职位描述： 1.按照PTSG的Gate review流程要求作为指导方针领导项目，同时也需要满足客户及行业标准（IATF16949, VDA RGA, APQP, ANPQP等） 2.负责完整收集项目相关文件，如需要可以要求项目成员提供相关文件。 3.领导APQP gate review同时监督开口问题。 4.制作和监控项目开发时间计划（包括“是什么”，“时间”及客户时间节点），与客户及内部利益相关人沟通项目进展。 5.管理进度，与所有相关人沟通项目状态，关闭项目。 6.领导项目范畴内的变更管理，协调实施与项目团队及利益相人相关的措施。 7.确保项目目标的达成，例如利润率，成本，性能目标，满足SOR中的技术规范，时间和关键节点（包括正式工装件，PPAP件和量产件）。 业务流程支持 1.支持审核（包括IATF16949,客户特殊审核等）。 2.在整个组织架构中通过使用PTSG的Gate review流程促进有纪律性的项目管理。项目投产 1.组织项目核心人员完成TFC评审。 2.与产品分析工程师，制造工程师及财务紧密合作分析SAP成本并申请SAP成本释放。 3.管理和监控试生产并确保手工样件，工装样件交付。 4.负责新业务的报价。 5.创建和维护新业务的的SAP基础数据，其中包括材料清单、工艺路线。职位要求： 1、必须为工程类或类似专业； 2、英语CET-6及以上；英语口语流利； 3、非常丰富的项目管理经验； 4、适应定期的短期出差； 5、有很好的会议组织、协调沟通能力；需要与各部门（包含组织内部各部门，及外部沟通）极强的抗压能力、思维敏捷等。...
JLL empowers you to shape a brighter way. Our people at JLL are shaping the future of real estate for a better world by combining world class services, advisory and technology for our clients. We are
Job Description: JOB DESCRIPTION JOB INFORMATION Job Title: Cross-Plant (XP) for TAKT team Type of Contract: Local Hire Location: Tianjin Company: ATFAC Department: Siglum: ACOLSX1 Report to: HO Cross-Plant(XP) Operations in TAKT Team for L1 Band
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JLL empowers you to shape a brighter way. Our people at JLL are shaping the future of real estate for a better world by combining world class services, advisory and technology for our clients. We are
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Assisting PI to administer the clinical trials in accordance with the SOP, ensuring the clinical trials are conducted in accordance with GCP guidelines and quality. Novotech is a global full-service clinical Contract Research Organization (CRO). At
Assisting PI to administer the clinical trials in accordance with the SOP, ensuring the clinical trials are conducted in accordance with GCP guidelines and quality. About the role Assisting PI to administer the clinical trials in
Assisting PI to administer the clinical trials in accordance with the SOP, ensuring the clinical trials are conducted in accordance with GCP guidelines and quality. About the role Assisting PI to administer the clinical trials in
Assisting PI to administer the clinical trials in accordance with the SOP, ensuring the clinical trials are conducted in accordance with GCP guidelines and quality. About the role Assisting PI to administer the clinical trials in
Assisting PI to administer the clinical trials in accordance with the SOP, ensuring the clinical trials are conducted in accordance with GCP guidelines and quality. About the role Assisting PI to administer the clinical trials in
Assisting PI to administer the clinical trials in accordance with the SOP, ensuring the clinical trials are conducted in accordance with GCP guidelines and quality. About the role Assisting PI to administer the clinical trials in
Assisting PI to administer the clinical trials in accordance with the SOP, ensuring the clinical trials are conducted in accordance with GCP guidelines and quality. About the role Assisting PI to administer the clinical trials in