生产部工艺工程师 (职位编号：84795526)
天津百特医疗用品有限公司
- 公司规模：500-1000人
- 公司性质：外资(欧美)
- 公司行业：医疗设备/器械
职位信息
- 发布日期：2021-01-11
- 工作地点：天津-北辰区
- 招聘人数：1人
- 工作经验：3-4年经验
- 学历要求：本科
- 职位类别：药品生产/质量管理
职位描述
Responsibility
To be responsible for supervising all process activities in production area to ensure the manufacturing goals and projects are met to maintain the compliance with GMP, EHS guidelines and any other regulations. Continually optimize the current processes and update related documents, including the procedure of material handling, operation, equipment, inspection and so on.
- Write/update the production processes and procedure according to the cGMP requirement and Baxter requirement.
- As the key player to complete all the validation activities according to cGMP requirement and Baxter quality system.
- Continuously optimize the operational and quality processes and equipment to achieve the company strategy target.
- Participate and present documents/process as the key player in production area if the audit or inspection, ensure to pass the inspections or audit, take the effective actions if any findings related to production area.
-Handle the non-conformity and CR cases for the validation and daily operation.
-Train employees, e.g. operators, technicians and engineers
- Capable of operating the equipment and other operational procedure.
-Use the LEAN tools to improve the current process and operation, ensure that the production provides cost-effective and high quality product timely and efficiently.
- Assist dept. manager to achieve the KPIs and VIP project.
- Understand and implement Baxter, division and regulatory EHS requirements as applicable to process engineer, report incidents of noncompliance with EHS laws and requirements or failure to carry out EHS responsibilities, which endanger the environment or people.
Requirement
- At least a bachelor in Pharmacy or Engineering.
- More than 3 year of production experience in a manufacturing environment preferably in the pharmaceutical, medical or similar industry.
- Familiar with the processes of pharmaceutical manufacturing and GMP management.
- Good oral and written English level.
- High level of attention to detail.
- Independent and honest.
- Have good leadership and communication skills. Demonstrate a strong trouble shooting ability and a desire to learn new things.
- Excellent manufacturing skill, to use the LEAN tools to solve the practical problem during the daily operation.
To be responsible for supervising all process activities in production area to ensure the manufacturing goals and projects are met to maintain the compliance with GMP, EHS guidelines and any other regulations. Continually optimize the current processes and update related documents, including the procedure of material handling, operation, equipment, inspection and so on.
- Write/update the production processes and procedure according to the cGMP requirement and Baxter requirement.
- As the key player to complete all the validation activities according to cGMP requirement and Baxter quality system.
- Continuously optimize the operational and quality processes and equipment to achieve the company strategy target.
- Participate and present documents/process as the key player in production area if the audit or inspection, ensure to pass the inspections or audit, take the effective actions if any findings related to production area.
-Handle the non-conformity and CR cases for the validation and daily operation.
-Train employees, e.g. operators, technicians and engineers
- Capable of operating the equipment and other operational procedure.
-Use the LEAN tools to improve the current process and operation, ensure that the production provides cost-effective and high quality product timely and efficiently.
- Assist dept. manager to achieve the KPIs and VIP project.
- Understand and implement Baxter, division and regulatory EHS requirements as applicable to process engineer, report incidents of noncompliance with EHS laws and requirements or failure to carry out EHS responsibilities, which endanger the environment or people.
Requirement
- At least a bachelor in Pharmacy or Engineering.
- More than 3 year of production experience in a manufacturing environment preferably in the pharmaceutical, medical or similar industry.
- Familiar with the processes of pharmaceutical manufacturing and GMP management.
- Good oral and written English level.
- High level of attention to detail.
- Independent and honest.
- Have good leadership and communication skills. Demonstrate a strong trouble shooting ability and a desire to learn new things.
- Excellent manufacturing skill, to use the LEAN tools to solve the practical problem during the daily operation.
职能类别：药品生产/质量管理
公司介绍
百特是全球领先的医疗用品公司，百特专注于危重治疗领域，在肾科、药物输注和生物科技等领域通过提供先进的多样化的产品和服务。
百特总部设在美国芝加哥，是***进入中国医疗市场的大型跨国公司之一，目前已在中国多个城市建立了办事处，并建立了五家大规模的合资和独资生产企业，一家研发中心。
天津百特医疗用品有限公司于1995年成立，占地面积10,496平米，其中实验室2,400平方米，500余名员工。目前主要产品是以葡萄糖、氯化钠为代表的大输液产品。
未来两年内，百特天津工厂将投产肾科相关腹膜透析产品，目前正在进行项目建设中，诚邀各方英才的加入！
百特总部设在美国芝加哥，是***进入中国医疗市场的大型跨国公司之一，目前已在中国多个城市建立了办事处，并建立了五家大规模的合资和独资生产企业，一家研发中心。
天津百特医疗用品有限公司于1995年成立，占地面积10,496平米，其中实验室2,400平方米，500余名员工。目前主要产品是以葡萄糖、氯化钠为代表的大输液产品。
未来两年内，百特天津工厂将投产肾科相关腹膜透析产品，目前正在进行项目建设中，诚邀各方英才的加入！
联系方式
- Email：TTA@baxter.com
- 公司地址：百特天津工厂