Gary Hartman Email & Phone Number
Principal Consultant @ Independent Consultant
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Gary Hartman Location
- Coeur d'Alene, ID, US
Gary Hartman Work
- 2026 - now Principal Consultant @
- 2019 - 2023 Global Quality Head of Device, Combination Products, and Software as a Medical Device (Sr. Director) @
- 2017 - 2019 Head of Device Quality (Senior Director) @
- 2015 - 2017 Director Quality Engineering, Combination Products @
- 2013 - 2015 Sr Quality Assurance Manager, Device Contract Manufacturing @
- 2011 - 2013 Global Supplier Quality Manager, Surgical Division @
- 2009 - 2011 Sr. Quality Systems Manager, Neuromodulation Division @
- 2005 - 2009 Global CAPA Program Manager @
- 2004 - 2005 Sr. Qualty Engineer @ Heartport
- 1996 - 2004 Sr. Supplier Quality Manager @
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 Independent Consultant. Gary Hartman brings experience from previous roles at AstraZeneca and Amgen. With a robust skill set that includes QSR, ISO 13485, CAPA, Design Control, Process Validation and more. Gary Hartman has 4 emails and 3 mobile phone numbers on RocketReach.
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