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Responsibility主要职责
· Work to support the creation and
revision of procedures in support of process improvements to Dizal’s Quality
System.
· Responsible for document management
activities, including but not limited to document lifecycle management and
archives management.
· Responsible for training activities,
including but not limited to maintain training matrix, coordinate to complete
training task, maintain training material and training record, track and
analyze training implementation
· Support change control and supplier
quality management work.
· Coordination with all functions
regarding compliance and quality issues
· Participate in the establishing and
maintaining of the quality system & compliance program to ensure
regulatory compliance.
Requirement任职要求
迪哲医药(股票代码:688192)是一家创新型生物医药企业,专注于恶性肿瘤、免疫性疾病领域创新疗法的研究、开发和商业化。公司坚持源头创新的研发理念,以推出全球首创药物(First-in-class)和具有突破性潜力的治疗方法为目标,旨在填补全球未被满足的临床需求。基于行业领先的转化科学和新药分子设计与筛选技术平台,公司已建立了五款具备全球竞争力的产品管线,两大领先产品处于全球关键性临床试验阶段,其中一款已获批上市。
Dizal Pharmaceutical Co., Ltd (Ticker: 688192 ) is a commercial stage biopharmaceutical company. At Dizal we aspire to discover and develop differentiated therapeutics for the treatment of cancer and immunological diseases. Building on our extensive expertise in translational science and molecular design, we have established an internationally competitive portfolio of five clinical-stage assets with two leading assets in global pivotal studies and one already approved.