Senior Regulatory Affairs Specialist, Global Submissions

Cure Talent is seeking a Senior Regulatory Affairs Specialist in Crewe, England, to join a renowned medical device company. In this hands-on role, you'll support regulatory strategies, manage global submissions, and ensure compliance with EU MDR and US FDA regulations. Successful candidates will have strong experience in regulatory affairs and document review, supporting continuous improvement processes. Join the team and contribute to life-saving technologies in an impactful environment.
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