Marie Doyle Email & Phone Number
Director, GLP and GCLP R and D Quality @ Teva Pharmaceuticals
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Marie Doyle Location
- Philadelphia, PA, US
Marie Doyle Work
- 2020 -now Director, GLP and GCLP R and D Quality @
- 1996 -now Quality Assurance and Regulatory Compliance @
- 2016 -2020 Director, Global Quality Compliance Excellence - Inspection Analytics and Compliance @
- 2011 -2016 Director, Global Quality Compliance @
- 2011 -2011 Director, Head of Global Risk Assessment @ Teva Pharmaceutical Industries Ltd.
- 2009 -2011 Continuous Improvement Black Belt @
- 2008 -2009 Associate Director, QA @
- 2007 -2008 Director, Quality Assurance @
- 2006 -2007 Associate Director, Alliance QA @
- 2004 -2006 Manager, Alliance Quality Assurance @
- 2001 -2004 Associate Manager, QA Contracts and Services @
- 2001 -2001 Supervisor, QA Contracts @
- 2000 -2001 Auditor, QA Contracts @
- 1998 -2000 Product Safety Associate, Pharmacovigilance @
- 1997 -1998 Associate Auditor, Regulatory Compliance @
- 1996 -1997 Associate Auditor, QA Contracts @
Marie Doyle Education
- Temple University
MS (Quality Assurance/Regulatory Affairs)
2008-2010 - Saint Joseph's University
MBA (Pharmaceutical Marketing)
2002-2006 - Penn State University
BS (Major: Life Science; Minor: Anthropology)
1990-1994
Marie Doyle Skills
- Leadership
- Six Sigma
- Quality Management
- Clinical Trials
- Good Laboratory Practice Glp
- Cross Functional Team
- GMP
- GxP
- Biotechnology
- Change Control
- Regulatory Affairs
- Life Sciences
- Process Improvement
- Trackwise
- Validation
- Medical Devices
- Quality Assurance
- Cleaning Validation
- Corrective And Preventive Action Capa
- Regulatory Requirements
- Generic Programming
- Pharmacovigilance
- Quality System
- Analytical Chemistry
- Lifesciences
- SOP development
- Laboratory Information Management System Lims
- V&V
- Biopharmaceuticals
- GCP
- Quality Auditing
- Cross Functional Team Leadership
- Drug Development
- U.S. Food And Drug Administration Fda
- Regulatory Submissions
- Vaccines
- Management
- Standard Operating Procedure Sop
- Pharmaceutical Industry
- Technology Transfer
- Aseptic Processing
- Continuous Improvement
- GLP
- LIMS
- CAPA
- FDA
- Sop
- 21 CFR Part 11
- ISO 13485
- u.s. Food and Drug Administration
- Corrective and Preventive Action
- Standard Operating Procedure
- Good Laboratory Practice
- Laboratory Information Management System
Marie Doyle Summary
- Marie Doyle, based in Philadelphia, PA, US, is currently a Director, GLP and GCLP R and D Quality at Teva Pharmaceuticals. Marie Doyle brings experience from previous roles at Teva Pharmaceuticals and Teva Pharmaceutical Industries Ltd.. Marie Doyle holds a 2008 - 2010 MS in Quality Assurance/Regulatory Affairs @ Temple University. With a robust skill set that includes Leadership, Six Sigma, Quality Management, Clinical Trials, Good Laboratory Practice Glp and more. Marie Doyle has 3 emails and 1 mobile phone numbers on RocketReach.
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