Summary
Lamonte Fields is a Senior Associate in Quality Systems with 11 years of experience streamlining document control and compliance for biotech and pharmaceutical manufacturers. He has deep expertise with Part 11-compliant EDMS platforms (MasterControl, SmartSolve, PDOCs) and a track record of automating workflows that saved over 1,200 annual labor hours for manufacturing teams. Lamonte pairs meticulous document lifecycle management—from batch records and SOPs to audit support—with hands-on training and onboarding to boost organizational adoption. He has supported high-stakes campaigns including COVID-19 scale-up efforts and managed regulatory audit deliverables for FDA, EMA, and Health Canada. Known for practical productivity tooling and cross-functional collaboration, he excels at turning complex regulatory requirements into efficient, auditable processes.
10 years of coding experience
5 years of employment as a software developer
Rensselaer Polytechnic Institute