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标题：2013默沙东中国校园招聘正式启动！
亲爱的同学们，
2013默沙东中国校园招聘自2012年9月正式启动！
今年默沙东中国为应届毕业生提供了近200个销售培训生职位（全国），3个工程师职位（杭州/上海工厂），和近15个北京研发中心的职位。我们将在上海、北京、广州、杭州、南京、沈阳、天津、郑州、济南、武汉、南昌、成都、重庆、西安、昆明、兰州16个城市举办宣讲会，我们期待宣讲会现场与同学们的互动交流！
此次默沙东中国校园招聘的官方网站是http://campus.51job.com/msd, 欢迎大家点击访问，关注网申职位详情、招聘流程及各高校宣讲会时间安排！
远见，我们共同穿越！
加入我们，成为世界领先制药企业的一员，为人类健康事业造福。
默沙东中国人力资源部门
<关于默沙东>
今天的默沙东正致力于为全世界带来健康的福音。我们为全球140多个国家提供药物、疫苗、生物制剂、健康消费品和动物保健产品，并与客户一起提供创新的健康解决方案。同时，我们还致力于通过各种意义深远的项目向需要帮助的人们捐赠和提供产品，从而扩展人们进入医疗卫生的途径。默沙东，健康是福。
默沙东中国的总部设在上海，目前中国大陆地区共有16个办公室和2座工厂，超过5000名员工。目前，我们在中国提供涵盖心血管、抗感染、男性健康、女性健康、骨科、疼痛、皮肤、呼吸、糖尿病、专科药品、疫苗等领域的38种人用药品和4种疫苗。我们还向中国市场提供46种动物保健产品，用以预防、治疗和控制家禽家畜以及宠物的疾病。
了解更多公司信息，请访问公司全球网站www.merck.com，或其中国网站www.msdchina.com.cn
招聘职位：
销售培训生 (全国200名)
我们的销售培训生计划，有机会让您成为一名为医生和病人提供药品及健康知识的专业人才。您将有机会同富有经验的团队并肩作战，只要您具备：
 本科及以上学历
 良好的人际交往和沟通能力
 良好的团队合作精神
 有效的计划和组织能力
 良好的承压能力并自我激励
工作职责：
通过专业的产品推广和学术交流，为医生提供具有价值的产品和治疗领域信息，为公司业务发展做出贡献。
 为所负责的产品制定区域业务计划
 制定目标客户及客户分类计划
 与目标客户建立合作关系
 改变和强化客户行为
 贯彻品牌策略
 进行销售跟踪及跟进工作
每位同学可最多申请两个志愿地点，最终将按照志愿顺序录取。具体地点如下：
北京，上海，江苏，安徽，浙江，广东，深圳，海南，辽宁，吉林，黑龙江，内蒙古，山西，河南，河北，山东，天津，新疆，兰州，陕西，四川，重庆，云南， 湖南，湖北，福建，江西
MMDP专员、MMDP工程师 --“制造健康”职业起航轮岗计划（杭州2名、上海1名）
MMDP（默沙东“制造健康”职业启航计划）是MSD Manufacturing Development Program的缩写。为了帮助制造部员工在职业初级阶段奠定技术、商业和领导能力的基础，默沙东制造部制定了两年的多个职位轮岗计划，为职场新人提供了一个进入默沙东公司职业发展通道的平台。
轮岗地点包括杭州和上海的制造基地，轮岗将从以下职能中选出：生产运营、质量控制、质量保证、精益/六西格玛、工程/维护等。
在两年的职业启航计划中，公司提供三次轮岗机会。期间，新员工将获得来自导师和工作伙伴的支持。在轮岗顺利完成后，公司将根据业务需求和个人发展目标，为新员工提供更为挑战的工作机会， 工作地点为杭州、上海。由此，新员工进入默沙东公司的职业发展通道，在帮助公司实现“制造健康”目标的同时保持自身的学习与发展，根据默沙东职业地图，通过定期的发展计划，持续拓展职业生涯！
MMDP Overview
• MSD Manufacturing Development Program: a 2-year program with multiple rotations.
• A portfolio of rotation experiences to develop technical, business and leadership capabilities.
• An entry step to diverse career paths across MSD Manufacturing division.
MMDP Components
• Assignments span technical, operations, and business areas. Rotations will be chosen from the following areas:
1. Production Operations
2. Quality Control
3. Quality Assurance
4. Lean/Six Sigma
5. Engineering/Maintenance (only for chemical engineering and engineering background)
6. Other relevant areas
• Buddy and mentor support
• Potential Rotation Locations: Hangzhou and Shanghai
Post MMDP Assignment
• A new job is assigned from the 3rd year in a way to best balance individual goals and business needs of the division.
• Periodical employee development plans following MSD career maps
• Work Location: Hangzhou, Shanghai
MMDP Candidates Requirements
• Bachelor's/master's degree, graduating in 2013 (major: Engineering, Pharmacy, Chemical Engineering)
• Fluent English (minimum: CET-6)
• Outstanding academic records of achievement and demonstrated leadership abilities;
• Individuals who are analytical and inquisitive about the interrelationships of various components;
• Quick learners committed to making a difference in the pursuit of manufacturing high-quality, market-leading products.
北京研发中心职位（15名）：
Associate Data Coordinator-PV
Primary Activities:
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 worldwide.
• Participate/perform in training and certification activities for PV GDMS.
Other activities that the Coordinator can be assuming depending of the role: PV lead
• Provide franchise 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.
• Oversee redistribution of workload within franchise and across franchise with manager support to ensure reporting timelines are met.
• Assist management to ensure key performance indicator targets are met. Assist with root cause analysis and oversee implementation of actions plans when appropriate.
• Identify coordinator, team, franchise, training and/or processes related issues and escalate to PV liaison, PV trainer or DMC PV management as appropriate.
• Actively participate and ensure effective communication with different roles in Global Safety, DMCs and other areas.
Reviewer
 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.
Requirements:
 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 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
Associate Data Coordinator-CT
Primary activities:
His/Her tasks depend on the Process/Role Assigned: Data Enterer, Data Reviewer, Manual Encoder, and Data Project Lead (DPL).
Data Enterer
• Performs Sponsor Data Entry as applicable per protocol-specific Data Management Plan (DMP) following protocol-specific eCRF Entry Guidelines.
Data Reviewer
• Runs data integrity check reports in accordance with protocol-specific Data Review Plan (DRP) to identify data missing, inconsistencies or departures from protocol-specific eCRF Entry Guidelines.
• Raises queries with investigational site staff and reviews responses and corresponding data corrections to confirm identified issue resolution.
• Escalates overdue items including but not limited to outstanding queries and missing visits and reports the outstanding items resolution status to the DPL.
• Assists the DPL with data management activities to ensure all identified data issues are resolved and data are clean prior to study database lock.
Manual Encoder
• Encodes medical terminologies as applicable per protocol-specific DMP and Global Encoding Practices Document.
• Runs encoding check reports in accordance with protocol-specific data review plan to identify encoding issues including but not limited to unspecified encoded terms, encoded term inconsistencies or departures from protocol-specific eCRF Entry Guidelines.
• Raises query with investigational site staff and reviews responses and corresponding data corrections to confirm resolution.
DPL is the Lead Data Reviewer for a protocol within a Data Management Center (DMC). His/her responsibilities include but not are not limited to:
• Ensure compliance of standard key performance indicators according to process expectations at protocol level.
• Monitors data quality and cycle-time performance measures to ensure compliance and perform root cause analysis and implement action plan as needed.
• Coordinates and mentors data reviewers who work in his/ her protocol to ensure their compliance with SOPs, protocol-specific DMP and DRP.
• Communicates with sites and country Clinical Research Associates to ensure timely resolution of data issues and overdue items including but not limited to outstanding queries and missing visits.
• Works with the global study DPL team to provide protocol data management progress update at DMC level and discuss identified scientific and technical issues for resolution.
• Proactively communicates with DMC management to share project status, risk assessment and outstanding item resolution status.
Requirements:
Education:
 At least B.A. or B.S. degree, preferably in Medicine, Pharmacy, Nursing, Biological Sciences, or health care related discipline
Knowledge and Skills:
 Self-motivated, excellent in work planning and time management
 Fluent oral and written English skills
 Good sense and awareness of regulations and policies
 Able to work under pressure and change environment with flexibility
 Good communication skills with the ability to communicate with both the technical and business areas.
宣讲会行程
具体行程安排请以网站公布为准http://campus.51job.com/msd
城市 宣讲学校 宣讲会日期 时间 宣讲会场地
上海 复旦大学医学院（枫林校区） 10月17日 18:30 明道楼二楼多功能厅
上海 上海大学（宝山校区） 10月18日 18:30 J101室
杭州 浙江大学（紫金港校区） 10月16日 18:30 国会中心138
南京 中国药科大学（江宁校区） 10月16日 18:30 江宁校区C101教室
广州 中山大学（南校区） 10月15日 19:00 岭南学院陈捷荣三楼报告厅
广州 南方医科大学 10月16日 18:30 春江厅
广州 广东药学院（大学城校区） 10月17日 18:30 国际会议中心(大学城校区)
西安 西安交通大学 10月29日 19:00 本部教2-100（德育基地）
兰州 兰州大学（医学校区） 10月15日 19:00 大学生活动中心
南昌 南昌大学 10月16日 18:30 国际交流中心多功能厅
武汉 武汉大学 10月18日 19:00 学生就业服务中心第二报告厅
重庆 西南大学 10月16日 18:30 招就处楼报告厅1(北校区)
昆明 云南大学 10月18日 18:30 科学馆一楼报告厅
成都 四川大学（望江校区） 10月22日 18:30 文华活动中心二楼报告厅（望江校区）
天津 天津大学 10月9日 18:30 多媒体教室24楼405
济南 山东大学（中心校区） 10月18日 18:30 邵逸夫科学馆报告厅
郑州 河南中医学院 10月11日 18:30 河南中医学院新校区A区353教室
沈阳 沈阳药科大学 10月23日 18:30 本部新二教室
北京 北京中医药大学 10月24日 19:00 逸夫馆一层报告厅 |
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