制剂产品研发总监/副总监

职位描述/Job Description

1.    The individual in this position will lead a group of scientists responsible for providing formulation services for products in early phase development through clinical trial material manufacturing.

领导早期制剂开发到临床用药品生产团队。

 

2.    Qualified candidate should have experience in oral solid dosage form development from concept through technology transfer and will be knowledgeable of cGMP manufacturing.

负责口服固体制剂从概念,技术转移到cGMP临床药品生产。

 

3.    The candidate must have experience handling multiple projects at various stages of development simultaneously.

能够同时管理多个不同研发阶段的项目。

 

4.    Good written and verbal communication skills are a must, experience in clinical trial material manufacturing pilot plan is desirable and the individual must be able to work in a fast-paced, team environment.

必须有良好的英语写作和口语能力,有临床实验用药品生产经验者优先,必须能够适应快节奏,团队合作的工作环境。

 

任职资格/Qualifications

1.    The candidate must have a Ph.D. in Pharmaceutics/Pharmaceutical Technology or other related discipline, as well as a minimal of 3 years of working experience in formulation research and development. Prior supervisory experience is desired. An M.S. with a minimal of 5 years of industrial experience will be considered too.

具有药学/药学技术相关专业的博士学位以及三年以上制剂研发领域的工作经验或者具有药学相关专业的硕士学位以及五年以上的制剂研发领域的工作经验;有团队管理经验的优先。


工作地点:上海—浦东张江地区

薪资待遇:面议

简历发至:HR@xihuasci.com(请注明应聘职位)


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