Lisa Liu

About Lisa Liu

Direct and lead multiple teams to fulfill fast pace analytical development tasks and manage teams to maintain best GMP compliance requirements.• Supervise analytical development teams to provide comprehensive support for drug product development. Lead method development, validation, transfer, stability studies and regulatory/CMC filing.• Manage a group of scientists and specialists in the fields of software system support, metrology, documentation review, stability management, reference standards, and raw material procurement and release to enable the analytical development department activities in full GMP compliance and continuous quality improvement.• Lead a clinical/consumer study analytical team to support wide range of clinical/consumer studies• Organize product development projects in analytical development area to meet constantly changed and aggressive timelines

Experience

1. Sr Associate Director, Analytical Development, Compliance and Clinical Support

   Bayer

   Sep 2019 — Present · Morristown, NJ, US

Education

• The University of Western Australia

  Ph.D., Organic Chemistry

  1992 — 1996

• Wuhan University

  B.Sc, M.Sc, Chemistry

Skills

• Method Development
• Method Transfer
• Drug Development
• Ich Guidelines
• Chromatography
• Pharmaceutical Industry
• Sop
• Fda
• Pharmaceutical Development
• Analytical Chemistry
• Quality Control
• Gmp
• Dissolution
• Validation
• Project Management
• Technical Leadership
• Cross-Functional Team Leadership
• Hplc
• Analytical Method Validation
• Glp
• Organic Synthesis
• Stability Studies
• Product Development
• Technology Transfer