QC CHEMIST III
$62,400–$72,800 year
On-site · Irvine, California, United States
Job Summary
Perform method validation, verification, transfer, and analytical testing for clinical submission materials (raw materials, finished products, stabilities, and cleaning validation). Maintain and troubleshoot analytical instrumentation; conduct laboratory investigations and peer review data; develop, validate, and troubleshoot analytical methods; perform method transfers from other facilities; author SOPs and analytical methods; assist with equipment calibrations/qualification; train laboratory staff; support internal, customer, and agency audits. Requires a Bachelor's degree in chemistry or related discipline and 5+ years' experience in a chemistry laboratory with instrumentation (HPLC, GC, CE, ICP, FTIR, dissolution). Knowledge of GLP/GMP preferred; strong communication, organization, and attention to detail essential.
Required Qualifications
- Bachelor's degree in chemistry or related discipline
- 5+ years' experience in a chemistry laboratory
- 5+ years' experience with analytical instrumentation (HPLC, GC, CE, ICP, FTIR, dissolution)
- 2+ years' experience in GLP or GMP (preferred)
- Strong communication skills (written and verbal)
- Ability to follow standard operating procedures
- Ability to organize, prioritize and multitask with minimal supervision
- Strong attention to detail
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