Resumes
Resumes
Garth Nobis
View pageLocation:
3508 Chuparosa Dr, Santa Barbara, CA 93105
Industry:
Medical Devices
Work:
Allergan - Santa Barbara, California Area Feb 2011 - Sep 2012
Director, Compliance and Quality Management
Consulting, Medical Device 2010 - Feb 2011
Consultant--Quality Systems, Compliance, and Regulatory Affairs
Oraya Therapeutics, Inc. - San Francisco Bay Area Dec 2007 - Nov 2009
Vice President, Regulatory Affairs/Quality Assurance
Accuray Incorporated - San Francisco Bay Area 2002 - 2007
Vice President, Regulatory/Quality
Guidant Corporation (Vascular Intervention Group) - San Francisco Bay Area 1997 - 2002
Director, Regulatory Compliance
Director, Compliance and Quality Management
Consulting, Medical Device 2010 - Feb 2011
Consultant--Quality Systems, Compliance, and Regulatory Affairs
Oraya Therapeutics, Inc. - San Francisco Bay Area Dec 2007 - Nov 2009
Vice President, Regulatory Affairs/Quality Assurance
Accuray Incorporated - San Francisco Bay Area 2002 - 2007
Vice President, Regulatory/Quality
Guidant Corporation (Vascular Intervention Group) - San Francisco Bay Area 1997 - 2002
Director, Regulatory Compliance
Education:
Kettering University
BIE University of Dayton
MBA
BIE University of Dayton
MBA
Skills:
Fda
Medical Devices
Iso 13485
Quality System
Regulatory Affairs
Design Control
Gmp
Fda Udi Unique Device Identification
Cross Functional Team Leadership
Quality Assurance
Regulatory Submissions
Validation
Quality Management
Clinical Research
U.s. Food and Drug Administration
V&V
Clinical Trials
Process Improvement
Quality Auditing
Iso 14971
Pma
Gcp
Iso 9000
Capa
R&D
Quality Control
Iso
Strategy
21 Cfr Part 11
Testing
Ce Marking
Research and Development
Glp
Corrective and Preventive Action
Medical Devices
Iso 13485
Quality System
Regulatory Affairs
Design Control
Gmp
Fda Udi Unique Device Identification
Cross Functional Team Leadership
Quality Assurance
Regulatory Submissions
Validation
Quality Management
Clinical Research
U.s. Food and Drug Administration
V&V
Clinical Trials
Process Improvement
Quality Auditing
Iso 14971
Pma
Gcp
Iso 9000
Capa
R&D
Quality Control
Iso
Strategy
21 Cfr Part 11
Testing
Ce Marking
Research and Development
Glp
Corrective and Preventive Action
Interests:
Collecting Antiques
Exercise
Nascar
Home Improvement
Reading
Gourmet Cooking
Sports
The Arts
Home Decoration
Health
Cooking
Electronics
Crafts
Fitness
Music
Movies
Collecting
Medicine
Career
Investing
Exercise
Nascar
Home Improvement
Reading
Gourmet Cooking
Sports
The Arts
Home Decoration
Health
Cooking
Electronics
Crafts
Fitness
Music
Movies
Collecting
Medicine
Career
Investing
Languages:
English
Medical Device Quality Asssurance And Regulatory Affairs, Seeking New Opportunity, Either Short Or Long Term
View pageLocation:
Santa Barbara, California Area
Industry:
Medical Devices
Work:
Allergan - Santa Barbara, California Area Feb 2011 - Sep 2012
Director, Compliance and Quality Management
Consulting, Medical Device 2010 - Feb 2011
Consultant--Quality Systems, Compliance, and Regulatory Affairs
Oraya Therapeutics, Inc. - San Francisco Bay Area Dec 2007 - Nov 2009
Vice President, Regulatory Affairs/Quality Assurance
Accuray Incorporated - San Francisco Bay Area 2002 - 2007
Vice President, Regulatory/Quality
Guidant Corporation (Vascular Intervention Group) - San Francisco Bay Area 1997 - 2002
Director, Regulatory Compliance
Director, Compliance and Quality Management
Consulting, Medical Device 2010 - Feb 2011
Consultant--Quality Systems, Compliance, and Regulatory Affairs
Oraya Therapeutics, Inc. - San Francisco Bay Area Dec 2007 - Nov 2009
Vice President, Regulatory Affairs/Quality Assurance
Accuray Incorporated - San Francisco Bay Area 2002 - 2007
Vice President, Regulatory/Quality
Guidant Corporation (Vascular Intervention Group) - San Francisco Bay Area 1997 - 2002
Director, Regulatory Compliance
Education:
Kettering University
BIE University of Dayton
MBA
BIE University of Dayton
MBA
Skills:
FDA
Design Control
ISO 13485
Medical Devices
Quality System
Regulatory Affairs
GMP
FDA UDI Unique Device Identification
Design Control
ISO 13485
Medical Devices
Quality System
Regulatory Affairs
GMP
FDA UDI Unique Device Identification