Establish the timetable for the execution of projects linked to the development and manufacture of medical devices.
Create, update and monitor planning to reduce the risk of delays.
Create, update and monitor planning to reduce the risk of delays.
JOB DESCRIPTION
RELATIONSHIPS AND/ OR FUNCTIONAL
Reporting to the Program Director
exchange information with internal R&D and Production departments to collect and analyze status and progress data
and also with cross-functional departments: Quality, Regulatory Affairs, Industrialization and Clinical
exchange information with internal R&D and Production departments to collect and analyze status and progress data
and also with cross-functional departments: Quality, Regulatory Affairs, Industrialization and Clinical
MAIN MISSIONS & ACTIVITIES
- Lead the program planning process based on the plannings of the various program projects
- Build and set up plannings for the program’s various projects
- Highlight and communicate to stakeholders the connections between the various plannings
- Anticipate and analyze deviations and identify the consequences in terms of delays
- Adjust plannings and alert parties concerned
RESPONSIBILITIES
Keeps program schedules up to date.
Ensures program planning is consistent with activities, projects and the program roadmap.
Ensures program planning is consistent with activities, projects and the program roadmap.
AUTONOMY
Alert the program Director in case of delay
SKILLS REQUIRED
- Theoretical knowledge
Formation supérieure technique et ou scientifique (type ingénieur)
Bachelor’s / Master’s degree Engineering
- Practical knowledge
1 to 3 years’ experience, which may include years of apprenticeship
Knowledge of implantable medical device design would be a plus
Good command of IT tools (MS project, pack office)
English (reading, writing, speaking)
CANDIDATE
To apply for this vacancy, please send your application to jobopportunities@affluentmedical.com