1. Undergraduate degree in pharmaceutical, biological, chemical sciences, or engineering 药学、生物学、化学科学或工程学相关本科学位。
2.Relevant advanced degree preferred 相关高级学位优先。
3. Supervisory experience 8 or more years 管理经验8年或8年以上。
4.Minimum of 10 years progressive experience in the technical, quality control, sterile preparations for human health products 至少10年在技术、质量保证、无菌制剂方面的经验。
5.Deep knowledge & experience of cGMP’s & effective quality management and demonstrated leadership of Regulatory Inspection Management and Regulatory Affairs. 对cGMP 有深入了解，有效的质量管理经验并在法规检查管理方面有丰富经验。
6.Deep knowledge / Expertise in Pharmaceutical/Bio-Pharmaceutical Manufacturing Processes 丰富的药品/ 生物制药生产流程方面的专业知识。
7. Fluent in English (written and spoken) 有一定的英语水平（书面和口语）。