Posted:1 day ago|
Platform:
On-site
Full Time
Conduct visual, dimensional, and functional inspections per defined procedures.
Review inspection records, drawings, and specifications.
Document results accurately in inspection reports and quality systems.
Identify nonconformances and support root cause analysis.
Ensure inspection equipment calibration and proper handling.
Maintain compliance with ISO 13485 and FDA 21 CFR 820 requirements.
Diploma/Bachelor’s degree in Engineering, Mechanical or related field.
2–4 years’ experience in quality inspection (medical device preferred).
Knowledge of measuring instruments (calipers, micrometers, gauges).
Understanding of ISO 13485 and GMP requirements.
Strong attention to detail and documentation accuracy.
Cyient
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