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人才招募

和黄医药的目标是成为一家为中国和全球市场开发创新药物的领先的医药公司。我们诚邀有志人士加入我们的团队。我们致力于让每一名员工能够发挥才干,并提供互相协作的工作环境以回报您的才能和热情。如果您希望成为我们团队的一员,请将您的简历发送给我们

职能团队
临床及注册
商业化
商务开发
生产
药学
药物研究与发展
行政支持
工作地点
上海
中国其他地区
亚洲(中国外)
北京
欧洲
美国
苏州
香港
找到相关结果: 30
Job Title: Associate Director of Statistician Location: Shanghai   Position Overview HUTCHMED Clinical & Regulatory Stats team is responsible for the development and implementation of trial designs, data a
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职位: Medical Advisor/Senior Medical Science Liaison, Oncology 工作地点: Chengdu/Jinan/Guangzhou/Changsha   Position Overview Medical Advisor (MA) or Senior Medical Science Liaison (Sr MSL) serves as
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职位: (高级)抗体偶联药物(ADC)研发研究员 工作地点: 上海   岗位职责:  负责创新抗体偶联药物(Antibody-Drug Conjugate, ADC)的药物发现,以及创新
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Job Title: Senior Director of Novel Antibody Group Location: Shanghai   Major Responsibilities and Duties Develop internal novel antibody technology platform, including but not limited to bispecific, multi
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Job Title: Clinical Project Manager Location: Shanghai/Guangzhou   Primary Function Quality and Compliance Management in clinical product development. Major Responsibilities and Duties Implement an
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Job Title: Senior Product Manager Location: Hong Kong   Tasks and Responsibilities Responsible for analyzing the market of HUTCHMED products and therapeutic areas. Analyze, coordinate and support the i
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职位 抗体工程研究员 工作地点 上海   岗位职责: 从事抗体药研发工作,负责推进项目运行,及时、高效、完成创新研发目标。 负责抗体工程、单克隆抗体改造、人源化、
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Job Title: Sr. Manager / Manager, GCP auditor Location: Beijing/Guangzhou Summary of Relevant Job Responsibilities Contribute to Quality and Risk Management Framework / Program across C&R. Drive continu
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职位 (Sr.) CTA / 临床试验助理 工作地点 上海   职责 临床试验的合同及付款 临床试验的文件维护 临床试验的物品资料供应 临床试验的内部沟通协调 临床试验的会
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Job Title: Clinical Research Associate (CRA) Location: Shanghai / Beijing / Guangzhou / Hangzhou / Nanjing / Suzhou / Chengdu / Jinan / Changsha / Haerbin / Changchun / Shenyang / Zhengzhou / Xi’an   Primary Act as principal link be
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Job Title: CRA Line Manager Location: Shanghai   Responsibilities Be responsible for CRA team management and operational management system. Oversees the performance of the CRAs within their specified team. Implements professional develop
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Job Title: Senior Director / Executive Director, Formulation Development Location: Shanghai   Responsibilities Supervise and support formulation development team to develop, optimize, scale-up, and manufacture CTM in support of IND
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Job Title: Senior Manager / Manager, Analytical Location: Shanghai   COMPETENCIES; Knowledge, Skills and Abilities Must have a strong Quality Control mind-set with extensive knowledge and experience of c
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Job Title: Manager, Analytical R&D Location: Shanghai   Primary The primary function for this position is to oversee analytical development’s daily activities, such as method development and validation, analytical testing and stabil
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Job Title: Clinical Research Physician Location: Shanghai   Responsibilities Support medical director in drafting clinical trial protocol and study report. Contribute to  the  medical/scientific  input  given  for  the  de
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Job Title: Senior Statistician Location: Shanghai   Primary Function The Senior statistician is responsible for all statistical aspects of a clinical development project of one compound, from early clinical
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Job Title: Clinical Project Manager Location: Shanghai / Beijing / Guangzhou / Nanjing / Hangzhou / Suzhou / Tianjin   Primary Function Management of clinical research project. Vendor (CRO, Lab, drug storage, etc.) supervision and manage
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Job Title: Drug Safety Specialist/Senior Drug Safety Specialist Location: Shanghai   Primary The Drug Safety Specialist/Senior Drug Safety Specialist is responsible for the collection, processing, follow-up, and regulatory reporting o
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Job Title: Director of Novel Antibody Group Location: Shanghai   Major Responsibilities and Duties Develop internal novel antibody technology platform, including but not limited to bispecific, multi-spec
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Job Title: Medical Science Liaison Location: Beijing / Nanjing   Position Overview & Key Results Areas The Medical Science Liaison serves as an advocate for company science within the healthcare community.  By virtue of his/her train
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Job Title: Senior Database Developer Department/Group: Clinical & Regulatory Department Location: Shanghai   Primary Functions Responsible for executing end to end clinical database setup and management activities pertaining to
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Job Title: Production Engineer Location: Suzhou   Responsibilities Participate in or responsible for qualification of process equipment. Participate in or responsible for production related process validation, cleaning validation
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Job Title: Formulation Engineer Location: Suzhou   Principle Roles & Responsibility Participate in the work related to new product introduction and organize the drafting of R&D related contracts. Perform process transfer, process
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职位名称 QC 分析员 部门 QC 工作地点 苏州   岗位描述 负责QC实验室理化检测 主要职责/责任 严格遵守实验室相关的各项标准操作规程及检测操作规程; 执行原辅料、包装材料、
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Job Title: Associate Director (AD), Regulatory Affairs Location: Beijing Major Responsibilities and Duties Review product registration dossier and relevant documents Obtain IND & NDA approval as well
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Key Responsibilities: Responsible for analyzing the market of HUTCHMED products and therapeutic areas. Analyze, coordinate and support the information needs of preparing new product launch; Formulate the of marketing strategy and roadmap from pr
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Key Responsibilities: Develop and execute market access strategies and commercialization plan aligned with country objectives; Work across functionally with global and local medical and commercial functions to develop value propositions and mess
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Responsibilities Prepare process R&D related documents and reports to support IND and NDA. Update technical documents and effectively communicate with process R&D team. Support process R&D team to provide documentation for IND, NDA, I
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Primary Function The Statistical programmer/Senior Statistical Programmer is responsible for all statistical programming aspects at project level. The position is a key contributor with biostatistics in ensuring that pharmaceutical drug-developmen
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Responsibilities Review product registration dossier and relevant documents Obtain IND & NDA approval as well as product registration license renewal as planed Coordinate with each function within HMPL from registration pathway Establish and
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