Beschreibung
This is the opportunity to join a world leading medical device company for a 9-12 month contract. You will be working across all stages of the product lifecycle for a portfolio of high-risk devices.Requirements:
- Minimum 3 years experience: Providing product development support throughout all product lifecycles stages for high risk devices (class IIb minimum).
- Participate in all regulatory activities in various phases of design controls.
- Minimum 3 years experience: Technical files: new and existing products, STED, declaration of conformity.
- Minimum 3 submissions: USA (FDA) 510(k) submission (drafted, submitted and reviewed).
If you or someone you know is interested, please get in touch with your CV to