

A global engineering and technology solutions provider specializing in digital, manufacturing, GIS and semiconductor services.
Ensure inspection equipment calibration and proper handling.
Document results accurately in inspection reports and quality systems.
Identify nonconformances and support root cause analysis.
Maintain compliance with ISO 13485 and FDA 21 CFR 820 requirements.
Review inspection records, drawings, and specifications.
Conduct visual, dimensional, and functional inspections per defined procedures.
2–4 years’ experience in quality inspection (medical device preferred).
Understanding of ISO 13485 and GMP requirements.
Strong attention to detail and documentation accuracy.
Diploma/Bachelor’s degree in Engineering, Mechanical or related field.
Knowledge of measuring instruments (calipers, micrometers, gauges).