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Job description
Trinity Biotech seeks a Site Head of Quality to oversee the development, implementation, and maintenance of the Quality Management System ensuring compliance with ISO 13485 and FDA 21 CFR Part 820. This role drives continuous improvement and upholds the highest quality standards for medical devices.
You will lead the QA team, manage supplier relationships, monitor KPIs, supervise audits and CAPA, and collaborate with R&D, manufacturing, and regulatory affairs to ensure quality is embedded across
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Worksite address
kansas city, MO, 64101, US
Who can apply
Review the original listing for work authorization, qualifications and employer requirements.