Job deｓｃｒｉｐｔion:

Establish and maintain the quality systems related to QA batch disposition and record review in compliance with Chinese veterinary pharmacopoeia and local cGMP and company's quality manual chapters.Responsible for setting up production quality oversight and management system, encompassing production workshops, processes and Utility Systems for routine oversight and management. Provide support to ensure process and related support system meet GMP and company's quality manual. Ensure alignment of owned quality systems with the intent of the company's quality manual, and where required, develop and document rationale for differences between local requirement and quality manual core requirement.Provide timely final review and disposition of batch records. Release of finished products and raw materials in time for the product supply.Work directly with IPT staff, supporting and at times leading significant investigations to provide an efficient and effective service to support the timely and compliant disposition of materials, components, and products.Acquire and maintain knowledge of current local and international regulatory and legislative requirements and trends to ensure that expert advice and appropriate technical support on quality related matters is provided to the site.Provide leadership and coaching to both quality and production staff in relation to quality performance and improvement.Ensure that any product quality / supply issues are communicated timely to management as required and are remediated appropriately