武汉招聘

岗位描述：
? Participate in the daily activities of the purification Manufacturing Group. Apply proper PPE (Personal Protective Equipment) to all work in the facility;
参与纯化组的日常生产活动，应用适当的个人防护用品去完成在厂房内的所有工作；
? Participate in the evaluation of new technology, new production process and new production technology;
参与评估新工艺、新生产流程和新生产技术；
? Escalate process issues as necessary to ensure resolution;
根据需要上报工艺中的问题并保证解决问题；
? Author MGF-DSP GMP documents, ensure GMP training requirements are complete and current;
起草生产部纯化组的GMP文件，确保完成和更新GMP培训要求；
? Familiar with the handle process of quality events such as deviation, CAPA and change control;
熟悉偏差，CAPA和变更等质量事件的处理流程；
? Ensure operations strictly adhere to all SOPs and cGMP/Quality requirements;
保证严格根据所有的SOPs和cGMP/质量要求来操作；
? Ensure all work is performed in safe manner, the operation complies with EHS requirements and meets the specifications for each service request;
确保安全的方式去执行所有的工作，操作符合EHS要求，并符合各个服务请求的标准；
? Clean and maintain the GMP facility and production equipment, maintenance of environmental and personal hygiene;
清洁和维护GMP厂房和生产设备,保持环境和个人卫生；
? Participate in the internal auditing program for company as required; Serve as department representative on cross-functional teams;
根据需要参与公司的内部审计计划；能够担任跨职能团队的部门代表；
? Other work arranged by superior leaders.
上级领导安排的其他工作。

鼎康生物是一家领先的CDMO公司，可提供一站式的CMC解决方案，支持从早期药物开发到后期临床研究和商业化cGMP生产。鼎康引进了全球***模块化生物制药工厂Kubio；为客户开发的多个产品已经在全球20多个国家进行临床试验。在不久的将来，鼎康生物总产能将超过140,000L。我们承诺通过技术和生产创新，使全球患者都能负担得起具有国际标准的生物药物，提高治疗水平以改善人类健康。