue growth, and partnerships Identify and execute commercial opportunities across FMCG sectors (food, beverages, beauty, household, pharma, alcohol) Lead senior-level negotiations with FMCG brands, agencies, and distributors Build and maintain long-term relationships with key decision-makers (Marketing, Trade Marketing, Digital, Innovation) Define and execute go-to-market strategy together with founders Work closely with the product team to localize and adapt solutions to market needs Manage sales pipeline, forecasting, and performance reporting Represent the company at industry events, conferences, and client meetings Over time, build and lead a local commercial team Requirements Senior experience in Business Development, Commercial Leadership, or Country Management within FMCG or MarTech Trade Marketing experience is a must Strong understanding of FMCG market dynamics and decision-making processes Proven ability to close complex, high-value commercial deals Strategic mindset combined with hands-on execution Excellent communication and negotiation skills Spanish (native or fluent) and strong English Based in Spain and available for periodic travel What We Offer Director-level role with real ownership of the Spanish market Direct access to founders and strong influence on product and strategy Clear growth path toward Head of Southern Europe Competitive compensation package (fixed + performance-based) Long-term incentives Opportunity to build and scale a market from an early stage

¿Estás preparado para diseñar soluciones innovadoras en la industria farmacéutica? ¡Estamos buscando un Ingeniero de Utilities apasionado y comprometido! En esta posición, tendrás la responsabilidad de diseñar los sistemas clave de instalaciones farmacéuticas, asegurando que cumplan con los requerimientos del usuario, normativa farmacéutica y estándares de seguridad y medio ambiente. Tus responsabilidades - Diseño de instalaciones mecánicas en la industria farmacéutica (piping, generaciones de frio/calor, vapor, agua purificada/inyectables...) - Generar documentos técnicos para entregar a cliente: P&Ids, listados, fichas técnicas, memorias técnicas, etc. - Preparación de documentos para licitación, comparativos técnicos y económicos - Realizar los proyectos garantizando el cumplimiento de las normativas - Preparación de las URS del proyecto en colaboración con el cliente - Realizar los proyectos de forma que se cumplan los hitos marcados en tiempos y calidad, que marcará el director de proyecto o el cliente - Para algunos proyectos, liderar el equipo del proyecto. Delegar responsabilidades a los miembros del equipo de proyecto, en especial a otros ingenieros de proyectos y al equipo de delineación. - En determinados proyectos, preparación de documentos de calidad: QMP, DQ, AR, etc. - Garantizar la correcta ejecución del proyecto con presencia en obra según necesidades del proyecto Conocimientos y experiencia - Experiencia previa como ingeniero de proyectos en el sector industrial / químico-farmacéutico o en la consecución de tareas relacionadas con el diseño de ingeniería conceptual, básica y de detalle u otros estudios técnicos del diseño. - Licenciado en ingeniería: química, ciencias de la vida... - Conocimiento fluido del español y del inglés. Se valorarán idiomas adicionales. - Usuario de Microsoft Office, Microsoft Project, Power Point, Adobe. Competencias - Excelentes habilidades de comunicación. - Excelente pensamiento analítico y resolución de problemas. - Capacidad para priorizar tareas y cumplir plazos estrictos. - Excelente conjunto de habilidades de gestión de clientes. - Capacidad para trabajar en varios proyectos en paralelo. - Capaz de trabajar en equipo, colaborativo, innovador y responsable. - Se requiere disponibilidad para viajar para visitar clientes. Conocimientos que suman puntos - Experiencia en los sectores de la salud/ciencias de la vida/farmacéutico. - Familiarizado con GMP, ISPE, FDA, OMS y otras directrices y regulaciones farmacéuticas. - Experiencia como ingeniero de proyectos en el diseño y construcción de plantas farmacéuticas. - Conocimiento técnico de HVAC, proceso, salas blancas, tuberías, control o electricidad en la industria farmacéutica. - Valorables capacidades previas adquiridas en el diseño de instalaciones industriales o como técnico(a) de puesta en marcha o como responsable entrega de dosieres técnicos. Razones para trabajar en KLINEA - Lugar de trabajo: Sant Quirze del Vallès. - Incorporación inmediata. - Salario competitivo según tu experiencia y habilidades. - Tiempo completo y contrato indefinido. - Horario flexible. - Día libre en tu cumpleaños. - Retribución flexible (seguro Adeslas y cheque restaurante/transporte/guardería) - Plan interno de formación y certificaciones. - Actividades de trabajo en equipo. - Un excelente entorno de trabajo con un equipo colaborativo, joven y dinámico. Si la calidad, la eficiencia y el profesionalismo te definen, ¡esta oportunidad es para ti!

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 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 as mother tongue is highly valued 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.

In a few words Position: SAP BASIS ADMINISTRATOR Location: Madrid-On site Experience: +3 years as SAP Basis Administrator, preferably in pharmaceutical industry Want to know more? INSUD PHARMA is undertaking a global project to implement and migrate its SAP ECC management system to S4/HANA. We seek an SAP PP-PI Expert Consultant to collaborate in this implementation by analyzing, supervising, and delivering solutions together with external partners working on the project. The consultant will liaise with key users, control project execution within their area, and ensure quality and adherence to the Core Model defined for INSUD PHARMA. What are we looking for? The SAP Basis Administrator provides first-level technical support on the company's SAP systems, ensuring optimal operation through preventive maintenance, continuous monitoring, incident management, user administration, and participation in system upgrades or new product installations. Collaborate with different teams to ensure continuity of service and contribute to digital transformation projects within a specialized SAP technology service environment. Specific responsabilities: Provide preventive, planned, and corrective technical support for SAP systems (NetWeaver, S/4 HANA, Business Objects). Manage and maintain optimal SAP system performance. Administer SAP landscape transports, jobs, printers, and print queues. Create, maintain, and manage users, profiles, and roles (including GRC tool; user/role lock and unlock). Monitor performance and availability of SAP systems. Troubleshoot technical issues and manage SAP Basis support tickets. Implement new SAP releases, patches, products, and software/certificate upgrades. Perform basic monitoring, database backup, and recovery tasks (Hana, Oracle, etc.). Create and maintain standard operational procedures (SOP) in collaboration with the Quality Assurance area. Collaborate with cross-functional teams and during audit processes, participating in digital transformation projects. What do you need? Basic knowledge of operating system administration (Linux/Windows) and databases (HANA, Oracle, etc.) Database communication: Configure and maintain communication between databases, manage memory, and handle the exchange of business data, including integrations with external systems. Understanding of SAP architecture (On-Premise, Cloud, and hybrid models). Analytical and problem-solving skills. Communication and teamwork skills. Our benefits! Permanent contract ⏰ Flexible schedule Health insurance coverage Professional development opportunities Selection process ️ Initial contact through phone or email. 1-2 interviews conducted virtually or in person. Continuous communication about the selection status. Not the right fit? Follow us on LinkedIn and Instagram for more exciting career opportunities at INSUD PHARMA. Stay connected and be ready for your next challenge! #InsudPharma #Challenger #InsudTalent COMMITMENT TO EQUAL OPPORTUNITY INSUD PHARMA promotes gender equality and does not discriminate based on ethnicity, religion, sexual orientation, disability, or any other condition. We foster a diverse, inclusive, and respectful work environment.

Whitewater Group is a leading provider of innovative and sustainable water treatment engineering systems operating in Ireland, 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 Bray, Co. The Group is experiencing significant growth due to its focus on off-site construction methods (OSM) of delivering turnkey projects, meaning on-site construction time is kept to a minimum. The successful candidate will be involved in planned preventative maintenance, repair and maintenance of existing water treatment plants, customer training, and delivering a high level of technical support. Whitewater provides quality engineering support, including root cause analysis and the implementation of corrective actions. All work is carried out in accordance with relevant Company and Customer Quality procedures. The role also includes managing customer relationships with a strong focus on communication and ensuring excellence in customer satisfaction. Collaboration with the customer service and administration teams is essential, including the provision of technical service reports and all relevant documentation for processing and invoicing. Perform planned preventative maintenance (PPM) and corrective repair on existing water treatment plants. Diagnose faults and implement root cause analysis and corrective actions. Troubleshoots and repairs pumps, instruments and control panels. Prepare and submit technical service reports. Complete all required documentation for customer service and administration, ensuring accurate processing and invoicing. Ensure all work complies with company and customer quality procedures. Work independently or as part of a small team with minimal supervision. Degree or equivalent qualification in Mechanical or Electrical background. Working with water treatment technologies such as Membranes, Ion Exchange, CDI, Filtration, Chemical Dosing Systems and UV. Fluent Spanish & English speaker with strong speaking skills. IT literate and proficiency in the use of Microsoft Office including Word, Excel, Powerpoint, Outlook.

Whitewater Group is a leading provider of innovative and sustainable water treatment engineering systems operating in Ireland, 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 Bray, Co. The Group is experiencing significant growth due to its focus on off-site construction methods (OSM) of delivering turnkey projects, meaning on-site construction time is kept to a minimum. The successful candidate will be involved in planned preventative maintenance, repair and maintenance of existing water treatment plants, customer training, and delivering a high level of technical support. Whitewater provides quality engineering support, including root cause analysis and the implementation of corrective actions. All work is carried out in accordance with relevant Company and Customer Quality procedures. The role also includes managing customer relationships with a strong focus on communication and ensuring excellence in customer satisfaction. Collaboration with the customer service and administration teams is essential, including the provision of technical service reports and all relevant documentation for processing and invoicing. Perform planned preventative maintenance (PPM) and corrective repair on existing water treatment plants. Diagnose faults and implement root cause analysis and corrective actions. Troubleshoots and repairs pumps, instruments and control panels. Prepare and submit technical service reports. Complete all required documentation for customer service and administration, ensuring accurate processing and invoicing. Ensure all work complies with company and customer quality procedures. Work independently or as part of a small team with minimal supervision. Degree or equivalent qualification in Mechanical or Electrical background. Working with water treatment technologies such as Membranes, Ion Exchange, CDI, Filtration, Chemical Dosing Systems and UV. Fluent Spanish & English speaker with strong speaking skills. IT literate and proficiency in the use of Microsoft Office including Word, Excel, Powerpoint, Outlook.

Whitewater Group is a leading provider of innovative and sustainable water treatment engineering systems operating in Ireland, 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 Bray, Co. The Group is experiencing significant growth due to its focus on off-site construction methods (OSM) of delivering turnkey projects, meaning on-site construction time is kept to a minimum. The successful candidate will be involved in planned preventative maintenance, repair and maintenance of existing water treatment plants, customer training, and delivering a high level of technical support. Whitewater provides quality engineering support, including root cause analysis and the implementation of corrective actions. All work is carried out in accordance with relevant Company and Customer Quality procedures. The role also includes managing customer relationships with a strong focus on communication and ensuring excellence in customer satisfaction. Collaboration with the customer service and administration teams is essential, including the provision of technical service reports and all relevant documentation for processing and invoicing. Perform planned preventative maintenance (PPM) and corrective repair on existing water treatment plants. Diagnose faults and implement root cause analysis and corrective actions. Troubleshoots and repairs pumps, instruments and control panels. Prepare and submit technical service reports. Complete all required documentation for customer service and administration, ensuring accurate processing and invoicing. Ensure all work complies with company and customer quality procedures. Work independently or as part of a small team with minimal supervision. Degree or equivalent qualification in Mechanical or Electrical background. Working with water treatment technologies such as Membranes, Ion Exchange, CDI, Filtration, Chemical Dosing Systems and UV. Fluent Spanish & English speaker with strong speaking skills. IT literate and proficiency in the use of Microsoft Office including Word, Excel, Powerpoint, Outlook.

Whitewater Group is a leading provider of innovative and sustainable water treatment engineering systems operating in Ireland, 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 Bray, Co. The Group is experiencing significant growth due to its focus on off-site construction methods (OSM) of delivering turnkey projects, meaning on-site construction time is kept to a minimum. The successful candidate will be involved in planned preventative maintenance, repair and maintenance of existing water treatment plants, customer training, and delivering a high level of technical support. Whitewater provides quality engineering support, including root cause analysis and the implementation of corrective actions. All work is carried out in accordance with relevant Company and Customer Quality procedures. The role also includes managing customer relationships with a strong focus on communication and ensuring excellence in customer satisfaction. Collaboration with the customer service and administration teams is essential, including the provision of technical service reports and all relevant documentation for processing and invoicing. Perform planned preventative maintenance (PPM) and corrective repair on existing water treatment plants. Diagnose faults and implement root cause analysis and corrective actions. Troubleshoots and repairs pumps, instruments and control panels. Prepare and submit technical service reports. Complete all required documentation for customer service and administration, ensuring accurate processing and invoicing. Ensure all work complies with company and customer quality procedures. Work independently or as part of a small team with minimal supervision. Degree or equivalent qualification in Mechanical or Electrical background. Working with water treatment technologies such as Membranes, Ion Exchange, CDI, Filtration, Chemical Dosing Systems and UV. Fluent Spanish & English speaker with strong speaking skills. IT literate and proficiency in the use of Microsoft Office including Word, Excel, Powerpoint, Outlook.

Greetings from Ubique Systems!!! We are looking for a Data Architect for one of our customer who has an expertise in:- Strong experience as an Information Architect in Pharma / Healthcare environments Proven expertise in: Data modeling (conceptual, logical, canonical) Metadata management Pharma R&D Master Data & Reference Data Management (MDRM) Data governance frameworks Deep understanding of Pharma Commercial data domains, such as: Sales & CRM Marketing & campaign data Customer (HCP/HCO) data Market access and commercial analytics Ability to operate at strategic and advisory level, influencing stakeholders across business and IT Experience driving enterprise-wide data standards and value realization Employment type:- B2B Contract. It would be hybrid working in Barcelona, Spain. Note:-Only apply if you have valid visa in the EU Region, Sponsorship will not be given.

Cognizant is a world leader in delivering digital transformation solutions to Life Sciences. Through our knowledge and expertise in Automation, MES & Digital, we deliver stable manufacturing systems that are optimized to improve operational efficiencies, whilst maintaining compliance. Our specialist engineering teams have the aptitude to deliver and support Pharma 4.0 architectures and solutions covering all IT, OT and IoT applications, infrastructures and services The AVEVA PI Engineer position offers the opportunity to join a multidisciplinary team that operates across multiple sites, providing support for the PI Historian Operational Service. The AVEVA PI Engineer will be an integral member of the support team, responsible for monitoring the system to ensure continuous production at the manufacturing site. Responsibilities: Support site vertical integration defined by the Project Manager or Lead Engineer. Create/Update the configuration and validation documents related to the PI system. Execute the validation as defined in the change control. Ensure data integrity and consistency by implementing data quality control measures and monitoring data validation processes. Collaborate within Automation Infra team to manage system upgrades, patches, and performance optimizations for the OSIsoft PI system. Handling and addressing tickets or issues associated with the PI system. Provide maintenance to the PI system to ensure system availability 24/7. Stay up-to-date with industry trends, emerging technologies, and regulatory requirements related to data engineering and manufacturing systems. Contribute to continuous improvement initiatives, identifying opportunities to enhance data management processes, system performance, and user experience To apply for this PI Software Engineer role, you will need an undergraduate degree in IT, Automation, Science or Engineering, or a related discipline, or equivalent work experience. You will also require the following: Experience working with the OSIsoft PI system, ideally within the pharmaceutical industry. Understanding of pharmaceutical manufacturing processes, including batch processing, equipment automation, and data acquisition systems. Proficiency in data engineering concepts, data integration, and data management best practices. Ability to multitask, manage multiple projects and prioritize tasks in a busy environment Experience with programming languages (e.g., Python, SQL) and scripting is advantageous. Experience with ticketing systems such as Service Now or similar The Cognizant community: We are a high caliber team who appreciate and support one another. Our people uphold an energetic, collaborative and inclusive workplace where everyone can thrive. Cognizant is a global community with more than 300,000 associates around the world. We don’t just dream of a better way – we make it happen. We take care of our people, clients, company, communities and climate by doing what’s right. We foster an innovative environment where you can build the career path that’s right for you. About us: Cognizant is one of the world's leading professional services companies, transforming clients' business, operating, and technology models for the digital era. Our unique industry-based, consultative approach helps clients envision, build, and run more innovative and efficient businesses. Headquartered in the U.S., Cognizant (a member of the NASDAQ-100 and one of Forbes World’s Best Employers 2024) is consistently listed among the most admired companies in the world. Learn how Cognizant helps clients lead with digital at

Cognizant is a world leader in delivering digital transformation solutions to Life Sciences. Through our knowledge and expertise in Automation, MES & Digital, we deliver stable manufacturing systems that are optimized to improve operational efficiencies, whilst maintaining compliance. Our specialist engineering teams have the aptitude to deliver and support Pharma 4.0 architectures and solutions covering all IT, OT and IoT applications, infrastructures and services The AVEVA PI Engineer position offers the opportunity to join a multidisciplinary team that operates across multiple sites, providing support for the PI Historian Operational Service. The AVEVA PI Engineer will be an integral member of the support team, responsible for monitoring the system to ensure continuous production at the manufacturing site. Responsibilities: Support site vertical integration defined by the Project Manager or Lead Engineer. Create/Update the configuration and validation documents related to the PI system. Execute the validation as defined in the change control. Ensure data integrity and consistency by implementing data quality control measures and monitoring data validation processes. Collaborate within Automation Infra team to manage system upgrades, patches, and performance optimizations for the OSIsoft PI system. Handling and addressing tickets or issues associated with the PI system. Provide maintenance to the PI system to ensure system availability 24/7. Stay up-to-date with industry trends, emerging technologies, and regulatory requirements related to data engineering and manufacturing systems. Contribute to continuous improvement initiatives, identifying opportunities to enhance data management processes, system performance, and user experience To apply for this PI Software Engineer role, you will need an undergraduate degree in IT, Automation, Science or Engineering, or a related discipline, or equivalent work experience. You will also require the following: Experience working with the OSIsoft PI system, ideally within the pharmaceutical industry. Understanding of pharmaceutical manufacturing processes, including batch processing, equipment automation, and data acquisition systems. Proficiency in data engineering concepts, data integration, and data management best practices. Ability to multitask, manage multiple projects and prioritize tasks in a busy environment Experience with programming languages (e.g., Python, SQL) and scripting is advantageous. Experience with ticketing systems such as Service Now or similar The Cognizant community: We are a high caliber team who appreciate and support one another. Our people uphold an energetic, collaborative and inclusive workplace where everyone can thrive. Cognizant is a global community with more than 300,000 associates around the world. We don’t just dream of a better way – we make it happen. We take care of our people, clients, company, communities and climate by doing what’s right. We foster an innovative environment where you can build the career path that’s right for you. About us: Cognizant is one of the world's leading professional services companies, transforming clients' business, operating, and technology models for the digital era. Our unique industry-based, consultative approach helps clients envision, build, and run more innovative and efficient businesses. Headquartered in the U.S., Cognizant (a member of the NASDAQ-100 and one of Forbes World’s Best Employers 2024) is consistently listed among the most admired companies in the world. Learn how Cognizant helps clients lead with digital at

Greetings from Ubique Systems!!! We are looking for a Data Architect for one of our customer who has an expertise in:- Strong experience as an Information Architect in Pharma / Healthcare environments Proven expertise in: Data modeling (conceptual, logical, canonical) Metadata management Pharma R&D Master Data & Reference Data Management (MDRM) Data governance frameworks Deep understanding of Pharma Commercial data domains, such as: Sales & CRM Marketing & campaign data Customer (HCP/HCO) data Market access and commercial analytics Ability to operate at strategic and advisory level, influencing stakeholders across business and IT Experience driving enterprise-wide data standards and value realization Employment type:- B2B Contract. It would be hybrid working in Barcelona, Spain. Note:-Only apply if you have valid visa in the EU Region, Sponsorship will not be given.

In a few words Position: SAP BASIS ADMINISTRATOR Location: Madrid-On site Experience: +3 years as SAP Basis Administrator, preferably in pharmaceutical industry Want to know more? INSUD PHARMA is undertaking a global project to implement and migrate its SAP ECC management system to S4/HANA. We seek an SAP PP-PI Expert Consultant to collaborate in this implementation by analyzing, supervising, and delivering solutions together with external partners working on the project. The consultant will liaise with key users, control project execution within their area, and ensure quality and adherence to the Core Model defined for INSUD PHARMA. What are we looking for? The SAP Basis Administrator provides first-level technical support on the company's SAP systems, ensuring optimal operation through preventive maintenance, continuous monitoring, incident management, user administration, and participation in system upgrades or new product installations. Collaborate with different teams to ensure continuity of service and contribute to digital transformation projects within a specialized SAP technology service environment. Specific responsabilities: Provide preventive, planned, and corrective technical support for SAP systems (NetWeaver, S/4 HANA, Business Objects). Manage and maintain optimal SAP system performance. Administer SAP landscape transports, jobs, printers, and print queues. Create, maintain, and manage users, profiles, and roles (including GRC tool; user/role lock and unlock). Monitor performance and availability of SAP systems. Troubleshoot technical issues and manage SAP Basis support tickets. Implement new SAP releases, patches, products, and software/certificate upgrades. Perform basic monitoring, database backup, and recovery tasks (Hana, Oracle, etc.). Create and maintain standard operational procedures (SOP) in collaboration with the Quality Assurance area. Collaborate with cross-functional teams and during audit processes, participating in digital transformation projects. What do you need? Basic knowledge of operating system administration (Linux/Windows) and databases (HANA, Oracle, etc.) Database communication: Configure and maintain communication between databases, manage memory, and handle the exchange of business data, including integrations with external systems. Understanding of SAP architecture (On-Premise, Cloud, and hybrid models). Analytical and problem-solving skills. Communication and teamwork skills. Our benefits! Permanent contract ⏰ Flexible schedule Health insurance coverage Professional development opportunities Selection process ️ Initial contact through phone or email. 1-2 interviews conducted virtually or in person. Continuous communication about the selection status. Not the right fit? Follow us on LinkedIn and Instagram for more exciting career opportunities at INSUD PHARMA. Stay connected and be ready for your next challenge! #InsudPharma #Challenger #InsudTalent COMMITMENT TO EQUAL OPPORTUNITY INSUD PHARMA promotes gender equality and does not discriminate based on ethnicity, religion, sexual orientation, disability, or any other condition. We foster a diverse, inclusive, and respectful work environment.

In a few words Position: SAP BASIS ADMINISTRATOR Location: Madrid-On site Experience: +3 years as SAP Basis Administrator, preferably in pharmaceutical industry Want to know more? INSUD PHARMA is undertaking a global project to implement and migrate its SAP ECC management system to S4/HANA. We seek an SAP PP-PI Expert Consultant to collaborate in this implementation by analyzing, supervising, and delivering solutions together with external partners working on the project. The consultant will liaise with key users, control project execution within their area, and ensure quality and adherence to the Core Model defined for INSUD PHARMA. What are we looking for? The SAP Basis Administrator provides first-level technical support on the company's SAP systems, ensuring optimal operation through preventive maintenance, continuous monitoring, incident management, user administration, and participation in system upgrades or new product installations. Collaborate with different teams to ensure continuity of service and contribute to digital transformation projects within a specialized SAP technology service environment. Specific responsabilities: Provide preventive, planned, and corrective technical support for SAP systems (NetWeaver, S/4 HANA, Business Objects). Manage and maintain optimal SAP system performance. Administer SAP landscape transports, jobs, printers, and print queues. Create, maintain, and manage users, profiles, and roles (including GRC tool; user/role lock and unlock). Monitor performance and availability of SAP systems. Troubleshoot technical issues and manage SAP Basis support tickets. Implement new SAP releases, patches, products, and software/certificate upgrades. Perform basic monitoring, database backup, and recovery tasks (Hana, Oracle, etc.). Create and maintain standard operational procedures (SOP) in collaboration with the Quality Assurance area. Collaborate with cross-functional teams and during audit processes, participating in digital transformation projects. What do you need? Basic knowledge of operating system administration (Linux/Windows) and databases (HANA, Oracle, etc.) Database communication: Configure and maintain communication between databases, manage memory, and handle the exchange of business data, including integrations with external systems. Understanding of SAP architecture (On-Premise, Cloud, and hybrid models). Analytical and problem-solving skills. Communication and teamwork skills. Our benefits! Permanent contract ⏰ Flexible schedule Health insurance coverage Professional development opportunities Selection process ️ Initial contact through phone or email. 1-2 interviews conducted virtually or in person. Continuous communication about the selection status. Not the right fit? Follow us on LinkedIn and Instagram for more exciting career opportunities at INSUD PHARMA. Stay connected and be ready for your next challenge! #InsudPharma #Challenger #InsudTalent COMMITMENT TO EQUAL OPPORTUNITY INSUD PHARMA promotes gender equality and does not discriminate based on ethnicity, religion, sexual orientation, disability, or any other condition. We foster a diverse, inclusive, and respectful work environment.

In a few words Position: SAP BASIS ADMINISTRATOR Location: Madrid-On site Experience: +3 years as SAP Basis Administrator, preferably in pharmaceutical industry Want to know more? INSUD PHARMA is undertaking a global project to implement and migrate its SAP ECC management system to S4/HANA. We seek an SAP PP-PI Expert Consultant to collaborate in this implementation by analyzing, supervising, and delivering solutions together with external partners working on the project. The consultant will liaise with key users, control project execution within their area, and ensure quality and adherence to the Core Model defined for INSUD PHARMA. What are we looking for? The SAP Basis Administrator provides first-level technical support on the company's SAP systems, ensuring optimal operation through preventive maintenance, continuous monitoring, incident management, user administration, and participation in system upgrades or new product installations. Collaborate with different teams to ensure continuity of service and contribute to digital transformation projects within a specialized SAP technology service environment. Specific responsabilities: Provide preventive, planned, and corrective technical support for SAP systems (NetWeaver, S/4 HANA, Business Objects). Manage and maintain optimal SAP system performance. Administer SAP landscape transports, jobs, printers, and print queues. Create, maintain, and manage users, profiles, and roles (including GRC tool; user/role lock and unlock). Monitor performance and availability of SAP systems. Troubleshoot technical issues and manage SAP Basis support tickets. Implement new SAP releases, patches, products, and software/certificate upgrades. Perform basic monitoring, database backup, and recovery tasks (Hana, Oracle, etc.). Create and maintain standard operational procedures (SOP) in collaboration with the Quality Assurance area. Collaborate with cross-functional teams and during audit processes, participating in digital transformation projects. What do you need? Basic knowledge of operating system administration (Linux/Windows) and databases (HANA, Oracle, etc.) Database communication: Configure and maintain communication between databases, manage memory, and handle the exchange of business data, including integrations with external systems. Understanding of SAP architecture (On-Premise, Cloud, and hybrid models). Analytical and problem-solving skills. Communication and teamwork skills. Our benefits! Permanent contract ⏰ Flexible schedule Health insurance coverage Professional development opportunities Selection process ️ Initial contact through phone or email. 1-2 interviews conducted virtually or in person. Continuous communication about the selection status. Not the right fit? Follow us on LinkedIn and Instagram for more exciting career opportunities at INSUD PHARMA. Stay connected and be ready for your next challenge! #InsudPharma #Challenger #InsudTalent COMMITMENT TO EQUAL OPPORTUNITY INSUD PHARMA promotes gender equality and does not discriminate based on ethnicity, religion, sexual orientation, disability, or any other condition. We foster a diverse, inclusive, and respectful work environment.

Position: Data Platform Architect INSUD PHARMA operates across the entire pharmaceutical value chain, providing specialized knowledge and experience in scientific research, development, manufacturing, sales, and marketing of a wide range of active pharmaceutical ingredients (API), finished dosage forms (FDF), and branded pharmaceutical products, adding value to human and animal health. The activities of INSUD PHARMA are organized into three synergistic business areas: Industrial (Chemo), Branded (Exeltis), and Biotech (mAbxience), with over 9,000 professionals in more than 50 countries, 20 state-of-the-art facilities, 15 specialized R&D centers, 12 commercial offices, and more than 35 pharmaceutical subsidiaries, serving 1,150 customers in 96 countries worldwide. INSUD PHARMA believes in innovation and sustainable development. We are looking for a highly skilled Data Architect to take ownership of permissions management, cost optimization, and operational stability across our Snowflake data platform and associated orchestration tools such as Airflow and dbt. This role is critical to ensuring secure, efficient, and governed data access and processing, aligned with the Cosmos architecture and corporate policies. The candidate will also lead the definition and promotion of best practices and methodologies across the data platform lifecycle. Manage and control permissions and access in Snowflake, ensuring compliance with data security and governance policies, including RBAC design and enforcement integrated into CI/CD pipelines. Monitor and optimize costs associated with Snowflake and related cloud services, implementing strategies for efficient and controlled consumption. Oversee the operation, monitoring, and stability of the entire data platform, including Snowflake, Airflow orchestration, and dbt transformations. Manage CI/CD processes using GitLab, defining, executing, and maintaining pipelines for automated deployments across Snowflake, Airflow, dbt, and related components. Lead deployments in production and pre-production environments, ensuring quality, stability, and compliance with SLAs. Diagnose and resolve technical issues related to permissions, deployments, orchestration workflows, and resource consumption. Collaborate with architecture and development teams to define and apply best practices in data management, security, development, orchestration, and transformation. Define and promote development methodologies and quality control aligned with the Platform architecture. Implement and maintain integrated monitoring dashboards for end-to-end visibility of platform health, data pipeline executions, and operational metrics; Collaborate with AWS teams to manage permissions, network configurations, and inter-system connectivity, escalating issues as needed. Coordinate with Datasphere teams for SAP data ingestion and integration with Snowflake. Document processes, configurations, policies, and architectural decisions related to permissions, costs, orchestration, deployments, and platform governance. Proven experience in Snowflake administration and management, especially in access control, RBAC, and cost optimization. Experience with Airflow for orchestration, including monitoring, troubleshooting, and deployment. Strong knowledge and hands-on experience with dbt for data modeling and transformation, with the ability to define and promote best practices. Experience managing CI/CD pipelines with GitLab, including automated deployments and integration with orchestration tools. Solid understanding of cloud data architectures and services (AWS, Azure, Google Cloud), including permissions and networking aspects. Experience troubleshooting complex technical issues related to deployments, permissions, orchestration workflows, and resource usage. Familiarity with development methodologies, quality assurance, and governance in data environments. Ability to implement and maintain integrated monitoring and alerting solutions, preferably using Power BI. Advanced technical English proficiency Flexible start time from Monday to Friday (full-time). # Permanent contract.

Position: Data Platform Architect INSUD PHARMA operates across the entire pharmaceutical value chain, providing specialized knowledge and experience in scientific research, development, manufacturing, sales, and marketing of a wide range of active pharmaceutical ingredients (API), finished dosage forms (FDF), and branded pharmaceutical products, adding value to human and animal health. The activities of INSUD PHARMA are organized into three synergistic business areas: Industrial (Chemo), Branded (Exeltis), and Biotech (mAbxience), with over 9,000 professionals in more than 50 countries, 20 state-of-the-art facilities, 15 specialized R&D centers, 12 commercial offices, and more than 35 pharmaceutical subsidiaries, serving 1,150 customers in 96 countries worldwide. INSUD PHARMA believes in innovation and sustainable development. We are looking for a highly skilled Data Architect to take ownership of permissions management, cost optimization, and operational stability across our Snowflake data platform and associated orchestration tools such as Airflow and dbt. This role is critical to ensuring secure, efficient, and governed data access and processing, aligned with the Cosmos architecture and corporate policies. The candidate will also lead the definition and promotion of best practices and methodologies across the data platform lifecycle. Manage and control permissions and access in Snowflake, ensuring compliance with data security and governance policies, including RBAC design and enforcement integrated into CI/CD pipelines. Monitor and optimize costs associated with Snowflake and related cloud services, implementing strategies for efficient and controlled consumption. Oversee the operation, monitoring, and stability of the entire data platform, including Snowflake, Airflow orchestration, and dbt transformations. Manage CI/CD processes using GitLab, defining, executing, and maintaining pipelines for automated deployments across Snowflake, Airflow, dbt, and related components. Lead deployments in production and pre-production environments, ensuring quality, stability, and compliance with SLAs. Diagnose and resolve technical issues related to permissions, deployments, orchestration workflows, and resource consumption. Collaborate with architecture and development teams to define and apply best practices in data management, security, development, orchestration, and transformation. Define and promote development methodologies and quality control aligned with the Platform architecture. Implement and maintain integrated monitoring dashboards for end-to-end visibility of platform health, data pipeline executions, and operational metrics; Collaborate with AWS teams to manage permissions, network configurations, and inter-system connectivity, escalating issues as needed. Coordinate with Datasphere teams for SAP data ingestion and integration with Snowflake. Document processes, configurations, policies, and architectural decisions related to permissions, costs, orchestration, deployments, and platform governance. Proven experience in Snowflake administration and management, especially in access control, RBAC, and cost optimization. Experience with Airflow for orchestration, including monitoring, troubleshooting, and deployment. Strong knowledge and hands-on experience with dbt for data modeling and transformation, with the ability to define and promote best practices. Experience managing CI/CD pipelines with GitLab, including automated deployments and integration with orchestration tools. Solid understanding of cloud data architectures and services (AWS, Azure, Google Cloud), including permissions and networking aspects. Experience troubleshooting complex technical issues related to deployments, permissions, orchestration workflows, and resource usage. Familiarity with development methodologies, quality assurance, and governance in data environments. Ability to implement and maintain integrated monitoring and alerting solutions, preferably using Power BI. Advanced technical English proficiency Flexible start time from Monday to Friday (full-time). # Permanent contract.

Position: Data Platform Architect INSUD PHARMA operates across the entire pharmaceutical value chain, providing specialized knowledge and experience in scientific research, development, manufacturing, sales, and marketing of a wide range of active pharmaceutical ingredients (API), finished dosage forms (FDF), and branded pharmaceutical products, adding value to human and animal health. The activities of INSUD PHARMA are organized into three synergistic business areas: Industrial (Chemo), Branded (Exeltis), and Biotech (mAbxience), with over 9,000 professionals in more than 50 countries, 20 state-of-the-art facilities, 15 specialized R&D centers, 12 commercial offices, and more than 35 pharmaceutical subsidiaries, serving 1,150 customers in 96 countries worldwide. INSUD PHARMA believes in innovation and sustainable development. We are looking for a highly skilled Data Architect to take ownership of permissions management, cost optimization, and operational stability across our Snowflake data platform and associated orchestration tools such as Airflow and dbt. This role is critical to ensuring secure, efficient, and governed data access and processing, aligned with the Cosmos architecture and corporate policies. The candidate will also lead the definition and promotion of best practices and methodologies across the data platform lifecycle. Manage and control permissions and access in Snowflake, ensuring compliance with data security and governance policies, including RBAC design and enforcement integrated into CI/CD pipelines. Monitor and optimize costs associated with Snowflake and related cloud services, implementing strategies for efficient and controlled consumption. Oversee the operation, monitoring, and stability of the entire data platform, including Snowflake, Airflow orchestration, and dbt transformations. Manage CI/CD processes using GitLab, defining, executing, and maintaining pipelines for automated deployments across Snowflake, Airflow, dbt, and related components. Lead deployments in production and pre-production environments, ensuring quality, stability, and compliance with SLAs. Diagnose and resolve technical issues related to permissions, deployments, orchestration workflows, and resource consumption. Collaborate with architecture and development teams to define and apply best practices in data management, security, development, orchestration, and transformation. Define and promote development methodologies and quality control aligned with the Platform architecture. Implement and maintain integrated monitoring dashboards for end-to-end visibility of platform health, data pipeline executions, and operational metrics; Collaborate with AWS teams to manage permissions, network configurations, and inter-system connectivity, escalating issues as needed. Coordinate with Datasphere teams for SAP data ingestion and integration with Snowflake. Document processes, configurations, policies, and architectural decisions related to permissions, costs, orchestration, deployments, and platform governance. Proven experience in Snowflake administration and management, especially in access control, RBAC, and cost optimization. Experience with Airflow for orchestration, including monitoring, troubleshooting, and deployment. Strong knowledge and hands-on experience with dbt for data modeling and transformation, with the ability to define and promote best practices. Experience managing CI/CD pipelines with GitLab, including automated deployments and integration with orchestration tools. Solid understanding of cloud data architectures and services (AWS, Azure, Google Cloud), including permissions and networking aspects. Experience troubleshooting complex technical issues related to deployments, permissions, orchestration workflows, and resource usage. Familiarity with development methodologies, quality assurance, and governance in data environments. Ability to implement and maintain integrated monitoring and alerting solutions, preferably using Power BI. Advanced technical English proficiency Flexible start time from Monday to Friday (full-time). # Permanent contract.

Position: Data Platform Architect INSUD PHARMA operates across the entire pharmaceutical value chain, providing specialized knowledge and experience in scientific research, development, manufacturing, sales, and marketing of a wide range of active pharmaceutical ingredients (API), finished dosage forms (FDF), and branded pharmaceutical products, adding value to human and animal health. The activities of INSUD PHARMA are organized into three synergistic business areas: Industrial (Chemo), Branded (Exeltis), and Biotech (mAbxience), with over 9,000 professionals in more than 50 countries, 20 state-of-the-art facilities, 15 specialized R&D centers, 12 commercial offices, and more than 35 pharmaceutical subsidiaries, serving 1,150 customers in 96 countries worldwide. INSUD PHARMA believes in innovation and sustainable development. We are looking for a highly skilled Data Architect to take ownership of permissions management, cost optimization, and operational stability across our Snowflake data platform and associated orchestration tools such as Airflow and dbt. This role is critical to ensuring secure, efficient, and governed data access and processing, aligned with the Cosmos architecture and corporate policies. The candidate will also lead the definition and promotion of best practices and methodologies across the data platform lifecycle. Manage and control permissions and access in Snowflake, ensuring compliance with data security and governance policies, including RBAC design and enforcement integrated into CI/CD pipelines. Monitor and optimize costs associated with Snowflake and related cloud services, implementing strategies for efficient and controlled consumption. Oversee the operation, monitoring, and stability of the entire data platform, including Snowflake, Airflow orchestration, and dbt transformations. Manage CI/CD processes using GitLab, defining, executing, and maintaining pipelines for automated deployments across Snowflake, Airflow, dbt, and related components. Lead deployments in production and pre-production environments, ensuring quality, stability, and compliance with SLAs. Diagnose and resolve technical issues related to permissions, deployments, orchestration workflows, and resource consumption. Collaborate with architecture and development teams to define and apply best practices in data management, security, development, orchestration, and transformation. Define and promote development methodologies and quality control aligned with the Platform architecture. Implement and maintain integrated monitoring dashboards for end-to-end visibility of platform health, data pipeline executions, and operational metrics; Collaborate with AWS teams to manage permissions, network configurations, and inter-system connectivity, escalating issues as needed. Coordinate with Datasphere teams for SAP data ingestion and integration with Snowflake. Document processes, configurations, policies, and architectural decisions related to permissions, costs, orchestration, deployments, and platform governance. Proven experience in Snowflake administration and management, especially in access control, RBAC, and cost optimization. Experience with Airflow for orchestration, including monitoring, troubleshooting, and deployment. Strong knowledge and hands-on experience with dbt for data modeling and transformation, with the ability to define and promote best practices. Experience managing CI/CD pipelines with GitLab, including automated deployments and integration with orchestration tools. Solid understanding of cloud data architectures and services (AWS, Azure, Google Cloud), including permissions and networking aspects. Experience troubleshooting complex technical issues related to deployments, permissions, orchestration workflows, and resource usage. Familiarity with development methodologies, quality assurance, and governance in data environments. Ability to implement and maintain integrated monitoring and alerting solutions, preferably using Power BI. Advanced technical English proficiency Flexible start time from Monday to Friday (full-time). # Permanent contract.

Vincle es una empresa especializada en el proceso comercial con más de 30 años de experiencia en los sectores del Gran Consumo y Pharma con proyectos a nivel internacional. ¿Quieres conocer más? Entra en nuestra web: &##Queremos ampliar nuestro equipo PMO con un/a Consultor/ Analista Técnico-Funcional de Implementación CRM que haya tenido experiencia previa. ¿Qué esperamos de ti? ~ Formación Superior en áreas relacionadas con IT/ informática (Ingenieria, Informática, Ciclos formativos de Informática y/o programación, ...) ~+5 años de experiencia en análisis y puesta en marcha de proyectos de Applications (CRM, ERP, BI, etc.). ~ Inglés y Español fluidos. Mínimo C1 en ambos. ~ Capacidad Analítica, de trabajo en detalle y resolución de problemas, así como y buenas habilidades comunicativas y de trabajo en equipo. &##Reunirse con los socios comerciales y técnicos de nuestros clientes para tomar los requisitos de sus necesidades. Realizar el análisis funcional, técnico y orgánico en los nuevos proyectos en los que participes. Elaborar documentación técnica para los equipos de desarrollo de nuestra Fábrica de Software. Desarrollo de proyectos y seguimiento del rendimiento de los proyectos. Desarrollar documentación de datos de uso y prueba del sistema para verificar la calidad de los desarrollos. Proponer soluciones óptimas a cualquier problema de funcionamiento que surja y sugerir el desarrollo de nuevas aplicaciones o funcionalidades. Proporcionar soporte técnico a nuestro Departamento de Atención al Cliente N3 con la base de clientes actual. &##Modelo híbrido oficina (3 días/semana)-remoto (2 días/semana). - Oficinas en Madrid - Pozuelo de Alarcón. ~ Flexibilidad horaria de entrada y salida. ~ Contrato indefinido. ~ Jornada intensiva Viernes y verano (1/2 Julio y Agosto). ~23 días laborables de vacaciones. ~ Formación activa dentro de la empresa. ~ Ven a un equipo donde se transmite el buen rollo y no nos asusta ningún reto! ¿

Job Title: Information Protection Analyst Location: Barcelona, Spain - Hybrid: 3 Days to Office Every Week Duration: 6 Months - Extendable Employment Type: Contract B2B Roles & Responsibilities: We are hiring an Information Protection Analyst (Data Security) to support enterprise information protection and risk reduction initiatives. We require strong Information Protection and Data Security domain experience . Role Focus Drive delivery of information protection and data security changes Engage IT, Security, Compliance, and Business stakeholders Define clear, testable technical and process requirements Manage and prioritise security change backlogs Conduct impact and risk assessments Coordinate UAT, pilots, and control validation Progress governance approvals (security reviews, DPIAs, compliance sign-off) Support adoption and measure control effectiveness Mandatory Skills & Experience Proven experience as an Information Protection Analyst Strong Data Security domain knowledge Practical understanding of: Data Classification DLP (Data Loss Prevention) Encryption & Key Management Identity & Access Management (IAM) Secure collaboration & data monitoring Knowledge of GDPR, SCCs, ISO 27001, NIST Experience in risk-based analysis and governance navigation Strong stakeholder management (IT, Compliance, Security, Business) Experience working in Agile / hybrid delivery environments Desirable Life Sciences / Pharma experience DPIAs, risk assessments, control testing, audit evidence collection Tools: Jira, Azure DevOps, Confluence Experience running UAT, usability testing, and adoption activities

Sobre Strategic Pharma Strategic Pharma es una consultora especializada en gestión y desarrollo estratégico de farmacias comunitarias. Con más de 20 años de experiencia en el sector farmacéutico, ayudamos a titulares y equipos a mejorar la rentabilidad, la organización y la eficiencia de su farmacia mediante auditorías, formación práctica y programas de mentoría. Nuestra metodología combina el análisis de datos con la experiencia real del día a día en la oficina de farmacia, para transformar la gestión en decisiones estratégicas que generan resultados sostenibles y equipos más comprometidos. Con el lanzamiento de nuestra plataforma de formación online, buscamos profesionales con vocación docente que contribuyan al desarrollo de programas orientados a la práctica de la farmacia comunitaria actual. Descripción: Strategic Pharma selecciona farmacéuticos/as titulados/as con formación avanzada en estrés e insomnio para colaborar en la formación online dirigida a farmacéuticos comunitarios que quieren especializarse en consejo sobre estrés e insomnio. Buscamos un perfil con conocimiento profundo de la fisiología del estrés y del sueño , experiencia real en el abordaje de estrés e insomnio desde la farmacia comunitaria y capacidad para trasladar el conocimiento científico a la práctica diaria del mostrador . Requisitos imprescindibles (excluyentes): Grado en Farmacia (imprescindible). Experiencia en abordaje del estrés, insomnio o fatiga en farmacia comunitaria . Conocimientos avanzados en fisiología del sueño y regulación del estrés . Dominio de suplementación, fitoterapia y adaptógenos relacionados con el descanso y el manejo del estrés . Capacidad para analizar casos clínicos y trasladar el razonamiento al consejo farmacéutico en mostrador . Se valorará especialmente Formación avanzada en sueño, estrés, micronutrición y suplementación. Experiencia en docencia o formación dirigida a farmacéuticos . Experiencia en creación de contenidos técnicos o programas formativos . Participación en formación online o programas educativos estructurados . Funciones Diseño y elaboración de contenidos formativos especializados en estrés e insomnio . Impartición de formación online dirigida a farmacéuticos . Colaboración en proyectos de consultoría técnica en el área de bienestar y sueño . Condiciones Colaboración profesional (autónomo/a) o contrato indefinido discontinuo . Trabajo 100 % online . Compatible con actividad profesional en farmacia .

Sobre Strategic Pharma Strategic Pharma es una consultora especializada en gestión y desarrollo estratégico de farmacias comunitarias. Con más de 20 años de experiencia en el sector farmacéutico, ayudamos a titulares y equipos a mejorar la rentabilidad, la organización y la eficiencia de su farmacia mediante auditorías, formación práctica y programas de mentoría. Nuestra metodología combina el análisis de datos con la experiencia real del día a día en la oficina de farmacia, para transformar la gestión en decisiones estratégicas que generan resultados sostenibles y equipos más comprometidos. Con el lanzamiento de nuestra plataforma de formación online, buscamos profesionales con vocación docente que contribuyan al desarrollo de programas orientados a la práctica de la farmacia comunitaria actual. Descripción: Strategic Pharma selecciona farmacéuticos/as titulados/as con formación avanzada en estrés e insomnio para colaborar en la formación online dirigida a farmacéuticos comunitarios que quieren especializarse en consejo sobre estrés e insomnio. Buscamos un perfil con conocimiento profundo de la fisiología del estrés y del sueño, experiencia real en el abordaje de estrés e insomnio desde la farmacia comunitaria y capacidad para trasladar el conocimiento científico a la práctica diaria del mostrador. Requisitos imprescindibles (excluyentes): • Grado en Farmacia (imprescindible)., • Experiencia en abordaje del estrés, insomnio o fatiga en farmacia comunitaria., • Conocimientos avanzados en fisiología del sueño y regulación del estrés., • Dominio de suplementación, fitoterapia y adaptógenos relacionados con el descanso y el manejo del estrés., • Capacidad para analizar casos clínicos y trasladar el razonamiento al consejo farmacéutico en mostrador. Se valorará especialmente • Formación avanzada en sueño, estrés, micronutrición y suplementación., • Experiencia en docencia o formación dirigida a farmacéuticos., • Experiencia en creación de contenidos técnicos o programas formativos., • Participación en formación online o programas educativos estructurados. Funciones • Diseño y elaboración de contenidos formativos especializados en estrés e insomnio., • Impartición de formación online dirigida a farmacéuticos., • Colaboración en proyectos de consultoría técnica en el área de bienestar y sueño. Condiciones • Colaboración profesional (autónomo/a) o contrato indefinido discontinuo., • Trabajo 100 % online., • Compatible con actividad profesional en farmacia.

Who We Are: Whitewater Group is a leading provider of innovative and sustainable water treatment engineering systems operating in Ireland, 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 Bray, Co. Wicklow and operates from European bases in Spain, Sweden, Finland and UK, with plans for further offices to open in Germany, Denmark and Italy. The Group is experiencing significant growth due to its focus on off-site construction methods (OSM) of delivering turnkey projects, meaning on-site construction time is kept to a minimum. Role Description: The successful candidate will be involved in planned preventative maintenance, repair and maintenance of existing water treatment plants, customer training, and delivering a high level of technical support. Whitewater provides quality engineering support, including root cause analysis and the implementation of corrective actions. All work is carried out in accordance with relevant Company and Customer Quality procedures. The role also includes managing customer relationships with a strong focus on communication and ensuring excellence in customer satisfaction. Collaboration with the customer service and administration teams is essential, including the provision of technical service reports and all relevant documentation for processing and invoicing. Main Duties and Responsibilities: • Perform planned preventative maintenance (PPM) and corrective repair on existing water treatment plants., • Diagnose faults and implement root cause analysis and corrective actions., • Troubleshoots and repairs pumps, instruments and control panels., • Provide high-level technical assistance to customers., • Prepare and submit technical service reports., • Complete all required documentation for customer service and administration, ensuring accurate processing and invoicing., • Ensure all work complies with company and customer quality procedures., • Work independently or as part of a small team with minimal supervision. Required Experience & Qualifications: • Degree or equivalent qualification in Mechanical or Electrical background., • Working with water treatment technologies such as Membranes, Ion Exchange, CDI, Filtration, Chemical Dosing Systems and UV., • Fluent Spanish & English speaker with strong speaking skills., • Strong detail-oriented work style, and an accommodating and proactive attitude., • IT literate and proficiency in the use of Microsoft Office including Word, Excel, Powerpoint, Outlook., • Permit to Work in the EU., • Full clean driving license.

In a nutshell 📌 Position: Launch Specialist – New Product Introduction (NPI) Location: INSUD PHARMA Headquarters, Sanchinarro (Madrid) – On-site Experience: 3-5 years in project management, preferably in the pharmaceutical industry or regulated sectors Want to know more? 👇 INSUD PHARMA operates across the entire pharmaceutical value chain, providing specialized knowledge and experience in scientific research, development, manufacturing, sales, and commercialization of a wide range of active pharmaceutical ingredients (APIs), finished dosage forms (FDF), and branded pharmaceutical products, adding value to both human and animal health. INSUD PHARMA’s activity is organized into three synergistic business areas: Industrial (Chemo), Branded (Exeltis), and Biotech (mAbxience), with more than 9,000 professionals in over 50 countries, 20 state-of-the-art facilities, 15 specialized R&D centers, 12 commercial offices, and more than 35 pharmaceutical subsidiaries, serving 1,150 clients in 96 countries worldwide. INSUD PHARMA believes in innovation and sustainable development. Ready to be a #Challenger? 💪 What are we looking for? 🔎 As a Launch Specialist at INSUD PHARMA, you will be the bridge between development and industrialization, ensuring every new product is ready for its first commercial production. Your mission will be to coordinate all key functions to guarantee successful launches, meeting the highest standards of quality, cost, and service. Key Responsibilities: • Manage and maintain launch plans for new products, ensuring milestones, dependencies, and timelines are met., • Coordinate cross-functional teams (Engineering, QA, QC, Production, Supply Chain, Planning, Regulatory Affairs, Finance, etc.) for timely execution of launch activities., • Lead follow-up meetings, facilitating communication and alignment among all stakeholders., • Serve as the operational point of contact for internal and external clients for assigned launches., • Proactively identify risks, constraints, or deviations, and propose mitigation plans., • Manage documentation, progress reports, and ensure data accuracy in the launch database., • Prioritize and sequence activities to maximize speed, service level, and business value., • Capture lessons learned and contribute to continuous improvement of launch processes. The challenge! 🚀 • Coordinate and oversee the execution of multiple launch projects simultaneously., • Ensure delivery ON TIME, IN FULL, AT THE RIGHT COST, and with the HIGHEST QUALITY., • Drive collaboration between departments and operational excellence. What do you need? 🤓 • University degree in Pharmacy, Chemistry, Engineering, Life Sciences, or similar., • 3-5 years of experience in project management, preferably in the pharmaceutical, chemical, or regulated sectors., • Experience coordinating cross-functional teams and managing stakeholders., • Solid knowledge of technology transfer processes, quality assurance, and supply chain., • High level of English (minimum B2); other languages are a plus., • Proficiency in project management tools (MS Project, Excel, etc.)., • Outstanding communication, organizational, analytical, and problem-solving skills. Our benefits! 👏 📜 Permanent contract 🌍 International and dynamic environment 🎓 Professional development plan and continuous training 🍽️ Subsidized canteen at headquarters 🅿️ Free parking 💼 Private health insurance What will the selection process be like? 🕵️ • Initial contact by phone or email., • 1-2 on-site/virtual interviews, • Ongoing communication about your application status. 🔷Think this offer isn’t for you?🔷 Follow us on LinkedIn and Instagram to discover more career opportunities at INSUD PHARMA! #InsudPharma #Challenger #Insuder #InsudTalent 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.

At ASTEK Iberia, we are looking for a senior Solution Architect with deep expertise in Risk, Audit & Compliance, strong knowledge of ServiceNow IRM/GRC modules, and solid background in SaaS, integrations and cloud architecture (AWS/Azure) for our pharma partner. The role will design and govern end-to-end solution architecture, translate business requirements into technical solutions, manage vendors, and ensure alignment with Roche enterprise IT standards in a global, multicultural environment. 💪 Main responsibilities: • Design solutions aligned with enterprise architecture standards and business priorities, • Lead cross-solution architecture discussions with developers, vendors, and internal/external stakeholders, • Review existing solutions to drive continuous improvement and manage technical debt, • Research, evaluate, and run proof-of-concepts for new technologies and solutions, • Define non-functional requirements and assess vendor and integration capabilities, • Translate business requirements into technical architecture and own solution architecture documentation, • Identify opportunities to optimize and improve business processes, • Partner with Product Managers and Enterprise Architects to define high-level solution intent and value 👀 Who are you? • Bachelor’s degree in Computer Science, Systems Analysis, or equivalent experience, • Deep expertise in Risk, Audit & Compliance management, • 7–10 years of experience designing and implementing IT solutions, • Strong knowledge of ServiceNow platform, especially IRM / GRC modules (TPRM / LSD), • Experience working with SaaS platforms (ServiceNow, Salesforce, SAP Cloud, etc.), • Strong understanding of integration architectures (APIs REST/SOAP, ESB/EAI, MQ, point-to-point), • Experience with cloud architectures (AWS and/or Azure), • Knowledge of middleware, security, infrastructure, and DevOps layers, • Ability to create clear architectural documentation (e.g. UML), • Strong communication skills and ability to explain complex technical concepts clearly, • Experience working in multicultural and international environments 💼 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.

Who We Are: Whitewater Group is a leading provider of innovative and sustainable water treatment engineering systems operating in Ireland, 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 Bray, Co. Wicklow and operates from European bases in Spain, Sweden, Finland and UK, with plans for further offices to open in Germany, Denmark and Italy. The Group is experiencing significant growth due to its focus on off-site construction methods (OSM) of delivering turnkey projects, meaning on-site construction time is kept to a minimum. Role Description: The successful candidate will be involved in planned preventative maintenance, repair and maintenance of existing water treatment plants, customer training, and delivering a high level of technical support. Whitewater provides quality engineering support, including root cause analysis and the implementation of corrective actions. All work is carried out in accordance with relevant Company and Customer Quality procedures. The role also includes managing customer relationships with a strong focus on communication and ensuring excellence in customer satisfaction. Collaboration with the customer service and administration teams is essential, including the provision of technical service reports and all relevant documentation for processing and invoicing. Main Duties and Responsibilities: • Perform planned preventative maintenance (PPM) and corrective repair on existing water treatment plants., • Diagnose faults and implement root cause analysis and corrective actions., • Troubleshoots and repairs pumps, instruments and control panels., • Provide high-level technical assistance to customers., • Prepare and submit technical service reports., • Complete all required documentation for customer service and administration, ensuring accurate processing and invoicing., • Ensure all work complies with company and customer quality procedures., • Work independently or as part of a small team with minimal supervision. Required Experience & Qualifications: • Degree or equivalent qualification in Mechanical or Electrical background., • Working with water treatment technologies such as Membranes, Ion Exchange, CDI, Filtration, Chemical Dosing Systems and UV., • Fluent Spanish & English speaker with strong speaking skills., • Strong detail-oriented work style, and an accommodating and proactive attitude., • IT literate and proficiency in the use of Microsoft Office including Word, Excel, Powerpoint, Outlook., • Permit to Work in the EU., • Full clean driving license.

En Shakers estamos buscando un/a Data QA Engineer freelance para incorporarse a un proyecto internacional dentro del sector pharma intelligence, trabajando junto a equipos de Data Engineering y Software Engineering en la entrega de soluciones estratégicas basadas en datos. 📅 Duración: 6–12 meses (alta probabilidad de extensión) 💼 Modelo: Freelance / Contractor 🌍 Ubicación: Remote desde España (valorado EU timezone) 🧩 ¿Qué harás? • Definir y ejecutar casos de prueba orientados a datos sobre distintas bases y tablas SQL., • Validar calidad, integridad y consistencia de datos., • Diseñar procesos de data testing automatizado., • Revisar estructuras de datos, métricas y reglas de validación., • Documentar test plans y resultados de validación., • Colaborar estrechamente con equipos de Data Engineers, Developers y Arquitectura., • Impulsar buenas prácticas Agile y DevOps dentro del delivery de datos. ✅ Requisitos clave • Experiencia en Data QA / Data Testing / QA orientado a datos., • Buen manejo de SQL y Stored Procedures., • Experiencia trabajando en entornos Microsoft Azure (idealmente Azure Data Factory)., • Experiencia validando datasets, integridad y calidad de datos., • Uso de archivos de configuración (JSON, YAML o similares). ⭐ Nice to have • Python para automatización., • Experiencia con Git (GitHub, GitLab, Bitbucket)., • Background trabajando con equipos de Data Engineering o ETL pipelines. 💡 Buscamos a alguien que… • Sea detallista y orientado/a a calidad., • Disfrute trabajando de forma colaborativa., • Tenga mentalidad proactiva y enfoque en aportar valor real al negocio. 👉 Si te interesa o conoces a alguien que le interese, no dudéis en aplicar

En Shakers estamos buscando un/a Data QA Engineer freelance para incorporarse a un proyecto internacional dentro del sector pharma intelligence, trabajando junto a equipos de Data Engineering y Software Engineering en la entrega de soluciones estratégicas basadas en datos. 📅 Duración: 6–12 meses (alta probabilidad de extensión) 💼 Modelo: Freelance / Contractor 🌍 Ubicación: Remote desde España (valorado EU timezone) 🧩 ¿Qué harás? • Definir y ejecutar casos de prueba orientados a datos sobre distintas bases y tablas SQL., • Validar calidad, integridad y consistencia de datos., • Diseñar procesos de data testing automatizado., • Revisar estructuras de datos, métricas y reglas de validación., • Documentar test plans y resultados de validación., • Colaborar estrechamente con equipos de Data Engineers, Developers y Arquitectura., • Impulsar buenas prácticas Agile y DevOps dentro del delivery de datos. ✅ Requisitos clave • Experiencia en Data QA / Data Testing / QA orientado a datos., • Buen manejo de SQL y Stored Procedures., • Experiencia trabajando en entornos Microsoft Azure (idealmente Azure Data Factory)., • Experiencia validando datasets, integridad y calidad de datos., • Uso de archivos de configuración (JSON, YAML o similares). ⭐ Nice to have • Python para automatización., • Experiencia con Git (GitHub, GitLab, Bitbucket)., • Background trabajando con equipos de Data Engineering o ETL pipelines. 💡 Buscamos a alguien que… • Sea detallista y orientado/a a calidad., • Disfrute trabajando de forma colaborativa., • Tenga mentalidad proactiva y enfoque en aportar valor real al negocio. 👉 Si te interesa o conoces a alguien que le interese, no dudéis en aplicar

Sobre la Empresa: ¿Qué hacemos en el Grupo Cibernos? Ayudamos a pequeñas y grandes empresas a desarrollar sus ideas innovadoras. Gracias a nuestro bagaje y know-how, nos sabemos adaptar a las necesidades de los clientes de cualquier tipología y en cualquier ámbito del desarrollo tecnológico, ya que se dispone de áreas de conocimiento en todos ellos. Sobre el Rol: Forma parte de nuestra estrategia de expansión El Grupo Cibernos continua su estrategia de expansión, reforzando su catálogo de servicios y soluciones, así como su presencia a nivel nacional, y para ello estamos Reforzando nuestros equipos de Comerciales IT, para ampliar y crear sinergias en el grupo. El candidato/a, se ocupará de: • Identificar oportunidades de negocio y prospectar clientes potenciales con necesidades en el área de SISTEMAS (Infraestructura, comunicaciones, redes, ciberseguridad, servicios cloud, etc), • Comprender las necesidades técnicas de los clientes y ofrecer soluciones adecuadas., • Presentar a los clientes nuestros servicios/productos/soluciones., • Negociar condiciones comerciales y cerrar acuerdos de venta., • Realizar el seguimiento de las ventas y mantener relaciones duraderas con los clientes. Habilidades y competencias necesarias: • Experiencia de al menos 2 años desarrollando nuevo negocio, realizando una venta consultiva para ofrecer la mejor solución de nuestro portfolio., • Aportar experiencia en llevar un offering con propuestas diversas en el ámbito de los sistemas, • Habilidad para establecer relaciones sólidas y generar confianza con los clientes., • Orientación al cliente y capacidad para ofrecer soluciones personalizadas., • Habilidad para negociar y cerrar acuerdos comerciales., • Capacidad para trabajar de manera autónoma y gestionar el ciclo completo de venta., • Conocimientos en técnicas de ventas y habilidades de comunicación efectiva., • Aportar una red de contactos activos en alguno de los sectores en los que queremos crecer: BANCA, SEGUROS, INDUSTRIA, AAPP, ENERGÍA, TELECOMUNICACIONES, PHARMA Ofrecemos: • Contrato Indefinido, • Salario fijo + variable y poder acogerte a un plan de retribución flexible, • Modalidad de trabajo: 2 Teletrabajo y 3 Presenciales (con flexibilidad) 50 años en el mercado IT. Nos distingue nuestra experiencia más de 50 años en el mercado tecnológico. El esfuerzo, el entusiasmo, la pasión y la capacidad de innovar que nos caracterizan, nos llevan a emprender proyectos motivadores que convierten nuestro día a día en un reto.

About Xebia With over 20 years of experience, our global network of passionate technologists and pioneering craftsmen deliver cutting-edge technology and game-changing consulting to companies on the brink of transformation. Since 2001, we have grown from a Java company into a full-service digital consulting company with 4500+ professionals working on a worldwide ambition. We are organized in complementary chapters – teams with a tremendous amount of knowledge and experience within a particular field, such as Agile, DevOps, Data and AI, Cloud, Software Technology, Functional Programming, Low Code, and Microsoft. We help the world’s top 250 companies and category leaders overcome digital challenges, embrace innovation, adopt new technology, and implement new business models. In addition to high-quality consulting, we also provide offshoring and nearshoring services. For more details please visit Role Summary The Scientific Product Manager (SPM) owns the strategy, roadmap, and delivery of scientific workspace products across multiple domains. You will identify the highest-value scientific use cases, define product requirements, align cross-functional teams, and drive successful adoption and measurable outcomes for scientists. Key Responsibilities • Own product vision and multi-quarter roadmap across a portfolio of scientific use cases and personas, • Define prioritization frameworks to balance scientific impact, feasibility, time to value, and platform scalability, • Partner with leadership and stakeholders to align product direction with business goals and customer success metrics, • Track competitive landscape and market trends; propose roadmap trade-offs between parity and differentiated innovation, • Develop deep understanding of end-to-end scientific workflows and identify implementation-ready use cases with the highest impact, • Expand the pipeline of new use cases through direct engagement with scientists and teams across functions and modalities, • Standardize how use cases are defined, scoped, and evaluated (problem statement, target user, workflow fit, success metrics, risks, dependencies), • Ensure use cases can be delivered as reusable platform patterns rather than one-off solutions where possible, • Translate scientific needs into clear, testable product requirements for engineering and design (epics, user stories, acceptance criteria), • Lead discovery to delivery execution with engineering, design, data science, and scientific stakeholders in an Agile environment, • Drive dependency management, trade-off decisions, and release planning across multiple concurrent initiatives, • Partner with engineering on validation and testing strategies for deployments in customer environments, including workflow realism and data constraints, • Define go-to-market readiness with stakeholders: documentation, training needs, enablement, and rollout strategy, • Post-launch, measure adoption and outcomes; iterate to improve usability, performance, and scientific value delivered, • Ensure product delivery against challenging scientific goals by maintaining tight feedback loops with end users and adjusting roadmap as needed Basic Qualifications • Bachelor’s or Master’s degree in bioinformatics, biology, or a related scientific discipline plus at least 5 years of relevant experience (PhD preferred), • Product management experience shipping software products, ideally across complex workflows and multiple user personas, • Ability to translate ambiguous scientific problems into structured product plans and engineering-ready requirements Preferred Qualifications • Experience in pharma, biotech, and or digital health environments, • Strong analytical and critical thinking skills; ability to synthesize complex inputs into clear decisions and narratives, • Working knowledge of data analysis and experimentation; Python, R, or MATLAB beneficial, • Excellent communication and collaboration skills in cross-functional, global teams, • Experience working in Agile or Scrum environments, • Foundation in biology across discovery concepts such as target discovery, NGS, small molecule discovery, and large molecule discovery

About Xebia With over 20 years of experience, our global network of passionate technologists and pioneering craftsmen deliver cutting-edge technology and game-changing consulting to companies on the brink of transformation. Since 2001, we have grown from a Java company into a full-service digital consulting company with 5,500+ professionals working on a worldwide ambition. We are organized in complementary service lines – teams with a tremendous amount of knowledge and experience within a particular field, such as Agile, DevOps, Data and AI, Cloud, Software Technology, Functional Programming, Intelligent Automation, and Microsoft. We help the world’s top 250+ companies and category leaders overcome digital challenges, embrace innovation, adopt new technology, and implement new business models. In addition to high-quality consulting, we also provide offshoring and nearshoring services. For more details, please visit About the role We’re seeking a Scientific Product Manager (SPM) to lead the strategy, roadmap, and delivery of GenAI products across scientific domains. This role identifies high-impact scientific use cases, translates them into scalable product solutions, and drives measurable adoption and value for scientists. What You’ll Do • Own product vision and multi-quarter roadmap aligned to business and scientific goals, • Identify, prioritize, and standardize high-value scientific use cases across workflows, • Translate complex scientific needs into clear product requirements for engineering and design, • Lead cross-functional execution (engineering, data science, design, scientific stakeholders) in an Agile environment, • Drive launch readiness, adoption, and continuous improvement based on user feedback and outcomes, • Build strong partnerships with customers and internal scientific teams What You Bring • BS/MS (PhD preferred) in bioinformatics, biology, or related field, • 5+ years’ relevant experience, including product management for software products, • Ability to turn ambiguous scientific challenges into structured product plans, • Experience in pharma, biotech, or digital health preferred, • Strong analytical, communication, and cross-functional leadership skills

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.