QC分析员
上海卡乐康包衣技术有限公司
- 公司规模:150-500人
- 公司性质:合资(欧美)
- 公司行业:制药/生物工程
职位信息
- 发布日期:2017-12-07
- 工作地点:上海-闵行区
- 招聘人数:1人
- 工作经验:无工作经验
- 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 化学分析测试员
职位描述
职位描述:
Job Summary
This position is responsible for inspection and processing of all finished product and intermediate, including Batch Manufacturing Sheet preparations which are based on small sample testing and material usage controls, and product label printing & reconciliation. Individual maintains both the FG laboratory and the legal retain room. Additional support is also required including customer complaint investigation, validation protocol executions and technical support of manufacturing process study such as coating trail and some analytical testing, and administrative supports.
Main Responsibilities
Performs testings on the samples of finished products, intermediates, technical service,validation, stability and complaints etc. in accordance with established procedures or protocols.
按照规定的规程或方案检验原料、成品、中间体、实验样品、验证样品、稳定性样品和投诉样品等。
Maintains good housekeeping, order, and safety in the laboratory and retain sample room.
保持实验室和留样室处于整洁、有序和安全的状态。
Submits accurate, precise and complete reports in a timely fashion. Exhibits a working knowledge of Colorcon Oracle database applications to maintain accuracy of records.
及时提交准确完整的报告,应用卡乐康的数据系统保持记录的准确性。
Prepares Batch Manufacturing Sheets and product labels generation。
批生产制造单的签发和产品标签的打印、发放。
Maintains an awareness of cGMP and cGLP and maintains compliance with those
regulations; documents all activities associated with cGMP compliance (i.e. QC tests, instrument checks/calibration, OOS investigations etc.).
熟悉药品生产质量管理规范和实验室管理规范,记录与规范符合性相关的如QC检验、仪器的校验,检验结果不符合的实验室调查等各项活动。
Demonstrates the ability to set own priorities based on operations schedule and deadlines.
有能力根据生产计划和时限安排自己工作的优先次序。
Interdepartmental communication with Operation team concerning the own work related issues.
和工作相关的各部门保持良好的沟通。
Other tasks are assigned by Supervisor or Shift Team Leader.
其它主管或班组长安排的工作。
Measurement - Refer to BSC
Requirements:
College or above in pharmacy or chemical related.
Minimum one years experience in a pharmaceutical work environment with knowledge of cGMPs.
Must have organizational skills, decision-making skills, and communication skills.
Have chemical analysis or instrumental analysis background.
Good computer and English skills
举报
分享
Job Summary
This position is responsible for inspection and processing of all finished product and intermediate, including Batch Manufacturing Sheet preparations which are based on small sample testing and material usage controls, and product label printing & reconciliation. Individual maintains both the FG laboratory and the legal retain room. Additional support is also required including customer complaint investigation, validation protocol executions and technical support of manufacturing process study such as coating trail and some analytical testing, and administrative supports.
Main Responsibilities
Performs testings on the samples of finished products, intermediates, technical service,validation, stability and complaints etc. in accordance with established procedures or protocols.
按照规定的规程或方案检验原料、成品、中间体、实验样品、验证样品、稳定性样品和投诉样品等。
Maintains good housekeeping, order, and safety in the laboratory and retain sample room.
保持实验室和留样室处于整洁、有序和安全的状态。
Submits accurate, precise and complete reports in a timely fashion. Exhibits a working knowledge of Colorcon Oracle database applications to maintain accuracy of records.
及时提交准确完整的报告,应用卡乐康的数据系统保持记录的准确性。
Prepares Batch Manufacturing Sheets and product labels generation。
批生产制造单的签发和产品标签的打印、发放。
Maintains an awareness of cGMP and cGLP and maintains compliance with those
regulations; documents all activities associated with cGMP compliance (i.e. QC tests, instrument checks/calibration, OOS investigations etc.).
熟悉药品生产质量管理规范和实验室管理规范,记录与规范符合性相关的如QC检验、仪器的校验,检验结果不符合的实验室调查等各项活动。
Demonstrates the ability to set own priorities based on operations schedule and deadlines.
有能力根据生产计划和时限安排自己工作的优先次序。
Interdepartmental communication with Operation team concerning the own work related issues.
和工作相关的各部门保持良好的沟通。
Other tasks are assigned by Supervisor or Shift Team Leader.
其它主管或班组长安排的工作。
Measurement - Refer to BSC
Requirements:
College or above in pharmacy or chemical related.
Minimum one years experience in a pharmaceutical work environment with knowledge of cGMPs.
Must have organizational skills, decision-making skills, and communication skills.
Have chemical analysis or instrumental analysis background.
Good computer and English skills
职能类别: 药品生产/质量管理 化学分析测试员
关键字: QC分析员
公司介绍
卡乐康(Colorcon)是全球药剂开发领域的领导者,总部位于美国费城,成立于1961年,至今已有50年以上的历史。卡乐康以优质的产品、领先的制药技术及全面的增值服务,成为全球制药企业配方的合作伙伴。
卡乐康自1993年近入中国市场,并于1996年正式注册上海卡乐康包衣技术有限公司。在进入中国20年间,卡乐康推动了薄膜包衣及配方技术在中国制药领域的快速发展。我们的专利产品欧巴代(Opadry)系列,已经成为该领域中运用最广泛的产品之一,代表了当今薄膜包衣技术的最高水平,从而也为中国市场提供了与世界同步的选择。
经过多年的磨练,我们在中国的生产规模、员工队伍、销售利润都有了快速地增长,同时确立了在行业中的领导地位。欢迎你查看我们的网站——www.colorcon.com, www.colorcon.com.cn 来获得对公司情况的进一步了解。你会对我们是药用辅料领域的全球领先者以及我们将面临的巨大发展机会而感到兴奋!
因公司业务发展需要诚聘英才,如感兴趣者请联系我们
邮件:rying@colorcon.com
卡乐康自1993年近入中国市场,并于1996年正式注册上海卡乐康包衣技术有限公司。在进入中国20年间,卡乐康推动了薄膜包衣及配方技术在中国制药领域的快速发展。我们的专利产品欧巴代(Opadry)系列,已经成为该领域中运用最广泛的产品之一,代表了当今薄膜包衣技术的最高水平,从而也为中国市场提供了与世界同步的选择。
经过多年的磨练,我们在中国的生产规模、员工队伍、销售利润都有了快速地增长,同时确立了在行业中的领导地位。欢迎你查看我们的网站——www.colorcon.com, www.colorcon.com.cn 来获得对公司情况的进一步了解。你会对我们是药用辅料领域的全球领先者以及我们将面临的巨大发展机会而感到兴奋!
因公司业务发展需要诚聘英才,如感兴趣者请联系我们
邮件:rying@colorcon.com
联系方式
- Email:rying@colorcon.com
- 公司地址:地址:span春东路588号(近银都路)