Manufacturing quality engineering
L&T Technology Services
Contract: 12+ months with possible extension
Lead RCA using 5 Whys, Fishbone, Fault Tree Analysis, 8D, and DMAIC .
Ensure CAPA and Quality System documentation meets ISO 13485 and FDA 21 CFR 820 requirements.
Partner with Manufacturing, Operations, R&D, and Supplier Quality teams to implement corrective actions.
Perform data trending/statistical analysis to verify CAPA effectiveness and support audit readiness.
Key Requirements: 5-7+ years of relevant Quality Engineering experience.
Bachelor's degree in Engineering preferred/required based on client requirements.
Medical device or regulated manufacturing experience.
Vacancy posted 2 days ago
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