Sustaining Activities & Continuous Improvement Performing RCA using Lean Manufacturing tools to reduce manufacturing failures and improve process performance.
Coordinate ECOs implementation to support process optimization and controlled manufacturing changes.
Coordinate operator training activities supporting successful implementation of manufacturing process changes.
Analyze Yield, Failure Rate, and Scrap metrics to identify improvement opportunities and support data-driven decision making.
Engineering Changes & Project Implementation Lead and coordinate manufacturing process improvements through the implementation of new materials, EFTs, fixtures, and process enhancements, ensuring successful integration into MPIs, BOMs, and Travelers.
Update IQ/OQ/PQ validation protocols to support manufacturing process changes.
Lead cross-functional projects and Management of Change (MOC) activities.
Lead scrap and failure rate reduction projects, achieving reductions in several initiatives.
Quality & Compliance Investigations and support resolution of NCRs and VRs.




Perform traceability reviews and risk assessments using PFMEA documentation.
Ensure compliance with WIs, SOPs, DOPs, and Quality System requirements. Required Skills and Experience 3 years at least as Manufacturing engineer in a medical device company (preferred)
Must be able to speak, read and write in English 85%.
Strong RCA experience
Lean manufacturing tools(yellow belt is a preferred)
Strong communications skills across team organizations and cultures.
Strong IQ/QO/PQ Validation protocols background
PFMEA
Experience with SAP transactions and Agile.
Review and/or approve ECO (Engineering Change Orders) Required Education and Training
Bachelor of Engineering in Industrial Engineering, Mechanical Engineering, Mechatronics Engineering, Electrical Engineering, Electronic Engineering or equivalent.
*the start date for this position is in January 2027 Q1
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📌 Manufacturing Engineer Ii (Centro Cívico)
🏢 Intuitive Surgical, S. De R. L De C. V.
📍 Centro Cívico