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上海罗氏制药招制程控制（现场QA）
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Responsibilities: Responsible for in-process control of repacking product (Cold chain products) in warehouse. 负责在仓库中进行的冷链产品的重包装过程中的制程控制。 By taking the ID sample for all the material added according to ID sampling role, ensuring each pack of raw material are used in correct. 按照ID取样计划，对所有的物料进行ID采样，确保每包原料的正确使用。 By taking the test sample of bulk and finished products according to the sampling role, to ensure the sample can delegate the whole batch. 按照采样任务，采集需要进行测试的半成品和成品的样品，确保所采集的样品可以代表整批产品。 By checking and sampling retention sample for each finished batch. 对每个完成的批次进行留样取样及检查。 Qualification: 1 Years work experience in quality control, assurance, analysis or equivalent 一年质量控制，质量保证，分析及相关工作经验 At least 1 year experience of technical position in pharmaceutical company 至少一年药厂技术岗位工作经验 Knowledge of GMP GMP知识 Skills and experience of pharmaceutical production process and in-process control 药品生产与制程控制的技能与经验 Knowledge of Quality management 质量管理的知识 PC skill: word, excel, Lims 电脑技能: word, excel, Lims Pharmacy, Chemistry, Biochemistry and equivalent 药学、化学、生物化学及相关学科优先 |
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