cmdr , Documentation Skills, FDA 21 CFR 820, Iso 13485, Analytical problem-solving, Capa

equipment qualification, Documentation, Sops, calibration verification, audits, Capa, GxP regulations

Ms Office, APQP, Iso 13485, Iso 9001, Fmea, Ppap, quality management software tools, IATF 16949

statistical data analysis , Process Control Systems, Risk Analysis, CAPA Systems, quality engineering, Report Writing

calipers , Micrometers, Quality standards, Root-cause investigations, Iso 13485, Inspection procedures, microsoft software, Safety

IQ OQ PQ, Root Cause Analysis, NPI Validations, Cmm, MSA Calibration, Cnc Machining, Optical Surface Roughness Gauges, FAI, Machining Transfers, Ppap, Inspection and Measurement Systems, CAPA Management, Quality Control

Iso 27001, Microsoft Office, Rca, Iso 14001, Iso 9001, presentation tools, 8D, RBA code of conduct, Capa

Iso 13485, Iso 9001, Root Cause Analysis, Validation and Verification Principles, Supplier Audits, Quality Management System, Corrective Actions, Supplier Quality Management, Technical Writing

Adverse Event Reporting, Iso 13485, FDA 21 CFR Part 820, Document Control, Non-conformance management