Audrey Sanchez

Document Control Specialist III at AGC Biologics

Audrey Sanchez is a skilled professional with extensive experience in document control and training within the pharmaceutical sector. Currently serving as a Document Control Specialist III and Quality Systems Training Associate II at AGC Biologics since November 2020, Audrey is responsible for managing GMP document changes in accordance with FDA standards, as well as creating and implementing training programs. Previous roles include Document Management and Training Specialist at STAQ PHARMA and Operations and Packaging Training Coordinator at Novartis, where Audrey maintained high training standards for over 200 employees. With a strong background in document management, including significant contributions to system migrations and the maintenance of compliance for numerous products, Audrey's career spans over two decades with key positions at leading companies such as Sandoz and Terumo BCT. Audrey is a graduate of South High School Pueblo.

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AGC Biologics

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AGC Biologics is a leading global Contract Development and Manufacturing Organization (CDMO), with a relentless commitment to deliver the highest standard of service to our clients and partners.


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1,001-5,000

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