
Project QA Manager - Asia

職位描述
Main Tasks:
? Assure execution, maintenance and improvement of the Quality Management System at all plants within the Asia GO together with the Plant QA Manager.
? Assure compliance with the Quality Management System at all plants in Asia together with the Plant QA Manager.
? Assure GMP/regulatory compliance at all plants in Asia together with the Plant Manager and Plant QA Manager.
o Assure together with Local Quality Management by means of regular Quality audits that the Plant Quality Systems comply with FK Corporate procedures and all relevant regulatory and certification requirements.
? Oversight of LIMS project implementation in GO Asia
o Provision of management support and guidance to LIMS SME
? Support the Plant QA Manager in quality investigation projects arising at the plants.
? Escalate Quality issues to the GO QA Head
? Quality metrics data review on a monthly basis
o Review of the monthly Quality Key Performance Indicators reported by plant.
o Regular review of the KabiTrack data to ensure the events/actions are closed in a timely manner.
o Review of the effectiveness check data generated against CAPAs.
? Where possible, harmonise the common Operating Procedures related to the quality system at all the plants in Asia GO.
? Assure that the Global and Divisional SOPs, WIs and GDs are implemented in the Region.
? Where possible, harmonise and centralise the procedure and qualification activities for vendors shared by plants in Asia. Support the vendor audit programme.
? Support the plants in the inspection readiness programme prior to regulatory inspections. In addition, provide support in the preparation and review of responses.
? Support the plants during and after Fresenius-Kabi internal audits
? Enhance quality educational level at all plants within the Asia region.
? Liaise with Quality organizations of other GOs, I&D Centres and Divisions with the purpose of benchmarking against each other and share lessons learned.
? Ensure that the procedures/Manufacturing processes filed with regulatory agencies are followed on a routine basis
? Assist in the audits of third party manufacturing sites and implementation of technical agreements
? Propose and support quality related investment projects
? Ensure data integrity procedures and implemented at the plants in Asia GO
Requirements:
? An independent working personality with high skills and experience (+ 7 years) in pharmaceutical manufacturing and experience in an international operating pharmaceutical company is preferred. University degree in pharmaceutical/biological or chemical science is a requirement and experience in aseptic manufacturing and understanding of microbiological topics is a prerequisite.
? Open and positive character with excellent communication skills that is able to motivate people.
? Due to the regional nature of the position the role will involve travel nationally and internationally.
? Compliance with the FK Code of Conduct
? Proven leadership, high integrity and communication skills
? Fluent in English
企業(yè)簡介
華瑞制藥有限公司(SSPC)是中德合資的現(xiàn)代化制藥企業(yè),總投資4510萬美元,生產(chǎn)和銷售全套臨床營養(yǎng)系列產(chǎn)品。公司秉承“關愛生命、造福人類”的理念,致力于臨床營養(yǎng)產(chǎn)品的研究開發(fā)和科學應用。公司獲國家藥品監(jiān)督管理局及歐盟頒發(fā)的GMP證書,并通過ISO14001認證,是國內(nèi)較早向歐洲出口大容量注射劑和凍干粉針劑的企業(yè)。
職位發(fā)布企業(yè)
華瑞制藥有限公司
企業(yè)性質(zhì):合資企業(yè)
企業(yè)規(guī)模:500-999人
成立年份:1982
企業(yè)網(wǎng)址:http://www.sspc.com.cn
企業(yè)地址:建國門北大街8號華潤大廈1801-1805室
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職位發(fā)布日期: 2019-04-15