东莞招聘

The position is open to all the locations in China

The Sr. Professional, Manufacturing Intelligence (MI) Global Solution Delivery position within Manufacturing Solutions provides functional and technical expertise for manufacturing intelligence solutions for the Pfizer Global Supply (PGS). The incumbent will report to the Sr. Manager , MI Global Solution Owner, Manufacturing Solutions BT.

The Sr. Professional, MI Solution Delivery position will be responsible for technical requirements, solution development, solution problem management, and functional application expertise.
? Analyze processes and make recommendations for improving efficiency, product or service delivery; and constantly strive to reduce expenses;
? Must be able to work independently as well as with a team.
？ Working as a part of a global team, the incumbent will be responsible for providing production support for the various Manufacturing Intelligence (MI) systems supported by the global Manufactured Solutions (MS) domain.
？ Working as a part of a global team, the incumbent will be responsible for providing application development, including new programs, enhancements and bug fixes for the various MI systems supported by the global MS domain.
？ Incumbent will work with Business Application Owners and members of the broader MS teams to translate business requirements into functional design documents and system configuration for system enhancements.
？ Incumbent will be responsible for managing system test and regression test activities. This may include maintenance of existing scenarios/scripts and creation of new scenarios/scripts.
？ Incumbent will be required to maintain and/or create system design and support documentation that meets Pfizer GMP standards.
？ Incumbent may be required to work with vendors and offshore partners in order to perform these duties.
？ Working with Site and MS Domain teams to delivery MI vision.
？ Ensure compliance with Global standards for application development, including documentation standards as per GMP.
？ Regulatory Compliance Methodology (GRC and SDLC)
Work / partner with:
? Manufacturing Solutions Client Partner regional teams to partner with users and gather voice of the customer;
? Work with Global Engineering to understand customer needs and align to OpU/Site informatics plans;
? Coordinate with other Manufacturing Solution GSD teams to leverage SMEs as required to support business needs;
? Work with Solutions Management and Continuous Improvement teams to understand trends in problem management and leverage CI capabilities to drive better utilization of the core solutions with the business;
? Coordinate with other solution ERP & PGS BT solutions owners to define, build, and deliver new sources of data;
? Work with BT Compliance to ensure solutions meet GMP requirements, as necessary.
Organization Accountability
? An external partner for consulting and development services

Qualifications:

Minimum of 5 years related work experience, 2 years of which is in a pharmaceutical environment. The following qualifications are required:
o Experience with at least one of the MI systems by the global Mfg. Solutions domain.
o Minimum 1 year of experience with testing methodology (Developer, Unit, System and Regression testing)
o Focused experience in Compliance, Business Functional Requirements, Operational Reporting, and Visualization. Experience to include all stages of system and application GRC/SDLC from concept through business case development, system build & deploy, system support and system retirement.

Education:
Bachelor’s degree – Required
Computer Science, or similar sciences, Degree – Preferred
Master of Business Administration – A plus

A thorough understanding of system GMP requirements in deailed knowledge of IT system deisgn and the maintenacnce lifecycle in GMP environments.

? Must have knowledge and understanding of GE Plant Apps (PEPS), Rockwell Automation VantagePoint (PPRS), SAP xMII (DART), Oracle Application Express (MIND2), and Catalyst;
? Strong process and procedure skills, most particularly regarding SDLC, functional enhancement governance, and stakeholder management;
? Knowledge of SDLC/ELC/GRC and project management processes;
? Experience supporting the implementation of IT solutions;
? Prior experience gathering and defining requirements for reporting and analytics;
? Excellent verbal and written communications skills and the ability to effectively communicate with the appropriate project stakeholders and senior business leadership;
? Ability to interact effectively with people at all levels of the organization who possess varying levels of technical expertise;
? Ability to work independently with minimal supervision and manage multiple priorities;
? Demonstrated ability to successfully manage interpersonal relationships;
? Demonstrated ability to articulate technical concepts to non-technical personnel;
? Previous experience in conflict resolution;
? An equitable balance between basic managerial skills, service delivery focus and business acumen;
? Must have the ability to work across multiple concurrent operations and projects and be flexible to adapt to changing priorities.
? Ability to speak and write Chinese and Japanese.
Some travel required (10 – 15%).

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.