职位描述
QS SPECIALIST
Main Responsibilities:
1、To support the Quality Manager to ensure robust quality systems are developed, implemented and maintained in adherence with Good Manufacturing Practices (GMP) of the applicable regulatory requirements (e.g., EDQM) for the manufacturing and distribution of GMP materials to the applicable markets;
2、To deploy and maintain the core quality systems and to administer the day-to-day activities associated with CAPA, Change Control, Complaints, Supplier & Material Management, and Audit systems/ processes;
3. To act as the competent Quality representative on Quality Compliance topics; To develop, maintain, and update applicable Quality related SOPs and documents to assure the procedures are compliant with company policies/ standards and regulatory expectations;
4. To support effective management of all internal (including Self-Inspection) and external audits; To track the progress and completion of all audit-CAPAs;
5. To promote and improve GMP culture in the site;
6. To back up for material & product release and on-site QA management.
Qualification:
1.At least bachelor degree in Chemical, Pharmaceutical Engineering, Bio-pharma or related;
2.Minimum 5 years of direct (i.e., hands-on) QA/ QS experience in Pharma industry; Specific experience with non-sterile manufacturing processes (APIs, intermediates, or bulk chemicals) would be an asset;
3. Proven experience in the application and interpretation of cGMP requirements of various regulatory authorities/ guidelines (e.g., ICH, EU, US FDA, NMPA, etc.);
4. Detail-oriented to assure accuracy of data and information;
5. Excellent technical writing, analytical, problem-solving and communication
skills;
6. Proven time management and organizational skills to work in a fast pace
regulated environment;
7. Proficient in computing (e.g., Microsoft Word, Excel, PowerPoint, Minitab,
etc.) and in performing appropriate data analysis, gap/ risk assessment;
8.Good at English communication (both oral and written skills at a professional level, capable of communicating with non-Chinese speakers independently without the need of an interpreter).
1、To support the Quality Manager to ensure robust quality systems are developed, implemented and maintained in adherence with Good Manufacturing Practices (GMP) of the applicable regulatory requirements (e.g., EDQM) for the manufacturing and distribution of GMP materials to the applicable markets;
2、To deploy and maintain the core quality systems and to administer the day-to-day activities associated with CAPA, Change Control, Complaints, Supplier & Material Management, and Audit systems/ processes;
3. To act as the competent Quality representative on Quality Compliance topics; To develop, maintain, and update applicable Quality related SOPs and documents to assure the procedures are compliant with company policies/ standards and regulatory expectations;
4. To support effective management of all internal (including Self-Inspection) and external audits; To track the progress and completion of all audit-CAPAs;
5. To promote and improve GMP culture in the site;
6. To back up for material & product release and on-site QA management.
Qualification:
1.At least bachelor degree in Chemical, Pharmaceutical Engineering, Bio-pharma or related;
2.Minimum 5 years of direct (i.e., hands-on) QA/ QS experience in Pharma industry; Specific experience with non-sterile manufacturing processes (APIs, intermediates, or bulk chemicals) would be an asset;
3. Proven experience in the application and interpretation of cGMP requirements of various regulatory authorities/ guidelines (e.g., ICH, EU, US FDA, NMPA, etc.);
4. Detail-oriented to assure accuracy of data and information;
5. Excellent technical writing, analytical, problem-solving and communication
skills;
6. Proven time management and organizational skills to work in a fast pace
regulated environment;
7. Proficient in computing (e.g., Microsoft Word, Excel, PowerPoint, Minitab,
etc.) and in performing appropriate data analysis, gap/ risk assessment;
8.Good at English communication (both oral and written skills at a professional level, capable of communicating with non-Chinese speakers independently without the need of an interpreter).
工作地点
江苏省泰州市泰兴市新港南路20号

公司信息
公司介绍
泰兴扬子医药化工有限公司是生产医药中间体的专业企业,地处长江下游泰兴市沿江经济开发区。区内实行集中供电、供气和供水,公用设施齐全,水陆交通方便。 公司占地面积80000平方米,固定资产5.21亿元。现有职工380人,其中工程技术人员100多名。我公司年产对氨基苯酚35000吨,对硝基苯酚10000吨。 我公司检测手段齐全,产品质量上乘。产品畅销全十几个省市,并出口到日本、欧美、东南亚及非洲等地区,年外贸销售额超三亿元。 我厂管理严格,经营灵活,致力创新,同时注重新产品的开发。热忱欢迎国内外客户选用我公司产品。我们将以优良的产品质量、可靠的信誉、合理的价格为您提供优良的服务。
工商信息
企业名称 泰兴市扬子医药化工有限公司
企业类型 有限责任公司(港澳台投资、非独资)
法人代表 袁俊
经营状态 存续
成立时间 2001-06-15
注册资本 36.5万美元
认证资质
营业执照信息

更新于 今天



