Teams at US Pharma Lab

Leads quality assurance compliance programs for a dietary supplement manufacturing or CDMO environment. Responsibilities include developing SOPs, managing GMP and GLP compliance, overseeing audits and regulatory inspections, driving CAPA and deviation resolution, reviewing specifications and quality documents, managing vendor qualification and quality agreements, training QA staff, and implementing quality metrics and continuous improvement initiatives. The role requires strong knowledge of dietary supplement GMP regulations and hands-on audit readiness experience.

Supports Lean Six Sigma and continuous improvement initiatives across manufacturing operations. Responsibilities include workflow analysis, root cause analysis, process and cell design improvements, cost reduction, KPI reporting, SYSPRO ERP support, employee training, and project coordination. The role collaborates with leadership and cross-functional teams to implement Lean programs, improve productivity and safety, and develop systems for measuring project performance.