Import/Export Manager(J21693)社

面议

市辖区本科及以上4年及以上

发布时间：2023-09-06

职位描述

工作职责:
The primary role of the DBO Asia Clinical Supply Import Export Manager in DBO Asia is to utilize knowledge of supply chain processes and project management to provide strategic and operational Import/Export planning for clinical trials and continuously improve processes to best utilize our digital clinical supply chain for logistics activities. This position utilizes their knowledge of distribution, logistics, import/export processes and global clinical supply requirements to ensure efficient tools are in place to manage international logistics within the clinical supply chain.
The role is responsible for implementing innovative solutions within DBO / GCS. The role is responsible for ensuring quality and compliance through risk identification, mitigation, and strategic planning for all projects and programs throughout the life of the clinical trial.
This position develops and executes analysis of processes, trends and procedures to triage issues and proactively build enhanced tools to allow for evolution of our physical and digital clinical supply chain. Excellent customer service skills, root cause analysis and data-driven decision making are utilized daily in this position.
Liaises with: DBO ,DBO Asia, Dev Japan , Dev China, Regulatory, Legal, CSL colleagues and project management personnel at third party logistics providers, Quality Assurance, Supply Chain Leads & Clinical Supply & Strategy Management, Global Import/Export, Packaging Coordinators and Inventory Management personnel. The position functions from a Pfizer office.
ROLE RESPONSIBILITIES
Establishes effective mechanisms for providing Import/Export expertise to colleagues, customers and other stakeholders in the development and execution of Inventory Management Import/Export solutions and processes
Ensure that Import/Export strategies are compliant with GMP & GCP guidelines and principles, 21CFR Part 11, and applicable regulations including all (global) country specific legislation regarding Valuation, Value for Customs, shipment of hazardous goods, Importer of Record information, tariff codes, Import and Export licenses, Value Added Tax& Duty
Provide Import/Export technical and process expertise to Medicinal Sciences colleagues
Support global relationships with Medicinal Sciences and non-Medicinal Sciences partners including Legal, Quality, Global Trade Compliance, Pfizer Global Supply Logistics, Indirect and Corporate Tax, Global Pricing & Reimbursement, Corporate insurance, global distribution vendors, freight forwarders and customs brokers
Point of contact with senior management (customer groups, stakeholders and supply chain) on Import/Export issues and opportunities, especially for communicating compliance issues, strategic direction, and assuring integrated issue resolution
Maintain GMP/GDP compliant operations and deliver logistics strategies that improve cost, efficiency and quality for Clinical Supply Operations
Ensure both business and patient continuity for all Pfizer active clinical trials to enable commercial licensure of Pfizer’s investigational medicines
Liaise with US-based team members to streamline and standardize CSL global SOPs
DIGITAL RESPONSIBILITIES
Identify, lead, and manage innovative approaches to business chall********n support of Global Clinical Supply culture of innovation
Build a network of contacts to foster personal and professional developments
Support the implementation of innovative solutions that aims at simplifying operations
任职资格:
BASIC QUALIFICATIONS
Minimum BSc/BA degree. and proven relevant experience in Import/Export clinical supply chain operations and/or commercial supply organizations, customs brokerage or transportation related industries.
Experience in pharmaceutical supply chain management, GMP, GCP, business administration, and people development skills are desirable.

其他要求

招聘人数：1人
职能类别：供应链经理/主管

公司介绍

On October 31, 2005, Pfizer announced the official opening of China Research and Development Center (CRDC) in Shanghai. Pfizer Global Research and Development’s Center is mainly engaged in drug development activities. Much of the facility's capacity is devoted to the study design, data management and statistical analysis of global phase I-IV clinical trials, as well as the clinical study report process. In addition, CRDC is a part of Pfizer global Safety and Risk Management and covers the functions of safety data processing and assessment. The center also trains Pfizer employees in China and throughout the Asia region in internationally recognized Good Clinical Practice standards.
辉瑞公司于2005年10月31日宣布辉瑞中国研发中心正式在上海揭幕。辉瑞中国研发中心主要为全球辉瑞药物开发提供支持工作。大部分的功能是围绕在I-IV期临床试验研究设计、数据管理和生物统计分析、以及临床试验报告的部分准备工作。此外，该中心是辉瑞全球安全和风险管理部的一个分支，负责安全数据处理和评估工作。研发中心还将为辉瑞公司在中国及亚洲的其它运营部门的员工提供国际标准的临床试验管理规范(GCP)的技术培训。