1. At least 8 years of relevant working experience in the pharmaceutical industry, with at least 5 years spent in a Quality role.

2. Working knowledge of Validation principles and knowledge of Computerized System Validation/ Cleaning/ Process Validation is preferred

3. Strong oral and writing English (Chinese and German is a plus)

4. Solid understanding of GMP and European regulations (German drug law is a plus)

5. Results oriented and ability to deliver under pressure in a fast paced environment

6. Think individually with a strong sense of service, decisiveness and responsibility. Good knowledge of Microsoft Office – Powerpoint, Word, Excel