IA-Production Associate Manager-Beijing
赛诺菲(北京)制药有限公司
- 公司规模:150-500人
- 公司性质:外资(欧美)
- 公司行业:制药/生物工程
职位信息
- 发布日期:2021-01-12
- 工作地点:北京-大兴区
- 招聘人数:1人
- 工作经验:5-7年经验
- 学历要求:本科
- 职位月薪:20-30万/年
- 职位类别:生产主管
职位描述
Key Accountabilities:
Responsible for the activities of new products launch project in production, including training, technical confirmation and related validation execution etc.
负责新产品上市项目中生产相关的工作,包括培训、技术确认和相关验证工作执行。
Optimize the production process, improve the equipment and system, consistantly supply high quality production.
优化生产工艺,改进设备和系统,保证始终如一地生产出合格产品。
Coordinate with SMS to improve OEE, yield and productivity with SMS tools and methodologies.
协调SMS部门,利用SMS相关工具和方法论提高OEE、收率和生产率。
Management of the production environment, process, hygiene, facilities to make sure all production activities comply with SOPs and GMP requirements.
生产环境、工艺、卫生、设施等的管理,确保生产活动符合SOP和GMP要求。
To review the batch production records and batch packaging records and improve the right first time.
审核批生产记录和批包装记录并提高一次通过率。
To implement the equipment qualification, process validation according to the master plan.
按照计划完成区域内的设备的确认和工艺验证。
To execute and follow the required initial and continous trainings of production operators.
对生产相关人员进行必要的上岗前培训和继续培训,并根据实际需要调整培训内容。
Organize daily production meeting, coordinate all shifts and keep closely communication with planning, QA, maintenance and warehouse ect, to optimize production plan, ensure right Plant Service Level and reduce production cycle time.
组织日常生产协调会,协调各生产班组的活动及与质量、计划、维修、仓库间的沟通,优化生产计划,确保生产计划完成率及缩短生产周期。
Follow up the actions of Change Control, CAPA for deviations or complaints related to production.
确保生产中所有变更、偏差及生产相关的投诉问题纠正措施和预防措施的及时落实及有效性。 Develop necessary SOPs and ensure the implementation and improvement.
组织制定相关的岗位操作规程并确保执行及持继改进 Implement SMS standards and continuously improve in 5S/HSE aspects and waste minimization.
贯彻落实赛诺菲制造系统标准,在HSE、精益生产等方面持续改进。
Other tasks temporarily assigned by department manager.
按时完成上级临时交办的或部门间合作的其他工作任务。
HSE ACCOUNTABILITIES / HSE职责
Participate dept. HSE targets establishment and implement.
参与制定本部门HSE管理目标并实施。
To ensure HSE requirements and procedures implementation, operation as per SOPs with properly PPE .
落实HSE规章制度,确保部门员工按照操作规程生产,确保个人防护用品的正确使用。
To ensure dept. personnel to complete HSE before and during operation.
确保部门员工完成岗前HSE教育和持续培训。
Attend to dept. onsite inspection monthly, HSE monthly meeting. implement dept. HSE defects inspection, report HSE issue, assist to investigate and implement correction actions.
参加部门月度现场检查,HSE月度会议,落实部门HSE隐患排查治理工作,及时报告安全、环保和职业健康事故,协助事故调查、分析,落实事故防范措施。
ENERGY SAVING ACCOUNTABILITIES 能源管理职责
Actively participate in and support energy-saving projects, raise energy-saving proposal based on production practice, attend to audit of energy management system.
积极参与、支持公司节能减排项目,根据生产经验提出节能方案,参与能源管理体系的内部评审。
Key Requirements:
Bachelor degree education or above, with major on pharmaceutical or related. 本科及以上学历, 制药或相关专业
5+ years related the working experience of pharmaceutical industry. 5年以上制药管理岗位工作经验。
GMP, 5S 、Lean etc. related training.
GMP、5S、Lean及其他相关培训
Good command of English both spoken and written
良好的英语听、说、读、写能力
Excellent MS office skills
能够熟练使用办公软件
Strong analytical and problem solving skills
较强的分析能力和问题解决能力
Excellent communication and coordination skills.
卓越的沟通和组织协调能力
Excellent team work / team player and people management
skills.
卓越的团队合作与人员管理技能
Be good at continuous improvement.
善于发现并推进持续改进
At Sanofi diversity and inclusion is foundational to how we operate and embedded in our Core Values. We recognize to truly tap into the richness diversity brings we must lead with inclusion and have a workplace where those differences can thrive and be leveraged to empower the lives of our colleagues, patients and customers. We respect and celebrate the diversity of our people, their backgrounds and experiences and provide equal opportunity for all.
职能类别:生产主管
公司介绍
尊重:我们认同和尊重员工、患者和合作伙伴的需求及其多样性。我们承诺在互信的基础上开展透明且具有建设性的沟通。
创新:我们鼓励所有的员工和合作伙伴发挥创业精神、探索创新思路。
信心:我们充满自信,恪守原则。我们一心一意、永不气馁,敢于挑战常规。
齐心:我们对我们的行为、我们的员工、我们的患者和我们生存的环境负责。共同的责任让我们走到一起。
正直:我们承诺,坚持最严格的道德操守和质量标准,决不妥协。
赛诺菲(北京)制药有限公司
赛诺菲(北京)制药有限公司坐落于北京经济技术开发区,占地4万多平方米,现有员工100名左右。公司于2002年12月通过了国家GMP认证,认证范围包括小容量注射剂的分包装,片剂和胶囊的分包装和生产。公司产品于2003年3月开始投放国内市场。
联系方式
- 公司地址:地址:span亦庄经济技术开发区兴盛街7号