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Responsibilities:
1. 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。
2. 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。
3. 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。
4. Regular collection and analysis for production data;
定期收集与分析产品的工艺数据及参数。
5. 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。
6. Participation in deviation investigation;
参与变更或异常状况调查。
7. Participation in new product introduction
参与新品引入工作。
Qualification:
1. 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
2. 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
3. Good English command & Good Computer skill.
良好的英文和电脑技能
4. Working under pressure
抗压
5. Innovation , challenge, Deeply think about , not just follow
创新挑战,善于思考
6. 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
Position Hilights:
1. Leading platform of Bayer plant site.
拜耳领先的工厂平台。
2. Hands on working experience to do the practice.
提供实战平台增加实践能力。
3. Top interns will have the fast pass to join in Bayer after internship.
实习期结束,表现突出者立即录用为拜耳的员工。