上海招聘

岗位职责：

• Be responsible for tracing all quality questions in the GMP manufacturing process.

• Be responsible for maintaining the relationship both the client and company and communicating with the client smoothly.

• Attend the daily quality meeting with the client and raise/ solve the relevant quality questions.

• Be responsible for answering the questions between client QA and internal QA.

• Be responsible for tracing the relevant deviation, CAPA and change control for the project.

• Attend the audit work for project.

• Attend the daily CMC meeting on time.

• Be responsible for reviewing the executive MBR, collecting the relevant documents to complete the batch releasing.

• Assistant to optimize the releasing process and update the relevant SOPs.

• Organize the release meeting periodically and trace the progress.

• Be responsible for the release testing

• Complete the temporary work by the director.

任职资格：

• College degree or above with a major in chemistry, biology, biochemistry, chemical engineering, bioengineering, or related field.

• More than 6 years working the relevant biological pharmacy industry and be familiar with the progress.

• More than 4 years direct working experience in QA in pharmaceuticals/biotech/medical device manufacturing or related fields.

• Good communication and coordination skills.

• Listening and speaking fluently, be good at reading and writing.

• More than 4 years for quality management experience.

• Manage the team with more than 2 years experiences.

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