
Packing QA

職位描述
Responsibilities:
- Handling, investigation and assessing of quality issues
- Establish, execute and track CAPA
- To be involved in regulatory inspections and self-inspection
- Ensure to fulfil the KPIs of QA
- Identify the quality risk during daily work, improve continuously
- Support PET business processes regarding compliance and quality
- Communicate with other AZ sites regarding to quality issues
- Coach team member managing QA affairs
- Review production sheet and release product
- Maintain a smooth product release procedure
- Returned goods handling
- To take part in vendor audit
- Draft and review document to make sure in compliance with GMP requirement
- Annual product review
- Own QA procedure, section operation GMP compliance
- Lead and execute Change Control
- Quality continuous improvement
- Lead daily QA work in Packing QA Team
- Work instruction and help to team members
- Build and develop team capability
- Provide daily performance feedback to team members
- SHE responsibilities
Requirements:
- University graduate, major in pharmaceutical or related subjects
- 5 years plus experience as quality assurance
- Good GMP and quality system management knowledge
- Knowledge of product process and typical equipment
- Knowledge of process control methodology and statistics, for example Cpk, FMEA
- Working knowledge of Microsoft applications, SAP or similar system
- Good English
- Good Computer skill
- Good communication skills, proactive leadership, strong quality minds and strong service minds
企業(yè)簡(jiǎn)介
阿斯利康是全球領(lǐng)先制藥公司之一,總部位于英國(guó)倫敦。公司主要從事處方藥品的研究、開(kāi)發(fā)、生產(chǎn)、銷(xiāo)售以及提供醫(yī)療服務(wù),在消化、心血管、中樞神經(jīng)、呼吸、腫瘤和抗感染領(lǐng)域處于領(lǐng)先地位。2006年公司銷(xiāo)售額超過(guò)264億美元。阿斯利康中國(guó)區(qū)總部位于上海,在中國(guó)大陸20多個(gè)主要城市設(shè)有辦事處,現(xiàn)有超過(guò)2900名員工。
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阿斯利康
企業(yè)性質(zhì):合資企業(yè)
企業(yè)規(guī)模:2000-4999人
成立年份:1999
企業(yè)網(wǎng)址:https://www.astrazeneca.com.cn/zh/
企業(yè)地址:上海
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職位發(fā)布日期: 2019-04-16

