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Automation Engineer For our Grifols in Parets, we are looking for an Automation Engineer. This is a key hire for the successful implementation of a newly introduced equipment. We are seeking a professional with strong expertise and proven technical leadership skills. Main Requirements: • Minimum of 5 years of experience in industrial automation projects., • Advanced knowledge of Siemens TIA Portal and Siemens AWL Step7., • Hands-on experience with the commissioning of new machines/lines, troubleshooting, and process validation., • Desirable: knowledge of Rockwell and Zenon SCADA systems. Additional Skills (highly valued for this project): • Experience in the integration of equipment within GMP/pharma or other highly regulated environments., • Ability to prepare technical documentation and contribute to qualification processes (IQ/OQ)., • Strong team-player mindset to collaborate across engineering, maintenance, production, and quality teams., • Excellent problem-solving, analytical skills, and ability to liaise with external suppliers. This role will be essential in ensuring the successful start-up, optimization, and validation of the new machine, bringing expertise in both programming and systems integration. 📍 Location: Parets (Barcelona Area) Travelling may not be requiered at the begining but we need flexible travelling according the project is moving on -international-.

International Sales Area Manager International Role | Medical Devices | Hybrid Work | Fast-Growing Team ___ is an innovative technological company dedicated to the development and commercialization of medical devices in the fields of neuro, spinal and cardiac surgery. Offices based in Cerdanyola del Valles (Barcelona).Their mission is to provide worldwide surgeon with innovative solutions. As Sales Area Manager, you will be responsible for driving business growth in assigned territories, managing distributor relationships, and supporting the adoption of their innovative products in hospitals across the globe. You will work closely with surgeons and distributors, combining sales drive with hands-on product application support. This is an exciting opportunity to join a small but highly dynamic team and where your work will have direct impact on our growth. Your Role & Responsibilities: • Build and maintain strong relationships with distributors, creating added value through business growth., • Manage the full sales cycle in your assigned territories: from identifying opportunities and negotiating contracts to closing deals., • Support distributors with joint hospital visits, sales model reviews, product trainings, and assistance during surgeries., • Travel occasionally to meet clients, attend congresses, and represent NEOS Surgery internationally., • Identify new sales channels, expand distributor databases, and support overall business development., • Stay ahead of industry trends: analyse competitors, benchmark the market, and share insights with the team., • Collaborate closely with Marketing, Clinical, R&D, Quality, and Regulatory departments., • Master our product portfolio and work hand-in-hand with our product specialist to resolve customer queries., • Co-create marketing tools and solutions tailored to specific customer needs. What We’re Looking For: • Degree in Life/Health Sciences, Economics, or Business Administration., • 2–4 years of professional experience, ideally in the medical device sector., • Strong ambition to develop a career in business development and sales., • Previous commercial/sales experience is a plus, but not essential., • Fluent English, • Willingness to travel internationally Why Join NEOS Surgery? • Be part of a young, dynamic, and ambitious team where entrepreneurship and initiative are valued., • Work in the fast-growing medical devices sector with an international presence in 20+ countries., • Experience a flexible and hybrid work environment, designed to empower high performance and personal growth., • Join a company on the rise, where you will have real impact and grow alongside the business.

The Siegfried Group is a global life science company with a network of 13 sites in Europe, the USA and Asia. Siegfried offers contract development and manufacturing of active pharmaceutical ingredients, intermediates, and drug products and has sales more than CHF 1.3 billion Swiss Franks. Siegfried Holding AG employs over 3,900 people and is listed on the SIX Swiss Exchange (SIX: SFZN). Are you a Senior Manager Business Applications (SAP Data Migration) looking for a new challenge in a dynamic CDMO Pharmaceutical Industry in our Barberà del Vallès site? Reporting to the Head Data Intelligence and SAP-Basis, you will be responsible for replacing the existing system to migrate data, selecting and evaluating data migration designs, governing scalable data migration architectures and standards across SAP programs. Your role: • Technical and functional lead for SAP data migration and master data projects, including architectural transition from R/3 (ECC 6.0) to the S/4HANA landscape., • Convert business needs and design scalable, compliant data migration solutions and roadmaps, ensuring end-to-end consistency and auditability across all Siegfried sites., • Design and govern scalable data migration architectures and standards to ensure quality, compliance, and consistency across SAP programs., • Select and evaluate data migration (e.g., SAP Data Services, LSMW) and master data tools to ensure reusability, compliance, and fit-for-purpose solutions., • Coordination and management of external consulting resources in term of project management, • Conduct internal trainings on data migration and master data, promoting best practices and knowledge sharing. Your profile: • Educational background in Information Technology or equivalent qualification., • Led at least one complex data migration project to SAP S/4HANA., • At least 7 years experience in delivering services related to data migration, transformation, and support for mergers, acquisitions, and divestitures, • Served as an enterprise architect or advisor, guiding customers in building IT roadmaps using SAP products and services., • Experience with Data Management solutions (e.g., MDG, ILM) or SAP Industry Solutions is an added advantage, • Experience with SQL is a plus., • Solution-oriented with strong communication skills., • Willingness to work on a broad range of topics in the area of SAP Master data ., • Resilient team player with high flexibility., • Fluent in Spanish and English, both written and spoken. 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. Who we are 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.

Desde ManpowerGroup Talent Solutions estamos buscando un Experto en implementaciones desde cero de LIMS, para una empresa multinacional del sector pharma, referente en medicamentos genéricos de valor añadido, ubicada en Martorelles. Dentro del departamento de IT Quality and Compliance, tus funciones principales serán: • Implementar un sistema LIMS desde cero para gestionar integralmente los laboratorios de Control de Calidad e I+D, eliminando por completo el uso de papel., • Diseñar y desarrollar una arquitectura modular que permita la integración escalonada de los diferentes módulos del LIMS, garantizando flexibilidad y adaptabilidad a las necesidades del negocio., • Automatizar la captura de datos conectando equipos e instrumentos de laboratorio al LIMS para mejorar la trazabilidad, minimizar errores y optimizar la eficiencia operativa., • Implementar un Sistema de Ejecución de Laboratorio (LES) que digitalice los flujos de trabajo del laboratorio, incluyendo la gestión de muestras, reactivos, análisis e informes., • Implementar un cuaderno electrónico de laboratorio (ELN) en el área de I+D, facilitando la documentación estructurada y el cumplimiento normativo de la investigación., • Garantizar la integración del LIMS con otros sistemas corporativos (ERP, MES, sistemas de calidad, etc.) para lograr una gestión eficiente y centralizada de la información., • Responsable de supervisar el mantenimiento de la aplicación LIMS, optimizando las nuevas funcionalidades como herramientas de IA. Trabajar en un entorno regulado, garantizando el cumplimiento de las normativas aplicables al sector farmacéutico, como GMP, FDA 21 CFR Parte 11, GAMP 5 e ISO., • Colaborar en la validación del sistema LIMS, siguiendo las mejores prácticas de Validación de Sistemas Informáticos (CSV) para garantizar el cumplimiento de los requisitos normativos., • Gestionar la seguridad y la accesibilidad de los datos, estableciendo los controles y permisos adecuados., • Capacitar a los usuarios y gestionar la adopción del sistema, asegurándose de que los equipos de laboratorio estén familiarizados con el LIMS y sus funcionalidades., • Colaborar estrechamente con equipos multidisciplinares (TI, Calidad, Producción, I+D, proveedores) para garantizar el éxito del proyecto. Requisitos: • Mínimo 3 años como Consultor o Técnico LIMS., • Sistemas LIMS. Configuración o programación de estos sistemas., • Empower, LabX, LIMS (distintos fabricantes)., • Inglés nivel B2 a nivel comprensión, • Se valorará la experiencia en el cumplimiento de regulaciones de la industria farmacéutica como GMP, FDA 21 CFR Parte 11, GAMP 5 e ISO., • Project Management Methodology. Competencias: • Liderazgo y mentalidad orientada a resultados, • Trabajo en equipo y comunicación efectiva, • Adaptabilidad y gestión del cambio, • Resolución de problemas y proactividad, • Atención al detalle, • Autonomía y toma de decisiones, • Compromiso y responsabilidad Qué te ofrecemos: • Entorno de trabajo que promueve el aprendizaje y desarrollo., • Contrato indefinido directamente con cliente, • Modelo de trabajo híbrido (3 días de teletrabajo a la semana, con flexibilidad si hay que acudir algún día extra, de forma esporádica), • Seguro de vida y accidentes, • Retribución Flexible (Seguro Médico, Ticket Restaurant, Tarjeta Transporte, Guardería y Formación), • E-Learning (Acceso a una plataforma de E-learning gratuita con más de 100 cursos, • Idiomas: Clases en Plataforma Online Gratuita, • Flexibilidad Horaria, de vacaciones y teletrabajo, • Horario: Lunes a Jueves flexibilidad 7:00-9:30h. Salida a partir de las 16:00h en adelante. Viernes a partir de les 15:30h, • Cantina 4 euros al menú. En los procesos de selección garantizamos la igualdad de oportunidades. Trabajamos para crear equipos diversos y estamos convencidos de que una cultura y un entorno inclusivos nos ayudan a hacer realidad nuestro propósito: mejorar la vida de las personas, empezando por nosotros mismos

At Siegfried, we offer more than just a job — we provide a platform for you to thrive, grow, and shape your future. With locations across the globe, we empower our employees to build meaningful, international careers in a truly dynamic and collaborative environment. We believe in the power of multidisciplinary teamwork and encourage every individual to take ownership of their personal and professional development. At Siegfried, your ideas matter, your voice is heard, and your contribution drives real impact. Our culture of innovation, continuous learning, and shared success makes Siegfried not just a workplace — but a place where you can growth professionally. Your Role: • Technical and functional consultant for Data Intelligence, including the implementation of reporting and analytics solutions in the SAP BW/4HANA and SAP Analytics Cloud environments (SAP Datasphere and SAP Analytics Cloud Planning as a plus)., • Translate business needs and design scalable, compliant Data Intelligence solutions by implementing roadmaps, ensuring end-to-end consistency and auditability across all Siegfried sites., • Design and govern scalable Data Intelligence solutions with the focus on reporting and analytics based on standards to ensure quality, compliance, and consistency across Siegfried's business areas., • Support evaluation of the new reporting and analytics tools (SAP Business Data Cloud, SAP DataSphere, SAP Analytics Cloud for Excel, and others)within data intelligence area to ensure reusability, compliance, and fit-for-purpose solutions., • Coordination and management of external consulting resources in term of project and resource management, • Conduct internal trainings on data intelligence (reporting/analytics), promoting best practices and knowledge sharing. Your Profile: • Educational background in Information Technology or equivalent qualification., • At least 10 years of previous experience in a similar role., • Proven project and hando-on expertise in reporting and analytics, predominantly within the SAP environment., • Proven experience in delivering services related to data extraction, data modelling, and building highly appealing user interfaces, • Experience with Data Management solutions (e.g., MDG, ILM) or SAP Industry Solutions is an added advantage, • Experience with programming languages like ABAP, AMDP, and JavaScript is a plus, • Solution-oriented personality with strong communication skills., • Willingness to work on a broad range of topics around Data Intelligence, • Resilient team player with high flexibility., • Fluent in Spanish and English, both written and spoken.

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.

Sales Area Manager - Medical Device International Role | Medical Devices | Hybrid Work | Fast-Growing Team NEOS Surgery is an innovative technological company dedicated to the development and commercialization of medical devices in the fields of neuro, spinal and cardiac surgery. Offices based in Cerdanyola del Valles (Barcelona).Their mission is to provide worldwide surgeon with innovative solutions. As Sales Area Manager, you will be responsible for driving business growth in assigned territories, managing distributor relationships, and supporting the adoption of their innovative products in hospitals across the globe. You will work closely with surgeons and distributors, combining sales drive with hands-on product application support. This is an exciting opportunity to join a small but highly dynamic team and where your work will have direct impact on our growth. Your Role & Responsibilities: Build and maintain strong relationships with distributors, creating added value through business growth. Manage the full sales cycle in your assigned territories: from identifying opportunities and negotiating contracts to closing deals. Support distributors with joint hospital visits, sales model reviews, product trainings, and assistance during surgeries. Travel occasionally to meet clients, attend congresses, and represent NEOS Surgery internationally. Identify new sales channels, expand distributor databases, and support overall business development. Stay ahead of industry trends: analyse competitors, benchmark the market, and share insights with the team. Collaborate closely with Marketing, Clinical, R&D, Quality, and Regulatory departments. Master our product portfolio and work hand-in-hand with our product specialist to resolve customer queries. Co-create marketing tools and solutions tailored to specific customer needs. What We’re Looking For: Degree in Life/Health Sciences, Economics, or Business Administration. 2–4 years of professional experience, ideally in the medical device sector. Strong ambition to develop a career in business development and sales. Previous commercial/sales experience is a plus, but not essential. Fluent English Willingness to travel internationally Why Join NEOS Surgery? Be part of a young, dynamic, and ambitious team where entrepreneurship and initiative are valued. Work in the fast-growing medical devices sector with an international presence in 20+ countries. Experience a flexible and hybrid work environment, designed to empower high performance and personal growth. Join a company on the rise, where you will have real impact and grow alongside the business.

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. Benefits: • Annual Bonus: 7.5%, • Two days of home office per week, • Free parking, • Good public transport available to reach the site, • Subsidized canteen on-site or restaurant ticket: to use when eating out or working from home, • Medical, life, and accident insurance 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.

Colaborar con otros departamentos, como ventas y almacén, para asegurar una coordinación efectiva y una experiencia del cliente sin inconvenientes. Experiencia previa en roles administrativos o de soporte, preferiblemente en el sector de servicios técnicos o atención al cliente. Gestionar la doc

Somos la firma global de talento: Selección, headhunting, formación y consultoría de Eurofirms Group.En Claire Joster creemos en el talento único de cada persona y sabemos que la diversidad aporta valor a los equipos, impulsando organizaciones más innovadoras, creativas y eficientes.Por eso, co

You will validate any new parts or suppliers against production and customer requirements as well as our quality standards. Analyze and evaluate special customer-relevant quality requirements. Supplier Quality Management from acquisition phase to SOP and during production.

Como ingeniero/a de calidad tu misión principal será el desarrollo de documentación PPAP para una de las principales OEMS y contribuir al crecimiento de la industria de la automoción.

Importante empresa del sector metalúrgico dedicada a la creación de piezas de automóviles situada en Barberà del Vallés, precisa incorporar personal como operario/a en la sección de verificación.Medición con herramientas como pie de rey o gramil.Disponibilidad para trabajar de Lunes a Vierne

Please add a text and explain the position.Join multidisciplinary adhesives operations team.Develop skills in industrial maintenance in a high quality standards environment.Support maintenance responsible to fix assets and maintenance strategy in a plant.Support maintenance responsible with internat

Please add a text and explain the position.Join multidisciplinary adhesives operations team.Develop skills in industrial maintenance in a high quality standards environment.Support maintenance responsible to fix assets and maintenance strategy in a plant.Support maintenance responsible with internat

Please add a text and explain the position.Join multidisciplinary adhesives operations team.Develop skills in industrial maintenance in a high quality standards environment.Support maintenance responsible to fix assets and maintenance strategy in a plant.Support maintenance responsible with internat

Develop practicable, sustainable actions at shopfloor, compliant to Quality standard requirements, alignment with Production, Engineering .CP moderation, outline risk reduct.Participate in ADP/MOC projects and support processes requiring Quality involvement .Root-cause-analysis, corrective action, p

Please add a text and explain the position.Join multidisciplinary adhesives operations team.Develop skills in industrial maintenance in a high quality standards environment.Support maintenance responsible to fix assets and maintenance strategy in a plant.Support maintenance responsible with internat

Empresa logística ubicada en Sabadell Sud precisa incorporar mozo/a manipulador/a con carretilla, transpaleta electrica.Funciones: Entradas, salidas, preparación de pedidos, picking con PDA, ubicación de material, etiquetado, encajado, manipulación en almacén entre otras tareas derivadas del p

Please add a text and explain the position.Join multidisciplinary adhesives operations team.Develop skills in industrial maintenance in a high quality standards environment.Support maintenance responsible to fix assets and maintenance strategy in a plant.Support maintenance responsible with internat

Experiencia demostrable mínimo de 6 meses desarrollando las funciones descritas. Te apasiona el mundo de la automoción y tienes experiencia gestionando equipos en linea de montaje y manipulación de piezas?. Organización de personal en linea de producción.

Please add a text and explain the position.Join multidisciplinary adhesives operations team.Develop skills in industrial maintenance in a high quality standards environment.Support maintenance responsible to fix assets and maintenance strategy in a plant.Support maintenance responsible with internat

Develop practicable, sustainable actions at shopfloor, compliant to Quality standard requirements, alignment with Production, Engineering .CP moderation, outline risk reduct.Participate in ADP/MOC projects and support processes requiring Quality involvement .Root-cause-analysis, corrective action, p

Conduct quality “GEMBA” walks to ensure correct operation and compliance with specifications across all production lines. Participate in continuous improvement and cost reduction projects.

Mantenir actualitzada la documentació, arxius i registres de les persones treballadores, amb els antecedents i informació relativa a la plantilla (altes, baixes, contractes i clàusules, liquidacions, horaris, calendaris laborals, canvis de dades de pagament, justificants, etc. Empresa ubicada a S

Develop practicable, sustainable actions at shopfloor, compliant to Quality standard requirements, alignment with Production, Engineering .CP moderation, outline risk reduct.Participate in ADP/MOC projects and support processes requiring Quality involvement .Root-cause-analysis, corrective action, p

Empresa logística ubicada en Sabadell Sud precisa incorporar mozo/a manipulador/a.Funciones: Entradas, salidas, preparación de pedidos, picking con PDA, ubicación de material, etiquetado, encajado, manipulación en almacén entre otras tareas derivadas del puesto.Buscamos personal polivalente y

Empresa logística ubicada en Sabadell Sud precisa incorporar mozo/a manipulador/a para campaña textil y libros:.Funciones: Entradas, salidas, preparación de pedidos, picking con PDA, ubicación de material, etiquetado, encajado, manipulación en almacén entre otras tareas derivadas del puesto.B

Per empresa ubicada a Sabadell dedicada a la promoció i defensa dels drets de les persones precisen:.Administrativo/a àrea de gestió de persones.Mantenir actualitzada la documentació, arxius i registres de les persones treballadores, amb els antecedents i informació relativa a la plantilla (alt

Operates machines and production equipment safely in accordance with instructions .Sets up or adjusts equipment according to manufacturing specifications .Monitors the quality of output to identify or discard re-manufacture faulty products .Maintains accurate daily production records so that manufac

Operates machines and production equipment safely in accordance with instructions .Sets up or adjusts equipment according to manufacturing specifications .Monitors the quality of output to identify or discard re-manufacture faulty products .Maintains accurate daily production records so that manufac

Operates machines and production equipment safely in accordance with instructions .Sets up or adjusts equipment according to manufacturing specifications .Monitors the quality of output to identify or discard re-manufacture faulty products .Maintains accurate daily production records so that manufac

Empresa cárnica en Montornés precisa incorporar a un mozo/peon para mover, paletizar y almacenar mercancía congelada.

Empresa logística ubicada en Sabadell Sud precisa incorporar mozo/a manipulador/a.Funciones: Entradas, salidas, preparación de pedidos, picking con PDA, ubicación de material, etiquetado, encajado, manipulación en almacén entre otras tareas derivadas del puesto.Buscamos personal polivalente y

Empresa logística ubicada en Sabadell Sud precisa incorporar mozo/a manipulador/a.Funciones: preparación de pedidos, picking con PDA, ubicación de material, etiquetado, encajado, manipulacion en almacén entre otras tareas derivadas del puesto.Buscamos personal polivalente y con compromiso.IMPRES

Working on leading-edge AWS-hosted applications, the QA Engineer will develop and execute both automated and manual testing scenarios to ensure the delivery of high-quality software products.

Software Quality Assurance Engineer / 6 months / Barcelona (Hybrid) / €300 -€345per day. I am currently looking for a Software Quality Assurance Engineer.

Quieres dar tus primeros pasos en el mundo laboral y desarrollar tu vocación? ¡¡Ha llegado tu momento!! En.Lidera tu camino y únete a nuestro Talent Program Pathfinder! Una experiencia en la que TÚ serás protagonista.Pero no te preocupes, no lo harás en solitario.Tendrás guías que te acompa

Are you enthusiastic about becoming a highly skilled quality engineer? If so, this position may pique your interest. As a Quality Engineer in the automotive sector, you will be responsible for developing a plan and implementing a systematic approach to ensure that all defined automotive standards, p

Servicios de Executive Search, RPO y Soluciones de Talento.Nuestra misión es impulsar el crecimiento y la realización tanto de personas como de organizaciones.Facilitamos a las personas la búsqueda de oportunidades inspiradoras y ayudamos a las organizaciones a identificar profesionales que las l

This role involves developing, implementing, and maintaining quality assurance protocols to ensure supplier compliance and product quality. Create and maintain supplier quality evaluation and control systems to ensure consistent quality standards. Takes initiative in identifying and addressing quali

The Quality Assurance Specialist will provide support to QA team by contributing to all activities involving quality assurance and compliance with applicable regulatory requirements and assuring that Company standards are maintained, and product integrity is preserved. At Adalvo, we're not just a co

Estamos buscando un/a Senior Quality Technician.

The electronics quality manager ensures that electronic products meet required quality and reliability standards. Bitron is a multinational, family-owned industrial group with a clear vision: to create products and systems that help improve the quality of people's lives and the world around them. Kn

Ready to lead quality at the infrastructure level of travel?.