Trabajos quality en Caldes De MontbuiCrear alertas

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.

Job Summary Under direction of the immediate supervisor, the Specialist participates in the execution and coordination of manufacturing processes following quality, safety, and environmental rules. He/She interprets analytical data, may review existing procedures and methods and in some cases may write laboratory procedures. He/She performs and/or supervises a variety of routine and specialized tasks, prepares materials, reagents, and equipment, runs specialized laboratory tests and procedures for which he/she has been adequately trained, and compiles data. He/She performs and/or coordinates routine equipment and laboratory maintenance. Specifically for this job, He/She willcarry out an intensive follow-up of the lyophilization equipment both in its operation rutine and in possible preventive actions, as well as collaborate in research tasks related to lyophilization tasks. Regarding the relation ship with others areas of the manufacturing services section, He/She will collaborate in those routine tasks and improvement projects for which He/She will be required. Key Accountabilities • Conducts manufacturing processes and laboratory tests according to approved instructions., • Operates a variety of laboratory equipment., • Compiles manufacturing data, performs the required calculations and complete the corresponding manufacturing and testing records., • Maintains a clean, sanitary and well resourced work area in accordance with approved practices and the regulations in place., • Follow strict laboratory, quality, safety and environmental procedures according to regulations in place., • Under the supervision of his manager and with the support -if needed- of other colleagues, can collaborate in the transfer & set up of new processes and systems., • Participates in activities related to continuous improvement, 5S and Lean Six-Sigma., • Mentor or Support the training of newcomers., • Support other colleagues, specially in some complex processes, tests and tasks., • Based on his/her expertise, he/she will review the new manufacturing processes and related documents prior to their implementation., • Collaborate in the resolution of technical incidences, non-conformances and change-controls as well as in the preparation of validation lots., • Assume the coordination of a certain group of colleagues in the absence if is necessary. Networking/Key relationships To be determined based on the department needs, to include interactions such as: • Mainly with R&D, Quality and Operations colleagues. Minimum Knowledge & Experience required for the position: • Education:, • Required: Ciclo Formativo de Grado Superior in Science or Health-related field, completed with experience in chemical, biological, or health-related laboratory Degree may be substituted by relevant skills and work experience., • Valuable: Any additional degree higher than that required in the previous section., • Experience:, • Specific experience will be required in freeze, drying, use of laboratory equipment., • Additional Skills/Knowledge:, • Software: Fluency in Office Tools (Excel & Word), Valuable Basic knowledge in SAP., • Language: Fluency in Spanish or Catalan. Medium knowledge of English (reading and speaking). Skills & Capabilities: The ideal candidate for this position willexhibit the following skills and competencies: • Ability to learn specific, practical techniques and apply this knowledge to solve technical problems., • Ability to maintain, calibrate and use technical equipment with accuracy., • Time management skills in order to work on several different projects at the same time., • Flexibility in order to work with and provide support for a number of people., • Experience in providing demonstrations and writing technical reports., • Teamwork and interpersonal skills., • Attention to detail., • Oral and written communication skills., • Flexibility in the management of the schedule to be able to adapt to the productive processes., • Reflects values of Werfen in the quality of work and working relationship. Travel requirements: Sporadic travel or short-term assigment to an external lab may be requested.

En Fluidra estamos buscando un/a Customer Quality Engineer para incorporarse de forma temporal a nuestro equipo de Quality EMEA, cubriendo una baja de paternidad desde finales de mayo hasta enero de 2027. Si te interesa participar en proyectos de desarrollo de producto, colaborar con equipos internacionales y aportar valor a la calidad desde las primeras fases del NPD hasta la industrialización, esta posición puede ser una excelente oportunidad para ti. LO QUE APORTARÁS La persona que ocupe esta posición dará soporte al área de Calidad durante el periodo de cobertura, colaborando estrechamente con equipos multifuncionales de I+D, Supply Chain, Manufactura y Proveedores. Tu contribución será clave para asegurar la calidad del producto y los procesos durante distintas fases del ciclo de vida, participando en iniciativas relacionadas con nuevos productos, cambios de ingeniería, validaciones y mejora continua. El puesto reportará directamente a la Quality Director EMEA, y estará integrado en un entorno técnico, dinámico y de alcance internacional. LAS RESPONSABILIDADES PRINCIPALES: • Desarrollar y mantener relaciones efectivas y colaborativas con equipos multifuncionales en la resolución de Quality Hot Topics, Engineering Change Orders, New Product Introductions, Supplier Scorecards y transferencias de producto., • Evaluar documentación de Production Part Approval Process (PPAP) y revisar First Article Inspection Reports (FAIR)., • Proporcionar soporte avanzado de Ingeniería de Calidad durante la introducción de nuevos procesos en proveedores, aplicando metodología APQP u otros modelos de New Product Development (NPD)., • Aportar indicadores clave de calidad (KPIs) a los planes de Design Validation Testing (DVT) de los proyectos., • Colaborar en la definición de criterios realistas de aceptación (pass/fail) y promover acciones para alcanzar los objetivos establecidos., • Liderar actividades de Design for Manufacturing (DFM) dentro de los proyectos, impulsando planes de acción para mejorar deficiencias detectadas., • Contribuir a la mejora continua de los procesos NPD, desarrollando e implementando herramientas que faciliten una comunicación clara y una resolución eficaz de incidencias de calidad. LO QUE BUSCAMOS Educación • Grado universitario en Ingeniería Mecánica, Industrial o de Procesos. Experiencia • Se valora contar con aproximadamente 2 años de experiencia en entornos de Manufactura, Calidad o Sourcing., • También se considerarán perfiles junior, siempre que cuenten con una base sólida en Calidad y capacidad de adaptación a la dinámica de un centro de I+D. Conocimientos técnicos • Buen entendimiento del control de procesos de fabricación, especialmente en entornos de pruebas manuales o semi‑automatizadas., • Experiencia en metodologías 8D (RCA) y/o modelos de resolución de problemas según AIAG., • Conocimiento y uso de herramientas AIAG como Control Plan, PFMEA, MSA y Layered Process Audits., • Conocimientos de procesos de fabricación de chapa metálica y/o componentes plásticos en entornos de ensamblaje., • Conocimiento de planes de validación de Firmware (Hardware/Software) para producción en serie. Competencias • Habilidades de comunicación e interpersonales, con capacidad para interactuar eficazmente con distintos niveles de la organización a nivel regional y global., • Perfil dinámico y flexible, con buena capacidad de planificación y organización., • Capacidad para gestionar múltiples responsabilidades en un entorno de trabajo dinámico., • Sólidos conocimientos de shop-math aplicados a ensayos e inspecciones de calidad de componentes mecánicos, plásticos y subconjuntos eléctricos. Idiomas • Español: nativo., • Inglés: nivel alto (imprescindible). LO QUE OFRECEMOS • Oportunidad temporal para formar parte de una compañía multinacional líder en el sector de piscina y wellness., • Participación directa en proyectos de desarrollo de producto, calidad de proveedores y preparación para producción dentro del ámbito EMEA., • Entorno colaborativo e internacional, con exposición a diferentes áreas técnicas y de negocio., • Jornada laboral de 40 horas semanales., • Posibilidad de aprendizaje y desarrollo profesional incluso en una posición temporal. SOBRE FLUIDRA Fluidra es un grupo multinacional líder global en la industria de la piscina y el wellness, cotizado en la Bolsa de España. Fundada en 1969, la compañía desarrolla soluciones innovadoras para piscinas residenciales y comerciales. Con presencia en más de 45 países y un equipo de más de 7.000 personas, Fluidra cuenta con un amplio portfolio de marcas reconocidas como Zodiac, Polaris, Jandy, CMP, S.R. Smith, Cover‑Pools e iAquaLink, impulsando la innovación en áreas como eficiencia energética, robótica, IA e IoT. El propósito de Fluidra es transformar el agua en un mundo mejor, actuando siempre bajo valores de colaboración, excelencia, aprendizaje continuo, inclusión y trabajo en equipo. ¿No cumples con todos los requisitos? En Fluidra apostamos por un entorno inclusivo. Si esta posición te interesa, te animamos a postular igualmente. Podrías ser la persona adecuada para este puesto o para futuras oportunidades dentro de la organización. Fluidra promueve la igualdad de oportunidades, independientemente de origen, edad, género, orientación sexual, religión u otras características protegidas.

Job Summary The mission of this position is to guarantee that the Standards under which the Quality System is based are aligned with the requirements of the different Regulations of the Countries and Organizations where Biokit sells the products. Assure that all products manufactured at Biokit are designed, manufactured and released according to established procedures. In addition this role works with specific manufacturing teams to drive continuous improvement of Quality within manufacturing – seeking defect rate reduction, increased manufacturing efficiency,reduced costs and enhanced customer satisfaction. Key Accountabilities • Review and approval of manufacturing and general procedures, • Development of Quality Improvement plan for manufacturing area of responsibility, • Measurement and reporting of Quality KPIs and metrics for manufacturing area of responsibility., • Change Management: evaluate the impact of the proposed changes and management of change control., • Validation: Be able to establish a strategy to validate changes. Review and approve validation strategies and the corresponding documentation (protocol and report)., • Risk Assessment: perform, review and approve the risk assessment performed at Biokit to evaluate the impact of changes and non-conformances in the final product., • Participate in Internal and External Audits., • Perform Quality Training to all personnel at Biokit., • Management of Non-Conformities and CAPA., • Review of product Batch Record as needed. Networking/Key relationships The main interactions are with: • Operations area., • Quality Control. Minimum Knowledge & Experience required for the position: Education: • Required: Bachelor's degree (Diplomatura) in Chemistry, Biotechnology or other Sciences., • Degree may be substituted by relevant skills and work experience. Valuable: Any additional degree higher than the required Experience: • Required: 3 years in a similar position Additional Skills/Knowledge: • Software: Fluency in Office Tools (Excel & Word), Valuable Basic knowledge in SAP., • Language: Fluency in Spanish or Catalan. Advanced knowledge of English (reading and speaking)., • Standards: Knowledge of Quality standards. Skills & Capabilities: The ideal candidate for this position will exhibit the following skills and capabilities: • Management of decisions under pressure., • Methodical and well-organized person., • Teamwork., • Time management skills., • Ability to express information clearly and concisely to the staff, ensuring their understanding., • Ability to apply a systematic approach and constant control, follow-up and verification of the results., • Ability to collaborate, participate and coordinate actively with working groups, • Reflects values of Werfen in the quality of work and working relationship Travel requirements: Not Required.

¿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 🌍. Buscamos una persona para incorporarse en el departamento de Quality Control como Analistaa para el Turno de Tarde (14h a 22h). ¿Te apuntas? Como Analista de Control de Calidad, formarás parte de un equipo clave para garantizar que todos los productos cumplen los más altos estándares de calidad farmacéutica. Tu trabajo tendrá un impacto directo en la seguridad, eficacia y excelencia de los productos que llegan al paciente. ¿Qué funciones harás? • Realizar análisis físico-químicos, con técnicas como cromatografía, HPLC/UPLC, test de disolución, disgregación, friabilidad, dureza, pH, punto fusión, determinación nitrógeno, IR, NIR, UV, Karl-Fischer, estufas, muflas, valoración potenciométrica, viscosidad, conductividad, fluorimetría, o granulometría y registrar correctamente los resultados obtenidos., • Colaborar en la revalidación de los métodos analíticos, • Poner a punto, verificar, calibrar y mantener los equipos., • Realizar muestreos de materias primas y producto acabado., • Realizar, cuando corresponda muestreo y análisis del sistema de agua de la Planta., • Conocer y cumplir los PNT y las normativas GMP y los PNT del sistema de gestión de Seguridad, Salud y Medioambiente, así como las medidas preventivas indicadas en la ficha de riesgos del puesto de trabajo. ¿Qué perfil buscamos? • Formación superior en Laboratorio de Análisis y Control de Calidad., • Experiencia como analista en el sector farmacéutico o químico-farmacéutico en entorno GMP. ¿Qué ofrecemos? ⚙️Trabajarás dentro de un gran equipo de profesionales con muy buen ambiente laboral. 📍Oficinas ubicadas en Palau solità i Plegamans. 💼Proyecto temporal 🕒Horario en turno de tarde (Horario de 14:00h a 22:00h) 🌱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 cumples la mayoría de los requisitos y te motiva el proyecto, ¡te esperamos!

Job Summary Reporting to Global Systems Support Group Manager, will be responsible for providing technical support for the Werfen AID products. The System support manager will be responisble for providing support to the Buisness unit, Affiliates, and Customers worldwide. The Primary area of focus will be in Europe and EEMEA but global travel will be required. Key Accountabilities • To be the intermediary between software/hardware developers and the company stakeholders, during product/software development and launching., • Conduct training for Werfen Autoimmunity applications and services. Training of customers and product demonstrations to external and internal customers as needed., • Provide telephone, email, and on-site technical support as requested, • Be the subject matter expert for escalated troubleshooting, product investigations and global service improvements, • GSS representative in meetings related instrument line projects, these can extend into work hours that support the US PST and EST zones., • Participate in industry conferences and set up and breakdown at trade shows (EU, EEMEAI)., • Draft documents and reports when it is needed. Collaberate with department collueges, global affilates, OEM partners and customers to minimize downtime and interruptions of the equipment., • Ensure proper communication and documentation of product claims based on SOP and FDA regulations., • Support key buisness needs for Werfen AID. Networking/Key relationships This position requires cooperation with: • Werfen Clinical Software: To provide them field feedback experience and to execute internal tests on interim software versions or during software development/validation., • Quality Assurance: to coordinate equipment and facilities qualifications, • Technical Support: to support them with escalated support request, • Werfen Affiliates/Distributors:, • To provide escalated support remotely, in-house installations and deep troubleshooting, • To provide in-house support for instrument evaluation during product launches, • To organize calls/focus group meetings for product development and improvements Minimum Knowledge & Experience required for the position: Education: • Required: Bachelor's degree (Diplomatura) in Mechanical, Electrical, Electronic, Biomedical and/or Chemical Engineering., • Degree may be substituted by relevant skills and work experience, • Reading and interpretation of documents such as safety standards, operating and maintenance instructions, technical documents, procedures manuals and SOPs., • Valuable: Ability to perform chemiluminescence immunoassays procedures or solid phase chemistry – ideally the candidate will come from in vitro diagnostic companies or manufacturers of machinery. Experience: • Required: 3 years in a similar position, • Adavanced knowledge in IFA, EIA technology perfered. Additional Skills/Knowledge: • Software: Fluency in Office Tools (Excel & Word), Valuable Basic knowledge in SAP, • Language: Fluency in Spanish. Advanced knowledge of English (reading and speaking), • Standards: Knowledge in programming, developing bat files, etc Skills & Capabilities: The ideal candidate for this position will exhibit the following skills and capabilities: • Management of decisions under pressure., • Methodical and well-organized person., • Teamwork, • Analytical skills to troubleshoot Biomedical devices, • A good understanding of Autoimmunity – Diseases & Biomarkers, • Time management skills, • Ability to express information clearly and concisely to the developers, colleagues and customers, ensuring their understanding., • Ability to apply a systematic approach and constant control, follow-up and maintenance of the scheduled & assigned tasks, • Ability to collaborate, participate and coordinate actively with working groups, • Reflects values of Werfen in the quality of work and working relationship Travel requirements: Up to 35% of time.

ITW (Illinois Tool Works Inc.) is a Fortune 200 company and is one of the world’s leading diversified manufacturers of specialized industrial equipment, automotive components, consumables, and related service businesses. ITW businesses serve local customers and markets around the globe, with operations in 55 countries and an employee base of more than 48,000 women and men who adhere to the highest ethical standards. These talented individuals, many of whom have specialized engineering or scientific expertise, contribute to our global leadership in innovation. We are proud of our broad portfolio of more than 17,000 granted and pending patents. The Seats & Motion Division within the ITW Automotive Segment delivers highly differentiated, precision-engineered plastic solutions to our “80” global OEMs & Tiers across North America and Europe through customer back innovation, targeted at addressing the emerging pain points associated with passenger seating & comfort, and ensuring best-in-class quality & delivery through our commitment to 80/20 operational excellence. Position Summary: Responsible for developing and validating new products through our Customer Back Innovation process, using advanced materials, rapid prototyping, CAD tools and creative thinking bridging early-stage innovation with feasible engineering solutions. Responsibilities: Develop innovative concepts and generate new ideas by applying analytical methods and creative problem-solving tools to identify optimal technical solutions. Manage, lead, and coordinate local activities related to innovation projects within the ITW framework, under the direction of the EU Innovation Manager. Support the integration of innovative product development projects into the company CBI process, ensuring compliance as well as proper documentation, storage, and communication of project data and information. Build strong relationships with key internal stakeholders and departments to foster an open-minded culture and facilitate the adoption of innovative concepts, processes, and technologies. Develop plastic-compatible 3D CAD designs, including components and assemblies, and create technical drawings according to design requirements, installation constraints, and specifications. Apply and/or coordinate engineering analysis methods (e.g., CAE/FEM simulations) to define, evaluate, and optimize future product concepts into high-performance solutions. Research, evaluate, and recommend materials and manufacturing processes, leveraging internal expertise and external investigation of emerging technologies and industry developments. Plan, organize, and execute concept verification activities, ranging from initial proof-of-concept assessments with 3D-printed samples to prototype testing aligned with key DVP validation requirements. Provide clear and concise project updates to the Innovation Team, ensuring regular communication of progress and supporting the preparation of technical reviews and project meetings. Apply ITW Toolbox principles to ensure structured and effective execution of innovation projects from concept design through manufacturing readiness Actively contributes to technology scouting, competitive benchmarking, and identification of emerging solutions that can expand the company’s innovation pipeline Position Skills and Experience Requirements: Bachelor’s degree in Engineering or Engineering Technology, preferably in Mechanical / Mechatronics / Electronics Engineering, Industrial Design Engineering, or a related field (or equivalent professional experience). 1–3 years of experience in engineering and product design, preferably within an industrial or automotive environment. Experience with CAD tools such as CATIA V5 or Siemens NX; familiarity with CAE tools, Moldflow analysis, and dynamic simulation is considered a strong advantage. Ability to create both concept-level and detailed CAD models suitable for prototyping, visualization, and technical evaluation. Automotive industry experience is highly preferred. Knowledge of plastic injection molding processes, including basic understanding of assembly methods and tooling technologies. Experience creating technical drawings for injection-molded plastic components, including appropriate tolerances and design considerations. Strong structured problem-solving capability, with the ability to challenge conventional solutions and propose innovative alternatives. Comfort working with ambiguity and early-stage concepts typical of innovation and advanced engineering projects. Hands-on mindset with interest in rapid prototyping, experimentation, and development of proof-of-concept solutions Excellent organizational and interpersonal skills, with the ability to collaborate effectively across functions. Strong verbal and written communication skills in a technical environment. Ability to work independently, exercising sound judgment and effective decision-making. Proficient in standard engineering and office software tools What we are offering: Thrive in an international environment with genuine growth opportunities! Enjoy flexible working hours. Enjoy subsidized lunches. Receive 100% supplementary insurance coverage in case of illness. Comprehensive health insurance. Life insurance coverage. Enjoy organic fruit in the office every Tuesday & Thursday Access our social fund for orthodontics, orthopedics, schoolbooks, and more for parents and children. Discounts on physiotherapy

Buscamos una persona para incorporarse en el departamento de Quality Control como Analistaa para el Turno de Tarde (14h a 22h).

Buscamos una persona para incorporarse en el departamento de Quality Control como Analistaa para el Turno de Tarde (14h a 22h).

We are currently looking for a Clinical R&D Quality Assurance Technician to join Noucor’s Quality team. 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 activiti

We are currently looking for a Clinical R&D Quality Assurance Technician to join Noucor’s Quality team. 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 activiti

Key Accountabilities Review and approval of manufacturing and general procedures Development of Quality Improvement plan for manufacturing area of responsibility Measurement and reporting of Quality KPIs and metrics for manufacturing area of responsibility. In addition this role works with specific

Key Accountabilities Review and approval of manufacturing and general procedures Development of Quality Improvement plan for manufacturing area of responsibility Measurement and reporting of Quality KPIs and metrics for manufacturing area of responsibility. Perform Quality Training to all personnel

Job Summary The mission of this position is to guarantee that the Standards under which the Quality System is based are aligned with the requirements of the different Regulations of the Countries and Organizations where Biokit sells the products. Assure that all products manufactured at Biokit are designed, manufactured and released according to established procedures. In addition this role works with specific manufacturing teams to drive continuous improvement of Quality within manufacturing – seeking defect rate reduction, increased manufacturing efficiency,reduced costs and enhanced customer satisfaction. Key Accountabilities Review and approval of manufacturing and general procedures Development of Quality Improvement plan for manufacturing area of responsibility Measurement and reporting of Quality KPIs and metrics for manufacturing area of responsibility. Change Management: evaluate the impact of the proposed changes and management of change control. Validation: Be able to establish a strategy to validate changes. Review and approve validation strategies and the corresponding documentation (protocol and report). Risk Assessment: perform, review and approve the risk assessment performed at Biokit to evaluate the impact of changes and non-conformances in the final product. Participate in Internal and External Audits. Perform Quality Training to all personnel at Biokit. Management of Non-Conformities and CAPA. Review of product Batch Record as needed. Networking/Key relationships The main interactions are with: • Operations area. • Quality Control. Minimum Knowledge & Experience required for the position: Education: Required: Bachelor's degree (Diplomatura) in Chemistry, Biotechnology or other Sciences. Degree may be substituted by relevant skills and work experience. Valuable: Any additional degree higher than the required Experience: ~ Required: 3 years in a similar position Additional Skills/Knowledge: Software: Fluency in Office Tools (Excel & Word), Valuable Basic knowledge in SAP. Language: Fluency in Spanish or Catalan. Advanced knowledge of English (reading and speaking). Standards: Knowledge of Quality standards. Skills & Capabilities: The ideal candidate for this position will exhibit the following skills and capabilities: Management of decisions under pressure. Methodical and well-organized person. Teamwork. Time management skills. Ability to express information clearly and concisely to the staff, ensuring their understanding. Ability to apply a systematic approach and constant control, follow-up and verification of the results. Ability to collaborate, participate and coordinate actively with working groups Reflects values of Werfen in the quality of work and working relationship Travel requirements: Not Required.

Key Accountabilities Review and approval of manufacturing and general procedures Development of Quality Improvement plan for manufacturing area of responsibility Measurement and reporting of Quality KPIs and metrics for manufacturing area of responsibility. Perform Quality Training to all personnel

Responsibilities include overseeing the Quality System, ensuring compliance with Good Distribution Practices (GDP), managing training plans, and coordinating product recalls.

Una empresa internacional de servicios tecnológicos busca un/a Ingeniero/a de Calidad Proyecto en Polinyà, España.Siga leyendo para comprender completamente lo que este trabajo requiere en cuanto a habilidades y experiencia.Si su perfil encaja, presente su candidatura.Se requiere experiencia mín

Actualmente, buscamos incorporar un Director de Garantía de Calidad en nuestras oficinas centrales de Sentmenat, para liderar e impulsar nuestro sistema integrado de gestión y garantizar la excelencia en todos los procesos de la compañía. Experiencia de al menos 5 años liderando sistemas de ges

We are a world leader in plasma‑derived medicines with a presence in more than 100 countries, and a growing global team of over 20,000 people.Envíe su CV y cualquier información adicional requerida después de haber leído esta descripción, haciendo clic en el botón de solicitud.The role invol

A global healthcare company in Spain seeks a Data Product Owner to design high-quality data models and lead product strategy.Haga clic en "Solicitar" a continuación para enviar su candidatura.Asegúrese de que su CV está actualizado y de que ha leído primero las especificaciones del puesto.The su

An international healthcare company is seeking a Data Product Owner in Parets del Vallès, Spain.Si le interesa solicitar este empleo, por favor, asegúrese de cumplir los siguientes requisitos que se enumeran a continuación.You will design high-quality data models and define product strategy to en

A global healthcare company is seeking an Instruments Quality Engineer to ensure the quality of diagnostic instruments.Está pensando en solicitar este empleo? No se demore, desplácese hacia abajo y envíe su solicitud lo antes posible para no perder la oportunidad.You will participate in various q

A global healthcare company is seeking a Data Product Owner to design and maintain high-quality data models that align with business objectives.Por favor, presente su candidatura sin demora si su perfil encaja bien con este puesto, debido al alto nivel de interés.The ideal candidate will possess ov

We are looking for a Quality Systems Specialist to join Quality department at Biomat SA, company dedicated to analyzing and controlling the plasma used by Instituto Grifols SA as raw material for the production of plasma derivatives. Participate in the company’s global quality projects. You have 3

Would you like to join an international team working to improve the future of healthcare? Grifols is a global healthcare company that since 1909 has been working to improve the health and well‑being of people around the world. We are looking for an Instruments Quality Engineer responsible for ensu

A leading healthcare company in Spain seeks a Quality Auditor to oversee GMP audits and provide regulatory compliance guidance.

Would you like to join an international team working to improve the future of healthcare? Do you want to enhance the lives of millions of people? Grifols is a global healthcare company that since 1909 has been working to improve the health and well-being of people around the world. We are looking fo

A global healthcare company in Parets del Vallès is seeking a Quality Systems Specialist to manage change control processes and quality assurance tasks.

Grifols is a global healthcare company that since 1909 has been working to improve the health and well-being of people around the world.We are leaders in plasma-derived medicines and transfusion medicine, developing, producing, and marketing innovative medicines, solutions, and services in more than

A global healthcare company in Parets del Vallès seeks an Instruments Quality Engineer to join their Diagnostic division. The role involves ensuring quality throughout the lifecycle of diagnostic instruments and compliance with various regulations.

A global healthcare company is seeking a Project Manager to coordinate pharmaceutical engineering projects in Parets del Vallès, Spain, ensuring compliance with technical quality and regulatory standards.Asegúrese de presentar su candidatura con toda la información solicitada, tal como se expone

Una empresa del sector salud busca un/a Trainee en Control de Calidad para ayudar en la elaboración y estandarización de procedimientos, evaluación técnica de proveedores y gestión de no conformidades.Es usted el solicitante adecuado para esta oportunidad? Descúbralo leyendo el resumen del pue

The mission of this position is to guarantee that the Standards under which the Quality System is based are aligned with the requirements of the different Regulations of the Countries and Organizations where Biokit sells the products. In addition this role works with specific manufacturing teams to

Experience in customer quality or product quality in an industrial environment. Act as the main point of contact with the customer for quality incidents, field failures, and warranty claims. Lead quality investigations using the 8D methodology.

Únete a CELSA GROUP™! Líderes en Europa en producción de acero circular y bajas emisiones, y uno de los fabricantes más diversificados e integrados verticalmente del sector.Actualmente buscamos un/a Comercial Industrial de sector metal para nuestras instalaciones de Ferimet (Sabadell).Misión