实验室仪器管理工程师

性别要求：不限性别 Job responsibilities including but not limited to:1.负责QC实验室的验证和再验证工作。Be responsible for QC laboratory computerized system validation and revalidation.2.负责QC实验室验证计划制定及修订。Be responsible for establishing and revising of VP for QC laboratory computerized system.3.主导计算机验证前的风险评估。Lead risk assessment before computerized system validation.4.负责计算机验证方案和报告等验证文件的审核。Responsible for review of the validation documents, such as validation protocols and validation summary reports.5.参与验证过程中偏差的调查分析及变更的评估。Participate in deviation investigation, analysis and change assessment.任职要求：1.本科或以上学历，计算机，自动化，软件工程，制药工程等相关学科。Bachelor Degree or abovemajor in computer, automation, software engineering ,pharmaceutical engineering and related subjects.2.3年以上工作经验，制药企业QC实验室经验尤佳。At least three years’ working experience，preferred in pharmaceutical industry QC labs.3.分析化学/生物化学方面的基础知识。Basic knowledge of Analytical chemistry/Biochemistry .4.IT网络、域控、数据库方面的基础知识。Basic knowledge of IT network, domain control and database.5.有较强的分析问题能力及良好的沟通技巧、工作认真、细致，具有良好的团队合作精神。Excellent communication, problem-solving, and organization skills, attentive, careful and meticulous, with strong team-work ability.6.学习能力强，喜欢钻研，对于新的系统能够快速入手。Quick learner, be familiar with new systems with ease.