High School Diploma or GED required.
Minimum one (1) year of experience in manufacturing, quality, laboratory, or FDA-regulated environments.
Experience reviewing documentation for accuracy, completeness, and compliance.
Working knowledge of GMPs, GDP, and quality system requirements.
Proficiency with Microsoft Office and electronic quality systems.
Ability to work non-standard hours as business needs require.
Regular and predictable onsite attendance required.
Ability to sit, stand, walk, and perform computer-based work throughout the workday.
Ability to lift up to 20 pounds occasionally.
Requires visual acuity and attention to detail for review of electronic and paper records.