Job Description:
Quality Control Chemist5 days on-site
Support a well-established CDMO in Irvine, CA, while expanding on your analytical experience in a cGMP environment.
Day to day:
- Analytical testing of raw materials, in-process samples, and final products
- Predominately utilize HPLC, as well as other analytical instrumentation
- Adhere to all SOPs and cGMP regulations
- Provide peer review for other technician's data
- Maintain and troubleshoot HPLC and other analytical instrumentation
- Support equipment calibrations
- Additional relevant tasks as needed
Experience:
- Bachelor of Science in Chemistry or related field
- Experience in pharmaceutical/biotech environment
- Exposure to working with small molecules
- Experience working with HPLC