To participate in the new product development process and work closely with the engineer team to ensure that suppliers meet the different requirements of the new product development phase.
2、项目试制阶段,参与工艺过程的讨论与确认。
To participate in the discussion and confirmation of the process during the trial production stage of the project.
3、产品验收检验的方法制定、确认和执行。
To be responsible for the formulation, confirmation and implementation of inspection methods for product acceptance
4、参与供应商的评估,选择,以及战略供应商的过程改善。
To participate in supplier evaluation, selection and process improvement of strategic suppliers.
5、监控供应商的质量表现,推动供应商的持续改善。
To monitor supplier's quality performance and promote supplier's continuous improvement.
6、负责监控制造过程、产品和物料质量,保证与研发部门的质量接口进行合适的设计转移。
To be responsible for monitoring the quality of manufacturing process, products and materials, and ensuring proper design transfer of quality interface with R&D department.
7、主导不合格产品和物料的处置,发起产品和制造相关过程的CAPA, 与运营部门持续推动质量改进。
Lead the disposal of non-conforming products and materials, initiate CAPA for products and manufacturing related processes, and continuously promote quality improvement with operation departments.
8、其他未尽事宜。
Other tasks assigned by the leader.
任职要求:
1、本科及以上学历,工科类相关专业。
Bachelor degree or above, major in engineering.
2、5年以上的医疗行业工作经验。
Over 5 years working experience in medical industry.
3、具备丰富的质量体系知识,具有审核员资质。
Abundant knowledge of quality system and have certification of qualified auditors.
4、具备良好的解决问题及团队合作能力。
Good cordination ability and teamwork spirit.
5、具有良好的英文听、说、读、写能力。
Good command of English in listening, speaking, reading and writing.