Uceda Science & Technology Job Listings - OK

Browse

Antiques Collectibles

Baby Kids Items

Books · Movies And Music

Home Improvement Supplies

Musical Instruments

Office Supplies

Administration & Office Support

Advertising · Arts & Media

Banking & Financial Services

Call Center & Customer Service

CEO & General Management

Community Services & Development

Consulting & Strategy

Design & Architecture

Education & Training

Farming · Animals & Conservation

Government & Defense

Healthcare & Medical

Hospitality & Tourism

Human Resources & Recruitment

Information & Communication Technology

Manufacturing · Transport & Logistics

Marketing & Communications

Mining · Resources & Energy

Real Estate & Property

Retail & Consumer Products

Science & Technology

Self Employment

Sport & Recreation

Trades & Services

Property For Sale

Property For Rent

Home Improvement

Repair And Technical Support

Writing · Translation · And Transcription

Activities & Groups

Artists & Musicians

Classes & Lessons

Friendship & Networking

Travel & Travel Partners

Skills & Language Swap

···

Log in / Register

Science & Technology in Uceda

Best Match

Filter·1

Science & Technology

Uceda

Salary

Job Type

Workplace type

Unit

Location:Uceda

Category:Science & Technology

Science Teacher – Baccalaureate (Long-term replacement)65174530059523120

Science Teacher – Baccalaureate (Long-term replacement)

Position Summary: The SEK Ciudalcampo International School is seeking a Science Teacher – Biology for the Baccalaureate programme to deliver innovative and motivating lessons, fostering a dynamic, future-oriented learning environment. Key Highlights: 1. Teaching Biology and Geology (National Baccalaureate and IB) 2. Use of active methodologies and laboratory as an essential resource 3. Tutoring of MYP5 group (4th year of ESO) and collaboration with teaching staff The **SEK Ciudalcampo International School** requires the immediate incorporation of a **Science Teacher – Biology for the Baccalaureate programme**, for a **long-term replacement**, within its Science Department. ### **Mission:** Deliver lessons using an innovative and motivating approach, fostering a dynamic, future-oriented learning environment that inspires students to achieve their maximum academic and personal potential. ### **Responsibilities:** * Teach **Biology and Geology in the National Baccalaureate** and **Biology in the International Baccalaureate (DP)**, ensuring rigorous instruction aligned with the curriculum. * Employ active methodologies and the **laboratory as an essential resource** for practical learning and applied understanding of scientific content. * Assume **tutoring responsibilities for an MYP5 group (4th year of ESO)**, including academic monitoring, personalised guidance, and support for students’ holistic development. * Collaborate with the teaching team in designing educational strategies and academic performance improvement plans. * Create a positive, stimulating classroom environment consistent with SEK values and the SEK profile. ### **Subjects to be taught:** **National Baccalaureate (BTO):** * Biology and Geology – BTO 1 * General Biology – BTO 1 * Biology – BTO 2 **International Baccalaureate (DP):** * Environmental Systems and Societies (ESS) – DP1 and DP2 ### **Requirements:** * **Qualification:** Bachelor’s or Master’s degree in Biology or related fields. * **Experience:** Prior experience in National Baccalaureate and/or International Baccalaureate (DP) will be valued. * **Languages:** Instruction in Spanish (English proficiency not required). * **Digital competencies:** Basic proficiency in Microsoft Office and educational applications. * **Competency profile:** Flexible, motivated individual with a vocation for teaching, a positive attitude, and alignment with the **SEK profile**. ### **What we offer:** * **Long-term replacement contract**. * **Immediate start**. * **Full-time schedule**, Monday to Friday (9:00–17:00). * International, innovative, and collaborative educational environment. **Location:** SEK Ciudalcampo International School **#LI-AG1**

C. del Camino del Sur, 6, 28109 Alcobendas, Madrid, Spain

Biology Teacher65156655996546121

Biology Teacher

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

P32P+C5 Cerceda, Spain

Laboratory Technician65156659209859122

Laboratory Technician

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

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

Laboratory Equipment Sales Representative65156656500610123

Laboratory Equipment Sales Representative

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

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

ELECTRICAL ENGINEER65137707951875124

ELECTRICAL ENGINEER

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

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

Mathematics, Physics, and Chemistry Teacher for 1st Year of Bachillerato near Hospital Infanta Sofía Metro Station65137459541761125

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

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

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

Food Safety and Quality Technician65137459057282126

Food Safety and Quality Technician

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

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

Sustainability Intern65137331750018127

Sustainability Intern

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

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

Revenue Financial Controller - Laboratorio Central Health Diagnostics Quirónsalud (Alcobendas)65106073484547128

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

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

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

Intern65106073466754129

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

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

Associate Clinical Trial Manager (PhD) - Neuroscience / Ophthalmology650936654097931210

Associate Clinical Trial Manager (PhD) - Neuroscience / Ophthalmology

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

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

Energy Efficiency Engineer650936652145931211

Energy Efficiency Engineer

* **About Us** Our engineering firm is seeking to strengthen its team with a certified professional capable of leading energy efficiency projects. * **Position** We are hiring an Architect or Engineer in Spain, duly authorized to issue and sign Energy Efficiency Certificates (EECs) under the CAE scheme. * **Main Responsibilities** · Preparation and signing of EECs in accordance with Spanish regulations. · Energy diagnosis and audit of buildings (new and existing). · Development of energy efficiency improvement projects. · Administrative and regulatory follow-up of certifications. · Collaboration with internal engineers and technicians. · Participation in construction, rehabilitation, and sustainable renovation projects. * **Candidate Profile** · Degree in Architecture or Engineering recognized in Spain. · Current registration with the Official College of Architects (or equivalent for engineers). · Legal authorization to prepare and sign EECs. · Experience in energy audits or sustainable design is valued. · Knowledge of Spanish energy efficiency regulations (RD 390/2021, etc.). · Proficiency in energy certification software (CE3X, HULC, etc.). · French language required. · Rigor, autonomy, and ability to work as part of a team. * **Terms** · Contract: CDD (fixed-term) · Location: MADRID · Remuneration: commensurate with profile and experience · Start date: as soon as possible * **Applications** Send CV to: contact@energestia.es Employment type: Full-time Work location: On-site

C. de Alonso Heredia, 14, Salamanca, 28028 Madrid, Spain

Data Analyst (wind sector) - Remote650935380776981212

Data Analyst (wind sector) - Remote

DESCRIPTION **Data Analyst (Wind Sector) \- Remote** ---------------------------------------- **Company:** Eosol Group **Location:** Remote **Experience Level:** 2\+ Years Eosol Group is seeking a highly analytical and detail\-oriented Data Analyst to join our growing team, focusing on the dynamic wind energy sector. This remote position offers an exciting opportunity to contribute significantly to strategic decision\-making by providing robust data\-driven insights. You will work closely with the VP of Tower Sourcing, playing a pivotal role in optimizing our sourcing workflows and cost structures. **About the Role:** As a Data Analyst at Eosol Group, you will be instrumental in transforming raw data into actionable intelligence. You will immerse yourself in the intricacies of tower sourcing, meticulously analyzing data to identify trends, inefficiencies, and opportunities for enhancement. Your responsibilities will include ensuring data integrity, developing insightful reports, and recommending process improvements to foster greater transparency and efficiency within the organization. **Key Responsibilities:** * **Strategic Support:** Provide comprehensive analytical and data\-driven support to the VP of Tower Sourcing, influencing key strategic decisions. * **Workflow Understanding:** Develop a deep and nuanced understanding of tower sourcing workflows, including associated cost structures and data flows. * **Data Cleaning \& Structuring:** Proactively identify inconsistencies, errors, and gaps within existing datasets. Perform thorough data cleaning, organization, and standardization to ensure the reliability and accuracy of all reporting. * **Data Analysis \& Insight Generation:** Conduct in\-depth analysis of sourcing and cost data to detect emerging trends, pinpoint inefficiencies, and uncover opportunities for improvement. This includes meticulous tracking of Risks \& Opportunities (R\&O). * **Reporting \& Visualization:** Design, develop, and maintain dashboards and reports using Power BI and advanced Excel techniques. Effectively present complex data findings in a clear, concise, and easily understandable format for various stakeholders. * **Process Improvement:** Recommend and implement enhancements to data management and reporting processes. Drive initiatives that lead to improved data quality, accessibility, and actionable insights, ultimately enabling better transparency across the organization. * **Collaboration:** Work collaboratively with cross\-functional teams to gather data requirements and deliver insights that support business objectives. * **Problem\-Solving:** Address data\-related challenges and develop innovative solutions to improve data accuracy and reporting effectiveness. **Qualifications:** * Bachelor's degree in a quantitative field such as Statistics, Mathematics, Economics, Computer Science, or a related discipline. * A minimum of 3 years of professional experience in a Data Analyst role, preferably within the energy sector or a related industry. * Proven experience in data cleaning, transformation, and manipulation. * Demonstrated ability to analyze complex datasets and derive meaningful insights. * Proficiency in data visualization tools, particularly Power BI. * Advanced proficiency in Microsoft Excel, including complex formulas, pivot tables, and data modeling. * Strong understanding of database concepts and SQL. * Excellent analytical, problem\-solving, and critical\-thinking skills. * Exceptional communication and presentation skills, with the ability to explain technical concepts to non\-technical audiences. * Self\-motivated and able to work independently in a remote environment. **Preferred Skills:** * Experience with Python or R for data analysis. * Familiarity with data warehousing concepts. * Knowledge of the wind energy sector, including sourcing and supply chain dynamics. * Experience with cloud data platforms (e.g., Azure, AWS). * Understanding of statistical modeling and forecasting techniques. **Join Eosol Group:** If you are a passionate Data Analyst looking to make a significant impact in the renewable energy sector, we encourage you to apply. Eosol Group is committed to fostering a collaborative and innovative work environment where your contributions are valued and recognized. This is an excellent opportunity to grow your career with a forward\-thinking company.

Senior Medical Writer - Sponsor dedicated - Remote role based in Europe650854635635211213

Senior Medical Writer - Sponsor dedicated - Remote role based in Europe

**Description** Senior Medical Writer \- Sponsor dedicated \- Remote role based in Europe 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** * Leads the clear and accurate completion of medical writing deliverables, ensuring scientific information is presented clearly and accurately. Manages medical writing activities associated with individual studies, coordinating medical writing activities within and across departments with minimal supervision. Leads the resolution of comments from the client. * Completes a variety of documents that may include clinical study protocols and clinical study protocol amendments; clinical study reports; patient narratives; annual reports; investigator brochures; informed consents; annual reports; plain language summaries; periodic safety update reports, clinical development plans; IND submissions; integrated summary reports; NDA and eCTD submissions; journal manuscripts; and abstracts, posters, and presentations for scientific meetings. * Adheres to established regulatory standards, including, but not limited to, ICH E3 guidelines, as well as company standard operating procedures, client standards, and company and/or client approved\-templates, authorship requirements, and style and formatting guides, when completing medical writing projects, on time and on budget. * Coordinates quality and editorial reviews. Ensures source documentation is managed appropriately. Leads team document reviews, and reviews documents as needed. * Acts as peer reviewer for internal team to ensure document scientific content, clarity, overall consistency, and proper format. * Reviews statistical analysis plans and table/figure/listing specifications for appropriate content, and for grammar, format, and consistency. Provides feedback to further define statistical output required and document needs. * Interacts and builds good working relations with clients, department head, and peers in data management, biostatistics, regulatory affairs, and medical affairs, as necessary, to produce writing deliverables. * Performs online clinical literature searches and complies with copyright requirements. * Identifies and proposes solutions to resolve issues, escalating as appropriate. Provides technical support, training, and consultation to department and other company staff. May contribute to development of internal materials and presentations or changes to internal process, standard practices, and capabilities. * Mentors and leads less experienced medical writers on complex projects, as necessary. * Develops deep expertise on key topics in the industry and the regulatory requirements and guidelines that affect medical writing. * Aware of budget specifications for assigned projects, working within the budgeted hours and communicating status and changes to medical writing leadership. * Completes required administrative tasks within the specified timeframes. * Performs other work\-related duties as assigned. * Minimal travel may be required (less than 25%). Qualifications: * 3\-5 years of relevant experience in science, technical, or medical writing. * Experience working in the biopharmaceutical, device, or contract research organization industry required. * Strong understanding of FDA and ICH regulations, other regulatory guidelines, and/or good publication practices strongly required. * Experience writing relevant document types required. * Extensive knowledge of English grammar and ability to communicate clearly; strong familiarity with AMA Manual of Style. **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** Roles within the Medical Writing job family are responsible for writing and editing manuscripts and other medical communications on clinical studies and/or scientific reports including special summaries from raw data for submission to regulatory agencies or for in\-company use, monographs, comprehensive reviews, scientific exhibits, and other projects requiring skill in medical communication such as screening, analyzing, and summarizing additional data from other sources as needed. Conducts systematic literature searches and reviews. Prepares literature for new products and revises existing medical communication. Reviews and analyzes statistical outputs to prepare results\-based documents such as clinical study reports and development safety update reports. Supports engagement and interaction with regulatory agencies through preparation of briefing books and response documents to health authority questions.Impact and ContributionIndividual contributors with responsibility in a professional or technical discipline or specialty, but may manage two or fewer employees. May direct the work of lower level professionals or manage processes and programs. The majority of time is spent contributing to the design, implementation or delivery of processes, programs, and policies, using knowledge and skills typically acquired through advanced education. Individual contributor with developing subject matter expertise and responsibility for processes. In\-depth knowledge and skills within a professional discipline, understanding the impact of work on related areas. May be responsible for entire projects or processes within area of responsibility.

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

Industrial Water Treatment Technician650713364327691214

Industrial Water Treatment Technician

Do you have experience in industrial water treatment plants (WWTPs, WTPs, etc.)? Have you worked with pumps, valves, dosing systems, and purification processes? At this time, as a recruitment consultancy, we are looking for an **Industrial Water Treatment Technician** for our client, located in **Madrid**. The **job** focuses on **operating, controlling, and maintaining** wastewater or industrial water treatment facilities, ensuring the process runs correctly and complies with regulatory parameters. **FUNCTIONS AND RESPONSIBILITIES** * Operation, supervision, and maintenance of industrial water treatment systems. * Monitoring and control of processes such as **filtration, sedimentation, chemical dosing, chlorination, pumping, and automation**. * Preventive and corrective maintenance of associated equipment (pumps, valves, instrumentation, sensors, etc.). * Conducting basic water analyses and making adjustments based on results. * Supporting commissioning activities, resolving incidents, and providing technical support to clients when required. * Coordinating with the plant’s technical team and office staff to ensure proper facility operation. **REQUIREMENTS** * Vocational training (FP) in electromechanics, electricity, or industrial maintenance. * Minimum 2 years’ experience in hydraulic or electrical installations. * Knowledge of advanced water treatment technologies (RO, EDI, MBR, etc.). * Valid driver’s license type B. **What does the company offer?** * Permanent contract. * Working hours: Monday to Friday, 8–3 p.m., and Saturdays, either 8–1 p.m. or 9–2 p.m. * Salary: €30–32K (negotiable). * **Company car.** Reclut is a boutique recruitment and headhunting consultancy. It offers personalized services tailored to each client’s specific needs. Its mission is to help companies find the best talent, as well as to provide new career opportunities for job seekers.

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

€ 30,000-32,000/year

Product Analyst | Remoto650604909585951215

Product Analyst | Remoto

DESCRIPTION At **KENOS Technology**, we are looking for a **Product Analyst** with at least **3 years of experiencie** to join a complex project in the **automotive** sector within an **international** team. **This is a remote position based in Spain.** **What you will do** * **Analyze and translate business \& user needs** into clear requirements, user stories, and acceptance criteria in collaboration with the Product Owner. * **Facilitate alignment and drive prioritization** of the product backlog based on value, impact, and strategic goals. * **Identify and drive process optimizations** and improvements within the team and its workflows. * **Develop metrics and KPIs** to enable data\-driven decisions, continuous improvement, and transparent reporting. * **Proactively identify and mitigate product risks** (e.g., legal, data privacy) in collaboration with relevant departments. REQUIREMENTS **At least 3 years of experiencie with...** * **Strong** **analytical and problem\-solving skills**. * Proficient user of website and user behaviour analytics tools such as **Google Analytics****,** **Adobe Analytics** **or similar** and solid understanding of **Data Layers****.** * Knowledge of **data visualisation** and reporting tools such as **Google Looker Studio.** * A **collaborative approach** and ability to support strong team dynamics. * **Fluent in English** (C1 required). If you meet the requirements and are interested in joining our team, we look forward to receiving your application!

Cook/Cook - Residential Center DomusVi Alcalá de Henares650600312160011216

Cook/Cook - Residential Center DomusVi Alcalá de Henares

**Description:** ---------------- At DomusVi, caring means **sharing humanity**, growing as a professional, and being part of work that transcends everyday life. We are looking for professionals who wish to practice their vocation in an environment where empathy, innovation, and respect are part of every working day. **Why DomusVi?** Because we are the largest network of socio-healthcare centers and services in Spain, with over **28,000 committed professionals**. We operate from a close, professional, and human perspective, where each user, employee, and family member matters. **Our values define us:** * **The art of caring:** We apply knowledge and humanity to care and well-being. * **Pioneering spirit:** Innovation and technology are part of our daily routine. * **Innate empathy:** We value active and empathetic listening. * **Shared trust:** We foster relationships based on commitment and mutual trust. * **Emotional sincerity:** We bring authenticity to every relationship. **What you’ll find at DomusVi** * A culture centered on caring for and respecting people (users, employees, families). * An interdisciplinary and collaborative team that supports you, listens to you, and helps you develop. * Job stability and conditions adapted to your needs. * Time to devote to what matters most: high-quality care. * Spaces to develop and grow professionally. **What will you do as a cook?** * Support and assist the Head Chef and/or Kitchen Manager. * Receive orders: control products upon receipt, verify raw materials. * Prepare menus following the Technical Sheets for each dish included in the menu. * Know and ensure compliance with current regulations regarding food service. * Ensure the established service is delivered to maximize user satisfaction. * Access and use the DOMUSCHEF tool to: generate daily production reports and place orders for raw materials needed to prepare menus (in the absence of the Kitchen Manager/Head Chef). **What we offer:** * **Contract: temporary, 3 to 6 months, with conversion to permanent contract** * **Working hours: 89%** * **Shifts: rotating, 08:30–15:00 / 15:30–21:30** * **Start date:** immediate * **Work environment:** collaborative and respectful * **Work-life balance** * **Continuous training, Social Benefits, and Professional Development:** enabling you to grow within a company in constant evolution. **Requirements:** --------------- * Candidate with training in Hospitality and Catering and at least 12 months’ experience in a similar position, preferably in Collective Catering. * Positive consideration will be given to candidates holding Food Handler certification and training on the safe use of cleaning chemicals. * Positive consideration will be given to candidates holding additional training related to the field, as well as complementary training promoting Equality. **Would you like to work somewhere your vocation and professional development go hand in hand?** At DomusVi, **we share humanity**, caring for both those we serve and those who form part of our team. **We look forward to welcoming you!**

C. de Santiago, 22, 28801 Alcalá de Henares, Madrid, Spain

Clinical Research Physician650493813260811217

Clinical Research Physician

Job Summary : We are seeking Clinical Research Physicians to join our dynamic team. The Clinical Research Physician will have overall responsibility for providing medical, scientific, and strategic leadership for the successful planning, execution, and reporting of clinical trials. Additionally, this role acts as the Medpace internal medical expert and will serve as a medical resource for the review, presentation, and interpretation of results in the Clinical Study Report. The Clinical Research Physician will also be involved in the development of new clinical projects, including study design, protocol, and project plans as required. We are currently seeking Clinical Research Physicians in the following Therapeutic Areas: * Psychiatry * Pediatric / Neuromuscular Neurology * GI / Hepatology * Dermatology * Metabolic / Endocrinology \*\*All Medical Directors have hybrid WFH flexibility. Responsibilities : * Provide medical management and expertise for clinical trials; * Contribute medical expertise to study reports, regulatory documents, and manuscripts; * Manage safety issues in clinical trials and work closely with associates in evaluation and assessment of the trials; * Participate in new business development through involvement in proposal and sponsor meetings as requested; * Coordinate with other departments in all phases of the studies and trials including feasibility assessments, design processes, educational efforts, management of medical information, and reviewing and editing of medical documents; * Follow specific research related protocol and lead others in strict adherence to the policies. Qualifications : * Must have an M.D. degree or equivalent. Board certification and current medical licensure are preferred; * Must have prior clinical trial research experience; and * Previous experience in pharmaceutical\-related clinical research is preferred. **Travel**: up to 20% Medpace Overview : Medpace is a full\-service clinical contract research organization (CRO). We provide Phase I\-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti\-viral and anti\-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40\+ countries. Why Medpace? : People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today. The work we’ve done over the past 30\+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future. **Medpace Perks** * Flexible work environment * Competitive compensation and benefits package * Competitive PTO packages * Structured career paths with opportunities for professional growth * Company\-sponsored employee appreciation events * Employee health and wellness initiatives **Awards*** Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024 * Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility **What to Expect Next** A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.

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

Pediatric / Neuromuscular Neurologist650493813096981218

Pediatric / Neuromuscular Neurologist

Job Summary : We are seeking a Pediatric / Neuromuscular Neurologist to join our dynamic team. The Medical Director will have overall responsibility for providing medical, scientific, and strategic leadership for the successful planning, execution, and reporting of clinical trials. Additionally, this role acts as the Medpace internal medical expert and will serve as a medical resource for the review, presentation, and interpretation of results in the Clinical Study Report. The Medical Director will also be involved in the development of new clinical projects, including study design, protocol, and project plans as required. We are currently seeking Medical Directors in different locations. \*\*All Medical Directors have hybrid WFH flexibility. Responsibilities : * Provide medical management and expertise for clinical trials; * Contribute medical expertise to study reports, regulatory documents, and manuscripts; * Manage safety issues in clinical trials and work closely with associates in evaluation and assessment of the trials; * Participate in new business development through involvement in proposal and sponsor meetings as requested; * Coordinate with other departments in all phases of the studies and trials including feasibility assessments, design processes, educational efforts, management of medical information, and reviewing and editing of medical documents; * Follow specific research related protocol and lead others in strict adherence to the policies. Qualifications : * Must have an M.D. degree or equivalent. Board certification and current medical licensure are preferred; * Prior clinical trial research experience preferred; and * Previous experience in pharmaceutical\-related clinical research is preferred. Travel: up to 20% Medpace Overview : Medpace is a full\-service clinical contract research organization (CRO). We provide Phase I\-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti\-viral and anti\-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40\+ countries. Why Medpace? : People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today. The work we’ve done over the past 30\+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future. **Medpace Perks** * Flexible work environment * Competitive compensation and benefits package * Competitive PTO packages * Structured career paths with opportunities for professional growth * Company\-sponsored employee appreciation events * Employee health and wellness initiatives **Awards*** Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024 * Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility **What to Expect Next** A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.

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

Hepatology - Medical Director650493812925471219

Hepatology - Medical Director

Job Summary : We are seeking a Hepatologist to join our team in London. The Medical Director will have overall responsibility for providing medical, scientific, and strategic leadership for the successful planning, execution, and reporting of clinical trials. Additionally, this role acts as the Medpace internal medical expert and will serve as a medical resource for the review, presentation, and interpretation of results in the Clinical Study Report. The Medical Monitor will also be involved in the development of new clinical projects, including study design, protocol, and project plans as required. \*\*All Medical Monitors have hybrid WFH flexibility. Responsibilities : * Provide medical management and expertise for clinical trials; * Contribute medical expertise to study reports, regulatory documents, and manuscripts; * Manage safety issues in clinical trials and work closely with associates in evaluation and assessment of the trials; * Participate in new business development through involvement in proposal and sponsor meetings as requested; * Coordinate with other departments in all phases of the studies and trials including feasibility assessments, design processes, educational efforts, management of medical information, and reviewing and editing of medical documents; * Follow specific research related protocol and lead others in strict adherence to the policies. Qualifications : * Must have an M.D. degree or equivalent. Board certification and current medical licensure are preferred; * Prior clinical trial research experience preferred; and * Previous experience in pharmaceutical\-related clinical research is preferred. Travel: up to 20% Medpace Overview : Medpace is a full\-service clinical contract research organization (CRO). We provide Phase I\-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti\-viral and anti\-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40\+ countries. Why Medpace? : People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today. The work we’ve done over the past 30\+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future. **Medpace Perks** * Flexible work environment * Competitive compensation and benefits package * Competitive PTO packages * Structured career paths with opportunities for professional growth * Company\-sponsored employee appreciation events * Employee health and wellness initiatives **Awards*** Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024 * Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility **What to Expect Next** A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.

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

Psychiatry - Medical Director650493812759071220

Psychiatry - Medical Director

Job Summary : We are seeking a Psichiatry Medical Director to join our dynamic team. The Medical Director will have overall responsibility for providing medical, scientific, and strategic leadership for the successful planning, execution, and reporting of clinical trials. Additionally, this role acts as the Medpace internal medical expert and will serve as a medical resource for the review, presentation, and interpretation of results in the Clinical Study Report. The Medical Director will also be involved in the development of new clinical projects, including study design, protocol, and project plans as required. We are currently seeking Medical Directors in different locations. \*\*All Medical Directors have hybrid WFH flexibility. Responsibilities : * Provide medical management and expertise for clinical trials; * Contribute medical expertise to study reports, regulatory documents, and manuscripts; * Manage safety issues in clinical trials and work closely with associates in evaluation and assessment of the trials; * Participate in new business development through involvement in proposal and sponsor meetings as requested; * Coordinate with other departments in all phases of the studies and trials including feasibility assessments, design processes, educational efforts, management of medical information, and reviewing and editing of medical documents; * Follow specific research related protocol and lead others in strict adherence to the policies. Qualifications : * Must have an M.D. degree or equivalent. Board certification and current medical licensure are preferred; * Prior clinical trial research experience preferred; and * Previous experience in pharmaceutical\-related clinical research is preferred. Travel: up to 20% Medpace Overview : Medpace is a full\-service clinical contract research organization (CRO). We provide Phase I\-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti\-viral and anti\-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40\+ countries. Why Medpace? : People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today. The work we’ve done over the past 30\+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future. **Medpace Perks** * Flexible work environment * Competitive compensation and benefits package * Competitive PTO packages * Structured career paths with opportunities for professional growth * Company\-sponsored employee appreciation events * Employee health and wellness initiatives **Awards*** Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024 * Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility **What to Expect Next** A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.

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

Dermatologist - Medical Director650493812591371221

Dermatologist - Medical Director

Job Summary : We are seeking an Dermatologist \- Medical Director to join our dynamic team. The Medical Director will have overall responsibility for providing medical, scientific, and strategic leadership for the successful planning, execution, and reporting of clinical trials. Additionally, this role acts as the Medpace internal medical expert and will serve as a medical resource for the review, presentation, and interpretation of results in the Clinical Study Report. The Medical Director will also be involved in the development of new clinical projects, including study design, protocol, and project plans as required. We are currently seeking Medical Directors in different locations. \*\*All Medical Directors have hybrid WFH flexibility. Responsibilities : * Provide medical management and expertise for clinical trials; * Contribute medical expertise to study reports, regulatory documents, and manuscripts; * Manage safety issues in clinical trials and work closely with associates in evaluation and assessment of the trials; * Participate in new business development through involvement in proposal and sponsor meetings as requested; * Coordinate with other departments in all phases of the studies and trials including feasibility assessments, design processes, educational efforts, management of medical information, and reviewing and editing of medical documents; * Follow specific research related protocol and lead others in strict adherence to the policies. Qualifications : * Must have an M.D. degree or equivalent. Board certification and current medical licensure are preferred; * Prior clinical trial research experience preferred; and * Previous experience in pharmaceutical\-related clinical research is preferred. Travel: up to 20% Medpace Overview : Medpace is a full\-service clinical contract research organization (CRO). We provide Phase I\-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti\-viral and anti\-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40\+ countries. Why Medpace? : People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today. The work we’ve done over the past 30\+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future. **Medpace Perks** * Flexible work environment * Competitive compensation and benefits package * Competitive PTO packages * Structured career paths with opportunities for professional growth * Company\-sponsored employee appreciation events * Employee health and wellness initiatives **Awards*** Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024 * Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility **What to Expect Next** A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.

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

Personal warehouse laboratory650493701854751222

Personal warehouse laboratory

Warehouse assistant sought for a major pharmaceutical laboratory in Meco. The position focuses on the distribution area, where the candidate will actively participate in organizing and ensuring the smooth operation of the warehouse. Main responsibilities include ensuring compliance with the laboratory's quality standards, as well as performing cleaning and maintenance tasks for the facility. The candidate will also be responsible for order preparation, including labeling and strapping, and will maintain thorough documentation of delivery notes, managing goods receipts and dispatches. A substitution contract is offered with a fixed night shift, Monday to Friday, from 23:00 to 07:00 hours. **Requirements:** * Minimum education level: high school diploma, vocational training level 1 (FP1), vocational training level 2 (FP2) or higher (the relevant diploma/certificate of grades will be requested; official recognition/homologation is not required). * Minimum 1 year of experience as a warehouse assistant in the pharmaceutical or food sector (preferably). * The job involves a high physical workload.

C. Reino Unido, 7, 28880 Meco, Madrid, Spain

Investment banking intern649860656184331223

Investment banking intern

Join an intellectually rigorous finance internship designed for high\-performing individuals who are serious about launching a career in investment banking. This internship is tailored for ambitious individuals seeking real\-world exposure in financial modeling, transaction analysis, and strategic advisory. You'll work alongside experienced professionals and gain front\-line exposure to capital markets, company valuation, and deal execution workflows. **Key Learning Areas \& Tasks:** * Build and maintain detailed financial models using Excel, including DCF, precedent transaction, and comparables analysis. * Conduct industry\-specific market research and macroeconomic analysis to support transaction opportunities. * Participate in the preparation of pitch materials, investor memos, and strategic presentations. * Assist in developing client\-ready documents including deal decks and financial summaries. * Analyze company fundamentals and trends using earnings reports, M\&A data, and public filings. * Support business case development, sensitivity testing, and transaction structuring across live deals and internal projects. **What We’re Looking For:*** Currently studying or recently completed a degree in Finance, Economics, Business, or a quantitative discipline (or equivalent experience). * Strong interest in investment banking, corporate finance, and financial markets. * Familiarity with Excel modeling, PowerPoint presentations, and financial statement analysis. * Sharp analytical mind, attention to detail, and strong communication skills. * A proactive, resourceful, and self\-motivated work ethic. * International or multicultural experience is advantageous but not required. **What You'll Gain:*** Practical training in valuation, M\&A analysis, and financial strategy. * Mentorship and structured feedback from professionals with experience at top\-tier investment firms. * A results\-oriented environment that simulates real\-world investment banking workflows. * Flexible working arrangements — remote opportunities available. **Compensation:*** Paid internship route accessible **Ideal For:** Aspiring investment bankers, finance enthusiasts, and high\-agency individuals eager to gain elite experience before entering full\-time analyst roles at investment banks and private equity firms. F4BSnKchuM

Calle de Diego de León, 34, Salamanca, 28006 Madrid, Spain

Analista Funcional de Comercio Electrónico649711768296991224

Analista Funcional de Comercio Electrónico

En ABB ayudamos a la industria a adelantarse a la competencia: operar de forma más eficiente y ecológica. Para nosotros, el progreso es el estándar —para ti, tu equipo y todo el mundo. Como líder global, te brindamos lo que necesitas para lograrlo. No siempre será fácil; el desarrollo exige determinación. Pero en ABB nunca actuarás solo. Gestiona aquello que impulsa al mundo. Este puesto depende de: Chapter Lead (Piloto ELSP) Como Analista Funcional de Negocio, formarás parte de la Unidad Ágil de Procesos y Herramientas Comerciales para la Habilitación Empresarial, dentro del Capítulo de Análisis Funcional de Comercio Electrónico. Trabajarás en el Equipo Ágil «Gestionar el Marco de Colaboración y Compartición de Conocimiento», cuya misión es gestionar el marco de colaboración de la División para apoyar la planificación, la generación de ideas y la compartición de conocimientos sobre diseños estándar, mejores prácticas y directrices. Tendrás la oportunidad de ser responsable del análisis, gestión, desarrollo y mejora de procesos comerciales globales e integrados de extremo a extremo. Al colaborar con los interesados del negocio y de Sistemas de Información (IS), serás responsable de cerrar la brecha entre el entorno empresarial y el técnico, recopilando requisitos comerciales y utilizando el análisis de datos para evaluar procesos y definir desafíos, oportunidades y soluciones, con el fin de respaldar las decisiones relativas a nuevas soluciones o servicios de IS, o a su mejora. Este puesto contribuye a nivel mundial a **Electrificación Inteligente de Energía**. Ubicación preferida: Europa El modelo de trabajo para este puesto es: Híbrido **Serás principalmente responsable de:** * Identificar, recopilar, analizar y priorizar los requisitos comerciales, traduciéndolos hábilmente en historias de implementación para el desarrollo de herramientas destinadas a la Planificación Estratégica y de Cartera, la Ejecución y Entrega del Backlog, así como herramientas y plataformas de tickets para la compartición de conocimiento * Traducir los requisitos comerciales en especificaciones para equipos de desarrollo internos y externos * Colaborar estrechamente con los usuarios finales y el equipo de desarrollo para establecer planes de desarrollo claros y criterios de aceptación verificables, garantizando una alineación perfecta y aprovechando las mejores prácticas para cumplir los requisitos comerciales * Brindar análisis específicos para funciones comerciales, aportando experiencia técnica y en procesos comerciales/datos para respaldar las decisiones relativas a nuevas soluciones o servicios de IS, o a sus modificaciones * Trabajar junto con desarrolladores y el área de IS para estimar y supervisar el esfuerzo de desarrollo, incluyendo capacidad, estado y velocidad, en todos los desarrollos y lanzamientos planificados * Confirmar si la solución entregada cumple con la especificación real durante las Pruebas de Aceptación por el Usuario * Brindar capacitación y orientación a los usuarios de las herramientas * Informar y actualizar a los principales interesados sobre el avance del proyecto **Requisitos del puesto:** * Título universitario en Ingeniería, Ciencias de la Computación, Matemáticas, Física o Estadística * 3+ años de experiencia en puestos técnicos o de liderazgo similares * Competencia técnica en Salesforce y herramientas impulsadas por IA; habilidades en Python (programación orientada a objetos) y conocimientos prácticos de Docker, GitLab CI/CD, Azure DevOps, Jira y Linux * Amplios conocimientos de metodologías ágiles, ofreciendo liderazgo y orientación a los equipos en la gestión del backlog y la entrega * Excelentes capacidades analíticas y de gestión de riesgos, con una sólida comprensión financiera para estimar costos, esfuerzos y gestionar la demanda de soluciones de IS * Conocimiento de tecnologías de IA y su aplicación para optimizar procesos comerciales y la toma de decisiones * Dominio fluido del inglés, con excelentes habilidades comunicativas y de gestión de interesados **¿Qué obtienes tú?** Te empoderamos para asumir la iniciativa, compartir ideas audaces y dar forma a resultados reales. Crecerás mediante experiencia práctica, tutoría y aprendizaje adaptado a tus objetivos. Aquí, tu trabajo no solo importa: impulsa el progreso. **Más sobre nosotros** ABB Smart Power ofrece soluciones de distribución energética para centros de datos, plantas industriales y de fabricación, infraestructuras críticas y edificios comerciales. Los equipos técnicos de la División trabajan en estrecha colaboración con socios industriales, entregando soluciones avanzadas que apoyan un crecimiento acelerado, la transición energética y los objetivos de sostenibilidad. El portafolio de la División incluye interruptores automáticos industriales, sistemas de baja tensión, aplicaciones de arranque de motores y dispositivos de seguridad como interruptores y relés. Su unidad Power Protection brinda a las mayores empresas mundiales de centros de datos soluciones avanzadas de UPS eficientes desde el punto de vista energético. El ABB Ability™ Energy Manager de la División ofrece una plataforma escalable y fácil de usar que ayuda a las organizaciones a ahorrar energía y reducir sus emisiones de CO2. **Llamado a la acción** Guía el futuro. Aquí es donde la innovación se acelera, las industrias se reinventan y tu impacto impulsa al mundo hacia adelante. Run What Runs the World. #ABBCareers #RunwithABB #Runwhatrunstheworld #Agile #Electrification #SmartPower #FunctionalAnalyst #BusinessDeveloper Valoramos la diversidad de experiencias. ¿Podría ser esta tu historia? ¡Postúlate ya o visita www.abb.com para conocer más sobre nosotros y descubrir el impacto de nuestras soluciones en todo el mundo.

C. de Sangenjo, 37, Fuencarral-El Pardo, 28034 Madrid, Spain

Quality Technician648429715078421225

Quality Technician

At Fiesta, we are leaders in the manufacturing and sale of sweets and confectionery; our origins date back to the 1940s. Among our most iconic products are the authentic Kojak—the first lollipop with a stick filled with chewing gum—the original heart-shaped lollipop, the fun Fresquitos, the chewable lollipop Lolipop, and a wide range of licorice and gummy candies. We are currently seeking a person to join **our quality team** in Alcalá de Henares. Could that be you? Keep reading… Once you join our team, these are the **tasks** you will carry out: * Perform established quality verifications, ensuring compliance with defined standards. * Plan, execute, and implement complaint control and design improvement actions. * Handle customer complaints and propose solutions to identified issues. * Support training programs. * Design and implement processes and procedures. * Other duties associated with the position. **What do you need to perform this role?** * Availability to work different shifts (morning or afternoon) * Minimum education: bachelor’s degree or equivalent. A master’s degree in the food industry is recommended. * Formal training in BRCGS V9, Allergens, and Good Manufacturing Practices will be highly valued. * Minimum 3 years of relevant experience. * Proficiency in Microsoft Office tools. At Fiesta Colombina, we commit to evaluating candidates applying to our job openings solely based on their competencies, technical skills, and experience. All applications will be treated equally, without regard to race, nationality, gender, age, gender identity, or any other classification protected by law.

Av. de Madrid, 46, 28802 Alcalá de Henares, Madrid, Spain

Electrical Technician or Senior Engineer – Trillo Nuclear Power Plant (Guadalajara)648423219472651226

Electrical Technician or Senior Engineer – Trillo Nuclear Power Plant (Guadalajara)

Eurocontrol (Apave Group) is seeking an **Electrical Technician** or **Senior Engineer** to work at the Trillo Nuclear Power Plant in Guadalajara. **Minimum requirements** for the profile: * 2 years of experience in similar positions. * Possession of a Technical Engineering degree. * Desirable: experience in electrical project installation work. * Desirable: experience in the nuclear sector and knowledge of nuclear systems. If you believe your profile matches this position, please do not hesitate to apply. We look forward to receiving your application! *Statement on equality, diversity, and inclusion:* *We are committed to equality, diversity, and inclusion, and welcome applications from all sectors of the community, as we believe a diverse workforce brings greater depth to our work.* **Minimum requirements** for the profile: * 2 years of experience in similar positions. * Possession of a Technical Engineering degree. * Desirable: experience in electrical project installation work. * Desirable: experience in the nuclear sector and knowledge of nuclear systems.

C. Mayor, 10, 19001 Guadalajara, Spain

Senior Product Analyst648423211064341227

Senior Product Analyst

At **Joyteractive**, we’re on a mission to dominate the world of puzzle games. Our flagship title, *Cryptogram: Word Brain Puzzle*, is already one of the top word games in the US. We’re a focused and driven team of 60 professionals, passionate about building outstanding mobile puzzle experiences. We're on the hunt for a skilled Senior Product Analyst with previous successful experience in games. **What are you working on?** * Genres: Puzzle, Casual * Platforms: iOS, Android, Mobile **For which tasks (responsibilities)?** * Collect, analyze and present data for product management and marketing decisions; * Construct and visualize key product metrics and indicators; * Design of product/marketing features experiments, impact estimation (A/B testing); * Diligently monitor user behavior and provide insights. * Conduct deep\-dive analyses both upon request and proactively to uncover hidden product opportunities. * Propose product improvements based on data insights to drive key metrics. **What kind of professional are we looking for?** * 3\+ years of experience in product analytics in gamedev; * Knowledge of statistics (experiment design, statistical tests etc); * Knowledge of SQL; * Python or R programming experience (Python preferred); * Experience in business intelligence software (Tableau/Power BI) **Will be a plus:** * Experience with PostgreSQL, Redshift, RDS; * Experience in projects in the genre of match3, puzzles, casual, midcore * Experience in marketing \& monetization analytics * Experience in calculating LTV and forecasting * Experience at business intelligence / game design position in mobile gaming industry (Word/Board/Puzzle) **What are the conditions and bonuses?** * 18 business days of compensated day\-offs * 8 paid Personal Days a year \+ 1 day is added every year * Flexible Public Holidays policy * Individual budget for training and growth * 100% Sick Leave compensation * Payment for wear and tear on equipment while using a personal computer * Remote work

REACH-CLP and Biocides Technician648422619827231228

REACH-CLP and Biocides Technician

**Company Description** At SGS, our mission is to deliver value to society by providing a sustainable environment. Through our work, we ensure safety and quality, building trust across all sectors of society—even those that are not visible. We employ the most highly qualified professionals, working as one large team across more than 140 countries every day—making us industry leaders. We encourage you to join this human team, where you will train and develop within an environment characterized by camaraderie, flexibility, respect, and equality. At SGS, you will find: The opportunity to make a difference. A place where you can contribute your value to society. An international, innovative environment full of challenges, where you can share and learn alongside the best. You define us—you make SGS! **Job Description** We strive to hire the best professionals and value integrity, curiosity, excellence, respect, inclusion, and collaboration. Among many things, what makes SGS special is our culture. Would you like to join an industry-leading company? Currently, we are seeking a **REACH-CLP and Biocides Technician** for our Environmental team based in Madrid. If you join us, your day-to-day responsibilities will include: * Participating in the coordination of national and international REACH/CLP/Biocides projects with various stakeholders—including clients, laboratories, competent authorities, etc. * Reviewing chemical analyses for substance identification. * Managing various chemical and web-based applications such as IUCLID and Reach-IT, and software for preparing Safety Data Sheets. * Preparing PCN (Harmonized Process) dossiers. **Requirements** The qualifications we expect you to meet include: * Education: Bachelor’s degree in Chemical Engineering, Biochemistry, Industrial Chemistry, Environmental Sciences, or related fields. * Prior experience of at least one year in a similar role or in regulatory affairs will be viewed favorably. * Advanced level of English (B2–C1). **Additional Information** **What will you find at SGS?** * We are a multinational industry leader operating across virtually all industrial sectors. * SGS employees consistently highlight our positive workplace atmosphere as the most valued aspect. * We provide technical and soft-skills training to support continued professional growth. * We offer Flexible Compensation and special discounts for SGS employees. * We are a sustainable company actively engaged in addressing social issues. * We are committed to equality and diversity within our teams. At SGS, as part of our firm commitment to promoting equal opportunities and respecting diversity, we ensure that all our selection processes are conducted objectively, impartially, and fairly—and free from any form of bias or discrimination.

C. Trespaderne, 29, Barajas, 28042 Madrid, Spain

Site Engineer648412448011551229

**Site Name:** GSK Tres Cantos, Madrid **Posted Date:** Dec 16 2025 **Site Engineer** ================= **Location****:** Tres Cantos **Fecha límite para aplicar: 08/01/2026** GSC R\&D Engineering Services delivers facilities management and capital projects for R\&D sites. We are looking for a proactive Site Engineer to support site operations, ensuring safe, reliable and compliant facilities. You will manage engineering and capital projects, drive reliability and sustainability improvements, and work closely with operations, EHS, service partners and suppliers. Key responsibilities * Lead and support engineering capital projects from initiation to handover, ensuring compliance with statutory and GSK engineering standards. * Monitor engineering performance (maintenance adherence, MTTR, disruptions) and act as first escalation point for on‑site issues. Deliver risk mitigation plans from engineering gap assessments and manage corrective actions. * Champion engineering controls: Permit to Work, Change Control, Operational Occurrence Reporting and EHS improvement initiatives. * Support audits and implement improvements from findings, CAPAs and alerts. * Drive energy‑efficiency and sustainability projects to improve facility performance. Serve as technical authority/deputy for the site where competent, and oversee vendor/service‑partner delivery. * Establish robust maintenance regimes and PPMs with local/regional teams and service partners. Deputize for the Site Operations Manager/Director when required and participate in site crisis response on rotation. What we’re looking for * Degree in Engineering (Mechanical, Industrial or Electrical). Master’s preferred. * Proven experience in facilities engineering, operations or capital delivery (R\&D or pharmaceutical environment desirable). * Strong knowledge of HVAC, utilities and site infrastructure. * Experience with project delivery, risk management, audits and CAPA. * Solid stakeholder management and vendor oversight skills. * Excellent communication in Spanish and English. * Analytical, pragmatic and safety‑focused mindset. Why join us * Work on high‑visibility projects that directly impact site performance and sustainability. * Cross‑functional role with autonomy and opportunity to influence technical standards. * Development opportunities within a global organization. **Why GSK?** **Uniting science, technology and talent to get ahead of disease together.** GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2\.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases – to impact health at scale. People and patients around the world count on the medicines and vaccines we make, so we’re committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people. Should you require any reasonable adjustments or arrangements to support you during the recruitment process, specific to your individual needs, please contact us on esp\-inclusion.recruitment@gsk.com. Please note should your enquiry not relate to adjustments, we will not be able to support you through these channels. GSK is an Equal Opportunity Employer. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), parental status, national origin, age, disability, genetic information (including family medical history), military service or any basis prohibited under federal, state or local law. **Important notice to Employment businesses/ Agencies** GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK's commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site. Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license, GSK may be required to capture and report expenses GSK incurs, on your behalf, in the event you are afforded an interview for employment. This capture of applicable transfers of value is necessary to ensure GSK’s compliance to all federal and state US Transparency requirements. For more information, please visit the Centers for Medicare and Medicaid Services (CMS) website at https://openpaymentsdata.cms.gov/

C. de Santiago Grisolía, 4, 28760 Tres Cantos, Madrid, Spain

Previous
1(current)
2
3
More
9
Next

Popular Cities

Marcilla Science & Technology Recruitment La Rioja Science & Technology Recruitment Cascante Science & Technology Recruitment Cantabria Science & Technology Recruitment Canary Islands Science & Technology Recruitment Molins de Rei Science & Technology Recruitment El Ejido Science & Technology Recruitment Riudellots de la Selva Science & Technology Recruitment Benahadux Science & Technology Recruitment Asturias Science & Technology Recruitment

Help

Support and feedback

Cookie

Cookie Settings

Our Apps

Download on the

APP Store

Download

Get it on

Google Play

© 2025 Servanan International Pte. Ltd.