Senior Regulatory Affairs – EU IVDR Perf. Studies; Remote
Milton Keynes, Buckinghamshire, MK10 0BX, England, UK
Listed on 2026-09-18
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Healthcare
Medical Science Liaison
EPM Scientific, in partnership with a Global Diagnostics Manufacturer, seeks a Sr. Regulatory Affairs Specialist to support EU Competent Authorities and MHRA with performance study applications for CDx programs.
This contract role is 12 months, predominantly remote with occasional on-site presence in the north of England. You will plan and coordinate regulatory submissions, maintain IVDR documentation, and align strategy with cross-functional teams (Clinical, QA, R&D, and Regulatory).
The Senior Regulatory Affairs – EU IVDR Perf. Studies (Remote) role at EPM Scientific is now open for applications in United Kingdom.
Learn more about the Senior Regulatory Affairs – EU IVDR Perf. Studies (Remote) role in the description above.
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