Regulatory Affairs Supervisor
職位描述
Role Overview:
1. Responsible for setting up the product registration plan per marketing’s registration request
2. Responsible for registration of Recon product according to the timeframe of registration plan
3. Responsible for following up type testing, preparing submission documents, communicating with CFDA authority during technical evaluation period, conducting in compliance with local regulatory agency requirements and relevant SOP.
4. Responsible for good documentation management.
5. Responsible for providing regulatory support to relevant department
6. Responsible for establishment of good working relationship with regulatory agencies and GBU supporting team
Please include specific internal and external relationships, product focus (if any), regulatory requirements, etc.
Responsibilities: (Please specify % amount against each responsibility)
This is the key position of Recon product registration in China. Anna is the RABP to support Recon business unit and lead a registration team with two team members. Under that postion, the staff needs to:
1. Set up the registration plan for Recon products according to marketing launch plan or expiration date of original certificate, keep good communication with supervisor and co-worker, provide monthly update for the projects (15%);
2. Follow up testing and technical review for the registration ( 30%)
3. Cooperate with local marketing and sourcing company, push the whole registration process going forward as planed following the SOP requirement. ( 20 %)
4. Set up good relationship with authority from testing centre and technical evaluation centre. (10 %)
5. Lead Recon registration team to proceed all initial and renewal registration in China according to the plan to support Recon business growth in China, review the registration process with team member and coach junior team member as well(10%)
6. Keep good documentation management for the registered products. ( 5%)
7. Provide the regulatory support to other departments in daily work ( 5%)
8. Lead RA project and make sure it’s completed as planning ( 5%)
Location: Beijing commercial
Education: Bachelor and above
Licenses/ Certifications:
Experience: 5 years+ registration experience
Competences:
Physical Demands:
Medical or biological background, come from science department in a college is preferred.
English communication ability, read and write fluently, simple spoken English at least
Team work spirits
企業(yè)簡介
施樂輝公司(smith&nephew)是由英國專業(yè)藥劑師Thomas John Smith 于1856年在英格蘭北部的赫爾(Hull)所創(chuàng)立,總部設(shè)于英國倫敦。1994年,施樂輝(smith&nephew)進(jìn)駐中國,總部設(shè)在上海,并陸續(xù)在北京、廣州、香港、成都等地設(shè)立辦事處;1999年施樂輝在上海外高橋保稅區(qū),成立了在中國的第一家全資子公司——施樂輝醫(yī)用產(chǎn)品國際貿(mào)易(上海)有限公司Smith & Nephew Medical (Shanghai) Limited,并逐步在全國各大城市設(shè)立分銷機(jī)構(gòu)。通過多年努力,施樂輝已將世界最先進(jìn)的技術(shù)及產(chǎn)品引進(jìn)中國,以堅(jiān)定信念和優(yōu)質(zhì)產(chǎn)品,幫助中國數(shù)以萬計(jì)人民重新獲得健康新生活。
自創(chuàng)始以來,施樂輝 (smith&nephew)一向以敢于創(chuàng)新、保持優(yōu)質(zhì)傳統(tǒng)為宗旨。至今,在全球醫(yī)療和健康護(hù)理領(lǐng)域位居領(lǐng)導(dǎo)地位。全球員工超過9,000名,業(yè)務(wù)分布于34個國家,集團(tuán)生產(chǎn)超過1400類產(chǎn)品,銷售廣達(dá)100個國家,是業(yè)界卓有口碑的領(lǐng)導(dǎo)者。施樂輝 (smith&nephew)不斷創(chuàng)新和研發(fā)臨床所信賴的產(chǎn)品,其產(chǎn)品線中三大類產(chǎn)品:骨科、內(nèi)鏡、傷口護(hù)理系列,均是全球業(yè)界的佼佼者。
施樂輝 (smith&nephew)于2007年6月收購普魯斯貿(mào)易(北京)有限公司專業(yè)從事高品質(zhì)的髖、膝、脊柱等外科植入物及配套手術(shù)器械的生產(chǎn)和銷售。
公司主頁:http://www.smith-nephew.com
職位發(fā)布企業(yè)
施樂輝醫(yī)用產(chǎn)品國際貿(mào)易(上海)有限公司
企業(yè)性質(zhì):外資企業(yè)
企業(yè)規(guī)模:1-49人
成立年份:1999
企業(yè)網(wǎng)址:http://www.smith-nephew.com
企業(yè)地址:黃浦區(qū)西藏中路168號12樓
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職位發(fā)布日期: 2019-05-31