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 25 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 Proficient in Microsoft Office