Job Description: The Process Engineer is responsible for the support of the Unit of Production (UP), regarding the control testing of formula, WIP, and finished goods. Work with the UP Production management and others as necessary. Assist UP in continuous improvement of manufacturing operations using problem solving tools and through formula and process inspection. Responsible for ensuring that suppliers and manufacturers (internal and external) of bulk and WIPs provide the specified quality in accordance with the accepted L’Oréal methods and standards. The PE will identify and resolve quality related problems or issues that arise in process, systems, methods or procedures used to produce these formulas, WIP, or finished goods. Job Responsibilities: Use of Quality Charts, control methods and standards (including the use of gages, instruments, personal computers and SPC tools) to determine cause and effect in quality problem solving; Manages non-conformance/blocked lots of AC, PF, WIP, and Bulk; Interface between UP and provides input regarding corrective actions; Work to improve flow and efficiency of the laboratory; Perform Line validations; Manage OTC paperwork and investigation; Work with the UP to resolve production related issues; Know, understand, and implement L’Oréal rules; Knowledgeable of the Quality Manual, Quality Procedures, area work instructions, and test methods; Responsible for enduring testing performed by personnel is in compliance with DGO methods; Responsible for writing documents related to the Laboratory functions (work instructions, forms, etc.); Involved in the purchase and implementation of new lab equipment and their effect on quality; Troubleshoots non-conformance in components, bulk and finished goods proposes solutions; Interact closely with processing/production on daily production needs; Has the ability to perform varying functions (components, bulk, finished goods, etc.) of the lab; Understand the urgency of the business, and is able to serve the UP in a timely manner; Uphold the values of the Compass; Performs any other duties as directed. Actively engaged in the safety initiatives of the plant (MESURE, etc.) Good knowledge of ISO and GMP requirements; Ensure DGO/GMP compliance of UP by performing routine audits. Responsible for safe practices in the laboratory; Responsible for taking part in SHAP assessments; Issues rejects on non-conforming lots; Responsible for verification of lab equipment; Job Details: Company: L'Oréal Vacancy Type: Full Time Job Location: North Little Rock, AR, US Application Deadline: N/A Apply Here instantcareers.net
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