Regulatory CMC Consultant - Device/Combination Product

We are looking to identify experienced regulatory professionals for a new consultation project that will begin in January 2026.

This consultant will provide expertise and advice on CMC regulatory aspect related to devices / combination products. This will relate specifically from a development perspective across global markets.

The position can be fully remote, working European hours and the initial duration of the contract will be 6 months - although, there is a high likelihood of renewal.

What do you need to bring?

* 10 years+ experience in the development and registration of medical devices / combination products

In submitting your profile, please share the following details:

* Specific CMC experience within device / combination products

* Global market experience

* Location

* Expected daily rate

* Location

For further details, please contact Mark Bux-Ryan or apply.

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