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QA Specialist
Join a Leading Centre of Excellence in Clinical Research
A unique part-time opportunity has opened up for a detail-oriented and proactive Quality Assurance Specialist to contribute to a world-renowned research hub driving breakthroughs in cancer diagnostics and treatment.
In this pivotal role, you’ll be part of a specialised team ensuring compliance with Good Clinical Practice (GCP) in clinical trials. From managing internal audits and non-conformances to guiding teams on regulatory standards, you’ll be at the heart of initiatives that directly support patient-focused research.
The Role:
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Ensure compliance with GCP and clinical trial regulations
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Conduct internal audits and manage documentation reviews
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Handle non-conformances and support CAPA implementation
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Maintain and improve Quality Management System (QMS)
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Activate and track projects in the Laboratory Information Management System (LIMS)
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Provide QA guidance and basic training to staff
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Support external audit preparation and regulatory inspections
You’ll Bring
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Experience in QA or compliance in GxP-regulated labs
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Working knowledge of GCP, CAPA, internal audits, and quality systems like LIMS and QPulse
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A science background (BSc or equivalent experience) and a meticulous eye for detail
This is more than a job—it’s your chance to make a meaningful impact while working with brilliant minds on some of the most exciting challenges in biomedical science today.
Apply now and be part of something that matters
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