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Global Responsibility Execute UpStream (USP) activities in the Cell Culture area of the production department, following operational procedures and GMP regulations. Specific Responsibilities • Execute the cell culture activities, according to process specifications and quality standards., • Write SOPs related to the equipment and activities of USP department., • Write batch records., • Prepare the production equipment prior to its use and after it (cleaning, inactivation, etc.)., • Register all the productive activities in logbooks, batch records (BRs) or other documents, according to the Company’s quality procedures., • Prepare culture means and process, filtering and sterilization solutions., • Provide support in preparation activities, reconditioning and materials sterilization., • Install and qualify equipment and support its maintenance, calibration and requalification., • Participate and promote improvements in the productive processes, records and activities of the Company, encouraging the continuous improvement., • Provide information and support in researches related to quality deviations and participate in the follow up of the subsequent implementation of corrective and preventive measures. Requirements and personal skills • Education: Degree in Pharmacy or similar., • Languages: Fluent Spanish and English, knowledge of other languages will be an asset., • Experience (years/area): +2 years of experience in a similar position., • Specific Knowledge: USP activities, GMP and SHE regulations., • Work shifts: 2 work shifts Morning - Evening., • Personal skills: Attention to detail, accuracy and reliability. At mAbxience, we provide equal opportunities to all regardless of race, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, or gender identity.

Position: QA Specialist (PRD) – Investigations, CRs, CAPAs & Floor Oversight Location: León (on-site) Experience: At least 3 years’ experience in similar roles within the Quality department in pharmaceutical industrial settings Want to find out more? 👇 LEONFARMA is part of INSUD PHARMA, a global leader in the pharmaceutical value chain and a benchmark in the research, development, manufacture and marketing of pharmaceutical products that contribute to human and animal health. Our purpose is to transform the industry through innovation, excellence and a commitment to sustainable development. Ready to be a #Challenger at LEONFARMA? 💪 What are we looking for? 🔎 We are looking for a QA Specialist (PRD) – Investigations, CRs, CAPAs & Floor Oversight who is passionate about the industrialisation of new products. General Responsibility Ensure quality oversight of production-related activities in a GMP-regulated manufacturing environment, acting as a key quality partner for operations on the shop floor. The role is responsible for leading and coordinating investigations, change controls and CAPAs, ensuring appropriate risk assessment, impact evaluation and timely closure in compliance with quality and regulatory requirements. In addition, the position provides real-time QA support to production, reinforcing GMP compliance, issue resolution and continuous improvement across daily manufacturing operations. Specific Responsibilities • Lead and manage quality investigations related to deviations associated with production activities., • Perform and support root cause analysis, ensuring robust identification of underlying causes and appropriate documentation of findings., • Evaluate the impact of deviations on product quality, manufacturing processes and GMP/regulatory compliance., • Coordinate cross-functional investigation activities with Production, Engineering, Quality Control, Maintenance and other relevant departments., • Review, assess and approve change requests/change controls, ensuring proper justification, impact assessment and implementation in line with GMP requirements., • Ensure that change controls are adequately evaluated, approved, implemented and closed within established timelines., • Review and approve CAPA plans derived from investigations, audits and inspections, ensuring actions are appropriate and sustainable., • Monitor CAPA implementation and verify effectiveness prior to closure., • Provide routine QA floor oversight through regular presence in production areas, supporting real-time decision-making and compliance with approved procedures., • Support production teams during critical operations, helping resolve GMP issues promptly and reinforcing quality culture on the shop floor. Experience (area) Quality Assurance in GMP-regulated pharmaceutical or biotechnology manufacturing environments, with strong exposure to production-related quality activities. Personal skills • Adaptability to change and flexibility, • Speed without compromising on quality, • Leadership and teamwork, • Effective communication, • Compliance, integrity and sustainability, • Growth mindset, • Business focus Our benefits! 👏 📜 Permanent contract 🎯 Career progression and development within a growing international group 🏆 Ongoing training and an innovative working environment 🍏 Subsidised canteen and other employee benefits What will the recruitment process be like? 🕵️ Initial contact by phone or email with our Talent Acquisition team. 1 or 2 face-to-face interviews at our premises in León. Regular updates on the progress of the process. 🔷Do you think this role isn’t for you? 🔷 Follow us on LinkedIn and Instagram so you don’t miss out on future career opportunities! #Leonfarma #Challenger #InsudPharma #InsudTalent COMMITMENT TO EQUAL OPPORTUNITIES AT LEONFARMA, we believe in and act to promote genuine equality of opportunity. We do not discriminate on the basis of gender, ethnicity, religion, sexual orientation, disability or any other characteristic. We value diversity and talent. We’d love to meet you!

Desde mAbxience, compañía especializada en el desarrollo y fabricación de medicamentos biosimilares incorporamos un/a técnico de QA Manufacturing para nuestra planta en León (España). Responsabilidad Global Reportando a la Coordinación de QA manufacturing se encarga de la revisión de las operaciones de fabricación y documentación relacionada con el proceso productivo. Las fabircaciones se centran en API formulado de Biosimilares (anticuerpos monoclanares) de desarrollo propio y productos CMO (Biosimilares/Innovadores). Responsabilidades específicas • Quality Oversight de las operaciones en planta., • Revisión de guías de fabricación y cuadernos de registro., • Revisión y cierre de guías de fabricación cumplimentadas., • Gestión del sistema de eventos de calidad. Revisión de investigaciones de causa raíz, evaluaciones de imapcto, análisis de riesgos relacionados con fabricaciones e instalaciones., • Utilización de la herramineta trackwise para la gestión de la documentación de calidad (Eventos de calidad, controles de cambios, reclamaciones, sistema documental y de entrenamientos)., • Revisión de procedimientos normalizados de trabajo, nuevas ediciones de guías de fabricación, métodos cromatográficos, etc., • Notificación de eventos durante las fabricaciones CMO., • Colaboración en la generación de los APQR y PQR de fabricación de sustancia activa formulada., • Participación / colaboración en la elaboración de métricas del departamento., • Emisión de copias controladas de BRs, seguimiento de documentación, entrenamientos, etc., • Notificar de todos aquellos problemas potenciales o reales detectados a través de su área de responsabilidad y ayudar a implantar las acciones correctivas / preventivas necesarias junto con los responsables locales., • Impulsar la innovación en sus áreas de interés y proponer mejoras respecto a los sistemas de Calidad., • Asistencia a reuniones de departamento / sección según aplique. En adición se podrán seleccionar otro tipo de reuniones con el fin de ampliar el conocimiento del dia a día de una empresa referente del sector biotecnológico. Requisitos y habilidades personales • Formación: Grado en Farmacia, Químicas, Biotecnología, Ciencias de la salud..., • Idiomas: inglés, • Experiencia: 2-3 años en posición similar Ofrecemos contratación indefinida para entrar a formar parte de una Compañía biofarmacéutica en plena expansión. • Seguro de vida y accidente., • Comedor gratuito de empresa., • Plataforma online de formación gratuita., • Biblioteca online gratuita., • Plataforma de bienestar social, físico y emocional. Mabxience es una Empresa comprometida con la igualdad de oportunidades, por lo que todxs lxs candidatxs serán consideradxs sin distinción de raza, color, género, edad, orientación sexual, religión, origen, estado civil, ciudadanía o capacidad diferentes.

Role: QA EBR Technician Location: León Experience: 1–3 years. Want to find out more? 👇 INSUD PHARMA operates across the entire pharmaceutical value chain, providing specialist knowledge and expertise in scientific research, development, manufacturing, sales and marketing of a wide range of active pharmaceutical ingredients (APIs), finished dosage forms (FDFs) and branded pharmaceutical products, adding value to human and animal health. INSUD PHARMA’s activities are organised into three synergistic business areas: Industrial (Chemo), Branded (Exeltis) and Biotechnology (mAbxience), with over 9,000 professionals in more than 50 countries, 20 state-of-the-art facilities, 15 specialised R&D centres, 12 sales offices and more than 35 pharmaceutical subsidiaries, serving 1,150 customers in 96 countries worldwide. INSUD PHARMA believes in innovation and sustainable development. Global Responsibility Comply with the GMP standards for medicinal and combination products for human use. Review, control and ensure compliance of Electronic Batch Records (EBR) and related manufacturing documentation in accordance with internal procedures, GMP rules and Authority and customers requirements, ensuring data integrity, traceability, accuracy and completeness of batch documentation prior to batch disposition and/or release activities. Specific Responsibilities · Develop standard operating procedures (general quality and departmental) related to batch record review, good documentation practices and electronic batch record management to ensure that all steps are properly defined and comply with internal and external regulations applicable in each case. · Review and approve internal SOPs related to EBR management, documentation review and GMP documentation practices. · Review Electronic Batch Records and associated manufacturing documentation to ensure completeness, accuracy, consistency and compliance with approved procedures and manufacturing instructions. · Verify that all critical process steps, controls, calculations, material reconciliations and manufacturing data are correctly documented in the EBR system and related records. · Ensure that all entries, corrections, comments and changes in the electronic records are properly documented and compliant with data integrity and GMP requirements. · Manage discrepancies identified during batch record review and coordinate with Production and other involved departments their investigation, correction and closure in accordance with internal procedures. · Support root cause analysis and trend analysis related to documentation errors, batch record discrepancies and recurring issues detected during EBR review. · Coordinate with Production, Engineering, Maintenance, Validation and other departments to ensure that any issue impacting batch documentation is properly assessed and resolved. · Review and verify that deviations, change controls or other quality events impacting the batch are properly linked, assessed and documented in the batch record package when applicable. · Ensure the proper management, traceability and archive of GMP documentation related to batch manufacturing records. · Support the implementation, maintenance and continuous improvement of electronic batch record systems and associated documentation workflows. · Participate in training activities related to Good Documentation Practices, GMP requirements and proper use/completion of Electronic Batch Records. · Support external audits and inspections according to the Annual Plan to assess compliance of batch documentation practices, data integrity requirements and the GMP system. · Participate in internal audits related to documentation practices, EBR processes and manufacturing records. · Support the Qualified Person and batch release activities through timely and accurate review of manufacturing documentation. · Support on quality investigations, batch documentation assessments and product quality issues related to manufacturing records. · Support to quality activities according to the appropriate training. Competencies/Career level Innovation, customer oriented, communication, team work, adaptability/flexibility, productivity, self-development, sense of urgency, initiative. Attention to detail, analytical mindset, compliance mindset, documentation rigor and organizational skills are especially valuable for this position. Requirements and personal skills · Education: Degree in Pharmacy or Chemistry or Sciences. · Languages: Intermediate or high level of English and bilingual in Spanish. · Experience (years/area): A minimum of 3 years' experience in similar position for a senior position. Experience in GMP documentation review, manufacturing records, batch record review or pharmaceutical production quality activities is highly valuable. · Specific Knowledge: Knowledge of GMP documentation systems, good documentation practices, batch record review processes, deviations/non-conformities, data integrity principles and quality systems in production plants. Experience with Electronic Batch Records (EBR) systems will be highly valued. · Travels: Not required. · Personal skills: Good communication skills, proactivity, good working under pressure, team working, problem-solving, good organizational skills, persistence and high attention to detail. COMMITMENT TO EQUAL OPPORTUNITIES The InsudPharma Group recognises that business management must be aligned with the needs and demands of society, and therefore is committed to equal opportunities and equal treatment for men and women, as set out in the relevant legislation in force – Organic Law 3/2007 – and we do not discriminate against anyone on the grounds of ethnicity, religion, age, sex, nationality, marital status, emotional or sexual orientation, gender identity or expression, disability, or any other personal or social circumstance.

We're looking for you! At HP SCDS, we're looking for a Senior Full Stack Engineer (Python & React) to join our Data & AI team within Sales Operations, supporting HP’s Graphics Solutions Business. You’ll help build an AI-powered assistant designed to enable Account Managers to work more efficiently, access relevant information faster, and make better business decisions. This is an exciting opportunity to contribute to a product with global reach, combining modern software engineering, data platforms, and AI technologies in a collaborative and innovative environment. What will you do? • Design, develop, and evolve full-stack applications for AI-powered solutions., • Build and maintain backend services using Python and FastAPI., • Develop modern, intuitive, and high-performing user interfaces with React and Vite., • Work closely with Data Scientists, AI Engineers, and Product Owners to transform business requirements into scalable solutions., • Participate in architecture discussions, technical design, and key technology decisions., • Ensure code quality, maintainability, scalability, and performance through engineering best practices., • Contribute to the growth and evolution of a product used by global sales teams., • Take an active role in code reviews, continuous improvement initiatives, and knowledge sharing within the team. What are we looking for? • Approximately 4-5 years of experience in software development., • Strong experience as a Full Stack Software Engineer., • Hands-on experience developing with Python, FastAPI, and React + Vite., • Experience designing, building, and consuming APIs., • Solid understanding of modern application architectures and software engineering best practices., • Experience working with relational databases., • English level B2 minimum, with the ability to communicate effectively in an international environment and collaborate with global teams., • Ability to work successfully in multidisciplinary teams., • Strong communication skills and a proactive, solution-oriented mindset., • Experience with Databricks or similar Data & AI platforms will be highly valued., • Knowledge of PostgreSQL is a plus., • Familiarity with the Python and JavaScript ecosystems, including relevant libraries and frameworks, will be appreciated., • Experience building cloud-native applications would be considered an advantage., • Product-oriented mindset with a strong focus on delivering business value., • Ability to thrive in dynamic environments and tackle open-ended challenges., • High level of ownership, autonomy, and execution capability., • Excellent collaboration skills across both technical and business stakeholders. What do we offer? You'll join an international, collaborative, and supportive team, working on innovative solutions with a real impact on HP’s business. This role offers the opportunity to contribute to cutting-edge AI and data-driven products while continuing to grow professionally in a stable environment that promotes continuous learning and development. • Flexible working hours, • Meal Allowance, • Private Health Insurance, • Annual Performance Bonus, • ...and much more! Position Details Location: León Work model: Hybrid (minimum 3 days per week in the office) Application: Apply directly via LinkedIn Discover more about our culture and life at HP SCDS: 📸 _ 💼 _ 🎥 _

QA Specialist (PRD) – Investigations, CRs, CAPAs & Floor Oversight.At least 3 years’ experience in similar roles within the Quality department in pharmaceutical industrial settings.LEONFARMA is part of INSUD PHARMA, a global leader in the pharmaceutical value chain and a benchmark in the researc

Role: QA EBR Technician Location: León Experience: 1–3 years. Want to find out more? 👇 INSUD PHARMA operates across the entire pharmaceutical value chain, providing specialist knowledge and expertise in scientific research, development, manufacturing, sales and marketing of a wide range of active pharmaceutical ingredients (APIs), finished dosage forms (FDFs) and branded pharmaceutical products, adding value to human and animal health. INSUD PHARMA’s activities are organised into three synergistic business areas: Industrial (Chemo), Branded (Exeltis) and Biotechnology (mAbxience), with over 9,000 professionals in more than 50 countries, 20 state-of-the-art facilities, 15 specialised R&D centres, 12 sales offices and more than 35 pharmaceutical subsidiaries, serving 1,150 customers in 96 countries worldwide. INSUD PHARMA believes in innovation and sustainable development. Global Responsibility Comply with the GMP standards for medicinal and combination products for human use. Review, control and ensure compliance of Electronic Batch Records (EBR) and related manufacturing documentation in accordance with internal procedures, GMP rules and Authority and customers requirements, ensuring data integrity, traceability, accuracy and completeness of batch documentation prior to batch disposition and/or release activities. Specific Responsibilities · Develop standard operating procedures (general quality and departmental) related to batch record review, good documentation practices and electronic batch record management to ensure that all steps are properly defined and comply with internal and external regulations applicable in each case. · Review and approve internal SOPs related to EBR management, documentation review and GMP documentation practices. · Review Electronic Batch Records and associated manufacturing documentation to ensure completeness, accuracy, consistency and compliance with approved procedures and manufacturing instructions. · Verify that all critical process steps, controls, calculations, material reconciliations and manufacturing data are correctly documented in the EBR system and related records. · Ensure that all entries, corrections, comments and changes in the electronic records are properly documented and compliant with data integrity and GMP requirements. · Manage discrepancies identified during batch record review and coordinate with Production and other involved departments their investigation, correction and closure in accordance with internal procedures. · Support root cause analysis and trend analysis related to documentation errors, batch record discrepancies and recurring issues detected during EBR review. · Coordinate with Production, Engineering, Maintenance, Validation and other departments to ensure that any issue impacting batch documentation is properly assessed and resolved. · Review and verify that deviations, change controls or other quality events impacting the batch are properly linked, assessed and documented in the batch record package when applicable. · Ensure the proper management, traceability and archive of GMP documentation related to batch manufacturing records. · Support the implementation, maintenance and continuous improvement of electronic batch record systems and associated documentation workflows. · Participate in training activities related to Good Documentation Practices, GMP requirements and proper use/completion of Electronic Batch Records. · Support external audits and inspections according to the Annual Plan to assess compliance of batch documentation practices, data integrity requirements and the GMP system. · Participate in internal audits related to documentation practices, EBR processes and manufacturing records. · Support the Qualified Person and batch release activities through timely and accurate review of manufacturing documentation. · Support on quality investigations, batch documentation assessments and product quality issues related to manufacturing records. · Support to quality activities according to the appropriate training. Competencies/Career level Innovation, customer oriented, communication, team work, adaptability/flexibility, productivity, self-development, sense of urgency, initiative. Attention to detail, analytical mindset, compliance mindset, documentation rigor and organizational skills are especially valuable for this position. Requirements and personal skills · Education: Degree in Pharmacy or Chemistry or Sciences. · Languages: Intermediate or high level of English and bilingual in Spanish. · Experience (years/area): A minimum of 3 years' experience in similar position for a senior position. Experience in GMP documentation review, manufacturing records, batch record review or pharmaceutical production quality activities is highly valuable. · Specific Knowledge: Knowledge of GMP documentation systems, good documentation practices, batch record review processes, deviations/non-conformities, data integrity principles and quality systems in production plants. Experience with Electronic Batch Records (EBR) systems will be highly valued. · Travels: Not required. · Personal skills: Good communication skills, proactivity, good working under pressure, team working, problem-solving, good organizational skills, persistence and high attention to detail. COMMITMENT TO EQUAL OPPORTUNITIES The InsudPharma Group recognises that business management must be aligned with the needs and demands of society, and therefore is committed to equal opportunities and equal treatment for men and women, as set out in the relevant legislation in force – Organic Law 3/2007 – and we do not discriminate against anyone on the grounds of ethnicity, religion, age, sex, nationality, marital status, emotional or sexual orientation, gender identity or expression, disability, or any other personal or social circumstance.

En Exceltic somos una empresa de ingeniería y consultoría tecnológica en fuerte crecimiento, con presencia internacional y proyectos en sectores como energía, industria, ferroviario, infraestructuras, tecnología y Data Centers. Experiencia en implementación y seguimiento de Planes de Calidad d

React Native Mobile Developer 📍 Salamanca, Spain (On-site) About the Role We're looking for a React Native Mobile Developer to build and maintain mobile applications for iOS and Android. You'll work closely with designers and developers to deliver high-quality mobile solutions. Requirements • 3+ years of React Native experience, • Strong knowledge of JavaScript (ES6+) and TypeScript, • Experience with REST APIs, • Experience publishing apps on iOS and Android, • Familiarity with Git, • Strong problem-solving and communication skills Nice to Have • Native mobile development experience, • CI/CD and automated testing experience, • Performance optimization knowledge Benefits • Career development opportunities, • On-site gym with 24/7 access, • Free snacks, fruit, and coffee, • Provident fund, • Free parking, • Regular team events and outings

We're hiring: React Native Developers Spain (On-site in Salamanca) | Full-time At Silicon Dali, we're looking for 2 React Native Developers to join our engineering team in Salamanca, Spain, and help us build high-quality mobile applications for iOS and Android. This is an on-site role, so candidates must already be based in Spain or willing to relocate to Salamanca. Candidates must already be eligible to work in Spain. We are currently unable to provide visa sponsorship or work permit support for this position. We build custom software products for startups and enterprises, with strong expertise in iGaming, forex, fintech, and crypto. Our focus is on performance, scalability, security, and building software that lasts. We're looking for engineers with strong software engineering fundamentals, proven React Native experience, and a modern development mindset using AI-powered engineering tools like Claude, Cursor, GitHub Copilot, or similar. • Build and maintain production-grade React Native applications, • Integrate REST APIs, backend services, WebSockets, and real-time systems, • Improve app performance, reliability, and release quality, • Collaborate closely with backend engineers, QA, product, and design teams, • Support App Store and Google Play releases, • Use AI-assisted development tools to improve productivity and code quality, • Professional experience building production React Native applications, • Strong JavaScript and TypeScript skills, • Solid understanding of software engineering fundamentals, debugging, and clean code principles, • Experience with Redux, Zustand, or similar state management solutions, • Performance optimization and debugging experience, • Familiarity with mobile CI/CD and release pipelines, • Comfortable using AI tools like Claude, Cursor, GitHub Copilot, or similar in daily development workflows, • Git experience, • Strong English communication skills, • Career growth and continuous learning opportunities, • Health insurance, • Experienced and collaborative engineering team, • Interesting and technically challenging projects, • Positive and supportive work environment, • Regular team events and outings, • On-site offices in Salamanca near Plaza Mayor If you're passionate about mobile engineering, care about software quality, and want to work with a strong team building ambitious products, we'd love to hear from you. #J-18808-Ljbffr

React Native Mobile Developer 📍 Salamanca, Spain (On-site) About the Role We're looking for a React Native Mobile Developer to build and maintain mobile applications for iOS and Android. You'll work closely with designers and developers to deliver high-quality mobile solutions. Requirements • 3+ years of React Native experience, • Strong knowledge of JavaScript (ES6+) and TypeScript, • Experience with REST APIs, • Experience publishing apps on iOS and Android, • Familiarity with Git, • Strong problem-solving and communication skills Nice to Have • Native mobile development experience, • CI/CD and automated testing experience, • Performance optimization knowledge Benefits • Career development opportunities, • On-site gym with 24/7 access, • Free snacks, fruit, and coffee, • Provident fund, • Free parking, • Regular team events and outings

At HP SCDS, we're building a brand-new team and we're looking for a Senior Software Engineer to join us as a founding member. This is a unique opportunity to help shape the future of how our teams work by designing and developing innovative software solutions that drive transformation and modernization. Based in León, you'll play a key role in defining the architecture, technology stack, and technical direction of a high-impact initiative from day one. • Design and develop robust, scalable, and well-architected software solutions., • Apply data architecture best practices and software design patterns to create maintainable and efficient systems., • Integrate existing AI models into business applications to optimize internal processes and workflows., • Collaborate closely with stakeholders to identify opportunities for digital transformation., • Contribute to technical decision-making, helping define the team's architecture and technology stack., • Ensure high standards of software quality through code reviews, testing, and engineering best practices., • Actively participate in building a new team culture focused on innovation, collaboration, and continuous improvement., • 5+ years of experience in software engineering., • Strong knowledge of software architecture, data architecture principles, and design patterns., • Experience integrating AI models or AI-powered capabilities within software solutions., • Solid understanding of modern software development practices and methodologies., • Ability to work autonomously in an evolving and fast-paced environment., • Strong problem-solving and communication skills., • Fluent English (C1 level or higher). Join a collaborative and innovative environment where you'll have the opportunity to build solutions with real impact from the ground up. You'll work alongside talented professionals, contribute to strategic initiatives, and enjoy continuous learning and professional growth opportunities. • Private health insurance, • Annual performance bonus, • And much more! Work model: Hybrid (minimum 3 days per week in the office) #J-18808-Ljbffr

We're looking for you! At HP SCDS, we're looking for a Senior Full Stack Engineer (Python & React) to join our Data & AI team within Sales Operations, supporting HP’s Graphics Solutions Business. You’ll help build an AI-powered assistant designed to enable Account Managers to work more efficiently, access relevant information faster, and make better business decisions. This is an exciting opportunity to contribute to a product with global reach, combining modern software engineering, data platforms, and AI technologies in a collaborative and innovative environment. What will you do? • Design, develop, and evolve full-stack applications for AI-powered solutions., • Build and maintain backend services using Python and FastAPI., • Develop modern, intuitive, and high-performing user interfaces with React and Vite., • Work closely with Data Scientists, AI Engineers, and Product Owners to transform business requirements into scalable solutions., • Participate in architecture discussions, technical design, and key technology decisions., • Ensure code quality, maintainability, scalability, and performance through engineering best practices., • Contribute to the growth and evolution of a product used by global sales teams., • Take an active role in code reviews, continuous improvement initiatives, and knowledge sharing within the team. What are we looking for? • Approximately 4-5 years of experience in software development., • Strong experience as a Full Stack Software Engineer., • Hands-on experience developing with Python, FastAPI, and React + Vite., • Experience designing, building, and consuming APIs., • Solid understanding of modern application architectures and software engineering best practices., • Experience working with relational databases., • English level B2 minimum, with the ability to communicate effectively in an international environment and collaborate with global teams., • Ability to work successfully in multidisciplinary teams., • Strong communication skills and a proactive, solution-oriented mindset., • Experience with Databricks or similar Data & AI platforms will be highly valued., • Knowledge of PostgreSQL is a plus., • Familiarity with the Python and JavaScript ecosystems, including relevant libraries and frameworks, will be appreciated., • Experience building cloud-native applications would be considered an advantage., • Product-oriented mindset with a strong focus on delivering business value., • Ability to thrive in dynamic environments and tackle open-ended challenges., • High level of ownership, autonomy, and execution capability., • Excellent collaboration skills across both technical and business stakeholders. What do we offer? You'll join an international, collaborative, and supportive team, working on innovative solutions with a real impact on HP’s business. This role offers the opportunity to contribute to cutting-edge AI and data-driven products while continuing to grow professionally in a stable environment that promotes continuous learning and development. • Flexible working hours, • Meal Allowance, • Private Health Insurance, • Annual Performance Bonus, • ...and much more! Position Details Location: León Work model: Hybrid (minimum 3 days per week in the office) Application: Apply directly via LinkedIn Discover more about our culture and life at HP SCDS: 📸 Instagram 💼 LinkedIn 🎥 Youtube

Who are we: Antolin is a leading global automotive supplier; we are experts in designing, manufacturing and supplying innovative solutions for vehicles around the world. Our product portfolio includes trim, headliners, and cockpits, as well as lighting and other interior systems. We offer comprehensive solutions with a focus on quality, safety, and sustainability. Our products are used in many of the world’s leading car brands. In fact, Antolin equips nearly 700 vehicle models around the world. With 136 manufacturing plants and offices in 23 countries, Antolin has achieved this strong industry presence through 75 years of working with our customers in order to develop a complete cycle of component manufacturing, from their conception and design, through the development and validation stages, to their industrialisation and sequenced delivery. We are working hard on spearheading the transformation that the automotive industry is currently experiencing with regard to vehicle interiors by collaborating with our customers. We do so in order to develop more sustainable and technologically advanced vehicles that are also adapted to the new needs and requirements of their passengers. As part of this transformation, Antolin is committed to a sustainable business model that focuses on and creates value for all its stakeholders, including its customers, employees, investors, suppliers, and society as a whole. Mission: Lead APQP and PPAP dossiers related to supplier components, coordinating all required activities with suppliers and cross-functional teams to ensure component qualification and approval are achieved on time and in compliance with customer and quality requirements. Responsibilities: • Lead and manage APQP and PPAP dossiers thoughout component development and industrialization phases., • Coordinate supplier and internal activities to ensure project milestones and qualification requirements are achieved., • Monitor component validation and approval plans., • Review and validate APQP/PPAP documentation required for component qualification., • Identify risks and drive corrective actions to ensure quality, cost, and timing objectives are met., • Act as the liaison between suppliers and internal departments such as Quality, Purchasing, Engineering, and Manufacturing., • Ensure compliance with customer requirements, quality standards, and corporate procedures., • Support problem-solving and continuous improvement initiatives related to supplier quality. We are looking for: We are looking for a proactive and results-oriented proffesional with experience in APQP and PPAP processes, capable of coordinating suppliers and cross-functional teams within a dynamic industrial environment. This temporary oportunity has been created to provide maternity leave cover, ensuring continuity and support within the Supplier Manufacturing Quality team. • Minimum 2 years of experience in APQP and PPAP processes., • Engineering degree preferred; other educational backgrounds will also be considered if supported by relevant experience., • Professional working proficiency in English., • Knowledge of quality tools and methodologies related to component development and industrialization., • Strong planning, organization, and project management skills., • Excellent communication and teamwork abilities. What can we offer you: • You will be part of a highly engaged multinational with international career opportunities., • We offer you a learning journey adapted to your professional experience., • You will work on international projects for world- renowned companies in Automotive sector., • You can find an Open Environment to learn new technologies., • We can offer you a competitive salary, benefits and valuable OEM discounts. Here at Antolin, we are an equal opportunity employer and value diversity in our workplace. We do not discriminate based on race, religion, colour, national origin, gender, sexual orientation, age, marital status, or disability status. All qualified applicants will receive consideration for employment without regard to any of these protected characteristics. We encourage applications from all individuals and strongly support diversity in our workplace. We strive to create an inclusive environment for everyone, and we are committed to treating everyone in a fair and equitable manner. We are proud to be an equal opportunity employer and are committed to fostering a diverse and inclusive work environment. This job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities. The Company reserves the right to revise the job description at any time. Duties, responsibilities or activities may change, or new ones may be assigned at any time with or without notice. The employee must be able to perform the essential functions of the position satisfactorily. If requested, reasonable accommodations may be made to enable employees with disabilities to perform the essential functions of the job, absent undue hardship. DREAM. DARE. DO

Position: QA Specialist (PRD) – Investigations, CRs, CAPAs & Floor Oversight Location: León (on-site) Experience: At least 3 years’ experience in similar roles within the Quality department in pharmaceutical industrial settings Want to find out more? LEONFARMA is part of INSUD PHARMA, a global leader in the pharmaceutical value chain and a benchmark in the research, development, manufacture and marketing of pharmaceutical products that contribute to human and animal health. Our purpose is to transform the industry through innovation, excellence and a commitment to sustainable development. Ready to be a #Challenger at LEONFARMA? What are we looking for? We are looking for a QA Specialist (PRD) – Investigations, CRs, CAPAs & Floor Oversight who is passionate about the industrialisation of new products. General Responsibility Ensure quality oversight of production-related activities in a GMP-regulated manufacturing environment, acting as a key quality partner for operations on the shop floor. The role is responsible for leading and coordinating investigations, change controls and CAPAs, ensuring appropriate risk assessment, impact evaluation and timely closure in compliance with quality and regulatory requirements. In addition, the position provides real-time QA support to production, reinforcing GMP compliance, issue resolution and continuous improvement across daily manufacturing operations. Specific Responsibilities • Lead and manage quality investigations related to deviations associated with production activities., • Perform and support root cause analysis, ensuring robust identification of underlying causes and appropriate documentation of findings., • Evaluate the impact of deviations on product quality, manufacturing processes and GMP/regulatory compliance., • Coordinate cross-functional investigation activities with Production, Engineering, Quality Control, Maintenance and other relevant departments., • Review, assess and approve change requests/change controls, ensuring proper justification, impact assessment and implementation in line with GMP requirements., • Ensure that change controls are adequately evaluated, approved, implemented and closed within established timelines., • Review and approve CAPA plans derived from investigations, audits and inspections, ensuring actions are appropriate and sustainable., • Monitor CAPA implementation and verify effectiveness prior to closure., • Provide routine QA floor oversight through regular presence in production areas, supporting real-time decision-making and compliance with approved procedures., • Support production teams during critical operations, helping resolve GMP issues promptly and reinforcing quality culture on the shop floor. Experience (area) Quality Assurance in GMP-regulated pharmaceutical or biotechnology manufacturing environments, with strong exposure to production-related quality activities. Personal skills • Adaptability to change and flexibility, • Speed without compromising on quality, • Leadership and teamwork, • Effective communication, • Compliance, integrity and sustainability, • Growth mindset, • Business focus Our benefits! Permanent contract Career progression and development within a growing international group Ongoing training and an innovative working environment Subsidised canteen and other employee benefits What will the recruitment process be like? ️ Initial contact by phone or email with our Talent Acquisition team. 1 or 2 face-to-face interviews at our premises in León. Regular updates on the progress of the process. Do you think this role isn’t for you? Follow us on LinkedIn and Instagram so you don’t miss out on future career opportunities! #Leonfarma #Challenger #InsudPharma #InsudTalent COMMITMENT TO EQUAL OPPORTUNITIES AT LEONFARMA, we believe in and act to promote genuine equality of opportunity. We do not discriminate on the basis of gender, ethnicity, religion, sexual orientation, disability or any other characteristic. We value diversity and talent. We’d love to meet you!

Everything you are looking for and more The APM technician perform on-site service and maintenance visits. The ideal candidate will be responsible for identifying and resolving technical, software or mechanical issues on our Lockers, ensuring minimal downtime and maximum customer satisfaction. The role includes replacing components, repairing parts, and coordinating tasks with the support and dispatching teams. The APM technician is based in Salamanca area, carries out on-site interventions in the whole Castilla y León region, also covering nearby cities/regions (Ávila, Badajoz, Cáceres, Valladolid, Oviedo etc.). What responsibilities and objectives will you have? - Perform scheduled and emergency service visits, complying with the SLA. - Diagnose technical issues and implement effective solutions on-site. - Perform root cause analysis of reported problems. - Replace defective components and carry out mechanical and/or electrical repairs. - Communicate with the dispatching team to align on planning and priorities. - Follow safety and quality standards during all service activities. - Coordinate with the internal support team to ensure smooth execution of tasks. - Document interventions and report findings accurately and timely. - Use internal software to monitor the performance and operation of the Lockers network. - Use the spare parts in the assigned car kit responsibly and efficiently. - Ensure that the stock level of the car kit is always adequate and replenished as needed. - Conduct training sessions and periodic audits. Well, what will the requirements be? - Technical diploma or equivalent experience in mechanics, electronics, or related fields. - Strong mechanical/electrical aptitude and the ability to understand complex systems. - Previous experience in hardware and software maintenance roles for electronic equipment. - Ability to read, interpret, and analyse monitoring dashboards and system logs. - Ability to read technical drawings and manuals. - Problem-solving mindset and hands-on attitude - Ability to work independently and as part of a team. - Strong field presence: this is a field-based role requiring regular daily on-site operations. - Good written and spoken English. - Valid driving license (type B). Experience level: At least 2 or 3 years of experience in a similar position. Qualifications: - Preference for technical diplomas or similar. What do we offer? - Language platform - Wellbeing programme - Flexible working hours - Online platform for lifelong learning - Competitive salary - Flexible remuneration services can be contracted Why join us? At InPost, you will play a key role in shaping how millions of customers interact with last-mile delivery solutions. You will work in a fast-growing, innovative environment where your contributions directly support the company’s expansion and market presence. Our culture is built around five key behaviours, driven by a strong “Go Go Go” mindset focused on speed and determination. - CHAMPION THE CUSTOMER: We put the customer at the center of everything we do and strive to exceed expectations. - OWN IT: We take responsibility, act with initiative, and proactively drive solutions. - DARE TO DISRUPT: We embrace innovation, ambition, and continuous learning to grow and improve together. - MAKE IT HAPPEN: We adapt quickly, learn constantly, and move forward with Smart execution. - WIN TOGETHER: We achieve great results through collaboration, recognition, and a shared winning mindset. Inclusive Culture At InPost, we are committed to building a diverse and inclusive workplace. We welcome applications from all backgrounds and believe that different perspectives strengthen our teams and drive better results.

Who are we: Antolin is a leading global automotive supplier; we are experts in designing, manufacturing, and supplying innovative solutions for vehicles around the world. Our product portfolio includes trim, headliners, and cockpits, as well as lighting and other interior systems. We offer comprehensive solutions with a focus on quality, safety, and sustainability. Our products are used in many of the world’s leading car brands. In fact, Antolin equips nearly 700 vehicle models around the world. With 136 manufacturing plants and offices in 23 countries, Antolin has achieved this strong industry presence through 75 years of working with our customers in order to develop a complete cycle of component manufacturing, from their conception and design, through the development and validation stages, to their industrialisation and sequenced delivery. We are working hard on spearheading the transformation that the automotive industry is currently experiencing with regard to vehicle interiors by collaborating with our customers. We do so in order to develop more sustainable and technologically advanced vehicles that are also adapted to the new needs and requirements of their passengers. As part of this transformation, Antolin is committed to a sustainable business model that focuses on and creates value for all its stakeholders, including its customers, employees, investors, suppliers, and society as a whole. Mission: The successful candidate will be responsible for defining, evolving, and optimizing business processes related to Sales and Finance in SAP, with a particular focus on the end-to-end order-to-cash cycle. The role aims to ensure proper integration between the SD and FI modules and to contribute to the continuous improvement of processes and solutions, aligning them with business needs and the company’s strategy. Responsibilities: • Participate in the evolution of the full order-to-cash cycle., • Collaborate with business stakeholders to identify improvement opportunities and define functional solutions., • Take part in implementation projects, roll-outs, and S/4HANA transformation initiatives., • Coordinate with technical and functional teams for the implementation of developments and enhancements., • Prepare functional documentation and support testing activities (UAT, integration testing). We are looking for: • Minimum of 4–5 years of experience as an SAP SD and/or FI consultant., • Cross-functional knowledge of both modules, with emphasis on:, • SD billing, • SD–FI integration (FI-AR), • Proven experience in end-to-end order-to-cash processes, from design through to implementation., • Experience participating in SAP projects (implementations, roll-outs, or enhancements)., • Hands-on experience with S/4HANA and migration projects from SAP ECC., • Experience in the automotive sector. What can we offer you: • You will be part of a highly engaged multinational with international career opportunities., • We offer you a learning journey adapted to your professional experience., • You will work on international projects for world- renowned companies in Automotive sector., • You can find an Open Environment to learn new technologies., • We can offer you a competitive salary, benefits and valuable OEM discounts. Here at Antolin, we are an equal opportunity employer and value diversity in our workplace. We do not discriminate based on race, religion, colour, national origin, gender, sexual orientation, age, marital status, or disability status. All qualified applicants will receive consideration for employment without regard to any of these protected characteristics. We encourage applications from all individuals and strongly support diversity in our workplace. We strive to create an inclusive environment for everyone, and we are committed to treating everyone in a fair and equitable manner. We are proud to be an equal opportunity employer and are committed to fostering a diverse and inclusive work environment. This job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities. The Company reserves the right to revise the job description at any time. Duties, responsibilities or activities may change, or new ones may be assigned at any time with or without notice. The employee must be able to perform the essential functions of the position satisfactorily. If requested, reasonable accommodations may be made to enable employees with disabilities to perform the essential functions of the job, absent undue hardship. DREAM. DARE. DO

Identify risks and drive corrective actions to ensure quality, cost, and timing objectives are met. Act as the liaison between suppliers and internal departments such as Quality, Purchasing, Engineering, and Manufacturing. Ensure compliance with customer requirements, quality standards, and corporat

Role: QA EBR Technician Location: León Experience: 1–3 years. Want to find out more? 👇 INSUD PHARMA operates across the entire pharmaceutical value chain, providing specialist knowledge and expertise in scientific research, development, manufacturing, sales and marketing of a wide range of active pharmaceutical ingredients (APIs), finished dosage forms (FDFs) and branded pharmaceutical products, adding value to human and animal health. INSUD PHARMA’s activities are organised into three synergistic business areas: Industrial (Chemo), Branded (Exeltis) and Biotechnology (mAbxience), with over 9,000 professionals in more than 50 countries, 20 state-of-the-art facilities, 15 specialised R&D centres, 12 sales offices and more than 35 pharmaceutical subsidiaries, serving 1,150 customers in 96 countries worldwide. INSUD PHARMA believes in innovation and sustainable development. Global Responsibility Comply with the GMP standards for medicinal and combination products for human use. Review, control and ensure compliance of Electronic Batch Records (EBR) and related manufacturing documentation in accordance with internal procedures, GMP rules and Authority and customers requirements, ensuring data integrity, traceability, accuracy and completeness of batch documentation prior to batch disposition and/or release activities. Specific Responsibilities · Develop standard operating procedures (general quality and departmental) related to batch record review, good documentation practices and electronic batch record management to ensure that all steps are properly defined and comply with internal and external regulations applicable in each case. · Review and approve internal SOPs related to EBR management, documentation review and GMP documentation practices. · Review Electronic Batch Records and associated manufacturing documentation to ensure completeness, accuracy, consistency and compliance with approved procedures and manufacturing instructions. · Verify that all critical process steps, controls, calculations, material reconciliations and manufacturing data are correctly documented in the EBR system and related records. · Ensure that all entries, corrections, comments and changes in the electronic records are properly documented and compliant with data integrity and GMP requirements. · Manage discrepancies identified during batch record review and coordinate with Production and other involved departments their investigation, correction and closure in accordance with internal procedures. · Support root cause analysis and trend analysis related to documentation errors, batch record discrepancies and recurring issues detected during EBR review. · Coordinate with Production, Engineering, Maintenance, Validation and other departments to ensure that any issue impacting batch documentation is properly assessed and resolved. · Review and verify that deviations, change controls or other quality events impacting the batch are properly linked, assessed and documented in the batch record package when applicable. · Ensure the proper management, traceability and archive of GMP documentation related to batch manufacturing records. · Support the implementation, maintenance and continuous improvement of electronic batch record systems and associated documentation workflows. · Participate in training activities related to Good Documentation Practices, GMP requirements and proper use/completion of Electronic Batch Records. · Support external audits and inspections according to the Annual Plan to assess compliance of batch documentation practices, data integrity requirements and the GMP system. · Participate in internal audits related to documentation practices, EBR processes and manufacturing records. · Support the Qualified Person and batch release activities through timely and accurate review of manufacturing documentation. · Support on quality investigations, batch documentation assessments and product quality issues related to manufacturing records. · Support to quality activities according to the appropriate training. Competencies/Career level Innovation, customer oriented, communication, team work, adaptability/flexibility, productivity, self-development, sense of urgency, initiative. Attention to detail, analytical mindset, compliance mindset, documentation rigor and organizational skills are especially valuable for this position. Requirements and personal skills · Education: Degree in Pharmacy or Chemistry or Sciences. · Languages: Intermediate or high level of English and bilingual in Spanish. · Experience (years/area): A minimum of 3 years' experience in similar position for a senior position. Experience in GMP documentation review, manufacturing records, batch record review or pharmaceutical production quality activities is highly valuable. · Specific Knowledge: Knowledge of GMP documentation systems, good documentation practices, batch record review processes, deviations/non-conformities, data integrity principles and quality systems in production plants. Experience with Electronic Batch Records (EBR) systems will be highly valued. · Travels: Not required. · Personal skills: Good communication skills, proactivity, good working under pressure, team working, problem-solving, good organizational skills, persistence and high attention to detail. COMMITMENT TO EQUAL OPPORTUNITIES The InsudPharma Group recognises that business management must be aligned with the needs and demands of society, and therefore is committed to equal opportunities and equal treatment for men and women, as set out in the relevant legislation in force – Organic Law 3/2007 – and we do not discriminate against anyone on the grounds of ethnicity, religion, age, sex, nationality, marital status, emotional or sexual orientation, gender identity or expression, disability, or any other personal or social circumstance.

QA Specialist (PRD) – Investigations, CRs, CAPAs & Floor Oversight.At least 3 years’ experience in similar roles within the Quality department in pharmaceutical industrial settings.LEONFARMA is part of INSUD PHARMA, a global leader in the pharmaceutical value chain and a benchmark in the researc

QA Specialist (PRD) – Investigations, CRs, CAPAs & Floor Oversight.At least 3 years’ experience in similar roles within the Quality department in pharmaceutical industrial settings.LEONFARMA is part of INSUD PHARMA, a global leader in the pharmaceutical value chain and a benchmark in the researc

React Native Mobile Developer 📍 Salamanca, Spain (On-site) About the Role We're looking for a React Native Mobile Developer to build and maintain mobile applications for iOS and Android. You'll work closely with designers and developers to deliver high-quality mobile solutions. Requirements • 3+ years of React Native experience, • Strong knowledge of JavaScript (ES6+) and TypeScript, • Experience with REST APIs, • Experience publishing apps on iOS and Android, • Familiarity with Git, • Strong problem-solving and communication skills Nice to Have • Native mobile development experience, • CI/CD and automated testing experience, • Performance optimization knowledge Benefits • Career development opportunities, • On-site gym with 24/7 access, • Free snacks, fruit, and coffee, • Provident fund, • Free parking, • Regular team events and outings

Who are we: Antolin is a leading global automotive supplier; we are experts in designing, manufacturing, and supplying innovative solutions for vehicles around the world. Our product portfolio includes trim, headliners, and cockpits, as well as lighting and other interior systems. We offer comprehensive solutions with a focus on quality, safety, and sustainability. Our products are used in many of the world’s leading car brands. In fact, Antolin equips nearly 600 vehicle models around the world. With over 120 plants in 25 countries, Antolin has achieved this strong industry presence through over seventy years of working with our customers in order to develop a complete cycle of component manufacturing, from their conception and design, through the development and validation stages, to their industrialization and sequenced delivery. We are working hard on spearheading the transformation that the automotive industry is currently experiencing with regard to vehicle interiors by collaborating with our customers. We do so in order to develop more sustainable and technologically advanced vehicles that are also adapted to the new needs and requirements of their passengers. As part of this transformation, Antolin is committed to a sustainable business model that focuses on and creates value for all its stakeholders, including its customers, employees, investors, suppliers, and society as a whole. Mission: This position is responsible for managing identity governance, access control, and modern workplace technologies to support productivity, collaboration, and compliance. Responsibilities: • Lead the design and implementation of identity and access management (IAM) solutions, including Azure Active Directory, Single Sign-On (SSO), and Multi-Factor Authentication (MFA)., • Oversee endpoint and device management using tools such as Microsoft Intune, SCCM, ..., • Ensure seamless integration of workplace technologies including Microsoft 365, Teams, SharePoint, and other collaboration platforms assuring compliance with contracts in place., • Define and enforce policies for secure access to corporate resources across hybrid and remote environments., • Collaborate with cybersecurity, infrastructure, IT operations and HR teams to align identity lifecycle processes with organizational needs., • Drive adoption of Zero Trust principles and modern workplace strategies., • Manage vendor relationships and evaluate emerging technologies to enhance workplace capabilities. What we are looking for: • Bachelor’s or Master’s degree in Information Technology, Telecommunication engineering, or related field., • Proven experience in identity management, endpoint administration, and workplace technology deployment., • Strong knowledge of Microsoft 365 ecosystem, Azure AD, and enterprise mobility solutions., • Excellent communication, & project management skills. What can we offer you: • You will be part of a highly engaged multinational with international career opportunities., • We offer you a learning journey adapted to your profile., • You will work on international projects for world- renowned companies in Automotive sector., • You can find an Open Environment to learn new technologies. Here at Antolin, we are an equal opportunity employer and value diversity in our workplace. We do not discriminate based on race, religion, colour, national origin, gender, sexual orientation, age, marital status, or disability status. All qualified applicants will receive consideration for employment without regard to any of these protected characteristics. We encourage applications from all individuals and strongly support diversity in our workplace. We strive to create an inclusive environment for everyone, and we are committed to treating everyone in a fair and equitable manner. We are proud to be an equal opportunity employer and are committed to fostering a diverse and inclusive work environment. This job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities. The Company reserves the right to revise the job description at any time. Duties, responsibilities or activities may change or new ones may be assigned at any time with or without notice. The employee must be able to perform the essential functions of the position satisfactorily. If requested, reasonable accommodations may be made to enable employees with disabilities to perform the essential functions of the job, absent undue hardship. DREAM. DARE. DO

Junior Quality Engineer (1-2 years of experience) Company: ARAN EUROPE Location: Villanubla, Valladolid, Spain Contract Type: Permanent Working Hours: Full-time Job Description We are looking for a dynamic and growth-oriented Junior Quality Engineer to permanently join our industrial plant. Working closely with the Quality Manager, you will ensure compliance with production standards and actively participate in continuous improvement initiatives. Key Responsibilities • Process Control: Oversee quality controls on production lines and approve finished product releases., • Non-Conformance Management: Identify deviations, analyze root causes, and monitor corrective actions., • Audits and Regulations: Assist in maintaining the quality management system (ISO 9001 and applicable food safety regulations)., • Customer & Supplier Relations: Support the handling of complaints and the approval of raw materials. Minimum Requirements • Education: Bachelor's Degree in Engineering (Industrial, Chemical, Materials, or similar)., • Experience: 1 to 2 years in quality departments within the industrial, packaging, or automotive sectors., • Skills: Analytical mindset, technical rigor, proactivity, and strong teamwork skills in factory environments., • Languages: Intermediate to advanced level of English (valuable for documentation and customer relations). What We Offer • Permanent contract and job stability., • Development plan and continuous learning within a solid industrial company., • Competitive salary based on the candidate's qualifications. Interested candidates should send their CV directly to: Esther Arcos HR Manager Email: Mob: +34 618 477 100 Address: C/ Guarnicioneros, 4 (Polígono Ind. San Cosme), 47620 Villanubla, Valladolid, Spain

Who are we: Antolin is a leading global automotive supplier; we are experts in designing, manufacturing, and supplying innovative solutions for vehicles around the world. Our product portfolio includes trim, headliners, and cockpits, as well as lighting and other interior systems. We offer comprehensive solutions with a focus on quality, safety, and sustainability. Our products are used in many of the world’s leading car brands. In fact, Antolin equips nearly 700 vehicle models around the world. With 136 manufacturing plants and offices in 23 countries, Antolin has achieved this strong industry presence through 75 years of working with our customers in order to develop a complete cycle of component manufacturing, from their conception and design, through the development and validation stages, to their industrialisation and sequenced delivery. We are working hard on spearheading the transformation that the automotive industry is currently experiencing with regard to vehicle interiors by collaborating with our customers. We do so in order to develop more sustainable and technologically advanced vehicles that are also adapted to the new needs and requirements of their passengers. As part of this transformation, Antolin is committed to a sustainable business model that focuses on and creates value for all its stakeholders, including its customers, employees, investors, suppliers, and society as a whole. Mission: The successful candidate will be responsible for defining, evolving, and optimizing business processes related to Sales and Finance in SAP, with a particular focus on the end-to-end order-to-cash cycle. The role aims to ensure proper integration between the SD and FI modules and to contribute to the continuous improvement of processes and solutions, aligning them with business needs and the company’s strategy. Responsibilities: • Participate in the evolution of the full order-to-cash cycle., • Collaborate with business stakeholders to identify improvement opportunities and define functional solutions., • Take part in implementation projects, roll-outs, and S/4HANA transformation initiatives., • Coordinate with technical and functional teams for the implementation of developments and enhancements., • Prepare functional documentation and support testing activities (UAT, integration testing). We are looking for: • Minimum of 4–5 years of experience as an SAP SD and/or FI consultant., • Cross-functional knowledge of both modules, with emphasis on:, • SD billing, • SD–FI integration (FI-AR), • Proven experience in end-to-end order-to-cash processes, from design through to implementation., • Experience participating in SAP projects (implementations, roll-outs, or enhancements)., • Hands-on experience with S/4HANA and migration projects from SAP ECC., • Experience in the automotive sector. What can we offer you: • You will be part of a highly engaged multinational with international career opportunities., • We offer you a learning journey adapted to your professional experience., • You will work on international projects for world- renowned companies in Automotive sector., • You can find an Open Environment to learn new technologies., • We can offer you a competitive salary, benefits and valuable OEM discounts. Here at Antolin, we are an equal opportunity employer and value diversity in our workplace. We do not discriminate based on race, religion, colour, national origin, gender, sexual orientation, age, marital status, or disability status. All qualified applicants will receive consideration for employment without regard to any of these protected characteristics. We encourage applications from all individuals and strongly support diversity in our workplace. We strive to create an inclusive environment for everyone, and we are committed to treating everyone in a fair and equitable manner. We are proud to be an equal opportunity employer and are committed to fostering a diverse and inclusive work environment. This job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities. The Company reserves the right to revise the job description at any time. Duties, responsibilities or activities may change, or new ones may be assigned at any time with or without notice. The employee must be able to perform the essential functions of the position satisfactorily. If requested, reasonable accommodations may be made to enable employees with disabilities to perform the essential functions of the job, absent undue hardship. DREAM. DARE. DO

Who are we: Antolin is a leading global automotive supplier; we are experts in designing, manufacturing, and supplying innovative solutions for vehicles around the world. Our product portfolio includes trim, headliners, and cockpits, as well as lighting and other interior systems. We offer comprehensive solutions with a focus on quality, safety, and sustainability. Our products are used in many of the world’s leading car brands. In fact, Antolin equips nearly 600 vehicle models around the world. With over 120 plants in 25 countries, Antolin has achieved this strong industry presence through over seventy years of working with our customers in order to develop a complete cycle of component manufacturing, from their conception and design, through the development and validation stages, to their industrialization and sequenced delivery. We are working hard on spearheading the transformation that the automotive industry is currently experiencing with regard to vehicle interiors by collaborating with our customers. We do so in order to develop more sustainable and technologically advanced vehicles that are also adapted to the new needs and requirements of their passengers. As part of this transformation, Antolin is committed to a sustainable business model that focuses on and creates value for all its stakeholders, including its customers, employees, investors, suppliers, and society as a whole. Mission: This position is responsible for managing identity governance, access control, and modern workplace technologies to support productivity, collaboration, and compliance. Responsibilities: • Lead the design and implementation of identity and access management (IAM) solutions, including Azure Active Directory, Single Sign-On (SSO), and Multi-Factor Authentication (MFA)., • Oversee endpoint and device management using tools such as Microsoft Intune, SCCM, ..., • Ensure seamless integration of workplace technologies including Microsoft 365, Teams, SharePoint, and other collaboration platforms assuring compliance with contracts in place., • Define and enforce policies for secure access to corporate resources across hybrid and remote environments., • Collaborate with cybersecurity, infrastructure, IT operations and HR teams to align identity lifecycle processes with organizational needs., • Drive adoption of Zero Trust principles and modern workplace strategies., • Manage vendor relationships and evaluate emerging technologies to enhance workplace capabilities. What we are looking for: • Bachelor’s or Master’s degree in Information Technology, Telecommunication engineering, or related field., • Proven experience in identity management, endpoint administration, and workplace technology deployment., • Strong knowledge of Microsoft 365 ecosystem, Azure AD, and enterprise mobility solutions., • Excellent communication, & project management skills. What can we offer you: • You will be part of a highly engaged multinational with international career opportunities., • We offer you a learning journey adapted to your profile., • You will work on international projects for world- renowned companies in Automotive sector., • You can find an Open Environment to learn new technologies. Here at Antolin, we are an equal opportunity employer and value diversity in our workplace. We do not discriminate based on race, religion, colour, national origin, gender, sexual orientation, age, marital status, or disability status. All qualified applicants will receive consideration for employment without regard to any of these protected characteristics. We encourage applications from all individuals and strongly support diversity in our workplace. We strive to create an inclusive environment for everyone, and we are committed to treating everyone in a fair and equitable manner. We are proud to be an equal opportunity employer and are committed to fostering a diverse and inclusive work environment. This job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities. The Company reserves the right to revise the job description at any time. Duties, responsibilities or activities may change or new ones may be assigned at any time with or without notice. The employee must be able to perform the essential functions of the position satisfactorily. If requested, reasonable accommodations may be made to enable employees with disabilities to perform the essential functions of the job, absent undue hardship. DREAM. DARE. DO

Junior Quality Engineer (1-2 years of experience) Company: ARAN EUROPE Location: Villanubla, Valladolid, Spain Contract Type: Permanent Working Hours: Full-time Job Description We are looking for a dynamic and growth-oriented Junior Quality Engineer to permanently join our industrial plant. Working closely with the Quality Manager, you will ensure compliance with production standards and actively participate in continuous improvement initiatives. Key Responsibilities • Process Control: Oversee quality controls on production lines and approve finished product releases., • Non-Conformance Management: Identify deviations, analyze root causes, and monitor corrective actions., • Audits and Regulations: Assist in maintaining the quality management system (ISO 9001 and applicable food safety regulations)., • Customer & Supplier Relations: Support the handling of complaints and the approval of raw materials. Minimum Requirements • Education: Bachelor's Degree in Engineering (Industrial, Chemical, Materials, or similar)., • Experience: 1 to 2 years in quality departments within the industrial, packaging, or automotive sectors., • Skills: Analytical mindset, technical rigor, proactivity, and strong teamwork skills in factory environments., • Languages: Intermediate to advanced level of English (valuable for documentation and customer relations). What We Offer • Permanent contract and job stability., • Development plan and continuous learning within a solid industrial company., • Competitive salary based on the candidate's qualifications. Interested candidates should send their CV directly to: Esther Arcos HR Manager Email: Mob: +34 618 477 100 Address: C/ Guarnicioneros, 4 (Polígono Ind. San Cosme), 47620 Villanubla, Valladolid, Spain

Global Responsibility Execute UpStream (USP) activities in the Cell Culture area of the production department, following operational procedures and GMP regulations. Specific Responsibilities • Execute the cell culture activities, according to process specifications and quality standards., • Write SOPs related to the equipment and activities of USP department., • Write batch records., • Prepare the production equipment prior to its use and after it (cleaning, inactivation, etc.)., • Register all the productive activities in logbooks, batch records (BRs) or other documents, according to the Company’s quality procedures., • Prepare culture means and process, filtering and sterilization solutions., • Provide support in preparation activities, reconditioning and materials sterilization., • Install and qualify equipment and support its maintenance, calibration and requalification., • Participate and promote improvements in the productive processes, records and activities of the Company, encouraging the continuous improvement., • Provide information and support in researches related to quality deviations and participate in the follow up of the subsequent implementation of corrective and preventive measures. Requirements and personal skills • Education: Degree in Pharmacy or similar., • Languages: Fluent Spanish and English, knowledge of other languages will be an asset., • Experience (years/area): +2 years of experience in a similar position., • Specific Knowledge: USP activities, GMP and SHE regulations., • Work shifts: 2 work shifts Morning - Evening., • Personal skills: Attention to detail, accuracy and reliability. At mAbxience, we provide equal opportunities to all regardless of race, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, or gender identity.

Global Responsibility Execute UpStream (USP) activities in the Cell Culture area of the production department, following operational procedures and GMP regulations. Specific Responsibilities • Execute the cell culture activities, according to process specifications and quality standards., • Write SOPs related to the equipment and activities of USP department., • Write batch records., • Prepare the production equipment prior to its use and after it (cleaning, inactivation, etc.)., • Register all the productive activities in logbooks, batch records (BRs) or other documents, according to the Company’s quality procedures., • Prepare culture means and process, filtering and sterilization solutions., • Provide support in preparation activities, reconditioning and materials sterilization., • Install and qualify equipment and support its maintenance, calibration and requalification., • Participate and promote improvements in the productive processes, records and activities of the Company, encouraging the continuous improvement., • Provide information and support in researches related to quality deviations and participate in the follow up of the subsequent implementation of corrective and preventive measures. Requirements and personal skills • Education: Degree in Pharmacy or similar., • Languages: Fluent Spanish and English, knowledge of other languages will be an asset., • Experience (years/area): +2 years of experience in a similar position., • Specific Knowledge: USP activities, GMP and SHE regulations., • Work shifts: 2 work shifts Morning - Evening., • Personal skills: Attention to detail, accuracy and reliability. At mAbxience, we provide equal opportunities to all regardless of race, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, or gender identity.

Who are we: Antolin is a leading global automotive supplier; we are experts in designing, manufacturing and supplying innovative solutions for vehicles around the world. Our product portfolio includes trim, headliners, and cockpits, as well as lighting and other interior systems. We offer comprehensive solutions with a focus on quality, safety, and sustainability. Our products are used in many of the world’s leading car brands. In fact, Antolin equips nearly 700 vehicle models around the world. With 136 manufacturing plants and offices in 23 countries, Antolin has achieved this strong industry presence through 75 years of working with our customers in order to develop a complete cycle of component manufacturing, from their conception and design, through the development and validation stages, to their industrialisation and sequenced delivery. We are working hard on spearheading the transformation that the automotive industry is currently experiencing with regard to vehicle interiors by collaborating with our customers. We do so in order to develop more sustainable and technologically advanced vehicles that are also adapted to the new needs and requirements of their passengers. As part of this transformation, Antolin is committed to a sustainable business model that focuses on and creates value for all its stakeholders, including its customers, employees, investors, suppliers, and society as a whole. Mission: Lead APQP and PPAP dossiers related to supplier components, coordinating all required activities with suppliers and cross-functional teams to ensure component qualification and approval are achieved on time and in compliance with customer and quality requirements. Responsibilities: • Lead and manage APQP and PPAP dossiers thoughout component development and industrialization phases., • Coordinate supplier and internal activities to ensure project milestones and qualification requirements are achieved., • Monitor component validation and approval plans., • Review and validate APQP/PPAP documentation required for component qualification., • Identify risks and drive corrective actions to ensure quality, cost, and timing objectives are met., • Act as the liaison between suppliers and internal departments such as Quality, Purchasing, Engineering, and Manufacturing., • Ensure compliance with customer requirements, quality standards, and corporate procedures., • Support problem-solving and continuous improvement initiatives related to supplier quality. We are looking for: We are looking for a proactive and results-oriented proffesional with experience in APQP and PPAP processes, capable of coordinating suppliers and cross-functional teams within a dynamic industrial environment. This temporary oportunity has been created to provide maternity leave cover, ensuring continuity and support within the Supplier Manufacturing Quality team. • Minimum 2 years of experience in APQP and PPAP processes., • Engineering degree preferred; other educational backgrounds will also be considered if supported by relevant experience., • Professional working proficiency in English., • Knowledge of quality tools and methodologies related to component development and industrialization., • Strong planning, organization, and project management skills., • Excellent communication and teamwork abilities. What can we offer you: • You will be part of a highly engaged multinational with international career opportunities., • We offer you a learning journey adapted to your professional experience., • You will work on international projects for world- renowned companies in Automotive sector., • You can find an Open Environment to learn new technologies., • We can offer you a competitive salary, benefits and valuable OEM discounts. Here at Antolin, we are an equal opportunity employer and value diversity in our workplace. We do not discriminate based on race, religion, colour, national origin, gender, sexual orientation, age, marital status, or disability status. All qualified applicants will receive consideration for employment without regard to any of these protected characteristics. We encourage applications from all individuals and strongly support diversity in our workplace. We strive to create an inclusive environment for everyone, and we are committed to treating everyone in a fair and equitable manner. We are proud to be an equal opportunity employer and are committed to fostering a diverse and inclusive work environment. This job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities. The Company reserves the right to revise the job description at any time. Duties, responsibilities or activities may change, or new ones may be assigned at any time with or without notice. The employee must be able to perform the essential functions of the position satisfactorily. If requested, reasonable accommodations may be made to enable employees with disabilities to perform the essential functions of the job, absent undue hardship. DREAM. DARE. DO

Desde mAbxience, compañía especializada en el desarrollo y fabricación de medicamentos biosimilares incorporamos un/a técnico de QA Manufacturing para nuestra planta en León (España). Responsabilidad Global Reportando a la Coordinación de QA manufacturing se encarga de la revisión de las operaciones de fabricación y documentación relacionada con el proceso productivo. Las fabircaciones se centran en API formulado de Biosimilares (anticuerpos monoclanares) de desarrollo propio y productos CMO (Biosimilares/Innovadores). Responsabilidades específicas • Quality Oversight de las operaciones en planta., • Revisión de guías de fabricación y cuadernos de registro., • Revisión y cierre de guías de fabricación cumplimentadas., • Gestión del sistema de eventos de calidad. Revisión de investigaciones de causa raíz, evaluaciones de imapcto, análisis de riesgos relacionados con fabricaciones e instalaciones., • Utilización de la herramineta trackwise para la gestión de la documentación de calidad (Eventos de calidad, controles de cambios, reclamaciones, sistema documental y de entrenamientos)., • Revisión de procedimientos normalizados de trabajo, nuevas ediciones de guías de fabricación, métodos cromatográficos, etc., • Notificación de eventos durante las fabricaciones CMO., • Colaboración en la generación de los APQR y PQR de fabricación de sustancia activa formulada., • Participación / colaboración en la elaboración de métricas del departamento., • Emisión de copias controladas de BRs, seguimiento de documentación, entrenamientos, etc., • Notificar de todos aquellos problemas potenciales o reales detectados a través de su área de responsabilidad y ayudar a implantar las acciones correctivas / preventivas necesarias junto con los responsables locales., • Impulsar la innovación en sus áreas de interés y proponer mejoras respecto a los sistemas de Calidad., • Asistencia a reuniones de departamento / sección según aplique. En adición se podrán seleccionar otro tipo de reuniones con el fin de ampliar el conocimiento del dia a día de una empresa referente del sector biotecnológico. Requisitos y habilidades personales • Formación: Grado en Farmacia, Químicas, Biotecnología, Ciencias de la salud..., • Idiomas: inglés, • Experiencia: 2-3 años en posición similar Ofrecemos contratación indefinida para entrar a formar parte de una Compañía biofarmacéutica en plena expansión. • Seguro de vida y accidente., • Comedor gratuito de empresa., • Plataforma online de formación gratuita., • Biblioteca online gratuita., • Plataforma de bienestar social, físico y emocional. Mabxience es una Empresa comprometida con la igualdad de oportunidades, por lo que todxs lxs candidatxs serán consideradxs sin distinción de raza, color, género, edad, orientación sexual, religión, origen, estado civil, ciudadanía o capacidad diferentes.

En Exceltic somos una empresa de ingeniería y consultoría tecnológica en fuerte crecimiento, con presencia internacional y proyectos en sectores como energía, industria, ferroviario, infraestructuras, tecnología y Data Centers. Ser la persona responsable de las actividades de Aseguramiento y Co

Desde mAbxience, compañía especializada en el desarrollo y fabricación de medicamentos biosimilares incorporamos un/a técnico de QA Manufacturing para nuestra planta en León (España). Responsabilidad Global Reportando a la Coordinación de QA manufacturing se encarga de la revisión de las operaciones de fabricación y documentación relacionada con el proceso productivo. Las fabircaciones se centran en API formulado de Biosimilares (anticuerpos monoclanares) de desarrollo propio y productos CMO (Biosimilares/Innovadores). Responsabilidades específicas • Quality Oversight de las operaciones en planta., • Revisión de guías de fabricación y cuadernos de registro., • Revisión y cierre de guías de fabricación cumplimentadas., • Gestión del sistema de eventos de calidad. Revisión de investigaciones de causa raíz, evaluaciones de imapcto, análisis de riesgos relacionados con fabricaciones e instalaciones., • Utilización de la herramineta trackwise para la gestión de la documentación de calidad (Eventos de calidad, controles de cambios, reclamaciones, sistema documental y de entrenamientos)., • Revisión de procedimientos normalizados de trabajo, nuevas ediciones de guías de fabricación, métodos cromatográficos, etc., • Notificación de eventos durante las fabricaciones CMO., • Colaboración en la generación de los APQR y PQR de fabricación de sustancia activa formulada., • Participación / colaboración en la elaboración de métricas del departamento., • Emisión de copias controladas de BRs, seguimiento de documentación, entrenamientos, etc., • Notificar de todos aquellos problemas potenciales o reales detectados a través de su área de responsabilidad y ayudar a implantar las acciones correctivas / preventivas necesarias junto con los responsables locales., • Impulsar la innovación en sus áreas de interés y proponer mejoras respecto a los sistemas de Calidad., • Asistencia a reuniones de departamento / sección según aplique. En adición se podrán seleccionar otro tipo de reuniones con el fin de ampliar el conocimiento del dia a día de una empresa referente del sector biotecnológico. Requisitos y habilidades personales • Formación: Grado en Farmacia, Químicas, Biotecnología, Ciencias de la salud..., • Idiomas: inglés, • Experiencia: 2-3 años en posición similar Ofrecemos contratación indefinida para entrar a formar parte de una Compañía biofarmacéutica en plena expansión. • Seguro de vida y accidente., • Comedor gratuito de empresa., • Plataforma online de formación gratuita., • Biblioteca online gratuita., • Plataforma de bienestar social, físico y emocional. Mabxience es una Empresa comprometida con la igualdad de oportunidades, por lo que todxs lxs candidatxs serán consideradxs sin distinción de raza, color, género, edad, orientación sexual, religión, origen, estado civil, ciudadanía o capacidad diferentes.

En Exceltic somos una empresa de ingeniería y consultoría tecnológica en fuerte crecimiento, con presencia internacional y proyectos en sectores como energía, industria, ferroviario, infraestructuras, tecnología y Data Centers. Contamos con un equipo de profesionales apasionados por la ingenier

Junior Quality Engineer (1-2 years of experience) Company: ARAN EUROPE Location: Villanubla, Valladolid, Spain Contract Type: Permanent Working Hours: Full-time Job Description We are looking for a dynamic and growth-oriented Junior Quality Engineer to permanently join our industrial plant. Working closely with the Quality Manager, you will ensure compliance with production standards and actively participate in continuous improvement initiatives. Key Responsibilities • Process Control: Oversee quality controls on production lines and approve finished product releases., • Non-Conformance Management: Identify deviations, analyze root causes, and monitor corrective actions., • Audits and Regulations: Assist in maintaining the quality management system (ISO 9001 and applicable food safety regulations)., • Customer & Supplier Relations: Support the handling of complaints and the approval of raw materials. Minimum Requirements • Education: Bachelor's Degree in Engineering (Industrial, Chemical, Materials, or similar)., • Experience: 1 to 2 years in quality departments within the industrial, packaging, or automotive sectors., • Skills: Analytical mindset, technical rigor, proactivity, and strong teamwork skills in factory environments., • Languages: Intermediate to advanced level of English (valuable for documentation and customer relations). What We Offer • Permanent contract and job stability., • Development plan and continuous learning within a solid industrial company., • Competitive salary based on the candidate's qualifications. Interested candidates should send their CV directly to: Esther Arcos HR Manager Email: Mob: +34 618 477 100 Address: C/ Guarnicioneros, 4 (Polígono Ind. San Cosme), 47620 Villanubla, Valladolid, Spain

Who are we: Antolin is a leading global automotive supplier; we are experts in designing, manufacturing, and supplying innovative solutions for vehicles around the world. Our product portfolio includes trim, headliners, and cockpits, as well as lighting and other interior systems. We offer comprehensive solutions with a focus on quality, safety, and sustainability. Our products are used in many of the world’s leading car brands. In fact, Antolin equips nearly 600 vehicle models around the world. With over 120 plants in 25 countries, Antolin has achieved this strong industry presence through over seventy years of working with our customers in order to develop a complete cycle of component manufacturing, from their conception and design, through the development and validation stages, to their industrialization and sequenced delivery. We are working hard on spearheading the transformation that the automotive industry is currently experiencing with regard to vehicle interiors by collaborating with our customers. We do so in order to develop more sustainable and technologically advanced vehicles that are also adapted to the new needs and requirements of their passengers. As part of this transformation, Antolin is committed to a sustainable business model that focuses on and creates value for all its stakeholders, including its customers, employees, investors, suppliers, and society as a whole. Mission: This position is responsible for managing identity governance, access control, and modern workplace technologies to support productivity, collaboration, and compliance. Responsibilities: • Lead the design and implementation of identity and access management (IAM) solutions, including Azure Active Directory, Single Sign-On (SSO), and Multi-Factor Authentication (MFA)., • Oversee endpoint and device management using tools such as Microsoft Intune, SCCM, ..., • Ensure seamless integration of workplace technologies including Microsoft 365, Teams, SharePoint, and other collaboration platforms assuring compliance with contracts in place., • Define and enforce policies for secure access to corporate resources across hybrid and remote environments., • Collaborate with cybersecurity, infrastructure, IT operations and HR teams to align identity lifecycle processes with organizational needs., • Drive adoption of Zero Trust principles and modern workplace strategies., • Manage vendor relationships and evaluate emerging technologies to enhance workplace capabilities. What we are looking for: • Bachelor’s or Master’s degree in Information Technology, Telecommunication engineering, or related field., • Proven experience in identity management, endpoint administration, and workplace technology deployment., • Strong knowledge of Microsoft 365 ecosystem, Azure AD, and enterprise mobility solutions., • Excellent communication, & project management skills. What can we offer you: • You will be part of a highly engaged multinational with international career opportunities., • We offer you a learning journey adapted to your profile., • You will work on international projects for world- renowned companies in Automotive sector., • You can find an Open Environment to learn new technologies. Here at Antolin, we are an equal opportunity employer and value diversity in our workplace. We do not discriminate based on race, religion, colour, national origin, gender, sexual orientation, age, marital status, or disability status. All qualified applicants will receive consideration for employment without regard to any of these protected characteristics. We encourage applications from all individuals and strongly support diversity in our workplace. We strive to create an inclusive environment for everyone, and we are committed to treating everyone in a fair and equitable manner. We are proud to be an equal opportunity employer and are committed to fostering a diverse and inclusive work environment. This job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities. The Company reserves the right to revise the job description at any time. Duties, responsibilities or activities may change or new ones may be assigned at any time with or without notice. The employee must be able to perform the essential functions of the position satisfactorily. If requested, reasonable accommodations may be made to enable employees with disabilities to perform the essential functions of the job, absent undue hardship. DREAM. DARE. DO

Collaborate with functional teams in IT across SAP and other Business Application stakeholders and all relevant business representatives to ensure compliance and/or project quality. The ideal candidate will bring deep CSV and Test Management expertise for Enterprise Business Applications like SAP, e

UNIQLO’s LifeWear philosophy consist of offering clothing that comes from the Japanese values of simplicity, quality and longevity, constantly being innovated to bring more warmth, more lightness, better design, and better comfort to people’s lives. Formar parte de un equipo unido, colaborar act

Collaborate with functional teams in IT across SAP and other Business Application stakeholders and all relevant business representatives to ensure compliance and/or project quality. Key role for defining, driving and implementation of Test Management for Business Application and other major initiati

These hotels are marketed under four brands that allow us to provide our guests with a clear differentiating value in terms of both quality and service: ### Royal Hideaway Luxury Hotels & Resorts ### Barceló Hotels & Resorts ### Occidental Hotels & Resorts ### Allegro HotelsAll of the above, co

Identify, create and facilitate process design changes by conducting business and systems process analysis and design at a complex level; focusing on quality improvement and data management; ensuring data is reliable and valid; developing process improvements; integrating new systems and processes w

Reports to: Executive Chef and Executive Sous Chef. Keep the Executive Chef and Executive Sous Chef fully informed of significant operational matters, challenges, or accomplishments. The Pastry Chef is responsible for delivering high-quality, efficient, individualized, and technically excellent past