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About Bilinear Labs At Bilinear Labs, we do Research and Software Engineering for blockchain and finance. Rooted in the north of Spain, we bridge blockchain innovation and traditional finance, driven by a belief in transparency, verifiability, privacy, and cybersecurity. What You’ll Do • 💻 Work with us on your Master’s thesis in close contact with the founder and with the support of the team., • ✍️ Write reports and blog posts showcasing your work to the world., • 🧑‍💻 Write clean, maintainable, and high-performance code (Go, Rust, or Solidity)., • 🧪 Design and execute tests to ensure the reliability, security, and scalability of your software., • 📏 Profile and benchmark to crush latency and resource usage., • 🏗️ Own the full software lifecycle: requirements, design, architecture, implementation, testing, deployment, and monitoring. About You • 📚 Master’s student in Computer Science, Telecommunications, or a related technical field., • 📍 Living in the north of Spain and able to commute to León once every couple of weeks., • 🇺🇸 Comfortable working day-to-day in English., • 🎯 Pragmatic decision-maker: able to evaluate trade-offs based on constraints., • 🛠️ Able to work independently with minimal supervision., • 💻 Experience with at least two of C/C++, Go, Rust, or Python., • 🗄️ Experience with databases and Git., • 🐳 Experience with Docker and containers., • 🛜 Familiar with blockchain fundamentals, consensus algorithms, smart contracts, peer-to-peer networks, and data structures such as Merkle trees., • 🌐 International experience living abroad. What We Offer • 💸 Paid Cursor license. We expect you to use AI daily in your workflow., • 🧠 Smart colleagues to learn from., • 🌍 Global impact while working with international clients., • 🎓 One fully covered conference per year to keep your skills sharp., • 🚀 Help shape the company’s future, processes, and technical vision from Day 1., • 🌆 Hybrid work in a vibrant city boasting Spain’s most beautiful cathedral, exceptional quality of life, wallet-friendly tapas, and a rich tapestry of history. Thesis Topics • 🔗 Implementation of a Hash Time-Locked Contracts (HTLC) protocol over two EVM-compatible blockchains., • 🔐 Integration of ECDSA threshold signatures in a wallet., • 🛡️ Implementation of a cybersecurity algorithm to prevent address-poisoning scams., • 🌲 Implementation of a Rust-based indexer directly reading the Ethereum state., • 🎯 Wildcard application: If you have an idea, we’re all ears. Our Hiring Process • ☕️ Chat with the Founder. Share your background, aspirations, and mutual fit., • 📑 HR Partner Interview. Deep dive into culture and work style., • 🔧 Technical Interview. Programming and system-design discussion. We don’t see a Master’s thesis as a box to tick, and you shouldn’t either. If you’re looking for an easy project just to wrap up your degree, this is not the place for you. But if you want to work hard, solve real problems, and build a thesis that becomes the foundation of your future career, then we want to hear from you. This is your chance to create work you’ll be proud to show, and to grow alongside people who care about pushing boundaries. If this sounds like your kind of challenge, we’d love to hear from you! 🚀

We’re Hiring! Do you have a passion for software development and quality assurance? At HP SCDS , we’re looking for a talented professional to join our team as a QA Hardware Development Engineer to design diagnostic solutions for large-format printers and develop automated tests to ensure the highest product quality. What You’ll Do Develop diagnostic tools for HP large-format printers. Design and implement automated tests to validate diagnostics. Collaborate with a multidisciplinary team on quality-driven projects. Contribute to continuous improvement of QA processes and tools. ✅ What We’re Looking For Degree in Computer Science, Telecommunications, or a related technical field. Strong foundation in Object-Oriented Programming (OOP) and SOLID principles. Passion for high-quality work and attention to detail. Creativity, proactivity, and strong teamwork skills. Nice to Have Knowledge of Python. Experience with automated testing frameworks and tools (Robot Framework, Selenium, etc.). English proficiency to collaborate in international environments. What We Offer Be part of a dynamic team with direct impact on HP product quality. Hybrid work model with flexibility. (Minimum 3 days per ween in the office) Continuous training and professional growth opportunities. Restaurant Ticket. Health insurance. Annual performance bonus. And much more! Location: León, Spain Find out more about our culture and daily life at HP SCDS on our social networks: Instagram HP SCDS YouTube HP SCDS

Mantell Associates is partnered with a forward-thinking biopharmaceutical company, who is seeking a driven Planning Consultant to join their newly established planning team in Spain. Planning Consultant - Responsibilities: Map, document and optimise the full planning process flow - from demand management through manufacturing plans for APIs, semi-finished and finished products Propose and deploy planning frameworks to align demand forecasts, production capacities and inventory strategies with business objectives Coordinate demand and manufacturing planning for active pharmaceutical ingredients (APIs) and finished/semi-finished products, ensuring integration across supply, operations and commercial teams Define and monitor key planning performance indicators (KPIs) such as inventory turnover, coverage, production cycle times and service level metrics Work with team members to establish inventory targets, coverage models and production schedules based on business needs and supply constraints Utilise advanced Excel modelling and support the implementation/configuration of MRP systems to drive accurate planning output and transparency Collaborate cross-functionally with Supply Chain, Manufacturing, Procurement and Finance to ensure planning decisions align with cost, quality and timeline objectives Drive continuous improvement in planning practices, translating data and performance insights into actionable process optimisations Planning Consultant - Requirements: Proven experience (5+ years) in demand management, manufacturing planning or supply chain planning in the pharmaceutical industry, specifically with APIs, semi-finished and finished dosage forms Hands-on experience in mapping process flows, implementing or improving planning systems, and developing KPI-driven planning performance frameworks Advanced Excel skills (modelling, analysis, dashboards) and experience working with MRP/ERP systems in a manufacturing environment Strong analytical mindset, problem-solving skills and ability to translate planning data into meaningful business actions Excellent communication and collaboration skills in English; proficiency in Spanish or willingness to work in Spanish-speaking environment is advantageous

From mAbxience, a company specialized in the development and manufacture of biosimilar medicines, we are incorporating a un Quality Control Projects Supervisor (Bio) for our plant in León.General Responsibility Along with Quality Control Manager, implementation and maintenance of all biochemical

Mantell Associates is partnered with a forward-thinking biopharmaceutical company, who is seeking a driven Planning Consultant to join their newly established planning team in Spain. Planning Consultant - Responsibilities: Map, document and optimise the full planning process flow - from demand management through manufacturing plans for APIs, semi-finished and finished products Propose and deploy planning frameworks to align demand forecasts, production capacities and inventory strategies with business objectives Coordinate demand and manufacturing planning for active pharmaceutical ingredients (APIs) and finished/semi-finished products, ensuring integration across supply, operations and commercial teams Define and monitor key planning performance indicators (KPIs) such as inventory turnover, coverage, production cycle times and service level metrics Work with team members to establish inventory targets, coverage models and production schedules based on business needs and supply constraints Utilise advanced Excel modelling and support the implementation/configuration of MRP systems to drive accurate planning output and transparency Collaborate cross-functionally with Supply Chain, Manufacturing, Procurement and Finance to ensure planning decisions align with cost, quality and timeline objectives Drive continuous improvement in planning practices, translating data and performance insights into actionable process optimisations Planning Consultant - Requirements: Proven experience (5+ years) in demand management, manufacturing planning or supply chain planning in the pharmaceutical industry, specifically with APIs, semi-finished and finished dosage forms Hands-on experience in mapping process flows, implementing or improving planning systems, and developing KPI-driven planning performance frameworks Advanced Excel skills (modelling, analysis, dashboards) and experience working with MRP/ERP systems in a manufacturing environment Strong analytical mindset, problem-solving skills and ability to translate planning data into meaningful business actions Excellent communication and collaboration skills in English; proficiency in Spanish or willingness to work in Spanish-speaking environment is advantageous

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. Travels: Personal skills : Result oriented, attention to detail, Teamwork oriented mAbxience is committed to equal opportunities. We do not discriminate against any person on the grounds of ethnicity, religion, age, sex, nationality, marital status, affective or sexual orientation, gender identity or expression, disability, or any other personal or social circumstance.

Global Responsibility 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

Mantell Associates is partnered with a forward-thinking biopharmaceutical company, who is seeking a driven Planning Consultant to join their newly established planning team in Spain. This role offers a unique opportunity to map process flows, coordinate demand and manufacturing plans for active ingredients (APIs), and help structure the planning function from the ground up. Planning Consultant - Responsibilities: Map, document and optimise the full planning process flow - from demand management through manufacturing plans for APIs, semi-finished and finished products Propose and deploy planning frameworks to align demand forecasts, production capacities and inventory strategies with business objectives Coordinate demand and manufacturing planning for active pharmaceutical ingredients (APIs) and finished/semi-finished products, ensuring integration across supply, operations and commercial teams Define and monitor key planning performance indicators (KPIs) such as inventory turnover, coverage, production cycle times and service level metrics Work with team members to establish inventory targets, coverage models and production schedules based on business needs and supply constraints Utilise advanced Excel modelling and support the implementation/configuration of MRP systems to drive accurate planning output and transparency Collaborate cross-functionally with Supply Chain, Manufacturing, Procurement and Finance to ensure planning decisions align with cost, quality and timeline objectives Drive continuous improvement in planning practices, translating data and performance insights into actionable process optimisations Planning Consultant - Requirements: Proven experience (5+ years) in demand management, manufacturing planning or supply chain planning in the pharmaceutical industry, specifically with APIs, semi-finished and finished dosage forms Hands-on experience in mapping process flows, implementing or improving planning systems, and developing KPI-driven planning performance frameworks Advanced Excel skills (modelling, analysis, dashboards) and experience working with MRP/ERP systems in a manufacturing environment Strong analytical mindset, problem-solving skills and ability to translate planning data into meaningful business actions Excellent communication and collaboration skills in English; proficiency in Spanish or willingness to work in Spanish-speaking environment is advantageous Mantell Associates is a specialist Pharmaceutical and Life Science headhunting firm. For more information on this opportunity, contact us at +44 (0)20 3854 7700.

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

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. Travels: Personal skills : Result oriented, attention to detail, Teamwork oriented mAbxience is committed to equal opportunities. We do not discriminate against any person on the grounds of ethnicity, religion, age, sex, nationality, marital status, affective or sexual orientation, gender identity or expression, disability, or any other personal or social circumstance.

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

From Mabxience, a company specialized in the development and manufacture of biosimilar medicines, we are incorporating a temporary MSAT technician for our plant in León. Global Responsabilities Organize the implementation of manufacturing processes in any of the producing lines at mAbxience (León); identification and proposal of continuous improvement programs in production; scientific support on deviation and non-conformity solving as well as assessment and implementation of new technologies in producing lines. Specific responsabilities Follow and participate in process developments by R&D in order to ensure that their execution at industrial scale will be possible as for infrastructures, materials, operations and costs, exposing all with a process risk assessment in regards of facilities and scale applicable to these. Technology transfers performed in between company units or with external customers, in order to ensure that their execution at industrial scale will be possible as for infrastructures, materials, operations and costs. Write and verify documentation needed to start up manufacturing process in producing lines. For instance: Process descriptions. List of materials and Raw Materials and their specifications. Manufacturing Versions and roadmaps. Initial Master Batch Records. Scale-up rationale and report. Additional scale-up protocols/reports such as stability studies of intermediate products among others. Coordinate and provide training courses on new operations to the different production sections. Coordinate and provide scientific support to production throughout execution of engineering batches and early GMP batches, following up process trending as well as analytical product parameters: data gathering. Coordinate and support to R&D for studies included in Process validation stages, including DSM, viral clearance, and resin lifetime studies, as well as process characterisation. Follow up of process or product deviations, identifying possible root causes, potential impacts, proposing corrective and preventive actions, as indicated in the corresponding quality procedure. Coordinate with other departments sampling plans for first batches manufactured in GMP facility for new process under implementation. Identification and evaluation of process improvement and optimization opportunities. Asses their impact and coordinate their implementation with the different involved departments (Engineering, R&D, Quality, Supply Chain, Purchases…). Suggest and assess implementation of new technologies, equipment, or different usages of these, functioning as Operations interface with the departments of Engineering, R&D, Quality, Supply Chain, Purchases… Support and organization of the writing, execution, and reporting, as it may correspond, for the different experiments and studies associated to batch implementation, researching on any incidence or proposal of process improvement. Qualifications Education: University degree oriented to biology or chemistry Languages: Intermediate English level (fluency valued) Experience (years/area): ≥2 years in Operations, R&D, MSAT Specific Knowledge: Work in GMP environment, UPS-DSP experience, Tech transfer, process validation. Travels: 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.

Company Description Silicon Dali is a preferred partner for leading enterprises, SMEs, and technology challengers, specializing in custom software development, product design, QA, and consultancy services. Role Description This is a full-time on-site .NET Backend Developer role located in Salamanca, Spain. The .NET Backend Developer will be responsible for the day-to-day tasks associated with backend development, collaborating closely with front-end developers and other team members to implement designs and functionalities. If you are passionate about clean code and user experience, this is a great opportunity to grow and contribute to exciting projects. If you’re passionate about clean code, scalable architectures, and modern backend development practices, we want to meet you! Key Responsibilities Develop services using .NET Create scalable architectures and maintainable codebases. Work closely with product managers and front-end developers. Ensure application quality through unit and integration testing. Participate in code reviews and propose technical improvements. Stay current with backend best practices and emerging trends. Required Qualifications Strong English communication (written and spoken) is essential. Work involves English communication. 3+ years of experience working with .NET / C# Solid understanding of API development and integration Experience with databases (SQL / NoSQL) Knowledge of services and backend communication patterns Experience working with websocket connections Nice to Have Experience with containers (Docker) Knowledge of Kubernetes or other orchestration tools Experience with CI/CD pipelines, release processes, or cloud environments Familiarity with microservices architecture Other backend languages Why Join Us? Work in a growing and collaborative environment Opportunities to innovate and work with modern technologies Professional development and career growth Competitive salary based on experience A creative and collaborative workspace in the heart of Salamanca

At mAbxience, a company specialized in the development and manufacturing of biosimilar medicines, we are hiring a Bioassay Scientist for our Manufacturing Site in León (Spain). GLOBAL RESPONSIBILITY This individual will be responsible to co-ordinate the work of the Bioassay group inside analytical development. The main task will be development, qualification and validation of new bioanalytical methods, co-ordination of sample testing to support process and formulation development and other developments activities of biotherapeutics drug candidates at all stages of development. Review of external development and qualification & validation reports. Bioanalytical techniques include but are not limited to high complexity cell based test assays (ADCC, CDC, neutralization, apoptosis, etc.), SPR, target binding ELISA, Flow Cytometer based binding assays as well residual impurities analysis in compliance with GLP/GMP and regulatory guidance as it relate to drug substance and drug product development. This individual will be required to present and interpret scientific data, write technical reports, and represent the team in matrix team or R&D group meetings when needed. SPECIFIC RESPONSIBILITIES Performs the assigned analytical tasks individually if needed in support of product development, registration lot release, pre and post regulatory submission activities. Performs activities within the assigned timelines and in compliance with GLP/GMP, regulatory requirements and company practices and procedures. -Co-ordinate and supervise the work of the Bioassay group (Technicians and Analysts). -Develop, implement, and qualify high complexity Surface Plasmon Resonance (SPR), cell-based test assays (ADCC, CDC, neutralization, apoptosis etc.) as well in process impurities in compliance with GLP/GMP and regulatory guidance to support process and formulation development with minimum supervision. -Identifies technical challenges during analytical method development and perform method trouble shooting. -Proactively participates in activities in support of process development and process changes -Designs, follows, and reviews protocols, scientific methods, and departmental procedures; Organizes and interprets scientific data. -Documents analytical activities and results accurately, in a timely manner and right-first time. -Reviews and checks analytical data generated by peers and maintains integrity of data. -Communicates effectively with peers, supervisor, and management about the status of the assigned activities, maintaining supervisor constantly updated. -Write and review technical and data analysis reports, SOPs, Tech Transfer documents and maintain accurate, precise, legible documentations. -Supporting quality control during tech transfer and Validation. REQUIREMENTS AND PERSONAL SKILLS Education: Master’s degree or PhD with major in Biological Sciences or another science-related major.  Languages: Excellent communication and interpersonal skills in English and Spanish, both written and verbal are required. (Spanish is not a must).  Experience (years/area): o PhD with 5-year industry experience or MS with minimum 8-10 year of relevant experience in biopharmaceutical/biotechnology industry. Graduation gained from chemistry, analytical chemistry, biology, biochemistry, immunology, bioengineering, Pharmacology, or other related disciplines preferred. o Min of 5-7 years’ experience with development, validation of bioanalytical assay methods in a regulated Good Laboratory Practices (GLP) and/or Good Manufacturing Practices (GMP) environment. o Hands-on experience and proficiency with the use of various bioanalytical and biochemical tools including but not limited to SPR, ELISA, Western blot, enzymatic assays, cell-based assays. o Hands-on experience with Flow Cytometry.  Specific Knowledge: o Knowledge of Surface Plasmon Resonance (SPR) platform. o Knowledge of biologics and industry experience in biologics research / development Mabxience is a company committed to equal opportunities, and therefore, all candidates will be considered without distinction of race, color, gender, age, sexual orientation, religion, origin, marital status, citizenship, or disability.

En pocas palabras Posición : QA Coordinator (Release - QC) Localización: León Experiencia: Mínimo 4 años en posición similar en QA o QC ¿Quieres saber más? Chemo, parte de INSUD PHARMA, es una empresa líder en la cadena de valor farmacéutica, comprometida con la innovación y la calida

At mAbxience, a company specialized in the development and manufacturing of biosimilar medicines, we are hiring a Bioassay Scientist for our Manufacturing Site in León (Spain). GLOBAL RESPONSIBILITY This individual will be responsible to co-ordinate the work of the Bioassay group inside analytical development. The main task will be development, qualification and validation of new bioanalytical methods, co-ordination of sample testing to support process and formulation development and other developments activities of biotherapeutics drug candidates at all stages of development. Review of external development and qualification & validation reports. Bioanalytical techniques include but are not limited to high complexity cell based test assays (ADCC, CDC, neutralization, apoptosis, etc.), SPR, target binding ELISA, Flow Cytometer based binding assays as well residual impurities analysis in compliance with GLP/GMP and regulatory guidance as it relate to drug substance and drug product development. This individual will be required to present and interpret scientific data, write technical reports, and represent the team in matrix team or R&D group meetings when needed. SPECIFIC RESPONSIBILITIES Performs the assigned analytical tasks individually if needed in support of product development, registration lot release, pre and post regulatory submission activities. Performs activities within the assigned timelines and in compliance with GLP/GMP, regulatory requirements and company practices and procedures. -Co-ordinate and supervise the work of the Bioassay group (Technicians and Analysts). -Develop, implement, and qualify high complexity Surface Plasmon Resonance (SPR), cell-based test assays (ADCC, CDC, neutralization, apoptosis etc.) as well in process impurities in compliance with GLP/GMP and regulatory guidance to support process and formulation development with minimum supervision. -Identifies technical challenges during analytical method development and perform method trouble shooting. -Proactively participates in activities in support of process development and process changes -Designs, follows, and reviews protocols, scientific methods, and departmental procedures; Organizes and interprets scientific data. -Documents analytical activities and results accurately, in a timely manner and right-first time. -Reviews and checks analytical data generated by peers and maintains integrity of data. -Communicates effectively with peers, supervisor, and management about the status of the assigned activities, maintaining supervisor constantly updated. -Write and review technical and data analysis reports, SOPs, Tech Transfer documents and maintain accurate, precise, legible documentations. -Supporting quality control during tech transfer and Validation. REQUIREMENTS AND PERSONAL SKILLS Education: Master’s degree or PhD with major in Biological Sciences or another science-related major. Languages: Excellent communication and interpersonal skills in English and Spanish, both written and verbal are required. (Spanish is not a must). Experience (years/area): o PhD with 5-year industry experience or MS with minimum 8-10 year of relevant experience in biopharmaceutical/biotechnology industry. Graduation gained from chemistry, analytical chemistry, biology, biochemistry, immunology, bioengineering, Pharmacology, or other related disciplines preferred. o Min of 5-7 years’ experience with development, validation of bioanalytical assay methods in a regulated Good Laboratory Practices (GLP) and/or Good Manufacturing Practices (GMP) environment. o Hands-on experience and proficiency with the use of various bioanalytical and biochemical tools including but not limited to SPR, ELISA, Western blot, enzymatic assays, cell-based assays. o Hands-on experience with Flow Cytometry. Specific Knowledge: o Knowledge of Surface Plasmon Resonance (SPR) platform. o Knowledge of biologics and industry experience in biologics research / development Mabxience is a company committed to equal opportunities, and therefore, all candidates will be considered without distinction of race, color, gender, age, sexual orientation, religion, origin, marital status, citizenship, or disability.

Do you have at least 15 years of experience as a Project Manager in Powertrain environments? At ALTEN, we know that the success of our projects is due to the people who make up our team. That’s why we are committed to supporting your talent, meeting your career expectations, and making you feel at home. Do you want to help build tomorrow’s world today? Keep reading! What will your mission be? Coordinate technical and project management activities across the main client, industrial partners, and the different departments involved. Ensure the proper application of internal development and quality processes (project management methodologies, design, validation, and homologation). Consolidate and report QCDP indicators (Quality, Cost, Deadline, Performance) at each project milestone. Oversee the technical convergence of mechanical components within your area of responsibility, from early phases through technical maturity (P0–P4). Participate in defining objectives, risk analysis, and overall project planning. Prepare the technical documentation required for development (specifications, functional analyses, validation plans, quality dossiers, QCDP reports, among others). Ensure problem-solving and technical traceability using structured methodologies (LUP, 8D, QC Story, PDCA). Coordinate the technical transfer to the series production phase. Participate in training sessions and updates of internal development and quality tools. Ideal candidate profile: Degree in Engineering (preferably Industrial, Mechanical, Automotive, or similar). At least 15 years of experience in technical project management, especially in the automotive/Powertrain sector. Deep technical knowledge of combustion and electric engines. Proven experience in technical coordination between departments and cross-functional project management. High level of English (C1) is essential, both spoken and written. Strong interpersonal skills to facilitate agreements and decision-making in complex and multicultural environments. Leadership skills, global project vision, and a results-oriented mindset. What can we offer you? A position in a competitive multinational company in continuous growth. ✌️ Integration into a highly qualified team of professionals, with a good work atmosphere, innovative and dynamic. Specialized training and continuous professional development. Social benefits and a Flexible Compensation Plan. Competitive compensation. Who are we? We are a team. We are part of ALTEN, a European multinational specialized in providing consulting, IT, and engineering services to major companies in the Spanish market. If you’re into numbers, here are some: in Spain, we have a turnover of 217 million euros, 9 offices, and a team of 5,240 people. At ALTEN, we are also proud to offer equal opportunities regardless of gender, age, diverse abilities, or country of origin. Our commitment is to talent—and to the people who have it. If you believe you’ve got talent, apply now!

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

Ingeniería de Proyecto: Generar documentos técnicos para entregar a cliente: P&Ids, listados, fichas técnicas, memorias técnicas, etc. • Preparación de documentos para licitación, comparativos técnicos y económicos • Gestionar el mantenimiento preventivo y correctivo de las instalaciones • Preparación de las URS del proyecto en colaboración con el cliente. • Supervisar la ejecución de protocolos IQ/OQ de cada sistema. • Realizar los proyectos de forma que se cumplan los hitos marcados en tiempos y calidad, que marcará el director de proyecto o el cliente • En determinados proyectos, preparación de documentos de calidad: QMP, DQ, AR, etc. • Ø Formación y conocimientos • Experiencia previa mínima de 2 años como ingeniero de proyectos o de proceso en el sector biotecnológico / farmacéutico. • Licenciado en ingeniería química, ingeniería industrial química o formación afín. • Formación posgrado o conocimientos de equipos de bioprocesos y procesos biotecnológicos a nivel piloto o industrial. • Conocimiento fluido del español y del inglés. • Usuario de Microsoft Office, Microsoft Project, Power Point, AdobeAcrobat. Excelente conjunto de habilidades de gestión de clientes. • Capacidad para trabajar bajo presión, responsable de múltiples proyectos importantes en paralelo. • Capaz de trabajar en equipo, colaborativo, innovador y responsable. Ø Formación y conocimientos valorables • Formación de posgrado (Máster y/o Doctorado) relacionada con la biotecnología, ingeniería de proceso o ciencias de la vida. • Experiencia en los sectores biotecnológico/farmacéutico. • Experiencia en el diseño de instalaciones farmacéuticas: HVAC, proceso, salas blancas, servicios auxiliares limpios, servicios auxiliares industriales, control o electricidad en la industria farmacéutica, dependiendo de la especialización • Experiencia como ingeniero de proyectos en el diseño y construcción de plantas farmacéuticas. • Amplio conocimiento técnico de bioproceso a nivel upstream y downstream. • Conocimientos de procesos productivo implicando microorganismos, células animales y terapias avanzadas. • Se valorará positivamente dominio de AutoCAD.

At mAbxience, a company specialized in the development and manufacturing of biosimilar medicines, we are hiring a Bioassay Scientist for our Manufacturing Site in León (Spain). GLOBAL RESPONSIBILITY This individual will be responsible to co-ordinate the work of the Bioassay group inside analytical development. The main task will be development, qualification and validation of new bioanalytical methods, co-ordination of sample testing to support process and formulation development and other developments activities of biotherapeutics drug candidates at all stages of development. Review of external development and qualification & validation reports. Bioanalytical techniques include but are not limited to high complexity cell based test assays (ADCC, CDC, neutralization, apoptosis, etc.), SPR, target binding ELISA, Flow Cytometer based binding assays as well residual impurities analysis in compliance with GLP/GMP and regulatory guidance as it relate to drug substance and drug product development. This individual will be required to present and interpret scientific data, write technical reports, and represent the team in matrix team or R&D group meetings when needed. SPECIFIC RESPONSIBILITIES Performs the assigned analytical tasks individually if needed in support of product development, registration lot release, pre and post regulatory submission activities. Performs activities within the assigned timelines and in compliance with GLP/GMP, regulatory requirements and company practices and procedures. -Co-ordinate and supervise the work of the Bioassay group (Technicians and Analysts). -Develop, implement, and qualify high complexity Surface Plasmon Resonance (SPR), cell-based test assays (ADCC, CDC, neutralization, apoptosis etc.) as well in process impurities in compliance with GLP/GMP and regulatory guidance to support process and formulation development with minimum supervision. -Identifies technical challenges during analytical method development and perform method trouble shooting. -Proactively participates in activities in support of process development and process changes -Designs, follows, and reviews protocols, scientific methods, and departmental procedures; Organizes and interprets scientific data. -Documents analytical activities and results accurately, in a timely manner and right-first time. -Reviews and checks analytical data generated by peers and maintains integrity of data. -Communicates effectively with peers, supervisor, and management about the status of the assigned activities, maintaining supervisor constantly updated. -Write and review technical and data analysis reports, SOPs, Tech Transfer documents and maintain accurate, precise, legible documentations. -Supporting quality control during tech transfer and Validation. REQUIREMENTS AND PERSONAL SKILLS Education: Master’s degree or PhD with major in Biological Sciences or another science-related major.  Languages: Excellent communication and interpersonal skills in English and Spanish, both written and verbal are required. (Spanish is not a must).  Experience (years/area): o PhD with 5-year industry experience or MS with minimum 8-10 year of relevant experience in biopharmaceutical/biotechnology industry. Graduation gained from chemistry, analytical chemistry, biology, biochemistry, immunology, bioengineering, Pharmacology, or other related disciplines preferred. o Min of 5-7 years’ experience with development, validation of bioanalytical assay methods in a regulated Good Laboratory Practices (GLP) and/or Good Manufacturing Practices (GMP) environment. o Hands-on experience and proficiency with the use of various bioanalytical and biochemical tools including but not limited to SPR, ELISA, Western blot, enzymatic assays, cell-based assays. o Hands-on experience with Flow Cytometry.  Specific Knowledge: o Knowledge of Surface Plasmon Resonance (SPR) platform. o Knowledge of biologics and industry experience in biologics research / development Mabxience is a company committed to equal opportunities, and therefore, all candidates will be considered without distinction of race, color, gender, age, sexual orientation, religion, origin, marital status, citizenship, or disability.

Mantell Associates is partnered with a forward-thinking biopharmaceutical company, who is seeking a driven Planning Consultant to join their newly established planning team in Spain. Planning Consultant - Responsibilities: Map, document and optimise the full planning process flow - from demand management through manufacturing plans for APIs, semi-finished and finished products Propose and deploy planning frameworks to align demand forecasts, production capacities and inventory strategies with business objectives Coordinate demand and manufacturing planning for active pharmaceutical ingredients (APIs) and finished/semi-finished products, ensuring integration across supply, operations and commercial teams Define and monitor key planning performance indicators (KPIs) such as inventory turnover, coverage, production cycle times and service level metrics Work with team members to establish inventory targets, coverage models and production schedules based on business needs and supply constraints Utilise advanced Excel modelling and support the implementation/configuration of MRP systems to drive accurate planning output and transparency Collaborate cross-functionally with Supply Chain, Manufacturing, Procurement and Finance to ensure planning decisions align with cost, quality and timeline objectives Drive continuous improvement in planning practices, translating data and performance insights into actionable process optimisations Planning Consultant - Requirements: Proven experience (5+ years) in demand management, manufacturing planning or supply chain planning in the pharmaceutical industry, specifically with APIs, semi-finished and finished dosage forms Hands-on experience in mapping process flows, implementing or improving planning systems, and developing KPI-driven planning performance frameworks Advanced Excel skills (modelling, analysis, dashboards) and experience working with MRP/ERP systems in a manufacturing environment Strong analytical mindset, problem-solving skills and ability to translate planning data into meaningful business actions Excellent communication and collaboration skills in English; proficiency in Spanish or willingness to work in Spanish-speaking environment is advantageous

At mAbxience, a company specialized in the development and manufacturing of biosimilar medicines, we are hiring a Supply Planner & External Manufacturing Specialist for our Manufacturing Site in León (Spain). GLOBAL RESPONSIBILITY The Supply Planner & External Manufacturing Specialist is responsible for managing production of pharmaceutical products performed in external vendors (CMOs). Its main responsibility is secure a smooth and efficient production as per Supply chain demand. The Drug Product collaborates with cross-functional departments to plan, manage and drive Fill & Finish activities within agreed quality, scope, budget and time. Builds and maintains productive relationships with a wide variety of internal and external stakeholders. Ensures fluent communication between API and CMO sites, building and managing a solid process flow. SPECIFIC RESPONSIBILITIES Drug Product Supply responsibilities: · Ensure that Finish Products planning, manufacturing and supply in external vendors (CMO) meets commercial and non-commercial demand (clinical, developments). · Working closely with Launch department, technical MSAT teams and CMO Supply teams to support Implementation of new drug product (DP) and new launches/NPI. · Oversite and optimization of aseptic fill/finish processes and plans for mAbxience products. · Deploy and align with CMO a robust manufacturing plan with 12-18 months horizon that is align with customer demand, critical resource capacity and business plan. · Track evolution of manufacturing performance. Establish and report KPI to support Supply Chain and business targets. · Prepare and communicate timelines associated to pre commercialization DP manufacturing. · Generate and communicate data and information with necessary departments like regulatory, Quality or Supply Chain. Support during evaluation of quality deviations and corrective actions. · Support the pre commercial manufacturing activities (demo runs, engineering runs, PPQs, etc) · Develop effective forecasts based on customer demand and support the commercial team. Conduct monthly forecast maintenance. Track Demand vs Forecasts. · Coordination of new launches and ongoing production together with third parties and internal stakeholders. Governance and oversight: · Establish a robust governance process of CMO, including capacity assessment, KPI measure and Supply Planning to support S&OP process. · Identify risks and define/track actions together with stakeholders to mitigate the risks. · Generate information, measurement and follow up performance indicators in Drug Product, including Lead Times, Schedule adherence, and others to support proper inventory management. Continuous Improvement & Innovation: · Lead initiatives to improve supply chain efficiency, cost-effectiveness, and quality. · Identify opportunities for automation and data-driven decision-making to enhance supply chain performance. REQUIREMENTS AND PERSONAL SKILLS · Education: University Degree and preferably Master in Supply Chain. A degree in Pharmacy or similar is an asset. · 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: Manufacturing Support activities, GMP and SHE regulations. Strong Customer focus and relationship building. Basic knowledge in medication registries. Logistics knowledge in the pharmaceutical industry and SAP R3 and APO. · Travels: Willingness to travel. · Personal skills: Good organizational and communication skills, accuracy and reliability. Good interaction and team working capacity, ability to multi-tasks, demonstrated strong organizational skills and ability to independently prioritize work, attention to detail, excellent communication skills, accuracy, flexibility and openness to changes. Keeping focus in changing environments and experience in conflict resolution and negotiation skills. 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.

Site Manager – Industrial Greenfield EPC Project Location: Salamanca, Castile and Leon, Spain About the Role A leading organisation in the industrial engineering sector is seeking an experienced Site Manager to oversee the full on-site construction, installation, and delivery of a major greenfield EPC project in Salamanca. You will lead all multidisciplinary site teams, contractors, and subcontractors across civil, mechanical, electrical, structural, instrumentation, and commissioning scopes. This role is central to the successful delivery of one of the company’s flagship capital investments and offers the opportunity to work on a complex, large-scale build from early construction through mechanical completion, commissioning, and handover. Key Responsibilities Site Leadership & Construction Management Lead and manage all construction, installation, and build activities from the initial site set-up through to project completion. Drive on-site execution plans, ensuring safety, quality, schedule, and budget targets are achieved. Represent the project at site level and act as the primary interface between contractors, project engineering teams, and senior leadership. Multidisciplinary Team Oversight Coordinate and supervise all technical disciplines on site including civil, structural, M&E, process, safety, and commissioning personnel. Monitor subcontractor performance, labour allocation, resourcing, and daily activity planning. Ensure seamless integration between work packages and construction phases. Planning, Scheduling & Progress Control Implement daily and weekly construction coordination meetings. Monitor progress against the project schedule and identify constraints, risks, and mitigation actions. Control site documentation including drawings, permits, method statements, and inspection records. Quality, Compliance & Safety Enforce strong HSE culture and compliance with Spanish construction law and EU standards. Oversee site inspections, QA/QC checks, and acceptance criteria for all installed equipment and works. Maintain permit-to-work systems, risk assessments, toolbox talks, and incident reporting processes. Contractor & Supplier Management Lead contractor kick-off, mobilisation, and performance reviews. Manage site logistics, deliveries, lifting operations, storage, and material handling. Support procurement decisions and vendor verification in coordination with the project team. Commissioning & Hand-Over Support pre-commissioning and commissioning activities including punch lists, checksheets, and equipment readiness. Work closely with OEM representatives, installation specialists, and commissioning engineers. Ensure all site works meet handover documentation and quality standards. Required Experience Proven experience managing greenfield industrial construction projects. Background in at least one of the following sectors: Oil & gas, chemicals, biofuels, distillery, pharmaceutical, process manufacturing, or large industrial EPC builds. Strong track record overseeing multidisciplinary contractor teams on complex construction sites. Demonstrated ability to deliver large industrial plant installations from groundworks through mechanical completion. Fluent Spanish; strong English communication skills. Excellent site documentation and construction reporting capabilities. Valid driving licence preferred.

At mAbxience, a company specialized in the development and manufacturing of biosimilar medicines, we are hiring a Bioassay Scientist for our Manufacturing Site in León (Spain). GLOBAL RESPONSIBILITY This individual will be responsible to co-ordinate the work of the Bioassay group inside analytical development. The main task will be development, qualification and validation of new bioanalytical methods, co-ordination of sample testing to support process and formulation development and other developments activities of biotherapeutics drug candidates at all stages of development. Review of external development and qualification & validation reports. Bioanalytical techniques include but are not limited to high complexity cell based test assays (ADCC, CDC, neutralization, apoptosis, etc.), SPR, target binding ELISA, Flow Cytometer based binding assays as well residual impurities analysis in compliance with GLP/GMP and regulatory guidance as it relate to drug substance and drug product development. This individual will be required to present and interpret scientific data, write technical reports, and represent the team in matrix team or R&D group meetings when needed. SPECIFIC RESPONSIBILITIES Performs the assigned analytical tasks individually if needed in support of product development, registration lot release, pre and post regulatory submission activities. Performs activities within the assigned timelines and in compliance with GLP/GMP, regulatory requirements and company practices and procedures. -Co-ordinate and supervise the work of the Bioassay group (Technicians and Analysts). -Develop, implement, and qualify high complexity Surface Plasmon Resonance (SPR), cell-based test assays (ADCC, CDC, neutralization, apoptosis etc.) as well in process impurities in compliance with GLP/GMP and regulatory guidance to support process and formulation development with minimum supervision. -Identifies technical challenges during analytical method development and perform method trouble shooting. -Proactively participates in activities in support of process development and process changes -Designs, follows, and reviews protocols, scientific methods, and departmental procedures; Organizes and interprets scientific data. -Documents analytical activities and results accurately, in a timely manner and right-first time. -Reviews and checks analytical data generated by peers and maintains integrity of data. -Communicates effectively with peers, supervisor, and management about the status of the assigned activities, maintaining supervisor constantly updated. -Write and review technical and data analysis reports, SOPs, Tech Transfer documents and maintain accurate, precise, legible documentations. -Supporting quality control during tech transfer and Validation. REQUIREMENTS AND PERSONAL SKILLS Education: Master’s degree or PhD with major in Biological Sciences or another science-related major.  Languages: Excellent communication and interpersonal skills in English and Spanish, both written and verbal are required. (Spanish is not a must).  Experience (years/area): o PhD with 5-year industry experience or MS with minimum 8-10 year of relevant experience in biopharmaceutical/biotechnology industry. Graduation gained from chemistry, analytical chemistry, biology, biochemistry, immunology, bioengineering, Pharmacology, or other related disciplines preferred. o Min of 5-7 years’ experience with development, validation of bioanalytical assay methods in a regulated Good Laboratory Practices (GLP) and/or Good Manufacturing Practices (GMP) environment. o Hands-on experience and proficiency with the use of various bioanalytical and biochemical tools including but not limited to SPR, ELISA, Western blot, enzymatic assays, cell-based assays. o Hands-on experience with Flow Cytometry.  Specific Knowledge: o Knowledge of Surface Plasmon Resonance (SPR) platform. o Knowledge of biologics and industry experience in biologics research / development Mabxience is a company committed to equal opportunities, and therefore, all candidates will be considered without distinction of race, color, gender, age, sexual orientation, religion, origin, marital status, citizenship, or disability.

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: This role is part of our ADAS software development project for one of the largest automotive manufacturers. Key Responsibilities: Test Coordination & Implementation Track test sheet deliveries from the system team. Develop and debug CAPL-based test scripts in the Vector CANoe environment. Validate tests on HIL (Hardware-in-the-Loop) benches . Generate validation reports and meet project deadlines. Project Communication & Coordination Provide weekly progress reports . Prepare for Quality Gates and software release acceptance. Coordinate debug sessions with external suppliers. Participate in bug reviews and backlog grooming with the project team. Team & Process Management Monitor task progress via Kanban , Jira . Estimate and track team workload. Actively participate in SAFe Agile ceremonies (e.g., PI planning, sprints, retrospectives). Required Knowledge & Skills: Technical Skills Proficiency in Vector CANoe and CAPL scripting . Experience with Lauterbach TRACE32 for debugging. Familiarity with DDT2000 for flashing/configuration. Configuration of Vector tool environments . Scripting with Bash . Version control using Git , GitLab (CI/CD pipelines) . Tools & Collaboration Platforms Jira, Confluence, SharePoint for agile and document collaboration. Microsoft Excel for reporting or data handling. Languages Fluent in Spanish and English (both written and spoken). Soft Skills Excellent problem-solving, communication, and creativity. Strong coordination skills in multi-disciplinary teams. Qualifications: Degree in Computer Engineering or Telecommunications . Scrum certification (Scrum Master or Product Owner) is a plus. Good to Have / Bonus: General understanding of ADAS features (like ACC, LKA, AEB, etc.). Experience working directly with automotive OEMs or Tier-1 suppliers. 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.

In a few words Position: Packaging Material Specialist. Location: León. Experience:+ 5 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: The individual will be responsible for supporting the development, testing and implementation of new packaging materials and designs. This includes working with manufacturing, engineering, supply chain, and design team. Specific Responsibilities: • Be the packaging expert for the organization., • Own all packaging related activities for assigned products., • Ensure that packaging is developed and specified to meet the needs – lead material and supplier qualification efforts., • Be the contact with procurement for supplier allocation across packaging lines., • Ensure that all packaging activities are properly documented (specs, drawings, qualifications, change controls, etc.)., • Technical Support for quality discussions with material and equipment suppliers – handle the complaint process (oversight investigations, follow-up CAPAs)., • Improve finished product palletization efficiency., • Reduce stops and OEE loss due to materials quality – drive improvement projects., • Reduce the Number of complaints related with packaging material and propose improvements, • Create the Technical documentation of packaging material., • Education: BS or MS in a scientific or engineering discipline., • Languages: Fluent Spanish, English is a plus. o with artworks, keylines, and labelling –this is going to be a separate team o packaging equipment – Blister, labelers, cartoners, etc. o writing and manage documentation (specs, drawings, qualifications). • Specific Knowledge: Pharmaceutical experience and regulatory knowledge is valuable for the position. 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.

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

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

At mAbxience, a company specialized in the development and manufacturing of biosimilar medicines, we are hiring a Bioassay Scientist for our Manufacturing Site in León (Spain). GLOBAL RESPONSIBILITY This individual will be responsible to co-ordinate the work of the Bioassay group inside analytical development. The main task will be development, qualification and validation of new bioanalytical methods, co-ordination of sample testing to support process and formulation development and other developments activities of biotherapeutics drug candidates at all stages of development. Review of external development and qualification & validation reports. Bioanalytical techniques include but are not limited to high complexity cell based test assays (ADCC, CDC, neutralization, apoptosis, etc.), SPR, target binding ELISA, Flow Cytometer based binding assays as well residual impurities analysis in compliance with GLP/GMP and regulatory guidance as it relate to drug substance and drug product development. This individual will be required to present and interpret scientific data, write technical reports, and represent the team in matrix team or R&D group meetings when needed. SPECIFIC RESPONSIBILITIES Performs the assigned analytical tasks individually if needed in support of product development, registration lot release, pre and post regulatory submission activities. Performs activities within the assigned timelines and in compliance with GLP/GMP, regulatory requirements and company practices and procedures. -Co-ordinate and supervise the work of the Bioassay group (Technicians and Analysts). -Develop, implement, and qualify high complexity Surface Plasmon Resonance (SPR), cell-based test assays (ADCC, CDC, neutralization, apoptosis etc.) as well in process impurities in compliance with GLP/GMP and regulatory guidance to support process and formulation development with minimum supervision. -Identifies technical challenges during analytical method development and perform method trouble shooting. -Proactively participates in activities in support of process development and process changes -Designs, follows, and reviews protocols, scientific methods, and departmental procedures; Organizes and interprets scientific data. -Documents analytical activities and results accurately, in a timely manner and right-first time. -Reviews and checks analytical data generated by peers and maintains integrity of data. -Communicates effectively with peers, supervisor, and management about the status of the assigned activities, maintaining supervisor constantly updated. -Write and review technical and data analysis reports, SOPs, Tech Transfer documents and maintain accurate, precise, legible documentations. -Supporting quality control during tech transfer and Validation. REQUIREMENTS AND PERSONAL SKILLS Education: Master’s degree or PhD with major in Biological Sciences or another science-related major.  Languages: Excellent communication and interpersonal skills in English and Spanish, both written and verbal are required. (Spanish is not a must).  Experience (years/area): o PhD with 5-year industry experience or MS with minimum 8-10 year of relevant experience in biopharmaceutical/biotechnology industry. Graduation gained from chemistry, analytical chemistry, biology, biochemistry, immunology, bioengineering, Pharmacology, or other related disciplines preferred. o Min of 5-7 years’ experience with development, validation of bioanalytical assay methods in a regulated Good Laboratory Practices (GLP) and/or Good Manufacturing Practices (GMP) environment. o Hands-on experience and proficiency with the use of various bioanalytical and biochemical tools including but not limited to SPR, ELISA, Western blot, enzymatic assays, cell-based assays. o Hands-on experience with Flow Cytometry.  Specific Knowledge: o Knowledge of Surface Plasmon Resonance (SPR) platform. o Knowledge of biologics and industry experience in biologics research / development Mabxience is a company committed to equal opportunities, and therefore, all candidates will be considered without distinction of race, color, gender, age, sexual orientation, religion, origin, marital status, citizenship, or disability.

Mantell Associates is partnered with a forward-thinking biopharmaceutical company, who is seeking a driven Planning Consultant to join their newly established planning team in Spain. Planning Consultant - Responsibilities: Map, document and optimise the full planning process flow - from demand management through manufacturing plans for APIs, semi-finished and finished products Propose and deploy planning frameworks to align demand forecasts, production capacities and inventory strategies with business objectives Coordinate demand and manufacturing planning for active pharmaceutical ingredients (APIs) and finished/semi-finished products, ensuring integration across supply, operations and commercial teams Define and monitor key planning performance indicators (KPIs) such as inventory turnover, coverage, production cycle times and service level metrics Work with team members to establish inventory targets, coverage models and production schedules based on business needs and supply constraints Utilise advanced Excel modelling and support the implementation/configuration of MRP systems to drive accurate planning output and transparency Collaborate cross-functionally with Supply Chain, Manufacturing, Procurement and Finance to ensure planning decisions align with cost, quality and timeline objectives Drive continuous improvement in planning practices, translating data and performance insights into actionable process optimisations Planning Consultant - Requirements: Proven experience (5+ years) in demand management, manufacturing planning or supply chain planning in the pharmaceutical industry, specifically with APIs, semi-finished and finished dosage forms Hands-on experience in mapping process flows, implementing or improving planning systems, and developing KPI-driven planning performance frameworks Advanced Excel skills (modelling, analysis, dashboards) and experience working with MRP/ERP systems in a manufacturing environment Strong analytical mindset, problem-solving skills and ability to translate planning data into meaningful business actions Excellent communication and collaboration skills in English; proficiency in Spanish or willingness to work in Spanish-speaking environment is advantageous

Si buscas una nueva oportunidad laboral que impulse tu carrera, no lo dudes, en NTT DATA te estamos esperando. En NTT DATA desarrollamos ecosistemas a través de tecnologías de vanguardia, potenciando nuestra creatividad, respetando la diversidad y apostando por una cultura inclusiva. Contamos con diferentes iniciativas que ayudan a potenciar nuestro "diversity mindset". Estamos ampliando nuestros equipos de Quality Services y nos interesa conocer perfiles muy variados. ¿Cuáles serán tus responsabilidades? Diseñar y ejecutar planes de prueba funcionales y seguir la trazabilidad de los mismos. Diseñar y desarrollar soluciones automatizadas para aplicaciones web y móviles en un entorno ágil y multifuncional. Diseñar y desarrollar soluciones automatizadas para el backend (APIs, microservicios). Ejecutar y supervisar el conjunto de pruebas y abordar los problemas detectados. Mejorar continuamente el conjunto de pruebas y aumentar la cobertura. Trabajar con los diferentes miembros de los equipos para optimizar la calidad de la automatización de pruebas. Supervisión cruzada del código con sus compañeros. Compartir y prestar apoyo a otros miembros del equipo de ingenieros de automatización de control de calidad con el desarrollo de pruebas. Trabajar con DevOps para sugerir mejoras en los procesos y el ciclo de integración continua de Jenkins/Bamboo. ¿Cuáles son los requisitos? Si tienes un enfoque funcional, conocimiento en la creación de casos y planes de prueba. Si tienes experiencia en QA automatizado, haber trabajado con Frameworks como Selenium, WebdriverIO, Playwright o Appium (valoramos otros, siendo estos los principales). Buen nivel en Java y/o Python. Valoramos el nivel de inglés. Si tienes a partir de un B2, quizás te interese formar parte de nuestros proyectos internacionales. Además, ¿qué ofrecemos? Plan de carrera personalizado. Beneficios sociales. Flexibilidad horaria. Modelo híbrido de trabajo, a elegir. Acceso al programa de certificaciones oficiales. Incorporación a una comunidad de profesionales altamente cualificados. ¡NTT DATA es tu sitio! Porque hemos obtenido en España, por 10º año consecutivo, la certificación Top Employer, que nos reconoce como una de las mejores empresas en las que trabajar, gracias a nuestro compromiso por el talento. Únete a un equipo que apuesta por el desarrollo integral de sus profesionales, elige el modelo de trabajo que mejor se adapte a ti, y colabora en un entorno diverso, donde cada persona tiene su propia singularidad.

Oversees biochemical activities for new molecules, manages analytical tasks, ensures method implementation, and provides technical support during audits.

Responsable de Calidad y Medio Ambiente para liderar proyectos, asegurar la calidad, gestionar incidencias y mantener certificaciones.

Mínimo 4 años en posición similar en QA o QC.Chemo, parte de INSUD PHARMA, es una empresa líder en la cadena de valor farmacéutica, comprometida con la innovación y la calidad en el desarrollo y fabricación de principios activos y productos farmacéuticos.En Chemo, valoramos el compromiso, la

Mínimo 4 años en posición similar en QA o QC.Chemo, parte de INSUD PHARMA, es una empresa líder en la cadena de valor farmacéutica, comprometida con la innovación y la calidad en el desarrollo y fabricación de principios activos y productos farmacéuticos.En Chemo, valoramos el compromiso, la

En pocas palabras Posición: QA Coordinator (Release - QC)Localización: LeónExperiencia: Mínimo 4 años en posición similar en QA o QC¿Quieres saber más? Chemo, parte de INSUD PHARMA, es una empresa líder en la cadena de valor farmacéutica, comprometida con la innovación y la calidad en e

In coordination with Quality Control Manager, suitable day-to-day organization within area and designated technicians and analysts. Manage all analytical tasks for Quality Control Projects bio related to new projects such as:. Quality Control Projects Supervisor (Bio).

En Capitole seguimos creciendo!.Y queremos que tú formes parte de uno de nuestros proyectos más estratégicos.Estamos buscando un/a QA Engineer Senior para incorporarse a un producto digital core de uno de nuestros clientes TOP.Si te apasiona la calidad, la automatización y formar parte de equipo

Along with Quality Control Manager, implementation and maintenance of all biochemical activities related to new molecules. In coordination with Quality Control Manager, suitable day-to-day organization within area and designated technicians and analysts. Manage all analytical tasks for Quality Contr

Buscas un nuevo reto donde desarrollar tu carrera y aprender nuevas tecnologías?.Entonces sigue leyendo porque esto te puede interesar.Scalian es una empresa de más de 6.Estamos especializados en dar servicios a diferentes clientes enfocados en Data, Cloud e Inteligencia Artificial.Buscamos un/a p

Specific ResponsibilitiesManage all analytical tasks for Quality Control Projects bio related to new projects such as:Projects follow up, using a suitable tool easy to follow Collaborate with R&D in design, adjustment, implementation, transfer of analytical methodsCollaborate with MSAT in process va

Quality & Patient Experience Manager.

The selected candidate will support the management and follow-up of quality activities related to the vehicle, working closely with the customer’s internal quality team. This role is ideal for candidates who have recently completed an internship in the automotive industry or who have approximately

Drive further adoption of unit, integration, and system testing; metrics to monitor code coverage; bug prevention strategies; and other quality measures. BS/BA in Computer Science or a related field, or equivalent years of experience in quality assurance.

Manage quality incidents and coordinate with the Client quality/buying team to resolve issues. As a Garment Quality Team Leader, you ensure that all garment quality standards of our global fashion client are consistently met. Evaluate and select optimal ironing and finishing methods, reporting quali

As our Quality Control Engineer, you will be the critical guardian of quality for our high-performance, AI-driven solutions and LLM services. Create and standardise quality control and reporting across projects. Act as the point of contact for quality validation on final deliverables.

Take your career to the next level with Amaris Consulting as a QA Hybrid Tester.Become part of an international team, thrive in a.Join Amaris Consulting, where you can.Identify, log and track defects.Join our dynamic team of talented individuals and experience a world of growth and opportunities.Gro

This role is ideal for those candidates who enjoy hands-on laboratory work, operating under GMP standard, and contributing to high-quality, safe production processes. Strong attention to detail, documentation accuracy and commitment to quality.