3-5 years of quality experience within a pharmaceutical, dietary supplement, food, or related regulated manufacturing environment.
Knowledge of FDA regulations and current Good Manufacturing Practices (cGMPs), including 21 CFR Part 111 for dietary supplements.
Experience with quality systems, internal and external audits, Root Cause Analysis, and Corrective and Preventive Actions (CAPA).
Knowledge of quality requirements for dietary supplements, vitamins, and wellness products.
Demonstrated experience in project planning, project management, and continuous improvement initiatives.
Ability to read, interpret, and apply technical documents, procedures, safety requirements, quality standards, and government regulations.
Proficient mathematical and statistical skills, including the ability to calculate percentages, proportions, and other quality-related metrics.
Physical ability to stand, walk, bend, climb, and occasionally lift materials in a manufacturing and packaging environment.