Guadalajara Laboratory & Technical Services Job Listings

Quality Control Technician64960905206530120

We are looking for a Quality Control Technician to join our team in Tielmes de Tajuña. Your responsibilities will include comprehensive supervision of production processes to ensure adherence to the highest quality standards. You will carry out detailed inspections—both visual and analytical—of products to ensure they meet all required specifications. You will also perform necessary laboratory analyses to assess the quality of products and raw materials. You will play a key role in implementing and maintaining quality procedures, ensuring compliance with current regulations. In addition, you will participate in staff training on quality guidelines and standards, investigate incidents and complaints, and actively seek opportunities to improve the overall efficiency and quality of our processes. * Minimum 6 months’ experience in similar positions. * We are seeking a proactive, organized, and dynamic individual. * Proximity of residence to the workplace is desirable. Completed ESO or equivalent studies.

6MPX+8P Tielmes, Spain

Negotiable Salary

Indeed

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

Negotiable Salary

Ink Application Technology Engineer64706413646595122

Indeed

Ink Application Technology Engineer

**Your responsibilities – What can you expect as an Ink Application Technology Engineer?** * You will manage projects to deliver technological solutions, applications, and services defined according to agreed timelines, budgets, and standards. * You will conduct laboratory studies to develop technological solutions aligned with customer and market needs, in cooperation with the technology and analytical laboratory, including on-site support at customer facilities. * You will carry out research activities, including on-site support at customer facilities, as well as execution of various R&D projects. * You will identify technical requirements, raw materials, and processes, and supervise any technical activities related to product development. * You will provide technical advice and support for decision-making, as well as support to colleagues in the Commercial Department. * You will prepare technical and test reports. **Your profile – What do you bring as an Ink Application Technology Engineer?** * You hold a university degree in Chemistry or a related field. * You possess knowledge of liquid inks and/or printing processes such as gravure or flexography, or knowledge of polymeric materials. * You have experience with dosing systems, colorimetry, and use of spectrophotometers, as well as other quality control equipment used in the graphic arts industry. * You are a dynamic and innovative professional, customer- and results-oriented, with a high degree of flexibility and initiative. * You are a strong communicator with a high level of English proficiency. * You have good proficiency in office software and SAP. * Willingness to travel occasionally.

9HMX+8X Loeches, Spain

Negotiable Salary

Director - Strategy and Integration64749999694465123

Indeed

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

Negotiable Salary

Indeed

Quality Intern

**Title:** **Quality Intern** ============================= Location: Arganda del Rey, ES *At Tetra Pak we commit to making food safe and available, everywhere; and we protect what's good – protecting food, protecting people, and protecting the planet. By doing so we touch millions of people's lives every day.* *And we need people like you to make it happen.* ***We empower you to reach your potential with opportunities to make an impact to be proud of – for food, people and the planet.*** **Job Summary** --------------- We are looking for an Quality Intern to join Tetra Pak factory based in Spain, Arganda del Rey. This is a paid internship opportunity for a 6\-month \+ 6\-month period. You will be contracted through the Business School or University with a collaboration agreement signed and in force with Tetra Pak Envases S.A. Therefore, a **valid student status** is a must for this position. **What you will do** -------------------- * You will actively collaborate in the implementation and maintenance of the World Class Manufacturing methodology, especially in Quality. * You will be incorporated into the Quality department and will actively collaborate in all functions and tasks aimed at the development of quality methodology: Audits to groups / participation in the weekly strategic meetings of the group, collaboration in the analysis of defects and in the establishment of the conditions for 0 defects. * You will participate in the tasks and projects of the Quality Department, actively collaborating in the management of the quality. * You will gain a deep insight into the WCM (TPM) philosophy of continuous improvement and deep knowledge of one of the main pillars of WCM. **We believe you have** ----------------------- * Active student status at a university or Higher Educational / Business School within the Industrial Engineering / Quality / Manufacturing area * Fluent language skill in English and Spanish * Strong interest and passion to learn more about WCM and Quality methodology * Keen eye for details and highly responsible person **We Offer You** * A variety of exciting challenges with ample opportunities for development and training in a truly global landscape * A culture that pioneers a spirit of innovation where our industry experts drive visible results * An equal opportunity employment experience that values diversity and inclusion * Market competitive compensation and benefits with flexible working arrangements **Apply Now** If you are inspired to be part of our promise to protect what’s good; for food, people, and the planet, apply through our careers page at https://jobs.tetrapak.com/. This job posting expires on **25th December 2025\.** If you have any questions about your application, please contact **Turan Abdullazade at Turan.Abdullazade@tetrapak.com** *Diversity, equity, and inclusion is an everyday part of how we work. We give people a place to belong and support to thrive, an environment where everyone can be comfortable being themselves and has equal opportunities to grow and succeed. We embrace difference, celebrate people for who they are, and for the diversity they bring that helps us better understand and connect with our customers and communities worldwide.*

P.º de la Estación, 28D, 28500 Arganda del Rey, Madrid, Spain

Negotiable Salary

Laboratory Technician | Clinical Analysis | Madrid64685280168195125

Indeed

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

€ 500/week

Integrated Research - Senior Principal64685280010881126

Indeed

Integrated Research - Senior Principal

Madrid, Spain \| Full time \| Hybrid \| R1492192**Job available in additional locations** **Location:** EU\-Wide (hybrid/remote)**Real World Commercial Solutions to Create a Healthier World** In RWCS we’re passionate about improving the life sciences ecosystem and making decisions that accelerate innovation for a healthier world. Every day our team develops evidence\-based strategies that are used in published research, clinical guidelines, and market access decisions, to improve healthcare at every touchpoint. We design and deliver Commercial Analytics, supported by our world\-class proprietary data assets, solve complex client challenges through strategic consulting, and use leading edge market research techniques to support clients brand strategy, planning and measurement. We’re purpose\-driven problem solvers, that do what we love to make a greater impact on human health.**Integrated Research***We focus on understanding the behaviours and attitudes of Health Care Professionals and patients, and supporting international pharmaceutical companies to understand them as people. This is across the product lifecycle.**We explore and measure what Health Care Professionals and patients say and do using different behavioural frameworks to deliver actionable insights and clear answers to our clients’ business questions. We typically use IQVIA data to contextualise our research and collaborate with other IQVIA teams to provide our clients with comprehensive solutions to their business issues.***The Role** In this role, you’ll be a senior lead in the Integrated Research team. You will drive the growth of the team across multiple different areas, and be a leadership role model to the other seniors in the group. You’ll work directly with multiple clients to develop business opportunities and provide valuable input to solutions, take pride in your work and relationships, and exceed targets. You will also have a strong focus on developing future talent in the team and ensuring the next generation of leaders has clear guidance and growth pathways**What You’ll Be Doing*** Proactively bringing solutions to ensure the business is well functioning and the teams have what they need to deliver * Owning significantly sized accounts and meeting or exceeding revenue targets by developing and delivering insightful, value\-added solutions that address complex issues * Supporting the evolution of what the team does and how we talk about it to ensure the offering is always compelling to clients * Seeking out and identifying new revenue opportunities and ensuring a continuous flow of business from clients * Applying consultative problem\-solving skills to be an Integrated Solutions expert (based on a foundation of market research) * Developing new, tangible and commercial offerings * Bringing solutions to growth barriers in the business and taking responsibility for their implementation * Contributing to the awareness of IQVIA Integrated Research in the marketplace through speaking engagements, client meetings, and publications * Mentoring, coaching, and sharing expertise **Who You Are*** A degree holder with 15\+ years’ experience in life sciences or healthcare consulting * Expertise in primary market research methodologies and delivery processes * Proven seller of complex engagements to the top Pharma/Life Sciences companies * An established leader, typically of multiple or significantly sized teams, with a record of management and people development * An expert in the identified teams’ solutions, that can produce new and creative ideas * A successful mentor, talent retainer and confident leader that can enable creativity in others **Benefits** Visit our **benefits page** for information on everything from perks to well\-being initiatives and career enhancement. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com

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

Negotiable Salary

Integrated Research - Senior Consultant64685280026883127

Indeed

Integrated Research - Senior Consultant

Madrid, Spain \| Full time \| Hybrid \| R1505719**Job available in additional locations** **Location:** Portugal, Spain, Greece**Real World Commercial Solutions to Create a Healthier World** In RWCS we’re passionate about improving the life sciences ecosystem and making decisions that accelerate innovation for a healthier world. Every day our team develops evidence\-based strategies that are used in published research, clinical guidelines, and market access decisions, to improve healthcare at every touchpoint. We design and deliver Commercial Analytics, supported by our world\-class proprietary data assets, solve complex client challenges through strategic consulting, and use leading edge market research techniques to support clients brand strategy, planning and measurement. We’re purpose\-driven problem solvers, that do what we love to make a greater impact on human health.**Integrated Research***We focus on understanding the behaviours and attitudes of Health Care Professionals and patients, and supporting international pharmaceutical companies to understand them as people. This is across the product lifecycle.**We explore and measure what Health Care Professionals and patients say and do using different behavioural frameworks to deliver actionable insights and clear answers to our clients’ business questions. We typically use IQVIA data to contextualise our research and collaborate with other IQVIA teams to provide our clients with comprehensive solutions to their business issues.***The Role** In this role, you’ll be ensuring on\-time and on\-budget delivery of completed projects for high client satisfaction. We need insightful, detail\-oriented people that can identify and elevate new business opportunities and assist in sales, so we can work with our clients to make a difference in the life science industry.**What You’ll Be Doing*** Providing day\-to\-day client management of projects, including leading update meetings, and participating in delivery workshops. Participation in key aspects of project delivery, such as interview moderation, designing, structuring and delivering client reports and presentations * Leading the definition of research design and planning for proposal purposes * Leadership of extended project teams to execute high quality research across multiple methodologies (RWD, PMR, AIML etc) and analysis on time and within budget * Planning, organising and managing all aspects of project delivery (scope, quality, resources, risk and timelines) to successfully complete specific project goals and objectives. Proactively identifying project related delivery risks and suggesting and implementing mitigating actions * Preparing and facilitating decision making on project related questions, internally as well as with clients. Recommending improvements and alternative solutions to resolve client challenges * Identifying new business opportunities for follow\-on work * Supporting business development activities, including proposal writing, pitch development and delivery * Contributing to the EMEA community through networking and cross\-team working * Raising the external profile of IQVIA by attending conferences and generating thought leadership pieces **Who You Are*** A university degree holder with 5\+ years of experience in life science or healthcare consulting * Previous work experience of at least 6/7 years in consultancy and / or market research. Preferential consideration will be given to candidates with experience in carrying out consulting and market research projects in the pharmaceutical area at an international/cross\-country level. * Project management experience with client\-influencing and relationship\-building skills * High skills of interpretation and analysis (quantitative, qualitative and integration of different sources of data assets) * Experienced in developing relationships with senior roles at our client organisations * Knowledgeable of developments in the life science industry * Excellent at presenting and communicating * Fluent in English IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com

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

Negotiable Salary

Pharmaceutical Sr Market Research – French Speaker64685280060675128

Indeed

Pharmaceutical Sr Market Research – French Speaker

Madrid, Spain \| Full time \| Home\-based \| R1479538 We are looking for a passionate a**Pharmaceutical Sr Market Research – French Speaker** to join our dynamic team in Madrid or Barcelona. You will play a key role in managing and delivering primary market research projects, supporting our clients in their strategic decision\-making.**Your responsibilities:*** Lead or contribute to consulting projects from design to delivery. * Analyze client needs and propose tailored, cost\-effective, and innovative solutions. * Supervise and support analysts and consultants throughout project execution. * Conduct qualitative and quantitative analyses to identify key insights. * Produce and present clear, impactful reports adapted to different stakeholders. * Participate in identifying business opportunities and developing client relationships. * Ensure post\-delivery follow\-up to guarantee client satisfaction. * Develop your sector and methodological expertise within our Center of Excellence. **Requirements:*** Ideally, a scientific background and/or graduate from a business school or university. * 5 to 8 years of experience in market research, preferably in a research institute, consulting firm, or within the life sciences industry. * Strong project management and client relationship skills. * Ability to work in teams and manage multiple projects simultaneously. * Excellent verbal and written communication skills, with strong presentation abilities (in French and English). * Good knowledge of consulting methodologies and industry challenges. * Established professional network in the life sciences field is a plus. **Why join us?*** Exciting projects with key industry players. * Collaborative and supportive work environment. * Opportunities for professional growth and specialization. * Flexible hybrid work model. * IQVIA recognized as a LinkedIn Top Employer. * Rich and diverse training offerings. IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com. At IQVIA, we believe that diversity, inclusion, and belonging empower our mission to accelerate innovation for a healthier world. We create a culture of belonging by valuing the perspectives of all talented employees worldwide and providing them with the opportunity to power smarter healthcare for everyone, everywhere. When our talented employees bring their authentic selves and their diverse experiences to work, they enable us to accomplish extraordinary things. Multifaceted thought processes spark innovation. Multi\-talented collaboration harnesses innovation to deliver superior outcomes.

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

Negotiable Salary

Associate Biostatistics Director - FSP (Permanent Home-based)64685280077058129

Indeed

Associate Biostatistics Director - FSP (Permanent Home-based)

Madrid, Spain \| Full time \| Home\-based \| R1503450**Job available in additional locations** * Lead full scope of Biostatistics conduct for the responsible program within a therapeutic area. Define statistical strategy and ensure appropriate statistical methodologies applied to study design and data analysis for clinical trials and regulatory submissions. * Influence and contribute to clinical development plans, collaborate with cross\-functional team for governance reviews. Lead statistical strategy for planning and study execution (member of Study Executive Team, Clinical Development Team) and quantitative evaluation to clinical trials, regulatory submissions, and related documents. * Provide statistical thought partnership for innovative study design and clinical development plans, including Go\-No Go criteria and probability of technical success calculations. * Provide for project\-wide planning of analyses; quality and timely delivery of interim and final results, including integrated analyses for submissions. * Represent Biostatistics in interactions with regulatory authorities (eg, FDA, EMA, PMDA) * Be responsible for interpreting analysis results and ensuring reporting accuracy in study reports and regulatory documents. * Prepare abstracts, posters, oral presentations and written reports to effectively communicate results of clinical programs and studies to internal and external stakeholders and colleagues with varying levels of clinical research knowledge **Education**+ PhD or MS in Biostatistics, Statistics or related field **Experience*** Minimum of 8 years of experience in clinical trial statistics, preferably within a pharmaceutical or CRO setting. *  **Technical Expertise:** * Advanced proficiency in SAS / R for data analysis and statistical programming. * Experience with Bayesian methods, predictive modeling, and simulation techniques. * Proven track record in strategic study design, including adaptive designs, sample size calculations, and interim analysis planning. * Familiarity with regulatory guidance on statistical methodologies (e.g., FDA, EMA, PMDA). * Solid experience in applications of advanced statistical methodologies * Leading roles in regulatory submissions * Experience in interactions with major regulatory authorities preferred * Demonstrated statistical expertise and leadership in facilitating and optimizing the (pre/early/full\-) clinical development strategy *  **Study Design and Strategy:** * Ability to lead statistical discussions during protocol development and study planning. * Skilled in defining statistical analysis plans (SAP) and developing strategic approaches for complex study designs. * Experience in strategy discussions involving adaptive design, go/no\-go criteria, and futility analyses. *  **Collaboration and Communication:** * Strong communication skills to effectively present statistical concepts to cross\-functional teams. * Proven experience in collaborating with clinical and regulatory teams to align statistical strategy with overall program objectives. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com

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

Negotiable Salary

Sr Medical Writer - Narrative Writer646172586382101210

Indeed

Sr Medical Writer - Narrative Writer

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

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

Negotiable Salary

Copy of Agro-Food Laboratory Technician645509424788491211

Indeed

Copy of Agro-Food Laboratory Technician

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

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

Negotiable Salary

Lead UI/UX Product Designer645225215430411212

Indeed

Lead UI/UX Product Designer

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

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

€ 80,000-100,000/year

Market Access Specialist645225139024671213

Indeed

Market Access Specialist

**Market Access Specialist** ============================ **What are we looking for?** We are seeking a highly motivated individual with strong work capacity, analytical skills, attention to detail, initiative, and flexibility, who enjoys working in a team and is interested in building a career in the Market Access field, to fill a vacancy within the Market Access and Pricing department. This is a position whose primary mission is to manage activities related to pricing and reimbursement processes, national and regional access, as well as research projects in health economics and outcomes research (HEOR) for products within the assigned therapeutic area. **Main responsibilities** : * Design market access strategy, build and maintain an integrated value story targeted at payers, and prepare value dossiers to be submitted during pricing and reimbursement (P\&F) procedures for products under responsibility. * Adapt economic models to the Spanish setting or develop them from scratch (such as budget impact tools, cost-effectiveness analyses, etc.), as well as conduct literature reviews, meta-analyses, and other Health Economics and Outcomes Research (HEOR) works such as Real-World Evidence (RWE) studies focused on information gaps relevant to payers. * Create materials to effectively communicate value stories and generated studies tailored to payer needs. * Lead technical responses in Health Technology Assessment processes in Spain to position products under responsibility regarding P\&F conditions and/or regional access (e.g., Therapeutic Positioning Reports from the Spanish Medicines Agency at national level or CatSalut product assessments at regional level). * Stay up to date on the competitive landscape and the evolution of the Spanish National Health System to inform market access strategies. * Collaborate with central and local teams to drive continuous improvements. Work closely with internal cross-functional teams (sales, marketing, medical, government affairs, regulatory, etc). **Requirements** * University degree in health sciences, economics, statistics or related fields. * Experience in market access, health economics and outcomes research (HEOR) departments. * Knowledge of pricing and reimbursement processes, as well as national and regional access under Spanish legislation. * Strong analytical skills. * Influence and communication abilities. * Fluent spoken and written English (C1\). * Proficiency in MS Office tools. **Desirable:** * Master’s degree in Market Access and HEOR preferred. * Initiative and creativity to propose solutions. Deadline: 28/11/2025 **Why GSK?** **Uniting science, technology and talent to get ahead of disease together.** GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2\.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases – to impact health at scale. People and patients around the world count on the medicines and vaccines we make, so we’re committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people. If you require an accommodation or other assistance to apply for a job at GSK, please contact the GSK Service Centre at 1\-877\-694\-7547 (US Toll Free) or \+1 801 567 5155 (outside US). GSK is an Equal Opportunity Employer. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), parental status, national origin, age, disability, genetic information (including family medical history), military service or any basis prohibited under federal, state or local law. **Important notice to Employment businesses/ Agencies** GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK's commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site. Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license, GSK may be required to capture and report expenses GSK incurs, on your behalf, in the event you are afforded an interview for employment. This capture of applicable transfers of value is necessary to ensure GSK’s compliance to all federal and state US Transparency requirements. For more information, please visit the Centers for Medicare and Medicaid Services (CMS) website at https://openpaymentsdata.cms.gov/

C. de Dolores Ibárruri, 1, 28760 Tres Cantos, Madrid, Spain

Negotiable Salary

Management Controller - Central Laboratory Health Diagnostics Quirónsalud (Alcobendas)645212543156491214

Indeed

Management Controller - Central Laboratory Health Diagnostics Quirónsalud (Alcobendas)

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

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

Negotiable Salary

Indeed

Testing engineer

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

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

Negotiable Salary

Waste Technical Management Internship643298356757771216

Indeed

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

€ 950/biweek

Technical Management Internship in Municipal Waste643298356908821217

Indeed

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

€ 950/biweek

Principal Data Operations Analyst641693958206741218

Indeed

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

Negotiable Salary

Junior Quality Assurance Inspector641625054048031219

Indeed

Junior Quality Assurance Inspector

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

Negotiable Salary

Dermatologist - Medical Director641507664698911220

Indeed

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., specialization in dermatology and current medical licensure; * Board certification; * 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

Negotiable Salary

Psychiatry - Medical Director641507664500491221

Indeed

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., specialization in psychiatry and current medical licensure; * Board certification; * 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

Negotiable Salary

Senior Data Operations Analyst641507655837471222

Indeed

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

Negotiable Salary

CPS Statistical Operations Analyst641501772568351223

Indeed

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

Negotiable Salary

MOZO/A MANIPULACION -LABORATORIO641493906784011224

Indeed

MOZO/A MANIPULACION -LABORATORIO

#### **Salario:** **A convenir**#### **Tipo de contrato:** De duracion determinada #### **Jornada:** Jornada Completa #### **Experiencia:** 1 año de experiencia En TEMPS llevamos 30 años encontrando oportunidades profesionales para la gente que busca trabajo.Tenemos experiencia y estamos comprometidos. En este momento tenemos esta posición vacante. ¿Te encaja?Seleccionamos mozos/as de almacén con experiencia en manipulación de dispositivos electrónicos (cámaras de seguridad, móviles, tablets, alarmas.). También con experiencia en manipulación y revisión con otro tipo de productos pequeños.FUNCIONES: \- Montaje y desmontaje de alarmas \- Testing Tool: Meter equipos en jigs y seguir una secuencia de pasos sencilla y guiada por pantalla.\- Recuperación de componentes: Inspeccionar visualmente baterías, soportes de pared, tapas de batería, pantallas para buscar arañazos, etc.\- Proceso de pulido: reparación o limpieza de la cámara de seguridad a través de una máquina, o incluso de manera manual.Se ofrece\- Contrato temporal por ETT \+ posibilidades reales de paso a plantilla.\- Salario: 9,36 brutos por hora trabajada.\- Turnos rotativos de Lunes a Viernes

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

€ 9/hour

Project Management Engineer641476241196831225

Indeed

Project Management Engineer

**Company Description** At SGS, our mission is to add value to society by providing a sustainable environment. Through our work, we guarantee safety and quality, bringing trust to all areas of society, even in those that are not visible. We have the most qualified professionals working as one great team across more than 140 countries every day, making us leaders in the industry. We encourage you to become part of this human team, where you will train and grow in an atmosphere of camaraderie, flexibility, respect, and equality. At SGS, you will find: The opportunity to make a difference. A place where you can contribute your value to society. An international environment with an innovative spirit, full of challenges where you can share and learn with the best. You define us, you make SGS. **Job Description** We strive to hire the best professionals and value integrity, curiosity, excellence, respect, inclusion, and collaboration. What's special about SGS, among other things, is our culture. Would you like to join a leading company in its sector? **We are looking for you!** Currently, we are seeking a **Project Management Engineer** for our laboratory design and installation department, SGS EPC LABORATORY SERVICES. You will be part of a dynamic and multidisciplinary team carrying out laboratory projects worldwide. Our clients are large companies and engineering firms undertaking "green field" or "upgrading" projects seeking SGS's specialization in the laboratory area. Within this team, you will perform the **following responsibilities:** * Review of requisitions, coordination, activation, planning, and collaboration with technical departments. * Liaising with the client and providing periodic reports. * Supplier sourcing. * Preparation of technical proposals and budgets. * Project documentation control. * Site visits for monitoring and supervision, both within and outside Spain. **Requirements** The **requirements** for this position are as follows: * Degree in Mechanical, Electrical, or Chemical Engineering. * Experience in construction, engineering, FEED, process, etc. projects. * Willingness to travel. * Advanced level of English. **Additional Information** **What will you find at SGS?** * We are a multinational leader in our sector, operating in virtually all industrial sectors. * What SGS employees value most is our positive work environment. * We offer technical and skills training to continue professional growth. * We provide Flexible Compensation and special discounts for SGS staff. * We are a Sustainable company involved in social issues. At SGS, as part of our strong commitment to promoting equal opportunities and respect for diversity, we ensure that all our selection processes are conducted objectively, impartially, and fairly, and are free from any kind of bias or discrimination.

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

Negotiable Salary

Junior Quality Control Laboratory Technician641476240375071226

Indeed

Junior Quality Control Laboratory Technician

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. **Educational Requirements:** Bachelor's degree in Chemical Sciences. **Language Requirements:** Fluent spoken and written English (C1 level). **Experience Requirements:** Prior experience not required. **Additional Information:** Availability to work afternoon shifts from Monday to Friday. **Personal Skills:** * Interpersonal skills: Teamwork, customer orientation (internal/external), initiative and decision-making, strong oral and written communication, active listening, problem-solving ability. * Organizational skills: Ability to organize workspace and daily activities to ensure maximum quality. Ensure a safe environment to prevent incidents and/or accidents. Attention to detail. Ability to handle multiple tasks simultaneously and prioritize objectives... * Technical skills: Knowledge of Good Manufacturing Practices regulations, GMP policies and procedures. Ability to work in a highly regulated environment. * Computer skills: Proficiency in office software at user level, as well as knowledge of computer systems controlling daily operational activities. **Key Responsibilities:** * Ensure training completion for all assigned tasks. Recognize deviations and initiate, participate in, and/or conduct root cause investigations. * Conduct and/or approve analytical investigations and deviations. * Develop and/or review Quality Control technical documentation required for the role based on learning and experience, ensuring compliance with applicable quality standards. * Develop and/or review laboratory change controls related to the position (e.g., analytical documentation, equipment). * Manage internal Quality Control documents (e.g., laboratory notebooks, analytical methods). * Collaborate in the review of analytical data for release of finished product batches, raw materials, stability studies, and Quality Control service samples. * Promptly and properly report any incidents arising in the area’s activities to the group supervisor. * Participate in audits and self-inspections. * Identify job-related improvements and support implementation efforts. * Contribute to quality system improvements through creation and review of documentation. * Participate in and propose Continuous Improvement initiatives within the team. * Ensure compliance with safety regulations and wear appropriate work attire and necessary personal protective equipment for each task. * Perform job-related tasks safely, complying with all safety and hygiene requirements. * Identify and report any situation that could pose a risk to personnel. * Participate in behavior observations and company initiatives aimed at identifying potential risks. 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

Negotiable Salary

Electronic Engineer for Hardware Testing641476239790101227

Indeed

Electronic Engineer for Hardware Testing

**ARQUIMEA** is a **technology company** operating globally, providing innovative solutions and products in highly demanding sectors. Our business areas include **Aerospace, Defense and Security, Big Science, Biotechnology, and Fintech**. Currently, we are seeking an **Electronic Engineer for Hardware Testing** to perform electrical tests on ASICs under ionizing radiation to characterize the degradation of key parameters within the framework of qualification according to ESCC 9000. **Main Responsibilities:** * + Preparation, execution, and analysis of electrical tests on ASICs during TID campaigns. + Understanding and use of the internal system developed for signal control, generation, and acquisition. + Processing and analysis of data to produce clear and concise reports. + Preparation of technical reports in accordance with ESCC 9000 and related standards. + Design of electronic support solutions for the characterization of high-performance ASICs. + Use of laboratory instrumentation (oscilloscopes, SMUs, analyzers, generators, etc.). + Collaboration with design, reliability, and quality teams. + Compliance with safety protocols in irradiation environments. **Requirements:** * + Experience in electrical testing of semiconductors/ASICs. + Knowledge and application of ESCC 9000 and ESCC 22900 standards. + Familiarity with irradiation campaigns (gamma, protons, heavy ions). + Ability to process and present data concisely. + Ability to quickly understand and apply internal measurement systems. + Experience in electronic design for device characterization. + Advanced technical English. **Education and Experience:** * University degree in Telecommunications, Electrical/Electronic Engineering. * Bachelor's degree in Electronic Engineering, Telecommunications, Physics, or similar. The position is **located** at our headquarters in **Madrid City, at** Serrano Galvache, 56. We are looking for **curious**, **creative**, **tenacious**, and **collaborative** individuals eager to achieve results and unafraid to take on challenges to help improve the society in which we live. #### **Think Big, Do the Job & Enjoy Life** *At ARQUIMEA, we value diversity and inclusion. We do not discriminate based on race, color, religion, gender, sexual orientation, gender identity, nationality, age, disability, or other protected factors by law. All candidates will be considered equally based on their skills and experience.*

C. de Serrano Galvache, 20, Cdad. Lineal, 28033 Madrid, Spain

Negotiable Salary

Indeed

LABORATORY TECHNICIAN

Position: laboratory technician for clinical analysis. Schedule: Monday to Friday, from 8 to 12h. Salary: 11\.639,35€ gross/year for the first 6 months. 12\.251,96€ gross/year from the 7th month onwards. Type of position: Part-time, Permanent contract Salary: 11\.639,35€\-12\.251,96€ per year Expected hours: 20 per week Work location: On-site employment

C/ Constitución, 16, 19003 Guadalajara, Spain

€ 11,639-12,251/month

Laboratory Technician for R&D641451014186261229

Indeed

Laboratory Technician for R&D

We are looking for a Laboratory Technician to join the R&D team at a pharmaceutical company located in Azuqueca de Henares. This position offers a Monday to Friday work schedule with flexible start times and a full-time workload of 40 hours. In addition to an indefinite contract, benefits include an attractive salary package, life and accident insurance, free on-site cafeteria, co-payment for voluntary health insurance, and access to a benefits and savings club. Professional development plans and internal mobility opportunities are also provided. The main responsibilities of the role involve organizing the daily work of analysts, determining necessary tests and equipment to use. It is also essential to review documentation for each analysis and research reports, ensuring compliance with GMP standards. You will participate in the development, verification, and validation of methods for analyzing new materials or existing assays, documenting the entire process and its results. Additionally, out-of-specification (OOS) results will be investigated, and tests performed by analysts will be supervised, resolving any doubts to ensure proper test execution. * Education: Bachelor's degree in Chemistry. * Languages: Fluent English. * Experience (years/area): 2\-5 years of experience in the pharmaceutical industry in an analytical role involving validations and technology transfer. * Specific Knowledge: PNTs, European Pharmacopoeia (EP), USP regulations, and GMP.

Av. Francisco Vives, 4, 19200 Azuqueca de Henares, Guadalajara, Spain

Negotiable Salary