• 招聘类型：社招
• 工作性质：全职

职位描述

Responsibilities:

• Finish the routine analytical work accurately and timely
• Conduct the maintenance and validation for instrument periodically based on plan and keep it in good status
• Double-check the BAR
• Responsible for the management of chemical reagents/ reference standard/ consumables, including purchase and maintenance of safety inventory
• Responsible for the handling and disposal of lab wasted articles/expire reagent/toxic substances
• Report any deviation timely and assist in investigation
• Stability study and test
• Equipment & Column routine maintenance
• Issue and revise specification, test method and batch analysis record of starting materials and finished products, and purchasing specification, test method for PQ, CQ etc.
• Prepare specification for application (draft) and specification explanation
• Check specification and test method for import products together with Regulatory department
• Technology transfer and method validation/verification
• Fill in related documentation such as BAR, other logbook etc., timely to ensure the accuracy of content as per requirement of SOPs
• Take part in actively in correction to the observations found in self-inspection
• Assist and support the group leader in leading the associated teams when required
• SHE responsibilities

任职条件

Requirements:

• University or above
• Basic GMP, GLP knowledge; Experience in QC
• More than 3-4 years working experience in pharmaceutical company or related industry
• Good English command
• Good computer skill
• Good teamwork spirit
• Sense of responsibility and work actively

阿斯利康声明：

1. 本公司招聘工作均由本公司人力资源部主持，在面试流程中，无需候选人提交除简历之外的其他个人信息，无需缴纳任何保证金或费用，无需付费参加任何培训课程。请求职者谨防诈骗信息。

2. 本公司所有招聘均通过直接面谈、电话沟通、EMAIL（以@astrazeneca.com为后缀）方式进行。

3. 对于未经本公司允许发出相关招聘信息的行为，阿斯利康公司保留追究其法律责任的权利。

4. 请关注阿斯利康官方微信公共帐号“阿斯利康招聘号”（中国地区唯一官方微信招聘渠道），了解更多职位信息。如您对招聘信息的真实性有任何疑问，请上传截图反馈至此微信号。

职位要求

• 学历要求：本科及以上
• 工作经验：3年以上
• 外语要求：英语熟练