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Gary Hartman Location
Coeur d'Alene, ID, US
Gary Hartman Work
Principal Consultant @ (April 2026 - Present)
Principal Consultant @ (March 2026 - April 2026)
Global Quality Head of Device, Combination Products, and Software as a Medical Device (Sr. Director) @ (October 2019 - October 2023)
Head of Device Quality (Senior Director) @ (March 2017 - October 2019)
Director Quality Engineering, Combination Products @ (March 2015 - March 2017)
Sr Quality Assurance Manager, Device Contract Manufacturing @ (September 2013 - March 2015)
Global Supplier Quality Manager, Surgical Division @ (April 2011 - September 2013)
Sr. Quality Systems Manager, Neuromodulation Division @ (January 2009 - January 2011)
Global CAPA Program Manager @ (January 2005 - January 2009)
Sr. Qualty Engineer @ Heartport (January 2004 - January 2005)
Sr. Supplier Quality Manager @ (January 1996 - January 2004)
Gary Hartman Skills
QSR
ISO 13485
CAPA
Design Control
Process Validation
Supplier Quality
Supplier Management
Supplier Auditing
Regulatory Compliance
Quality System
V&V
Supply Management
FDA
Medical Devices
Validation
Auditing
ISO 14971
Quality Auditing
CE marking
21 CFR
21 CFR Part 11
Manufacturing
DMAIC
GMP
FDA GMP
Design of Experiments
Change Control
CQE
Root Cause Analysis
FMEA
ISO
Medical Device Directive
PMA
Quality Assurance
SPC
Quality Control
GxP
Computer System Validation
Regulatory Affairs
Iso 9000
Verification and Validation V&V
Combination Products
Corrective and Preventive Action Capa
ISO Standards
Regulatory Requirements
Corrective and Preventive Action
Verification and Validation
Gary Hartman Summary
Gary Hartman, based in Coeur d'Alene, ID, US, is currently a Principal Consultant at Gerard Consulting, LLC. Gary Hartman brings experience from previous roles at Independent Consultant, AstraZeneca and Amgen. With a robust skill set that includes QSR, ISO 13485, CAPA, Design Control, Process Validation and more. Gary Hartman has 3 emails and 4 mobile phone numbers on RocketReach.
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