Associate Manager(Packaging)包装和生产副经理

在罗氏，我们鼓励每位同事展现真实的自己；我们欣赏独特且出众的品质。罗氏的文化鼓励积极的表达、开放的对话和真诚的连结，在这里，你将因为做自己而被重视、接纳和尊重，并得到个人的提升和职业的发展。所有的这一切，都是为了更好地预防、阻止和治愈疾病，并确保医疗资源的可及性和可持续性。欢迎加入罗氏，一个重视每种声音的地方。 职位 Roles &

Responsibilities / Accountabilities 主要职责/责任 (Major functions of the position) （职位的首要职能） 1. 精益生产、数字化运营与包装流程优化 / Lean Production, Digitalization &

• Process Optimization ● Lead LPS (Lean Production System) promotion and digital lean initiatives within the packaging area to foster a culture of operational excellence. 主导 LPS（精益生产系统）在包装区域的推广，并推动 数字化精益落地，打造卓越运营文化。 ● Lead and implement Kaizen (continuous improvement) initiatives, utilizing SMED (Single-Minute Exchange of Die) to optimize changeover time, line clearance, and material logistics flow. 主导并实 施 Kaizen（持续改进）项目，利用 SMED 工具重点优化设备换线时间、清场流程及物料物流动线。 ● Design and deploy low-cost automation (LCIA) and ergonomic solutions to eliminate shop floor wastes and optimize workplace layout. 引入低成本自动化（LCIA）与人机工程学（Ergonomics）解 决方案，消除车间浪费并优化现场布局。 ● Lead TPM (Total Productive Maintenance) and OAC (Operator Asset Care) programs to cross-train operators, establishing multi-skilled teams to improve packaging agility. 主导 TPM（全员生产维护） 与 OAC（操作工设备自主维护）项目的开展，建立员工多技能矩阵，以提高包装生产的灵活性。 ● Establish, standardize, and continuously optimize workflows (SOPs/Work Instructions) to sustain improvement results and ensure operational consistency. 建立、规范并持续优化工作流程标准化 （SOP/工作指南），以巩固精益改进成果并确保生产操作的一致性。 ● Monitor and analyze packaging line performance metrics, track OEE, perform root-cause analysis for downtimes, and coordinate with external departments to develop effective recovery action plans. 监控并分析包装线的绩效指标，追踪 OEE（整体设备效率）及停机根本原因，并协调外部门制定有效的 改善行动计划。 Track and trend all KPI data to identify potential process gaps/risks; take necessary remediation actions with relevant departments to ensure the process remains stable and under control. 对包装的 KPI 进行趋势分析，基于分析结果联合相关部门采取必要的纠正行动，以确保生产过程的稳定可控。 2. 质量、合规与技术风险控制 / Quality, Compliance &
• Technical Risk Control ● Take ownership of the management, periodic review, and lifecycle updating for general SOPs within the packaging department. 负责包装通用 SOP 的管理、定期审阅及全生命周期更新。 ● Assist superiors in handling packaging production quality deviations and investigations; provide support to solve product complaints and establish robust mitigation actions. 协助主管处理包装生产现 场的质量偏差与调查；支持生产部的投诉处理，并通过制定合适的补救与纠正措施来解决问题。 ● Support QRM (Quality Risk Management) activities within production, overviewing the end-to-end (E2E) risk assessment and mitigation for each product. 支持生产部质量风险管理（QRM）的相 关行动，确保每个产品端到端（E2E）的风险评估与控制。 ● Manage and support CAPA (Corrective and Preventive Action) and Change Control execution within the production workshop. 支持并负责生产部内 CAPA（纠正预防措施）与变更管理的日常执行。 ● Ensure all process changes and optimization projects fully comply with GMP regulations, data integrity standards, and global change control procedures. 确保所有的流程变更与优化项目完全符合 GMP 规范、数据完整性要求及变更控制流程。 ● Support cross-functional teams (Engineering, QA, Validation) in equipment qualification, packaging material validation, and advanced technical troubleshooting. 配合跨职能团队（工程、QA、验证）完 成设备确认、包装材料验证以及现场技术疑难问题的排查。 ● Review and update batch records, logbooks, and master data in related IT systems (such as MES, SAP, Veeva, Cornerstone) affected by process updates. 针对流程与精益更新，负责审查和更新受影 响的批记录、日志及相关 IT 系统（如 MES、SAP、Veeva、Cornerstone）中的主数据。 3.项目独立主导与跨部门项目用户角色 / Project Leadership &
• Cross-Functional Project User Role ● Independently own, lead, and execute internal optimization and modification projects within the packaging department (e.g., OEE boost, changeover optimization, and waste reduction projects). 独立承担并主导包装部门内部的改良型与优化类项目（如 OEE 提升、换线优化、降本增效等部门内项 目），负责从立项、方案设计到落地执行的全周期管理。 ● Act as the core Business/User Role (Key User) in cross-functional projects 在跨部门项目作为包装 部门的核心业务用户（Key User）深度参与。 4. 团队赋能与精益文化建设 / Capability Development &
• Lean Culture ● Conduct on-site technical training and OJT (On-the-Job Training) for shop floor operators to enhance their understanding of standardized workflows and Lean concepts. 对车间操作员工进行培训，提升 一线员工对标准化工作流及精益理念的认知与实操能力。 ● Foster a shop floor continuous improvement culture by coaching frontline teams on how to identify wastes, submit, and execute Kaizen suggestions. 指导一线团队识别现场浪费，培训并鼓励其提交与 执行 Kaizen 建议，在车间内营造全员积极参与持续改进的文化氛围。 5. SHE（安全、健康、环境） / SHE Act as the packaging SPOC (Single Point of Contact) for SHE-related matters, conducting safety assessments and STARI tracking. 作为 SHE（安全、健康、环境）相关的包装接口人/评估人，负责 安全评估及 STARI 的跟踪。 Qualification and Experience 能力与经验 Education/Qualifications 教育程度/所获资格证书 University or above 本科及以上 Pharmacy, Chemistry, Biochemistry and equivalent 药学、化学、生物化学及相关学科 Leadership Competencies,As the individual contributor and self-leader, self-motivation and good communication skill is preferred 作为一个个人贡献者和自我领导，自我激励和良好的交流能力是必须的 Job Required Competencies 岗位所需胜任力 1.3 Years work experience in quality control, assurance, analysis or equivalent 三年质量控制，质量保证，分析及相关工作经验 2.At least 3 year experience of technical position in pharmaceutical company manufacturing. 至少三年药厂技术岗位工作经验 3.Expertise in the using of PMP & lean tools is preferred 能够熟练运用项目管理和精益生产工具更好 4.Knowledge of GMP GMP 知识 Skills and experience of pharmaceutical production process and in-process control 药品生产与制程控制的技能与经验 Skills of carrying physical test and operating normal instruments 实验与仪器操作的能力 5.Knowledge of Quality management 质量管理的知识 6.Language skill: Good at English, listening, speaking, reading and writing. 语言技能: 具有良好的英语听说读写能力 7.PC skill: Office, Minitab (or equivalent software) 电脑技能: Office, Minitab (or equivalent software) 我们是谁 打造更健康的未来是促使我们创新的动力。全球超过100,000名员工共同致力于推进科学，确保今天和明天的人们，都能获得高质量的医疗资源。我们的努力帮助了2600多万人使用我们的药物进行治疗，我们的诊断产品运行超过300亿次检测。罗氏通过赋能探索新的可能、激发创造力并保持高标准以提供突破传统的医疗解决方案，对全球的医疗环境带去推动和影响。 让我们一起，构建更健康的未来。 罗氏提供平等的职业发展机会。