Process Engineer

Revlon•Oxford, NC

1d•Onsite

About The Position

A Manufacturing Process Engineer designs, implements, monitors, and improves manufacturing processes in a regulated GMP environment. The role focuses on improving efficiency, maintaining product quality, ensuring safety and compliance, and reducing production costs while supporting product design, quality systems, validation activities, and factory operations. This is an onsite role requiring full-time presence at Revlon’s Oxford, North Carolina office. The engineer works with R&D and design teams to scale products from prototypes to full production and supports factory operations, process validation, documentation, and regulatory compliance.

Requirements

Bachelor’s degree in Chemical, Mechanical, Industrial, or Manufacturing Engineering, or a closely related technical discipline.
2 to 5+ years of hands-on engineering experience in a manufacturing, industrial, or regulated production environment.
Direct experience working under Good Manufacturing Practices (GMP).
Strong knowledge of Lean Manufacturing, Six Sigma, and Continuous Improvement practices.
Proficiency with CAD platforms such as SolidWorks or AutoCAD, statistical tools such as Minitab, and ERP/MES systems.
Experience performing Failure Mode and Effects Analysis (FMEA) and safety hazard assessments.
Working knowledge of GMP documentation, change control, deviation investigations, CAPA support, audit readiness, and validated manufacturing systems.
Strong analytical problem-solving ability to resolve complex technical issues under production deadlines.
Ability to communicate technical direction clearly to cross-functional teams, from operators to senior leaders.
Must be legally authorized to work in the United States without current or future visa support; Revlon cannot sponsor or transfer employment visas.

Responsibilities

Evaluate manufacturing workflows to reduce waste, shorten cycle times, and improve yields using Lean Manufacturing and Six Sigma methods.
Plan equipment layouts, select manufacturing tools, and support integration of automated machinery.
Identify root causes of production disruptions, equipment failures, and product defects.
Develop, execute, and support process validation protocols, including Installation, Operational, and Performance Qualifications (IQ/OQ/PQ), in accordance with GMP requirements.
Create, revise, and maintain SOPs, work instructions, batch records, and manufacturing specifications.
Track process capability using Statistical Process Control (SPC) tools and performance dashboards.
Partner with R&D and design teams to scale products from prototypes to full production.
Ensure manufacturing processes meet applicable safety, environmental, quality, FDA, ISO, and GMP standards; support audit readiness and corrective actions.