Newark Metro Area, NJ
Contributes to the development of priority drug candidates through the development, validation, and implementation of analytical methods involving modern analytical instrumentation including HPLC/UPLC, GC, dissolution, FT-IR, Karl Fischer titrations, etc.
Transfers validated methods to customer labs, and partner-owned quality control (QC) labs.
Performs testing for development and clinical materials and stability samples in accordance with established methods, specifications and protocols under supervision.
BS/MS Chemistry (or relevant discipline).
Minimum 3 years cGMP / GLP pharmaceutical laboratory experience