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ppPerfil académico Licenciatura o grado en Biología, Biología Celular, Microbiología, Biotecnología, Bioquímica o área equivalente. /ppValorable máster relacionado con biología molecular, biomedicina o enfermedades infecciosas. /ppNivel intermedio de inglés (lectura, hablado y escrito). Conocimientos básicos de herramientas de análisis de datos (por ejemplo Excel). /ph3Responsabilidades principales /h3ulliIntegrarte en la unidad de in vitro de Global Health Medicines RD y apoyar los proyectos activos relacionados con biología molecular in vitro. /liliPlanificar y ejecutar experimentos de biología molecular: PCR (convencional y cuantitativa), clonaje, preparación y manejo de ácidos nucleicos, y apoyo a ensayos de secuenciación. /liliRealizar manipulación y análisis de proteínas utilizando ensayos de cuantificación (por ejemplo, BCA) y técnicas de western blot. /liliEjecutar y mantener cultivos de líneas celulares de macrófagos (por ejemplo, THP-1 u otras líneas relevantes), incluyendo mantenimiento rutinario y preparación de ensayos funcionales. /liliTrabajar con enterobacterias, incluyendo manejo y cultivo de E. coli y Salmonella, siguiendo estrictamente los procedimientos de bioseguridad establecidos. /liliColaborar en la puesta a punto y caracterización de vesículas extracelulares (aislamiento, cuantificación y análisis básico). /liliTrabajar en laboratorios de bioseguridad nivel 2 y 3, siguiendo los procedimientos de seguridad, las normas de calidad y la documentación asociada. /liliManejar lectores de placas, dispensadores, lavadores y otros equipos de laboratorio automatizados necesarios para los ensayos. /liliProcesar, analizar y comprobar la calidad de los datos experimentales utilizando Excel y otras herramientas de análisis de datos disponibles en el equipo. /liliRecopilar datos, preparar informes y presentaciones de resultados experimentales para reuniones internas. /li /ulh3Requisitos mínimos /h3ulliExperiencia práctica en laboratorio adquirida mediante asignaturas prácticas, trabajo fin de grado/máster o estancias previas. /liliConocimientos básicos y manejo práctico de técnicas de biología molecular y celular. /liliHabilidades de comunicación escrita y oral en español, y nivel intermedio de inglés para leer bibliografía, discutir resultados y trabajar con equipos internacionales. /liliDisponibilidad para trabajar de forma presencial en el laboratorio. /liliCapacidad de trabajo en equipo y adaptación a un entorno multidisciplinar. /liliCompromiso con el cumplimiento de las normas de seguridad y calidad en laboratorio BSL2 y BSL3. /li /ulh3Cualificaciones deseables /h3ulliExperiencia previa con cultivos celulares y trabajo con bacterias como E. coli y Salmonella. /liliFamiliaridad con técnicas avanzadas de análisis de ácidos nucleicos y proteínas. /liliExperiencia o interés en el manejo y caracterización de vesículas extracelulares. /liliConocimientos básicos de ensayos basados en placas (ensayos de viabilidad, curvas dosis–respuesta, cinéticas de acción de compuestos). /liliManejo básico de herramientas de análisis de datos (Excel, Spotfire u otras herramientas estadísticas/gráficas). /liliExperiencia previa en laboratorios de bioseguridad nivel 2 o 3*, o formación específica en bioseguridad. /li /ulh3Lo que valoramos en ti /h3ulliMentalidad resolutiva y ganas de aprender. /liliCuriosidad científica e iniciativa para proponer mejoras en ensayos y procesos. /liliAtención al detalle y rigurosidad en la ejecución de experimentos y el análisis de datos. /liliCapacidad para trabajar de forma autónoma una vez formado, manteniendo una comunicación fluida con el equipo. /li /ulh3¿Qué ofrecemos? /h3ulliBolsa de ayuda de 900,00€ brutos mensuales 8h. diarias en Jornada completa /liliBeca de 1 año de duración /lili25 días de vacaciones durante todo el año /liliComedor gratuito en las instalaciones /liliCentro de prácticas en España: Severo Ochoa, 2 Tres Cantos (Madrid) /liliLa beca incluye matrícula en Programa CITIUS de Iniciación profesional en la Empresa (Universidad Autónoma de Madrid) /li /ulpSkills Biotechnology, Cell Biology, Data Quality, Following Instructions, Interpersonal Communication, Life Science, Listening Effectively, Molecular Biology, Proper Documentation, Scientific Research /ppThis is a temporary internship opportunity focused on professional development. Any reimbursement, scholarship, allowance, or financial support will be provided in accordance with applicable local laws, regulations, and GSK site policies. More detailed information will be provided during the recruitment process. /ppSe trata de una oportunidad de prácticas de carácter temporal, orientada al desarrollo profesional. Los gastos elegibles, así como las becas o tasas podrán ser reembolsados de acuerdo con la legislación local aplicable, la normativa vigente o la política del centro de GSK. Se proporcionará información más detallada durante el proceso de selección. /ppWhy GSK? Uniting science, technology and talent to get ahead of disease together. GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases – to impact health at scale. People and patients around the world count on the medicines and vaccines we make, so we’re committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people. /ppShould you require any reasonable adjustments or arrangements to support you during the recruitment process, specific to your individual needs, please contact us on Please note should your enquiry not relate to adjustments, we will not be able to support you through these channels. GSK is an Equal Opportunity Employer. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), parental status, national origin, age, disability, genetic information (including family medical history), military service or any basis prohibited under federal, state or local law. /ppWe are a global biopharma company with a special purpose – to unite science, technology and talent to get ahead of disease together – so we can positively impact the health of billions of people and deliver stronger, more sustainable shareholder returns – as an organisation where people can thrive. Getting ahead means preventing disease as well as treating it, and we aim to impact the health of 2.5 billion people around the world in the next 10 years. Our success absolutely depends on our people. While getting ahead of disease together is about our ambition for patients and shareholders, it’s also about making GSK a place where people can thrive. We want GSK to be a place where people feel inspired, encouraged and challenged to be the best they can be. A place where they can be themselves – feeling welcome, valued and included. Where they can keep growing and look after their wellbeing. So, if you share our ambition, join us at this exciting moment in our journey to get Ahead Together. Find out more on our career site. /p /p #J-18808-Ljbffr

pulliExperience: Minimum 2 years of relevant experience /li /ul pbWant to know more? /b /p pAt Algenex, we are passionate about advancing biotechnology through the development and manufacturing of recombinant proteins for the formulation of biological medicines. /p pWe are currently looking for an Analytical Development Technician to join our team in Tres Cantos, Madrid. This is an excellent opportunity for a laboratory professional who wants to contribute to analytical development activities in a growing and innovative environment, supporting projects with real impact on the future of biologic products. /p pIf you enjoy combining scientific rigor, technical execution, problem-solving, cross-functional collaboration, and high-quality analytical work in a regulated environment, this role could be your next challenge. /p h3What are we looking for? /h3 pWe are looking for a proactive, detail-oriented, and scientifically driven professional with experience in analytical development, analytical validation, or quality control within the biopharmaceutical or biotechnology industry. /p pIn this role, you will contribute to the development, qualification, and validation of analytical methods, support product development across different stages, and help ensure robust, reliable, and compliant analytical data. /p h3The challenge! /h3 ul liDevelop, qualify, and validate new analytical methods, identifying technical challenges and performing troubleshooting, optimization, and robustness activities. /li liExecute analytical tasks autonomously in support of different stages of Analytical Development and/or Analytical Validation. /li liDesign, follow, review, and contribute to analytical protocols, methods, and departmental procedures. /li liOrganize, analyze, and interpret scientific data, ensuring the technical consistency and reliability of results. /li liDocument activities and results accurately and on time in accordance with cGxP, regulatory requirements, and internal procedures. /li liPlan, execute, analyze, and document stability and validation studies. /li liDraft and review technical documentation such as SOPs, analytical methods, validation protocols, stability plans/protocols, and technical reports. /li liParticipate in the training and onboarding of new team members in analytical techniques, equipment, documentation best practices, safety, and internal workflows. /li liManage and maintain the inventory and status of reagents, standards, and samples, ensuring operational availability. /li liCommunicate effectively with peers, supervisors, and management regarding activity status, risks, and potential deviations. /li liExecute sample testing to support development activities across all product stages, including process development, formulation, characterization, and comparability, when applicable. /li liGenerate and execute validation and stability protocols/plans and associated reports, including sampling point tracking, trending, and result evaluation. /li liPrepare and manage solutions, buffers, standards, and controls. /li liRecord results and observations in a timely and accurate manner, ensuring data integrity and right-first-time documentation. /li liReview and consolidate documentation and results generated by the team when applicable, ensuring complete and consistent records, traceability, and compliance with ALCOA+ principles. /li liProvide support to other company areas depending on business needs and company priorities. /li /ul h3What do you need? /h3 ul liMS, BS, or Higher Vocational Training in Clinical and Biomedical Laboratory or other Life Sciences-related disciplines. /li liMinimum 2 years of relevant experience in the biopharmaceutical or biotechnology industry in analytical development, analytical validation, or quality control. /li liKnowledge and hands-on experience in the development, qualification, and validation of analytical methods for biological products. /li liPractical experience working with biological samples and analytical techniques, including: /li liHPLC: SEC, IEX, Reverse Phase, and Normal Phase /li liELISA: direct, indirect, sandwich, and inhibition /li licIEF /li liCE-SDS /li liWestern Blot /li liSDS-PAGE /li liqPCR /li liUV/Vis /li liOther relevant analytical techniques /li liExperience working in regulated environments and managing technical documentation accordingly. /li liStrong scientific data analysis and interpretation skills. /li liExperience with cGxP, ALCOA+, and technical documentation will be highly valued. /li /ul pFlexible start time from Monday to Friday (full-time) /p ul liBenefits and Savings Club /li liTraining and language learning platform /li liWellness platform with unlimited free psychologist sessions /li liDevelopment plans and internal mobility policy /li /ul h3What will the selection process look like? /h3 ul liInitial contact by phone /li li2 interview stages /li liFinal feedback at the end of the process /li /ul h3Do you think this role is not for you? /h3 pStay connected with Algenex and follow our upcoming opportunities. The right next step in your career might be just around the corner. /p h3EQUAL OPPORTUNITY COMMITMENT /h3 pAt Algenex, we are committed to equal opportunities and to fostering a diverse, inclusive, and respectful workplace. All applications will be considered without discrimination based on gender, gender identity or expression, ethnicity, nationality, religion, sexual orientation, age, disability, or any other characteristic protected by applicable law. /p /p #J-18808-Ljbffr