Jobs at Codexis

Lead analytical method transfer and validation for oligonucleotide and enzyme products; author protocols, SOPs and regulatory reports; manage analytical methods and instruments lifecycle for GMP readiness; perform advanced QC testing; oversee stability programs; troubleshoot and investigate deviations/OOS; support QC systems, documentation, and lab buildout for GMP-compliant operations.

Lead hands-on process development and scale-up of Codexis' ECO Synthesis® oligonucleotide manufacturing platform. Drive tech transfer, process characterization, equipment selection, safety and documentation (SOPs, batch records), and mentor early-career staff while collaborating with R&D, Operations, Quality, and external vendors to enable GMP-ready production.

Perform analytical method development, validation, and transfer for product development. Execute experiments, process and interpret data, test finished and development samples, present results cross-functionally, and maintain laboratory operations and instrumentation.