At a Glance
- Tasks: Lead regulatory strategies for FDA approvals and international clearances in medical devices.
- Company: DEKA Research and Development, a leader in innovative medical technology.
- Benefits: Competitive salary, flexible work options, and opportunities for professional growth.
- Other info: Join a dynamic team dedicated to advancing medical technology.
- Why this job: Make a difference in healthcare by ensuring safe and effective medical devices reach the market.
- Qualifications: Experience in regulatory affairs and strong project management skills.
The predicted salary is between 60000 - 80000 £ per year.
DEKA Research and Development is seeking a Regulatory Affairs Project Manager to develop and execute regulatory strategies for FDA approvals and international clearances. The role involves leading submission efforts (510(k)s, PMAs, IDEs) and guiding regulatory compliance.
We think you need these skills to ace Regulatory Strategy Lead, Medical Devices
Regulatory Strategy Development
FDA Approval Processes
International Clearances
Submission Management
510(k) Submissions
PMA Submissions
IDE Submissions
