At Daiichi Sankyo, we are united by a single purpose, to improve lives around the world through innovative medicines. With a legacy of innovation since 1899, a presence in more than 30 countries, and more than 19,000 employees, we are advancing breakthrough therapies in oncology, cardiovascular disease, rare diseases, and immune disorders. Guided by our 2030 vision to "be an innovative global healthcare company contributing to the sustainable development of society", we are shaping a healthier, more hopeful future for patients, their families, and society. Purpose of the function LOCATION: SWITZERLAND The Manager, Global Quality Management System (Global RandD and PV QA), supports the oversight and continuous improvement of Daiichi Sankyo's QMS, including Master Data/Data Lake reporting, Veeva Quality Docs management, Global SOP governance, training management, quality metrics, and inspection support. The role ensures that GxP procedural documents, training frameworks, and reporting processes comply with global regulatory requirements and Daiichi Sankyo policies, while driving harmonisation and continuous improvement across R&D, PV, MA, a Roles and Responsibilities CoMET Quality Docs Vault Management Provide System And Process Support, Including Supporting the review, approval, and publication of GxP procedural documents in the CoMET QualityDocs Vault.
Acting as Subject Matter Expert (SME) for the electronic document management system, contributing to system requirements and configuration.
Reviewing and executing User Acceptance Testing (UAT) scripts for document management system changes.
Ensuring document lifecycle activities comply with global quality and system governance requirements. Global SOP Committee (GSOPC) Office Activities Providing QA oversight and coordination for GSOPC office activities.
Facilitating timely review and approval of Global RandD, Pharmacovigilance, and Medical Affairs procedural documents.
Overseeing Global SOP lifecycle management a...