01 April 2018
01 October 2019
2690€ (Non-contractual allowance laid down by decree and order, whose amount may vary in particular depending on the changes to the reference scale, the location of the position and the cases for deductions set out in the texts)
Sanofi is a global life sciences company committed to improving access to healthcare and supporting the people we serve throughout the continuum of care. From prevention to treatment, Sanofi transforms scientific innovation into healthcare solutions, in human vaccines, rare diseases, multiple sclerosis, oncology, immunology, infectious diseases, diabetes and cardiovascular solutions and consumer healthcare. More than 110,000 people at Sanofi are dedicated to make a difference in patients’ daily life, wherever they live and enable them to enjoy a healthier life.
Program SaVIE (VIE of Sanofi) is available to citizens of the European Economic Area (EU + Norway, Liechtenstein and Iceland) aged between 18 and 28.
PLEASE NOTE that since the VIE Program is primarily an international development program, candidates cannot apply to a VIE assignment in their own country of citizenship.
PLEASE NOTE that applications that are only submitted in French cannot be considered by our non-French speaking partners at Sanofi worldwide. Therefore, only applications that are submitted in English will be considered.
We are looking for a candidate for a VIE mission of:
Regulatory Affairs Consultant - VIE Contract (W/M)
Full integration into the Regulatory Affairs team of the Swiss affiliate.
The VIE will benefit from the experience of the team in place and will be trained in all the Swiss regulatory activities required for the position.
The VIE will participate in the daily activities, meetings and strategic thinking of the Regulatory Affairs Department and will be in charge of managing a product portfolio.
He will be in direct contact with the Swiss health authorities (Swissmedic).
Participation in the main activities and responsibilities of the Regulatory Affairs Department:
- Preparation and submission of regulatory variations (Labeling, CMC) to Swissmedic
- Follow-up of submissions
- Management of Corporate requests concerning registered files
- Preparation and submission of special requests (co-marketings, Marketing Authorisation renewals, etc.)
- Participation in strategic registration discussions (within the department, with marketing, medical, logistics, etc.)
- Participation in specific projects (related to service, subsidiary or new products)
- Update or drafting of internal procedures
- Continuous updating of the Group and local databases
- Initiation and handling of submissions in eCTD (publishing)
- Scientific university education (Master's degree required), preferably pharmacy studies, industry option
- Previous experience in Regulatory Affairs would be an asset
- At ease with computers in general and the use of common software (Word, Excel, PowerPoint)
- Good oral and written communication in French and English required, knowledge in German would be an asset
Job related skills required:
- Critical mind
- Conscientious, accurate, with a sense of organization and analysis
- Team spirit