崗位職責(zé):
1.負(fù)責(zé)相關(guān)樣品的純化工藝開發(fā)和優(yōu)化工作,完成實(shí)驗(yàn)記錄的規(guī)范書寫(純化工藝包括但不限于融合蛋白、單抗、多抗)。
Responsible for the development and optimization of purification process of relevant samples, and complete the standard writing of experimental records (purification process includes but is not limited to fusion protein, monoclonal antibody and polyclonal antibody).
2.負(fù)責(zé)起草相關(guān)文件,包括工藝規(guī)程、儀器操作等。
Responsible for drafting relevant documents, including process regulations, instrument operation, etc.
3.負(fù)責(zé)純化方案的調(diào)研,設(shè)計,撰寫及優(yōu)化。
Responsible for the investigation, design, writing and optimization of purification scheme.
4.參與純化成本的核算。
Participate in the accounting of purification cost.
5.負(fù)責(zé)管理、維護(hù)保養(yǎng)檢驗(yàn)設(shè)備,確保檢驗(yàn)設(shè)備可正常運(yùn)行且在有效期內(nèi)。協(xié)助主管完成對新設(shè)備的安裝、調(diào)試、校準(zhǔn)、確認(rèn)以及設(shè)備檔案的建立工作。
Responsible for the management and maintenance of the inspection equipment to ensure that the inspection equipment can operate normally and within the validity period. Assist supervisor to complete the installation, debugging, calibration, confirmation of new equipment and the establishment of equipment files.
6.完成純化主管分配的其他工作和職責(zé)。
Complete other duties and responsibilities assigned by purification supervisor.
任職要求:
1. 至少三年以上從事純化相關(guān)工作(至少包括親和層析、陰陽離子層析、超濾、納濾等)的實(shí)踐經(jīng)驗(yàn)。
At least three years of practical experience in purification related work (including at least affinity chromatography, anion and cation chromatography, ultrafiltration, nanofiltration, etc.).
2. 能夠閱讀相關(guān)的英文資料。
Be able to read related English materials.