Teams at Codexis

Perform analytical method development, validation, and testing for finished products and development samples. Design and execute experiments, process and interpret data, present results, maintain instruments and lab supplies, and support cross-functional teams in a fast-paced laboratory environment.

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.