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I’ve done a little bit of everything in Pharma, but I love the huge amount of opportunities and challenges that the industry brings. Over 1,000,000 people work in the industry and still no one has the blueprint to get a product to market with a perfect process. That there is always something to be improved and achieved gets me up and out every day. I’ve worked in numerous capacities in the industry, and I have found each one enormously interesting and me more knowledgeable than when I started: process development for a Safety Division, taking a site from paper-based to electronic, heading up Quality for a CDMO site, commissioning pilot plants for clinical trail manufacture, leading an Analytical Testing team—it all has helped me build my knowledge and skills and hasn’t been boring for a single moment. I think if the industry can smooth out some of the edges and increase its efficiencies—and eliminate fraud—it will continue to help society and the world in ways that hardly even seem possible. I am happy to be a part of it.
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Director Of Quality AssuranceCambrexChapel Hill, Nc, Us
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Director Of QualityRecipharm Feb 2018 - PresentHeads Quality Assurance, Stability Mgmt, Peer Review and Data Integrity teams for RTP site of global, industry-leading CDMO performing clinical-phase product testing, focusing on inhaled dosage forms. Manages QMS, makes quality decisions for site and sits on site leadership team, inputing on company direction. Strives for a quality and on-time product, done efficiently.
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Assoc. Director, Quality AssuranceRecipharm Sep 2015 - Feb 2018*Heads QA team at the RTP site for Recipharm, a global CDMO, managing all aspects of Quality and Compliance*Updated QMS to raise standard to meet with GMP manufacture requirements (revised 60% of SOPs in 8 months)*Oversaw dramatic improvement in QMS metrics, and instituted Quality Council*Leads GMP Suite team to enable manufacture of Phase 1&2 clinical trial supplies (inhaled, topical and solutions), including managing engineering fixes, writing validation documentation, and writing SOPs*Performs internal audits for R&D and hosts sponsor audits*Leads major continuous improvement projects, such as Computer System Validation for electronic notebook application*Sits on Site Management Team, inputting on direction of company
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Manager, R&D Qa Gmp And OperationsGlaxosmithkline Aug 2012 - Sep 2015Brentford, Middlesex, GbLed and provided day-to-day direction of global QA team of release officers and specialists. Responsible for QA oversight and quality management system compliance for Skin Health business unit. -
Sr. Analyst, R&D Qa OperationsGlaxosmithkline Jan 2011 - Aug 2012Brentford, Middlesex, GbManaged operations and validation activities for QA team. Took on responsibilities of departing QA Director of Validation after 3 months in position, and quickly became validation expert for the site.
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Validation Business Analyst, R&D ItGlaxosmithkline Sep 2010 - Jan 2011Brentford, Middlesex, GbLed computer system validation efforts for multiple key R&D computer systems, using expertise in 21 CFR Part 11, with focus on both quality and meeting timelines.
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Validation Business Analyst, R&D ItStiefel, A Gsk Company Jan 2008 - Sep 2010Rtp, Nc, UsResponsible for validation of key R&D computer systems to support regulatory filings. -
Manager, Process DocumentationPfizer Pharmaceuticals Dec 2006 - Dec 2007New York, New York, UsManaged Documentum repository used by 700+ person Safety Dept, and led the transition of this repository to a unified platform. -
Senior Documentation Associate, Process DocumentationPfizer Pharmaceuticals Nov 2002 - Dec 2006New York, New York, UsAuthored and edited standard operating procedures for Safety Department. Responsibilities included editing, writing, project management, and management of a Documentum repository for SOPs.
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Copy EditorWine Spectator Oct 2000 - Nov 2002Copy editor for popular wine magazine, 18 issues annually.
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Editorial AssistantThe Chronicle Of Higher Education 1997 - 2000Washington, Dc, Us
George Chase Skills
George Chase Education Details
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University Of Mary WashingtonBa
Frequently Asked Questions about George Chase
What company does George Chase work for?
George Chase works for Cambrex
What is George Chase's role at the current company?
George Chase's current role is Director of Quality Assurance.
What is George Chase's email address?
George Chase's email address is ge****@****ail.com
What is George Chase's direct phone number?
George Chase's direct phone number is +191988*****
What schools did George Chase attend?
George Chase attended University Of Mary Washington.
What skills is George Chase known for?
George Chase has skills like Quality Assurance, Pharmaceutical Industry, Validation, Software Documentation, Gmp, Document Management, Gxp, Computer System Validation, Sop, Cross Functional Team Leadership, Project Management, 21 Cfr Part 11.
Who are George Chase's colleagues?
George Chase's colleagues are Abhi Salunia, Preston Harms, Sören Olsson, Emelie Enger, Corey Trankel, Edward Tutu, Drew Canning.
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