Onsite QC Director - Lab Leadership & Compliance

Revlon; Oxford (NC); On-site; USD 136,000 - 170,000; Full time

Job summary

Revlon is seeking a Director of Quality Control at its Oxford, NC site to lead QC laboratory operations, ensuring timely and compliant testing and release of materials and finished goods for FDA-regulated cosmetics and OTC products.

The role provides hands-on technical and people leadership in analytical testing, microbiology, stability, method validation, investigations, data integrity, and continuous improvement, partnering across QA, Manufacturing, R&D, Regulatory, and Supply Chain.

Qualifications

• 15+ years in QC, laboratory, analytical, or manufacturing quality in FDA-regulated manufacturing (cosmetics/pharmaceuticals)
• Strong leadership experience
• Knowledge of cGMP, FDA expectations, investigations, and data integrity
• Experience supporting regulatory inspections and audits

Responsibilities

• Lead day-to-day QC laboratory operations (chemical, physical, analytical, microbiological, raw material, bulk, packaging, stability, finished goods testing)
• Ensure testing, documentation, review, and release meet FDA, cGMP, internal and customer requirements
• Maintain inspection-ready practices, equipment, documentation, and records
• Manage budget and capex for the QC department
• Oversee method qualification, validation, verification, transfer, and lifecycle management
• Provide direction for investigations (OOS/OOT) and troubleshooting
• Partner with R&D, QA, Regulatory, and Manufacturing on new product launches and tech transfers

Skills

Leadership

Quality control

FDA-regulated

cGMP

Data integrity

Analytical chemistry

Microbiology

Education

Bachelor's degree in Chemistry, Biology, Microbiology, Pharmaceutical Sciences, Engineering, or related field

Tools

Laboratory equipment systems

Job description

Revlon is seeking a Director of Quality Control at its Oxford, NC site to lead QC laboratory operations, ensuring timely and compliant testing and release of materials and finished goods for FDA-regulated cosmetics and OTC products.

The role provides hands-on technical and people leadership in analytical testing, microbiology, stability, method validation, investigations, data integrity, and continuous improvement, partnering across QA, Manufacturing, R&D, Regulatory, and Supply Chain.