M&S-Country Quality Supervisor-Shanghai

Job title职位名称 : Country Quality Supervisor • Location工作地点： Shanghai 上海 About the job工作职 责 We are an innovative global healthcare company with one purpose: to chase the miracles of science to improve people’s lives. We’re also a company where you can flourish and grow your career, with countless opportunities to explore, make connections with people, and stretch the limits of what you thought was possible. Ready to get started?   Main responsibilities职责描述： Management of the Country Quality Management System 分公司质量体系管理 • Implement, manage, and control a Country Quality Management system for GxP activities from development to commercialisation of all products and related GxP services, in compliance with Sanofi requirements, as well as applicable local regulatory requirements. • undefined • Participate in the Oversee of all country GxP operation and compliance (including PV, regulatory, market supply chain, medical, etc.) through robust quality management system, to ensure fulfilment of post-market management , GSP/GDP quality management and MAHD accountability. • undefined • Understand Quality culture and promote Quality mindset into the country governance, working principles, and ways of operating. • undefined • Ensure appropriate communication of key messages pertaining to Quality across the country organization, highlighting their possible business impact. • undefined • Assure that a process for management of GxP documents and records is in use in all GxP areas, considering data integrity and data privacy principles. • undefined Country Quality documentation system 本地质量文件系统 ： • Organize a consistent life cycle management of Country GxP documents (except for Clinical Study Unit (CSU)) using the global content management system. • undefined • Ensure and coordinate across GxP functions the direct use of global documents or the creation of country GxP documents, based on the Advanced Content Template (ACT) in case of any regulatory requirement. • undefined Country Quality audits and GxP regulatory country inspections 本地质量审计和GxP监管检查： • Collaborate to ensure country inspection readiness. • undefined • Participate in the Management of country regulatory inspections related to GxP processes owned by the CQH and provide support and coordination with other GxP country functions in country regulatory inspections for processes in their respective areas of responsibilities, ensuring contribution of concerned functions at global level, as needed. • undefined • Where applicable, in accordance with local regulations and/or the expectations of local regulatory authorities, collaborate with the Regulatory Affairs, Pharmacovigilance, and other relevant functional departments to support regulatory inspections of marketing authorization holders, overseas sites, and MAHD(s). • undefined • Implement a strategy for local quality audits, based on Quality risk management criteria, of key local GxP service providers directly managed by the country, including the outsourced hybrid processes (non-GxP processes with GxP impact) with safety reporting components. • undefined Personnel Qualification and Training 人员资质和培训： • Organize information sharing, training sessions or programs related to processes under the responsibility of the CQH for concerned country associates, according to Sanofi and regulatory requirements. • undefined • Ensure that there are system, process and procedure in use for the personnel qualification (e.g. CV, job description, training curricula and records) and the management of GxP trainings across the country by each GxP function. • undefined Country Quality Review分公司质量回顾： • If required by local regulations, support the Annual Country Quality Review as per Sanofi requirements. • undefined • undefined • u