Global Clinical Supply - Distribution Specialist(职位编号:980111_1365759019)
辉瑞制药有限公司
- 公司规模:5000-10000人
- 公司性质:外资(欧美)
- 公司行业:制药/生物工程
职位信息
- 发布日期:2013-05-14
- 工作地点:北京
- 招聘人数:1
- 工作经验:五年以上
- 学历要求:本科
- 语言要求:英语熟练
- 职位类别:临床协调员
职位描述
Responsibilities
*Makes use of expertise in Clinicopia, CSDS, IVR/IWR and other distribution related systems to: effect drug transfers, request shipments and enter key data.
*Supports IVRS/IWRS process (for both internal (Impala) and external systems) related to inventory management and monitoring reports at depots; provides information needed for forecasting / maintaining drug plan to SCM; collaborate with SCC, IGOT and vendor IVRS project managers to address distribution requirements for studies run by an IVR provide; ensure adequate reporting is established at study set up to provide visibility of supplies to customers
*Provides standard tracking information, documents and reports on inventory levels and expiry dates and shipping history to ensure proactive triaging/trouble shooting and enabling flow of material transfers or drug shipments.
*Interact with distribution center's making recommendations where appropriate to ensure compliance with Distribution Network procedures, study requirements and Technical Plans.
*Collaboration with other areas of the Global Supply Chain to coordinate shipping activities to ensure timely delivery of clinical supplies.
*Establish Program and protocol level distribution plans with Supply Chain Lead (SCL), Packaging Coordinator (PC), and Clinical Teams during study planning and required document creation/revisions and providing ongoing support while acting as single point of contact for SCM on all distribution areas. Contribute to decisions on country feasibility and strategy discussions well in advance of the protocol decisions. Ownership of timing and challenges on country movements in order to meet study requirements.
*Provide input to distribution strategies for Pharm Sci Depots. Assist Distribution Network Lead with project work and strategic development of the group.
*Utilize vendor and Pfizer systems to ensure supplies are in the appropriate distribution center and are available for use.
*Determine the use of appropriate distribution center through evaluation of warehousing needs against capacity and capability.
*Develop strong relationship with and local distribution centers & couriers to facilitate timely delivery of clinical supplies.
*Utilize vendor and Pfizer systems to request and manage movement of drug product to packaging/ distribution locations.
*Interface with Distribution Center's:
oFacilitate set up of distribution strategies for protocols/programs and provide ongoing support at distribution centres.
oManage and provide resolution to distribution center issues and deviations in partnership with Quality Assurance and other Supply Chain colleagues.
oReinforce implementation of the established country shipment timelines, SOPs and Technical Plans for material moves with colleagues at distribution centers.
oCapture and trend issue log data. Make recommendations for process improvements based on trend data. Develop expertise and mentor colleagues.
oCapture suggested revisions and supporting data for Technical Plans.
oPerform oversight visits to distribution centres where applicable to ensure contractor compliance with global procedures and Distribution Instructions.
oOversee order processing and ensure delivery of supplies at right time and place.
*Interface directly with SCLs, and other groups within the supply chain in order to provide timely and responsive guidance and issue resolution regarding distribution activities.
*Evaluate current processes on an on-going basis and make recommendations for continuous improvement in the Distribution operating model.
*Provide guidance and leadership to members of the distribution organization on strategic decisions and operational development.
Qualifications
*Considerable knowledge of interdependencies of supply chain principles, practices and concepts and an understanding of the practices, concepts and operations in other relevant disciplines.
*Familiar with Supply Chain databases and systems.
*Familiar with IVRS/ IWRS systems
*Experience in management of a third party contractor.
*Recognized as an internal expert in their discipline and/or role.
*Knowledge of Distribution role and international distribution experience in the Pharmaceutical industry.
*Understanding of project management concepts.
*Competent in using information systems including MS Office products.
*Effective in both verbal and written communication.
*Ability to multi-task, manage personal time and manage multiple priorities.
*Proven ability to negotiate and problem-solve.
*Demonstrated ability to apply process improvements and procedures.
*Experience and working knowledge of Clinical Supply Systems.
*Experienced colleagues would be expected to have prior experience with development & implementation of strategic plans in research and development operations within the pharmaceutical industry as well as a solid understanding of interdependencies of supply chain and logistical processes.
must include implementation of strategic plans in the pharmaceutical industry and solid understanding of interdependencies of supply chain and logistical processes
Understanding of overall WWPTX activities
*Makes use of expertise in Clinicopia, CSDS, IVR/IWR and other distribution related systems to: effect drug transfers, request shipments and enter key data.
*Supports IVRS/IWRS process (for both internal (Impala) and external systems) related to inventory management and monitoring reports at depots; provides information needed for forecasting / maintaining drug plan to SCM; collaborate with SCC, IGOT and vendor IVRS project managers to address distribution requirements for studies run by an IVR provide; ensure adequate reporting is established at study set up to provide visibility of supplies to customers
*Provides standard tracking information, documents and reports on inventory levels and expiry dates and shipping history to ensure proactive triaging/trouble shooting and enabling flow of material transfers or drug shipments.
*Interact with distribution center's making recommendations where appropriate to ensure compliance with Distribution Network procedures, study requirements and Technical Plans.
*Collaboration with other areas of the Global Supply Chain to coordinate shipping activities to ensure timely delivery of clinical supplies.
*Establish Program and protocol level distribution plans with Supply Chain Lead (SCL), Packaging Coordinator (PC), and Clinical Teams during study planning and required document creation/revisions and providing ongoing support while acting as single point of contact for SCM on all distribution areas. Contribute to decisions on country feasibility and strategy discussions well in advance of the protocol decisions. Ownership of timing and challenges on country movements in order to meet study requirements.
*Provide input to distribution strategies for Pharm Sci Depots. Assist Distribution Network Lead with project work and strategic development of the group.
*Utilize vendor and Pfizer systems to ensure supplies are in the appropriate distribution center and are available for use.
*Determine the use of appropriate distribution center through evaluation of warehousing needs against capacity and capability.
*Develop strong relationship with and local distribution centers & couriers to facilitate timely delivery of clinical supplies.
*Utilize vendor and Pfizer systems to request and manage movement of drug product to packaging/ distribution locations.
*Interface with Distribution Center's:
oFacilitate set up of distribution strategies for protocols/programs and provide ongoing support at distribution centres.
oManage and provide resolution to distribution center issues and deviations in partnership with Quality Assurance and other Supply Chain colleagues.
oReinforce implementation of the established country shipment timelines, SOPs and Technical Plans for material moves with colleagues at distribution centers.
oCapture and trend issue log data. Make recommendations for process improvements based on trend data. Develop expertise and mentor colleagues.
oCapture suggested revisions and supporting data for Technical Plans.
oPerform oversight visits to distribution centres where applicable to ensure contractor compliance with global procedures and Distribution Instructions.
oOversee order processing and ensure delivery of supplies at right time and place.
*Interface directly with SCLs, and other groups within the supply chain in order to provide timely and responsive guidance and issue resolution regarding distribution activities.
*Evaluate current processes on an on-going basis and make recommendations for continuous improvement in the Distribution operating model.
*Provide guidance and leadership to members of the distribution organization on strategic decisions and operational development.
Qualifications
*Considerable knowledge of interdependencies of supply chain principles, practices and concepts and an understanding of the practices, concepts and operations in other relevant disciplines.
*Familiar with Supply Chain databases and systems.
*Familiar with IVRS/ IWRS systems
*Experience in management of a third party contractor.
*Recognized as an internal expert in their discipline and/or role.
*Knowledge of Distribution role and international distribution experience in the Pharmaceutical industry.
*Understanding of project management concepts.
*Competent in using information systems including MS Office products.
*Effective in both verbal and written communication.
*Ability to multi-task, manage personal time and manage multiple priorities.
*Proven ability to negotiate and problem-solve.
*Demonstrated ability to apply process improvements and procedures.
*Experience and working knowledge of Clinical Supply Systems.
*Experienced colleagues would be expected to have prior experience with development & implementation of strategic plans in research and development operations within the pharmaceutical industry as well as a solid understanding of interdependencies of supply chain and logistical processes.
must include implementation of strategic plans in the pharmaceutical industry and solid understanding of interdependencies of supply chain and logistical processes
Understanding of overall WWPTX activities
公司介绍
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.
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.
联系方式
- Email:chinahrwest@Pfizer.com
- 公司地址:南京西路中信泰富