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. CMC, regulatory, drug, device, development, registration, submission, consultant, freelance, interim, advice, affairs