某知名医疗公司
Process Engineer
医疗器械及设备
工程
常州
经验不限
本科
¥10 - 20K/月
职位描述
Main responsibilities主要职责：
1. Participate in new product design, review the manufacturability of design and review drawings.
参与新产品设计，评审设计的可制造性，评审图纸
2. Responsible for the design and verification of process tooling for batch trial production of new products, set up production lines, improve trial production reports and relevant process data, and complete operator training.
负责新产品批量试制的工艺工装设计和验证，建立生产线，完善试制报告和有关工艺资料，并完成操作工的培训
3. When making samples and opening new molds, conduct technical communication with suppliers to ensure that technical problems are clarified and solved at the beginning.
在样品制作和新开模具的时候，和供应商进行技术沟通，确保技术问题在开始时得到澄清和解决
4. Maintain mass production products, go deep into the production site, grasp the quality situation, guide the workshop production, and timely solve the technical problems in production.
维护量产产品，深入生产现场，掌握质量情况，指导车间生产，及时解决生产中出现的技术问题
5. Continuously and proactively improve the design or process, initiate and track changes to implementation.
持续主动地改善设计或工艺过程，发起变更并跟踪至实施
7. Maintain cross-departmental communication and look for opportunities to reduce product design and manufacturing costs.
保持跨部门的沟通，寻找降低产品设计成本和制造成本的机会
8. Respond quickly to customer complaints related to product quality and propose solutions until closure.
对产品质量相关的客户抱怨做出快速反应，并提出解决措施，直至关闭
9. Process validation, including preparation of validation plans, programs and reports.
过程确认（清洗、焊接、包装、灭菌、洁净室、纯化水系统等），包括编制确认计划、方案、报告，协调验证/确认过程中问题的解决，以及偏差的处理，执行确认活动中的风险分析（PFMEA）
10. Perform NC evaluation, complete root cause investigation, and close CAPA in time
执行NC评估，完成根本原因调查，并及时关闭CAPA
11. Participate in supplier audit and evaluate the technical capabilities of new suppliers.
参与供应商审核，评估新供应商引进的技术能力
12. Complete and record related design defects.
完成并记录相关的设计缺陷