Number of recruits：1 person
1. Ph.D., have more than 2 years of experience in vaccine and drug R&D and industrialization, get familiar with relevant processes;
2. Get familiar with relevant requirements of GMP production quality management systems for drugs and test methods of Chinese Pharmacopoeia;
3. Have experience in review and registration of packing materials of drugs;
4. Have strong communication and coordination skills, writing and analytical abilities and subjective initiative.
1. Responsible for investigating specific application scenarios of laboratory consumables and other products in bio-pharmaceuticals, biological product and other fields, and collecting the requirements of regulations and standards for applicability, biosafety and biocompatibility of products in this field;
2. Analyze the feasibility of existing consumables and new products for supervision of packing materials of drugs;
3. Guide and participate in tests of related products as packing materials of drugs and consumables of medical instruments;
4. Guide the preparation, communication and review of product market access certification data;
5. Coordinate the work of internal related departments and external application units;
6. Complete other tasks assigned by superior leaders.