At a Glance
- Tasks: Lead the EU regulatory strategy for a new Class III medical device under MDR.
- Company: Global medical device organisation with a strong focus on innovation.
- Benefits: Competitive salary, health benefits, and opportunities for professional growth.
- Other info: Join a dynamic team and contribute to groundbreaking medical advancements.
- Why this job: Make a significant impact in the medical field by ensuring device compliance and safety.
- Qualifications: Experience in regulatory affairs and knowledge of EU MDR requirements.
The predicted salary is between 60000 - 80000 £ per year.
Cure Talent is partnered with a global medical device organisation to recruit a Regulatory Affairs Manager to lead the EU regulatory strategy for a new Class III device under MDR.
The role focuses on project leadership within a large, international regulatory function.
You will define approval pathways under MDR 2017/745, manage interactions with Notified Bodies and authorities, and collaborate with R&D, Clinical and Global RA teams to drive submissions from concept to approval.
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Regulatory Affairs Lead: EU MDR for Class III Devices 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.
