主要职责： 方法开发与验证：基于中国药典、ICH、ISO等要求，完成专属性、准确性、精密度、线性、范围、定量/检测限、稳定性等验证；搭建核酸定量/定性、基因测序、PCR/qPCR/数字PCR、CE、HPLC等分析方法。 实验与优化：独立开展核酸提取、酶活/分子标记检测、电泳等实验；排查并优化方法，提升灵敏度、重复性与效率。 文档与合规：撰写方案、报告、SOP与技术转移文件；配合项目申报与审计资料准备。 仪器与协作：负责qPCR/数字PCR、分光光度计、CE、HPLC等设备的使用与维护；与QC/研发协作完成检测、数据复核与问题处理；遵循生物与数据安全规范；参与方法研讨与培训。 任职要求： 学历专业：分子生物学/生物化学与分子生物学/细胞生物学/生物技术/生物工程等相关专业，本科及以上；硕士优先。 技能：熟练核酸分析、PCR/qPCR、电泳等；能独立进行方法开发与验证；熟悉中国药典、ICH Q2与合规要求；能撰写验证文件与SOP；熟练使用基因分析与数据处理软件，具备图谱解读与统计分析能力；熟悉相关仪器操作与故障排查。 经验：本科2年以上相关科研/研发经验；硕士及以上可接收应届；有高校实验室、药企或生物技术公司经验者优先。 综合能力：严谨细致、责任心强；问题解决与快速响应能力佳；良好的文档与沟通协作能力，支持跨部门与技术转移；学习能力强，跟进行业技术与法规；具备良好英文读写能力。 Date Posted19-Aug-2026 Closing Date29-Nov-2026 AstraZeneca embraces diversity and equality of opportunity. We are committed to building an inclusive and diverse team representing all backgrounds, with
Purpose & Overall Relevance for the Organization: Manage a team of product developers in the creation and commercialization of assigned products. Actively monitors development calendars to ensure deadlines, costing KPIs and quality standards are met. Acts as
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Your mission Lead and coordinate licensing activities directed to China, with the goal to enhance Midas Group’s track record of licensing deals in the territory, i.e. Identify and search for niche and complex products needed in
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