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Importante empresa multinacional de automoción, con 59 sedes alrededor del mundo y más de 17.500 empleados, ubicada en la zona de Ágreda-Soria precisa incorporar a su equipo a un/a Responsable de Calidad y Medio Ambiente. Buscamos un profesional que, habiéndose desarrollado en entorno industrial, preferiblemente en el sector de automoción, lidere un proyecto estable y un equipo multidisciplinar, estableciendo relaciones de sinergia con el resto de departamentos con habilidades demostradas en motivación y desarrollo de equipos. Al formar parte del equipo de dirección, deberá ser capaz de aportar soluciones y espíritu constructivo en temas generales y transversales de la planta, liderando procesos de cambio internos a través de aportaciones constructivas y una excelente comunicación. Tus principales responsabilidades serán: • Establecer pautas y estándares para el aseguramiento de los requisitos de calidad de los clientes y normativa en planta, partners o proveedores. Elaborar y mantener los PFMEAs, • Colaboración con la central en el desarrollo de proveedores y monitorización de los mismos., • Supervisar y mantener el Sistema y las certificaciones de Calidad, y Medio Ambiente, • Optimizar, rentabilizar y mejora continua de la Gestión de la Calidad y del Medio Ambiente, • Analizar y gestionar las incidencias y reclamaciones, analizando de forma coordinada con el resto de los departamentos con la utilización de sistemas de resolución de problemas y asegurando una relación de colaboración., • Planificar, coordinar y asistir en las auditorias, tanto internas como externas, auditorías inter-plantas, así como en proveedores (necesarios certificación de auditor interno VDA 6.3 y 6.5), • Comunicación continua con el cliente y mantenimiento de portales actualizados., • Seguimiento de garantías de cliente, participando y liderando la negociación de factores técnicos., • Elaborar informes regulares necesarios para el seguimiento de los indicadores de calidad para la planta y la central., • Planificar, definir y hacer el seguimiento de las necesidades de formación, cualificación y desarrollo profesional y personal para la mejora continua asegurando el seguimiento de la Política de Calidad y Medio Ambiente de toda la plantilla., • Organizar y coordinar los laboratorios de ensayos de durabilidad, corrosión y metalografía, • Comunicación entre plantas, participando activamente en las plataformas de calidad. Requisitos mínimos: • Diplomatura técnica y/o experiencia asimilable a las funciones y responsabilidades del puesto., • Al menos 3-5 años en sector industrial con experiencia en liderazgo de equipos., • Conocimiento y experiencia con procesos VDA 6.3 y 6.5 en Core Tools (PFMEA, SPC, MSA, CP, PPAP), ANPQP, APQP, PSCR, ISO 14001, ISO IATF16949, ERPs (SAP nivel usuario), • Experiencia en problem solving (A3, Isikawa, 8D, etc.), • Nivel de inglés Medio/Alto. Valorable otros idiomas (francés, alemán), • Disponibilidad para viajes (principalmente para visitar a clientes y a casa matriz) Competencias personales clave: • Enfoque a la mejora continua., • Habilidades demostradas para el liderazgo y el trabajo en equipo, • Capacidades para toma de decisiones, • Proactividad, • Buenas habilidades de comunicación, • Apertura a los cambios. Te ofrecemos la oportunidad de unirte a un equipo sólido y comprometido, en una organización líder en su sector, con un entorno de trabajo estimulante y oportunidades de desarrollo profesional. Fecha de incorporación inmediata. Duración del contrato: indefinido

Our goal is to strengthen the brand in Spain. We are looking for you to work as Automation Engineer! Partner with local site project teams to scope changes on the PLC system Maintain Inventory and control upgrades to PLC/SCADA systems Follow the SDLC Procedure to implement changes (covering RS updates, RTM Change control, Implementation, and test) To prepare and approve Quality assurance plans and close out reports To partner with local site project teams to scope changes and prep relevant documentation In the review and approval of automation documents Support Field testing Equipment and support commissioning Ensure implement is implemented in a safe fashion with quality a necessary output. Educate local project teams on automation standards as they relate to technology selection, system configuration, SDLC, validation, hardware, software environments and business processes. Kneat, Siemens WinCC/S7, Aveva System Platform/Intouch, Aveva (OSI) PI, Microsoft 365 products and Windows core WFI Generation & Distribution, Building management systems, Cleaning and Sterilization (Parts washers & Autoclaves), Blending and Formulation, Filling, Packaging and Inspection We are HCLTech, one of the fastest-growing large tech companies in the world and home to 225,000+ people across 60 countries, supercharging progress through industry-leading capabilities centered around Digital, Engineering and Cloud. The driving force behind that work, our people, are diverse, creative, and passionate, raising the bar for excellence on a regular basis. We, in turn, work hard to bring out the best in them as we strive to help them find their spark and become the best version of themselves that they can be. Join us on our journey in advancing the technological world through innovation and creativity. We offer End-to-end digital transformation expertise that helps clients from strategy through execution. We work with the biggest brands, offering the opportunity to be a part of industry-leading work. We are invested in your growth, offering learning and career development opportunities at every level to help you find your spark. We offer a virtual-first work environment, promoting a good work-life balance and real flexibility Our company is extremely diverse with representation of 165 nationalities. To achieve all our objectives, it intends to attract, develop, and retain different profiles, assuming diversity as a key factor and differentiator of fundamental innovation in our organization. All qualified applicants will receive consideration for employment without regard to age, ancestry, color, family or medical care leave, gender identity or expression, genetic information, marital status, medical condition, national origin, physical or mental disability, political affiliation, protected veteran status, race, religion, sex (including pregnancy), sexual orientation, or any other characteristic protected by applicable laws, regulations, and ordinances.

Job Title: Senior CQV Engineer Location: Salamanca, Spain Duration: 1 Year (Starting May/June 2026) with potential extension Language Requirements: Spanish (essential) Company Overview: Adryan is an internationally operating services group. From our offices in The Netherlands and Switzerland, we offer a full range of services for the (bio)pharmaceutical and high-end food industry. We are specialised in the areas of project management, engineering, CQV and compliance. Position Overview: The Senior CQV Engineer is responsible for executing and supporting Commissioning, Qualification & Validation (CQV) activities for equipment, systems, and facilities, ensuring compliance with Good Manufacturing Practices (GMP), regulatory requirements, and applicable quality standards, while meeting project timelines and objectives. Key Responsibilities: Commissioning • Participate in commissioning activities for equipment and systems (FAT, SAT, functional testing)., • Participate actively in construction and/or equipment walkdowns and follow up on open action items., • Verify that systems are installed and operate in accordance with design requirements., • Prepare, review, and execute CQV documentation (URS, DQ, IOQ, PQ)., • Develop and execute qualification and/or validation protocols and reports., • Ensure appropriate requirements traceability., • Identify, document, and follow up on deviations and issues., • Ensure compliance with GMP, FDA, EMA, GAMP 5, ICH, and internal policies and procedures., • Participate in internal and external audits (regulatory and/or client audits)., • Coordinate CQV activities with multidisciplinary teams (QA, Engineering, Production, Automation)., • Report progress, risks, and issues to the CQV Lead and/or Project Manager., • Ensure compliance with project schedules and agreed deliverables., • Prepare and review system lists, impact assessments, quality tracking tools, and overall project plans developed throughout the project lifecycle. Qualifications & Experience: • Bachelor’s degree in Engineering (Industrial, Chemical, Mechanical, Electrical, Biomedical, or similar)., • A Master’s degree or specific training in Validation and/or Quality is considered an asset., • Proven experience in CQV activities within sterile pharmaceutical manufacturing facilities., • Experience with systems and equipment such as HVAC, Utilities (PW, WFI, gases), process equipment, and automated systems is desirable., • Experience in reviewing technical and validation documentation, especially in Spanish., • Knowledge of GMP regulations and applicable regulatory guidelines., • Experience with risk-based validation methodologies., • Ability to generate and manage technical documentation and CQV protocols., • Knowledge of automation systems and CSV is considered a plus., • Excellent organizational and coordination skills to keep tasks on track., • Fluency in Spanish; proficiency in English is a plus., • Ability to work independently and as part of a multidisciplinary team. Start Date: May/June 2026 Duration: 1 year with potential for extension If you meet these qualifications and are interested in contributing to a cutting-edge sterile manufacturing environment, please apply with your updated CV. Note: On-site presence will be discussed; partly remote working arrangements are possible. Documentation and systems are accessible online for your convenience.

🚀 Únete a NTT DATA En NTT DATA trabajamos para transformar el futuro a través de la tecnología. Somos más de 190.000 profesionales en más de 50 países, impulsando proyectos que conectan innovación, talento y un claro enfoque hacia la evolución digital de nuestros clientes. Operamos en múltiples industrias, pero en el mundo Telco jugamos en la liga de los grandes: virtualización, automatización, cloud telco y reconversión de infraestructuras críticas definen buena parte de nuestro día a día. 📡 ¿Dónde vas a trabajar? Formarás parte del área de Telecom & Media, en un proyecto estratégico de innovación y vanguardia, donde se probarán nuevas tecnologías y se implementarán las soluciones más punteras del sector. 💡 Buscamos Un/a especialista en Tecnología y Certificación de Servicios de Voz y Datos, con foco en plataformas de Mensajería (SMS/MMS/RCS), Presencia y Buzones de Voz (VMS). 🧩 ¿Qué nos gustaría que aportaras? Más de 5 años de experiencia en certificación, validación e integración de servicios y plataformas Telco, con especialización en: • Localización (ENL, GMLC, servicios basados en posición), • Mensajería (SMS, USSD, RCS, plataformas de mensajería Web), • Presencia, Perfil de Usuario y Plataformas de Buzones, • Arquitecturas SDF/SOA, OSB y WebLogic, • Pruebas de performance, resiliencia y alta disponibilidad en servicios críticos Experiencia transversal en plataformas de red, middleware y servicios de valor añadido, capaz de abordar certificación extremo a extremo en entornos complejos y de alta exigencia. • Redes móviles: GSM, GPRS, UMTS, IMS y red de señalización., • Sistemas: Linux/Unix y Windows (administración básica)., • Bases de datos (consultas y modelado)., • Protocolos: TCP/IP, HTTP/HTTPS, FTP/SFTP, TELNET, SSH/SSH2., • Scripting: Shell, Batch., • Virtualización: VMware, Red Hat Enterprise Virtualization, etc., • Manejo de Quality Center (QC)., • Análisis de trazas con herramientas tipo Nethawk. 🛠️ Tus principales funciones • Asegurar la interoperabilidad de protocolos de señalización y la entrega de servicios multimedia., • Garantizar la alta disponibilidad y la experiencia de usuario en servicios críticos de red. 🧭 Soft skills que marcan la diferencia • Foco en resultados y calidad del servicio en entornos críticos., • Capacidad analítica y visión transversal de los proyectos., • Mentalidad resolutiva y orientación a la ejecución. 🎯 ¿Qué te ofrecemos? 💼 Contrato indefinido y participación en proyectos estratégicos dentro del sector Telco. 📈 Retribución competitiva con revisiones periódicas. 🔝 Plan de desarrollo profesional y mentoring técnico. 📝 Acceso a formación continua en tecnologías clave: certificaciones, cursos... 👩🏽 💻 Modalidad híbrida y flexibilidad horaria. 🏥 Beneficios corporativos y programas de bienestar. 🌏 Iniciativas sociales y proyectos de impacto tecnológico. 🌍 Nuestra cultura En NTT DATA creemos en personas que cuestionan, proponen, crean y evolucionan. Nos encanta el talento que busca crecer, aprender y dejar huella en proyectos de gran impacto. Queremos que formes parte de un entorno donde puedas ser auténtico/a y desarrollar tu mejor versión. #WeAreAllUnique #YouMakeUsUnique

Mantell Associates is partnered with a global biopharmaceutical organisation based in León, specialising in the development, manufacturing, and commercialisation of biosimilars, alongside offering integrated CDMO services worldwide. Following significant recent investment, the business is experiencing rapid growth and expanding its Quality Assurance function with the hire of a QA Consultant. This is a fully onsite opportunity, offering the chance to play a key role in a high-growth environment. QA Consultant - Responsibilities: • Manage deviations, investigations, and root cause analysis, • Lead and track CAPAs to ensure timely and effective resolution, • Review and approve GMP documentation and batch records, • Support audits and ensure inspection readiness What’s on offer: • Join an investment-backed, rapidly scaling biopharma organisation, • High-impact role within a growing QA team, • Exposure to complex biologics and biosimilars manufacturing, • Competitive daily rate Mantell Associates is a specialist Pharmaceutical and Life Science headhunting firm. For more information on this opportunity, contact us at +44 (0)20 3854 7700.

From Mabxience, a company specialized in the development and manufacture of biosimilar medicines, we are incorporating a temporary MSAT technician for our plant in León. Global Responsabilities Organize the implementation of manufacturing processes in any of the producing lines at mAbxience (León); identification and proposal of continuous improvement programs in production; scientific support on deviation and non-conformity solving as well as assessment and implementation of new technologies in producing lines. Specific responsabilities • Follow and participate in process developments by R&D in order to ensure that their execution at industrial scale will be possible as for infrastructures, materials, operations and costs, exposing all with a process risk assessment in regards of facilities and scale applicable to these., • Technology transfers performed in between company units or with external customers, in order to ensure that their execution at industrial scale will be possible as for infrastructures, materials, operations and costs., • Write and verify documentation needed to start up manufacturing process in producing lines. For instance:, • Process descriptions., • List of materials and Raw Materials and their specifications., • Manufacturing Versions and roadmaps., • Initial Master Batch Records., • Scale-up rationale and report., • Additional scale-up protocols/reports such as stability studies of intermediate products among others., • Coordinate and provide training courses on new operations to the different production sections., • Coordinate and provide scientific support to production throughout execution of engineering batches and early GMP batches, following up process trending as well as analytical product parameters: data gathering., • Coordinate and support to R&D for studies included in Process validation stages, including DSM, viral clearance, and resin lifetime studies, as well as process characterisation., • Follow up of process or product deviations, identifying possible root causes, potential impacts, proposing corrective and preventive actions, as indicated in the corresponding quality procedure., • Coordinate with other departments sampling plans for first batches manufactured in GMP facility for new process under implementation., • Identification and evaluation of process improvement and optimization opportunities. Asses their impact and coordinate their implementation with the different involved departments (Engineering, R&D, Quality, Supply Chain, Purchases…)., • Suggest and assess implementation of new technologies, equipment, or different usages of these, functioning as Operations interface with the departments of Engineering, R&D, Quality, Supply Chain, Purchases…, • Support and organization of the writing, execution, and reporting, as it may correspond, for the different experiments and studies associated to batch implementation, researching on any incidence or proposal of process improvement. Qualifications • Education: University degree oriented to biology or chemistry, • Languages: Intermediate English level (fluency valued), • Experience (years/area): ≥2 years in Operations, R&D, MSAT, • Specific Knowledge: Work in GMP environment, UPS-DSP experience, Tech transfer, process validation., • Personal skills : Result oriented, attention to detail, Teamwork oriented mAbxience is committed to equal opportunities. We do not discriminate against any person on the grounds of ethnicity, religion, age, sex, nationality, marital status, affective or sexual orientation, gender identity or expression, disability, or any other personal or social circumstance.

In a few words Position: R&D QA Techinician. Location: León. Experience: Between 1-3 years. Want to know more? 👇 INSUD PHARMA operates across the entire pharmaceutical value chain, providing specialized knowledge and experience in scientific research, development, manufacturing, sales, and marketing of a wide range of active pharmaceutical ingredients (API), finished dosage forms (FDF), and branded pharmaceutical products, adding value to human and animal health. The activities of INSUD PHARMA are organized into three synergistic business areas: Industrial (Chemo), Branded (Exeltis), and Biotech (mAbxience), with over 9,000 professionals in more than 50 countries, 20 state-of-the-art facilities, 15 specialized R&D centers, 12 commercial offices, and more than 35 pharmaceutical subsidiaries, serving 1,150 customers in 96 countries worldwide. INSUD PHARMA believes in innovation and sustainable development. The challenge: Collaborate with the Head of QA-R&D of Chemo in order to assure the activities of R&D Department are performed in compliance with the internal SOPs, the GMP and EMEA and FDA legislation. Specific Responsibilities: • Collaborate with the Head of QA-R&D in the implementation and maintenance of a Corporate Quality System in R&D in compliance with GMP., • Write and review corporate procedures which allow to standardize the R&D Department activities and to assure their adaptation to the correspondent Good Manufacturing Practices., • Review and approve documents generated by R&D (i.e. Analytical validations, master batch records, procedures, and analytical methods)., • Review and approve executed batch records and analytical results of R&D before their release., • Issue and review R&D analytical specifications., • Perform internal and external audits., • Collaborate with the Head of QA-R&D in the preparation and attendance of clients audits and Health Authorities inspections., • Issue and organize the documentation sent from QA to RA for new submission of MA and to answer DL., • Collaborate in GMP training of R&D employees., • Train the new incorporations in the specific activities and functions of the position in which you are an expert. Requirements and personal skills: • Education: Degree in Health Sciences (e.g. Chemistry, Pharmacy, Biology or Medicine) with supplementary knowledge of Quality and GMP., • Languages: Fluent Spanish and English, knowledge of other languages will be an asset., • Experience (years/area): +2 years in Quality Assurance and desirable experience in R&D., • Specific Knowledge: Quality procedures and GMP., • Travels: Not required, may occur occasionally., • Personal skills: Good communication skills, customer orientation, proactivity, organizational skills. COMMITMENT TO EQUAL OPPORTUNITIES The InsudPharma group is aware that business management must align with the needs and demands of society, and therefore assumes the commitment to equal opportunities and treatment between men and women, as stated in the current regulations on the matter - Organic Law 3/2007, and we do not discriminate against any person on the grounds of ethnicity, religion, age, sex, nationality, marital status, affective or sexual orientation, gender identity or expression, disability, or any other personal or social circumstance.

In a few words Position: R&D QA Techinician. Location: León. Experience: Between 1-3 years. Want to know more? 👇 INSUD PHARMA operates across the entire pharmaceutical value chain, providing specialized knowledge and experience in scientific research, development, manufacturing, sales, and marketing of a wide range of active pharmaceutical ingredients (API), finished dosage forms (FDF), and branded pharmaceutical products, adding value to human and animal health. The activities of INSUD PHARMA are organized into three synergistic business areas: Industrial (Chemo), Branded (Exeltis), and Biotech (mAbxience), with over 9,000 professionals in more than 50 countries, 20 state-of-the-art facilities, 15 specialized R&D centers, 12 commercial offices, and more than 35 pharmaceutical subsidiaries, serving 1,150 customers in 96 countries worldwide. INSUD PHARMA believes in innovation and sustainable development. The challenge: Collaborate with the Head of QA-R&D of Chemo in order to assure the activities of R&D Department are performed in compliance with the internal SOPs, the GMP and EMEA and FDA legislation. Specific Responsibilities: • Collaborate with the Head of QA-R&D in the implementation and maintenance of a Corporate Quality System in R&D in compliance with GMP., • Write and review corporate procedures which allow to standardize the R&D Department activities and to assure their adaptation to the correspondent Good Manufacturing Practices., • Review and approve documents generated by R&D (i.e. Analytical validations, master batch records, procedures, and analytical methods)., • Review and approve executed batch records and analytical results of R&D before their release., • Issue and review R&D analytical specifications., • Perform internal and external audits., • Collaborate with the Head of QA-R&D in the preparation and attendance of clients audits and Health Authorities inspections., • Issue and organize the documentation sent from QA to RA for new submission of MA and to answer DL., • Collaborate in GMP training of R&D employees., • Train the new incorporations in the specific activities and functions of the position in which you are an expert. Requirements and personal skills: • Education: Degree in Health Sciences (e.g. Chemistry, Pharmacy, Biology or Medicine) with supplementary knowledge of Quality and GMP., • Languages: Fluent Spanish and English, knowledge of other languages will be an asset., • Experience (years/area): +2 years in Quality Assurance and desirable experience in R&D., • Specific Knowledge: Quality procedures and GMP., • Travels: Not required, may occur occasionally., • Personal skills: Good communication skills, customer orientation, proactivity, organizational skills. COMMITMENT TO EQUAL OPPORTUNITIES The InsudPharma group is aware that business management must align with the needs and demands of society, and therefore assumes the commitment to equal opportunities and treatment between men and women, as stated in the current regulations on the matter - Organic Law 3/2007, and we do not discriminate against any person on the grounds of ethnicity, religion, age, sex, nationality, marital status, affective or sexual orientation, gender identity or expression, disability, or any other personal or social circumstance.

In a few words Position: QC Analyst Temporary Location: León Experience: 1-2 years Want to know more? 👇 INSUD PHARMA operates across the entire pharmaceutical value chain, providing specialized knowledge and experience in scientific research, development, manufacturing, sales, and marketing of a wide range of active pharmaceutical ingredients (API), finished dosage forms (FDF), and branded pharmaceutical products, adding value to human and animal health. The activities of INSUD PHARMA are organized into three synergistic business areas: Industrial (Chemo), Branded (Exeltis), and Biotech (mAbxience), with over 9,000 professionals in more than 50 countries, 20 state-of-the-art facilities, 15 specialized R&D centers, 12 commercial offices, and more than 35 pharmaceutical subsidiaries, serving 1,150 customers in 96 countries worldwide. INSUD PHARMA believes in innovation and sustainable development. Ready to be a #Challenger? What are we looking for? 🔎 We are recruiting a new INSUDER as an analyst to join the QC team at our site based in León. The challenge! • Analyze, using different analytical techniques (GC, HPLC, TLC, KF), API, intermediate samples or final samples and stability samples, in order to ensure good quality (meet the specifications) of different products., • Complete analytical documentation for each product to meet GMP standards., • Store and control of stock chemical reagents, following established rules to ensure order and location., • Take intermediate or final production and cleaning samples., • Take samples for microbiological analysis of water, air and surfaces of manufacturing facilities and equipment., • Follow approved analytical methods and SOP in place. What do you need? • Education: FP II Chemistry or Chemical Degree., • Languages: Fluent Spanish, medium level English is a plus., • Experience (years/area): Minimum 2 year experience in the functions mentioned above is recommended. Experience in HPLC, GC, Physico-chemical analysis., • Specific Knowledge: Knowledge of GMP and GLP regulations. Our benefits! • 📜 Temporary contract., • 💸 Attractive salary package., • 🕒 Temporary work with rotating shifts to balance your work and family life., • 🧪 Training and experience in a strategic and constantly growing sector., • 👨‍👩‍👧 We are characterized by a professional, close-knit, and team-oriented work environment. What will the Selection process be like? 🕵️ ➡️ Stay tuned to your phone and email! The first thing we will likely do is contact you through one of the two channels. ➡️ Prepare well! We will continue with an in-person/virtual interview depending on availability and what we agree upon; there may be one or two interviews in the process, and depending on the type of process, there may also be some kind of test. ➡️ Wait for the result! We care that you feel guided throughout each selection process and know what to expect from us, so we will always try to inform you of the status of the process. 🔷 Do you think this offer is not for you? 🔷 Follow us on social media like LinkedIn/Instagram and stay tuned for any offers we may release; the opportunity to be a new Insuder is waiting! #InsudPharma #Challenger #Insuder #InsudTalent COMMITMENT TO EQUAL OPPORTUNITIES The InsudPharma group is aware that business management must align with the needs and demands of society, and therefore assumes the commitment to equal opportunities and treatment between men and women, as stated in the current regulations on the matter - Organic Law 3/2007, and we do not discriminate against any person on the grounds of ethnicity, religion, age, sex, nationality, marital status, affective or sexual orientation, gender identity or expression, disability, or any other personal or social circumstance.

In a few words Position: QC Analyst Temporary Location: León Experience: 1-2 years Want to know more? 👇 INSUD PHARMA operates across the entire pharmaceutical value chain, providing specialized knowledge and experience in scientific research, development, manufacturing, sales, and marketing of a wide range of active pharmaceutical ingredients (API), finished dosage forms (FDF), and branded pharmaceutical products, adding value to human and animal health. The activities of INSUD PHARMA are organized into three synergistic business areas: Industrial (Chemo), Branded (Exeltis), and Biotech (mAbxience), with over 9,000 professionals in more than 50 countries, 20 state-of-the-art facilities, 15 specialized R&D centers, 12 commercial offices, and more than 35 pharmaceutical subsidiaries, serving 1,150 customers in 96 countries worldwide. INSUD PHARMA believes in innovation and sustainable development. Ready to be a #Challenger? What are we looking for? 🔎 We are recruiting a new INSUDER as an analyst to join the QC team at our site based in León. The challenge! • Analyze, using different analytical techniques (GC, HPLC, TLC, KF), API, intermediate samples or final samples and stability samples, in order to ensure good quality (meet the specifications) of different products., • Complete analytical documentation for each product to meet GMP standards., • Store and control of stock chemical reagents, following established rules to ensure order and location., • Take intermediate or final production and cleaning samples., • Take samples for microbiological analysis of water, air and surfaces of manufacturing facilities and equipment., • Follow approved analytical methods and SOP in place. What do you need? • Education: FP II Chemistry or Chemical Degree., • Languages: Fluent Spanish, medium level English is a plus., • Experience (years/area): Minimum 2 year experience in the functions mentioned above is recommended. Experience in HPLC, GC, Physico-chemical analysis., • Specific Knowledge: Knowledge of GMP and GLP regulations. Our benefits! • 📜 Temporary contract., • 💸 Attractive salary package., • 🕒 Temporary work with rotating shifts to balance your work and family life., • 🧪 Training and experience in a strategic and constantly growing sector., • 👨‍👩‍👧 We are characterized by a professional, close-knit, and team-oriented work environment. What will the Selection process be like? 🕵️ ➡️ Stay tuned to your phone and email! The first thing we will likely do is contact you through one of the two channels. ➡️ Prepare well! We will continue with an in-person/virtual interview depending on availability and what we agree upon; there may be one or two interviews in the process, and depending on the type of process, there may also be some kind of test. ➡️ Wait for the result! We care that you feel guided throughout each selection process and know what to expect from us, so we will always try to inform you of the status of the process. 🔷 Do you think this offer is not for you? 🔷 Follow us on social media like LinkedIn/Instagram and stay tuned for any offers we may release; the opportunity to be a new Insuder is waiting! #InsudPharma #Challenger #Insuder #InsudTalent COMMITMENT TO EQUAL OPPORTUNITIES The InsudPharma group is aware that business management must align with the needs and demands of society, and therefore assumes the commitment to equal opportunities and treatment between men and women, as stated in the current regulations on the matter - Organic Law 3/2007, and we do not discriminate against any person on the grounds of ethnicity, religion, age, sex, nationality, marital status, affective or sexual orientation, gender identity or expression, disability, or any other personal or social circumstance.

At mAbxience, a company specialized in the development and manufacturing of biosimilar medicines, we are hiring a AD Bioassay Analyst for our Manufacturing Site in León (Spain). GLOBAL RESPONSIBILITY Performs and directs assays according to and in compliance with Good Laboratory Practices (GLP), current Good Manufacturing Practices (cGMP) guidelines and Standard Operating Procedures (SOPs). Sufficiently competent in science to initiate and carry out scientific development projects related to the development of new assays, initiation of new programs, assay validations and associated projects. Schedules and directs assays under the supervision of the Study Director. Assists with training junior staff members. Performs Research & Development activities as required. SPECIFIC RESPONSIBILITIES Conducts and directs assays and lab procedures according to and in compliance with GLP, cGMP, guidelines and SOPs. Accurately completes batch records and other required documentation according to and in compliance with GLP, cGMP guidelines and SOPs. Follows all general and laboratory SOPs. Maintains a laboratory notebook for Research & Development activities as required. Communicates with supervisor and other colleagues re: daily lab activities. Prepares reagents and completes reagent batch records. Checks reagents for expired chemicals and disposes of any expired reagents. Performs laboratory maintenance (i.e. decontaminates and disposes of medical and other waste as appropriate, maintains laboratory supply inventories, keeps work surfaces clean and neat) and keeps records of maintenance according to guidelines and SOPs. Performs routine equipment monitoring and cleaning (i.e. centrifuges, biosafety and chemical hoods, refrigerators, incubators and freezers) and keeps records according to guidelines and SOPs. Completes all requisite training (Quality Assurance, safety, etc.). Correctly analyzes scientific data with accuracy and precision. Performs daily work activities with minimal supervision. Communicates inventory needs to Materials Management personnel and contacts suppliers for technical information as needed. REQUIREMENTS AND PERSONAL SKILLS ·Education: Master’s degree or bachelor’s degree with major in Biological Sciences or other science-related major, plus. Languages: Fluent Spanish, working knowledge in English, knowledge of other languages will be an asset. Experience (years/area): 1-2 or more years of experience. Specific Knowledge: Knowledge of molecular biology and immunology. mAbxience is a company committed to equal opportunities, and therefore, all candidates will be considered without distinction of race, color, gender, age, sexual orientation, religion, origin, marital status, citizenship, or disability.

From Mabxience, a company specialized in the development and manufacture of biosimilar medicines, we are incorporating a temporary MSAT technician for our plant in León. Global Responsabilities Organize the implementation of manufacturing processes in any of the producing lines at mAbxience (León); identification and proposal of continuous improvement programs in production; scientific support on deviation and non-conformity solving as well as assessment and implementation of new technologies in producing lines. Specific responsabilities • Follow and participate in process developments by R&D in order to ensure that their execution at industrial scale will be possible as for infrastructures, materials, operations and costs, exposing all with a process risk assessment in regards of facilities and scale applicable to these., • Technology transfers performed in between company units or with external customers, in order to ensure that their execution at industrial scale will be possible as for infrastructures, materials, operations and costs., • Write and verify documentation needed to start up manufacturing process in producing lines. For instance:, • Process descriptions., • List of materials and Raw Materials and their specifications., • Manufacturing Versions and roadmaps., • Initial Master Batch Records., • Scale-up rationale and report., • Additional scale-up protocols/reports such as stability studies of intermediate products among others., • Coordinate and provide training courses on new operations to the different production sections., • Coordinate and provide scientific support to production throughout execution of engineering batches and early GMP batches, following up process trending as well as analytical product parameters: data gathering., • Coordinate and support to R&D for studies included in Process validation stages, including DSM, viral clearance, and resin lifetime studies, as well as process characterisation., • Follow up of process or product deviations, identifying possible root causes, potential impacts, proposing corrective and preventive actions, as indicated in the corresponding quality procedure., • Coordinate with other departments sampling plans for first batches manufactured in GMP facility for new process under implementation., • Identification and evaluation of process improvement and optimization opportunities. Asses their impact and coordinate their implementation with the different involved departments (Engineering, R&D, Quality, Supply Chain, Purchases…)., • Suggest and assess implementation of new technologies, equipment, or different usages of these, functioning as Operations interface with the departments of Engineering, R&D, Quality, Supply Chain, Purchases…, • Support and organization of the writing, execution, and reporting, as it may correspond, for the different experiments and studies associated to batch implementation, researching on any incidence or proposal of process improvement. Qualifications • Education: University degree oriented to biology or chemistry, • Languages: Intermediate English level (fluency valued), • Experience (years/area): ≥2 years in Operations, R&D, MSAT, • Specific Knowledge: Work in GMP environment, UPS-DSP experience, Tech transfer, process validation., • Personal skills: Result oriented, attention to detail, Teamwork oriented mAbxience is committed to equal opportunities. We do not discriminate against any person on the grounds of ethnicity, religion, age, sex, nationality, marital status, affective or sexual orientation, gender identity or expression, disability, or any other personal or social circumstance.

From Mabxience, a company specialized in the development and manufacture of biosimilar medicines, we are incorporating a temporary MSAT technician for our plant in León. Global Responsabilities Organize the implementation of manufacturing processes in any of the producing lines at mAbxience (León); identification and proposal of continuous improvement programs in production; scientific support on deviation and non-conformity solving as well as assessment and implementation of new technologies in producing lines. Specific responsabilities • Follow and participate in process developments by R&D in order to ensure that their execution at industrial scale will be possible as for infrastructures, materials, operations and costs, exposing all with a process risk assessment in regards of facilities and scale applicable to these., • Technology transfers performed in between company units or with external customers, in order to ensure that their execution at industrial scale will be possible as for infrastructures, materials, operations and costs., • Write and verify documentation needed to start up manufacturing process in producing lines. For instance:, • Process descriptions., • List of materials and Raw Materials and their specifications., • Manufacturing Versions and roadmaps., • Initial Master Batch Records., • Scale-up rationale and report., • Additional scale-up protocols/reports such as stability studies of intermediate products among others., • Coordinate and provide training courses on new operations to the different production sections., • Coordinate and provide scientific support to production throughout execution of engineering batches and early GMP batches, following up process trending as well as analytical product parameters: data gathering., • Coordinate and support to R&D for studies included in Process validation stages, including DSM, viral clearance, and resin lifetime studies, as well as process characterisation., • Follow up of process or product deviations, identifying possible root causes, potential impacts, proposing corrective and preventive actions, as indicated in the corresponding quality procedure., • Coordinate with other departments sampling plans for first batches manufactured in GMP facility for new process under implementation., • Identification and evaluation of process improvement and optimization opportunities. Asses their impact and coordinate their implementation with the different involved departments (Engineering, R&D, Quality, Supply Chain, Purchases…)., • Suggest and assess implementation of new technologies, equipment, or different usages of these, functioning as Operations interface with the departments of Engineering, R&D, Quality, Supply Chain, Purchases…, • Support and organization of the writing, execution, and reporting, as it may correspond, for the different experiments and studies associated to batch implementation, researching on any incidence or proposal of process improvement. Qualifications • Education: University degree oriented to biology or chemistry, • Languages: Intermediate English level (fluency valued), • Experience (years/area): ≥2 years in Operations, R&D, MSAT, • Specific Knowledge: Work in GMP environment, UPS-DSP experience, Tech transfer, process validation., • Personal skills : Result oriented, attention to detail, Teamwork oriented mAbxience is committed to equal opportunities. We do not discriminate against any person on the grounds of ethnicity, religion, age, sex, nationality, marital status, affective or sexual orientation, gender identity or expression, disability, or any other personal or social circumstance.

GLOBAL RESPONSIBILITY The Process Data Analyst is responsible for supporting our biosimilar development programs through advanced data evaluation. The primary focus of this position is to apply statistical methodologies to support decision-making in biosimilar development. While the core of the role is statistical analysis, the ability to assist in data engineering and the structuring of datasets from various sources is highly desirable to ensure seamless analytical workflows. SPECIFIC RESPONSIBILITIES · Analyzing, interpreting, and displaying data to identify process variables that most significantly impact production yield and product quality attributes. · Using statistical tools (e.g., Python, Minitab, SPSS) to identify, analyze, and interpret patterns and trends in complex datasets for process diagnosis and prediction. · Performing analysis to assess the quality, meaning, and integrity of experimental data. · Preparing reports for management stating trends, patterns, and predictions using relevant data visualizations and dashboards. · Participating in troubleshooting studies and root cause analysis by evaluating multi-variable correlations. · Organizing and structuring data related to process development (CLD, Upstream, Downstream, CMC and Analytical) into readable and actionable formats. · Providing technical support across different R&D units regarding data interpretation and statistical significance. REQUIREMENTS AND PERSONAL SKILLS · Education: Bachelor’s degree in Statistics, Mathematics, Biochemistry, Bioprocess Engineering, or a related field. Languages: Fluent Spanish, working knowledge in English, knowledge of other languages will be an asset. · Experience (years/area): +1 year of relevant expertise in laboratory activities working, and +3 years of relevant expertise in statistics. · Specific Knowledge: o Proficiency in statistics and statistical packages like Minitab, SPSS, SAS to be used for analyzing datasets. o Knowledge in developing reports and dashboards. o Analyzing and visualizing data. o Knowledge of programming languages like Python, R or MATLAB. o Technical knowledge regarding database design development, data models, techniques for data mining, and segmentation. o Knowledge of selecting and applying the appropriate algorithms to datasets in order to find solutions. o Proven working experience in data analysis. · Travels: Not required. · Personal skills: o High level communications skills with other departments. o Excellent problem-solving skills as well as time management and organizational skills. o Adept at queries, writing reports, and making presentations. o Ability to communicate effectively with others internally (up, down, and laterally) and externally to the organization. o A logical and investigative mind. o A methodical approach to work. o Teamworking skills. 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.

Role Summary: Permanent Full Time Position Revise detenidamente toda la documentación de la solicitud antes de hacer clic en el botón de solicitar al final de esta descripción. About Us: Huxley is an IT recruitment firm specializing in connecting top software engineers with leading technology companies across the APAC region. About the Company Publicly listed MNC Product company operating multiple large-scale consumer services and data-driven platforms. We’re hiring a Technical Lead to lead complex, multi-team software initiatives within our advertising and partner marketing platforms. You will own end-to-end delivery—from scoping and requirements through launch and post‑release improvement—working closely with engineering, product, quality, SRE/DevOps, and PMO/governance stakeholders across regions. This is a hands-on delivery role for someone who is comfortable driving clarity from ambiguity, orchestrating distributed teams, and landing business outcomes on schedule and within budget. What You’ll Do • Program Ownership: Define scope, timelines, and measurable outcomes for large, cross-functional software efforts; create delivery plans that balance speed, quality, and risk., • Requirements & Alignment: Facilitate requirement definition with Product and Engineering; lead trade-off discussions; drive consensus on priorities and acceptance criteria., • Delivery Governance: Manage execution using Agile/Scrum and scaled practices; run ceremonies, track dependencies, and resolve blockers across multiple squads., • Stakeholder Management: Communicate progress, risks, and decisions to managers, senior leaders, and executive stakeholders; prepare clear status reports and readouts., • Budget & Resources: Coordinate with PMO on cost, resourcing, and governance; forecast needs and optimize utilization across global teams., • Quality & Readiness: Partner with QA and SRE/DevOps on test strategy, reliability, release readiness, and post‑launch follow‑up., • Process Improvement: Identify gaps in workflow; implement pragmatic process and tooling improvements that accelerate delivery without sacrificing quality., • Bachelor’s degree in Computer Science, Engineering, Business, or a related field (or equivalent practical experience)., • 7–10+ years of progressive experience managing complex software development or platform delivery programs using Java., • Proven success delivering large-scale, cross-functional projects on time and within budget., • Practical expertise with project methodologies (Agile/Scrum, Scaled Scrum, Waterfall/Hybrid) and delivery tools (e.g., Jira, Confluence; plus Asana or Microsoft Project a bonus)., • Experience leading distributed/global teams with strong stakeholder management and negotiation skills across cultures and seniority levels., • Solid understanding of cloud technologies (e.g., GCP, AWS, or Azure) and modern SDLC practices. xcskxlj, • Excellent communication skills in English (written and spoken).

HBX Group is the world’s leading technology partner, connecting and empowering the world of travel. We’re game-changers, disruptors, the people who bring together local and global brands in accommodation, transport, activities and payments through our network of 300,000 hotels worldwide, 60,000 hard to reach high value clients such as tour operators, travel agents and loyalty schemes across 140 source markets. We are tech-driven, with a customer-first philosophy, and commercial teams whose knowledge and relationships on the ground are second to none. And of course we have an amazing team! Our people, Team HBX Group, are the beating heart of the company who we encourage to ‘move fast, dream big and make the difference’ every day. In fact, we believe that it is tech + data + people that truly sets us apart in the market, alongside our ‘global approach, local touch’ mentality. We’re headquartered in Palma, Mallorca and employ around 3,500 people worldwide. Es posible que un gran número de candidatos se presenten a este puesto, así que asegúrese de enviar su CV y su solicitud lo antes posible. JOB DESCRIPTION: Lead the end-to-end design and execution of high-impact strategic initiatives (“Big Bets”) across the organization’s ecosystem, blending strategic vision, cross-functional leadership, and operational excellence to deliver measurable business results. Collaborate closely with business unit leaders and centers of excellence to co-create strategies for each vertical, launch and scale key growth initiatives, and ensure all efforts are fully aligned with HBX’s overarching priorities and long-term ambitions. Responsibilities: • Lead the E2E design and delivery of selected Big Bets across the full Ecosystem by working together with commercial and business unit leaders., • Works closely together with Business Unit (BUs) leaders (e.g. Sourcing, Distribution, Fintech, Mobility & Experiences, HotelTech) and Sales & Sourcing Centers of Excellence to (i) redesign BU strategies under new context of verticalization and (ii) define and launch the main initiatives that will support growth (internally and leveraging partners)., • Identifies market trends alongside the Corporate Strategy team and assesses their impact on BU strategy & HBX positioning to ensure a strong and competitive value proposition within selected BUs, • Develops the strategy, performance and status reporting of specific big bets to be presented in leadership group meetings, Transformation Office, Executive Committee and Advisory Committee Skills • Strategic Planning: Design BU strategies with HBX’s overall strategic priorities and ensuring consistency and quality., • Conceptual Problem Solving: Structuring and solving complex ambiguous challenges such as commercial, partnership & Target Operating Models, • Analytical Problem Solving: Applying structured, data-driven approaches to break down complex business challenges, identify root causes, and quantify impact—supporting strategic decisions with robust financial, operational, and market analysis, • Business Plan Development: Create comprehensive business plans that articulate strategic objectives, synergy areas, and financial projections., • Communication: Strong presentation skills to synthesize complex topics into actionable insights (for senior stakeholders), • Stakeholder Engagement: Influencing senior stakeholders and navigating ambiguity to deliver high-impact outcomes., • Results Orientation: Drive initiatives to completion, maintaining focus on measurable outcomes and continuous improvement., • Project Management: Lead and coordinate cross-functional projects, ensuring effective planning, execution, and delivery within scope, time, and budget., • Judgment and Decision-Making: Exercise sound judgment to make timely, well-informed decisions in dynamic environments., • Financial Acumen: Demonstrate strong understanding of financial principles, budgeting processes, and the ability to interpret and act on financial data., • Coaching and Leadership: Delegate, train, and motivate team members to foster development and high performance., • Interpersonal Skills: Build strong relationships and communicate effectively with stakeholders at all levels, adapting style to audience and context. Experience • Minimum of 7 years of relevant experience managing strategy & transformation projects at a global organization or in a Strategy Consulting firm, • Minimum 3 years managing Strategy / Transformation projects within a corporate environment, with direct accountability on the financial results of such programs – examples include: value creation plan in post-merger integrations, BU strategic transformations, etc., • Experience managing and developing people in a multicultural and global organization Qualifications • Master’s degree in Engineering, Business Administration or related At HBX Group, we believe that diversity drivesinnovation and makestravel a force for good. We're committed to creatinganinclusive workplace where everyone feels valued and respected, embracing different backgrounds, perspectives and talents. Join us and be part of a team where diversity and equal opportunities really do make a difference. You will have the opportunity to work for a company that is going through significant change in becoming the world´s leading travel services provider. We are looking for people that are ready to ride the wave in this exciting journey. As well as an attractive benefits package you will be able to work: • Within an innovative, engaging and multicultural environment., • Have the opportunity to build strong and lasting business relationships and friendships from around the world. xcskxlj, • Have the opportunity in developing your career locally or within one of our beautiful working locations across the globe.

IF YOU ARE INTERESTED, PLEASE SHARE YOUR CV IN ENGLISH LANGUAGE ONLY! Por favor, lea detenidamente la siguiente descripción del puesto para asegurarse de que encaja con el perfil antes de enviar su solicitud. Who are we? We are a technology-led healthcare solutions provider. We are driven by our purpose to enable healthcare organizations be future ready. We offer accelerated, global growth opportunities for talent that’s bold, industrious, and nimble. With Indegene, you gain a unique career experience that celebrates entrepreneurship, and is guided by passion, innovation, collaboration, and empathy. To explore exciting opportunities at the convergence of healthcare and technology, check out if we told you that you can move to an exciting role in an entrepreneurial organization without the usual risks associated with it? We understand that you are looking for growth in your career at this point and we would love for you to join us in our journey and grow with us. At Indegene, our roles come with the excitement you require at this stage of your career with the reliability you seek. We believe in creating leaders of tomorrow and mentor our leads to help them grow and nurture them as people managers and account managers. We are a rapidly growing global organization and are scouting for the best talent for this phase of growth. With us, you are at the intersection of two of the most exciting industries of healthcare and technology. We offer global opportunities with fast-track careers while you work with a team that is fueled by purpose. The combination of this will lead to a truly differentiated experience for you. If this excites you, then apply below. Role: Architect IF YOU ARE INTERESTED, PLEASE SHARE YOUR CV IN ENGLISH LANGUAGE ONLY! Job Description: Role Overview The Architect – MarTech & Digital Ecosystem serves as the enterprise technology and solution design authority for marketing, web, and data platforms within a global delivery model. This role is responsible for defining and governing a scalable, compliant, and fully integrated MarTech architecture spanning marketing automation, CRM, web platforms, DAMs, and enterprise data ecosystems. The Architect ensures seamless interoperability between platforms such as Salesforce Marketing Cloud (SFMC), Veeva, WordPress VIP, DAM systems, and enterprise data layers (data warehouses, data lakes, MDM, CMP), while enabling automation, AI-driven use cases, and compliant activation across markets. The role blends architecture leadership, integration strategy, governance ownership, and stakeholder orchestration. Key Responsibilities: A. Enterprise MarTech & Platform Architecture o Veeva CRM & Veeva PromoMats o WordPress VIP (component-based architecture) o DAM and content supply chain systems o Enterprise data platforms (warehouses, lakes, MDM, CMP) • Translate commercial and marketing requirements into scalable, compliant, and reusable technical solutions., • Define reusable templates, modular components, metadata structures, and shared taxonomies to enable cross-market standardization. o WordPress VIP ↔ DAMs & metadata layers o Workflow tools ↔ Production & MLR systems o MarTech platforms ↔ Enterprise data warehouses, CDPs, and consent platforms • Architect API-first, middleware-enabled, cloud-native integrations., • Enable automated content syndication, consent-based activation, and data-driven personalization., • Define data models supporting segmentation, personalization, and omnichannel orchestration. o Lineage o Access controls o Compliant activation • Ensure adherence to regulatory frameworks such as GDPR and HIPAA., • Embed consent management workflows via CMP integrations., • Act as the final architecture authority for campaign and platform compliance., • Enforce MLR-aligned templates and metadata-driven content workflows., • Drive defect reduction through standardized QA frameworks and automation tools. Collaborate closely with: • Key Account Managers, • Market Liaisons, • Onsite Delivery Teams, • Regional Governance & Program Management, • Lead technical design workshops, intake governance forums, and architecture reviews., • Translate complex technical constructs into commercially meaningful insights., • Provide strategic advisory on platform investments, scalability, and operational efficiency. Skills & Experience Required • 7–12 years of experience in MarTech, Enterprise Architecture, or Digital Engineering. o WordPress VIP & component-based web design o Veeva CRM & Veeva PromoMats workflows o API design, webhooks, middleware, and cloud-native integration patterns o Metadata frameworks and tagging structures o CDPs and marketing analytics pipelines (e.g., GA integrations) o Data warehouses, lakes, and MDM architectures o QA automation frameworks • · Language proficiency required in Spanish (for Spain market), • · Based in Madrid or already residing in Spain with ability for regular on-site work. Leadership & Behavioural Competencies • Strong client-facing communication and executive presence., • Ability to translate architectural complexity into business value., • Multi-stakeholder orchestration across global delivery models., • Strategic thinking with focus on scalability, profitability, and operational efficiency., • Governance-driven mindset with risk anticipation capability. EQUAL OPPORTUNITY: Indegene is proud to be an Equal Employment Employer and is committed to the culture of Inclusion and Diversity. We do not discriminate on the basis of race, religion, sex, colour, age, national origin, pregnancy, sexual orientation, physical ability, or any other characteristics. All employment decisions, from hiring to separation, will be based on business requirements, candidate’s merit and qualification. We are an Equal Opportunity Employer. xcskxlj All qualified applicants will receive consideration for employment without regard to race, colour, religion, sex, national origin, gender identity, sexual orientation, disability status, protected veteran status, or any other characteristics.

GLOBAL RESPONSIBILITY The Process Data Analyst is responsible for supporting our biosimilar development programs through advanced data evaluation. The primary focus of this position is to apply statistical methodologies to support decision-making in biosimilar development. While the core of the role is statistical analysis, the ability to assist in data engineering and the structuring of datasets from various sources is highly desirable to ensure seamless analytical workflows. SPECIFIC RESPONSIBILITIES · Analyzing, interpreting, and displaying data to identify process variables that most significantly impact production yield and product quality attributes. · Using statistical tools (e.G., Python, Minitab, SPSS) to identify, analyze, and interpret patterns and trends in complex datasets for process diagnosis and prediction. · Performing analysis to assess the quality, meaning, and integrity of experimental data. · Preparing reports for management stating trends, patterns, and predictions using relevant data visualizations and dashboards. · Participating in troubleshooting studies and root cause analysis by evaluating multi-variable correlations. · Organizing and structuring data related to process development (CLD, Upstream, Downstream, CMC and Analytical) into readable and actionable formats. · Providing technical support across different R&D units regarding data interpretation and statistical significance. REQUIREMENTS AND PERSONAL SKILLS · Education: Bachelor’s degree in Statistics, Mathematics, Biochemistry, Bioprocess Engineering, or a related field. Languages: Fluent Spanish, working knowledge in English, knowledge of other languages will be an asset. · Experience (years/area): +1 year of relevant expertise in laboratory activities working, and +3 years of relevant expertise in statistics. · Specific Knowledge: o Proficiency in statistics and statistical packages like Minitab, SPSS, SAS to be used for analyzing datasets. o Knowledge in developing reports and dashboards. o Analyzing and visualizing data. o Knowledge of programming languages like Python, R or MATLAB. o Technical knowledge regarding database design development, data models, techniques for data mining, and segmentation. o Knowledge of selecting and applying the appropriate algorithms to datasets in order to find solutions. o Proven working experience in data analysis. · Travels: Not required. · Personal skills: o High level communications skills with other departments. o Excellent problem-solving skills as well as time management and organizational skills. o Adept at queries, writing reports, and making presentations. o Ability to communicate effectively with others internally (up, down, and laterally) and externally to the organization. o A logical and investigative mind. o A methodical approach to work. o Teamworking skills. 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.

Una empresa en crecimiento en el sector de energías renovables busca un Responsable de Calidad para su oficina en Madrid.Esta es una excelente oportunidad para unirse a una compañía en expansión y desempeñar un papel esencial en la gestión de calidad, asegurando el cumplimiento de normativas I

In a few words Position: QC Analyst Temporary Location: León Experience: 1-2 years Want to know more? 👇 INSUD PHARMA operates across the entire pharmaceutical value chain, providing specialized knowledge and experience in scientific research, development, manufacturing, sales, and marketing of a wide range of active pharmaceutical ingredients (API), finished dosage forms (FDF), and branded pharmaceutical products, adding value to human and animal health. The activities of INSUD PHARMA are organized into three synergistic business areas: Industrial (Chemo), Branded (Exeltis), and Biotech (mAbxience), with over 9,000 professionals in more than 50 countries, 20 state-of-the-art facilities, 15 specialized R&D centers, 12 commercial offices, and more than 35 pharmaceutical subsidiaries, serving 1,150 customers in 96 countries worldwide. INSUD PHARMA believes in innovation and sustainable development. Ready to be a #Challenger? What are we looking for? 🔎 We are recruiting a new INSUDER as an analyst to join the QC team at our site based in León. The challenge! • Analyze, using different analytical techniques (GC, HPLC, TLC, KF), API, intermediate samples or final samples and stability samples, in order to ensure good quality (meet the specifications) of different products., • Complete analytical documentation for each product to meet GMP standards., • Store and control of stock chemical reagents, following established rules to ensure order and location., • Take intermediate or final production and cleaning samples., • Take samples for microbiological analysis of water, air and surfaces of manufacturing facilities and equipment., • Follow approved analytical methods and SOP in place. What do you need? • Education: FP II Chemistry or Chemical Degree., • Languages: Fluent Spanish, medium level English is a plus., • Experience (years/area): Minimum 2 year experience in the functions mentioned above is recommended. Experience in HPLC, GC, Physico-chemical analysis., • Specific Knowledge: Knowledge of GMP and GLP regulations. Our benefits! • 📜 Temporary contract., • 💸 Attractive salary package., • 🕒 Temporary work with rotating shifts to balance your work and family life., • 🧪 Training and experience in a strategic and constantly growing sector., • 👨👩👧 We are characterized by a professional, close-knit, and team-oriented work environment. What will the Selection process be like? 🕵️ ➡️ Stay tuned to your phone and email! The first thing we will likely do is contact you through one of the two channels. ➡️ Prepare well! We will continue with an in-person/virtual interview depending on availability and what we agree upon; there may be one or twointerviews in the process, and depending on the type of process, there may also be some kind of test. ➡️ Wait for the result! We care that you feel guided throughout each selection process and know what to expect from us, so we will always try to inform you of the status of the process. 🔷 Do you think this offer is not for you? 🔷 Follow us on social media like LinkedIn/Instagram and stay tuned for any offers we may release; the opportunity to be anew Insuder is waiting! #InsudPharma #Challenger #Insuder #InsudTalent COMMITMENT TO EQUAL OPPORTUNITIES The InsudPharma group is aware that business management must align with the needs and demands of society, and therefore assumes the commitment to equal opportunities and treatment between men and women, as stated in the current regulations on the matter - Organic Law 3/2007, and we do not discriminate against any person on the grounds of ethnicity, religion, age, sex, nationality, marital status, affective or sexual orientation, gender identity or expression, disability, or any other personal or social circumstance.

AI-Assisted Software Engineer / AI Coding Enablement Engineer (Remote) ¿Quiere enviar su solicitud? Lea toda la información sobre este puesto a continuación y luego pulse el botón de solicitar. Project summary We are looking for a Software Engineer with strong experience in AI-assisted development to help drive the adoption of AI coding practices across the organization. This role combines hands-on engineering, technical coaching, and governance, ensuring the effective, secure, and scalable use of AI tools within the software development lifecycle. You will work closely with engineering teams to standardize AI-assisted workflows, define best practices, and help transform AI-generated code into production-ready solutions. Main responsibilities AI Engineering & Development Enablement • Define and standardize best practices for AI-assisted software development, • Establish guidelines for AI tool usage (code generation, refactoring, testing, and documentation), • Create reusable playbooks, development patterns, and prompt libraries, • Support engineering teams in building applications using AI-assisted workflows, • Define quality standards for AI-generated code, • Ensure compliance with security, licensing, and data privacy requirements, • Implement guardrails and governance frameworks for AI usage in development, • Evaluate risks and limitations of LLM-generated outputs, • Evaluate, select, and integrate AI coding tools, • Embed xcskxlj AI capabilities into the development lifecycle (IDE, CI/CD, code reviews), • Build internal tooling to standardize usage and measure adoption, • Provide technical coaching on AI-assisted development practices, • Train engineering teams on AI coding tools and workflows, • Create onboarding materials and internal documentation, • Mentor engineers on how to transform AI outputs into production-ready code

¿Te apasiona la calidad , la seguridad alimentaria y el trabajo en entornos industriales altamente automatizados ? Usted podría ser el solicitante perfecto para este trabajo. Lea toda la información asociada y asegúrese de presentar su candidatura. Si buscas un proyecto con impacto real en la calidad del producto y en la mejora continua de una planta productiva, esta oportunidad puede ser para ti. Buscamos incorporar un/a Plant Quality Manager que lidere la implantación y seguimiento de los sistemas de gestión de calidad y seguridad alimentaria, garantizando los estándares exigidos por clientes, consumidores y normativas internacionales. ¿Cuál será tu misión? Asegurar la correcta ejecución del plan de calidad en planta. Supervisar indicadores, estándares y material en proceso, proponiendo medidas correctivas. Ser el referente durante auditorías internas y externas ( IFS, BRC, AIB… ). Liderar la implantación y actualización del APPCC . Gestionar no conformidades y planes de acción. Asegurar el cumplimiento de Food Defense . Impulsar la formación del equipo en sistemas de calidad y seguridad alimentaria. Participar en proyectos de mejora y soporte técnico ante reclamaciones. Gestionarás 20 personas. Perfil que buscamos 2–3 años de experiencia en calidad dentro de la industria alimentaria. Formación en Ciencia y Tecnología de los Alimentos, Ingeniería Química o afines. Inglés alto. Conocimiento de normativas y auditorías (IFS, BRC, AIB). xiphteb Habilidades de liderazgo, orientación a resultados y toma de decisiones.

Solutions Engineer Ultralytics•Villaornate y Castro, León, ES Descripción del trabajo At Ultralytics, we relentlessly drive innovation in AI, building the world's leading YOLO models. We're looking for passionate individuals obsessed with AI, eager to make a global impact, and ready to excel in a dynamic, high‑energy environment. Join our team and help shape the future of Vision AI. ¿Todo listo para enviar su solicitud? Asegúrese de comprender todas las responsabilidades y tareas asociadas a este puesto antes de continuar. Location and Legalities This full‑time Solutions Engineer position is based onsite in our brand‑new Ultralytics office in London, UK. What You'll Do As a Solutions Engineer at Ultralytics, you will be the technical face of our organization. You will work directly with clients to design, prototype, and deploy computer vision solutions powered by Ultralytics YOLO. You will help bridge the gap between client needs and our powerful AI tooling, guiding them through every stage from ideation to deployment. Collaborate with clients to understand their use cases and challenges, and architect end‑to‑end solutions using the YOLO ecosystem. Deliver high‑quality technical demos, onboarding sessions, proof‑of‑concepts, and technical workshops that illustrate how to build with YOLO and demonstrate the power of Ultralytics tooling. Design annotation strategies and model training pipelines tailored to the client’s data, goals, and deployment constraints. Debug client issues and deliver effective solutions with a strong understanding of the YOLO package, Python, OpenCV, and model behavior. Support pre‑sales efforts by participating in technical discovery calls and helping shape proposals and SLAs. Serve as a key technical advisor during customer engagements, ensuring successful integration and continued satisfaction. Interface regularly with Sales, Marketing, Engineering, and Product teams to advocate for customer needs and influence roadmap priorities. Act as a strategic technical advisor to clients, shaping computer vision solutions that drive tangible business outcomes with YOLO models. Enable the sales and marketing teams with technical expertise, competitive insights, and field learnings to support campaign effectiveness and messaging accuracy. Represent Ultralytics at conferences, webinars, and customer events, and contribute to technical blog posts, customer stories, and educational materials. Your strategic vision and technical expertise will be essential in supporting Ultralytics' mission of delivering top‑tier machine learning tools and models like YOLO11 to the community. Skills and Experience 5+ years of experience in Computer Vision, Machine Learning, or applied AI roles. Excellent client‑facing skills: patient, resilient, and able to communicate clearly with technical and non‑technical stakeholders. Proficiency in Python and familiarity with the YOLO ecosystem. Hands‑on experience with OpenCV, PyTorch, and classical ML/CV concepts. Strong understanding of end‑to‑end model lifecycles, including data collection, preparation, training, evaluation, and deployment. Experience with Docker and comfort working across Linux, macOS, and Windows environments. Demonstrated ability to teach or mentor teams and developers through courses, bootcamps, workshops, or community engagement. Comfort leading workshops, writing technical guides, or presenting to developer audiences. Cultural Fit - Intensity Required Ultralytics is a high‑performance environment for world‑class talent obsessed with achieving extraordinary results. We operate at a relentless pace, demanding exceptional dedication and an unwavering commitment to excellence. Our team thrives on audacious goals and absolute ownership. This is not a conventional workplace. If your priority is predictable comfort or a standard work‑life balance over the relentless pursuit of progress, Ultralytics is not for you. We seek driven individuals prepared for the profound personal investment required to make a defining contribution to the future of AI. Compensation and Benefits Competitive Salary: Highly competitive based on experience. Startup Equity: Participate directly in our company's growth and success. Hybrid Flexibility: 3 days per week in our brand‑new office – 2 days remote. Generous Time Off: 24 days vacation, your birthday off, plus local holidays. Flexible Hours: Tailor your working hours to suit your productivity. Tech: Engage with cutting‑edge AI projects and our Ultralytics HUB. Gear: Brand‑new Apple MacBook Air and Apple Display provided. Team: Become part of a supportive and passionate team environment. If you are driven to redefine the capabilities of machine learning and eager to make a significant impact, Ultralytics offers an exceptional career opportunity. #J-18808-Ljbffr

The ideal candidate is always looking for ways to improve a product or service to make it better, faster, and more user-friendly.You are responsible for producing technology solutions from concept to delivery that satisfy customer needs in alignment with our overall strategy.Serve as a product exper

We’re Hiring: Quality Assurance (QA) Specialist.

Responsable de Calidad de Procesos y Producto.La persona seleccionada tendrá un papel clave garantizando el cumplimiento de los estándares de calidad en los procesos de fabricación y en el producto final, contribuyendo a la mejora continua y a la satisfacción del cliente.Funciones principales: -

Responsable de Calidad de Procesos y Producto.La persona seleccionada tendrá un papel clave garantizando el cumplimiento de los estándares de calidad en los procesos de fabricación y en el producto final, contribuyendo a la mejora continua y a la satisfacción del cliente.Funciones principales: -

HSE Manager Your role will encompass Take overall responsibility for the.Health, Safety, and Environmental performance.Lead and manage the site HSE team.HSE supervisors and officers, ensuring effective implementation of HSE procedures and company standards.Develop, implement, and enforce project HSE

Responsable de Calidad de Procesos y Producto.La persona seleccionada tendrá un papel clave garantizando el cumplimiento de los estándares de calidad en los procesos de fabricación y en el producto final, contribuyendo a la mejora continua y a la satisfacción del cliente.Funciones principales: -

Una empresa líder en aparatología médica busca un Quality Director para garantizar el cumplimiento normativo y la excelencia técnica de sus productos.

Importante empresa multinacional de automoción, con 59 sedes alrededor del mundo y más de 17.Ágreda-Soria precisa incorporar a su equipo a un/a Responsable de Calidad y Medio Ambiente.Tiene las siguientes habilidades, experiencia e impulso para tener éxito en este puesto? Descúbralo a continuac

Importante empresa multinacional de automoción, con 59 sedes alrededor del mundo y más de 17.Ágreda-Soria precisa incorporar a su equipo a un/a Responsable de Calidad y Medio Ambiente.Tiene las siguientes habilidades, experiencia e impulso para tener éxito en este puesto? Descúbralo a continuac

Desde Adecco Selección , buscamos un / a Responsable de Calidad de Procesos y Producto para una empresa industrial dedicada a la fabricación de transformadores de distribución y potencia, para su sede en Salamanca.Siga leyendo para descubrir lo que necesitará para tener éxito en este puesto, in

Asegurar la calidad y el cumplimiento normativo en los procesos de la planta, gestionando sistemas de calidad, documentación, controles de cambio, reclamaciones, desviaciones y auditorías.

Busca Responsable de Calidad para liderar y garantizar el cumplimiento normativo y estándares de seguridad alimentaria en planta, con experiencia en industria cárnica y conocimientos de APPCC y Norma de Calidad del Ibérico.

Todas las habilidades, cualificaciones y experiencia relevantes que necesitará un candidato seleccionado se enumeran en la siguiente descripción.Perform physicochemical analysis of injectable products.Perform analysis of raw materials, packaging materials, intermediate products, and final products

Desde Arturo Sanchez buscamos incorporar Responsable de Calidad para liderar y garantizar el cumplimiento normativo y los estándares de seguridad alimentaria en planta.No deje pasar esta oportunidad, inscríbase rápidamente si su experiencia y habilidades coinciden con lo que se indica en la sigui

Importante empresa multinacional de automoción, con 59 sedes alrededor del mundo y más de 17.Ágreda-Soria precisa incorporar a su equipo a un/a Responsable de Calidad y Medio Ambiente.Tiene las siguientes habilidades, experiencia e impulso para tener éxito en este puesto? Descúbralo a continuac

Importante empresa multinacional de automoción, con 59 sedes alrededor del mundo y más de 17.Ágreda-Soria precisa incorporar a su equipo a un/a Responsable de Calidad y Medio Ambiente.Tiene las siguientes habilidades, experiencia e impulso para tener éxito en este puesto? Descúbralo a continuac

En Indra Group buscamos un Quality Assurance Engineer para reforzar la planta de León.

Una empresa del sector cárnico en Castilla y León busca un Responsable de Calidad para liderar el cumplimiento normativo y garantizar los estándares de seguridad alimentaria.Usted podría ser el solicitante perfecto para este trabajo.Lea toda la información asociada y asegúrese de presentar su

Following significant recent investment, the business is experiencing rapid growth and expanding its Quality Assurance function with the hire of a QA Consultant.

Importante empresa multinacional de automoción, con 59 sedes alrededor del mundo y más de 17.Responsable de Calidad y Medio Ambiente.Todas las habilidades, cualificaciones y experiencia relevantes que necesitará un candidato seleccionado se enumeran en la siguiente descripción.Buscamos un profes

With continued investment driving growth, they are looking to expand their Quality Control team with an experienced QC Consultant.

Importante empresa multinacional de automoción, con 59 sedes alrededor del mundo y más de 17.Responsable de Calidad y Medio Ambiente.Buscamos un profesional que, habiéndose desarrollado en entorno industrial, preferiblemente en el sector de automoción, lidere un proyecto estable y un equipo mult