M&S Graduate Program-Quality Lead-Beijing

Job title 职位名称 : M&S Graduate Program-Quality Trainee Location工作地点： Beijing 北京 About Sanofi We’re an R&D-driven, AI-powered biopharma company committed to improving people’s lives and delivering compelling growth. Our deep understanding of the immune system – and innovative pipeline – enables us to invent medicines and vaccines that treat and protect millions of people around the world. Together, we chase the miracles of science to improve people’s lives. About Manufacturing & Supply (M&S) J oin a global network that powers how Sanofi delivers — seamlessly, purposefully, and at scale. In Manufacturing & Supply, you’ll help reimagine how life-changing treatments reach people everywhere, faster, reliably, sustainably and affordably, at the quality levels expected. About the Program Your Journey to Manufacturing Leadership Starts Here The M&S Graduate Program is Sanofi's flagship early career accelerator, designed to fast-track exceptional talent into M&S China's core leadership pipeline. Over 3 years, you will gain cross-regional, cross-functional business immersion across critical M&S operations — building deep operational expertise, strategic thinking, and global perspective through real-world challenges. With industry-leading executive support — including a Site Head as your Career Sponsor and a Global M&S Leader as your dedicated mentor — you will benefit from direct access to M&S China Cluster and Global Business Leaders through regular executive dialogues, a personalized development journey with external professional coaching, and targeted capability building in Digital & AI, critical thinking, and leading change. This is your express lane to becoming a strong successor in M&S China's core leadership team. Main responsibilities： Quality control lab operational support & Oversight & continuous improvement Perform routine and non-routine analytical testing of raw materials, in-process samples, finished products, and stability samples in compliance with SOPs, GxP, and regulatory requirements Support QC laboratory equipment qualification, calibration, and preventive maintenance activities Assist in analytical method verification and validation activities under supervision Document test results accurately and in a timely manner in full compliance with data integrity standards Participate in deviation investigations, root cause analysis (RCA), and corrective/preventive action (CAPA) follow-up Contribute to laboratory housekeeping, safety compliance, and 5S/continuous improvement initiatives Support trend analysis of QC data and escalate anomalies to senior managers QC Regulatory Compliance & Inspection Readiness Support inspection readiness activities for national and international regulatory agencies (NMPA, FDA, EMEA), learning to implement agency-specific requirements Participate in self-audits, global audits, and regulatory inspections, building knowledge of compliance expectations and audit response strategies Contribute to the development of a robust contamination control strategy and sterility assurance system for sterile and non-sterile products Cross-functional Collaboration & Stakeholder Engagement Collaborate cross-functionally with Production, Quality Assurance, and Regulatory Affairs teams Partner with Production, Quality Assurance, Engineering, and Supply Chain teams to ensure quality control operation align across all manufacturing operations Provide QC support during product launches, technical studies, and validation activities, practicing influence without direct authority Team Development & Quality Culture Building Support the training and development of QC team members, building coaching and people leadership skills Promote a culture of quality throughout the organization, reinforcing GMP awareness and continuous learning Progressively take on people management responsibilities, including performance evaluation and individual development planning by Year 3 Actively engage in the Early Talent Program's learning curriculum, mentoring sessions, and rotational assessments About you 任职资格: List here ideally the must-haves criteria to be successful on the role. 请列出胜任该职位所必须具备的条件。 Education : Master's Degree required in Pharmaceutical Sciences, Biotechnology, Chemical Engineering, Life Sciences, or related technical disciplines; top MBA with relevant manufacturing exposure also considered Experience At least 2–3 years of experience in pharmaceutical quality assurance, quality control, manufacturing, or related regulatory/compliance roles — ideally within GMP-regulated environments Demonstrated exposure to cGMP operations, quality event investigations (deviations, OOS, CAPA), and regulatory compliance over years of tenure alone Experience or strong interest in sterile manufacturing, contamination control, or biologics quality systems is highly valued Familiarity with Chinese cGMP (NMPA), FDA, and/or EMEA regulatory frameworks is a strong plus Fluency in English required; strong written and verbal communication skills essential for regulatory documentation and cross-functional collaboration Soft skills Collaborate effectively with peers, stakeholders, partners across the organization to positively impact business results. Act for innovation, initiating new and improved ways of working. Develop teams in anticipation of future business needs. LEAN oriented, problem solving & new way of working. Open minded and curios to learn new tools. Technical skills In-depth knowledge of the biologic product license application process, and the associated regulatory requirements. Know-how in Quality systems, Quality Risk Management, Continuous improvement management, GxP and health regulated regulations, International and FDA exposure, KNEAT solution is a plus. What You'll Gain 你会获得 This program is designed to give you an advantage in your leadership career. Here is what you can expect: A structured 3-year leadership accelerator with clear milestones, defined rotations, and a guaranteed landing role — no ambiguity about where you are headed Real-World Business Immersion: Cross-regional, cross-functional rotations in live business environments, building operational expertise, business acumen, and strategic thinking Industry-Leading Executive Support: Dual mentorship from a Site Head and Global M&S Leader, with direct access to top leadership through regular executive dialogues Personalized Development: Customized career roadmap, external professional co