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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.

From mAbxience, a company specialized in the development and manufacture of biosimilar medicines, we are incorporating a Upstream technician for our plant in León. Global Responsibility Responsible for proper execution of cell culture process development and cell clarification activities of antibody and non-antibody protein biosimilar molecules production processes. Provide technical leadership for analysts involved in upstream process development. Contribute for interacting extensively with process development group (UPS and DSP). Specific Responsibilities • Responsible for organizing laboratory activities on daily bases, giving support for good execution of the different projects (II, III)., • Perform laboratory operation at AMBR, 1L, 5L and 50L scale bioreactors, disposable “WAVE” and depth filtration harvest clarification equipment., • Execution of upstream activities such as cell banking, seed train, production process (fed-batch and batch), cell line stability studies., • Applied DOE & multivariate analysis tools for experimental planning, data analysis (II, III)., • Data gathering, analyses and creating appropriate statistical presentations, including graphs and charts (I)., • Data analyses, formulate conclusions and create appropriate statistical presentations, including graphs and charts, and prepare and present written or oral progress reports regarding studies (II, III)., • Working according to GLP standards., • Maintenance and redaction of Standards Operating Procedures., • Continuous Improvement - will support process improvements throughout the development process. Requirements and personal skills • Education: Degree or HNC in relevant Biochemistry/chemistry specialty, Phd is a plus., • Languages: Fluent Spanish, working knowledge in English, knowledge of other languages will be an asset., • Experience (years/area): +1 (I), 3-6 (II) or +6 (III) years of relevant expertise in the upstream activities working with biologics pharmaceuticals and biotech environments., • Specific Knowledge:, • Knowledge on laboratory operation at AMBR, 1L, 5L and 50L scale bioreactors, disposable “WAVE” and depth filtration harvest clarification equipment., • Experienced (I, II) or Expert (III) in upstream activities such as cell banking, seed train, production process (fed-batch and batch), cell line stability studies., • Knowledge on mammalian cell line metabolism as well as structure, function of monoclonal antibodies (I, II) with specific understanding of post-translational modifications (III)., • Travels: Not required., • Personal skills:, • Ability to lead, motivate and train team members and establish priorities and manage competing deadlines for self and others (III)., • Ability to read and carefully follow instructions., • Communication skills to other departments., • Excellent problem solving abilities and organization skills (II, III)., • Leadership skills in staff supervision (II, III)., • Willingness to work extended and, at times unusual hours to meet business needs. We offer a permanent contract to join a growing pharmaceutical company. • Life and accident insurance., • Free company canteen., • Free online training platform., • Free online library., • Social, physical and emotional well-being platform. mAbxience is committed to equal opportunities. We do not discriminate against any person on the grounds of ethnicity, religion, age, sex, nationality, marital status, affective or sexual orientation, gender identity or expression, disability, or any other personal or social circumstance.

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

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 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.

Are you ready to join a world leader in the exciting and dynamic fields of the Pharmaceutical and Medical Device industries? PQE Group has been at the forefront of these industries since 1998, with 40 subsidiaries and more than 2000 employees in Europe, Asia and the Americas. We are currently seeking an experienced Commissioning, Qualification & Validation (CQV) Consultant in León, Spain. This role will focus on the qualification and validation of equipment and systems in biotechnological production facilities. Responsibilities include, but are not limited to: • Execute commissioning, qualification, and validation activities for pharmaceutical/biotech equipment and systems., • Prepare, review, and execute C&Q and validation documentation (URS, DQ, IQ, OQ, PQ protocols, test scripts, and summary reports)., • Collaborate with cross-functional teams (Engineering, QA, Validation, Manufacturing) to ensure compliance with GMP, regulatory guidelines, and project timelines., • Review technical documentation, P&IDs, FAT/SAT protocols, and vendor manuals., • Identify, troubleshoot, and document deviations, ensuring timely resolution., • Ensure all activities meet GMP, FDA, EMA, and ICH requirements., • Provide project updates and progress reports to stakeholders. Required Qualifications: • Bachelor’s degree in Engineering, Life Sciences, or related field., • 5 year of experience in IQ/OQ/PQ protocol development and execution and C&Q for pharmaceutical/biotech facilities, including construction of production plants, • Strong knowledge of GMP, FDA, and EU regulations., • Excellent analytical, problem-solving, and communication skills., • Ability to work independently and collaboratively in a project environment., • Spanish native, English fluent (at least B2) Next Steps Upon receiving your application, if a match is found, the Recruiting department will contact you for an initial HR interview. If there's a positive match, a technical interview with the Hiring Manager will be arranged. In the case of a positive outcome coming from Hiring Manager interview, recruiter will contact you for further steps or to discuss our proposal. Alternatively, if the outcome is negative, we will contact you to halt the recruitment process. Working at PQE Group As a member of the PQE team, you will be part of a challenging, multicultural company that values collaboration and innovation. PQE Group gives you the opportunity to work on international projects, improve your skills and interact with colleagues from all corners of the world. If you are looking for a rewarding and exciting career, PQE Group is the perfect place for you. Apply now and take the first step towards an amazing future with us.

Position: Analista I+D / R&D Analyst Location: León Experience: Minimum 1-4 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 incorporating a new INSUDER as Analista I+D / R&D Analyst at our plant in León. The challenge! • Assign any sample with an ID according to the SOP to ensure sample traceability., • Perform tests in developing, verify and validate analytical methods for API, excipients and Pharmaceutical Product Development R&D., • Register the analytical results of the tests and produce reports with the results and conclusions., • Inform the Analytical Development Scientist about the results obtained, and any incident occurring during the analysis., • Propose changes and / or variations in analytical tests carried out to improve methodologies., • Inform, investigate and document OOS and OOT in a timely manner., • Calibrate if applicable and maintain R & D as per specific SOP. Review and maintain stock levels of materials, consumables, reagents (standard and other products). What do you need? • Education: Basic Studies in Chemical Analysis., • Languages: High level of Spanish and medium level of English., • Experience (years/area): Minimum 1-4 years’ experience in the functions mentioned above as analyst in the pharma industry, working with drugs. Handling Equipment of Liquid Chromatography. Knowledge in other analytical techniques., • Specific Knowledge: GMP regulations., • Personal skills: Analytical skills, reliability and patience. Our benefits! 💸 Attractive salary package. 🧪 Training and experience in a strategic and constantly growing sector. 👨 👩 👧 We are characterized by a professional, close, and teamwork-oriented environment. What will the Selection process be like? 🕵️ ➡️ Stay tuned to your phone and email! The first thing we will likely do is contact you through one of the two channels. ➡️ Prepare well! We will continue with an in-person/virtual interview depending on availability and what we agree upon; there may be one or two interviews in the process, and depending on the type of process, there may also be some kind of test. ➡️ Wait for the result! We care that you feel guided throughout each selection process and know what to expect from us, so we will always try to inform you of the status of the process. 🔷 Do you think this offer is not for you? 🔷 Follow us on social media like LinkedIn/Instagram and stay tuned for any offers we may release; the opportunity to be a new Insuder is waiting! #InsudPharma #Challenger #Insuder #InsudTalent COMMITMENT TO EQUAL OPPORTUNITIES The InsudPharma group is aware that business management must align with the needs and demands of society, and therefore assumes the commitment to equal opportunities and treatment between men and women, as stated in the current regulations on the matter - Organic Law 3/2007, and we do not discriminate against any person on the grounds of ethnicity, religion, age, sex, nationality, marital status, affective or sexual orientation, gender identity or expression, disability, or any other personal or social circumstance.

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

🚀 We’re Hiring at HP SCDS (León)! 🧪 QA Automation – Hardware & Solutions 📍 León, Spain Are you motivated by quality assurance and test automation? At HP SCDS, we are expanding our Quality Assurance team with two open positions to work on HP 3D and Large Format printers, contributing to highly technical projects with global impact. 🔍 Open Positions (2 roles) Test Automation – HP 3D Printing Solutions Focused on automating the testing of 3D solutions, designing robust and repeatable tests to ensure reliability and consistency. What you’ll do: • Design and implement automated tests to validate 3D solutions., • Collaborate with the team on quality initiatives and continuous improvement. Diagnostics Development & Automation – Large Format Printers Focused on developing diagnostics for large format printers and automating tests to ensure the highest quality of those diagnostics. What you’ll do: • Develop diagnostics for HP large format printers., • Design and implement automated tests to validate those diagnostics., • Contribute to improving the hardware quality of large format printers within a multidisciplinary team. ✅ Basic Requirements • Degree in Computer Science, Telecommunications, or equivalent technical background (including vocational training)., • Solid foundation in Object-Oriented Programming (OOP) and SOLID principles., • Passion for well-crafted work, attention to detail, proactivity, and teamwork., • English proficiency to collaborate in international environments. ➕ Nice to Have Experience or knowledge in: • TypeScript, • Python, • Automation tools/frameworks (WebDriverIO, Selenium, Robot Framework), • Agile methodologies (Scrum, Kanban) 👉 Interested? Apply now and become part of a QA team working on cutting-edge HP printing technologies. Feel free to apply directly or reach out for more information.

🚀 We’re looking for you! Do you enjoy programming in C++ and feel motivated to learn new things? At HP SCDS, within the Large Format team, we’re looking for a Firmware Developer to join the development of the firmware used by our large-format printers. 🧠 What will you do in your day-to-day? • Develop and maintain firmware for large-format printers., • Participate in the design, implementation, and continuous improvement of new features., • Collaborate with multidisciplinary teams to evolve our solutions and take them one step further. ✅ What are we looking for? • Solid knowledge of object-oriented programming (OOP) and design patterns., • Experience with C++., • Willingness to learn, technical curiosity, and a proactive attitude., • Ability to work in a team., • Good level of English to collaborate in an international environment., • Strong communication skills, both written and verbal. 💼 What do we offer? • Being part of a specialized technical team, with a direct impact on our products., • Continuous learning and support in your professional development., • A collaborative, close, and very positive work environment. 🌱 Benefits • Meal voucher, • Health insurance, • Annual performance bonus, • …and much more! 📍 Location: León (on-site) 📌 Application: Apply directly through LinkedIn 🔍 Discover more about our day-to-day at HP SCDS: 📸 Instagram HP SCDS 🎥 YouTube HP SCDS

🤖 Senior AI Engineer We’re looking for a professional with strong expertise in Artificial Intelligence and hands-on experience with AI model lifecycle management platforms. This is a great opportunity to join a valuable AI solution used by both internal and external customers, with plenty of room to grow 🚀 In this role, you’ll focus on identifying the key features needed for the platform, guiding the team through their implementation, and staying up to date with the latest advances in AI—bringing a strategic mindset to shaping the product roadmap. You’ll also play an important role in user adoption (both internal and external), gathering feedback to help define and continuously improve the platform’s capabilities. You’ll be joining a highly autonomous team of software and ML engineers working for the AI Models business unit, led from Palo Alto, and collaborating in a truly international environment 🌍 ✅ Must-have requirements • Bachelor’s degree in an AI/ML-related field: Computer Science, Mathematics, Physics, etc., • Ability to keep up with the state of the art in AI, understanding and applying scientific papers., • Experience applying ML, NLP, GenAI, or data science solutions in real use cases., • Advanced knowledge of Python 🐍, • Experience with some of the following AI & data science frameworks: PyTorch, Hugging Face Transformers, vLLM, MLflow, SGLang, etc., • Fluent English (minimum B2, C1 preferred)., • Strong skills in communicating scientific results, both orally and in writing. 🌟 Nice to have (a big plus!) • PhD or Master’s degree in an AI/ML-related field., • Knowledge of MLOps: deployment, monitoring, testing, AI solutions in the Cloud (Azure, AWS, etc.)., • Experience with other programming languages: Go, JavaScript, React, etc., • Familiarity with tools such as Git, Docker, Bash scripting, and more., • Publications in scientific journals or conferences 📚, • Experience working with agile methodologies. ✨ If you’re passionate about AI, enjoy combining research with real-world impact, and want to help shape a growing platform used across the organization and beyond—we’d love to hear from you!

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.

We’re Hiring at HP SCDS (León)! QA Automation – Hardware & Solutions León, Spain Are you motivated by quality assurance and test automation ? At HP SCDS , we are expanding our Quality Assurance team with two open positions to work on HP 3D and Large Format printers , contributing to highly technical projects with global impact . Open Positions (2 roles) Test Automation – HP 3D Printing Solutions Focused on automating the testing of 3D solutions, designing robust and repeatable tests to ensure reliability and consistency. What you’ll do: Design and implement automated tests to validate 3D solutions. Collaborate with the team on quality initiatives and continuous improvement. Diagnostics Development & Automation – Large Format Printers Focused on developing diagnostics for large format printers and automating tests to ensure the highest quality of those diagnostics. What you’ll do: Develop diagnostics for HP large format printers. Design and implement automated tests to validate those diagnostics. Contribute to improving the hardware quality of large format printers within a multidisciplinary team. ✅ Basic Requirements Degree in Computer Science, Telecommunications, or equivalent technical background (including vocational training). Solid foundation in Object-Oriented Programming (OOP) and SOLID principles . Passion for well-crafted work, attention to detail, proactivity, and teamwork. English proficiency to collaborate in international environments. ➕ Nice to Have Experience or knowledge in: TypeScript Python Automation tools/frameworks (WebDriverIO, Selenium, Robot Framework) Agile methodologies (Scrum, Kanban) Interested? Apply now and become part of a QA team working on cutting-edge HP printing technologies . Feel free to apply directly or reach out for more information .

We’re Hiring at HP SCDS (León)! QA Automation – Hardware & Solutions León, Spain Are you motivated by quality assurance and test automation ? At HP SCDS , we are expanding our Quality Assurance team with two open positions to work on HP 3D and Large Format printers , contributing to highly technical projects with global impact . Open Positions (2 roles) Test Automation – HP 3D Printing Solutions Focused on automating the testing of 3D solutions, designing robust and repeatable tests to ensure reliability and consistency. What you’ll do: Design and implement automated tests to validate 3D solutions. Collaborate with the team on quality initiatives and continuous improvement. Diagnostics Development & Automation – Large Format Printers Focused on developing diagnostics for large format printers and automating tests to ensure the highest quality of those diagnostics. What you’ll do: Develop diagnostics for HP large format printers. Design and implement automated tests to validate those diagnostics. Contribute to improving the hardware quality of large format printers within a multidisciplinary team. ✅ Basic Requirements Degree in Computer Science, Telecommunications, or equivalent technical background (including vocational training). Solid foundation in Object-Oriented Programming (OOP) and SOLID principles . Passion for well-crafted work, attention to detail, proactivity, and teamwork. English proficiency to collaborate in international environments. ➕ Nice to Have Experience or knowledge in: TypeScript Python Automation tools/frameworks (WebDriverIO, Selenium, Robot Framework) Agile methodologies (Scrum, Kanban) Interested? Apply now and become part of a QA team working on cutting-edge HP printing technologies . Feel free to apply directly or reach out for more information .

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.

We’re Hiring at HP SCDS (León)! QA Automation – Hardware & Solutions León, Spain Are you motivated by quality assurance and test automation ? At HP SCDS , we are expanding our Quality Assurance team with two open positions to work on HP 3D and Large Format printers , contributing to highly technical projects with global impact . Open Positions (2 roles) Test Automation – HP 3D Printing Solutions Focused on automating the testing of 3D solutions, designing robust and repeatable tests to ensure reliability and consistency. What you’ll do: Design and implement automated tests to validate 3D solutions. Collaborate with the team on quality initiatives and continuous improvement. Diagnostics Development & Automation – Large Format Printers Focused on developing diagnostics for large format printers and automating tests to ensure the highest quality of those diagnostics. What you’ll do: Develop diagnostics for HP large format printers. Design and implement automated tests to validate those diagnostics. Contribute to improving the hardware quality of large format printers within a multidisciplinary team. ✅ Basic Requirements Degree in Computer Science, Telecommunications, or equivalent technical background (including vocational training). Solid foundation in Object-Oriented Programming (OOP) and SOLID principles . Passion for well-crafted work, attention to detail, proactivity, and teamwork. English proficiency to collaborate in international environments. ➕ Nice to Have Experience or knowledge in: TypeScript Python Automation tools/frameworks (WebDriverIO, Selenium, Robot Framework) Agile methodologies (Scrum, Kanban) Interested? Apply now and become part of a QA team working on cutting-edge HP printing technologies . Feel free to apply directly or reach out for more information .

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.

Responsibilities: Manage high-volume inbound and outbound sales motions across all stages of the sales funnel via phone, email, video and social media outreach for B2B (business to business) Ability to identify key point of contacts through Sales Navigator as well as all forms of desk targets Actively manage sales pipeline with a focus on moving all prospects through the sales funnel Document all relevant prospect and customer interactions on CRM (Salesforce) Transition qualified leads from pipeline to onboarding team to finalize the transaction Review and report daily, monthly and quarterly metrics to help achieve sales goals Additional information: Working Hours: Monday–Friday, 10am–7pm, with a 1‑hour fully paid break Hybrid role: 3 days home office (Wed & Thu office) Training: 23.04.2026 Salary Bulgaria: 1670.39 Euro gross a month + performance bonus 1537.20 euro gross (quaterly) Salary Greece: 1150 Euro gross a month + project bonus 150 Euro a month + performance bonus 1000 Euro gross (quaterly) Relocation: relocation to Greece/Bulgaria. Remote work outside of Greece/Bulgaria is not permitted Relocation package: We provide full support with relocation to Greece/Bulgaria - including flight reimbursement, 2 weeks hotel and advanced payment. Requirements: Knowledge of English and Spanish at min. C1 level (speaking and writing) Min. 2.5 years and up to 5 years of directly relevant customer facing experience in sales or customer service role, ideally in tech. advertising sales sector Ability to think creatively and react quickly to tailor messaging to different conversations Ambition, confidence, fearless outgoing attitude – a self-starter with a competitive growth mindset Strong time-management skills and the ability to work independently Salesforce experience/ prior exposure to a CRM tool Previous experience within sales (working on warm leads, cold outreaches, research)

Responsibilities: Manage high-volume inbound and outbound sales motions across all stages of the sales funnel via phone, email, video and social media outreach for B2B (business to business) Ability to identify key point of contacts through Sales Navigator as well as all forms of desk targets Actively manage sales pipeline with a focus on moving all prospects through the sales funnel Document all relevant prospect and customer interactions on CRM (Salesforce) Transition qualified leads from pipeline to onboarding team to finalize the transaction Review and report daily, monthly and quarterly metrics to help achieve sales goals Additional information: Working Hours: Monday–Friday, 10am–7pm, with a 1‑hour fully paid break Hybrid role: 3 days home office (Wed & Thu office) Training: 23.04.2026 Salary Bulgaria: 1670.39 Euro gross a month + performance bonus 1537.20 euro gross (quaterly) Salary Greece: 1150 Euro gross a month + project bonus 150 Euro a month + performance bonus 1000 Euro gross (quaterly) Relocation: relocation to Greece/Bulgaria. Remote work outside of Greece/Bulgaria is not permitted Relocation package: We provide full support with relocation to Greece/Bulgaria - including flight reimbursement, 2 weeks hotel and advanced payment. Requirements: Knowledge of English and Spanish at min. C1 level (speaking and writing) Min. 2.5 years and up to 5 years of directly relevant customer facing experience in sales or customer service role, ideally in tech. advertising sales sector Ability to think creatively and react quickly to tailor messaging to different conversations Ambition, confidence, fearless outgoing attitude – a self-starter with a competitive growth mindset Strong time-management skills and the ability to work independently Salesforce experience/ prior exposure to a CRM tool Previous experience within sales (working on warm leads, cold outreaches, research)

Responsibilities: Manage high-volume inbound and outbound sales motions across all stages of the sales funnel via phone, email, video and social media outreach for B2B (business to business) Ability to identify key point of contacts through Sales Navigator as well as all forms of desk targets Actively manage sales pipeline with a focus on moving all prospects through the sales funnel Document all relevant prospect and customer interactions on CRM (Salesforce) Transition qualified leads from pipeline to onboarding team to finalize the transaction Review and report daily, monthly and quarterly metrics to help achieve sales goals Additional information: Working Hours: Monday–Friday, 10am–7pm, with a 1‑hour fully paid break Hybrid role: 3 days home office (Wed & Thu office) Training: 23.04.2026 Salary Bulgaria: 1670.39 Euro gross a month + performance bonus 1537.20 euro gross (quaterly) Salary Greece: 1150 Euro gross a month + project bonus 150 Euro a month + performance bonus 1000 Euro gross (quaterly) Relocation: relocation to Greece/Bulgaria. Remote work outside of Greece/Bulgaria is not permitted Relocation package: We provide full support with relocation to Greece/Bulgaria - including flight reimbursement, 2 weeks hotel and advanced payment. Requirements: Knowledge of English and Italian at min. C1 level (speaking and writing) Min. 2.5 years and up to 5 years of directly relevant customer facing experience in sales or customer service role, ideally in tech. advertising sales sector Ability to think creatively and react quickly to tailor messaging to different conversations Ambition, confidence, fearless outgoing attitude – a self-starter with a competitive growth mindset Strong time-management skills and the ability to work independently Salesforce experience/ prior exposure to a CRM tool Previous experience within sales (working on warm leads, cold outreaches, research)

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.

Responsibilities: Manage high-volume inbound and outbound sales motions across all stages of the sales funnel via phone, email, video and social media outreach for B2B (business to business) Ability to identify key point of contacts through Sales Navigator as well as all forms of desk targets Actively manage sales pipeline with a focus on moving all prospects through the sales funnel Document all relevant prospect and customer interactions on CRM (Salesforce) Transition qualified leads from pipeline to onboarding team to finalize the transaction Review and report daily, monthly and quarterly metrics to help achieve sales goals Additional information: Working Hours: Monday–Friday, 10am–7pm, with a 1‑hour fully paid break Hybrid role: 3 days home office (Wed & Thu office) Training: 23.04.2026 Salary Greece: €1350.00 gross per month + quarterly bonus 1350.00 gross Salary Bulgaria: €2198.56 gross per month + quarterly bonus 1537.20 gross Relocation: relocation to Greece/Bulgaria. Remote work outside of Greece/Bulgaria is not permitted Relocation package: We provide full support with relocation to Greece/Bulgaria - including flight reimbursement, 2 weeks hotel and advanced payment. Requirements: Knowledge of English and German at min. C1 level (speaking and writing) Min. 2.5 years and up to 5 years of directly relevant customer facing experience in sales or customer service role, ideally in tech. advertising sales sector Ability to think creatively and react quickly to tailor messaging to different conversations Ambition, confidence, fearless outgoing attitude – a self-starter with a competitive growth mindset Strong time-management skills and the ability to work independently Salesforce experience/ prior exposure to a CRM tool Previous experience within sales (working on warm leads, cold outreaches, research)

From mAbxience, a company specialized in the development and manufacture of biosimilar medicines, we are incorporating a Upstream technician for our plant in León. Global Responsibility Responsible for proper execution of cell culture process development and cell clarification activities of antibody and non-antibody protein biosimilar molecules production processes. Provide technical leadership for analysts involved in upstream process development. Contribute for interacting extensively with process development group (UPS and DSP). Specific Responsibilities Responsible for organizing laboratory activities on daily bases, giving support for good execution of the different projects (II, III). Perform laboratory operation at AMBR, 1L, 5L and 50L scale bioreactors, disposable “WAVE” and depth filtration harvest clarification equipment. Execution of upstream activities such as cell banking, seed train, production process (fed-batch and batch), cell line stability studies. Applied DOE & multivariate analysis tools for experimental planning, data analysis (II, III). Data gathering, analyses and creating appropriate statistical presentations, including graphs and charts (I). Data analyses, formulate conclusions and create appropriate statistical presentations, including graphs and charts, and prepare and present written or oral progress reports regarding studies (II, III). Working according to GLP standards. Maintenance and redaction of Standards Operating Procedures. Continuous Improvement - will support process improvements throughout the development process. Requirements and personal skills Education: Degree or HNC in relevant Biochemistry/chemistry specialty, Phd is a plus. Languages: Fluent Spanish, working knowledge in English, knowledge of other languages will be an asset. Experience (years/area): +1 (I), 3-6 (II) or +6 (III) years of relevant expertise in the upstream activities working with biologics pharmaceuticals and biotech environments. Specific Knowledge: Knowledge on laboratory operation at AMBR, 1L, 5L and 50L scale bioreactors, disposable “WAVE” and depth filtration harvest clarification equipment. Experienced (I, II) or Expert (III) in upstream activities such as cell banking, seed train, production process (fed-batch and batch), cell line stability studies. Knowledge on mammalian cell line metabolism as well as structure, function of monoclonal antibodies (I, II) with specific understanding of post-translational modifications (III). Travels: Not required. Personal skills: Ability to lead, motivate and train team members and establish priorities and manage competing deadlines for self and others (III). Ability to read and carefully follow instructions. Communication skills to other departments. Excellent problem solving abilities and organization skills (II, III). Leadership skills in staff supervision (II, III). Willingness to work extended and, at times unusual hours to meet business needs. We offer a permanent contract to join a growing pharmaceutical company. Life and accident insurance. Free company canteen. Free online training platform. Free online library. Social, physical and emotional well-being platform. mAbxience is committed to equal opportunities. We do not discriminate against any person on the grounds of ethnicity, religion, age, sex, nationality, marital status, affective or sexual orientation, gender identity or expression, disability, or any other personal or social circumstance.

Global Responsibility 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.

Responsibilities: Manage high-volume inbound and outbound sales motions across all stages of the sales funnel via phone, email, video and social media outreach for B2B (business to business) Ability to identify key point of contacts through Sales Navigator as well as all forms of desk targets Actively manage sales pipeline with a focus on moving all prospects through the sales funnel Document all relevant prospect and customer interactions on CRM (Salesforce) Transition qualified leads from pipeline to onboarding team to finalize the transaction Review and report daily, monthly and quarterly metrics to help achieve sales goals Additional information: Working Hours: Monday–Friday, 10am–7pm, with a 1‑hour fully paid break Hybrid role: 3 days home office (Wed & Thu office) Training: 23.04.2026 Salary Greece: €1350.00 gross per month + quarterly bonus 1350.00 gross Salary Bulgaria: €2198.56 gross per month + quarterly bonus 1537.20 gross Relocation: relocation to Greece/Bulgaria. Remote work outside of Greece/Bulgaria is not permitted Relocation package: We provide full support with relocation to Greece/Bulgaria - including flight reimbursement, 2 weeks hotel and advanced payment. Requirements: Knowledge of English and German at min. C1 level (speaking and writing) Min. 2.5 years and up to 5 years of directly relevant customer facing experience in sales or customer service role, ideally in tech. advertising sales sector Ability to think creatively and react quickly to tailor messaging to different conversations Ambition, confidence, fearless outgoing attitude – a self-starter with a competitive growth mindset Strong time-management skills and the ability to work independently Salesforce experience/ prior exposure to a CRM tool Previous experience within sales (working on warm leads, cold outreaches, research)

Responsibilities: Manage high-volume inbound and outbound sales motions across all stages of the sales funnel via phone, email, video and social media outreach for B2B (business to business) Ability to identify key point of contacts through Sales Navigator as well as all forms of desk targets Actively manage sales pipeline with a focus on moving all prospects through the sales funnel Document all relevant prospect and customer interactions on CRM (Salesforce) Transition qualified leads from pipeline to onboarding team to finalize the transaction Review and report daily, monthly and quarterly metrics to help achieve sales goals Additional information: Working Hours: Monday–Friday, 10am–7pm, with a 1‑hour fully paid break Hybrid role: 3 days home office (Wed & Thu office) Training: 23.04.2026 Salary Greece: €1350.00 gross per month + quarterly bonus 1350.00 gross Salary Bulgaria: €2198.56 gross per month + quarterly bonus 1537.20 gross Relocation: relocation to Greece/Bulgaria. Remote work outside of Greece/Bulgaria is not permitted Relocation package: We provide full support with relocation to Greece/Bulgaria - including flight reimbursement, 2 weeks hotel and advanced payment. Requirements: Knowledge of English and German at min. C1 level (speaking and writing) Min. 2.5 years and up to 5 years of directly relevant customer facing experience in sales or customer service role, ideally in tech. advertising sales sector Ability to think creatively and react quickly to tailor messaging to different conversations Ambition, confidence, fearless outgoing attitude – a self-starter with a competitive growth mindset Strong time-management skills and the ability to work independently Salesforce experience/ prior exposure to a CRM tool Previous experience within sales (working on warm leads, cold outreaches, research)

We’re Hiring at HP SCDS (León)! QA Automation – Hardware & Solutions León, Spain Are you motivated by quality assurance and test automation ? At HP SCDS , we are expanding our Quality Assurance team with two open positions to work on HP 3D and Large Format printers , contributing to highly technical projects with global impact . Open Positions (2 roles) Test Automation – HP 3D Printing Solutions Focused on automating the testing of 3D solutions, designing robust and repeatable tests to ensure reliability and consistency. What you’ll do: Design and implement automated tests to validate 3D solutions. Collaborate with the team on quality initiatives and continuous improvement. Diagnostics Development & Automation – Large Format Printers Focused on developing diagnostics for large format printers and automating tests to ensure the highest quality of those diagnostics. What you’ll do: Develop diagnostics for HP large format printers. Design and implement automated tests to validate those diagnostics. Contribute to improving the hardware quality of large format printers within a multidisciplinary team. ✅ Basic Requirements Degree in Computer Science, Telecommunications, or equivalent technical background (including vocational training). Solid foundation in Object-Oriented Programming (OOP) and SOLID principles . Passion for well-crafted work, attention to detail, proactivity, and teamwork. English proficiency to collaborate in international environments. ➕ Nice to Have Experience or knowledge in: TypeScript Python Automation tools/frameworks (WebDriverIO, Selenium, Robot Framework) Agile methodologies (Scrum, Kanban) Interested? Apply now and become part of a QA team working on cutting-edge HP printing technologies . Feel free to apply directly or reach out for more information .

From mAbxience, a company specialized in the development and manufacture of biosimilar medicines, we are incorporating a Upstream technician for our plant in León. Global Responsibility Responsible for proper execution of cell culture process development and cell clarification activities of antibody and non-antibody protein biosimilar molecules production processes. Provide technical leadership for analysts involved in upstream process development. Contribute for interacting extensively with process development group (UPS and DSP). Specific Responsibilities Responsible for organizing laboratory activities on daily bases, giving support for good execution of the different projects (II, III). Perform laboratory operation at AMBR, 1L, 5L and 50L scale bioreactors, disposable “WAVE” and depth filtration harvest clarification equipment. Execution of upstream activities such as cell banking, seed train, production process (fed-batch and batch), cell line stability studies. Applied DOE & multivariate analysis tools for experimental planning, data analysis (II, III). Data gathering, analyses and creating appropriate statistical presentations, including graphs and charts (I). Data analyses, formulate conclusions and create appropriate statistical presentations, including graphs and charts, and prepare and present written or oral progress reports regarding studies (II, III). Working according to GLP standards. Maintenance and redaction of Standards Operating Procedures. Continuous Improvement - will support process improvements throughout the development process. Requirements and personal skills Education: Degree or HNC in relevant Biochemistry/chemistry specialty, Phd is a plus. Languages: Fluent Spanish, working knowledge in English, knowledge of other languages will be an asset. Experience (years/area): +1 (I), 3-6 (II) or +6 (III) years of relevant expertise in the upstream activities working with biologics pharmaceuticals and biotech environments. Specific Knowledge: Knowledge on laboratory operation at AMBR, 1L, 5L and 50L scale bioreactors, disposable “WAVE” and depth filtration harvest clarification equipment. Experienced (I, II) or Expert (III) in upstream activities such as cell banking, seed train, production process (fed-batch and batch), cell line stability studies. Knowledge on mammalian cell line metabolism as well as structure, function of monoclonal antibodies (I, II) with specific understanding of post-translational modifications (III). Travels: Not required. Personal skills: Ability to lead, motivate and train team members and establish priorities and manage competing deadlines for self and others (III). Ability to read and carefully follow instructions. Communication skills to other departments. Excellent problem solving abilities and organization skills (II, III). Leadership skills in staff supervision (II, III). Willingness to work extended and, at times unusual hours to meet business needs. We offer a permanent contract to join a growing pharmaceutical company. Life and accident insurance. Free company canteen. Free online training platform. Free online library. Social, physical and emotional well-being platform. mAbxience is committed to equal opportunities. We do not discriminate against any person on the grounds of ethnicity, religion, age, sex, nationality, marital status, affective or sexual orientation, gender identity or expression, disability, or any other personal or social circumstance.

From mAbxience, a company specialized in the development and manufacture of biosimilar medicines, we are incorporating a Upstream technician for our plant in León. Global Responsibility Responsible for proper execution of cell culture process development and cell clarification activities of antibody and non-antibody protein biosimilar molecules production processes. Provide technical leadership for analysts involved in upstream process development. Contribute for interacting extensively with process development group (UPS and DSP). Specific Responsibilities Responsible for organizing laboratory activities on daily bases, giving support for good execution of the different projects (II, III). Perform laboratory operation at AMBR, 1L, 5L and 50L scale bioreactors, disposable “WAVE” and depth filtration harvest clarification equipment. Execution of upstream activities such as cell banking, seed train, production process (fed-batch and batch), cell line stability studies. Applied DOE & multivariate analysis tools for experimental planning, data analysis (II, III). Data gathering, analyses and creating appropriate statistical presentations, including graphs and charts (I). Data analyses, formulate conclusions and create appropriate statistical presentations, including graphs and charts, and prepare and present written or oral progress reports regarding studies (II, III). Working according to GLP standards. Maintenance and redaction of Standards Operating Procedures. Continuous Improvement - will support process improvements throughout the development process. Requirements and personal skills Education: Degree or HNC in relevant Biochemistry/chemistry specialty, Phd is a plus. Languages: Fluent Spanish, working knowledge in English, knowledge of other languages will be an asset. Experience (years/area): +1 (I), 3-6 (II) or +6 (III) years of relevant expertise in the upstream activities working with biologics pharmaceuticals and biotech environments. Specific Knowledge: Knowledge on laboratory operation at AMBR, 1L, 5L and 50L scale bioreactors, disposable “WAVE” and depth filtration harvest clarification equipment. Experienced (I, II) or Expert (III) in upstream activities such as cell banking, seed train, production process (fed-batch and batch), cell line stability studies. Knowledge on mammalian cell line metabolism as well as structure, function of monoclonal antibodies (I, II) with specific understanding of post-translational modifications (III). Travels: Not required. Personal skills: Ability to lead, motivate and train team members and establish priorities and manage competing deadlines for self and others (III). Ability to read and carefully follow instructions. Communication skills to other departments. Excellent problem solving abilities and organization skills (II, III). Leadership skills in staff supervision (II, III). Willingness to work extended and, at times unusual hours to meet business needs. We offer a permanent contract to join a growing pharmaceutical company. Life and accident insurance. Free company canteen. Free online training platform. Free online library. Social, physical and emotional well-being platform. 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.

Responsibilities: Manage high-volume inbound and outbound sales motions across all stages of the sales funnel via phone, email, video and social media outreach for B2B (business to business) Ability to identify key point of contacts through Sales Navigator as well as all forms of desk targets Actively manage sales pipeline with a focus on moving all prospects through the sales funnel Document all relevant prospect and customer interactions on CRM (Salesforce) Transition qualified leads from pipeline to onboarding team to finalize the transaction Review and report daily, monthly and quarterly metrics to help achieve sales goals Additional information: Working Hours: Monday–Friday, 10am–7pm, with a 1‑hour fully paid break Hybrid role: 3 days home office (Wed & Thu office) Training: 23.04.2026 Salary Greece: €1350.00 gross per month + quarterly bonus 1350.00 gross Salary Bulgaria: €2198.56 gross per month + quarterly bonus 1537.20 gross Relocation: relocation to Greece/Bulgaria. Remote work outside of Greece/Bulgaria is not permitted Relocation package: We provide full support with relocation to Greece/Bulgaria - including flight reimbursement, 2 weeks hotel and advanced payment. Requirements: Knowledge of English and German at min. C1 level (speaking and writing) Min. 2.5 years and up to 5 years of directly relevant customer facing experience in sales or customer service role, ideally in tech. advertising sales sector Ability to think creatively and react quickly to tailor messaging to different conversations Ambition, confidence, fearless outgoing attitude – a self-starter with a competitive growth mindset Strong time-management skills and the ability to work independently Salesforce experience/ prior exposure to a CRM tool Previous experience within sales (working on warm leads, cold outreaches, research)

Responsibilities: Manage high-volume inbound and outbound sales motions across all stages of the sales funnel via phone, email, video and social media outreach for B2B (business to business) Ability to identify key point of contacts through Sales Navigator as well as all forms of desk targets Actively manage sales pipeline with a focus on moving all prospects through the sales funnel Document all relevant prospect and customer interactions on CRM (Salesforce) Transition qualified leads from pipeline to onboarding team to finalize the transaction Review and report daily, monthly and quarterly metrics to help achieve sales goals Additional information: Working Hours: Monday–Friday, 10am–7pm, with a 1‑hour fully paid break Hybrid role: 3 days home office (Wed & Thu office) Training: 23.04.2026 Salary Bulgaria: 1670.39 Euro gross a month + performance bonus 1537.20 euro gross (quaterly) Salary Greece: 1150 Euro gross a month + project bonus 150 Euro a month + performance bonus 1000 Euro gross (quaterly) Relocation: relocation to Greece/Bulgaria. Remote work outside of Greece/Bulgaria is not permitted Relocation package: We provide full support with relocation to Greece/Bulgaria - including flight reimbursement, 2 weeks hotel and advanced payment. Requirements: Knowledge of English and Spanish at min. C1 level (speaking and writing) Min. 2.5 years and up to 5 years of directly relevant customer facing experience in sales or customer service role, ideally in tech. advertising sales sector Ability to think creatively and react quickly to tailor messaging to different conversations Ambition, confidence, fearless outgoing attitude – a self-starter with a competitive growth mindset Strong time-management skills and the ability to work independently Salesforce experience/ prior exposure to a CRM tool Previous experience within sales (working on warm leads, cold outreaches, research)

Responsibilities: Manage high-volume inbound and outbound sales motions across all stages of the sales funnel via phone, email, video and social media outreach for B2B (business to business) Ability to identify key point of contacts through Sales Navigator as well as all forms of desk targets Actively manage sales pipeline with a focus on moving all prospects through the sales funnel Document all relevant prospect and customer interactions on CRM (Salesforce) Transition qualified leads from pipeline to onboarding team to finalize the transaction Review and report daily, monthly and quarterly metrics to help achieve sales goals Additional information: Working Hours: Monday–Friday, 10am–7pm, with a 1‑hour fully paid break Hybrid role: 3 days home office (Wed & Thu office) Training: 23.04.2026 Salary Greece: €1350.00 gross per month + quarterly bonus 1350.00 gross Salary Bulgaria: €2198.56 gross per month + quarterly bonus 1537.20 gross Relocation: relocation to Greece/Bulgaria. Remote work outside of Greece/Bulgaria is not permitted Relocation package: We provide full support with relocation to Greece/Bulgaria - including flight reimbursement, 2 weeks hotel and advanced payment. Requirements: Knowledge of English and German at min. C1 level (speaking and writing) Min. 2.5 years and up to 5 years of directly relevant customer facing experience in sales or customer service role, ideally in tech. advertising sales sector Ability to think creatively and react quickly to tailor messaging to different conversations Ambition, confidence, fearless outgoing attitude – a self-starter with a competitive growth mindset Strong time-management skills and the ability to work independently Salesforce experience/ prior exposure to a CRM tool Previous experience within sales (working on warm leads, cold outreaches, research)

Responsibilities: Manage high-volume inbound and outbound sales motions across all stages of the sales funnel via phone, email, video and social media outreach for B2B (business to business) Ability to identify key point of contacts through Sales Navigator as well as all forms of desk targets Actively manage sales pipeline with a focus on moving all prospects through the sales funnel Document all relevant prospect and customer interactions on CRM (Salesforce) Transition qualified leads from pipeline to onboarding team to finalize the transaction Review and report daily, monthly and quarterly metrics to help achieve sales goals Additional information: Working Hours: Monday–Friday, 10am–7pm, with a 1‑hour fully paid break Hybrid role: 3 days home office (Wed & Thu office) Training: 23.04.2026 Salary Bulgaria: 1670.39 Euro gross a month + performance bonus 1537.20 euro gross (quaterly) Salary Greece: 1150 Euro gross a month + project bonus 150 Euro a month + performance bonus 1000 Euro gross (quaterly) Relocation: relocation to Greece/Bulgaria. Remote work outside of Greece/Bulgaria is not permitted Relocation package: We provide full support with relocation to Greece/Bulgaria - including flight reimbursement, 2 weeks hotel and advanced payment. Requirements: Knowledge of English and Spanish at min. C1 level (speaking and writing) Min. 2.5 years and up to 5 years of directly relevant customer facing experience in sales or customer service role, ideally in tech. advertising sales sector Ability to think creatively and react quickly to tailor messaging to different conversations Ambition, confidence, fearless outgoing attitude – a self-starter with a competitive growth mindset Strong time-management skills and the ability to work independently Salesforce experience/ prior exposure to a CRM tool Previous experience within sales (working on warm leads, cold outreaches, research)

Are you ready to join a world leader in the exciting and dynamic fields of the Pharmaceutical and Medical Device industries? PQE Group has been at the forefront of these industries since 1998 , with 40 subsidiaries and more than 2000 employees in Europe, Asia and the Americas. We are currently seeking an experienced Commissioning, Qualification & Validation (CQV) Consultant in León, Spain . This role will focus on the qualification and validation of equipment and systems in biotechnological production facilities . Responsibilities include, but are not limited to: Execute commissioning, qualification, and validation activities for pharmaceutical/biotech equipment and systems . Prepare, review, and execute C&Q and validation documentation ( URS, DQ, IQ, OQ, PQ protocols , test scripts , and summary reports ). Collaborate with cross-functional teams ( Engineering, QA, Validation, Manufacturing ) to ensure compliance with GMP , regulatory guidelines , and project timelines . Review technical documentation , P&IDs , FAT/SAT protocols , and vendor manuals . Identify, troubleshoot , and document deviations , ensuring timely resolution . Ensure all activities meet GMP , FDA , EMA , and ICH requirements . Provide project updates and progress reports to stakeholders . Required Qualifications: Bachelor’s degree in Engineering, Life Sciences , or related field. + 5 year of experience in IQ/OQ/PQ protocol development and execution and C&Q for pharmaceutical/biotech facilities, including construction of production plants Strong knowledge of GMP , FDA , and EU regulations . Excellent analytical , problem-solving , and communication skills . Ability to work independently and collaboratively in a project environment . Spanish native, English fluent (at least B2) Next Steps Upon receiving your application, if a match is found, the Recruiting department will contact you for an initial HR interview. If there's a positive match, a technical interview with the Hiring Manager will be arranged. In the case of a positive outcome coming from Hiring Manager interview, recruiter will contact you for further steps or to discuss our proposal. Alternatively, if the outcome is negative, we will contact you to halt the recruitment process. Working at PQE Group As a member of the PQE team, you will be part of a challenging, multicultural company that values collaboration and innovation . PQE Group gives you the opportunity to work on international projects, improve your skills and interact with colleagues from all corners of the world. If you are looking for a rewarding and exciting career, PQE Group is the perfect place for you. Apply now and take the first step towards an amazing future with us.

Are you ready to join a world leader in the exciting and dynamic fields of the Pharmaceutical and Medical Device industries? PQE Group has been at the forefront of these industries since 1998 , with 40 subsidiaries and more than 2000 employees in Europe, Asia and the Americas. We are currently seeking an experienced Commissioning, Qualification & Validation (CQV) Consultant in León, Spain . This role will focus on the qualification and validation of equipment and systems in biotechnological production facilities . Responsibilities include, but are not limited to: Execute commissioning, qualification, and validation activities for pharmaceutical/biotech equipment and systems . Prepare, review, and execute C&Q and validation documentation ( URS, DQ, IQ, OQ, PQ protocols , test scripts , and summary reports ). Collaborate with cross-functional teams ( Engineering, QA, Validation, Manufacturing ) to ensure compliance with GMP , regulatory guidelines , and project timelines . Review technical documentation , P&IDs , FAT/SAT protocols , and vendor manuals . Identify, troubleshoot , and document deviations , ensuring timely resolution . Ensure all activities meet GMP , FDA , EMA , and ICH requirements . Provide project updates and progress reports to stakeholders . Required Qualifications: Bachelor’s degree in Engineering, Life Sciences , or related field. + 5 year of experience in IQ/OQ/PQ protocol development and execution and C&Q for pharmaceutical/biotech facilities, including construction of production plants Strong knowledge of GMP , FDA , and EU regulations . Excellent analytical , problem-solving , and communication skills . Ability to work independently and collaboratively in a project environment . Spanish native, English fluent (at least B2) Next Steps Upon receiving your application, if a match is found, the Recruiting department will contact you for an initial HR interview. If there's a positive match, a technical interview with the Hiring Manager will be arranged. In the case of a positive outcome coming from Hiring Manager interview, recruiter will contact you for further steps or to discuss our proposal. Alternatively, if the outcome is negative, we will contact you to halt the recruitment process. Working at PQE Group As a member of the PQE team, you will be part of a challenging, multicultural company that values collaboration and innovation . PQE Group gives you the opportunity to work on international projects, improve your skills and interact with colleagues from all corners of the world. If you are looking for a rewarding and exciting career, PQE Group is the perfect place for you. Apply now and take the first step towards an amazing future with us.

Are you ready to join a world leader in the exciting and dynamic fields of the Pharmaceutical and Medical Device industries? PQE Group has been at the forefront of these industries since 1998 , with 40 subsidiaries and more than 2000 employees in Europe, Asia and the Americas. We are currently seeking an experienced Commissioning, Qualification & Validation (CQV) Consultant in León, Spain . This role will focus on the qualification and validation of equipment and systems in biotechnological production facilities . Responsibilities include, but are not limited to: Execute commissioning, qualification, and validation activities for pharmaceutical/biotech equipment and systems . Prepare, review, and execute C&Q and validation documentation ( URS, DQ, IQ, OQ, PQ protocols , test scripts , and summary reports ). Collaborate with cross-functional teams ( Engineering, QA, Validation, Manufacturing ) to ensure compliance with GMP , regulatory guidelines , and project timelines . Review technical documentation , P&IDs , FAT/SAT protocols , and vendor manuals . Identify, troubleshoot , and document deviations , ensuring timely resolution . Ensure all activities meet GMP , FDA , EMA , and ICH requirements . Provide project updates and progress reports to stakeholders . Required Qualifications: Bachelor’s degree in Engineering, Life Sciences , or related field. + 5 year of experience in IQ/OQ/PQ protocol development and execution and C&Q for pharmaceutical/biotech facilities, including construction of production plants Strong knowledge of GMP , FDA , and EU regulations . Excellent analytical , problem-solving , and communication skills . Ability to work independently and collaboratively in a project environment . Spanish native, English fluent (at least B2) Next Steps Upon receiving your application, if a match is found, the Recruiting department will contact you for an initial HR interview. If there's a positive match, a technical interview with the Hiring Manager will be arranged. In the case of a positive outcome coming from Hiring Manager interview, recruiter will contact you for further steps or to discuss our proposal. Alternatively, if the outcome is negative, we will contact you to halt the recruitment process. Working at PQE Group As a member of the PQE team, you will be part of a challenging, multicultural company that values collaboration and innovation . PQE Group gives you the opportunity to work on international projects, improve your skills and interact with colleagues from all corners of the world. If you are looking for a rewarding and exciting career, PQE Group is the perfect place for you. Apply now and take the first step towards an amazing future with us.

Who are we? At STACBOND, our vision is global. Present in over 90 countries, we continue to grow and expand our influence in the architecture and construction sector. Our commitment to internationalization has positioned us as a global reference in aluminum panel manufacturing and related solutions. We are looking for professionals with an international mindset and the drive to take on new challenges. If you want to join a dynamic, innovative, and constantly evolving team, we are waiting for you! What are we looking for? STACBOND is seeking an Export Area Manager to support and grow our international business. Main Responsibilities: • Develop and implement sales strategies for international markets. • Conduct market research to identify new business opportunities. • Maintain and strengthen relationships with existing clients. • Visit potential new customers. • Attend international trade fairs and events to promote our products. What We Offer: • Competitive salary package (fixed + variable), open to negotiation. • Summer intensive working hours and Friday afternoons off. • New flexible compensation plan: meal vouchers, transportation, and childcare. • Specialized in-house training provided by the company. • Social benefits and partnership agreements (health insurance, training, etc.). • International working environment with exposure to different countries. Desired Profile: • A degree in international trade, business, or a related field will be valued. • 2–3 years of proven experience in similar positions. • Advanced level of English. • Advanced skills in Microsoft Office and internal management software (ERP, CRM, etc.). • Availability to travel is essential. Join STACBOND’s growth and be part of our vision for the future! Commitment to Gender Equality: Our company is deeply committed to promoting equal treatment and opportunities for everyone in the workplace. All employment decisions are made based on fairness and non-discrimination, regardless of gender, race, beliefs, or any other personal characteristic. Commitment to Diversity and Inclusion: A disability or health condition should never be a barrier to taking part in a selection process. STACBOND upholds the principle of inclusion in recruitment and offers all candidates equal opportunities to demonstrate their skills by identifying and removing any barriers or obstacles that may arise due to a disability or health condition.

Are you ready to join a world leader in the exciting and dynamic fields of the Pharmaceutical and Medical Device industries? PQE Group has been at the forefront of these industries since 1998 , with 40 subsidiaries and more than 2000 employees in Europe, Asia and the Americas. We are currently seeking an experienced Commissioning, Qualification & Validation (CQV) Consultant in León, Spain . This role will focus on the qualification and validation of equipment and systems in biotechnological production facilities . Responsibilities include, but are not limited to: Execute commissioning, qualification, and validation activities for pharmaceutical/biotech equipment and systems . Prepare, review, and execute C&Q and validation documentation ( URS, DQ, IQ, OQ, PQ protocols , test scripts , and summary reports ). Collaborate with cross-functional teams ( Engineering, QA, Validation, Manufacturing ) to ensure compliance with GMP , regulatory guidelines , and project timelines . Review technical documentation , P&IDs , FAT/SAT protocols , and vendor manuals . Identify, troubleshoot , and document deviations , ensuring timely resolution . Ensure all activities meet GMP , FDA , EMA , and ICH requirements . Provide project updates and progress reports to stakeholders . Required Qualifications: Bachelor’s degree in Engineering, Life Sciences , or related field. + 5 year of experience in IQ/OQ/PQ protocol development and execution and C&Q for pharmaceutical/biotech facilities, including construction of production plants Strong knowledge of GMP , FDA , and EU regulations . Excellent analytical , problem-solving , and communication skills . Ability to work independently and collaboratively in a project environment . Spanish native, English fluent (at least B2) Next Steps Upon receiving your application, if a match is found, the Recruiting department will contact you for an initial HR interview. If there's a positive match, a technical interview with the Hiring Manager will be arranged. In the case of a positive outcome coming from Hiring Manager interview, recruiter will contact you for further steps or to discuss our proposal. Alternatively, if the outcome is negative, we will contact you to halt the recruitment process. Working at PQE Group As a member of the PQE team, you will be part of a challenging, multicultural company that values collaboration and innovation . PQE Group gives you the opportunity to work on international projects, improve your skills and interact with colleagues from all corners of the world. If you are looking for a rewarding and exciting career, PQE Group is the perfect place for you. Apply now and take the first step towards an amazing future with us.

Responsibilities: • Manage high-volume inbound and outbound sales motions across all stages of the sales funnel via phone, email, video and social media outreach for B2B (business to business), • Ability to identify key point of contacts through Sales Navigator as well as all forms of desk targets, • Actively manage sales pipeline with a focus on moving all prospects through the sales funnel, • Document all relevant prospect and customer interactions on CRM (Salesforce), • Transition qualified leads from pipeline to onboarding team to finalize the transaction, • Review and report daily, monthly and quarterly metrics to help achieve sales goals Additional information: Working Hours: Monday–Friday, 10am–7pm, with a 1‑hour fully paid break Hybrid role: 3 days home office (Wed & Thu office) Training: 23.04.2026 Salary Greece: €1350.00 gross per month + quarterly bonus 1350.00 gross Salary Bulgaria: €2198.56 gross per month + quarterly bonus 1537.20 gross Relocation: relocation to Greece/Bulgaria. Remote work outside of Greece/Bulgaria is not permitted Relocation package: We provide full support with relocation to Greece/Bulgaria - including flight reimbursement, 2 weeks hotel and advanced payment. Requirements: • Knowledge of English and German at min. C1 level (speaking and writing), • Min. 2.5 years and up to 5 years of directly relevant customer facing experience in sales or customer service role, ideally in tech. advertising sales sector, • Ability to think creatively and react quickly to tailor messaging to different conversations, • Ambition, confidence, fearless outgoing attitude – a self-starter with a competitive growth mindset, • Strong time-management skills and the ability to work independently, • Salesforce experience/ prior exposure to a CRM tool, • Previous experience within sales (working on warm leads, cold outreaches, research)

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.

Would you like to work with the latest technology in the automotive sector? Bertrandt AG Spain is an innovative German multinational company that provides engineering solutions in the automotive sector. Teamwork is the fuel that drives us to excellence, working side by side with the client. We are people who share the same passion. Do you want to join our team? Rol: Benchmarking the costs of powertrain systems and components by systematically comparing internal cost structures to those of competitors. The primary objective is to provide actionable insights that inform Design and Process teams about engineering and cost optimization efforts, ensuring the company’s offerings remain competitive in the global automotive market. This position is designed to develop and leverage internal expertise. Tasks: Collect necessary data for Costing, using internal and external teardown information. Identify cost drivers, material choices, manufacturing processes, and sourcing strategies used by competitors. Maintain a database of benchmarked cost data for use in ongoing and future projects. Formalize detailed should costs analyses and gap analyses Work closely with engineering, procurement, and finance teams to validate benchmarking assumptions and ensure data accuracy. Prepare detailed reports and presentations summarizing findings, cost differentials, and strategic recommendations for management and engineering teams. Required Knowledge & Skills: Technical Skills • Bachelor’s or Master’s degree in Engineering, or a related field, • Minimum 7 years of experience in powertrain costing within the automotive industry, • Experience with cost benchmarking, teardown analysis, and competitive intelligence in the automotive sector., • Knowledge of Costing Software, including preferably Siemens Costing SW., • Strong analytical skills and proficiency with cost modelling tools and techniques., • Ability to interpret technical and financial data from diverse sources, • Excellent communication and presentation skills for conveying complex benchmarking findings., • Project management experience., • Knowledge of the latest trends in automotive powertrain., • Fluency in English. Fluency in Spanish and/or French, to effectively communicate in our diverse work environment. What can we offer you? 🌏 Permanent contract 🕓 Flexible working hours 📚 Language training programs and continuous learning 🚑 Flexible compensation plan (health insurance) 🌴 23 working days of vacation 🎉 Company events – we like to have fun! 💖 A great work environment – open and inclusive If you believe this role is for you and want to work in a dynamic and continuously learning environment, apply now – we’re excited to meet you! We are BERTRANDT. And you? We’re waiting for you! At Bertrandt AG Spain, we are committed to creating a diverse and inclusive workplace and believe in equal opportunities for all qualified individuals, regardless of gender, age, disability, sexual orientation, gender identity or expression, religion, ethnicity, marital status, or any other personal or social circumstance.

From mAbxience, a company specialized in the development and manufacture of biosimilar medicines, we are incorporating a Upstream technician for our plant in León. Global Responsibility Responsible for proper execution of cell culture process development and cell clarification activities of antibody and non-antibody protein biosimilar molecules production processes. Provide technical leadership for analysts involved in upstream process development. Contribute for interacting extensively with process development group (UPS and DSP). Specific Responsibilities • Responsible for organizing laboratory activities on daily bases, giving support for good execution of the different projects (II, III)., • Perform laboratory operation at AMBR, 1L, 5L and 50L scale bioreactors, disposable “WAVE” and depth filtration harvest clarification equipment., • Execution of upstream activities such as cell banking, seed train, production process (fed-batch and batch), cell line stability studies., • Applied DOE & multivariate analysis tools for experimental planning, data analysis (II, III)., • Data gathering, analyses and creating appropriate statistical presentations, including graphs and charts (I)., • Data analyses, formulate conclusions and create appropriate statistical presentations, including graphs and charts, and prepare and present written or oral progress reports regarding studies (II, III)., • Working according to GLP standards., • Maintenance and redaction of Standards Operating Procedures., • Continuous Improvement - will support process improvements throughout the development process. Requirements and personal skills • Education: Degree or HNC in relevant Biochemistry/chemistry specialty, Phd is a plus., • Languages: Fluent Spanish, working knowledge in English, knowledge of other languages will be an asset., • Experience (years/area): +1 (I), 3-6 (II) or +6 (III) years of relevant expertise in the upstream activities working with biologics pharmaceuticals and biotech environments., • Specific Knowledge:, • Knowledge on laboratory operation at AMBR, 1L, 5L and 50L scale bioreactors, disposable “WAVE” and depth filtration harvest clarification equipment., • Experienced (I, II) or Expert (III) in upstream activities such as cell banking, seed train, production process (fed-batch and batch), cell line stability studies., • Knowledge on mammalian cell line metabolism as well as structure, function of monoclonal antibodies (I, II) with specific understanding of post-translational modifications (III)., • Travels: Not required., • Personal skills:, • Ability to lead, motivate and train team members and establish priorities and manage competing deadlines for self and others (III)., • Ability to read and carefully follow instructions., • Communication skills to other departments., • Excellent problem solving abilities and organization skills (II, III)., • Leadership skills in staff supervision (II, III)., • Willingness to work extended and, at times unusual hours to meet business needs. We offer a permanent contract to join a growing pharmaceutical company. • Life and accident insurance., • Free company canteen., • Free online training platform., • Free online library., • Social, physical and emotional well-being platform. 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.

Would you like to work with the latest technology in the automotive sector? Bertrandt AG Spain is an innovative German multinational company that provides engineering solutions in the automotive sector. Teamwork is the fuel that drives us to excellence, working side by side with the client. We are people who share the same passion. Do you want to join our team? Rol: Benchmarking the costs of powertrain systems and components by systematically comparing internal cost structures to those of competitors. The primary objective is to provide actionable insights that inform Design and Process teams about engineering and cost optimization efforts, ensuring the company’s offerings remain competitive in the global automotive market. This position is designed to develop and leverage internal expertise. Tasks: Collect necessary data for Costing, using internal and external teardown information. Identify cost drivers, material choices, manufacturing processes, and sourcing strategies used by competitors. Maintain a database of benchmarked cost data for use in ongoing and future projects. Formalize detailed should costs analyses and gap analyses Work closely with engineering, procurement, and finance teams to validate benchmarking assumptions and ensure data accuracy. Prepare detailed reports and presentations summarizing findings, cost differentials, and strategic recommendations for management and engineering teams. Required Knowledge & Skills: Technical Skills • Bachelor’s or Master’s degree in Engineering, or a related field, • Minimum 7 years of experience in powertrain costing within the automotive industry, • Experience with cost benchmarking, teardown analysis, and competitive intelligence in the automotive sector., • Knowledge of Costing Software, including preferably Siemens Costing SW., • Strong analytical skills and proficiency with cost modelling tools and techniques., • Ability to interpret technical and financial data from diverse sources, • Excellent communication and presentation skills for conveying complex benchmarking findings., • Project management experience., • Knowledge of the latest trends in automotive powertrain., • Fluency in English. Fluency in Spanish and/or French, to effectively communicate in our diverse work environment. What can we offer you? 🌏 Permanent contract 🕓 Flexible working hours 📚 Language training programs and continuous learning 🚑 Flexible compensation plan (health insurance) 🌴 23 working days of vacation 🎉 Company events – we like to have fun! 💖 A great work environment – open and inclusive If you believe this role is for you and want to work in a dynamic and continuously learning environment, apply now – we’re excited to meet you! We are BERTRANDT. And you? We’re waiting for you! At Bertrandt AG Spain, we are committed to creating a diverse and inclusive workplace and believe in equal opportunities for all qualified individuals, regardless of gender, age, disability, sexual orientation, gender identity or expression, religion, ethnicity, marital status, or any other personal or social circumstance.

Responsibilities: • Manage high-volume inbound and outbound sales motions across all stages of the sales funnel via phone, email, video and social media outreach for B2B (business to business), • Ability to identify key point of contacts through Sales Navigator as well as all forms of desk targets, • Actively manage sales pipeline with a focus on moving all prospects through the sales funnel, • Document all relevant prospect and customer interactions on CRM (Salesforce), • Transition qualified leads from pipeline to onboarding team to finalize the transaction, • Review and report daily, monthly and quarterly metrics to help achieve sales goals Additional information: Working Hours: Monday–Friday, 10am–7pm, with a 1‑hour fully paid break Hybrid role: 3 days home office (Wed & Thu office) Training: 23.04.2026 Salary Greece: €1350.00 gross per month + quarterly bonus 1350.00 gross Salary Bulgaria: €2198.56 gross per month + quarterly bonus 1537.20 gross Relocation: relocation to Greece/Bulgaria. Remote work outside of Greece/Bulgaria is not permitted Relocation package: We provide full support with relocation to Greece/Bulgaria - including flight reimbursement, 2 weeks hotel and advanced payment. Requirements: • Knowledge of English and German at min. C1 level (speaking and writing), • Min. 2.5 years and up to 5 years of directly relevant customer facing experience in sales or customer service role, ideally in tech. advertising sales sector, • Ability to think creatively and react quickly to tailor messaging to different conversations, • Ambition, confidence, fearless outgoing attitude – a self-starter with a competitive growth mindset, • Strong time-management skills and the ability to work independently, • Salesforce experience/ prior exposure to a CRM tool, • Previous experience within sales (working on warm leads, cold outreaches, research)

We are interviewing for an English teaching position, in-person, face to face, starting on April 6th in Ávila (Spain). We currently have a request from a client to teach in-person English company classes in P.I. Vicolozano : 4 hours a week in the mornings. • Days: Mondays and Fridays, • Timetable: Mondays (11:00 - 13:00) and Fridays (12:30 - 14:30), • Location: Ávila (P.I. Vicolozano), • Type of classes: In-company group class (3-7 students), • Levels: A1 and A2 Materials and support are provided Support and ongoing teacher development program Pay: 14-20€ / hour Contract options: laboral (work contract) or autónomo (freelance contract) Requirements: • Teachers need to have their work visa (or student visa that allows to work) ready., • Native or bilingual in English.