Gabriela Cabral is a high-level expert, working in Biosense Webster main office of which is in 285. as a Director, External Manufacturing and Supplier Quality from 2015. Gabriela gained professional experience in more than seven positions at different companies. Dallas, Texas is the area, where this professional was lastly known to be settled. This person's phone and email are accessed through this website by request.
Name variants:
Gabrielle Cabral
Last updated May 15, 2024
Contact Information
Workplace
Director, External Manufacturing and Supplier Quality
Diamond Bar, CA
Industry
Medical Devices, Design, Mfg, Mkt & Sales Of Electrophysiology Catheters, Mfg Electromedical Equipment Mfg Surgical/Medical Instruments, Surgical and Medical Instruments, Electromedical Equipment
Colleagues
Work History
Director, External Manufacturing and Supplier Quality
3333 south Diamond Canyon Rd, Diamond Bar, CA 91768
Ensures company supplier-related processes are robust, compliant and aligned with strategic priorities, while driving needed improvements in performance across the supply base.
Aug 2015 — Aug 2018
Director, Quality and Compliance
201 Mentor Dr, Santa Barbara, CA 93111
from Jul 2018
Quality Director
5452 Betsy Ross Dr, Santa Clara, CA 95054
Direct the Quality Systems and Operations for Cordis de Mexico, Biosence Webster and Codman Manufacturing operations in Juarez facility, interacting with three different medical devices fran...
Jul 2013 — Jul 2015
Plant Quality Manager
4545 Creek Rd, Cincinnati, OH 45242
Responsible for the Quality Systems and Quality operations of Ethicon Inc. operations at Juarez facility.
May 2009 — Jul 2013
Ww Quality Unit Manager, Failure Analysis
5452 Betsy Ross Dr, Santa Clara, CA 95054
Responsible for the Failure Analysis laboratories operations in Netherlands, Miami Florida and Juarez Mexico.
Jan 2004 — Jul 2006
Education
1996 — 1998
1991 — 1995
Occupations
Executive
Director
Sales Specialist
Supplier
Operations Manager
Services Professional
Sales Representative
Skills
Quality System
Iso 13485
Medical Devices
Quality Control
Fda
Continuous Improvement
Capa
Design Control
V&V
Six Sigma
Dmaic
Fmea
Minitab
Design of Experiments
Gmp
Iso 14971
Lean Manufacturing
Root Cause Analysis
Spc
Supplier Quality
Validation
Product Launch
21 Cfr Part 11
Change Control
Failure Analysis
Quality Auditing
Cqe
Iso
21 Cfr
Cqa