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Si tienes experiencia como Técnico de Soporte o Helpdesk en ERP o plataformas digitales y te gustaría formar parte del equipo de una importante multinacional del sector alimentario ¡Sigue leyendo! Vas a trabajar como IT Support de una empresa multinacional ubicada en Sant Cugat del Vallès. Tus funciones serán: • Facilitar la comunicación directa con proveedores nuevos en EDI, ayudándoles a comprender el proceso de implementación., • Asistir en la configuración del software necesario para el intercambio de datos en los sistemas de los proveedores., • Asegurar el correcto funcionamiento del sistema EDI mediante la definición de requisitos técnicos en cuanto a documentos, formatos, datos a intercambiar y estándares a utilizar., • Proveer orientación y apoyo continuo a los proveedores en todas las fases del proceso de implementación., • Diagnosticar y resolver incidencias en la interacción., • Recopilar datos y hacer seguimiento para garantizar una recepción y procesamiento eficiente de los mensajes., • Documentar interacciones con proveedores, asegurando un seguimiento adecuado y resolución de dudas e incidencias., • Colaborar en la definición y cálculo de indicadores de rendimiento (KPIs) para la dirección de la empresa. Requisitos: • Experiencia como Técnico de Soporte o Helpdesk en ERP o plataformas digitales., • Experiencia dando soporte mediante sistemas de ticketing., • Buena organización en el día a día para gestionar relaciones con múltiples proveedores., • Capacidad de análisis y buenas habilidades de comunicación para interactuar efectivamente con proveedores. -Valorable conocimientos de EDI. -Nivel de inglés medio. -Persona enfocada a tratar con cliente interno. -Interés por continuar desarrollando tu carrera profesional en el ámbito tecnológico de la mano de una multinacional del sector retail. -Disposición para colaborar con la compañía mediante una oportunidad laboral de duración determinada. ¿Qué se ofrece? Se ofrece un contrato temporal a través de Adecco hasta el 31 de Marzo de 2026, con posibilidades de ampliación. Con un horario será de Lunes a Viernes de 9.00h a 18.00h. El salario será alrededor de los 20-21k brutos anuales. Si consideras que podrías encajar en la vacante, ¡esta es tu oportunidad, inscríbete, te estamos esperando!

Gi Group es la multinacional Italiana líder en el mundo que ofrece soluciones integrales para el desarrollo del mercado laboral. Nuestra misión es contribuir con una visión global al desarrollo del mercado laboral con el objetivo principal de aumentar la empleabilidad, basándonos siempre en el valor personal y social del trabajo. Trabajamos día a día con nuestros candidatos y trabajadores para guiarles en su carrera profesional, y con nuestros clientes, para lograr un crecimiento y consecución de éxitos conjunta. Conoce más en Desde Gi Group trabajamos para una reconocidísima empresa multinacional del sector gran consumo. Nuestro cliente ofrece productos y experiencia en el sector de las masas congeladas de grandes superficies en más de 80 países de todo el mundo a través de sus 22 fábricas y sus 33 oficinas de ventas. Buscamos a un GESTOR/A DE REAPROVISIONAMIENTO INTERNO. Su misión principal será la de realizar el reaprovisionamiento de los centros logísticos, teniendo en cuenta el stock y controlando tanto las necesidades como la capacidad de cada centro. Se ofrece: • Contrato indefinido, • Jornada completa en Sant Cugat, en horario de 09:00 a 18:00 h., • Interesantes beneficios sociales. Funciones principales: • Seguimiento de la demanda y reaprovisionamiento., • Soporte en el seguimiento del stock de producto terminado para optimizar el nivel de servicio a clientes y minimizar obsoletos., • Controlar la ocupación de los almacenes, ajustando a los niveles óptimos., • Colaborar en la gestión de roturas de stock de producto para clientes, intentado minimizar estas., • Mantenimiento del mapa de picking, ajustando este a la necesidad de la compañía., • Retornos de producto fuera del mapa para evitar obsoletos. Requisitos: • Experiencia laboral previa en planificación y/o previsión de la demanda, • Gran dominio de Excel, • Capacidad de toma de decisiones, resolución de problemas y de trabajo en equipo. Muy valorable: • Inglés medio-avanzado, • Formación especializada en logística o grado en ingeniería., • Experiencia en empresas de Alimentación y gran consumo ¡Si te interesa esta enorme oportunidad y cumples con los requisitos, estaremos encantad@s de conocerte

Sales Manager Grow Your Career with a Leading International Company Would you like to advance your career in a highly successful international company and seize the opportunity for continuous growth? Are you a natural leader with a passion for sales and the food manufacturing industry? If so, this is the opportunity you've been looking for. We are a globally operating company specializing in the refining of oils and fats. As a key supplier to major manufacturing industries, we offer high-quality products and uphold the highest sustainability standards. Position Overview: • Manage assigned strategic customer accounts, reporting directly to the Sales Director., • Develop and implement strategies to become a trusted partner to our clients, monitoring KPIs to achieve company targets., • Maintain regular communication with customer accounts, keeping them informed of our product portfolio, market prices, and relevant industry insights., • Conduct market analysis to identify and develop new customer opportunities. Candidate Profile: • University degree in Economics, Finance, Engineering, or a related field., • Relevant postgraduate qualifications preferred., • Proven sales experience in the food industry or B2B environment., • Knowledge of fats and oils applications., • Proficiency in English is required; additional languages are a plus. What We Offer: • A well-defined career path within a robust, growing company with a strong market presence.

¿Quieres formar parte de una multinacional en expansión dentro del sector de la alimentación? ¿Tienes experiencia previa como Administrativo/a de Compras? ¿Buscas estabilidad y crecimiento profesional? Si todas tus respuestas son positivas, ¡Sigue leyendo! Desde Adecco estamos colaborando con una multinacional del sector de la Alimentación, ubicada en Sant Cugat del Vallès, que se encuentra en la búsqueda de un/a Administrativo/a de Compras, para que de soporte en la distribución y archivo de la documentación de proveedores, y los procedimientos establecidos, con el objetivo de facilitar la consecución de objetivos del departamento. ¿Cuáles serán tus funciones? ·Dar soporte en la distribución de la documentación contractual de compras recibida que le sea asignada. ·Realizar la verificación de la información y documentación de la publicación comercial asignada. ·Llevar cabo el archivo de la documentación de los proveedores y de las hojas de negociación. ·Revisión y corrección de contratos. ·Revisión y corrección de precios de artículos. ·Registro y revisión de condiciones contractuales. ·Resolver las incidencias de su ámbito de responsabilidad relacionadas con artículos, precios y proveedores. ·Revisar el uso del logo corporativo en las comunicaciones, el packaging y el etiquetado de los productos que le sean asignados. ·Resolver las incidencias de su ámbito de responsabilidad. ·Velar por el cumplimiento de los plazos establecidos en aquellas acciones que así lo requieren. ¿Qué necesitas? Formación en ADE, Comercio Internacional, Administración y Finanzas o similar. Al menos 2 años de experiencia en administración, preferiblemente en gestión documental. Salario en función de experiencia y valía demostrable. Nivel alto de Excel. Inglés nivel mínimo B2. Capacidad para gestionar altos volúmenes de documentación con atención al detalle. ¿Qué ofrecemos? Contrato indefinido directamente por empresa. Posibilidad de hacer teletrabajo. Horario flexible con jornada presencial en Sant Cugat. Posibilidades de crecimiento dentro de la empresa. Descuentos en productos de la empresa. Plan de retribución flexible. Formación continua. Excelente ambiente de trabajo.

Desde GRUPO GALLO estamos buscando un/a Responsable de Contabilidad y Administración, con la misión de: liderar, dirigir, supervisar y ejecutar la contabilidad de las empresas que forman del grupo. Serás responsable de registrar las operaciones financieras según la normativa legal vigente y las políticas internas con el objetivo de conseguir el análisis de la situación financiera y la toma de decisiones por parte de la Dirección Financiera. Reportando a la CFO del grupo, estas serán tus funciones: • Revisar y coordinar el proceso de cierre contable mensual., • Ejecutar el proceso consolidación contable del grupo., • Relación con las entidades bancarias., • Revisar y coordinar la tesorería del grupo: pagos, cobros, conciliaciones bancarias., • Supervisar los procesos de presentación de obligaciones fiscales mensuales & anuales., • Supervisar con responsable del área de cuentas a pagar que esté al día y coordinar los días de ejecución de pagos y sus cuantías., • Supervisar con responsable del área de cuentas a cobrar el estado de los vencimientos y partidas, la compensación de deducciones y reclamaciones de retrasos, control del Riesgo, la información trimestral a suministrar y la liquidación anual del seguro., • Ejecutar y contabilizar todo el proceso de cierre de la contabilidad anual con el resultado final del ejercicio, en coordinación con Controlling y Dirección Financiera, • Coordinar y ejecutar la aportación de información para la auditoría externa., • Coordinar y liderar mejoras en el área contable/administrativa tanto de procesos como sistemas., • Gestión de un equipo de 9 personas. Requisitos: • Mínimo de 8 años de experiencia en el área de Contabilidad y Administración., • Titulación universitaria en ADE, Economía o similares. Valorable Master en Dirección Contable/Financiera., • Nivel de inglés C1., • Experiencia en SAP., • Conocimientos de ESG. Qué esperamos de ti: • Que tengas experiencia implementando SAP., • Que aportes capacidad de organización, analítica y comunicación., • Que te apasione trabajar en un equipo., • Deseable experiencia en Gran Consumo. Ofrecemos: • Oportunidad de desarrollo profesional en una empresa líder., • Buen ambiente de trabajo, en equipo dinámico y colaborativo., • Jornada flexible., • Retribución flexible. Si cumples con los requisitos y quieres seguir desarrollándote en una empresa líder en el sector, ¡esta es tu oportunidad!

Gi Group es la multinacional Italiana líder en el mundo que ofrece soluciones integrales para el desarrollo del mercado laboral. Nuestra misión es contribuir con una visión global al desarrollo del mercado laboral con el objetivo principal de aumentar la empleabilidad, basándonos siempre en el valor personal y social del trabajo. Conoce más en Desde Gi Group buscamos a un/a Supply Planner para nuestro cliente, importante empresa multinacional dedicada al sector alimentación con ubicación en Sant Cugat del Vallès. Su misión será coordinar y planificar los programas de producción para garantizar el nivel de servicio y la eficiencia de las plantas dentro del presupuesto. Funciones: • Alcanzar el KPI de Nivel de Servicio desarrollando y manteniendo cronogramas de producción para garantizar que los productos se produzcan de manera oportuna y eficiente., • Coordinar las actividades de producción con otros departamentos, como compras, inventario y calidad, para garantizar que los cronogramas de producción estén alineados con las necesidades de la cadena de suministro., • Monitorear el progreso de la producción y ajustar los cronogramas según sea necesario para cumplir con los requisitos cambiantes o los retrasos., • Contribuir a lograr el KPI de OEE de las plantas de producción mediante la anticipación y la prevención de cambios de último momento en la producción., • Detectar brechas de capacidad y elaborar escenarios para anticipar y prevenir desafíos de capacidad en nuestras plantas de producción., • Gestionar los niveles de inventario para garantizar el nivel de servicio., • Comunicar de manera proactiva dentro de los departamentos de Servicio al Cliente y Ventas sobre cualquier posible evento imprevisto que pueda afectar el servicio., • Detectar desviaciones en la previsión para escalarla al equipo de planificación de la demanda y obtener nuevos conocimientos sobre el comportamiento del mercado. Requisitos: • Grado o Máster en Ingeniería, • Experiencia en planificación de la demanda, producción o Compras, • Nivel intermedio-alto de inglés, al menos B2., • Fuertes habilidades analíticas y de resolución de problemas, • Dominio de Paquete Office, • Valorable experiencia en software de planificación de la producción, • Capacidad para trabajar en un entorno de ritmo rápido y con plazos de entrega Se ofrece: • Proyecto estable., • Jornada completa., • Posibilidades de crecimiento y desarrollo profesional., • Incorporación en empresa líder en su sector, • Interesantes beneficios sociales ¡Si cumples con los requisitos y quieres conocer en detalle la oferta, estaremos encantad@s de conocerte!

Gi Group es la multinacional Italiana líder en el mundo que ofrece soluciones integrales para el desarrollo del mercado laboral. Nuestra misión es contribuir con una visión global al desarrollo del mercado laboral con el objetivo principal de aumentar la empleabilidad, basándonos siempre en el valor personal y social del trabajo. Trabajamos día a día con nuestros candidatos y trabajadores para guiarles en su carrera profesional, y con nuestros clientes, para lograr un crecimiento y consecución de éxitos conjunta. Conoce más en ___ Actualmente, nos encontramos en busca de jefe/a de turno, para importante empresa ubicada en Barberà del Vallès. Funciones: • Organización del turno, • Control y gestión de operarios/as (entre 15 y 20 operarios/as), • Resolución de incidencias, • Soporte a la línea de producción Requisitos: • Residencia cercana a Barberá del Vallés, • Vehículo propio, • Disponibilidad para realizar turnos rotativos de mañana, tarde y noche semanales y/o 4o turno, • Disponer de experiencia previa consolidada como jefe/a de turno, • Valorable positivamente experiencia en sector alimentación, • Buena actitud, organización y capacidad para trabajar en quipo Y por nuestra parte, ¿qué podemos ofrecerte? • Contratación estable directamente por empresa., • Horario de lunes a viernes en turnos rotativos de mañana, tarde y noche semanales y/o 4o turno, • Salario entre 28.000e brutos/anuales y 30.000e brutos/anuales ¡Si cumples los requisitos y quieres valorar esta enorme oportunidad de empleo, estaremos más que encantad@s de conocerte!

Desde Paul Marlex, estamos colaborando con una empresa líder en el desarrollo y suministro de soluciones químicas especializadas para diversas aplicaciones industriales, ubicada en Montcada i Reixac, que actualmente busca incorporar a su equipo a un/a Técnico/a de Gestión de Calidad y Medio Ambiente. ¿Cuál será tu misión en la empresa? • Dar soporte en la gestión documental del Sistema Integrado de Calidad y Medio Ambiente., • Mantener y actualizar los sistemas de gestión según las normas ISO 9001, ISO 14001 y FSSC 22000., • Asegurar el cumplimiento de las normativas aplicables en materia de calidad y seguridad alimentaria., • Colaborar en la aplicación y seguimiento de procedimientos, instrucciones y requisitos internos del sistema de calidad., • Dar soporte en auditorías internas y externas, así como en la mejora continua de los procesos. A la persona seleccionada se le ofrece: • Oportunidad de crecimiento profesional en una compañía líder en su sector., • Incorporación directa a la empresa con contrato indefinido., • Horario flexible: De lunes a jueves: entrada entre 7:30 y 9:00 h y salida entre 16:15 y 18:00 h. Viernes: entrada entre 7:00 y 8:00 h y salida a partir de las 14:45 h. Requisitos: • Formación en Ciencias de la Vida, Ingeniería de los Alimentos, Ciencias Ambientales o similar., • Conocimientos o experiencia previa en sistemas de gestión de calidad y seguridad alimentaria., • Familiaridad con normativas como ISO 9001, ISO 14001 y FSSC 22000., • Se valorará positivamente experiencia o formación en industria farmacéutica o alimentaria.

At its locations around the world, Siegfried offers employees exciting career opportunities in international settings. We cultivate multidisciplinary cooperation and encourage our staff to actively shape and influence their careers. This approach, coupled with our dynamic working environment, make Siegfried an attractive employer. Your role: • Comprehensive Product Management: Oversee the entire commercial lifecycle of the product, from its transfer by development to the present date, acting as the Single Point of Contact (SPOC)., • Risk Analysis and Quality Control: Create, update, and monitor the product-specific Quality Risk Analysis (QRA) and ensure compliance with quality standards., • Data Monitoring and Analysis: Evaluate critical and key variables through statistical analysis, track data trends, and review the Annual Product Quality Review (APQR) to make informed decisions regarding control status., • Inspection Readiness: Ensure all aspects related to the product process are prepared for audits and regulatory inspections., • Performance Monitoring and Improvement: Identify trends, detect issues, and lead the implementation of corrective and preventive actions (CAPAs) to enhance products., • Deviation Management and Improvement Projects: Investigate process deviations, lead optimization projects, and engage cross-functional teams in improvement initiatives., • In-Process Controls (IPC) Monitoring: Ensure the tracking of critical parameters in laboratories and guarantee that data is visible and communicated at the plant level., • Technical Change Assessment: Analyze the impact of process modifications, determine their feasibility, and manage the quotations associated with these changes., • Process and Product Validation: Ensure continuous validation status, alignment with the APQR, and implementation of control strategies based on Critical Quality Attributes (CQA), Critical Process Parameters (CPP), and Critical Material Attributes (CMA)., • Product Launch and Transfer: Facilitate product transfers by ensuring technical documentation and providing necessary support to the receiving plant., • Manufacturing Optimization and Excellence: Lead improvement projects to enhance the robustness and sustainability of pharmaceutical processes in collaboration with Operational Excellence (OPEX). Your profile: • University degree in a scientific field or related, or a higher vocational training degree in a scientific field with previous experience in a similar position., • High level of English., • Experience in a similar technical position and in the pharmaceutical sector., • Knowledge of data management and application of statistical techniques. Working at Siegfried Siegfried's work environment is dynamic and international. With a highly professional and motivated team, the company operates in a future-oriented business field. Siegfried possesses a unique culture that leverages cultural differences to create a competitive advantage. Siegfried places highest priority on providing a flexible, diverse and discrimination-free working environment in which employees can develop personally and professionally, advance innovation and deliver superior performance. We strive to provide a work environment where employees can take on challenging jobs and associated responsibilities that best serve their personal and technical development and can benefit from the success of our company. The company regulations in respect of compensation and career development opportunities apply to all Siegfried sites. Additional conditions of employment are governed by location-specific circumstances, legislation and customs. In the Midst of People’s Lives – Across the Globe The Siegfried Group is one of the world’s leading Custom Development and Manufacturing Organizations (CDMOs) developing and producing active pharmaceutical ingredients (API), intermediates and finished dosage forms. As our core competence, we successfully integrate chemical and pharmaceutical capabilities into a single business model. The Siegfried name stands for highest quality, efficiency, flexibility and safety. Present in Europe, Asia and North America, we serve a broad global customer base from major international pharmaceutical companies down to small biologic-pharmaceutical organizations. For them we develop and produce product innovations on a large scale to finished products. We integrate our offer seamlessly into the customers’ value chain. Our comprehensive services range from early-stage Research & Development services such as synthesis, scale-up, formulation development, stability studies and method development all the way through to manufacturing services, ranging from preclinical R&D material for clinical trial purposes to commercial production. We are able to produce about 200 of the approximately 1500 registered drug substances used in medicine. Moreover, we produce 20 percent of global demand for caffeine. Consequently, nearly 1 billion individuals come into contact with Siegfried products.

At its locations around the world, Siegfried offers employees exciting career opportunities in international settings. We cultivate multidisciplinary cooperation and encourage our staff to actively shape and influence their careers. This approach, coupled with our dynamic working environment, make Siegfried an attractive employer. Your role: • Comprehensive Product Management: Oversee the entire commercial lifecycle of the product, from its transfer by development to the present date, acting as the Single Point of Contact (SPOC)., • Risk Analysis and Quality Control: Create, update, and monitor the product-specific Quality Risk Analysis (QRA) and ensure compliance with quality standards., • Data Monitoring and Analysis: Evaluate critical and key variables through statistical analysis, track data trends, and review the Annual Product Quality Review (APQR) to make informed decisions regarding control status., • Inspection Readiness: Ensure all aspects related to the product process are prepared for audits and regulatory inspections., • Performance Monitoring and Improvement: Identify trends, detect issues, and lead the implementation of corrective and preventive actions (CAPAs) to enhance products., • Deviation Management and Improvement Projects: Investigate process deviations, lead optimization projects, and engage cross-functional teams in improvement initiatives., • In-Process Controls (IPC) Monitoring: Ensure the tracking of critical parameters in laboratories and guarantee that data is visible and communicated at the plant level., • Technical Change Assessment: Analyze the impact of process modifications, determine their feasibility, and manage the quotations associated with these changes., • Process and Product Validation: Ensure continuous validation status, alignment with the APQR, and implementation of control strategies based on Critical Quality Attributes (CQA), Critical Process Parameters (CPP), and Critical Material Attributes (CMA)., • Product Launch and Transfer: Facilitate product transfers by ensuring technical documentation and providing necessary support to the receiving plant., • Manufacturing Optimization and Excellence: Lead improvement projects to enhance the robustness and sustainability of pharmaceutical processes in collaboration with Operational Excellence (OPEX). Your profile: • University degree in a scientific field or related, or a higher vocational training degree in a scientific field with previous experience in a similar position., • High level of English., • Experience in a similar technical position and in the pharmaceutical sector., • Knowledge of data management and application of statistical techniques. Working at Siegfried Siegfried's work environment is dynamic and international. With a highly professional and motivated team, the company operates in a future-oriented business field. Siegfried possesses a unique culture that leverages cultural differences to create a competitive advantage. Siegfried places highest priority on providing a flexible, diverse and discrimination-free working environment in which employees can develop personally and professionally, advance innovation and deliver superior performance. We strive to provide a work environment where employees can take on challenging jobs and associated responsibilities that best serve their personal and technical development and can benefit from the success of our company. The company regulations in respect of compensation and career development opportunities apply to all Siegfried sites. Additional conditions of employment are governed by location-specific circumstances, legislation and customs. In the Midst of People’s Lives – Across the Globe The Siegfried Group is one of the world’s leading Custom Development and Manufacturing Organizations (CDMOs) developing and producing active pharmaceutical ingredients (API), intermediates and finished dosage forms. As our core competence, we successfully integrate chemical and pharmaceutical capabilities into a single business model. The Siegfried name stands for highest quality, efficiency, flexibility and safety. Present in Europe, Asia and North America, we serve a broad global customer base from major international pharmaceutical companies down to small biologic-pharmaceutical organizations. For them we develop and produce product innovations on a large scale to finished products. We integrate our offer seamlessly into the customers’ value chain. Our comprehensive services range from early-stage Research & Development services such as synthesis, scale-up, formulation development, stability studies and method development all the way through to manufacturing services, ranging from preclinical R&D material for clinical trial purposes to commercial production. We are able to produce about 200 of the approximately 1500 registered drug substances used in medicine. Moreover, we produce 20 percent of global demand for caffeine. Consequently, nearly 1 billion individuals come into contact with Siegfried products.

At its locations around the world, Siegfried offers employees exciting career opportunities in international settings. We cultivate multidisciplinary cooperation and encourage our staff to actively shape and influence their careers. This approach, coupled with our dynamic working environment, make Siegfried an attractive employer. Your role: • Comprehensive Product Management: Oversee the entire commercial lifecycle of the product, from its transfer by development to the present date, acting as the Single Point of Contact (SPOC)., • Risk Analysis and Quality Control: Create, update, and monitor the product-specific Quality Risk Analysis (QRA) and ensure compliance with quality standards., • Data Monitoring and Analysis: Evaluate critical and key variables through statistical analysis, track data trends, and review the Annual Product Quality Review (APQR) to make informed decisions regarding control status., • Inspection Readiness: Ensure all aspects related to the product process are prepared for audits and regulatory inspections., • Performance Monitoring and Improvement: Identify trends, detect issues, and lead the implementation of corrective and preventive actions (CAPAs) to enhance products., • Deviation Management and Improvement Projects: Investigate process deviations, lead optimization projects, and engage cross-functional teams in improvement initiatives., • In-Process Controls (IPC) Monitoring: Ensure the tracking of critical parameters in laboratories and guarantee that data is visible and communicated at the plant level., • Technical Change Assessment: Analyze the impact of process modifications, determine their feasibility, and manage the quotations associated with these changes., • Process and Product Validation: Ensure continuous validation status, alignment with the APQR, and implementation of control strategies based on Critical Quality Attributes (CQA), Critical Process Parameters (CPP), and Critical Material Attributes (CMA)., • Product Launch and Transfer: Facilitate product transfers by ensuring technical documentation and providing necessary support to the receiving plant., • Manufacturing Optimization and Excellence: Lead improvement projects to enhance the robustness and sustainability of pharmaceutical processes in collaboration with Operational Excellence (OPEX). Your profile: • University degree in a scientific field or related, or a higher vocational training degree in a scientific field with previous experience in a similar position., • High level of English., • Experience in a similar technical position and in the pharmaceutical sector., • Knowledge of data management and application of statistical techniques. Working at Siegfried Siegfried's work environment is dynamic and international. With a highly professional and motivated team, the company operates in a future-oriented business field. Siegfried possesses a unique culture that leverages cultural differences to create a competitive advantage. Siegfried places highest priority on providing a flexible, diverse and discrimination-free working environment in which employees can develop personally and professionally, advance innovation and deliver superior performance. We strive to provide a work environment where employees can take on challenging jobs and associated responsibilities that best serve their personal and technical development and can benefit from the success of our company. The company regulations in respect of compensation and career development opportunities apply to all Siegfried sites. Additional conditions of employment are governed by location-specific circumstances, legislation and customs. In the Midst of People’s Lives – Across the Globe The Siegfried Group is one of the world’s leading Custom Development and Manufacturing Organizations (CDMOs) developing and producing active pharmaceutical ingredients (API), intermediates and finished dosage forms. As our core competence, we successfully integrate chemical and pharmaceutical capabilities into a single business model. The Siegfried name stands for highest quality, efficiency, flexibility and safety. Present in Europe, Asia and North America, we serve a broad global customer base from major international pharmaceutical companies down to small biologic-pharmaceutical organizations. For them we develop and produce product innovations on a large scale to finished products. We integrate our offer seamlessly into the customers’ value chain. Our comprehensive services range from early-stage Research & Development services such as synthesis, scale-up, formulation development, stability studies and method development all the way through to manufacturing services, ranging from preclinical R&D material for clinical trial purposes to commercial production. We are able to produce about 200 of the approximately 1500 registered drug substances used in medicine. Moreover, we produce 20 percent of global demand for caffeine. Consequently, nearly 1 billion individuals come into contact with Siegfried products.

At its locations around the world, Siegfried offers employees exciting career opportunities in international settings. We cultivate multidisciplinary cooperation and encourage our staff to actively shape and influence their careers. This approach, coupled with our dynamic working environment, make Siegfried an attractive employer. Your role: • Comprehensive Product Management: Oversee the entire commercial lifecycle of the product, from its transfer by development to the present date, acting as the Single Point of Contact (SPOC)., • Risk Analysis and Quality Control: Create, update, and monitor the product-specific Quality Risk Analysis (QRA) and ensure compliance with quality standards., • Data Monitoring and Analysis: Evaluate critical and key variables through statistical analysis, track data trends, and review the Annual Product Quality Review (APQR) to make informed decisions regarding control status., • Inspection Readiness: Ensure all aspects related to the product process are prepared for audits and regulatory inspections., • Performance Monitoring and Improvement: Identify trends, detect issues, and lead the implementation of corrective and preventive actions (CAPAs) to enhance products., • Deviation Management and Improvement Projects: Investigate process deviations, lead optimization projects, and engage cross-functional teams in improvement initiatives., • In-Process Controls (IPC) Monitoring: Ensure the tracking of critical parameters in laboratories and guarantee that data is visible and communicated at the plant level., • Technical Change Assessment: Analyze the impact of process modifications, determine their feasibility, and manage the quotations associated with these changes., • Process and Product Validation: Ensure continuous validation status, alignment with the APQR, and implementation of control strategies based on Critical Quality Attributes (CQA), Critical Process Parameters (CPP), and Critical Material Attributes (CMA)., • Product Launch and Transfer: Facilitate product transfers by ensuring technical documentation and providing necessary support to the receiving plant., • University degree in a scientific field or related, or a higher vocational training degree in a scientific field with previous experience in a similar position., • High level of English., • Experience in a similar technical position and in the pharmaceutical sector. Siegfried's work environment is dynamic and international. With a highly professional and motivated team, the company operates in a future-oriented business field. Siegfried possesses a unique culture that leverages cultural differences to create a competitive advantage. Siegfried places highest priority on providing a flexible, diverse and discrimination-free working environment in which employees can develop personally and professionally, advance innovation and deliver superior performance. We strive to provide a work environment where employees can take on challenging jobs and associated responsibilities that best serve their personal and technical development and can benefit from the success of our company. The company regulations in respect of compensation and career development opportunities apply to all Siegfried sites. Additional conditions of employment are governed by location-specific circumstances, legislation and customs. In the Midst of People’s Lives – Across the Globe The Siegfried Group is one of the world’s leading Custom Development and Manufacturing Organizations (CDMOs) developing and producing active pharmaceutical ingredients (API), intermediates and finished dosage forms. As our core competence, we successfully integrate chemical and pharmaceutical capabilities into a single business model. The Siegfried name stands for highest quality, efficiency, flexibility and safety. Present in Europe, Asia and North America, we serve a broad global customer base from major international pharmaceutical companies down to small biologic-pharmaceutical organizations. For them we develop and produce product innovations on a large scale to finished products. We integrate our offer seamlessly into the customers’ value chain. Our comprehensive services range from early-stage Research & Development services such as synthesis, scale-up, formulation development, stability studies and method development all the way through to manufacturing services, ranging from preclinical R&D material for clinical trial purposes to commercial production. We are able to produce about 200 of the approximately 1500 registered drug substances used in medicine. Moreover, we produce 20 percent of global demand for caffeine. Consequently, nearly 1 billion individuals come into contact with Siegfried products.

At its locations around the world, Siegfried offers employees exciting career opportunities in international settings. We cultivate multidisciplinary cooperation and encourage our staff to actively shape and influence their careers. This approach, coupled with our dynamic working environment, make Siegfried an attractive employer. Your role: • Comprehensive Product Management: Oversee the entire commercial lifecycle of the product, from its transfer by development to the present date, acting as the Single Point of Contact (SPOC)., • Risk Analysis and Quality Control: Create, update, and monitor the product-specific Quality Risk Analysis (QRA) and ensure compliance with quality standards., • Data Monitoring and Analysis: Evaluate critical and key variables through statistical analysis, track data trends, and review the Annual Product Quality Review (APQR) to make informed decisions regarding control status., • Inspection Readiness: Ensure all aspects related to the product process are prepared for audits and regulatory inspections., • Performance Monitoring and Improvement: Identify trends, detect issues, and lead the implementation of corrective and preventive actions (CAPAs) to enhance products., • Deviation Management and Improvement Projects: Investigate process deviations, lead optimization projects, and engage cross-functional teams in improvement initiatives., • In-Process Controls (IPC) Monitoring: Ensure the tracking of critical parameters in laboratories and guarantee that data is visible and communicated at the plant level., • Technical Change Assessment: Analyze the impact of process modifications, determine their feasibility, and manage the quotations associated with these changes., • Process and Product Validation: Ensure continuous validation status, alignment with the APQR, and implementation of control strategies based on Critical Quality Attributes (CQA), Critical Process Parameters (CPP), and Critical Material Attributes (CMA)., • Product Launch and Transfer: Facilitate product transfers by ensuring technical documentation and providing necessary support to the receiving plant., • Manufacturing Optimization and Excellence: Lead improvement projects to enhance the robustness and sustainability of pharmaceutical processes in collaboration with Operational Excellence (OPEX). Your profile: • University degree in a scientific field or related, or a higher vocational training degree in a scientific field with previous experience in a similar position., • High level of English., • Experience in a similar technical position and in the pharmaceutical sector., • Knowledge of data management and application of statistical techniques. Working at Siegfried Siegfried's work environment is dynamic and international. With a highly professional and motivated team, the company operates in a future-oriented business field. Siegfried possesses a unique culture that leverages cultural differences to create a competitive advantage. Siegfried places highest priority on providing a flexible, diverse and discrimination-free working environment in which employees can develop personally and professionally, advance innovation and deliver superior performance. We strive to provide a work environment where employees can take on challenging jobs and associated responsibilities that best serve their personal and technical development and can benefit from the success of our company. The company regulations in respect of compensation and career development opportunities apply to all Siegfried sites. Additional conditions of employment are governed by location-specific circumstances, legislation and customs. In the Midst of People’s Lives – Across the Globe The Siegfried Group is one of the world’s leading Custom Development and Manufacturing Organizations (CDMOs) developing and producing active pharmaceutical ingredients (API), intermediates and finished dosage forms. As our core competence, we successfully integrate chemical and pharmaceutical capabilities into a single business model. The Siegfried name stands for highest quality, efficiency, flexibility and safety. Present in Europe, Asia and North America, we serve a broad global customer base from major international pharmaceutical companies down to small biologic-pharmaceutical organizations. For them we develop and produce product innovations on a large scale to finished products. We integrate our offer seamlessly into the customers’ value chain. Our comprehensive services range from early-stage Research & Development services such as synthesis, scale-up, formulation development, stability studies and method development all the way through to manufacturing services, ranging from preclinical R&D material for clinical trial purposes to commercial production. We are able to produce about 200 of the approximately 1500 registered drug substances used in medicine. Moreover, we produce 20 percent of global demand for caffeine. Consequently, nearly 1 billion individuals come into contact with Siegfried products.

At its locations around the world, Siegfried offers employees exciting career opportunities in international settings. We cultivate multidisciplinary cooperation and encourage our staff to actively shape and influence their careers. This approach, coupled with our dynamic working environment, make Siegfried an attractive employer. Your role: • Comprehensive Product Management: Oversee the entire commercial lifecycle of the product, from its transfer by development to the present date, acting as the Single Point of Contact (SPOC)., • Risk Analysis and Quality Control: Create, update, and monitor the product-specific Quality Risk Analysis (QRA) and ensure compliance with quality standards., • Data Monitoring and Analysis: Evaluate critical and key variables through statistical analysis, track data trends, and review the Annual Product Quality Review (APQR) to make informed decisions regarding control status., • Inspection Readiness: Ensure all aspects related to the product process are prepared for audits and regulatory inspections., • Performance Monitoring and Improvement: Identify trends, detect issues, and lead the implementation of corrective and preventive actions (CAPAs) to enhance products., • Deviation Management and Improvement Projects: Investigate process deviations, lead optimization projects, and engage cross-functional teams in improvement initiatives., • In-Process Controls (IPC) Monitoring: Ensure the tracking of critical parameters in laboratories and guarantee that data is visible and communicated at the plant level., • Technical Change Assessment: Analyze the impact of process modifications, determine their feasibility, and manage the quotations associated with these changes., • Process and Product Validation: Ensure continuous validation status, alignment with the APQR, and implementation of control strategies based on Critical Quality Attributes (CQA), Critical Process Parameters (CPP), and Critical Material Attributes (CMA)., • Product Launch and Transfer: Facilitate product transfers by ensuring technical documentation and providing necessary support to the receiving plant., • Manufacturing Optimization and Excellence: Lead improvement projects to enhance the robustness and sustainability of pharmaceutical processes in collaboration with Operational Excellence (OPEX). Your profile: • University degree in a scientific field or related, or a higher vocational training degree in a scientific field with previous experience in a similar position., • High level of English., • Experience in a similar technical position and in the pharmaceutical sector., • Knowledge of data management and application of statistical techniques. Working at Siegfried Siegfried's work environment is dynamic and international. With a highly professional and motivated team, the company operates in a future-oriented business field. Siegfried possesses a unique culture that leverages cultural differences to create a competitive advantage. Siegfried places highest priority on providing a flexible, diverse and discrimination-free working environment in which employees can develop personally and professionally, advance innovation and deliver superior performance. We strive to provide a work environment where employees can take on challenging jobs and associated responsibilities that best serve their personal and technical development and can benefit from the success of our company. The company regulations in respect of compensation and career development opportunities apply to all Siegfried sites. Additional conditions of employment are governed by location-specific circumstances, legislation and customs. In the Midst of People’s Lives – Across the Globe The Siegfried Group is one of the world’s leading Custom Development and Manufacturing Organizations (CDMOs) developing and producing active pharmaceutical ingredients (API), intermediates and finished dosage forms. As our core competence, we successfully integrate chemical and pharmaceutical capabilities into a single business model. The Siegfried name stands for highest quality, efficiency, flexibility and safety. Present in Europe, Asia and North America, we serve a broad global customer base from major international pharmaceutical companies down to small biologic-pharmaceutical organizations. For them we develop and produce product innovations on a large scale to finished products. We integrate our offer seamlessly into the customers’ value chain. Our comprehensive services range from early-stage Research & Development services such as synthesis, scale-up, formulation development, stability studies and method development all the way through to manufacturing services, ranging from preclinical R&D material for clinical trial purposes to commercial production. We are able to produce about 200 of the approximately 1500 registered drug substances used in medicine. Moreover, we produce 20 percent of global demand for caffeine. Consequently, nearly 1 billion individuals come into contact with Siegfried products.

Empresa del sector hostelería busca un/a camarero/a de pisos para trabajar en Montcada i Reixac y realizar las siguientes tareas: * Mantenimiento del orden y limpieza, de pisos, habitaciones, áreas comunes, y otras dependencias del hotel.

Nuevas vacantes para camareros y baristas en Badalona en agosto.