北京招聘

The position is open to all the locations in China

Requirements:
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

Financial Accountability
Capital Project Management
? None

Qualification:
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%).

大连工厂是辉瑞制药有限公司在大连开发区的生产基地，也是辉瑞全球生产集团(PGM)在中国的一个区域性供应组织。工厂占地面积82,000平方米，其中厂房设施占地20,586平方米。大连工厂拥有世界上最先进的生产设施和检测技术。产品包括多种片剂、粉针剂、粉剂和胶囊等多种剂型的制剂药。工厂率先于1997年4月获得国家GMP认证委员会颁发的中华人民共和国第0001号GMP认证证书，其综合生产能力已居国内领先水平。由于工厂拥有世界一流的检测分析手段和辉瑞全球统一的完善的质量保障体系，使工厂的产品全部达到或者超过了中国药典和美国药典标准。此外，大连工厂的产品还分别于1994年、1997年、2000年和2002年通过了澳大利亚TGA检验，已获准出口日本、澳大利亚、菲律宾、巴基斯坦及欧洲等地。并于2004年4月获得由德国莱茵认证公司颁发的ISO14001环境管理体系认证证书，同时获得了中国国家认证机构认可委员会的认可。

作为辉瑞全球生产集团的一部分，大连工厂一直致力于生产高质量的创新药品，百分之百地满足客户的需求。同时，不断改进和创新，努力降低生产成本，创造并保持其在本行业内最优异的环保、健康和安全方面的业绩。