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.