Resumes
Resumes

Quality Systems Manager
View pageLocation:
1605 Englewood Dr, Poway, CA
Industry:
Biotechnology
Work:
Amedica Biotech (via Aerotek contract assignment) - San Jose, CA Sep 2012 - May 2013
Quality Systems Professional
Implementing Excellence - Greater San Diego Area Apr 2012 - Sep 2012
Quality Systems Professional
LIAI - La Jolla, CA Jun 2009 - Apr 2012
Quality Systems Manager
Implementing Excellence - Greater San Diego Area Jan 2009 - Jun 2009
Quality Systems Professional
Artes Medical - Greater San Diego Area Sep 2007 - Nov 2008
QA Compliance Manager
Quality Systems Professional
Implementing Excellence - Greater San Diego Area Apr 2012 - Sep 2012
Quality Systems Professional
LIAI - La Jolla, CA Jun 2009 - Apr 2012
Quality Systems Manager
Implementing Excellence - Greater San Diego Area Jan 2009 - Jun 2009
Quality Systems Professional
Artes Medical - Greater San Diego Area Sep 2007 - Nov 2008
QA Compliance Manager
Education:
San Diego State University-California State University 2008 - 2009
Advanced Certificate, Biomedical Quality Systems UCSD Extension
Virginia (Northern) Community College, Southwestern Junior College
Advanced Certificate, Biomedical Quality Systems UCSD Extension
Virginia (Northern) Community College, Southwestern Junior College
Skills:
Iso 13485
Quality System
Quality Assurance
Capa
Medical Devices
Design Control
Gmp
Iso
Iso 9000
Change Control
Quality Control
Document Management
V&V
R&D
Regulatory Submissions
Sop
Quality Auditing
Validation
Glp
Process Improvement
Manufacturing
Gxp
Iso 14971
Biotechnology
Supplier Quality
Biopharmaceuticals
Team Leadership
21 Cfr Part 11
Computer System Validation
Regulatory Affairs
Regulatory Requirements
Quality Management
Continuous Improvement
Fda Gmp
Corrective and Preventive Action
21 Cfr Part 820
Process Development
Problem Analysis
Spc
Design of Experiments
Iso Management Representative
European Medical Device Directive
Canadian Medical Device Regulations
Taiwan Medical Device Regulatory Requirements
Supplier Evaluation
Qc Inspection
Non Conforming Materials Management
Quality System
Quality Assurance
Capa
Medical Devices
Design Control
Gmp
Iso
Iso 9000
Change Control
Quality Control
Document Management
V&V
R&D
Regulatory Submissions
Sop
Quality Auditing
Validation
Glp
Process Improvement
Manufacturing
Gxp
Iso 14971
Biotechnology
Supplier Quality
Biopharmaceuticals
Team Leadership
21 Cfr Part 11
Computer System Validation
Regulatory Affairs
Regulatory Requirements
Quality Management
Continuous Improvement
Fda Gmp
Corrective and Preventive Action
21 Cfr Part 820
Process Development
Problem Analysis
Spc
Design of Experiments
Iso Management Representative
European Medical Device Directive
Canadian Medical Device Regulations
Taiwan Medical Device Regulatory Requirements
Supplier Evaluation
Qc Inspection
Non Conforming Materials Management
Interests:
Beach
Collecting Antiques
Exercise
Home Improvement
Geeky Technology
Animals
Reading
Sports
The Arts
History
Home Decoration
Cooking
Electronics
Biking
Music
Movies
Collecting
Kids
Parenting
Automobiles
Walking
Travel
Career
Traveling
Science
Collecting Antiques
Exercise
Home Improvement
Geeky Technology
Animals
Reading
Sports
The Arts
History
Home Decoration
Cooking
Electronics
Biking
Music
Movies
Collecting
Kids
Parenting
Automobiles
Walking
Travel
Career
Traveling
Science
Languages:
English