立即投递该职位 职位名称：物流合规专员-上海-上海市 职位描述/要求：PRINCIPLE DUTIES AND RESPONSIBILITIES: Location: Shanghai, China You have honed your knowledge, functional breadth and technical skills. This is your opportunity to join our dynamic Supply Chain team as a Compliance Program Lead, providing guidance, expertise and services to ensure process and product quality for Global Logistics Operations. Here, you'll implement your vision by transforming broad concepts and business strategies into structured projects, lead the design and delivery of new programs and provide solutions to complex, high impact issues. In this role, you will: ? Establish, maintain, review, and improve Global Logistics programs, policies, and procedures to ensure compliance to all applicable standards and regulations, consistent with corporate objectives. ? Manage and maintain Global internal and exceptional shipping processes, ensuring full compliance to applicable financial, legal, trade, and regulatory requirements. Lead routine monitoring and improvement projects to improve compliance and adapt to business needs. ? Identify opportunities and lead initiatives for continuous improvement compliance in Global Logistics processes. Work with multi-functional groups and apply global business view to develop enterprise-wide compliance solutions. ? Coordinate with cross-functional stakeholders to assure Agilent Global Logistics operational compliance to ISO 9001, ISO 13485, and Medical Device regulations, per-country and global customs and trade regulations, and other regulations as applicable. 2 ? Support the resolution of critical Logistics compliance issues. ? Raise compliance awareness through trainings and communication ? Work independently and exert strong leadership and decision-making skills. QUALIFICATION ? Over 4 years of experience in a Quality, Compliance, or Supply Chain operations role. ? Experience leading problem solving and continuous improvement initiatives, in-depth knowledge and practical application of Quality problem solving systems and tools e.g. 8D, PDCA, 5 whys RCA, FMEA, etc. is highly desired. ? Strong knowledge of ISO 9001 certification standard, audit methods and quality improvement tools required. Knowledge of ISO 13485 and Medical Device regulations highly desired. Understanding of logistics compliance and trade regulations desired. ? Knowledge of the principles and practices of computer applications including word processing, spreadsheet, database management, and presentation software and internet search engines. ? Requires excellent oral, written, and communication skills ? Must display strong analytical and problem-solving skills ? Self-motivated and able to function effectively within team ? Ability to prioritize, manage multiple projects at the same time ? Requires leadership & transformation/change management sklls. 公司介绍： 美国安捷伦科技公司是一家多元化的高科技跨国公司，它于1999年从惠普公司分离出来，主要致力于通讯和生命科学两个领域内产品的研制开发、生产销售和技术服务等工作。 安捷伦科技公司是分析仪器系统的领导供应商，其产品正在化学、环保、食品、医药和生命科学领域中广泛使用。安捷伦具有世界最先进的化学分析仪器，丰富的法规适应性和专业技术经验，以及优良的支持服务系统，这些都能够帮助您的实验室超前...查看全部
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