Quality Control Chemist III
5 days on-site (fully on-site)
A small, well-established CDMO in Irvine, CA, wants to add a QC Chemist to their team. Join this team to expand on your analytical experience in a cGMP environment. The organization supports its employees' growth and development, helping employees succeed in the pharmaceutical industry while supporting their network of clients.
Currently, the team is only considering candidates local to Irvine, CA, or candidates with a sustainable commute to their labs.
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
Experience:
- Bachelor of Science in Chemistry or related field
- 5+ years of experience in the pharmaceutical/biotech environment
- Exposure to working with small molecules
- 5+ years of experience working with HPLC in industry
