At BioTalent, we are working with a client to fill their newly created RA specialist position. They are a transformative Device company focused on large range of products with a large customer base
This role will offer you
* To work in a fast-paced environment and the ability to take a huge impact.
* A chance to work across both NPD and an existing product line.
* Exposure to high visibility from the senior leadership team.
You will be responsible for
* Produce new and updating CE marking for local and international registrations
* Support with writing new risk management activities
* Be part of the team for their MDR transition
You will bring the following
* Hands on Regulatory experience within a device or IVD products in an ISO13485
* CE marking within EU with ideally international experience
* Experienced in ISO14971 risk management
* Both German and English speaking
If you want to be part of an innovative thinking, growing company where you can grow and expand your current knowledge, GET IN TOUCH - Please email me at michael.kakoullis@biotalent.com or on +41215608532 if you think you could be a good match.