职位诱惑实习期结束,表现突出者立即录用为拜耳的员工。领先的工厂平台,实战平台
Ensure production and all production documents are corresponding to Chinese GMP and related regulations.
确保生产及所有生产文件都遵循中国GMP相关标准。
Responsible for drafting and revising process specification, SOP, batch record etc. for launched products;
负责草拟或修改产品的工艺标准,SOP,批记录等。
Production on-site inspection, ensure the validated process being conducted in commercial manufacture.
负责工厂工艺流程巡查,确保产品工艺流程合规操作。
Regular collection and analysis for production data;
定期收集与分析产品的工艺数据及参数。
Assists process senior technician for process validation, cleaning validation and equipment qualification;
协助资深工艺技术人员进行工艺验证,清洁验证与设备验证。
Participation in deviation investigation;
参与变更或异常状况调查。
Participation in new product introduction
参与新品引入工作。
[要求]:
Bachelor or above, major in pharmaceutical or related subjects.
药学/制药工程/化学工艺或相关专业本科,或本科以上
4 days a week for 6 months working is preferred.
优先考虑6个月实习期,每周能到岗4天
Good English command & Good Computer skill.
良好的英文和电脑技能
Working under pressure
抗压
Innovation , challenge, Deeply think about , not just follow
创新挑战,善于思考
Team work spirit, good communication and logical analysis.
良好的团队合作,良好的沟通能力和逻辑思维
昆明市高新技术开发区科医路45号昆明科医工厂
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