1. 实验室与质量监督(Laboratory & Quality Supervision)：
1.1 管理配方方案、原材料验证及生产过程控制，确保质量达标。
Manage formulation protocols, raw material validation, and in-process controls to ensure quality standards.
1.2 监督产品稳定性研究、取样检测及质量控制文档编制，保障 QC 流程合规。
Supervise product stability studies, sampling/testing, and QC documentation to maintain
compliance.
1.3 确保生产全流程符合内部质量程序及兽药/制药法规要求。
Ensure full compliance with internal quality procedures and veterinary/pharmaceutical regulations throughout
production.
2. 生产管理(Production Management)：
2.1 领导粉末配方、混合、定量、包装等生产流程。
Lead the manufacturing process: powder formulation, blending, dosing, and packaging
2.2 监督、培训生产操作员，提升团队技能与操作规范性。
Supervise and train production operators to enhance skills and operational standardization.
2.3 维护生产计划、生产库存、批次追溯体系。
Maintain production schedules, inventory levels, and batch traceability.
2.4 识别并解决生产偏差，减少停机时间。
Identify and resolve production deviations, ensuring minimal downtime.
3. 文档与合规管理(Documentation & Compliance)：
3.1 维护批次记录、QC 报告、偏差报告及清洁日志，确保文档完整准确。
Maintain batch records, QC reports, deviation reports, and cleaning logs for accuracy/completeness.
3.2 执行 GMP 及生物安全标准。
Enforce GMP and biosafety standards throughout the facility.
3.3 协调内部审核、CAPA（纠正和预防措施）及客户投诉调查。
Coordinate internal audits, CAPAs, and customer complaint investigations.
4. 跨部门协作(Cross-functional Collaboration)：
4.1 与研发、质量、供应链团队对接，推动工艺优化与资源协同。
Liaise with R&D, Quality, and Supply Chain teams to drive process optimization and resource alignment.
4.2 向上级（工厂经理）汇报生产进度、质量状况及重大问题。
Report production progress, quality status, and critical issues to line manager (Plant Manager).