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GARDENER (DISABILITY CERTIFICATE REQUIRED)65161642086787120

GARDENER (DISABILITY CERTIFICATE REQUIRED)

Job Summary: We are seeking a Gardener to maintain landscaped areas, applying gardening techniques and operating specialized machinery. Key Points: 1. Gardening tasks and maintenance of green spaces 2. Use of appropriate machinery and tools 3. Performing delicate tasks such as application of phytosanitary products AFANIAS, the Association of Families, was founded in 1964 and works daily to become a leading organization in Intellectual Disability (ID), with social presence and influence, facilitating autonomy and quality of life for people with ID and their families, while addressing their life cycle needs. In this context, we are announcing the Gardener position at AFANIAS. MAIN RESPONSIBILITIES * Gardening tasks: watering and fertilizing plants, pruning trees and shrubs, fertilizing and mowing lawns, removing weeds from gardens, preserving green spaces, and keeping pathways free of debris, etc. * Maintaining landscaped areas in good condition. * Using appropriate machinery and tools for each task. * Organizing and cleaning tools, equipment, facilities, and machinery. * Operating machinery and self-propelled vehicles. * Performing more delicate tasks. For example: applying chemical/phytosanitary products REQUIRED PROFILE * Disability certificate of 33% or higher * Experience in gardening and use of gardening machinery. * Mobility and autonomy in performing tasks. * Positive attitude and willingness to work. * Work permit in Spain. * Driving license type B. Schedule: Mon-Fri, 7:30-15:00

Prta del Sol, 4, 2ºC, Centro, 28013 Madrid, Spain

TECHNICIAN/CONSTRUCTION SITE MANAGER FOR VENTILATION65161638439937121

TECHNICIAN/CONSTRUCTION SITE MANAGER FOR VENTILATION

Job Summary: We are looking for an Engineer/Construction Site Manager for stable, innovative and continuously growing projects, focused on project execution, budgeting and technical office work. Key Points: 1. Integration into a diverse, committed and high-performing team 2. Market-leading company in major electrical works and renewable energy 3. Opportunities for professional growth and development We are expanding our team of ENGINEERS/CONSTRUCTION SITE MANAGERS for a stable, innovative and continuously growing project; your mission will be project execution and budgeting, technical office work. We are a company specialized in major electrical works and renewable energy; we are pioneers in team management and offer a pleasant working environment. We invite you to join this distinctive, committed and high-performing team; thanks to the passion and development of this talent, we have continued growing and become leaders in our sector. **Requirements:** * Forced ventilation * PCI (Fire Prevention Code) * Air conditioning * Heating **Offered:** * Immediate incorporation * Employment contract * 40-hour workweek, Monday to Friday * Professional development: Middle management team members have been promoted internally. Integration into an excellent working environment, loyalty program and socially responsible company. **Benefits** Opportunities for professional growth and development * Initial and ongoing training program fully covered by the company (Prior experience valued). **Position Type** Full-time Salary: €1,200–1,600 per month Expected Hours: 40 hours per week Schedule: * Monday to Friday **Experience Required in:** \- Technical office \- Projects and budgeting \- Proficiency in AutoCAD and Microsoft Office suite is mandatory. We seek a candidate with at least 1 year of experience in a similar position. Work Location: On-site position (Rivas-Vaciamadrid) Position Type: Full-time Salary: Up to €34,000.00 per year Work Location: On-site position

C. Antonio Gaudí, 17, 28521 Rivas-Vaciamadrid, Madrid, Spain

€ 1,200-1,600/month

Compliance Assistant65161465063043122

Compliance Assistant

Summary: This role supports the compliance Partner Onboarding team by assisting with onboarding new partners and services, ensuring adherence to AML policies and regulatory requirements. Highlights: 1. Support compliance partner onboarding and network expansion 2. Conduct due diligence research and sanction screening 3. Contribute to creating new compliance policies and procedures **Description** Dandelion may be a new platform, but we’re not new to the industry. Backed by Euronet’s 35 years of experience in electronic payments, money transfers, and compliance, Dandelion is the largest, most diverse cross\-border payments platform, delivering real\-time payments across bank accounts, wallets, and cash. Today, our network spans more than 600,000 cash locations and over 4\.1 billion bank accounts and 3\.1 billion mobile wallets. We reach 170 countries around the world with over 90% of payments delivered in real\-time. **ABOUT THIS ROLE** **The main purpose of the role is to support the compliance Partner Onboarding team in the onboarding of new partners, services and expansions of the network as well as understanding the business to ensure compliance with our current AML Policies and procedures responsibilities and regulatory requirements.** **ROLES \& RESPONSIBILITIES** * Compliance due diligence and approval of New Partners globally * Review and approval of all expansion and service modifications related to Existing Partners, including: network expansions, business model expansions, or other modifications to the Partner Agreement. * Conduct due diligence research over available internal systems, the internet and other external data bases, including sanction screening and open\-source investigations. * When needed, assist with the on\-going due diligence process of existing Partners, including visits, KYC refresh and reporting. * Assist with the internal and external Audit management. * Contribute to creation of new policies and procedures, collaborating with supervisors and managers. **POSITION REQUIREMENTS** * Communication Skills * Strong research, analytical and reporting skills. * Excellent communications skills in English and Spanish, both oral and written. * Good planning and time management/prioritization skills. Ria Money Transfer offers a competitive salary and benefits package. **.** Actual compensation is based upon factors such as the candidate’s skills, qualifications, and experience. In addition, Ria Money Transfer offers a wide range of best in class, comprehensive and inclusive employee benefits for this role including healthcare, dental and vision benefits, Paid Vacation/ Sick Leave and more. Ria Money Transfer is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. Check out our website to learn more about the company at: http://www.riamoneytransfer.com/ The position responsibilities outlined above are intended to define the general contents and requirements to perform this job. It is not to be taken as a complete statement of responsibilities or requirements. This job description does not restrict the Company’s right to assign or reassign duties and responsibilities to this job as needed.

C. Sol, 1, 28950 Moraleja de Enmedio, Madrid, Spain

Demand and Supply Manager65161428062083123

Demand and Supply Manager

Summary: Join our Clinical Trials Division to design, implement, and interpret inventory management plans for global clinical trials, ensuring efficient supply chain operations. Highlights: 1. Discover meaningful work making a positive global impact. 2. Contribute to making the world healthier, cleaner, and safer. 3. Develop solutions for challenging global issues. **Work Schedule** Standard (Mon\-Fri)**Environmental Conditions** Office**Job Description** As part of the Thermo Fisher Scientific team, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner, and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world’s toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer. Question \- Could you be the right addition to our organization? **Location/Division Specific Information** **We are the Clinical Trials Division (CTD): We Supply the Hope that Changes Lives \- Global (remote)** CTD partners with pharmaceutical and biotech customers around the world to ensure the right patients get the right therapies in the right doses at the right time \- a concept that we internally adopt as "There is a Patient Waiting." Our unique blend of services includes project management, packaging, distribution, transportation management and specialty logistics, ancillary supply management, clinical supply optimization, bio\-repository storage and much more. Our more than 4000 employees in over 15 countries work hard every day knowing that what they do matters. **A Day in the Life:** * Design, Implement, Interpret and Review inventory management plan to forecast supply plan of study drugs to global clinical trials, using sound supply chain techniques. * Provide input into User Requirement Specifications of Interactive Response Technology (IRT) medication management module and complete User Acceptance Testing if required. * Review IRT strategy to ensure it supports the strategic supply plans and that IRT settings are adjusted to optimize the supply and demand. * Ensures plans are robust and optimizes global and regional supply strategies to ensure continuity of subject supply in the most effective and efficient manner. * Develop and provide clients with reports on actual project spend versus budget. * Establishes connections between demand planning team and S\&OP ensuring the latest forecast information is aggregated and integrated into the divisional S\&OP process. * Partners with the Enterprise Project Manager, along with global and site project management teams and/or directly with the customer to proactively share key client data to facilitate an effective supply chain planning cycle. * Ensure temperature excursion process is performed as required. * Establish and maintain financial forecasts and monthly billing processes for assigned client projects. * Assist in training and on boarding of new employees (buddy concept) * Stay on top of relevant cGMPs, GCPs, and other regulatory requirements and ensure study management activities are aligned. * Demonstrate and promote company vision. * Conduct activities in a safe and efficient manner. **As Demonstrated By:** **Project Management** * Structures demand plans in line with client strategy —starting from an identified need, sets objectives and specific goals. * Speaks and writes in a clear, concise, and organized way. Listens carefully to others to ensure understanding and effective communication. **Technical Knowledge** * Independently digests data that is applicable to project results and collaborators. * Handles the demand planning part of projects efficiently in different systems and maintains their own as well as the team’s accountability for using Thermo Fisher tools to help the team be successful. * Demonstrates technical proficiency and uses innovations to advance the efficiency and effectiveness of work processes, procedures, and outputs. * Knowledge of general inventory and billing principles, good documentation practices, and report generation. **Project Management Leadership** * Works with colleagues to quickly resolve or raise solutions to problems. Develops a sense of urgency among cross\-functional teams to influence project timelines. * Communicates at the proper time, understands boundaries, respects differences, and confronts tension. Ensures that all communications are clear, focused, and based on a solid understanding of needs, using the most appropriate medium. * To champion a sense of belonging and connection, remote employees are expected to keep their camera on and participate in video calls both internally and externally, as appropriate. **Keys to Success:** **Education** * Bachelor's degree in supply chain, business/operations management preferred. * High school diploma or equivalent required. **Experience** * 4 to 5 years of supply chain and/or planning experience leading global supply chain design and logistics management, preferably as they relate to clinical program design and execution. * Understanding of clinical supply requirements, phases of clinical development, and the factors that influence study designs preferred. **Knowledge, Skills, Abilities** * Requires strong eye for business including the ability to understand the manufacturing process and how cost impacts the overall business. * Requires enhanced PC knowledge and skills using Microsoft Office (Word, Excel, Access, PowerPoint) products. * Requires interpersonal social skills and the ability to lead and work in teams including client services, technical, planning, and financial expertise. * Requires excellent analytical and interpersonal skills. * APICS certification or equivalent preferred.

C. de Garganta de los Montes, 2-6, Arganzuela, 28045 Madrid, Spain

Data Engineer Consultant65156831131905124

Data Engineer Consultant

Job Summary: We are looking for a Data Engineer with at least 2 years of experience in data-oriented backend projects to design and develop end-to-end data pipelines. Key Highlights: 1. Design and development of end-to-end data pipelines 2. Implementation of data ingestion and transformation processes 3. Collaboration with BI, analytics, and business teams Shall we continue walking together? What Are We Looking For? We are seeking a Data Engineer with at least 2 years of experience in data-oriented backend projects who has participated in the design and development of end\-to\-end data pipelines, covering the various layers of ingestion, transformation, and storage. What Will Your Responsibilities Be? Design, develop, and maintain end\-to\-end data pipelines, from ingestion through to the consumption layer. Implement data ingestion processes from multiple sources (APIs, databases, files, external systems). Develop data transformation and enrichment processes ensuring quality, traceability, and efficiency. Design and optimize data models oriented toward analytics and reporting. **Work with Azure services such as:** Azure Data Factory for pipeline orchestration. Azure Data Lake Storage for data storage. Azure Synapse, Databricks, and/or Microsoft Fabric for processing and transformation. Implement best practices for versioning, error handling, logging, and pipeline monitoring. Collaborate with BI, analytics, and business teams to understand requirements and translate them into technical solutions. Participate in data architecture decisions and continuous improvement of existing solutions. Document developments and data flows clearly and maintainably. **Requirements:** At least 2 years of experience in Data Engineering or data-oriented backend projects. Experience with Azure or AWS. Proficiency in Python and SQL programming. Knowledge of data modeling and architectures such as Data Lake / Data Warehouse / Lakehouse. Intermediate level of English. What Do We Offer You? You will benefit from a hybrid-flexible work model. You may opt for a flexible compensation system, medical service, health insurance, life insurance, and accident insurance. You will have access to a professional development training plan throughout your career. You will grow within a feedback-driven culture that fosters your continuous learning. If interested, you may participate in national and international social action and volunteering programs. You will enjoy a cultural and sports offering. Now the decision is yours! If you believe this position is right for you, click ‘Apply’ and complete your profile so we can assess your application. If your profile fits, our recruitment team will contact you to get to know you. From there, we will guide you through our selection process and your Deloitte journey will begin. What impact will you make? Deloitte is a professional services firm firmly committed to equal opportunity. In this regard, the Firm accepts and processes applications from all sectors of society without discrimination on grounds of sex, gender expression, race, religion or beliefs, ethnic or national origin, disability, illness or health condition, genetic predisposition to disease, age, citizenship, marital status, sexual orientation or gender identity, socioeconomic status, or any other personal or social condition or circumstance. **Location:** Madrid **Position Type:** Experienced Professionals **Service Line:** TAX \& LEGAL **Req Id:** 46000

Prta del Sol, 4, 2ºC, Centro, 28013 Madrid, Spain

Senior Assurance Public Sector with French65156830152066125

Senior Assurance Public Sector with French

Job Summary: Participate in the transformation of national and international organizations by supporting the management and verification of projects funded by public funds and collaborating with public entities on financial reporting and audits. Key Highlights: 1. High-impact projects and continuous learning 2. Positive work environment with cultural and sports activities 3. Feedback-oriented culture and professional development Can you imagine yourself contributing to the transformation of leading national and international organizations? At Deloitte, we are committed to generating impact for society, our clients, and you. What types of projects do we undertake in the Public Sector? We primarily work with public sector entities, supporting them in managing and verifying projects funded by national public resources as well as funds from the European Union. We collaborate with public entities to obtain such public funding, reviewing and drafting their financial reports. Additionally, we support internal audits and assist with documentation, technical reports, and economic reports. What responsibilities would you assume? Management of multidisciplinary and international teams to carry out audit and related assignments. Client interaction to deliver financial services such as auditing, financial advisory, and non-financial information advisory. Proactively support client management by keeping managers and senior staff informed and establishing effective working relationships. Understanding, analysis, and review of business processes, financial statements, and associated controls. Advisory services related to financial transformation. Development and application of various regulations (primarily the Spanish General Accounting Plan [PGC] and IFRS). What are we looking for? Individuals with a strong desire to learn, teamwork capability, organizational skills, an innovative mindset, clear results orientation, proactivity, and critical thinking. Graduates in Economics, Business Administration and Management (ADE), Finance and Accounting, or other degrees with a focus on finance. A Master’s degree in Accounting and Auditing is considered a plus. Two to four years’ experience in the responsibilities outlined above. Prior team management experience is highly valued. Proficiency in English (minimum B2 level) is required; knowledge of additional languages is advantageous. Proficiency in Microsoft Office (Word, Excel, PowerPoint). Willingness to travel and possession of a valid driver’s license. What is it like to work at Deloitte? High-impact projects offering long-term career progression and continuous learning **️ Hybrid-flexible daily routine:** flexible working hours and a balanced mix of remote work and in-person collaboration—either at our offices or at client sites **Positive atmosphere both inside and outside the office:** enjoy multiple team-building events per year, cultural and sports activities… and much more! **‍ ️ Holistic wellbeing:** take care of your physical, mental, and financial health through our comprehensive wellness program… including on-site medical staff at our offices! **Social impact:** participate in numerous national and international volunteering initiatives and pro-bono projects, dedicating your time and talent to those who need it most **️ Feedback culture and continuous learning:** grow within an inclusive environment where equal opportunity and your personalized learning plan will drive your development. Can you already picture yourself at the Deloitte University in Paris? **Exclusive benefits as a Deloitte professional:** access a wide range of benefits and a comprehensive flexible compensation plan **If this resonates with you, here’s what to do next:** Apply to this role by clicking ‘Submit Application Now’ and completing your profile If your profile matches our requirements, our Talent team will contact you to learn more about you Start the process! We’ll guide you through each step until your onboarding. Deloitte is a professional services firm firmly committed to equal opportunity. In this regard, the Firm accepts and processes applications from all sectors of society, without discrimination based on gender, gender expression, race, religion or beliefs, ethnic or national origin, disability, illness or health condition, genetic predisposition to disease, age, citizenship, marital status, sexual orientation or gender identity, socioeconomic status, or any other personal or social condition or circumstance. **Location:** Madrid **Position Type:** Experienced Professionals **Service Line:** AUDIT & ASSURANCE **Req Id:** 46018

Prta del Sol, 4, 2ºC, Centro, 28013 Madrid, Spain

Expert Product Auditor | Industrial Products and Construction Materials Sector | Autonomy65156667263490126

Expert Product Auditor | Industrial Products and Construction Materials Sector | Autonomy

Position Summary: Evaluates and audits industrial and construction products to ensure safe and compliant solutions meeting high standards, with autonomy and expert support. Key Highlights: 1. Autonomy to organize visits and audits with full freedom. 2. Flexibility and work-life balance tailored to you. 3. Continuous learning, applying technical criteria in real-world settings. Would you like to evaluate key products in industrial and construction environments, directly contributing to ensuring the market has safe, efficient, and strictly compliant solutions? At AENOR, you’ll have the opportunity to audit products impacting major construction and industrial projects. You’ll operate with autonomy, backed by expert support and within an environment where technical knowledge is valued and shared. If you’re seeking a role with growth potential, direct impact, and a network of professionals who add value… AENOR is your place. ### **What will your experience be like as a Product Certification Auditor at AENOR?** **Genuine camaraderie from day one** You won’t be alone here. The team is always ready to help—even if they don’t yet know you. A strong, cross-functional, and authentic support network forms naturally. **Autonomy to manage your own pace** You’ll manage your visits and audits with full freedom. Your professional judgment is trusted to decide how, when, and where to plan your work. **Flexibility and work-life balance tailored to you** After a week of travel, you can work remotely. You’ll be able to adjust your schedule to balance your personal life, family, or downtime. **Continuous learning with direct impact** From day one, you’ll apply technical criteria in real-world settings. Each evaluation is an opportunity to grow further as a sector reference. **Top-tier clients exposing you to the sector’s most advanced developments** You’ll collaborate with industry-leading construction and industrial companies, applying standards that set benchmarks for quality, safety, and sustainability. **Purpose and continuous improvement** Your work ensures products and services meet rigorous technical standards, delivering safety, trust, and continuous market improvement. ️ **A trusted brand that positions you strongly** Carrying the AENOR name opens doors. Clients value your expertise from the very first minute, and you establish yourself as a sector reference. **Benefits that make the difference** Intensive working hours for three months in summer, company car (including personal use), childcare allowances, per diems, language courses, laptop, discounts, covered travel, and flexible compensation, among others. ### **What will make you successful in this position** **University degree or higher vocational training (FP Superior) in engineering or chemistry** This enables you to apply objective, technically grounded, and professional product evaluation criteria. ️ **Minimum 2 years’ experience in quality management and industrial product evaluation** Essential to conduct audits competently and with technical credibility from the outset. ️ **Knowledge of construction and industrial products** Helps you understand the technical evaluation contexts and engage confidently with process owners. ️ **High level of spoken, written, and reading English** Required to handle technical documentation and communicate with international clients or internal teams. **High level of French (highly valued)** Facilitates communication with French-speaking companies and international sector projects. ### **Your mission as a Product Certification Auditor at AENOR** As an auditor, you’ll ensure that products used in construction and industry meet the highest standards of safety, quality, and reliability. You’ll carry out technical audits, verifications, and conformity assessments, helping manufacturers, distributors, and sector stakeholders deliver safe and reliable products to the market. Your work improves processes and protects people. Your signature builds trust. **Will you join our mission?** If you’re motivated to work with freedom, technical judgment, and purpose in the construction sector… this is your opportunity. Apply now and become part of the leading team in product certification.

Calle de Génova, 6, 4ª Planta, Centro, 28004 Madrid, Spain

Expert Product Auditor | Plastics Sector | Autonomy65156667018881127

Expert Product Auditor | Plastics Sector | Autonomy

Job Summary: This role offers the opportunity to assess key plastic products in construction, contributing to safe and compliant solutions that meet stringent standards within a supportive and professionally developing environment. Key Highlights: 1. Autonomy to organize visits and audits 2. Continuous learning and long-term development 3. Genuine camaraderie and a strong support network Would you like to assess key plastic materials used in construction and on-site installations—directly contributing to ensuring the market has safe, efficient, and rigorously standard-compliant solutions? At AENOR, you’ll have the opportunity to audit plastic products impacting major construction projects. You’ll operate with autonomy, backed by expert guidance and in an environment where technical knowledge is valued and shared. If you’re seeking a role with growth potential, direct impact, and a network of professionals who add real value… AENOR is the place for you. ### **What will your experience be like as a Product Certification Auditor at AENOR?** **Genuine camaraderie from day one** You won’t be alone here. The team is always ready to help—even if they don’t yet know you. A strong, cross-functional, and authentic support network is fostered. **Autonomy to manage your own pace** You’ll fully manage your visits and audits. Your professional judgment is trusted to decide how, when, and where to plan your work. **Flexibility and work-life balance tailored to you** After a week of travel, you can work remotely. You’ll be able to adjust your schedule to balance your personal life, family, or downtime. **Continuous learning with direct impact** From day one, you’ll apply technical criteria in real-world settings. Each evaluation is an opportunity to grow further as a sector reference. **Top-tier clients exposing you to the sector’s most advanced developments** You’ll collaborate with leading construction and building companies, applying standards that set benchmarks for quality, safety, and sustainability. **Real training and long-term development** If you already have experience, you’ll continue growing here—becoming IRCA-certified (if not already), and taking on new technical challenges. **Purpose and continuous improvement** Your work ensures products and services meet rigorous technical standards, bringing safety, trust, and continuous improvement to the market. ️ **A trusted brand that positions you** Carrying the AENOR name opens doors. Clients value your expertise from the very first minute—and you position yourself as a sector reference. **Benefits that make a difference** Intensive summer schedule (3 months), company car (also for private use), childcare allowances, per diems, language courses, laptop, discounts, covered travel, and flexible compensation, among others. ### **What will make you successful in this position** **University-level technical education in engineering or chemistry** This enables you to apply objective, technically grounded, and professional product evaluation criteria. ️ **Minimum 2 years’ experience in quality management and conformity assessment** Essential to conduct audits with technical competence and credibility from day one. ️ **Knowledge of plastic products, manufacturing processes, traceability, and recyclability.** This helps you understand technical assessment contexts and confidently engage with process owners. ️ **High level of spoken, written, and reading English** Required to handle technical documentation and communicate with international clients or internal teams. **Official IRCA auditor certification (highly valued)** Provides additional recognition and the ability to conduct audits with a global, rigorous perspective. ### **Your mission as a Product Certification Auditor at AENOR** As an auditor, you’ll ensure plastic products used in construction, building, and installations meet the highest standards of safety, quality, and reliability. You’ll perform technical audits, verifications, and conformity assessments—helping manufacturers, distributors, and sector stakeholders deliver safe and reliable products to the market. Your work improves processes and protects people. Your signature builds trust. **Will you join our mission?** If working with freedom, technical judgment, and purpose in the plastics sector motivates you… this is your opportunity. Apply now and become part of the leading product certification team.

Calle de Génova, 6, 4ª Planta, Centro, 28004 Madrid, Spain

Talent Sourcer (f/m/x)65156658960513128

Talent Sourcer (f/m/x)

Summary: Join AUTO1 Group's Country Operations Team as a Talent Sourcer to build strong talent pipelines through research and active sourcing for current and future staffing needs. Highlights: 1. Be part of an international Talent Sourcing Team on recruitment projects 2. Develop creative ideas for direct approach of specialists and executives 3. Grow and learn about sourcing tools and techniques to find great talents **Company Description** ----------------------- Join our Country Operations Team at AUTO1 Group as a Talent Sourcer. Your main responsibility will be to source talent and build a strong pipeline for current and future staffing needs. If you're interested in research and excited about recruiting, we want to meet you. AUTO1 Group is Europe’s leading digital automotive platform. We revolutionize the used car market with our well\-known brands **Autohero** , **wirkaufendeinauto.de** and **AUTO1\.com** . **Your new Role** ----------------- * Be part of our international Talent Sourcing Team and work on recruitment projects to find the best talents for the AUTO1 Group. * Develop creative ideas for the direct approach of specialists and executives \& become an expert for active sourcing. * Beyond the classic direct approach, you will regularly try out new tools and methods to identify interested candidates. * Be in charge of research projects and find innovative ways to attract and find candidates. * Ensure a strong talent pipeline for current and future staffing needs by building long\-lasting relationships with internal and external partners. **Your Skills** --------------- * A university degree in HR or in other related fields. * Experience in Talent Acquisition, sourcing or research. * Excellent communication skills in English. * Solutions and results oriented approach. * Fast\-adapting personality with a desire to grow and learn about sourcing tools and techniques to find great talents. **Our Offer** ------------- * Truly international (over 100 nationalities) and diverse working environment, transparency, clear communication and supportive, open\-minded team where you can be exactly who you are. * Our dynamic startup environment offers new challenges for personal growth with the contribution of own ideas. * Work remotely \- anywhere from Spain! * You get the chance to develop yourself personally and will be supported in achieving your goals through frequent feedback talks. * Flexible working hours. You will be able to adjust your daily journey around our core\-hours, making your start and end of the day compatible with your personal life. Join us, building the best way to buy and sell cars! You do not meet 100% of the requirements? Take your shot and apply anyway! We offer room for growth and challenges to learn from. Contact Anita Mare *At AUTO1 Group we live an open culture, believe in direct communication, and value diversity. We welcome every applicant; regardless of gender, ethnic origin, religion, age, sexual identity, disability, or any other non\-merit factor.* \#LI\-A1

Prta del Sol, 4, 2ºC, Centro, 28013 Madrid, Spain

Senior CRA65156658720898129

Summary: This Senior Clinical Research Associate role involves overseeing and managing clinical trial activities to ensure protocol adherence, regulatory compliance, and data integrity. Highlights: 1. Oversee and manage clinical trial activities 2. Ensure data integrity, participant safety, and compliance 3. Monitor clinical trial sites and provide support Senior Clinical Research Associate Oncology Home based Spain ICON plc is a world\-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development We are currently seeking a Senior Clinical Research Associate (CRA) to join our diverse and dynamic team. As a Senior CRA at ICON Plc, you will play a critical role in overseeing and managing clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards. You will contribute to the success of clinical trials by ensuring data integrity, participant safety, and compliance throughout the study lifecycle. What You Will Be Doing:* Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards. * Conducting site visits to assess site performance, resolve issues, and provide support to ensure successful trial execution. * Collaborating with cross\-functional teams to ensure timely and accurate data collection and reporting. * Providing training and guidance to site staff and other CRAs to maintain high standards of clinical trial conduct. * Building and maintaining effective relationships with site personnel and stakeholders to facilitate smooth trial operations. Your Profile:* Advanced degree in a relevant field such as life sciences, nursing, or medicine. * Extensive experience as a Clinical Research Associate, with a strong understanding of clinical trial processes and regulatory requirements. * Proven ability to manage multiple sites and projects simultaneously, with strong organizational and problem\-solving skills. * Expertise in monitoring practices, data integrity, and site management, with proficiency in relevant clinical trial software and tools. * Excellent communication, interpersonal, and stakeholder management skills, with the ability to influence and drive compliance within a complex environment. * Ability to travel at least 60% of the time (international and domestic \- fly and drive) and should possess a valid driver’s license What ICON can offer you: Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent. In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well\-being and work life balance opportunities for you and your family. Our benefits examples include:* Various annual leave entitlements * A range of health insurance offerings to suit you and your family’s needs. * Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead. * Global Employee Assistance Programme, TELUS Health, offering 24\-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family’s well\-being. * Life assurance * Flexible country\-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others. Visit our careers site to read more about the benefits ICON offers. At ICON, inclusion \& belonging are fundamental to our culture and values. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.

Prta del Sol, 4, 2ºC, Centro, 28013 Madrid, Spain

Biology Teacher651566559965461210

Biology Teacher

Job Summary: Colegio Montesclaros is seeking a Biology Teacher for a maternity leave replacement, focused on students’ intellectual and personal development. Key Points: 1. Maternity leave replacement opportunity. 2. Join a school that values students’ holistic development. 3. Emphasis on quality processes and personalized attention. **Company Information** ----------------------- * **Company Name:** Colegio Montesclaros * **Website:** https://www.colegiomontesclaros.es/ * **Description:** Colegio Montesclaros is a coeducational, private subsidized school founded in the 2009\-2010 academic year by Grupo Educare, with the primary objective of helping students develop intellectual capabilities as well as human and spiritual values through quality processes and personalized attention. **Job Posting Information** ------------------------ * **Job Title:** Biology Teacher * **Posting Period:** 13\-01\-2026 to 28\-01\-2026 * **Province:** Madrid * **Town:** Boalo, El * **Description:** Maternity leave replacement **Requirements** -------------- * **Requirements:** TEACHING MASTER'S DEGREE C1 * **Teaching Master's Degree or CAP (Certificado de Aptitud Pedagógica)** **Contract Information** --------------------------------- * **Working Hours:** Full-time * **Contract Type:** Maternity leave replacement * **Salary:** CAM Collective Agreement ##### **Share this job posting**

P32P+C5 Cerceda, Spain

Laboratory Technician651566592098591211

Laboratory Technician

Job Summary: We are seeking a Laboratory Technician to perform quality testing and analysis at the plant, ensuring the accuracy and reliability of results to meet high standards. Key Highlights: 1. Essential role in on-site quality testing and analysis 2. Responsible for rigorous control of laboratory documentation 3. Ensures compliance with high product quality standards We are looking for a Laboratory Technician in O Grove for a leading company in the canned food industry. Your role will be essential in conducting quality tests and analyses directly on-site, carefully recording all data obtained. You will be responsible for maintaining rigorous control over laboratory-generated documentation, ensuring analytical results are accurate and reliable. Your work will guarantee that the final product meets the highest quality standards required by our customers. A background in laboratory work and quality control is valued, as well as at least one year of prior experience in similar roles, preferably within the food industry. Shifts are rotating, Monday through Friday, covering mornings (07:00\-15:00h) and afternoons (15:00\-23:00h). * Education related to laboratory work and quality control. * At least one year of prior experience in the position, preferably in the food sector.

Rúa da Praza, 19, 36980 O Grove, Pontevedra, Spain

Laboratory Equipment Sales Representative651566565006101212

Laboratory Equipment Sales Representative

Job Summary: We are seeking a professional to manage, strengthen, and prospect a client portfolio in laboratories and research centers, providing technical and commercial advisory services. Key Responsibilities: 1. Management and enhancement of the existing client portfolio 2. Prospecting and identification of new business opportunities 3. Specialized technical and commercial advisory services We are seeking a professional to manage and enhance the existing client portfolio, covering both laboratories and research centers, whether public or private. The main responsibility will be prospecting and identifying new business opportunities in the market, analyzing competitors to optimize commercial strategies. This role involves presenting innovative laboratory equipment and solutions, providing specialized technical and commercial advisory services. Additionally, it is essential to prepare, negotiate, and follow up on commercial proposals, maintaining close collaboration with technical and after-sales teams to ensure customer satisfaction and achievement of established sales targets. A higher technical education in fields such as chemistry, biology, health sciences, or pharmacy is required, along with a valid driver’s license and availability for travel. Strong organizational skills, autonomy, and excellent communication abilities are important. Intermediate-level technical English proficiency is desirable.

98MM+88 Pola de Siero, Municipality of Siero, Spain

Field Quality Surveyor in Madrid651377081419531213

Field Quality Surveyor in Madrid

On-site Surveyor in the Central Area of Madrid. This is an extra assignment three times per month, always during morning hours. A work contract is offered. Knowledge of languages will be valued. Type of position: Permanent contract Work location: On-site employment

C. de la Abada, 6, Centro, 28013 Madrid, Spain

ELECTRICAL ENGINEER651377079518751214

ELECTRICAL ENGINEER

At ADYD Group, we continue to grow and invest in top talent within the field of engineering. We are opportunity and talent—a company specializing in engineering services, offering design, project engineering, outsourcing, and training. We are seeking an Electrical Engineer to work in Alcobendas for a company providing packaging services to the pharmaceutical sector. The main responsibilities will include panel layout, single-line diagram drafting, cable sizing calculations, bill of materials preparation, and technical specifications for low-voltage (LV) and medium-voltage (MV) projects. **Requirements:** * Education: Degree in Electrical Engineering or related field. * Proven experience in the responsibilities described above. * Proficiency with tools such as NEPLAN, ETAP, and DigSILENT. * Technical English. **Conditions:** * Work for a rapidly growing company with multidisciplinary and highly qualified teams. * Opportunities for professional development and continuous improvement—we are expanding across all departments. * Committed to our employees’ well-being. * Close-knit team, positive working environment, and strong camaraderie. Join our team! …

C. de Luis Carlos Vázquez, 14, Cdad. Lineal, 28043 Madrid, Spain

Mathematics, Physics, and Chemistry Teacher for 1st Year of Bachillerato near Hospital Infanta Sofía Metro Station651374595417611215

Mathematics, Physics, and Chemistry Teacher for 1st Year of Bachillerato near Hospital Infanta Sofía Metro Station

We are looking for a teacher to provide Mathematics, Physics, and Chemistry tutoring at the student’s home for a 1st-year Bachillerato student. The student lives near Hospital Infanta Sofía Metro Station. Fee: 19.50 euros (13 euros/hour) Job type: Permanent contract Salary: €12.00–€13.00 per hour Scheduled hours: 1.5 hours per week Work location: On-site employment

P.º Gregorio Marañón, 7, 28702 San Sebastián de los Reyes, Madrid, Spain

Food Safety and Quality Technician651374590572821216

Food Safety and Quality Technician

We are looking for an experienced food safety technician for a prestigious company in Madrid, Las Tablas area, in the collective catering sector. Your responsibilities will include maintaining the center's HACCP plan, attending internal and external audits, planning and monitoring corrective actions, training staff... A university degree in health sciences or food technology and a master's degree in food safety are required. We offer flexible working hours, meal allowances, and a pleasant work environment. Salary to be agreed upon. This position runs from February to October to cover a maternity leave. Interested candidates should contact us to schedule an interview. Job type: Full-time Benefits: * Meals at the company * Flexible working hours * Company laptop * Company phone Work location: On-site employment

C. del Arroyo de Valdebebas, 17, Hortaleza, 28050 Madrid, Spain

CRA II651373319289631217

Clinical Research Associate Home based Spain ICON plc is a world\-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development We are currently seeking a Clinical Research Associate II to join our diverse and dynamic team. As a Clinical Research Associate II at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies. What you will be doing* Conducting site qualification, initiation, monitoring, and close\-out visits for clinical trials. * Ensuring protocol compliance, data integrity, and patient safety throughout the trial process. * Collaborating with investigators and site staff to facilitate smooth study conduct. * Performing data review and resolution of queries to maintain high\-quality clinical data. * Contributing to the preparation and review of study documentation, including protocols and clinical study reports Your profile* Bachelor's degree in a scientific or healthcare\-related field. * Minimum of 2 years of experience as a Clinical Research Associate. * In\-depth knowledge of clinical trial processes, regulations, and ICH\-GCP guidelines. * Strong organizational and communication skills, with attention to detail. * Ability to work independently and collaboratively in a fast\-paced environment. * Ability to travel at least 60% of the time (international and domestic \- fly and drive) and should possess a valid driver’s license What ICON can offer you: Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent. In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well\-being and work life balance opportunities for you and your family. Our benefits examples include:* Various annual leave entitlements * A range of health insurance offerings to suit you and your family’s needs. * Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead. * Global Employee Assistance Programme, TELUS Health, offering 24\-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family’s well\-being. * Life assurance * Flexible country\-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others. Visit our careers site to read more about the benefits ICON offers. At ICON, inclusion \& belonging are fundamental to our culture and values. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.

Prta del Sol, 4, 2ºC, Centro, 28013 Madrid, Spain

Clinical Research Associate651373319118101218

Clinical Research Associate

Clinical Research Associate ICON plc is a world\-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development We are currently seeking a Clinical Research Associate II to join our diverse and dynamic team. As a Clinical Research Associate II at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies. What you will be doing* Conducting site qualification, initiation, monitoring, and close\-out visits for clinical trials. * Ensuring protocol compliance, data integrity, and patient safety throughout the trial process. * Collaborating with investigators and site staff to facilitate smooth study conduct. * Performing data review and resolution of queries to maintain high\-quality clinical data. * Contributing to the preparation and review of study documentation, including protocols and clinical study reports Your profile* Bachelor's degree in a scientific or healthcare\-related field. * Minimum of 2 years of experience as a Clinical Research Associate. * In\-depth knowledge of clinical trial processes, regulations, and ICH\-GCP guidelines. * Strong organizational and communication skills, with attention to detail. * Ability to work independently and collaboratively in a fast\-paced environment. * Ability to travel at least 60% of the time (international and domestic \- fly and drive) and should possess a valid driver’s license What ICON can offer you: Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent. In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well\-being and work life balance opportunities for you and your family. Our benefits examples include:* Various annual leave entitlements * A range of health insurance offerings to suit you and your family’s needs. * Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead. * Global Employee Assistance Programme, TELUS Health, offering 24\-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family’s well\-being. * Life assurance * Flexible country\-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others. Visit our careers site to read more about the benefits ICON offers. At ICON, inclusion \& belonging are fundamental to our culture and values. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.

Prta del Sol, 4, 2ºC, Centro, 28013 Madrid, Spain

Medical Monitor (Gastroenterology)651373318789141219

Medical Monitor (Gastroenterology)

**Company Description** PSI is a leading Contract Research Organization with 30 years experience in the industry, offering a perfect balance between stability and innovation to both clients and employees. We focus on delivering quality and on\-time services across a variety of therapeutic indications. **Job Description** PSI **Medical Monitors** provide medical input to global clinical studies and advise the teams and business partners, while always focusing on patients' safety and well\-being. **Responsibilities:** * Serve as medical point of contact for internal project team, study sites and study sponsor for medical matters related to the conduct of clinical trials per protocol and per GCP guidelines * Advise clients, project teams, sites, regulatory agencies and third\-party vendors on medical matters * Collaborate with internal departments in the preparation of clinical development plans, protocols, investigator brochures, annual reports, clinical study reports, patient narratives, and scientific presentations * Review and analysis of clinical data to ensure the safety of study participants in clinical trials * Ensure that the reported trial data is accurate, complete, and verifiable, and that the conduct of the trial is in compliance with the currently approved protocol/amendments * Address safety issues across the trial from sites and the study team * Provide support for medical data review * Participate in bid defense meetings and proposal activities * Assist in Pharmacovigilance activities * Identify trial risks, and create and implement mitigation strategies with other relevant departments * Organize and lead clinical development advisory boards and safety monitoring boards * Ensure Study team compliance with FDA, EMEA, ICH and GCP guidelines **Qualifications** * Medical Doctor degree * Gastroenterology Fellowship certification is a must * Prior experience as a practicing MD (minimum of 10 years) * Prior research and/or industry experience is a plus * Full working proficiency in English * Proficiency with MS Office applications * Communication, presentation and analytical skills * Able to work in teams, problem\-solving, and detail\-oriented **Additional Information** As part of PSI's Medical Monitoring team, you will join our international group of medical professionals, build a career on the frontline of medical science and use your knowledge and expertise to help bring new medications to patients.

Prta del Sol, 4, 2ºC, Centro, 28013 Madrid, Spain

Sustainability Intern651373317500181220

Sustainability Intern

**Join Ferrovial: Where Innovation Meets Opportunity** ====================================================== Are you ready to elevate your career with a global leader in infrastructure solving complex problems and generating a positive outcome on people’s lives? At **Ferrovial**, we are not just a company; we are a community of innovators and trailblazers. Listed on three major stock markets: Nasdaq (US), Euronext Amsterdam (Netherlands) and IBEX 35 (Spain), we are also member of the Dow Jones Sustainability Index and FTSE4Good. We operate in more than 15 countries and have a workforce of over 24,000 professionals worldwide. Ferrovial’s activity is carried out through our business units, including Highways, Airports, Construction, and Energy. Our **Corporate** organization oversees business activities, providing strategic planning, communication, legal, finance and human resources services to the business units. As a member of our corporate organization, you will have a broad view of our company, further supporting your career development. **Why Ferrovial?** * **Global presence, local impact**: Be part of a company that is shaping the future of infrastructure worldwide, with challenging roles and projects that make a real difference. * **Collaborative excellence**: Work alongside talented professionals in a collaborative environment where your ideas and contributions are valued. * **Inclusive Culture:** Thrive in an innovative and respectful workplace that values every voice, celebrates what makes us unique and turns differences into innovation. * **Career growth**: Benefit from global and cross\-business unit mobility, with development processes designed to ensure your professional growth. * **Compelling benefits and employee wellbeing**: Enjoy a comprehensive benefits package that rewards your hard work and dedication and take advantage of initiatives designed to support your physical and psychological health. * **Productivity tools**: Utilize cutting\-edge tools like Microsoft Copilot to enhance your productivity and efficiency. **Job Description:** ==================== **About the Role** The selected candidate will join **Ferrovial’s Sustainability team**, supporting the **development and implementation** of the company’s environmental strategy at a **global level**. This role contributes to advancing Ferrovial’s commitment to climate action, natural capital preservation, circular economy, and water resource management. The intern will collaborate in analyzing environmental performance, preparing sustainability reports, and supporting key initiatives aimed at reducing the company’s environmental footprint and enhancing its sustainability ratings. **Key Responsibilities** * Development and implementation of environmental projects related to climate change, natural capital, circular economy, and water. * Calculation of Carbon Footprint, Water Footprint, and biodiversity impact. * Preparation of Non\-Financial Information Statements (EINF) and sustainability reports. **Qualifications** * Environmental background: Environmental Sciences, Biology, or Engineering (Forestry, Agricultural, Industrial, etc.). * High level of English (C1\). * Knowledge in climate change (carbon footprint, climate risks, biodiversity, environmental impacts). * Advanced level in Office tools. * Ability to work in a team, influencing skills, results orientation, adaptability, and proactivity. * Support with environmental and sustainability ratings (Dow Jones Sustainability Index – Best in Class, CDP, etc.). * Analysis of environmental and sustainability legislation. **Seize the challenge. Move the world together!** Innovative, creative, respectful, and diverse are some of the ways we describe ourselves. We are motivated by challenges, and we collaborate across our business units to move the world together. Your journey to a fulfilling career starts here! Ferrovial is an equal opportunity employer. We treat all jobs applications equally, regardless of gender, color, race, ethnicity, religion, national origin, age, disability, pregnancy, sexual orientation, gender identity and expression, covered veteran status or protected genetic information (each, a “Protected Class”), or any other protected class in accordance with applicable laws. **\#WeAreFerrovial**

Av. de América, 27, local A, Chamartín, 28002 Madrid, Spain

Flight Test & Integration Engineer - COMMS / Datalink Systems651369669344011221

Flight Test & Integration Engineer - COMMS / Datalink Systems

Madrid Flight Test & Integration Engineer - COMMS / Datalink Systems Capgemini Engineering, a global leader in engineering services, brings together teams of engineers, scientists and architects to help the world’s most innovative companies unlock their potential and contribute to a better future. From autonomous vehicles to life-saving robots, our experts in digital technologies and software think outside the box, delivering unique R&D and engineering services across all industries. Join the team and advance your career at a company offering growth opportunities where you can make a difference—and no two days are ever the same! Are you passionate about the aerospace industry, tactical communication systems and working in test environments? At Capgemini Engineering, we are seeking a **Flight Test & Integration Engineer – COMMS / Datalink Systems** for a strategic aerospace sector project in Madrid. **What will you do in this role?** You will join the team responsible for **Flight Test Analysis**, laboratory testing and integration of communication systems (COMMS / Datalink). Your responsibilities will include: * Conducting **Lab Test Program Requirement Analysis**, including definition of test points, test conditions, database preparation and environment configuration. * Executing **integration tests** on **L2 and L1 rigs**. * Analyzing test data and participating in incident investigations **(snags/SARs)**. * Preparing **Lab Test Reports**, including the necessary technical analysis for their development. * Working with **Link 16/22 (TDMS)** protocols and test development, qualification and certification tools. * Collaborating with multidisciplinary teams in a highly technological environment focused on mission systems and datalinks. **What are we looking for?** * Degree in **Telecommunications**, **Electronics**, **Aeronautics**, **Industrial Engineering** or related field. * Knowledge of programming/scripting (highly desirable). * Experience or interest in communication system integration and testing. * Familiarity with laboratory environments, rigs and mission systems. * Prior experience with **TDMS / Link16 / Link22** is a plus. * **Technical English**. **Valued Skills** * System Testing * Integration Testing * Communication Systems * Navigation / Datalink * Flight Test Analysis * Programming & Scripting * Data Analysis * Laboratory Testing * L1/L2 Support Candidates holding a disability certificate will be positively considered within our inclusion and diversity policy. All applications are valued. We offer extensive training opportunities—both in-person and online—including certifications. Even if you don’t meet 100% of the desired qualifications, we’d love to meet you! Our commitment to inclusion and equal opportunity is reflected in our Equality Plan and Code of Ethics, which guarantee professional development for employees and equal opportunity in recruitment—within a discrimination-free environment based on ethnicity, nationality, social origin, age, sexual orientation, gender expression, religion or any other personal, physical or social circumstance. **What do we offer?** * A unique work environment highly rated by our professionals in periodic evaluations. * Wellbeing HUB: Includes policies and initiatives for physical health (Wellhub) and mental wellbeing. * 24 vacation days + 2 personal days + 24 and 31 December + option to purchase up to 7 additional vacation days per year. * FlexAbroad: possibility to work remotely from another country for up to 45 days. * Flexible Compensation Plan (medical insurance, transportation, training, meal card or food allowance, childcare…) * Continuous learning: access to Mylearning, Capgemini University, Digital Campuses and Professional Communities. You’ll also have access to platforms such as Coursera, Udemy, Pluralsight, Harvard Manager Mentor, Education First for languages (English, French, German…) and more! * Participation in Volunteering and Social Action initiatives through our Sustainability, Inclusion and Equality Groups. * Onboarding support through our Buddies program. * Life and Accident Insurance **Why choose us?** Capgemini is a global leader in transforming clients’ businesses by harnessing the full power of technology. Guided by our purpose—to create an inclusive and sustainable future through technology and the energy of those who build it—we are a responsible, diverse company and an international leader in IT and engineering services, with over 360,000 professionals across 50+ countries. With a strong 55-year heritage and deep industry expertise, clients trust Capgemini to address their full business needs—from strategy and design to operations—powered by the fast-evolving worlds of cloud, data, AI, connectivity, software, platforms and digital engineering. In 2022, the Group reported global revenues of €22 billion. Rewrite your future and **join the team!** #LI-CS21 Ref. code 393575-es_ES Posted on 18 Jan 2026 Experience level Experienced Professionals Contract type Permanent Location Madrid Business unit Engineering and R&D Services Brand Capgemini Engineering Professional communities Products & Systems Engineering

Prta del Sol, 4, 2ºC, Centro, 28013 Madrid, Spain

Ingeniero/a de apoyo al desarrollo de bancos automáticos de radiofrecuencia651064885515541222

Ingeniero/a de apoyo al desarrollo de bancos automáticos de radiofrecuencia

**Ubicación:**Madrid, MD, ES **Perfil profesional:** Ingeniería D\&S, Mobility y ATM **Experiencia requerida:** Más de 2 años de experiencia **Modalidad del puesto:** Híbrido 744643\-01/25

Prta del Sol, 4, 2ºC, Centro, 28013 Madrid, Spain

Head of Data - Senior Data Scientist651064880881931223

Head of Data - Senior Data Scientist

We are searching for a Data \& Analytics Leader with at least 8\+ years of experience driving AI and Data strategies in banking, fintech, and/or outsourcing sectors with proven ability to lead high\-performance teams, align data strategy with business goals, and deliver measurable impact through innovation and governance. Working alongside the CEO she/he will be responsible for Data governance and its accuracy as well as the elaboration of reports to improve the efficiency of the organization, including predictive models. Core Skills * Data Strategy \& Governance * Executive Stakeholder Management * Business Impact through AI \& BI * High\-Performance Team Leadership * Financial Services Expertise Education Mathematician / Statistics / Engineering with experience in Finance ***If you think you can fit...please apply!*** **Auxadi** is the leading firm for International Accounting, Reporting, Compliance, Payroll Solutions CoSec \& Transfer Pricing management powered by Technology and amazing People. We support our clients by becoming an international extension of their accounting departments. Our Single Point of Contact model and cloud\-based technology platform are clear differentiators of our value proposition. At Auxadi you’ll be part of a team of over 300 professionals in 22 jurisdictions, serving clients in more than 50 countries and being part of multi\-country projects. You will work side by side with colleagues from all over the world developing your professional life in a multicultural environment. Auxadi is an equal opportunity employer and is strongly committed to promoting equal opportunities in the workplace, providing the means to assist all employees in their professional and personal development, without tolerating any discrimination. **Auxadi’s spirit is global!**

Prta del Sol, 4, 2ºC, Centro, 28013 Madrid, Spain

IT Demand Management Manager. Remote651064861306891224

IT Demand Management Manager. Remote

**Description:** ---------------- At Grupo NS we are looking for **an IT Demand Management Manager** with a **solid technical profile in infrastructure** and strong **management capabilities, to lead and coordinate the IT services demand** of a banking sector entity. The selected candidate will be responsible for acting as the central point of demand, ensuring that proposals and offers align with service development and quality. **Main responsibilities:** * **Centralize and manage the IT demand** of a banking entity. * **Analyze and understand customer needs** regarding **infrastructure and IT services.** * **Prepare technical and economic proposals**, **ensuring their feasibility** and alignment with the service model. * **Defend** and present proposals to the entity. * **Track submitted proposals** and **coordinate** with the **involved teams.** * **Ensure the proper transition of approved proposals** into service development. **We offer:** * Joining a **stable, high-impact project.** * Participation in managing a relevant entity within the banking sector. * A collaborative and dynamic professional environment. **If you are motivated to join a strategic project where your technical vision and management skills make the difference, this is your opportunity. We want to meet you and have you on board!** **Requirements:** --------------- **Requirements:** * **Solid technical knowledge** of IT infrastructure. * **Previous experience in demand management**, service management or similar roles. * **Ability to combine technical vision** **with** **management skills.** * Experience in **preparing and defending proposals.** * Strong **communication skills** and **customer orientation.** * Organizational, analytical and follow-up capabilities.

Prta del Sol, 4, 2ºC, Centro, 28013 Madrid, Spain

Paint Preparation Technician651062213306901225

Paint Preparation Technician

From Talleres Gámez Sánchez, the official Ford service center, we are seeking a methodical, detail-oriented paint preparation technician with good coordination skills for their duties, always prioritizing safety and health when working with chemical products, as well as possessing manual dexterity for repetitive tasks—all to assist the lead painter and ensure a perfect finish. Responsibilities: \-Disassembly and reassembly of parts (bumpers, handles, etc.). \-Hand or machine sanding and smoothing. Application of filler to repair imperfections. \-Priming (application of primer) to ensure paint adhesion. \-Masking and protecting areas not to be painted using specialized tapes and papers. \-Preparing and mixing paint to precisely match the existing color. \-Assisting in paint application on repaired areas or specific parts. \-Initial polishing and inspection for possible defects. \-Stock control of materials (fillers, tapes, solvents) and placing orders. \-Maintaining cleanliness, order, and maintenance of the work area, paint booth, and tools. \-Monitoring temperature and humidity records, and paint equipment parameters. Job Type: Full-time, Permanent contract Work Location: On-site employment

C/ de la Constitución, 1, 28943 Fuenlabrada, Madrid, Spain

Associate Director, Patient Recruitment Strategy651060735132171226

Associate Director, Patient Recruitment Strategy

Madrid, Spain \| Full time \| Home\-based \| R1523996 **Be the strategic force behind patient‑centric trial success at IQVIA** At IQVIA, we are reimagining how clinical trials reach, engage, and support patients. Our Patient and Site Centric Solutions (PSCS) team partners with experts across the business to design strategies that help sponsors enroll and retain the right patients — while ensuring sites feel supported and empowered every step of the way. If you are passionate about improving the patient experience in research and want to influence global trial performance, this role offers a unique opportunity to make meaningful impact.**What you will do*** Develop and implement best‑in‑class patient recruitment, retention, and site‑engagement strategies to support customer enrollment goals. * Partner cross‑functionally to shape PSCS strategy both pre‑ and post‑award. * Lead elements of solution innovation to enhance our global recruitment and retention offerings. * Present strategy recommendations and insights during client bid‑defense meetings. * Create data‑driven budget estimates for proposed solutions. * Represent IQVIA at industry events, conferences, or webinars as a thought leader. * Collaborate with internal stakeholders to ensure all solutions meet quality and regulatory standards. * Mentor and coach team members to support development and team excellence. * Drive process improvement initiatives within PSCS. * Serve as a trusted liaison for internal teams and clients on recruitment strategy topics. **What you need to succeed*** Bachelor’s degree required. * 10\+ years of relevant experience, including 5\+ years in leadership roles. * Strong understanding of clinical development, patient recruitment, and site engagement. * In‑depth knowledge of GCP/ICH and applicable regulatory guidelines. * Demonstrated ability to analyze data and translate insights into effective strategies. * Solid understanding of clinical research financial parameters and budget management. * Excellent communication and presentation skills with the ability to influence stakeholders. * Strong leadership capabilities with a collaborative, relationship‑oriented style. * Proficiency in Microsoft PowerPoint, Excel, and Word. * Strong organizational and problem‑solving skills with the ability to manage competing priorities. **Why join IQVIA** At IQVIA, you’ll be part of a global team driving smarter healthcare for everyone, everywhere. You’ll work alongside innovators, clinicians, analysts, and strategists who are committed to improving patient outcomes and shaping the future of clinical development. Expect a culture built on collaboration, continuous learning, and opportunities for growth — supported by tools and insights that help you do your best work. IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com. At IQVIA, we believe that diversity, inclusion, and belonging empower our mission to accelerate innovation for a healthier world. We create a culture of belonging by valuing the perspectives of all talented employees worldwide and providing them with the opportunity to power smarter healthcare for everyone, everywhere. When our talented employees bring their authentic selves and their diverse experiences to work, they enable us to accomplish extraordinary things. Multifaceted thought processes spark innovation. Multi\-talented collaboration harnesses innovation to deliver superior outcomes.

C/ de Juan Esplandiú, 11-13, Retiro, 28007 Madrid, Spain

Revenue Financial Controller - Laboratorio Central Health Diagnostics Quirónsalud (Alcobendas)651060734845471227

Revenue Financial Controller - Laboratorio Central Health Diagnostics Quirónsalud (Alcobendas)

**At Quirónsalud, your career has a purpose.** At **Quirónsalud**, we do not just lead the healthcare sector; we are **transforming** it. With state-of-the-art technology and a network of over **58 hospitals in Spain and more than 180 healthcare centres across Europe**, backed by **Fresenius-Helios**, we work with a clear mission: **improving lives**. We are looking for professionals who want to **grow, innovate and be part of a team where excellence is part of everyday life.** **Join our team** **Position:** Revenue Financial Controller **Location:** Laboratorio Central Health Diagnostics (Alcobendas) **Key responsibilities:** * Lead the preparation of the annual revenue + activity budget and monitor its execution. * Monitor contracts and ensure correct tariff application. * Participate in defining and improving revenue and activity dashboards (KPIs_Power BI). * Contribute ideas and innovation to improve existing processes and systems. * Perform revenue closing and reconciliation with various profit centres and business units. * Prepare monthly and annual closing reports on revenue figures (billing/provisions/activity/KPIs). * Monitor monthly performance versus prior year and budget, analyse variances and propose improvements. * Monitor and evaluate profitability. * Analyse balance sheet accounts (revenue, bad debts). * Support audits. **What we offer:** * **Immediate onboarding** into a collaborative and specialised team. * **Attractive, competitive and market-aligned remuneration package.** * **An environment that fosters your development** * You will benefit from the support of an experienced team that will help you strengthen your skills and advance your career. * **Continuous training**: we will stimulate your learning and development through our **Quirónsalud University** and our **specific training plans**, enabling your personal and professional growth. **We care about your wellbeing** * **Access to our Health and Wellbeing Programme**, including initiatives such as: * + **Healthcare:** physical and mental wellbeing programmes (access to medical services, health maintenance programmes, psychological support). + **Financial wellbeing:** flexible compensation schemes, salary management facilities and exclusive discounts. + **Volunteering programme.** We’re waiting for you! *At Quirónsalud, we promote integration and respect for diversity. Therefore, our selection processes are conducted under these principles. Likewise, the company declares its commitment to establishing and developing practices that drive and foster equal treatment and opportunities between men and women, without discrimination—direct or indirect—based on gender. This principle forms part of our Corporate and People Policy, aligned with Organic Law 3/2007, of 22 March, on Effective Equality between Women and Men.* * Bachelor’s degree in Business Administration and Management (ADE), Economics, Business Studies, etc. * Minimum three years’ experience in similar roles. * Knowledge of SQL, Power Query, Power BI. * Proficiency in Excel. * Hospital or industrial sector experience is desirable.

Pl. Mayor, nº 1, 28100 Alcobendas, Madrid, Spain

Intern651060734667541228

**WHO WE ARE:** Plug and Play Tech Center is the ultimate innovation platform, bringing together the best startups and the world’s largest corporations to create the most meaningful connections that bring innovation to anyone, anywhere. We are on a mission to bring the benefits of Silicon Valley to all corners of the world. Each year, hundreds of entrepreneurs join our vertical\-specific accelerator programs to team up with our corporate members or receive a direct investment from Plug and Play. Plug and Play has over 45 locations across the world and our corporate members include: Daimler, Prologis, PG\&E, Nissan, Volvo, BP, Walmart, Nokia, Coca Cola, Doosan Bobcat, and over 500 more. Plug and Play’s corporate members utilize Plug and Play to identify the best startups to meet their challenges. Plug and Play’s proven investment track record includes Honey, Dropbox, Lending Club, Kustomer, Einride, and many more. **WHO WE’RE LOOKING FOR:** We’re an exceptional team with backgrounds in technology and entrepreneurship and we’re growing rapidly to deliver on our mission. We’re actively seeking an Intern to continuously deliver value to our partners under our fintech vertical in Madrid. An ideal candidate is highly strategic, ambitious, detail oriented, and able to effectively influence both within the organization and with our external partners. **HOW YOU’LL MAKE A DIFFERENCE:** As we live the startup spirit ourselves, no one in the team is exclusively limited to their main tasks. Rather, we are a dynamic team of all\-rounders who work closely together in all projects. However, your main role will be in supporting our team with the following tasks: Sourcing startups * Research and analyse the market and industry trends to identify the best early\-stage companies and founding teams with a specific focus. * Identify and reach out to promising startups. * Assist the senior team in evaluating startups from various sources. * Create meaningful and positive relationships with the startups and scale\-ups. Corporate facing * Coordinate the Plug and Play open\-innovation\-based deal flow and startup evaluation process together with our corporate partners. * Identify great startup offerings meeting corporate tech and business needs. * Funneling all individual interests of our corporate partners into the outline of the program and timeline (e.g. Workshops, Dealflow Sessions, Innovation Days, Demo Days etc.). * Introducing start\-ups to our corporate partners and helping our corporate partners engage with startups when there is a potential match or opportunity. Community Facing * Build and maintain an ecosystem of relevant stakeholders around innovation, venture capital and startups (incl. clusters, government representatives, universities, mentors, keynote speakers, etc.). Project \& Client Management * Support the end\-to\-end execution of open innovation programs, coordinating timelines, deliverables, and stakeholders across multiple projects. * Act as a day\-to\-day support point for corporate partners and startups, ensuring clear communication, follow\-ups, and alignment throughout the program lifecycle. * Track progress, prepare client\-facing materials, and contribute to continuous improvement of internal project management processes. **REQUIRED EXPERIENCE:** * Bachelor’s degree in Business Administration, engineering, economics or related field preferred. * Fluency in English and in Spanish is essential. * Detail oriented, highly organized, and comfortable working in a fast\-paced environment. * Strong process and analytical skills to identify inefficiencies and create improvements. * Excellent communication skills and proficiency in public speaking. * Passionate about technology with some background in the Startup ecosystem (research, courses, projects, etc…) * Project management and startup experience is a plus. * Ability to work with all levels of management is crucial. * Demonstrate integrity, responsibility, accountability, self\-awareness, work ethic, and empathy. * **All CVs must be submitted in English**

Calle de Lagasca, 37, Salamanca, 28001 Madrid, Spain

Associate Clinical Trial Manager (PhD) - Neuroscience / Ophthalmology650936654097931229

Associate Clinical Trial Manager (PhD) - Neuroscience / Ophthalmology

Job Summary : Medpace is currently seeking candidates with **PhDs and/or Post\-Doctoral Research experience** for a full\-time, office\-based Associate Clinical Trial Manager (aCTM) to join our Clinical Trial Management team. The aCTM will be a part of the Clinical Trial Management team working with Project Coordinators and Clinical Trial Managers in performance of clinical trial management activities. Candidate must have a desire to transfer and apply analytical and academic skills in clinical project administration and management. A fantastic opportunity for recent PhD graduates to enter the industry, receive solid foundational training, work in an international environment, and **develop their career in the research and development of cutting\-edge therapeutics**. Candidates should expect to have an intensive training period and show the desire and aptitude for an accelerated career path into Clinical Trial Management (CTM). Responsibilities : * Communicate and collaborate on global study activities; working closely with the project coordinator and clinical trial manager * Ensure timely delivery of recurrent tasks consistently with a high degree of accuracy * Compile and maintain project\-specific status reports within the clinical trial management system * Interact with the internal project team, Sponsor, study sites, and third\-party vendors * Manage and perform quality control of our internal regulatory filing system * Provide oversight and management of study supplies * Create and maintain project timelines * Coordinate project meetings and produce quality minutes Qualifications : * PhD in Life Sciences * Fluency in English with solid presentation skills * Ability to work in a fast\-paced dynamic industry within an international team * Prior experience within the CRO or pharmaceutical industry not required but will be advantageous Medpace Overview : Medpace is a full\-service clinical contract research organization (CRO). We provide Phase I\-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti\-viral and anti\-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40\+ countries. Why Medpace? : People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today. The work we’ve done over the past 30\+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future. **Medpace Perks** * Flexible work environment * Competitive compensation and benefits package * Competitive PTO packages * Structured career paths with opportunities for professional growth * Company\-sponsored employee appreciation events * Employee health and wellness initiatives **Awards*** Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024 * Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility **What to Expect Next** A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.

C. de Santiago Bernabéu, 12, Chamartín, 28036 Madrid, Spain

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