At a Glance
- Tasks: Lead regulatory affairs for medical devices and establish core processes across EMEA.
- Company: Join a forward-thinking company dedicated to innovation in healthcare.
- Benefits: Attractive salary, flexible working options, and opportunities for professional growth.
- Other info: Collaborative environment with a focus on quality and compliance.
- Why this job: Shape the future of medical device regulation and make a real impact.
- Qualifications: Proven experience in regulatory affairs and strong leadership skills.
The predicted salary is between 60000 - 80000 £ per year.
Jobtailor is seeking an experienced Regulatory Affairs leader to set up the EMEA function, establish core processes and an in-region quality management system, and take on the UK Responsible Person role with MHRA. The role involves building scalable expansion processes, aligning UK/EU regulatory positions, and shaping both EMEA and global RA strategy for future growth.
You will work in close partnership with the Quality team to drive post-market activities, and drive governance across UK and EU.
We think you need these skills to ace EMEA Regulatory Lead: Build & Scale Medical Devices RA
Regulatory Affairs Expertise
Quality Management Systems
Process Development
UK Responsible Person Role
EMEA Regulatory Compliance
Strategic Planning
Post-Market Surveillance
