Erika Brandon
Regulatory Affairs Post-Approval Group Leader@ Lannett Company, Inc.
Philadelphia, Pennsylvania, United States
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Erika Brandon is a highly experienced professional with over 20 years of work experience. She has a strong background in validation, GMP, FDA, and SOAP. Currently, she holds the position of Regulatory Affairs Post-Approval Group Leader at Lannett Company in the United States. Erika has also worked as a Regulatory Affairs Associate and R&D Chemist at Lannett Company, Inc. and Hemispherx Biopharma, Inc. She has a proven track record in the pharmaceutical manufacturing industry and has worked with a wide range of customers, including patients, healthcare providers, and government agencies.
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Emails and Phone Numbers

@aol.com
@lannett.com
+1 215333****
+1 215333****
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About

Regulatory Affairs Post-Approval Group Leader at Lannett Company

Work Experience

1150 Northbrook Dr, Trevose, Pennsylvania, 19053, US

Pharmaceutical Manufacturing

473
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Erika Brandon's Professional Milestones

  • Regulatory Affairs Post-Approval Group Leader (2013-06-01~): Successfully executed regulatory compliance programs across the post-appaval group, ensuring compliance on a timely and cost-effective scale.
  • Qc Chemist (2003-04-01~2005-09-01): Consistently accurate and efficient testing, improving product quality and reliability.
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Education

Penn State University
Penn State University

Biology,

Bachelors,

Bachelor Of Science