Job Purpose:
Our client a medical device company are seeking a QA Technician to provide day-to-day quality support on the manufacturing lines.
This role ensures compliance with ISO *****, FDA 21 CFR Part 820, EU MDR, and the internal Quality Management System.
You will be responsible for production audits, non-conformance handling, quality metrics reporting, and supporting continuous improvement and compliance activities.
Key Responsibilities:
Perform production audits, inspections, and ensure Good Manufacturing & Documentation Practices (GMP/GDP)
Manage non-conforming materials and support root cause investigations
Maintain and report quality metrics
Support internal/external audits and regulatory compliance
Assist in documentation, process improvements, and lean initiatives
Education and Experience:
Degree in a quality-related discipline is desirable
2–5 years' experience in a regulated manufacturing environment (Medical Device or Pharma)
Strong knowledge of ISO *****, FDA 21 CFR Part 820, and EU MDR
Excellent communication and documentation skills
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