What are the responsibilities and job description for the Manufacturing Quality Engineer position at L&T Technology Services?
Position: Engineering – Sr Engr
Contract: 12 months with possible extension
Role Overview:
- Own CAPA records end-to-end, including investigation, root cause, corrective actions, effectiveness checks, and closure.
- 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.
- Maintain accurate records in eQMS systems such as TrackWise, MasterControl, or equivalent.
Key Requirements:
- 5–7 years of relevant Quality Engineering experience.
- Bachelor's degree in Engineering preferred/required based on client requirements.
- Strong CAPA, NCR/NCMR, RCA, and technical documentation experience.
- Medical device or regulated manufacturing experience.
- Experience with ISO 13485 and FDA 21 CFR 820.
Salary : $50 - $55