Quality Control Analyst II - Analytical Chemistry

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