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/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) employer: Cure Talent
As a leading global medical device company based in Crewe, we pride ourselves on fostering a collaborative and innovative work culture that empowers our employees to excel. With a strong focus on professional development, we offer mentorship opportunities and support for continuous learning, ensuring that our team members grow alongside the company. Our commitment to employee well-being is reflected in our comprehensive benefits package and a supportive environment that values work-life balance.
