Jobs at Revance

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.

Lead design and execution of an enterprise intelligence platform: architect knowledge graphs, entity resolution, vector DBs and feature stores; deliver production AI/ML driving commercial outcomes; build and lead data, AI and analytics teams; own governance, observability, and MLOps; embed intelligence into CRM and commercial workflows to measurably lift revenue.

Lead and grow Revance's digital engineering capability across Salesforce and modern headless web stacks. Hands-on manager who debugs production issues, enforces code quality and standards, manages vendor partnerships, hires and develops engineers, drives technical debt remediation, and owns platform reliability and cross-pod engineering consistency.

Drive retail sales and brand presence across Ulta Beauty territory through in-store events, product training, freelance talent scheduling, expense management, relationship building with store teams and management, consistent in-store presence, and weekly sales performance analysis to meet or exceed targets.

Lead design, build, and operate email and SMS programs in Salesforce Marketing Cloud. Create multi-touch journeys, dynamic personalized content, SQL/AMPscript-driven data extensions, responsive HTML/CSS email templates, testing strategies, segmentation, tracking with UTMs, and cross-functional collaboration to optimize performance and reporting.

Lead formulation development of skincare, cosmetics, OTC and personal care products from concept through commercialization. Serve as technical SME in emulsion, surfactant and sunscreen chemistries; design and analyze experiments; support scale-up and tech transfer; collaborate cross-functionally; mentor junior scientists; and document research and regulatory considerations.

Manage a portfolio of 10+ corporate and consumer websites, driving CMS improvements, content governance, UX/CRO/SEO optimization, analytics-driven enhancements, cross-functional project delivery, and day-to-day site operations to support B2B and B2C objectives.

Support inventory and cost accounting in a manufacturing environment: assist monthly close, reconcile inventory and accruals, analyze cost variances, prepare journal entries and reports, coordinate physical inventories, and provide audit support while helping improve processes and maintain internal controls.

Support the revenue cycle by generating invoices, applying payments, reconciling accounts, investigating discrepancies, managing deductions, coordinating customer payments, assisting month-end close, and maintaining AR documentation.

Review and approve laboratory analytical data, investigations, and dispositions to ensure cGMP and ALCOA+ compliance. Drive timely resolution of lab deviations, OOS/OOTs, and nonconformances; recommend CAPAs and procedural improvements; approve raw material specifications and finished product COAs; revise QA SOPs and support QA oversight of analytical data and final batch disposition. Collaborate with QC and Quality leadership to report metrics and support material release workflows.

Operate and maintain wastewater treatment equipment in a cGMP pharmaceutical manufacturing facility: add disinfectants, collect and test samples, record meter/gauge readings, inspect and clean equipment, ensure safety and procedural compliance, and assist other departments as needed.

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.

Plan and execute employee engagement and customer-facing events at HQ and off-site; manage logistics, vendors, contracts, budgets, event staffing, inventory, parking, and administrative tasks. Support cross-functional teams, conduct site visits, and attend community events; occasional travel and nights/weekends for larger events.

Field-based role driving retail sales and brand presence at Ulta Beauty. Plan and execute in-store events and trainings, manage freelance talent and budgets, build retailer relationships, analyze weekly sales to identify opportunities, and consistently achieve territory sales targets.

Perform on-floor QA checks during manufacturing, filling, and packaging to ensure cGMP and SOP compliance. Document inspections, assist with batch record review, support deviations and investigations, help prepare controlled documents, and aid audits under senior QA supervision. Build quality oversight skills and regulatory knowledge through training.

Lead end-to-end design, development, validation, and lifecycle management of R&D lab informatics systems. Own lab modernization roadmap, ensure CSV, data integrity, system security, and regulatory compliance (cGMP, Part 11, Annex 11). Manage validation engineers and system administrators, coordinate cross-functional stakeholders, drive system rollouts, audits, monitoring, vendor management, and operational performance reporting.

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.

Support washroom manufacturing operations including sanitizing equipment, preventing cross-contamination, hose and pump sanitation, disassembly/assembly and troubleshooting of pumps, cleaning packing/filling equipment, performing preventative maintenance, and maintaining documentation and cGMP/SOP compliance on a 4x12 day shift schedule.

Lead and oversee analytical QC testing for clinical and commercial drug substance and drug product in a GMP and select-agent regulated lab. Manage laboratory capacity, method lifecycle (validation/transfer), stability and release testing, regulatory inspection readiness, biosafety/biosecurity, investigations (OOS/OOT/CAPA), and develop QC staff to ensure compliant, timely product release and continual process improvement.