Quality jobs in Parets Del VallèsCrear alertas

Responsibilities: • Carry out process audits and approval of new suppliers for their incorporation into the group's panel., • Pilot the technical support to supplier with the technical departments of the group., • Carry out the homologation of the purchase components., • Pilot the action plan of the deviations detected in the homologation phase of the purchase components., • Define and maintain KPI's for monitoring the position., • Define the reception control plan for the purchase components., • Take active roles in the work of internal-external issues, risk& opportunity studies, D/FMEA studies etc., • Inform and educate to suppliers about all the requests and expectations which are introduced in hand manuals, agreements, instructions and so on. Follow-up suppliers' project documentations and take these documents convenient format and timely • Track the serial projects and supplier’s parts failure trends, take necessary actions to reduce these failure quantities and rates, • Manage suppliers’ 8D processes which are escalated, get suitable respond in each step of 8D and on time. Minimum Required Knowledge and Skills: • High School Degree • Using ability MS Office Programs, • Have at least 3 years experiences in quality departments, 1 year of experience as a SQE within productive companies, • Knowledge of ISO 9001 is required. ISO 14001 and ISO 22163 etc. systems are positively valued., • Knowledge of any of these production processes, plastic injection, aluminum casting, stamping, welding, gluing, fabric manufacturing processes, painting, machining, foaming, upholstering, cutting and sewing, press, folding, laser cutting, is valued positively., • Knowledge of Core Tools (APQP-PPAP, SPC, MSA, PFMEA, 8D), • Auditing knowledge is required, • Knowledge of: English, Spanish. We offer: • position, • for professional growth, • Salary aligned with the candidate's value, • Flexible working hours, • 30% home office

Quieres formar parte de un equipo con impacto real en la salud global? En Noucor, compañía químico-farmacéutica, te ofrecemos la oportunidad de liderar proyectos que llegan a más de 100 países 🌍. En esta ocasión, buscamos una persona para incorporarse en el departamento de Quality Assurance. ¿Te apuntas? ¿Qué funciones harás? • Participación en proyectos de Cualificación de equipos, servicios e intalaciones, revisión y aprobación de las mismas., • Participación en proyectos de Validación de sistemas informáticos, revisión y aprobación de las mismas., • Evaluación de proveedores de sistemas informaticos, mantenimiento y calibraciones de equipos , servicios e instalaciones., • Revisión de SOPs' de departamentos de Inginiería , mantenimiento e IT., • Revisión de planes de cualificación, validación de sistemas informáticos , mantenimientos y calibraciónes., • Elaboración y aprobación de SOP`s relacionados con validaciones de sistemas y cualificaciones de equipos, instalaciones y serivcios., • Aseguramiento del Data Integrity., • Gestión de desviaciones , CAPAS y controles de cambios., • Realización de autoinspecciones., • Participación en auditorias de clientes para asgurar el cumplimiento de las normas GxP ( FDA, EU ), • Conocer cumplir y hacer cumplir los PNT's y las normativas GXP. ¿Qué perfil buscamos? • Grado o Licenciatura en Farmacia, Biomedicina, Química, Ciencias de la Salud, Ingeniería o afines., • Mínimo 2 años de experiencia en una posición similar en el sector farmacéutico o sector de la alimentación., • Se valorará positivamente formación complementaria: Posgrado en sistemas de Calidad en la Industria Farmacéutica y afines, Posgrado en estadística aplicada a la industria farmacéutica y afines y/o gestión de equipos de laboratorio., • Nivel de inglés alto ¿Qué ofrecemos? ⚙️Trabajarás dentro de un gran equipo de profesionales con muy buen ambiente laboral. 🚀Tendrás aprendizaje y desarrollo continuo. 📍Oficinas ubicadas en Palau-solità i Plegamans. ❤️Política Flex&Work con horario flexible y 1 día de home office. 💼Proyecto indefinido y salario competitivo. 🌱Servicio de comedor subvencionado y parking gratuito. 🧘🏻 ♀️Nos preocupamos por tu Bienestar – el Plan Wellness incluye fisioterapia, psicología online, eventos deportivos, entre otros. En Noucor creemos en el poder de los equipos diversos. Por eso, valoramos todas las candidaturas sin distinción de género, edad, origen, orientación sexual, identidad de género o cualquier otra condición. Si te interesa aportar tu granito de arena al ecosistema de la salud y al bienestar de las personas, esta es tu oportunidad, no lo dudes, ¡te estamos esperando!

Do you want to be part of a team with a real impact on global health? At Noucor, a chemical and pharmaceutical company, we offer you the opportunity to lead projects that reach more than 100 countries worldwide 🌍. We are currently looking for a Clinical R&D Quality Assurance Technician to join Noucor’s Quality team. Main Tasks: • Ensure that all processes related to clinical trials are performed in compliance with GCP (Good Clinical Practice) and applicable quality standards., • Provide QA support to clinical trial activities, including documentation review and quality oversight of internal teams and external partners (CROs, service providers)., • Evaluate and manage quality issues, deviations, CAPAs, change controls and complaints related to Clinical Trials., • Support quality activities related to Investigational Medicinal Products (IMPs) in collaboration with Pharmaceutical Development and Analytical Development., • Maintain awareness of applicable quality regulations and compliance requirements impacting clinical development and R&D activities. Requirements: • Degree in Pharmacy, Chemistry, Biology, or similar., • Fluent in English and Spanish., • Experience in Good Clinical Practices (GCP); knowledge of GMP requirements for IMPs in clinical trials (formerly Annex 13)., • Good command of MS Office., • High willingness to learn and take on new challenges and responsibilities., • Motivation, teamwork, and good communication skills. We Offer: 🤩 Work within a great team of professionals with a very good work environment. ⚙️ Innovative work environment focused on continuous improvement. 🚀 Continuous learning and development. 💼 Competitive benefits package and flexible schedule. 📍 Offices in Palau-solità i Plegamans. 💰 Competitive salary. Interested in joining us? At Noucor, we believe in the value of diverse teams. We therefore welcome and consider all applications regardless of gender, age, background, sexual orientation, gender identity, or any other personal characteristic. If you meet most of the requirements and are motivated by the project, we would be pleased to hear from you.

Misión del puesto: Dar soporte en las tareas, proyectos y seguimiento para asegurar el cumplimiento de los requisitos del Sistema de Calidad y Medio Ambiente, así como contribuir a las actividades internas del departamento para alcanzar los objetivos definidos. Responsabilidades: • Gestionar y mejorar los Sistemas de Calidad (ISO 9001, IATF 16949, EN9100) y Medio Ambiente (ISO 14001)., • Coordinar auditorías internas, externas, de proveedores y clientes., • Supervisar y analizar datos de calidad y ambientales, proponiendo acciones de mejora., • Garantizar el cumplimiento legal y normativo vigente, tanto nacional como internacional., • Apoyar en sostenibilidad, gestión de ciclo de vida de productos y programas de formación interna., • Delegar funciones del Quality & Env Manager cuando sea necesario. Requisitos: • Grado en Química, Ingeniería Industrial o Ciencias Ambientales., • Imprescindible conocimientos en IATF 16949 e ISO 9001; valorable EN9100 e ISO 14001., • Informática a nivel usuario (Office, SAP)., • Idiomas: Español, Catalán e Inglés (mínimo B2)., • Experiencia mínima de 2 años en puestos similares en industria de automoción y/o aeronáutica. Podrás contribuir directamente en la mejora de procesos y la sostenibilidad de la empresa, trabajando en un entorno profesional y dinámico.

Join Our Team as a Manufacturing Engineer at Multi-Wing in la Roca del Vallès, Catalonia, Spain. Are you passionate about transforming engineering designs into real, manufacturable products? Do you enjoy working at the intersection of design, production, and data accuracy? At Multi-Wing, we’re looking for a Manufacturing Engineer to help bridge the gap between product design and production — ensuring our world-class airflow solutions are built with precision and efficiency. 🚀 What You’ll Do As part of our Engineering team, you’ll: • Create and maintain product codifications, Bills of Materials (BoMs), and routings in Microsoft Dynamics 365., • Ensure manufacturing data is always accurate, consistent, and aligned with approved drawings and standards., • Collaborate closely with Design, Planning, Production, and Quality to release new products into manufacturing., • Execute and document engineering changes (ECN/ECO), ensuring timely updates across systems., • Support data governance, monitor master-data quality, and drive continuous improvement in processes and standards. This role is perfect for someone who thrives on precision, loves structure, and enjoys turning complex product data into clear, reliable manufacturing information. 🔧 What We’re Looking For • Education: BSc/MSc in Mechanical, Industrial, or Management Engineering (or equivalent)., • (A technical diploma with hands-on experience in manufacturing will also be considered.), • Experience:, • Entry-level candidates with internships/traineeships in manufacturing are welcome., • 1–3 years of experience in manufacturing engineering or master-data management (BoMs, routings) is a plus., • Skills:, • Strong understanding of production cycles, BoMs, and technical drawings., • Accuracy-focused, analytical, and comfortable with data-driven problem solving., • Advanced Excel skills and experience with ERP systems (preferably Microsoft Dynamics 365)., • Solid communication and documentation habits in a cross-functional environment., • Languages:, • English and Spanish – working proficiency (B2+). 💡 Nice to Have • Exposure to Lean / Continuous Improvement principles., • Familiarity with ECN/ECO processes and master-data quality KPIs., • Knowledge of variant/configuration management and data validation tools (e.g., Power Query, SQL). 🌍 Why Join Multi-Wing? At Multi-Wing, we’re proud to design and manufacture customized axial fans that help shape a more energy-efficient world. Joining us means becoming part of a global engineering community that values innovation, precision, and teamwork. You’ll have the opportunity to grow your technical expertise, contribute to process excellence, and make a visible impact in a dynamic, international manufacturing environment. 👉 Ready to take the next step? Apply now and help us drive excellence from design to production.

Delegar funciones del Quality & Env Manager cuando sea necesario.

A leading global healthcare company is seeking a Microbiological Control Technical Manager to lead a technical team focused on Quality Control activities.This position requires 3-5 years of experience in process validation, strong analytical skills, and the ability to collaborate effectively.The suc

A leading beauty company in Granollers seeks an experienced Master Data Governance and Analytics Manager to enhance data quality and governance processes.The ideal candidate will have significant experience in data management, process improvement, and project management, ensuring high-quality data u

Accomplishes tasks as directed by supervisor(s) .Supports processes/operations of the respective Henkel team .Complies with Henkel's internal guidelines, rules and regulations.Join multidisciplinary adhesives operations team.Develop skills in industrial maintenance in a high quality standards enviro

Accomplishes tasks as directed by supervisor(s) .Supports processes/operations of the respective Henkel team .Complies with Henkel's internal guidelines, rules and regulations.Join multidisciplinary adhesives operations team.Develop skills in industrial maintenance in a high quality standards enviro

Accomplishes tasks as directed by supervisor(s) .Supports processes/operations of the respective Henkel team .Complies with Henkel's internal guidelines, rules and regulations.Join multidisciplinary adhesives operations team.Develop skills in industrial maintenance in a high quality standards enviro

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

Develop and deliver training and workshops related to quality, safety, and environment. Collaborate with other departments to integrate quality, safety, and environmental policies across all areas of the organization. Specific training in quality management systems, environmental management, and occ

Global tech company founded in 2011.Our mission is to shape the future through technology.We are looking for a highly organized.Quality Management System (QMS) Technician.Your primary mission is to maintain our QMS based on ISO9001, IATF 16949, ISO13485 and ISO14001.You will ensure that our internal

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

Become part of the team and bring your uniqueness to us! We welcome all applications across different genders, origins, cultures, religions, sexual orientations, disabilities, and generations. Monitor and communicate changes in Integrated Management System to impacted stakeholders. Chemical Engineer

Accomplishes tasks as directed by supervisor(s) .Supports processes/operations of the respective Henkel team .Complies with Henkel's internal guidelines, rules and regulations.Join multidisciplinary adhesives operations team.Develop skills in industrial maintenance in a high quality standards enviro

Accomplishes tasks as directed by supervisor(s) .Supports processes/operations of the respective Henkel team .Complies with Henkel's internal guidelines, rules and regulations.Join multidisciplinary adhesives operations team.Develop skills in industrial maintenance in a high quality standards enviro

Accomplishes tasks as directed by supervisor(s) .Supports processes/operations of the respective Henkel team .Complies with Henkel's internal guidelines, rules and regulations.Join multidisciplinary adhesives operations team.Develop skills in industrial maintenance in a high quality standards enviro

Experience in production environments, preferably in the automotive industry. Modify and update manufacturing instructions and other production-related documents. Conduct quality “GEMBA” walks to ensure correct operation and compliance with specifications across all production lines.

Experience in production environments, preferably in the automotive industry. Modify and update manufacturing instructions and other production-related documents. Conduct quality “GEMBA” walks to ensure correct operation and compliance with specifications across all production lines.

Modify and update manufacturing instructions and other production-related documents.Prepare quotations for new parts following the established procedure.Prepare documentation and follow up on online tests.Prepare and manage test shipments.Conduct quality “GEMBA” walks to ensure correct operation

Empresa logística ubicada en Sabadell Sud precisa incorporar mozo/a manipulador/a.Funciones: Clasificación de mercancía, embolsado, etiqeutado, preparación de pedidos, ubicación de material, encajado, manipulación en almacén entre otras tareas derivadas del puesto.Buscamos personal polivalen

Participate in the development and maintenance of quality procedures related to complaints, vigilance system and post-market surveillance. You have 2 years of experience in Quality Assurance within pharmaceutical industry and/or medical devices.

We are currently looking for a Clinical R&D Quality Assurance Technician to join Noucor’s Quality team. Maintain awareness of applicable quality regulations and compliance requirements impacting clinical development and R&D activities. Ensure that all processes related to clinical trials are perfo

We are currently looking for a Clinical R&D Quality Assurance Technician to join Noucor’s Quality team. Main Tasks: Ensure that all processes related to clinical trials are performed in compliance with GCP (Good Clinical Practice) and applicable quality standards. Provide QA support to clinical tr

We are currently looking for a Clinical R&D Quality Assurance Technician to join Noucor’s Quality team. Evaluate and manage quality issues, deviations, CAPAs, change controls and complaints related to Clinical Trials. Support quality activities related to Investigational Medicinal Products (IMPs)

Delegar funciones del Quality & Env Manager cuando sea necesario.

Tienes experiencia liderando equipos en entornos de calidad? ¿Te apasiona mejorar procesos y asegurar la excelencia en el servicio? ¿Hablas inglés con fluidez?.Somos una empresa en plena expansión, especializada en ofrecer soluciones de calidad en el entorno servicios.Apostamos por la mejora con

Delegar funciones del Quality & Env Manager cuando sea necesario.

Qué buscamos? Buscamos un/a Service Quality Manager que quiera liderar el área y asumir el reto de garantizar la excelencia operativa.

Tienes experiencia liderando equipos en entornos de calidad? ¿Te apasiona mejorar procesos y asegurar la excelencia en el servicio? ¿Hablas inglés con fluidez?.Somos una empresa en plena expansión, especializada en ofrecer soluciones de calidad en el entorno servicios.Apostamos por la mejora con

Delegar funciones del Quality & Env Manager cuando sea necesario.

Hola! Desde AXPE Consulting , estamos gestionando una nueva oportunidad para QA Tester (Manual / API).Buscas un reto en QA dentro de un entorno corporativo, con foco en testing de APIs y componentes digitales ? &##128161; ¿Qué estamos buscando? ✅ Perfil Senior con +4 años de experiencia

Tienes experiencia liderando equipos en entornos de calidad? ¿Te apasiona mejorar procesos y asegurar la excelencia en el servicio? ¿Hablas inglés con fluidez?.Le gusta esta oportunidad? Asegúrese de inscribirse rápido, ya que se espera un gran volumen de solicitudes.Desplácese hacia abajo par

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

This position oversees the Quality Control, Quality Assurance, and Regulatory Affairs functions, ensuring that operations, systems, and products consistently meet applicable GxP and global regulatory requirements. The Director of Quality and Regulatory Affairs will play a central role in defining an

As a Garment Quality Team Leader, you ensure that all garment quality standards of our global fashion client are consistently met. Manage quality incidents and coordinate with the Client quality/buying team to resolve issues. Plan, coordinate, and follow up on daily quality activities and workload.

We are looking for a Language Data and Quality Reviewer with proficiency in Galician to join our team. While prior experience in similar roles is beneficial, we encourage candidates with some experience in data analysis, quality assurance, or related fields to apply, especially those looking to grow

BS/BA in Computer Science or a related field, or equivalent years of experience in quality assurance. Drive further adoption of unit, integration, and system testing; metrics to monitor code coverage; bug prevention strategies; and other quality measures.

This role is ideal for those candidates who enjoy hands-on laboratory work, operating under GMP standard, and contributing to high-quality, safe production processes. Strong attention to detail, documentation accuracy and commitment to quality.

As our Quality Control Engineer, you will be the critical guardian of quality for our high-performance, AI-driven solutions and LLM services. As a Quality Control Engineer, you will:. Evaluate system quality for scalability, latency, and data integrity.

Chief Data Office en la línea de trabajo de calidad de datos.El objetivo principal será implementar y supervisar controles de calidad de datos, asegurando el cumplimiento de requisitos funcionales y regulatorios.Zona horaria NY (flexibilidad para España).Traducir requisitos funcionales y regulato

Quality Control Engineer – AI & LLM Services. Want to be on the front line of real-world AI quality, validating systems that power next-generation LLMs, chatbots, and AI services used globally?. A fast-scaling European deep-tech company at the intersection of AI and advanced computing is hiring a

This position oversees the Quality Control, Quality Assurance, and Regulatory Affairs functions, ensuring that operations, systems, and products consistently meet applicable GxP and global regulatory requirements. The Director of Quality and Regulatory Affairs will play a central role in defining an

It is a fixed-term contract to work until 30th June 2026What You'll Do:As our Quality Control Engineer, you will be the critical guardian of quality for our high-performance, AI-driven solutions and LLM services. Evaluate system quality for scalability, latency, and data integrity. Create and standa

This role is ideal for those candidates who enjoy hands-on laboratory work, operating under GMP standard, and contributing to high-quality, safe production processes. Responsibilities: Analytical tests on production materialsComplete laboratory documentation in line with GMP requirementsMaintain lab

Own quality validation for AI & LLM-based applications (chatbots, RAG, APIs, data pipelines). Quality Control Engineer – AI & LLM Services. Want to be on the front line of real-world AI quality, validating systems that power next-generation LLMs, chatbots, and AI services used globally?.