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p3PBiovian is seeking an Automation Engineer to join their Engineering team in Navarra. The role focuses on programming manufacturing equipment and robotic systems, ensuring safe, compliant operations and seamless interfaces between machinery and control systems. /ppYou will drive process improvements, support upgrades, troubleshoot issues across pre- and post-sales, and manage technical and financial aspects of projects while complying with GMP standards. /p #J-18808-Ljbffr

ppWe are looking for a proactive, hands-on, and motivated bMaintenance Specialist /b to join our bMaintenance Department /b and support the reliable operation of our biopharmaceutical manufacturing facilities. /ph3Key Responsibilities: /h3pAs a bMaintenance Specialist /b, you will: /pulliEnsure accurate completion of maintenance records to guarantee full traceability of production-related activities in compliance with GMP requirements. /liliContribute to continuous improvement initiatives focused on enhancing quality, cost-efficiency, productivity, safety, and environmental performance. /liliMaintain facilities and equipment in optimal operating condition, following manufacturer guidelines and internal procedures. /liliExecute the annual preventive maintenance plan to ensure the proper functioning of plant equipment and utilities. /liliComplete and maintain equipment control records, validation logs, usage books, and departmental performance indicators. /liliDraft and update Standard Operating Procedures (SOPs) related to maintenance activities when assigned. /liliPerform corrective maintenance interventions across manufacturing equipment and facility systems. /liliCarry out maintenance operations required to ensure uninterrupted plant performance while complying with GMP standards. /li /ulh3Assessment Criteria: /h3h3Education: /h3ulliHigher Vocational Training (CFGS) in Mechanical, Electrical, Electronic, Electromechanical Engineering or a related technical field. /li /ulh3Languages: /h3ulliIntermediate English level (B1) is desirable. /li /ulh3Work Experience: /h3ulliMinimum 2 years of experience in industrial maintenance environments. /li /ulh3Nice to Have: /h3ulliPrevious experience working under GMP-regulated environments. /liliExperience maintaining industrial machinery and facility systems. /li /ulh3Key Competencies: /h3ulliTeamwork and collaboration skills. /liliQuick learning ability. /liliProactive attitude and problem-solving mindset. /li /ulh3Why 3PBiovian? /h3ulliA permanent and stable position in a competitive growing company. /liliA competitive time off package with 41 paid days of vacation. /liliFlexible compensation plan, allowing all employees to allocate up to 30% of their gross annual salary to daily services exempt from income taxes (childcare, health insurance, academic training etc.) /liliAll new hires who reside outside Navarra are provided with a relocation service and/or assistance. /liliCompany benefits club, which allows 3PBIOVIAN employees to obtain exclusive prices and discounts on a multitude of products and services (Booking, FNAC, Rituals, El Corte Inglés etc.) /lili3PBio is committed to the continuous, updated and personalized improvement of our personnel's learning. To this end, we have Learning Development department, who is in charge of creating personalized, individualized and differentiating career plans for our employees. /liliThe company continues to focus on internal talent and stable employment, focusing on upskilling and reskilling. We offer opportunities for professional growth and take an environment of trust. /liliWe encourage the participation of our employees in solidarity events such as charity races, social donations... /liliWe have several programs aimed at improving the physical, psychological and emotional well-being of our employees. In this context, we participate in the Corporate Challenge, promote healthy lunches and comfortable and safe work spaces. /liliWe have a high-impact work environment with flat hierarchies and short decision-making processes. /lili...And so much more! /li /ulh3Why us? /h3pWe know it takes people with passion and a shared purpose to manufacture advanced medicines. /ppWe specialize in process development and GMP manufacturing of biologics and cell therapy products using microbial and mammalian expression systems. We are with you on your biologics journey, growing with you and supporting you with process and analytical development, preclinical and clinical supply, and commercial production. With a focus on biotechnology applications in both human and animal health sectors, we offer customized solutions that meet the specific needs of all our clients /ppFrom development to product delivery, we are with you on your biologics journey. We are a leading global CDMO and preferred partner for pharmaceutical and biotech companies. We have what it takes to help you improve lives. /ph3It's within us. /h3 /p #J-18808-Ljbffr

ppTécnico/a de Desarrollos informático (H/M/D) /p ul liUbicación: Navarra, Imárcoain (CP 31119) /li liTipo de contrato: Eventual (6 meses) + posibilidad transformación a indefinido /li liJornada: Completa (Lunes a Viernes) /li liSalario: 24.000 – 27.000 € brutos/año /li /ul h3Qué harás en tu día a día /h3 ul liDesarrollar y mantener aplicaciones utilizando C# y .NET. /li liDesarrollar, integrar y consumir Web Services y APIs REST. /li liDiseñar y mantener consultas, procedimientos y desarrollos sobre bases de datos Oracle y SQL. /li liAnalizar y resolver incidencias técnicas de las aplicaciones existentes. /li liMantener y evolucionar aplicaciones desarrolladas en VB / VB.NET. /li liIntegrar aplicaciones con diferentes sistemas y servicios externos. /li liColaborar con el equipo técnico en el análisis de requisitos y la definición de soluciones. /li liElaborar y mantener la documentación técnica de los desarrollos realizados. /li /ul h3¿Qué buscamos? /h3 ul liExperiencia desarrollando con C# y .NET. /li liConocimientos de Web Services y APIs REST. /li liExperiencia trabajando con bases de datos Oracle y SQL. /li liConocimientos de VB / VB.NET para el mantenimiento de aplicaciones existentes. /li liCapacidad analítica, orientación a la resolución de problemas y trabajo en equipo. /li /ul h3Valoraremos especialmente /h3 ul liExperiencia con .NET Framework, .NET Core y versiones .NET 6, 7, 8 o superiores. /li liConocimientos de ASP.NET y ASP.NET Core. /li liExperiencia en integración de sistemas y aplicaciones empresariales. /li liManejo de Git como sistema de control de versiones. /li liExperiencia administrando o desplegando aplicaciones mediante IIS. /li liConocimientos de JSON, XML y otros formatos de intercambio de información. /li liExperiencia utilizando herramientas de Inteligencia Artificial aplicadas al desarrollo de software, como asistentes de programación, generación y revisión de código, depuración y optimización de aplicaciones. /li /ul h3¿Qué te ofrecemos? /h3 ul liProyecto estable con contratación eventual + posibilidad transformación a indefinido /li liDesarrollo profesional y oportunidades de crecimiento dentro de un grupo logístico en constante evolución. /li liUn entorno de trabajo dinámico, colaborativo y cercano, donde las personas marcan la diferencia. /li liLa oportunidad de participar en proyectos tecnológicos con impacto real en todas las delegaciones y unidades de negocio del Grupo. /li liFormación continua y posibilidad de seguir desarrollando tus conocimientos en un entorno innovador. /li liRetribución competitiva, acorde a tu experiencia y trayectoria profesional /li /ul h3Requisitos mínimos /h3 ul liExperiencia de al menos 2 años desarrollando aplicaciones con C# y .NET. /li liGrado en Ingeniería Informática, Ingeniería del Software o similar; o Ciclo Formativo de Grado Superior en Desarrollo de Aplicaciones Multiplataforma (DAM), Desarrollo de Aplicaciones Web (DAW) o titulaciones equivalentes. /li /ul pG1 /p p#Disayt /p /p #J-18808-Ljbffr

ppWe are looking for a proactive, rigorous and adaptable bQuality Control Biological Laboratory Manager /b to join our Quality Control Department. /p pMain Responsibilities: /p pAs a bQuality Control Biological Laboratory Manager /b, your responsibilities will include: /p ul liPlanning and coordination of laboratory activities, ensuring compliance and effective management of human resources according to operational needs. /li liGuarantee the accuracy of the results issued by the Laboratory. /li liManage, supervise and generate technical documentation associated such as: SOPs and CoAs. /li liCoordinate the correct state of work equipment according to GMP requirements and technical data sheets. /li liManage and investigate OOS and deviations as needed. /li liEnsure the application of GMP requirements and the correct training of the personnel in charge. /li /ul pAssesment criteria: /p pEducation: /p ul liUniversity degree or equivalent in Chemistry, Biochemistry; Biology; Biotechnology or related areas. /li liMaster's degree in Chemistry; Biochemistry; Biology; Biotechnology or related areas. /li liPhD in related areas is desirable, but not necessary /li /ul pLanguages: Fluent in Spanish. Intermediate level of English (Level B2 / First Certificate). /p pAt least 4 years of experience with/ in: /p ul liExperience on GMP regulations. /li liExtensive technical knowledge on molecular biology assays (SDS-Page, ELISA, qPCR, microbiology, bioassays). /li liExperience in international environments is a plus. /li liExperience on cell bioassay is a plus. /li liManaging a technical team in a Laboratory. /li /ul pWhy 3PBiovian? /p ul liYou will have 26 paid days off: 23 vacation days + 2 personal days + 1 day off set by the company. /li liFlexible compensation plan, allowing all employees to allocate up to 30% of their gross annual salary to daily services exempt from income tax (childcare, health insurance, training, etc.). /li liCompany benefits club, which allows 3P employees to obtain exclusive prices and discounts on a multitude of products and services (Booking, Fnac, Rituals, El Corte Inglés, etc.). /li liFlexible working hours during the week and a reduce work day on Friday of 7h. /li liSpecial Summer working day of 7 hours during July and August, as well as 7-hour working days during the first week of September and the last week of December. /li li3PBio is committed to the continuous, updated and personalized improvement of our personnel's learning. To this end, we have Learning Development department, who is in charge of creating personalized, individualized and differentiating career plans for our employees. /li liThe company continues to focus on internal talent and stable employment, focusing on upskilling and reskilling. We offer opportunities for professional growth and take an environment of trust. /li liWe encourage the participation of our employees in solidarity events such as charity races, social donations... /li liWe have several programs aimed at improving the physical, psychological and emotional well-being of our employees. In this context, we participate in the Corporate Challenge, promote healthy lunches and comfortable and safe work spaces. /li liWe have a high-impact work environment with flat hierarchies and short decision-making processes. /li liAll new hires who reside outside of Navarra are provided with a relocation service and/or assistance. /li /ul pWhy us? /p pWe know it takes people with passion and a shared purpose to manufacture advanced medicines. /p pWe specialize in process development and cGMP manufacturing of biologics and cell therapy products using microbial and mammalian expression systems. We are with you on your biologics journey, growing with you and supporting you with process and analytical development, preclinical and clinical supply, and commercial production. With a focus on biotechnology applications in both human an animal health sectors, we offer customized solutions that meet the specific needs of all our clients. /p pFrom development to product delivery, we are with you on your biologics journey. We are a leading global CDMO and preferred partner for pharmaceutical and biotech companies. We have what it takes to help you improve lives. /p pIt's within us. /p /p #J-18808-Ljbffr

pp We are looking for a results-driven, enthusiastic and proactive bUpstream Technician /bto join our Manufacturing Operations Department. /p pAs a bUSP Manufacturing Technician /b, your responsibilities will include: /p ul liEnsure the timely compliance with the planning of the USP Scale-Up and Manufacturing department previously made by a Team leader. /li liEnsure the correct training of the personnel in charge. /li liPrepare, control and develop processes for the production of recombinant proteins, monoclonal antibodies or similar biological molecules in microorganisms. /li liParticipate in internal / external audits as required by the Quality Assurance Department. /li liComply and ensure compliance with GMP standards within the work team. /li liRecord and manage any quality indicators associated with a scale-up and manufacturing process. Participate in the investigation of the same together with the Team Leader USP (FAB). /li liInvestigate and propose new methods or process innovations to optimize and improve the work in the area. /li liEnsure proper compliance with regulations and correct completion of current documentation. /li liParticipate in the correct transfer of technologies and resources between companies related to 3P Biopharmaceuticals in collaboration with other departments and their manager. /li liPerform the entry documentation of new equipment from the USP Scale-up and Manufacturing area under the supervision of the Team Leader USP (FAB). /li liSupervise the correct completion of the new equipment entry documentation. /li liSupervise the correct training of the personnel in charge, if any. /li liCarry out the distribution and supervision of daily activities. /li liWrite and keep updated the documentation associated with the production processes carried out in the USP area. /li liControl / monitoring of orders placed in the USP production area using ERP software. /li /ul pbEducation: /bBachelor's degree in Pharmacy; Biology; Biochemistry; Biotechnology; Chemistry; IPPA; Chemical Engineering, cell culture etc . Desirable but not required Master's degree or equivalent in related fields. /p pbLanguages: /bFluent in Spanishb. /bIntermediate level of English (Level B2 / First Certificate). /p pbBetween 1 and 2 years of experience in/with: /b /p ul liGMP/GLP regulations /li liWith bioreactors /li liCell Cultures /li liMicrobiological analysis techniques /li liUpstream production positions /li liBiotechnology / Biopharmaceutical Sector /li /ul pbOther requirements: /b /p ul liOpen to work in shifts. /li liA permanent and stable position in a competitive growing company. /li liA competitive time off package with 41 paid days of vacation. /li liFlexible compensation plan, allowing all employees to allocate up to 30% of their gross annual salary to daily services exempt from income taxes (childcare, health insurance, academic training etc.) /li liAll new hires who reside outside Navarra are provided with a relocation service and/or assistance. /li liCompany benefits club, which allows 3PBIOVIAN employees to obtain exclusive prices and discounts on a multitude of products and services (Booking, FNAC, Rituals, El Corte Inglés etc.) /li li3PBio is committed to the continuous, updated and personalized improvement of our personnel's learning. To this end, we have Learning Development department, who is in charge of creating personalized, individualized and differentiating career plans for our employees. /li liThe company continues to focus on internal talent and stable employment, focusing on upskilling and reskilling. We offer opportunities for professional growth and take an environment of trust. /li liWe encourage the participation of our employees in solidarity events such as charity races, social donations... /li liWe have several programs aimed at improving the physical, psychological and emotional well-being of our employees. In this context, we participate in the Corporate Challenge, promote healthy lunches and comfortable and safe work spaces. /li liWe have a high-impact work environment with flat hierarchies and short decision-making processes. /li li...And so much more! /li /ul pWe know it takes people with passion and a shared purpose to manufacture advanced medicines. /p pWe specialize in process development and GMP manufacturing of biologics and cell therapy products using microbial and mammalian expression systems. We are with you on your biologics journey, growing with you and supporting you with process and analytical development, preclinical and clinical supply, and commercial production. With a focus on biotechnology applications in both human and animal health sectors, we offer customized solutions that meet the specific needs of all our clients /p pFrom development to product delivery, we are with you on your biologics journey. We are a leading global CDMO and preferred partner for pharmaceutical and biotech companies. We have what it takes to help you improve lives. /p /p #J-18808-Ljbffr

p3PBIOVIAN is seeking a proactive Maintenance Specialist to join our Maintenance Department and support the reliable operation of our biopharmaceutical manufacturing facilities. You will execute preventive maintenance, maintain records, and contribute to GMP-compliant processes while driving continuous improvement and ensuring plant uptime. /ppThe role offers a permanent position with growth opportunities, relocation assistance for candidates outside Navarra, and a comprehensive benefits package /p #J-18808-Ljbffr

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