Regulatory Affairs Project Manager
Closing Date: 23rd February 2023
* Proven experience of EU and US medical devices regulations* Experience of ISO 13485 QMS.* Compilation of Technical Files/Documentation to MDD 93/42/EEC or MDROur client is seeking a Projects Manager - Regulatory Affairs to provide leadership and oversight of regulatory projects and staff including new or renewed product registrations and claims in accordance with regulatory requirements. This role will be reporting to ...