Posted:2 months ago|
Platform:
Work from Office
Full Time
Role & responsibilities Knowledge on Design, develop, and improve manufacturing processes for medical devices. Support and implement lean manufacturing and Six Sigma methodologies to enhance efficiency and reduce waste. Ensure manufacturing processes comply with FDA (21 CFR 820), ISO 13485, and other relevant medical device regulations Develop and maintain process validation (IQ, OQ, PQ) and documentation. Support root cause analysis (RCA) and corrective/preventive actions (CAPA) Provide technical support for new product introductions (NPI) and process transfers Knowledge on lean tools and techniques EXPERTISE AND QUALIFICATION S VSM, process improvement, layout design
Larsen & Toubro (L&T)
Upload Resume
Drag or click to upload
Your data is secure with us, protected by advanced encryption.
My Connections Larsen & Toubro (L&T)
5.0 - 10.0 Lacs P.A.