Experience with learning management systems, particularly ComplianceWire.
Proficiency in Excel and data entry.
Experience supporting training programs in a regulated environment.
LMS administration experience.
Knowledge in quality assurance, pharma, and medical devices.
Strong verbal and written communication skills.
Ability to manage multiple priorities and work cross-functionally.
Bachelor's degree or equivalent combination of education and experience.
0-1+ years of experience in pharmaceutical, biotechnology, or medical device environments.
LMS Administrator certification or equivalent hands-on experience.
Familiarity with quality systems training requirements and documentation.
Knowledge of regulatory standards including 21 CFR Part 820, 21 CFR Part 211, and ISO.
Experience supporting regulatory inspections and quality compliance initiatives.