China Pharma R&D Quality & Compliance Specialist
職位描述
職位描述:
Quality Processes
Process, systems and documentation
? Support the local impact assessment of global R&D procedural documents and, if applicable, support development and management of associated local procedural documents
? Support to take oversight for local procedural documents in close collaboration with functional owners in China R&D/SAF and BRQC process and development
Training and knowledge management
? Support onboarding of new hires to provide general onboarding training package
? Coordinate local workshops to support QMS and compliance awareness, Lessons Learned, etc.
? Provide advice regarding SOP, system and GxP(GMP excluded) questions
? Coordinate the availability of local training curricula, if applicable, for China R&D/SAF in collaboration with local and global training partners such as regional Q&C, LOC e-University
? Support development of training materials for China R&D/SAF functional departments in collaboration with content owners.
Quality monitoring & compliance
? Support development of the Annual Quality Plan with remediation activities addressing compliance issues and risk signals
? Coordinate and/or perform QC checks and remediation actions specified in Annual Quality Plan. Monitor progress and effectiveness of remediation actions
? Support local and central business partners to facilitate (local) inspections and office audits as needed
? Support local and central business partners in timely CAPA setting and implementation
? On an ad hoc basis, perform activities such as On-Site Quality Monitoring and file checks
Data Quality, Metrics & Reporting
? Support disclosure of clinical data on local public web, if applicable (CT.gov excluded)
? Support to take oversight for system related data quality, e.g., TMS, CTMS
Regulatory Compliance
Local regulatory intelligence
? Support RA Quality representative to perform impact assessments of new/revised local regulations, guidance and standards
? Coordinate or support special investigation and issue remediation activities
Business Development
Vendor management
? Support local vendor assessments, if applicable
? Support activities related to annual DD update, certification and training of local vendors, if applicable
Business Quality
Management Review
? Support monitoring of compliance metrics, audit findings and issues (including appropriate escalation)
? Support LOC Management Review in collaboration with LOC quality partners
? Coordinate and/or participate in quality committee, if applicable
Others
? If applicable, support country specific quality management activities including but not limited to organizing cross-departmental quality meetings
企業(yè)簡(jiǎn)介
美國(guó)強(qiáng)生公司創(chuàng)建于1886年,目前在全球60個(gè)國(guó)家建立了250多家分公司,是目前世界上最具綜合性、業(yè)務(wù)分布范圍最廣的衛(wèi)生保健產(chǎn)品的制造商和相關(guān)服務(wù)提供商,業(yè)務(wù)領(lǐng)域主要包括制藥,醫(yī)療器械和消費(fèi)品。
西安楊森制藥有限公司是美國(guó)強(qiáng)生公司在華最大的子公司,成立于1985年。公司管理中心在北京,生產(chǎn)基地位于西安,在全國(guó)28個(gè)城市設(shè)有辦事處,在華員工超過(guò)3000人。在過(guò)去的25年中,西安楊森保持持續(xù)穩(wěn)定發(fā)展,成為了中國(guó)領(lǐng)先的合資制藥企業(yè)。
西安楊森不斷引進(jìn)和生產(chǎn)多種創(chuàng)新的、高品質(zhì)的藥品,其產(chǎn)品包括多種高質(zhì)量的處方藥,以及廣受患者信賴的非處方藥物。西安楊森依托強(qiáng)生公司全球強(qiáng)大的研究開(kāi)發(fā)體系,著眼于未來(lái),不斷引進(jìn)新的藥品,計(jì)劃上市生物制劑、腫瘤、心血管、風(fēng)濕和泌尿等更多領(lǐng)域的產(chǎn)品以服務(wù)于中國(guó)的廣大患者。
西安楊森公司遵從強(qiáng)生信條的原則,致力于公司的長(zhǎng)期發(fā)展。這是公司在過(guò)去取得成功的基石,也是未來(lái)成長(zhǎng)的保障。
西安楊森公司獲得眾多獎(jiǎng)項(xiàng)和贊譽(yù),比如《財(cái)富》雜志評(píng)選的“中國(guó)最受贊賞的外資企業(yè)”及“人力資源經(jīng)理眼中的熱門(mén)雇主”;中國(guó)中央電視臺(tái) “2005CCTV中國(guó)年度雇主”;CRF評(píng)選的2007-2008年度北京地區(qū)“中國(guó)杰出雇主”;2008年與強(qiáng)生在華公司一起榮獲“第六屆中國(guó)大學(xué)生最佳雇主獎(jiǎng)和進(jìn)步飛速獎(jiǎng)”稱號(hào),和2009年“第七屆中國(guó)大學(xué)生最佳雇主獎(jiǎng)”,并位列醫(yī)藥行業(yè)第一名。2010年強(qiáng)生在華公司榮獲“第八屆中國(guó)大學(xué)生最佳雇主制藥/醫(yī)療行業(yè)最佳雇主第一名”。這是繼上屆強(qiáng)生公司獲得醫(yī)藥行業(yè)第一名后再次蟬聯(lián)這項(xiàng)榮譽(yù)。
職位發(fā)布企業(yè)
西安楊森制藥有限公司
企業(yè)性質(zhì):民營(yíng)企業(yè)
企業(yè)規(guī)模:1000-1999人
成立年份:1985
企業(yè)網(wǎng)址:www.xian-janssen.com.cn/
企業(yè)地址:陜西省西安市新城區(qū)萬(wàn)壽北路34號(hào)
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職位發(fā)布日期: 2016-11-23