Jobs at Revance

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.

Provides quality assurance oversight for GxP facilities, utilities, equipment, analytical instruments, and computerized systems supporting biologic drug products. Coordinates change controls, deviations, CAPAs, investigations, validation activities, audits, quality metrics, inspection readiness, and data integrity programs. Partners with Quality Control, Manufacturing, Facilities, IT, Supply Chain, and Regulatory Affairs to maintain compliance with US and international cGMP requirements and continuously improve quality systems.

Leads the supply chain planning function, including strategic planning, S&OP, supply and demand forecasting, inventory optimization, replenishment, scenario planning, and cross-functional collaboration. Drives continuous improvement, process optimization, performance measurement, and cost reduction while managing supply chain planning and warehouse teams. Requires pharmaceutical operations or GMP experience, CMO and 3PL relationship knowledge, planning software proficiency, and substantial management experience.

Hands-on analytical development role supporting biologics characterization: develop, validate, and execute analytical methods; author protocols and reports; operate and maintain instrumentation; ensure compliance with ICH/GxP; interact with CDMOs and testing labs; support regulatory submissions and train staff.

Lead strategy and execution for the RHA injectable HA filler portfolio: launch new indications, drive market share growth, partner cross-functionally, manage product launches, medical marketing, KOL relationships, budget and team leadership, and assess commercial performance.

Supports clinical development strategy and designs, executes, and evaluates Phase 1–3 studies for therapeutic products and indications. Develops protocols and regulatory documents, supports IND/BLA submissions, collaborates with clinical operations, biometrics, safety, medical affairs, and CROs, and engages investigators, KOLs, regulators, and scientific organizations. Ensures GCP and SOP compliance while contributing to product strategy, publications, presentations, and clinical leadership.