- 公司介绍我的客户是一家由国家顶级科研机构深度孵化的“大国重器”领军企业，代表着国产高端医疗装备自主创新的最高水平。该公司依托全球领先的加速器物理技术，专注于填补国内空白的重离子癌症治疗系统及核药产业链的研发与制造。目前，公司正在苏州高新区全力打造总投资达十亿元的华东总部及现代化生产基地，标志着其从科研成果转化正式迈向大规模产业化的关键跨越。这一标志性项目涉及高度复杂的GMP洁净空间、放射性核素工作场所及精密电磁屏蔽工程，为具备专业深度的工程合规人才提供了极具挑战性的实战平台。加入该项目将深度参与国家级战略装备从建设到投产的全生命周期，是在硬核医疗科技赛道实现个人职业价值与履历升华的绝佳契机。岗位核心目标负责苏州基地从“蓝图设计”到“正式投产”全过程的GMP合规管理。确保厂房设计、设备选型、系统验证（IQ/OQ/PQ）及质量管理体系（QMS）完全符合国家药监局（NMPA）对放射性药品的监管要求，并最终通过GMP符合性检查。关键职责描述一、建设与验证期设计合规审查（DQ）： 参与工厂概念设计及详细设计评审，确保公司介绍我的客户是一家由国家顶级科研机构深度孵化的“大国重器”领军企业，代表着国产高端医疗装备自主创新的最高水平。该公司依托全球领先的加速器物理技术，专注于填补国内空白的重离子癌症治疗系统及核药产业链的研发与制造。目前，公司正在苏州高新区全力打造总投资达十亿元的华东总部及现代化生产基地，标志着其从科研成果转化正式迈向大规模产业化的关键跨越。这一标志性项目涉及高度复杂的GMP洁净空间、放射性核素工作场所及精密电磁屏蔽工程，为具备专业深度的工程合规人才提供了极具挑战性的实战平台。加入该项目将深度参与国家级战略装备从建设到投产的全生命周期，是在硬核医疗科技赛道实现个人职业价值与履历升华的绝佳契机。岗位核心目标负责苏州基地从“蓝图设计”到“正式投产”全过程的GMP合规管理。确保厂房设计、设备选型、系统验证（IQ/OQ/PQ）及质量管理体系（QMS）完全符合国家药监局（NMPA）对放射性药品的监管要求，并最终通过GMP符合性检查。关键职责描述一、建设与验证期设计合规审查（DQ）： 参与工厂概念设计及详细设计评审，确保
- about the company.A leading global oncology biotech founded in 2010, it now employs over 11,000 staff worldwide and has its products approved in more than 75 countries.about the team.Led by world-renowned scientific leaders and seasoned industry experts, the team integrates cutting-edge expertise in targeted therapies, immuno-oncology, and next-generation platforms (e.g., ADCs, CDACs).about the job.As a Principal Scientist in Physicochemical Analysis, youabout the company.A leading global oncology biotech founded in 2010, it now employs over 11,000 staff worldwide and has its products approved in more than 75 countries.about the team.Led by world-renowned scientific leaders and seasoned industry experts, the team integrates cutting-edge expertise in targeted therapies, immuno-oncology, and next-generation platforms (e.g., ADCs, CDACs).about the job.As a Principal Scientist in Physicochemical Analysis, you
- About the CompanyWe are a premier healthcare complex incubated by a leading publicly listed corporation specializing in high-end integrated medical facilities. Our mission is to establish iconic, international medical landmarks that redefine the standard of care. Currently in a phase of aggressive national expansion, we offer a sophisticated platform where technology and medical excellence converge, providing an unparalleled environment for visionary healtAbout the CompanyWe are a premier healthcare complex incubated by a leading publicly listed corporation specializing in high-end integrated medical facilities. Our mission is to establish iconic, international medical landmarks that redefine the standard of care. Currently in a phase of aggressive national expansion, we offer a sophisticated platform where technology and medical excellence converge, providing an unparalleled environment for visionary healt
- The client is a listed company. Responsibilities:1.Design and perform physicochemical analytical support to biologics development from early to late stage.2.Analytical method development, transfer and troubleshooting for product quality control and stability study.3.Draft protocol/report and execute study to support IND/NDA filings.4.Participate in projects as ARD subject matter expert (SME) and provide professional guidance whenever needed.5.ContinuouslyThe client is a listed company. Responsibilities:1.Design and perform physicochemical analytical support to biologics development from early to late stage.2.Analytical method development, transfer and troubleshooting for product quality control and stability study.3.Draft protocol/report and execute study to support IND/NDA filings.4.Participate in projects as ARD subject matter expert (SME) and provide professional guidance whenever needed.5.Continuously
- 【公司简介】我的客户是一家由海外顶尖核酸药物专家与人工智能科学家联合创立的锐意生物医学高新技术企业。公司独辟蹊径，依托自主研发的 “AI算法 + 游离RNA（microRNA）” 大数据平台，死磕阿尔兹海默病（AD）等全球重大神经退行性疾病的超早期标志物发现与核酸药物转化。目前，公司已获得国内顶级投资机构近亿元的资本加持，并在全球多地设有联合研发中心。在这里，您将作为核心骨干，深度参与从前沿新靶点筛选到创新核酸药物（ASO/siRNA）一体化验证的颠覆性研发全流程。【岗位职责】1、主导 miRNA/siRNA、ASO 或其他核酸类药物的靶点发现、验证及候选分子筛选（PCC selection）；2、负责体外高通量筛选平台（如96通量）的搭建、优化与国产化替代；3、设计并执行 free uptake 等功能性筛选实验，评估 小核酸活性与特异性；4、支持体内药效研究，包括小鼠模型构建、人源化模型调研、外包项目管理及数据解读；5、参与 IND 申报相关生物学数据整理、理论支持及专利撰写；6、协同 BD 团队提供科【公司简介】我的客户是一家由海外顶尖核酸药物专家与人工智能科学家联合创立的锐意生物医学高新技术企业。公司独辟蹊径，依托自主研发的 “AI算法 + 游离RNA（microRNA）” 大数据平台，死磕阿尔兹海默病（AD）等全球重大神经退行性疾病的超早期标志物发现与核酸药物转化。目前，公司已获得国内顶级投资机构近亿元的资本加持，并在全球多地设有联合研发中心。在这里，您将作为核心骨干，深度参与从前沿新靶点筛选到创新核酸药物（ASO/siRNA）一体化验证的颠覆性研发全流程。【岗位职责】1、主导 miRNA/siRNA、ASO 或其他核酸类药物的靶点发现、验证及候选分子筛选（PCC selection）；2、负责体外高通量筛选平台（如96通量）的搭建、优化与国产化替代；3、设计并执行 free uptake 等功能性筛选实验，评估 小核酸活性与特异性；4、支持体内药效研究，包括小鼠模型构建、人源化模型调研、外包项目管理及数据解读；5、参与 IND 申报相关生物学数据整理、理论支持及专利撰写；6、协同 BD 团队提供科
