Paul Wanback

About Paul Wanback

Educated in chemical and biological laboratory analysis techniques.• Knowledge of pharmaceutical laboratory testing, analysis and documentation, SOP, cGLP, cGMP, and FDA regulations and guidelines.• Performed HPLC Method Development/ Validation and GC and HPLC Method Transfers.• Adepted to stability and release testing in a quality Control environment.• Experience using instruments such as, GC, HPLC, UPLC, TOC, Mettler Titrators, Mettler Scales and Brookfield Viscometers.• SME in Empower 2 & 3 chromatography software.• Highly motivated. Eager to understand and learn results of experiments performed.• Proficient in computer programs such as Windows 7, Microsoft Word, Excel, Access, PowerPoint, and the Internet.

Experience

1. Laboratory Investigator

   Lotus Pharmaceutical Co., Ltd

   Feb 2026 — Present · Cantau, TW

Education

• State University of New York at Plattsburgh

  BS, Cellular Biochemistry

  1998 — 2001

• S.U.N.Y Plattsburgh

  Bachelor of Science, Cellular Biochemistry

  1998 — 2001

• S.U.N.Y Plattsburgh

  Master of Arts, Natural Science

  2003 — 2004

Skills

• Viscosity
• Uv/Vis
• Assay Development
• Dissolution
• Cleaning Validation
• High-Performance Liquid Chromatography (Hplc)
• Gas Chromatography
• Quality Control
• Gmp
• Pharmaceutical Industry
• Sop
• Toc
• Fda
• U.s. Food and Drug Administration (Fda)
• Glp
• Usp
• Empower
• Hplc
• Standard Operating Procedure (Sop)
• Chemistry
• Capa
• Tlc
• Organic Synthesis
• Analytical Chemistry
• Uv
• V&V
• Method Development
• Validation
• Gc-Fid
• Elisa
• Laboratory
• Biochemistry
• Lims
• Gc-Headspace
• Ftir
• Wet Chemistry