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Production GMP Engineer

薪资面议  /  5年  /   惠州

2025-12-24 更新

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职位属性

招聘类型:社招
工作性质:全职

职位描述

1.       生产管理Production work management

  • 负责相关区域WI的编写,培训,监控和年度回顾Responsible for the writing, training, monitoring, and annual review of relevant regional Wis.
  • 监督负责卫生情况和现场5S系统的管理和维持Supervise the management and maintenance of hygiene and on-site 5S.
  • 确保负责的相关操作规程得到审核批准,并得到严格执行Ensure that responsible SOP are reviewed, approved, and strictly enforced.
  • 配合GMP新产品的开发、转移及在产产品的工艺优化工Cooperate with the Technical Research Department to complete the development and transfer of GMP new products, as well as the optimization of the process for products in production.
  • 负责制定GMP相关的改造文件的编写或者审核Responsible for developing or reviewing GMP related modification documents.
  • 参与生产技术质量分析会,提倡合理化建议,降低产品成本Participate in production technology quality analysis meetings, advocate for rational suggestions, and reduce product costs.
  • 定期审核关于本部门的投诉,聆听客户的意见Regularly review complaints about our department and listen to customer feedback.


2.       安全生产Safety management

  • 确保生产部在安全体系的引导下进行安全生产Ensure that the production department conducts safety production under the guidance of the safety system.
  •  重视安全生产,并组织安全自查或与有关部门进行安全生产检查,发现问题及时采取各种有效措施,消除事故隐患Pay attention to safety production and organize safety self-inspection or conduct safety production inspections with relevant departments. If problems are found, take various effective measures in a timely manner to eliminate accident hazards.
  • 配合安全环保部,落实工厂安全、环保、职业健康管理体系工作Cooperate with the Safety and Environmental Protection Department to implement the factory's safety, environmental protection, and occupational health management system work.

   

3.       生产部GMP体系管理Quality control

  • 确认负责的GMP相关记录填写完整并审核;负责相关GMP文件的编写,培训,执行,跟进和年度的回顾Confirm that the responsible GMP related records are completed and reviewed; Responsible for the preparation, training, execution, follow-up, and annual review of relevant GMP documents.
  • 负责产品、工艺、设备、厂房等拟作的变更/验证,并监督实施Responsible for the proposed changes/verifications of products, processes, equipment, factories, etc., and supervising their implementation.
  • 确保有及时有效的沟通机制和逐级汇报程序,将质量问题传递到适当的管理层Ensure timely and effective communication mechanisms and step-by-step reporting procedures are in place to convey quality issues to appropriate management levels.
  • 识别并管理部门内部产生的风险,定期回顾、分析风险控制措施并不断改进Identify and manage internal risks within the department, regularly review and analyze risk control measures, and continuously improve them.
  • 负责GMP相关设备的异常处理,偏差调查Responsible for abnormal handling and deviation investigation of GMP related equipment.

任职条件

  • 本科以上学历,药学相关专业。Bachelor degree or above, major in pharmaceutical engineering, pharmacy or related
  • 5年以上医药API生产经验。More than 5 years practical experience in Pharma API production
  • 英语良好。Good English skill both in spoken and written 

职位要求

  • 学历要求:本科
  • 工作经验:5年

公司福利

  • 员工体检
  • 商业保险
  • 带薪年假
  • 绩效奖金
  • 交通福利
  • 午餐福利