AR-CMMD高级主管/AR-CMMDSD

面议

天津市

刷新时间：2023-03-03

职位描述

领导AR-CMMD团队承接处于不同治疗领域各个阶段的ADC，多肽，核苷酸，多糖和聚合物辅料等生物药项目分析技术和项目分析管理工作，保证项目分析进度与质量，参与分析项目报价。
Lead AR-CMMD organization in handling analytical techniques and project management of ADC, Peptide, oligonucleotide, polysaccharides and polymer ingredients at various stages from different therapeutic areas, ensured project schedule and quality, and participated in project quotation.
作为团队负责人，负责ADC，多肽，核苷酸生物药项目分析平台能力建设，包括强大的分析团队建设和项目承接能力建设。
Act as the organizational leader with responsibility to build a strong ADC, Peptide, oligonucleotide, polysaccharides and polymer ingredients analytical team and platform to deliver various ADC, Peptide, oligonucleotide, polysaccharides and polymer ingredients projects.
ADC，多肽，核苷酸生物药项目分析方法开发/确认/验证/转移方案和计划的制定和组织执行，相关的技术指导和复核，保证项目顺利开展。
Be responsible for formulating and implementing analytical method development/confirmation/validation/ transfer plan for ADC, peptide, nucleotide biological drug project, providing relevant technical guidance and review to ensure the smooth implementation of the project.
快速响应实验室调查，推动调查进展，协助制定调查方案和调查文件的技术性复核，与客户沟通实验室调查内容。
Quick response to laboratory investigation, promote the progress of survey, assist in the formulation of investigation plan and technical review of investigation documents, and communicate with customers about laboratory investigation document.
对接客户技术参观/访问以及客户/法规机构的实验室参观和审计工作。
Responsible for customer technical visits/visits and laboratory visits and audits to customer/regulatory agencies
部门内工作沟通管理，梯队人员培养，团队建设工作，重点进行实验室人员分析技能培训与提升。
Responsible for communication and management within the department, echelon personnel training, team building, focusing on the training and improvement of analytical skills of laboratory staff.
负责资源协调和预算管理。
Responsible for management of resourcing and budget planning.

任职资质/ Qualification：

硕士/博士学历，至少5-8年寡核苷酸/多肽/或蛋白分析相关工业界经验，有团队管理经验者优先。
Master degree above, PhD preferred, at least 5-8yrs of industry experience in oligonucleotide/peptide/ protein analysis; Team leader's experience preferred.
有扎实的分析专业知识，具有较强的cGMP法规和数据完整性意识并且对法规更新有敏捷的感知识别能力。
Strong analytical expertise, strong awareness of cGMP regulations and data integrity and quick awareness of regulatory updates.
有良好的组织沟通和协调管理能力，以及团队合作意识和大局观念，思路清晰。
Good organization, communication, coordination and management skills, team spirit and overall picture concept, strong logical thinking.
英语流利，可以胜任客户沟通工作；有海外工作或留学经验优先。
Fluent in English, able to communicate with customers; Overseas working or studying experience is preferred.

其他要求

招聘人数：1人
职能类别：药物分析/药品检验

公司介绍

诗迈医药猎头是一家专业从事医药行业猎头服务的科技型企业，总部位于杭州，下属有上海、南京、广州、武汉等多家分公司，同时自主开发国内领先的猎头办公系统及医药人才网站，全面致力于海内外制药、生物、医疗、器械等行业线上线下人力资源整合。
公司与全国各地研发企业、生产企业及销售经营等企业及业内同行建立了良好互动平台，在欧、美、日等国家建立了海归引进平台，同时积极开展医药高等院校公益系列讲座，搭建了以人力、企业为主体的立体化咨询服务网，为医药企业人才队伍建设发挥了积极重要作用，为很多医药企业解决了高端人力之困。