Errington Legal is partnering with a global biotech to hire a European Regulatory Lead, based in London or Cambridge with hybrid working. The role focuses on regulatory and quality matters for medical‑device products, including RUO and clinical offerings, and advises the business on complex frameworks across the EMEALA region.
You will collaborate with Reg Affairs, Med Affairs, Marketing and Compliance, and support regional submissions, market access strategies and post‑market matters.
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