Company Description

Technopath Clinical Diagnostics, part of LGC Clinical Diagnostics, develops and manufactures a comprehensive range of diagnostic quality solutions used by laboratories across the life sciences industry.

Our work supports confidence in diagnostic results and contributes directly to improved patient outcomes. We do this by combining scientific expertise, robust quality systems and a culture shaped by our values: Passion, curiosity, integrity, brilliance and respect.

Job Description

This is a hands‑on regulatory role where your expertise directly supports product compliance, patient safety and business continuity.

As Regulatory Affairs Specialist, you will partner closely with Quality, R&D and Operations teams to apply regulatory requirements across our in‑vitro diagnostic portfolio. During this fixed‑term period, you’ll play an important role in sustaining CE marking, supporting IVDR activities...