Can Read And Comprehend Production Prints, Standards, And Check Sheets. Proficient With Creating\Writing Various Quality Documentation I.E. Ppaps (Production Part Approval Process) Levels 1 Through 5 And, Supporting Information, Depending On Level Of Submission Required. Design Records, (Ballooned Part Drawing To Match Inspection Results) Engineering Change Documents, (Showing Detailed Description Of A Change), Customer Engineering Approval, (Engineering Trial Of Sample Production Parts Done By Customer "Temporary Deviation" Is Required To Send Parts Before Ppap Is Complete), Design Fmea, (Failure Mode And Effect Analysis, Specific To The Design Stage, Allows Design Team Documentation Of Predicted Failures), Process Flow Diagrams, (Shows All Steps Required In Manufacturing Of The Part), Process Fmea, (Evaluates Each Step In The Process To Indicate What Could Go Wrong), Control Plan, ( Provides More Details On How Issues Are Checked In Inspection, Assembly Process And Finished Product Then Pfmea) ,Measurement System Analysis Studies, Gauge R&R, Dimensional Results, Material Performance Test Results, Initial Process Studies, Qualified Laboratory Documentation, Appearance Approval Report, Sample Product, Master Sample, Checking Aids, Records Of Compliance With Customer- Specific Requirements, And Psw(Part Submission Warrant) Isir (Initial Sample Inspection Report), Inspection Standards, Operation Standards, Material Certificates. I Have Many Years Of Experience With A Vast Range Of Quality Test Equipment And Processes To Include But Not Limited To:
