New Production Import Manager世界500强欧美制药公司，新建工厂职位
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：2013-07-11
- 工作地点：上海
- 招聘人数：1
- 职位类别：药品生产/质量管理
职位描述
Division: Technical
Location: HQ, Shanghai
Job Summary:
? Work as a single point of contact with global functions (e.g. supply chain team, new introduction team etc.), and locally coordinate with relevant parties (e.g. Registration dept,. Planning etc.) To identify at early stage global changes which need regulatory approval in China, and will impact SRPL's supply chain. In Shanghai, lead cross function task force, to make risk assessment, develop scenarios and options, to make sure uninterrupted supply for upcoming global changes to be implemented in SRPL.
? Coordinate cross functions within Technical Division to meet the product launch target in supporting business development in SRPL.
Responsibilities:
? Working closely with relative functions, identify at early stage relevant global changes which need regulatory approval in China, and will impact SRPL's supply chain.
? Closely contact with HQ functions, coordinate with relevant parties within SRPL, and organize cross-function discussion, to develop scenarios and options for related global changes to be implemented in SRPL to make sure the uninterrupted supply.
? Work as the local change leader for the global changes impacting on local supply chain.
? Lead task force to work out the action plan in consideration of all risks, and follow up with all relevant parties to take actions according to action plan.
? Coordinate product launch activities within Technical.
Requirements:
? Bachelor or above
? Pharmaceutical related area preferred
? CET-6 or above
? At least 5 years' working experience
? At least 4 years' experience in supply chain/ or technical registration/ registration area of pharmaceutical industry.
? Good at English, listening, speaking, reading and writing.
Location: HQ, Shanghai
Job Summary:
? Work as a single point of contact with global functions (e.g. supply chain team, new introduction team etc.), and locally coordinate with relevant parties (e.g. Registration dept,. Planning etc.) To identify at early stage global changes which need regulatory approval in China, and will impact SRPL's supply chain. In Shanghai, lead cross function task force, to make risk assessment, develop scenarios and options, to make sure uninterrupted supply for upcoming global changes to be implemented in SRPL.
? Coordinate cross functions within Technical Division to meet the product launch target in supporting business development in SRPL.
Responsibilities:
? Working closely with relative functions, identify at early stage relevant global changes which need regulatory approval in China, and will impact SRPL's supply chain.
? Closely contact with HQ functions, coordinate with relevant parties within SRPL, and organize cross-function discussion, to develop scenarios and options for related global changes to be implemented in SRPL to make sure the uninterrupted supply.
? Work as the local change leader for the global changes impacting on local supply chain.
? Lead task force to work out the action plan in consideration of all risks, and follow up with all relevant parties to take actions according to action plan.
? Coordinate product launch activities within Technical.
Requirements:
? Bachelor or above
? Pharmaceutical related area preferred
? CET-6 or above
? At least 5 years' working experience
? At least 4 years' experience in supply chain/ or technical registration/ registration area of pharmaceutical industry.
? Good at English, listening, speaking, reading and writing.
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