Teams at Revance

Entry-level QA Specialist supporting manufacturing floor to ensure cGMP compliance through in-process quality checks, batch record review, deviation documentation, SOP support, and audit assistance. Performs inspections, documents per GDP, aids investigations, learns root-cause analysis, and collaborates with operations under QA supervision to maintain product quality and patient safety.

Manage high-volume Concur expense audits, corporate card reconciliation, T&E inbox support, reporting/analysis, fraud and SOX audit support, and drive T&E process improvements and cost savings.

Prepare, compile, and submit medical device regulatory dossiers (e.g., FDA 510(k), EU MDR) and manage international registrations, labeling/UDI compliance, and regulatory inspections. Interpret global regulations, support change control, maintain registrations and certificates, and advise cross-functional teams on market entry and regulatory strategy.