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Imagina formar parte de una empresa en constante movimiento, donde las soluciones surgen de la escucha y se materializan a través del aporte de cada persona que conforma nuestro ecosistema. Nuestro propósito es claro: gestionar el textil para crear valor con soluciones sostenibles. Construimos un modelo empresarial diferente que impulsa un cambio social y ambiental positivo, transformando la diversidad en inclusión, donde #TODOSSUMAMOS. Contamos con un equipo de más de 6.400 personas distribuidas en 45 plantas industriales, la mayoría Centros Especiales de Empleo, superando el 75% de personas con discapacidad y, ofreciendo cobertura total en España, Colombia y Portugal. En el transcurso de este crecimiento, queremos que nos acompañes como Jefe/a de Producción, teniendo la oportunidad de incorporarte al equipo de Beriain. ✅ Marcarás la diferencia: Te encargarás de supervisar las líneas de producción durante todo el proceso garantizando el flujo de la cadena, cumpliendo el plan de trabajo establecido y controlando el desempeño del personal, así como el de la maquinaria. Además, entre tus funciones estarán las siguientes: • Elaboración de cuadrantes, teniendo en cuenta turnos y horarios., • Participación en el informe de accidentes y registros de prevención de riesgos laborales., • Control del uso y stock de los EPIS., • Control de Calidad, atención a clientes/as y resolución de incidencias., • Supervisión del proceso de producción y la calidad del producto., • Coordinación con mantenimiento de posibles paradas preventivas y técnicas que afecten a producción., • Mantenimiento de la herramienta de gestión de la producción y análisis de sus informes, mejoras en procesos, maquinaría, personal, etc., • Favorecer la integración de los trabajadores/as en los Centros Especiales de Empleo. 🏆 ¿Qué te hará triunfar en esta posición? Si eres la persona que buscamos, graduado/a en ingeniería química o industrial, con conocimientos informáticos en Office y SAP, y experiencia mínima de 2 años, esta oportunidad puede ser para ti. Además, valoramos otras formaciones regladas con experiencia demostrable en el área, y que dispongas del certificado de discapacidad igual o superior al 33%. 🌟 Ventajas de ser parte de este reto • Cultura inclusiva: Un ambiente colaborativo donde valoramos la diversidad y el desarrollo de las personas, impactando positivamente en nuestros clientes y la sociedad., • Retribución flexible: organiza tu retribución con PayFlow., • Cultura de aprendizaje: El desarrollo profesional es clave. Ofrecemos formación continua para tu crecimiento., • Beneficios: Programa de Ayuda al Empleado, talleres relacionados con la salud y el bienestar, Tarjeta +ONCE y descuentos por pertenecer a ILUNION. 🚀 ¿Esta vacante te entusiasma? ¡Inscríbete ahora! Y si piensas que hay alguien más a quien podría interesarle, recuerda: ¡Compartir es cuidar!

📢We are looking for a Technical Services Technician to join our Technical Services Team. 🚀Main Responsibilities: As Technical Services Technician, your responsibilities will include: • Responsible of the execution of the Tech Transfer Policies of the department according to the in-force SOP’s., • Responsible of design of process scale up according to the in-force SOP’s., • Responsible of the execution of the Validation activities in agreement with the in-force SOP’s., • Prepare and execute the protocols corresponding to the Tech Transfer policies in a Biotech industry, not only from customer to facility but also among departments., • Evaluate the technical documentation of the potential processes to be transferred., • Follow-up the Tech Transfer runs and Scale-Up batches in order to assure the right performance of these batches. Prepare the Tech Transfer report., • Prepare and execute Cleaning, Process and Analytical Validation Protocols., • Coordinate the execution of the Validation Campaigns., • Lead the risk analysis sessions following HAZOP/FMEA methodologies., • Prepare URS’s of the equipment needed for the execution of a certain project as well as the internal documentation for the right management of the equipment., • Comply and assure the compliance of the GMP regulations. 📚Assessment Criteria: • Bachelor’s degree in Science, Chemical Engineering, or any other related discipline is required., • 5 years of experience in tech transfer activities of Biological processes, internal and external tech transfer., • At least 5 years of experience in process validation and cleaning validation activities, desirable in a biotech company., • Experience in risk analysis and HAZOP/FMEA methodologies., • Expert in GMP regulations., • Fluent in English 💊Why 3PBiovian? • You will have 26 paid days off: 23 vacation days + 2 personal days + 1 day off set by the company., • Flexible 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.)., • Company 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.)., • Flexible working hours during the week and a reduce work day on Friday of 7h., • Special Summer working day of 7h during July and August., • 3PBio 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., • The 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., • We encourage the participation of our employees in solidarity events such as charity races, social donations..., • We 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., • We have a high-impact work environment with flat hierarchies and short decision-making processes., • All new hires who reside outside of Navarra are provided with a relocation service and/or assistance. 💥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.

📢The successful candidate will join 3PBiovian as a Senior Quality Assurance Technician. 🚀Main responsibilities: • Achieve the objectives set by the Quality Assurance and Regulatory Affairs Department., • Cooperate in compliance with the NCFs and the Quality System implemented at 3PBiovian., • Prepare and review deviations, change controls, risk management, corrective or preventive actions, AMB, OOS, OOT, OOL, customer and supplier claims, etc., or those documents that are considered to require a review by Quality Assurance. ., • Provide support to the Quality Assurance department in audits of clients and regulatory authorities., • To carry out the functions assigned and for which training has been received, of the job position. Specifically: • Review the documentation associated with the GMP lot., • Review the documentation associated with the Cellular Bank batch., • Prepare GMP stability studies: review protocols and reports., • Issue quality system documentation to carry out the activities of other departments. Methodical, DPR, MPR, etc., • Review the Process In Progress Verification and the Cleaning In Progress Verification., • Prepare: Product Quality Review., • Review product specifications. 📖Assessment criteria: • Bachelor’s degree in Pharmacy, Chemical Engineering, Biochemistry or any other related discipline is required., • Previous experience working for a CDMO is desirable., • 5 years of experience in quality assurance activities., • Expert in GMP regulations., • Fluent in English is desirable. ❗️❗️Why 3PBiovian? • You will have 26 paid days off: 23 vacation days + 2 personal days + 1 day off set by the company., • Flexible 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.)., • Company 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.)., • Flexible working hours during the week and a reduce work day on Friday of 7h., • Special Summer working day of 7h during July and August., • 3PBio 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., • The 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., • We encourage the participation of our employees in solidarity events such as charity races, social donations..., • We 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., • We have a high-impact work environment with flat hierarchies and short decision-making processes., • All new hires who reside outside of Navarra are provided with a relocation service and/or assistance. 💥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.

📢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 Manufacturing Operations Department? The successful candidate will join 3PBiovian as a DSP Manufacturing Technician. 🚀 Responsibilities: • Achieve the objectives set by the Team Leader and the DSP manufacturing manager. Prepare, control and develop processes for the production of recombinant proteins, monoclonal antibodies or similar biological molecules in microorganisms., • Comply with good manufacturing practice (GMP), as well as occupational health and safety standards., • Maintain equipment and facilities in perfect state of repair, ensuring that they are operated according to the manuals provided by the manufacturer. Perform the incoming documentation of new equipment from the Scaling and Manufacturing DSP area under the supervision of the Team Leader DSP (FAB)., • Ensure the maintenance of up to date technical documentation of the DSP process, as well as all documentation related to assigned tasks., • Record and manage any quality indicators associated with a scaling and manufacturing process. Participate in the investigation of the same together with the Team Leader DSP (FAB)., • Oversee and write SOPs that correspond to the activities carried out in the Scaling and Manufacturing DSP department., • Conduct and/or supervise chromatographic runs, as well as all other manufacturing operations., • Ensure that the necessary material orders are scheduled in the SAP system to meet the production schedule according to the project and the weekly production plan. Carry out the control and supervision, the stock of materials needed to perform the daily activities., • Prepare, pack, evaluate and unpack chromatography columns, as well as supervise these operations performed by Operators., • Program chromatography methods in UNICORN to ensure the correct execution of DSP processes., • Prepare the documentation related to the quality system associated with the DSP Scale-up and Manufacturing plant: Deviations; Change Controls; Action Plans; Corrective, preventive and improvement actions, etc.)., • Prepare and ensure the correct preparation of solutions required for the performance of manufacturing activities., • Participate in internal / external audits as required by the Quality Assurance Department., • Participate in the correct transfer of technologies and resources between companies related to 3P Biopharmaceuticals in collaboration with other departments and your manager. 📖 Assessment criteria: • Advanced Vocational Training or equivalent in related areas (Biology, Biochemistry, Biotechnology, Chemistry, Health, Clinical Laboratory, etc.)., • University Degree or equivalent in related areas (Biology; Biochemistry; Biotechnology; Chemistry; IPPA; Chemical Engineering, etc.)., • Master's Degree in related areas (Biology; Biochemistry; Biotechnology; Chemistry; IPPA, etc.) is valued but not required., • Intermediate level of English (Level B2 / First Certificate)., • Open to work in shifts., • Office Software Package: User Level., • Unicorn Software Package: User Level. Between 1 and 2 years of experience in/with: • GMP/GLP regulations, • Chromatographic equipment, • Packed chromatographic columns, • Experience with ÄKTA, • Experience with Unicorn ❗️❗️ 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 Quality Control department? The successful candidate will join 3PBiovian as a Quality Control Technician – Physico-chemical Laboratory. 🚀Main responsibilities: • Evaluate and review the technical documentation corresponding to the Quality Control of the physico-chemical area, as well as the analytical results in routine manufacturing, validation and transfer activities in the established times., • Prepare and/or review documentation related to the average life cycle of analytical QC methods, such as validation, transfer or verification protocols and reports, change controls... in the established times., • Perform active participation in project teams, including internal and customer meetings if applicable., • Review and approve project documentation (Sampling Plans; Flow charts) required for operations., • Carry out the drafting and supervision of Standard Operating Procedures (SOP's)., • Conduct investigation of OOTs, OOSs and deviations., • Manage CAPAS (corrective and preventive actions) arising from deviations and applicable effectiveness verification., • Support stability studies agreed with our customers in collaboration with other technicians. 📖 Assessment criteria: • University Degree or equivalent in Chemistry, Pharmacy, Biotechnology, Biochemistry or similar., • Master's degree related to the area of study., • PhD with specialization in Biotechnology is valued but not necessary. Between 3 and 4 years of experience in/with: • Performing protein analysis., • Development /qualification/ validation of non-complementary analytical methods., • Specific molecular biology techniques for protein characterization and microbiology techniques., • Recombinant proteins, mAbs, Biosimilar, ADCs., • Knowledge of analytical equipment: HPLC, UV, IR, etc. and GMP regulations., • Pharmaceutical regulatory guidelines. Languages: • High level of spoken and written English (Level C1 / Advanced). ❗️❗️Why 3PBiovian? • You will have 26 paid days off: 23 vacation days + 2 personal days + 1 day off set by the company., • Flexible 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.)., • Company 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.)., • Flexible working hours during the week and a reduce work day on Friday of 7h., • Special Summer working day of 7h during July and August., • 3PBio 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., • The 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., • We encourage the participation of our employees in solidarity events such as charity races, social donations..., • We 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., • We have a high-impact work environment with flat hierarchies and short decision-making processes., • All new hires who reside outside of Navarra are provided with a relocation service and/or assistance. 💥Why us? We know it takes people with passion and a shared purpose to manufacture advanced medicines. We 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 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.

📢The successful candidate will join 3PBiovian as a LIMS Technician - Quality Control. 🚀Main responsibilities: • Carry out improvements in the workflows already implemented in the STARLIMS application for the different management and analytical activities. In implementation stages in the Project Phase., • Resolve user incidents arising from the use of LIMS., • Ensure the proper use in Routine of the system., • Train the different users in the correct use of the application and its maintenance of the new activities developed in the project phase in the successive product expansions until its passage to routine., • Participate in the development and validation of new functionalities., • Write unit tests, drafting of the User SOP, drafting of the configuration SOP, of new functionalities to be implemented., • Develop, maintain and update the generation of analytical notebooks (ELN) for analytical methods performed in Quality Control. 📖Assessment criteria: • Advanced Vocational Training, Intermediate Level Training Cycle or University Degree related to the area: Computer Science, Information Technology or a related field., • Experience with SQL language., • Knowledge of creating and modifying reports with Crystal Reports software (for editing labels and certificates), • Knowledge of laboratory workflows., • Knowledge of ELN and scripts., • Perform URS and technical data sheets. Between 3 and 4 years of experience in/with: • GMP regulations., • Biotechnology industry., • Laboratory computer applications., • Management and organization of electronic files and documentation. ❗️❗️Why 3PBiovian? • You will have 26 paid days off: 23 vacation days + 2 personal days + 1 day off set by the company., • Flexible 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.)., • Company 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.)., • Flexible working hours during the week and a reduce work day on Friday of 7h., • Special Summer working day of 7h during July and August., • 3PBio 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., • The 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., • We encourage the participation of our employees in solidarity events such as charity races, social donations..., • We 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., • We have a high-impact work environment with flat hierarchies and short decision-making processes., • All new hires who reside outside of Navarra are provided with a relocation service and/or assistance. 💥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.

FERCHAU Spain, provee servicios de ingeniería avanzada en el sector aeroespacial, automoción, ferroviario, IT, maquinaria industrial y plantas. Formamos parte de un grupo alemán fuertemente consolidado, reconocido por ser uno de los líderes de la ingeniería alemana y con presencia en Alemania, Austria, Francia, Polonia y Reino Unido. FERCHAU lo forman alrededor de 11.000 empleados con más de 100 Oficinas técnicas. En FERCHAU Spain contamos actualmente con un equipo de 300 ingenieros y técnicos, con oficinas en Madrid, Sevilla, Barcelona, Valencia y Bilbao donde estamos ampliando nuestra presencia, gracias a nuestro conocimiento, la realización de proyectos innovadores y de alto valor añadido. Seleccionamos a personas clave que quiera formar parte de una empresa como FERCHAU. Nuestra oferta incluye incorporarse en un grupo líder de Ingeniería y TI europeo en constante crecimiento, adquirir un desarrollo profesional, trabajar en iniciativas de alto contenido tecnológico y optar a proyectos con proyección internacional. Con nosotros encontrarás proyectos desafiantes y un entorno internacional, con las mejores perspectivas para tu desarrollo personal. Necesitamos incorporar a nuestro equipo de proyectos MODELADOR/AS BIM Y CAD con experiencia en el manejo de REVIT y AUTOCAD para ampliar nuestro equipo de Oficina Técnica en Obra. Funciones: • Manejo BIM 360 y REVIT., • Manejo AutoCAD., • Modelado instalaciones MEP, modificadas por los contratistas por cambios en el proyecto o indicaciones : PCI, mecánicas, pluviales, lixiviados, fecales, eléctricas (bandejas y cuadros)., • Modelado y/o grafiado de detalles en 2D integrados en el modelo para suministro a obra y AATT de SCPSA., • Asistencia técnica a los técnicos, modeladores y diseñadores de obra., • Mediciones, toma de datos y seguimiento de obra para reflejar las modificaciones y ajustes en tiempo real en los modelos y planos., • Reportaje fotográfico para su volcado al ACC por sistemas y volúmenes para registro y trazabilidad de la obra., • Actualización de modelos y publicación de planos asbuilt Requisitos: • Formación: CFGS ó Grado en Arquitectura, Ingeniería Civil o similar., • Experiencia: mínima de 2 años en tareas similares., • Experiencia con Revit y AutoCAD., • Persona con iniciativa, proactividad, capacidad de trabajo en equipo, capacidad de comunicación, planificación y organización. Ofrecemos contratación estable y plan de carrera individualizado. Si crees que reúnes los requisitos, quieres incorporarte en Empresa Multinacional alemana, líder en el sector industrial europeo con posibilidades reales de crecer profesionalmente en un proveedor de Servicios de Ingeniería de primer orden, estaremos encantados de recibir tu candidatura y que formes parte de nuestro equipo y de nuestro proyecto.

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 Quality Control Technician - Biology Laboratory.Ensure GMP activities in the biological department.Evaluate and review the technical document

FERCHAU Spain, provee servicios de ingeniería avanzada en el sector aeroespacial, automoción, ferroviario, IT, maquinaria industrial y plantas. Formamos parte de un grupo alemán fuertemente consolidado, reconocido por ser uno de los líderes de la ingeniería alemana y con presencia en Alemania, Austria, Francia, Polonia y Reino Unido. FERCHAU lo forman alrededor de 11.000 empleados con más de 100 Oficinas técnicas. En FERCHAU Spain contamos actualmente con un equipo de 300 ingenieros y técnicos, con oficinas en Madrid, Sevilla, Barcelona, Valencia y Bilbao donde estamos ampliando nuestra presencia, gracias a nuestro conocimiento, la realización de proyectos innovadores y de alto valor añadido. Seleccionamos a personas clave que quiera formar parte de una empresa como FERCHAU. Nuestra oferta incluye incorporarse en un grupo líder de Ingeniería y TI europeo en constante crecimiento, adquirir un desarrollo profesional, trabajar en iniciativas de alto contenido tecnológico y optar a proyectos con proyección internacional. Con nosotros encontrarás proyectos desafiantes y un entorno internacional, con las mejores perspectivas para tu desarrollo personal. Necesitamos incorporar a nuestro equipo de proyectos MODELADOR/AS BIM Y CAD con experiencia en el manejo de REVIT y AUTOCAD para ampliar nuestro equipo de Oficina Técnica en Obra. Funciones: • Manejo BIM 360 y REVIT., • Manejo AutoCAD., • Modelado instalaciones MEP, modificadas por los contratistas por cambios en el proyecto o indicaciones : PCI, mecánicas, pluviales, lixiviados, fecales, eléctricas (bandejas y cuadros)., • Modelado y/o grafiado de detalles en 2D integrados en el modelo para suministro a obra y AATT de SCPSA., • Asistencia técnica a los técnicos, modeladores y diseñadores de obra., • Mediciones, toma de datos y seguimiento de obra para reflejar las modificaciones y ajustes en tiempo real en los modelos y planos., • Reportaje fotográfico para su volcado al ACC por sistemas y volúmenes para registro y trazabilidad de la obra., • Actualización de modelos y publicación de planos asbuilt Requisitos: • Formación: CFGS ó Grado en Arquitectura, Ingeniería Civil o similar., • Experiencia: mínima de 2 años en tareas similares., • Experiencia con Revit y AutoCAD., • Persona con iniciativa, proactividad, capacidad de trabajo en equipo, capacidad de comunicación, planificación y organización. Ofrecemos contratación estable y plan de carrera individualizado. Si crees que reúnes los requisitos, quieres incorporarte en Empresa Multinacional alemana, líder en el sector industrial europeo con posibilidades reales de crecer profesionalmente en un proveedor de Servicios de Ingeniería de primer orden, estaremos encantados de recibir tu candidatura y que formes parte de nuestro equipo y de nuestro proyecto.

📢We are looking for an innovative, and motivated Human Resources Technician to join our Human Resources team. In this role, you will be responsible for driving the full recruitment cycle and supporting global mobility initiatives. You will partner with hiring managers to attract and retain top talent, while also managing international assignments, ensuring compliance with global mobility requirements, and providing a seamless relocation experience for employees. 🚀Main Responsibilities: As a Human Resources Technician, your responsibilities will include: • To lead the recruitment process from start to finish, designing and executing effective recruitment strategies to attract both active and passive candidates., • To create and implement new talent attraction initiatives to engage top talent., • To conduct direct searches, headhunting, screening, and shortlisting the best candidates for various roles, and carry out all necessary assessments (interviews, assessment centers, language tests, etc.)., • To act as a trusted advisor to the business in talent attraction and recruitment matters., • To coordinate and negotiate relocation allowances for selected international candidates., • To keep job descriptions updated and aligned with company needs., • To collaborate with hiring managers to plan annual recruitment needs and identify key talent within teams for retention., • To partner with universities and business schools on employer branding initiatives., • To ensure a positive candidate experience at every stage of the recruitment process., • To continuously improve our talent acquisition function, refining processes, and implementing best practices., • To manage global mobility processes, including visa and immigration procedures, legal compliance and relocation support (housing, schooling, family assistance). 📚Assessment Criteria: • Education: Degree in Labor Relations & Human Resources, Law, Psychology or a related field. A Master’s in Human Resources is a plus., • Languages: Fluent in Spanish and English. Knowledge of additional languages is an advantage., • Experience: 3+ years of experience in talent acquisition and mobility processes for Life Sciences companies. Experience in recruitment agencies or headhunting is highly valuable., • Skills: Familiarity with job boards and LinkedIn Recruiter tools., • Strong management and communication skills with the ability to build trusted relationships., • Results-driven and solution-oriented with a focus on continuous improvement. 💊Why 3PBiovian? • You will have 26 paid days off: 23 vacation days + 2 personal days + 1 day off set by the company., • Flexible 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.)., • Company 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.)., • Flexible working hours during the week and a reduce work day on Friday of 7h., • Special Summer working day of 7h during July and August., • 3PBio 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., • The 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., • We encourage the participation of our employees in solidarity events such as charity races, social donations..., • We 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., • We have a high-impact work environment with flat hierarchies and short decision-making processes., • All new hires who reside outside of Navarra are provided with a relocation service and/or assistance. 💥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.

Gracias a nuestra plataforma de gestión de clientes, podrás aceptar o descartar solicitudes de trabajos en tu área, enviando presupuestos solo a los clientes que más te interesen. Pertenecer a la red de profesionales de Cronoshare no tiene coste y recibirás nuevos clientes según tus preferenci

Cronoshare es una plataforma online para profesionales que quieren encontrar nuevos clientes.Buscamos Tejados en Biurrun y alrededores.Pertenecer a la red de profesionales de Cronoshare no tiene coste y recibirás nuevos clientes según tus preferencias, de forma personalizada.Conocimientos previos

About the Role We are seeking an experienced Senior Quality Assurance Technician to join our team. As a key member of our quality assurance department, you will be responsible for ensuring the quality of our products and services.

We are seeking a skilled Technical Services Specialist to execute tech transfer policies, design process scale-ups and conduct validation activities in compliance with standard operating procedures. • Prepare and Execute Protocols for Tech Transfer policies in a biotech industry, including customer-to-facility transfers and departmental transfers., • Evaluate technical documentation of potential processes to be transferred., • Follow up on Tech Transfer runs and Scale-Up batches to ensure proper performance and prepare Tech Transfer reports., • Prepare and Execute Cleaning, Process, and Analytical Validation Protocols., • Coordinate the execution of Validation Campaigns., • Lead Risk Analysis Sessions using HAZOP/FMEA methodologies., • Prepare User Requirements Specifications (URS) for equipment needed for project execution and internal documentation for equipment management., • Ensure Compliance with Good Manufacturing Practices (GMP) regulations., • Bachelor's degree in Science, Chemical Engineering or related discipline required., • At least 5 years of experience in tech transfer activities, including internal and external tech transfer, process validation and cleaning validation., • Experience in risk analysis and HAZOP/FMEA methodologies., • Expertise in GMP regulations., • 26 paid days off per year., • Flexible compensation plan allowing employees to allocate up to 30% of their gross annual salary to daily services exempt from income tax., • Company benefits club offering exclusive prices and discounts on various products and services., • Flexible working hours during the week and reduced workday on Fridays., • Special summer working day of 7 hours during July and August., • Comprehensive Learning & Development program providing personalized career plans and opportunities for professional growth., • Environment of trust and stability, focusing on upskilling and reskilling., • Participation in solidarity events and programs promoting physical, psychological and emotional well-being., • Flat hierarchies and short decision-making processes., • Relocation assistance for new hires residing outside of Navarra.

Te apasiona el contacto con personas?.Eres una persona humilde, trabajadora y honesta?.Tienes buenas habilidades de negociación?.Te gustaría trabajar por objetivos?.Te gusta detectar las necesidades de los clientes y ofrecerles lo que necesitan?.Si la mayoría de las respuestas han sido afirmativa

Soldadura MIG MAG Interpretación de planos Horario: Turnos rotativos Duración: 6 meses Jornada: Completa.

Nuevas vacantes para mantenimiento industrial en Noáin en septiembre.

Elaboración de menús del día, menús fin de semana y pinchos.Horario: De lunes a domingos con los descansos establecidos en la ley.A turnos: principalmente de mañana.Turno partido el viernes y sábado según necesidades.

Empresa del sector textil busca un/a auxiliar/a administrativo/a para trabajar en Beriain y realizar las siguientes tareas: * Gestión de compras.

La persona seleccionada realizará las siguientes funciones: - Operario de máquina. Empresa del sector metal situada en Noáin necesita incorporar un/a operario/a de máquina.

Empresa del sector metal busca un/a electricista para trabajar en la zona de Pamplona y realizar las siguientes tareas: * Instalaciones eléctricas.

Montador/a de muebles Las tareas principales incluyen la recepción cuidadosa y la inspección detallada de la mercancía que llega.

Empresa del sector textil busca un/a operario/a textil para trabajar en Beriain y realizar las siguientes tareas: * Cortes de telas.

Nuevas vacantes para marketing y ventas en Galar en septiembre.

Estamos en búsqueda de un/a operario/a de máquina con carretilla y puente grúa para trabajar en una empresa del sector del metal ubicada en la zona de Noain.

Empresa dedicada a fabricación necesita la incorporación de un/a mozo/a de almacén - carretillero/a en Noain.Las tareas a desempeñar son las siguientes: * Carga y descarga de camiones.Jornada completa de 40 horas semanales entre lunes y viernes en turno sw mañana en horario entre 08:00h y 15:

Empresa dedicada a la publicidad necesita la incorporación de un/a comercial en Pamplona.

Tenemos un/a hijo/a (1 Nia, 5 aos).No dudes en ponerte en contacto conmigo para conocernos.

Tenemos 2 hijos (1 Nio y 1 Nia, 1 y 5 aos).No dudes en ponerte en contacto conmigo para conocernos.

Tenemos un/a hijo/a (1 Nia, 2 aos).No dudes en ponerte en contacto conmigo para conocernos.

We have 1 child (1 boy, 7 years old).Feel free to contact me so we can make an appointment.

Hola, tengo una nia de 7 meses y voy a necesitar ayuda de forma ocasional, por semanas completas de lunes a jueves, y el a horario sera entre las 16:15 y las 18:15.Mi marido y yo trabajamos, por lo que uno de nosotros siempre estara en la habitacin del al lado para cualquier necesidad.Busco una pers

Oier tiene 5 aos es muy buen chico y muy fcil de llevar Nagore va a cumplir 3 aos y es muy movida traviesa pero con la que te res mucho,es incansable y le gusta maquillarse sobretodo pintarse las uas.

Camarero de barra, servicio de mesas y reposición de cámaras.

Coordinación con el entorno de las personas usuarias referentes: centro de salud, familia, etc.

Reparto de mercancía en diferentes puntos de Navarra.Realizar las rutas pactadas en el día mediante tacógrafo.Descarga y carga de materiales.Horario: De lunes a viernes de 08:00 a 13:00 y de 14:00 a 17:00h Duración: De 2 a 3 meses Jornada: Completa.

Diversas actividades, incluyendo: - Interpretación de planos.Horario: Turnos de mañana 06:00h a 14:00h y tarde 14:00h a 22:00h.

Asistir en la recepción e inspección de mercancía, apoyar en el montaje de muebles, colaborar en la instalación tanto en tienda como en domicilio, ayudar en la revisión de calidad, organizar herramientas y materiales, realizar tareas básicas de mantenimiento, asistir al montador principal dura

FERCHAU Spain, provee servicios de ingeniería avanzada en el sector aeroespacial, automoción, ferroviario, IT, maquinaria industrial y plantas.Formamos parte de un grupo alemán fuertemente consolidado, reconocido por ser uno de los líderes de la ingeniería alemana y con presencia en Alemania, A

Cada profesional de nuestra empresa es importante para nosotros, nos ayudan a crecer de manera diversa y gracias a ellos somos más de 13.Si eres una persona entusiasta, te apasiona la tecnología y buscas un nuevo reto profesional ¡Este es tu sitio!.Buscamos ampliar nuestro equipo con.Anímate a d

En Mutua Navarra trabajamos por un bienestar sostenible, ayudando a que las personas se sientan mejor.Buscamos incorporar un/a profesional sanitario/a con titulación de Grado o Licenciatura en Medicina homologada para trabajar en España, sede en Pamplona (Navarra).Si eres médico/a, te apasiona la

Nuestro cliente NUEVO SISTEMA MODULAR, empresa líder en construcción modular industrializada, busca incorporar a su equipo a un/a Técnico/a de Estudios y Licitaciones para sus instalaciones ubicadas en la comarca de Pamplona.Análisis de pliegos técnicos y administrativos.Elaboración de presupu

Desde EULEN Flexiplán Selección colaboramos con.ÉCNICO/A AYUDANTE DE LABORATORIO.Dirección de Medicina Personalizada y Laboratorios.Te encargarás de ejecutar ( bajo supervisión) tareas relacionadas con la prestación de unos servicios analíticos en el ámbito agrario o agroalimentario.Mantend

Como personal de ventas tendras las siguientes responsabilidades: -Servicio de atención al cliente, garantizando la calidad durante todo el proceso.Preparación de todo tipo de café, bebidas y servicios (desayunos, meriendas, take away, etc.Velar por el buen mantenimiento y limpieza de la tienda.R

Somos Timac AGRO la multinacional líder en nutrición vegetal, animal y humana, con productos diferenciados y de alta tecnología y estamos buscando incorporar un/a:.GESTOR/A DE PROVEEDORES EXTERNOS (FABRICACIÓN Y LOGISTICA).La persona incorporada dependerá del Responsable de Administración de V

QUIERES TENER LA OPORTUNIDAD DE ENTRAR EN UN PROYECTO CON CRECIMIENTO CONTINUO?.Únete al #TeamTRIGO y sé la pieza fundamental en proyectos punteros de automoción!.Por qué trabajar con nosotros?.Invertirás en tu crecimiento personal y profesional a través de.Quieres formar parte de este #TeamTr

If you are an Elementary Teacher wanting to work in one of the most popular teaching destinations in Europe, then this could be your chance!.Become an Elementary Teacher in historical Barcelona and take advantage of the historical Architecture, scrumptious Spanish Cuisine and lively nightlife.With i