Patty George Email and Phone Number
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Quality Professional skilled in oversight of a GMP manufacturing facility.Experience with small molecule parenteral drug products and biologics drug substance.Strong QC Laboratory background in raw materials, finished goods, commercial stability, LIMS, instrumentation, documentation, and personnel training. Strengths in Quality Records and review of change controls, non-conformances, lab investigations, and CAPAs, Provides quality review of product and equipment validation protocols and reports.Experience working with controlled substances as well as select agent materials Skilled in increasing efficiency and working with cross functional teams. Assures compliance with GMPs.CertificationsASQ Manager of Quality/Organizational Excellence - CMQ/OEASQ Pharmaceutical GMP Professional - CPGPASQ Supplier Quality CertificationASQ Quality AuditorSpecialties: LabWare LIMSTrackwise Quality Records WorkflowsInstrumental Analysis
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Director Of QualityCaps® (Central Admixture Pharmacy Services, Inc.)Peoria, Az, Us
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Associate Director Quality AssuranceB. Braun Medical Inc. (Us) Jan 2024 - PresentBethlehem, Pa, Us -
Associate Director Quality At AbbvieAbbvie Nov 2015 - Mar 2023North Chicago, Illinois, UsSite Quality Head for biologics drug substance manufacturing. Oversee Quality Assurance, Quality Control and Validation Departments. -
Quality Control ManagerAllergan Nov 2013 - Nov 2015Dublin, Coolock, Ie -
Manager Analytical ChemistryIrvine Pharmaceutical Services Jul 2011 - Nov 2013Manage staff chemists and support personnel in the testing of raw materials, finished product and stability samples using compendial and internal methods. Responsible for sample administration of incoming materials. Managed stability personnel and perform review of protocols and reports. Responsible for the writing of laboratory investigations, deviations, CAPAs, and impact assessments as well as method transfer, method validation, and compendial method verification protocols and reports. Interact with clients regarding samples and project work. Represent the raw material in laboratory and client audits.
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District Commissioner (Volunteer)Boy Scouts Of America Jan 2010 - Sep 2012Irving, Tx, Us -
Associate Director Quality Control ChemistryTeva Pharmaceuticals 1997 - Dec 2010Tel-Aviv, IlManaged a staff of over 50 chemists and support personnel in testing and release of raw materials and finished parenteral drug products with oversight of the commercial stability program. Reviewed department CAPAs, laboratory investigations and deviation reports. Supported customer audits and FDA inspections for the chemistry laboratory. -
Supervisor Quality Control ChemistrySteris Laboratories 1990 - 1997Supervised a group of chemists on two shifts for in-process and finished product release. Wrote laboratory investigations for non-conforming data.
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Analytical ChemistNaturally Vitamin Supplements Sep 1986 - Feb 1990Analyze Vitamin Supplements per USP monographsWrote department SOPs
Patty George Skills
Patty George Education Details
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Northern Arizona UniversityChemistry -
Asq Certifications
Frequently Asked Questions about Patty George
What company does Patty George work for?
Patty George works for Caps® (Central Admixture Pharmacy Services, Inc.)
What is Patty George's role at the current company?
Patty George's current role is Director of Quality.
What is Patty George's email address?
Patty George's email address is p_****@****cox.net
What is Patty George's direct phone number?
Patty George's direct phone number is +194945*****
What schools did Patty George attend?
Patty George attended Northern Arizona University, Asq Certifications.
What are some of Patty George's interests?
Patty George has interest in Masters Swimming.
What skills is Patty George known for?
Patty George has skills like Gmp, Fda, Lims, Pharmaceutical Industry, Analytical Chemistry, Hplc, Quality Control, Sop, Validation, Capa, Gas Chromatography, Chemistry.
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