Senior Quality Control Chemist - 5 days on-site
A small, well-established CDMO in Irvine, CA, wants to add a Senior 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 who have a sustainable commute to their labs.
Day to day:
- Analytical testing of raw materials, in-process samples, and final products
- Predominately utilize analytical instrumentation, and ensure proper functioning
- Carry out the development of analytical methods, and author SOPs
- Provide peer review for other technician's data
- Maintain and troubleshoot HPLC and other analytical instrumentation, and maintain equipment calibration and qualification
- Support management with training of team members, laboratory investigations, and internal/external audits
Experience:
- Bachelor of Science in Chemistry or related field
- 8+ years of experience in the pharmaceutical/biotech environment
- Exposure to working with small molecules
- Experience working with HPLC, GC, CE, ICP, FTIR, and dissolution apparatus.
