The primary responsibility of this position is to advise and implement quality systems for medical device manufacturers. This position requires independent utilization of Quality Management System methods, including but not limited to: quality system implementation, project management, design controls, validation (design, process, and/or software), risk management, design verification, and post-market activities. Must interact with consultants, clients, suppliers, and experts outside QA Consulting in order to communicate and implement QA Consulting’s objectives. Client/ supplier management, delegation and project management skills are required.
Principal Duties and Responsibilities
Knowledge, Skills, and Abilities