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Entegris is seeking a Quality Lab Supervisor for the CMP Pads Manufacturing team at the Aurora, IL facility. The role leads Quality Lab Technicians, ensuring safe, compliant, and timely lab execution on the 2:00pm–10:00pm shift, Monday through Friday onsite.
You will drive safety, quality, and continuous improvement, coach staff, manage performance, and ensure proper documentation across COA and LIMS, with weekend support as needed.
Supervisor, Quality Lab
Entegris is seeking a driven and collaborative Quality Lab Supervisor to join the CMP Pads Manufacturing team at the Aurora, Illinois facility. In this role, you will be accountable for safe, compliant, and timely day-to-day laboratory execution for the shift by leading Quality Lab Technicians who perform visual inspection and testing for manufacturing, product development, engineering, and customer‑failure analysis. Your role will ensure a strong focus on safety, quality, efficiency, and continuous improvement while fostering an environment where teamwork, innovation, and accountability thrive. This 2nd Shift position is onsite, Monday through Friday, leading a team that operates 2:00pm to 10:00pm, with extended shift support and weekend oversight as business needs require.
Model safe work practices and monitor quality areas to ensure cleanliness, housekeeping, and EHS procedures are followed; support plant safety and housekeeping initiatives as assigned
Provide clear communication regarding goals, expectations, and daily priorities; collaborate with other supervisors, engineering and management to ensure alignment and escalat
Train, certify, coach, and develop laboratory technicians; address performance issues with proper documentation and manage performance reviews and corrective actions in a timely manner
Provide day-to-day direction and respond to shift-level concerns, including safety incidents, quality issues, and personnel matters
Ensure test results, Certificates of Analysis, and Laboratory Information Management System records are complete, accurate, timely, and traceable
Ensure technicians recognize, contain, document, and elevate product, instrument, method, and quality‑standard deviations or nonconformances in a timely manner
Support corrective action and nonconformance investigations, including containment, data collection, root‑cause analysis, effectiveness checks, and documentation of results
Apply Lean and Six Sigma concepts, including Kanban, 6S, PDCA, and visual management, to improve resource planning, schedule attainment, workplace organization, and daily execution.
Prepare the laboratory for internal, customer, and external audits and ensure identified actions are completed
Identify and pursue opportunities for safety improvements, 6S, labor, cost reduction, waste elimination, improved material flow, and greater equipment and process efficiency.
Bachelor's degree in Chemistry, Biology, Engineering, Quality, or another related technical field, or an equivalent combination of education and relevant manufacturing quality laboratory experience
Typically 5 or more years of quality laboratory or manufacturing experience, including demonstrated experience leading a team