如约见 · 医疗健康 · 药学/药物研发

DP 8-制剂生产助理工程师

药明生物 · 杭州市 · 薪资面议 · 更新于 2026/10/20

任职要求

经验:2年以上学历:大专

岗位描述

岗位职责 Responsibilities无菌生产操作负责无菌制剂生产相关工作,包括配液、灌装、灯检、贴签等生产操作。Aseptic Manufacturing OperationsPerform aseptic drug product manufacturing activities, including solution preparation, filling, visual inspection, and labeling operations.设备操作与维护负责生产设备的操作、日常维护,并配合设备维修、校验及验证工作,确保设备处于良好运行状态。Equipment Operation & MaintenanceOperate manufacturing equipment, perform routine maintenance, and support equipment repair, calibration, and qualification activities to ensure reliable equipment performance.生产文件管理负责批生产记录、设备使用台账及相关生产文件的填写、审核与管理,确保生产记录真实、完整、可追溯。Production Documentation ManagementComplete, review, and maintain batch production records, equipment logbooks, and related manufacturing documents, ensuring accuracy, completeness, and traceability.洁净区与物料管理负责洁净区的清洁、消毒及生产物料管理,确保生产环境和物料状态符合GMP要求。Cleanroom & Material ManagementPerform cleanroom cleaning and disinfection activities and manage production materials to ensure compliance with GMP requirements.EHS与合规执行严格遵守GMP、EHS、数据完整性及公司相关管理要求,确保生产活动符合质量、安全及合规标准。EHS & Regulatory ComplianceAdhere to GMP, EHS, data integrity, and company compliance requirements to ensure safe, compliant, and high-quality manufacturing operations.任职要求 Qualifications教育背景制药、生物工程、药学等相关专业专科或本科毕业;应届毕业生或具有2年以上制药行业相关工作经验。EducationAssociate or Bachelor's degree in Pharmaceutical Sciences, Biological Engineering, Pharmacy, or other related disciplines. Fresh graduates are welcome to apply; candidates with more than 2 years of relevant experience in the pharmaceutical industry are preferred.专业经验了解无菌制剂生产工艺,有无菌药品生产经验者优先。Professional ExperienceBasic knowledge of aseptic drug product manufacturing processes; experience in sterile pharmaceutical manufacturing is preferred.设备知识了解无菌制剂生产设备。Equipment KnowledgeKnowledge of aseptic manufacturing equipment.团队协作能力具备较强的责任心、执行力和团队协作能力,能够适应生产现场工作节奏。Teamwork & ExecutionDemonstrate a strong sense of responsibility, effective execution capability, and excellent teamwork skills in a manufacturing environment.办公软件技能熟练使用Office等常用办公软件,能够完成生产记录、数据整理及相关文件编制工作。Computer SkillsProficient in Microsoft Office and other standard business applications, with the ability to complete production documentation, data management, and related record preparation.综合能力工作认真细致,具备良好的沟通能力、学习能力和问题解决能力,能够在GMP环境下高效开展工作。Core CompetenciesDetail-oriented with strong communication, learning, and problem-solving skills, and capable of working effectively in a GMP-regulated environment.

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