Faith E Fraley
from Cary, NC
- Also known as:
-
- Faith Erica Fraley
- Phone and address:
- 2523 Pickett Branch Rd, Cary, NC 27519
Faith Fraley Phones & Addresses
- 2523 Pickett Branch Rd, Cary, NC 27519
Work
-
Company:Sanofi pasteurNov 2009
-
Position:Manager, equipment engineering
Education
-
School / High School:Rochester Institute of Technology2001 to 2008
-
Specialities:Mechanical / Electrical Engineering
Skills
Gmp • Validation • Change Control • Quality System • Capa • Fda • V&V • Quality Control • Quality Assurance • Pharmaceutical Industry • Sop • Manufacturing • Process Simulation • Biotechnology • 21 Cfr Part 11 • Engineering • Biopharmaceuticals • Automation • Cleaning Validation • Root Cause Analysis • Software Documentation • Process Engineering • Aseptic Processing • Lean Manufacturing • Project Engineering • Glp • Medical Devices • Continuous Improvement • Gxp • Gamp • Quality Management • Computer System Validation • Cross Functional Team Leadership • Lifesciences • Iso 13485 • Quality Auditing • Good Laboratory Practice • U.s. Food and Drug Administration • Commissioning
Industries
Biotechnology
Resumes
Director, Cqv Engineering
view sourceLocation:
Cary, NC
Industry:
Biotechnology
Work:
Sanofi Pasteur since Nov 2009
Manager, Equipment Engineering
L.R. Costanzo Co. Inc. Jan 2008 - Dec 2009
Commissioning/Qualification Engineer
Isec Inc. 2006 - 2008
Project Engineer
Cambrex 1998 - 2005
Project Engineer
Cambrex Bio Science 1998 - 2005
Project Engineer
Manager, Equipment Engineering
L.R. Costanzo Co. Inc. Jan 2008 - Dec 2009
Commissioning/Qualification Engineer
Isec Inc. 2006 - 2008
Project Engineer
Cambrex 1998 - 2005
Project Engineer
Cambrex Bio Science 1998 - 2005
Project Engineer
Education:
Rochester Institute of Technology 2001 - 2008
University of Maryland Baltimore County 1997 - 2001
photography, photography
University of Maryland Baltimore County 1997 - 2001
photography, photography
Skills:
Gmp
Validation
Change Control
Quality System
Capa
Fda
V&V
Quality Control
Quality Assurance
Pharmaceutical Industry
Sop
Manufacturing
Process Simulation
Biotechnology
21 Cfr Part 11
Engineering
Biopharmaceuticals
Automation
Cleaning Validation
Root Cause Analysis
Software Documentation
Process Engineering
Aseptic Processing
Lean Manufacturing
Project Engineering
Glp
Medical Devices
Continuous Improvement
Gxp
Gamp
Quality Management
Computer System Validation
Cross Functional Team Leadership
Lifesciences
Iso 13485
Quality Auditing
Good Laboratory Practice
U.s. Food and Drug Administration
Commissioning
Validation
Change Control
Quality System
Capa
Fda
V&V
Quality Control
Quality Assurance
Pharmaceutical Industry
Sop
Manufacturing
Process Simulation
Biotechnology
21 Cfr Part 11
Engineering
Biopharmaceuticals
Automation
Cleaning Validation
Root Cause Analysis
Software Documentation
Process Engineering
Aseptic Processing
Lean Manufacturing
Project Engineering
Glp
Medical Devices
Continuous Improvement
Gxp
Gamp
Quality Management
Computer System Validation
Cross Functional Team Leadership
Lifesciences
Iso 13485
Quality Auditing
Good Laboratory Practice
U.s. Food and Drug Administration
Commissioning
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