Senior Technical Operations Consultant at EPM Scientific
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
4+ years of experience in pharmaceutical/biotech environment
Exposure to working with small molecules
4+ years of experience working with HPLC in industry
Seniority level
Associate
Employment type
Full-time
Job function
Science
Industries
Biotechnology Research and Pharmaceutical Manufacturing
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