职位描述
该职位还未进行加V认证,请仔细了解后再进行投递!
职位描述:
responsibilities:
- establish and maintain document control process, including origin of internal or external, to ensure only valid and current version can be used;
- maintain all quality related records well controlled to ensure a good record practice is implemented through routine training and monitoring in on-line document system;
-support to monitor and follow up the capa status and support on internal audit program to ensure the system is consistently complying to applicable standards/regulations;
-responsible for quality system data collection and analysis to detect any abnormal trending or opportunity for improvement
-responsible to support product registration per request
-other responsibility defined in related company procedures or assigned by qara supervisor
qualifications:
-bachelor’s degree or above
-iso13485:2016 internal auditor certificate
-3-year above similar quality system management experience in medical device or pharmaceutical industry
-solid understanding on iso13485; and familiar with gmp&gsp or other medical device related regulations
-good capa management ability
-good command of english and mandarin
-good knowledge with pc application
-on-line document control system experience
-accountability, learning agile, “can do” attitude, teamwork spirit
-down to earth capability
-qara team at both corporate and regional levels as well as the functional departments in shanghai
分享
微信邮件
responsibilities:
- establish and maintain document control process, including origin of internal or external, to ensure only valid and current version can be used;
- maintain all quality related records well controlled to ensure a good record practice is implemented through routine training and monitoring in on-line document system;
-support to monitor and follow up the capa status and support on internal audit program to ensure the system is consistently complying to applicable standards/regulations;
-responsible for quality system data collection and analysis to detect any abnormal trending or opportunity for improvement
-responsible to support product registration per request
-other responsibility defined in related company procedures or assigned by qara supervisor
qualifications:
-bachelor’s degree or above
-iso13485:2016 internal auditor certificate
-3-year above similar quality system management experience in medical device or pharmaceutical industry
-solid understanding on iso13485; and familiar with gmp&gsp or other medical device related regulations
-good capa management ability
-good command of english and mandarin
-good knowledge with pc application
-on-line document control system experience
-accountability, learning agile, “can do” attitude, teamwork spirit
-down to earth capability
-qara team at both corporate and regional levels as well as the functional departments in shanghai
分享
微信邮件
工作地点
地址:上海徐汇区上海-徐汇区
以担保或任何理由索取财物,扣押证照,均涉嫌违法,请提高警惕
职位发布者
林亮HR
上海萌黎国际贸易有限公司
- 医疗设备·器械
- 200-499人
- 公司性质未知
- 虹桥路3号港汇中心二座1803室