Quality Assurance Engineer

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 Oxford, NC office.

Overview: This role will drive culture change in the organization to that of a harmonized, consistent Quality Unit and expectation.

Key Responsibilities

: Quality Assesses the impact of deviations, CAPAs, and associated change request on the validation status of equipment and/or systems.

Requirements

Support and review Quality Investigations, Nonconformance(s) and Quality Complaint(s) assigned to the Oxford location. Identify and lead continuous improvement opportunities within quality systems and other areas as appropriate.

, and regulatory

Monitor production quality performance through audits, inspections, and statistical analysis. Develop and maintain quality procedures, work instructions, and control plans. Lead continuous improvement initiatives focused on reducing defects, waste, rework, and downtime.

Contributes to the development of process controls to maintain consistent product quality.

and best practices. Promote a culture of continuous improvement and operational excellence. Participate in cross-functional teams to resolve quality and process-related issues.

Minimal to no travel required Strong analytical and problem-solving skills. Ability to manage multiple projects simultaneously. Strong collaboration and stakeholder management skills.

Results-driven with a focus on continuous improvement. Culture Drive culture change, to one that is data-driven, fact-based, and quality-oriented, without sacrificing plant capacities and output. Required Knowledge & Skills: Bachelor of Science degree, such as Engineering, Microbiology, Chemistry and minimum of 5 years of experience Experience working in a cGMP environment and good understanding of regulations and industry guidance including but not limited to FDA, Ability to manage time and workload so that the goals and objectives for each role are met, using appropriate prioritization strategies.

Proficiency in standard business software (Word, Excel, Outlook, PowerPoint) Excellent oral and written skills coupled with the ability to succeed in a teamwork-oriented atmosphere.