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人才招募

和黃醫藥的目標是成為一家為中國和全球市場開發創新藥物的領先的醫藥公司。我們誠邀有志人士加入我們的團隊。我們致力於讓每一名員工能夠發揮才幹,並提供互相協作的工作環境以回報您的才能和熱情。如果您希望成為我們團隊的一員,請將您的簡歷發送給我們

職能團隊
临床开发
信息技术部
商務開發
商業化
生產
臨床及註冊
藥學
藥物研究與發展
行政支持
工作地點
上海
中國其他地區
亞洲(中國外)
北京
歐洲
美國
蘇州
香港
找到相關結果: 31
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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職位: Medical Advisor/Senior Medical Science Liaison, Oncology 工作地點: Chengdu/Jinan/Guangzhou/Changsha   Position Overview Medical Advisor (MA) or Senior Medical Science Liaison (Sr MSL) serves as
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職位: (高級)抗體偶聯藥物(ADC)研發研究員 工作地點: 上海   職責:  負責創新抗體偶聯藥物(Antibody-Drug Conjugate, ADC)的藥物發現,以及
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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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職位 抗體工程研究員 工作地點 上海   崗位職責: 從事抗體藥研發工作,負責推進項目運行,及時、高效、完成創新研發目標。 負責抗體工程、單克隆抗體改造、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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職位 (Sr.) CTA / 臨床試驗助理 工作地點 上海   職責 臨床試驗的合同及付款 臨床試驗的文件維護 臨床試驗的物品資料供應 臨床試驗的內部溝通協調
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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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職位名稱 QC 分析員 部門 QC 工作地黠 蘇州   崗位描述 負責QC實驗室理化檢測 主要職責/責任 嚴格遵守實驗室相關的各項標準操作規程及檢測操作規程; 執行原輔料、包裝材料、
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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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Primary Functions The mission of Hutchison MediPharma (US) Inc. Regulatory Affairs is to develop innovative global registration strategies that advance our pipeline products through approval in US and EU In this position, the Regulatory Affairs S
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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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