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1、2023年制药行业岗位职责3篇 书目 第1篇制药行业岗位职责 第2篇生物制药行业岗位职责 第3篇制药行业销售岗位职责 制药行业销售岗位职责 制药行业销售工程师 宝帝流体限制系统 宝帝流体限制系统(上海)有限公司,宝帝,宝帝流体限制系统,流体限制系统,宝帝 职责描述: 1、负责气动过程阀门,工业用传感器类的产品推广 2、负责销售工作整体运作的有效执行,完成公司业绩和达成预期市场占有率目标 3、开发区域内及制药行业内新客户 4、维护,巩固,提升与老客户的关系 5、熟识行业动态,供应行业趋势分析,为客户供应技术支持,并擅长发觉新商机 任职要求: 1、本科(全日制)及以上; 2、机械、机电、机械自动化
2、、电气自动化、仪表自动化、化工工程工艺、制药工程工艺、发酵等相关专业优先; 3、3年以上阀门、仪表等相关产品的销售阅历,制药行业的工程公司、设备成套商、卫生管道相关工作阅历; 4、制药行业,尤其是生物制药、疫苗、血液制品德业销售阅历优先。 生物制药行业岗位职责 技术支持工程师(生物制药行业) 安诺 杭州安诺过滤器材有限公司,安诺,安诺 岗位职责: 1、负责与客户的技术沟通工作,收集客户的技术要求,并进行初步分析和分解; 2、负责产品应用背景评估和技术分析,依据客户需求和产品性能供应合适的解决方案; 3、负责本行业过滤技术应用前景及市场分析,使产品开发落地; 4、负责解答客户对产品运用、投诉等相
3、关问题; 5、负责本行业的内、外技术沟通和培训。 任职要求: 1、生物化工、生物制药相关专业硕士及以上学历。 2、具有优秀的沟通表达实力及组织协调实力。 3、熟识原料药、无菌制剂等产品制造工艺。 4、能协作公司适应短期出差。 制药行业岗位职责 qa manager-制药行业 responsibilities: in charge site quality control, quality system management. set up the company quality goal and regularly review the status of quality target. tr
4、ain and guide the team to reach functional quality goal. manage engineers and inspectors team of qa section, coordinate with other dept./team. define the quality assurance policy and process, lead the implementation of quality assurance models and system that can guarantee to the organization custom
5、er satisfaction, continuous improvement and organizational effectiveness in order to achieve maximum competitiveness. prepare weekly and monthly quality reports, make continuous quality improvement through good team work connect customer needs with the conditions of the production process and define
6、 product guidelines and criteria and the conditions of the manufacturing process. quality management system implement, monitor and maintain. conduct regular internal quality audits to ensure its effectiveness and suitability. ensure that the quality management system (qms) is effectively established
7、, implemented and maintained to be in compliance with iso9001, iso13485, 21 cfr 820, ce standards and chinese gmp. manage all inspection instrument, inspection gages, and test fixtures/tooling/equipment. requirement: 10+ quality management experience,5+ site quality control experience in pharmaceuti
8、cal, ivd or medical device industry people management experience experienced in iso 13485, 21 cfr 820,gmp,qsr fda inspection experience sound knowledge in process quality control and risk management strong in leadership good at communication, coordination fluent in english responsibilities: in charg
9、e site quality control, quality system management. set up the company quality goal and regularly review the status of quality target. train and guide the team to reach functional quality goal. manage engineers and inspectors team of qa section, coordinate with other dept./team. define the quality as
10、surance policy and process, lead the implementation of quality assurance models and system that can guarantee to the organization customer satisfaction, continuous improvement and organizational effectiveness in order to achieve maximum competitiveness. prepare weekly and monthly quality reports, ma
11、ke continuous quality improvement through good team work connect customer needs with the conditions of the production process and define product guidelines and criteria and the conditions of the manufacturing process. quality management system implement, monitor and maintain. conduct regular interna
12、l quality audits to ensure its effectiveness and suitability. ensure that the quality management system (qms) is effectively established, implemented and maintained to be in compliance with iso9001, iso13485, 21 cfr 820, ce standards and chinese gmp. manage all inspection instrument, inspection gage
13、s, and test fixtures/tooling/equipment. requirement: 10+ quality management experience,5+ site quality control experience in pharmaceutical, ivd or medical device industry people management experience experienced in iso 13485, 21 cfr 820,gmp,qsr fda inspection experience sound knowledge in process quality control and risk management strong in leadership good at communication, coordination fluent in english
