About the role
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Job Description
- 负责分析方法的转移,确认和验证,起草相应的研究验证文件,保证方法学验证的科学性、合规性,并审核方案和报告。
- 负责实验室相关项目规划,相关活动的统筹和安排,追踪项目进度,确保按时完成项目。
- 负责建立实验室对新产品的检验能力,新的分析技术,深入掌握检验关键点。
- 实验室分析方法SME,维护实验室分析方法管理文件,解决验证工作中的异常情况,熟悉实验室调查流程。
- 支持和带领实验室精益管理,推进实验室持续改进。
- 定期参与Global Quality 组织的QC相关会议,清晰的知晓会议内容并根据会议内容对实际情况进行分析、跟进和提高。
- 根据实验室不同时期的业务需求,必要时支持其他小组的工作,保证常规放行和项目的交付。
- 对实验室仪器设备进行综合性管理,包括设备日常使用、清洁、点检、确认、数据可靠性等。
- 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。
Locations
Tianjin, ChinaWorker Type
EmployeeWorker Sub-Type
RegularTime Type
Full timeAplyr's read
Takeda is a global leader in pharmaceuticals, focusing on research-driven innovation. It attracts professionals dedicated to advancing healthcare worldwide.
What's promising
- •Takeda invests heavily in R&D, driving innovation in pharmaceuticals.
- •Global presence offers diverse career opportunities across various regions and functions.
- •Strong focus on employee development with roles in technical and data-driven learning.
What to watch
- •Pharmaceutical industry faces regulatory challenges that can impact operations.
- •Global operations may lead to complex organizational structures.
- •High competition in the pharma sector can pressure market share and innovation.
Why Takeda
- •Takeda emphasizes research-driven innovation, setting it apart in the pharma industry.
- •Commitment to global health initiatives reflects its broader mission beyond profit.
- •Diverse role offerings, from AI engineering to quality assurance, highlight its multifaceted approach.
Aplyr’s read is generated by AI from public sources. Was it useful?
About Takeda
Takeda Pharmaceutical Company is a global, research and development-driven pharmaceutical company committed to bringing better health and a brighter future to people worldwide.
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