Senior QC Specialist
Full-timeSenior
Description
<p>By clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda’s <a href="https://jobs.takeda.com/privacynotice" target="_blank">Privacy Notice</a> and <a href="https://www.takeda.com/terms-and-conditions/" target="_blank">Terms of Use</a>. I further attest that all information I submit in my employment application is true to the best of my knowledge.</p><p></p><p style="text-align:inherit"></p><h2><b>Job Description</b></h2><p style="text-align:inherit"></p><p>1. 完成所分配的日常产品的检验工作,严格执行检验标准和流程,遵循数据可靠性要求,确保实验过程合规性和结果的准确性。</p><p>2. 对Gobal SOP 或本地法规进行gap 分析,并完成相关行动。</p><p>3. 起草分析方法确认/验证方案,并按照批准的方案,实施分析方法转移/确认/验证。</p><p>4. 维护相关SOP、质量标准、检验记录等文件。</p><p>5. 执行相关仪器和系统的日常清洁、维护、点检、定期确认、定期回顾等,保证仪器设备处于正常使用状态。</p><p>6. 参与和执行相关的分析方法/流程优化等持续改进项目。</p><p>7. 执行新分析仪器的AIQ验证和计算机化系统回顾和升级等活动。</p><p>8. 实验室试剂和耗材管理,包括采购、接收、盘点、废弃等。</p><p>9. 遵守公司EHS的管理规定,严格执行实验室相关的化学品管理、个人防护用品、危险废弃报废等各项要求。</p><p style="text-align:inherit"></p><h2><b>Locations</b></h2>Tianjin, China<p style="text-align:inherit"></p><h2><b>Worker Type</b></h2>Employee<p style="text-align:inherit"></p><h2><b>Worker Sub-Type</b></h2>Regular<p style="text-align:inherit"></p><h2><b>Time Type</b></h2>Full time
Takeda
PHARMACEUTICAL
Small Molecule, Enzymes
LocationTOKYO, Japan
Employees49,000
Open Jobs1373
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