一、公司簡介
今天的默沙東正致力于為全世界帶來健康的福音。我們?yōu)槿?40多個國家提供藥物、疫苗、生物制劑、健康消費品和動物保健產(chǎn)品，并與客戶一起提供創(chuàng)新的健康解決方案。同時，我們還致力于通過各種意義深遠(yuǎn)的項目向需... 今天的默沙東正致力于為全世界帶來健康的福音。我們?yōu)槿?40多個國家提供藥物、疫苗、生物制劑、健康消費品和動物保健產(chǎn)品，并與客戶一起提供創(chuàng)新的健康解決方案。同時，我們還致力于通過各種意義深遠(yuǎn)的項目向需要幫助的人們捐贈和提供產(chǎn)品，從而擴(kuò)展人們進(jìn)入醫(yī)療衛(wèi)生的途徑。默沙東，健康是福。
默沙東中國的總部設(shè)在上海，目前中國大陸地區(qū)共有10個分公司和3座工廠，分別在上海，杭州和南京。員工總?cè)藬?shù)超過5100人。
目前，我們在中國提供涵蓋心血管、抗感染、男性健康、女性健康、骨科、疼痛、皮膚、呼吸、?？扑幤贰⑤o助生殖、疫苗等領(lǐng)域的46種人用藥品。默沙東在中國建有三座工廠，擁有技術(shù)水平全球的生產(chǎn)設(shè)施，一流的環(huán)境標(biāo)、優(yōu)秀的生產(chǎn)工人以及高水平的管理能力，符合中國藥品生產(chǎn)質(zhì)量管理規(guī)范(gimp標(biāo)準(zhǔn))。我們還向中國市場提供46種動物健康產(chǎn)品，用以預(yù)防、治療和控制家禽家畜以及寵物的疾病。
“我們應(yīng)當(dāng)永遠(yuǎn)銘記，藥物是為人類而生產(chǎn)，不是為追求利潤而制造的。只要我們堅守這一信念，利潤必將隨之而來。僅僅發(fā)明了一種新藥，并非已經(jīng)大功告成，我們還要探索有效途徑，使默沙東的科研成果，能夠造福于全人類?！?BR> 喬治默克 一九五零年十二月一日
二、招聘職位
Safety Data Specialist(默沙東中國研發(fā)中心，研發(fā)部)
工作地點：北京
有效日期：2015年04月16日
招聘人數(shù)：多人
職位性質(zhì)：全職
職位描述：
Position Overview - Basic Functions & Responsibility
Essential function(s) includes, but is not limited to:
Under the direction of the Associate Manager/Manager, the Safety Data Specialist is responsible for analyzing, triaging, and processing all adverse experience information received for investigational and marketed products according to standard operating procedures for further reporting to the PMDA by PV of MSD. KK.
In addition, collaborates with staff within the organization as well as cross-functionally.
Primary Activities
Primary activities include, but are not limited to
1.His/Her tasks depend on the Process/role assigned: Registry and Case Processing, Junior PV Lead, Reviewer.
•Perform registry and case assignment tasks as needed.
•Perform data entry/review of all adverse experience information received and processed within internal database within the established timeframes.
•Through daily case prioritization activities, reports are completed within the established timeframes to ensure compliance with internal, business partner, and regulatory agency reporting requirements.
•Participate/perform in training and certification activities for JPV.
Other activities that the Safety Data Specilaist can assume depending of the role:
•Provide team support by ensuring the appropriate resources such as SOPs and product/protocol guidelines are available and routinely updated to ensure the quality of reports.
•Identify coordinator, team, training and/or processes related issues and escalate to JPV liaison, JPV trainer or DMC JPV management as appropriate.
•Actively participate and ensure effective communication with different roles in Japan PV Safety, DMCs and other areas.
•Perform case review of adverse experience information within the established timeframes to be compliant with internal, business partner, and regulatory agency reporting requirements worldwide.
•Assist managers with reviewing individual coordinator report quality.
2.Skills (include specific skill levels required to apply Merck Leadership Principles)
•A bachelor’s degree, preferably in a medicine, pharmacy, nursing or biological science
•Excellent organizational, workload prioritization and time management skills
•Excellent overall communication skills with advanced oral and written Japanese skills
•Excellent overall communication skills with advanced written English skills
•Advanced computer skills
•Independent, strong analytical and problem solving skills
•Good sense and awareness of regulations and policies
•Able to work under the pressure, strong sense of responsibility and accountability
•Prefer students,whose graduation years is 2015.
If you are interested in our position, please apply through https://merck.taleo.net/careersection/msd_external_career_section/jobdetail.ftl?job=RES001486&lang=en&sns_id=mailto
Senior Safety Data Specialist(默沙東中國研發(fā)中心，研發(fā)部)
工作地點：北京
有效日期：2015年04月16日
招聘人數(shù)：多人
職位性質(zhì)：全職
職位描述：
Position Overview - Basic Functions & Responsibility:
Under the direction of the Associate Manager/Manager, the Senior Safety Data Specialist is responsible for analyzing, triaging, and processing all adverse experience information received for investigational and marketed products according to standard operating procedures for further reporting to the PMDA by PV of MSD. KK .
In addition, collaborates with staff within the organization as well as cross-functionally.
Primary Activities
Primary activities include, but are not limited to:
1.His/Her tasks depend on the Process/role assigned: Trainer, Liaison, JPV Lead, Expert Reviewer, workload lead and Technical Experts.
•Perform registry and case assignment tasks as needed.
•Perform data entry/review of all adverse experience information received and processed in internal database within the established timeframes.
•Through daily case prioritization activities, reports are completed within the established timeframes to ensure compliance with internal, business partner, PMDA requirements.
•Participate/perform in training and certification activities for DMC JPV.
•Serve as local expert by ensuring the appropriate resources such as SOPs and product/protocol guidelines are available and suggesting to MSD.KK for routinely updated. Stay abreast of updates to act as resource for questions/clarifications.
•Develop and support different strategies to improve team performance.
•Continually monitor for opportunities for process improvement to improve efficiency and effectiveness and implement changes as appropriate.
Other activities that the Coordinator can be assuming depending of the role:
•Perform case review of adverse experience information within the establish timeframe to be compliant with internal, business partners, PMDA requirements.
•Assist management to ensure key performance indicator targets are met. Assist with root cause analysis and oversee implementation of actions plans when appropriate. Provide technical level process expertise and conduct periodic assessments to ensure established processes are being followed in a consistent and appropriate manner.
•Ensure the development, organization and implementation of the basic and PV Specific Training Plans for the Team.
•Perform and coordinate mentoring activities for JPV coordinators as appropriate based on operation and business needs.
•Support solve technical issues related to PV process
•Actively participate in and ensure effective communications with MSD. KK and JPV leads/ JPV reviewers/ trainers/liaisons of other DMC JPV locations to guarantee standard procedures are aligned.
2.Skills (include specific skill levels required to apply Merck Leadership Principles)
•Additional to the skills of the Safety Data Specialist,
•At least two years experience or the skill that is equal to in Pharmacovigilance.
•Excellent organizational skill.
•Be able to effectively organize, review, interpret and communicate adverse event information.
•Good sense and awareness of regulations and policies
•Excellent oral and written Japanese skills.
•Excellent written English skills.
•Prefer students,whose graduation year of 2015.
If you are interested our position, please apply via
https://merck.taleo.net/careersection/msd_external_career_section/jobdetail.ftl?job=RES001487&lang=en&sns_id=mailto
今天的默沙東正致力于為全世界帶來健康的福音。我們?yōu)槿?40多個國家提供藥物、疫苗、生物制劑、健康消費品和動物保健產(chǎn)品，并與客戶一起提供創(chuàng)新的健康解決方案。同時，我們還致力于通過各種意義深遠(yuǎn)的項目向需... 今天的默沙東正致力于為全世界帶來健康的福音。我們?yōu)槿?40多個國家提供藥物、疫苗、生物制劑、健康消費品和動物保健產(chǎn)品，并與客戶一起提供創(chuàng)新的健康解決方案。同時，我們還致力于通過各種意義深遠(yuǎn)的項目向需要幫助的人們捐贈和提供產(chǎn)品，從而擴(kuò)展人們進(jìn)入醫(yī)療衛(wèi)生的途徑。默沙東，健康是福。
默沙東中國的總部設(shè)在上海，目前中國大陸地區(qū)共有10個分公司和3座工廠，分別在上海，杭州和南京。員工總?cè)藬?shù)超過5100人。
目前，我們在中國提供涵蓋心血管、抗感染、男性健康、女性健康、骨科、疼痛、皮膚、呼吸、?？扑幤贰⑤o助生殖、疫苗等領(lǐng)域的46種人用藥品。默沙東在中國建有三座工廠，擁有技術(shù)水平全球的生產(chǎn)設(shè)施，一流的環(huán)境標(biāo)、優(yōu)秀的生產(chǎn)工人以及高水平的管理能力，符合中國藥品生產(chǎn)質(zhì)量管理規(guī)范(gimp標(biāo)準(zhǔn))。我們還向中國市場提供46種動物健康產(chǎn)品，用以預(yù)防、治療和控制家禽家畜以及寵物的疾病。
“我們應(yīng)當(dāng)永遠(yuǎn)銘記，藥物是為人類而生產(chǎn)，不是為追求利潤而制造的。只要我們堅守這一信念，利潤必將隨之而來。僅僅發(fā)明了一種新藥，并非已經(jīng)大功告成，我們還要探索有效途徑，使默沙東的科研成果，能夠造福于全人類?！?BR> 喬治默克 一九五零年十二月一日
二、招聘職位
Safety Data Specialist(默沙東中國研發(fā)中心，研發(fā)部)
工作地點：北京
有效日期：2015年04月16日
招聘人數(shù)：多人
職位性質(zhì)：全職
職位描述：
Position Overview - Basic Functions & Responsibility
Essential function(s) includes, but is not limited to:
Under the direction of the Associate Manager/Manager, the Safety Data Specialist is responsible for analyzing, triaging, and processing all adverse experience information received for investigational and marketed products according to standard operating procedures for further reporting to the PMDA by PV of MSD. KK.
In addition, collaborates with staff within the organization as well as cross-functionally.
Primary Activities
Primary activities include, but are not limited to
1.His/Her tasks depend on the Process/role assigned: Registry and Case Processing, Junior PV Lead, Reviewer.
•Perform registry and case assignment tasks as needed.
•Perform data entry/review of all adverse experience information received and processed within internal database within the established timeframes.
•Through daily case prioritization activities, reports are completed within the established timeframes to ensure compliance with internal, business partner, and regulatory agency reporting requirements.
•Participate/perform in training and certification activities for JPV.
Other activities that the Safety Data Specilaist can assume depending of the role:
•Provide team support by ensuring the appropriate resources such as SOPs and product/protocol guidelines are available and routinely updated to ensure the quality of reports.
•Identify coordinator, team, training and/or processes related issues and escalate to JPV liaison, JPV trainer or DMC JPV management as appropriate.
•Actively participate and ensure effective communication with different roles in Japan PV Safety, DMCs and other areas.
•Perform case review of adverse experience information within the established timeframes to be compliant with internal, business partner, and regulatory agency reporting requirements worldwide.
•Assist managers with reviewing individual coordinator report quality.
2.Skills (include specific skill levels required to apply Merck Leadership Principles)
•A bachelor’s degree, preferably in a medicine, pharmacy, nursing or biological science
•Excellent organizational, workload prioritization and time management skills
•Excellent overall communication skills with advanced oral and written Japanese skills
•Excellent overall communication skills with advanced written English skills
•Advanced computer skills
•Independent, strong analytical and problem solving skills
•Good sense and awareness of regulations and policies
•Able to work under the pressure, strong sense of responsibility and accountability
•Prefer students,whose graduation years is 2015.
If you are interested in our position, please apply through https://merck.taleo.net/careersection/msd_external_career_section/jobdetail.ftl?job=RES001486&lang=en&sns_id=mailto
Senior Safety Data Specialist(默沙東中國研發(fā)中心，研發(fā)部)
工作地點：北京
有效日期：2015年04月16日
招聘人數(shù)：多人
職位性質(zhì)：全職
職位描述：
Position Overview - Basic Functions & Responsibility:
Under the direction of the Associate Manager/Manager, the Senior Safety Data Specialist is responsible for analyzing, triaging, and processing all adverse experience information received for investigational and marketed products according to standard operating procedures for further reporting to the PMDA by PV of MSD. KK .
In addition, collaborates with staff within the organization as well as cross-functionally.
Primary Activities
Primary activities include, but are not limited to:
1.His/Her tasks depend on the Process/role assigned: Trainer, Liaison, JPV Lead, Expert Reviewer, workload lead and Technical Experts.
•Perform registry and case assignment tasks as needed.
•Perform data entry/review of all adverse experience information received and processed in internal database within the established timeframes.
•Through daily case prioritization activities, reports are completed within the established timeframes to ensure compliance with internal, business partner, PMDA requirements.
•Participate/perform in training and certification activities for DMC JPV.
•Serve as local expert by ensuring the appropriate resources such as SOPs and product/protocol guidelines are available and suggesting to MSD.KK for routinely updated. Stay abreast of updates to act as resource for questions/clarifications.
•Develop and support different strategies to improve team performance.
•Continually monitor for opportunities for process improvement to improve efficiency and effectiveness and implement changes as appropriate.
Other activities that the Coordinator can be assuming depending of the role:
•Perform case review of adverse experience information within the establish timeframe to be compliant with internal, business partners, PMDA requirements.
•Assist management to ensure key performance indicator targets are met. Assist with root cause analysis and oversee implementation of actions plans when appropriate. Provide technical level process expertise and conduct periodic assessments to ensure established processes are being followed in a consistent and appropriate manner.
•Ensure the development, organization and implementation of the basic and PV Specific Training Plans for the Team.
•Perform and coordinate mentoring activities for JPV coordinators as appropriate based on operation and business needs.
•Support solve technical issues related to PV process
•Actively participate in and ensure effective communications with MSD. KK and JPV leads/ JPV reviewers/ trainers/liaisons of other DMC JPV locations to guarantee standard procedures are aligned.
2.Skills (include specific skill levels required to apply Merck Leadership Principles)
•Additional to the skills of the Safety Data Specialist,
•At least two years experience or the skill that is equal to in Pharmacovigilance.
•Excellent organizational skill.
•Be able to effectively organize, review, interpret and communicate adverse event information.
•Good sense and awareness of regulations and policies
•Excellent oral and written Japanese skills.
•Excellent written English skills.
•Prefer students,whose graduation year of 2015.
If you are interested our position, please apply via
https://merck.taleo.net/careersection/msd_external_career_section/jobdetail.ftl?job=RES001487&lang=en&sns_id=mailto