Flow Specialist / 生产专员
上海勃林格殷格翰药业有限公司
- 公司规模:1000-5000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:2013-07-11
- 工作地点:上海-浦东新区
- 招聘人数:1
- 学历要求:大专
- 语言要求:英语良好
- 职位类别:药品生产/质量管理 生产文员
职位描述
Position: Flow Specialist
Department: Ops(PhP-Tech&Ops)
Report to: Flow Manager
Location: Zhangjiang Plant Shanghai (1 person)
Basic Purpose of the Position
岗位的基本目标
1. To assist production manager and supervisor to ensure an efficiency management for all packaging processes in connection with packaging products, beginning with material receipt over processing and ending with finished product
协助生产经理和主管有效控制整个包装过程,从材料接收到成品的全部包装过程;
2. Effective and efficient management of available resources to meet the operational requirements of GMP, corporate guidelines, policies, procedures and industry standards to ensure ongoing compliance of pharmaceutical production;
有效整合已有资源,确保药品生产与GMP,公司政策法规,行业标准方面保持一致;
3. To continuously improve the performance and reliability of service of production within agreed safety, quality and cost standards;
在已达成一致的安全,质量和成本标准下,持续提高生产的绩效及服务的可靠性;
4. Establish team objectives, targets and standards within the context of the overall organizational strategy in order to meet Boehringer Ingelheims operational and corporate objectives.
在总体战略下制定团队的目标和标准,以达到勃林格殷格翰的运营和公司目标。
Accountabilities
职责
1. Safety management
安全管理
To achieve compangy safety target, ensure the manufacturing environment, machine and operation is under a safe and reliable control, carry out effective supervising and instruction for safety during shift work, report any accident or near miss case immediately.
为了实现公司安全目标,确保生产区域环境,设备,和员工操作在安全可靠的条件下进行,翻班期间对现场进行安全检查及督导,并对发生的安全事故和险肇事故及时进行报告
2. People development
人员发展
To develop multi-skilled staffs, participate training and evaluation work with training team support.
为了培养多技能的员工,在培训团队的协助下参与培训考核工作的开展。
3. People management
人员管理
Responsible for the arrangement of shift work, management of attendance, leave and sick leave of staff.
负责员工翻班工作安排、考勤、休假和病假管理。
4. Quality management
质量管理
To achieve company quality target, ensure the operation system of production and packaging accord with GMP, the law for medicine management and company internal requirements, enhance RFT and reduce quality complaint and deviation, carryout effective shop floor management in shift work, review production batch documents. Meanwhile, report any defective material complaint and deviation immediately, participate investigation and CAPA establish.
为了实现公司质量目标,保证生产和包装的运行体系符合GMP、药品管理法和公司内部要求,提高一次正确率,降低投诉率和生产质量事故的发生,翻班期间进行有效的现场管理和人员培训,对批生产文件进行复核,同时对区域内发生的偏差、物料缺陷及时报告,参与调查并制定切实有效的CAPA措施。
5. Shift work management
翻班管理
Responsible for general coordination in shift work, ensure the shift performance dialogue carry out effectively.
负责本区域翻班期间一切生产工作的总协调,负责交接班会议的有效开展。
6. Customer service
客户服务
*To enhance customer service level sustained,
为了持续提高客户服务水平,
*Producton adhere to plan, summary production data and working hour statistic.
按计划生产,汇总生产数据并进行工时统计;
*Responsible for the transfer of material and finished products with material group.
和物料部门衔接物料和成品收发;
*Fulfill the equipment maintenance work with engineer team.
协助生产设备团队开展设备维护工作;
*Assist supplier exploitation and managaement to purchasing department
协助采购部门开发供应商和管理;
*Assist work related new product launch
协助新产品上市的各项工作;
*Fulfill other tasks arranged by superior
完成上级交给的其他任务。
7. CHINA LEAN implementation
精益生产项目实施
To get sustained improvement for equipment efficiency, operator efficiency and product yield, be fully involved in CHINA LEAN implementation, optimize production process, reduce non-value added step, to shorten production throughput time.
为了持续的提高设备效率(0EE),人员效率(OOE),产品收率(Yield),降低产品成本,积极参与CHINA LEAN各项目,通过优化和改进生产流程,减少无效的操作和支出,缩短生产周期。
Required Education
所需的教育背景
1. Pharmacy background and related;
药学或者相关专业
2. Office soft skill;
熟练的OFFICE 软件应用技能
3. Good people management skill and effective communication skill;
良好的人员管理技能和有效沟通技能
4. Good people management skill
良好的人员管理技能
5. Effective communication skill in both Chinese and English.
有效的中英文沟通技能
6. Clear understanding of the regulatory requirements of the Pharmaceutical Industry including a good working knowledge of GMP standards
对制药行业的政策规章有清晰的理解,包括能对GMP标准
7. Better to have experience of shop floor management within the international pharmaceutical industry.
最好有跨国制药行业一线管理方面的经验。
8. Willing to work in shift
愿意做翻班工作
Department: Ops(PhP-Tech&Ops)
Report to: Flow Manager
Location: Zhangjiang Plant Shanghai (1 person)
Basic Purpose of the Position
岗位的基本目标
1. To assist production manager and supervisor to ensure an efficiency management for all packaging processes in connection with packaging products, beginning with material receipt over processing and ending with finished product
协助生产经理和主管有效控制整个包装过程,从材料接收到成品的全部包装过程;
2. Effective and efficient management of available resources to meet the operational requirements of GMP, corporate guidelines, policies, procedures and industry standards to ensure ongoing compliance of pharmaceutical production;
有效整合已有资源,确保药品生产与GMP,公司政策法规,行业标准方面保持一致;
3. To continuously improve the performance and reliability of service of production within agreed safety, quality and cost standards;
在已达成一致的安全,质量和成本标准下,持续提高生产的绩效及服务的可靠性;
4. Establish team objectives, targets and standards within the context of the overall organizational strategy in order to meet Boehringer Ingelheims operational and corporate objectives.
在总体战略下制定团队的目标和标准,以达到勃林格殷格翰的运营和公司目标。
Accountabilities
职责
1. Safety management
安全管理
To achieve compangy safety target, ensure the manufacturing environment, machine and operation is under a safe and reliable control, carry out effective supervising and instruction for safety during shift work, report any accident or near miss case immediately.
为了实现公司安全目标,确保生产区域环境,设备,和员工操作在安全可靠的条件下进行,翻班期间对现场进行安全检查及督导,并对发生的安全事故和险肇事故及时进行报告
2. People development
人员发展
To develop multi-skilled staffs, participate training and evaluation work with training team support.
为了培养多技能的员工,在培训团队的协助下参与培训考核工作的开展。
3. People management
人员管理
Responsible for the arrangement of shift work, management of attendance, leave and sick leave of staff.
负责员工翻班工作安排、考勤、休假和病假管理。
4. Quality management
质量管理
To achieve company quality target, ensure the operation system of production and packaging accord with GMP, the law for medicine management and company internal requirements, enhance RFT and reduce quality complaint and deviation, carryout effective shop floor management in shift work, review production batch documents. Meanwhile, report any defective material complaint and deviation immediately, participate investigation and CAPA establish.
为了实现公司质量目标,保证生产和包装的运行体系符合GMP、药品管理法和公司内部要求,提高一次正确率,降低投诉率和生产质量事故的发生,翻班期间进行有效的现场管理和人员培训,对批生产文件进行复核,同时对区域内发生的偏差、物料缺陷及时报告,参与调查并制定切实有效的CAPA措施。
5. Shift work management
翻班管理
Responsible for general coordination in shift work, ensure the shift performance dialogue carry out effectively.
负责本区域翻班期间一切生产工作的总协调,负责交接班会议的有效开展。
6. Customer service
客户服务
*To enhance customer service level sustained,
为了持续提高客户服务水平,
*Producton adhere to plan, summary production data and working hour statistic.
按计划生产,汇总生产数据并进行工时统计;
*Responsible for the transfer of material and finished products with material group.
和物料部门衔接物料和成品收发;
*Fulfill the equipment maintenance work with engineer team.
协助生产设备团队开展设备维护工作;
*Assist supplier exploitation and managaement to purchasing department
协助采购部门开发供应商和管理;
*Assist work related new product launch
协助新产品上市的各项工作;
*Fulfill other tasks arranged by superior
完成上级交给的其他任务。
7. CHINA LEAN implementation
精益生产项目实施
To get sustained improvement for equipment efficiency, operator efficiency and product yield, be fully involved in CHINA LEAN implementation, optimize production process, reduce non-value added step, to shorten production throughput time.
为了持续的提高设备效率(0EE),人员效率(OOE),产品收率(Yield),降低产品成本,积极参与CHINA LEAN各项目,通过优化和改进生产流程,减少无效的操作和支出,缩短生产周期。
Required Education
所需的教育背景
1. Pharmacy background and related;
药学或者相关专业
2. Office soft skill;
熟练的OFFICE 软件应用技能
3. Good people management skill and effective communication skill;
良好的人员管理技能和有效沟通技能
4. Good people management skill
良好的人员管理技能
5. Effective communication skill in both Chinese and English.
有效的中英文沟通技能
6. Clear understanding of the regulatory requirements of the Pharmaceutical Industry including a good working knowledge of GMP standards
对制药行业的政策规章有清晰的理解,包括能对GMP标准
7. Better to have experience of shop floor management within the international pharmaceutical industry.
最好有跨国制药行业一线管理方面的经验。
8. Willing to work in shift
愿意做翻班工作
公司介绍
关于勃林格殷格翰
加入勃林格殷格翰,与我们一起携手并肩,共创未来。我们深信每一位员工的成长都将铸就公司的发展,每一位员工的努力也都将成就公司的美好明天。130余年来,研发驱动型制药公司勃林格殷格翰作为全球前20大制药企业之一,持续致力于人用药品、动物保健和生物制药合同生产三大业务领域,力争为人类和动物带来更多健康。加入勃林格殷格翰,将是您实现“创新展现价值”的绝佳机会!在工作中,您将通过与内外部伙伴的通力合作,站在知识迭代的最前沿;科研过程中,您将不断探索新型科学发现,切实提高全人类的生活质量;与此同时,您也将助力公司成为未来行业当之无愧的领导者。
我们的业务正处在持续高速发展之中,是中国业内发展最快的公司之一。我们诚邀您加入勃林格殷格翰,共同携手向前,成为实现2025愿景的一份子。
作为业内的领导企业,热情、创新和独立是驱动我们不懈前行的动力,我们为每一位努力热忱、恪尽职守的员工提供成长机会,实现其个人价值。作为连续七年通过“中国杰出雇主”认证的企业,我们通过提供高质量的职业发展规划、参与或领导国际项目的机会,为每一位员工的成功之路夯实基础。
让我们彼此成就,引领未来!
想获取更多信息,有以下方式:
1. 访问************************************/或
2. 关注我们领英账号, 或
3. 关注我们的微信公众号:BI招聘
行为准则
-责任心:即使情况不明朗,我们总是在自己的决策和行为中展现主人翁精神
-敏锐度:面对内外部变化时,我们以开放的心态快速应对
-内部企业家精神:我们与客户携手构筑创新理念,以应对瞬息万变的市场
联系我们
如果你坚信自己就是我们要找的人,不要犹豫,马上申请吧!
加入勃林格殷格翰,与我们一起携手并肩,共创未来。我们深信每一位员工的成长都将铸就公司的发展,每一位员工的努力也都将成就公司的美好明天。130余年来,研发驱动型制药公司勃林格殷格翰作为全球前20大制药企业之一,持续致力于人用药品、动物保健和生物制药合同生产三大业务领域,力争为人类和动物带来更多健康。加入勃林格殷格翰,将是您实现“创新展现价值”的绝佳机会!在工作中,您将通过与内外部伙伴的通力合作,站在知识迭代的最前沿;科研过程中,您将不断探索新型科学发现,切实提高全人类的生活质量;与此同时,您也将助力公司成为未来行业当之无愧的领导者。
我们的业务正处在持续高速发展之中,是中国业内发展最快的公司之一。我们诚邀您加入勃林格殷格翰,共同携手向前,成为实现2025愿景的一份子。
作为业内的领导企业,热情、创新和独立是驱动我们不懈前行的动力,我们为每一位努力热忱、恪尽职守的员工提供成长机会,实现其个人价值。作为连续七年通过“中国杰出雇主”认证的企业,我们通过提供高质量的职业发展规划、参与或领导国际项目的机会,为每一位员工的成功之路夯实基础。
让我们彼此成就,引领未来!
想获取更多信息,有以下方式:
1. 访问************************************/或
2. 关注我们领英账号, 或
3. 关注我们的微信公众号:BI招聘
行为准则
-责任心:即使情况不明朗,我们总是在自己的决策和行为中展现主人翁精神
-敏锐度:面对内外部变化时,我们以开放的心态快速应对
-内部企业家精神:我们与客户携手构筑创新理念,以应对瞬息万变的市场
联系我们
如果你坚信自己就是我们要找的人,不要犹豫,马上申请吧!
联系方式
- Email:HRTACampusWest.CN@boehringer-ingelheim.com
- 公司地址:地址:span张江李时珍路257号