Trabajos auditor en Barberà Del VallèsCrear alertas

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 leaders in plasma-derived medicines and transfusion medicine and develop, produce and market innovative medicines, solutions and services in more than 110 countries and regions. We believe that diversity adds value to our business, our teams, and our culture. We are committed to equal employment opportunities, fostering an inclusive environment where diversity makes us outstanding. Help us lead one of the world’s largest pharmaceutical companies. 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. That’s why we need R&D QA Specialist & Auditor like you. Provide quality oversight of SIO pre-clinical activities to ensure that studies, processes, systems and documentation comply with applicable regulatory requirements, company standards and the R&D Quality System. Review of study documentation and data, quality oversight of SIO pre-clinical activities, execution of internal and external audits, qualification and oversight of vendors and management of quality system processes such as deviations, CAPAs, change controls and controlled documentation. Support development programs through independent quality oversight and audit activities, identify compliance risks, drive continuous improvement initiatives and provide QA guidance to cross-functional teams to ensure the integrity, reliability, and regulatory acceptability of SIO pre-clinical activities for plasma and non-plasma products. To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skills, education, and/or ability required. Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions). Bachelor’s degree in a Health Sciences-related field, such as Biology, Biochemistry, Chemistry, Biomedical Engineering, or a similar discipline. You have 2-5 years of experience in the pharmaceutical industry in a similar Quality Assurance (QA) role or within scientific research environments applying GLP regulations. Strong knowledge of GCLP, GMP and GLP quality standards and regulatory requirements. Advanced English proficiency. Advanced user of Microsoft Office tools, including Word, Excel and Outlook, with solid knowledge of Quality Management Systems (QMS), particularly within SAP environments and Document Management Systems (DMS). It is a brilliant opportunity for you, Grifols is fully aware that its employees are one of its major assets. We are committed to maintaining an atmosphere that encourages all our employees to develop their professional careers in an excellent working environment. Information about Grifols is available at www.grifols.com. We believe in diverse talent and want to remove any barriers that may hinder your participation. If you require any adjustments in our selection process, please do not hesitate to inform us when applying. We are here to help. Grifols is an equal opportunity employer. Monday-Thursday 7-10 to 16-19h and Friday 8-15h (with the same flexible start time). Contract of Employment: Permanent position Flexibility for U Program: Hybrid Location: Sant Cugat del Vallès Type: Indefinido tiempo completo www.grifols.com Learn more about Grifols #J-18808-Ljbffr

That’s why we need R&D QA Specialist & Auditor like you.

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. It is a brilliant

Grifols is seeking an R&D QA Specialist & Auditor to oversee pre-clinical activities for plasma and non-plasma products.

R&D QA Specialist & Auditor to provide quality oversight of SIO pre-clinical activities, ensuring studies, processes and documentation comply with regulatory requirements and Grifols standards.

Grifols is seeking a QA Specialist & Auditor to join its international team in Sant Cugat del Vallès.

Desde la unidad de Estrategia y Transformación de Auditoría nos encontramos buscando un/a Auditor/Auditora.Desplegarás las iniciativas que sustentan la definición de la estrategia de auditoría.Liderarás grupos de trabajo creados para tal fin, el desarrollo metodológico de las iniciativas, def

Banco Sabadell busca un/a Auditor/a para liderar la definición y ejecución de la estrategia de auditoría, coordinando equipos y desarrollando políticas y procedimientos acorde a normativas bancarias internacionales.

Manejar el sistema de gestión hotelera (PMS) y realizar cobros o cierres de caja cuando sea necesario. Experiencia mínima de 1 año en recepción de hoteles. Te apasiona la hospitalidad y el servicio al cliente? Estamos buscando un/a Auditor/a Nocturno/a para uno de nuestros hoteles en Cerdanyola.

Plan de crecimiento para formarte como auditor. Realizar auditorías técnicas a los clientes. Experiencia previa: orientación a cliente y enfocado a trabajos de auditorías/inspecciones y revisión documental.

Realizarás auditorías para clientes según la normativa de referencia aplicable (preparación y ejecución de auditorías in situ, redacción de informes, gestión del expediente). Auditor/a de Certificación de Sistemas. Experiencia mínima de 1 año realizando auditorías de certificación.

Se valorará formación universitaria, alto xcskxlj nivel de inglés, experiencia en auditorías y revisión documental, conocimientos ENAC, ATEX y normativas CE.

Te apasiona el sector agroalimentario y quieres que tu trabajo tenga un impacto directo en el bienestar animal y la seguridad de lo que consumimos?. Certificar estándares de bienestar animal:. La base técnica indispensable para comprender la realidad de los productores y los criterios de salud/bie

OCA Global busca un Auditor/a de Bienestar Animal para certificar esquemas como Bienestar Animal y contribuir a una cadena alimentaria más segura y sostenible en Cataluña.

No necesitas experiencia previa en auditoría:. Redactarás los resultados e incidencias de cada auditoría de forma clara y rigurosa, aportando la información clave para que los productores puedan aplicar una mejora continua en sus instalaciones. Planificarás tus rutas, visitas y tiempos para gar

En RSM, como Auditor/a Senior en auditoría financiera, dirigirás y ejecutarás procesos de revisión de estados financieros para clientes de diversos sectores, aportando rigor técnico y valor agregado. Trabajarás dentro de un equipo con enfoque en sostenibilidad y desarrollo profesional, alinean

In this role you will lead and perform GMP audits to ensure compliance with Novartis Quality System and current regulations.You will work on internal and external audits across sites, functions, and suppliers, shaping a global audit strategy and supporting risk-based improvements.You will mentor sta

Colaborarás en presupuestos anuales y en la detección y análisis de tarifas, elaborando informes para direcciones y participando en auditorías. Colaboración en auditorías de cuentas anuales. Experiencia mínima de 2–3 años en auditoría, administración o contabilidad.

En KPMG Auditores, colaborarás en auditoría de estados financieros y análisis de riesgos dentro de un equipo global en expansión. Auditoría de estados financieros.

En RSM Barcelona buscamos un/a Auditor/a Junior en auditoría financiera para integrarse al equipo local. Será responsable de apoyar procesos de auditoría en diferentes sectores para clientes de la firma, dentro de una estructura internacional y orientada a la sostenibilidad.

As a Global GCP/PV Auditor, you will ensure clinical and pharmacovigilance activities meet regulations and Novartis standards.

As a Senior Auditor at Zurich Group Audit, you help deliver high-quality audits in a fast-moving, international setting.

In this role you will lead and perform GMP audits to ensure compliance with Novartis Quality System and current regulations.You will work on internal and external audits across sites, functions, and suppliers, shaping a global audit strategy and supporting risk-based improvements.You will mentor sta

As a Senior Auditor at Zurich Group Audit, you help deliver high-quality audits in a fast-moving, international setting.

As a Global GCP/PV Auditor, you will ensure clinical and pharmacovigilance activities meet regulations and Novartis standards.

En KPMG Auditores, colaborarás en auditoría de estados financieros y análisis de riesgos dentro de un equipo global en expansión. Auditoría de estados financieros.