Teams at Revance

Prepares and manages domestic and international medical device regulatory submissions, registrations, renewals, and amendments. Interprets global regulations, evaluates product changes, develops regulatory strategies, reviews labeling and promotional materials, and supports audits and inspections. The role manages documentation for FDA, EU, and multiple international authorities while monitoring evolving regulatory requirements and coordinating cross-functional compliance activities.

Leads global quality control across drug development, clinical manufacturing, commercialization, analytical development, microbiology, testing, stability, release, and regulatory compliance. Oversees internal and contract laboratories and manufacturers, ensures adherence to GxP regulations and data integrity requirements, supports regulatory submissions and inspections, manages quality agreements, and chairs quality reviews. Develops departmental budgets and resources while building and mentoring QC leadership teams.

Leads Revance’s enterprise business intelligence function, including the Power BI platform, BI development team, semantic layer, reporting standards, and self-service natural-language analytics. Partners with stakeholders and Data Engineering to deliver trusted, decision-ready insights. Oversees BI strategy, governance, data integrity, platform operations, project prioritization, and distributed team leadership while driving dashboard quality, adoption, and modernization.