The Role:
An Active Device company that is specialised in ophthalmic active devices working with Class II and Class IIB products is seeking for a RA consultant.
The project is for 12-months to ensure the RA documentation is aligned with FDA regulations- the position will be based in the Frankfurt area.
Responsibilities:
- Working with active devices class II / IIB products and FDA Regulations
- Maintaining of Regulatory Files
- Provide support for currently required products and registration with distributors
- Collating necessary information for global regulatory registrations
- Working with license renewals
Skills and Experience Required
- FDA Regulations experience
- Home-based working flexibility
- Able to start immediately
- Fluent in German and English
What this Job Offers You
- An opportunity to work on a RA project specialising in Class lla and Class 2b products, with some flexibility for home-based working.
- Gain experience working with FDA regulations
How to apply
Apply here if you are interested in this opportunity please apply on the link below or if you would like a confidential discussion about your career opportunities please contact a member of EPM Scientific.
Disclaimers if necessary: Must have the rights to Work in Germany.
