Gary Stephenson

Director, Quality Systems and Compliance

Gary Stephenson is a qualified expert, working in Maquet Getinge Group as a Director of Quality and Compliance since 2007. Gary Stephenson has earned professional experience in more than six positions at different companies. Gary Stephenson went to the San Jose State University and received education. Dayton, Ohio is the area, where this expert was lastly known to live. Gary Stephenson's email address and phone can be accessed through SoftwareOfficial by request.
Name variants:
Garrett Stephenson
Last updated May 16, 2024

Contact Information

Last Update
Jul 6, 2022
Email
ga**@varian.com, ge**@gmail.com
Location
Dayton, OH
Company
Maquet Getinge Group

Workplace

Director of Quality and Compliance

Work History

Director of Quality and Compliance

Developed and managed all aspects of Quality/Compliance in three different manufacturing locations that included Document Control, CAPA, Internal Auditing, Failure Investigations, Complaints...
2007 — 2012

Director, Quality Systems and Compliance

3100 Hansen Way, Palo Alto, CA 94304
Managing all aspects of Quality/Compliance including Document Control, NPI Quality Engineering, Corporate and Internal Auditing, Supplier Quality, Quality Assurance and Control, Corrective A...
from 2012

Director Quality and Compliance

100 Boston Scientific Way, Marlborough, MA 01752
2004 — 2007

Corporate Director of Quality

2000 — 2004

Vice President Regulatory and Quality

2971 Spring St, Redwood City, CA 94063
Jan 1999 — Dec 2000

Corporate Director of Quality

1995 — 1999

Occupations

Executive
Director
Sales Specialist
Supplier
IT Professional
Software Tester
Operations Manager
Services Professional
Sales Representative
Computer Specialist

Skills

Iso 13485
Design Control
Capa
Medical Devices
Iso 14971
Quality System
Fda
Quality Assurance
Quality Auditing
Design of Experiments
V&V
Validation
Gmp
Root Cause Analysis
Fmea
Continuous Improvement
Dmaic
Manufacturing
Iso
Biomedical Engineering
21 Cfr Part 11
Corrective and Preventive Action
Pma
Regulatory Affairs
21 Cfr
Quality System Compliance
U.s. Food and Drug Administration
Process Simulation
Fda Gmp
Change Control
Failure Mode and Effects Analysis
Login