东莞招聘

Responsibilities
Import Export Specialist - Global Brokerage Team Member Core Responsibilities
*Support team lead through operational management and issue resolution related to Customs and Other Government Agency (OGA) clearance of Pfizer products for clinical trial activities.
*Interface directly with the Customs Broker and/or Government Agencies to resolve issues with entries or provide additional information as required.
*Interface directly with Supply Chain Pack/Label Distribute (PLD) vendors to ensure distribution centers understand operational processes as they relate to customs clearance, and provide any necessary training to the PLD Vendors.
*Interface with Pfizer Development Operations, Worldwide Regulatory and/or Alliance Partner organizations to verify import licensure for importation of clinical trial medications.
oObtain copies of Import Licenses from either existing Pfizer country office resources or designated Alliance Partner resources.
oEstablish notification process for license renewal based on Country's clearance difficulties/base clearance timelines.
oAdvise Global Broker on requirements for management of actual import quantities against the Import License's authorized maximum levels.
oNotify PFE Country Office or designated Strategic Alliance Partner when Import License remaining levels reach predefined thresholds for reapplication/submission of new license.
*Provide issue resolution for clinical trial logistics as it relates to customs clearance and broker operations.
*Manage the Country Specifications documents
oDevelop and implement country specification system for provision of import/export requirements between broker and distribution operations.
oMaintain Country Specifications going forward with the input/support of the Global Broker.
*Support global distribution of Pfizer clinical trial materials as it relates to customs clearance and global broker operations.
oApprove shipping documents issued by either Pfizer Sites or Core Vendors.
oProvide tracking of shipments where normal AWB data cannot be leveraged by customer base.
oMonitor global shipments through the destination country's clearance process all the way through to final delivery to the ultimate consignee.
oAssist in resolving any destination clearance issues/problems.
oAudit invoices received to ensure proper cross charging to the appropriate Project Code (or alternatively, review/approve all invoices and code for appropriate Project Code.
*Duty/VAT Payment & Reclamation
oAssist PFE Country Office or designated Strategic Alliance Partner with any Duty payment issues or queries from government authorities.
oAssist PFE Country Office or designated Strategic Alliance Partner with regularly scheduled VAT payments (either shipment-by-shipment or periodically (i.e., quarterly)).
oAssist PFE Country Office or designated Strategic Alliance Partner with VAT reclamation recovery/issues.
*Obtain compliant valuations, HTS codes, FDA product codes and country of origins and ensure these are applied to documentation for international movements.
*Provide Import/Export guidance and direction to WWPTx Supply Chain Lines.
*Where necessary, interface directly with the Customs Broker and/or government agencies to resolve issues with entries or provide additional information as required.
*Maintain and enhance appropriate networking relationships with pharmaceutical companies, trade organizations and government personnel.
*Continue individual and organizational development to ensure currency and compliance with global import/export requirements.
*Provide back up to other Import/Export Specialists at PGRD sites.
*Serve as the primary point of contact between the Clinical Supply Logistics organization and strategic partners such as Customs Brokers, Transportation providers, Warehouse, Storage, and domestic distribution providers to ensure safe and secure movement of clinical supplies to patients. This colleague would serve as the primary POC for the following AsiaPac countries: Hong Kong; Indonesia; Malaysia; Philippines; Singapore; South Korea; Taiwan; and Thailand.

Import Export Specialist - Global Brokerage Team Member (China) Specific Responsibilities
*Surveillance and communication of Chinese Regulatory requirements relating to the importation, storage, and distribution of investigational medicines.
*Assist with the capture of Import licenses for investigational medicines, commercial medicines and equipment related to Pharmaceutical Sciences business in support of Pfizer clinical trials and related work in China.
*Support material logistics (API, excipients, packages, standards, analytical columns etc) for pilot batches productions and analytical tech transfer for other Pfizer China sites).
*Perform logistics duties associated with Samples obtained for Pharmaceutical equivalence, Bioequivalence and Clinical Trials.
*Manage and/or support financial process related to VAT/Duty payment for imported clinical supplies, samples and equipment.
*Serve as the primary point of contact between the Clinical Supply Logistics organization and strategic partners such as Customs Brokers, Transportation providers, Warehouse, Storage, and domestic distribution providers to ensure safe and secure movement of clinical supplies to patients. This colleague would serve as the primary POC for the following AsiaPac countries: Hong Kong; Indonesia; Malaysia; Pakistan; Philippines; Singapore; South Korea; Taiwan; and Thailand.
*Provide support for routine queries and inspections by regulatory agencies as they related to importation, storage, and distribution of clinical supplies and equipment (e.g. Customs, etc.).
*Support quality investigations and recall activities (product collection) related to clinical trials in China.
*Liaise with Pharmaceutical Sciences teams in China as well as other functional groups such as Development Operations, Strategic External Partners, and members of the Emerging Markets Business Unit.
*Assist in the local purchase of clinical trial supplies as determined by the Local Sourcing Initiative.
*Support Medical Affairs in the acquisition (e.g. invoice approval, etc.) process of clinical trial material for IIR Grant Studies and Compassionate Use Shipments.
*Serve as a valued Global Clinical Supply Team member by building strong relationships with key customer groups and external partners.

Strategic deliverables within the center of emphasis:
*Provide advice/guidance on the customs, regulatory, and company requirements for shipping materials between global WWPTx sites.
*Interface closely with Import/Export colleagues, Inventory Management, and Global Operations, as needed on international shipment of materials.
*Maintain strong links with Import/Export Specialists at other WWPTx sites to: (a) contribute to the development of more efficient processes, and (b) joint resolution to issues affecting international movement of WWPTx materials.
*Develop and deploy metrics program for measure of departmental performance against stated goals for operations responsibilities.
*Develop & deliver training to WWPTx Supply Chain colleagues.
*Prepare and or provide guidance on preparation of controlled substance import/export licenses for US DEA where appropriate. Provide guidance on Controlled Substance shipping requirements to international destinations where possible.

Qualifications
*Experienced colleagues would be expected to have prior experience with import/export regulations which may include focused expertise with government agencies such as U.S. FDA, U.S. CBP, U.S.D.A, U.S. DEA, HMRC, MHRA, Home Office Agency, SFDA, AQSIQ, and the various Government Agencies involved in the additional AsiaPac countries for which they are the primary POC for.
*Experienced colleagues would have prior experience with an FDA regulated industry and can understand the requirements for associated Customs and OGA clearances. Having experience with pharmaceutical industry operations, the development & implementation of strategic plans in Research & Development as well as an understanding of the interdependencies between Supply Chain and logistical processes is an added benefit.

辉瑞公司（Pfizer Inc.）创建于1849年，迄今已有160多年的历史，总部位于美国纽约，是目前全球***的以研发为基础的生物制药公司。辉瑞致力于运用创新的科学技术以及全球资源来改善每个生命阶段的健康和福祉。
我们的目标是“不断创新为患者带来能显著改善其健康的药物”。我们的使命是“成为一家卓越的创新型生物制药公司”。
2012年辉瑞公司全年合计收入590亿美元，研发投入78亿美元。辉瑞在全球拥有9万多名员工，59家生产基地，业务遍及全球150多个国家和地区。2012年财富全球500强企业中辉瑞排名126位。
目前辉瑞公司的产品覆盖了包括化学药物、生物制剂、疫苗、健康药物、动物保健品等用于人类、动物和消费者保健等诸多广泛而极具潜力的治疗及健康领域，同时其卓越的研发和生产能力处于全球领先地位。
在人类和动物药品的发现、开发和生产过程中，辉瑞始终致力于奉行严格的质量、安全和价值标准。每天，分布在世界各地的辉瑞员工致力于促进当地医疗卫生的发展以及探索能够应对当今最为棘手疾病的预防和治疗方案。
辉瑞还与世界各地的医疗卫生专业人士、政府和社区合作，支持世界各地的人们能够获得更为可靠和可承付的医疗卫生服务。这与辉瑞作为一家世界领先的生物制药公司的责任是一致的。160多年来，辉瑞一直努力为人们提供更好、更优质的服务。
辉瑞生物制药目前在华上市的创新药物已超过50个，其治疗领域涵盖了心脑血管及代谢、抗感染、中枢神经、抗炎镇痛、抗肿瘤、泌尿、疫苗及等诸多领域。其中如立普妥®、络活喜®、万艾可®、舒普深®、希舒美®、沛儿®、索坦®许多产品在市场上处于领先地位。为了让中国的广大患者能及时接受与全球同步的先进的药物治疗，辉瑞未来将进一步加大和加快在华新药引进和上市的力度和速度。
辉瑞健康药物旗下的善存®、钙尔奇®、惠菲宁®等消费保健产品也在中国市场家喻户晓，并以其优异的品质深受广大消费者的青睐；辉瑞旗下的硕腾动物保健品*为中国的动物保健市场提供各类领先的动物疫苗和动物药品。

At Pfizer, we apply science and our global resources to improve health and well-being at every stage of life. We strive to set the standard for quality, safety and value in the discovery, development and manufacturing of medicines for people and animals. Our diversified global health care portfolio includes human and animal biologic and small molecule medicines and vaccines, as well as nutritional products of healthcare industry and many of the world's best-known healthcare products such as Centrum. Every day, Pfizer colleagues work across developed and emerging markets to advance wellness, prevention, treatments and cures that challenge the most feared diseases of our time. Consistent with our responsibility as the world's leading biopharmaceutical company, we also collaborate with health care providers, governments and local communities to support and expand access to reliable, affordable health care around the world. For more than 160 years, Pfizer has worked to make a difference for all who rely on us.