深圳招聘

职位描述：
Responsibilities:
- Set up and maintain the documentation control system to support the quality management system running.
- Issue and print the hard copies of the documents, forms, logbooks in the GMP requirement.
- To be responsible for the electronic document management system.
- To run the other quality databases.
- Management the projects and equipment archive.
- Manage the GMP archive.
- Conduct the training to employees in the field of GMP requirement on document control.

Requirements:
- University degree on relevant majors.
- Good at English writing, reading and speaking skills.
- At least 5 years working experience in the relevant position.
- Experience from a cGMP pharmaceutical company is preferred.
- Strong ability to work collaboratively in a team based environment.
- Strong communication skills.
- Strong ability to work in an effective and flexible way. 举报 分享

  杰科生物成立于2015年，公司坐落于天津滨海新区中新生态城。

  杰科生物产业定位于高端生物医药，产品涵盖单克隆抗体、重组蛋白、溶瘤病毒、免疫毒素、疫苗等。依托于我们可持续的强大创新研发实力、备受业界推崇的设备设施配置、遵循GMP的全过程管理体系以及最重要的——不断壮大的优秀人才团队，我们从研发、生产到上市，覆盖生物医药产业全链条。

  杰科生物致力于研发生产创新医药，在满足自身发展的同时，我们积极面向全球客户展开共赢合作，为客户定制和提供优质产品和增值服务，乃至完整的解决方案。