We have a current opportunity for a Regulatory Affairs Consultant on a contract basis for 12 month, starting as soon as possible in the Basel area.
Responsibilities:
- Create, prepare, and update regulatory documents
- Experience with pharmaceutical and medical device products (IVD)
- Liaise with clients/customers to minimize risks and assure that products meet up-to-date requirements
- Vigilance and technical documentation
- Ensure GMP qualified production and compliance
If you are available to start a new project, please apply directly online via the link.
