JUNIOR MANAGER REGULATORY AFFAIRS

Job description

Enterprise:
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.
At Sanofi diversity and inclusion is foundational to how we operate and is embedded in our Core Values. We respect the diversity of our people, their backgrounds and experiences. We recognize to truly tap into the richness diversity brings we must lead with inclusion and have a workplace where those differences can thrive and be leveraged to empower the lives of our employees, patients and customers.
We are looking for a candidate for a VIE mission of:
Junior Manager Regulatory Affairs
- VIE Contract (W/M)
Job Details:
- Support lifecycle management for vaccine portfolio
- Preparation of labelling changes and supporting the implementation in packaging material
- Support the business unit with regulatory guidance
- Interaction with national competent health authority as required
- Database management
- Work within an international team
- Other key responsibilities as assigned
Candidate:
Education/ Experience:
- Master Degree in Natural Sciences, Pharmaceutical or Health related field
- Experience & knowledge of regulatory affairs/ lifecycle management of pharmaceutical products is a plus
- Ability to work effectively within cross-functional teams as well as independently
Languages:
- English is a must with German on advanced level, French is a plus