Director, Quality Control

Revlon•Oxford, NC

4d•Onsite

About The Position

At Revlon, we create beauty innovations for everyone that inspire confidence and ignite joy every day. Breaking beauty boundaries is in our company’s DNA. Since its game-changing launch of the first opaque nail enamel in 1932 (and later, the first long-wear foundation), Revlon has provided consumers with high-quality product innovation, performance, and sophisticated glamour. Elizabeth Arden made waves as a woman-led beauty company in the 1920s. In 1931, Almay became the original hypoallergenic, fragrance-free beauty brand. Today, Revlon resiliently continues its legacy as a leading global beauty company. Our diverse portfolio—which consists of some of the world’s most iconic brands and product offerings in color cosmetics, skincare, hair color & care, personal care, and fragrances—is sold around the world through prestige, professional, mass, and direct-to-consumer retail channels. These brands include Revlon, Revlon Professional, Elizabeth Arden, Almay, American Crew, CND, Cutex, Mitchum, Sinful Colors, Creme of Nature, Christina Aguilera, John Varvatos, Juicy Couture, Ed Hardy and more. We honor our heritage, embrace change, and applaud diversity. We champion our employees and celebrate our consumers. We are Revlon, together, transforming beauty. This role is an Onsite Role: This role requires full-time presence at our North Carolina office. Revlon is seeking a Director, Quality Control to lead Quality Control laboratory operations at the Oxford, NC manufacturing site. This role is responsible for ensuring timely, accurate, compliant testing and release of raw materials, bulk product, packaging materials, labels, and finished goods in support of FDA-regulated cosmetics and OTC manufacturing. The Director will provide hands-on technical and people leadership for QC laboratory operations, analytical testing, microbiology, stability, method validation, laboratory investigations, data integrity, and continuous improvement. The role will strengthen lab performance, build capability, improve right-first-time execution, and ensure the QC organization operates in a perpetual state of inspection readiness. This leader will partner closely with Quality Assurance, Manufacturing, R&D, Regulatory, Engineering, Supply Chain, and site leadership to support compliant production, timely product release, and sustained quality performance.

Requirements

Bachelor’s degree in Chemistry, Biology, Microbiology, Pharmaceutical Sciences, Engineering, or related scientific field; advanced degree preferred.
15+ years of progressive Quality Control, laboratory, analytical, or manufacturing quality experience in FDA-regulated manufacturing, preferably OTC, cosmetics, pharmaceuticals, personal care, or consumer health.
Significant leadership experience in QC laboratory operations, including analytical chemistry and/or microbiology.
Strong knowledge of cGMP, FDA expectations, laboratory investigations, data integrity, analytical method validation, stability, and laboratory equipment systems.
Experience supporting regulatory inspections, customer audits, and internal audits.
Demonstrated ability to lead teams through change, improve performance, and build technical capability.
Candidates must be legally authorized to work in the United States without current or future visa support.

Nice To Haves

Advanced degree preferred.

Responsibilities

Lead day-to-day QC laboratory operations, including chemical, physical, analytical, microbiological, raw material, bulk, packaging, stability, and finished goods testing.
Ensure testing, documentation, review, and release activities are completed accurately, efficiently, and in compliance with applicable FDA, cGMP, internal, and customer requirements.
Establish priorities, staffing plans, workflows, and laboratory schedules to support manufacturing operations and business needs.
Maintain inspection-ready laboratory practices, equipment, documentation, and records.
Manage the budget and capex for QC department.
Oversee analytical method qualification, validation, verification, transfer, and lifecycle management.
Ensure laboratory methods are scientifically sound, fit for purpose, and consistently executed.
Provide technical direction for OOS, OOT, atypical result, deviation, and laboratory investigations.
Partner with R&D, QA, Regulatory, and Manufacturing on new product launches, reformulations, technology transfers, and troubleshooting.
Ensure QC operations comply with applicable FDA, cGMP, cGLP, data integrity, ISO 22716, internal quality, and site procedures.
Maintain robust laboratory documentation, sample management, specifications, testing records, equipment logs, and controlled procedures.
Oversee laboratory equipment qualification, calibration, maintenance, and readiness.
Support regulatory inspections, customer audits, internal audits, and inspection response activities related to QC operations.
Establish and monitor QC performance metrics, including testing cycle time, release performance, right-first-time, invalid assay rate, OOS/OOT trends, backlog, and investigation aging.
Identify and implement process improvements to increase laboratory efficiency, reduce rework, improve throughput, and strengthen compliance.
Drive standardization, simplification, digital enablement, and improved use of laboratory systems and data.
Partner with site leadership to resolve quality, manufacturing, material, and supply constraints affecting product release.
Lead, coach, and develop QC managers, supervisors, analysts, microbiologists, technicians, and laboratory support personnel.
Build a culture of scientific rigor, accountability, collaboration, urgency, and continuous learning.
Assess team capability, create development plans, strengthen succession, and ensure appropriate training and qualification.
Serve as a visible, engaged leader who connects laboratory priorities to Oxford’s broader operational and quality transformation.