长沙招聘

工作内容：

制药GMP质量体系文件管理，OA vender的沟通及供应商相关资质等的确认及管理，系统流程及数据维护

Description:

Support GMP daily archiving, retrieving, issuing and/or reconciliation of GMP documents.

Collect QA KPI relevant performance data, e.g. deviation, CAPA, change control etc. on biweekly basis for further presentation compilation.

Support master data entry for quality view in MDM.

Support ongoing supplier qualification project.

Duties & Responsibilities:

Coordinate, controlled issue and reconcile SOP and other quality documentations. Handle document creation, revision, review and approval of workflow in electronic document management system. Execute tasks timely and accurately to meet the documentation management requirements.

Support with KPI collection and trending analysis in GO Track system.

Support with QM module in GBS including Master Data Maintenance and QIR collection.

Maintain access control and folder structure in Share Room and QA Share Folder.

Controlled issue and reconcile label, logbook and cleaning records.

Archive and retrieve GMP documents.

Support with supplier qualification MSO to manage supplier qualification.

应聘条件：

学历/专业：本科学历，生物工程/制药/化学工程等相关专业必须

工作经验： 1年左右经验，工作中了解或熟悉制药GMP条例体系

英语要求：书面邮件及系统Workable，口语的最低要求是能用简单的沟通表述清楚自身的意思

能力要素：工作细致，与同事间沟通良好流畅

上海中智项目外包咨询服务有限公司是中智上海全资子公司，发展至今，经与几千家各个行业的企业成功合作，服务网络覆盖全国300多个城市。以服务外包的形式为企业提供“优质、高效、便捷”的灵活用工、项目管理、办公室商务服务等，其中全球500强企业占比超过50%，涉及制造、金融、化工、医药、奢侈品与消费品、进出口贸易等行业，并且与服务客户建立了良好的合作伙伴关系。
中智将以不懈追求卓越的精神，坚持传承与创新，积极探索企业发展的新方向、新路径，推动企业实现新发展，继续强化质量意识，加强质量管理，落实质量责任，提高服务质量，进而为将上海建设成“具有国际竞争力的质量高地”作出更大的贡献。