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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.

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.

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.

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.

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.

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.

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. With continued investment driving growth, they are looking to expand their Quality Control team with an experienced QC Consultant. This is a fully onsite role within a GMP-regulated laboratory environment. QC Consultant - Responsibilities: • Perform analytical testing in line with GMP requirements, • Support stability studies and routine QC testing, • Prepare and manage reagents, solutions, and laboratory materials, • Ensure accurate and compliant documentation of all laboratory activities What’s on offer: • Opportunity to join a high-growth, investment-backed CDMO, • Work on advanced biopharmaceutical products, • Collaborative and fast-paced environment, • 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.

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.

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.

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.

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.

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.

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.

¿Y si tu próximo paso profesional te colocara en el centro de los proyectos que están transformando la industria? ⚙️ Imagina ser una pieza clave en garantizar que los procesos, productos o soluciones cumplan con los más altos estándares de calidad, innovación y rendimiento. En TRIGO , no buscamos solo experiencia. Buscamos personas con actitud, compromiso y ganas de dejar huella en lo que hacen. Bajo nuestro lema QUALITY IS OUR MINDSET , nuestro propósito es permitir a las personas viajar con total tranquilidad y confianza, asegurando que cada método de transporte cumpla con los más altos estándares de calidad y seguridad. ¿Te atreves a dar el siguiente paso? Gestor de Proyectos Junior | Automoción Proyecto de alto impacto en automoción industrial Estabilidad garantizada: Indefinido Modalidad presencial en Valladolid ¿Por qué trabajar con nosotros? Innovación constante: aquí cada día plantea nuevos desafíos, nuevas ideas y nuevas soluciones. Crecimiento real: te acompañamos a crecer desde dentro con formación y promociones internas. Cultura colaborativa: trabajamos en equipo, celebramos los logros juntos y aprendemos de los errores. Como gestor/a de proyectos, serás el referente técnico para la gestión de actividades y soporte tecnológico para proyectos de Calidad como proyectos de seguimiento y animación de Joint Ventures, Digitalización, Actividades de mejora continua, Acciones de ruptura y transformación y reorganización en uno de los cliente líder en el sector automoción. Los retos a los que te enfrentarás: Gestión y coordinación de proyectos digitales, asegurando la correcta planificación, ejecución y seguimiento de las iniciativas. Coordinación entre las diferentes entidades del cliente Alineación de procesos y estándares Soporte a industrialización / producción de powertrain Gestión de proyectos o actividades dentro del perímetro de actuación Interacción con plantas, ingeniería o calidad dentro del nuevo modelo organizativo Gestión de documentación técnica de motor/powertrain y procedimientos de calidad o producción Definición de KPIs comunes y estructuración de datos de producción/calidad, presentación de planes de acción Soporte a proyectos de analítica o IA; y conectar iniciativas digitales (DMS, visión artificial) Asistencia a reuniones mensuales del grupo con realización de informes posteriores y envió internamente Redacción del protocolo de calidad y seguimiento de lista de prioridades Implantación de la metodología 6 Sigma. Qué te hará triunfar en el puesto: ✅ 3-5 años de experiencia en funciones similares ✅Conocimientos en pilotaje de presentación, formalización y seguimiento de decisiones ✅ Experiencia en seguimiento de avance de proyecto (objetivos, indicadores, reporting) ✅ Nivel alto de Office 365 ✅ Inglés mínimo B2. Así será tu proceso de selección: Llamada breve para alinear tus expectativas y conocerte (15 min). Entrevista online con el equipo de Talent Acquisition (40 min). Validación técnica presencial con el equipo de operaciones/responsables de departamento para conocer cómo es el día a día (45 min). Porque sabemos que lo que haces importa, hazlo en un lugar donde de verdad deje huella. Inscríbete y sigamos formando juntos el #TeamTRIGO. En TRIGO fomentamos la igualdad de oportunidades y la diversidad. Todas las candidaturas serán evaluadas sin discriminación por razones de género, origen, orientación sexual, discapacidad u otras circunstancias.

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.

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.

Our goal is to strengthen the brand in Spain. We are looking for you to work as Automation Engineer! What do you need to fulfill this job? 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) SDLC common tasks but not limited to: 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 protocol generation, execution, and approval 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. Use and update of development system if required Educate local project teams on automation standards as they relate to technology selection, system configuration, SDLC, validation, hardware, software environments and business processes. Ensure SLA’s are in place for OEM systems with appropriate support available as back-up if necessary Build and maintain relationships with key OEM vendors ensuring reliability of supply and cost effective support model Partner with internal IT departments (GIO etc) ensuring standard and secure implementation in line with MSD Standards Core Competencies (Technical): Experience with any of the following Applications Kneat, Siemens WinCC/S7, Aveva System Platform/Intouch, Aveva (OSI) PI, Microsoft 365 products and Windows core Experience with any of the following processes: WFI Generation & Distribution, Building management systems, Cleaning and Sterilization (Parts washers & Autoclaves), Blending and Formulation, Filling, Packaging and Inspection About HCLTech: 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. If all this sounds like an environment you’ll thrive in, then you’re in the right place. Join us on our journey in advancing the technological world through innovation and creativity. Why Us? 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 freedom and flexibility on the job, empowering our employees to make decisions. 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. We offer the opportunity to work with colleagues across the globe. We are a certified great place to work and a top employer in 25 countries including Romania, offering a positive work environment that values employee recognition and respect. If you have a valid disability certificate, Certificate of Disability in Force, please contact us. Among HCLs principles we would like to highlight diversity and inclusion as a strength in our values and practices. 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. We welcome and value all people, and we are committed to the inclusion and sense of belonging of each person who is part of HCL. HCL is an equal opportunity employer. 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.

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

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.

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.

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. Collaborate with Engineering, Automation, and vendors during start-up activities. Qualification & Validation 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. Support requalification activities and change management processes. Regulatory Compliance & Quality 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). Support change impact assessments and Change Control activities. Project Management & Collaboration 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.

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.

💡 ¿Y si tu próximo paso profesional te colocara en el centro de los proyectos que están transformando la industria? ⚙️ Imagina ser una pieza clave en garantizar que los procesos, productos o soluciones cumplan con los más altos estándares de calidad, innovación y rendimiento. En TRIGO, no buscamos solo experiencia. Buscamos personas con actitud, compromiso y ganas de dejar huella en lo que hacen. Bajo nuestro lema QUALITY IS OUR MINDSET, nuestro propósito es permitir a las personas viajar con total tranquilidad y confianza, asegurando que cada método de transporte cumpla con los más altos estándares de calidad y seguridad. ¿Te atreves a dar el siguiente paso? Gestor de Proyectos Junior | Automoción 📍 Proyecto de alto impacto en automoción industrial 🌱 Desarrollo profesional real 💼 Modalidad presencial en Valladolid ¿Por qué trabajar con nosotros? 🔹Innovación constante: aquí cada día plantea nuevos desafíos, nuevas ideas y nuevas soluciones. 🔹Crecimiento real: te acompañamos a crecer desde dentro con formación y promociones internas. 🔹Cultura colaborativa: trabajamos en equipo, celebramos los logros juntos y aprendemos de los errores. Como gestor/a de proyectos, serás el referente técnico para la gestión de actividades y soporte tecnológico para proyectos de Calidad como proyectos de seguimiento y animación de Joint Ventures, Digitalización, Actividades de mejora continua, Acciones de ruptura y transformación y reorganización en uno de los cliente líder en el sector automoción. Los retos a los que te enfrentarás: • Gestión y coordinación de proyectos digitales, asegurando la correcta planificación, ejecución y seguimiento de las iniciativas., • Coordinación entre las diferentes entidades del cliente, • Alineación de procesos y estándares, • Soporte a industrialización / producción de powertrain, • Gestión de proyectos o actividades dentro del perímetro de actuación, • Interacción con plantas, ingeniería o calidad dentro del nuevo modelo organizativo, • Gestión de documentación técnica de motor/powertrain y procedimientos de calidad o producción, • Definición de KPIs comunes y estructuración de datos de producción/calidad, • Soporte a proyectos de analítica o IA; y conectar iniciativas digitales (DMS, visión artificial) Qué te hará triunfar en el puesto: ✅ 3-5 años de experiencia en funciones similares ✅Conocimientos en pilotaje de presentación, formalización y seguimiento de decisiones ✅ Experiencia en seguimiento de avance de proyecto (objetivos, indicadores, reporting) ✅ Nivel alto de Office 365 ✅ Inglés mínimo B2. Así será tu proceso de selección: • 📞 Llamada breve para alinear tus expectativas y conocerte (15 min)., • 💻 Entrevista online con el equipo de Talent Acquisition (40 min)., • 🏢 Validación técnica presencial con el equipo de operaciones/responsables de departamento para conocer cómo es el día a día (45 min). Porque sabemos que lo que haces importa, hazlo en un lugar donde de verdad deje huella. Inscríbete y sigamos formando juntos el #TeamTRIGO. En TRIGO fomentamos la igualdad de oportunidades y la diversidad. Todas las candidaturas serán evaluadas sin discriminación por razones de género, origen, orientación sexual, discapacidad u otras circunstancias.

At Altorecruit , we are a consultancy specialized in selection and executive search for industrial and manufacturing companies . We work closely with our clients to understand their business, organizational context and operational challenges in order to identify leaders capable of driving sustainable performance and long-term growth. Currently, we are supporting an international industrial group in the search for a Plant Manager to lead one of its manufacturing facilities located in Soria, Spain . This position reports directly to the Business Unit Manager and plays a key role in ensuring operational excellence, production performance and the continuous development of the plant organization. Position Summary The Plant Manager is responsible for the overall management of the manufacturing facility, ensuring efficient production operations, high product quality, cost control, and compliance with safety and regulatory standards. The role leads plant personnel, optimizes operational performance, and drives continuous improvement to achieve business objectives. Key Responsibilities • Oversee daily plant operations, including production, maintenance, quality, and logistics., • Ensure production targets are met in terms of volume, quality, cost, and delivery schedules., • Develop and implement operational strategies to improve efficiency, productivity, and profitability., • Lead, mentor, and develop plant staff and department managers., • Monitor and control operating budgets, production costs, and resource allocation., • Ensure compliance with health, safety, environmental, and regulatory standards., • Implement and promote continuous improvement initiatives (Lean Manufacturing, Six Sigma, etc.)., • Coordinate closely with supply chain, engineering, quality, and commercial teams., • Analyze production data and KPIs to identify areas for improvement and optimization., • Manage maintenance programs to ensure equipment reliability and minimize downtime., • Culture of safety, teamwork, and operational excellence. Requirements Education • Bachelor’s degree in Engineering, Industrial Management, Manufacturing, or related field., • Minimum 8 years of experience in manufacturing or industrial operations., • At least 3–5 years in a leadership role within a production environment., • Strong leadership and team management skills., • Solid understanding of manufacturing processes and industrial operations., • Experience with Lean Manufacturing, Six Sigma, or other operational excellence methodologies., • Strong analytical and problem-solving abilities., • Excellent organizational and decision-making skills., • Ability to work under pressure and manage multiple priorities., • Financial skills and understanding., • Excellent organizational and communication skills Languages • Spanish: Native or fluent., • English: Professional proficiency preferred. Compensation & Benefits • Competitive salary package., • Performance-based bonus.

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.

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.

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.

Global ResponsibilityExecute UpStream (USP) activities in the Cell Culture area of the production department, following operational procedures and GMP regulations.Specific ResponsibilitiesExecute 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 skillsEducation: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.

Our goal is to strengthen the brand in Spain. We are looking for you to work as Automation Engineer! What do you need to fulfill this job? • 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), • SDLC common tasks but not limited to:, • 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 protocol generation, execution, and approval, • 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., • Use and update of development system if required, • Educate local project teams on automation standards as they relate to technology selection, system configuration, SDLC, validation, hardware, software environments and business processes., • Ensure SLA’s are in place for OEM systems with appropriate support available as back-up if necessary Core Competencies (Technical): • Experience with any of the following Applications, • Kneat, Siemens WinCC/S7, Aveva System Platform/Intouch, Aveva (OSI) PI, Microsoft 365 products and Windows core, • Experience with any of the following processes:, • WFI Generation & Distribution, Building management systems, Cleaning and Sterilization (Parts washers & Autoclaves), Blending and Formulation, Filling, Packaging and Inspection About HCLTech: 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. If all this sounds like an environment you’ll thrive in, then you’re in the right place. Join us on our journey in advancing the technological world through innovation and creativity. Why Us? • 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 freedom and flexibility on the job, empowering our employees to make decisions., • 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., • We offer the opportunity to work with colleagues across the globe., • We are a certified great place to work and a top employer in 25 countries including Romania, offering a positive work environment that values employee recognition and respect. If you have a valid disability certificate, Certificate of Disability in Force, please contact us. Among HCL's principles we would like to highlight diversity and inclusion as a strength in our values and practices. 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. We welcome and value all people, and we are committed to the inclusion and sense of belonging of each person who is part of HCL. • HCL is an equal opportunity employer. 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.

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.

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.

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. With continued investment driving growth, they are looking to expand their Quality Control team with an experienced QC Consultant. This is a fully onsite role within a GMP-regulated laboratory environment. QC Consultant - Responsibilities: • Perform analytical testing in line with GMP requirements, • Support stability studies and routine QC testing, • Prepare and manage reagents, solutions, and laboratory materials, • Ensure accurate and compliant documentation of all laboratory activities What’s on offer: • Opportunity to join a high-growth, investment-backed CDMO, • Work on advanced biopharmaceutical products, • Collaborative and fast-paced environment, • 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.

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. With continued investment driving growth, they are looking to expand their Quality Control team with an experienced QC Consultant. This is a fully onsite role within a GMP-regulated laboratory environment. QC Consultant - Responsibilities: • Perform analytical testing in line with GMP requirements, • Support stability studies and routine QC testing, • Prepare and manage reagents, solutions, and laboratory materials, • Ensure accurate and compliant documentation of all laboratory activities What’s on offer: • Opportunity to join a high-growth, investment-backed CDMO, • Work on advanced biopharmaceutical products, • Collaborative and fast-paced environment, • 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.

At Altorecruit, we are a consultancy specialized in selection and executive search for industrial and manufacturing companies. We work closely with our clients to understand their business, organizational context and operational challenges in order to identify leaders capable of driving sustainable performance and long-term growth. Currently, we are supporting an international industrial group in the search for a Plant Manager to lead one of its manufacturing facilities located in Soria, Spain. This position reports directly to the Business Unit Manager and plays a key role in ensuring operational excellence, production performance and the continuous development of the plant organization. Position Summary The Plant Manager is responsible for the overall management of the manufacturing facility, ensuring efficient production operations, high product quality, cost control, and compliance with safety and regulatory standards. The role leads plant personnel, optimizes operational performance, and drives continuous improvement to achieve business objectives. Key Responsibilities • Oversee daily plant operations, including production, maintenance, quality, and logistics., • Ensure production targets are met in terms of volume, quality, cost, and delivery schedules., • Develop and implement operational strategies to improve efficiency, productivity, and profitability., • Lead, mentor, and develop plant staff and department managers., • Monitor and control operating budgets, production costs, and resource allocation., • Ensure compliance with health, safety, environmental, and regulatory standards., • Implement and promote continuous improvement initiatives (Lean Manufacturing, Six Sigma, etc.)., • Coordinate closely with supply chain, engineering, quality, and commercial teams., • Analyze production data and KPIs to identify areas for improvement and optimization., • Manage maintenance programs to ensure equipment reliability and minimize downtime., • Culture of safety, teamwork, and operational excellence. Requirements Education • Bachelor’s degree in Engineering, Industrial Management, Manufacturing, or related field., • Minimum 8 years of experience in manufacturing or industrial operations., • At least 3–5 years in a leadership role within a production environment., • Strong leadership and team management skills., • Solid understanding of manufacturing processes and industrial operations., • Experience with Lean Manufacturing, Six Sigma, or other operational excellence methodologies., • Strong analytical and problem-solving abilities., • Excellent organizational and decision-making skills., • Ability to work under pressure and manage multiple priorities., • Financial skills and understanding., • Excellent organizational and communication skills Languages • Spanish: Native or fluent., • English: Professional proficiency preferred. Compensation & Benefits • Competitive salary package., • Performance-based bonus.

At mAbxience, a company specialized in the development and manufacturing of biosimilar medicines, we are hiring a Bioassay Scientist for our Manufacturing Site in León (Spain). GLOBAL RESPONSIBILITY This individual will be responsible to co-ordinate the work of the Bioassay group inside analytical development. The main task will be development, qualification and validation of new bioanalytical methods, co-ordination of sample testing to support process and formulation development and other developments activities of biotherapeutics drug candidates at all stages of development. Review of external development and qualification & validation reports. Bioanalytical techniques include but are not limited to high complexity cell based test assays (ADCC, CDC, neutralization, apoptosis, etc.), SPR, target binding ELISA, Flow Cytometer based binding assays as well residual impurities analysis in compliance with GLP/GMP and regulatory guidance as it relate to drug substance and drug product development. This individual will be required to present and interpret scientific data, write technical reports, and represent the team in matrix team or R&D group meetings when needed. SPECIFIC RESPONSIBILITIES Performs the assigned analytical tasks individually if needed in support of product development, registration lot release, pre and post regulatory submission activities. Performs activities within the assigned timelines and in compliance with GLP/GMP, regulatory requirements and company practices and procedures. -Co-ordinate and supervise the work of the Bioassay group (Technicians and Analysts). -Develop, implement, and qualify high complexity Surface Plasmon Resonance (SPR), cell-based test assays (ADCC, CDC, neutralization, apoptosis etc.) as well in process impurities in compliance with GLP/GMP and regulatory guidance to support process and formulation development with minimum supervision. -Identifies technical challenges during analytical method development and perform method trouble shooting. -Proactively participates in activities in support of process development and process changes -Designs, follows, and reviews protocols, scientific methods, and departmental procedures; Organizes and interprets scientific data. -Documents analytical activities and results accurately, in a timely manner and right-first time. -Reviews and checks analytical data generated by peers and maintains integrity of data. -Communicates effectively with peers, supervisor, and management about the status of the assigned activities, maintaining supervisor constantly updated. -Write and review technical and data analysis reports, SOPs, Tech Transfer documents and maintain accurate, precise, legible documentations. -Supporting quality control during tech transfer and Validation. REQUIREMENTS AND PERSONAL SKILLS Education: Master’s degree or PhD with major in Biological Sciences or another science-related major.  Languages: Excellent communication and interpersonal skills in English and Spanish, both written and verbal are required. (Spanish is not a must).  Experience (years/area): o PhD with 5-year industry experience or MS with minimum 8-10 year of relevant experience in biopharmaceutical/biotechnology industry. Graduation gained from chemistry, analytical chemistry, biology, biochemistry, immunology, bioengineering, Pharmacology, or other related disciplines preferred. o Min of 5-7 years’ experience with development, validation of bioanalytical assay methods in a regulated Good Laboratory Practices (GLP) and/or Good Manufacturing Practices (GMP) environment. o Hands-on experience and proficiency with the use of various bioanalytical and biochemical tools including but not limited to SPR, ELISA, Western blot, enzymatic assays, cell-based assays. o Hands-on experience with Flow Cytometry.  Specific Knowledge: o Knowledge of Surface Plasmon Resonance (SPR) platform. o Knowledge of biologics and industry experience in biologics research / development 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.

At Altorecruit, we are a consultancy specialized in selection and executive search for industrial and manufacturing companies. We work closely with our clients to understand their business, organizational context and operational challenges in order to identify leaders capable of driving sustainable performance and long-term growth. Currently, we are supporting an international industrial group in the search for a Plant Manager to lead one of its manufacturing facilities located in Soria, Spain. This position reports directly to the Business Unit Manager and plays a key role in ensuring operational excellence, production performance and the continuous development of the plant organization. Position Summary The Plant Manager is responsible for the overall management of the manufacturing facility, ensuring efficient production operations, high product quality, cost control, and compliance with safety and regulatory standards. The role leads plant personnel, optimizes operational performance, and drives continuous improvement to achieve business objectives. Key Responsibilities • Oversee daily plant operations, including production, maintenance, quality, and logistics., • Ensure production targets are met in terms of volume, quality, cost, and delivery schedules., • Develop and implement operational strategies to improve efficiency, productivity, and profitability., • Lead, mentor, and develop plant staff and department managers., • Monitor and control operating budgets, production costs, and resource allocation., • Ensure compliance with health, safety, environmental, and regulatory standards., • Implement and promote continuous improvement initiatives (Lean Manufacturing, Six Sigma, etc.)., • Coordinate closely with supply chain, engineering, quality, and commercial teams., • Analyze production data and KPIs to identify areas for improvement and optimization., • Manage maintenance programs to ensure equipment reliability and minimize downtime., • Culture of safety, teamwork, and operational excellence. Requirements Education • Bachelor’s degree in Engineering, Industrial Management, Manufacturing, or related field., • Minimum 8 years of experience in manufacturing or industrial operations., • At least 3–5 years in a leadership role within a production environment., • Strong leadership and team management skills., • Solid understanding of manufacturing processes and industrial operations., • Experience with Lean Manufacturing, Six Sigma, or other operational excellence methodologies., • Strong analytical and problem-solving abilities., • Excellent organizational and decision-making skills., • Ability to work under pressure and manage multiple priorities., • Financial skills and understanding., • Excellent organizational and communication skills Languages • Spanish: Native or fluent., • English: Professional proficiency preferred. Compensation & Benefits • Competitive salary package., • Performance-based bonus.

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.

Our goal is to strengthen the brand in Spain. We are looking for you to work as Automation Engineer! What do you need to fulfill this job? • 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), • SDLC common tasks but not limited to:, • 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 protocol generation, execution, and approval, • 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., • Use and update of development system if required, • Educate local project teams on automation standards as they relate to technology selection, system configuration, SDLC, validation, hardware, software environments and business processes., • Ensure SLA’s are in place for OEM systems with appropriate support available as back-up if necessary Core Competencies (Technical): • Experience with any of the following Applications, • Kneat, Siemens WinCC/S7, Aveva System Platform/Intouch, Aveva (OSI) PI, Microsoft 365 products and Windows core, • Experience with any of the following processes:, • WFI Generation & Distribution, Building management systems, Cleaning and Sterilization (Parts washers & Autoclaves), Blending and Formulation, Filling, Packaging and Inspection About HCLTech: 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. If all this sounds like an environment you’ll thrive in, then you’re in the right place. Join us on our journey in advancing the technological world through innovation and creativity. Why Us? • 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 freedom and flexibility on the job, empowering our employees to make decisions., • 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., • We offer the opportunity to work with colleagues across the globe., • We are a certified great place to work and a top employer in 25 countries including Romania, offering a positive work environment that values employee recognition and respect. If you have a valid disability certificate, Certificate of Disability in Force, please contact us. Among HCL's principles we would like to highlight diversity and inclusion as a strength in our values and practices. 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. We welcome and value all people, and we are committed to the inclusion and sense of belonging of each person who is part of HCL. • HCL is an equal opportunity employer. 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.

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.

🚀 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 Ingeniero/a de Certificación OCS altamente cualificado para unirse a nuestro equipo de telecomunicaciones. Esta persona será responsable de liderar la validación y pruebas de extremo a extremo de los sistemas de tarificación online. 🧩 ¿Qué nos gustaría que aportaras? Más de 5 años de experiencia en Certificación y/o en el dominio OCS. Se requiere experiencia en el ámbito de: • Redes móviles: GSM, GPRS, UMTS, IMS, 5GSA; red de señalización., • Sistemas operativos: Unix/Linux Redhat y Windows (administración)., • Bases de datos: consultas y modelado., • Protocolos de red: TCP/IP, HTTP/HTTPS, FTP/SFTP, TELNET, SSH/SSH2, SOAP, REST., • Scripting: Shell, Batch., • Entornos virtualizados: VMware, Red Hat Enterprise Virtualization, Openshift, etc., • Análisis de trazas con herramientas tipo Nethawk., Wireshark., • Arquitectura OCS: estructura y operación del nodo, modelo de datos, distribución de servicios y provisión., • Lógica de tarificación (voz, datos, contenidos, mensajería)., • Sistemas Red Hat (v7)., • Bases de datos Oracle RAC, CRS, Dataguard, REDIS/Valkey., • Almacenamiento HP 3PAR (Snapshot/Remote Copy)., • Interfaces de provisión: SDP‑SG en ASN.1., SOAP/REST., • Interfaces hacia red: SS7/CS1+/INAP, SS7/MAP, TCP/IP/Diameter Ro/SBI (N40), • Análisis de CDRs (ASN.1)., • Arquitectura de tráfico GSM/UMTS, IMS, 5GSA., • Information Framework (SID) TMForum. 🛠️ Tus principales funciones Serás el/la responsable de validar: • Asegurar la integridad de los ingresos y la correcta integración entre el Core de red y los sistemas de facturación., • Nuevas versiones de SW., • Planes de precios., • Cuotas de datos y servicios de valor añadido. 🧭 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

🚀 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 Ingeniero/a de Certificación OCS altamente cualificado para unirse a nuestro equipo de telecomunicaciones. Esta persona será responsable de liderar la validación y pruebas de extremo a extremo de los sistemas de tarificación online. 🧩 ¿Qué nos gustaría que aportaras? Más de 5 años de experiencia en Certificación y/o en el dominio OCS. Se requiere experiencia en el ámbito de: • Redes móviles: GSM, GPRS, UMTS, IMS, 5GSA; red de señalización., • Sistemas operativos: Unix/Linux Redhat y Windows (administración)., • Bases de datos: consultas y modelado., • Protocolos de red: TCP/IP, HTTP/HTTPS, FTP/SFTP, TELNET, SSH/SSH2, SOAP, REST., • Scripting: Shell, Batch., • Entornos virtualizados: VMware, Red Hat Enterprise Virtualization, Openshift, etc., • Análisis de trazas con herramientas tipo Nethawk., Wireshark., • Arquitectura OCS: estructura y operación del nodo, modelo de datos, distribución de servicios y provisión., • Lógica de tarificación (voz, datos, contenidos, mensajería)., • Sistemas Red Hat (v7)., • Bases de datos Oracle RAC, CRS, Dataguard, REDIS/Valkey., • Almacenamiento HP 3PAR (Snapshot/Remote Copy)., • Interfaces de provisión: SDP‑SG en ASN.1., SOAP/REST., • Interfaces hacia red: SS7/CS1+/INAP, SS7/MAP, TCP/IP/Diameter Ro/SBI (N40), • Análisis de CDRs (ASN.1)., • Arquitectura de tráfico GSM/UMTS, IMS, 5GSA., • Information Framework (SID) TMForum. 🛠️ Tus principales funciones Serás el/la responsable de validar: • Asegurar la integridad de los ingresos y la correcta integración entre el Core de red y los sistemas de facturación., • Nuevas versiones de SW., • Planes de precios., • Cuotas de datos y servicios de valor añadido. 🧭 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

🚀 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

🚀 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 Ingeniero/a de Certificación OCS altamente cualificado para unirse a nuestro equipo de telecomunicaciones. Esta persona será responsable de liderar la validación y pruebas de extremo a extremo de los sistemas de tarificación online. 🧩 ¿Qué nos gustaría que aportaras? Más de 5 años de experiencia en Certificación y/o en el dominio OCS. Se requiere experiencia en el ámbito de: • Redes móviles: GSM, GPRS, UMTS, IMS, 5GSA; red de señalización., • Sistemas operativos: Unix/Linux Redhat y Windows (administración)., • Bases de datos: consultas y modelado., • Protocolos de red: TCP/IP, HTTP/HTTPS, FTP/SFTP, TELNET, SSH/SSH2, SOAP, REST., • Scripting: Shell, Batch., • Entornos virtualizados: VMware, Red Hat Enterprise Virtualization, Openshift, etc., • Análisis de trazas con herramientas tipo Nethawk., Wireshark., • Arquitectura OCS: estructura y operación del nodo, modelo de datos, distribución de servicios y provisión., • Lógica de tarificación (voz, datos, contenidos, mensajería)., • Sistemas Red Hat (v7)., • Bases de datos Oracle RAC, CRS, Dataguard, REDIS/Valkey., • Almacenamiento HP 3PAR (Snapshot/Remote Copy)., • Interfaces de provisión: SDP‑SG en ASN.1., SOAP/REST., • Interfaces hacia red: SS7/CS1+/INAP, SS7/MAP, TCP/IP/Diameter Ro/SBI (N40), • Análisis de CDRs (ASN.1)., • Arquitectura de tráfico GSM/UMTS, IMS, 5GSA., • Information Framework (SID) TMForum. 🛠️ Tus principales funciones Serás el/la responsable de validar: • Asegurar la integridad de los ingresos y la correcta integración entre el Core de red y los sistemas de facturación., • Nuevas versiones de SW., • Planes de precios., • Cuotas de datos y servicios de valor añadido. 🧭 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

🚀 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

💡 ¿Y si tu próximo paso profesional te colocara en el centro de los proyectos que están transformando la industria? ⚙️ Imagina ser una pieza clave en garantizar que los procesos, productos o soluciones cumplan con los más altos estándares de calidad, innovación y rendimiento. En TRIGO, no buscamos solo experiencia. Buscamos personas con actitud, compromiso y ganas de dejar huella en lo que hacen. Bajo nuestro lema QUALITY IS OUR MINDSET, nuestro propósito es permitir a las personas viajar con total tranquilidad y confianza, asegurando que cada método de transporte cumpla con los más altos estándares de calidad y seguridad. ¿Te atreves a dar el siguiente paso? Gestor de Proyectos Junior | Automoción 📍 Proyecto de alto impacto en automoción industrial 🌱 Desarrollo profesional real 💼 Modalidad presencial en Valladolid ¿Por qué trabajar con nosotros? 🔹Innovación constante: aquí cada día plantea nuevos desafíos, nuevas ideas y nuevas soluciones. 🔹Crecimiento real: te acompañamos a crecer desde dentro con formación y promociones internas. 🔹Cultura colaborativa: trabajamos en equipo, celebramos los logros juntos y aprendemos de los errores. Como gestor/a de proyectos, serás el referente técnico para la gestión de actividades y soporte tecnológico para proyectos de Calidad como proyectos de seguimiento y animación de Joint Ventures, Digitalización, Actividades de mejora continua, Acciones de ruptura y transformación y reorganización en uno de los cliente líder en el sector automoción. Los retos a los que te enfrentarás: • Gestión y coordinación de proyectos digitales, asegurando la correcta planificación, ejecución y seguimiento de las iniciativas., • Coordinación entre las diferentes entidades del cliente, • Alineación de procesos y estándares, • Soporte a industrialización / producción de powertrain, • Gestión de proyectos o actividades dentro del perímetro de actuación, • Interacción con plantas, ingeniería o calidad dentro del nuevo modelo organizativo, • Gestión de documentación técnica de motor/powertrain y procedimientos de calidad o producción, • Definición de KPIs comunes y estructuración de datos de producción/calidad, • Soporte a proyectos de analítica o IA; y conectar iniciativas digitales (DMS, visión artificial) Qué te hará triunfar en el puesto: ✅ 3-5 años de experiencia en funciones similares ✅Conocimientos en pilotaje de presentación, formalización y seguimiento de decisiones ✅ Experiencia en seguimiento de avance de proyecto (objetivos, indicadores, reporting) ✅ Nivel alto de Office 365 ✅ Inglés mínimo B2. Así será tu proceso de selección: • 📞 Llamada breve para alinear tus expectativas y conocerte (15 min)., • 💻 Entrevista online con el equipo de Talent Acquisition (40 min)., • 🏢 Validación técnica presencial con el equipo de operaciones/responsables de departamento para conocer cómo es el día a día (45 min). Porque sabemos que lo que haces importa, hazlo en un lugar donde de verdad deje huella. Inscríbete y sigamos formando juntos el #TeamTRIGO. En TRIGO fomentamos la igualdad de oportunidades y la diversidad. Todas las candidaturas serán evaluadas sin discriminación por razones de género, origen, orientación sexual, discapacidad u otras circunstancias.

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