上海招聘

工作职责:

1. Be responsible for GMP/Quality Assurance related training.

2. Be responsible for following up the CAPA, deviation, change control and complaint’s status.

3. Be responsible for coordinating deviation/CAPA to ensure corrective and preventative actions are carried out and documented.

4. Be responsible for maintaining current and history specification/analytical method /protocol/memo

5. Be responsible for distributing new effective specification/analytical method / protocol/Memo.

6. Be responsible for distributing QA controlled logbook/forms and allocating ASU record sequential No., log No. or form No.

7. Be responsible for getting CoA/RoA effective, distributing ID chromatogram.

8. Be responsible for the preparing the GMP area access list.

任职资格:

1. Must be trained in or have experience with the requirement of GMP regulation.

2. Strong communication skills, both written and verbal, and outstanding interpersonal skills.

3. Good at coordination and communication at all levels of employees

4. Good skill of micro office software.

合全（sta）是药明康德全资子公司，其中包括：上海合全药物研发有限公司( 原药明康德工艺研发部，上海外高桥)，合全药物公司是sta 专门从事工艺合成路线研发及放大实验的研发团队；合全药业金山公司和常州公司是sta 提供符合cgmp 标准的中式放大及商业化生产的基地。
shanghai syntheall pharmaceutical co., ltd. is a wholly-owned subsidiaries of wuxi app tec, including:
sta r&d is professional in route selection and process scaled up r&d;sta jinshan and changzhou are the pilot plants and commercial production base under cgmp.

sta 公司愿景 sta vision：
改变创新药api 的工艺研发和生产模式，加快新药研发速度，降低新药成本，造福人类健康。
transform how industry develops and manufactures apis, shorten the time and lower the cost of new drug developments, improve the quality of life.

sta 公司使命 sta mission：
不断创新、不断完善创新药api 的工艺研发以及研发和商业化生产的一体化平台，为全球新药研发机构提供最优质***效的api 工艺研发和生产一体化服务和***解决方案。
constantly enhance the capabilities of our fully-integrated api development and manufacturing platform from preclinical batches to commercial supplies, provide highly efficient and cost-effective solutions to our partners worldwide.