About Xebia With over 20 years of experience, our global network of passionate technologists and pioneering craftsmen deliver cutting-edge technology and game-changing consulting to companies on the brink of transformation. Since 2001, we have grown from
Would you like to start a new professional adventure as a Regional C-PMO Lead in one of our opportunities within the Healthcare & Digital Transformation industry ? Your missions? Act as a strategic PMO partner for
Overview As QA Officer you ensure quality oversight across GMP activities at the site. You will support validation/qualification efforts, manage quality documentation, and supervise batch release activities. Working in shifts, you contribute to audits, inspections, and
As QA Officer you ensure quality oversight across GMP activities at the site. You will support validation/qualification efforts, manage quality documentation, and supervise batch release activities. Working in shifts, you contribute to audits, inspections, and continuous
Overview Inscríbase (haciendo clic en el botón correspondiente) después de revisar toda la información relacionada con el trabajo a continuación. As QA Officer you ensure quality oversight across GMP activities at the site. You will support
Overview Inscríbase (haciendo clic en el botón correspondiente) después de revisar toda la información relacionada con el trabajo a continuación. As QA Officer you ensure quality oversight across GMP activities at the site. You will support
The Senior Director, Regulatory Affairs is responsible for leading regulatory strategy and execution for assigned development programs, with a primary focus on oncology and broader disease areas as needed. This role will serve as the Global Regulatory