At a Glance
- Tasks: Lead regulatory activities and oversee document reviews for medical devices.
- Company: Global medical device company with a focus on innovation.
- Benefits: Competitive salary, mentorship opportunities, and a collaborative team environment.
- Other info: Join a small team with great potential for professional growth.
- Why this job: Make a real impact in the medical field while advancing your career.
- Qualifications: Experience in Regulatory Affairs and knowledge of EU MDR and US FDA.
The predicted salary is between 60000 - 80000 £ per year.
Cure Talent is thrilled to partner with a global medical device company seeking a Regulatory Affairs Lead in Crewe. This hands-on role involves supporting regulatory activities, with a focus on document review and international registrations.
Candidates should have proven experience in Regulatory Affairs and familiarity with EU MDR and US FDA frameworks. The successful candidate will oversee regulatory strategy, perform comprehensive document reviews, and guide submissions across various markets. Mentorship within a small team will also be part of the responsibilities.
Global Regulatory Lead – Medical Devices (EU MDR/US FDA) in Crewe employer: Cure Talent
Join a dynamic and innovative medical device manufacturer in Slough, where your role as Procurement Manager will not only enhance your career but also contribute to meaningful healthcare solutions. With a strong focus on employee development, a collaborative work culture, and the opportunity to manage significant procurement budgets, this position offers a unique chance to make a real impact while enjoying a supportive environment that values growth and excellence.
