Benjamin La Bonte

I specialize in ensuring product quality, regulatory compliance, and operational excellence across pharmaceutical, biotech, and manufacturing environments. With over 17 years of experience, I’ve supported batch record review, deviation investigations, CAPA coordination, audits, and document control initiatives that drive continuous improvement and on-time product release. I bring a hands-on approach to quality systems, root cause analysis, and cross-functional collaboration that helps organizations meet cGMP and ISO standards efficiently and effectively.