Associate Quality Validation Manager/副质量验证经理-500强医药企业，丰厚的薪资和广阔的职业发展空间
上海帝博企业管理咨询有限公司
- 公司规模：少于50人
- 公司性质：外资(欧美)
- 公司行业：专业服务(咨询、人力资源、财会)
职位信息
- 发布日期：2013-06-20
- 工作地点：上海
- 招聘人数：1
- 工作经验：三年以上
- 学历要求：本科
- 语言要求：英语熟练
- 职位类别：质量管理/测试主管(QA/QC主管) 质量管理/测试工程师(QA/QC工程师)
职位描述
Primary Purpose of Job
§ Ensure qualification and validation activities in Technical compliance with relevant company policy, headquarter guideline and regulatory requirements.
Principle Roles & Responsibilities
? Oversight the planning and execution of projects in Technical
Ø By performing quality oversight on the aspects of Pharma projects from plan to design, build and test phase to monitor the compliance of project progress with company operating procedures, global standard and processes, and to verify the intended user requirement can be met and critical aspects are identified for further verification.
? Review related project quality documents and qualification documents
Ø By compliance review of qualification plans and reports, and project related quality documents for document completeness, GMP compliance and data acceptability.
? Oversight of qualification activities' execution
Ø By governance the execution progress of qualification activities to assure the compliance with company operating procedures, global guidelines, and regulatory.
? Support activities
Ø By providing support to other quality validation activities as required by superior.
Qualification and Experience
? Education/Qualifications
Ø Bachelor of Engineering Degree or above
? Job Required Competencies
Ø Project management skills
Ø Professional knowledge of qualification, validation and pharma production
Ø Knowledge of China/EU/FDA GMP requirements
Ø Language skills - English & Chinese
§ Ensure qualification and validation activities in Technical compliance with relevant company policy, headquarter guideline and regulatory requirements.
Principle Roles & Responsibilities
? Oversight the planning and execution of projects in Technical
Ø By performing quality oversight on the aspects of Pharma projects from plan to design, build and test phase to monitor the compliance of project progress with company operating procedures, global standard and processes, and to verify the intended user requirement can be met and critical aspects are identified for further verification.
? Review related project quality documents and qualification documents
Ø By compliance review of qualification plans and reports, and project related quality documents for document completeness, GMP compliance and data acceptability.
? Oversight of qualification activities' execution
Ø By governance the execution progress of qualification activities to assure the compliance with company operating procedures, global guidelines, and regulatory.
? Support activities
Ø By providing support to other quality validation activities as required by superior.
Qualification and Experience
? Education/Qualifications
Ø Bachelor of Engineering Degree or above
? Job Required Competencies
Ø Project management skills
Ø Professional knowledge of qualification, validation and pharma production
Ø Knowledge of China/EU/FDA GMP requirements
Ø Language skills - English & Chinese
公司介绍
DB Talent is a European based recruitment company. Our Shanghai office opened in the 2001, and we have continually provided excellent professional service to our clients and candidates.
联系方式
- 联系人：resume
- 电话：13701722965