這篇《2013年輝瑞（中國(guó)）研究開(kāi)發(fā)有限公司上海校園招聘簡(jiǎn)章》是為大家整理的，希望對(duì)大家有所幫助。以下信息僅供參考！
公司簡(jiǎn)介：
輝瑞(中國(guó))研究開(kāi)發(fā)有限公司2005年10月31日在上海成立，位于有“藥谷”之稱(chēng)的浦東張江。輝瑞中國(guó)研發(fā)中心主要為全球輝瑞藥物開(kāi)發(fā)提供支持工作。大部分的功能是圍繞在I-IV期臨床試驗(yàn)研究設(shè)計(jì)、數(shù)據(jù)管理和生物統(tǒng)計(jì)分析、以及臨床試驗(yàn)報(bào)告和藥品注冊(cè)的準(zhǔn)備工作。此外，該中心是輝瑞全球安全和風(fēng)險(xiǎn)管理部的一個(gè)分支，負(fù)責(zé)安全數(shù)據(jù)處理和評(píng)估工作。研發(fā)中心還將為輝瑞公司在中國(guó)及亞洲的其它運(yùn)營(yíng)部門(mén)的員工提供國(guó)際標(biāo)準(zhǔn)的臨床試驗(yàn)管理規(guī)范(GCP)的技術(shù)培訓(xùn)。
招聘崗位：藥品注冊(cè)申報(bào)專(zhuān)員(Publishing Manager)
工作地點(diǎn)：上海市浦東區(qū)
招聘人數(shù)：14人
要求：生物醫(yī)藥、化學(xué)背景，英文好的面試者優(yōu)先考慮，本科、碩士均可，工作經(jīng)驗(yàn)不限。
采用內(nèi)部人員直薦方式，如感興趣，請(qǐng)將簡(jiǎn)歷投至： Fang.Wang7@pfizer.com
英文招聘資料如下：
Division/Organization:
Position Purpose
This role works within a team to create Regulatory Agency Submission Packages(Dossier) using a number of build and publishing tools. The Dossiers are compiled in paper and/or electronic format with documentation received from Submission co-ordinators and submitted to Regulatory agencies (often within very tight timelines) to seek clinical trial and/or marketing authorization approval for pharmaceutical products.
Primary Responsibilities
Responsible for the building, publishing, archiving activities and associated tasks for assigned Regulatory submissions within agreed timelines.
Adhering to quality control procedures and standards related to submission publishing.
Adhering to the appropriate use of document management systems, publishing and validation tools, through the use of working practices and quality control steps to ensure Regulatory compliance.
Support other team members with submission workload when necessary to provide flexible support for the submissions portfolio.
Support global/local teams by completing tasks assigned by submission co-ordinators
Adhere to Pfizer compliance standards.
Technical Skill Requirements
Computer literacy in MS Word/Outlook/Excel/Adobe Acrobat.
Proven technical aptitude and ability to quickly learn and use new software, regulations and quality standards
Functional and technical knowledge and skills to do the job at a high level of accomplishment
Qualifications (i.e., preferred education, experience, attributes)
Proven technical aptitude
Quick learner with ability to multi-task
Ability to work with accuracy and attention to detail
Ability to work with autonomy and/or part of a team in a busy environment
Demonstrated ability to work in a highly regulated environment
Demonstration of experience working in a customer service environment
生物醫(yī)藥、化學(xué)背景，英文好的面試者優(yōu)先考慮，本科、碩士均可
請(qǐng)把簡(jiǎn)歷投至： Fang.Wang7@pfizer.com
公司簡(jiǎn)介：
輝瑞(中國(guó))研究開(kāi)發(fā)有限公司2005年10月31日在上海成立，位于有“藥谷”之稱(chēng)的浦東張江。輝瑞中國(guó)研發(fā)中心主要為全球輝瑞藥物開(kāi)發(fā)提供支持工作。大部分的功能是圍繞在I-IV期臨床試驗(yàn)研究設(shè)計(jì)、數(shù)據(jù)管理和生物統(tǒng)計(jì)分析、以及臨床試驗(yàn)報(bào)告和藥品注冊(cè)的準(zhǔn)備工作。此外，該中心是輝瑞全球安全和風(fēng)險(xiǎn)管理部的一個(gè)分支，負(fù)責(zé)安全數(shù)據(jù)處理和評(píng)估工作。研發(fā)中心還將為輝瑞公司在中國(guó)及亞洲的其它運(yùn)營(yíng)部門(mén)的員工提供國(guó)際標(biāo)準(zhǔn)的臨床試驗(yàn)管理規(guī)范(GCP)的技術(shù)培訓(xùn)。
招聘崗位：藥品注冊(cè)申報(bào)專(zhuān)員(Publishing Manager)
工作地點(diǎn)：上海市浦東區(qū)
招聘人數(shù)：14人
要求：生物醫(yī)藥、化學(xué)背景，英文好的面試者優(yōu)先考慮，本科、碩士均可，工作經(jīng)驗(yàn)不限。
采用內(nèi)部人員直薦方式，如感興趣，請(qǐng)將簡(jiǎn)歷投至： Fang.Wang7@pfizer.com
英文招聘資料如下：
Division/Organization:
Position Purpose
This role works within a team to create Regulatory Agency Submission Packages(Dossier) using a number of build and publishing tools. The Dossiers are compiled in paper and/or electronic format with documentation received from Submission co-ordinators and submitted to Regulatory agencies (often within very tight timelines) to seek clinical trial and/or marketing authorization approval for pharmaceutical products.
Primary Responsibilities
Responsible for the building, publishing, archiving activities and associated tasks for assigned Regulatory submissions within agreed timelines.
Adhering to quality control procedures and standards related to submission publishing.
Adhering to the appropriate use of document management systems, publishing and validation tools, through the use of working practices and quality control steps to ensure Regulatory compliance.
Support other team members with submission workload when necessary to provide flexible support for the submissions portfolio.
Support global/local teams by completing tasks assigned by submission co-ordinators
Adhere to Pfizer compliance standards.
Technical Skill Requirements
Computer literacy in MS Word/Outlook/Excel/Adobe Acrobat.
Proven technical aptitude and ability to quickly learn and use new software, regulations and quality standards
Functional and technical knowledge and skills to do the job at a high level of accomplishment
Qualifications (i.e., preferred education, experience, attributes)
Proven technical aptitude
Quick learner with ability to multi-task
Ability to work with accuracy and attention to detail
Ability to work with autonomy and/or part of a team in a busy environment
Demonstrated ability to work in a highly regulated environment
Demonstration of experience working in a customer service environment
生物醫(yī)藥、化學(xué)背景，英文好的面試者優(yōu)先考慮，本科、碩士均可
請(qǐng)把簡(jiǎn)歷投至： Fang.Wang7@pfizer.com