Job Description SummaryIn this role you will lead, support and report independent GMP audits according to the Novartis Quality System and the current GMP regulations to assess compliance with applicable regulations, standards, and guidance documents. Review
Job Description SummaryThe Product Quality Lead plays a crucial role in ensuring the quality and consistency of our products throughout their lifecycle. This role encompasses a wide range of responsibilities that bridges clinical, development, and technical
In a nutshell Position: Business Development Associate – CDMO Biologics Location: Madrid, Hibrid Experience: 3+ Want to know more? mAbxience is a global biopharmaceutical company committed to innovation and excellence in the development and manufacturing of biotechnological
León, Castilla and Leon, Spain 8 months ago ¿Todo listo para enviar su solicitud? Por favor, lea la descripción al menos una vez antes de hacer clic en Solicitar. Técnico de control de calidad en fisicoquímica
Responsibilities Desplácese hacia abajo para obtener una visión general completa de lo que requerirá este trabajo. ¿Es usted el candidato adecuado para esta oportunidad? Supports and helps in order fulfillment and overall inventory Maintains the cleanliness
Business Development Associate – CDMO Biologics Location: Madrid, Hibrid mAbxience is a global biopharmaceutical company committed to innovation and excellence in the development and manufacturing of biotechnological medicines. We operate with a strong focus on quality, regulatory
Business Development Associate – CDMO Biologics Location: Madrid, Hibrid mAbxience is a global biopharmaceutical company committed to innovation and excellence in the development and manufacturing of biotechnological medicines. We operate with a strong focus on quality, regulatory
Clinical Project Support Specialist We are looking for a Clinical Project Support Specialist to work in a multinational company. Its products and services are designed to benefit people and improve their quality of life. Position purpose:
Summary ¿Quiere enviar su solicitud? Lea toda la información sobre este puesto a continuación y luego pulse el botón de solicitar. In this role you will lead, support and report independent GMP audits according to the
Responsibilities Si sus habilidades, experiencia y cualificaciones coinciden con las de esta descripción del puesto, no demore su solicitud. Assist/advise project teams on all regulatory requirements for clinical studies Perform compliance assessments according to country requirements