About this role
Support laboratory testing, method development and quality operations at a global pharmaceutical manufacturer in Fort Worth, Texas. What you'll do Run routine and non-routine analyses of raw materials, in-process, environmental, finished goods and stability samples. Develop, qualify, validate and transfer analytical methods.
Interpret results against specifications and recommend release. Participate in OOS and failure investigations; write reports, protocols and SOPs. Calibrate and troubleshoot lab equipment; coordinate with contract labs.
Bachelor's degree in Chemistry, Biochemistry, Biology or related. Analytical method development, validation and transfer. HPLC/GC and capillary electrophoresis preferred. OOS/deviation investigations and GMP/GDP.
Contract: 12 months, with possible extension Shift: Administrative, Monday–Friday (40 hours/week) Start: Immediate