生产经理、总监、或运营总

面议

常州市本科及以上

刷新时间：2020-02-25

职位描述

岗位职责：
主持生产管理工作，负责生物药GMP生产的人员、文件、物料、厂房设备设施以及实施过程的全方位管理，确保生产系统的有效运作，保质保量完成年度生产目标；
Production management, all-round management of staff, documents, materials, facility equipment and operations during biological drugs GMP production, effective manufacturing system operations assurance, and annual production target completion with quality and quantity;

建立和完善各类生产需要的政策制度，cGMP标准文档系统包括日常操作流程以及生产批记录。
Establishment and improvement of all manufacturing-related policies & regulations, and cGMP standard documentation system including daily operation flowchart and production batch record.

依据公司年度目标，组织编制生产部年度工作计划和生产目标，以及年度生产预算，并监督执行；
Preparation of annual work plan, production target and production budget of production department according to company’s annual target, and supervision over execution;

负责组建、培养和激励生产系统的技术和管理团队，做好部门绩效考核，不断提升团队效能；
Technical and management team organization, training and inspiration for production system, department performance evaluation, and team efficiency and ability upgrade;

严格按照美国、欧盟、中国GMP法规对工厂生产体系和生产活动等进行管理，组织领导生产员工严格执行相关工作标准；
Factory management of production system and production activity in strict accordance with USA, EU and China’s GMP regulations, leadership of production staff to comply with work-related standards strictly;

负责生产成本、质量、过程、产能的评估和控制；准备和控制部门预算；
Evaluation and control of production cost, quality, process and capacity; preparation and control of department budget;

定期组织召开生产例会，协调各部门之间的沟通与合作，及时解决生产出现的各种技术及工艺问题，指导处理生产偏差；
Regular production meeting organization, coordination for departments’ communication & cooperation, all technical and process problems solutions during production timely, and production deviance control and guidance;

协助生产厂房和车间的设计、建造、验证直至启动生产；
Facility and workshop design, construction and validation assistance till production started;

协助生产工艺放大和转移、验证及持续监控；
Production process amplification, transfer and validation assistance, and continuous surveillance;

负责公司生产系统的安全生产工作，配合EHS专管部门定期组织安全教育和安全检查，确保安全零事故；
Safety production assurance of production system, regular safety training and inspections organization with EHS to make sure zero accident;

完成领导交办的其它临时工作。
Completion of other temporary work assigned by supervisor.

岗位要求：
生物化学、生物技术或药学相关专业，本科及以上学历；
Major in biochemistry, biotechnology, or other related to pharmaceuticals, with bachelor’s and above degree;

10年以上大型跨国制药企业生产相关经验以及至少5年以上管理经验，熟悉生物科技行业及生物药生产；参与过生产车间设计、建设经验者优先；
Over 10 years’ production or related experience in large multinational pharmaceutical companies and at least 5 years’ management experience, familiar with biotechnology industry and biological drugs manufacturing; experience in workshop design and construction is preferred;

熟悉美国、欧盟、中国的GMP对于生物药生产的规范和质量标准要求；有国内大中型制药企业或国外生物企业任职经历，有EMA或FDA认证经验者优先；
Familiar with GMP regulations and quality requirements for biological drugs manufacturing in USA, EU, and China; experience in domestic medium and large pharmaceutical companies or foreign biological companies; experience in EMA or FDA authentication is preferred;

具有良好的语言表达能力和沟通协调能力，团队协作能力，计划与执行能力；英语文字书写能力及口语突出者优先；
Good language competence, communication & coordination skill, teamwork, and planning & execution ability; proficiency in written and oral English is preferred;

具有分析判断能力、业务管理能力和组织领导能力及持续改善意识；思路清晰，具有高度的责任心、原则性强，为人正直、自律，工作严谨。
With analysis and judgment ability, business management ability, organization leadership ability, and sense of continuous improvement; clear thinking, strong sense of responsibility, principled, honest, self-disciplined, and meticulous in work.

其他要求

招聘人数：1人
职能类别：生产经理

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。