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职能类别:医药技术研发人员
(1) Responsible for purification process development of antibody drugs, recombinant protein drugs and other biopharmaceuticals.
(2) Assist department manager to resolve the technical problems about technology transfer, scale-up and production, improve and optimize the production process.
(3) Write and revise SOP, batch record and other technical documentation as necessary.
(4) Effective communication of data/results through written documentation and oral presentations.
(5) Accountable for completing the assigned tasks and communicate results in a timely manner.
(4) Perform other duties as assigned by department manager. .
Basic requirements:
(1) Master degree inFermentation Engineering or Bio-engineering or Bio-chemistry.
(2) Knowledge and experience in downstream purification process development and/or manufacturing for protein therapeutics products
(3) Familiar with downstream purification unit operations, such as chromatography, ultrafiltration, depth filtration, etc.
(4) Experience with scale-up, process improvement and optimization.
(5) Must have a ability to read, write and speak English.
(6) Must be able to write effectively as demonstrated through authorship of batch records, SOPs and technical reports.
(7) Strong team work and communication skill.
(8) Ability to work independently, with minimal supervision, and to manage multiple projects at one time.
(9) 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。