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1年经验
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硕士
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招若干人
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11-09 发布
职位描述
职位描述: Responsibilities:?Perform protein characterization and validation using a variety of analytical and biophysical methods including but not limited to HPLC, CE, CD, DLS, DSC, UV/Vis following established SOPs;?Carry out industrial forensic analysis and identification of extraneous matters such as fibers, particles, contaminants using microscopic and spectroscopic methods including optical microscope, IR, Raman and SEM/EDS;?Acquire, review and archive data and prepare reports in a timely manner to meet project deadlines or milestones.?Develop, improve, validate and transfer analytical methods to support product release and regulatory submissions.?Communicate and interact with internal colleagues from many other functional areas to solve project related issues or challenges;?Report and update project progresses with domestic and international clients in Chinese and/or English as necessary.?Guide junior scientists and new employees to carry out sample testing, data analysis and documentation.Qualifications:?M.S or Ph.D. in analytical chemistry or relevant physical sciences with 1-2 years of industrial or research lab experiences with proven scientific achievement.?Hands on experiences in HPLC, CE, DSC, CD, UV/Vis, particle counting and sizing, vibrational spectroscopy (IR, Raman) and microscopy (Optical, SEM and EDS, XPS) are expected.?Familiar with compliance requirements in sample preparation and testing, experimental design and execution, and data analysis and documentation;?Efficient team player and be able to work in cross-functional and fast-paced work environment;?Competitive communication skills (both verbal and written) and interpersonal skills; Fluent in Chinese and English.?Work experiences in pharmaceutical or biotech industries are advantageous. 职能类别: 生物工程/生物制药 关键字: 单抗 蛋白分析
联系方式
东平街188号
公司信息
苏桥医药(苏州)有限公司是一家致力于抗体及融合蛋白类生物药物的研发、工艺开发、及中试生产的高科技企业,服务范围全面覆盖临床前研究、临床研究、及商业化生产阶段。总投资额为4,640万美元。 苏桥医药是苏州生物纳米科技园(BioBay)重点扶持的企业之一。苏桥在园区内的建造面积共占地7,000平方米,目标产能1期实现69批次,2期实现92批次。 苏桥将严格遵守国际主流药品监管机构的质量标准,包括CFDA、USA (21-CFR) 、EMA (Eurdralex)、PIC/S以及 WHO。苏桥交付的生产样品能够满足客户在全球多个国家临床试验申请的CMC要求。
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