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Laboratory & Technical Services in Uceda

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Laboratory & Technical Services

Uceda

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Location:Uceda

Category:Laboratory & Technical Services

Laboratory Technician65156659209859120

Laboratory Technician

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

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

Food Safety and Quality Technician65137459057282121

Food Safety and Quality Technician

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

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

Revenue Financial Controller - Laboratorio Central Health Diagnostics Quirónsalud (Alcobendas)65106073484547122

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

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

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

Intern65106073466754123

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

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

Associate Clinical Trial Manager (PhD) - Neuroscience / Ophthalmology65093665409793124

Associate Clinical Trial Manager (PhD) - Neuroscience / Ophthalmology

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

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

Senior Medical Writer - Sponsor dedicated - Remote role based in Europe65085463563521125

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

**Description** Senior Medical Writer \- Sponsor dedicated \- Remote role based in Europe Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities. Our Clinical Development model brings the customer and the patient to the center of everything that we do. We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to work with, but to make us easier to work for. Whether you join us in a Functional Service Provider partnership or a Full\-Service environment, you’ll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals. We are agile and driven to accelerate the delivery of therapies, because we are passionate to change lives. Discover what our 29,000 employees, across 110 countries already know: **WORK HERE MATTERS EVERYWHERE** Why Syneos Health * We are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program. * We are committed to our Total Self culture – where you can authentically be yourself. Our Total Self culture is what unites us globally, and we are dedicated to taking care of our people. * We are continuously building the company we all want to work for and our customers want to work with. Why? Because when we bring together diversity of thoughts, backgrounds, cultures, and perspectives – we’re able to create a place where everyone feels like they belong. **Job Responsibilities** * Leads the clear and accurate completion of medical writing deliverables, ensuring scientific information is presented clearly and accurately. Manages medical writing activities associated with individual studies, coordinating medical writing activities within and across departments with minimal supervision. Leads the resolution of comments from the client. * Completes a variety of documents that may include clinical study protocols and clinical study protocol amendments; clinical study reports; patient narratives; annual reports; investigator brochures; informed consents; annual reports; plain language summaries; periodic safety update reports, clinical development plans; IND submissions; integrated summary reports; NDA and eCTD submissions; journal manuscripts; and abstracts, posters, and presentations for scientific meetings. * Adheres to established regulatory standards, including, but not limited to, ICH E3 guidelines, as well as company standard operating procedures, client standards, and company and/or client approved\-templates, authorship requirements, and style and formatting guides, when completing medical writing projects, on time and on budget. * Coordinates quality and editorial reviews. Ensures source documentation is managed appropriately. Leads team document reviews, and reviews documents as needed. * Acts as peer reviewer for internal team to ensure document scientific content, clarity, overall consistency, and proper format. * Reviews statistical analysis plans and table/figure/listing specifications for appropriate content, and for grammar, format, and consistency. Provides feedback to further define statistical output required and document needs. * Interacts and builds good working relations with clients, department head, and peers in data management, biostatistics, regulatory affairs, and medical affairs, as necessary, to produce writing deliverables. * Performs online clinical literature searches and complies with copyright requirements. * Identifies and proposes solutions to resolve issues, escalating as appropriate. Provides technical support, training, and consultation to department and other company staff. May contribute to development of internal materials and presentations or changes to internal process, standard practices, and capabilities. * Mentors and leads less experienced medical writers on complex projects, as necessary. * Develops deep expertise on key topics in the industry and the regulatory requirements and guidelines that affect medical writing. * Aware of budget specifications for assigned projects, working within the budgeted hours and communicating status and changes to medical writing leadership. * Completes required administrative tasks within the specified timeframes. * Performs other work\-related duties as assigned. * Minimal travel may be required (less than 25%). Qualifications: * 3\-5 years of relevant experience in science, technical, or medical writing. * Experience working in the biopharmaceutical, device, or contract research organization industry required. * Strong understanding of FDA and ICH regulations, other regulatory guidelines, and/or good publication practices strongly required. * Experience writing relevant document types required. * Extensive knowledge of English grammar and ability to communicate clearly; strong familiarity with AMA Manual of Style. **Get to know Syneos Health** Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and 675,000\+ Trial patients. No matter what your role is, you’ll take the initiative and challenge the status quo with us in a highly competitive and ever\-changing environment. Learn more about Syneos Health. http://www.syneoshealth.com **Additional Information** Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description. The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. Further, nothing contained herein should be construed to create an employment contract. Occasionally, required skills/experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees. The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job. **Summary** Roles within the Medical Writing job family are responsible for writing and editing manuscripts and other medical communications on clinical studies and/or scientific reports including special summaries from raw data for submission to regulatory agencies or for in\-company use, monographs, comprehensive reviews, scientific exhibits, and other projects requiring skill in medical communication such as screening, analyzing, and summarizing additional data from other sources as needed. Conducts systematic literature searches and reviews. Prepares literature for new products and revises existing medical communication. Reviews and analyzes statistical outputs to prepare results\-based documents such as clinical study reports and development safety update reports. Supports engagement and interaction with regulatory agencies through preparation of briefing books and response documents to health authority questions.Impact and ContributionIndividual contributors with responsibility in a professional or technical discipline or specialty, but may manage two or fewer employees. May direct the work of lower level professionals or manage processes and programs. The majority of time is spent contributing to the design, implementation or delivery of processes, programs, and policies, using knowledge and skills typically acquired through advanced education. Individual contributor with developing subject matter expertise and responsibility for processes. In\-depth knowledge and skills within a professional discipline, understanding the impact of work on related areas. May be responsible for entire projects or processes within area of responsibility.

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

Clinical Research Physician65049381326081126

Clinical Research Physician

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

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

Pediatric / Neuromuscular Neurologist65049381309698127

Pediatric / Neuromuscular Neurologist

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

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

Hepatology - Medical Director65049381292547128

Hepatology - Medical Director

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

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

Psychiatry - Medical Director65049381275907129

Psychiatry - Medical Director

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

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

Dermatologist - Medical Director650493812591371210

Dermatologist - Medical Director

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

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

Personal warehouse laboratory650493701854751211

Personal warehouse laboratory

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

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

Quality Technician648429715078421212

Quality Technician

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

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

Director - Strategy and Integration647499996944651213

Director - Strategy and Integration

Expedia Group brands power global travel for everyone, everywhere. We design cutting\-edge tech to make travel smoother and more memorable, and we create groundbreaking solutions for our partners. Our diverse, vibrant, and welcoming community is essential in driving our success. **Why Join Us?** To shape the future of travel, people must come first. Guided by our Values and Leadership Agreements, we foster an open culture where everyone belongs, differences are celebrated and know that when one of us wins, we all win. We provide a full benefits package, including exciting travel perks, generous time\-off, parental leave, a flexible work model (with some pretty cool offices), and career development resources, all to fuel our employees' passion for travel and ensure a rewarding career journey. We’re building a more open world. Join us. Expedia Group B2B is looking for a strategic forward\-looking **Director, Strategy and Integration** to play a meaningful role in evolving our business and redefining the travel industry. Do you want to help people go places? Come travel with us! In this role, you will accelerate the execution of Expedia Group fast growth B2B branch, starting by leading the business integration of acquired companies into our Expedia Group portfolio. Besides this you will be responsible for strategic projects that drive transformational change for our B2B partners across our Lodging, Air and Ground Transport businesses. This includes defining objectives and priorities, evaluating investment priorities and ensuring results. If you have a passion for M\&A, enjoy being results\-oriented, collaborative, and owning end\-to\-end strategic projects then join this dynamic and mighty team! **What you'll do:** ------------------- * Collaborating with key functional leaders, corporate, HR and finance, lead business, product and tech, strategy and commercial integration of acquired company for Expedia Group * Work with third party suppliers for the execution of the integration * Recognize and frame strategic opportunities for Expedia B2B, with a focus on external, in a structured, analytical way to clearly communicate options, risks, and trade\-offs * Drive decision\-making and alignment by working across E4B and Expedia Group * Lead strategic projects and lead investigations to drive the business forward * Travel required, in Amsterdam in year 1 **Who you are:** ---------------- * You have a solid track record of Post Merger Integration and M\&A * You bring excellent quantitative, analytical and critical thinking skills and an ability to translate metrics, research and trends into viable strategies * You have excellent oral and written communication skills to communicate issues and influence others, including experience communicating complex information to senior leaders * You see the 'big picture' and to effectively prioritize and drive multiple projects * You are a self\-starter who can excel in a fast\-paced and fluid environment * You are a team player who actively promotes \& encourages diversity of thought * 10\+ years’ experience in strategy consulting and / or similar role in a leading technology company; MBA a plus * Expert level knowledge of Microsoft Excel and PowerPoint and proven experience in modeling, analysis, research and presentation creation **Accommodation requests** If you need assistance with any part of the application or recruiting process due to a disability, or other physical or mental health conditions, please reach out to our Recruiting Accommodations Team through the Accommodation Request. We are proud to be named as a Best Place to Work on Glassdoor in 2024 and be recognized for award\-winning culture by organizations like Forbes, TIME, Disability:IN, and others. Expedia Group's family of brands includes: Brand Expedia®, Hotels.com®, Expedia® Partner Solutions, Vrbo®, trivago®, Orbitz®, Travelocity®, Hotwire®, Wotif®, ebookers®, CheapTickets®, Expedia Group™ Media Solutions, Expedia Local Expert®, CarRentals.com™, and Expedia Cruises™. © 2024 Expedia, Inc. All rights reserved. Trademarks and logos are the property of their respective owners. CST: 2029030\-50 Employment opportunities and job offers at Expedia Group will always come from Expedia Group’s Talent Acquisition and hiring teams. Never provide sensitive, personal information to someone unless you’re confident who the recipient is. Expedia Group does not extend job offers via email or any other messaging tools to individuals with whom we have not made prior contact. Our email domain is @expediagroup.com. The official website to find and apply for job openings at Expedia Group is careers.expediagroup.com/jobs. Expedia is committed to creating an inclusive work environment with a diverse workforce. All qualified applicants will receive consideration for employment without regard to race, religion, gender, sexual orientation, national origin, disability or age.

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

Laboratory Technician | Clinical Analysis | Madrid646852801681951214

Laboratory Technician | Clinical Analysis | Madrid

Would you like to join **Novasalud Global Health**, a leading company in corporate health services, clinical analysis, and healthcare assistance? We are seeking a **Senior Laboratory Technician** to join our team in **Madrid** for **clinical analysis and blood draws** at a **medical center**, for an **approximate period of 6 months**, from **Monday to Friday (working days).** **Main responsibilities:** * Performing clinical analyses, blood draws, and collection of biological samples. * **Pre-analytical procedures** and **sample preparation** for shipment to the laboratory. * **Incident management** and **order management**. **Requirements:** * Qualification as a **Senior Technician in Clinical and Biomedical Laboratory** or equivalent. * Prior experience in **clinical analysis and blood draws**. * Availability of a **personal vehicle** is desirable. **Job conditions:** * Working schedule: **Monday to Friday (working days).** * Working hours: **8:30 a.m. to 10:30 a.m.** * Contract type: **Fixed-term intermittent contract.** * Start date: **Immediate.** * Duration: **Approximately 6 months; possible extension.** * Gross salary: **€500/month** **What we offer:** * Job stability and flexibility. * A dynamic and professional work environment. * Ongoing training in clinical analysis. * Compatibility with another job. **How to apply:** Submit your updated CV by clicking "Apply now" and join our team. **Also...** Join our WhatsApp channel (we post job openings daily) here → https://goo.su/q3nXnLh Job type: Part-time, Fixed-term intermittent contract Contract duration: 6 months Salary: €500.00 per month Work location: On-site

Ronda del Caballero de la Mancha, 68, Fuencarral-El Pardo, 28034 Madrid, Spain

Sr Medical Writer - Narrative Writer646172586382101215

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

Copy of Agro-Food Laboratory Technician645509424788491216

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

Lead UI/UX Product Designer645225215430411217

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 Specialist645225139024671218

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

Management Controller - Central Laboratory Health Diagnostics Quirónsalud (Alcobendas)645212543156491219

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

Testing engineer643857925159701220

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

Waste Technical Management Internship643298356757771221

Waste Technical Management Internship

**Job Description** At Veolia Spain, we are looking to hire a person to carry out an internship in Waste Technical Management at our central offices in Madrid. If you are interested in participating in the selection process, apply here! Responsibilities * You will actively participate in monitoring and optimizing waste business lines (plastics, commercial and industrial, and municipal waste), collaborating in defining investment solutions, work procedures, and operational support. * You will support the implementation of strategic projects such as lean management by providing cross-functional support to the rest of the team. * Monitoring waste plant operations. Tracking KPIs, analyzing production and efficiency data, assisting in report preparation. * Support for industrial risk control activities (risk assessments, etc…). * Coordination and Presentation: Coordinate with various internal departments, suppliers, and others to obtain necessary information within established deadlines. We offer: * Working hours: Flexible, arrival time between 07:30 and 09:30 * Duration: 6 months * Financial allowance: 950 euros / 40 hr week **Requirements** * Education: Bachelor’s degree in Engineering or related field * English level: B2 * Work location: Madrid **Additional Information** As an inclusive company, Veolia is committed to diversity and values all applications without discrimination.

C. de Serrano Galvache, 56, Cdad. Lineal, 28033 Madrid, Spain

Technical Management Internship in Municipal Waste643298356908821222

Technical Management Internship in Municipal Waste

**Job Description** At Veolia España, we are looking to hire a person for an internship in the Technical Management of Municipal Waste at our central offices in Madrid. If you are interested in participating in the selection process, apply here! Responsibilities: * Support in tender analysis: Collaborate in reviewing tender documents, identifying basic requirements and deadlines under the supervision of the technical manager. * Support during site visits and data collection: Accompany teams on visits to waste management facilities for data gathering and learning about operational processes. * Preparation of basic documentation: Draft spreadsheets, comparative tables, and simple technical documents following established templates. * Assistance in coordination: Support communication with internal departments and suppliers to collect necessary information. * Administrative follow-up: Keep records of submitted bids, deadlines, and tender statuses updated in databases. * Operational data analysis: Assist in collecting and performing basic analysis of KPIs and production indicators from facilities under supervision. We offer: * Working hours: Flexible, arrival time between 07:30 and 09:30 * Duration: 6 months * Financial allowance: 950 euros / 40 hours per week **Requirements** * Education: Bachelor's degree in Engineering or related field * English level: B2 * Work location: Madrid **Additional Information** As an inclusive company, Veolia is committed to diversity and values all applications without discrimination.

C. de Serrano Galvache, 56, Cdad. Lineal, 28033 Madrid, Spain

Senior Product Manager - Core Distributed Platform - East Coast to EMEA643184839171851223

Senior Product Manager - Core Distributed Platform - East Coast to EMEA

Location Spain, United States, Canada, United Kingdom, Hungary, Germany, Sweden, Belgium, Netherlands, Switzerland Employment Type Full time Location Type Remote Department Products Product Management Camunda is the **leader in enterprise agentic automation, orchestrating complex business processes**, including high\-value knowledge work, across agents, people, and systems. By creating production\-ready, enterprise\-grade agents with built\-in governance, Camunda uniquely delivers trusted AI agents for business\-critical processes. **Over 700 leading innovators like Atlassian, ING, and Vodafone, rely on Camunda** to slash time\-to\-value from months to days, boost operational efficiency, and elevate customer experiences. **As a fully remote, global company, we’re rewriting the rules of modern business.** Named GP Bullhound’s 2024 Top 100 Next Unicorn list, certified as a **Great Place to Work**, and recognized by Flexa for true flexibility, we’re growing fast and looking for top talent to join our team. If you’re excited to do meaningful work and make real impact, keep reading, **this role could be the one you’ve been waiting for.** **About the role:** We are seeking a talented and technically proficient Senior Product Manager to lead the development and evolution of our Core Distributed Platform, which includes Zeebe, the cloud\-native workflow engine at the heart of Camunda. This critical role is both technical and product\-focused, requiring a deep understanding of customer needs, system scalability, performance, reliability, and security. As the Senior Product Manager for the Core Distributed Platform, you will work closely with engineering teams, customers, and stakeholders to define and execute the product strategy for our distributed workflow orchestration engine. You will drive the roadmap for foundational platform capabilities and ensure the platform meets the complex requirements of distributed systems at scale. *Curious about the kind of challenges you'll work on at Camunda? Watch this quick* *30\-minute talk* *from our engineers to learn more about the new Camunda Exporter and how we’re solving complex problems at scale* **What You’ll Be Doing:** * Define market\-driven vision, strategy, and product requirements focused on improving the Camunda product portfolio. * Manage community, customer, partner, and internal feedback with an emphasis on successfully driving innovation to improve our customers experience with Camunda’s core platform. * Fully evaluate and prioritize incoming feature requests * Keep the self\-managed team equipped to work on the appropriate epics. * Continuous assessment of Camunda demand, market differentiation and the competitive landscape as well as close collaboration with our Pre\-Sales Engineers, Solution Architects, and other Field teams. **What You Bring:** * Ability and/or willingness to use our product * Experience working with platform products used by IT departments at large enterprise companies (e.g., developers, automation engineers, ops teams). * 5\+ years of product management experience, ideally in distributed systems, technical SaaS products, PaaS, or cloud\-native products. * Experience of OKRs, customer research techniques, product design, Go\-To\-Market planning, backlog management, and working in Agile teams. * Strong communication skills \- internally collaborating with others and externally presenting to customers. * Strong understanding of distributed systems concepts, including scalability, fault tolerance, event\-driven architecture, and performance optimization. **Nice\-to\-haves:** * Familiarity with technologies such as Kubernetes, Docker, cloud services (AWS, GCP, Azure), and message brokers (e.g., Kafka, RabbitMQ). * Experience working with IT platforms in banking, financial services, and insurance sector. * Technical knowledge of configuring, deploying, managing the life cycle of platform products. \#LI\-SK1 \#LI\-Remote \#EMEA \#USEAST **What We Have to Offer:** **Compensation** We offer competitive, fair, and transparent compensation. Salary ranges are location\-based, with Standard and Major markets (global tech hubs) reflecting local competition. **The Annual Total Target Cash** (base salary \+ 100% variable target, where applicable) shown below spans from the minimum in a Standard market to the maximum in a Major market. Final offers depend on **skills**, **experience**, and **location**, and we typically hire in the first half of the range to allow room for growth: * United States: $143,800\.00 to $231,900\.00 * Germany: €92,900\.00 to €153,700\.00 * United Kingdom: £90,300\.00 to £148,500\.00 * Singapore: S$178,600\.00 to S$267,900\.00 If you’re based elsewhere, you’ll be hired via **Remote.com** (our global employer partner), and your Talent Acquisition Partner will provide a personalized **Total Rewards Calculator** after your first interview. **Equity:** We also offer equity (where applicable) through our **Virtual Stock Option Plan (VSOP)**. **Benefits \& Perks** We invest in your wellbeing, growth, and ability to connect, along with perks that support you no matter where you’re based. Our benefits are globally designed and locally delivered where applicable. * **Remote \& Flexible:** Work from anywhere with the setup that suits you, **home office budget, co\-working space support, and flexible time off** to recharge when you need it. * **In Person Connection:** We invest in meaningful face time through our **Annual Kickoff** (Vienna in 2025, Madrid in 2026!), **team offsites, and Camundi Connection Budgets**, including contributing to meetups while travelling,, and local gatherings with fellow Camundi. * **Health \& Wellbeing:** Access locally tailored healthcare, **Modern Health for global mental wellbeing, and an annual fitness reimbursement.** * **Financial Security:** Retirement and pension plans (often with company contributions), plus life and disability insurance where relevant. * **Professional Growth:** Up to $/€/£1,000 per year for self\-driven learning: courses, certifications, books, you decide! *”Everyone is welcome at Camunda”* — *it’s a celebrated component of our culture. We strive to create an inclusive environment that empowers our people. At Camunda, we honour diverse cultures and backgrounds and are proud to be an equal opportunity employer. All qualified applicants will receive consideration without regard to gender, race, ethnicity, religion, belief, sexual orientation, age, disability or any other protected characteristics under applicable law. We are looking forward to your application!* ***Come join us and be part of Camunda’s incredible journey: Make an impact at a pivotal moment in our story!***

AI Design Systems & Product Designer (Freelance)642962796227871224

AI Design Systems & Product Designer (Freelance)

DESCRIPTION ### **What we're looking for…** We are looking for someone capable of exploring, defining, and executing the strategy to integrate AI capabilities into design systems, based on the objectives and experiments established in our transformation project. A person with a practical, visual, and implementation-focused mindset. A profile who will lead the team to ensure that our design components and patterns are not only scalable and consistent, but also adaptive and intelligent. * **Flexible collaboration format (fractional advisory/part\-time).** ### **Specifically, here’s what you’ll do:** * Lead Strategy: Drive the evolution of the design system by defining the roadmap for AI integration, aligned with project goals. * Research and Experimentation: Promote experimentation with new AI tools and workflows (generative, predictive) to optimize and enhance the design system. * Define Patterns: Develop and document new design patterns and components that incorporate AI in an ethical, accessible, and user-centered way. * Interdisciplinary Collaboration: Work closely with engineering, product, and data science teams to implement and validate AI solutions within the system. * Management and Mentorship: Guide and mentor the design team, fostering a culture of innovation and excellence at the intersection of design and AI. ### **For this, you should have experience in…** * Product or UI/UX designer with strong proficiency in Figma and Design Systems. * Experience in AI-powered interface projects (assistive UIs, generative tools, LLMs). * Solid understanding of responsible and accessible design frameworks. * Ability to produce clear and structured documentation. * Professional English, remote work experience, and collaborative skills. ### **At Garaje, we appreciate people who…** Take pride in their work, give their best, always have fun, are brave and take risks, learn from mistakes, and love what they do. Our attitude is defined by the passion with which we engage in our projects, the empathy and closeness we show to our clients, and our ambition to go beyond just being correct. ### **At Garaje...We are \| We are not:** We are humble and approachable people \[but not subservient or simplistic] We are passionate and expert people \[but not overwhelming or pretentious] We are purposeful makers \[but not mere doers or gurus] We are brave and consistent people \[but not reckless or irresponsible] We are self-demanding \[but not obstructive] ### **What happens next?** If this sounds good to you, click "apply"—we’re excited to receive your application! If your profile matches what we’re looking for, we’ll contact you soon to schedule an initial introductory call. If you progress, you’ll likely meet someone from the team.

Principal Data Operations Analyst641693958206741225

Principal Data Operations Analyst

**Job Description** This position executes the Onshore processes of Stat Operations and associated project work for their country. This includes understanding and representing the local market conditions in the operations processes, as well as executing the local country “onshore” work. This entails engaging local partners like IO and CSE teams to ensure smooth hand\-offs in operations. **Job Responsibilities** * Execute the Statistical Operations processes and related project work for the designated country. Onshore project work involves tasks that require a local presence, such as understanding the local landscape, sample design, and conducting data queries that necessitate local inspections, contacts, or language proficiency. * Collaborate with the country’s Onshore Operations team to meet execution requirements as outlined in the Operations process playbooks and associated project work. * Maintain close collaboration with the country’s Offshore Statistical Operations and Input Validation team. * Engage with the Client Services Executive (CSE) and Data Science teams on specific Operations and project work to ensure smooth operations. * Act as a contact point for local deliverables and for specific Operations and project work, addressing data inquiries or challenges with local teams and offshore Operations regarding processes or methods. * Work with the CPS EU IV/SO Hub Leader, Coordinators, or Client Operations leaders/teams to harmonize processes, methods, and applications in order to implement optimized best practices. **Qualifications:** Essential Requirements: * Fluency in English * Bachelor's degree (B.S. or B.A.), preferably in a statistical, mathematical, or technical field * Working knowledge of SQL and database structures * Ability to work in a cross\-functional environment with multiple interacting teams * Experience in handling, manipulating, and analyzing data * Ability to document work and effectively prioritize documentation tasks * Excellent analytical and problem\-solving skills, with strong attention to detail * Ability to work both independently and collaboratively in a team setting * Strong organizational, communication, and interpersonal skills Preferred Qualifications: * Fluency in Spanish * Master’s degree * 1–3 years of experience in quantitative analysis * Experience with R and Python * Ability to execute research projects and translate findings into operational or analytical solutions * Ability to manage multiple projects simultaneously, while adapting to shifting priorities and deadlines * Capacity to integrate technical, marketing, and business perspectives \#LI\-Hybrid\-LN **Additional Information** **Our Benefits** * Flexible working environment * Volunteer time off * LinkedIn Learning * Employee\-Assistance\-Program (EAP) **About NIQ** NIQ is the world’s leading consumer intelligence company, delivering the most complete understanding of consumer buying behavior and revealing new pathways to growth. In 2023, NIQ combined with GfK, bringing together the two industry leaders with unparalleled global reach. With a holistic retail read and the most comprehensive consumer insights—delivered with advanced analytics through state\-of\-the\-art platforms—NIQ delivers the Full View™. NIQ is an Advent International portfolio company with operations in 100\+ markets, covering more than 90% of the world’s population. For more information, visit NIQ.com Want to keep up with our latest updates? Follow us on: LinkedIn \| Instagram \| Twitter \| Facebook **Our commitment to Diversity, Equity, and Inclusion** At NIQ, we are steadfast in our commitment to fostering an inclusive workplace that mirrors the rich diversity of the communities and markets we serve. We believe that embracing a wide range of perspectives drives innovation and excellence. All employment decisions at NIQ are made without regard to race, color, religion, sex (including pregnancy, sexual orientation, or gender identity), national origin, age, disability, genetic information, marital status, veteran status, or any other characteristic protected by applicable laws. We invite individuals who share our dedication to inclusivity and equity to join us in making a meaningful impact. To learn more about our ongoing efforts in diversity and inclusion, please visit the https://nielseniq.com/global/en/news\-center/diversity\-inclusion

C. de Salvador de Madariaga, 1, Cdad. Lineal, 28027 Madrid, Spain

Junior Quality Assurance Inspector641625054048031226

Junior Quality Assurance Inspector

At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life\-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We’re looking for people who are determined to make life better for people around the world. **Primary Purpose and Objective of the Position:** * Ensure that quality systems directly related to materials, purchased intermediates, and finished products are managed according to established quality standards. * Ensure that physical inspection of packaging materials, medical devices, vials, purchased intermediates, and finished products is carried out in accordance with established procedures, approved specifications, and required timelines. **Educational Requirements (Studies):** Higher Degree in Quality Analysis and Control. **Personal Skills:** The following qualities are required: * Interpersonal skills: teamwork, customer orientation (internal/external), decision making, good oral and written communication. * Organizational skills: ability to prioritize objectives. * Technical skills: knowledge of Good Manufacturing Practices, quality concepts, and their application in the pharmaceutical industry is desirable. * Computer skills: proficiency in commonly used office software at user level, as well as knowledge of computer systems controlling business processes. **Key Responsibilities:** * **Ensure proper review, approval, and detection of potential rejections of packaging materials, and review and detection of potential rejections of purchased intermediates, vials, bulk products, and medical devices, for subsequent use in production.** ---------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------- * **Perform identification of purchased intermediates prior to receipt, as well as sampling of bulk materials for receipt and analysis.** ------------------------------------------------------------------------------------------------------------------------------------------------------ * **Collaborate in the creation and review and/or develop GMP procedures for the area in accordance with standards under our responsibility.** -------------------------------------------------------------------------------------------------------------------------------------------------- * **Ensure communication of quality issues to other members of the Incoming Quality Assurance \& Product Disposition team and other Quality Assurance teams.** ---------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------- **Key Responsibilities:** * No experience required. **Schedule:** Availability to work morning shift from Monday to Friday. Lilly is dedicated to helping individuals with disabilities actively engage in the workforce, ensuring equal opportunities when applying for positions. If you require accommodation to submit a resume for a position at Lilly, please complete the accommodation request form (https://careers.lilly.com/us/en/workplace\-accommodation) for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response. Lilly does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status. \#WeAreLilly

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

Senior Data Operations Analyst641507655837471227

Senior Data Operations Analyst

This position executes the Onshore processes of Stat Operations and associated project work for their country. This includes understanding and representing the local market conditions in the operations processes, as well as executing the local country “onshore” work. This entails engaging local partners like IO and CSE teams to ensure smooth hand\-offs in operations. **Job Responsibilities** * Execute the Statistical Operations processes and related project work for the designated country. Onshore project work involves tasks that require a local presence, such as understanding the local landscape, sample design, and conducting data queries that necessitate local inspections, contacts, or language proficiency. * Collaborate with the country’s Onshore Operations team to meet execution requirements as outlined in the Operations process playbooks and associated project work. * Maintain close collaboration with the country’s Offshore Statistical Operations and Input Validation team. * Engage with the Client Services Executive (CSE) and Data Science teams on specific Operations and project work to ensure smooth operations. * Act as a contact point for local deliverables and for specific Operations and project work, addressing data inquiries or challenges with local teams and offshore Operations regarding processes or methods. * Work with the CPS EU IV/SO Hub Leader, Coordinators, or Client Operations leaders/teams to harmonize processes, methods, and applications in order to implement optimized best practices. **Qualifications:** Essential Requirements: * Fluency in English * Bachelor's degree (B.S. or B.A.), preferably in a statistical, mathematical, or technical field * Working knowledge of SQL and database structures * Ability to work in a cross\-functional environment with multiple interacting teams * Experience in handling, manipulating, and analyzing data * Ability to document work and effectively prioritize documentation tasks * Excellent analytical and problem\-solving skills, with strong attention to detail * Ability to work both independently and collaboratively in a team setting * Strong organizational, communication, and interpersonal skills Preferred Qualifications: * Fluency in Spanish * Master’s degree * 1–3 years of experience in quantitative analysis * Experience with R and Python * Ability to execute research projects and translate findings into operational or analytical solutions * Ability to manage multiple projects simultaneously, while adapting to shifting priorities and deadlines * Capacity to integrate technical, marketing, and business perspectives **We offer:** * Meal allowance * Life insurance * Vacation days (22\) * Hybrid work mode * Volunteer time off * LinkedIn Learning * Employee\-Assistance\-Program (EAP) \#LI\-LN\-Hybrid **Additional Information** -------------------------- **Our Benefits** * Flexible working environment * Volunteer time off * LinkedIn Learning * Employee\-Assistance\-Program (EAP) **About NIQ** NIQ is the world’s leading consumer intelligence company, delivering the most complete understanding of consumer buying behavior and revealing new pathways to growth. In 2023, NIQ combined with GfK, bringing together the two industry leaders with unparalleled global reach. With a holistic retail read and the most comprehensive consumer insights—delivered with advanced analytics through state\-of\-the\-art platforms—NIQ delivers the Full View™. NIQ is an Advent International portfolio company with operations in 100\+ markets, covering more than 90% of the world’s population. For more information, visit NIQ.com Want to keep up with our latest updates? **Our commitment to Diversity, Equity, and Inclusion** At NIQ, we are steadfast in our commitment to fostering an inclusive workplace that mirrors the rich diversity of the communities and markets we serve. We believe that embracing a wide range of perspectives drives innovation and excellence. All employment decisions at NIQ are made without regard to race, color, religion, sex (including pregnancy, sexual orientation, or gender identity), national origin, age, disability, genetic information, marital status, veteran status, or any other characteristic protected by applicable laws. We invite individuals who share our dedication to inclusivity and equity to join us in making a meaningful impact. To learn more about our ongoing efforts in diversity and inclusion, please visit the https://nielseniq.com/global/en/news\-center/diversity\-inclusion

C. de Salvador de Madariaga, 1, Cdad. Lineal, 28027 Madrid, Spain

CPS Statistical Operations Analyst641501772568351228

CPS Statistical Operations Analyst

**Job Description** This position executes the Onshore processes of Stat Operations and associated project work for their country. This includes understanding and representing the local market conditions in the operations processes, as well as executing the local country “onshore” work. This entails engaging local partners like IO and CSE teams to ensure smooth hand\-offs in operations. **Job Responsibilities** * Execute the Statistical Operations processes and related project work for the designated country. Onshore project work involves tasks that require a local presence, such as understanding the local landscape, sample design, and conducting data queries that necessitate local inspections, contacts, or language proficiency. * Collaborate with the country’s Onshore Operations team to meet execution requirements as outlined in the Operations process playbooks and associated project work. * Maintain close collaboration with the country’s Offshore Statistical Operations and Input Validation team. * Engage with the Client Services Executive (CSE) and Data Science teams on specific Operations and project work to ensure smooth operations. * Act as a contact point for local deliverables and for specific Operations and project work, addressing data inquiries or challenges with local teams and offshore Operations regarding processes or methods. * Work with the CPS EU IV/SO Hub Leader, Coordinators, or Client Operations leaders/teams to harmonize processes, methods, and applications in order to implement optimized best practices. **Qualifications:** Essential Requirements: * Fluency in English * Bachelor's degree (B.S. or B.A.), preferably in a statistical, mathematical, or technical field * Working knowledge of SQL and database structures * Ability to work in a cross\-functional environment with multiple interacting teams * Experience in handling, manipulating, and analyzing data * Ability to document work and effectively prioritize documentation tasks * Excellent analytical and problem\-solving skills, with strong attention to detail * Ability to work both independently and collaboratively in a team setting * Strong organizational, communication, and interpersonal skills Preferred Qualifications: * Fluency in Spanish * Master’s degree * 1–3 years of experience in quantitative analysis * Experience with R and Python * Ability to execute research projects and translate findings into operational or analytical solutions * Ability to manage multiple projects simultaneously, while adapting to shifting priorities and deadlines * Capacity to integrate technical, marketing, and business perspectives **We offer:** * Meal allowance * Life insurance * Vacation days (22\) * Hybrid work mode * Volunteer time off * LinkedIn Learning * Employee\-Assistance\-Program (EAP) \#LI\-LN\-Hybrid **Additional Information** **Our Benefits** * Flexible working environment * Volunteer time off * LinkedIn Learning * Employee\-Assistance\-Program (EAP) **About NIQ** NIQ is the world’s leading consumer intelligence company, delivering the most complete understanding of consumer buying behavior and revealing new pathways to growth. In 2023, NIQ combined with GfK, bringing together the two industry leaders with unparalleled global reach. With a holistic retail read and the most comprehensive consumer insights—delivered with advanced analytics through state\-of\-the\-art platforms—NIQ delivers the Full View™. NIQ is an Advent International portfolio company with operations in 100\+ markets, covering more than 90% of the world’s population. For more information, visit NIQ.com Want to keep up with our latest updates? Follow us on: LinkedIn \| Instagram \| Twitter \| Facebook **Our commitment to Diversity, Equity, and Inclusion** At NIQ, we are steadfast in our commitment to fostering an inclusive workplace that mirrors the rich diversity of the communities and markets we serve. We believe that embracing a wide range of perspectives drives innovation and excellence. All employment decisions at NIQ are made without regard to race, color, religion, sex (including pregnancy, sexual orientation, or gender identity), national origin, age, disability, genetic information, marital status, veteran status, or any other characteristic protected by applicable laws. We invite individuals who share our dedication to inclusivity and equity to join us in making a meaningful impact. To learn more about our ongoing efforts in diversity and inclusion, please visit the https://nielseniq.com/global/en/news\-center/diversity\-inclusion

C. de Salvador de Madariaga, 1, Cdad. Lineal, 28027 Madrid, Spain

Staff ML Engineer (LLMS, NLP)641494104759071229

Staff ML Engineer (LLMS, NLP)

**Who we are is what we do.** Deel is the all\-in\-one payroll and HR platform for global teams. Our vision is to unlock global opportunity for every person, team, and business. Built for the way the world works today, Deel combines HRIS, payroll, compliance, benefits, performance, and equipment management into one seamless platform. With AI\-powered tools and a fully owned payroll infrastructure, Deel supports every worker type in 150\+ countries—helping businesses scale smarter, faster, and more compliantly. Among the largest globally distributed companies in the world, our team of 6,000 spans more than 100 countries, speaks 74 languages, and brings a connected and dynamic culture that drives continuous learning and innovation for our customers. **Why should you be part of our success story?** As the fastest\-growing Software as a Service (SaaS) company in history, Deel is transforming how global talent connects with world\-class companies – breaking down borders that have traditionally limited both hiring and career opportunities. We're not just building software; we're creating the infrastructure for the future of work, enabling a more diverse and inclusive global economy. In 2024 alone, we paid $11\.2 billion to workers in nearly 100 currencies and provided healthcare and benefits to workers in 109 countries—ensuring people get paid and protected, no matter where they are. Our momentum is reflected in our achievements and customer satisfaction: CNBC Disruptor 50, Forbes Cloud 100, Deloitte Fast 500, and repeated recognition on Y Combinator’s top companies list – all while maintaining a 4\.83 average rating from 15,000 reviews across G2, Trustpilot, Captera, Apple and Google. Your experience at Deel will be a career accelerator. At the forefront of the global work revolution, you'll tackle complex challenges that impact millions of people's working lives. With our momentum—backed by a $12 billion valuation and $1 B in Annual Recurring Revenue (ARR) in just over five years—you'll drive meaningful impact while building expertise that makes you a sought\-after leader in the transformation of global work. **Get ready to:** * Design and deploy advanced LLM\-powered applications that support our Payroll product lines and operations. * Lead architecture decisions, cost optimization, and observability efforts for mission\-critical AI workflows. * Collaborate with ML researchers, product managers, and application engineers. * Create massive impact by doing ground breaking work in an already high\-scale product. You'll bring: * 12\+ years of engineering experience, ideally in ML systems or large\-scale software, with a strong foundation in system design and architecture. * Hands\-on experience implementing research and algorithms in Python, focused on information retrieval, text processing, NLP, LLMs, and machine learning. * Experience building production\-grade LLM applications, including fine\-tuning or adapting base models for domain\-specific tasks. * Deep understanding of vector databases (e.g. Pinecone, Weaviate, FAISS) and how they fit into retrieval\-augmented generation and context retrieval pipelines. * Python expertise for AI/ML development and Node.js familiarity for integration with product and application teams. * Knowledge of prompt engineering, LLM API integration, and system reliability patterns for scaling AI in production. * Experience with observability and cost optimization across AI infrastructure (tracing, metrics, performance tuning). **Bonus** * Cost tracking and model optimization for AI workloads. * RAG implementations, LangChain/CrewAI experience. * Background in classical ML or pre\-LLM NLP. * Exposure to multimodal systems. **Total Rewards** Our workforce deserves fair and competitive pay that meets them where they are. With scalable benefits, rewards, and perks, our total rewards programs reflect our commitment to inclusivity and access for all. **Some things you’ll enjoy** * Stock grant opportunities dependent on your role, employment status and location * Additional perks and benefits based on your employment status and country * The flexibility of remote work, including optional WeWork access At Deel, we’re an equal\-opportunity employer that values diversity and positively encourage applications from suitably qualified and eligible candidates regardless of race, religion, sex, national origin, gender, sexual orientation, age, marital status, veteran status, disability status, pregnancy or maternity or other applicable legally protected characteristics. *Unless otherwise agreed, we will communicate with job applicants using Deel\-specific emails, which include @**deel.com* *and other acquired company emails like @**payspace.com* *and @**paygroup.com**. You can view the most up\-to\-date job listings at Deel by visiting**our careers page**.* *Deel is an equal\-opportunity employer and is committed to cultivating a diverse and inclusive workplace that reflects different abilities, backgrounds, beliefs, experiences, identities and perspectives.* *Deel will provide accommodation on request throughout the recruitment, selection and assessment process for applicants with disabilities. If you require accommodation, please inform our Talent Acquisition Team at recruiting@deel.com of the nature of the accommodation that you may require, to ensure your equal participation.* We use Covey as part of our hiring and/or promotional processes. As part of the evaluation process, we provide Covey with job requirements and candidate\-submitted applications. Certain features of the platform may qualify it as an Automated Employment Decision Tool (AEDT) under applicable regulations. For positions in New York City, our use of Covey complies with NYC Local Law 144\. We began using Covey Scout for Inbound on March 30, 2025\. For more information about our data protection practices, please visit our Privacy Policy. You can review the independent bias audit report covering our use of Covey here: https://getcovey.com/nyc\-local\-law\-144

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