Regulatory Specialist

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 or on if you think you could be a good match.