Manufacturing quality activities, Iso 13485, Regulatory submission preparation, Design Verification, Fmea, Validation and usability testing, Risk Management per ISO 14971, Medical device software development per IEC 62304, Design Software

Rca, PLM Team Center, Globus, Capa, Six-Sigma

Quality Assurance, UI automation using Selenium, Agile DevOps delivery models, Automated test execution through Jenkins, Test design techniques

APQP, Root Cause Analysis, Supplier Audits, iso standards, Fmea, Data Analysis

regulatory standards , Version Control, Iso 13485, Fmea, Statistical testing, Reliability Testing, Capa, Risk Management, Qms, Six Sigma, CFR820, Electronic document control, Fixture qualification, Design Verification, Complaint Handling, Post Market Survey, Design Validation, Test method validation

8d problem solving , Power Bi, Microsoft Excel, Fmea, Supplier Quality Improvement, Spc, audit management, Lean Six Sigma, APQP, Regulatory and QMS Compliance, 7 Qc Tools, Minitab, KPI Analysis and Reporting, Ppap, Msa

Quality Assurance Control, Vendor Contractor Coordination, Quality documentation, Non-Conformance Reports, Civil structural finishing, QA QC procedures, Daily Quality Reports, Material Test Certificates, Inspection reports, MEP works

APQP, Iso 9001, Msa, Product Drawings, Fmea, Ppap, Spc, Measuring Instruments, 8D Reports, IATF