Kattia A.
Supplier QA at Bourns, Inc.- Claim this Profile
Click to upgrade to our gold package
for the full feature experience.
Topline Score
Bio
Credentials
-
Auditor Interno IATF 16949:2016
Soluciones Integrales a Sistemas de Calidad y Ambiente (QESS) -
Auditor Interno ISO 14001:2015
Soluciones Integrales a Sistemas de Calidad y Ambiente (QESS) -
Core Tools Overview
Quality House Automotive & Aerospace Division -
Fundamentals of GD&T 2009 Skills Assessment
Effective Training Inc., an SAE International Company -
IATF 16949:2016 para Mandos Medios
Soluciones Integrales a Sistemas de Calidad y Ambiente (QESS) -
Solución de Problemas en Equipo 8 DG
Quality House Automotive & Aerospace Division
Experience
-
Bourns, Inc.
-
Appliances, Electrical, and Electronics Manufacturing
-
700 & Above Employee
-
Supplier QA
-
Mar 2014 - Present
• Supplier Quality System Development for Automotive Industry• Quality Management System: Internal and External Audits, Corrective and Preventive Actions.• Calibrations Program Supervisor • Incoming Inspection Coordinator • Shelf life for the products used in the process. • Supplier Quality System Development for Automotive Industry• Quality Management System: Internal and External Audits, Corrective and Preventive Actions.• Calibrations Program Supervisor • Incoming Inspection Coordinator • Shelf life for the products used in the process.
-
-
-
Vention Medical
-
United States
-
Medical Equipment Manufacturing
-
100 - 200 Employee
-
Quality Engineer
-
Feb 2009 - Feb 2014
• Supervisor• Problem Solving Tools• Corrective and Preventive Actions• Participation in the implementation of new manufacturing lines (Validation process) • Supervisor• Problem Solving Tools• Corrective and Preventive Actions• Participation in the implementation of new manufacturing lines (Validation process)
-
-
-
Horizon International
-
India
-
Machinery Manufacturing
-
1 - 100 Employee
-
Quality Supervisor
-
Jan 2008 - Feb 2009
• Develop procedures for the different operations and inspections of the process• Training for operators regarding process and quality• Develop incoming inspection procedures• Release the product is going to ship. • Develop procedures for the different operations and inspections of the process• Training for operators regarding process and quality• Develop incoming inspection procedures• Release the product is going to ship.
-
-
-
Hospira
-
United States
-
Pharmaceutical Manufacturing
-
700 & Above Employee
-
Validation Administration Engineer & Validation Engineer
-
Mar 2005 - Nov 2007
• Equipment validation• Regulatory documentation for clean rooms, as Validation Periodic Review• Validation plans.• User requirements• Design specifications• Traceability Matrix• Validation process as IQ, IOQ, PQ, PV.• Changes control (VCR)• Training coordinator• Product use facilitator. • Equipment validation• Regulatory documentation for clean rooms, as Validation Periodic Review• Validation plans.• User requirements• Design specifications• Traceability Matrix• Validation process as IQ, IOQ, PQ, PV.• Changes control (VCR)• Training coordinator• Product use facilitator.
-
-
Education
-
Universidad de Ciencias Empresariales UCEM
Bachelor's degree, Industrial Engineer