Job Description:
- $50-66/hr
- Schedule: Monday-Friday
- This position is a 6 ½ -month assignment with the possibility of extension.
- Position will be mainly responsible for transferring, developing, validating, and executing analytical methods in a cGMP Quality Control environment.
- Position will be responsible for supporting analytical investigations, troubleshooting methods and instrumentation, and reviewing OOS/OOT results, deviations, and CAPAs.
- Position will also be responsible for supporting instrument qualification, raw material testing and qualification, QC data analysis, technical documentation, and special projects.
- Bachelor's degree at a minimum is Required!
- Minimum of 3 years of analytical development or validation experience in a GMP pharmaceutical, biopharmaceutical, or related manufacturing environment is Required!
- Knowledge of analytical methods, method validation, and cGMP/regulatory requirements is Required!
- Experience with statistical analysis, QC data trending, and laboratory investigations is Preferred!
- Experience with analytical instrumentation qualification, troubleshooting, and raw material qualification is Preferred!
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