职位描述
该职位还未进行加V认证,请仔细了解后再进行投递!
岗位职责: The Manager External Supply Quality is accountable for providing quality assurance management of key contractors for Pfizer and for assuring that the products supplied to our patients are manufactured, tested in accordance with c-GMPs, the registration file and any additional country specific requirements. This is highly independent position operating with minimal supervision, interacting with high levels of management both at contract manufacturers and within Pfizer. Will operate as spokesperson for External Supply Quality and will spend a significant period of time developing relationships, independently negotiating, developing and communicating Pfizer quality requirements with contract manufacturers. The Manager External Supply Quality will have significant interactions with many internal business and manufacturing organizations (e.g., ES, GCMC, GTE, QO Center, PGS sites and PGRD) and will lead virtually based cross functional teams. 任职要求: Minimally BA/BS Science, Engineering, or related technical discipline with at least 8 years in a GXP setting. At least 4 years of Product Quality Assurance experience in a GMP environment. More than 2 years-experience with API/DS (Drug Substance) /DP (Drug Product) manufacturing and/or testing of large molecule products is required. Experience with external suppliers/contractors is preferred. Deep understanding of sterile operation is preferred. Advanced computer skills, MS Office and enterprise systems such as SAP, QTS, and Documentum platforms. Command of English language required and multi-lingual is beneficial. Strong verbal and written communication including presentation skills. Shows strong negotiation skills and is diplomatic in communication with internal and external customers. Demonstrated ability to manage multiple projects. Demonstrated ability to prioritize work, to act and work independently and to report items as required to Team leader. Have excellent organization skills. Demonstrated experience managing complex quality and compliance activities in a manufacturing plant or with a contractor. Developing personal leadership to manage cross functional projects. Developing ability to resolve conflicts. Takes initiatives and is proactive, persistent. Has a broad GMP and technical know-how to handle emerging issues.
工作地点
地址:台州台州
求职提示:用人单位发布虚假招聘信息,或以任何名义向求职者收取财物(如体检费、置装费、押金、服装费、培训费、身份证、毕业证等),均涉嫌违法,请求职者务必提高警惕。
职位发布者
HR
辉瑞制药有限公司
- 制药·生物工程
- 1000人以上
- 外商独资·外企办事处
- 碑林区和平路116号金鼎大厦303