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Leanbio is a leading Biopharmaceutical CDMO offering end-to-end services in the field of recombinant proteins, mRNA and pDNA. With over a decade of expertise, we have a proven track record in development and manufacturing of therapeutic molecules such as antibodies, Fab fragments, ADCs, enzymes, complex proteins, mRNA and pDNA. Leanbio has already worked with over 100 candidates over these years, some already in late clinical stages. Leanbio is expanding its development and manufacturing capabilities with a new GMP site in Barcelona with over 4,000 sqm. and three manufacturing areas: one for mammalian expression systems up to 2000L, another for microbial and yeast up to 1000L, and a third are for mRNA up to 50L. The new facility includes state-of-the-art development laboratories, oustanding Quality control rooms and warehouse. Leanbio is a global service provider for the development and manufacturing of biologics. Our commitment to excellence is evident in everything we do: • Prioritizing customer satisfaction., • Providing cutting-edge end-to-end services., • Utilizing state-of-the-art facilities., • Offering extensive expertise in biologics. We are looking for a new person to join the QC as an analyst to work in our brand new facilities in Sant Quirze del Vallès: MAIN RESPONSIBILITIES: • Perform routine and non-routine physicochemical analyses of raw materials, intermediates, and finished products using techniques such as:HPLC (High-Performance Liquid Chromatography), Karl Fischer titration (moisture determination), FTIR / IR (identification of materials), Loss on Drying (LOD), Potentiometric titrations, Residue on Ignition (ROI), pH, conductivity, osmolality, TOC, etc., • Carry out sampling and analysis of water systems, including:Water for Injection (WFI), • Support environmental monitoring activities, including:surface and air sampling in classified areas., • Ensure strict adherence to GMP and ALCOA++ data integrity principles, maintaining complete, accurate, and traceable documentation., • Document all activities clearly and contemporaneously in lab notebooks, logbooks, or electronic systems (e.g., LIMS), in compliance with internal SOPs., • Participate in quality system activities, such as investigation of OOS / OOT results reporting of deviations and support in CAPA implementation., • Maintain and calibrate laboratory equipment, performing routine checks and informing of any malfunction or need for maintenance., • Follow safety protocols and contribute to keeping the lab in a clean condition at all times., • Collaborate with cross-functional teams, including QA, production, and validation, when needed. REQUIREMENTS: • Advanced Training in Laboratory Analysis and Control with 2–5 years of experience in Quality Control in a GMP-regulated pharmaceutical environment., • Practical experience in physicochemical testing including HPLC, Karl Fischer, IR, Loss on Drying, potentiometric titrations, and Residue on Ignition., • Skilled in sampling and analysis of pharmaceutical water systems (WFI, Purified Water) following USP/EP methods., • Familiarity with environmental monitoring in cleanroom environments is an asset., • Strong knowledge of ALCOA++ principles and GMP documentation practices., • Experience with quality systems (OOS, deviations, CAPAs, change control)., • Proactive team player with good organizational skills and the ability to work independently., • Fluent in Spanish with basic to intermediate English communication skills (reading/writing preferred).

Leanbio is a leading Biopharmaceutical CDMO offering end-to-end services in the field of recombinant proteins, mRNA and pDNA. With over a decade of expertise, we have a proven track record in development and manufacturing of therapeutic molecules such as antibodies, Fab fragments, ADCs, enzymes, complex proteins, mRNA and pDNA. Leanbio has already worked with over 100 candidates over these years, some already in late clinical stages. Leanbio is expanding its development and manufacturing capabilities with a new GMP site in Barcelona with over 4,000 sqm. and three manufacturing areas: one for mammalian expression systems up to 2000L, another for microbial and yeast up to 1000L, and a third are for mRNA up to 50L. The new facility includes state-of-the-art development laboratories, oustanding Quality control rooms and warehouse. Leanbio is a global service provider for the development and manufacturing of biologics. Our commitment to excellence is evident in everything we do: • Prioritizing customer satisfaction., • Providing cutting-edge end-to-end services., • Utilizing state-of-the-art facilities., • Offering extensive expertise in biologics. We are looking for a new person to join the QC as a Bioassay analyst to work in our brand new facilities in Sant Quirze del Vallès: MAIN RESPONSIBILITIES: • Perform cell proliferation methods and others bioassays to verify the potency of biotechnology products, according to to USP, EP, and internal methodologies., • Cell bank production, caracterization and release management., • Maintain detailed and contemporaneous records in laboratory notebooks, logbooks, or electronic systems (LIMS)., • Participate in quality system activities including investigation of OOS/OOT microbiological results, deviation reporting, and support in CAPA implementation., • Maintain laboratory equipment calibration and functionality and promptly report any malfunctions or maintenance needs., • Follow all biosafety and safety protocols contributing to maintaining a clean, organized, and compliant laboratory environment., • Collaborate effectively with QA, production, validation, and other cross-functional teams to support quality assurance and compliance. REQUIREMENTS: • Advanced training in bioassays analysis with 2 to 5 years of proven experience in Quality Control within a GMP-regulated pharmaceutical environment., • Practical expertise in bioassays used in biotechnology, including cell proliferation assay, following USP and EP methods., • Skilled in cell culture. Strong knowledge of ALCOA++ data integrity principles and GMP documentation practices., • Experienced in managing quality systems including Out of Specification (OOS) investigations, deviation reporting, CAPA implementation, and change control., • Proactive team player with strong organizational skills and the ability to work independently while ensuring strict compliance with regulatory requirements., • Fluent in Spanish with basic to intermediate English communication skills (reading and writing preferred).

Leanbio is a leading Biopharmaceutical CDMO offering end-to-end services in the field of recombinant proteins, mRNA and pDNA. With over a decade of expertise, we have a proven track record in development and manufacturing of therapeutic molecules such as antibodies, Fab fragments, ADCs, enzymes, complex proteins, mRNA and pDNA. Leanbio has already worked with over 100 candidates over these years, some already in late clinical stages. Leanbio is expanding its development and manufacturing capabilities with a new GMP site in Barcelona with over 4,000 sqm. and three manufacturing areas: one for mammalian expression systems up to 2000L, another for microbial and yeast up to 1000L, and a third are for mRNA up to 50L. The new facility includes state-of-the-art development laboratories, oustanding Quality control rooms and warehouse. Leanbio is a global service provider for the development and manufacturing of biologics. Our commitment to excellence is evident in everything we do: • Prioritizing customer satisfaction., • Providing cutting-edge end-to-end services., • Utilizing state-of-the-art facilities., • Offering extensive expertise in biologics. We are looking for a new person to join the QA as a Specialist to work in our brand new facilities in Sant Quirze del Vallès: MAIN RESPONSIBILITIES: • To build, with the Head of Quality Assurance oversight, the Quality Management System creating and/or approving Standard Operating Procedures to support GMP manufacturing activities., • To build and manage the Documentation Management System and associated training., • To lead the supplier qualification program, approving new suppliers and managing supplier status during its life cycle., • To review Technical Agreements between the company and suppliers/clients., • To review batch documentation for release purposes., • To support facility, utilities and equipment qualification activities, approving protocols and final reports as well as managing related change control records. REQUIREMENTS: • Bachelor’s degree in a Science field with proven experience in GMP Quality Assurance roles., • In-depth knowledge managing Quality Management Systems (deviations, CAPA, change controls, audits and supplier qualification)., • Experience in batch release activities acting as QP deputy will be a plus., • Experience in facilities, utilities and equipment qualification., • Outstanding problem-solving and decision-making skills., • Team player, excellent verbal and written comunication skills (both Spanish and English) and strong analytical and organizatonal skills.

En Grupo IMAN, compañía nacional con amplia trayectoria y presencia multisectorial, buscamos incorporar a un/a Comercial para reforzar nuestro equipo en la zona del Vallès Occidental. Descripción del Puesto: La persona seleccionada será la encargada de la captación y desarrollo de nuevos clientes para cualquiera de las unidades de negocio del Grupo (trabajo temporal, selección, outsourcing, formación, prevención de riesgos laborales, facility services, etc.), adaptando nuestras soluciones a las necesidades específicas de cada cliente. Funciones principales: • Prospección activa de clientes potenciales en la zona asignada., • Presentación y comercialización de los servicios de las diferentes divisiones del grupo., • Elaboración de propuestas comerciales personalizadas., • Seguimiento continúo de las oportunidades abiertas hasta su cierre., • Negociación y cierre de acuerdos comerciales., • Coordinación con los equipos operativos para asegurar la correcta implantación del servicio., • Registro de la actividad comercial en el CRM., • Reporte de resultados a la dirección comercial. Requisitos: • Valorable Ciclo Formativo de Grado Superior o estudios universitarios, preferentemente en áreas de Empresariales, Recursos Humanos, Marketing o similares., • Experiencia mínima de 2 años en funciones comerciales B2B, valorándose especialmente en el sector servicios (ETT, outsourcing, RRHH, facility services, etc.)., • Residir en el Vallès Occidental., • Disponer de carnet B., • Conocimiento del tejido empresarial del Vallès Occidental será considerado un plus., • Catalán y castellano nativo., • Capacidad de negociación y comunicación. Iniciativa, autonomía y capacidad de organización. Y habilidad para establecer relaciones comerciales de confianza. ¿Qué ofrecemos? • Contratación indefinida., • Jornada completa de Lunes a Viernes en turno partido de 9 a 18 con una hora para comer a medio día., • Viernes alternos jornada intensiva., • Puesto de trabajo en las oficinas centrales del grupo ubicadas en Terrassa., • Paquete retributivo según experiencia y expectativas., • Vehículo de empresa o compensación por uso de vehículo propio., • Posibilidades de desarrollo profesional dentro del grupo. En GRUPO IMAN estamos comprometidos con la igualdad de género, por lo que este proceso se llevará a cabo respetando el principio de no discriminación e igualdad de oportunidades, y se basará en los méritos y las capacidades de las/os candidatas/os.

Leanbio is a leading Biopharmaceutical CDMO offering end-to-end services in the field of recombinant proteins, mRNA and pDNA. With over a decade of expertise, we have a proven track record in development and manufacturing of therapeutic molecules such as antibodies, Fab fragments, ADCs, enzymes, complex proteins, mRNA and pDNA. Leanbio has already worked with over 100 candidates over these years, some already in late clinical stages. Leanbio is expanding its development and manufacturing capabilities with a new GMP site in Barcelona with over 4,000 sqm. and three manufacturing areas: one for mammalian expression systems up to 2000L, another for microbial and yeast up to 1000L, and a third are for mRNA up to 50L. The new facility includes state-of-the-art development laboratories, oustanding Quality control rooms and warehouse. Leanbio is a global service provider for the development and manufacturing of biologics. Our commitment to excellence is evident in everything we do: • Prioritizing customer satisfaction., • Providing cutting-edge end-to-end services., • Utilizing state-of-the-art facilities., • Offering extensive expertise in biologics. We are looking for a new person to join the team as a Marketing Manager in our brand new facilities in Sant Quirze del Vallès: MAIN RESPONSIBILITIES: • Marketing strategy development and execution., • Lead generation and campaign management (digital, events, etc)., • Measure ROI and performance of all marketing activities using KPIs and analytics., • Content Creation & Brand Messaging. Create compelling, scientifically accurate content for web, social media, brochures, whitepapers, case studies, and videos. Maintain brand consistency across all platforms and communications., • Digital Marketing & Website Management., • Plan and manage company participation in events and fairs. Coordinate logistics, branding, promotional material, and follow-up activities with BD. Fairs preparation, assistance and follow-up., • Work creatively and analytically in a problem-solving environment demonstrating teamwork, innovation and excellence., • Market Intelligence & Competitive Analysis: Monitor market trends, customer needs, and competitor positioning in the DS/CDMO space. Provide insights and strategic recommendations to BD and leadership teams., • Business Development Support: develop marketing collateral (presentations, flyers, technical overviews) for the BD team., • Budget & Vendor Management: Manage the marketing budget, external agencies, designers, and other vendors to deliver cost-effective campaigns., • Stakeholder Collaboration: Work closely with internal teams (BD, Technical, PM, Regulatory) to ensure accurate, aligned messaging., • Act as the marketing voice within cross-functional planning and client targeting., • Collaborate on RFP responses and client-specific materials, if needed., • Participate in establishing practices, templates, policies, tools and partnerships to expand and mature these capabilities for the organization., • Develop and deliver progress reports, proposals, requirements documentation and presentations to various audiences, including project team, BD Director, sponsors, and other key stakeholders., • Deliver appropriate and effective executive level communication., • Continue professional development in order to keep abreast of emerging technologies, methods and best practices., • Support in Business Plans. REQUIREMENTS: • Bachelor's Degree in Marketing, Communications, Life Sciences or equivalent work experience., • MBA or master’s in marketing, Life Sciences, or Business is a plus., • 5+ years of marketing experience for complex services. At least 2 years in CDMO, pharma, or biotech industry., • 5+ years of experience working with business stakeholders within a cross-functional matrix environment., • 3+ years of previous experience with Market research and analysis, Digital Marketing (SEO, social media, content marketing, etc), and Data-Driven Decisions to measure ROI and performance., • Technical skills are also desirable. It will be highly desirable Industry-Specific Knowledge and deep understanding of the pharmaceutical value chain, regulatory environment (e.g., FDA, EMA), and B2B marketing dynamics in a CDMO setting. Ability to grasp and communicate technical aspects of drug development, manufacturing, and analytical services., • High English level to understand complex technical and business discussions (written and spoken), communicate fluently and effectively in professional settings. Write clear, well-structured messages, communications, and emails. Present ideas for marketing activities and adapt the communication style for different audiences (scientific, commercial, regulatory)., • Intermediate level of proficiency with CRMs (PipeDrive, Salesforce, etc), MS Project, Excel, Visio, PowerPoint and SharePoint with experience presenting to stakeholders and / or Senior Leadership., • Proven ability to demonstrate a drive for results and accountability of business needs., • Proven ability to work in an ambiguous environment and collaborate across multiple areas in order to achieve a common business objective., • Interpersonal skills to influence and spur change, facilitate and enhance performance within a cross - functional environment., • Demonstrate decisiveness in resolving business problems, making decisions and identifying priorities.