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职能类别:医药技术研发人员
Job responsibilities:
(1) Develop and optimize analytical methods for characterization of biotherapeutics in pre-clinical and
clinical stages.
(2) Write Standard Operation Procedure (SOP)
(3) Develop analytical methods for intermediates as part of PAT (Process Analytical Technology)
(4) Involved in analytical method transfer from other companies.
(5) Perform all experiments under applicable safety and regulatory compliances.
(6) Generate high quality results in support of analytical testing of growing drug pipeline.
(7) Document data/results according to applicable compliances, such as GMP.
(8) Effective communication of data/results through written documentation and oral presentations.
(9) Accountable for completing the assigned tasks and communicate results in a timely manner.
Basic requirements:
(1) A master degree with 5+ years or a Ph.D.
(2) Strong hands-on experience in HPLC (SEC, IEX, RP), LC-MS (peptide mapping and N-linked glycan) and CE (cIEF and CE-SDS).
(3) Ability to work independently and to manage multiple projects at one time.
(4) Good written and oral communication skills in English.
(5) Eager and quick to learn, self-driven and motivated.
公司简要介绍:
公司名称:杰科(天津)生物医药有限公司
公司类型:合资
公司规模:50-150人
公司介绍:杰科(天津)生物医药有限公司是一家中美合资的生物制药公司,坐落于天津中新生态城。公司正在筹建包括研发、中试、质控及GMP生产等功能的大型生产基地,并陆续从国内外招聘优秀人才,组建一流的研发及生产团队。公司正在筹建的是中国规模最大之一的生物药物生产设施,其研发、生产及质量控制等设施均达到欧美设计建造标准。第一期工程将在三年内投产运行。杰科生物预计未来一期、二期共建设十条生产线,满足十多个生物药物的大规模GMP生产,达到1000-1500人的规模,产品包括单克隆抗体、抗体融合蛋白、细胞因子、重组蛋白或DNA疫苗等。