Alcorcon Laboratory & Technical Services Job Listings

Secondary School Teacher of Biology and Physics-Chemistry

We are seeking a qualified secondary school teacher to teach Biology and Physics-Chemistry in ESO and Bachillerato at our school located in Pozuelo. The subject is taught in Spanish. We offer full-time employment and a permanent contract. Start date: End of January Requirements: -Bachelor's degree or equivalent in Biology, Physics, Chemistry, or related fields -CAP or Master's degree in Secondary Education -Availability starting in January Position type: Full-time, Permanent contract Work location: On-site employment

C. Tomás Pierri, 1, 28223 Pozuelo de Alarcón, Madrid, Spain

Negotiable Salary

Study Support Assistant64629068405378121

Indeed

Study Support Assistant

Study Support Assistant ICON plc is a world\-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development As a Study Support Assistant, you’ll play an important role in helping our clinical studies get up and running efficiently. This is an ideal position for someone looking to begin a career in clinical research, offering hands\-on experience in a global organization and the chance to learn from experts in the field. Your main responsibilities will include:* Supporting Study Start\-Up activities by tracking, filing, collating and verifying submission documentation for Ethics Committees (EC), Regulatory Authorities (CA), and other relevant bodies * Assisting with translation and coordination of submission documents * Updating and maintaining tracking systems to ensure accurate study progress records * Assisting in the setup, maintenance, and quality review of the Trial Master File (TMF) to ensure completeness and inspection readiness * Helping set up and maintain electronic filing systems and study documentation * Coordinating and attending team meetings, preparing presentations and materials when required * Assisting with payments to regulatory or ethics bodies as needed * Ensuring compliance with ICH\-GCP, ICON Standard Operating Procedures (SOPs) and study requirements What You Need* A Bachelor diploma (or local equivalent) is required; a background in research or healthcare is an advantage but not essential * Excellent attention to detail and strong organizational skills * Effective written and verbal communication skills in English * A proactive attitude with the ability to collaborate and support multiple team members * Good computer literacy and willingness to learn ICON systems, including CTMS and TMF tools \#LI\-PD1 What ICON can offer you: Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent. In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well\-being and work life balance opportunities for you and your family. Our benefits examples include:* Various annual leave entitlements * A range of health insurance offerings to suit you and your family’s needs. * Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead. * Global Employee Assistance Programme, TELUS Health, offering 24\-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family’s well\-being. * Life assurance * Flexible country\-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others. Visit our careers site to read more about the benefits ICON offers. At ICON, inclusion \& belonging are fundamental to our culture and values. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.

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

Negotiable Salary

Sr Medical Writer - Narrative Writer64617258638210122

Indeed

Sr Medical Writer - Narrative Writer

**Description** Sr Medical Writer \- Narrative Writer 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

Negotiable Salary

Quality Systems Technician64609799366273123

Indeed

Quality Systems Technician

Capgemini Engineering, a global leader in engineering services, brings together teams of engineers, scientists, and architects to help the world’s most innovative companies unlock their full potential. From autonomous vehicles to life-saving robots, our digital technology and software experts think beyond convention, delivering unique R&D and engineering services across all industries. We are seeking a Quality Technician for the Pharmaceutical Sector in Madrid, within our Quality department. What will you do? * Quality Management Systems management. * Administration and tracking of deviations and CAPAs affecting the engineering area. * Technical documentation management and control. * Ensuring compliance with GMP regulations and internal standards. * SAP management. * Basic user-level administration of the SAP Maintenance Module (Plant Maintenance, Quality Management). * User onboarding and offboarding (operators, technicians, etc.), profile and permission assignment. * Reviewing and assigning work orders within the system. What profile are we looking for? * Vocational training (FP) or Engineering degree. * Minimum 3 years’ experience in roles similar to the one offered. * English level B2. * SAP and document management experience is desirable. * Pharmaceutical industry experience is mandatory. Candidates with a disability certificate will be positively considered under our inclusion and diversity policy. We welcome all applications. We offer an extensive training portfolio—including classroom, online, and certification programs. Even if you don’t meet 100% of the desired qualifications, we’d love to meet you! Our commitment to inclusion and equal opportunity is reflected in our Equality Plan and Code of Ethics, which guarantee professional development for all employees and ensure fair, non-discriminatory selection processes—regardless of ethnicity, nationality, social origin, age, sexual orientation, gender expression, religion, or any other personal, physical, or social circumstance. Why will you enjoy working here? We offer a comprehensive suite of Development and Work-Life Balance measures, including: * A uniquely positive workplace environment, highly rated by our professionals in periodic evaluations. * 24 vacation days + 2 personal days + December 24 and 31 + option to purchase up to 7 additional vacation days per year. * Flexible Compensation Plan (health insurance, transportation, training, meal card or food allowance, childcare support, etc.). * Continuous learning opportunities through MyLearning, Capgemini University, Digital Campuses, and Professional Communities. You’ll also have access to platforms such as Coursera, Udemy, Pluralsight, Harvard Manager Mentor, and Education First for language learning (English, French, German, etc.)—among others! * Life and Accident Insurance. Why Capgemini Engineering? Capgemini is a global leader in partnering with organizations to transform and manage their businesses by harnessing the power of technology. Every day, the Group is guided by its purpose: to unleash human energy through technology for an inclusive and sustainable future. Capgemini is a responsible and diverse organization of over 360,000 team members across more than 50 countries. With a solid 55-year heritage and broad industry expertise, Capgemini is trusted by clients to address their full business needs—from strategy and design to operations—powered by the fast-evolving worlds of cloud, data, AI, connectivity, software, digital engineering, and platforms. In 2022, the Group reported global revenues of €22 billion. Apply now! 'Get the future you want! #LI-AD14 Ref. code 372666-es_ES Posted on 02 Dec 2025 Experience level Experienced Professionals Contract type Permanent Location Madrid Business unit Engineering and R&D Services Brand Capgemini Engineering Professional communities Manufacturing & Operations Engineering

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

Negotiable Salary

Predoctoral researcher in training.64561991103874124

Indeed

Predoctoral researcher in training.

A 4-year predoctoral training contract is offered for the completion of a doctoral thesis at the Center for Metabolomics and Bioanalysis (CEMBIO), Faculty of Pharmacy, San Pablo CEU University, within the framework of the project: ADVANCED DEVELOPMENTS AND STRATEGIES FOR CURRENT CHALLENGES: UNCOVERING HIDDEN INFORMATION IN METABOLOMICS (CHALLENGEMET), whose objective is to improve and consolidate methodologies, expand the amount of information obtained, and enhance the understanding of biological mechanisms underlying health and disease conditions through metabolomics and lipidomics. Job responsibilities:* Conducting research tasks related to the project: Preparation of biological samples and metabolite analysis by mass spectrometry coupled with chromatographic techniques and related methods, data processing and reprocessing using innovative strategies, interpretation and discussion of results. Reading and writing scientific and outreach texts. * Preparation and defense of a doctoral thesis. * Participation in meetings, seminars, and scientific dissemination activities. * Integration into a multidisciplinary and highly competitive team with international recognition. * Collaboration with leading research groups in their respective fields. Educational requirements:* Degree in Chemistry, Pharmacy, Bioinformatics, Biomedicine, or related sciences that qualifies the candidate for doctoral studies. * Not having previously held a predoctoral contract for more than 12 months. * Knowledge of bioinformatics will be valued. * Proficiency in English at C1 level or equivalent is required. Conditions* Type of contract: Predoctoral (Article 21 of Law 14/2011, of June 1, and Royal Decree 103/2019, of March 1). * Start date: The first day of the corresponding month. * Duration: Up to 4 years. * Working hours: Full-time. * Salary: The call establishes in its article 12.4 the minimum remuneration for predoctoral contracts. * Workplace: Center for Metabolomics and Bioanalysis (CEMBIO), Faculty of Pharmacy, San Pablo CEU University. Required documentation* Updated CV. * Academic transcript. * Motivation letter. * Certificate of English proficiency (optional)

Ctra.Majadahonda-Av.Adolfo Suárez, 28660 Boadilla del Monte, Madrid, Spain

Negotiable Salary

Copy of Agro-Food Laboratory Technician64550942478849125

Indeed

Copy of Agro-Food Laboratory Technician

**Job Opportunity: Agro-Food Laboratory Technician – AENOR** Are you passionate about food safety and technical laboratory analysis? Do you want to be part of a team that ensures the quality of products reaching millions of people? At **AENOR**, we are looking for an **Agro-Food Laboratory Technician** to strengthen our team in Madrid, directly contributing to the reliability of our testing and control services. **What will your experience at AENOR be like?** **Reference technical environment** You will work with advanced technology and accredited methodologies in physicochemical and microbiological testing. **Collaborative and specialized team** You will join a multidisciplinary team experienced in food legislation, quality, and safety. **Continuous learning** You will have access to technical training and professional development opportunities in the agri-food sector. **Real impact on food quality** Your work will directly contribute to ensuring the safety of products reaching consumers. **Differentiating benefits** Intensive working hours during summer, flexible compensation, childcare assistance, language training, laptop, meal allowances, and more. **What are we looking for?** * **Technical education**: Higher Vocational Training in Analysis and Control, Clinical Diagnostic Laboratory, Chemistry, or similar. * **Experience**: At least 2 years in an agri-food laboratory performing physicochemical and microbiological tests. * **Regulatory knowledge**: Familiarity with standards such as ISO 17025. * **Rigour and organization**: Ability to follow procedures, record results, and maintain traceability. * **Commitment to quality**: Attention to detail and a vocation for continuous improvement. * **Availability to work shifts and flexible working hours**. **Your mission in the laboratory** You will perform quality control tests on food products, following accredited protocols. You will collaborate in method validation, equipment maintenance, and process improvement. You will actively participate in internal and external audits, ensuring regulatory compliance. **Are you interested?**

C. de Miguel Yuste, 12, San Blas-Canillejas, 28037 Madrid, Spain

Negotiable Salary

Research Engineer Intern (Video/Multimodal LLM)64550942446082126

Indeed

Research Engineer Intern (Video/Multimodal LLM)

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

Negotiable Salary

Food Quality Technician with English64550942397187127

Indeed

Food Quality Technician with English

At Cominport Distribución SLU, a multinational specializing in the import and distribution of Japanese food products, we are seeking a food quality technician with English proficiency specialized in the food sector for our Madrid headquarters. Main responsibilities: management of quality procedures related to food products, monitoring ISO 22000 regulations, conducting analyses, supplier control (labeling, etc.). Participation in internal training and dissemination of company regulations regarding handling food products, among others. **Requirements** Bachelor's degree in Food Science and Technology or similar fields. Intermediate/advanced level in English reading and writing. Minimum of 1 year of experience in the quality department of the food industry. Additional training such as related master's degrees will be valued. Intermediate level in **Office** (primarily Excel and Word). **We Offer** Stable full-time employment contract within a positive work environment. Standard working hours: 07.00-08.00 to 16.00-17.00 with a break for lunch. **Area - Position** Quality Department. Position type: Full-time Position type: Full-time, Permanent contract Salary: 18.000,00€-21.000,00€ per year Experience: * Food quality department: 1 year (Required) Language: * English (Required) Job location: On-site

Av. Marconi, 1 - PAE Neisa Sur, Villaverde, 28021 Madrid, Spain

€ 18,000/year

Indeed

CNC MACHINING

Join EDIBON, a leading Spanish company internationally recognized for designing and manufacturing educational and research equipment with over 45 years of experience. Headquartered in Móstoles, Spain, and with a young and dynamic team of more than 120 professionals, EDIBON exports approximately 98% of its products to over 140 countries, offering a broad international perspective and direct contact with clients worldwide. Responsibilities * Operate and program CNC lathes for component production, ensuring precision and quality in each manufactured part. * Read and interpret technical drawings and specifications to set up machines. * Perform preventive and corrective maintenance on CNC equipment to ensure proper operation and minimize downtime. * Program the lathe using the machine's own language and interface. Prepare materials and carry out machining operations. Requirements * Minimum of 2 years' experience as a CNC Turner in the industrial sector. * Advanced knowledge in reading technical drawings and using measuring instruments. * Experience with FANUC-type CNC lathes is desirable. * Experience with other types of machining workshop tools and/or milling machines is a plus. Benefits * Friday afternoons off. * Flexible time-off allowance. * Employee parking. * Fixed salary plus performance-based bonus. * Stable position (permanent contract). Join EDIBON as a CNC TURNER and enjoy a high-quality, committed, and professional environment, working with an innovative team in Móstoles.

C. Julio Cervera, 10, 28935 Móstoles, Madrid, Spain

Negotiable Salary

AI Video & Visual Designer "Proteos Biotech"64533856752129129

Indeed

AI Video & Visual Designer "Proteos Biotech"

**AI Creative Specialist – Visual Storytelling (Proteos Biotech)** **Department:** Global Marketing **Reports to:** Global Marketing Director **Location:** Madrid **Contract type:** Full\-time **Position summary:** At Proteos Biotech, we are seeking a creative professional with solid experience in AI-generated visuals (Midjourney, DALL·E, Leonardo.ai, Runway or others) to transform scientific and medical concepts into impactful visual content aligned with the brand’s defined positioning. You will be responsible for leading AI-based visual creative direction, producing images, renders, key visuals, and moodboards that communicate biotechnology, regeneration, and medical aesthetics in an emotional, aspirational, and rigorous manner. **Main responsibilities:** * Create visual concepts and graphic assets using generative AI (Midjourney, DALL·E, etc.) aligned with the global branding of pbserum. * Design key visuals and moodboards for global line-specific campaigns. * Collaborate with design and medical affairs teams to translate scientific evidence into clear, visually appealing imagery. * Generate product image libraries and emotional storytelling assets for reels, websites, training, and PR. * Develop advanced AI prompts (e.g., Midjourney/ChatGPT) to maximize aesthetic consistency, texture, lighting, and visual tone. * Support the creation of realistic 3D renders of vials and packaging, applying the look \& feel defined in the Brandbook. * Maintain consistency with the global visual tone and brand narrative: visible science, authentic beauty. * Participate in brainstorming sessions with external agencies and contribute disruptive visual solutions. * Develop reusable AI templates for the team (e.g., concepts of “emotional bioremodeling,” skin, enzymes, laboratory, natural beauty). **Requirements:** * Proven experience in art direction or digital design using generative AI (advanced-level experience in Midjourney or similar platforms is mandatory). * Strong knowledge of Adobe Creative Suite, Canva, and AI editing platforms (Runway, Leonardo.ai or similar). * Ability to interpret medical and scientific briefs and translate them into compelling visual storytelling. * Aesthetic sensitivity and mastery of composition, color, lighting, and texture. * Knowledge of the beauty\-tech, aesthetic medicine, or dermocosmetic sectors is a plus. * Professional-level English (reading and writing prompts in English). * Proactive, curious attitude with a focus on visual innovation. **We especially value:** * Experience in global aesthetic or health\-tech campaigns. * Portfolio showcasing AI-generated work (mandatory). * Familiarity with the visual language of pbserum (visible science, elegance, real beauty, natural light). * Ability to work under pressure and manage simultaneous projects. **What we offer:** * Join the leading biotechnology lab in recombinant enzymes. * Integration into a multidisciplinary marketing team (scientific, digital, and creative). * Innovative environment with international projects (LATAM, MENA, Europe, USA). * Ongoing training in AI applied to marketing. * Competitive salary based on experience. Position type: Full-time, Permanent contract Salary: €20\.000,00\-€35\.000,00 per year Benefits: * Christmas basket * Company events * Flexible working hours * Summer reduced working day * Reduced working day on Fridays * Company laptop * Free parking * Private medical insurance * Company phone * Meal vouchers Work location: On-site

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

€ 20,000-35,000/year

Waste Management Technician - Quirónsalud University Hospital Madrid (Pozuelo de Alarcón)645332510465301210

Indeed

Waste Management Technician - Quirónsalud University Hospital Madrid (Pozuelo de Alarcón)

**At Quirónsalud, your career has a purpose.** At **Quirónsalud**, we're not only leading the healthcare sector; we're **transforming** it. With cutting-edge technology and a network of over **58 hospitals in Spain and more than 180 healthcare centers 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 everyday practice.** **Join our team** * **Position:** Waste Management Technician * **Location:** Quirónsalud University Hospital Madrid \- Pozuelo de Alarcón. **Responsibilities:** * Open and close the goods loading dock gate. * Receive various waste collection companies. * Weigh waste materials. * Classify and label waste. * Properly document all waste. * Maintain constant contact with companies to schedule pickup days and times. * Participate in various quality audits by providing requested documentation. * Support the maintenance department when placing orders. **What we offer:** * Temporary contract. * Immediate incorporation. * Full-time split-shift contract (from 08\.00 to 17\.00 hours)**.** **An environment that enhances your development** * You will have the support of an experienced team that will help strengthen your skills and advance your career. * **Continuous training**: we will stimulate your learning and development through our **Quirónsalud University** and our specific **training programs**, enabling your personal and professional growth. **We care about your well-being** * **Access to our health and well-being program**, including initiatives such as: * + **Health care:** physical and mental wellness plans (access to medical services, health maintenance programs, and psychological support) + **Financial care:** flexible compensation programs, salary management assistance, and exclusive discounts. + **Family care:** initiatives focused on promoting healthy living and work-life balance. + **Volunteer program.** We're waiting for you! *At Quirónsalud, we promote integration and respect for diversity. Therefore, our selection processes will be conducted under these principles. Likewise, the company declares its commitment to establishing and developing practices that promote equal treatment and opportunities between men and women, without direct or indirect discrimination based on sex. This principle is part of our Corporate and People policy, in line with Organic Law 3/2007, of March 22, on effective equality between genders.* **REQUIRED QUALIFICATIONS** * Professional certification, CFGM or CFGS in Environmental Control, Waste Management, or similar. * Proficiency in Office, especially Excel. * Minimum six months of experience in a similar role. * Availability for immediate incorporation. * Interest in a substitution contract.

C. Tomás Pierri, 1, 28223 Pozuelo de Alarcón, Madrid, Spain

Negotiable Salary

Indeed

Chemical Engineer

We are looking for a professional with a completed higher degree or bachelor's degree in Chemical Engineering to join a team. Key responsibilities include supervision and management of manufacturing processes, direct interaction and negotiation with suppliers, and specialized technical advisory. Additionally, the candidate will be responsible for inventory management, resource optimization, and organization of personnel in charge of the technical department. The formulation of new products or improvement of existing ones, monitoring of regulations and legal requirements, as well as calculation and control of manufacturing costs, will also be part of the duties. Proven experience in the manufacturing of products such as detergents, soaps, degreasers, air fresheners, alcohols, solvents, or glycols, along with a positive attitude, proactivity, consistency, and strong organizational skills in a similar position for at least two years is highly valued.

Calle del Dr. Benito, 12, 28341 Valdemoro, Madrid, Spain

Negotiable Salary

Researcher (Fluent Turkish)645332510312971212

Indeed

Researcher (Fluent Turkish)

The aim of compliance\-driven due diligence is to assess our clients’ actual or potential counterparties, looking for any issues that might pose a reputational or other risk to them. As part of a dedicated team (VANTAGE), the compliance due diligence researcher role involves media research, working with databases, primary documents and other sources to uncover reputational and criminal issues and ultimate beneficial ownership, as well as making sense of complex corporate structures and identifying possible political and sanctions exposure. Your main task will be to review, coordinate and report the findings of OSINT and HUMINT research concisely within short timeframes. A meticulous eye for detail is a must in this challenging, fast\-paced role. The right candidate will be a team player who can maintain a positive attitude under pressure. You will be required to make sense of complex information and have a clear and crisp writing style. **Please submit a copy of your CV in English.** **Tasks and Responsibilities** * Work on a range of due diligence assignments, which include corporate compliance/ABAC/ESG and financial crime/IPO/KYC projects * Conduct media and database research using complex search criteria and following a strict methodology * Liaise with in\-country source networks to obtain relevant compliance\-related information not available via OSINT sources. * Analyse search results within the context of the project and the country, * Distil conclusions and identify indirect connections from research findings * Rate findings based on standard or tailored risk assessment methodologies * Summarise all relevant findings in a report * When required, brief and present findings to internal colleagues * Collaborate with team members across the firm to deliver joint projects **Requirements** * **Essential** * + Knowledge of research techniques, databases, networks, online registers and archives, and research in the general internet + Knowledge of the business, political, and social context of a geographical area + Native or equivalent fluency in English and Turkish + Excellence in research and writing in English and clear communication style + Communicate complex topics verbally and in writing effectively + Ability to summarise large amounts of information in a clear and concise manner + Ability to manage and prioritise multiple tasks to tight deadlines + Curiosity, attention to detail and problem\-solving skills + Ability to work independently and in a team + Education to degree level **Preferred** * + Demonstrated professional experience + Fluency in another European language or Arabic **Benefits** * Control Risks offers a competitively positioned compensation and benefits package that is transparent and summarised in the full job offer. * We operate a discretionary global bonus scheme that incentivises, and rewards individuals based on company and individual performance. * Control Risks supports hybrid working arrangements, wherever possible, that emphasise the value of in\-person time together \- in the office and with our clients \- while continuing to support flexible and remote working. * Working with our clients, from day one our people are given direct responsibility, career development and the opportunity to work collaboratively on fascinating projects in a rewarding and inclusive global environment. * The Company is committed to further its diversity, inclusion and equity agenda and as an employee you have access to various business resource groups in the Company including the Company's LGBT\+ network called MOSAIC, the Women's Network, and Synergy \- a people network to celebrate and promote ethnic diversity at Control Risks *Control Risks is committed to a diverse environment and is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, colour, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability, age or veteran status.* *If you require any reasonable adjustments to be made in order to participate fully in the interview process, please let us know and we will be happy to accommodate your needs.*

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

Negotiable Salary

Indeed

CRA II or Senior

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

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

Negotiable Salary

Senior researcher to lead the Catalysis and Energy Materials group - Investigador senior645234008240651214

Indeed

Senior researcher to lead the Catalysis and Energy Materials group - Investigador senior

Scientist position in Catalysis and Energy Materials **OTHER DETAILS** **Ref. num.** 2025\-JLL\-R3 R4\-306 #### **Senior researcher to lead the Catalysis and Energy Materials group \- Investigador senior** IMDEA Materials Institute is a public research organization founded in 2007 by Madrid’s regional government to carry out research of excellence in Material Science and Engineering by attracting talent from all over the world to work in an international and multidisciplinary environment. IMDEA Materials has grown rapidly since its foundation and currently includes more than 120 researchers from 22 nationalities and has become one of the leading research centers in materials in Europe which has received the María de Maeztu seal of excellence from the Spanish government. The research activities have been focused on the areas of materials for transport, energy, and health care and the Institute has state\-of\-the\-art facilities for processing, characterization and simulation of advanced materials. **Description** IMDEA Materials has opened a new position of Senior Researcher in the following area: Design and development of heterogeneous catalysts for energy conversion and transformation processes at the interface of electro\- and photocatalysis, with a particular emphasis on water electrolysis and the exploration of halide perovskite–based photocatalysts. The successful candidate should not only excel in research but also demonstrate strong leadership and management skills. Experience in planning, executing, and monitoring complex R\&D projects, as well as efficient resource allocation, will be key aspects of the role. A proven track record as Principal Investigator (PI) in competitive research projects and securing funding is highly desirable. The successful candidate must demonstrate strong leadership, communication, and teamwork skills to foster a collaborative research environment. Experience in supervising PhD students and early\-career researchers, as well as engaging with stakeholders in academia and industry, will be essential. Candidates with expertise in technology transfer, industrial collaboration, and science communication will be highly valued. Additionally, they will be expected to contribute to the strategic development of the Institute, ensuring efficient resource management and long\-term growth. Familiarity with the research ecosystem at IMDEA Materials and demonstrated ability to integrate effectively into similar multidisciplinary environments will be considered an advantage. The Institute is looking for dynamic researchers with the ability to drive new research lines, foster innovation, and contribute to the long\-term scientific strategy of the center. **Requirements** PhD in Chemistry, Material Science or related discipline (compulsory). Fluent English (oral and written) (compulsory). **Scholarship**: Well\-established international reputation and continued professional growth and recognition, demonstrated by: * Publication and citation record. * Technology transfer record: patents, software, industrial partnerships. * Principal investigator of research projects funded by national or international bodies or industry. * Awards and honours. * Invited/keynote/plenary lectures at national and international conferences. * International experience and international research network. **Leadership**: * Ability to develop an independent research group with internationally recognized scientific and/or technological achievements. * Funding record. * Advising of doctoral and master thesis. * Organization of national and international conferences and workshops. * Coordination of National and/or European research projects. **Experience and contributions in the area of Catalysis and Energy Materials:** * Proven expertise in heterogeneous catalysis for energy\-transition applications. The research background and activities should clearly address key challenges in both electrocatalytic and photocatalytic processes. This includes the design and development of tailor\-made nanostructured materials—particularly for water electrolysis—as well as the exploration and advancement of halide perovskite semiconductors for catalytic energy conversion. ***Submission of all required documents is mandatory.*** *A valid Spanish national ID (DNI) or residence permit is a mandatory requirement.* **Conditions** Contrato indefinido con cargo a la tasa de reposición para 2024 autorizada por la Consejería de Economía, Hacienda y Empleo de la Comunidad de Madrid. Permanent contract under the 2024 replacement rate authorised by the Department of Economy, Finance and Employment of the Community of Madrid. Applications are processed upon reception. The position might be closed once ten working days have passed since publication, so **we encourage early application.** The working language of the Institute is English. Full command of the English language is required in all positions. **WHAT YOU WILL FIND AT IMDEA**: Stimulating environment where you can grow professionally. IMDEA Materials Institute is committed to equal opportunities, diversity and the promotion of a healthy work environment and work\-life balance. **Female applicants are encouraged to apply** to our research and technical positions. Besides on\-the\-job technical training, IMDEA Materials Institute is committed to training the Institute’s scientists and staff in “soft” or transversal skills

C. Cuestas Bajas, 12A, 28901 Getafe, Madrid, Spain

Negotiable Salary

Sports Data Editor - English (ES)645233619393311215

Indeed

Sports Data Editor - English (ES)

### **About Simply.TV** At **Simply.TV**, we’re redefining how the world experiences **TV and sports metadata**. As a leading provider of advanced, AI\-driven metadata solutions, we empower broadcasters, streaming platforms, and telecom operators to deliver smarter, more engaging content discovery experiences. From next\-gen EPG (Electronic Program Guide) data to rich content enrichment, we enable our partners to stay ahead in a rapidly evolving media landscape. Headquartered in Copenhagen, but supported by 400\+ employees worldwide, our data fuels user interfaces that are used by millions of viewers every day — and we’re just getting started. Whether you're passionate about **media technology, sports, or data**, Simply.TV is the place to shape the future of content discovery — and have fun doing it. **Join us, and let’s make content discovery simple, powerful, and inspiring!** **The Role** Simply.TV is looking for a **Sports Data Editor (Spanish Market)** who lives and breathes sports. This role focuses almost entirely on the Spanish sports market, from major channels like **LaLiga TV** or **Teledeporte** to niche channels such as **Gol Televisión**. You’ll be responsible for maintaining and expanding our sports database, ensuring that our clients and their viewers receive **accurate, complete, and timely sports data**. We’re seeking someone who knows the market inside out, can anticipate competitions. This position is ideal for someone who loves sports, data, and precision, and who takes pride in delivering high\-quality information that enhances the viewing experience. **Key Tasks** * Research and create detailed data entries for sports events, tournaments, and leagues. * Track programs and competitions on Spanish sports channels; create new entries in the database when needed. * Collect and verify all relevant background information about sports events. * Merge duplicate or identical programs to ensure clean datasets. * Double\-check your work to correct inconsistencies and errors. * Ensure that clients receive **complete, accurate, and timely sports data**, twice error\-checked. **Requirements** * + **Deep knowledge of the Spanish sports market**, including major channels (LaLiga TV, Teledeporte) and niche channels (Gol Televisión). * + Solid understanding of sports competitions and ability to anticipate key events. + Strong knowledge of Spanish sports (LaLiga, Copa del Rey, national competitions). + Basic understanding of major international sports events (Tennis Grand Slams, NBA, Formula 1, NFL, Olympic Games, Tour de France). + University degree in a relevant area (Sports Management, Journalism, Business, or Data). + Exceptional written and spoken English. Spanish is a must. + Highly structured, detail\-oriented, and comfortable spotting errors. + Proficient with databases, online research tools, and data handling. + Thrives in a fast\-paced, dynamic environment. + Motivated to learn new tools and processes daily. + Collaborative mindset — enjoys working in an international team. + Passionate about sports, metadata, and delivering excellent user experiences. **Please note \- we can only accept CVs in English!**

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

Negotiable Salary

Lead UI/UX Product Designer645225215430411216

Indeed

Lead UI/UX Product Designer

#### **What You’ll Do** As the Lead UI/UX Product Designer at InteractiveAI, you will own and drive all design functions across the company, from the core product experience to our marketing website, brand visuals, and communication touchpoints. You will shape how users interact with our AI\-driven platform and how the world perceives our product and brand. This is a strategic, end\-to\-end design leadership role where you will transform complex AI\-native workflows into intuitive interfaces, build and scale our design system, define our brand expression, and ensure consistency across product, website, and communication. You will work closely with product, engineering, marketing, and leadership to deliver a cohesive, modern, and category\-defining experience across every surface. * **Product Design \& UX Ownership** + Lead the full design lifecycle: research, concepting, flows, wireframes, prototypes, and polished UI. + Transform complex AI workflows into simple, elegant, intuitive interfaces for technical and enterprise users. * **Design Vision \& Strategy** + Define the design vision for the product, platform, website, and brand in partnership with product and leadership. + Build a clear design strategy that balances usability, aesthetics, scalability, and business needs. * **Design System Leadership** + Build and maintain a scalable, modern design system used across product and marketing. + Establish guidelines for UI patterns, components, typography, color, and interaction principles. * **Marketing Website \& Brand Execution** + Own the UI/UX of our company website and landing pages, ensuring they reflect our brand, value proposition, and ecosystem. + Partner with marketing to design visuals, communication assets, and brand expressions. * **Cross\-Functional Collaboration** + Work closely with product managers to translate requirements into clear user experiences. + Collaborate with engineering to ensure accurate and high\-quality implementation. + Align with marketing and leadership to ensure visual and experiential coherence across channels. * **Prototyping \& Iteration** + Build high\-fidelity interactive prototypes to validate and refine ideas quickly. + Run user tests and incorporate feedback from internal teams, clients, and stakeholders. * **Mentorship \& Best Practices** + Champion design excellence across the company. + Establish processes, workflows, design reviews, and best practices for a high\-performance design culture. #### **What We’re Looking For** * 5\+ years of experience in product design, UI/UX, or digital design, with ownership of complex SaaS products. * A portfolio demonstrating strong UX, UI, and visual design craft—across both product and website work. * Proficiency with modern design tools (Figma required; Sketch, Adobe Suite optional). * Experience conducting user research, usability tests, and synthesizing insights into design decisions. * Proven experience building or scaling a design system from scratch. * Strong visual design skills: typography, layout, color, motion, and interaction patterns. * Understanding of front\-end development concepts (HTML/CSS/JS) to collaborate effectively with engineers. * Experience designing for technical audiences, developer tools, workflows, or data\-rich interfaces. * Ability to drive brand expression: website design, communication assets, and digital touchpoints. * Exceptional communication skills; strong ability to present design decisions convincingly. * Experience working in fast\-paced startup environments. * Nice\-to\-have: contributions to the design community (writing, speaking, open\-source). #### **What You’ll Get** * Competitive base salary (€80,000/yr to €100,000/yr) \+ performance bonuses * Access to equity/share plan as it rolls out * Health \& wellness allowances * Private health insurance * Flexible work setup \+ travel when needed (Hybrid in Lisbon or Madrid preferred) * 25 days of holidays/paid time off (excluding local public holidays) #### **Who You Are** * User\-Centric: You deeply understand user needs and design experiences that solve real problems. * A Systems Thinker: You instinctively turn complexity into clarity, structure, and usability. * Proactive \& Self\-Directed: You identify opportunities, own your impact, and move quickly. * Highly Creative: You bring modern, polished aesthetics and innovative interactions to the table. * High\-Ownership: You treat the platform, website, and brand as your own. * Collaborative: You work effectively with product, engineering, and marketing teams—and elevate others through feedback. * Startup\-Minded: You thrive in ambiguity and move rapidly without sacrificing craft. #### **Interview Process** We keep our process focused and respectful of your time. Most candidates complete it in 2–3 weeks. Here’s what to expect: * Intro Call – 30 minutes to align on fit and expectations * Portfolio Review – Deep dive into your work, design decisions, and process * Take\-Home Challenge – Practical design task inspired by real product needs * Cultural \& Values Interview – Discussion on motivations, working style, and collaboration * Offer – Final conversation and offer We’re forming a team of builders — people who care about impact, quality, and growth. If that’s you, let’s talk — careers@interactive.ai#### **About us** InteractiveAI is a fast\-growing startup on a mission to empower enterprises with fully managed AI agent lifecycles. We are building the next generation of enterprise\-AI solutions, delivering an end\-to\-end Agentic IDE alongside an extensible ecosystem of agentic resources and solutions. Our platform allows companies to orchestrate, monitor, evaluate, deploy and improve AI agents—and soon fine\-tune and own their own models. We value autonomy, speed, and innovation, and we’re building a world\-class team to match. Our squads are lean, focused, and execution\-driven. If you thrive in high\-performance environments and want to be part of a company that rewards transformational outcomes, this is for you.

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

€ 80,000-100,000/year

Market Access Specialist645225139024671217

Indeed

Market Access Specialist

**Market Access Specialist** ============================ **What are we looking for?** We are seeking a highly motivated individual with strong work capacity, analytical skills, attention to detail, initiative, and flexibility, who enjoys working in a team and is interested in building a career in the Market Access field, to fill a vacancy within the Market Access and Pricing department. This is a position whose primary mission is to manage activities related to pricing and reimbursement processes, national and regional access, as well as research projects in health economics and outcomes research (HEOR) for products within the assigned therapeutic area. **Main responsibilities** : * Design market access strategy, build and maintain an integrated value story targeted at payers, and prepare value dossiers to be submitted during pricing and reimbursement (P\&F) procedures for products under responsibility. * Adapt economic models to the Spanish setting or develop them from scratch (such as budget impact tools, cost-effectiveness analyses, etc.), as well as conduct literature reviews, meta-analyses, and other Health Economics and Outcomes Research (HEOR) works such as Real-World Evidence (RWE) studies focused on information gaps relevant to payers. * Create materials to effectively communicate value stories and generated studies tailored to payer needs. * Lead technical responses in Health Technology Assessment processes in Spain to position products under responsibility regarding P\&F conditions and/or regional access (e.g., Therapeutic Positioning Reports from the Spanish Medicines Agency at national level or CatSalut product assessments at regional level). * Stay up to date on the competitive landscape and the evolution of the Spanish National Health System to inform market access strategies. * Collaborate with central and local teams to drive continuous improvements. Work closely with internal cross-functional teams (sales, marketing, medical, government affairs, regulatory, etc). **Requirements** * University degree in health sciences, economics, statistics or related fields. * Experience in market access, health economics and outcomes research (HEOR) departments. * Knowledge of pricing and reimbursement processes, as well as national and regional access under Spanish legislation. * Strong analytical skills. * Influence and communication abilities. * Fluent spoken and written English (C1\). * Proficiency in MS Office tools. **Desirable:** * Master’s degree in Market Access and HEOR preferred. * Initiative and creativity to propose solutions. Deadline: 28/11/2025 **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. If you require an accommodation or other assistance to apply for a job at GSK, please contact the GSK Service Centre at 1\-877\-694\-7547 (US Toll Free) or \+1 801 567 5155 (outside US). 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 Dolores Ibárruri, 1, 28760 Tres Cantos, Madrid, Spain

Negotiable Salary

Senior GRC Specialist (Cybersecurity) - Hybrid Madrid645212975470091218

Indeed

Senior GRC Specialist (Cybersecurity) - Hybrid Madrid

1 Opening Alcorcon ### **Role description** **We are still looking for the very Top Talent…and we would be delighted if you were to join our team!** More in details, UST is a multinational company based in North America, certified as a Top Employer and Great Place to Work company with over 35\.000 employees all over the world and presence in more than 35 countries. We are leaders on digital technology services, and we provide large\-scale technologic solutions to big companies. **What we look for?** We are looking for a GRC Specialist contribute for a project with one of our global customers in the cybersecurity team. **Skills:** * 4 years’ experience in audits and compliance and assessments based on national and international standards (ISO27001, ISO22301, ENS, NIST, DORA, NIS2\) * Knowledge/certifications in ISO27001 is a must. It is also desirable knowledge in ENS, ISO 27005, ISO22301, ISO 42001, NIST CSF 2\.0, NIST, SOC 2, GDPR, DORA, NIS2, CMMC 2\.0 * Proficiency with a variety of instruments for assessing and controlling risk (ex. ISO 31000, Magerit v3, COSO) * Experience in implementation of best practices, compliance with information security policies and standards. * Technical experience or applicable knowledge in security architectures for different environments. * Experience related to Cybersecurity ecosystem, deployment experience of security technologies. * Knowledge of different security solutions/technologies: FW, DLP, IDS/IPS, EDR… * Experience in incident response plans and exercises * Fluent in English * Computer Engineering/Telecommunications and/or Master in Cybersecurity It is also desirable and will be considered to hold certifications such as CISM, CISSP, CISA, ISO/IEC 27001 Lead Auditor / Lead Implementer. We will also consider knowledge of HIPAA, ARC\-AMPE or OT Cybersecurity (ISO 27019 / IEC 62443\) for the more senior role **Tasks:** * Handle the assigned tasks from the allocated domain with minimal guidance from the leads. (Domain Examples: BCMS, ISMS, Risk assessment (AARR \& BIAs), GAP Analysis, Incident management, Awareness activities, Data Privacy, etc.) * Independently handle (with very minimal guidance from the supervisors) internal audits or GAP Analysis to ensure compliance with security standards (ex. ISO 27001/ISO 22301/ISO 27701, NIST CSF 2\.0, ..) requirement as well as process specific requirements * Responsible for the effective documentation of projects individually. * Point out the non\-conformance areas and suggest measures to improve the information security individually. * Ensure that risk management is effectively conducted across the organization, business processes and information systems. * Involve and contribute to customer assurance activities. * Coordinate information security awareness training programs for all the employees, contractors and approved system users. * Coordinate and Review the technical assessments of IT systems and processes to identify potential risks. Submit recommendations to mitigate any risks identified and ensure controls that they are implemented. * Design, plan and execute the Cybersecurity activities. * Directly Interact with customer and communicate detailed technical requirement to the team. * Use independent judgement and discretion to analyze the system security. * Prepare detailed description of user requirements and steps required to perform a compliance project in basis a standard or regulation. * Learn and understand existing regulations or standards requirements. * Independently handle the evidence collection from multiple teams as part of any internal audits. * Policy/Procedure creation activities and process improvement ideas to be implemented. * Research and analytical skills, including the ability to convert complex policy issues into simple briefings and communicate to the audience. **Location**: 4 days remote 1 day at the office. **Schedule**: Office working hours **What can we offer?** * 23 days of Annual Leave plus the 24th and 31st of December as discretionary days! * Numerous benefits (Heath Care Plan, Internet Connectivity, Life and Accident Insurances). * \`Retribución Flexible´ Program: (Meals, Kinder Garden, Transport, online English lessons, Heath Care Plan…) * Free access to several training platforms * Professional stability and career plans * UST also, compensates referrals from which you could benefit when you refer professionals. * The option to pick between 12 or 14 payments along the year. * Real Work Life Balance measures (flexibility, WFH or remote work policy, compacted hours during summertime…) * UST Club Platform discounts and gym Access discounts **In UST we are committed to equal opportunities in our selection processes and do not discriminate based on race, gender, disability, age, religion, sexual orientation or nationality. We have a special commitment to Disability \& Inclusion, so we are interested in hiring people with disability certificate.** ### **Skills** Cyber Security,GRC,GDPR,Compliance ### **About UST** UST is a global digital transformation solutions provider. For more than 20 years, UST has worked side by side with the world’s best companies to make a real impact through transformation. Powered by technology, inspired by people and led by purpose, UST partners with their clients from design to operation. With deep domain expertise and a future\-proof philosophy, UST embeds innovation and agility into their clients’ organizations. With over 30,000 employees in 30 countries, UST builds for boundless impact—touching billions of lives in the process.

C. Polvoranca, 44, 28921 Alcorcón, Madrid, Spain

Negotiable Salary

GRC Project Manager (Cybersecurity) (Hybrid Madrid)645212975641621219

Indeed

GRC Project Manager (Cybersecurity) (Hybrid Madrid)

1 Opening Alcorcon ### **Role description** **We are looking for the very Top Talent…and we would be delighted if you were to join our team!** More in details, UST is a multinational company based in North America, certified as a Top Employer and Great Place to Work company with over 35\.000 employees all over the world and presence in more than 35 countries. We are leaders on digital technology services, and we provide large\-scale technologic solutions to big companies. **What are we looking for?** We are looking for a **GRC** **Project Manager**, with experience in cibersecurity projects, working close to one of our main clients in cybersecurity sector. **Main tasks and accountabilities will be:** * Handle the assigned tasks from the allocated domain with minimal guidance from the leads. (Domain Examples: BCMS, ISMS, Risk assessment (AARR \& BIAs), GAP Analysis, Incident management, Awareness activities, Data Privacy, etc.) * Independently handle (with very minimal guidance from the supervisors) internal audits or GAP Analysis to ensure compliance with security standards (ex. ISO 27001/ISO 22301/ISO 27701, NIST CSF 2\.0, ..) requirement as well as process specific requirements * Responsible for the effective documentation of projects individually. * Point out the non\-conformance areas and suggest measures to improve the information security individually. * Ensure that risk management is effectively conducted across the organization, business processes and information systems. * Involve and contribute to customer assurance activities. * Coordinate information security awareness training programs for all the employees, contractors and approved system users. * Coordinate and Review the technical assessments of IT systems and processes to identify potential risks. * Submit recommendations to mitigate any risks identified and ensure controls that they are implemented. * Design, plan and execute the Cybersecurity activities. * Directly Interact with customer and communicate detailed technical requirement to the team. * Use independent judgement and discretion to analyze the system security. * Prepare detailed description of user requirements and steps required to perform a compliance project in basis a standard or regulation. * Learn and understand existing regulations or standards requirements. * Independently handle the evidence collection from multiple teams as part of any internal audits. * Policy/Procedure creation activities and process improvement ideas to be implemented. * Research and analytical skills, including the ability to convert complex policy issues into simple briefings and communicate to the audience. **What UST expects from you?** * At least 5 years’ experience in audits and compliance and assessments based on national and international standards (ISO27001, ISO22301, ENS, NIST, DORA, NIS2\) * Knowledge/certifications in ISO27001\. * Proficiency with a variety of instruments for assessing and controlling risk (ex. ISO 31000, Magerit v3, COSO) * Experience in implementation of best practices, compliance with information security policies and standards. * Technical experience or applicable knowledge in security architectures for different environments. * Experience related to Cybersecurity ecosystem, deployment experience of security technologies. * Knowledge of different security solutions/technologies: FW, DLP, IDS/IPS, EDR… * Experience in incident response plans and exercises. * Computer Engineering/Telecommunications and/or Master in Cybersecurity. * Good english level (C1\) you will be working with international teams. Desired Skills: * Knowledge in ENS, ISO 27005, ISO22301, ISO 42001, NIST CSF 2\.0, NIST, SOC 2, GDPR, DORA, NIS2, CMMC 2\.0 * Hold certifications such as CISM, CISSP, CISA, ISO/IEC 27001 Lead Auditor / Lead Implementer. We will also consider knowledge of HIPAA, ARC\-AMPE or OT Cybersecurity (ISO 27019 / IEC 62443\) for the more senior role. **Work Location** Hybrid Madrid. 1\-2 days a week in the office or customer site. **Work schedule** Business Hours. No intensive working days for friday or summer. **What can we offer?** * 23 days of Annual Leave plus the 24th and 31st of December as discretionary days! * Numerous benefits (Health Care Plan, teleworking compensation, Life and Accident Insurances). * \`Retribución Flexible´ Program: (Meals, Kinder Garden, Transport, online English lessons, Health Care Plan…) * Free access to several training platforms * Professional stability and career plans * UST also, compensates referrals from which you could benefit when you refer professionals. * The option to pick between 12 or 14 payments along the year. * Real Work Life Balance measures (flexibility, WFH or remote work policy, compacted hours during summertime…) * UST Club Platform discounts and gym Access discounts **If you would like to know more, don’t hesitate to apply and we’ll get in touch to fill you in detail. We are waiting for you!** **In UST we are committed to equal opportunities in our selection processes and do not discriminate based on race, gender, disability, age, religion, sexual orientation or nationality. We have a special commitment to Disability \& Inclusion, so we are interested in hiring people with disability certificate.** ### **Skills** Business Intelligence,Iso 27001,GRC,Cyber Security ### **About UST** UST is a global digital transformation solutions provider. For more than 20 years, UST has worked side by side with the world’s best companies to make a real impact through transformation. Powered by technology, inspired by people and led by purpose, UST partners with their clients from design to operation. With deep domain expertise and a future\-proof philosophy, UST embeds innovation and agility into their clients’ organizations. With over 30,000 employees in 30 countries, UST builds for boundless impact—touching billions of lives in the process.

C. Polvoranca, 44, 28921 Alcorcón, Madrid, Spain

Negotiable Salary

INTEGRATED MANAGEMENT SYSTEM TECHNICIAN645212974670101220

Indeed

INTEGRATED MANAGEMENT SYSTEM TECHNICIAN

Join EDIBON, a leading company in research and education services with over 45 years of experience. Based in Móstoles, Madrid, we are recognized worldwide for our innovative educational equipment and research systems. We are seeking a Management Systems Technician to ensure that our products, services, and processes meet internal and external quality standards. Responsibilities * Maintenance and improvement of current ISO 9001, 14001, 27001, and 45001 certifications. Manage related tasks and documentation, analyze data, define and follow action plans, including internal and external audits. Coordinate with all involved departments. * Tracking and closure of non-conformities. * Internal regulatory compliance and monitoring of laws and new regulations regarding Quality, Environment, Occupational Health and Safety, and Information Security. * Control of waste generation and treatment. * Monitoring preventive planning and facility inspections. * Preparation of compliance reports required by legislation. * Control and monitoring of occupational risk prevention within the company and related documentation. Requirements Advanced level of English is essential. Candidate experienced in working within a certified Management System (ISO 9001, 14001, 45001, 27001). Experience in Occupational Risk Prevention. Minimum of 1 year of previous experience in similar roles. We are looking for a serious, rigorous individual with analytical skills, strong communication, organizational and planning abilities, capable of working independently and responsibly toward objectives. 100% on-site work. Benefits WHAT DO WE OFFER? Flexible working hours. Friday afternoons off. Bank of free hours. Employee parking. Stable position (permanent contract). Flexible compensation and possibility of private health insurance. Join EDIBON as a MANAGEMENT SYSTEMS TECHNICIAN. Work in an international, dynamic, and collaborative environment, developing innovative technological solutions with global impact.

C. Julio Cervera, 10, 28935 Móstoles, Madrid, Spain

Negotiable Salary

Indeed

CRA

### **Summary** This is a site relationship management role to ensure sustainable trial execution at site. The CRA will perform on\-site and remote monitoring activities related to initiation, conduct and timely completion of Phase I\-IV GDD trials within Spain in adherence with monitoring procedures and processes in accordance with ICH/GCP, local regulations and SOPs. Responsible for proactive site performance management (recruitment \& quality) and early identification of real site needs and issues as the single best point of contact (internally \& externally) for all sites. Location: Madrid: Provincial. ### **About the Role** **Key responsibilities but not limited to:** * Frontline liaison between Novartis and sites to ensure successful collaboration, meeting Novartis expectation on milestone and deliverables with true ownership mindset * Manage assigned study sites, conducting phase I\-IV protocols according to the monitoring plan and Novartis procedures * Perform site initiation visits, ensures site personnel is fully trained on all trial related aspects. * Perform continuous training for amendments and new site personnel as required. * Conduct continuous site monitoring activities (onsite and remote). * Implement site management activities to ensure compliance with protocol, global and local regulation including Health Authorities, data privacy requirements, global and local processes as applicable. * Identify deficiencies in site processes and monitor site processes performed outside the site, works in close collaboration with site on risks mitigation and process improvements * Promote a compliance culture advocating adherence to highest standards and ethical integrity, ensuring human subject protection and reliability of trial results at all times * Identify deficiencies in site process, work in close collaboration with site on risk mitigation * Establish a strong partnership and true collaboration with the site, to increase patient density and decrease issues at site. * Perform Site Closeout activities per SOPs and applicable regulations to ensure that site is aware of any follow up activity and archiving requirements * Attend onboarding\-, disease indication and project specific training and general CRA training as required **Essential criteria:** * Degree in scientific or healthcare discipline * Up to 2 years pharmaceutical industry experience or other relevant experience Central / in\-house monitoring or field monitoring experience is desirable **Desirable criteria:** * Decision capability * Excellent time management and organization capabilities, including ability to prioritize and multi\-task * Risk based mindset (from issue management to risk identification) supported by Novartis systems * Early adopter and open mindset across borders to support one study approach Good knowledge of drug development process specifically clinical trial/research Clinical and therapeutic knowledge * Knowledge of international standards (GCP/ICH, FDA, EMA) * Understanding the purpose of the CRA (Patient Safety; Data Integrity; PI oversight; GCP/ICH \& Protocol Compliance) **Languages:** * Fluent in both written and spoken English and country language **Why Novartis:** Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients’ lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people\-and\-culture **Join our Novartis Network:** Not the right Novartis role for you? Sign up to our talent community to stay connected and learn about suitable career opportunities as soon as they come up: https://talentnetwork.novartis.com/network **Benefits and Rewards:** Read our handbook to learn about all the ways we’ll help you thrive personally and professionally: https://www.novartis.com/careers/benefits\-rewards Division Development Business Unit Development Location Spain Site Madrid Provincial Company / Legal Entity ES06 (FCRS \= ES006\) Novartis Farmacéutica, S.A. Functional Area Research \& Development Job Type Full time Employment Type Regular Shift Work No Novartis is committed to building an outstanding, inclusive work environment and diverse teams' representative of the patients and communities we serve.

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

Negotiable Salary

Indeed

Contract Analyst II

Contract Analyst Home based Spain ICON plc is a world\-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development We are currently seeking a Contract Analyst II to join our diverse and dynamic team. As a Contract Analyst II at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of inNvative treatments and therapies. What you will be doing* Reviewing and analyzing contracts, agreements, and legal documents related to clinical trial activities and vendor relationships. * Negotiating contract terms and conditions with clients, vendors, and other stakeholders to ensure compliance with regulatory requirements and company policies. * Collaborating with cross\-functional teams to assess contract risks, identify opportunities for improvement, and develop strategies to mitigate potential issues. * Maintaining accurate and up\-to\-date records of contract status, milestones, and deliverables using contract management systems. * Providing guidance and support to internal teams on contract\-related matters, including contract interpretation, compliance, and dispute resolution. Your profile* Bachelor's degree in Business Administration, Legal Studies, or a related field; advanced degree or certification in Contract Management or a relevant discipline preferred. * Minimum of 2 years of experience in contract administration, contract management, or a related field, preferably in the pharmaceutical or clinical research industry. * Strong understanding of contract law, legal termiNlogy, and regulatory requirements related to clinical trials and vendor agreements. * Excellent analytical and problem\-solving skills, with the ability to evaluate complex contractual issues and propose effective solutions. * Strong attention to detail and organizational skills, with the ability to manage multiple tasks and prioritize work effectively in a fast\-paced environment. What ICON can offer you: Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent. In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well\-being and work life balance opportunities for you and your family. Our benefits examples include:* Various annual leave entitlements * A range of health insurance offerings to suit you and your family’s needs. * Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead. * Global Employee Assistance Programme, TELUS Health, offering 24\-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family’s well\-being. * Life assurance * Flexible country\-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others. Visit our careers site to read more about the benefits ICON offers. At ICON, inclusion \& belonging are fundamental to our culture and values. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.

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

Negotiable Salary

Research position in algorithmic design and LPBF of NiTi-based medical devices645212543002901223

Indeed

Research position in algorithmic design and LPBF of NiTi-based medical devices

IMDEA Materials is searching for a research engineer for the new line on "Bioinspired, Smart and Living Materials" for the design, prototyping, testing and certification of smart medical devices based on superelastic NiTi. **OTHER DETAILS** **Ref. num.** 2025\-AD\-R1\-305 #### **Research position in algorithmic design and LPBF of NiTi\-based medical devices** IMDEA Materials Institute is a public research organization founded in 2007 by Madrid’s regional government to carry out research of excellence in Material Science and Engineering by attracting talent from all over the world to work in an international and multidisciplinary environment. IMDEA Materials has grown rapidly since its foundation and currently includes more than 120 researchers from 22 nationalities and has become one of the leading research centers in materials in Europe which has received the María de Maeztu seal of excellence from the Spanish government. The research activities have been focused on the areas of materials for transport, energy, and health care and the Institute has state\-of\-the\-art facilities for processing, characterization and simulation of advanced materials. **Description** The selected candidate will work with Prof. Dr. Andrés Díaz Lantada supporting the settlement of a new research line, contributing to the engineering design of innovative medical (cardiovascular and neurological) medical devices based on smart alloys. Together with research and development tasks linked to innovative design and manufacturing approaches (DfAM strategies and LPBF for NiTi), support to dissemination and communication activities, impact promotion and fundraising are expected. The candidate will work with the PI of the research line focusing on a new generation of medical devices enabled by advanced personalized, AI\-based and algorithmic design methods together with high\-performance AM tools. **Requirements** Experience of at least 4 years working in the medical industry, especially in connection with R\&D projects linked to the design, prototyping, testing and certification of medical devices. Proficiency with algorithmic design tools (Rhino/Grasshopper \+ Python), computer\-aided design resources (Siemens NX) and finite\-element modelling of smart materials for medical devices, especially NiTi alloys, is required. Experience with laser powder bed fusion of NiTi alloys is also necessary. Evaluation will be based on 1\) CV, 2\) motivation letter, 3\) research portfolio highlighting experience in DfAM and LPBF, and 4\) selection of up to 5 publications. Candidates not providing the required documentation (points 1\-4\) will be automatically discarded. **Conditions** International working environment within a team of multidisciplinary researchers focused on transforming healthcare through materials research. Competitive salary based on fulfilment of requirements and according to IMDEA Materials standards. Start date: January 1st 2026\. Applications are processed upon reception. The position might be closed once ten working days have passed since publication, so **we encourage early application.** The working language of the Institute is English. Full command of the English language is required in all positions. **WHAT YOU WILL FIND AT IMDEA**: Stimulating environment where you can grow professionally. IMDEA Materials Institute is committed to equal opportunities, diversity and the promotion of a healthy work environment and work\-life balance. **Female applicants are encouraged to apply** to our research and technical positions. Besides on\-the\-job technical training, IMDEA Materials Institute is committed to training the Institute’s scientists and staff in “soft” or transversal skills

C. Cuestas Bajas, 12A, 28901 Getafe, Madrid, Spain

Negotiable Salary

Management Controller - Central Laboratory Health Diagnostics Quirónsalud (Alcobendas)645212543156491224

Indeed

Management Controller - Central Laboratory Health Diagnostics Quirónsalud (Alcobendas)

**At Quirónsalud, your career has a purpose.** At **Quirónsalud**, we don't just lead the healthcare sector; we are **transforming** it. With state-of-the-art technology and a network of more than **58 hospitals in Spain and over 180 healthcare centers 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 become part of a team where excellence is everyday practice.** **Join our team** **Position:** Controller \- Management Control **Location:** Central Laboratory Health Diagnostics (Alcobendas) **Job Functions and Responsibilities:** * Participation in the preparation of annual budgets and monitoring their compliance. * Involvement in the development of management dashboards (KPIs). * Performing monthly closing and reconciliation of accounting accounts with the various centers managed by the company. * Preparation of financial and economic reporting for monthly and annual closings of the company. * Cost control, budget follow-up, and variance analysis. * Identification and management of errors, variances, and improvement opportunities from an economic-financial perspective. * Monitoring and evaluation of profitability, margins, and results. * Analysis of financial statements, including balance sheets and profit/loss statements. * Analyze differences in accounts, ratios, revenues/expenses, and investment analyses. * Collaboration in preparing data for internal and external audits. **What we offer:** * **Immediate incorporation** into a collaborative and specialized team. * **Attractive salary package**, competitive and aligned with the market. **An environment that enhances your development** * You will have the support of an experienced team that will help strengthen your skills and advance your career. * **Continuous training**: we will stimulate your learning and development through our **Quirónsalud University** and our specific **training programs**, enabling personal and professional growth. **We care about your wellbeing** * **Access to our health and wellbeing program**, including initiatives such as: * + **Healthcare:** physical and mental wellness plans (access to medical services, health maintenance programs, and psychological support). + **Financial wellbeing:** flexible compensation programs, salary management assistance, and exclusive discounts. + **Volunteer program.** We're waiting for you! *At Quirónsalud, we promote integration and respect for diversity. Therefore, our selection processes will be conducted under these principles. Likewise, the company declares its commitment to establishing and developing practices that promote and encourage equal treatment and opportunities between men and women, without direct or indirect discrimination based on gender. This principle is part of our Corporate and People policy, in line with Organic Law 3/2007, of March 22, on effective equality between genders.* * Bachelor's degree in Business Administration, Economics, Business Studies, etc. * At least three years of experience in similar roles. * Knowledge of SQL, Power Query, Power BI. * Advanced Excel skills. * Experience in the hospital or industrial sector is a plus.

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

Negotiable Salary

Governance, Risk & Compliance Specialist - 100% Remote645212542538271225

Indeed

Governance, Risk & Compliance Specialist - 100% Remote

1 Opening Alcorcon ### **Role description** **CyberProof is a cyber security services and platform company whose mission is to help our customers react faster and smarter – and stay ahead of security threats, by creating secure digital ecosystems. CyberProof automates processes to detect and prioritize threats early and respond rapidly and decisively.** **CyberProof is part of the UST Global family. Some of the world’s largest enterprises trust us to create and maintain secure digital ecosystems using our comprehensive cyber security platform and mitigation services.** **What are we looking for?** We are looking for a Governance, Risk \& Compliance Specialist to contribute for a project with one of our global customers pioneer in the security field. **Work location**: Madrid **Work mode: 100% remote, with** **occasional on\-site presence (up to 1–2 times per month) at the Madrid office.** **Languages:** * English C1 **Experience \& Qualifications Required** * 4 years’ experience in audits and compliance and assessments based on national and international standards (ISO27001, ISO22301, ENS, NIST, DORA, NIS2\) • Knowledge/certifications in ISO27001 is a must. It is also desirable knowledge in ENS, ISO 27005, ISO22301, ISO 42001, NIST CSF 2\.0, NIST, SOC 2, GDPR, DORA, NIS2, CMMC 2\.0 * Proficiency with a variety of instruments for assessing and controlling risk (ex. ISO 31000, Magerit v3, COSO) * Experience in implementation of best practices, compliance with information security policies and standards. * Technical experience or applicable knowledge in security architectures for different environments. * Experience related to Cybersecurity ecosystem, deployment experience of security technologies. * Knowledge of different security solutions/technologies: FW, DLP, IDS/IPS, EDR… * Experience in incident response plans and exercises * Computer Engineering/Telecommunications and/or Master in Cybersecurity It is also desirable and will be considered to hold certifications such as CISM, CISSP, CISA, ISO/IEC 27001 Lead Auditor / Lead Implementer. We will also consider knowledge of HIPAA, ARC\-AMPE or OT Cybersecurity (ISO 27019 / IEC 62443\) for the more senior role **Key Roles \& Responsibilities:** * Handle the assigned tasks from the allocated domain with minimal guidance from the leads. (Domain Examples: BCMS, ISMS, Risk assessment (AARR \& BIAs), GAP Analysis, Incident management, Awareness activities, Data Privacy, etc.) * Independently handle (with very minimal guidance from the supervisors) internal audits or GAP Analysis to ensure compliance with security standards (ex. ISO 27001/ISO 22301/ISO 27701, NIST CSF 2\.0, ..) requirement as well as process specific requirements * Point out the non\-conformance areas and suggest measures to improve the information security individually. * Coordinate information security awareness training programs for all the employees, contractors and approved system users. * Coordinate and Review the technical assessments of IT systems and processes to identify potential risks. Submit recommendations to mitigate any risks identified and ensure controls that they are implemented. * Design, plan and execute the Cybersecurity activities. * Directly Interact with customer and communicate detailed technical requirement to the team. * Policy/Procedure creation activities and process improvement ideas to be implemented. * Research and analytical skills, including the ability to convert complex policy issues into simple briefings and communicate to the audience. **What can we offer?** 23 days of Annual Leave plus the 24th and 31st of December as discretionary days! Numerous benefits (Heath Care Plan, Internet Connectivity, Life and Accident Insurances). \`Retribución Flexible´ Program: (Meals, Kinder Garden, Transport, online English lessons, Heath Care Plan…) Free access to several training platforms Professional stability and career plans UST also, compensates referrals from which you could benefit when you refer professionals. The option to pick between 12 or 14 payments along the year. Real Work Life Balance measures (flexibility, WFH or remote work policy, compacted hours during summertime…) UST Club Platform discounts and gym Access discounts **If you would like to know more, do not hesitate to apply and we’ll get in touch to fill you in details. UST is waiting for you!** **In UST we are committed to equal opportunities in our selection processes and do not discriminate based on race, gender, disability, age, religion, sexual orientation or nationality. We have a special commitment to Disability \& Inclusion, so we are interested in hiring people with disability certificate.** ### **Skills** Business Intelligence,Iso 27001,GRC,Cyber Security ### **About UST** UST is a global digital transformation solutions provider. For more than 20 years, UST has worked side by side with the world’s best companies to make a real impact through transformation. Powered by technology, inspired by people and led by purpose, UST partners with their clients from design to operation. With deep domain expertise and a future\-proof philosophy, UST embeds innovation and agility into their clients’ organizations. With over 30,000 employees in 30 countries, UST builds for boundless impact—touching billions of lives in the process.

C. Polvoranca, 44, 28921 Alcorcón, Madrid, Spain

Negotiable Salary

tecnico de laboratorio mecanico644132401158411226

Indeed

tecnico de laboratorio mecanico

With our strong investment in research and development and our culture of continuous improvement, Hexcel is the industry leader in the manufacturing of advance composite materials, including carbon fiber, woven reinforcements, resins, prepregs, honeycombs and additive manufactured parts. We invite you to join the Hexcel team at various manufacturing sites, sales offices and R\&T centers around the globe. Become a part of the “strength within ". Hexcel is currently seeking Chemical lab Technician for our Parla location (Spain). The selected individual will be responsible for, but not limited, to the following obligations:* Collection and storage of test material. * Issuance of worksheets. * Realization of panels, vacuum bags, curing, machining of specimens, preparation of heels and tests according to the corresponding specifications. * Enter the data in the LIMS for the issuance of the Certificate of Analysis. * Maintenance of tools and tools. * Analysis of data obtained compared to the population. Qualifications:* Valuable experience in mechanical testing laboratory. * Internal learning. * Basic knowledge of Windows. Candidates must be eligible to work in the country where the position is based. Hexcel (NYSE: HXL) is a global leader in advanced composites technology, a leading producer of carbon fiber, and the world leader in honeycomb manufacturing for the commercial aerospace industry.

C. Alfonso XIII, 18, 28982 Parla, Madrid, Spain

Negotiable Salary

Indeed

Testing engineer

* If you are one of those who, after parking, double\-check that the car is closed… Your place is here! We are expanding our teams in the **space sector**. We´ll get to the point; we'll tell you what's not on the web. If you want to know more about us go to GMV website. **WHAT CHALLENGE WILL YOU BE TAKING ON?** In our team, you will **perform** various **tasks**, such as: * Inspections of purchased products. * Intermediate inspections of equipment, parts, and production processes. * Verification of finished products. * Creation of verification instructions. * Creation of production manuals. * Support for calibration and verification activities. **WHAT DO WE NEED IN OUR TEAM?** For this position, we are looking for **hardware technicians** (installations, repairs, laboratory, etc.) with knowledge of interpreting plans, handling measuring instruments, component assembly, and assembly. Knowledge of equipment calibration and verification, ESD environments, and Office software. The following will **be** **valued**: Experience in measuring and verifying machined and commercial parts. Verification of part quality. Control of production stock, verification of final product \- Packaging and labeling of final product for customer. Management of non\-compliant products. **WHAT DO WE OFFER?** **Hybrid working model** and **8 weeks** per year of **teleworking outside** your usual **geographical area.** **Flexible** start and finish **times**, and intensive working hours Fridays and in summer. **Personalized career plan** development, training and **language learning** support. National and international **mobility**. Do you come from another country? We can offer you a **relocation package**. **Competitive compensation** with ongoing **reviews**, flexible compensation and discount on brands. Wellbeing program: Health, dental and accident **insurance; free fruit and coffee**, physical, mental and financialhealth training, and much more! * ️ In our recruitment processes you will always have telephone and personal contact, face\-to\-face or online, with our talent acquisition team. In addition, bank transfers and bank cards will never be requested. If you are contacted through any other process, please write to our team at privacy@gmv.com ❤️We promote equal opportunities in recruitment, and we are committed to inclusion and diversity. **WHAT ARE YOU WAITING FOR? JOIN US** \#LI\-Hybrid If you have any questions please do not hesitate to contact **Ana Alonso Ruiz**, in charge of this vacancy. Ana Alonso Ruiz

Calle de la Aurora, 16, 28760 Tres Cantos, Madrid, Spain

Negotiable Salary

Senior Associate Venture Growth - 100% remote643742611695381228

Indeed

Senior Associate Venture Growth - 100% remote

***Join Tether and Shape the Future of Digital Finance*** At Tether, we’re not just building products, we’re pioneering a global financial revolution. Our cutting\-edge solutions empower businesses—from exchanges and wallets to payment processors and ATMs—to seamlessly integrate reserve\-backed tokens across blockchains. By harnessing the power of blockchain technology, Tether enables you to store, send, and receive digital tokens instantly, securely, and globally, all at a fraction of the cost. Transparency is the bedrock of everything we do, ensuring trust in every transaction. ***Innovate with Tether*** **Tether Finance:** Our innovative product suite features the world’s most trusted stablecoin, **USDT**, relied upon by hundreds of millions worldwide, alongside pioneering digital asset tokenization services. But that’s just the beginning: **Tether Power:** Driving sustainable growth, our energy solutions optimize excess power for Bitcoin mining using eco\-friendly practices in state\-of\-the\-art, geo\-diverse facilities. **Tether Data:** Fueling breakthroughs in AI and peer\-to\-peer technology, we reduce infrastructure costs and enhance global communications with cutting\-edge solutions like **KEET**, our flagship app that redefines secure and private data sharing. **Tether Education**: Democratizing access to top\-tier digital learning, we empower individuals to thrive in the digital and gig economies, driving global growth and opportunity. **Tether Evolution**: At the intersection of technology and human potential, we are pushing the boundaries of what is possible, crafting a future where innovation and human capabilities merge in powerful, unprecedented ways. ***Why Join Us?*** Our team is a global talent powerhouse, working remotely from every corner of the world. If you’re passionate about making a mark in the fintech space, this is your opportunity to collaborate with some of the brightest minds, pushing boundaries and setting new standards. We’ve grown fast, stayed lean, and secured our place as a leader in the industry. If you have excellent English communication skills and are ready to contribute to the most innovative platform on the planet, Tether is the place for you. **Are you ready to be part of the future?** **About the job** We’re currently looking for a Senior Associate to join our Venture Growth team. The position is 100% remote and will focus on expanding and accelerating Tether Ventures investment portfolio, ranging from seed and early stage investments to late stage, growth and strategic majorities. The Venture Growth team is currently a five person team that works closely with multiple other teams within Tether to assess investment opportunities, unlock synergies and create strategic value. This role will also work with external C\-level executives and board representatives on strategic planning, oversight and execution of key initiatives, monitoring, business planning/budgeting and KPIs. **Responsibilities** * Conduct screening and assessment of new investment opportunities in collaboration with the broader investment team, including market sizing, competitive analyses, and business model validation. * Participate in due diligence for new investments, with a focus on operational and strategic fit, scalability, and synergy potential. * Develop investment memos and strategic recommendations for internal and investor review, clearly articulating expected ROI and risks. Within the Portfolio: * Collaborate with senior leadership to assess and enhance their growth potential, operational effectiveness, and performance. * Partner with strategic leaders across business lines to set realistic key performance indicators (KPIs), design reporting templates, and engage in ongoing performance dialogue. * Map out competitive and adjacent industry landscapes, co\-develop strategic growth plans, and lead their execution. * Engaging with management teams on value\-creation initiatives such as go\-to\-market strategy, competitive threat assessments, cost synergy realization, and capital efficiency projects (including working capital optimization and procurement reviews). * Lead planning and forecasting processes to support company growth and regional expansion objectives. Build multi\-year business models to guide investments across capex, opex, M\&A, and human capital. * Support innovation efforts aimed at expanding revenue streams and improving profitability across the platform. * Contribute to inorganic growth initiatives by identifying, evaluating, and executing acquisition and partnership opportunities. * Ensure cross\-portfolio collaboration by promoting communication and alignment on shared initiatives, resources, and best practices. * Identify and coordinate human capital needs to support growth initiatives, leveraging internal teams for revenue generation and operational efficiency. * Drive a continuous improvement culture and operational excellence across the organization. * Bachelor’s degree or equivalent experience required. Master of Business Administration (or commensurate experience) preferred. * 5\+ years of experience required. Consulting, investment banking and/or PE experience preferred (e.g., 2\-3 yrs consulting \+ 2\-3 yrs in industry). * 2\+ years experience with the payments industry is preferred * Deep knowledge of resource planning, demand planning, budgeting, business planning, corporate strategy required. Prior exposure to the following areas is also valued: + Coordination of cross\-functional teams; + Direct reporting or direct interaction with C\-suite executives; + Strategic advisory projects for multinational groups including acquisitions, postmerger integrations, operational improvement plans; + Development of business plans, budgets, operating models, due diligence reports,investor reports and management presentations; + Acquisition due diligence (commercial, financial, legal, tax, technology, organizational, etc.) and/ or post\-acquisition support; + Exposure to communications, sales, business line or product management leadership, benchmarking, and forecasting functions. * Strong business sense, market research, analytical, and presentation skills required. Being reliable and organized: proven ability to work proactively to deliver high\-quality end\-results and outputs with attention to details even under pressure. * Must have strong verbal, written, and interpersonal communication skills to interact with all associates and key stakeholders, with the ability to communicate with tact and diplomacy. Able to present a proprietary standpoint / proposition and lead with influence. * Demonstrated ability to abide to commitments and protect confidential information. * Ability to develop and execute short and long\-term strategic plans; ability to develop and maintain external relations with a wide range of stakeholders and partners. * Ability to work day\-to\-day with management teams across different levels of seniority. * Limited travel may be required. **Important information for candidates** Recruitment scams have become increasingly common. To protect yourself, please keep the following in mind when applying for roles: * **Apply only through our official channels.** We do not use third\-party platforms or agencies for recruitment unless clearly stated. All open roles are listed on our official careers page: https://tether.recruitee.com/ * **Verify the recruiter’s identity.** All our recruiters have verified LinkedIn profiles. If you’re unsure, you can confirm their identity by checking their profile or contacting us through our website. * **Be cautious of unusual communication methods.** We do not conduct interviews over WhatsApp, Telegram, or SMS. All communication is done through official company emails and platforms. * **Double\-check email addresses.** All communication from us will come from emails ending in **@**tether.to **or @**tether.io * **We will never request payment or financial details.** If someone asks for personal financial information or payment at any point during the hiring process, it is a scam. Please report it immediately. **When in doubt, feel free to reach out through our official website.**

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

Negotiable Salary

Ink Application Technology Engineer643738684853791229

Indeed

Ink Application Technology Engineer

**Your Responsibilities – What to Expect as an Ink Application Technology Engineer** * You will manage projects to deliver defined technological solutions, applications, and services within agreed timelines, budgets, and standards. * You will conduct laboratory studies to develop technological solutions tailored to customer and market needs, in cooperation with the technology and analysis laboratory, including on-site support at customer facilities. * You will carry out research activities, including on-site support at customer sites, as well as execution of various R&D projects. * You will identify technical requirements, raw materials, processes, and oversee any technical activities related to product development. * You will provide technical advice and decision-making support, as well as assist colleagues in the Sales Department. * You will prepare technical and test reports. **Your Profile – What You Bring as an Ink Application Technology Engineer** * You hold a university degree in Chemistry or a related field. * You have knowledge of liquid inks and/or printing processes such as gravure or flexography, or expertise in polymeric materials. * You have experience with dosing systems, colorimetry, spectrophotometer usage, and other quality control equipment used in the printing industry. * You are a dynamic and innovative professional, customer/results-oriented, with a high level of flexibility and initiative. * You are an effective communicator with strong English language skills. * You have good knowledge of office software and SAP. * Occasional travel availability is required.

9HMX+8X Loeches, Spain

Negotiable Salary