Global Quality Systems Manager
HybridParis, Île-de-France, France
Job Summary
Conduct controlled document lifecycle activities and manage key Global Quality documentation within the electronic Document Management System. Maintain training matrices, Learning Objects, and user profiles as the LMS Administrator, while monitoring GxP training compliance and harmonizing practices across functions and sites. Lead defined activities in GxP document management and training, supporting the integration of newly acquired companies into the Ipsen QMS. This role reports to the Global Quality Systems Director and focuses on improving patients' lives through innovation and continuous improvement in a global biopharmaceutical environment.
Required Qualifications
- Knowledge of GxP requirements and Quality Assurance within the pharmaceutical, biotechnology or medical device industry
- Hands-on experience with an electronic Document Management System in a regulated GxP environment
- Hands-on experience with Learning Management Systems and GxP training administration
- Ability to connect, structure and analyse data from multiple sources and leverage digital tools such as Power BI, automation and AI-enabled solutions
- Problem-solving skills, with the ability to assess compliance risks and determine appropriate corrective or improvement actions
- Experience supporting Quality Systems improvement initiatives
- Experience working in a Global or cross-functional environment and coordinating activities with multiple stakeholders
- Bachelor's degree in Life Sciences, Quality or a related discipline
- Fluency in English
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