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.
Requirements
- 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.
Benefits
- Contract: 12 months, with possible extension
- Shift: Administrative, Monday–Friday (40 hours/week)
- Start: Immediate