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
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Quality Control Analyst II - Analytical Chemistry
BioPharma Consulting JAD Group
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