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Experienced Vice President of Quality with a demonstrated history of working in the pharmaceuticals industry. Skilled in U.S. Food and Drug Administration (FDA), Technology Transfer, Validation, cGMP, and Quality Assurance. Strong quality professional with a Bachelor's degree in Biology, from East Carolina University.
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Vice President Quality Audit And ComplianceGsk May 2014 - PresentResearch Triangle ParkLeading an audit team within Global Manufacturing and Supply with responsibility for GMP auditing of the global internal and external manufacturing network as well as all suppliers of production materials.Also responsible for Quality Regulatory Intelligence, pharmacopeial compliance, and inspection readiness. -
Project Director, Compliance ReviewGsk Sep 2012 - Apr 2014Research Triangle Park, NcLeading a project responsible for reviewing manufacturing practices against registered details to ensure compliance. Also responsible for developing and deploying an updated regulatory change management program within the manufacturing division to ensure future compliance. -
Production DirectorGlaxosmithkline Jun 2008 - Sep 2012Zebulon, NcResponsible for all manufacturing and packaging activities in the three production streams - solid dose, aerosols, and dry powders. -
Site Quality DirectorGlaxosmithkline Dec 2004 - Jun 2008Responsible for all aspects of Quality Assurance at the GSK Zebulon manufacturing site. -
Director, Regulatory Systems And ComplianceGlaxosmithkline Mar 2001 - Dec 2004Responsible for regulatory and compliance activities within the Quality team at the GSK Zebulon site. -
Principal Process EngineerGlaxowellcome Nov 2000 - Mar 2001Responsible for production technical support for solid oral dosage form products and product transfer activities. -
Assistant Director - Postapproval Regulatory AffairsGlaxowellcome Jul 1998 - Nov 2000Responsible for managing CMC components of post approval manufacturing changes and sNDA submissions. -
Section Head - International ComplianceGlaxowellcome Jul 1995 - Jun 1998Zebulon, NcResponsible for auditing international sites supplying the US market. Also responsible for PAI preparation activities and hosting FDA inspections at international manufacturing sites.
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Process EngineerGlaxo Jul 1993 - Jun 1995Zebulon, NcResponsible for technical support for solid oral dosage forms and technical support for solid, liquid, cream, and ointment products manufactured at CMO's
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Research ScientistGlaxo Jan 1988 - Jun 1993Worked in Pharmaceutical Development responsible for solid oral dosage form development, scale-up and validation.
Allen Moss Skills
Allen Moss Education Details
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Biology, General
Frequently Asked Questions about Allen Moss
What company does Allen Moss work for?
Allen Moss works for Gsk
What is Allen Moss's role at the current company?
Allen Moss's current role is Vice President Quality Audit and Compliance at GSK.
What is Allen Moss's email address?
Allen Moss's email address is al****@****gsk.com
What is Allen Moss's direct phone number?
Allen Moss's direct phone number is +44 20 8047*****
What schools did Allen Moss attend?
Allen Moss attended East Carolina University.
What are some of Allen Moss's interests?
Allen Moss has interest in Economic Empowerment, Politics, Science And Technology, Disaster And Humanitarian Relief, Human Rights, Health.
What skills is Allen Moss known for?
Allen Moss has skills like Validation, Gmp, Fda, Pharmaceutical Industry, Sop, Change Control, Quality Assurance, Regulatory Affairs, Capa, Technology Transfer, Quality Auditing.
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