Réf. : ALTO-CH-RAS 23/12/2021
context
Localisation
Neuchâtel (NE)
Start date
Ideal profile
Educational background
Academic degree(s) with focus in pharma, biotech, regulatory affairs or any other related field.
Fluency in English and French are required, German would be an asset.
Experience
First experience in regulatoy affairs in the pharmaceutical, biotech, chemical or similar industries.
You have good analytical and synthesis skills as well as diligence and team spirit
Only applicants with Swiss or EU/EFTA citizenship or candidates with an existing and valid residence and work permit in Switzerland will be considered.
Proposed project
To strengthen our team in Switzerland, we are currently looking for a Regulatory Affairs Specialist (m/f/x) to start asap.
About the job :
As a member of the Regulatory Department, you will support the project manager in charge of medical devices.
- Prepare approval files, check the technical file and design control (DHF) and work on the labelling of medical devices.
- Ensure vigilance and liaison with regulatory authorities and/or certification bodies.
- Apply MDR and ensure the regulatory and normative monitoring
- Participate in the management of the classification of products according to the CLP regulation.
WHAT WE OFFER
- A permanent contract and innovative projects
- An attractive remuneration policy
- Personalized management and continuous learning to develop your career
- Great team spirt and an integration within the "Tribe"
If you want to join a dynamic and ambitious company? Altogen is made for you. Send us your application.