1、 Perform all operations in cGMP production facilities to produce active pharmaceutical ingredients.

2、 Preparation of intermediates/solvents/buffer, cell culture (cell thawing, cell passage, cell delivery, cell expansion and cell isolation).

3、 Participation in equipment selection, further communication with raw material and equipment providers and business partners.

4、Participate in the development of cGMP documents such as SOPs, MBRs, validation/qualification protocols type and FAT/SAT documents.

5、Participate in cGMP training and follow cGMP rules.

1、College degree or above, majoring in biology and pharmacy.

2、Ability to review English literature.

3、Intention to work in Lingang for a long time.