Cure Talent, partnering with a global medical device company, is seeking a Regulatory Affairs Lead to drive regulatory strategy and execution across portfolios. You will act as a senior individual contributor, focusing on document review, international registrations, and defining regulatory pathways for Class III devices.
You will collaborate with senior stakeholders, mentor peers, and contribute to process improvements while navigating EU MDR and US FDA frameworks.
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Regulatory Affairs Lead — Medical Devices (EU MDR & FDA) in Coalville employer: Cure Talent
Join a leading global medical device company that is dedicated to innovation and excellence in life-saving technologies. As a Senior Regulatory Affairs Specialist, you will thrive in a collaborative work culture that values mentorship and continuous improvement, while enjoying opportunities for professional growth in a dynamic environment. Located in a vibrant area, this role offers the chance to make a meaningful impact on product portfolios and regulatory strategies, ensuring your contributions are recognised and valued.
