This business is in full growth mode.
They’re scaling internationally and tightening regulatory systems so they can keep pace.
And they need a Regulatory Lead to guide the way.
You won’t be buried under layers of sign-off here.
It’s a lean, ambitious team where RA is seen as a partner, not a blocker.
You’ll have direct access to leadership, commercial, R&D, and QA, influencing decisions before they’re set in stone.
What you’ll be doing:
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Keeping MDR technical documentation sharp and ready.
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Supporting UKCA, FDA 510(k), and global registrations across MEA, LATAM, APAC.
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Owning change control, being the voice of RA in NPD and design control.
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Handling distributor and notified body queries.
This position would suit someone who has been part of a small, fast paced organisation where priorities can shift and you have to adapt quickly. They’re looking for someone who is pragmatic and confident enough to influence without bulldozing.
The details:
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Senior RA Specialist / RA Lead – they aren’t rigid on title, you are the sole person responsible for regs here, but no team management.
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Salary: £65,000
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Hybrid: 3 days onsite, 2 WFH (with increase in products and NPD support, site presence is key here)
Curious? Let’s talk.
