崗位職責(zé):
1.落實(shí)上游工藝開發(fā)、技術(shù)轉(zhuǎn)移,開展上游工藝表征、工藝驗(yàn)證,進(jìn)行生產(chǎn)指導(dǎo)。
Implement cell line development, upstream process development, and technology transfer. Conduct upstream process characterization and process validation, and provide production guidance.
2.撰寫、審核項(xiàng)目研發(fā)、生產(chǎn)等申報相關(guān)工作。
Compose and review the declaration - related work for project R & D, production, etc.
3.負(fù)責(zé)上游工藝開發(fā)團(tuán)隊(duì)管理、人員招聘、人員培訓(xùn)等。
Be responsible for the management of the upstream process development team, staff recruitment, personnel training, etc.
4.細(xì)胞庫、上游工藝實(shí)驗(yàn)室統(tǒng)籌管理;
Overall management of the cell bank and the upstream process laboratory.
5.負(fù)責(zé)上游工藝開發(fā)年度預(yù)算申報、成本核算、儀器設(shè)備采購申請等事宜,確保上游工藝開發(fā)項(xiàng)目隨時運(yùn)行。
Be responsible for matters such as the annual budget declaration for upstream process development, cost accounting, and application for the procurement of instruments and equipment, to ensure the smooth operation of upstream process development projects at all times.
6.完成公司和上級領(lǐng)導(dǎo)下達(dá)的其它日常性和臨時性工作。
Completion of other daily and temporary work assigned by the company and higher management.
7.認(rèn)真貫徹執(zhí)行國家和公司制定的方針政策以及各項(xiàng)規(guī)章制度。
Conscientiously implement the guidelines and policies formulated by the state and the company, as well as various rules and regulations.
8.負(fù)責(zé)貫徹執(zhí)行國家藥品生產(chǎn)管理相關(guān)的法律、法規(guī)。
Responsible for the implementation of national laws and regulations related to drug production management.
任職要求:
1.5年以上抗體類藥物上游細(xì)胞培養(yǎng)工藝開發(fā)經(jīng)驗(yàn);有CDMO細(xì)胞培養(yǎng)工藝開發(fā)經(jīng)驗(yàn)優(yōu)先。生物制藥、生物技術(shù)、生物工程及相關(guān)專業(yè),本科以上學(xué)歷
More than 5 years of experience in upstream cell culture process development for antibody drugs; experience in CDMO cell culture process development is preferred.Bachelor
s degree or above in Biopharmaceuticals, Biotechnology, Bioengineering and related fields.
2.具有文獻(xiàn)檢索能力,熟悉抗體藥上游工藝開發(fā)流程,熟悉法規(guī)指導(dǎo)原則及操作規(guī)范。
Capable of literature search, familiar with the upstream process development of antibody drugs, familiar with regulatory guidance principles and operational norms.
3.具有一定的DoE實(shí)驗(yàn)設(shè)計(jì)與分析能力,熟悉JMP/Minitab等分析軟件。
Have certain ability in DoE experimental design and analysis, familiar with analysis software such as JMP/Minitab.
4.熟悉生物制藥工藝流程和相關(guān)技術(shù)。
Familiar with biopharmaceutical process and related technology.
5.做事細(xì)心,為人踏實(shí),責(zé)任心強(qiáng),有強(qiáng)烈的學(xué)習(xí)意愿。
Attentive in work, down-to-earth in personality, strong sense of responsibility, and a strong willingness to learn.