This position directs, guides and manages all aspects of Quality Assurance to achieve departmental execution and net value by optimizing risk, safety, financial, quality and productivity objectives, responsible for proactive and effective quality management. This position will be responsible for managing a staff of 20+ quality assurance inspectors and quality engineers in a Class 3 PMA medical device manufacturing company. An in-depth knowledge of FDA's Quality Management System Regulation and ISO 13485 Quality Management System and ISO 14971 is required. Areas of responsibility include, but are not limited to, the CAPA program, internal and external quality audits, and the nonconforming material process. The Manager will ensure sufficient staffing and resources are available to achieve business goals and compliance requirements. This position is also responsible for the creation and maintenance of written inspection instructions, performing trend analysis on various quality data, and presenting the reports to management.
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Job Type
Full-time
Career Level
Manager
Number of Employees
1,001-5,000 employees