- Understanding of GMP requirements and practices, familiar with analytical techniques such as HPLC, UPLC, GC, dissolution, particle size distribution, physical appearance, viscosity, rheometry and drug delivery system release profiles for drug products and/or drug substances.
- M.S. in Analytical Chemistry or related discipline with minimum 2 years of experience or B.S. in Analytical Chemistry or related discipline with minimum 5 years of experience in analysis of pharmaceutical products or pharmaceutical method development and validation.
- Minimum 2 years of experience in the analysis of data and writing of technical protocols, reports, and submission ready documents.