At a Glance
- Tasks: Lead the EU regulatory strategy for a groundbreaking Class III medical device.
- Company: Join a global leader in healthcare innovation and make a difference.
- Benefits: Competitive salary, flexible working options, and opportunities for professional growth.
- Other info: Collaborative environment with a focus on impactful regulatory programmes.
- Why this job: Shape the future of healthcare by ensuring compliance for innovative medical devices.
- Qualifications: Expertise in EU MDR 2017/745 and experience with Notified Bodies required.
The predicted salary is between 63000 - 77000 £ per year.
Cure Talent partners with a global medical device organisation recognised as a leader in healthcare innovation. This role leads the EU regulatory strategy for a brand new Class III device, from early development through to submission and approval, coordinating with global RA, Clinical Affairs and R&D teams.
The ideal candidate will have proven EU MDR 2017/745 expertise, experience with Notified Bodies, and a track record of delivering high-visibility regulatory programmes within a large.
EU Regulatory Lead – Class III Medical Device (MDR) in England 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.
