杭州招聘

1. Develop and maintain area/specific VPs
起草及维护区域/专题验证计划
2. Develop and maintain validation management procedures and SOPs
起草及维护验证管理程序及SOP
3. Writing and coordination of qualification/validation documentation according to VMPs or VPs
依据验证主计划和验证计划，起草及协调确认/验证文件
4. Evaluate and maintain validation related risks, such as process QRA, equipment RA, Cleaning RA, etc
评估和维护验证相关的风险，如工艺QRA、设备RA、清洁RA等
5. Execution of proper administration system of qualification/validation documents
执行良好的确认/验证文档管理
6. Be responsible for investigation, correction of deviations during validation execution.
负责验证执行中的偏差的调查及纠正。


具有质量保证和在规范的GMP制药行业中工作经验，有一定的无菌产品制造知识或生物制药经验。Have Quality Assurance and/or in a GMP regulated environment within the pharmaceutical industry. Certain sterile product manufacturing knowledge and Biopharmaceutical experience required.

Desired 有以下经验更佳:


Skills (e.g. IT)) 工作技能 (如IT技能等) ：
1) 可应用电脑办公软件，具备基本的网络知识。 Skilled in office software， have the basic knowledge of the network.
2) 了解GMP及相关规定。 Know with GMP and relevant regulations.
3) 有一定的沟通能力。 Certain organization and coordination and communication skills.

浙江天元生物药业有限公司 诚聘