岗位描述
Main Responsibilities
1.API CMO Management
· Oversee quality system assessment of CMOs and develop quality management strategies to ensure the quality system and quality management capabilities continuously meet HUTCHMED's expectations and requirements.
· Ensure effective management of API CMOs, including but not limited to participating in on-site audits (such as CMO quality audits, official GMP inspections, Pre-Approval Inspections), reviewing quality agreements, and evaluating annual quality management review reports.
· Ensure each batch of API is manufactured, tested, and released in accordance with approved documents and applicable regulatory requirements
· Ensure quality issues arising during API production and testing are properly addressed, with timely reporting to QA Head.
· Handle quality events including product complaint investigations, deviations, change controls, OOS/OOT, recalls, reprocessing, and rework.
· Review GMP documentation from CMOs to ensure compliance of GMP product documents
2. Material/Service Supplier Management
· Manage supplier selection, evaluation, qualification, and monitoring processes.
· Establish and maintain supplier audit processes and audit plans, implementing audits according to schedule.
· Establish supplier quality assurance agreement management processes and oversee drafting and signing of specific agreements.
· Communicate with suppliers regarding quality issues, track supplier quality problems, and implement corrective and preventive actions; regularly perform statistical analysis and trend reporting of supplier quality issues.
· Manage supplier change control assessments and activities, including related material evaluations and supplier qualification re-confirmation.
· Establish supplier files and participate in the maintenance and management of material master data.
· Supervise quality behaviors of relevant departments in the distribution of launched products to ensure compliance with
3.NMPA regulatory requirements.
· Review master data of tier-1 distributors for launched products
· Handle all commercial product quality complaints.
· Handle all returns of launched products, including quality returns and commercial returns.
· Assist related departments in product recalls to ensure distributors cooperate with HUTCHMED's recall actions.
4.Team Development & Capability Building
· Coach and develop team members to strengthen GMP awareness, technical competence, and digital literacy, fostering a culture of innovation and continuous improvement.
· Build organizational competency in AI-enabled quality tools and digital quality systems to ensure sustainable adoption and effective utilization.
Requirements
1.Education & Experience
• Bachelor's degree or above in pharmaceutical sciences or a relevant field.
• Minimum 15 years of experience in QA, Production, and/or QC within a pharmaceutical manufacturing site; multinational company experience preferred.
2.Regulatory & Technical Knowledge
• Solid GMP knowledge of non-sterile API and drug product, with working understanding of cGMP requirements across US, EU, and China regulations.
• Strong knowledge of Quality Risk Management (QRM) principles (ICH Q9) and risk-based approaches to quality decision-making.
3.Digital & AI Competency
• Proven experience in leading digital transformation initiatives within quality management, particularly with VEEVA Quality platform implementation and optimization.
• Demonstrated experience or strong strategic vision in applying AI and advanced analytics to quality management processes — including predictive analytics, automated trending, and intelligent decision support.
• Experience in establishing data-driven quality monitoring and early warning systems to proactively identify recurring deviations and systemic issues.
4.Leadership
• Strong leadership capability and strategic thinking; able to influence cross-functional stakeholders and drive organizational change.
5.Soft Skill
• Good communication skills.
• Fluent oral English and good written English skills.
• Good presentation capability.