- Process review
- Process development & optimization
- Scale up
- Technology transfer to production
- Impurity profile establishment
- Reference standard preparation
- Product specification establishment
- Project evaluation and management
- trouble-shooting
- relevant documentation (SOP document, derivation, OOS, DMF filling )
![台耀化學股份有限公司](https://www.biotech-edu.com/wp-content/uploads/2023/10/未命名-1-02.png)
全職
GMP原料藥, 實驗操作
待遇面議
研發-原料藥開發/(副)研究員
- 發布日期:
- 需求人數:1-2人
- 上班時段:日班,08:00-17:00
- 上班地點:桃園市蘆竹區和平街36號
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