Quality Process Manager

Quality Process ManagerCentral Package is a leading manufacturer of protective packaging for the medical device industry. Our customers view us as a trusted partner. Learn more at Quality Process Manager is responsible for the development, implementation, maintenance, and continuous improvement of the Quality Management System (QMS) in compliance with applicable customer requirements.

Key responsibilities include managing Document Control and CAPA functions, ensuring robust governance, timely execution, and effectiveness of quality system processes.

The role partners cross-functionally with Operation Managers and Spec Building to embed quality into all stages of the product lifecycle and to support audit readiness and inspection success. The compensation range for this role is $130,000-150,000 based on a candidates experience and proficiency levels.Responsibilities:Provide leadership oversight to customer audits, including preparation, execution, reporting, and closure of audit findings. Ensure sustained inspection of readiness and successful outcomes with customers.Provide leadership oversight the internal audit program, including auditor selection, training, audit scheduling, execution, and driving timely and effective corrective actions to strengthen the QMS.Develop, maintain, and continuously improve a robust Quality Management System and customer regulations.Lead CAPA functions and ensure effective management of customer complaints and internal CAPAs, including root cause analysis, corrective/preventive actions, effectiveness checks, and trend analysis.Sustain and continue to develop QMS training programs to drive compliance, enhance quality awareness, and build a culture of accountability and continuous improvement.Conduct process and product audits to identify gaps and drive continuous improvement initiatives using Lean and risk-based methodologies.Provide leadership as a key quality representative to customers, ensuring alignment with customer expectations. Complete all customer supplier audits, NAFTA, & Canadian export documentation.Represent Quality on the Supplier Qualification Team & supplier performance reviews, ensure that Approved Supplier List (ASL), and supplier audits meets standards.Partner with Design, Operations, and other departments to implement QMS improvements that enhance efficiency, compliance, and product quality.Implement, maintain, and optimize QMS records, ensuring system effectiveness, data integrity, and user adoption.Support preparation and presentation of Management Review inputs, ensuring clear visibility to QMS performance, risks, and improvement opportunities.