Our client is seeking a skilled and dynamic Senior Regulatory Affairs Specialist for a temporary position. As a pivotal member of their team, you will play a crucial role in ensuring compliance with medical device regulations, particularly the EU Medical Device Regulation (MDR). The ideal candidate for the Senior Regulatory Affairs Specialist role will possess 3-5 years of experience in regulatory affairs, with a strong background in EU MDR, regulatory change assessment, and submissions for both US and EU markets. If you are passionate about driving continuous improvement initiatives and thrive in a collaborative, cross-functional environment, we encourage you to apply for the Senior Regulatory Affairs Specialist position.Duties:Collaborate with multiple business units to develop, update, and enhance regulatory affair processes.Assist in implementing strategies and operations for regulatory affairs activities, including product registration submissions, progress reports, supplements, amendments, or periodic experience reports.Update and develop procedures for regulatory affairs to align with changes in the regulatory landscape, particularly EU MDR.Identify opportunities for regulatory affair process enhancement and drive changes to completion.