T Lakshmana Murthy

Experience

• 

  Dr. Reddy's Laboratories

  Apr 2001 - Jun 2008

  Deputy Manager

  Plant Quality Assurance, Global regulatory compliance.

• 

  Actavis (now Allergan)

  Jun 2008 - Sept 2010

  Manager, DQA & DRA

  End to end responsibility in providing Quality Management and regulatory guidance to associates in Analytical and R&D during development of APIs.

• 

  US Pharmacopeia

  Sept 2010 - now

  Responsible for Quality Assurance and GMP Audit function of Verification Programs. Lead auditor for GMP Audits across Southeast Asia and Product Documentation Review(QCM/CMC) for Dietary Supplement Manufacturers and Dietary/Pharmaceutical Ingredient Manufacturers Plan and execute GMP audits at various Dietary Supplements, Dietary Ingredients, Excipients and API manufacturers around the globe. Extensively travel to overseas. Perform CMC reviews. Compile audit reports and CAPA assessment reports.

  • Director-Global Quality Standards, VER and PQM+ at U.S.Pharmacopeia

    Aug 2023 - now

  • Director of Quality Assurance

    Aug 2015 - Aug 2023

  • Sr. GMP Auditor

    Jun 2013 - Jul 2015

  • GMP Auditor- Verification Programs,

    Sept 2010 - Jun 2013