Hover or tap a row for full statistics (EUR / month on this chart).
Salary analysis
Compared with the selected benchmark ("All roles in London, United Kingdom"), this listing's salary midpoint is about 94% lower. The offer sits below the benchmark range (€3,847–€15,737). The listed pay band (€459–€729) is tighter than the benchmark, which suggests lower salary variability. This benchmark is based on 10 comparable listings.
| Market | Lower bound (25th percentile) | Median | Upper bound (75th percentile) |
|---|---|---|---|
| All roles in London, United Kingdom | €3,847/per month | €7,124/per month | €15,737/per month |
This vacancy centers on building the EMEA Regulatory Affairs function from the ground up, including taking on the UK Responsible Person role, managing the MHRA relationship, and aligning regulatory strategy across UK, EU, and other jurisdictions. The candidate should have 8+ years in medical device regulatory affairs with at least 5 in UK/EU/EMEA-regulated devices, experience leading CE marking under EU MDR, and hands-on experience with AI-assisted regulatory tasks.
Job Details
Responsibilities
- Set up the EMEA RA function and in-region quality systems
- Hold the UK Responsible Person role and liaise with MHRA
- Develop country-by-country expansion processes
- Align regulatory positions across UK, EU and other jurisdictions
- Shape both EMEA and global RA strategy and future team
Requirements
- 8+ years in medical device regulatory affairs
- at least 5 focused on UK, EU or EMEA-regulated devices
- CE marking under EU MDR experience
- experience engaging with MHRA or other authorities in EMEA
- Statutory UK Responsible Person eligibility
- degree in a relevant field
Education Level
No degree required
| Location | Active listings |
|---|---|
| Remote - Global | 1 |
| Role type | Active listings |
|---|---|
| Quality Program Manager | 1 |
| Role level | Active listings |
|---|---|
| Senior | 1 |
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