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At a glance 📌 Position: Junior Data Analyst Location: Madrid Experience: Recent graduates or candidates with up to 1 year of experience Want to know more? 👇 Chemo is a global pharmaceutical company specialized in the development, manufacturing, and commercialization of active pharmaceutical ingredients, finished dosage forms, and generics. As part of the Insud Pharma group, Chemo plays a key role across the pharmaceutical value chain, with a strong focus on quality, innovation, and sustainable growth. If you have recently completed — or are about to complete — a Master’s in Data Analytics, Artificial Intelligence, Business Analytics, Data Science, or a related field, and you are looking to start your career in a role that combines data, business, and strategy, this opportunity could be for you 💪 At Chemo, we are looking for a Junior Data Analyst to support the Business Development & Portfolio team, helping analyze data and strategic information to identify, assess, and prioritize new product opportunities. This role is designed for someone with strong potential, analytical curiosity, and a willingness to learn, who wants to grow in an environment where data has a real impact on decision-making. What are we looking for? 🔎 We are looking for someone with an analytical mindset, an interest in working with data, and a business-oriented approach, who is eager to learn how to transform complex information into useful insights that support strategic decisions. We are not necessarily looking for extensive professional experience, but rather for a solid foundation, a learning mindset, and motivation to grow in an international pharma environment. The challenge 🚀 • Support the collection, organization, and analysis of market, competitor, and internal data., • Assist in the preparation and maintenance of reports, metrics, benchmarks, and dashboards., • Help structure, clean, and transform data for analysis., • Contribute to quantitative analyses aimed at identifying product opportunities and market trends., • Support the generation of insights for the Portfolio and Business Development teams., • Work closely with both technical and business stakeholders to understand needs and translate them into useful analyses., • Learn and progressively develop automation and data analysis capabilities within the team. What do you need? 🤓 • A recently completed — or nearly completed — Master’s degree in Data Analytics, Artificial Intelligence, Business Analytics, Data Science, or a related field., • Foundational knowledge of tools such as Python, SQL, and Excel., • Interest in applying data analysis to business decisions., • Strong analytical thinking, curiosity, and eagerness to learn., • Good organizational skills and attention to detail., • Ability to communicate ideas clearly and work with non-technical stakeholders., • A level of English that allows you to work in an international environment and handle documentation/information comfortably. It would be great if you also have ✅ • Knowledge of visualization tools such as Power BI or Tableau., • Experience with academic or personal projects related to data analysis., • Interest in the pharma, healthcare, or regulated industries., • Basic understanding of automation, ETL, or data preparation processes., • A genuine interest in combining data + business + strategy. What do we offer? 👏 📍 Hybrid position in Madrid (4/1) 🎓 A strong learning and development environment for junior profiles 🤝 Close support and mentoring from the team 📈 The opportunity to grow in a role with high business exposure 🚀 Involvement in analyses that have a real impact on strategic decisions 🌍 An international, dynamic, and innovative environment within the pharmaceutical industry Why could this be a great opportunity for you? • Because this is not a purely technical role or a purely business role — it is an opportunity to develop a broader profile, learning how to work with data in a real business context and how to turn information into actionable insights that support strategic decision-making., • It is a great first step if you want to grow at the intersection of analytics, business, and pharma. What does the selection process look like? 🕵️ • Initial contact by phone or email., • Interview with Talent Acquisition., • Interview with the Hiring Manager / team., • Communication and follow-up throughout the process. 🔷 Think this role may not be for you? 🔷 Follow us on LinkedIn and Instagram to stay updated on new opportunities. #Chemo #InsudPharma #Challenger #Insuder #InsudTalent EQUAL OPPORTUNITIES COMMITMENT At Chemo, we are committed to equal opportunities and non-discrimination. We welcome all applications regardless of gender, ethnic origin, religion, sexual orientation, disability, age, or any other personal or social condition protected by applicable law.

At a glance 📌 Position: Junior Data Analyst Location: Madrid Experience: Recent graduates or candidates with up to 1 year of experience Want to know more? 👇 Chemo is a global pharmaceutical company specialized in the development, manufacturing, and commercialization of active pharmaceutical ingredients, finished dosage forms, and generics. As part of the Insud Pharma group, Chemo plays a key role across the pharmaceutical value chain, with a strong focus on quality, innovation, and sustainable growth. If you have recently completed — or are about to complete — a Master’s in Data Analytics, Artificial Intelligence, Business Analytics, Data Science, or a related field, and you are looking to start your career in a role that combines data, business, and strategy, this opportunity could be for you 💪 At Chemo, we are looking for a Junior Data Analyst to support the Business Development & Portfolio team, helping analyze data and strategic information to identify, assess, and prioritize new product opportunities. This role is designed for someone with strong potential, analytical curiosity, and a willingness to learn, who wants to grow in an environment where data has a real impact on decision-making. What are we looking for? 🔎 We are looking for someone with an analytical mindset, an interest in working with data, and a business-oriented approach, who is eager to learn how to transform complex information into useful insights that support strategic decisions. We are not necessarily looking for extensive professional experience, but rather for a solid foundation, a learning mindset, and motivation to grow in an international pharma environment. The challenge 🚀 • Support the collection, organization, and analysis of market, competitor, and internal data., • Assist in the preparation and maintenance of reports, metrics, benchmarks, and dashboards., • Help structure, clean, and transform data for analysis., • Contribute to quantitative analyses aimed at identifying product opportunities and market trends., • Support the generation of insights for the Portfolio and Business Development teams., • Work closely with both technical and business stakeholders to understand needs and translate them into useful analyses., • Learn and progressively develop automation and data analysis capabilities within the team. What do you need? 🤓 • A recently completed — or nearly completed — Master’s degree in Data Analytics, Artificial Intelligence, Business Analytics, Data Science, or a related field., • Foundational knowledge of tools such as Python, SQL, and Excel., • Interest in applying data analysis to business decisions., • Strong analytical thinking, curiosity, and eagerness to learn., • Good organizational skills and attention to detail., • Ability to communicate ideas clearly and work with non-technical stakeholders., • A level of English that allows you to work in an international environment and handle documentation/information comfortably. It would be great if you also have ✅ • Knowledge of visualization tools such as Power BI or Tableau., • Experience with academic or personal projects related to data analysis., • Interest in the pharma, healthcare, or regulated industries., • Basic understanding of automation, ETL, or data preparation processes., • A genuine interest in combining data + business + strategy. What do we offer? 👏 📍 Hybrid position in Madrid (4/1) 🎓 A strong learning and development environment for junior profiles 🤝 Close support and mentoring from the team 📈 The opportunity to grow in a role with high business exposure 🚀 Involvement in analyses that have a real impact on strategic decisions 🌍 An international, dynamic, and innovative environment within the pharmaceutical industry Why could this be a great opportunity for you? • Because this is not a purely technical role or a purely business role — it is an opportunity to develop a broader profile, learning how to work with data in a real business context and how to turn information into actionable insights that support strategic decision-making., • It is a great first step if you want to grow at the intersection of analytics, business, and pharma. What does the selection process look like? 🕵️ • Initial contact by phone or email., • Interview with Talent Acquisition., • Interview with the Hiring Manager / team., • Communication and follow-up throughout the process. 🔷 Think this role may not be for you? 🔷 Follow us on LinkedIn and Instagram to stay updated on new opportunities. #Chemo #InsudPharma #Challenger #Insuder #InsudTalent EQUAL OPPORTUNITIES COMMITMENT At Chemo, we are committed to equal opportunities and non-discrimination. We welcome all applications regardless of gender, ethnic origin, religion, sexual orientation, disability, age, or any other personal or social condition protected by applicable law.

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.

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

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.

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

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

At a glance 📌 Position: Junior Data Analyst Location: Madrid Experience: Recent graduates or candidates with up to 1 year of experience Want to know more? 👇 Chemo is a global pharmaceutical company specialized in the development, manufacturing, and commercialization of active pharmaceutical ingredients, finished dosage forms, and generics. As part of the Insud Pharma group, Chemo plays a key role across the pharmaceutical value chain, with a strong focus on quality, innovation, and sustainable growth. If you have recently completed — or are about to complete — a Master’s in Data Analytics, Artificial Intelligence, Business Analytics, Data Science, or a related field, and you are looking to start your career in a role that combines data, business, and strategy, this opportunity could be for you 💪 At Chemo, we are looking for a Junior Data Analyst to support the Business Development & Portfolio team, helping analyze data and strategic information to identify, assess, and prioritize new product opportunities. This role is designed for someone with strong potential, analytical curiosity, and a willingness to learn, who wants to grow in an environment where data has a real impact on decision-making. What are we looking for? 🔎 We are looking for someone with an analytical mindset, an interest in working with data, and a business-oriented approach, who is eager to learn how to transform complex information into useful insights that support strategic decisions. We are not necessarily looking for extensive professional experience, but rather for a solid foundation, a learning mindset, and motivation to grow in an international pharma environment. The challenge 🚀 • Support the collection, organization, and analysis of market, competitor, and internal data., • Assist in the preparation and maintenance of reports, metrics, benchmarks, and dashboards., • Help structure, clean, and transform data for analysis., • Contribute to quantitative analyses aimed at identifying product opportunities and market trends., • Support the generation of insights for the Portfolio and Business Development teams., • Work closely with both technical and business stakeholders to understand needs and translate them into useful analyses., • Learn and progressively develop automation and data analysis capabilities within the team. What do you need? 🤓 • A recently completed — or nearly completed — Master’s degree in Data Analytics, Artificial Intelligence, Business Analytics, Data Science, or a related field., • Foundational knowledge of tools such as Python, SQL, and Excel., • Interest in applying data analysis to business decisions., • Strong analytical thinking, curiosity, and eagerness to learn., • Good organizational skills and attention to detail., • Ability to communicate ideas clearly and work with non-technical stakeholders., • A level of English that allows you to work in an international environment and handle documentation/information comfortably. It would be great if you also have ✅ • Knowledge of visualization tools such as Power BI or Tableau., • Experience with academic or personal projects related to data analysis., • Interest in the pharma, healthcare, or regulated industries., • Basic understanding of automation, ETL, or data preparation processes., • A genuine interest in combining data + business + strategy. What do we offer? 👏 📍 Hybrid position in Madrid (4/1) 🎓 A strong learning and development environment for junior profiles 🤝 Close support and mentoring from the team 📈 The opportunity to grow in a role with high business exposure 🚀 Involvement in analyses that have a real impact on strategic decisions 🌍 An international, dynamic, and innovative environment within the pharmaceutical industry Why could this be a great opportunity for you? • Because this is not a purely technical role or a purely business role — it is an opportunity to develop a broader profile, learning how to work with data in a real business context and how to turn information into actionable insights that support strategic decision-making., • It is a great first step if you want to grow at the intersection of analytics, business, and pharma. What does the selection process look like? 🕵️ • Initial contact by phone or email., • Interview with Talent Acquisition., • Interview with the Hiring Manager / team., • Communication and follow-up throughout the process. 🔷 Think this role may not be for you? 🔷 Follow us on LinkedIn and Instagram to stay updated on new opportunities. #Chemo #InsudPharma #Challenger #Insuder #InsudTalent EQUAL OPPORTUNITIES COMMITMENT At Chemo, we are committed to equal opportunities and non-discrimination. We welcome all applications regardless of gender, ethnic origin, religion, sexual orientation, disability, age, or any other personal or social condition protected by applicable law.

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

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

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

AI Labs is Insud Pharma’s transversal team for. 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 mat

¿Quiénes somos? Neotalent Conclusion es una de las mayores especialistas del mercado ibérico en captación y gestión de talento informático y de ingeniería. Como parte del grupo neerlandés Conclusion, que se compone por un ecosistema de 25 empresas y 3.600 empleados, nos centramos en aumentar la capacidad tecnológica de nuestros clientes y acelerar la transformación digital de los mismos. En Neotalent Conclusion, somos especialistas del talento. Atraemos a los mejores profesionales y los combinamos con los proyectos más ambiciosos, en el momento justo. Nuestro éxito radica en la inversión en innovación, orientación a resultados y, por encima de todo, en la garantía de que las personas tengan carreras felices y realizadoras. Con más de 25 años de experiencia, Neotalent Conclusion cuenta con oficinas en Madrid, Lisboa y Oporto. Nuestra compañía está formada por un equipo de más de 850 profesionales entre sus diferentes áreas de operación. Neotalent, the responsive people. Más información en www.neotalent.pt/es y https://neotalent.pt/es/oportunidades-de-carrera/. Descripción del puesto: En Neotalent Conclusion buscamos un/a Senior Full-Stack Developer para proyecto en el sector farmacéutico / Life Sciences. 🚀Cuáles serán tus funciones: • Desarrollo y mantenimiento de aplicaciones Full-Stack, • Diseño de soluciones backend con Python, • Gestión y optimización de bases de datos SQL, • Desarrollo de interfaces frontend (React / Vue / Angular), • Integración con sistemas industriales y datos en tiempo real, • Asegurar cumplimiento en entornos regulados (GMP/GAMP), • Participación en decisiones técnicas y code reviews 🔧 Requisitos clave: • Más de 5 años de experiencia en desarrollo Full-Stack, • Dominio avanzado de Python (Django, Flask o FastAPI), • Experiencia sólida en SQL (PostgreSQL/MySQL), • Amplio conocimiento de JavaScript + React / Vue / Angular, • Conocimientos de Git, Docker, CI/CD Valorable: Experiencia previa en entornos regulados / industria pharma 🌟 Por qué unirte a nosotros: • Trabajar en proyectos desafiantes para grandes clientes, • Aprender más sobre tecnologías emergentes, • Posibilidad de trabajar de forma remota, • Acceso a formación continua y certificaciones, • Disfrutar de un plan de compensación flexible, • ... ¡y mucho más!

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

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

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

In a few words • Position: Senior Backend Developer, • Location: Madrid (Chamberí area)., • +4 years of experience 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 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. Ready to be a #Challenger? What are we looking for? 🔎 We are AI Labs team, the applied AI department at Insud Pharma. We are a team of 30 professionals (AI Engineers, Data Scientists, Backend Engineers, DevOps Engineers, and Product Managers) working across the full breadth of the company, building products and systems that directly inform and shape decision-making. We are looking for a Senior Backend Developer with strong technical foundations who is eager to design, build, and scale robust backend systems that power real-world AI-driven products. You will work across diverse and complex domains (Clinical, R&D, manufacturing, and beyond), collaborating closely with Data Scientists, Product Managers, and DevOps to bring solutions from concept to production. You will take ownership of backend services end-to-end—defining architectures, designing APIs, ensuring performance and scalability, and delivering reliable systems in production environments. We are seeking someone curious enough to tackle complex engineering challenges (distributed systems, concurrency, scalability, observability), rigorous enough to apply best practices and make sound architectural decisions, and independent enough to deliver high-impact solutions with strong ownership. How the team works: AI Labs operates with a startup mindset within Insud Pharma. The department is young, and the culture reflects that: flat, collaborative, and fast-moving. Beyond the AI Engineering team, you will work alongside Data Scientists, DevOps Engineers, and Product Managers who are equally committed to delivering high-quality work. We hold regular demo days where teams present their work, as well as whiteboard sessions where we tackle problems together. The cross-disciplinary dynamic is genuinely strong. The office is located in central Madrid (Chamberí, near Eloy Gonzalo), well connected and situated in a vibrant part of the city. The challenge! • Design, develop, and maintain REST APIs (FastAPI, Flask, or similar)., • Define and evolve scalable and efficient backend architectures., • Build services considering concurrency, performance, and scalability., • Collaborate with frontend teams to define clear, consistent, and versioned API contracts., • Integrate backend services with SQL and/or NoSQL databases., • Ensure code quality through testing (unit and integration), code reviews, and best practices., • Participate in CI/CD pipelines and deployment processes., • Work with cloud environments (AWS and/or Azure) in production systems., • Implement monitoring and observability (logs, metrics, alerts)., • Identify and resolve performance, scalability, and security issues., • Contribute to technical standards and reusable components., • Mentor and support junior developers., • Collaborate closely with Product, Engineering, and DevOps teams., • Participate in architectural decisions and contribute to the evolution of the tech stack., • Ensure reliability, performance, and quality of backend services What do you need? • Fluency in Spanish and English., • Strong experience in Python and backend development in production environments., • Experience with FastAPI, Flask, or similar frameworks., • Proven experience designing APIs and scalable backend architectures., • Experience with SQL and/or NoSQL databases., • Experience with Docker and containerized environments., • Experience working with cloud platforms (AWS and/or Azure) for development and deployment., • Familiarity with CI/CD tools (e.g., GitHub Actions, Azure DevOps)., • Knowledge of authentication systems (OAuth2, JWT)., • Solid understanding of best practices (SOLID principles, clean architecture)., • Ability to work autonomously with strong ownership and results orientation Our benefits! ⏰ Flexible start time from Monday to Friday 📜 Permanent contract. 🥼 Life and accident insurance. 🍽️ Ticket restaurant 💻 Training and language learning platform 💆🏻 ♀️ Wellness platform with unlimited free psychologist sessions 🚕 Cabify transportation service for employee use 📈 Development plans, internal mobility policy. ⭐ Many more! What will the Selection process be like? 🕵️ ➡️ Stay tuned to your phone and email! The first thing we will likely do is contact you through one of the two channels. ➡️ Prepare well! We will continue with an in-person/virtual interview depending on availability and what we agree upon; there may be one or two interviews in the process, and depending on the type of process, there may also be some kind of test. ➡️ Wait for the result! We care that you feel guided throughout each selection process and know what to expect from us, so we will always try to inform you of the status of the process. 🔷 Do you think this offer is not for you? 🔷 Follow us on social media like LinkedIn/Instagram and stay tuned for any offers we may release; the opportunity to be a new Insuder is waiting! #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.

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

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

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

In a few words • Position: Senior Frontend Developer, • Location: Madrid (Chamberí area)., • +4 years of experience 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 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. Ready to be a #Challenger? What are we looking for? 🔎 We are AI Labs team, the applied AI department at Insud Pharma. We are a team of 30 professionals (AI Engineers, Data Scientists, Backend Engineers, DevOps Engineers, and Product Managers) working across the full breadth of the company, building products and systems that directly inform and shape decision-making. We are looking for a Senior Frontend Developer with a strong technical foundation and extensive experience in modern frontend technologies, particularly React. You will work on building high-quality interfaces and applications, translating complex business and technical requirements into intuitive, efficient, and scalable user experiences. You will take part in frontend architecture decisions, contribute to the definition and evolution of technical standards, design systems, and component libraries, and collaborate closely with backend, product, and design teams to build robust and maintainable end-to-end solutions. We are seeking someone curious enough to explore new tools, frameworks, and best practices within the frontend ecosystem; rigorous enough to ensure code quality, performance, and accessibility; and autonomous enough to take full ownership of solutions and drive them from concept to production with real impact How the team works: AI Labs operates with a startup mindset within Insud Pharma. The department is young, and the culture reflects that: flat, collaborative, and fast-moving. Beyond the AI Engineering team, you will work alongside Data Scientists, DevOps Engineers, and Product Managers who are equally committed to delivering high-quality work. We hold regular demo days where teams present their work, as well as whiteboard sessions where we tackle problems together. The cross-disciplinary dynamic is genuinely strong. The office is located in central Madrid (Chamberí, near Eloy Gonzalo), well connected and situated in a vibrant part of the city. The challenge! • Design and develop modern web applications using React and React Native., • Build scalable, reusable, and high-performance user interfaces., • Translate business requirements into high-quality user experiences., • Design and maintain design systems and UI component libraries., • Manage application state efficiently., • Integrate REST APIs and collaborate with backend teams on clear and maintainable contracts., • Optimize application performance (rendering, loading time, bundle size)., • Contribute to frontend architecture decisions (structure, modularity, scalability)., • Apply best practices in accessibility and usability., • Collaborate closely with product, design, and backend teams., • Ensure code quality through testing, code reviews, and best practices., • Contribute to defining technical standards and evolving the frontend stack., • Mentor and support junior developers. What do you need? • Fluency in Spanish and English., • Strong experience with React, React Native and the modern frontend ecosystem., • Solid knowledge of modern JavaScript and TypeScript., • Experience with state management solutions., • Experience integrating and consuming REST APIs., • Strong knowledge of HTML and CSS (responsive design, layouts, best practices)., • Experience with frontend development tools (bundlers, build tools, etc.)., • Familiarity with frontend testing (Jest, React Testing Library, or similar)., • Experience using Git in collaborative environments., • Understanding of software development best practices (clean code, frontend architecture)., • Ability to work autonomously with strong ownership and a product-oriented mindset. Our benefits! ⏰ Flexible start time from Monday to Friday 📜 Permanent contract. 🥼 Life and accident insurance. 🍽️ Ticket restaurant 💻 Training and language learning platform 💆🏻 ♀️ Wellness platform with unlimited free psychologist sessions 🚕 Cabify transportation service for employee use 📈 Development plans, internal mobility policy. ⭐ Many more! What will the Selection process be like? 🕵️ ➡️ Stay tuned to your phone and email! The first thing we will likely do is contact you through one of the two channels. ➡️ Prepare well! We will continue with an in-person/virtual interview depending on availability and what we agree upon; there may be one or two interviews in the process, and depending on the type of process, there may also be some kind of test. ➡️ Wait for the result! We care that you feel guided throughout each selection process and know what to expect from us, so we will always try to inform you of the status of the process. 🔷 Do you think this offer is not for you? 🔷 Follow us on social media like LinkedIn/Instagram and stay tuned for any offers we may release; the opportunity to be a new Insuder is waiting! #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 brief 📌 Position: Junior Demand Planner Location: Madrid (hybrid) Experience: 1–2 years of experience Want to know more? 👇 Exeltis is the branded business of Insud Pharma, an international pharmaceutical group operating across the entire value chain, from research and development to manufacturing, marketing, and distribution of value-added products for human and animal health. Insud Pharma’s activities are organized into three synergistic business areas: Industrial (Chemo), Branded (Exeltis), and Biotech (mAbxience). With 10,000 professionals across more than 50 countries, 20 industrial plants, 15 specialized R&D centers, 12 commercial offices, and over 35 pharmaceutical affiliates, Insud Pharma serves 1,150 customers in more than 110 countries worldwide. At Insud Pharma, we believe in innovation and sustainable development. At Exeltis, we are looking for someone with a foundation in planning, a strong analytical mindset, and a willingness to learn, to join the Supply Chain area and grow as a Junior Demand Planner in an international environment. What are we looking for? 🔎 We are looking for a junior professional who wants to grow within the demand planning area, contributing to forecast analysis, data monitoring, and cross-functional coordination to support more accurate and efficient planning. This is an ideal opportunity for someone with initial experience in Demand Planning, Forecasting, Supply Chain, or S&OP, who is eager to continue developing within the pharmaceutical sector. The challenge! 🚀 • Support the preparation and update of the demand forecast, consolidating information from markets, affiliates, or regions., • Collaborate in the analysis of sales history, trends, seasonality, and other factors impacting demand., • Participate in the preparation of information for monthly planning cycles such as S&OP / IBP., • Help monitor deviations between forecast and actual demand, identifying possible root causes together with the team., • Collaborate with Supply Planning to align forecasts, product availability, and supply needs., • Support the maintenance and review of planning-related information in systems, such as lead times, basic parameters, or product data., • Participate in the follow-up of product launches, transitions, discontinuations, and obsolescence control., • Prepare reports and KPIs to support analysis and decision-making., • Work closely with sales, marketing, finance, supply chain, and operations teams., • Contribute to the continuous improvement of processes, tools, and reporting within the area. What do you need? 🤓 • Degree in Engineering, Business Administration, Economics, Statistics, Supply Chain, Business Analytics, or a related field., • 1 to 2 years of experience in roles related to Demand Planning, Forecasting, Supply Chain, or S&OP., • High level of English, with the ability to work in an international environment., • Advanced Excel skills., • Experience or familiarity with ERP systems, ideally SAP., • Knowledge of planning or analytics tools such as APO, IBP, Anaplan, Power BI, or similar is a plus., • Strong analytical skills, attention to detail, and data-driven mindset., • Good communication and teamwork skills., • Interest in developing within the pharmaceutical sector. Our benefits! 👏 📜 Permanent contract ⏰ Flexible working hours 🍽️ Free canteen 🚗 Parking 🏥 Health insurance 📚 Professional development and continuous learning What will the selection process look like? 🕵️ • Initial contact by phone or email., • 1 or 2 virtual and/or in-person interviews., • Ongoing communication throughout the process. 🔷Do you think this opportunity is not for you? 🔷 Follow us on LinkedIn and Instagram to discover new career opportunities and stay updated on our open positions. #InsudPharma #Challenger #Insuder #InsudTalent EQUAL OPPORTUNITIES COMMITMENT At Exeltis, we promote equal opportunities and are committed to selection processes based on merit, skills, and experience. We guarantee non-discrimination on the basis of gender, age, ethnic or social origin, religion or beliefs, sexual orientation, gender identity, disability, or any other personal or social condition.

In a few words • Position: Senior Backend Developer, • Location: Madrid (Chamberí area)., • +4 years of experience 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 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. Ready to be a #Challenger? What are we looking for? 🔎 We are AI Labs team, the applied AI department at Insud Pharma. We are a team of 30 professionals (AI Engineers, Data Scientists, Backend Engineers, DevOps Engineers, and Product Managers) working across the full breadth of the company, building products and systems that directly inform and shape decision-making. We are looking for a Senior Backend Developer with strong technical foundations who is eager to design, build, and scale robust backend systems that power real-world AI-driven products. You will work across diverse and complex domains (Clinical, R&D, manufacturing, and beyond), collaborating closely with Data Scientists, Product Managers, and DevOps to bring solutions from concept to production. You will take ownership of backend services end-to-end—defining architectures, designing APIs, ensuring performance and scalability, and delivering reliable systems in production environments. We are seeking someone curious enough to tackle complex engineering challenges (distributed systems, concurrency, scalability, observability), rigorous enough to apply best practices and make sound architectural decisions, and independent enough to deliver high-impact solutions with strong ownership. How the team works: AI Labs operates with a startup mindset within Insud Pharma. The department is young, and the culture reflects that: flat, collaborative, and fast-moving. Beyond the AI Engineering team, you will work alongside Data Scientists, DevOps Engineers, and Product Managers who are equally committed to delivering high-quality work. We hold regular demo days where teams present their work, as well as whiteboard sessions where we tackle problems together. The cross-disciplinary dynamic is genuinely strong. The office is located in central Madrid (Chamberí, near Eloy Gonzalo), well connected and situated in a vibrant part of the city. The challenge! • Design, develop, and maintain REST APIs (FastAPI, Flask, or similar)., • Define and evolve scalable and efficient backend architectures., • Build services considering concurrency, performance, and scalability., • Collaborate with frontend teams to define clear, consistent, and versioned API contracts., • Integrate backend services with SQL and/or NoSQL databases., • Ensure code quality through testing (unit and integration), code reviews, and best practices., • Participate in CI/CD pipelines and deployment processes., • Work with cloud environments (AWS and/or Azure) in production systems., • Implement monitoring and observability (logs, metrics, alerts)., • Identify and resolve performance, scalability, and security issues., • Contribute to technical standards and reusable components., • Mentor and support junior developers., • Collaborate closely with Product, Engineering, and DevOps teams., • Participate in architectural decisions and contribute to the evolution of the tech stack., • Ensure reliability, performance, and quality of backend services What do you need? • Fluency in Spanish and English., • Strong experience in Python and backend development in production environments., • Experience with FastAPI, Flask, or similar frameworks., • Proven experience designing APIs and scalable backend architectures., • Experience with SQL and/or NoSQL databases., • Experience with Docker and containerized environments., • Experience working with cloud platforms (AWS and/or Azure) for development and deployment., • Familiarity with CI/CD tools (e.g., GitHub Actions, Azure DevOps)., • Knowledge of authentication systems (OAuth2, JWT)., • Solid understanding of best practices (SOLID principles, clean architecture)., • Ability to work autonomously with strong ownership and results orientation Our benefits! ⏰ Flexible start time from Monday to Friday 📜 Permanent contract. 🥼 Life and accident insurance. 🍽️ Ticket restaurant 💻 Training and language learning platform 💆🏻 ♀️ Wellness platform with unlimited free psychologist sessions 🚕 Cabify transportation service for employee use 📈 Development plans, internal mobility policy. ⭐ Many more! What will the Selection process be like? 🕵️ ➡️ Stay tuned to your phone and email! The first thing we will likely do is contact you through one of the two channels. ➡️ Prepare well! We will continue with an in-person/virtual interview depending on availability and what we agree upon; there may be one or two interviews in the process, and depending on the type of process, there may also be some kind of test. ➡️ Wait for the result! We care that you feel guided throughout each selection process and know what to expect from us, so we will always try to inform you of the status of the process. 🔷 Do you think this offer is not for you? 🔷 Follow us on social media like LinkedIn/Instagram and stay tuned for any offers we may release; the opportunity to be a new Insuder is waiting! #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 few words • Position: Senior Frontend Developer, • Location: Madrid (Chamberí area)., • +4 years of experience 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 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. Ready to be a #Challenger? What are we looking for? 🔎 We are AI Labs team, the applied AI department at Insud Pharma. We are a team of 30 professionals (AI Engineers, Data Scientists, Backend Engineers, DevOps Engineers, and Product Managers) working across the full breadth of the company, building products and systems that directly inform and shape decision-making. We are looking for a Senior Frontend Developer with a strong technical foundation and extensive experience in modern frontend technologies, particularly React. You will work on building high-quality interfaces and applications, translating complex business and technical requirements into intuitive, efficient, and scalable user experiences. You will take part in frontend architecture decisions, contribute to the definition and evolution of technical standards, design systems, and component libraries, and collaborate closely with backend, product, and design teams to build robust and maintainable end-to-end solutions. We are seeking someone curious enough to explore new tools, frameworks, and best practices within the frontend ecosystem; rigorous enough to ensure code quality, performance, and accessibility; and autonomous enough to take full ownership of solutions and drive them from concept to production with real impact How the team works: AI Labs operates with a startup mindset within Insud Pharma. The department is young, and the culture reflects that: flat, collaborative, and fast-moving. Beyond the AI Engineering team, you will work alongside Data Scientists, DevOps Engineers, and Product Managers who are equally committed to delivering high-quality work. We hold regular demo days where teams present their work, as well as whiteboard sessions where we tackle problems together. The cross-disciplinary dynamic is genuinely strong. The office is located in central Madrid (Chamberí, near Eloy Gonzalo), well connected and situated in a vibrant part of the city. The challenge! • Design and develop modern web applications using React and React Native., • Build scalable, reusable, and high-performance user interfaces., • Translate business requirements into high-quality user experiences., • Design and maintain design systems and UI component libraries., • Manage application state efficiently., • Integrate REST APIs and collaborate with backend teams on clear and maintainable contracts., • Optimize application performance (rendering, loading time, bundle size)., • Contribute to frontend architecture decisions (structure, modularity, scalability)., • Apply best practices in accessibility and usability., • Collaborate closely with product, design, and backend teams., • Ensure code quality through testing, code reviews, and best practices., • Contribute to defining technical standards and evolving the frontend stack., • Mentor and support junior developers. What do you need? • Fluency in Spanish and English., • Strong experience with React, React Native and the modern frontend ecosystem., • Solid knowledge of modern JavaScript and TypeScript., • Experience with state management solutions., • Experience integrating and consuming REST APIs., • Strong knowledge of HTML and CSS (responsive design, layouts, best practices)., • Experience with frontend development tools (bundlers, build tools, etc.)., • Familiarity with frontend testing (Jest, React Testing Library, or similar)., • Experience using Git in collaborative environments., • Understanding of software development best practices (clean code, frontend architecture)., • Ability to work autonomously with strong ownership and a product-oriented mindset. Our benefits! ⏰ Flexible start time from Monday to Friday 📜 Permanent contract. 🥼 Life and accident insurance. 🍽️ Ticket restaurant 💻 Training and language learning platform 💆🏻 ♀️ Wellness platform with unlimited free psychologist sessions 🚕 Cabify transportation service for employee use 📈 Development plans, internal mobility policy. ⭐ Many more! What will the Selection process be like? 🕵️ ➡️ Stay tuned to your phone and email! The first thing we will likely do is contact you through one of the two channels. ➡️ Prepare well! We will continue with an in-person/virtual interview depending on availability and what we agree upon; there may be one or two interviews in the process, and depending on the type of process, there may also be some kind of test. ➡️ Wait for the result! We care that you feel guided throughout each selection process and know what to expect from us, so we will always try to inform you of the status of the process. 🔷 Do you think this offer is not for you? 🔷 Follow us on social media like LinkedIn/Instagram and stay tuned for any offers we may release; the opportunity to be a new Insuder is waiting! #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 brief 📌 Position: Junior Demand Planner Location: Madrid (hybrid) Experience: 1–2 years of experience Want to know more? 👇 Exeltis is the branded business of Insud Pharma, an international pharmaceutical group operating across the entire value chain, from research and development to manufacturing, marketing, and distribution of value-added products for human and animal health. Insud Pharma’s activities are organized into three synergistic business areas: Industrial (Chemo), Branded (Exeltis), and Biotech (mAbxience). With 10,000 professionals across more than 50 countries, 20 industrial plants, 15 specialized R&D centers, 12 commercial offices, and over 35 pharmaceutical affiliates, Insud Pharma serves 1,150 customers in more than 110 countries worldwide. At Insud Pharma, we believe in innovation and sustainable development. At Exeltis, we are looking for someone with a foundation in planning, a strong analytical mindset, and a willingness to learn, to join the Supply Chain area and grow as a Junior Demand Planner in an international environment. What are we looking for? 🔎 We are looking for a junior professional who wants to grow within the demand planning area, contributing to forecast analysis, data monitoring, and cross-functional coordination to support more accurate and efficient planning. This is an ideal opportunity for someone with initial experience in Demand Planning, Forecasting, Supply Chain, or S&OP, who is eager to continue developing within the pharmaceutical sector. The challenge! 🚀 • Support the preparation and update of the demand forecast, consolidating information from markets, affiliates, or regions., • Collaborate in the analysis of sales history, trends, seasonality, and other factors impacting demand., • Participate in the preparation of information for monthly planning cycles such as S&OP / IBP., • Help monitor deviations between forecast and actual demand, identifying possible root causes together with the team., • Collaborate with Supply Planning to align forecasts, product availability, and supply needs., • Support the maintenance and review of planning-related information in systems, such as lead times, basic parameters, or product data., • Participate in the follow-up of product launches, transitions, discontinuations, and obsolescence control., • Prepare reports and KPIs to support analysis and decision-making., • Work closely with sales, marketing, finance, supply chain, and operations teams., • Contribute to the continuous improvement of processes, tools, and reporting within the area. What do you need? 🤓 • Degree in Engineering, Business Administration, Economics, Statistics, Supply Chain, Business Analytics, or a related field., • 1 to 2 years of experience in roles related to Demand Planning, Forecasting, Supply Chain, or S&OP., • High level of English, with the ability to work in an international environment., • Advanced Excel skills., • Experience or familiarity with ERP systems, ideally SAP., • Knowledge of planning or analytics tools such as APO, IBP, Anaplan, Power BI, or similar is a plus., • Strong analytical skills, attention to detail, and data-driven mindset., • Good communication and teamwork skills., • Interest in developing within the pharmaceutical sector. Our benefits! 👏 📜 Permanent contract ⏰ Flexible working hours 🍽️ Free canteen 🚗 Parking 🏥 Health insurance 📚 Professional development and continuous learning What will the selection process look like? 🕵️ • Initial contact by phone or email., • 1 or 2 virtual and/or in-person interviews., • Ongoing communication throughout the process. 🔷Do you think this opportunity is not for you? 🔷 Follow us on LinkedIn and Instagram to discover new career opportunities and stay updated on our open positions. #InsudPharma #Challenger #Insuder #InsudTalent EQUAL OPPORTUNITIES COMMITMENT At Exeltis, we promote equal opportunities and are committed to selection processes based on merit, skills, and experience. We guarantee non-discrimination on the basis of gender, age, ethnic or social origin, religion or beliefs, sexual orientation, gender identity, disability, or any other personal or social condition.

In a few words • Position: Senior Backend Developer, • Location: Madrid (Chamberí area)., • +4 years of experience 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 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. Ready to be a #Challenger? What are we looking for? 🔎 We are AI Labs team, the applied AI department at Insud Pharma. We are a team of 30 professionals (AI Engineers, Data Scientists, Backend Engineers, DevOps Engineers, and Product Managers) working across the full breadth of the company, building products and systems that directly inform and shape decision-making. We are looking for a Senior Backend Developer with strong technical foundations who is eager to design, build, and scale robust backend systems that power real-world AI-driven products. You will work across diverse and complex domains (Clinical, R&D, manufacturing, and beyond), collaborating closely with Data Scientists, Product Managers, and DevOps to bring solutions from concept to production. You will take ownership of backend services end-to-end—defining architectures, designing APIs, ensuring performance and scalability, and delivering reliable systems in production environments. We are seeking someone curious enough to tackle complex engineering challenges (distributed systems, concurrency, scalability, observability), rigorous enough to apply best practices and make sound architectural decisions, and independent enough to deliver high-impact solutions with strong ownership. How the team works: AI Labs operates with a startup mindset within Insud Pharma. The department is young, and the culture reflects that: flat, collaborative, and fast-moving. Beyond the AI Engineering team, you will work alongside Data Scientists, DevOps Engineers, and Product Managers who are equally committed to delivering high-quality work. We hold regular demo days where teams present their work, as well as whiteboard sessions where we tackle problems together. The cross-disciplinary dynamic is genuinely strong. The office is located in central Madrid (Chamberí, near Eloy Gonzalo), well connected and situated in a vibrant part of the city. The challenge! • Design, develop, and maintain REST APIs (FastAPI, Flask, or similar)., • Define and evolve scalable and efficient backend architectures., • Build services considering concurrency, performance, and scalability., • Collaborate with frontend teams to define clear, consistent, and versioned API contracts., • Integrate backend services with SQL and/or NoSQL databases., • Ensure code quality through testing (unit and integration), code reviews, and best practices., • Participate in CI/CD pipelines and deployment processes., • Work with cloud environments (AWS and/or Azure) in production systems., • Implement monitoring and observability (logs, metrics, alerts)., • Identify and resolve performance, scalability, and security issues., • Contribute to technical standards and reusable components., • Mentor and support junior developers., • Collaborate closely with Product, Engineering, and DevOps teams., • Participate in architectural decisions and contribute to the evolution of the tech stack., • Ensure reliability, performance, and quality of backend services What do you need? • Fluency in Spanish and English., • Strong experience in Python and backend development in production environments., • Experience with FastAPI, Flask, or similar frameworks., • Proven experience designing APIs and scalable backend architectures., • Experience with SQL and/or NoSQL databases., • Experience with Docker and containerized environments., • Experience working with cloud platforms (AWS and/or Azure) for development and deployment., • Familiarity with CI/CD tools (e.g., GitHub Actions, Azure DevOps)., • Knowledge of authentication systems (OAuth2, JWT)., • Solid understanding of best practices (SOLID principles, clean architecture)., • Ability to work autonomously with strong ownership and results orientation Our benefits! ⏰ Flexible start time from Monday to Friday 📜 Permanent contract. 🥼 Life and accident insurance. 🍽️ Ticket restaurant 💻 Training and language learning platform 💆🏻 ♀️ Wellness platform with unlimited free psychologist sessions 🚕 Cabify transportation service for employee use 📈 Development plans, internal mobility policy. ⭐ Many more! What will the Selection process be like? 🕵️ ➡️ Stay tuned to your phone and email! The first thing we will likely do is contact you through one of the two channels. ➡️ Prepare well! We will continue with an in-person/virtual interview depending on availability and what we agree upon; there may be one or two interviews in the process, and depending on the type of process, there may also be some kind of test. ➡️ Wait for the result! We care that you feel guided throughout each selection process and know what to expect from us, so we will always try to inform you of the status of the process. 🔷 Do you think this offer is not for you? 🔷 Follow us on social media like LinkedIn/Instagram and stay tuned for any offers we may release; the opportunity to be a new Insuder is waiting! #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.

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

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

In brief 📌 Position: Junior Demand Planner Location: Madrid (hybrid) Experience: 1–2 years of experience Want to know more? 👇 Exeltis is the branded business of Insud Pharma, an international pharmaceutical group operating across the entire value chain, from research and development to manufacturing, marketing, and distribution of value-added products for human and animal health. Insud Pharma’s activities are organized into three synergistic business areas: Industrial (Chemo), Branded (Exeltis), and Biotech (mAbxience). With 10,000 professionals across more than 50 countries, 20 industrial plants, 15 specialized R&D centers, 12 commercial offices, and over 35 pharmaceutical affiliates, Insud Pharma serves 1,150 customers in more than 110 countries worldwide. At Insud Pharma, we believe in innovation and sustainable development. At Exeltis, we are looking for someone with a foundation in planning, a strong analytical mindset, and a willingness to learn, to join the Supply Chain area and grow as a Junior Demand Planner in an international environment. What are we looking for? 🔎 We are looking for a junior professional who wants to grow within the demand planning area, contributing to forecast analysis, data monitoring, and cross-functional coordination to support more accurate and efficient planning. This is an ideal opportunity for someone with initial experience in Demand Planning, Forecasting, Supply Chain, or S&OP, who is eager to continue developing within the pharmaceutical sector. The challenge! 🚀 • Support the preparation and update of the demand forecast, consolidating information from markets, affiliates, or regions., • Collaborate in the analysis of sales history, trends, seasonality, and other factors impacting demand., • Participate in the preparation of information for monthly planning cycles such as S&OP / IBP., • Help monitor deviations between forecast and actual demand, identifying possible root causes together with the team., • Collaborate with Supply Planning to align forecasts, product availability, and supply needs., • Support the maintenance and review of planning-related information in systems, such as lead times, basic parameters, or product data., • Participate in the follow-up of product launches, transitions, discontinuations, and obsolescence control., • Prepare reports and KPIs to support analysis and decision-making., • Work closely with sales, marketing, finance, supply chain, and operations teams., • Contribute to the continuous improvement of processes, tools, and reporting within the area. What do you need? 🤓 • Degree in Engineering, Business Administration, Economics, Statistics, Supply Chain, Business Analytics, or a related field., • 1 to 2 years of experience in roles related to Demand Planning, Forecasting, Supply Chain, or S&OP., • High level of English, with the ability to work in an international environment., • Advanced Excel skills., • Experience or familiarity with ERP systems, ideally SAP., • Knowledge of planning or analytics tools such as APO, IBP, Anaplan, Power BI, or similar is a plus., • Strong analytical skills, attention to detail, and data-driven mindset., • Good communication and teamwork skills., • Interest in developing within the pharmaceutical sector. Our benefits! 👏 📜 Permanent contract ⏰ Flexible working hours 🍽️ Free canteen 🚗 Parking 🏥 Health insurance 📚 Professional development and continuous learning What will the selection process look like? 🕵️ • Initial contact by phone or email., • 1 or 2 virtual and/or in-person interviews., • Ongoing communication throughout the process. 🔷Do you think this opportunity is not for you? 🔷 Follow us on LinkedIn and Instagram to discover new career opportunities and stay updated on our open positions. #InsudPharma #Challenger #Insuder #InsudTalent EQUAL OPPORTUNITIES COMMITMENT At Exeltis, we promote equal opportunities and are committed to selection processes based on merit, skills, and experience. We guarantee non-discrimination on the basis of gender, age, ethnic or social origin, religion or beliefs, sexual orientation, gender identity, disability, or any other personal or social condition.

¿Quiénes somos? Neotalent Conclusion es una de las mayores especialistas del mercado ibérico en captación y gestión de talento informático y de ingeniería. Como parte del grupo neerlandés Conclusion, que se compone por un ecosistema de 25 empresas y 3.600 empleados, nos centramos en aumentar la capacidad tecnológica de nuestros clientes y acelerar la transformación digital de los mismos. En Neotalent Conclusion, somos especialistas del talento. Atraemos a los mejores profesionales y los combinamos con los proyectos más ambiciosos, en el momento justo. Nuestro éxito radica en la inversión en innovación, orientación a resultados y, por encima de todo, en la garantía de que las personas tengan carreras felices y realizadoras. Con más de 25 años de experiencia, Neotalent Conclusion cuenta con oficinas en Madrid, Lisboa y Oporto. Nuestra compañía está formada por un equipo de más de 850 profesionales entre sus diferentes áreas de operación. Neotalent, the responsive people. Más información en www.neotalent.pt/es y https://neotalent.pt/es/oportunidades-de-carrera/. Descripción del puesto: En Neotalent Conclusion buscamos un/a Senior Full-Stack Developer para proyecto en el sector farmacéutico / Life Sciences. 🚀Cuáles serán tus funciones: • Desarrollo y mantenimiento de aplicaciones Full-Stack, • Diseño de soluciones backend con Python, • Gestión y optimización de bases de datos SQL, • Desarrollo de interfaces frontend (React / Vue / Angular), • Integración con sistemas industriales y datos en tiempo real, • Asegurar cumplimiento en entornos regulados (GMP/GAMP), • Participación en decisiones técnicas y code reviews 🔧 Requisitos clave: • Más de 5 años de experiencia en desarrollo Full-Stack, • Dominio avanzado de Python (Django, Flask o FastAPI), • Experiencia sólida en SQL (PostgreSQL/MySQL), • Amplio conocimiento de JavaScript + React / Vue / Angular, • Conocimientos de Git, Docker, CI/CD Valorable: Experiencia previa en entornos regulados / industria pharma 🌟 Por qué unirte a nosotros: • Trabajar en proyectos desafiantes para grandes clientes, • Aprender más sobre tecnologías emergentes, • Posibilidad de trabajar de forma remota, • Acceso a formación continua y certificaciones, • Disfrutar de un plan de compensación flexible, • ... ¡y mucho más!

¿Quiénes somos? Neotalent Conclusion es una de las mayores especialistas del mercado ibérico en captación y gestión de talento informático y de ingeniería. Como parte del grupo neerlandés Conclusion, que se compone por un ecosistema de 25 empresas y 3.600 empleados, nos centramos en aumentar la capacidad tecnológica de nuestros clientes y acelerar la transformación digital de los mismos. En Neotalent Conclusion, somos especialistas del talento. Atraemos a los mejores profesionales y los combinamos con los proyectos más ambiciosos, en el momento justo. Nuestro éxito radica en la inversión en innovación, orientación a resultados y, por encima de todo, en la garantía de que las personas tengan carreras felices y realizadoras. Con más de 25 años de experiencia, Neotalent Conclusion cuenta con oficinas en Madrid, Lisboa y Oporto. Nuestra compañía está formada por un equipo de más de 850 profesionales entre sus diferentes áreas de operación. Neotalent, the responsive people. Más información en www.neotalent.pt/es y https://neotalent.pt/es/oportunidades-de-carrera/. Descripción del puesto: En Neotalent Conclusion buscamos un/a Senior Full-Stack Developer para proyecto en el sector farmacéutico / Life Sciences. 🚀Cuáles serán tus funciones: • Desarrollo y mantenimiento de aplicaciones Full-Stack, • Diseño de soluciones backend con Python, • Gestión y optimización de bases de datos SQL, • Desarrollo de interfaces frontend (React / Vue / Angular), • Integración con sistemas industriales y datos en tiempo real, • Asegurar cumplimiento en entornos regulados (GMP/GAMP), • Participación en decisiones técnicas y code reviews 🔧 Requisitos clave: • Más de 5 años de experiencia en desarrollo Full-Stack, • Dominio avanzado de Python (Django, Flask o FastAPI), • Experiencia sólida en SQL (PostgreSQL/MySQL), • Amplio conocimiento de JavaScript + React / Vue / Angular, • Conocimientos de Git, Docker, CI/CD Valorable: Experiencia previa en entornos regulados / industria pharma 🌟 Por qué unirte a nosotros: • Trabajar en proyectos desafiantes para grandes clientes, • Aprender más sobre tecnologías emergentes, • Posibilidad de trabajar de forma remota, • Acceso a formación continua y certificaciones, • Disfrutar de un plan de compensación flexible, • ... ¡y mucho más!

🚀 ¡Únete a VANTURE ESS y transforma el futuro digital! Somos una consultora tecnológica especializada en soluciones SAP y servicios integrales de transformación digital. Apostamos por el talento, la innovación, la flexibilidad y la confianza para impulsar el crecimiento de nuestros clientes en todos los sectores de negocio. Actualmente buscamos incorporar a nuestro equipo un/a Consultor/a Sénior SAP en el área Logística con una trayectoria sólida como Consultor/a, Team Lead y y Preventa, capaz de liderar iniciativas complejas E2E y aportar una visión funcional–técnica de alto valor. 🧩 ¿Qué harás en tu día a día? • Tendrás la oportunidad de dirigir proyectos estratégicos en entornos S/4 HANA, optimizar procesos logísticos y asegurar la correcta evolución de la plataforma SAP de nuestros clientes, • Serás responsable de orquestar todo el ciclo de vida de los proyectos SAP Logísticos: desde el análisis preliminar y la preventa hasta la planificación, ejecución, control presupuestario, comunicación con stakeholders y gestión del cambio., • Liderar proyectos SAP Logísticos E2E, desde la planificación hasta la puesta en producción., • Gestionar equipos internos y externos, garantizando la correcta ejecución según alcance, plazos y calidad., • Participar en actividades de preventa: demos, toma de requerimientos, dimensionamiento técnico y funcional., • Coordinar y ejecutar proyectos de migración de R/3 a S/4 HANA, rollouts y optimización de procesos., • Analizar, definir y mejorar procesos., • Asegurar una comunicación fluida con las áreas de negocio, dirección y partners tecnológicos., • Supervisar actividades de soporte, mantenimiento evolutivo y gestión de incidencias. 🎯 ¿Qué buscamos? Requisitos imprescindibles : • Experiencia demostrable como Consultor/a Sénior SAP en área logística ( Mínima de 10 años), • Background SAP PP- WM- y/o MM y SD, con visión funcional clara., • Participación real en proyectos de implementación, migración R/3 → S/4 HANA, rollouts y soporte., • Experiencia en gestión integral de proyectos (E2E) y metodologías clásicas/ágiles., • Capacidad para desempeñar funciones de preventa., • Experiencia en diferentes sectores : Servicios, Pharma, Químico, Industrial,etc.. 🔝 Valoraremos positivamente: • Certificaciones SAP (WM/MM/SD) o PMI/Scrum Master., • Conocimiento de módulos complementarios (EWM, LE, PP)., • Buen nivel de Inglés. 🌟 ¿Qué te ofrecemos? • 🤝 Contrato indefinido desde el primer día., • 📚 Plan de carrera y formación personalizada., • 💼 Paquete retributivo flexible: seguro médico privado, ticket restaurante, guardería y transporte., • 🕒 Horario de oficina de lunes a jueves + viernes intensivo., • 🏡 Proyecto 100% remoto (residencia en España imprescindible). Sólo se valorarán candidaturas para contratación en plantilla., • 📅 24 días laborables de vacaciones al año., • 💰 Salario competitivo según experiencia., • 🥰 Excelente clima laboral, basado en la confianza y el respeto. 🌈 En VANTURE ESS creemos en la igualdad de oportunidades Nuestro proceso de selección se basa en la objetividad, los méritos y la capacidad profesional, sin distinción por género, orientación sexual, edad, etnia o diversidad funcional. Si te apasiona el mundo SAP, buscas estabilidad y quieres formar parte de un equipo que apuesta por el talento... 📢 ¡Queremos conocerte! ¡Este es tu lugar! En VANTURE ESS apostamos por ti.

Mediance es un grupo empresarial en crecimiento especializado en la adquisición y desarrollo de compañías del sector sanitario. El grupo integra empresas que operan en diferentes ámbitos del healthcare, incluyendo la distribución de medicación, producto sanitario y equipamiento médico, así como a la optimización de procesos asistenciales y asesoramiento en la gestión a través del desarrollo de soluciones tecnológicas para el sector. El modelo de Mediance se basa en una estrategia buy & build, mediante la cual el grupo adquiere empresas especializadas y las impulsa mediante servicios centrales que aportan soporte estratégico en áreas como finanzas, recursos humanos, operaciones y tecnología. En este contexto, Mediance busca incorporar un Head of Technology / IT Director que lidere la estrategia tecnológica del grupo, impulsando la integración de sistemas entre las empresas participadas y construyendo una plataforma tecnológica común que permita mejorar la eficiencia operativa y escalar el crecimiento del grupo. Descripción del Puesto: El Head of Technology / IT Director será responsable de definir y ejecutar la estrategia tecnológica del grupo Mediance, con especial foco en la integración de sistemas, la estandarización de herramientas y la digitalización de las empresas participadas. Se trata de un rol con alto impacto estratégico, pero también con un enfoque hands-on, ideal para un perfil con mentalidad de constructor que quiera liderar la transformación tecnológica de un grupo sanitario en crecimiento. La persona seleccionada trabajará de forma transversal con los equipos directivos de las diferentes compañías del grupo, coordinando proveedores tecnológicos y apoyándose en los equipos técnicos existentes en las empresas participadas. Responsabilidades: • Definir la arquitectura tecnológica global del grupo Mediance., • Diseñar el roadmap de digitalización y evolución tecnológica., • Evaluar los sistemas y plataformas existentes en las empresas participadas., • Experiencia en implementaciones mediante APIs o middleware., • Liderar procesos de integración tecnológica tras adquisiciones., • Diseñar e implementar planes de unificación de sistemas., • Estandarizar herramientas y procesos tecnológicos entre compañías., • Seleccionar e implementar sistemas clave para el grupo (ERP, CRM, herramientas financieras, plataformas de reporting y business intelligence)., • Establecer estándares tecnológicos para todas las empresas participadas., • Definir la arquitectura de infraestructura y cloud del grupo., • Diseñar integraciones entre sistemas mediante APIs o middleware., • Garantizar la seguridad y escalabilidad de la plataforma tecnológica., • Seleccionar y coordinar consultoras y partners tecnológicos., • Supervisar proyectos tecnológicos y controlar calidad, tiempos y costes., • Garantizar una ejecución eficiente de las implementaciones., • Asesorar a los equipos técnicos existentes en las compañías del grupo., • Apoyar proyectos tecnológicos específicos en las empresas participadas., • Identificar oportunidades de mejora operativa mediante tecnología., • Definir estándares tecnológicos comunes., • Priorizar iniciativas tecnológicas con impacto en negocio., • Construir progresivamente una función tecnológica central para el grupo. Requisitos: • Entre 10 y 15 años de experiencia en tecnología, sistemas o transformación digital., • Experiencia liderando implementaciones de ERP o sistemas corporativos., • Experiencia en integración de sistemas entre diferentes empresas o unidades de negocio., • Conocimiento de arquitecturas cloud y sistemas empresariales., • Experiencia gestionando proveedores tecnológicos y consultoras., • Capacidad para liderar proyectos tecnológicos complejos con múltiples stakeholders., • Experiencia con Plataformas de Business Intelligence y reporting (Power BI, Tableau, etc.)., • Experiencia en implementaciones mediante APIs o middleware., • Disponibilidad para viajar a nivel nacional, con desplazamientos frecuentes por toda España (viajes semanales) para trabajar de forma presencial con las distintas compañías del grupo. Nice to have: • Experiencia en sectores como healthcare, pharma, distribución sanitaria o entornos industriales., • Experiencia en consultoría tecnológica o transformación digital., • Experiencia trabajando en grupos empresariales o empresas participadas por private equity., • Experiencia en procesos de integración tecnológica tras adquisiciones.

Mediance es un grupo empresarial en crecimiento especializado en la adquisición y desarrollo de compañías del sector sanitario. El grupo integra empresas que operan en diferentes ámbitos del healthcare, incluyendo la distribución de medicación, producto sanitario y equipamiento médico, así como a la optimización de procesos asistenciales y asesoramiento en la gestión a través del desarrollo de soluciones tecnológicas para el sector. El modelo de Mediance se basa en una estrategia buy & build, mediante la cual el grupo adquiere empresas especializadas y las impulsa mediante servicios centrales que aportan soporte estratégico en áreas como finanzas, recursos humanos, operaciones y tecnología. En este contexto, Mediance busca incorporar un Head of Technology / IT Director que lidere la estrategia tecnológica del grupo, impulsando la integración de sistemas entre las empresas participadas y construyendo una plataforma tecnológica común que permita mejorar la eficiencia operativa y escalar el crecimiento del grupo. Descripción del Puesto: El Head of Technology / IT Director será responsable de definir y ejecutar la estrategia tecnológica del grupo Mediance, con especial foco en la integración de sistemas, la estandarización de herramientas y la digitalización de las empresas participadas. Se trata de un rol con alto impacto estratégico, pero también con un enfoque hands-on, ideal para un perfil con mentalidad de constructor que quiera liderar la transformación tecnológica de un grupo sanitario en crecimiento. La persona seleccionada trabajará de forma transversal con los equipos directivos de las diferentes compañías del grupo, coordinando proveedores tecnológicos y apoyándose en los equipos técnicos existentes en las empresas participadas. Responsabilidades: • Definir la arquitectura tecnológica global del grupo Mediance., • Diseñar el roadmap de digitalización y evolución tecnológica., • Evaluar los sistemas y plataformas existentes en las empresas participadas., • Experiencia en implementaciones mediante APIs o middleware., • Liderar procesos de integración tecnológica tras adquisiciones., • Diseñar e implementar planes de unificación de sistemas., • Estandarizar herramientas y procesos tecnológicos entre compañías., • Seleccionar e implementar sistemas clave para el grupo (ERP, CRM, herramientas financieras, plataformas de reporting y business intelligence)., • Establecer estándares tecnológicos para todas las empresas participadas., • Definir la arquitectura de infraestructura y cloud del grupo., • Diseñar integraciones entre sistemas mediante APIs o middleware., • Garantizar la seguridad y escalabilidad de la plataforma tecnológica., • Seleccionar y coordinar consultoras y partners tecnológicos., • Supervisar proyectos tecnológicos y controlar calidad, tiempos y costes., • Garantizar una ejecución eficiente de las implementaciones., • Asesorar a los equipos técnicos existentes en las compañías del grupo., • Apoyar proyectos tecnológicos específicos en las empresas participadas., • Identificar oportunidades de mejora operativa mediante tecnología., • Definir estándares tecnológicos comunes., • Priorizar iniciativas tecnológicas con impacto en negocio., • Construir progresivamente una función tecnológica central para el grupo. Requisitos: • Entre 10 y 15 años de experiencia en tecnología, sistemas o transformación digital., • Experiencia liderando implementaciones de ERP o sistemas corporativos., • Experiencia en integración de sistemas entre diferentes empresas o unidades de negocio., • Conocimiento de arquitecturas cloud y sistemas empresariales., • Experiencia gestionando proveedores tecnológicos y consultoras., • Capacidad para liderar proyectos tecnológicos complejos con múltiples stakeholders., • Experiencia con Plataformas de Business Intelligence y reporting (Power BI, Tableau, etc.)., • Experiencia en implementaciones mediante APIs o middleware., • Disponibilidad para viajar a nivel nacional, con desplazamientos frecuentes por toda España (viajes semanales) para trabajar de forma presencial con las distintas compañías del grupo. Nice to have: • Experiencia en sectores como healthcare, pharma, distribución sanitaria o entornos industriales., • Experiencia en consultoría tecnológica o transformación digital., • Experiencia trabajando en grupos empresariales o empresas participadas por private equity., • Experiencia en procesos de integración tecnológica tras adquisiciones.

🚀 ¡Únete a VANTURE ESS y transforma el futuro digital! Somos una consultora tecnológica especializada en soluciones SAP y servicios integrales de transformación digital. Apostamos por el talento, la innovación, la flexibilidad y la confianza para impulsar el crecimiento de nuestros clientes en todos los sectores de negocio. Actualmente buscamos incorporar a nuestro equipo un/a Consultor/a Sénior SAP en el área Logística con una trayectoria sólida como Consultor/a, Team Lead y y Preventa, capaz de liderar iniciativas complejas E2E y aportar una visión funcional–técnica de alto valor. 🧩 ¿Qué harás en tu día a día? • Tendrás la oportunidad de dirigir proyectos estratégicos en entornos S/4 HANA, optimizar procesos logísticos y asegurar la correcta evolución de la plataforma SAP de nuestros clientes, • Serás responsable de orquestar todo el ciclo de vida de los proyectos SAP Logísticos: desde el análisis preliminar y la preventa hasta la planificación, ejecución, control presupuestario, comunicación con stakeholders y gestión del cambio., • Liderar proyectos SAP Logísticos E2E, desde la planificación hasta la puesta en producción., • Gestionar equipos internos y externos, garantizando la correcta ejecución según alcance, plazos y calidad., • Participar en actividades de preventa: demos, toma de requerimientos, dimensionamiento técnico y funcional., • Coordinar y ejecutar proyectos de migración de R/3 a S/4 HANA, rollouts y optimización de procesos., • Analizar, definir y mejorar procesos., • Asegurar una comunicación fluida con las áreas de negocio, dirección y partners tecnológicos., • Supervisar actividades de soporte, mantenimiento evolutivo y gestión de incidencias. 🎯 ¿Qué buscamos? Requisitos imprescindibles : • Experiencia demostrable como Consultor/a Sénior SAP en área logística ( Mínima de 10 años), • Background SAP PP- WM- y/o MM y SD, con visión funcional clara., • Participación real en proyectos de implementación, migración R/3 → S/4 HANA, rollouts y soporte., • Experiencia en gestión integral de proyectos (E2E) y metodologías clásicas/ágiles., • Capacidad para desempeñar funciones de preventa., • Experiencia en diferentes sectores : Servicios, Pharma, Químico, Industrial,etc.. 🔝 Valoraremos positivamente: • Certificaciones SAP (WM/MM/SD) o PMI/Scrum Master., • Conocimiento de módulos complementarios (EWM, LE, PP)., • Buen nivel de Inglés. 🌟 ¿Qué te ofrecemos? • 🤝 Contrato indefinido desde el primer día., • 📚 Plan de carrera y formación personalizada., • 💼 Paquete retributivo flexible: seguro médico privado, ticket restaurante, guardería y transporte., • 🕒 Horario de oficina de lunes a jueves + viernes intensivo., • 🏡 Proyecto 100% remoto (residencia en España imprescindible). Sólo se valorarán candidaturas para contratación en plantilla., • 📅 24 días laborables de vacaciones al año., • 💰 Salario competitivo según experiencia., • 🥰 Excelente clima laboral, basado en la confianza y el respeto. 🌈 En VANTURE ESS creemos en la igualdad de oportunidades Nuestro proceso de selección se basa en la objetividad, los méritos y la capacidad profesional, sin distinción por género, orientación sexual, edad, etnia o diversidad funcional. Si te apasiona el mundo SAP, buscas estabilidad y quieres formar parte de un equipo que apuesta por el talento... 📢 ¡Queremos conocerte! ¡Este es tu lugar! En VANTURE ESS apostamos por ti.

HAYS is collaborating with the leading company in the pharmaceutical sector. We are looking for a Paid Social Media Senior to join the team. What will your duties be? • Manage end-to-end paid media campaigns, ensuring alignment with global business objectives., • Develop and execute digital performance strategies tailored to each campaign and market., • Plan, implement, and optimize SEA and Paid Social campaigns focused on conversions, traffic, lead generation, and brand awareness., • Monitor campaign performance, including budget control, ongoing optimization, and detailed reporting., • Work with advertising platforms such as Google Ads, Bing Ads, Facebook Ads, LinkedIn Ads, SA360, and DV360., • Conduct benchmark analysis and competitive research to improve campaign performance., • Optimize campaigns for e-commerce, product and service promotion, and brand positioning., • Analyze performance data using tools like Adobe Analytics, Looker Studio, Power BI, and Semrush., • Create custom reports and dashboards, tailored to diverse stakeholders and international teams., • Implement and manage tracking infrastructure (pixels, tags, and events) to ensure accurate measurement., • Execute A/B testing and track key KPIs such as CPC, CTR, conversion rate, bounce rate, and cost per lead., • Leverage advanced analytics and AI-driven solutions (including prompt engineering and automation) to enhance targeting and maximize ROI., • Communicate and collaborate directly with stakeholders, global teams, and external suppliers., • Manage relationships with global partners, ensuring effective execution of international campaigns. Which are the requirements? • Proven experience managing paid media campaigns across key platforms: Meta (Facebook & Instagram) and LinkedIn Ads., • Previous experience working in a digital marketing agency environment., • Familiarity or willingness to work with emerging and alternative platforms such as: Reddit Ads and TikTok Ads is a plus., • Experience with X (Twitter) is a plus., • Experience managing campaigns or projects within the pharmaceutical (pharma) industry is highly desirable., • English fluent. What we offer? • Long term contract with Hays., • Participate in international projects., • Flexible remote work model (1 office day per month). Location: Barcelona., • Flexible Schedule: Monday to Friday from 8-9 to 5-6.

HAYS is collaborating with the leading company in the pharmaceutical sector. We are looking for a Paid Social Media Senior to join the team. What will your duties be? • Manage end-to-end paid media campaigns, ensuring alignment with global business objectives., • Develop and execute digital performance strategies tailored to each campaign and market., • Plan, implement, and optimize SEA and Paid Social campaigns focused on conversions, traffic, lead generation, and brand awareness., • Monitor campaign performance, including budget control, ongoing optimization, and detailed reporting., • Work with advertising platforms such as Google Ads, Bing Ads, Facebook Ads, LinkedIn Ads, SA360, and DV360., • Conduct benchmark analysis and competitive research to improve campaign performance., • Optimize campaigns for e-commerce, product and service promotion, and brand positioning., • Analyze performance data using tools like Adobe Analytics, Looker Studio, Power BI, and Semrush., • Create custom reports and dashboards, tailored to diverse stakeholders and international teams., • Implement and manage tracking infrastructure (pixels, tags, and events) to ensure accurate measurement., • Execute A/B testing and track key KPIs such as CPC, CTR, conversion rate, bounce rate, and cost per lead., • Leverage advanced analytics and AI-driven solutions (including prompt engineering and automation) to enhance targeting and maximize ROI., • Communicate and collaborate directly with stakeholders, global teams, and external suppliers., • Manage relationships with global partners, ensuring effective execution of international campaigns. Which are the requirements? • Proven experience managing paid media campaigns across key platforms: Meta (Facebook & Instagram) and LinkedIn Ads., • Previous experience working in a digital marketing agency environment., • Familiarity or willingness to work with emerging and alternative platforms such as: Reddit Ads and TikTok Ads is a plus., • Experience with X (Twitter) is a plus., • Experience managing campaigns or projects within the pharmaceutical (pharma) industry is highly desirable., • English fluent. What we offer? • Long term contract with Hays., • Participate in international projects., • Flexible remote work model (1 office day per month). Location: Barcelona., • Flexible Schedule: Monday to Friday from 8-9 to 5-6.

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

HAYS is collaborating with the leading company in the pharmaceutical sector. We are looking for a Paid Social Media Senior to join the team. What will your duties be? • Manage end-to-end paid media campaigns, ensuring alignment with global business objectives., • Develop and execute digital performance strategies tailored to each campaign and market., • Plan, implement, and optimize SEA and Paid Social campaigns focused on conversions, traffic, lead generation, and brand awareness., • Monitor campaign performance, including budget control, ongoing optimization, and detailed reporting., • Work with advertising platforms such as Google Ads, Bing Ads, Facebook Ads, LinkedIn Ads, SA360, and DV360., • Conduct benchmark analysis and competitive research to improve campaign performance., • Optimize campaigns for e-commerce, product and service promotion, and brand positioning., • Analyze performance data using tools like Adobe Analytics, Looker Studio, Power BI, and Semrush., • Create custom reports and dashboards, tailored to diverse stakeholders and international teams., • Implement and manage tracking infrastructure (pixels, tags, and events) to ensure accurate measurement., • Execute A/B testing and track key KPIs such as CPC, CTR, conversion rate, bounce rate, and cost per lead., • Leverage advanced analytics and AI-driven solutions (including prompt engineering and automation) to enhance targeting and maximize ROI., • Communicate and collaborate directly with stakeholders, global teams, and external suppliers., • Manage relationships with global partners, ensuring effective execution of international campaigns. Which are the requirements? • Proven experience managing paid media campaigns across key platforms: Meta (Facebook & Instagram) and LinkedIn Ads., • Previous experience working in a digital marketing agency environment., • Familiarity or willingness to work with emerging and alternative platforms such as: Reddit Ads and TikTok Ads is a plus., • Experience with X (Twitter) is a plus., • Experience managing campaigns or projects within the pharmaceutical (pharma) industry is highly desirable., • English fluent. What we offer? • Long term contract with Hays., • Participate in international projects., • Flexible remote work model (1 office day per month). Location: Barcelona., • Flexible Schedule: Monday to Friday from 8-9 to 5-6.

Ubicación Europa (preferiblemente España o ubicación estratégica dentro de la UE) – modalidad híbrida/remota con disponibilidad para viajes internacionales. Sobre la compañía Somos una Contract Research Organization (CRO) especializada en la gestión y ejecución de ensayos clínicos para compañías farmacéuticas, biotecnológicas y organizaciones del sector salud. Nuestro objetivo es ofrecer soluciones de alta calidad que aceleren el desarrollo de nuevas terapias y contribuyan al avance de la investigación clínica a nivel global. Posición Buscamos un/a Director/a de Desarrollo de Negocio con una trayectoria demostrada en el sector de investigación clínica y CROs, capaz de liderar la expansión comercial de la compañía en Europa y apoyar el crecimiento. La persona seleccionada deberá aportar un profundo conocimiento de la industria, experiencia en venta consultiva de servicios de investigación clínica y una sólida red de contactos en compañías farmacéuticas multinacionales, biotecnológicas y otros actores clave del ecosistema. Responsabilidades principales • Diseñar e implementar la estrategia de desarrollo de negocio para Europa, identificando nuevas oportunidades comerciales y alianzas estratégicas., • Desarrollar y gestionar relaciones de alto nivel con decisores clave en compañías farmacéuticas globales (Big Pharma), biotecnológicas, empresas de salud y sponsors de investigación clínica., • Generar nuevas oportunidades de negocio y liderar todo el ciclo comercial, desde la identificación del lead hasta el cierre contractual., • Representar a la compañía en congresos, eventos sectoriales, asociaciones de la industria y reuniones con clientes estratégicos., • Colaborar con los equipos operativos, científicos y de propuesta para desarrollar soluciones competitivas y adaptadas a las necesidades de los clientes., • Elaborar previsiones comerciales, seguimiento de pipeline y reporting periódico a la Dirección General., • Identificar oportunidades de expansión en Latinoamérica, aprovechando conocimiento del mercado y relaciones existentes en la región., • Mantener un profundo conocimiento de las tendencias del mercado, regulaciones, movimientos de la competencia y necesidades emergentes de la industria farmacéutica y biotecnológica. Requisitos Imprescindibles • Titulación universitaria en Ciencias de la Salud, Farmacia, Biología, Biotecnología, Medicina, Química o áreas afines., • Experiencia mínima de 8-10 años en desarrollo de negocio dentro de una CRO, organización de investigación clínica o sector relacionado., • Historial demostrable de generación de negocio y cierre de contratos relevantes en servicios de investigación clínica., • Red consolidada de contactos y capacidad de interlocución directa con responsables de Clinical Operations, Clinical Development, Outsourcing, Procurement, Medical Affairs y otras áreas clave dentro de grandes compañías farmacéuticas y biotecnológicas., • Conocimiento profundo de ensayos clínicos, desarrollo de medicamentos, regulación y modelos operativos de CRO., • Experiencia gestionando procesos comerciales complejos y negociaciones con clientes multinacionales., • Nivel profesional de inglés (C1 o superior). Muy valorable • Experiencia comercial en mercados europeos clave (Alemania, Reino Unido, Francia, Italia, España, Países Bajos y países nórdicos)., • Conocimiento y experiencia previa desarrollando negocio en Latinoamérica., • Red activa de contactos en compañías farmacéuticas globales, biotechs, sponsors y organizaciones de investigación clínica., • Experiencia en CROs medianas o internacionales con enfoque de crecimiento., • Dominio de español y portugués. Qué ofrecemos • Posición estratégica con impacto directo en el crecimiento de la compañía., • Paquete retributivo competitivo compuesto por salario fijo y variable vinculado a objetivos., • Flexibilidad laboral y entorno internacional., • Oportunidad de liderar la expansión comercial en mercados clave de Europa y Latinoamérica., • Participación activa en la definición de la estrategia corporativa y comercial de la organización.

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

Desde la división de Química&Pharma nos encontramos en la búsqueda de un/a Técnico/a HSE para una empresa del sector industrial con sede en Madrid. ¿Qué harás? • Coordinación del sistema de gestión PRL, planificación preventiva, supervisión de permisos de trabajo, investigación de accidentes y análisis de causa raíz., • Experiencia realizando evaluaciones higiénicas industriales (agentes químicos, APIs, etc.) y capacidad de análisis de resultados para garantizar condiciones seguras de trabajo., • Trayectoria mínima de 4-5 años en industria,trabajando en entornos ATEX y con conocimiento de normativa APQ/RD 1215/97., • Participación activa en trabajos especiales, coordinación de servicios de prevención ajenos, seguimiento de medidas correctoras y soporte en planes de seguridad y salud. ¿Qué buscamos? • Ingeniería en Ciencias Químicas o similar, Máster en PRL con las 3 especialidades (Seguridad, Higiene y Ergonomía) y mínimo 4-5 años de experiencia en entornos industriales. ¿Qué ofrecemos? • Contrato indefinido con cliente final., • Salario competitivo, • Retribución flexible.

Desde la división de Química&Pharma nos encontramos en la búsqueda de un/a Técnico/a HSE para una empresa del sector industrial con sede en Madrid. ¿Qué harás? • Coordinación del sistema de gestión PRL, planificación preventiva, supervisión de permisos de trabajo, investigación de accidentes y análisis de causa raíz., • Experiencia realizando evaluaciones higiénicas industriales (agentes químicos, APIs, etc.) y capacidad de análisis de resultados para garantizar condiciones seguras de trabajo., • Trayectoria mínima de 4-5 años en industria,trabajando en entornos ATEX y con conocimiento de normativa APQ/RD 1215/97., • Participación activa en trabajos especiales, coordinación de servicios de prevención ajenos, seguimiento de medidas correctoras y soporte en planes de seguridad y salud. ¿Qué buscamos? • Ingeniería en Ciencias Químicas o similar, Máster en PRL con las 3 especialidades (Seguridad, Higiene y Ergonomía) y mínimo 4-5 años de experiencia en entornos industriales. ¿Qué ofrecemos? • Contrato indefinido con cliente final., • Salario competitivo, • Retribución flexible.

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

Ubicación Europa (preferiblemente España o ubicación estratégica dentro de la UE) – modalidad híbrida/remota con disponibilidad para viajes internacionales. Sobre la compañía Somos una Contract Research Organization (CRO) especializada en la gestión y ejecución de ensayos clínicos para compañías farmacéuticas, biotecnológicas y organizaciones del sector salud. Nuestro objetivo es ofrecer soluciones de alta calidad que aceleren el desarrollo de nuevas terapias y contribuyan al avance de la investigación clínica a nivel global. Posición Buscamos un/a Director/a de Desarrollo de Negocio con una trayectoria demostrada en el sector de investigación clínica y CROs, capaz de liderar la expansión comercial de la compañía en Europa y apoyar el crecimiento. La persona seleccionada deberá aportar un profundo conocimiento de la industria, experiencia en venta consultiva de servicios de investigación clínica y una sólida red de contactos en compañías farmacéuticas multinacionales, biotecnológicas y otros actores clave del ecosistema. Responsabilidades principales • Diseñar e implementar la estrategia de desarrollo de negocio para Europa, identificando nuevas oportunidades comerciales y alianzas estratégicas., • Desarrollar y gestionar relaciones de alto nivel con decisores clave en compañías farmacéuticas globales (Big Pharma), biotecnológicas, empresas de salud y sponsors de investigación clínica., • Generar nuevas oportunidades de negocio y liderar todo el ciclo comercial, desde la identificación del lead hasta el cierre contractual., • Representar a la compañía en congresos, eventos sectoriales, asociaciones de la industria y reuniones con clientes estratégicos., • Colaborar con los equipos operativos, científicos y de propuesta para desarrollar soluciones competitivas y adaptadas a las necesidades de los clientes., • Elaborar previsiones comerciales, seguimiento de pipeline y reporting periódico a la Dirección General., • Identificar oportunidades de expansión en Latinoamérica, aprovechando conocimiento del mercado y relaciones existentes en la región., • Mantener un profundo conocimiento de las tendencias del mercado, regulaciones, movimientos de la competencia y necesidades emergentes de la industria farmacéutica y biotecnológica. Requisitos Imprescindibles • Titulación universitaria en Ciencias de la Salud, Farmacia, Biología, Biotecnología, Medicina, Química o áreas afines., • Experiencia mínima de 8-10 años en desarrollo de negocio dentro de una CRO, organización de investigación clínica o sector relacionado., • Historial demostrable de generación de negocio y cierre de contratos relevantes en servicios de investigación clínica., • Red consolidada de contactos y capacidad de interlocución directa con responsables de Clinical Operations, Clinical Development, Outsourcing, Procurement, Medical Affairs y otras áreas clave dentro de grandes compañías farmacéuticas y biotecnológicas., • Conocimiento profundo de ensayos clínicos, desarrollo de medicamentos, regulación y modelos operativos de CRO., • Experiencia gestionando procesos comerciales complejos y negociaciones con clientes multinacionales., • Nivel profesional de inglés (C1 o superior). Muy valorable • Experiencia comercial en mercados europeos clave (Alemania, Reino Unido, Francia, Italia, España, Países Bajos y países nórdicos)., • Conocimiento y experiencia previa desarrollando negocio en Latinoamérica., • Red activa de contactos en compañías farmacéuticas globales, biotechs, sponsors y organizaciones de investigación clínica., • Experiencia en CROs medianas o internacionales con enfoque de crecimiento., • Dominio de español y portugués. Qué ofrecemos • Posición estratégica con impacto directo en el crecimiento de la compañía., • Paquete retributivo competitivo compuesto por salario fijo y variable vinculado a objetivos., • Flexibilidad laboral y entorno internacional., • Oportunidad de liderar la expansión comercial en mercados clave de Europa y Latinoamérica., • Participación activa en la definición de la estrategia corporativa y comercial de la organización.

Ubicación Europa (preferiblemente España o ubicación estratégica dentro de la UE) – modalidad híbrida/remota con disponibilidad para viajes internacionales. Sobre la compañía Somos una Contract Research Organization (CRO) especializada en la gestión y ejecución de ensayos clínicos para compañías farmacéuticas, biotecnológicas y organizaciones del sector salud. Nuestro objetivo es ofrecer soluciones de alta calidad que aceleren el desarrollo de nuevas terapias y contribuyan al avance de la investigación clínica a nivel global. Posición Buscamos un/a Director/a de Desarrollo de Negocio con una trayectoria demostrada en el sector de investigación clínica y CROs, capaz de liderar la expansión comercial de la compañía en Europa y apoyar el crecimiento. La persona seleccionada deberá aportar un profundo conocimiento de la industria, experiencia en venta consultiva de servicios de investigación clínica y una sólida red de contactos en compañías farmacéuticas multinacionales, biotecnológicas y otros actores clave del ecosistema. Responsabilidades principales • Diseñar e implementar la estrategia de desarrollo de negocio para Europa, identificando nuevas oportunidades comerciales y alianzas estratégicas., • Desarrollar y gestionar relaciones de alto nivel con decisores clave en compañías farmacéuticas globales (Big Pharma), biotecnológicas, empresas de salud y sponsors de investigación clínica., • Generar nuevas oportunidades de negocio y liderar todo el ciclo comercial, desde la identificación del lead hasta el cierre contractual., • Representar a la compañía en congresos, eventos sectoriales, asociaciones de la industria y reuniones con clientes estratégicos., • Colaborar con los equipos operativos, científicos y de propuesta para desarrollar soluciones competitivas y adaptadas a las necesidades de los clientes., • Elaborar previsiones comerciales, seguimiento de pipeline y reporting periódico a la Dirección General., • Identificar oportunidades de expansión en Latinoamérica, aprovechando conocimiento del mercado y relaciones existentes en la región., • Mantener un profundo conocimiento de las tendencias del mercado, regulaciones, movimientos de la competencia y necesidades emergentes de la industria farmacéutica y biotecnológica. Requisitos Imprescindibles • Titulación universitaria en Ciencias de la Salud, Farmacia, Biología, Biotecnología, Medicina, Química o áreas afines., • Experiencia mínima de 8-10 años en desarrollo de negocio dentro de una CRO, organización de investigación clínica o sector relacionado., • Historial demostrable de generación de negocio y cierre de contratos relevantes en servicios de investigación clínica., • Red consolidada de contactos y capacidad de interlocución directa con responsables de Clinical Operations, Clinical Development, Outsourcing, Procurement, Medical Affairs y otras áreas clave dentro de grandes compañías farmacéuticas y biotecnológicas., • Conocimiento profundo de ensayos clínicos, desarrollo de medicamentos, regulación y modelos operativos de CRO., • Experiencia gestionando procesos comerciales complejos y negociaciones con clientes multinacionales., • Nivel profesional de inglés (C1 o superior). Muy valorable • Experiencia comercial en mercados europeos clave (Alemania, Reino Unido, Francia, Italia, España, Países Bajos y países nórdicos)., • Conocimiento y experiencia previa desarrollando negocio en Latinoamérica., • Red activa de contactos en compañías farmacéuticas globales, biotechs, sponsors y organizaciones de investigación clínica., • Experiencia en CROs medianas o internacionales con enfoque de crecimiento., • Dominio de español y portugués. Qué ofrecemos • Posición estratégica con impacto directo en el crecimiento de la compañía., • Paquete retributivo competitivo compuesto por salario fijo y variable vinculado a objetivos., • Flexibilidad laboral y entorno internacional., • Oportunidad de liderar la expansión comercial en mercados clave de Europa y Latinoamérica., • Participación activa en la definición de la estrategia corporativa y comercial de la organización.

Desde la división de Química&Pharma nos encontramos en la búsqueda de un/a Técnico/a HSE para una empresa del sector industrial con sede en Madrid. ¿Qué harás? • Coordinación del sistema de gestión PRL, planificación preventiva, supervisión de permisos de trabajo, investigación de accidentes y análisis de causa raíz., • Experiencia realizando evaluaciones higiénicas industriales (agentes químicos, APIs, etc.) y capacidad de análisis de resultados para garantizar condiciones seguras de trabajo., • Trayectoria mínima de 4-5 años en industria,trabajando en entornos ATEX y con conocimiento de normativa APQ/RD 1215/97., • Participación activa en trabajos especiales, coordinación de servicios de prevención ajenos, seguimiento de medidas correctoras y soporte en planes de seguridad y salud. ¿Qué buscamos? • Ingeniería en Ciencias Químicas o similar, Máster en PRL con las 3 especialidades (Seguridad, Higiene y Ergonomía) y mínimo 4-5 años de experiencia en entornos industriales. ¿Qué ofrecemos? • Contrato indefinido con cliente final., • Salario competitivo, • Retribución flexible.

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