Regulatory Affairs Manager
Regulatory ownership for a device portfolio across Gulf markets.
What the role involves
- Own submissions and renewals across GCC authorities.
- Keep technical files audit-ready as a standing state.
- Advise commercial teams on what can and cannot be claimed.
What we are looking for
- Medical device regulatory experience, ideally GCC or EU MDR.
- Comfort managing several authorities and timelines at once.
- Precision in written work — it is most of the job.
What happens after you apply.
Within 3 days
A consultant reads your application and calls you if there is a fit. If there is not, you get an email that says so plainly.
Screening call
Twenty to thirty minutes. The role in detail, the actual salary band, and what you need from your next move.
Structured interview
The same questions every candidate for this role is asked, so the comparison is fair. Bring two or three specific examples.
Submission, with your yes
Nothing goes to the employer until you agree to it. We brief you on the panel and the format before you meet them.
Apply for Regulatory Affairs Manager.
Four fields and your CV. A consultant — not an automated screen — reads every application and answers within three working days.
- Your CV goes nowhere without your explicit yes on this role.
- The salary band is disclosed on the first call.
- Feedback either way if you reach interview.
Similar mandates.
Not quite it?
Most of our mandates are never advertised. Register once and a consultant calls you when something matches.