Statistical Analysis, Process Capability Improvement, Iso 13485, Fmea, FDA QMSR 21 CFR Part 820, Spc, Gmp, validation protocols, Lean Kaizen, Msa, CAPA Management, Audit Participation

vision systems, Process Flow Diagrams, Fmea, Cmm, Spc, work instructions, Control Plans, IATF 16949, 8D, Micrometer, height gauge, 5-Why, Iso 9001, Doe, Ishikawa diagram, Msa, CPK

sop development , Iso 14971, Iso 13485, 21 CFR Part 820, Design Controls, Risk Management, Change Control, Document Management Systems, FDA Quality System Regulations, Quality Tools, Quality Documentation, Six Sigma

measurement tools , Ms Excel, ETQ, Sampling Plans, Engineering Drawings, Iso 13485, Iso 9001, Spc, basic statistical analysis, IATF 16949, inspection methods

Change Control, Iso 9001, Fmea, inspection and measurement equipment, Control Plans, Internal Auditing, 8D, FAI, Capa

Iso 9001, Iso 14001, Fmea, ISO 45001, Spc, Control Plan, 8D problem-solving methodology

Microsoft Office, Quality Management Systems, Statistical Tools, IEC 62941, 8D problem solving methodology, Iso 9001, Fmea, Spc, Msa

manufacturing processes , site operations , Emergency Response, Problem Solving, Quality Systems, Root Cause Analysis, CAPA management, Lean Management, Deviation investigation, Production Management, Project management, Digital Fluency, Risk Awareness, Electronic batch records, Project Coordination, data integrity, Technical transfer activities, Financial Acumen, Quality Compliance, Regulatory Compliance, SAP manufacturing execution systems, Validation trials

Non-Conformance Material Review (NCMR) Management, Non-Conformance Management, Quality Systems, Quality-related Process Product Change Notification, Quality Operations Process, Quality report management, Disposition direction on material under NCMR, Data analysis and trend reviews, Inventory transfer