Linda Cox
CMC Specialist@ GLOBAL
Philadelphia, Pennsylvania, United States
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Linda Cox is an experienced Regulatory Affairs Professional with 16.5 years of work experience in the pharmaceutical industry. She has expertise in drug development, investigational new drug applications, and FDA regulations. Linda has worked at GLOBAL, PharmaLex, Teva Pharmaceuticals, and GLOBAL, where she held positions such as Cmc Specialist and Senior Regulatory Affairs Specialist. She also has experience as a Junior Medical Writer and Scientist. Linda is skilled in regulatory affairs, GMP, cell culture, and project planning. She is currently based in the United States.
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Emails and Phone Numbers

@globalrwc.com
@globalmwt.com
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About

Experienced Regulatory Affairs Professional with a demonstrated history of working in the pharmaceuticals industry. Skilled in drug development, Investigational New Drug applications, New Drug Applications, GMP, Cell Culture, Pharmaceutical Industry, Abbreviated New Drug Application (ANDA), and U.S. Food and Drug Administration (FDA).

Work Experience

27721 105th Ave SE, Kent, WA, 98030, US

Biotechnology Research

71
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Linda Cox's Professional Milestones

  • Senior Regulatory Affairs Specialist (2016-12-01~2021-02-01): Successfully navigated complex regulatory landscapes, ensuring compliance and minimizing risk.
  • Product Release Auditor (2009-09-01~2011-01-01): Streamlined product release process, ensuring efficiency and accuracy in information retrieval.
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Education

Jefferson College
Jefferson College

Biology

2009-2017
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