Getafe Other Job Listings

Technical Applications Engineer64396339332865120

**Why Valvoline Global Operations?** At **Valvoline Global Operations**, we’re proud to be **The Original Motor Oil**, but we’ve never rested on being first. Founded in 1866, we introduced the world’s first branded motor oil, staking our claim as a pioneer in the automotive and industrial solutions industry. Today, as an affiliate of **Aramco**, one of the world’s largest integrated energy and chemicals companies, we are driven by innovation and committed to creating sustainable solutions for a better future. With a global presence, we develop **future\-ready products** and provide **best\-in\-class services** for our partners around the world. For us, originality isn’t just about where we began; it’s about where we’re headed and how we’ll lead the way. **We are originality in motion.** Our corporate values—**Care, Integrity, Passion, Unity, and Excellence**—are at the heart of everything we do. These values define how we operate, how we treat one another, and how we engage with our partners, customers, and the communities we serve. At Valvoline Global, we are united in our commitment to: * Treating everyone with care. * Acting with unwavering integrity. * Striving for excellence in all endeavors. * Delivering on our commitments with passion. * Collaborating as one unified team. When you join **Valvoline Global**, you’ll become part of a culture that celebrates creativity, innovation, and excellence. Together, we’re shaping the future of automotive and industrial solutions. **Job Overview** **The Technical Applications Engineer** will be a hands\-on individual who will report to the Technical Applications Team Manager. This role requires the individual to work with local marketing, and sales groups as well as fleet customers, industrial customers, and test partners. This role supports regional field test sites and provides data for new product development, industry approvals, and OEM support. Additionally, the individual will provide large customers with direct application support regarding lubricants, hydraulic fluids, chemicals, and coolants for passenger car, commercial and industrial applications. While some experience in tribology and lubricant formulation is preferred, it is more critical that a successful candidate have a strong mechanical aptitude, outstanding communication skills, working knowledge of Engineering principles and scientific methods, and demonstrable computer aptitude. The ability to analyze data and to author polished presentations/reports is key. **Primary Duties and Responsibilities** * Support the Valvoline channel partner team, their distributors and customers, Align with the needs of the regional sales team and VGO goals, prioritizing support linked to the goals of sales and marketing for your region. * Work with approved labs and our Technical Applications Team to develop and support oil analysis programs \& convert used oil data into effective reports for customer maintenance recommendations * Support, coordinate and manage local and regional field test projects focused on fluids such as engine oil, transmission oil, and gear oil to achieve industry approvals and support marketing claims as well as co\-ordinate and support customer demonstration/acceptance testing (less rigorous than field testing) * Investigate and resolve product application problems by conducting root cause analysis. May include supporting quality and supply chain with concerns of product quality. * Research regional key industry areas, including equipment design, technology changes and API, ACEA and ASTM standards to provide industry specific field knowledge to Sales, R\&D, and Marketing regarding product performance, customer needs, and industry trends. * Assist the European and regional marketing team in developing sales literature and differentiated offers * Provide proactive technical support to the regional Sales Team to grow business in various segments while developing strong customer relationships; support will encompass a wide range of industries, including PCMO, HDMO, Industrial, Trucking Fleet, Construction, Power Generation, Marine, Mining, and others. * Complete Lubricants Cross\-Referencing and input to support Sales opportunities. **Education** Engineering or Scientific background. Preferably a degree in Mechanical Engineering. Proficiency in English as well as local language. **Licenses and Certifications** Certified Lubrication Specialist (CLS) or Oil Monitoring Analysis (OMA) is a good to have **Knowledge, Skills, and** **Competencies** * Experience working on engines and vehicles (engine rebuilds, auto maintenance, modifications, heavy equipment maintenance, etc…) in a personal or professional capacity. A typical ‘Hands on Expertise’ approach * Excellent organizational, communication, and teamwork skill along with the ability to work independently. * Experience working directly with customer/field issues and following through to see resolutions impact cross functional teams (design, supply chain, quality assurance, etc...). * Experience with statistical software and/or data acquisition. * Prior technical sales or technical advisor field experience in petroleum, lubricants/base\-oils, or equipment industries. * Experience in tribology and lubricant development. * Experience in the mechanical development. * Experience in industrial/manufacturing lubricant applications. * Excellent time management skills * An exceptional safety mindset and ability to work safely at all times when unsupervised. Valvoline Global is an **equal opportunity employer**. We are dedicated to fostering an environment where every individual feels valued, respected, and empowered to contribute their unique perspectives and skills. We strictly prohibit discrimination and harassment of any kind, regardless of race, color, religion, age, sex, national origin, disability, genetics, veteran status, sexual orientation, gender identity, or any other legally protected characteristic. We are committed to ensuring accessibility throughout our recruitment process. If you require a reasonable accommodation to participate in any stage of the recruitment or selection process, please contact us at:. * **Email**: Valvolineglobalcareers@valvolineglobal.com This contact information is solely for accommodation requests. For inquiries about application status, please use the appropriate channels listed in your application materials. **Are You Ready to Make an Impact?** At Valvoline Global, we’re looking for passionate and talented individuals to join our journey of innovation and excellence. **Are you ready to shape the future with us? Apply today.** Requisition ID: 1698 \#LI\-KT1

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

Negotiable Salary

MSL CART - Norte (Galicia, Asturias o País Vasco)64374259355138121

Indeed

MSL CART - Norte (Galicia, Asturias o País Vasco)

At Johnson \& Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com **Job Function:** Medical Affairs Group**Job Sub Function:** Medical Science Liaison**Job Category:** Scientific/Technology**All Job Posting Locations:** Madrid, Spain**Job Description:** Johnson \& Johnson, compañía líder en el sector, busca incorporar un profesional de Medical Scientific Liaison para su unidad de **Terapia Celular\-CARTs con residencia en Norte.** Con el porfolio y pipeline más interesante del sector, J\&J ofrece la oportunidad de formar parte de un proyecto innovador, puntero y referente dentro de la industria farmacéutica. Como parte de Johnson \& Johnson, nuestra misión es transformar la vida de los pacientes mediante el descubrimiento y desarrollo de soluciones innovadoras para cubrir las necesidades médicas más importantes de nuestro tiempo. Buscamos incorporar profesionales con talento, ganas ilimitadas de contribuir, aprender, y buenos ¨team\-players¨, dispuestos a afrontar cualquier reto y a lograr resultados excelentes. Buscamos personas que sean capaces de encontrar oportunidades y proactivamente fomentar su propio desarrollo. **Principales funciones que desempeñar:** * To keep abreast of **medical and scientific knowledge.** + Continuous update on products, patient’s treatment trends, clinical activities and studies conducted within the therapeutic area in their region. * Development and maintenance of a **contact network with Leading Specialists**. + Understand their needs, key value drivers, practical treatment patterns and scientific activities within therapeutic area + Communicate value of company products, incl. clinical questionnaire discussions + Through scientific interactions, communicate medical benefits of products and contribute to foster innovative approaches + Represent the company within professional associations in the therapeutic area in cooperation with Medical Affairs/ Medical Education and other positions in the Medical Affairs Department * Proactive and reactive **communication of medical scientific data** according to following criteria * Proactive Scientific Communication to Leading Specialists must be consistent with the last approved Summary of Product Characteristics regarding the safe and effective use of approved products in approved indications. Content of Scientific Communication should be highly scientific, accurate, fair and objective, based on an up\-to\-date evaluation of all relevant evidence and reflect that evidence clearly, using neither marketing claims nor brand name. * In some very specific circumstances, the MSL can interact proactively with non\-Leading Specialists. The program should be clearly defined in the MSL Country Activity Plan, providing the rational, the objective, content, timelines and selection criteria of the HCPs to be involved. * Description of R\&D programs and discussing regulatory developments with no promotional intent are also part of Scientific Communication. * Reactive Communication of medical scientific data can be provided upon request to any Health Care Professional, within the approved label or off\-label. The request should come either directly from the HCP or via the Medical Information department. MSLs are required to document all off\-label information requests they receive from Leading Specialists and other HCPs that they may interact with. * Organization and participation in **Medical Education activities,** at local \&/regional level: + Identify/support/educate speakers + Build Medical Education programs with scientific third party + Collaborate with Medical Education manager in National Medical education activities + Provide scientific material under request. MSLs may initiate discussion with potential speakers, discussing documents/ slides which may be of help for future presentations. * Organization and participation in **Advisory Boards** in cooperation with Medical Affairs/Medical Education/other positions in the Medical Affairs Department. * **Market Access Discussions** MSLs can present highly scientific, accurate, fair and objective data to Payors (Hospital Formulary Committees, Health Insurers, Health Technology Assessment Committees, etc) to provide them with objective information about Company products. * **Pre\- Approval Activities** MSLs can engage in interactions with Payors to raise awareness so that payors can plan and budget so that patients can receive the product when it becomes available. MSLs can organize Speakers training to prepare speakers for delivering presentations to other HCP when the Marketing Authorization is granted. * Provision of **scientific support to company Sales Representatives** and other company representatives + Provide medical and product training and scientific support to Sales Representatives in coordination with Training/Medical Affairs Department as appropriate + Act as a reference point to Sales Representatives for any scientific query, in collaboration with Medical Information as appropriate. * **Local implementation of Medical Affairs Plan** in their areas: + Support the set up and follow up of local company sponsored studies, registries and other non\-interventional Medical Affairs studies + Propose investigators and sites for interventional and non\-interventional Medical Affairs studies. + Participate in investigator meetings preparation, recruitment follow\-up and study result presentation. + Receive investigator proposals for IIS and ensure they are discussed within the Medical Affairs department for decision. * Through scientific interactions, **gain valuable insight** into treatment patterns and scientific activities in the therapeutic area and provide input and a strategic view to the company Medical Affairs Plan / business decision\-making. * Observes and promotes all regulatory requirements as defined in applicable regulations, rules and procedures established by the Company, including but not limited to **Health Care Business Integrity and Pharmacovigilance** * Follow principles, procedures and training included in SAFE Fleet program. * GCO collaboration: Support GCO studies when needed through the identification of potential sites and facilitating a direct contact with leading specialists. * Report all suspected adverse reactions, serious or non serious, I may be aware of within a maximum of 24 hours after being aware of it and communicate it to the Pharmacovigilance Department. Additionally, for all employees involved in Research Related Activities (RRA): * Ensure safety reporting requirements (timely AE/PQC reporting) as set out in company policies and SOPs (Standard Operating Procedures) are met and appropriately managed when planning projects, developing materials, executing projects and contracting vendors. * Ensure HCC and legal requirements (Fair Market Value, Transfer of Value rules, Promotional Materials rules) are fully understood, appropriately managed and complied with when planning projects, developing materials, executing projects and contracting vendors. * Ensure inspection readiness with respect to personal training compliance, and availability of recent CV and individualized Job Description. **Qualifications** * Scientific degree: Medical Doctor, Pharmaceutical or Nature Science university degree, or related qualification (i.e. psychology degree) * Deep knowledge of the therapeutic area, strength in research and interpretation of medical data * Background to be accepted by the Leading Specialists in peer\-to\-peer relationship, i.e. relevant work experience, scientific acumen and/or communication skills. * Highly customer focused with an awareness of the importance of business results * Innovative with the ability to coordinate and drive a complex and changing environment * Awareness of, and adherence to, Johnson \& Johnson Credo values and International Health Care Business Integrity Guide. **Special Requirements** * Deep scientific knowledge in the therapeutic area **Required Skills:** **Preferred Skills:** Analytical Reasoning, Analytics Insights, Clinical Data Management, Clinical Trials, Collaborating, Communication, Data Reporting, Detail\-Oriented, Digital Culture, Digital Literacy, Execution Focus, Market Research, Medical Affairs, Medical Communications, Medical Compliance, Product Knowledge, Relationship Building, Scientific Research, Technologically Savvy

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

Negotiable Salary

Indeed

Transformation PMO

**Capgemini Engineering, a global leader in engineering services, brings together teams of Engineering, Science and Architecture 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 go beyond conventional boundaries, delivering unique R&D and engineering services across all industries.** **The Digital Continuity & Manufacturing (DC&M) team at Capgemini Engineering specializes in providing strategic solutions for the digitization of engineering and industrial processes, ensuring digital continuity throughout the entire product lifecycle, from design to maintenance. We focus on optimizing operational efficiency and driving innovation through the integration of advanced technologies such as automation, industrial IoT, and digital twins, helping companies rapidly adapt to the market and maintain a competitive edge.** **Currently, we are strengthening our team and are looking to hire a Transformation PM to join us in Madrid.** **What profile are we looking for?** * **Bachelor's, Master's or PhD in Engineering (preferably Electrical, Computer, Electronics or Telecommunications), Physics, Business Administration or related fields.** * **At least 4-5 years of experience in consulting projects, preferably in energy, manufacturing, pharmaceutical and healthcare sectors.** * **Experience in consulting projects in these sectors for various IT/OT, digital and/or transformation initiatives.** * **Knowledge of ISA95 and automation and control layer solutions.** * **Knowledge of MES solutions.** * **Process reengineering.** * **Experience in development and implementation projects using agile methodologies.** * **Knowledge of software and hardware solutions in these sectors.** **Having a disability certificate will be positively valued within the framework of our inclusion and diversity policy.** **We welcome all applications. We offer a wide range of training opportunities, both in-person and online, including certifications, etc. Even if you don’t meet 100% of the desired qualifications, we would love to hear from you!** **Our commitment to inclusion and equal opportunities means we have an Equality Plan and an Ethical Code that guarantee professional development and equal opportunities 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 can we offer you?** * **International Digital Continuity & Manufacturing Community, where you can collaborate with experts worldwide.** * **Career development plans and training programs tailored to your role.** * **Access to more than 400 internal training courses and platforms such as: Coursera, Udemy, Pluralsight, Harvard Manager Mentor, among others.** * **Language training in English, French and German through Education First (EF).** **Why Capgemini?** **Capgemini is a global leader in transforming clients’ businesses by harnessing the full power of technology. We are guided by the purpose of creating an inclusive and sustainable future through technology and the energy of those who develop it. We are a responsible and diverse company, a global leader in IT and Engineering services with over 360,000 professionals in more than 50 countries. With a solid 55-year heritage and extensive industry expertise, clients trust Capgemini to address their full business needs—from strategy and design to operations—powered by the fast-evolving world of cloud, data, AI, connectivity, software, platforms, and digital engineering. The Group reported global revenues of €22 billion in 2022.** **Rewrite your future. Join the team!** **www.capgemini.com/es-es** **\#LI-JA11**

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

Negotiable Salary

Bioinformatics Developer64282431251969123

Indeed

Bioinformatics Developer

At **Genestack** we are tackling the underlying computational and scientific challenges of bioinformatics in order to provide researchers with software tools that will streamline the discovery process and drive forward precision medicine, drug development, and bioinformatics research. We're looking for a **Bioinformatics Developer** to join our Professional Services team and deliver impactful, data\-driven solutions to life sciences clients. This hybrid role blends hands\-on scientific development, bioinformatics expertise, and systems integration work — helping research teams organize, analyze, and operationalize their omics data using our platform. You'll work closely with clients, product managers, and engineers to understand complex requirements and translate them into scalable, interoperable workflows. If you enjoy solving biological data challenges through a mix of analysis, automation, and architecture — this is your chance to make a difference in real\-world R\&D environments. **In this role, you will:** * Scope and lead bioinformatics projects. * Understand client needs and define project approaches, milestones, and outcomes across omics domains. * Process, curate, and harmonize omics data. * Design and implement integrations between our platform and external systems (cloud and on\-prem storage, pipeline execution engines, and analytical platforms). * Build and maintain bioinformatics connectors and pipelines for ingestion, transformation, and metadata normalization of structured and semi\-structured data. * Develop custom analytical and visualization tools using Python or R to support client\-specific reporting and exploration. * Collaborate with cross\-functional teams, including software engineers, product managers, and customer success, to ensure seamless client delivery and continuous improvement. * Translate technical insights into clear communication artifacts, including client documentation, training materials, and onboarding demos. * Provide pre\-sales and onboarding support, assisting with technical scoping, trial integrations, and early proof\-of\-value delivery. **We would like you to have:** * Bachelor's or Master's degree in Bioinformatics, Computational Biology, or a related scientific/technical field. * Strong experience managing and delivering bioinformatics projects, ideally in a services or consulting environment. * Proficiency in Python or R, with an emphasis on reproducible scientific code, APIs, and automation scripts. * Working knowledge of data integration, including protocols (e.g., HTTPS, S3, REST APIs), file formats (e.g., JSON, YAML, TSV), and data validation. * Familiarity with bioinformatics tools and pipelines (e.g., RNA\-seq, variant calling, multi\-omics integration). * Experience with data visualization frameworks, including Dash, Shiny, Plotly, or matplotlib. * Ability to manage multiple projects in parallel, balancing short\-term delivery and long\-term architectural thinking. * Excellent communication skills in English, with experience presenting technical work to both technical and non\-technical stakeholders. **It would be nice for you to have:** * Experience building custom connectors, ETL pipelines, or integrations across client infrastructures and cloud systems. * Familiarity with workflow orchestration tools like Nextflow, Airflow, etc. * Hands\-on experience with cloud environments (e.g., AWS, Azure), including secure access, bucket management, and environment provisioning. * Exposure to Java, Kotlin, or other JVM\-based languages for backend system integration. * Domain experience in oncology, immunology, single\-cell, microbiome, or other therapeutic areas and molecular data technologies. **We offer you:** * international team of professionals; * fully paid sick leaves; * onboarding and domain training for newcomers; * flexible work schedule.

2222+22 Yunclillos, Spain

Negotiable Salary

Cleaning Staff - VIP LOUNGES - T4 Airport64151478980739124

Indeed

Cleaning Staff - VIP LOUNGES - T4 Airport

**Company Description** DO \& CO is a gourmet catering company and our main activity in Spain is airline catering. We started more than forty years ago as a family restaurant, and although today we are a large company, we still maintain our traditions and family values. The most important ingredient in all our recipes is the people who are part of this company. Therefore, your well-being is our priority, and our Human Resources team works every day to improve the experience of our employees. Joining a new job is a very important moment, so we want everything to go perfectly as you begin your adventure with DO \& CO. **Job Description** What distinguishes us from other catering companies is our customer-facing service and our gourmet food. Customers rate our service through QR codes located throughout the lounge, which makes it essential for us to create high-quality experiences for all our guests. Everyone working in the VIP Lounges plays a key role in ensuring customer satisfaction. As a Cleaning Assistant, your duties/responsibilities will include: * Performing maintenance and cleaning of internal and external areas of Iberia's VIP Lounges. * Monitoring stock levels of cleaning supplies. * Operating light machinery to carry out cleaning procedures. * Completing an hourly checklist of tasks. * Handling chemical products. **Requirements** Requirements: * Availability to work rotating shifts (06:00 AM - 01:00 AM) * Immediate availability to start * Availability to work from Monday to Sunday * Experience working with chemical products required Languages: * Spanish Competencies: * Time Management * Attention to Detail * Teamwork * Flexibility and Adaptability **Additional Information** We believe our employees are the driving force behind our success, and we strive to create a positive and supportive work environment. As a member of our team, you will have access to a range of benefits, including: * Fuel your workday with delicious lunches and snacks—daily menu provided free of charge. * Join our dynamic company where your ideas are welcomed and valued. * Advance your career with genuine growth opportunities—even abroad! * Take advantage of the opportunity to work with a global leader in luxury gourmet entertainment and leave your mark on the industry. DO\&CO is an equal opportunity employer. All candidates will be considered without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran status, or disability.

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

Negotiable Salary

IT Procurement Consultant64147626184193125

Indeed

IT Procurement Consultant

**What do we do?** "Join the adventure at **BIP**! In our **Digital** **Consulting** area, we stand out for helping our clients navigate the exciting journey of digital transformation. We discover and implement the most innovative and emerging technologies aligned with business strategy, ensuring that every investment counts. Our services are the turbocharger driving change in business, and we're here to help our clients break barriers in the digital world. From changing ways of working to optimizing and automating processes, through economic management and technology supplier management, **we've got it all!** We are a diverse team joining forces to inject value into every project, combining our expertise in strategy and consulting with deep sector knowledge (energy, banking, insurance, etc.) to create tailored solutions our clients love. If you already have **at least two years of experience in the IT procurement field**, are passionate about information technology, possess negotiation and contract management skills, and enjoy working in teams to deliver top-tier solutions to our clients' challenges, **this is your place!** We are looking for people eager to communicate directly with clients and with a mindset ready to solve any puzzle that arises. **What will your day-to-day look like?** * Assist in defining procurement strategy by analyzing the evolution of the IT market to identify opportunities and risks. * Collaborate in drafting and reviewing specifications, as well as identifying new suppliers. * Execute tendering processes. * Lead negotiations with suppliers to establish agreements and contracts. * Coordinate contract drafting in collaboration with relevant departments. * Monitor contractual execution, ensuring service levels and resolving incidents. **What do we require?** * Minimum of 2 years of experience in IT Procurement. * Knowledge and proficiency with tools such as **Jaggaer** and **SAP**. * Strong negotiation and contract management skills. * Ability to work in teams and collaborate with different business areas. * Degree in STEM fields (Computer Science, Telecommunications, Industrial Engineering, Mathematics, Physics, Chemistry, etc.) or Business Administration. * Advanced level of English, as you will have the opportunity to work on international projects. * Hybrid work model, with availability to go to the office according to project needs. * **We will value:** * Possession of certifications such as ITIL, SCRUM, etc. * Knowledge of other languages. **What do we offer?** Become part of a young, fast-growing company with a close-knit, open-door culture, filled with talented professionals who regularly compete with the largest international consultancies—our slogan, after all, is: “Here to dare.” At Bip, we are committed to your personal and professional development. To support you, our culture promotes guidance from experienced professionals who will serve as mentors and inspiration, and we also offer training programs designed to help you reach your full potential. **As a summary, below are some programs and benefits enjoyed by Bip employees:** * Fixed and variable compensation based on individual performance * Personalized career development and training plans, including language courses (BIP Learning) * Mentorship and coaching programs based on role category (BIP Mentoring) * Continuous and personalized feedback (from your manager and your mentor) * Volunteering and social action programs * Sports and hiking programs, etc. (Club BIP) * Private medical insurance * Flexibility program (Flexible Compensation Plan) 23\+3 vacation days * *Bip Iberia, in compliance and alignment with the Comprehensive Law for Equal Treatment and Non-Discrimination, keeps all job openings available to any qualified individuals regardless of age, disability, gender, sexual or political orientation, race, or belief.* *BUSINESS INTEGRATION PARTNERS CONSULTING IBERIA, S.L., with tax ID B84701903 and contact Liliana Mendoza, will process the data received upon your application as Data Controller, for the purpose of managing the current selection process based on pre-contractual measures under GDPR Article 6\.1\. b), as well as for future selection processes if your profile is of interest, based on consent under Article 6\.1 a).* *BUSINESS INTEGRATION PARTNERS CONSULTING IBERIA, S.L. will not disclose your data to third parties unless legally required. The CV retention period is a maximum of 1 year, after which it will be destroyed.* *You may also exercise your rights of access, rectification, erasure, opposition, restriction of processing, data portability, and not to be subject to automated individual decisions, or request additional information about data processing via email: dpo\-bipspain@bip\-group.com*

Av. de Burgos, 12, Chamartín, 28036 Madrid, Spain

Negotiable Salary

Risk in Action Event - Madrid64147626164737126

Indeed

Risk in Action Event - Madrid

Join the crisis committee of a multinational company and face the challenge of Risk, Regulatory \& Forensic. Would you like to experience what it's like to work in risk consulting? If you are a third- or fourth-year undergraduate student or a master's student in a field related to Business Administration, Economics, Mathematics, Statistics, Data Science, Chemical Engineering, Industrial Engineering, Energy Engineering, or similar, this event is for you. We invite you to "Risk in Action", an event taking place on Friday, November 21, running from 09:00 to 15:00 in the morning, where you will tackle a crisis simulation case and get to know up close the Risk, Regulatory \& Forensic teams: Enterprise Risk, Financial Crime \& Forensic, Regulatory \& Financial Risk, and Non-Financial Regulation. What does the event involve? **Immerse yourself in the world of Risk, Regulatory \& Forensic:** Discover firsthand from our professionals what everyday life at Deloitte is like. **Test your skills:** Solve a crisis simulation case in a team, tackling real challenges in key risk areas. **Network with experts:** Connect with industry leaders, other students, and our talent team at an exclusive event. **Career opportunities:** If the experience motivates you, we may consider your application for future positions within our team. Are you ready to take on the challenge? Now it's up to you! If you believe this event is right for you, click 'Apply' and complete your profile so we can evaluate your application. What impact will you make? Deloitte is a professional services firm strongly committed to equal opportunities. In this regard, the firm will accept and process applications from all sectors of society, without discrimination based on sex, gender expression, race, religion or beliefs, ethnic or national origin, disability, illness or health condition, genetic predisposition to suffer pathologies, age, citizenship, marital status, sexual orientation or identity, socioeconomic situation, or any other personal or social condition or circumstance. **Location:** Madrid **Position Type:** Students and Recent Graduates **Service Line:** SRT **Req Id:** 44784

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

Negotiable Salary

Patent Adviser in the Chemistry field64147626205442127

Indeed

Patent Adviser in the Chemistry field

#### **Description** ABG Intellectual Property is one of Europe’s leading IP firms, working with clients across all technical fields and supporting innovation with high\-quality legal and technical expertise. We are looking for a Patent Adviser to join our Chemistry team. The role will involve discussing innovations with inventors and researchers, drafting and prosecuting patent applications, preparing responses to examiners, and providing advice on patentability, infringement and freedom\-to\-operate matters. The position offers the opportunity to work closely with clients in cutting\-edge areas of chemistry and materials science. #### **Requirements** * University degree in Chemistry (organic chemistry, inorganic chemistry, materials science or related fields). * Excellent written and oral communication skills. * High level of English (other languages will be valued). * Analytical skills, accuracy and rigor. * Client orientation, with a proactive and positive approach. #### **Why us?** Joining ABG means being part of one of Europe’s most respected IP firms, working side by side with highly qualified professionals in a collaborative and international environment. We combine scientific excellence with legal expertise and offer a culture based on continuous learning, teamwork and innovation. #### **What we offer?** * Opportunities for professional growth and ongoing training. * A collaborative and supportive working environment. * Flexibility and work\-life balance through our hybrid working model. * Health insurance and flexible compensation schemes. * A culture that values diversity, inclusion and equal opportunities. #### **Who we are?** **ABG Intellectual Property** is among the most prominent and fastest\-growing industrial property firms in Europe. We are a solid and reliable partner in obtaining effective industrial property protection across all technical fields, such as Engineering and Physics, Information and Communication Technologies, Biotechnology, Chemistry, Materials and Pharmaceuticals. ABG professionals share a passion for knowledge and possess training in cutting\-edge technologies to analyze our clients’ needs, offering the best technical and legal solutions to complex industrial property challenges. **Continuous learning** is an essential part of our culture. Excellence and service quality have always been ABG’s driving force since its foundation. To achieve this goal, it is essential that our professionals develop first\-class scientific, technical and legal knowledge. At ABG, we foster a learning culture that enables our patent and trademark attorneys, as well as our lawyers, to reach the highest professional standards. Our team regularly attends courses and seminars, both internal and external, to stay up to date with the latest advances in science and law. **Equal opportunities** ABG Intellectual Property maintains a firm commitment to equal treatment and non\-discrimination in all its processes, including recruitment. We guarantee equal opportunities regardless of gender, age, disability, sexual orientation, gender identity, or any other personal or social condition. We actively promote respect for diversity and inclusion, including towards the LGBTI community, as part of our corporate culture.

C. de Francisco Suárez, 7, Chamartín, 28036 Madrid, Spain

Negotiable Salary

Senior/Principal Clinical Database Manager64146411167491128

Indeed

Senior/Principal Clinical Database Manager

Precision for Medicine are hiring a Senior/Principal Clinical Database Manager to join our team, candidates can work remotely in the following locations: UK, Spain, Hungary, Poland, Romania, Serbia or Slovakia. Position Summary: The Senior/Principal Clinical Database Manager is responsible for the design, development, testing, implementation, maintenance and support of clinical databases and applications. Position will interface directly with the internal team (i.e. Data Management, Project Management, etc.), EDC vendor, clients and third\-party vendors to gather requirements and provide status updates. Provides operational and technical training to end users and junior staff. Additionally, the Senior/Principal Clinical Database Manager may play a lead role in internal software projects that require specialized programming and/or scripting. Qualifications: Minimum Required: * Must have experience in developing and customizing clinical data management databases in a clinical, scientific or health care discipline * Bachelor's and/or a combination of related experience * Rave API integration experience using external vendor modules * Rave Advanced Custom Function programming experience Other Required: * Proficiency in Microsoft Office: Word, Excel, PowerPoint, Outlook. * Able to handle a variety of clinical research tasks. * Excellent organizational and communication skills * Professional use of the English language; both written and oral. * Experience in Object Oriented Programming (C\#, C\+\+, VBS, etc.…), scripting language (PERL, etc.), SAS, R, SQL * Understanding of CDISC standards (CDASH, SDTM, ADaM, etc.) * Experience in clinical database management system development. * Experience in a clinical, scientific or healthcare discipline. * Experience in utilizing various clinical database management systems * Broad knowledge of drug, device and/or biologic development and effective data management practices * Strong leadership and interpersonal skills * Must be able to communicate effectively in the English language. Preferred: * Oncology and/or Orphan Drug therapeutic experience * Base SAS®, SAS/STAT and SAS/ACCESS software * SAS Macro programming language * Advanced experience in Database Management, object\-oriented programming * Veeva set up experience * Medidata Rave certification Precision medicine is revolutionizing the attack on cancer—and we are passionate about helping you harness its power. We strike tumours on a molecular level using biomarkers to link specific mutations to specific treatments. We combine deep science with deep data from advanced technological platforms, then layer on specialized expertise in the design and execution of targeted, adaptive clinical trials. Ultimately, we deliver robust insights that inform real\-time decisions—and optimize the oncology development pathway. \#LI\-NC1 \#LI\-Remote Any data provided as a part of this application will be stored in accordance with our Privacy Policy. For CA applicants, please also refer to our CA Privacy Notice. Precision Medicine Group is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, age, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status or other characteristics protected by law. If you are an individual with a disability and require a reasonable accommodation to complete any part of the application process or are limited in the ability or unable to access or use this online application process and need an alternative method for applying, you may contact Precision Medicine Group at QuestionForHR@precisionmedicinegrp.com. It has come to our attention that some individuals or organizations are reaching out to job seekers and posing as potential employers presenting enticing employment offers. We want to emphasize that these offers are not associated with our company and may be fraudulent in nature. Please note that our organization will not extend a job offer without prior communication with our recruiting team, hiring managers and a formal interview process.

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

Negotiable Salary

Senior Data Engineer - Hybrid Intelligence64146411055107129

Indeed

Senior Data Engineer - Hybrid Intelligence

**At Capgemini Engineering, the world leader in engineering services, we bring together a global team of engineers, scientists, and architects to help the world’s most innovative companies unleash their potential. From autonomous cars to life\-saving robots, our digital and software technology experts think outside the box as they provide unique R\&D and engineering services across all industries. Join us for a career full of opportunities. Where you can make a difference. Where no two days are the same.** **About the role** **At Hybrid Intelligence, we are looking for a** **Senior Data Engineer** **to join the team. You will work in a team of experts with whom you can learn and develop professionally while participating in the growth and expansion of the team. As a member of the Hybrid Intelligence team at Capgemini Engineering, you will work on a variety of innovative projects that make a difference. Our work is a fusion of applied mathematics, scientific computing, artificial intelligence, and software engineering.** **Your profile:** * **At least 4 years of experience developing** **ETLs** **,** **designing** **and modeling databases in a Cloud environment.** * **Hands on experience with** **AWS \& DBT.** * **Knowledge and experience with orchestration and automation tools such as** **Airflow, Luigi, Docker, and/or Kubernetes.** * **Data processing languages such as Python,** ***SCALA*** **, Java, and/or Pyspark.** * **Fluent level of** **English \& Spanish.** **We value all applications.** **We offer a wide range of training options, including in\-person, online certifications, etc. Even if you don't have 100% of the desired skills, we would love to meet you! Having a disability certificate will be positively valued, in line with our inclusion and diversity policy.** **Our commitment to inclusion and equal opportunities is reflected in our Equality Plan and Code of Ethics, which ensure the professional development of our staff and equal opportunities in their selection 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 will you like about working here?** **We have a very comprehensive catalog of Development and Work\-Life Balance measures, such as, for example, and among others:** * **Support at the beginning** **with the Buddies program.** * **24 vacation days** **\+ 2 personal days \+ December 24 and 31 \+ the option to buy up to 7 vacation days per year.** * **Continuous training** **, you can enjoy Mylearning, Capgemini University, and our Digital Campuses. You will have access to platforms such as Coursera, Udemy, Pluralsight, Harvard Manager Mentor, Education First for languages (English, French, German...) among others!** * **International DATA \& AI Community** **, where you can collaborate with experts from around the world.** **Capgemini is a global business and technology transformation partner, helping organizations to accelerate their dual transition to a digital and sustainable world, while creating tangible impact for enterprises and society. It is a responsible and diverse group of 340,000 team members in more than 50 countries. With its strong over 55\-year heritage, Capgemini is trusted by its clients to unlock the value of technology to address the entire breadth of their business needs. It delivers end\-to\-end services and solutions leveraging strengths from strategy and design to engineering, all fueled by its market leading capabilities in AI, generative AI, cloud and data, combined with its deep industry expertise and partner ecosystem.** **\#LI\-JJ1****\#LI\-Hybrid**

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

Negotiable Salary

Laboratory technician for the Molecular Genetics of Angiogenesis group “supervised by Dr. Rui Benedito641464109355551210

Indeed

Laboratory technician for the Molecular Genetics of Angiogenesis group “supervised by Dr. Rui Benedito

The Centro Nacional de Investigaciones Cardiovasculares Carlos III (F.S.P.) (CNIC) has been conceived to develop research of excellence, competitive and of international relevance in relation to cardiovascular diseases. The CNIC has a research center of 24,000 m2, located in Madrid, with more than 6,000 m2 for laboratories equipped with a state\-of\-the\-art infrastructure and equipment. The Molecular Genetics of Angiogenesis group of the Centro Nacional de Investigaciones Cardiovasculares Carlos III (F.S.P.) (CNIC) led by Dr. Rui Benedito, is looking for a laboratory technician to provide experimental support to the laboratory. This contract will be funded with the project “*Bridging the gap between cardiac and vascular regeneration*, *acronym: RESCUE*” exp: AC23\_2/00019, which has received funding of the Instituto de Salud Carlos III (ISCIII) and cofounded by the European Union NextGenerationEU in the framework of the ERA4Health Partnership: Fostering a European Research Area for Health Research (ERA4Health\-CARDINNOV). **Functions:** The selected candidate will be responsible for carrying out technical tasks related to molecular biology protocols (qPCR, cloning, genotyping, etc.), histological and immunohistochemical techniques (dissection and fixation of tissues, embedding and fluorescence immunostainings) and participate in the maintenance of experimental model colonies. Finally, they will collaborate with the rest of the technical staff in managing common stock, preparing reagents and solutions, as well as maintaining order and good laboratory practices. **Mandatory Requirements** * Title of “**Formación Profesional Grado Superior**”, with at least 2 years of experience in biomedical research centers or “**Formación Profesional Grado Medio**”, with at least 5 years of experience in biomedical research, or “**Bachiller Superior**” in Biomedical Sciences with at least 2 years of experience in biomedical research centers. **Valuable Requirements:** * C1\. Experience in molecular biology techniques (DNA extraction, genotyping, etc.) * C2\. Experience in histology and immunostaining techniques * C3\. Experience in tissue dissection, fixation and embedding * C4\. Experience in small experimental model management and *in vivo* experimental procedures. * C5\. Experience in laboratory management and organization * C6\. Interview. Positive action**:** a correction index of 1\.5 is established for each year of experience in the evaluation of the number of years in those criteria where experience is evaluated, in the event that the disable person greater than 66% and 1\.2 in the event that the disable person greater than 33%. **We offer:** * Joining a modern Research Center of international relevance in the scientific field. * Integration into young teams in an environment of scientific excellence. * Access to a modern infrastructure with the most advanced technology * Immediate incorporation * “Contrato de actividades científico‐técnicas, de duración indefinida (texto refundido Ley 14/2011, de 1 de junio, de la Ciencia, la Tecnología y la Innovación)”, according to the article 23‐bis de la Ley de la Ciencia”, funded by the project “*Bridging the gap between cardiac and vascular regeneration*”, funded by the ISCIII through the “Acciones complementarias de programación conjunta internacional 2023”, exp: AC23\_2/00019, as long as the selected candidate complies with the legal requirements for the formalization of the contract in accordance with the Spanish labor law. **Recruiment Plan:** The RESOLUTION OF THE SECRETARIAT OF STATE FOR PUBLIC FUNCTION APPROVING THE COMMON ACTION CRITERIA FOR THE RECRUITMENT PROCESSES IN THE STATE PUBLIC SECTOR ENTITIES of April 11, 2022, sets forth in point 6\.1 that “Unless a specific regulation establishes a merit\-bases recruitment system (“concurso”), the competition (“concurso\-oposición”) must be the recruitment system”. In CNIC, the specific regulations approved by the Foundation's board of trustees establish a merit\-based recruitment system (“concurso”) including a personal interview. At least the 3 candidates with the highest score (as long as they reach the minimum of 70 points as a sum of criteria C1‐C5\) will be interviewed. The candidate with the highest score will be hired given the total score (C1\-C6\) is 90 points or higher. **Recruitment Commission:** * Head of “Molecular Genetics Lab” * Research Office Manager * Research OfficeTechnician * PhD student in “Molecular Genetics Lab” * HR member The CNIC guarantees, in its field of action, the principle of equality in access to employment, and cannot establish any discrimination, direct or indirect, based on reasons of origin, including racial or ethnic, sex, age, marital status, religion or convictions, political opinion, sexual orientation and identity, gender expression, sexual characteristics, union affiliation, social condition, language within the State and disability, provided that the workers are in conditions of aptitude to carry out the work or employment for which try they are assigned. By participating in the selection process, the participant agrees that their data appear in the public resolutions of the selection process. Such resolutions (provisional list of admitted and excluded, definitive list of admitted and excluded and resolution of the process) are published on the CNIC website. Criterios de puntuación: C1 \- Experience in molecular biology techniques (DNA extraction, genotyping, etc.) (will be assessed as a whole on the basis of the time/specialty ratio) \- 15% C2 \- Experience in histology and immunostaining techniques (will be assessed as a whole on the basis of the time/specialty ratio) \- 15% C3 \- Experience in tissue dissection, fixation and embedding (will be assessed as a whole on the basis of the time/specialty ratio) \- 20% C4 \- Experience in small experimental model management and in vivo experimental procedures (will be assessed as a whole on the basis of the time/specialty ratio) \- 20% C5 \- Experience in laboratory management and organization (will be assessed as a whole on the basis of the time/specialty ratio) \- 10% C6 \- Interview \- 20%

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

Negotiable Salary

Senior Manager, Market Access641464108509471211

Indeed

Senior Manager, Market Access

**If you are a current Jazz employee please apply via the Internal Career site.** Jazz Pharmaceuticals is a global biopharma company whose purpose is to innovate to transform the lives of patients and their families. We are dedicated to developing life\-changing medicines for people with serious diseases — often with limited or no therapeutic options. We have a diverse portfolio of marketed medicines, including leading therapies for sleep disorders and epilepsy, and a growing portfolio of cancer treatments. Our patient\-focused and science\-driven approach powers pioneering research and development advancements across our robust pipeline of innovative therapeutics in oncology and neuroscience. Jazz is headquartered in Dublin, Ireland with research and development laboratories, manufacturing facilities and employees in multiple countries committed to serving patients worldwide. Please visit www.jazzpharmaceuticals.com for more information. **Brief** **Description** Reporting to the Market Access Director, Sr Manager Value \& Access will be responsible for developing and implementing the value proposition of the company’s product portfolio to ensure and maintain the optimal access conditions according to the local and global strategies. He/she will assist in the development and execution of optimal price and access strategies The candidate must be an expert in the Spanish healthcare system with a deep understanding of drug funding, pricing, and reimbursement policies, especially in oncology. **Essential** **Functions** * Lead the Access Strategy: Develop and execute strategic market access plans for Jazz Pharmaceuticals' oncology drugs at all stages, from pipeline to launch and post\-launch. * Develop P\&R dossiers for the Ministry of Health and other evaluating agencies according to the strategic positioning, value proposition and pricing guidance. * Definition of Pricing and Reimbursement Strategy: Negotiate and manage pricing and funding agreements, exploring shared value models and other innovative solutions to optimize access under Global pricing guidance. * Contribute to the definition of price assumptions for Business Planning purposes. * Collaborate with HEOR and Medical Affairs to develop clinical evidence, real\-world evidence (RWE), and pharmacoeconomic models that support the value of Jazz Pharmaceuticals' products. * Relationships with Key Stakeholders: Establish and maintain strong relationships with decision\-makers and opinion leaders in healthcare management, scientific societies, and representatives of health administrations (central and regional). * Identify and anticipate access barriers at the regional level, participating in the design and implementation of action plans tailored to each Autonomous Region, including regional and hospital access processes. * Lead the development of support materials for regional access and commercial teams (arguments, value presentations, competitive environment analysis). * Actively participate in the launch of new molecules or oncology indications, in coordination with Commercial, Medical, and Government Affairs teams. * Market Intelligence: Stay updated on the evolution of the healthcare environment, funding policies, market trends, and competitive activities that may impact the access of Jazz Pharmaceuticals' drugs, with a special focus on oncology. * Internal Training and Support: Act as an internal expert in Market Access, providing training and support to commercial teams to ensure the access strategy is integrated into all commercial activities. * Cross\-functional Collaboration: Work transversally with Medical, Commercial, Legal, and global Patient Access \& Value teams to ensure strategic alignment and coherent execution. * Behave ethically, responsibly, and professionally in accordance with Jazz Pharmaceuticals values and codes of practice. * Ensure compliance with all applicable Laws, Codes, corporate standards, and Procedures related to her/his area of relevance/responsibility. * Strictly observe and know Jazz Pharmacovigilance’s Policy. **Required Knowledge, Skills, and** **Abilities** * Experience in Market Access in the pharmaceutical industry in the oncology area. * Deep knowledge in health economics, health technology assessment and health outcomes. * Deep knowledge of the Spanish healthcare system, including national and regional pricing and reimbursement processes, as well as the Spanish and European regulatory environment. * Deep understanding of the Spanish oncology environment: decision circuits, reference hospitals, clinical trials, and influence networks. * Excellent communication, negotiation, and influence skills, both in technical and institutional environments with ability to communicate complex or technical content in an influential way to non\-technical audiences * Commercial acumen * Proven ability to build strong relationships with key stakeholders, both internal and external. * Strategic Thinking: Ability to analyse complex data, interpret market information, and develop innovative and evidence\-based access strategies. * High orientation to results and ability to lead cross\-functional projects * Solid understanding of commercial and medical functions and how these contribute to a successful patient access approach. **Others** * Computer skills and in particular Microsoft Office (Word, PowerPoint and Excel) and Microsoft Outlook; * Fluent in english both oral and written communications **Required/Preferred****Education****and****Licenses** * Scientific and/or economic degree * A post\-degree in Health Economics/HTA, market access is preferred \#LI\-SM1 \#LI\-remote *Jazz Pharmaceuticals is an equal opportunity/affirmative action employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any characteristic protected by law.* The successful candidate will also be eligible to participate in various benefits offerings, including, but not limited to, medical, dental and vision insurance, retirement savings plan, and flexible paid vacation. For more information on our Benefits offerings please click here: https://careers.jazzpharma.com/benefits.html.

C. de Sta. María Magdalena, 48, Chamartín, 28016 Madrid, Spain

Negotiable Salary

Business Development Engineer, Customer Relations641464107541791212

Indeed

Business Development Engineer, Customer Relations

Holtec is seeking an experienced professional with business development expertise to support existing projects and grow the company’s core business in the energy industry. This role requires specific focus on commercial nuclear power plants, custom fabrication, and clean energy technologies. The Business Development Engineer will report to the Holtec Europe Program Manager and will be based in Madrid, Spain. The position will require frequent travel to client offices, fabrication facilities, and power stations within Europe and internationally. The ideal candidate will be well\-rounded in technical and commercial aspects of Holtec’s core business areas and capable of operating independently. In addition to developing and maintaining relationships with clients, the position includes additional responsibilities such as support to proposal and pricing preparation, etc. The candidate must be highly motivated, results\-oriented and capable of interacting with business executives. **Minimum Responsibilities**:* Build and maintain relationships with new and existing clients and partners in Holtec’s core business areas. * Provide support to Holtec’s US\-based and Holtec Europe’s project teams during project execution of projects, supporting the resolution of any technical, contractual, or regulatory issues with the client and interfacing with local subcontractors. * Initiate and develop new opportunities to expand Holtec’s business. * Provide support to proposals preparation in collaboration with Holtec Europe and Holtec corporate offices. * Identify and attend conferences and marketing events in territory that result in new business. * Register with potential clients for RFPs, by preparing and submitting bid\-qualification responses. * Identify suitable vendors for projects, coordinate and manage communications with the vendors. * Provide weekly sales reports on potential business opportunities. **Additional Responsibilities (depending upon candidate’s technical capabilities and interests)*** Work with the project management team to ensure that all customer requirements are met in the design, manufacturing and installation stages. * Support review of contracts with Holtec’s legal team and add value with regards to risk identification and mitigation strategies. * Manage/Coordinate Quality Oversight of local subcontractors. **Job Requirements:*** Bachelor’s Degree in Mechanical, Nuclear, or related Engineering or Scientific discipline. * Minimum of 5 years’ experience in the energy industry, preferably in the nuclear industry. * Minimum of 5 years’ experience in business development. * Fluent in English language. * Excellent communication, organizational and interpersonal skills. To apply please email your resume and cover letter to r.marin@holtec.com. Holtec International is a U.S.\-based diversified energy technology company with its corporate technology center located in Camden, New Jersey, which is located in Camden, NJ, part of the Philadelphia metropolitan area. The company's corporate headquarters are located in Jupiter, Florida. The company maintains several operations centers around the world, including major bases of operation in Pittsburgh (Pennsylvania), Orrville (Ohio), Kiev (Ukraine), Leiston (England), Pune (India), Rio de Janeiro (Brazil) and Madrid (Spain). RioCdrMNm6

C. del Gral. Cabrera, 29, Tetuán, 28020 Madrid, Spain

Negotiable Salary

Clinical Program Manager641464107946271213

Indeed

Clinical Program Manager

**About us** Idoven is a European healthtech company using artificial intelligence to advance the early diagnosis of cardiovascular diseases, the leading cause of death worldwide. Our CE\-marked AI platform, Willem, analyzes electrocardiograms (ECGs) from any device, helping doctors detect heart conditions faster, more accurately and at scale. Backed by the European Innovation Council, Horizon 2020, and top\-tier investors, we’re building technology with the potential to save millions of lives. We collaborate with leaders like AstraZeneca, Abbott and EIT Health, and our work has been recognized by the European Seal of Excellence, the U.S. National Academy of Medicine, CB insights' Digital Health Lists, and South Summit as Most Disruptive Startup. Global icons Iker Casillas and Pau Gasol support our mission as brand ambassadors, helping raise awareness around heart health. If you're looking to build technology with real\-world impact at one of Europe’s most promising deep\-tech companies, Idoven is the place to do it. **About the Role** The Clinical Program Manager is responsible for the design, management, execution of the assigned clinical studies / projects for regulatory submission or evidence generation, in support of the development of artificial intelligence algorithms in the cardiology space to impact the next generation of patient care, to achieve team\-level goals. **Responsibilities** * Design clinical study protocols with the support of the Team Manager, and develops the project plan in consultation with Idoven clinical team and under the supervision of the Team Manager * Ensure the execution of assigned clinical studies with the goal of adhering to target timelines, budget and quality * Ensure the clinical studies are audit\-ready at all times (e.g. project team training records, central files, system validation, etc.) * Medical oversight during trials and functions as SME for scientific and medical questions during the trials * Support all investigators and centres involved in multi\-centre studies * Prepare the documentation required for Ethics Committee approvals under the supervision of the Team Manager * Conduct on\-site visits to support qualifications, training on implementation and conduct of study protocols * Provide oversight of clinical projects to ensure safety concerns and/or adverse events or trends in Field Events Reporting are identified and appropriate responses are developed and executed * Be involved in control of device distribution and allocation * Evaluate clinical data in preparation of study summary reports for presentations, publications and submissions * Engage with Key Opinion Leaders to collect their input as needed for the clinical project **Requirements** **What you need to succeed** * Minimum of 2 years directly supporting clinical research or similar experience in a medical/scientific area * Proven expertise in the writing of clinical and non\-clinical research protocols including trial design and methodology, and research publications. * Experience running multi\-centre studies from start to end * Proficient knowledge of medical terminology in cardiology * Expertise with Good Clinical Practices (GCPs) and regulatory compliance for clinical trials (e.g. applicable ISO Standards, CE Mark) * Bachelor's degree in Statistics, Science, Engineering or related field. PhD is a strong asset. * Spanish and English are a must. Other European languages are highly valued. * Excellent time management, planning, and organizational skills **Benefits** Be part of one of the most disruptive startups in HealthTech and AI and make a difference Personal and professional growth as part of a fast\-growing, international team No corners cut in having the best tech equipment to do your job Unlimited remote working environment, where you can choose to work from home and attend our Madrid office whenever you want to Learning and development opportunities and training budget Flexible Remuneration * ️ Health Insurance provided by IDOVEN Access to Wellhub (Gympass), empowering your physical and mental wellness! **️** Remote Work Allowance for your home office setup! 23 holidays, your birthday off, and December 24th and 31st half days to celebrate! Regular team events and Thursday happy hours And much more! At IDOVEN, we believe in hiring top talented people like you \- ambitious, forward thinkers who want to make a difference in the world and have an impact. **Diversity \& Inclusion** At Idoven, we believe diverse teams build better products. We are an equal opportunity employer and welcome applicants from all backgrounds, regardless of race, gender identity, age, religion, sexual orientation, or disability.

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

Negotiable Salary

Product Manager Endocutters & Bariatrics641464106398731214

Indeed

Product Manager Endocutters & Bariatrics

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

Negotiable Salary

Indeed

MSL HAP - Centro

At Johnson \& Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com **Job Function:** Medical Affairs Group**Job Sub Function:** Medical Science Liaison**Job Category:** Scientific/Technology**All Job Posting Locations:** Madrid, Spain**Job Description:** Job Description Johnson \& Johnson, a leader in the industry, is seeking to hire a Medical Scientific Liaison professional for its **Pulmonary Arterial Hypertension** unit **based in Madrid.** With the most compelling portfolio and pipeline in the sector, J\&J offers the opportunity to be part of an innovative, cutting-edge, and industry-leading project. As part of Johnson \& Johnson, our mission is to transform patients' lives through the discovery and development of innovative solutions addressing the most important medical needs of our time. We are looking for talented professionals with unlimited motivation to contribute, learn, and strong team players, willing to take on any challenge and achieve excellent results. We seek individuals who can identify opportunities and proactively drive their own development. **Main Responsibilities:** * To keep abreast of **medical and scientific knowledge.** + Continuous update on products, patient’s treatment trends, clinical activities and studies conducted within the therapeutic area in their region. * Development and maintenance of a **contact network with Leading Specialists**. + Understand their needs, key value drivers, practical treatment patterns and scientific activities within therapeutic area + Communicate value of company products, incl. clinical questionnaire discussions + Through scientific interactions, communicate medical benefits of products and contribute to foster innovative approaches + Represent the company within professional associations in the therapeutic area in cooperation with Medical Affairs/ Medical Education and other positions in the Medical Affairs Department * Proactive and reactive **communication of medical scientific data** according to following criteria * Proactive Scientific Communication to Leading Specialists must be consistent with the last approved Summary of Product Characteristics regarding the safe and effective use of approved products in approved indications. Content of Scientific Communication should be highly scientific, accurate, fair and objective, based on an up\-to\-date evaluation of all relevant evidence and reflect that evidence clearly, using neither marketing claims nor brand name. * In some very specific circumstances, the MSL can interact proactively with non\-Leading Specialists. The program should be clearly defined in the MSL Country Activity Plan, providing the rational, the objective, content, timelines and selection criteria of the HCPs to be involved. * Description of R\&D programs and discussing regulatory developments with no promotional intent are also part of Scientific Communication. * Reactive Communication of medical scientific data can be provided upon request to any Health Care Professional, within the approved label or off\-label. The request should come either directly from the HCP or via the Medical Information department. MSLs are required to document all off\-label information requests they receive from Leading Specialists and other HCPs that they may interact with. * Organization and participation in **Medical Education activities,** at local \&/regional level: + Identify/support/educate speakers + Build Medical Education programs with scientific third party + Collaborate with Medical Education manager in National Medical education activities + Provide scientific material under request. MSLs may initiate discussion with potential speakers, discussing documents/ slides which may be of help for future presentations. * Organization and participation in **Advisory Boards** in cooperation with Medical Affairs/Medical Education/other positions in the Medical Affairs Department. * **Market Access Discussions** MSLs can present highly scientific, accurate, fair and objective data to Payors (Hospital Formulary Committees, Health Insurers, Health Technology Assessment Committees, etc) to provide them with objective information about Company products. * **Pre\- Approval Activities** MSLs can engage in interactions with Payors to raise awareness so that payors can plan and budget so that patients can receive the product when it becomes available. MSLs can organize Speakers training to prepare speakers for delivering presentations to other HCP when the Marketing Authorization is granted. * Provision of **scientific support to company Sales Representatives** and other company representatives + Provide medical and product training and scientific support to Sales Representatives in coordination with Training/Medical Affairs Department as appropriate + Act as a reference point to Sales Representatives for any scientific query, in collaboration with Medical Information as appropriate. * **Local implementation of Medical Affairs Plan** in their areas: + Support the set up and follow up of local company sponsored studies, registries and other non\-interventional Medical Affairs studies + Propose investigators and sites for interventional and non\-interventional Medical Affairs studies. + Participate in investigator meetings preparation, recruitment follow\-up and study result presentation. + Receive investigator proposals for IIS and ensure they are discussed within the Medical Affairs department for decision. * Through scientific interactions, **gain valuable insight** into treatment patterns and scientific activities in the therapeutic area and provide input and a strategic view to the company Medical Affairs Plan / business decision\-making. * Observes and promotes all regulatory requirements as defined in applicable regulations, rules and procedures established by the Company, including but not limited to **Health Care Business Integrity and Pharmacovigilance** * Follow principles, procedures and training included in SAFE Fleet program. * GCO collaboration: Support GCO studies when needed through the identification of potential sites and facilitating a direct contact with leading specialists. * Report all suspected adverse reactions, serious or non serious, I may be aware of within a maximum of 24 hours after being aware of it and communicate it to the Pharmacovigilance Department. Additionally, for all employees involved in Research Related Activities (RRA): * Ensure safety reporting requirements (timely AE/PQC reporting) as set out in company policies and SOPs (Standard Operating Procedures) are met and appropriately managed when planning projects, developing materials, executing projects and contracting vendors. * Ensure HCC and legal requirements (Fair Market Value, Transfer of Value rules, Promotional Materials rules) are fully understood, appropriately managed and complied with when planning projects, developing materials, executing projects and contracting vendors. * Ensure inspection readiness with respect to personal training compliance, and availability of recent CV and individualized Job Description. **Qualifications** * Scientific degree: Medical Doctor, Pharmaceutical or Nature Science university degree, or related qualification (i.e. psychology degree) * Deep knowledge of the therapeutic area, strength in research and interpretation of medical data * Background to be accepted by the Leading Specialists in peer\-to\-peer relationship, i.e. relevant work experience, scientific acumen and/or communication skills. * Highly customer focused with an awareness of the importance of business results * Innovative with the ability to coordinate and drive a complex and changing environment * Awareness of, and adherence to, Johnson \& Johnson Credo values and International Health Care Business Integrity Guide. **Special Requirements** * Deep scientific knowledge in the therapeutic area

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

Negotiable Salary

Clinical Project Coordinator - Entry Level641464105116191216

Indeed

Clinical Project Coordinator - Entry Level

Job Summary : Due to continuous business growth and a strong study pipeline, we are looking for Project Coordinators to join our successful and growing Spanish team and engage in clinical trial management on a day to day level. This position will work with our operational teams to accomplish tasks and projects that are instrumental to the company’s success. Responsibilities : * Work closely with the Project Clinical Trial Manager for timely delivery of recurrent tasks consistently with a high degree of accuracy; * Maintain and track study supply inventory for study sites and coordinate shipping efforts of study materials; * Compile and maintain project\-specific status reports within the Clinical Trial Management System (CTMS); * Interact with the internal project team, Sponsor, study sites, and third\-party vendors; * Ownership of the Trial Master File; * Create and maintain project timelines and enrolment projections; and * Coordinate project meetings and produce quality minutes. Qualifications : * Clinical trial experience is beneficial; * Masters’ Degree in Life Sciences; * Excellent oral and written English Language communication skills; * Knowledge of Microsoft Office programs; * Excellent organisational and prioritisation skills; * Ability to work collaboratively on projects with others; * Strong attention to detail. **We ask that you please submit your CV in English.** Medpace Overview : Medpace is a full\-service clinical contract research organisation (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

Negotiable Salary

Nondestructive Testing (NDT) Technology Intern641464105564171217

Indeed

Nondestructive Testing (NDT) Technology Intern

**Nondestructive Testing (NDT) Technology Intern** -------------------------------------------------- **Welcome to the future of nuclear energy**, where Westinghouse Electric Company is leading the field with expertise and innovation to shape the power of tomorrow. At Westinghouse, innovation is in our DNA. We are creative. We think differently. We reimagine the possible across the nuclear industry every day. **About the role:** ------------------- As a Nondestructive Testing (NDT) Technology Intern you will report to the NDT Technology Manager and be located at the Madrid headquarters in San Sebastián de los Reyes with a hybrid work schedule (remote and in\-office). This is a part\-time and paid internship from September 2025, with the possibility to receive course credit. **Key Responsibilities:** ------------------------- * Participate in projects to develop inspection techniques for new plants under construction (Hinkley Point C (HPC)), plants in operation (Spain), and new reactors and fusion facilities (ITER or IFMIF\-Dones) * Perform simple tasks related to the development of Nondestructive testing techniques (ultrasounds) * Develop inspection techniques for metallic and composite materials * Verify the integrity of the main components and systems for Nuclear Power Plants for License Renewal, Life Extension, Long\-Term Operation, and the construction of new reactors based on new requirements * Conduct inspection of structures to verify the integrity of the components and locate and identify indications that may affect their correct operation **Qualifications:** ------------------- * Degree in Engineering (Physics, Chemistry, Math, or similar) * Experience with scientific software, AutoCAD, * Knowledge in wave propagation * Proficient in Spanish and English \#LI\-Hybrid **Why Westinghouse?** --------------------- We know that to put forth your best effort, you need to be challenged and enjoy what you do in a supportive and respectful environment. We aim to maintain this balance by offering our employees the amenities, benefits and training they need to reach personal and professional goals. **Below is an example of what employees in Spain can expect:** * Attractive stipend. * Hybrid model of work. * High flexibility and autonomy. * Learning and development opportunities. * We encourage our employees to participate in community service events and other team\-building activities to strengthen their bonds and inspire each other. **You can learn more about Westinghouse by visiting** http://www.westinghousenuclear.com. Westinghouse is an Equal Opportunity Employer including Veterans and Individuals with Disabilities.

G9VM+CM, 28703 San Sebastián de los Reyes, Madrid, Spain

Negotiable Salary

Indeed

VALUE OFFICE MANAGER

LAS ROZAS DE MADRID, M, ES, 28232 CaixaBank is a financial group with a socially responsible universal banking model with a long-term vision, based on quality, proximity and specialization, offering a tailored value proposition of products and services for each segment, embracing innovation as a strategic challenge and a distinctive feature of its culture, and whose leading position in retail banking in Spain and Portugal enables it to play a key role in contributing to sustainable economic growth. What projects do we develop? The manager's mission is to coordinate and execute the financial monitoring model for both investments/expenses and efficiencies of the Cosmos Program. Specifically, their responsibilities will be: * Generate information to ensure alignment of all project budgets with the overall financial plan of Cosmos * Execute the financial monitoring model for Cosmos projects, define metrics, establish KPIs, etc. * Carry out periodic financial monitoring, ensuring the collection of necessary information and generating the required financial management reports for the leadership of the Cosmos program and its governance bodies * Calculation and generation of information to track efficiencies included in the Cosmos financial plan * Definition and implementation of estimators that objectively assess projects * Definition and implementation of a framework enabling standardization, measurement and objective assessment of efficiencies and value contribution from COSMOS projects * Generate analytical information at project level to enable productivity measurement, considering all costs, efficiencies and value contributions arising from their execution. Minimum requirements * Knowledge of financial and accounting concepts * Proficiency and ease using presentation tools (PowerPoint) * Experience in implementing transformational projects * Advanced technological knowledge (Software Development, Infrastructure Management, Architecture) * Analytical skills with proven experience in cost allocation systems, cost savings, productivity measurement... Key competencies * Integrity * Focus on execution and results * Organizational ability * Autonomy and initiative * Capacity for analysis and conceptualization. * Adaptability to change and interest in professional development * Proactive attitude and strong work ethic * Teamwork skills * Negotiation skills (area managers, project leaders, etc.) * Strong analytical capability What do we offer? * Be part of the most innovative bank in Western Europe, according to The Innovators awards by the U.S. magazine Global Finance. * Onboarding program and personalized support for your professional development. * Individual training pathway with access to our online platform, which offers an extensive catalog of self-learning resources to foster your continuous growth. * You will have a comprehensive health insurance fully covered at no cost. Additionally, you will be enrolled in the Pension Plan, to which CaixaBank will make contributions focused on your future. * Flexible compensation applicable to transportation, training, languages, childcare, among others. * Flexibility measures (remote work, flexible start times). * We hold the Top Employer certification, recognizing us as one of the best companies to work for. Job profile Responsible for defining and implementing the functional application map, aligning application functionalities with business objectives. Additionally, they are responsible for the definition, coordination and monitoring of the technology strategic plan Competencies **HARD SKILLS** DEFINITION OF CUSTOMER VALUE PROPOSITION SOFTWARE, TECHNOLOGY AND MARKET TOOLS TECHNOLOGICAL ENVIRONMENTS BANKING AND/OR FINANCIAL PRODUCTS AND SERVICES PROJECT MANAGEMENT BUSINESS CASE TI PLATFORMS AND PROCESSES IT TRENDS NEGOTIATION ADVISORY ON SOLUTION PROJECTS CORPORATE STRATEGY API STRATEGY, ALM AND SYSTEM INTEGRATION WITH THIRD PARTIES RESEARCH ON TRENDS AND IMPACTS OF AI ON BUSINESS CONCEPTUALIZATION AND DESIGN OF DIGITALIZATION PROJECTS EXECUTIVE PRESENTATION DEVELOPMENT OPPORTUNITY IDENTIFICATION IT ARCHITECTURE**SOFT SKILLS** ALLIANCES – COMMUNICATION HUMANISM – COMMUNICATION AND EMPATHY ALLIANCES – COLLABORATION AND CROSS-FUNCTIONALITY ALLIANCES – INFLUENCE ALLIANCES – CUSTOMER ORIENTATION HUMANISM – LEADERSHIP AND TEAM DEVELOPMENT / SELF-LEADERSHIP ANTICIPATION – ANTICIPATION AND CHANGE MANAGEMENT EMPOWERMENT – FOCUS ON RESULTS DIVERSITY – PROMOTION OF DIVERSITY

C. del Caño, 9, 28231 Las Rozas de Madrid, Madrid, Spain

Negotiable Salary

Indeed

Energy Consultant

Are you looking for a professional challenge at a leading company? Join Bureau Veritas as an Energy Verifier! What will make you succeed in this position? * University degree: Engineer or Graduate in: Mining, Industrial, Chemical, Civil Engineering, Hydraulic Engineering, Public Works, Industrial Technical Engineer, Architect, Technical Architect, Degree in Energy Engineering or equivalent. * Experience in carrying out energy consultancy or audits. * Having the CEM® (Certified Energy Manager) certification awarded by the AEE (Association of Energy Engineers) will be valued. Also, having accredited certification in 'Measurement and Verification of Energy Savings from Energy Efficiency Projects'. * Knowledge and experience in regulations related to energy audits, particularly Royal Decree 56/2016\, will be valued. What will your main responsibilities be? * Conducting integral CAES verifications. * Strategic and risk analysis. * Preparation of technical reports. * Collection and analysis of information. * Management of findings and conclusions. What can we offer you? * Competitive salary according to the candidate's experience and skills. * Opportunities for professional development nationwide, an innovative environment and challenging projects. If you want to help us leave a mark and build together a safer and smarter society, alongside a united team and within a leading company with very large clients where you can see different things and keep learning... APPLY NOW! * *At Bureau Veritas we offer equal opportunities. No candidate or employee will receive less favorable treatment due to their gender, marital status, sexual orientation, color, race, ethnic origin, religion, disability or age.* *At Bureau Veritas we have a strict Code of Ethics that ensures diversity and inclusion and equal opportunities.*

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

Negotiable Salary

Industrial Safety Engineer - Technical Office Manager638412897152011220

Indeed

Industrial Safety Engineer - Technical Office Manager

Are you looking to lead a team of industrial safety experts and contribute to the development of innovative solutions? What will your responsibilities be? * Lead the technical office specialized in industrial safety engineering. * Perform industrial safety engineering and design assessments for large-scale industrial projects. * Act as chairperson in HAZID and HAZOP processes, and in risk assessment (quantitative risk analysis (QRA/FERA) and consequence analysis). * Use specialized safety software. * Ensure compliance with safety standards and regulations. * Supervise, train, and develop junior team members. * Support the commercial team in preparing proposals. What are the requirements? * University degree and/or master's in Industrial Engineering. * Master's in Industrial Engineering or similar and/or PhD is desirable. * Advanced level of English. French and/or Portuguese is desirable. * Minimum 10 years of experience in industrial safety engineering. Join a leading company that will invest in you and lead a team of experts, contributing to a safer future. Apply now!

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

Negotiable Salary

C/C++ Development La Marañosa638412895151371221

Indeed

C/C++ Development La Marañosa

**C/C\+\+ Developer La Marañosa** --------------------------------------- **C/C\+\+ Developer with experience in Database Design – Technology and Industrial Sector \| La Marañosa Campus (San Martin de la Vega, Madrid)** **Do you have experience in C/C\+\+ development and database design? Are you interested in joining innovative projects in sectors such as aerospace, industrial, or technology?** **At Capgemini Engineering, a global leader in engineering and R&D services, we are seeking a C/C\+\+ Developer to join a multidisciplinary technical team at the La Marañosa Campus in San Martin de la Vega (Madrid), participating in high-impact projects.** **What will you do?** * **Develop C/C\+\+ solutions for demanding technical environments.** * **Design and optimize databases for critical applications.** * **Apply object-oriented programming principles and UML modeling.** * **Collaborate with technical teams in an international environment.** **What are we looking for?** **\-University degree in Engineering (Aerospace, Industrial, Computer Science, Telecommunications, Naval), Architecture, Mathematics, Physics, or Data Science.** * **Minimum of 2 years of experience in C/C\+\+ development.** * **Minimum of 2 years of experience in database design.** * **Knowledge of UML and object-oriented programming.** * **Minimum English level B1 (technical communication and documentation).** **We also value:** * **Master's or official PhD in related fields.** * **English level C1 or higher.** **Technical certifications such as:** * **CLE – C Certified Entry\-Level Programmer** * **CPE – C\+\+/C\# Certified Entry\-Level Programmer** * **IBM – C\+\+/C\# Programming Essentials Professional Certificate** * **CPA – C\+\+/C\# Certified Associate Programmer** **What do we offer?** * **Permanent contract and involvement in stable, high-tech value projects.** * **Competitive salary aligned with your experience.** * **Social benefits: meal allowance, childcare voucher, continuous training.** * **Personalized career plan and real growth opportunities.** **\#LI\-LG1**

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

Negotiable Salary

AP1000 SRO training instructor638400066895391222

Indeed

AP1000 SRO training instructor

**Welcome to the future of nuclear energy**, where Westinghouse Electric Company is leading the field with expertise and progress to shape the power of tomorrow. At Westinghouse, innovation is in our DNA. We are creative. We think differently. We reimagine the possible across the nuclear industry every day. **About the role:** ------------------- As an AP1000 SRO Training Instructor you will deliver high\-level training, with passion for teaching, and your pedagogical skills. You should demonstrate organizational abilities such as teamwork, customer orientation and progress. You will report to the Operations and Technical Training Manager and be located at Madrid. Hybrid position with a mix of on\-site and off\-site model. **Main Responsibilities:** -------------------------- * Participate in all stages of the SAT process of the initial and continuing education programs of their specialty. * Manage the analysis, design and implementation of initial and continuous training needs in their specialty. * Design, development and implementation of the sessions corresponding to the initial and continuous training courses of licensed and non\-licensed operations personnel, including teaching sessions in the classroom, plant, and the simulator. * Collaborate in the analysis and implementation of corrections in the simulator when any type of malfunction is detected, and collaborate in the tests. * Coordinate training, providing support to training committees and planning training programs. * Define and collaborate in the development of advanced educational means (simulators, multimedia, videos, and models...) related to the assigned responsibilities; and in the maintenance and updating of those already available. **Requirements:** ----------------- Graduates of a University Degree or Master's Degree in scientific\-technical specialties (Engineering, Physics...). 7\+ years of experience as an operation instructor. Availability to establish residence in our Madrid Headquarters or a nearby location. Proficient in English language. Availability to travel and stay in national and international locations during participation in projects sporadically Driver's license required. Experience in power plants or industrial facilities valuable. \#LI\-Hybrid **Why Westinghouse?** --------------------- We know that to put forth your best effort, you need to be challenged and enjoy what you do in a supportive and respectful environment. We aim to maintain this balance by offering our employees the amenities, benefits and training they need to reach personal and professional goals. **Below is an example of what employees in Spain can expect:** * Great compensation * Hybrid model of work. * High flexibility and autonomy. * Great benefits for your convenience and safety: + Peer\-to\-peer recognition program. + Lunch allowance. + Private health insurance + Life insurance. + Employee Assistance Program: confidential counseling and resources for employees, eligible dependents, and household members * Learning and development opportunities. * We encourage our employees to participate in community service events and other team\-building activities to strengthen their bonds and inspire each other. **You can learn more about Westinghouse by visiting** http://www.westinghousenuclear.com. Westinghouse is an Equal Opportunity Employer including Veterans and Individuals with Disabilities.

G9VM+CM, 28703 San Sebastián de los Reyes, Madrid, Spain

Negotiable Salary

Field Service Engineer638400067256331223

Indeed

Field Service Engineer

**Bring more to life.** Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology? At Leica Microsystems, one of Danaher’s 15\+ operating companies, our work saves lives—and we’re all united by a shared commitment to innovate for tangible impact. You’ll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher’s system of continuous improvement, you help turn ideas into impact – innovating at the speed of life. Shape the Future with Us! At **Leica Microsystems**, we have been shaping the future for over 175 years with groundbreaking optical and digital solutions. With a culture rooted in customer focus, innovation, and teamwork, we lead the market in microscopy, imaging, and analysis, unveiling the invisible and empowering our customers to build a better, healthier world. Joining **Leica Microsystems** means contributing to scientific discoveries and supporting surgeons in making critical decisions. Our advanced microscopes and AI\-based image analysis solutions enable users to gain profound insights into development and engineering challenges. Here, you will work on meaningful projects alongside passionate colleagues, driving progress and pushing the boundaries of what’s possible. Learn about the Danaher Business System which makes everything possible. The **Field Service Engineer** is responsible for ensuring quick resolution of complex customers challenges and empowering team members with their functional knowledge. Working across all levels of the business, you will play a key role in contributing to the growth of overall business beyond service as well. This will require collaborating with team members at the point of impact and across the organization. Identify and implement opportunities to improve, while also operating as a change agent to ensure processes and standard work are being sustained and effective. This position reports to the Iberia Service Manager and is part of the Iberia Service Team. The FSE will be based in Madrid , however the role will be fully remote. **In this role, you will have the opportunity to:** * Delight customers through timely and competent response to their needs, coupled with clear communication \& Collaborate closely with the Service Team to ensure all customers in the region are provided a professional after\-sales service. * Support Sales Representatives in activities such as installations and demo/exhibitions. Conducts service, repair and/or installation of products or IT solutions at customer site, including electrical and mechanical testing, in accordance with maintenance contracts. * Responds to customer support calls within an assigned territory. Diagnoses system failures and determines most cost\-effective solution. Escalates complex issues to greater level of technical support or quality reporting system. * Help our organization grow by high quality support of our existing customers and by helping us identify new customers and opportunities during your time in the field **The essential requirements of the job include**: * Bachelor’s Engineer Degree Required or similar * Fluent in English and Spanish * Excellent Microsoft Office application skills (Word, Excel, PowerPoint) * Strong communication skills * Ability to travel within the Spain Central Region and eventually to the rest of Regions in Iberia. (Up to 70% travel). Must have a valid driver’s license with an acceptable driving record. Ability to lift, move or carry equipment \& tools. **It would be a plus if you also possess previous experience in:** Handling repairs, calibrations, upgrades and allied tasks. Networking, influencing, and communicating effectively across functions and at all levels. Excellent visual, written, and other communication skills. Training and/or coaching experience. Experience in maintaining, applying global processes. Track record of delivering standardization, simplification and continuous improvement across key business areas. Experience in working in a matrix organization including building relationships remotely and cross culturally. Leica Microsystems, a Danaher operating company, offers a broad array of comprehensive, competitive benefit programs that add value to our lives. Whether it’s a health care program or paid time off, our programs contribute to life beyond the job. Check out our benefits at Danaher Benefits Info. At Leica Microsystems we believe in designing a better, more sustainable workforce. This job is also eligible for bonus/incentive pay. We offer comprehensive package of benefits including paid time off, life insurance, pension plan, ticket restaurants and discount benefits webpage. Join our winning team today. Together, we’ll accelerate the real\-life impact of tomorrow’s science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life. For more information, visit www.danaher.com.

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

Negotiable Salary

Manager, Clinical Trial Management638400067610891224

Indeed

Manager, Clinical Trial Management

Precision for Medicine is growing! We are looking for a Manager, Clinical Trial Management to join our European team. The position could be covered fully remotely from Spain, Poland, Slovakia, Serbia, Hungary or Romania. **Position Summary:** * The Manager, Clinical Trial Management (MCTM) offers an additional development path for clinical research professionals. Responsibilities focus on the management and career development of the organization's Clinical Trial Managers (CTM, Sr. CTM, and Principal Clinical Trial Managers (PCTM) , as well as supporting the development of departmental initiatives to strengthen the quality and productivity of Clinical Trial Management operations. * This position requires the ability to independently lead, manage, and motivate a team of CTMs (employee and/or consultant) to a standard consistent with Precision for Medicine's values and overall focus on quality. The Manager will ensure studies are conducted in accordance with applicable SOPs, regulations, and ICH GCP principles. **Essential functions of the job include but are not limited to:** * Develop, mentor, coach and manage CTMs, and PCTMs to progress their skillset as per Precision for Medicine quality standards. Advocate individual growth and career development * Work with the Clinical Operations Management Team and management of other functional areas to continually improve and enhance CTM expectations and procedures to promote quality, consistency and efficiency while achieving established Key Performance Indicators (KPIs) * Collaborate with the Resourcing team to ensure Clinical Operations resource allocations and needs are appropriately met * Generate action plans and provide developmental/strategic oversight to optimize CTM services, with a focus on high quality delivery of individual/team/departmental goals * Provide on\-going feedback and development to manage the performance of direct reports. * Provide technical support and guidance (including scope definition, risk identification, escalation and mitigation, resource planning, goals, and deliverables) to assigned CTMs * Ensure all assigned CTMs have the proper resources, training, materials, and access to systems to deliver on the expectations of their position * Ensure CTMs uphold high quality standards and maintain compliance with established SOPs, working guidelines, project plans and all regulatory requirements * Ensure CTMs provide timely and accurate updates of all required administrative material (SOPs, T\&E, etc.) on company systems. * Recognize, exemplify, and adhere to Precision's values that center on our commitment to quality, our people, clients, and performance * Perform other duties and departmental initiatives as assigned by Leadership **Minimum Required:** * 4\-year college degree or equivalent experience ideally in a scientific or health related field * 5\+ years of industry experience in clinical research, including clinical operations experience in a pharmaceutical company or CRO, **with proven Line Management experience of the Clinical Trial Managers** * Experience in managing clinical aspects of complex and global trials * Working knowledge of ICH GCP guidelines and the clinical development process * Excellent communication and interpersonal skills to effectively interface with others in a team setting * Excellent organizational skills, attention to detail, and a customer service demeanor * Ability to travel domestically and internationally including overnight stays **Competencies:** * Direct work experience in a global, cross\-functional clinical management environment * Ability to develop, coach and mentor CTM staff and hold personnel accountable to achieve goals and address training needs * Proven experience in risk management and change management * High level of integrity and must inspire and demand the highest standards from assigned CTMs * Exhibits high self\-motivation, and the ability to work and plan independently as well as in a team environment * Excellent time management, negotiation, critical thinking, decision making, analytical and interpersonal skills * Excellent presentation, verbal, and written communications skills * Demonstrated successful independent negotiation and conflict management strategies * Demonstrates a high degree of professionalism, as evidenced by punctuality, ability to deliver on commitments, an understanding of the service culture and positive interactions with customers and team \#LI\-TB1 \#LI\-Remote Any data provided as a part of this application will be stored in accordance with our Privacy Policy. For CA applicants, please also refer to our CA Privacy Notice. Precision Medicine Group is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, age, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status or other characteristics protected by law. If you are an individual with a disability and require a reasonable accommodation to complete any part of the application process or are limited in the ability or unable to access or use this online application process and need an alternative method for applying, you may contact Precision Medicine Group at QuestionForHR@precisionmedicinegrp.com. It has come to our attention that some individuals or organizations are reaching out to job seekers and posing as potential employers presenting enticing employment offers. We want to emphasize that these offers are not associated with our company and may be fraudulent in nature. Please note that our organization will not extend a job offer without prior communication with our recruiting team, hiring managers and a formal interview process.

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

Negotiable Salary

Education Manager Iberia638400066384671225

Indeed

Education Manager Iberia

The Straumann Group is a global leader in tooth replacement and orthodontic solutions. Renowned for our innovative spirit and clinical excellence, we partner with dental professionals worldwide to enhance patient outcomes and quality of life. With a broad portfolio of products and services—including implants, clear aligners, biomaterials, and digital dentistry solutions—we are shaping the future of oral care. Our success is rooted in collaboration, trust, and a commitment to education and continuous learning. Reporting to the Head of Marketing, the Education Manager is responsible for executing Straumann’s Group customer education strategy in Iberia, with a strong focus on Key Opinion Leader (KOL) management. This role bridges internal and external stakeholders to deliver impactful education initiatives, optimize KOL utilization, and support continuous learning across the dental community and Straumann’s commercial teams. Key Responsibilities Key Opinion Leader (KOL) Management \& Speaker Coordination: * Lead the coordination of speaker deployment and KOL involvement in external educational initiatives, ensuring strategic alignment and value delivery. * Collaborate closely with the International Team for Implantology (ITI) to co\-develop local initiatives, study clubs, and support joint education formats. * Support the identification, development, and retention of high\-potential KOLs together with Brand Managers and the Head of Marketing \& Education. * Serve as the primary liaison for KOLs, both internally and externally. * Maintain a dynamic and trusted network of dental professionals to support study clubs, peer\-to\-peer events, and scientific exchange. * Collaborate with senior management and partners to enhance speaker content and performance through structured development programs. * Ensure consistent, high\-quality content delivery aligned with company goals across all KOL\-led activities. * Coordinate and align the key messages to be delivered by external speakers during company\-hosted events, ensuring consistency with brand strategy and educational objectives. Customer Education (External) * Execute and manage customer education programs tailored to the Iberia market for Straumann’s Group portfolio. * Collaborate with global HQ, regional teams and Iberia Brand Manager to localize and implement strategies for product launches and system updates. * Develop and maintain annual, quarterly, and monthly education calendars and reports. * Gather customer feedback and satisfaction data to evaluate and continuously improve the learning experience. * Plan, budget, and execute external education activities with a focus on effectiveness, quality, and ROI. Internal Training (Employees \& Commercial Teams) * Lead internal training initiatives to ensure the Iberian Team is fully equipped with up\-to\-date product and clinical knowledge. * Collaborate with global/regional training teams to ensure internal messaging and educational content consistency. * Support the onboarding of new employees and facilitate knowledge\-sharing across departments. * Represent the Iberian Region in global training sessions and contribute as a facilitator where needed. Qualifications \& Experience * Bachelor’s or Master’s degree in life science or related discipline. * 5\+ years of experience in customer education, KOL management, or clinical training—preferably within the dental or medtech industry. * Proven success in coordinating speaker engagement and curriculum\-driven educational programs. * Strong project management and stakeholder communication skills. * Fluent in English, written and verbal; local language is a must. * Familiarity with CRM systems, digital learning tools, and LMS platforms is preferred. Key Competencies * Excellent relationship\-building and interpersonal skills. * Strong communication and interpersonal abilities, with experience presenting to diverse audiences. * Customer\-focused mindset with a strong sense of initiative. * Comfortable managing multiple projects, deadlines, and budgets. * Willingness to travel regionally Excellent project management and organizational skills. At Straumann Group, we are committed to building a diverse and inclusive environment where every team member feels valued, heard, and empowered to contribute. We welcome applicants from all backgrounds and walks of life, and we believe that diverse perspectives lead to stronger innovation, better decision\-making, and a more meaningful impact on the communities we serve.

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

Negotiable Salary

Regulatory Affairs, Senior Specialist/Manager638400064235551226

Indeed

Regulatory Affairs, Senior Specialist/Manager

**Company Description** Ergomed Group is a rapidly expanding full service mid\-sized CRO specialising in Oncology and Rare Disease. Since its foundation in 1997 the company has grown organically and steadily by making strategic investments and landmark acquisitions, with operations in Europe, North America and Asia Our company allows for employee visibility (you have a voice!) creative contribution and realistic career development. We have nourished a true international culture here at Ergomed. We value employee experience, well\-being and mental health and we acknowledge that a healthy work life balance is a critical factor for employee satisfaction and in turn nurtures an environment from which a high\-quality client service can be achieved. Come and join us in this exciting journey to make a positive impact in patient’s lives. **Job Description** Ergomed is looking for a Regulatory Affairs professionals with in\-depth experience in managing global complex clinical studies. Opportunities are open to any geographical location; however, candidates will be required to possess excellent written and communication skills in English as well as good understanding of clinical trials environment/ICH GCP. Main responsibilities for the role are: * Assume leadership and functional representation for projects and/or deliverables of medium/high complexity ensuring effective and rapid coordination and management and execution of SSU/regulatory tasks, driving the team to meet the agreed targets and to comply with the agreed procedures, trackers and templates. * Develop strategy and manage set up activities (SSU RA Management Plan, procedures and core documents) ensuring compliance and consistency with department standards. Support team members in preparing project strategy, identifying issue and providing resolution. * Author/contribute towards the preparation and/or review of complex technical/scientific/legal documentation. * Ensure preparation, collection, review of regulatory information and documents to support submissions to FDA, EMA and national authorities (CTA/INDs, MAAs/NDAs/BLAs, ODDs, PIPs) as well as Ethic Committees/IRBs for initial authorisation and maintenance, in compliance with the applicable regulations. * Provide expert advice to Clients addressing complex regulatory queries ensuring consistent and high\-quality advice across all regions. * Ensure that all communications with Regulatory Authorities and Ethics Committees/IRBs are carefully tailored to the specific requirements and tale place only when essential guidance cannot be obtained through other available resources. * Ensure all team members assigned to the project for departmental deliverables are aware of the tasks and time allocated, monitor project budgets, hours spent vs budgeted and promptly identify and escalate any OoS. * Assist in securing new business or repeated business by participating to BDMs, developing and reviewing regulatory sections of proposals, regulatory costing and budgets. * Provide training, coaching and mentoring to junior members of staff. **Qualifications** * Bachelor's Degree in Chemistry, Life Sciences or Medicine * Minimum 3 years within CRO industry * Proven ability to successfully manage global projects * Expert knowledge of ICH GCP and/or GVP and comprehensive understanding of relevant legislation/ regulatory requirements globally * Very good written and verbal communication skills to clearly and concisely present information **Additional Information** We prioritize diversity, equity, and inclusion by creating an equal opportunities workplace and a human\-centric environment where people of all cultural backgrounds, genders and ages can contribute and grow. To succeed we must work together with a human first approach. Why? because our people are our greatest strength leading to our continued success on improving the lives of those around us. We offer: * Training and career development opportunities internally * Strong emphasis on personal and professional growth * Friendly, supportive working environment * Opportunity to work with colleagues based all over the world, with English as the company language **\#LI\-remote**

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

Negotiable Salary

Principal Global Feasibility Lead FSP EMEA. Sponsor dedicated.638400064604171227

Indeed

Principal Global Feasibility Lead FSP EMEA. Sponsor dedicated.

**Description** Principal Global Feasibility Lead FSP EMEA. Sponsor dedicated. Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities. Our Clinical Development model brings the customer and the patient to the center of everything that we do. We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to work with, but to make us easier to work for. Whether you join us in a Functional Service Provider partnership or a Full\-Service environment, you’ll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals. We are agile and driven to accelerate the delivery of therapies, because we are passionate to change lives. Discover what our 29,000 employees, across 110 countries already know: **WORK HERE MATTERS EVERYWHERE** Why Syneos Health * We are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program. * We are committed to our Total Self culture – where you can authentically be yourself. Our Total Self culture is what unites us globally, and we are dedicated to taking care of our people. * We are continuously building the company we all want to work for and our customers want to work with. Why? Because when we bring together diversity of thoughts, backgrounds, cultures, and perspectives – we’re able to create a place where everyone feels like they belong. **Job Responsibilities** * Is able to independently undertake the highest complexity level RFPs and Feasibility objectives across all therapeutic areas; confidently assesses the level of data and analysis required and proposes reasonable approaches for RFPs and individual paid or partnership feasibility assessments. + Proactively liaises with Business Units, Business Development, Medical Directors, Business Analysts, and other members of the team as needed to review RFP challenges and works collaboratively to a solution with no oversight required. + Proactively identifies solutions to non\-standard requests. Applies knowledge/skills to a range of moderately complex activities. Appropriate identification and escalation of issues from mentoring to management as needed. + Acts as representative of Global Feasibility in all interactions with internal and external stakeholders, with the highest degree of collaboration, professionalism, integrity, quality. + Capability to work efficiently within processes and undertake delivery of an average to higher number of assignments and complexity concurrently across all therapeutic areas as needed. * Development, analysis and delivery of pre\-award site level feasibility assessments into presentations and/or written reports for delivery to internal/external stakeholders, independently. + Upholds highest standards of Global Feasibility role; o Maintains comprehensive records of work and stores all relevant data within internal libraries in a timely manner, independently, without audit issues. o Excellent editing\-level verbal, written and visual communication skills. o Independently manages and performs research of scientific literature using internet and internal metrics and tools to provide background information, with a high degree of understanding and detail. o Independently supports the preparation of material for and attends bid defense teleconferences and meetings, under minimal review and supervision of a line manager or delegate. + May coordinate work of other team members as needed on larger joint projects, multi\-study assignments or alliance/ FSP partnerships. + Ability to mentor junior team members up to Senior Feasibility Lead, Global Feasibility level providing text and slide deck editing, data collection and processing insights across all therapeutic indications. + New team member mentoring upon discretion of the Line Manager. + Supports department management in development of group initiatives and achieving business objectives. May participate in and support activities related to department staff operations. + Actively participates in developing relevant metrics to measure the impact of data asset use, protocol feasibility assessments, other departmental activities. + May participate as departmental Subject Matter Expert (SME) or represent Feasibility in development of feasibility\-impacted processes and systems, including evaluation of departmental data asset assessments and support collection of associated metrics. + May be asked to develop, audit and maintain departmental systems for storage and retrieval and analysis of historical feasibility data in support of current RFPs and RFIs. **Get to know Syneos Health** Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and 675,000\+ Trial patients. No matter what your role is, you’ll take the initiative and challenge the status quo with us in a highly competitive and ever\-changing environment. Learn more about Syneos Health. http://www.syneoshealth.com **Additional Information** Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description. The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. Further, nothing contained herein should be construed to create an employment contract. Occasionally, required skills/experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees. The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job. **Summary** Feasibility Analytical Lead for the sponsor

C. del Gral. Cabrera, 29, Tetuán, 28020 Madrid, Spain

Negotiable Salary

Data Project Manager - Hybrid Intelligence638400063864351228

Indeed

Data Project Manager - Hybrid Intelligence

**At Capgemini Engineering** , the world leader in engineering services, we bring together a global team of engineers, scientists, and architects to help the world’s most innovative companies unleash their potential. From autonomous cars to life\-saving robots, our digital and software technology experts think outside the box as they provide unique R\&D and engineering services across all industries. Join us for a career full of opportunities. Where you can make a difference. Where no two days are the same. At Hybrid Intelligence, we are looking for a **Project Manager** to join the team. You will work in a team of experts with whom you can learn and develop professionally while participating in the growth and expansion of the team. As a member of the Hybrid Intelligence team at Capgemini Engineering, you will work on a variety of innovative projects that make a difference. Our work is a fusion of applied mathematics, scientific computing, artificial intelligence, and software engineering. ### **Your profile** * PhD or graduate degree in mathematics, physics, engineering, computer science, or a related field. * At least 4 years of previous experience as Project Manager. * Experience working with multidisciplinary teams. * Hands\-on experience managing AI solutions and agile methodologies. * Fluency in English and Spanish (C1\) and strong communication skills. Valuable technical knowledge and experience as a data scientist. * We value all applications. We offer a wide range of training options, including in\-person, online certifications, etc. Even if you don't have 100% of the desired skills, we would love to meet you! Having a disability certificate will be positively valued, in line with our inclusion and diversity policy. Our commitment to inclusion and equal opportunities is reflected in our Equality Plan and Code of Ethics, which ensure the professional development of our staff and equal opportunities in their selection 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 will you like about working here?** We have a very comprehensive catalog of Development and Work\-Life Balance measures, such as: * Support at the beginning with the Buddies program. * 24 vacation days \+ 2 personal days \+ December 24 and 31 \+ the option to buy up to 7 vacation days per year. * Continuous training: enjoy Mylearning, Capgemini University, and our Digital Campuses. You will have access to platforms such as Coursera, Udemy, Pluralsight, Harvard Manager Mentor, Education First for languages (English, French, German...), among others! International DATA \& AI Community, where you can collaborate with experts from around the world. * Capgemini is a global business and technology transformation partner, helping organizations to accelerate their dual transition to a digital and sustainable world, while creating tangible impact for enterprises and society. It is a responsible and diverse group of 340,000 team members in more than 50 countries. With its strong over 55\-year heritage, Capgemini is trusted by its clients to unlock the value of technology to address the entire breadth of their business needs. It delivers end\-to\-end services and solutions leveraging strengths from strategy and design to engineering, all fueled by its market\-leading capabilities in AI, generative AI, cloud and data, combined with its deep industry expertise and partner ecosystem. \#LI\-GV1

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

Negotiable Salary

Indeed

Trainee Architecture

Architecture Europe Region   MAD0000DV Requisition \# **Shape a future with purpose at Arup in Spain** **Highlighting project diversity in our Architecture Team in Spain** Arup’s purpose, shared values, and collaborative approach have set us apart for over 75 years, guiding how we shape a better world. We have been present in Spain since 1993 and we have a team of more than 300 engineers, consultants, and qualified technical personnel. We work for clients from the public and private sectors, providing creative and sustainable solutions based on the efficient use of resources. From lead design to technical specialist architecture, we have expertise in a wide range of sectors and design across all scales and types. Our teams help clients to develop exhilarating sporting venues, produce environmentally ambitious commercial developments, connect communities through intuitive and efficient transport systems, and deliver cutting edge scientific and industrial facilities. **The Opportunity** This is your chance to be part of the Architecture Team at Arup in Spain. It young and dynamic team that grows in an organic and agile way and is currently working on a wide variety of projects around the world. Building on our extensive global experience, we have established an architecture team in Madrid to enhance our ability to deliver multidisciplinary and integrated designs to our clients for a growing number of technically, socially and functionally complex projects. **As an Arcchitecture Trainee at Arup, you will:** * Participate in the ideation and presentation of Architecture and interior design proposals under the direction, assistance and supervision of the line manager. * Collaborate in writing effective and creative presentations. * Support in the completion of 3D modeling, images, diagrams, freehand drawings and mockups within a wide range of scales and project stages. * Have the possibility of going to site **Does this role inspire you?** We are looking for someone proactive and dynamic to develop their career in the Architecture field. Ideally, you’ll bring: * Currently studying a degree or master’s in architecture. * Fluent level of English and Spanish skills. * Ability to work as a team * Knowledge of Rhinoceros, AutoCAD, Office package, InDesign and Photoshop. **Bonus points if you:** * Have the ability to use rendering programs, such as VRay and/or similar. * Have an interest in digital tools and the use of other programs such as Illustrator **Conditions** * Be enrolled in the university to be able to establish an agreement with the University * Immediate incorporation * Duration: 6 months of extendable internship (possibility of joining after completing the internship) * Schedule: From 20 to 40 hours per week to be defined with the student * Remuneration: will depend on the student's level of training and the number of hours established. **How to apply for the internship?** To apply for this internship, register your updated CV,portfolio and a cover letter in English. **Why Arup?** At Arup, we offer a rewarding career with a global company committed to a better future. Our unique trust ownership structure allows us to prioritize meaningful work and invest in our people. We also offer a unique profit share program, allowing our members to share in the results of our collective efforts. **Benefits that work for you:** * **Professional Growth \& Development**: Benefit from continuous learning opportunities, training programs, and mentorship to enhance your skills and advance your career at Arup. * **Global Opportunities**: Collaborate with colleagues worldwide and explore potential short\-term or long\-term assignments at other Arup offices and project locations. * **Financial Well\-being \& Ownership**: Receive a competitive salary and benefits package and share in Arup's success through our global profit\-sharing programme. * **Work\-Life Balance**: We offer a hybrid working model and flexible working arrangements to support work\-life balance. * **Well\-being and Culture:** Access to a range of well\-being programs, including sports subsidies, social activities, and initiatives promoting a healthy work\-life balance. We foster a diverse and inclusive culture where everyone feels welcome, respected, and valued. Arup is recognized as one of the best companies to work for in Spain in 2024 by Actualidad Económica and Forbes magazine, thanks to our flexibility policies. We also adhere to the Code of Principles of Generational Diversity, committing to equal opportunities regardless of age. At Arup, you belong to an extraordinary collective where individuality is encouraged. Our strength comes from how we respect, share, and connect our diverse experiences, perspectives, and ideas. You’ll have the opportunity to do socially useful work that has meaning—to Arup, to your career, and to the clients and communities we serve. We are proud to be an equal opportunity employer and are committed to building a workplace that reflects the rich diversity of the world around us. We actively promote a culture of inclusion where everyone feels welcome, respected, and valued. We welcome applications from talented individuals of all backgrounds, regardless of age (within legal limits), gender identity or expression, disability, ethnicity, religion, sexual orientation, or any other protected characteristic. We are committed to making our recruitment process and workplaces accessible. If you need any assistance or adjustments, please contact beatriz.estefania@arup.com. We’re here to support you. **Do you want to join us in shaping a better world?**

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

Negotiable Salary