Faith Fraley

Engineering/Project lead for Site Viral Manufacturing

Faith Fraley is a qualified expert, who works in Sanofi Pasteur on the position of Engineering/Project lead for Site Viral Manufacturing since 2012. This expert has earned professional experience in more than 13 positions at different companies. Faith Fraley went to the Rochester Institute of Technology and received education from 2009. Cary, North Carolina is the city, where this expert was lastly known to settle. This professional's contacts can be accessed through this website on demand.
Name variants:
Fae Fraley, Fay Fraley, Faye Fraley
Last updated May 13, 2024

Contact Information

Last Update
Jul 12, 2022
Email
fa**@kymanox.com, ff**@yahoo.com, fa**@cambrex.com
Location
Cary, NC
Company
Sanofi Pasteur

Workplace

Engineering/Project lead for Site Viral Manufacturing

Work History

Engineering/Project lead for Site Viral Manufacturing

2012 — Jan 2012

Manager, Equipment Engineering

Swiftwater, PA
Nov 2009 — Sep 2013

Commissioning/Qualification Engineer

Scranton, PA
Feb 2008 — Nov 2009

Commissioning/Qualification Engineer

Jan 2008 — Dec 2009

Project Engineer/Manager

Columbia, MD
Aug 2006 — Feb 2008

Project Engineer

2006 — 2008

Project Engineer

2001 — 2005

Consultant/Contractor

2000 — Nov 2013

Lead - North American Viral Manufacturing Facility

2000 — Feb 2010
Baltimore, MD
Feb 1999 — Oct 2005

Project Engineer

1998 — 2005

Associate Project Engineer

1 Meadowlands Plz, East Rutherford, NJ 07073

Education

BS in Electrical/Mechanical Engineering

from 2009

Visual Arts

Baltimore, MD
1998 — 2001

AA in Engineering

from 1997

Occupations

Executive
Director
Manager
Sales Specialist
Equipment Tools Purchasing Agent
Scientist
Biotechnology Professional
Engineer
Operations Manager
Department Store Salesperson
Retail Salesperson
Biologist
Biological Scientist

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
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