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Comercial especialista de seguros de empresas en Santander Assurance Solutions, S.A. (SASA) Somos Santander Assurance Solutions (SASA), nacimos hace 4 años y estamos en pleno desarrollo, por ello, buscamos incorporar a especialistas de seguros para nuestro canal de empresas. Nuestra misión consiste en dinamizar y comercializar el portfolio de seguros de nuestros clientes, poniendo en marcha los planes de acción necesarios, que cubran los retos que se esperan de nuestra compañia. Actividades & Responsabilidades: • Comercialización directa de todo tipo de seguros a empresas., • Realización de simulaciones y proyectos para ofrecer soluciones personalizadas a clientes., • Acompañamiento en visitas comerciales para presentar propuestas y establecer relaciones sólidas con los clientes corporativos., • Fomento de buenas prácticas y cruce de experiencias positivas dentro del equipo de ventas., • Planificación de agenda para optimizar la gestión del tiempo y las actividades comerciales., • Preparación detallada de visitas, incluyendo recopilación de datos, campañas vigentes, coberturas obligatorias, y seguimiento de planes de acción comprometidos en visitas anteriores., • Seguimiento constante de los objetivos marcados por la Dirección Comercial, ajustando estrategias según los resultados obtenidos., • Formación en el producto y en técnicas comerciales a nuestros clientes. ¿Qué perfil estamos buscando? • Titulación Universitaria / Grado o similar, • Requisito imprescindible titulación mediador de seguros grupo B / valorable grupo A, • Experiencia en sector asegurador y/o banca, con exposición comercial., • Habilidades de comunicación efectiva y capacidad para establecer relaciones sólidas con clientes., • Orientación a resultados, con habilidad para trabajar con metas comerciales y demostrada capacidad para alcanzar y superar objetivos de ventas., • Capacidad analítica y visión estratégica para identificar oportunidades de negocio, adaptar estrategias comerciales y tomar decisiones basadas en datos., • Usuario avanzado de paquete Office. Y, ¿por qué SASA? Porque estamos comprometidos con el bienestar de las personas y esto define lo que hacemos y cómo lo hacemos. Nos encantan los retos y creemos en el desarrollo de las personas, que son las que hacen posible un futuro mejor y más sostenible. ¿Qué ofrecemos? • Contrato indefinido, • 25 días laborables de vacaciones + 1 extra por tu cumpleaños, • Seguro de vida y salud, • Horario flexible, • Recursos para que sigas formándote, • Jornada intensiva en época estival, • Y muchas cosas más!!!

📢Career Development Opportunity📢 Are you looking for an opportunity to develop your professional career in a CDMO Manufacturing Operations Department? From day one on, 3P Biovian has been inspired from the people that conforms it, and because of that matter, one of the main values of the company has always been the professional and personal growth of its employees in an international and biotechnological environment. Due to this prioritization, Navarra site of 3P Biovian is currently looking for professionals who want to focus their careers in Scale Up and Manufacturing department USP and DSP both. As 3P Biovian is committed to the continuous, updated and personalized improvement of our personnel´s learning, our Learning and Development department is focused in offering opportunities for professional growth and opting for an environment of trust. The successful candidate will join 3P Biovian, ini Navarra, Spain, as part of our Scale Up and Manufacturing department. The candidate will be expected to provide strategic development oversight know-how and technical input in specific tasks and in the group in general. In addition, the candidate will be involved in the manufacturing to obtain products (biomass or recombinant proteins) with the specifications required by our clients, in the execution of the tech transfer processes; as well as contribution to routine laboratory activities. What We´re looking for: • Experience in either Manufacturing departments in upstream and/or downstream processes, in the biotechnological industry., • People who have performed manufacturing activities in either the Upstream processing or Downstream processing area according to GMP guidelines, ensuring batch execution, evaluating test results, resolving issues and make proposals for resolution., • People who assists document preparation (e.g electronic batch records, SOPs) specific to the assigned manufacturing area., • Experience in working with bioreactor and filtration systems is desirable., • Experience in a GMP environment., • Proven initiative and independent thinking to deliver tasks on time, whilst working in a team environment., • A person capable to identify technical and scientific problems and discuss possible solutions., • Fluency in English is considered a plus., • Open to work in shifts. What We offer: • A permanent and stable position in a competitive growing company., • A competitive time off package with 39 paid days of vacation., • Additionally you will have an extra day off on the 26th of December., • Flexible 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.), • Company benefits club, which allows 3P Biovian employees to obtain exclusive prices and discounts on a multitude of products and services (Booking, FNAC, Rituals, El Corte Inglés etc.), • All new hires who reside outside Navarra are provided with a relocation service and/or assistance., • ...And so much more! Do you want to know us better? 🌟It´s within us.

📢 Are you looking for an opportunity to develop your professional career in a CDMO Quality Control Department? The successful candidate will join 3PBiovian as a QC Supervisor Technician Physicochemical Laboratory. 🚀Responsibilities: • Ensure GMP activities in the physicochemical laboratory., • Evaluate and review the technical documentation corresponding to the Quality Control of the physicochemical laboratory, as well as the analytical results in routine manufacturing, validation and transfer activities., • Organize and ensure compliance with the weekly program and coordinate human, material and technical resources to ensure its achievement., • Propose process improvements aimed at improving quality, cost, performance, time and safety of workers and the environment., • To train and qualify the analysts to carry out the controls correctly., • Maintain the installations in perfect state of conservation ensuring that they are operated according to the manuals provided by the manufacturer., • Carry out the drafting and supervision of standard operating procedures (SOP's)., • Carry out the resolution of deviations in the laboratory., • Coordinate the release of raw materials and the analysis of intermediates, drug substances and drug products., • Support stability studies agreed with our customers in collaboration with other technicians., • Provide production quality support in case of incidents that may arise., • Approve and close CAPAS (corrective and preventive actions) arising from deviations and applicable efficacy verification., • Check the correct traceability of the materials consumed in the analysis process., • Perform duties as assigned and for which job training has been received. 📖 Assesment criteria: • University Degree or equivalent in Chemistry; Biotechnology; Biology or similar., • Master's degree related to the area of study., • PhD in a related area is valued, but not necessary, • Intermediate level of English (B1 level / First Certificate), • Open to work in shifts. At least 4 years of work experience in/with: • Use of techniques such as HPLC, UV and IR Spectrophotometry, UPLC, Fluorescence, DAD, UV-VIS…, • Experience with recombinant proteins, mAbs, Biosimilar, ADCs (desirable)., • Experience with pharmaceutical regulatory guidelines., • Use of Agilent equipment with Empower 3 software. ❗️❗️Why 3PBiovian? • A permanent and stable position in a competitive growing company., • A competitive time off package with 39 paid days of vacation., • Additionally you will have an extra day off on the 26th of December., • Flexible 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.), • Company benefits club, which allows 3P Biovian employees to obtain exclusive prices and discounts on a multitude of products and services (Booking, FNAC, Rituals, El Corte Inglés etc.), • All new hires who reside outside Navarra are provided with a relocation service and/or assistance., • ...And so much more! 💥Why us? We know it takes people with passion and a shared purpose to manufacture advanced medicines. We 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 From 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. 🌟It's within us.

📢 Are you looking for an opportunity to develop your professional career in a CDMO Manufacturing Operations Department? The successful candidate will join 3PBiovian as a USP Manufacturing Technician. 🚀Responsibilities: • Ensure the timely compliance with the planning of the USP Scale-Up and Manufacturing department previously made by a Team leader., • Ensure the correct training of the personnel in charge., • Prepare, control and develop processes for the production of recombinant proteins, monoclonal antibodies or similar biological molecules in microorganisms., • Participate in internal / external audits as required by the Quality Assurance Department., • Comply and ensure compliance with GMP standards within the work team., • Record 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)., • Investigate and propose new methods or process innovations to optimize and improve the work in the area., • Ensure proper compliance with regulations and correct completion of current documentation., • Participate in the correct transfer of technologies and resources between companies related to 3P Biopharmaceuticals in collaboration with other departments and their manager., • Perform the entry documentation of new equipment from the USP Scale-up and Manufacturing area under the supervision of the Team Leader USP (FAB)., • Supervise the correct completion of the new equipment entry documentation., • Supervise the correct training of the personnel in charge, if any., • Carry out the distribution and supervision of daily activities., • Write and keep updated the documentation associated with the production processes carried out in the USP area., • Control / monitoring of orders placed in the USP production area using ERP software. 📖 Assesment criteria: • University Degree or equivalent in related areas (Pharmacy; Biology; Biochemistry; Biotechnology; Chemistry; IPPA; Chemical Engineering, cell culture etc.), • Desirable but not required Master's degree or equivalent in related fields (Biology; Biochemistry; Biotechnology; Chemistry; Organic Chemistry; IPPA; Chemical Engineering, etc.), • Intermediate level of English (Level B2 / First Certificate), • Open to work in shifts., • Software package: Office. User level. Between 1 and 2 years of experience in/with: • GMP/GLP regulations, • With bioreactors, • Cell Cultures, • Microbiological analysis techniques, • Upstream production positions, • Biotechnology / Biopharmaceutical Sector ❗️❗️Why 3PBiovian? • A permanent and stable position in a competitive growing company., • A competitive time off package with 41 paid days of vacation., • Additionally you will have an extra day off on the 23th of December., • Flexible 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.), • Company benefits club, which allows 3P Biovian employees to obtain exclusive prices and discounts on a multitude of products and services (Booking, FNAC, Rituals, El Corte Inglés etc.), • All new hires who reside outside Navarra are provided with a relocation service and/or assistance., • ...And so much more! 💥Why us? We know it takes people with passion and a shared purpose to manufacture advanced medicines. We 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 From 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. 🌟It's within us.

Incorpórate a una ingeniería líder en automatización industrial en Navarra En Gurpea Systems desarrollamos e integramos soluciones industriales avanzadas. Somos la ingeniería de referencia en Navarra, y lideramos proyectos de gran envergadura en los ámbitos de la robótica, la automatización, la visión artificial y la maquinaria especial. Trabajarás en una empresa consolidada, con reputación técnica contrastada y un equipo altamente cualificado. Participarás en proyectos líderes en innovación industrial, desarrollando soluciones para clientes de primer nivel. Somos una ingeniería en crecimiento constante, comprometida con la excelencia técnica y el desarrollo de nuestros profesionales. Buscamos incorporar a nuestro equipo un/a Técnico/a de Montaje y Puesta en Marcha Eléctrico/a con experiencia y una fuerte motivación por la tecnología y el trabajo bien hecho. Funciones: • Montaje eléctrico de maquinaria industrial según esquemas eléctricos y neumáticos., • Realización de pruebas de funcionamiento en taller., • Puesta en marcha en casa del cliente, garantizando la funcionalidad y calidad de la solución., • Montaje y ajuste de sistemas eléctricos y neumáticos., • Interpretación de documentación técnica, planos eléctricos y manuales. Ofrecemos: • Contrato indefinido desde el primer día., • Salario competitivo entre 32.000 y 36.000 euros brutos/año, en función de la experiencia, más variables (horas extra, plus de festivos, etc.) y paga adicional por beneficios., • Horario: jornada continua de lunes a viernes, de 7:00 a 15:00, con flexibilidad mutua según proyecto., • Conciliación: apostamos por la conciliación personal y profesional, siempre que la naturaleza del proyecto lo permita., • Convenio del Metal.14 pagas anuales (12 mensualidades más dos extras en junio y diciembre)., • Formación continua y desarrollo profesional dentro de un entorno técnico de alto nivel., • Retribución flexible: posibilidad de cheque guardería y seguro médico privado. Requisitos mínimos Requisitos: • Formación de Grado Superior en Mecatrónica Industrial, Automatización y Robótica, Sistemas Electrónicos o similar., • Experiencia en montaje eléctrico de maquinaria industrial., • Capacidad para leer e interpretar esquemas eléctricos y neumáticos., • Conocimiento en cableado de armarios (control, potencia, señales, comunicaciones)., • Persona responsable, con iniciativa y capacidad para resolver problemas técnicos., • Comprometida, con vocación técnica y orientación al trabajo en equipo., • Motivada por aprender, mejorar y participar en proyectos exigentes. Por qué Gurpea Systems: Trabajarás en una empresa consolidada, con reputación técnica contrastada y un equipo altamente cualificado. Participarás en proyectos líderes en innovación industrial, desarrollando soluciones de alto nivel para clientes de primer orden. Somos una ingeniería en crecimiento constante, comprometida con la excelencia técnica y el desarrollo de nuestros profesionales. Si buscas estabilidad, desarrollo y formar parte de un equipo técnico de referencia, esta es tu oportunidad.

Es un nio educado, muy alegre, sociable, divertido que acata con respeto las reglas y las normas establecidas, por lo que facilitar su manejo tanto en casa como en los paseos, necesitamos cuidado regular despus del cole y extra escolares mientras llegamos del trabajo.