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Manufacturing Supervisor

Apply now Job no: 615550
Work type: Permanent
Location: Chengdu
Categories: Manufacturing & Logistics, People Manager

Location工作地点:Xinglong Lake, Tianfu New Area, Chengdu, China 中国成都天府新区兴隆湖畔

The role is responsible for leading and developing a team to ensure production schedules are adhered to in a safe, efficient, and timely manner, in alignment with the Quality Management System.


Accountability 1: People 主要职责1: 人员

  • Plan the deployment of people and resources to best meet the requirements of the daily production plan.


  • Set team member expectations, motivate, and encourage employees to produce work to the standards required.


  • Provide coaching and advice to team members about the completion of their duties.


  • Review each team member’s performance periodically in line with the H.E.A.R. behaviours and development expectations.


  • Manage team flexibility & supervise the delivery of agreed training plans for team members and carry out assessments under the Core Skill and Flexibility matrices.


Accountability 2: Quality 主要职责2: 质量

  • Oversee quality of production throughput and organise the resolution of quality-related issues.


  • Ensure all manufacturing complies with Cochlear’s Quality Management System (QMS), meets quality standards and organise for the resolution of quality-related issues ensuring all production is carried out in accordance with Cochlear’s QMS procedures and standards.


Perform regular inspections on Quality records and policy adherence.


Accountability 3: Capacity / Productivity Improvement 主要职责3: 产能/生产率提升

  • Plan and organise work for the team members to execute the plan in the most efficient manner through the effective use of standard CMS processes, such as Kanban, First in First Out (FiFO), Short Interval Control, Rotation Plans, Shift Start-up/Shutdown, Production Daily Time Record, Exercise & Lateness tracking.

计划和组织团队成员的工作,以最有效的方式执行计划,通过有效使用标准的CMS流程,如看板, 先进先出(FiFO),短间隔控制,轮岗计划,班次开始/结束,生产每日时间记录,工间操和考勤跟踪。

  • Liaise with other departments and support functions to meet production and customer service objectives. Identify, escalate or resolve problems that may affect delivery of the production plan, and immediately escalate issues that cannot be resolved in line with CMS.

与其他部门和支持部门保持联系,以满足生产和客户服务需求目标。 识别、升级或解决可能影响生产交付的问题,并立即反馈不能通过CMS解决的问题。

  • Maintain and execute Leader Standard Work to CMS standards.


  • Ensure accurate recording of route times in the ERP (Enterprise Resource Planning, such as Oracle, SAP, or equivalent.) system by monitoring and improving team performance.

确保在ERP(企业资源计划,如Oracle, SAP,或类似的)系统,通过监控和提高团队绩效。

  • Proactively drive and sustain the culture of continuous improvement and Just in Time thinking through tools such as Visual Performance Management, 8 Waste (TIM WOODS), 5s, error proofing and set up time reduction in line with the CMS.

积极推动和维持持续改进的文化和JIT思维, 通过工具,如可视化管理,8浪费(TIM WOODS), 5s,防呆和快速换型符合CMS要求。

  • Recommend process improvements via the recommendation of updates to processes and procedures.


Accountability 4: Financial Management 主要职责4: 财务管理

  • Ensure inventory accuracy and traceability is always maintained within the manufacturing operations.


  • Ensure accurate ERP (Enterprise Resource Planning, such as Oracle, SAP, or equivalent.) job data for example: - scrap, assigned hours, consumables etc.

确保准确的ERP(企业资源计划,如Oracle, SAP或同等产品)工作数据例如:-废料,分配的工时,消耗品等。   

  • Advise relevant stakeholders on production downtime, and other inefficiencies.


Accountability 5: Workplace Health and Safety 主要职责: 工作现场健康和安全

  • Report incidents and support investigations in allocated timeframes.


  • Conduct workplace safety observations and participate in the development of appropriate risk controls for hazards identified.


  • Ensure team members adhere to all Workplace Health and Safety requirements.



  • Fluent in Mandarin and English 中英文流利
  • At least 5 years production management experience 5年以上生产管理经验
  • Experience in medical device assembly and manufacture. 有医疗器械组装和制造经验。
  • Knowledge of and exposure to lean manufacturing practices. 了解和接触精益生产实践。  
  • An ability to work in an environment with tight regulatory requirements and complex quality systems.能够在严格监管要求和复杂质量系统的环境中工作。 
  • Practical experience with an ERP system (Enterprise Resource Planning, such as Oracle,SAP, or equivalent).有ERP系统的实践经验(如Oracle,SAP或等效)。
  • Ability to display flexibility of approach in order to meet changing requirements and situations. 能够灵活运用方法以满足不断变化的需求和情况。

Advertised: China Standard Time
Anticipated Application Closing: China Standard Time

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