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
- Director, GLP and GCLP R and D Quality @ (April 2020 - Present)
- Quality Assurance and Regulatory Compliance @ (August 1996 - Present)
- Director, Global Quality Compliance Excellence - Inspection Analytics and Compliance @ (November 2016 - April 2020)
- Director, Global Quality Compliance @ (October 2011 - November 2016)
- Continuous Improvement Black Belt @ (April 2009 - February 2011)
- Associate Director, QA @ (August 2008 - April 2009)
- Associate Director, Alliance QA @ (March 2006 - October 2007)
- Manager, Alliance Quality Assurance @ (January 2004 - March 2006)
- Associate Manager, QA Contracts and Services @ (December 2001 - January 2004)
- Supervisor, QA Contracts @ (January 2001 - December 2001)
- Auditor, QA Contracts @ (February 2000 - January 2001)
- Product Safety Associate, Pharmacovigilance @ (May 1998 - February 2000)
- Associate Auditor, Regulatory Compliance @ (November 1997 - May 1998)
- Associate Auditor, QA Contracts @ (August 1996 - November 1997)
- Director, Head of Global Risk Assessment @ Teva Pharmaceutical Industries Ltd. (February 2011 - October 2011)
- Director, Quality Assurance @ (October 2007 - August 2008)
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. 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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